Hair coloring compositions suitable for facial hair

A hair coloring composition with 2-methoxymethyl-p-phenylenediamine and a controlled pH formulation addresses skin irritation and fading issues, delivering long-lasting color to facial hair.

FR3141071B1Active Publication Date: 2026-06-05LOREAL SA

Patent Information

Authority / Receiving Office
FR · FR
Patent Type
Patents
Current Assignee / Owner
LOREAL SA
Filing Date
2022-10-19
Publication Date
2026-06-05

AI Technical Summary

Technical Problem

Existing hair coloring compositions for permanent hair color change often cause skin irritation, damage to hair, and rapid fading of color, particularly when used on facial hair like beards and mustaches.

Method used

A hair coloring composition using 2-methoxymethyl-p-phenylenediamine as an oxidative dye precursor, combined with a developer composition, which is formulated to have a lower pH and includes specific ratios of surfactants, water-soluble solvents, and minimal alkalizing agents, ensuring gentle application and long-lasting color without skin irritation.

Benefits of technology

The composition provides long-lasting, vibrant color to facial hair while minimizing skin irritation and hair damage, maintaining color intensity over time.

✦ Generated by Eureka AI based on patent content.

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Abstract

Hair Coloring Compositions Suitable for Facial Hair: This disclosure relates to hair coloring base compositions and ready-to-use hair coloring compositions comprising 2-methoxymethyl-p-phenylenediamine, an oxidative dye precursor. The hair coloring base composition is mixed with a developer composition to form a ready-to-use hair coloring composition having a pH below the typical pH of 7. These compositions are effective for coloring hair, particularly beard hair. The color imparted to the hair is long-lasting (persistent), and skin sensitivity due to the coloring process is minimized or avoided. Processes for preparing the composition and processes for coloring hair, particularly beard hair, are also disclosed. Figure for abstract: none
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Description

Title of the invention: Hair coloring compositions suitable for facial hair. SCOPE OF DISCLOSURE

[0001] This disclosure relates to basic hair coloring compositions and ready-to-use hair coloring compositions comprising 2-methoxymethyl-p-phenylenediamine, an oxidative dye precursor. Methods for preparing the compositions and methods for coloring hair, particularly beard and moustache hair, are also disclosed. SUMMARY

[0002] There are various types of hair coloring compositions for temporary, semi-permanent, or permanent hair coloring. Most types of hair coloring compositions for permanently coloring hair are oxidative hair coloring compositions that use two parts. The first part is a hair coloring base composition that contains oxidative dye precursors (sometimes called "oxidative dyes") and couplers, which interact with the oxidative dye precursors. The second part is a developer composition containing an oxidizing agent such as hydrogen peroxide. The two parts are mixed immediately before use, forming a ready-to-use hair coloring composition that activates the hair coloring composition.Thus, ready-to-use hair coloring compositions can be called "active hair coloring compositions." The oxidative dye precursors and oxidizing agents in active hair coloring compositions diffuse into the hair shaft, where color formation occurs through a cascade of chemical reactions. The oxidative dye precursors are oxidized by the oxidizing agents, forming reactive intermediates. The couplers, which are relatively stable with respect to the oxidizing agents, react with these intermediates, leading to vibrant color molecules.

[0003] The hair coloring compositions of the present case include 2-methoxymethyl-p-phenylenediamine, an important oxidative dye precursor. Additional oxidative dye precursors, such as dimethylpiperazinium aminopyrazolopyridine and 2,3-diaminodihydropyrazolopyrazolone dimethosulfonate, etc., may also be included. The base hair coloring composition is combined with a developer composition to obtain a ready-to-use hair coloring composition having an inha- Typically low, in the range of approximately 6 to 8. These unique hair coloring compositions provide long-lasting color to hair while being gentle and non-irritating to the skin. They are useful for coloring all types of hair, including head hair, eyelashes, eyebrows, and body hair, but are particularly useful for coloring facial hair (beard and mustache).

[0004] The basic compositions for hair coloring include:

[0005] - of 2-methoxymethyl-P-phenylenediamine, and optionally one or more additional oxidative dye precursors;

[0006] - less than 3% by weight, preferably less than 2.5% by weight, in a way more preferred less than 2% by weight, even more preferred less than 1.5% by weight of one or more organic and / or mineral alkalizing agents, based on the total weight of the basic hair coloring composition;

[0007] - a combination of surfactants, water-soluble organic solvents and water constituting at least 70% by weight, preferably at least 75% by weight, more preferably at least 80% by weight of the base composition for hair coloring, based on the total weight of the base composition for hair coloring.

[0008] The pH of base hair coloring compositions is typically from about 7 to about 10, preferably from about 7.5 to about 9.5, and more preferably from about 8 to less than 9.5. A lower pH for the base hair coloring composition is useful for influencing the pH of a ready-to-use hair coloring composition formed by combining the base hair coloring composition with a developer composition. The pH of ready-to-use hair coloring compositions formed with base hair coloring compositions is from about 6 to about 8, preferably from about 6.1 to about 7.9, and more preferably from about 6.2 to about 7.8, which is lower than that of most ready-to-use hair coloring compositions.

[0009] Alkalizing agents have multiple roles in the coloring process, in addition to providing alkalinity to influence pH. Non-limiting examples of organic alkalizing agents include monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, N,N-dimethylethanolamine, 2-amino-2-methyl-l-propanol, 2-amino-2-methyl-l,3-propanediol, 3-amino-l,2-propanediol, 3-dimethylamino-l,2-propanediol, tris(hydroxymethyl)aminomethane, or mixtures thereof. Non-limiting examples of mineral alkalizing agents include ammonia, ammonium carbonates, sodium carbonates, potassium carbonates, ammonium bicarbonates, sodium bicarbonates, potassium bicarbonates, ammonium hydroxides, sodium hydroxides, potassium hydroxides, or mixtures thereof. However, in various embodiments, the basic hair coloring composition is free or essentially free of ammonia and / or ammonium ions, and / or ammonium hydroxide.

[0010] Surfactants may be nonionic, anionic, amphoteric (zwitterionic), or cationic. In various embodiments, the basic hair coloring compositions comprise one or more nonionic surfactants. In other embodiments, the basic hair coloring compositions comprise one or more nonionic surfactants and one or more anionic surfactants, for example, a fatty amide (nonionic surfactant) and a carboxylic ether (anionic surfactant).

[0011] The basic hair coloring compositions are aqueous. In addition to water, however, the hair coloring compositions may include one or more water-soluble organic solvents. Non-limiting examples of water-soluble organic solvents include glycerin, monoalcohols, polyols (polyhydric alcohols), glycols, and mixtures thereof, for example, glycerin, propylene glycol, butylene glycol, pentylene glycol, dipropylene glycol, hexylene glycol, ethanol, isopropanol, t-butyl alcohol, and mixtures thereof.

[0012] Additional components useful in basic hair coloring compositions include fatty alcohols, surfactants, and / or water-soluble organic solvents. In some embodiments, the fatty acids comprise from 12 to 24 carbon atoms. Non-limiting examples include cetyl alcohol, stearyl alcohol, cetearyl alcohol, behenyl alcohol, lauryl alcohol, myristic or myristyl alcohol, arachidyl alcohol, lignoceryl alcohol, and mixtures thereof.

[0013] In various embodiments, the basic hair coloring compositions include one or more reducing agents. Reducing agents are chemical species that lose an electron to another chemical species in a redox reaction. Non-limiting examples of reducing agents include ammonium bisulfite, ammonium sulfite, potassium metabisulfite, potassium sulfite, sodium hydrosulfite, sodium metabisulfite, sodium sulfite, sodium bisulfite, thioglycolic acid, thiolactic acid, dehydroascorbic acid, salts thereof, and mixtures thereof. In some embodiments, the basic hair coloring compositions include thioglycolic acid, thiolactic acid, salts thereof, and mixtures thereof.

[0014] In addition to the preceding, in various embodiments, the basic hair coloring composition includes:

[0015] (a) of 2-methoxymethyl-P-phenylenediamine, and optionally one or more additional oxidative dye precursors;

[0016] (b) one or more couplers;

[0017] (c) less than 3% by weight, preferably less than 2.5% by weight, in a way more preferably less than 2% by weight, even more preferably less than 1.5% by weight of one or more organic and / or mineral alkalizing agents, on the basis of the total weight of the basic hair coloring composition0;

[0018] (d) one or more fatty alcohols;

[0019] (e) one or more surfactants;

[0020] (f) optionally one or more water-soluble organic solvents;

[0021] (g) of water.

[0022] wherein (e), (f) and (g) are in quantities such that a combined quantity of (e), (f) and (g) constitutes at least 70% by weight, preferably at least 75% by weight, more preferably at least 80% by weight of the basic hair coloring composition; and

[0023] All percentages by weight are based on the total weight of the base composition for hair coloring.

[0024] In various embodiments, the basic hair coloring compositions are free or essentially free of ammonia and / or ammonium ions and / or ammonium hydroxide.

[0025] The base compositions for hair coloring are mixed with developer compositions to form ready-to-use hair coloring compositions having a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8. For example, the base compositions for hair coloring can be mixed with a developer composition in a weight ratio of about 5:1 to about 1:5, about 3:1 to about 1:3, or about 2:1 to about 1:2. The pH of the base compositions for hair coloring is typically about 7 to about 10, preferably about 7.5 to about 9.5, more preferably about 8 to less than 9.5.A lower pH for the base hair coloring composition is useful for influencing the pH of a ready-to-use hair coloring composition formed by combining the base hair coloring composition with a developer composition.

[0026] The hair coloring base compositions and the developer compositions are contained separately before mixing. Thus, the two compositions can be supplied in a kit. The kits according to this disclosure include one or more hair coloring base compositions and one or more developer compositions, in which the hair coloring base compositions and the developer compositions are contained separately. For example, the one or Several base compositions of hair coloring and one or more developer compositions may be included in separate containers which are packaged together.

[0027] The methods for preparing ready-to-use hair coloring compositions and the methods for coloring hair with these compositions involve combining the base hair coloring composition with a developer composition to form a ready-to-use hair coloring composition. The ready-to-use hair coloring composition is then applied to the hair for a period of time (for the treatment), for example, from approximately 1 to approximately 30 minutes, from approximately 1 to approximately 20 minutes, or from approximately 1 to approximately 15 minutes, from approximately 1 to 10 minutes, or from approximately 1 to 5 minutes. After the time period has elapsed, the hair coloring compositions can be removed from the hair by rinsing or washing, exposing the newly colored hair.The newly colored hairs retain their changed color permanently, suffer little or no unwanted chemical damage, and the underlying skin is not subjected to the burning and stinging associated with various oxidative coloring processes. Brief description of the designs.

[0028] Implementations of this technology will now be described, by way of example, with reference to the accompanying figures, in which:

[0029] [Fig-1] Fig. 1 is a graph showing the retention of gray hair color at 90% treated with a composition of the invention compared to hairs treated with two comparative compositions; and

[0030] [Fig.2] Fig.2 is a graph showing the color retention of hairs per- 90% of hairs treated with a composition of the invention compared to hairs treated with two comparative compositions.

[0031] The figures and the data they represent are not exhaustive and are provided simply to illustrate certain aspects of the technology. DETAILED DESCRIPTION

[0032] People often seek to permanently change the color of their hair using oxidative dyeing procedures. Complaints frequently associated with these procedures include the deposition of inadequate colors, damage to the hair and / or underlying skin, and hair discoloration over time. During the dyeing process, the hair coloring compositions often come into contact with the underlying skin. This can temporarily discolor the underlying skin, cause discomfort, and even, in some cases, damage the skin. Over time, the initial color imparted to the hair may fade. As the color fades, the hair may appear less vibrant, exhibit undesirable shades and appear neglected.

[0033] The hair coloring compositions and processes described in this case address the concerns raised above. They are gentle on the hair and the underlying skin while providing a fast, strong, and long-lasting color deposit. The hair coloring compositions are suitable for all hair types. However, due to their robust coloring ability and gentle nature, they are particularly well-suited for coloring facial hair (e.g., beard and mustache), which tends to be thicker than other hair.

[0034] Different types of hair grow on different parts of the body. Lanugo is the layer of fine down that covers most newborns. It tends to fall out soon after or just after birth. Down is short, fine, and slightly colored. It develops on the body during childhood, except for the lips, palms of the hands, soles of the feet, behind the ears, inside the navel, etc. This hair comes from follicles that are not connected to an oil gland. Terminal hairs grow mainly on the head. They are long, thick, and darker than the hair elsewhere on the body. When a person enters puberty, terminal hairs replace down in the pubic area and underarms. Males, in particular, may also develop terminal hairs instead of down on the chest, limbs, feet, back, and face.When they develop during puberty / adolescence, they are called androgenic hairs.

[0035] Scalp hair, like facial hair, grows in three stages, but facial hair has a much shorter growth phase. These stages include the active growth phase (anagen), the transitional phase (catagen, when growth stops), and the shedding phase (telogen). On the scalp, this cycle lasts for years; on the face, it is a matter of months. Beard and mustache hair (androgenic hair) can be very different from the hair that grew on the scalp, or from hair elsewhere on the body. Androgenic facial hair tends to be thicker and coarser in texture and may be a different color than scalp hair. A person may retain fully colored hair well into middle age, while the beard may turn partially or completely gray.Scalp hair can be straight; however, facial androgenic hair is thicker and curlier, partly due to the different shape of the follicles. Facial follicles are much more sensitive to androgens such as testosterone, which can cause them to twist and result in curly hair growth. The skin beneath facial androgenic hair is also different from the skin on the scalp.

[0036] As noted previously, hair coloring compositions intended to permanently alter hair color typically consist of a combination of two parts: a hair coloring base composition and a developer composition. The hair coloring base composition includes oxidative dye precursors, such as 2-methoxymethyl-p-phenylenediamine, and the developer composition includes oxidizing agents, such as hydrogen peroxide. The two parts are mixed to form a ready-to-use hair coloring composition.

[0037] Oxidative dye precursors are typically colorless or faintly colored compounds which, when combined with oxidizing agents, are converted into colored species via an oxidative condensation process. The shades obtained with oxidative dye precursors can be varied by combining them with one or more couplers. Couplers include, for example, aromatic meta-diamines, meta-aminophenols, meta-diphenols, and certain heterocyclic compounds, such as indole compounds.

[0038] The oxidizing agent(s) used in permanent hair dye compositions may degrade the melanin in the hair, which, depending on the nature of the oxidizing agent, may lead to less pronounced lightening of the fibers. A common oxidizing agent used in hair lightening and coloring is hydrogen peroxide. However, peroxygenated salts, such as persulfates, may be used, often in conjunction with hydrogen peroxide.

[0039] In general, hair coloring compositions are alkaline, having a high pH of approximately 9 and above, and may typically require the presence of an alkalizing agent such as ammonia or an ammonia-generating compound and / or an amine- or ammonium-based compound in sufficient quantities to achieve the desired alkalinity. The alkalizing agents help activate the oxidizing agents and cause the hair shaft to swell, allowing the small precursor molecules of oxidative dye to penetrate the cuticle and cortex before the completion of the oxidation condensation process. The larger color complexes resulting from the oxidative reaction are then trapped within the hair fiber, permanently altering the hair color.

[0040] In various embodiments, the basic hair coloring compositions of this disclosure include:

[0041] (a) of 2-methoxymethyl-P-phenylenediamine, and optionally one or more additional oxidative dye precursors;

[0042] (b) one or more couplers;

[0043] (c) less than 3% by weight, preferably less than 2.5% by weight, in a way more preferred less than 2% by weight, even more preferred less than 1.5% by weight of one or more organic and / or mineral alkalizing agents, based on the total weight of the base hair coloring composition0;

[0044] (d) about 0.1 to about 10% by weight of one or more fatty alcohols, for example, fatty alcohols containing 12 to 24 carbon atoms;

[0045] (e) approximately 15 to approximately 40% by weight of one or more surfactants;

[0046] (f) approximately 10 to approximately 40% by weight of one or more soluble organic solvents in the water;

[0047] (g) approximately 25 to approximately 60% by weight of water;

[0048] wherein (e), (f) and (g) are in quantities such that a combined quantity of (e), (f) and (g) constitutes at least 70% by weight of the basic hair coloring composition; and

[0049] All percentages by weight are based on the total weight of the base composition for hair coloring.

[0050] In various embodiments, the basic hair coloring compositions are free or essentially free of ammonia and / or ammonium ions, and / or ammonium hydroxide.

[0051] The pH of the hair coloring base composition will vary. However, the pH is typically such that when mixed with a developer composition to form a ready-to-use hair coloring composition, the ready-to-use hair coloring composition has a desired pH, for example, a pH of about 6 to about 8, preferably about 6.1 to about 7.9, more preferably about 6.2 to about 7.8. Developer compositions are typically acidic, for example, having a pH of 2 to about 6. Consequently, to obtain a ready-to-use hair coloring composition by mixing the developer composition with the hair coloring base composition, the hair coloring base composition must have a low pH, for example, about 7 to about 10, preferably about 7.5 to about 9.5, more preferably about 8 to less than 9.5.The pH of the hair coloring base composition, the pH of the developer composition, and the mixing ratio of the hair coloring base composition to the developer composition can influence the final pH of the ready-to-use hair coloring composition.

[0052] In various embodiments, the pH of the base composition for hair coloring is from about 7 to about 10, from about 7.5 to about 10, from about 8 to about 10, from about 8.5 to about 10, from about 7 to about 9.5, from about 7.5 to about 9.5, from about 8 to about 9.5, from about 8.5 to about 9.5, from about 7 to about 9, from about 7.5 to about 9, or from about 8 to about 9.

[0053] In various embodiments, the basic hair coloring compositions are free or essentially free of resorcinol and / or re- derivatives Sorcinol. Hair color modification compositions may, in certain embodiments, be free or substantially free of para-phenylenediamines (other than 2-methoxymethyl-p-phenylenediamine), resorcinol, and / or resorcinol derivatives. In certain embodiments, hair color modification compositions may be free or substantially free of one or more of the following: mineral oil, ammonia, ammonium hydroxide, ammonium thiolactate, para-phenylenediamines (other than 2-methoxymethyl-p-phenylenediamine), resorcinol, and / or resorcinol derivatives. In other embodiments, the hair color modification compositions may be free or substantially free of mineral oil, ammonia, ammonium hydroxide, ammonium thiolactate, para-phenylenediamines (other than 2-methoxymethyl-p-phenylenediamine), resorcinol, and / or resorcinol derivatives.

[0054] As noted, the base hair coloring compositions of this disclosure can be combined with a developer composition to form a ready-to-use hair coloring composition having a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8. The final pH of a ready-to-use hair coloring composition will depend on the content, pH, etc., of the base hair coloring composition.In various embodiments, the basic hair coloring compositions of this disclosure are such that they form a ready-to-use hair coloring composition having a pH of about 6 to about 8, about 6.1 to about 7.9, or about 6.2 to about 7.8, when mixed with a developer composition comprising hydrogen peroxide in a weight ratio of about 1:5 to about 5:1 (hair coloring composition developer composition).

[0055] Furthermore, the total amount of alkali-suppressing agent (e.g., monoethanolamine) in the base hair coloring composition is such that when mixed with a developer composition to form a ready-to-use hair coloring composition, the total amount of alkali-suppressing agent in the ready-to-use coloring composition is less than 2% by weight, preferably less than 1.5% by weight, more preferably less than 1% by weight.

[0056] For example, the hair coloring base compositions are such that they form a ready-to-use hair coloring composition having a pH of approximately 6 to approximately 8, approximately 6.1 to approximately 7.9, or approximately 6.2 to approximately 7.8, when mixed with a developer composition comprising hydrogen peroxide in a weight ratio of approximately 1:1 (hair coloring composition + developer composition), wherein the developer composition consists of:

[0057] (a) approximately 7.5% by weight of hydrogen peroxide;

[0058] (b) approximately 82% by weight of water;

[0059] (c) approximately 0.5% by weight of glycerin;

[0060] (d) approximately 2.3% by weight of cetearyl alcohol;

[0061] (e) approximately 0.9% by weight of trideceth-2 carboxamide MEA;

[0062] (f) approximately 0.6% by weight of ceteareth-25; and

[0063] in which all weight percentages for the components of the developer composition are based on the total weight of the developer composition.

[0064] The basic hair dye compositions include 2-methoxymethyl-p-phenylenediamine, which is an oxidative dye precursor, and optionally one or more additional oxidative dye precursors. Oxidative dye precursors are also called "primary intermediates" or "oxidation bases." Oxidative dye precursors are often colorless or weakly colored compounds, which, when combined with oxidizing agents, react via oxidative condensation to yield colored species.Non-limiting examples of oxidative dye precursors include aromatic diamines, polyhydric phenols, aminophenols, and derivatives of these compounds, such as, for example, N-substituted derivatives of amines, and phenol ethers, ortho- or para-aminophenols, ortho- or para-phenylenediamines, double bases, heterocyclic bases, and acid addition salts thereof. More specific non-limiting examples include dimethylpiperazinium aminopyrazolopyridine, 2,3-diaminodihydropyrazolopyrazolone dimethosulfonate, p-phenylenediamine, 2,5-diaminotoluene, N,N-bis(2-hydroxymethyl)-p-phenylenediamine, paminophenol, salts thereof, etc.

[0065] In some embodiments, in addition to 2-methoxymethyl-P-phenylenediamine, the basic hair coloring composition includes one or more oxidative dye precursors selected from dimethylpiperazinium aminopyrazolopyridine, 2,3-diaminodihydropyrazolopyrazolone dimethosulfonate, salts thereof, and combinations thereof.

[0066] A more exhaustive but not exhaustive list of useful oxidative dye precursors is described later, under the heading "Oxidative Dye Precursors".

[0067] The total amount of one or more oxidative dye precursors, including 2-methoxymethyl-p-phenylenediamine, will vary depending on the desired color and intensity of the hair to be treated. In various embodiments, the total amount of one or more oxidative dye precursors, including 2-methoxymethyl-p-phenylenediamine, is approximately 0.001 to approximately 12% by weight, approximately 0.001 to approximately 10% by weight, approximately 0.001 to approximately 8% by weight, approximately 0.001 to approximately 5% by weight, approximately 0.01 to approximately 10% by weight, from about 0.01 to about 8% by weight, from about 0.01 to about 6% by weight, or from about 0.01 to about 5% by weight, from about 0.1 to about 12% by weight, from about 0.1 to about 10% by weight, from about 0.1 to about 8% by weight, from about 0.1 to about 6% by weight, from about 0.1 to about 5% by weight, from about 0.5 to about 12% by weight, from about 0.5 to about 10% by weight, from about 0.5 to about 8% by weight, from about 0.5 to about 6% by weight, or from about 0.5 to about 5% by weight, based on the total weight of the base composition for hair coloring.

[0068] As for 2-methoxymethyl-p-phenylenediamine individually, in various embodiments, it is present in an amount of approximately 0.001 to approximately 10% by weight, approximately 0.001 to approximately 8% by weight, approximately 0.001 to approximately 5% by weight, approximately 0.001 to approximately 4% by weight, approximately 0.01 to approximately 10% by weight, approximately 0.01 to approximately 8% by weight, or approximately 0.01 to approximately 5% by weight, approximately 0.01 to approximately 4% by weight, approximately 0.1 to approximately 10% by weight, approximately 0.1 to approximately 8% by weight, approximately 0.1 to approximately 5% by weight, approximately 0.1 to approximately 4% by weight, approximately 0.1 to approximately 3.5% by weight. % by weight, from about 0.1 to about 3% by weight, from about 0.5 to about 8% by weight, or from about 0.5 to about 5% by weight, from about 0.5 to about 4% by weight, from about 0.5 to about 3.5% by weight, or from about 0.5 to about 3% by weight, based on the total weight of the base composition for hair coloring.

[0069] The colors obtained using oxidative dye precursors can be modified by combining them with one or more couplers. Thus, in some embodiments, the base hair dye compositions of this disclosure include one or more couplers. Non-limiting examples of couplers include aromatic meta-diamines, meta-aminophenols, meta-diphenols, and certain heterocyclic compounds, such as indole compounds. A more comprehensive but non-limiting list of couplers that can be included in the base hair dye compositions is provided later under the heading "Couplers." The variety of molecules used as oxidative dye precursors and couplers makes it possible to obtain a wide range of colors.

[0070] The total quantity of couplers, if any, will vary depending on the desired color of the hair to be treated. In various embodiments, the base hair coloring composition includes approximately 0.0001 to approximately 12% by weight, based on the total weight of the base hair coloring composition. In some cases, the total quantity of one or more couplers is approximately 0.001 to approximately 12% by weight, approximately 0.001 to approximately 10% by weight, approximately 0.001 to approximately 5% by weight, approximately 0.001 to approximately 3% by weight, approximately 0.01 to approximately 10% by weight, approximately 0.01 to approximately 8% by weight, approximately 0.01 to approximately 5% by weight, or approximately 0.01 to approximately 3% by weight, approximately 0.1 to approximately 10% by weight. weight, from about 0.1 to about 8% by weight, from about 0.1 to about 5% by weight, from about 0.1 to about 4% by weight, or from about 0.1 to about 3% by weight, based on the total weight of the base composition for hair coloring.

[0071] The weight ratio of the total amount of oxidative dye precursors (including 2-methoxymethyl-P-phenylenediamine) to the total amount of one or more couplers in the basic hair dye composition can be from about 1:1 to about 5:1, from about 1:1 to about 4:1, or from about 1:1 to about 3:1, from about 1:1 to about 2:1, or from about 1:1 to about 1.5:1.

[0072] In addition to oxidative dye precursors, and optionally couplers, the basic hair coloring composition, in certain embodiments, includes one or more direct dyes, pigments, and / or mixtures thereof. The total quantity of one or more direct dyes, pigments, and / or mixtures thereof, as applicable, will vary. However, in certain embodiments, the total quantity of one or more direct dyes, pigments, and / or mixtures thereof, as appropriate, is approximately 0.01 to approximately 5% by weight, approximately 0.01 to approximately 3% by weight, approximately 0.01 to approximately 2% by weight, approximately 0.1 to approximately 5% by weight, approximately 0.1 to approximately 3% by weight, approximately 0.1 to approximately 2% by weight, or approximately 0.1 to approximately 1% by weight, based on the total weight of the basic hair coloring composition.

[0073] Alkalinizing agents in the hair coloring base composition typically play multiple roles in the coloring process. For example, the alkalinizing agent(s) are useful for achieving a desired pH. In addition, the alkalinizing agent(s) help to cause swelling of the hair shaft, allowing small molecules of the oxidative dye precursor to penetrate the cuticle and cortex more easily. Furthermore, the alkalinizing agents can activate one or more oxidizing agents in the developer composition and contribute to the oxidative condensation process.Non-limiting examples of alkalizing agents include ammonia, ammonium hydroxide, ammonium carbonate, ammonium chloride, ammonium sulfate, ammonium nitrate, ammonium phosphate, ammonium acetate, ammonium hydrogen carbonate, ammonium carbamate, percarbonate salts, alkanolamines (such as monoethanolamine, diethanolamine, triethanolamine, monopropanolamine, dipropanolamine, tripropanolamine, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-methyl-1,3-propanol, and 2-amino-2-hydroxymethyl-1,3-propanediol), guanidium salts, alkali metal hydroxides (such as sodium hydroxide), and alkali metal carbonates, and mixtures thereof.

[0074] The basic hair coloring compositions according to this disclosure may include one or more alkalizing agents. According to various methods of preparation lisation, the alkalizing agent may include at least one organic alkalizing agent and / or at least one mineral alkalizing agent.

[0075] In some embodiments, the alkalizing agent comprises at least one organic alkalizing agent selected from monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, N,N-dimethylethanolamine, 2-amino-2-methyl-l-propanol, 2-amino-2-methyl-l,3-propanediol, 3-amino-l,2-propanediol, 3-dimethylamino-l,2-propanediol, tris(hydroxymethyl)amino-methane, or mixtures thereof.

[0076] In other embodiments, the alkali-forming agent comprises at least one mineral alkali-forming agent selected from ammonia, ammonium carbonates, sodium carbonates, potassium carbonates, ammonium bicarbonates, sodium bicarbonates, potassium bicarbonates, ammonium hydroxides, sodium hydroxides, potassium hydroxides, or mixtures thereof. In some embodiments, the alkali-forming component comprises ammonia and / or ammonium hydroxide.

[0077] In some embodiments, the alkali-forming agent comprises at least one organic alkali-forming agent and is free or substantially free of mineral alkali-forming agents. For example, the alkali-forming agent may comprise less than about 0.5%, less than about 0.4%, less than about 0.3%, less than about 0.2%, less than about 0.1%, or less than about 0.05% of mineral alkali-forming agents. In some embodiments, the alkali-forming agent comprises at least one organic alkali-forming agent and is free or substantially free of ammonia and / or ammonium ions and / or ammonium compounds. In various embodiments, the alkali-forming agent comprises monoethanolamine. In other embodiments, the alkali-forming agent comprises monoethanolamine and is free or substantially free of ammonia and / or ammonium ions and / or ammonium compounds.An "ammonium compound" in the context of this disclosure is a compound that produces ammonia when present in the composition at a particular pH. Examples of such compounds include ammonia and compounds that may be added in the form of ammonium hydroxide and ammonium salts (e.g., simple salts). Ammonium salts may include inorganic ammonium salts such as ammonium carbonate, ammonium bicarbonate, ammonium chloride, ammonium nitrate, ammonium sulfate, and ammonium phosphate; organic ammonium salts such as ammonium formate, ammonium acetate, and tetramethylammonium hydroxide; and mixtures thereof.

[0078] The total quantity of one or more alkalizing agents in the compositions of The base composition of the hair coloring agent will vary. However, in various embodiments, the base composition of the hair coloring agent includes less than approximately 3% by weight of alkalizing agents, based on the total weight of the base composition of the hair coloring agent. In other embodiments, the base composition of the hair coloring agent includes less than 3% by weight, less than 2.5% by weight, less than 2.2% by weight, less than 2% by weight, less than 1.8% by weight, less than 1.6% by weight, less than 1.5% by weight, less than 1.3% by weight, less than 1.1% by weight, or less than 1% by weight, based on the total weight of the base composition of the hair coloring agent.

[0079] The types of reducing agents that may be included in hair coloring base compositions can vary. Non-limiting examples of reducing agents include ammonium bisulfite, ammonium sulfite, potassium metabisulfite, potassium sulfite, sodium hydrosulfite, sodium metabisulfite, sodium sulfite, sodium bisulfite, thioglycolic acid, thiolactic acid, dehydroascorbic acid, salts thereof, and mixtures thereof. The salts referred to throughout the disclosure may include salts containing a counterion such as an alkali metal, an alkaline earth metal, or an ammonium counterion. This list of counterions, however, is not exhaustive. In various embodiments, preferred reducing agents include thiolactic acid, glycolic acid, salts thereof (e.g., ammonium thiolactate), and combinations thereof.

[0080] In various embodiments, one or more reducing agents may be derived from thiols such as thioglycolic acid or a salt thereof, thiolactic acid or a salt thereof, 3-mercaptopropionic acid, thiomalic acid, 2,3-dimercaptosuccinic acid, cysteine, N-glycyl-L-cysteine, L-cysteinylglycine and also esters and salts thereof, thioglycerol, cysteamine and the C1-C4 acyl derivatives thereof, N-mesylcysteamine, N-acetylcysteine, N-mercaptoalkylamides of sugars such as N-(mercapto-2-ethyl)gluconamide, pantetheine, N-(mercaptoalkyl)-Q-hydroxyalkylamides, N-mono- or N,N-dialkylmercapto-4-butyramides, aminomercaptoalkyl amides, N-(mercaptoalkyl)succinamic acids and N-(mercaptoalkyl)succinimides, al-kylamino mercaptoalkyl amides, mercaptoalkylamino amides, N-mercaptoalkylalkanediamides, ammonium bisulfite, ammonium sulfite, potassium metabisulfite,potassium sulfite, sodium hydrosulfite, sodium metabisulfite, sodium sulfite, sodium bisulfite, and mixtures thereof. In other embodiments, the basic hair-coloring composition includes one or more reducing agents selected from thioglycolic acid, thiolactic acid, 3-mercaptopropionic acid, salts thereof, and combinations thereof.

[0081] The reducing agent may also be selected from hydrides such as sodium or potassium borohydride or alkali metal or alkaline earth metal sulfites or bisulfites; or alternatively from phosphorus derivatives such as phosphines or phosphites. In various embodiments, one or more reducing agents are selected from ammonium bisulfite, ammonium sulfite, potassium metabisulfite, potassium sulfite, sodium hydrosulfite, sodium metabisulfite, sodium sulfite, sodium bisulfite, thioglycolic acid, thiolactic acid, dehydroascorbic acid, a salt thereof, and a mixture thereof.

[0082] The total amount of one or more reducing agents in the base composition for hair coloring can vary but is typically from about 0.01 to about 10% by weight, based on the total weight of the composition. The total amount of one or more reducing agents can be from about 0.01 to about 8% by weight, from about 0.01 to about 5% by weight, from about 0.1 to about 10% by weight, from about 0.1 to about 8% by weight, from about 0.1 to about 5% by weight, from about 0.1 to about 3% by weight, or from about 0.1 to about 2% by weight, based on the total weight of the base composition for hair coloring.

[0083] The term "fatty alcohol" refers to an alcohol comprising at least one hydroxyl group (OH), and comprising at least 8 carbon atoms, and which is neither oxy-alkylated (in particular neither oxyethylated nor oxypropylated) nor glycerolated. Fatty alcohols may be represented by: R-OH, in which R designates a saturated (alkyl) or unsaturated (alkenyl) group, linear or branched, comprising from 8 to 40 carbon atoms, preferably 10 to 30 carbon atoms, more preferably 12 to 24 carbon atoms, and even more preferably 14 to 22 carbon atoms.

[0084] Fatty alcohol(s) may be liquid(s) or solid(s). Non-limiting examples of solid fatty alcohols include those that are solid at room temperature and atmospheric pressure (25 °C, 780 mmHg) and are insoluble in water, i.e., they have a water solubility of less than 1 wt%, preferably less than 0.5 wt%, at 25 °C, 1 atm. Solid fatty alcohols may be represented by: R-OH, where R denotes a linear alkyl group, optionally substituted by one or more hydroxyl groups, comprising from 8 to 40 carbon atoms, preferably 10 to 30 carbon atoms, more preferably 12 to 24 carbon atoms, and even more preferably 14 to 22 carbon atoms.

[0085] In some embodiments, one or more fatty alcohols comprise from 12 to 24 carbon atoms. Specific, non-limiting examples include cetyl alcohol, stearyl alcohol, cetearyl alcohol, behenyl alcohol, lauryl alcohol, myristic or myristyl alcohol, arachidyl alcohol, lignoceryl alcohol, or mixtures thereof. Preferably, the cosmetic composition includes one or more fatty alcohols chosen from cetyl alcohol, stearyl alcohol, behenyl alcohol, oleyl alcohol, and mixtures thereof such as cetearyl or cetearyl alcohol.

[0086] Liquid fatty alcohols, particularly those containing C10-C34, preferably have branched carbon chains and / or one or more, preferably 1 to 3, double bonds. They are preferably branched and / or unsaturated (C=C double bond) and contain from 12 to 40 carbon atoms. Liquid fatty alcohols can be represented by: R-OH, where R denotes a C12-C24 branched alkyl group or an alkenyl group (comprising at least one C12-C24 C=C double bond), R optionally being substituted by one or more hydroxyl groups. Preferably, the liquid fatty alcohol is a branched saturated alcohol. Preferably, R does not contain a hydroxyl group. These include oleic alcohol, linoleic alcohol, linolenic alcohol, isocetyl alcohol, isostearyl alcohol, 2-octyl-l-dodecanol, 2-butyloctanol, 2-hexyl-l-decanol, 2-decyl-l-tetradecanol, 2-tetradecyl-l-cetanol and mixtures thereof.

[0087] In various embodiments, the hair coloring base composition includes one or more fatty alcohols selected from decyl alcohol, one-decyl alcohol, dodecyl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, cetearyl alcohol, isostearyl alcohol, isocetyl alcohol, behenyl alcohol, linalool, oleyl alcohol, myricyl alcohol, and a mixture thereof. In some cases, the hair coloring base compositions preferably include at least one oleyl alcohol.

[0088] The total quantity of one or more fatty alcohols, if any, will vary. In various embodiments, the basic hair coloring composition includes from about 0.1 to about 10% by weight, from about 0.1 to about 8% by weight, from about 0.1 to about 5% by weight, from about 0.5 to about 10% by weight, from about 0.5 to about 8% by weight, from about 0.5 to about 5% by weight, or from about 0.5 to about 3% by weight, based on the total weight of the basic hair coloring composition.

[0089] In various embodiments, the basic hair coloring composition includes one or more surfactants, for example, one or more anionic surfactants, nonionic surfactants, amphoteric surfactants (zwitterionic surfactants), cationic surfactants, and / or a mixture thereof. In a preferred embodiment, the basic hair coloring composition includes at least one or more nonionic surfactants and optionally, or preferably, one or more anionic surfactants. In some embodiments, the basic hair coloring composition is preferably free of, or essentially free of, cationic surfactants.

[0090] The total amount of one or more surfactants may vary but is typically about 1 to about 40% by weight, based on the total weight of the base hair coloring composition. The total quantity of one or more surfactants may be from about 1 to about 35% by weight, from about 1 to about 30% by weight, from about 5 to about 40% by weight, from about 5 to about 32% by weight, from about 10 to about 40% by weight, from about 10 to about 35% by weight, from about 10 to about 32% by weight, from about 15 to about 40% by weight, from about 15 to about 35% by weight, from about 15 to about 32% by weight, from about 20 to about 40% by weight, from about 20 to about 32% by weight, from about 20 to about 32% by weight, or from about 25 to about 32% by weight, based on the total weight of the base composition for hair coloring.

[0091] In various embodiments, the total quantity of one or more surfactants in the base composition for hair coloring is at least 10% by weight, at least 12% by weight, at least 15% by weight, at least 18% by weight, at least 20% by weight, at least 21% by weight, at least 22% by weight, at least 23% by weight, or at least 24% by weight, in each case having an optional maximum quantity of up to 30, 35 or 40% by weight, based on the total weight of the base composition for hair coloring.

[0092] In various embodiments, the basic hair-coloring composition includes one or more nonionic surfactants. Non-limiting examples of nonionic surfactants include oxyethylenated amides, oxyethylenated fatty alcohols, and sequenced (polycondensed) copolymer surfactants of ethylene oxide and propylene oxide, and a mixture thereof. In a preferred embodiment, the basic hair-coloring composition includes PEG-4 rapeseed amide (an oxyethylenated amide), deceth-3 (an oxyethylenated fatty alcohol), Poloxamer 338 (a sequenced (polycondensed) copolymer surfactant of ethylene oxide and propylene oxide), or a combination thereof.

[0093] Non-limiting examples of non-ionic oxyethylenated amides are those of the following formula: R—[(OCH2CH2)n-OCH2]p-CO—N(R )—(CH2CH2O)n H

[0094] in which:

[0095] p denotes 0 or 1,

[0096] n denotes a number in the range of 1 to 10 and preferably from 1 to 6,

[0097] n' denotes a number in the range of 1 to 100 and preferably from 1 to 60,

[0098] R' denotes a hydrogen atom or a CH2CH2OH radical and preferably a hydrogen atom, and

[0099] R denotes a C10-C30 alkyl or alkenyl radical, and preferably a C12-C22 radical.

[0100] Examples of such compounds include Amidet A15 sold by the Kao company. (INCI name: Trideceth-2 carboxamide MEA), Ethomid HP 60 sold by Akzo Nobel (INCI name: PEG-50 Hydrogenated Palmamide) and Amidet N sold by Kao (INCI name: PEG-4 Rapeseedamide).

[0101] In some cases, the basic hair coloring compositions include at least oxyethylenated rapeseed amide with 4 oxyethylene motifs (PEG-4 rapeseed amide).

[0102] Non-limiting examples of fatty alcohols include linear and branched alcohols, saturated or unsaturated, comprising from 6 to 30 carbon atoms and preferably from 8 to 30 carbon atoms, for example, cetyl alcohol, isostearyl alcohol, stearyl alcohol and mixtures thereof (cetylstearyl alcohol), octyldodecanol, 2-butyloctanol, 2-hexyldecanol, 2-undecylpentadecanol, oleyl alcohol, linolenylic alcohol, ricinoleyl alcohol, undecylenyl alcohol and linoleyl alcohol and mixtures thereof.

[0103] Non-limiting examples of oxyethylenated fatty alcohols include those comprising fewer than 10 OE motifs, preferably selected from oxyethylenated derivatives of saturated or unsaturated fatty alcohols, linear or branched, preferably linear, in C8-C30 and preferably in C12-C22, for example cetyl alcohol, oleyl alcohol, oleocetyl alcohol, lauryl alcohol, behenyl alcohol, cetearyl alcohol, stearyl alcohol and isostearyl alcohol, and mixtures thereof.

[0104] Examples of oxyethylenated fatty alcohols comprising fewer than 10 OE units include oxyethylenated fatty alcohols comprising 2 to 8, and preferably 2 to 6 OE units, for example, ethylene oxide and lauryl alcohol adducts, e.g., lauryl alcohol 2 OE (CTFA name: laureth-2), ethylene oxide and stearyl alcohol adducts, e.g., stearyl alcohol 2 OE (CTFA name: steareth-2), ethylene oxide and decyl alcohol adducts, e.g., decyl alcohol 3 OE (CTFA name: deceth-3), decyl alcohol 5 OE (CTFA name: deceth-5), and ethylene oxide and oleocetyl alcohol adducts, e.g., oleocetyl alcohol 5 OE (CTFA name: oleoceteth-5) and their mixtures. In some cases, deceth-3 can be particularly useful.

[0105] In addition, non-limiting examples of oxyethylenated fatty alcohols having an average degree of ethoxylation of 2 to 29 are, for example, laureth-2, oleth-2, ceteareth-2, laneth-2, laureth-3, oleth-3, ceteareth-3, laureth-4, oleth-4, ceteareth-4, laneth-4, laureth-5, oleth-5, ceteareth-5, laneth-5, deceth-4, deceth-7, laureth-7, oleth-7, coceth-7, ceteareth-7, ceteareth-7, Cl 1-15 pareth-7, laureth-9, oleth-9, ceteareth-9, laureth-10, oleth-10, beheneth-10, ceteareth-10, laureth-12, ceteareth-12, trideceth-12, ceteth-15, laneth-15, ceteareth-15, laneth-16, ceteareth-16, oleth-16, steareth-16, oleth-20, ceteareth-20, ceteareth-20, laneth-20, steareth-21, ceteareth-23, ceteareth-25, the ceteareth-27, and a mixture of these.

[0106] In some cases, the hair coloring composition includes both at least one nonionic surfactant selected from an oxyethylenated amide and at least one nonionic surfactant selected from an oxyethylenated fatty alcohol (OE) comprising fewer than 10 OE motifs, which may be selected from those described above.

[0107] In addition, the basic hair coloring composition may include one or more nonionic surfactants that are a sequenced (polycondensed) copolymer surfactant of ethylene oxide and propylene oxide. The sequenced (polycondensed) copolymer surfactant of ethylene oxide and propylene oxide may have a weight-average molecular weight ranging from 1000 to 20000, preferably from 1500 to 19000, from 2000 to 18000, or from 4000 to 17000.

[0108] Examples of usable sequenced copolymer (polycondensed) surfactants of ethylene oxide and propylene oxide include the tri-sequenced polyethylene glycol / polypropylene glycol / polyethylene glycol polycondensates sold under the names "Synperonic", such as "Synperonic PE / F32" (INCI name: Poloxamer 108), "Synperonic PE / F108" (INCI name: Poloxamer 338), "Synperonic PE / L44" (INCI name: Poloxamer 124), "Synperonic PE / L42" (INCI name: Poloxamer 122), "Synperonic PE / F127" (INCI name: Poloxamer 407), "Synperonic PE / F88" (INCI name: Poloxamer 238) or "Synperonic PE / L64" (INCI name: Poloxamer 184), by Croda, or also "Lutrol F68" (INCI name: Poloxamer 188), sold by BASF. In some cases, Poloxamer 338 may be particularly useful.

[0109] A more exhaustive list of useful non-ionic surfactants that can be included in the basic hair coloring composition is provided later, under the heading "Non-ionic surfactants".

[0110] The total amount of one or more non-ionic surfactants in the base composition of hair coloring may vary but is typically about 1 to about 40% by weight, based on the total weight of the base composition of hair coloring. The total amount of one or more nonionic surfactants may be from about 1 to about 35% by weight, from about 1 to about 30% by weight, from about 5 to about 40% by weight, from about 5 to about 32% by weight, from about 10 to about 40% by weight, from about 10 to about 35% by weight, from about 10 to about 32% by weight, from about 15 to about 40% by weight, from about 15 to about 35% by weight, from about 15 to about 32% by weight, from about 20 to about 40% by weight, from about 20 to about 32% by weight, from about 20 to about 32% by weight, or from about 25 to about 32% by weight, based on the total weight of the base composition for hair coloring.

[0111] In various embodiments, the total quantity of one or more non-ionic surfactants in the basic hair coloring composition is at least 10% by weight, at least 12% by weight, at least 15% by weight, at least 18% by weight, at least 20% by weight, at least 21% by weight, at least 22% by weight, at least 23% by weight, or at least 24% by weight, in each case having an optional maximum quantity of up to 30, 35 or 40% by weight, based on the total weight of the base composition for hair coloring.

[0112] In various embodiments, the hair coloring base composition includes one or more anionic surfactants. For example, in some embodiments, the hair coloring base composition includes one or more nonionic surfactants, one or more anionic surfactants, or a mixture thereof. In a preferred embodiment, the hair coloring base composition includes one or more nonionic surfactants and one or more anionic surfactants. The hair coloring base composition may also optionally include one or more amphoteric surfactants, one or more cationic surfactants, or a combination thereof. However, in some embodiments, the hair coloring base composition is free or substantially free of cationic surfactants and / or free or substantially free of amphoteric surfactants.

[0113] Non-limiting examples of anionic surfactants include alkyl carboxylic acids, alkyl ether carboxylic acids, alkyl phosphates, alkyl ether phosphates, alkyl sulfates, alkyl ether sulfates, alkyl sulfonates, alkyl ether sulfonates, and salts thereof. In some embodiments, the basic hair-coloring composition includes one or more alkyl ether carboxylic acids.Non-limiting examples of alkyl ether carboxylic acids include ceteareth-2 carboxylic acid, ceteareth-10 carboxylic acid, coceth-7 carboxylic acid, laureth-4 carboxylic acid, laureth-5 carboxylic acid, laureth-6 carboxylic acid, myreth-2 carboxylic acid, myreth-3 carboxylic acid, myreth-4 carboxylic acid, myreth-5 carboxylic acid, myreth-6 carboxylic acid, steareth-2 carboxylic acid, steareth-4 carboxylic acid, steareth-5 carboxylic acid, steareth-6 carboxylic acid, oleth-2 carboxylic acid, oleth-4 carboxylic acid, and mixtures and / or salts of these.

[0114] The total amount of one or more anionic surfactants, if any, will vary. In some embodiments, the hair coloring base composition includes approximately 0.1 to approximately 15% by weight of one or more anionic surfactants, based on the total weight of the hair coloring base composition. In other embodiments, the hair coloring base composition includes approximately 0.1 to approximately 12% by weight, approximately 0.1 to approximately 10% by weight, approximately 0.1 to approximately 8% by weight, approximately 0.1 to approximately 6% by weight, approximately 0.5 to approximately 15% by weight, approximately 0.5 to approximately 12% by weight, approximately 0.5 to approximately 10% by weight. weight, about 0.5 to about 8% by weight, about 0.5 to about 6% by weight, about 1 to about 15% by weight, about 1 to about 12% by weight, about 1 to about 10% by weight, about 1 to about 8% by weight, about 2 to about 10% by weight, about 3 to about 8% by weight, or about 4 to about 7% by weight, based on the total weight of the base composition for hair coloring.

[0115] In various embodiments, the basic hair-dyeing composition includes one or more water-soluble organic solvents (or simply "water-soluble solvents"). The term "water-soluble organic solvent" (or simply "water-soluble solvent") is interchangeable with the term "water-miscible solvent" and refers to an organic compound that is liquid at 25°C and atmospheric pressure (760 mmHg), and has a solubility of at least 50% in water under these conditions. In some embodiments, the water-soluble organic solvent(s) have a solubility of at least 60%, 70%, 80%, or 90% in water at 25°C and atmospheric pressure (760 mmHg). Non-limiting examples of water-soluble organic solvents include glycerin, alcohols (e.g., Ci-3o, Cms, Ci-10 or Ci-4 alcohols), polyols, glycols and mixtures thereof.In some embodiments, the water-soluble organic solvent(s) are selected from alcohols such as ethyl alcohol, isopropyl alcohol, propyl alcohol, benzyl alcohol and phenylethyl alcohol, or glycols or glycol ethers such as monomethyl, monoethyl and monobutyl ethers of ethylene glycol, propylene glycol or ethers thereof such as, for example, monomethyl ether of propylene glycol, butylene glycol, hexylene glycol, dipropylene glycol as well as alkyl ethers of diethylene glycol, for example monoethyl ether or monobutyl ether of diethylene glycol.

[0116] Other non-limiting but useful examples of water-soluble organic solvents include alkanediols (polyhydric alcohols) such as glycerin, 1,2,6-hexanetriol, trimethylolpropane, ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, pentaethylene glycol, dipropylene glycol, 2-butene-1,4-diol, 2-ethyl-1,3-hexanediol, 2-methyl-2,4-pentanediol, (caprylyl glycol), 1,2-hexanediol, 1,2-pentanediol and 4-methyl-1,2-pentanediol; alkyl alcohols having 1 to 4 carbon atoms such as ethanol, methanol, butanol, propanol and isopropanol;glycol ethers such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, ethylene glycol monomethyl ether acetate, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol mono-n-propyl ether, ethylene glycol mono-isopropyl ether, diethylene glycol mono-isopropyl ether, ethylene glycol mono-n-butyl ether, mono-t-butyl ether; ethylene glycol, diethylene glycol mono-t-butyl ether, 1-methyl-l-methoxybutanol, propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol mono-t-butyl ether, propylene glycol mono-n-propyl ether, propylene glycol mono-isopropyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, dipropylene glycol mono-n-propyl ether, and dipropylene glycol mono-isopropyl ether; 2-pyrrolidone, N-methyl-2-pyrrolidone, l,3-dimethyl-2-imidazolidinone, formamide, acetamide, dimethyl sulfoxide, sorbit, sorbitan, acetin, diacetinate, triacetin, sulfolane, and a mixture of the latter.

[0117] In various embodiments, the basic hair coloring composition includes one or more water-soluble organic solvents selected from glycols, CM alcohols, glycerin, and a mixture thereof; preferably the water-soluble organic solvent is selected from caprylyl glycol, glycerin, ethanol, isopropyl alcohol, dipropylene glycol, propylene glycol, hexylene glycol, caprylyl glycol, propylene glycol, glycerin, ethanol, and a mixture thereof.

[0118] In some embodiments, the basic hair coloring composition includes one or more polyhydric alcohols. Non-limiting examples of polyhydric alcohols include glycerin, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, 1,3-butanediol, 2,3-butanediol, 1,4-butanediol, 3-methyl-1,3-butanediol, 1,5-pentanediol, tetraethylene glycol, 1,6-hexanediol, 2-methyl-2,4-pentanediol, polyethylene glycol, 1,2,4-butanetriol, 1,2,6-hexanetriol, and mixtures thereof. Polyol compounds may also be used.Non-limiting examples include aliphatic diols, such as 2-ethyl-2-methyl-1,3-propanediol, 3,3-dimethyl-1,2-butanediol, 2,2-diethyl-1,3-propanediol, 2-methyl-2-propyl-1,3-propanediol, 2,4-dimethyl-2,4-pentanediol, 2,5-dimethyl-2,5-hexanediol, 5-hexene-1,2-diol and 2-ethyl-1,3-hexanediol, and mixtures thereof.

[0119] The total quantity of one or more water-soluble organic solvents will vary. In some embodiments, the base hair coloring composition includes approximately 1 to approximately 50% by weight of one or more water-soluble organic solvents, based on the total weight of the base hair coloring composition. In other embodiments, the base hair coloring composition includes approximately 1 to approximately 45% by weight, approximately 1 to approximately 40% by weight, approximately 1 to approximately 30% by weight, approximately 1 to approximately 25% by weight, approximately 5 to approximately 50% by weight, approximately 5 to approximately 40% by weight, approximately 5 to approximately 30% by weight, approximately 5 to approximately 25% by weight, approximately 10 to approximately 50% by weight, about 10 to about 40% by weight, about 10 to about 30% by weight, or about 10 to about 25% by weight, about 15 to about 50% by weight, about 15 to about 40% by weight, about 15 to about 30% by weight, about 15 to about 25% by weight, or about 18 to about 23% by weight of one or more water-soluble organic solvents, based on the total weight of the base composition for hair coloring.

[0120] In various embodiments, the total quantity of one or more water-soluble organic solvents in the base hair coloring composition is at least 10% by weight, at least 12% by weight, at least 15% by weight, at least 18% by weight, at least 20% by weight, in each case having an optional maximum quantity of up to 25, 30, 35 or 40% by weight, based on the total weight of the base hair coloring composition.

[0121] The hair coloring base composition includes varying amounts of water. The amount of water may vary depending on the desired consistency of the product, the amount of water (if any) in a developer composition with which the hair coloring base composition will be mixed, etc. In various embodiments, the hair coloring base composition includes approximately 5 to approximately 75% by weight, based on the total weight of the hair coloring base composition. In other embodiments, the total amount of water in the basic hair coloring composition is approximately 5 to approximately 70% by weight, approximately 5 to approximately 65% ​​by weight, approximately 5 to approximately 60% by weight, approximately 5 to approximately 50% by weight, approximately 10 to approximately 75% by weight, approximately 10 to approximately 70% by weight, approximately 10 to approximately 60% by weight, approximately 10 to approximately 50% by weight, approximately 15 to approximately 75% by weight,from approximately 15 to approximately 70% by weight, from approximately 15 to approximately 60% by weight, from approximately 15 to approximately 50% by weight, from approximately 20 to approximately 75% by weight, from approximately 20 to approximately 70% by weight, from approximately 20 to approximately 60% by weight, from approximately 20 to approximately 50% by weight, from approximately 25 to approximately 60% by weight, from approximately 25 to approximately 55% by weight, from approximately 30 to approximately 60% by weight, from approximately 30 to approximately 55% by weight, from approximately 30 to approximately 50% by weight, from approximately 35 to approximately 60% by weight, from approximately 35 to approximately 55% by weight, or from approximately 25 to approximately 50% by weight, based on the total weight of the base composition for hair coloring.

[0122] In various embodiments, the total amount of water in the base composition for hair coloring is at least 10% by weight, at least 15% by weight, at least 20% by weight, at least 25% by weight, at least 30% by weight, at least 35% by weight, or at least 40% by weight, in each case having an optional maximum amount of up to 45, 50, 55 or 60% by weight, based on the total weight of the base composition for hair coloring.

[0123] As mentioned above, the basic hair coloring compositions of this disclosure include varying amounts of surfactants, water-soluble organic solvents, water, etc. However, in some embodiments, the total amount (the combined amount) of surfactants, water-soluble organic solvents, and water in the basic hair coloring composition is about 60 to about 95% by weight, based on the total weight of the basic hair coloring composition.In other embodiments, the total quantity (combined quantity) of surfactants, water-soluble organic solvents, and water in the base hair coloring composition is approximately 65 to approximately 95% by weight, approximately 70 to approximately 95% by weight, approximately 75 to approximately 95% by weight, approximately 80 to approximately 95% by weight, approximately 85% to approximately 95% by weight, approximately 60 to approximately 90% by weight, approximately 65 to approximately 90% by weight, approximately 70 to approximately 90% by weight, approximately 75 to approximately 90% by weight, approximately 80 to approximately 90% by weight, or approximately 85 to approximately 90% by weight, based on the total weight of the base hair coloring composition.

[0124] In other embodiments, the total quantity (combined quantity) of surfactants, water-soluble organic solvents and water in the hair coloring base composition is at least 60% by weight, at least 65% by weight, at least 70% by weight, at least 75% by weight, at least 80% by weight, or at least 85% by weight, based on the total weight of the hair coloring base composition.

[0125] In various embodiments, the hair coloring composition may include one or more fatty compounds other than fatty alcohols, preferably one or more non-silicone fatty compounds. The term “non-silicone fatty compound” refers to a fatty compound that does not contain silicon (Si) atoms.Non-limiting examples of non-silicone fatty compounds include oils, mineral oils, fatty acids, fatty alcohol derivatives, fatty acid derivatives (such as alkoxylated fatty acids or polyethylene glycol esters of fatty acids or propylene glycol esters of fatty acids or butylene glycol esters of fatty acids or neopentyl glycol and fatty acid esters or polyglycerol / glycerol esters of fatty acids or glycol diesters or ethylene glycol and fatty acid diesters or fatty acid and fatty alcohol esters, short-chain alcohol and fatty acid esters), fatty alcohol esters, hydroxy-substituted fatty acids, waxes, triglyceride compounds, lanolin, and mixtures thereof. Non-limiting examples of fatty acids, fatty alcohol derivatives and fatty acid derivatives are listed in the International Cosmetic Ingredient Dictionary, Sixteenth Edition, 2016.A more comprehensive but not exhaustive list of fatty compounds is provided later, under the heading "Fatty compounds other than fatty alcohols".

[0126] In various embodiments, one or more fatty compounds other than fatty alcohols are liquid fatty compounds, also called "oils." The term "oil" is used here to refer to an organic compound other than a fatty alcohol that is insoluble in water at normal temperature (25 °C) and atmospheric pressure (760 mmHg), namely, it has a solubility in water of less than 5% by weight, or less than 1% by weight, or less than 0.1% by weight. The oils have in their structure a chain of at least two siloxane groups or at least one hydrocarbon chain comprising at least six carbon atoms. Furthermore, the oils are generally soluble in organic solvents under the same conditions of temperature and pressure, for example, in chloroform, ethanol, benzene, or decamethylcyclopentasiloxane. In addition, the oils are liquid at ordinary temperature (25 °C) and atmospheric pressure (760 mmHg).Oils preferably do not contain carboxylic acid functions, namely they do not contain -COOH or -COO- groups. As described throughout this disclosure, fatty alcohols are independent of fatty compounds and oils; that is, even if a fatty alcohol is present in the compositions of this disclosure, the compositions may nevertheless be free or substantially free of fatty compounds from oils (since fatty alcohols are not included in the definition of fatty compounds and oils).

[0127] The total amount of one or more fatty compounds in the hair coloring compositions, if any, will vary. Nevertheless, in various embodiments, the total amount of fatty compounds is from approximately 0.1 to approximately 20% by weight, based on the total weight of the hair coloring composition. In other embodiments, the total amount of fatty compounds is from approximately 0.1 to approximately 15% by weight, approximately 0.1 to approximately 10% by weight, and approximately 0.1 to approximately 5% by weight, based on the total weight of the base hair coloring composition.

[0128] The total amount of one or more oils (a type of fatty compound) in the hair coloring base compositions, if any, will vary. Nevertheless, in various embodiments, the total amount of oil is from about 0.1 to about 18% by weight, about 0.1 to about 15% by weight, about 0.1 to about 10% by weight, about 0.1 to about 5% by weight, about 0.1 to about 3% by weight, about 0.1 to about 2% by weight, based on the total weight of the hair coloring base composition.In other embodiments, the hair coloring compositions do not comprise more than 18% by weight of oils, not more than 15% by weight of oils, not more than 12% by weight of oils, not more than 10% by weight of oils, not more than 8% by weight of oils, not more than 5% by weight of oils, not more than 4% by weight of oils, not more than 3% by weight of oils, not more than 2% by weight of oils, not more than 1% by weight of oil, or may be free of or substantially free of oils.

[0129] In various embodiments, the hair coloring base compositions are free or substantially free of mineral oil, polybutene, hydrogenated polyisobutene, hydrogenated polydecene, polydecene, squalane, petrolatum, petroleum jelly (including liquid petroleum jelly), paraffin (including liquid paraffin), or isoparaffins, or mixtures thereof. In other embodiments, the hair coloring base compositions are at least free of petrolatum, petroleum jelly (including liquid petroleum jelly), paraffin (including liquid paraffin), isoparaffins, or mixtures thereof.

[0130] In various embodiments, the basic hair-coloring composition includes one or more cationic conditioning polymers. Non-limiting examples include cationic polysaccharide derivatives, cationic gum derivatives, diallyldimethyl ammonium chloride polymer derivatives, methacrylamidopropyltrimethylammonium chloride polymer derivatives, cationic cellulose derivatives, quaternized hydroxyethyl cellulose, cationic starch derivatives, cationic guar gum derivatives (hydroxypropyl guar hydroxypropyltrimonium chloride), acrylamide and dimethyldiallyammonium chloride copolymers, polyquatemiums, and mixtures thereof. A more comprehensive but non-limiting list of cationic conditioning polymers is included later under the heading "Cationic Conditioning Polymers".

[0131] The total amount of the cationic conditioning polymer(s), if present, will vary. However, in various embodiments, the total amount of one or more cationic conditioning polymers in the base hair coloring composition is approximately 0.01 to approximately 10% by weight, approximately 0.01 to approximately 5% by weight, approximately 0.01 to approximately 3% by weight, approximately 0.1 to approximately 10% by weight, approximately 0.1 to approximately 5% by weight, or approximately 0.1 to approximately 3% by weight, based on the total weight of the base hair coloring composition.

[0132] In various embodiments, the basic hair coloring composition includes one or more thickening agents. Non-limiting examples of thickening agents include crosslinked polyacrylate polymers or polyacrylate crosslinked polymers, cationic acrylate copolymers, anionic acrylic or carboxylic acid polymers, polyacrylamide polymers, polysaccharides, gums, polyquatemiums, vinylpyrrolidone homopolymers / copolymers, a C8-24 hydroxyl-substituted aliphatic acid, a C8-24 conjugated aliphatic acid, sugar fatty esters, polyglyceryl esters, and mixtures thereof. A more comprehensive but non-limiting list of thickening agents is included later under the heading "Thickening Agents".

[0133] The total quantity of one or more thickening agents, if present, will vary. For example, in various embodiments, the basic hair coloring composition includes one or more thickening agents in an amount of approximately 0.01 to approximately 10% by weight, approximately 0.01 to approximately 8% by weight, approximately 0.01 to approximately 5% by weight, approximately 0.01 to approximately 3% by weight, approximately 0.1 to approximately 10% by weight, approximately 0.1 to approximately 8% by weight, approximately 0.1 to approximately 5% by weight, or approximately 0.1 to approximately 3% by weight, based on the total weight of the basic hair coloring composition.

[0134] The hair coloring base composition may optionally include one or more additional conditioning agents. For example, hair coloring base compositions may optionally include one or more glyceryl ethers as conditioning agent(s). Non-limiting examples of glyceryl ethers include glyceryl butyl ether, glyceryl isobutyl ether, glyceryl tert-butyl ether, glyceryl pentyl ether, glyceryl isopentyl ether, glyceryl hexyl ether, glyceryl isohexyl ether, glyceryl heptyl ether, glyceryl octyl ether, glyceryl ethylhexyl ether, glyceryl nonyl ether, glyceryl decyl ether, glyceryl isodecyl ether, glyceryl lauryl ether, glyceryl myristyl ether, glyceryl palmitylic ether, glyceryl stearyl ether and glyceryl behenyl ether and mixtures thereof.Particularly useful glyceryl ethers also include glyceryl butyl ether, glyceryl isobutyl ether, glyceryl tert-butyl ether, glyceryl pentyl ether, glyceryl isopentyl ether, glyceryl hexyl ether, glyceryl isohexyl ether, glyceryl heptyl ether, glyceryl octyl ether, glyceryl ethylhexyl ether, glyceryl nonyl ether, glyceryl decyl ether, glyceryl isodecyl ether, glyceryl lauryl ether, and mixtures thereof. In some cases, glyceryl lauryl ether is particularly useful.

[0135] The total amount of one or more conditioning agents, if any, may vary but is typically from about 0.1 to about 15% by weight, based on the total weight of the base hair coloring composition. The total amount of one or more conditioning agents may be from about 0.1 to about 10% by weight, from 0.1 to about 5% by weight, from about 0.5 to about 15% by weight, from about 0.5 to about 10% by weight, from about 0.5 to about 5% by weight, or from about 1 to about 10% by weight, or from about 1 to about 5% by weight, based on the total weight of the base hair coloring composition.

[0136] The hair coloring compositions of this disclosure (hair coloring base compositions, developer compositions, and / or ready-to-use hair coloring compositions) may optionally include (or optionally exclude) one or more miscellaneous ingredients. Miscellaneous ingredients are ingredients that are compatible with the hair treatment composition but that do not do not disrupt or materially affect the basic and novel properties of the compositions. Non-limiting examples of ingredients include preservatives, fragrances, pH adjusters, salts, chelating agents, buffers, antioxidants, flavonoids, vitamins, botanical extracts, UV filtering agents, proteins, protein hydrolysates and / or isolates, fillers, composition colorants, cationic polymers, thickening agents, etc. In various embodiments, miscellaneous ingredients are selected from preservatives, fragrances, pH adjusters, salts, chelating agents, buffers, composition colorants, and mixtures thereof. For the purposes of this disclosure, a "composition colorant" is a compound that colors the composition but does not have an appreciable coloring effect on hair.In other words, the colorant is included to provide color to the formula for aesthetic appeal; it is not intended to impart coloring properties to the hair. Styling gels, for example, can be found in a variety of different colors (e.g., light blue, light pink, etc.); however, applying styling gel to hair does not change the hair color.

[0137] The total quantity of one or more miscellaneous ingredients, if any, will vary. However, in various embodiments, the compositions of this disclosure (hair coloring base compositions, developer compositions, and / or ready-to-use hair coloring compositions) include, where applicable, from about 0.001 to about 10% by weight of one or more miscellaneous ingredients. In other embodiments, the compositions of this disclosure include approximately 0.001 to approximately 5% by weight, approximately 0.001 to approximately 3% by weight, approximately 0.01 to approximately 10% by weight, approximately 0.01 to approximately 5% by weight, approximately 0.01 to approximately 3% by weight, approximately 0.1 to approximately 10% by weight, approximately 0.1 to approximately 5% by weight, or approximately 0.1 to approximately 3% by weight of one or more miscellaneous ingredients.

[0138] In various embodiments, the basic hair coloring composition comprises or consists of:

[0139] (a) of 2-methoxymethyl-P-phenylenediamine, and optionally one or more additional oxidative dye precursors;

[0140] (b) one or more couplers; and

[0141] (c) 3% by weight or less, preferably 2.5% by weight or less, in a manner more preferably 2% by weight or less, even more preferably 1.5% by weight or less of one or more alkalizing agents, wherein the one or more alkalizing agents are preferably monoethanolamine;

[0142] (d) about 0.1 to about 10% by weight, preferably about 0.1 to about 5% by weight, preferably about 0.5 to about 3% by weight of a or several fatty alcohols comprising 12 to 24 carbon atoms, preferably selected from cetyl alcohol, stearyl alcohol, cetearyl alcohol, behenyl alcohol, lauryl alcohol, myristic or myristyl alcohol, arachidyl alcohol, lignoceryl alcohol, oleyl alcohol and mixtures thereof;

[0143] (e) about 5 to about 40% by weight, preferably about 10 to about 30% by weight, more preferably about 15 to about 30% by weight of one or more surfactants, preferably one or more nonionic surfactants and optionally one or more anionic surfactants, in particular, wherein the one or more nonionic surfactants are selected from oxyethylenated amides, oxyethylenated fatty alcohols, and sequenced (polycondensed) copolymer surfactants of ethylene oxide and propylene oxide, and a mixture thereof, more preferably selected from oxyethylenated amides (e.g., PEG-4 rapeseed amide), oxyethylenated fatty alcohols (e.g., deceth-3), sequenced (polycondensed) copolymer surfactants of ethylene oxide and propylene oxide (e.g., Poloxamer 338), or a a combination of these.

[0144] (f) about 10 to about 40% by weight, preferably about 15 to about 35% by weight, more preferably about 15 to about 30% by weight of one or more water-soluble organic solvents, in particular, one or more water-soluble organic solvents selected from glycerin, mono-alcohols, polyols (polyhydric alcohols), glycols and a mixture thereof, preferably, the one or more water-soluble solvents are selected from glycerin, propylene glycol, butylene glycol, pentylene glycol, dipropylene glycol, hexylene glycol, ethanol, isopropanol, t-butyl alcohol, and a mixture thereof;

[0145] (g) about 25 to about 60% by weight, preferably about 30 to about 55% by weight, preferably about 35 to about 50% by weight of water;

[0146] wherein (e), (f) and (g) are in quantities such that a combined quantity of (e), (f) and (g) constitutes at least 70% by weight, preferably at least 75% by weight, more preferably at least 80% by weight and even more preferably at least 83% by weight of the basic hair coloring composition0;

[0147] (h) less than 15% by weight, preferably less than 10% by weight, in a way more preferred less than 5% by weight of oils;

[0148] (i) optionally, about 0.1 to about 10% by weight, preferably about 0.1 to about 5% by weight, more preferably about 0.1 to about 3% by weight of one or more reducing agents, for example selected from potassium metabisulfite, potassium sulfite, sodium hydrosulfite, sodium metabisulfite, sodium sulfite, sodium bisulfite, thioglycolic acid, thiolactic acid, dehydroascorbic acid, a salt of these, and a mixture of these, of preferably thioglycolic acid, thiolactic acid, salts thereof, and mixtures thereof; and

[0149] (j) optionally, about 0.01 to about 10% by weight, preferably about 0.01 at 5% by weight, more preferably about 0.1 to about 5% by weight of one or more miscellaneous ingredients, for example, preservatives, perfumes, pH adjusters, salts, chelating agents, buffers, antioxidants, flavonoids, vitamins, botanical extracts, UV filtering agents, proteins, protein hydrolysates and / or isolates, fillers, compositional colorants, cationic polymers, thickening agents, and mixtures thereof;

[0150] All percentages by weight are based on the total weight of the base composition for hair coloring.

[0151] The pH of the hair coloring base composition will vary. However, the pH is typically such that when mixed with a developer composition to form a ready-to-use hair coloring composition, the ready-to-use hair coloring composition has a desired pH, for example, a pH of about 6 to about 8, preferably about 6.1 to about 7.9, more preferably about 6.2 to about 7.8. Developer compositions are typically acidic, for example, having a pH of 2 to about 6. Consequently, to obtain a ready-to-use hair coloring composition by mixing the developer composition with the hair coloring base composition, the hair coloring base composition must have a low pH, for example, about 7 to about 10, preferably about 7.5 to about 9.5, more preferably about 8 to less than 9.5.The pH of the hair coloring base composition, the pH of the developer composition, and the mixing ratio of the hair coloring base composition to the developer composition can influence the final pH of the ready-to-use hair coloring composition.

[0152] In various embodiments, the pH of the base composition for hair coloring is from about 7 to about 10, from about 7.5 to about 10, from about 8 to about 10, from about 8.5 to about 10, from about 7 to about 9.5, from about 7.5 to about 9.5, from about 8 to about 9.5, from about 8.5 to about 9.5, from about 7 to about 9, from about 7.5 to about 9, or from about 8 to about 9.

[0153] In various embodiments, the basic hair coloring compositions are free or substantially free of resorcinol and / or resorcinol derivatives. The hair color modifying compositions may, in some embodiments, be free or substantially free of para-phenylenediamines (other than 2-methoxymethyl-p-phenylenediamine), resorcinol, and / or resorcinol derivatives. In some embodiments, the com Hair color modifying compositions may be free or substantially free of one or more of the following: mineral oil, ammonia, ammonium hydroxide, ammonium thiolactate, para-phenylenediamines (other than 2-methoxymethyl-p-phenylenediamine), resorcinol, and / or resorcinol derivatives. In other embodiments, hair color modifying compositions may be free or substantially free of mineral oil, ammonia, ammonium hydroxide, ammonium thiolactate, para-phenylenediamines (other than 2-methoxymethyl-p-phenylenediamine), resorcinol, and / or resorcinol derivatives.

[0154] As noted, the base hair coloring compositions of this disclosure can be combined with a developer composition to form a ready-to-use hair coloring composition having a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8. The final pH of a ready-to-use hair coloring composition will depend on the content, pH, etc., of the base hair coloring composition.In various embodiments, the basic hair coloring compositions of this disclosure are such that they form a ready-to-use hair coloring composition having a pH of about 6 to about 8, about 6.1 to about 7.9, or about 6.2 to about 7.8, when mixed with a developer composition comprising hydrogen peroxide in a weight ratio of about 1:5 to about 5:1 (hair coloring composition developer composition). For example, basic hair coloring compositions are such that they form a ready-to-use hair coloring composition having a pH of about 6 to about 8, about 6.1 to about 7.9, or about 6.2 to about 7.8, when mixed with a developer composition comprising hydrogen peroxide in a weight ratio of about 1:1 (hair coloring composition developer composition), in which the developer composition consists of: .

[0155] (a) about 7.5% by weight of hydrogen peroxide;

[0156] (b) about 82% by weight of water;

[0157] (c) about 0.5% by weight of glycerin;

[0158] (d) about 2.3% by weight of cetearyl alcohol;

[0159] (e) approximately 0.9% by weight of trideceth-2 carboxamide MEA;

[0160] (f) approximately 0.6% by weight of ceteareth-25; and

[0161] in which all weight percentages for the components of the developer composition are based on the total weight of the developer composition.

[0162] In various embodiments, this disclosure relates to a process comprising or consisting of:

[0163] (i) obtaining the basic hair coloring composition according to the present di- popularization;

[0164] (ii) obtaining a developer composition comprising:

[0165] (a) one or more oxidizing agents; and

[0166] (b) water;

[0167] (iii) mixing the base hair dye composition of (i) and the developer composition of (ii) in a weight ratio of about 1:5 to about 5:1, preferably about 1:3 to about 3:1, more preferably about 1:1, to form a ready-to-use hair dye composition having a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8; and

[0168] (iv) the application of the ready-to-use hair coloring composition to hair, preferably facial hair, more preferably beard or moustache hair;

[0169] (v) allowing the ready-to-use hair coloring composition to to remain on the hairs for a period of time, wherein the period of time is at least 1 minute but less than 30 minutes, preferably less than 15 minutes, more preferably less than 10 minutes, or even less than 5 minutes; and

[0170] (vi) after the time period has elapsed, rinsing the ready-to-use hair coloring composition to remove it from the hair.

[0171] The hair coloring base compositions according to this disclosure may be mixed at or near the time of use with a developer composition (also called an oxidizing composition) comprising at least one oxidizing agent. The oxidizing agent may be, for example, selected from peroxides, persulfates, perborates, percarbonates, alkali metal bromates, ferricyanides, peroxygenated salts, or a mixture thereof. Oxidizing agents that may also be used include at least one redox enzyme such as laccases, peroxidases, and 2-electron oxidoreductases, such as uricase, when appropriate in the presence of their respective donor or cofactor. Oxygen in the air may also be an oxidizing component.

[0172] In some embodiments, the oxidizing agent is hydrogen peroxide. In various embodiments, the hydrogen peroxide may be present in an aqueous solution with a concentration ranging from 1 to 40 volumes, such as 5 to 40 volumes, 5 to 30 volumes, or 5 to 20 volumes. In some embodiments, the oxidizing component is a 20 V, 30 V, or 40 V hydrogen peroxide developer composition.

[0173] In other embodiments, the oxidizing agent is a persulfate and / or a monopersulfate such as, for example, potassium persulfate, sodium persulfate, Ammonium persulfate, as well as mixtures thereof. In some embodiments, the oxidizing agents are chosen from hydrogen peroxide, potassium persulfate, sodium persulfate, or mixtures thereof.

[0174] The oxidizing agent may, in various embodiments, be present in the developer composition in an amount ranging from about 0.05% to about 50% by weight, such as from about 0.1% to about 30% by weight, from about 0.1% to about 20% by weight, from about 1% to about 20%, from about 1% to about 15%, from about 1% to about 12%, from about 3% to about 20%, from about 3% to about 15%, from about 3% to about 12%, from about 5% to about 20%, from about 5% to about 15%, from about 5% to about 12%, from about 7% to about 20%, from about 7% to about 15%, from about 7% to about 12%, from about 9% to about 20%, from about 9% to about 15%, or from about 9% to about 12% by weight, based on the total weight of the developer composition.

[0175] The developer composition may contain at least one solvent, for example water, water-soluble organic solvents, or mixtures thereof. Non-limiting examples of water-soluble organic solvents suitable for use in developer formulations, alone or in mixtures with water, include, but are not limited to, ethanol, isopropyl alcohol, propanol, benzyl alcohol, phenylethyl alcohol, glycols and glycol ethers, such as propylene glycol, hexylene glycol, monomethyl, monoethyl or monobutyl ethylene glycol ether, propylene glycol and its ethers, such as monomethyl propylene glycol ether, alkyl ethers of butylene glycol, dipropylene glycol, diethylene glycol, such as monoethyl and monobutyl diethylene ether, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, propane diol, glycerin,hydrocarbons such as linear-chain hydrocarbons, mineral oil, polybutene, hydrogenated polyisobutene, hydrogenated polydecene, polydecene, squalane, petrolatum, isoparaffins, or mixtures thereof.

[0176] Developer compositions may optionally include other components typically used in developer compositions, such as, for example, thickening agents, chelators, fatty substances, ceramides, pH correcting agents, preservatives, perfumes, surfactants, etc.

[0177] The developer composition may be in the form of a powder, gel, liquid, foam, lotion, cream, mousse, or emulsion. In some embodiments, the developer composition is aqueous and is in the form of a liquid, cream, or emulsion. In other embodiments, the developer composition is anhydrous or substantially anhydrous.

[0178] In various embodiments given by way of example, the composition of re The developer includes hydrogen peroxide. For example, hydrogen peroxide may be present in an amount of at least approximately 1% by weight, based on the total weight of the developer composition. In other embodiments, hydrogen peroxide is present in an amount ranging from approximately 0.1% to 80% by weight, such as approximately 1.0% to 75% by weight, or approximately 2% to 10% by weight, based on the total weight of the developer composition. In other embodiments given by way of example, hydrogen peroxide may be present in the developer composition in an amount ranging from approximately 2% to 25% by weight, such as approximately 4% to 20% by weight, approximately 6% to 15% by weight, or approximately 7% to 10%.

[0179] In variant embodiments, the developer composition is substantially anhydrous. The term “substantially anhydrous” means that the developer composition is either completely free of water or does not contain any appreciable amount of water, for example, not more than 5% by weight, or not more than 2% by weight, or not more than 1% by weight, based on the weight of the developer composition. It should be noted that this refers, for example, to bound water, such as the water of crystallization of salts or traces of water absorbed by the starting materials used in the preparation of the compositions according to the disclosure embodiments.

[0180] When the developer composition is substantially anhydrous, the developer composition may include at least one water-soluble organic solvent.Non-limiting examples include ethanol, isopropyl alcohol, propanol, benzyl alcohol, phenylethyl alcohol, glycols and glycol ethers, such as propylene glycol, hexylene glycol, monomethyl, monoethyl, or monobutyl ethylene glycol ether, propylene glycol and its ethers, such as monomethyl propylene glycol ether, alkyl ethers of butylene glycol, dipropylene glycol, and diethylene glycol, such as monoethyl and monobutyl diethylene ether, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, propane diol, glycerin, hydrocarbons such as linear-chain hydrocarbons, mineral oil, polybutene, hydrogenated polyisobutene, hydrogenated polydecene, polydecene, squalane, and petrolatum, isoparaffins, and mixtures thereof.

[0181] In a preferred embodiment, the developer composition includes:

[0182] (a) one or more oxidizing agents0;

[0183] - one or more surfactants; and

[0184] -water.

[0185] Developer compositions include one or more oxidizing agents present in sufficient quantity to develop a color when mixed with a hair coloring base composition. Non-limiting examples of agents Oxidizing agents include hydrogen peroxide, inorganic alkali metal peroxides (such as sodium periodate and sodium peroxide), organic peroxides (such as urea peroxide and melamine peroxide), inorganic perhydrate salts (such as alkali metal salts of perborates, percarbonates, perphosphates, persilicates, and persulfates), bromates, and mixtures thereof. In some cases, the developer composition includes hydrogen peroxide.

[0186] The total amount of one or more oxidizing agents in the developer composition may vary but is typically from about 0.5 to about 50% by weight, based on the total weight of the developer composition. In some cases, the total amount of one or more oxidizing agents is from about 0.5 to about 40% by weight, from about 1 to about 50% by weight, from about 1 to about 40% by weight, from about 1 to about 30% by weight, from about 1 to about 20% by weight, from about 1 to about 10% by weight, from about 5 to about 50% by weight, from about 5 to about 40% by weight, from about 5 to about 30% by weight, from about 5 to about 20% by weight, or from about 5 to about 10% by weight, based on the total weight of the developer composition.

[0187] The developer composition typically includes one or more surfactants. The one or more surfactants may be anionic, amphoteric, nonionic, zwitterionic, cationic, or a mixture thereof.

[0188] The total amount of one or more surfactants in the developer composition may vary but is typically from about 0.1 to about 25% by weight, based on the total weight of the developer composition for hair. The total amount of one or more surfactants may be from about 0.1 to about 20% by weight, from about 0.1 to about 15% by weight, from about 0.1 to about 10% by weight, from about 0.1 to about 5% by weight, from about 1 to about 25% by weight, from about 1 to about 20% by weight, from about 1 to about 15% by weight, from about 1 to about 10% by weight, or from about 1 to about 5% by weight, based on the total weight of the developer composition.

[0189] In some cases, the developer composition includes at least one or more nonionic surfactants. For example, developer compositions may include one or more nonionic surfactants selected from the group consisting of oxyethylenated amides, fatty alcohols, oxyethylenated fatty alcohols, and mixtures thereof. For example, the developer composition may include cetearyl alcohol (a fatty alcohol), trideceth-2 carboxamide MEA (an oxyethylenated amide), and ceteareth-25 (an oxyethylenated fatty alcohol), or a mixture thereof.

[0190] Non-limiting examples of non-ionic oxyethylenated amides are those of the following formula: R—[(OCH2CH2)n-OCH2]p-CO—N(R )—(CH2CH2O)n H

[0191] in which:

[0192] p denotes 0 or 1,

[0193] n denotes a number in the range of 1 to 10 and preferably from 1 to 6,

[0194] n' denotes a number in the range of 1 to 100 and preferably from 1 to 60,

[0195] R' denotes a hydrogen atom or a CH2CH2OH radical and preferably a hydrogen atom, and

[0196] R denotes an alkyl or alkenyl radical in C10-C30 and preferably in C12-C22.

[0197] Examples of these compounds include Amidet A15 sold by Kao (INCI name: Trideceth-2 carboxamide MEA), rEthomid HP 60 sold by Akzo Nobel (INCI name: PEG-50 Hydrogenated Palmamide), and Amidet N sold by Kao (INCI name: PEG-4 Rapeseedamide). In some cases, trideceth-2 carboxamide MEA may be particularly useful.

[0198] Non-limiting examples of fatty alcohols include linear and branched fatty alcohols, saturated or unsaturated, comprising from 6 to 30 carbon atoms and preferably from 8 to 30 carbon atoms, for example, cetyl alcohol, isostearyl alcohol, stearyl alcohol and mixtures thereof (cetylstearyl alcohol / cetearyl alcohol), octyldodecanol, 2-butyloctanol, 2-hexyldecanol, 2-undecylpentadecanol, oleyl alcohol, linolenylic alcohol, ricinoleyl alcohol, undecylenyl alcohol and linoleyl alcohol and mixtures thereof. In some cases, cetylstearyl / cetearyl alcohol may be particularly useful.

[0199] Non-limiting examples of oxyethylenated fatty alcohols include those comprising fewer than 10 OE motifs, preferably selected from oxyethylenated derivatives of saturated or unsaturated fatty alcohols, linear or branched, preferably linear, in C8-C30 and preferably in Ci2-C22, for example cetyl alcohol, oleyl alcohol, oleocetyl alcohol, lauryl alcohol, behenyl alcohol, cetearyl alcohol, stearyl alcohol and isostearyl alcohol, and mixtures thereof.

[0200] Oxyethylated fatty alcohols may have an average degree of ethoxylation of 2 to 29. Non-limiting examples of oxyethylated fatty alcohols having an average degree of ethoxylation of 2 to 29 are, for example, laureth-2, oleth-2, ceteareth-2, laneth-2, laureth-3, oleth-3, ceteareth-3, laureth-4, oleth-4, ceteareth-4, laneth-4, laureth-5, oleth-5, ceteareth-5, laneth-5, deceth-4, deceth-7, laureth-7, oleth-7, coceth-7, ceteth-7, ceteareth-7, Cl 1-15 pareth-7, laureth-9, oleth-9, ceteareth-9, laureth-10, oleth-10, beheneth-10, ceteareth-10, laureth-12, ceteareth-12, trideceth-12, ceteth-15, laneth-15, ceteareth-15, laneth-16, ceteareth-16, oleth-16, steareth-16, oleth-20, ceteareth-20, ceteareth-20, laneth-20, steareth-21, ceteareth-23, ceteareth-25, ceteareth-27, and a mixture of these.

[0201] Developer compositions may be free or substantially free of amphoteric surfactants and / or developer compositions may be free or essentially free of cationic surfactants and / or developer compositions may be free or essentially free of anionic surfactants.

[0202] The total amount of one or more nonionic surfactants in the developer composition may vary but is typically from about 0.1 to about 25% by weight, based on the total weight of the developer composition for hair. The total amount of one or more nonionic surfactants may be from about 0.1 to about 20% by weight, from about 0.1 to about 15% by weight, from about 0.1 to about 10% by weight, from about 0.1 to about 5% by weight, from about 1 to about 25% by weight, from about 1 to about 20% by weight, from about 1 to about 15% by weight, from about 1 to about 10% by weight, or from about 1 to about 5% by weight, based on the total weight of the developer composition.

[0203] The developer composition may include one or more water-soluble solvents. Non-limiting examples of water-soluble solvents include glycerin, alcohols (e.g., alcohols of the form Cl₃O, Cm₅, Cmo, or Cl₄), polyols, glycols, and mixtures thereof. Water-soluble solvents usable in the developer composition include those mentioned above with regard to the basic hair-staining composition, which, for the sake of brevity, are not repeated here.

[0204] The total amount of one or more water-soluble solvents in the developer composition, if any, may be from about 0.1 to about 25% by weight, from about 0.1 to about 20% by weight, from about 0.1 to about 15% by weight, from about 0.1 to about 10% by weight, or from about 0.1 to about 5% by weight, based on the total weight of the developer composition.

[0205] The viscosity of the developer composition is typically about 250 to about 2,000 cps at 25°C using a #4 spindle at 100 rpm. In some cases, the viscosity of the developer composition may be about 500 to about 2,500 cps, about 500 to about 2,000 cps, about 500 to about 1,500 cps, about 600 to about 1,300 cps, or about 650 to about 1,200 cps at 25°C using a #4 spindle at 100 rpm.

[0206] In one embodiment, the developer composition includes:

[0207] - approximately 1 to approximately 40% by weight, approximately 1 to approximately 25% by weight, or approximately 1 to about 15% by weight of one or more oxidizing agents, for example, one or more oxidizing agents selected from hydrogen peroxide, inorganic alkali metal peroxides (such as sodium periodate and sodium peroxide), organic peroxides (such as urea peroxide and melamine peroxide), inorganic perhydrate salts (such as alkali metal salts of perborates, per-carbonates, perphosphates, persilicates, persulfates), bromates, and a mixture of these, preferably hydrogen peroxide;

[0208] - approximately 0.1 to approximately 20% by weight, approximately 0.1 to approximately 10% by weight, or about 1 to about 10% by weight of one or more non-ionic surfactants, for example, one or more non-ionic surfactants selected from the group consisting of oxyethylenated amides, fatty alcohols, oxyethylenated fatty alcohols, and a mixture of these;

[0209] - optionally, about 0.1 to about 25% by weight, about 0.1 to about 15% by weight, or about 0.1 to about 10% by weight of one or more water-soluble solvents, for example, glycerin, alcohols, organic solvents, polyols, glycols, and mixtures thereof; and

[0210] - approximately 50 to approximately 92% by weight, approximately 60 to approximately 92% by weight, or approximately 75 to approximately 90% water by weight;

[0211] wherein the weight percentages are based on the total weight of the developer composition.

[0212] The hair dye base composition and the developer composition may be mixed in a ratio of approximately 1:5 to approximately 5:1 (hair dye base composition:developer composition). In some cases, the ratio is approximately 1:4 to approximately 4:1, approximately 1:3 to approximately 3:1, approximately 1:2 to approximately 2:1, or approximately 1:1 (hair dye base composition:developer composition).

[0213] As noted previously, the hair coloring base compositions of this disclosure can be combined with a developer composition to form a ready-to-use hair coloring composition having a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8. In various embodiments, the hair coloring base compositions of this disclosure are such that they form a ready-to-use hair coloring composition having a pH of about 6 to about 8, about 6.1 to about 7.9, or about 6.2 to about 7.8, when mixed with a developer composition comprising hydrogen peroxide.

[0214] In a preferred embodiment, the hair staining base compositions of this disclosure provide a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8 when mixed with a developer composition in a weight ratio of 1:1, wherein the developer composition consists of:

[0215] (a) about 7.5% by weight of hydrogen peroxide;

[0216] (b) about 82% by weight of water;

[0217] (c) about 0.5% by weight of glycerin;

[0218] (d) about 2.3% by weight of cetearyl alcohol;

[0219] (e) approximately 0.9% by weight of trideceth-2 carboxamide MEA;

[0220] (f) approximately 0.6% by weight of ceteareth-25; and

[0221] in which all the weight percentages for the components of the composition developer prices are based on the total weight of the developer composition.

[0222] A hair coloring base composition that provides a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8, when mixed with the specific developer composition described above, is not necessarily mixed with the specific developer composition described above during use. Instead, the specific developer composition described above may be used to evaluate the properties of the hair coloring base composition. In other words, the specific developer composition described above may be used in a process to determine whether a particular hair coloring base composition is capable of forming a ready-to-use hair coloring composition according to this disclosure.

[0223] This disclosure relates to a ready-to-use hair coloring composition comprising a combination of a hair coloring base composition according to this disclosure and a developer composition comprising an oxidizing agent. In various embodiments, the developer composition is selected from the developer compositions described throughout this disclosure. Non-limiting examples of oxidizing agents useful in developer compositions include hydrogen peroxide, inorganic alkali metal peroxides (such as sodium periodate and sodium peroxide), organic peroxides (such as urea peroxide and melamine peroxide), inorganic perhydrate salts (such as alkali metal salts of perborates, percarbonates, perphosphates, persilicates, persulfates), bromates, and mixtures thereof.In some embodiments, the oxidizing agent is a peroxo compound, preferably hydrogen peroxide. In various embodiments, the ready-to-use hair coloring composition comprises or consists of a hair coloring base composition and a developer composition combined in a weight ratio of approximately 5:1 to approximately 1:5, approximately 4:1 to approximately 1:4, approximately 3:1 to approximately 1:3, approximately 1:2 to approximately 2:1, or approximately 1:1.

[0224] In various embodiments, the ready-to-use hair coloring composition comprises or consists of a combination of a hair coloring base composition and a developer composition combined in a weight ratio of approximately 5:1 to approximately 1:5, approximately 4:1 to approximately 1:4, approximately 3:1 to approximately 1:3, approximately 1:2 to approximately 2:1, or approximately 1:1, in which

[0225] (I) the basic hair coloring composition comprises or is made up of°:

[0226] (a) of 2-methoxymethyl-P-phenylenediamine, and optionally one or more additional oxidative dye precursors;

[0227] (b) one or more couplers;

[0228] (c) less than 3% by weight, preferably less than 2.5% by weight, in a manner more preferably less than 2% by weight, even more preferably less than 1.5% by weight of one or more organic and / or mineral alkalizing agents, on the basis of the total weight of the basic hair coloring composition0;

[0229] (d) one or more fatty alcohols;

[0230] (e) one or more surfactants;

[0231] (f) optionally one or more water-soluble organic solvents;

[0232] (g) of water.

[0233] wherein (e), (f) and (g) are in quantities such that a combined quantity of (e), (f) and (g) constitutes at least 70% by weight, preferably at least 75% by weight, more preferably at least 80% by weight of the basic hair coloring composition; and

[0234] all percentages by weight are based on the total weight of the base composition for hair coloring; and

[0235] (II) The developer composition comprises or is made up of:

[0236] (a) one or more oxidizing agents, for example, one or more oxidizing agents selected from hydrogen peroxide, inorganic alkali metal peroxides (such as sodium periodate and sodium peroxide), organic peroxides (such as urea peroxide and melamine peroxide), inorganic perhydrate salts (such as alkali metal salts of perborates, percarbonates, per-phosphates, persilicates, persulfates), bromates, and a mixture of these, preferably hydrogen peroxide;

[0237] (b) one or more non-ionic surfactants, for example, of one or more ten non-ionic active ingredients selected from the group consisting of oxyethylenated amides, fatty alcohols, oxyethylenated fatty alcohols, and a mixture thereof;

[0238] -(c) optionally, one or more water-soluble solvents, for example, of glycerin, alcohols, organic solvents, polyols, glycols, and mixtures thereof; and

[0239] (d) about 50 to about 92% by weight, about 60 to about 92% by weight, or approximately 75 to approximately 90% water by weight;

[0240] wherein the weight percentages are based on the total weight of the developer composition; and

[0241] in which the hair coloring composition is ready for use:

[0242] (i) has a pH of about 6 to about 8, preferably of about 6.1 to about 7.9, of preferred method from about 6.2 to about 7.8;

[0243] (ii) comprises 2% by weight or less, preferably 1.5% by weight or less, more preferably 1% by weight or less, even more preferably 0.7% by weight or less of one or more alkalizing agents, in which the one or more alkalizing agents are preferably monoethanolamine; and

[0244] (iii) is optionally free or substantially free of ammonia, ammonium hydroxide and ammonium ions.

[0245] In other embodiments, the ready-to-use hair coloring composition comprises or consists of a combination of a hair coloring base composition and a developer composition combined in a weight ratio of approximately 5:1 to approximately 1:5, approximately 4:1 to approximately 1:4, approximately 3:1 to approximately 1:3, approximately 1:2 to approximately 2:1, or approximately 1:1, in which

[0246] (I) the basic hair coloring composition comprises or is made up of°:

[0247] (a) of 2-methoxymethyl-P-phenylenediamine, and optionally one or more additional oxidative dye precursors;

[0248] (b) one or more couplers; and

[0249] (c) 3% by weight or less, preferably 2.5% by weight or less, in a manner more preferably 2% by weight or less, even more preferably 1.5% by weight or less of one or more alkalizing agents, wherein the one or more alkalizing agents are preferably monoethanolamine;

[0250] (d) about 0.1 to about 10% by weight, preferably about 0.1 to about 5% by weight, more preferably about 0.5 to about 3% by weight of one or more fatty alcohols comprising 12 to 24 carbon atoms, preferably selected from cetyl alcohol, stearyl alcohol, cetearyl alcohol, behenyl alcohol, lauryl alcohol, myristic or myristyl alcohol, arachidyl alcohol, lignoceryl alcohol, oleyl alcohol and mixtures thereof;

[0251] (e) about 5 to about 40% by weight, preferably about 10 to about 30% by weight, more preferably about 15 to about 30% by weight of one or more surfactants, preferably one or more nonionic surfactants and optionally one or more anionic surfactants, in particular, wherein the one or more nonionic surfactants are selected from oxyethylenated amides, oxyethylenated fatty alcohols, and sequenced (polycondensed) copolymer surfactants of ethylene oxide and propylene oxide, and a mixture thereof, more preferably selected from oxyethylenated amides (e.g., PEG-4 rapeseed amide), oxyethylenated fatty alcohols (e.g., deceth-3), sequenced (polycondensed) copolymer surfactants of ethylene oxide and propylene oxide (e.g., Poloxamer 338), or a a combination of these.

[0252] (f) about 10 to about 40% by weight, preferably about 15 to about 35% by weight, preferably about 15 to about 30% by weight of one or more water-soluble organic solvents, in particular, one or more water-soluble organic solvents selected from glycerin, mono-alcohols, polyols (polyhydric alcohols), glycols and mixtures thereof, of Preferably, one or more water-soluble solvents are chosen from glycerin, propylene glycol, butylene glycol, pentylene glycol, dipropylene glycol, hexylene glycol, ethanol, isopropanol, t-butyl alcohol, and a mixture of these;

[0253] (g) about 25 to about 60% by weight, preferably about 30 to about 55% by weight, preferably about 35 to about 50% by weight of water;

[0254] wherein (e), (f) and (g) are in quantities such that a combined quantity of (e), (f) and (g) constitutes at least 70% by weight, preferably at least 75% by weight, more preferably at least 80% by weight and even more preferably at least 83% by weight of the basic hair coloring composition0;

[0255] (h) less than 15% by weight, preferably less than 10% by weight, in a way more preferred less than 5% by weight of oils;

[0256] (i) optionally, about 0.1 to about 10% by weight, preferably about 0.1 to about 5% by weight, more preferably about 0.1 to about 3% by weight of one or more reducing agents, for example selected from potassium metabisulfite, potassium sulfite, sodium hydrosulfite, sodium metabisulfite, sodium sulfite, sodium bisulfite, thioglycolic acid, thiolactic acid, dehydroascorbic acid, a salt thereof, and a mixture thereof, preferably thioglycolic acid, thiolactic acid, salts thereof, and mixtures thereof; and

[0257] (j) optionally, about 0.01 to about 10% by weight, preferably about 0.01 at 5% by weight, more preferably about 0.1 to about 5% by weight of one or more miscellaneous ingredients, for example, preservatives, perfumes, pH adjusters, salts, chelating agents, buffers, antioxidants, flavonoids, vitamins, botanical extracts, UV filtering agents, proteins, protein hydrolysates and / or isolates, fillers, compositional colorants, cationic polymers, thickening agents, and mixtures thereof;

[0258] wherein the weight percentages are based on the total weight of the base composition for hair coloring; and

[0259] (II) the developer composition comprises or is made up of:

[0260] (a) about 1 to about 40% by weight, about 1 to about 25% by weight, or about 1 to approximately 15% by weight of one or more oxidizing agents, for example, one or more oxidizing agents selected from hydrogen peroxide, inorganic alkali metal peroxides (such as sodium periodate and sodium peroxide), organic peroxides (such as urea peroxide and melamine peroxide), inorganic perhydrate salts (such as alkali metal salts of perborates, percarbonates, perphosphates, persilicates, persulfates), bromates, and a mixture of these, preferably hydrogen peroxide;

[0261] b) about 0.1 to about 20% by weight, about 0.1 to about 10% by weight, or about 1 to about 10% by weight of one or more nonionic surfactants, for example, one or more nonionic surfactants selected from the group consisting of oxyethylenated amides, fatty alcohols, oxyethylenated fatty alcohols, and a mixture thereof;

[0262] (c) optionally, about 0.1 to about 25% by weight, about 0.1 to about 15% by weight, or about 0.1 to about 10% by weight of one or more water-soluble solvents, for example, glycerin, alcohols, organic solvents, polyols, glycols, and mixtures thereof; and

[0263] (d) about 50 to about 92% by weight, about 60 to about 92% by weight, or approximately 75 to approximately 90% water by weight;

[0264] wherein the weight percentages are based on the total weight of the developer composition; and

[0265] in which the hair coloring composition is ready for use:

[0266] (i) has a pH of about 6 to about 8, preferably of about 6.1 to about 7.9, of preferred method from about 6.2 to about 7.8;

[0267] (ii) comprises 2% by weight or less, preferably 1.5% by weight or less, more preferably 1% by weight or less, even more preferably 0.7% by weight or less of one or more alkalizing agents, wherein the one or more alkalizing agents are preferably monoethanolamine; and

[0268] (iii) is optionally free or substantially free of ammonia, ammonium hydroxide and ammonium ions. Precursors of oxidative dyeing

[0269] Oxidative dyes are generally chosen from one or more oxidizing bases optionally combined with one or more couplers. By way of example, the oxidizing bases are chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases, and their addition salts.

[0270] Among the para-phenylenediamines that may be mentioned, for example, are para-phenylenediamine, para-toluenediamine, 2-chloro-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,5-dimethyl-para-phenylenediamine, N,N-dimethyl-para-phenylenediamine, N,N-diethyl-para-phenylenediamine, N,N-dipropyl-para-phenylenediamine, 4-amino-N,N-diethyl 1-3-methylaniline, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 4-N,N-bis(β-hydroxyethyl)amino-2-methylaniline, 4-N,N-bis(β-hydroxyethyl)amino-2-chloroaniline, 2-β-hydroxyethyl-para-phenylenediamine, 2-methoxymethyl-para-phenylenediamine, 2-fluoro-para-phenylenediamine, 2-isopropyl-para-phenylenediamine, N-(β-hydroxypropyl)-para-phenylenediamine, 2-hydroxymethyl-para-phenylenediamine, N,N-dimethyl-3-methyl-para-phenylenediamine, N-ethyl-N-(β-hydroxyethyl)-para-phenylenediamine, N-(β,γ-dihydroxypropyl)-para-phenylenediamine, N-(4'-aminophenyl)-para-phenylenediamine, N-phenyl-para-phenylenediamine, 2-β-hydroxyethyloxy-para-phenylenediamine, 2-β-acetylaminoethyloxy-para-phenylenediamine, N-(β-methoxyethyl)-para-phenylenediamine, 4-aminophenylpyrrolidine, 2-thienyl-para-phenylenediamine, 2-β-hydroxyethylamino-5-aminotoluene and 3-hydroxy-l-(4'-aminophenyl)pyrrolidine, and the addition salts of these with an acid.

[0271] Among the para-phenylenediamines mentioned above, para-phenylenediamine, para-toluenediamine, 2-isopropyl-para-phenylenediamine, 2-β-hydroxyethyl-para-phenylenediamine, 2-β-hydroxyethyloxy-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 2-chloro-para-phenylenediamine and 2-β-acetylaminoethyloxy-para-phenylenediamine, and the addition salts of these with an acid, are particularly preferred.

[0272] Among the bis(phenyl)alkylenediamines that may be mentioned, for example, are N,N'-bis(β-hydroxyethyl)-N,N'-bis(4'-aminophenyl)-1,3-diaminopropanol, N,N'-bis(β-hydroxyethyl)-N,N'-bis(4'-aminophenyl)ethylenediamine, N,N'-bis(4-aminophenyl)tetramethylenediamine, N,N'-bis(β-hydroxyethyl)-N,N'-bis(4-aminophenyl)tetramethylenediamine, N,N'-bis(4-methylaminophenyl)tetramethylenediamine, N,N'-bis(ethyl)-N,N'-bis(4'-amino-3'-methylphenyl)ethylenediamine and 1,8-bis(2,5-diaminophenoxy)-3,6-dioxaoctane, and the salts added to these.

[0273] Among the para-aminophenols that may be mentioned, for example, are para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 4-amino-3-chlorophenol, 4-amino-3-hydroxymethylphenol, the 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol, 4-amino-2-(β-hydroxyethylaminomethyl)phenol and 4-amino-2-fluorophenol, and the addition salts of these with an acid.

[0274] Among the ortho-aminophenols that may be mentioned, for example, are 2-aminophenol, 2-amino-5-methylphenol, 2-amino-6-methylphenol and 5-acetamido-2-aminophenol, and the addition salts of these.

[0275] Among the heterocyclic bases that can be mentioned, for example, are pyridine derivatives, pyrimidine derivatives and pyrazole derivatives.

[0276] Among the pyridine derivatives that may be mentioned are compounds such as 2,5-diaminopyridine, 2-(4-methoxyphenyl)amino-3-aminopyridine and 3,4-diaminopyridine, and the addition salts thereof. Other pyridine oxidation bases that are useful in this disclosure are the oxidation bases of 3-aminopyrazolo[l,5-a]pyridine or their addition salts described, for example, in French patent application FR 2 801 308. Examples that may be mentioned include pyrazolo[l,5-a]pyrid-3-ylamine, 2-acetylaminopyrazolo[l,5-a]pyrid-3-ylamine, 2-morpholin-4-ylpyrazolo[l,5-a]pyrid-3-ylamine, 3-aminopyrazolo[l,5-a]pyridine-2-carboxylic acid, 2-methoxypyrazolo[l,5-a]pyrid-3-ylamine, (3-aminopyrazolo[l,5-a]pyrid-7-yl)methanol, 2-(3-aminopyrazolo[l,5-a]pyrid-5-yl)ethanol, 2-(3-aminopyrazolo[l,5-a]pyrid-7-yl)ethanol, (3-aminopyrazolo[l,5-a]pyrid-2-yl)methanol, 3,6-diaminopyrazolo[l,5-a]pyridine, 3,4-Diaminopyrazolo[l,5-a]pyridine, pyrazolo[l,5-a]pyridine-3,7-diamine, 7-morpholin-4-ylpyrazolo[l,5-a]pyrid-3-ylamine, pyrazolo[l,5-a]pyridine-3,5-diamine, 5-morpholin-4-ylpyrazolo[l,5-a]pyrid-3-ylamine, 2-[(3-aminopyrazolo[l,5-a]pyrid-5-yl)(2-hydroxyethyl)amino]ethanol, 2-[(3-aminopyrazolo[l,5-a]pyrid-7-yl)(2-hydroxyethyl)amino]ethanol, 3-aminopyrazolo[l,5-a]pyridin-5-ol, 3-aminopyrazolo[l,5-a]pyridin-4-ol, 3-aminopyrazolo[l,5-a]pyridin-6-ol, 3-aminopyrazolo[l,5-a]pyridin-7-ol, 2-quadrature-hydroxyethoxy-3-aminopyrazolo[1,5-a]pyridine; 2-(4-dimethylpyrazinium-l-yl)-3-aminopyrazolo[l,5-a]pyridine; and their addition salts.

[0277] More specifically, the oxidation bases that are useful in this disclosure are chosen from among the 3-aminopyrazolo-[1,5-a]-pyridines and preferably substituted at carbon atom 2 by:

[0278] (a) a (di)(Ci-C6)(alkyl)amino group in which said alkyl group may be substituted by at least one hydroxy, amino, imidazolium group;

[0279] (b) a heterocycloalkyl group containing a chain of 5 to 7 links, and of 1 to 3 heteroatoms, potentially cationic, potentially substituted by one or more (Ci-C6-alkyls, such as a di(Cl-C4)alkylpiperazinium; or

[0280] (c) a (Ci-C6)alkoxy potentially substituted by one or more hydroxy groups such as α-hydroxyalkoxy, and their addition salts.

[0281] Among the pyrimidine derivatives that may be mentioned are compounds such as 2,4,5,6-tetraaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine, 2,5,6-triaminopyrimidine and their addition salts and their tautomeric forms, when a tautomeric equilibrium exists.

[0282] Among the pyrazole derivatives that may be mentioned are compounds such as 4,5-diamino-l-methyl-pyrazole, 4,5-diamino-l-(β-hydroxyethyl)pyrazole, 3,4-diamino-pyrazole, 4,5-diamino-l-(4'-chlorobenzyl)pyrazole, 4,5-diamino-l,3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyrazole, 4,5-diamino-l-methyl-3-phenylpyrazole, 4-amino-l,3-dimethyl-5-hydrazinopyrazole, l-benzyl-4,5-diamino-3-methyl-pyrazole, 4,5-diamino-3-tert-butyl-1-methylpyrazole, 4,5-diamino- l-tert-butyl-3-methylpyrazole, the 4,5-diamino- l-(β.-hydroxyethyl)-3-methylpyrazole, 4,5-diamino-l-ethyl-3-methylpyrazole, 4,5-diamino-l-ethyl-3-(4'-methoxyphenyl)pyrazole, 4,5-diamino-l-ethyl-3-hydroxymethylpyrazole, 4,5-diamino-3-hydroxymethyl-1-methylpyrazole, 4,5-diamino-3-hydroxymethyl-l-isopropylpyrazole, 4,5-diamino-3-methyl-1-isopropylpyrazole, 4-amino-5-(2'-aminoethyl)amino-l,3-dimethylpyrazole, 3,4,5-triaminopyrazole, l-methyl-3,4,5-triaminopyrazole, 3,5-diamino-l-methyl-4-methylaminopyrazole, 3,5-Diamino-4-(β-hydroxyethyl)amino-1-methylpyrazole, and its addition salts. 4,5-Diamino-1-(β-methoxyethyl)pyrazole may also be used.

[0283] Pyrazole derivatives that may also be mentioned include diamino-N,N-dihydropyrazolopyrazolones such as the following compounds and their addition salts: 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2-amino-3-ethylamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2-amino-3-isopropylamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2-amino-3-(pyrrolidin-1-yl)-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 4,5-diamino-1,2-dimethyl-1,2-dihydropyrazol-3-one, 4,5-diamino-1,2-diethyl-1,2-dihydropyrazol-3-one, 4,5-diamino-1,2-di-(2-hydroxyethyl)-1,2-dihydropyrazol-3-one, 2-amino-3-(2-hydroxyethyl)amino-6,7-dihydro-lH,5H-pyrazolo[l,2-a]pyrazol-l-one, 2-amino-3-dimethylamino-6,7-dihydro-lH,5H-pyrazolo[l,2-a]pyrazol-l-one, 2,3-diamino-5,6,7,8-tetrahydro-lH,6H-pyridazino[l,2-a]pyrazol-l-one, 4-amino-1,2-diethyl-5-(pyrrolidin-1 -yl)-1,2-dihydropyrazol-3-one, 4-amino-5-(3-dimethylaminopyrrolidin-1-yl)-1,2-diethyl-1,2-dihydropyrazol-3-one, 2,3-diamino-6-hydroxy-6,7-dihydro-1H,5H-pyrazolo[1H,2-α]pyrazol-1-one. 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1H,2-α]pyrazol-1-one and / or a salt thereof shall preferably be used. 4,5-diamino-1-(β-hydroxyethyl)pyrazole and / or 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1H,2-α]pyrazol-1-one and / or a salt thereof shall preferably be used as heterocyclic bases.

[0284] In various embodiments, the basic hair coloring composition is free or substantially free of resorcinol and / or resorcinol derivatives. Non-limiting examples of resorcinol derivatives that may be excluded from basic hair coloring compositions include 3,5-hydroxybenzyl, 3,5-dihydroxybenzylamine, 3,5-dihydroxyphenacetic acid, 2,4,5,6-tetraaminopyrimidine, p-phenylenediamine, p-toluylenediamine, 2,5-diaminoanisole, 2-chloro-o-phenylenediamine, N-ethyl-N-(2-hydroxyethyl)-p-phenylenediamine, N-butyl-N-sulfobutyl-p-phenylenediamine, N,N-bis-(2-hydroxyethyl)-p-phenylenediamine, N-methyl-p-phenylenediamine, N-(2-methoxyethyl)-p-phenylenediamine, N-(2-hydroxypropyl)-p-phenylenediamine, p-aminophenol, and combinations thereof. Couplers

[0285] Couplers include those conventionally used in oxidative hair coloring processes, for example, meta-aminophenols, meta-phenylenediamines and meta-diphenols, naphthols, mono- or polyhydroxylated naphthalene derivatives, and heterocyclic couplers such as, for example, indole derivatives, indoline derivatives, sesamol and its derivatives, pyridine derivatives, pyrazolotriazole derivatives, pyrazolones, indazoles, benzimidazoles, benzothiazoles, benzoxazoles, 1,3-benzodioxoles, quinolines, benzomorpholine derivatives, pyrazoloazole derivatives, pyr-roloazole derivatives, imidazoloazole derivatives, pyrazolopyrimidine derivatives, pyrazoline-3,5-dione derivatives, pyrrolo[3,2-d]oxazole derivatives, pyrazolo[3,4-d]thiazole derivatives, thiazoloazole S-oxide derivatives, derivatives of S,S-thiazoloazole dioxide, and the addition salts thereof.

[0286] Suitable color couplers include, for example, those conforming to the following general formula: 1 xx: 'T

[0287] wherein R1 is an unsubstituted hydroxy or amino group, or a hydroxy or amino group substituted by one or more hydroxyalkyl groups in C16; R3 and R5 are each independently hydrogen, hydroxy, amino, or amino groups substituted by an alkyl group in C16, an alkoxy group in C16, or a hydroxyalkyl group in C16; and R2, R4, and R6 are each independently an alkoxy group in C16, a hydroxyalkyl group in C16, or an alkyl group in C16. R3 and R4 may together form a methylenedioxy or ethylenedioxy group. Examples of such compounds include meta-derivatives such as phenols, meta-aminophenols, meta-phenylenediamines, and others, which may be unsubstituted, or substituted at the amino group or the benzene ring by alkyl, hydroxyalkyl, alkylamino, and other groups. Suitable couplers include m-aminophenol, 2,4-diaminotoluene, 4-amino, 2-hydroxytoluene, phenyl methyl pyrazolone, 3,4-methylenedioxyphenol, 3,4-methylenedioxy-l-[(beta-hydroxyethyl)amino]benzene,l-methoxy-2-amino-4-[(beta-hydroxyethyl)amino]benzene, l-hydroxy-3-(dimethylamino)benzene, 6-methyl-l-hydroxy-3[(beta-hydroxyethyl)amino]benzene, 2,4-dichloro-l-hydroxy-3-aminobenzene, l-hydroxy-3-(diethylamino)benzene, l-hydroxy-2-methyl-3-aminobenzene, 2-chloro-6-methyl-l-hydroxy-3-aminobenzene, 1,3-diaminobenzene, 6-methoxy-l,3-diaminobenzene, 6-hydroxyethoxy-1,3-diaminobenzene, 6-methoxy-5-ethyl-1,3-diaminobenzene, 6-ethoxy-1,3-diaminobenzene, l-bis(beta-hydroxyethyl)amino-3-aminobenzene, the 2-methyl-1,3-diaminobenzene, 6-methoxy-l-amino-3-[(beta-hydroxyethyl)amino]-benzene, 6-(beta-aminoethoxy)-1,3-diaminobenzene, 6-(beta-hydroxyethoxy)-l-amino-3-(methylamino)benzene, 6-carboxymethoxy-1,3-diaminobenzene, 6-ethoxy-l-bis(beta-hydroxyethyl)amino-3-aminobenzene, 6-hydroxyethyl-1,3-diaminobenzene, l-hydroxy-2-isopropyl-5-methylbenzene, , 1,3-Dihydroxybenzene, 2-chloro-1,3-dihydroxybenzene, 2-methyl-1,3-dihydroxybenzene, 4-chloro-1,3-dihydroxybenzene, 5,6-dichloro-2-methyl-1,3-dihydroxybenzene, L-hydroxy-3-aminobenzene, L-hydroxy-3-(carbamoylmethylamino)benzene, 6-Hydroxybenzomorpholine, 4-methyl-2,6-dihydroxypyridine, 2,6-dihydroxypyridine, 2,6-diaminopyridine, 6-aminobenzomorpholine, L-phenyl-3-methyl-5-pyrazolone, 1-Hydroxynaphthalene, 1,7-dihydroxynaphthalene, 1,5-dihydroxynaphthalene, 5-amino-2-methylphenol, 4-Hydroxyindole, 4-Hydroxyindoline, 6-hydroxyindole, 6-hydroxyindoline, 2,4-diaminophenoxyethanol, and mixtures thereof.

[0288] Other couplers may be chosen, for example, from the 2,4-Diamino-l-([3-hydroxyethyloxy)benzene, 2-methyl-5-aminophenol, 5-N-([3-hydroxyethyl)amino-2-methylphenol, 3-aminophenol, 1,3-dihydroxybenzene, l,3-dihydroxy-2-methylbenzene, 4-chloro-1,3-dihydroxybenzene, 2,4-diamino l-([3-hydroxyethyloxy)benzene, 2-amino-4-([3-hydroxyethylamino)-l-methoxybenzene, 1,3-diaminobenzene, l,3-bis(2,4-diaminophenoxy)propane, sesamol, l-amino-2-methoxy-4,5-methylenedioxybenzene, α-naphthol, 6-hydroxyindole, 4-hydroxyindole, 4-hydroxy-N-methylindole, the 6-hydroxyindoline, 2,6-dihydroxy-4-methylpyridine, 1H-3-methylpyrazol-5-one, 1-phenyl-3-methylpyrazol-5-one, 2-amino-3-hydroxypyridine, 3,6-dimethylpyrazolo[3,2-c]-1,2,4-triazole, 2,6-dimethylpyrazolo[1,5-b]-1,2,4-triazole, 6-methylpyrazolo[1,5-a]-benzimidazole, and acid addition salts thereof.

[0289] In one embodiment, the couplers include resorcinol, 1-naphtol, 2-methylresorcinol, 4-amino-2-hydroxytoluene, m-aminophenol, 2,4-diaminophenoxyethanol, phenyl methyl pyrazolone, rhydroxybenzomorpholine, 2-methyl-5-hydroxyethylaminophenol, 6-hydroxyindole, 2-amino-3-hydroxypyridine, 5-amino-6-chloro-o-cresol, 4-chlororesorcinol, their salts, and mixtures thereof.

[0290] In general, the acid addition salts of the oxidation bases and couplers can be chosen from hydrochlorides, hydrobromides, sulfates, tartrates, lactates and acetates. Non-ionic surfactants

[0291] Non-ionic surfactants are well-known compounds in themselves (see, for example, in this regard, the "Handbook of Surfactants" by MR Porter, Blackie & Son publishers (Glasgow and London), 1991, pages 116-178).

[0292] The nonionic surfactant may be, for example, chosen from alcohols, alpha- diols, alkylphenols and fatty acid esters, these compounds being ethoxylated, propoxylated or glycerolated and comprising at least one fatty chain including, for example, 8 to 18 carbon atoms, the number of ethylene oxide or propylene oxide groups ranging from 2 to 50, and the number of glycerol groups from 1 to 30. Maltose derivatives can also be mentioned.Other examples include, but are not limited to, copolymers of ethylene oxide and / or propylene oxide; condensates of ethylene oxide and / or propylene oxide with fatty alcohols; polyethoxylated fatty amides comprising, for example, 2 to 30 moles of ethylene oxide; polyglycerol fatty amides comprising, for example, 1.5 to 5 glycerol groups, such as 1.5 to 4; ethoxylated fatty acid esters of sorbitan comprising 2 to 30 moles of ethylene oxide; ethoxylated oils of vegetable origin; fatty acid esters of sucrose; fatty acid esters of polyethylene glycol; mono- or diesters of polyethoxylated fatty acids of glycerol; alkyl polyglycosides (C6-C24); N-alkylglucamine derivatives (C6-C24), amine oxides such as alkylamine oxides (C10-C14) or N-acylaminopropylmorpholine oxides (C10-C14) and mixtures thereof.

[0293] Nonionic surfactants may preferably be selected from polyoxyalkylated or polyglycerolated nonionic surfactants. The oxyalkylene motifs are more particularly oxyethylene or oxypropylene motifs, or a combination thereof, and are preferably oxyethylene motifs.

[0294] Examples of nonionic oxyalkylated surfactants that may be mentioned include: oxyalkylated (C8-C24) alkylphenols, saturated or unsaturated, linear or branched; oxyalkylated C8-C30 alcohols, saturated or unsaturated, linear or branched; oxyalkylated C8-C30 amides; esters of saturated or unsaturated, linear or branched C8-C30 acids and polyethylene glycols; polyoxyalkylated esters of saturated or unsaturated, linear or branched C8-C30 acids and sorbitol; saturated or unsaturated, oxyalkylated vegetable oils; condensates of ethylene oxide and / or propylene oxide, among others, alone or in mixtures.

[0295] Surfactants preferably contain a number of moles of ethylene oxide and / or propylene oxide between 2 and 100 and even better between 2 and 50.

[0296] In accordance with a preferred embodiment of the invention, the oxyalkylated non-ionic surfactants are selected from C8-C30 oxyethylened alcohols.

[0297] Examples of ethoxylated fatty alcohols (or C8-C30 alcohols) that may be mentioned include ethylene oxide adducts with lauryl alcohol, in particular those containing 9 to 50 oxyethylene groups and more particularly those containing 10 to 25 oxyethylene groups (laureth-10 to laureth-25); ethylene oxide adducts with behenyl alcohol, in particular those containing 9 to 50 groups oxyethylene (Beheneth-9 to Beheneth-50); ethylene oxide adducts with cetearyl alcohol (mixture of cetyl alcohol and stearyl alcohol), in particular those containing 10 to 30 oxyethylene groups (Ceteareth-10 to Ceteareth-30); ethylene oxide adducts with cetyl alcohol, in particular those containing 10 to 30 oxyethylene groups (Ceteth-10 to Ceteth-30); ethylene oxide adducts with stearyl alcohol, in particular those containing 10 to 30 oxyethylene groups (steareth-10 to steareth-30); ethylene oxide adducts with isostearyl alcohol, in particular those containing 10 to 50 oxyethylene groups (Isosteareth-10 to Isosteareth-50); and mixtures thereof.

[0298] As examples of non-ionic polyglycerol surfactants, C8-C40 polyglycerol alcohols are preferred.

[0299] In particular, C8-C40 polyglycerol alcohols correspond to the following formula:

[0300] RO-[CH2-CH(CH2OH)-O]mH or RO-[CH(CH2OH)-CH2O]mH

[0301] in which R represents a linear or branched alkyl or alkenyl radical, in C8-C40 and preferably in C8-C30, and m represents a number from 1 to 30 and preferably from 1.5 to 10.

[0302] By way of examples of suitable compounds in the context of the invention, we may mention lauryl alcohol containing 4 moles of glycerol (INCI name: Polyglyceryl-4 Lauryl Ether), lauryl alcohol containing 1.5 moles of glycerol, oleyl alcohol containing 4 moles of glycerol (INCI name: Polyglyceryl-4 Oleyl Ether), oleyl alcohol containing 2 moles of glycerol (INCI name: Polyglyceryl-2 Oleyl Ether), cetearyl alcohol containing 2 moles of glycerol, cetearyl alcohol containing 6 moles of glycerol, oleocetyl alcohol containing 6 moles of glycerol, and octadecanol containing 6 moles of glycerol.

[0303] Alcohol can represent a mixture of alcohols in the same way that the value of m represents a statistical value, meaning that, in a commercial product, several species of polyglycerol fatty alcohol can coexist as a mixture.

[0304] According to one of the embodiments of the present invention, the nonionic surfactant can be selected from polyol esters with saturated or unsaturated chain fatty acids containing, for example, 8 to 24 carbon atoms, preferably 12 to 22 carbon atoms, and their alkoxylated derivatives, preferably with an alkylene oxide number of 10 to 200, and even better from 10 to 100, such as glyceryl esters of one or more C8-C24 fatty acids, preferably Ci2-C22, and their alkoxylated derivatives, preferably with an alkylene oxide number of 10 to 200, and even better from 10 to 100; polyethylene glycol esters of one or more C8-C24 fatty acids, preferably C12-C22, and their alkoxylated derivatives, preferably with 10 to 200 alkylene oxides, and even better 10 to 100; esters of sorbitol of one or more C8-C24 fatty acids, preferably C12-C22, and their alkoxylated derivatives, preferably with 10 to 200 alkylene oxides, and better still from 10 to 100; sugar esters (sucrose, glucose, alkylglycose) of one or more C8-C24 fatty acids, preferably C12-C22, and their alkoxylated derivatives, preferably with 10 to 200 alkylene oxides, and better still from 10 to 100; fatty alcohol ethers; sugar ethers and one or more C8-C24 fatty alcohols, preferably C12-C22, and mixtures thereof.

[0305] Examples of ethoxylated fatty esters that may be mentioned include ethylene oxide adducts with esters of lauric acid, palmitic acid, stearic acid or behenic acid, and a mixture of the latter, in particular those containing 9 to 100 oxyethylene groups, such as PEG-9 to PEG-50 laurate; PEG-9 to PEG-50 palmitate; PEG-9 to PEG-50 stearate; PEG-9 to PEG-50 palmitostearate; PEG-9 to PEG-50 behenate; polyethylene glycol 100 EO monostearate and a mixture of the latter.

[0306] As examples of fatty acid glyceryl esters, glyceryl stearate (glyceryl mono-, di- and / or tristearate) or glyceryl ricinoleate and mixtures thereof may be cited in particular.

[0307] Examples of glyceryl esters of C8-C24 alkoxylated fatty acids include polyethoxylated glyceryl stearate (glyceryl mono-, di- and / or tristearate) such as PEG-20 glyceryl stearate.

[0308] Mixtures of these surfactants, such as for example the product containing glyceryl stearate and PEG-100 stearate, marketed under the name ARLACEL 165 by Croda, and a product containing glyceryl stearate (glyceryl mono- and distearate) and potassium stearate, may also be used.

[0309] Sorbitol esters of C8-C24 fatty acids and their alkoxylated derivatives may be selected from sorbitan palmitate, sorbitan trioleate and alkoxylated fatty acid and sorbitan esters containing, for example, 20 to 100 EO, such as, for example, polyethylene sorbitan trioleate (polysorbate 85) or compounds marketed under the trade names Tween 20 or Tween 60 by Croda.

[0310] Examples of esters of fatty acids and glucose or alkylglucose include, in particular, glucose palmitate, alkylglucose sesquistearates such as methylglucose sesquistearate, alkylglucose palmitates such as methylglucose or ethylglucose palmitate, fatty esters of methylglucoside, and more particularly methylglucoside and oleic acid diester (methylglucose dioleate), mixed ester of methylglucoside and oleic acid / hydroxystearic acid (methylglucose dioleate / hydroxystearate), methylglucoside and isostearic acid ester (methylglucose isostearate), methylglucoside and lauric acid ester (methylglucose laurate), and mixtures of monoester and diester of methyl- glucoside and isostearic acid (methylglucose sesqui-isostearate), the mixture of monoester and diester of methylglucoside and stearic acid (methylglucose sesquistearate) and in particular the product marketed under the name Glucate SS by Lubrizol, as well as mixtures thereof.

[0311] Examples of ethoxylated fatty acid and glucose or alkylglucose ethers include ethoxylated fatty acid and methylglucose ethers, and in particular polyethylene glycol ether of methylglucose and stearic acid diester with about 20 moles of ethylene oxide (PEG-20 methyl glucose distearate) such as the product marketed under the name Glucam E-20 distearate by Lubrizol, polyethylene glycol ether of the mixture of methyl glucose and stearic acid monoester and diester with about 20 moles of ethylene oxide (PEG-20 methyl glucose sesquistearate) and in particular the product marketed under the name Glucamate SSE-20 by Lubrizol and their mixture.

[0312] Examples of sucrose esters include sucrose palmitostearate, sucrose stearate and sucrose monolaurate.

[0313] Alkyl polyglucosides may be used as sugar ethers, for example decyl glucoside such as the product marketed under the name MYDOL 10 by Kao Chemicals, the product marketed under the name PLATAREN 2000 by BASF, and the product marketed under the name ORAMIX NS 10 by Seppic; caprylyl / capryl glucoside such as the product marketed under the name ORAMIX CG 110 by Seppic or under the name LUTENSOL GD 70 by BASF; lauryl glucoside such as the products marketed under the names PLANTAREN 1200 N and PLANTACARE 1200 by BASF; coco-glucoside such as the product marketed under the name PLANTACARE 818 / UP by BASF; and cetostearyl glucoside, possibly in a mixture with cetostearyl alcohol, marketed, for example, under the name MONTANOV 68 by Seppic, marketed under the name TEGO-CARE CG90 by Evonik, contains arachidyl glucoside,For example, in the form of the mixture of arachidyl and behenyl alcohols and arachidyl glucoside marketed under the name MONTANOV 202 by Seppic, cocoylethyl glucoside, for example in the form of the mixture (35 / 65) with cetyl and stearyl alcohols, marketed under the name MONTANOV 82 by Seppic, and a mixture of the latter may be cited in particular.

[0314] Mixtures of alkoxylated vegetable oil glycerides such as ethoxylated mixtures of palm (200 EO) and coconut (7 EO) glycerides may also be cited.

[0315] The nonionic surfactant may be selected from the group consisting of PEG-7 glyceryl cocoate, PEG-20 methylglucoside sesquistearate, PEG-20 glyceryl triisostearate, PG-5 dioleate, PG-4 diisostearate, PG-10 isostearate, PEG-8 isostearate and PEG-60 hydrogenated castor oil.

[0316] Mixtures of these oxyethylenated derivatives of fatty alcohols and fatty esters may also be used.

[0317] In some cases, the nonionic surfactant is a fatty alkanolamide. Non-limiting examples of fatty alkanolamides that may be used include cocamide MEA, cocamide DEA, sojamide DEA, lauramide DEA, oleamide MIPA, stearamide MEA, myristamide DEA, stearamide DEA, oleylamide DEA, suifamide DEA, lauramide MIPA, suifamide MEA, isostearamide DEA, isostearamide MEA, and a mixture thereof.

[0318] In some cases, the non-ionic surfactant is an oxyethylenated amide such as rapeseed PEG-4. Fatty compounds other than fatty alcohols

[0319] The fatty acids useful in this document include those having from about 10 to about 30 carbon atoms, from about 12 to about 22 carbon atoms, and from about 16 to about 22 carbon atoms. These fatty acids may be straight-chain or branched-chain and may be saturated or unsaturated. Also included are diacids, triacids, and other multiple acids that meet the carbon number requirement in this document. Salts of these fatty acids are also included in this document. Non-limiting examples of fatty acids include lauric acid, palmitic acid, stearic acid, behenic acid, arichidonic acid, oleic acid, isostearic acid, sebacic acid, and mixtures thereof. In some cases, fatty acids are chosen from the group consisting of palmitic acid, stearic acid and a mixture of these.

[0320] Fatty alcohol derivatives include alkyl fatty alcohol ethers, alkoxylated fatty alcohols, alkoxylated fatty alcohol alkyl ethers, fatty alcohol esters, and mixtures thereof. Non-limiting examples of fatty alcohol derivatives include materials such as methyl stearyl ether, 2-ethylhexyl dodecyl ether, stearyl acetate, cetyl propionate, the ceteth series of compounds such as ceteth-1 to ceteth-45, which are ethylene glycol cetyl alcohol ethers, where the numerical designation indicates the number of ethylene glycol fractions present; the series of steareth compounds such as steareth-1 to 10, which are ethylene glycol steareth alcohol ethers, where the numerical designation indicates the number of ethylene glycol fractions present;ceteareth-1 to ceteareth-10, which are ethylene glycol ceteareth alcohol ethers, i.e., a mixture of fatty alcohols containing mainly cetyl alcohol and stearyl alcohol, in which the numerical designation indicates the number of ethylene glycol fractions present; the C1-C30 alkyl ethers of the ceteth, steareth, and ceteareth compounds described above; the polyoxyethylenated ethers of branched alcohols such as octyldodecyl alcohol, dodecylpentadadecyl alcohol, hexyldecyl alcohol, and isostearyl alcohol; the polyoxy- ethers; ethylenates of behenyl alcohol; PPGs such as PPG-9-steareth-3, PPG-11 stearyl ether, PPG-8-ceteth-l and PPG-10 cetyl ether; and mixtures thereof.

[0321] Non-limiting examples of polyglycerol esters of fatty acids include those of the following formula: OR2 RMOCH.;Lh-CH^

[0322] wherein the average value of n is about 3 and R1, R2, and R3 can each independently be a fatty acid fraction or hydrogen, provided that at least one of the fractions R1, R2, and R3 is a fatty acid fraction. For example, R1, R2, and R3 can be saturated or unsaturated, linear or branched, and have a length in the range of Ci-C40, Ci-C30, CrC25, or Ci-C20, Ci-C6, or Ci-Ci0. For example, nonionic polyglyceryl esters of fatty acids include polyglyceryl-5 laurate,

[0323] Fatty acid derivatives are defined in this document to include fatty acid esters of fatty alcohols as defined above, fatty acid esters of fatty alcohol derivatives as defined above when such fatty alcohol derivatives have an esterifiable hydroxyl group, fatty acid esters of alcohols other than fatty alcohols and fatty alcohol derivatives described above, hydroxy-substituted fatty acids, and a mixture thereof.Non-limiting examples of fatty acid derivatives include ricinoleic acid, glyceryl monostearate, 12-hydroxystearic acid, ethyl stearate, cetyl stearate, cetyl palmitate, cetyl polyoxyethylenated ether stearate, polyoxyethylenated stearyl ether stearate, polyoxyethylenated lauryl ether stearate, ethylene glycol monostearate, polyoxyethylenated monostearate, polyoxyethylene distearate, propylene glycol monostearate, propylene glycol distearate, trimethylolpropane distearate, sorbitan stearate, polyglyceryl stearate, dimethyl sebacate, PEG-15 cocoate, PPG-15 stearate, glyceryl monostearate, glyceryl distearate, glyceryl tristearate, PEG-8 laurate, PPG-2 isostearate, PPG-9 laurate, and mixtures thereof. Glycerol monostearate, 12-hydroxystearic acid, and mixtures thereof are preferred for this use.

[0324] In some cases, the one or more fatty compounds may be one or more high-melting-point fatty compounds. A high-melting-point fatty compound is a fatty compound having a melting point of 25°C. Even higher-melting-point fatty compounds may also be used, for example, fatty compounds having a melting point of 40°C or higher, 45°C or higher, 50°C or higher. The high-melting-point fatty compound may be selected from the group consisting of fatty acids, fatty alcohol derivatives, fatty acid derivatives, and mixtures thereof. Non-limiting examples of High melting point compounds are listed in the International Cosmetic Ingredient Dictionary, Sixteenth Edition, 2016.

[0325] In some cases, fatty compounds include one or more waxes. Waxes generally have a melting point between 35 and 120°C at atmospheric pressure. Non-limiting examples of waxes in this category include, for example, synthetic wax, ceresin, paraffin, ozokerite, illipe butter, beeswax, camauba wax, microcrystalline wax, lanolin, lanolin derivatives, candelilla, cocoa butter, shellac wax, spermaceti, bran wax, capok wax, sugar cane wax, montan wax, whale wax, bay berry wax, sunflower (Helianthus annuus) seed wax, acacia deccurens flower wax, or a mixture thereof.

[0326] Among the waxes that can be used as non-silicone fatty compounds, we can mention animal waxes, such as beeswax; vegetable waxes, such as sunflower (helianthus annuus) seed wax, camauba, candelilla, ouricury or Japanese wax, or waxes from cork or sugar cane fibers; mineral waxes, for example paraffin or lignite wax, or microcrystalline waxes or ozokerites; synthetic waxes, including polyethylene waxes, and waxes obtained by Fischer-Tropsch synthesis.

[0327] In some cases, the fatty compounds include one or more non-silicone oils. Oils include, but are not limited to, natural oils, such as coconut oil; hydrocarbons, such as mineral oil and hydrogenated polyisobutene; fatty alcohols, such as octyldodecanol; esters, such as a C12-C15 alkyl benzoate; diesters, such as propylene dipelarganate; and triesters, such as glyceryl trioctanoate. Suitable low-viscosity oils have a viscosity of 5-100 mPas at 25°C and are generally esters having the structure RCO—OR', in which RCO represents the carboxylic acid radical and OR' is an alcohol residue.Examples of these low-viscosity oils include isotridecyl isononanoate, PEG-4 diheptanoate, isostearyl neopentanoate, tridecyl neopentanoate, cetyl octanoate, cetyl palmitate, cetyl ricinoleate, cetyl stearate, cetyl myristate, coco-dicaprylate / caprate, decyl isostearate, isodecyl oleate, isodecyl neopentanoate, isohexyl neopentanoate, octyl palmitate, dioctyl malate, tridecyl octanoate, myristyle myristate, octododecanol, or combinations of octyldodecanol, acetylated lanolin alcohol, cetyl acetate, of isododecanol, polyglyceryl-3-diisostearate, or combinations thereof. High viscosity oils typically have a viscosity of 200-1,000,000, or 100,000-250,000 mPas at 25°C.These oils include castor oil, lanolin and lanolin derivatives, triisocetyl citrate, sorbitan sesquioleate, Ci0-Ci8 triglycerides, caprylic / . Capricorn oil, coconut oil, corn oil, cottonseed oil, glyceryl triacetylhydroxystearate, glyceryl triacetyl ricinoleate, glyceryl trioctanoate, hydrogenated castor oil, linseed oil, mink oil, olive oil, palm oil, illipe butter, rapeseed oil, soybean oil, sunflower oil, tallow, tricaprine, trihydrostearine, triisostearine, trilaurin, trilinolein, trimyristine, triolein, tripalmitine, tristearine, walnut oil, wheat germ oil, cholesterol or combinations thereof.

[0328] Mineral oils, such as liquid paraffin or liquid petroleum, or animal oils, such as perhydrosqualene or arara oil, or vegetable oils, such as sweet almond, calophyllum, palm, castor, avocado, jojoba, olive, or cereal germ oil, can be used. Esters of these oils, for example jojoba esters, can also be used. Other useful esters include lanolic acid, oleic acid, lauric acid, stearic acid, or myristic acid; and esters of alcohols, such as oleyl alcohol, linoleyl or linolenic alcohol, isostearyl alcohol, or octyldodecanol. and / or acetylglycerides, octanoates, decanoates or ricinoleates of alcohols or polyalcohols.Alternatively, it is possible to use hydrogenated oils which are solid at 25°C, such as hydrogenated castor, palm or coconut oils, or hydrogenated tallow; mono-, di-, tri- or sucroglycerides; lanolins; or fatty esters which are solid at 25°C. Cationic conditioning polymers

[0329] Non-limiting examples of cationic polymers include copolymers of l-vinyl-2-pyrrolidine and l-vinyl-3-methylimidazolium salt (e.g., chloride salt) (called Polyquaternium-16); copolymers of l-vinyl-2-pyrrolidine and dimethylaminoethyl methacrylate (called Polyquaternium-11); cationic polymer containing a quaternary diallyl ammonium including, for example, dimethyldiallyammonium chloride homopolymer and acrylamide and dimethyldiallyammonium chloride copolymers (called Polyquaternium-6 and Polyquaternium-7); polysaccharide polymers, such as cationic cellulose derivatives and cationic starch derivatives. Cationic cellulose is available as hydroxyethylcellulose salts that have reacted with a trimethyl ammonium substituted epoxide (designated as Polyquatemium-10).Another type of cationic cellulose includes polymeric quaternary ammonium salts of hydroxyethylcellulose that have reacted with a lauryl dimethyl ammonium substituted epoxide (called Polyquatemium-24). In addition, or alternatively, cationic conditioning polymers may include, or be selected from, cationic derivatives of guar gum, such as hydroxypropyltrimonium guar chloride.

[0330] In certain embodiments, one or more polymers of condi Cationic polymers include cationic polysaccharide polymers, such as cationic cellulose, cationic starch, and cationic guar gum. In the context of this disclosure, cationic polysaccharide polymers include cationic polysaccharides and cationic polysaccharide derivatives (e.g., derivatized to be cationic), for example, resulting in cationic cellulose (cellulose derivatized to be cationic), cationic starch (derivatized to be cationic), and cationic guar gum (guar gum derivatized to be cationic).

[0331] Non-limiting examples of cationic celluloses include hydroxyethylcellulose (also known as HEC), hydroxymethylcellulose, methylhydroxyethylcellulose, hydroxypropylcellulose (also known as HPC), hydroxybutylcellulose, hydroxyethylmethylcellulose (also known as methyl hydroxyethylcellulose) and hydroxypropylmethylcellulose (also known as HPMC), cetyl hydroxyethylcellulose, polyquaternium-10, polyquaternium-24, and mixtures thereof, preferably polyquaternium-10, polyquaternium-24, and mixtures thereof.

[0332] Non-limiting examples of cationic guar include hydroxypropyltrimonium guar chloride, hydroxypropyltrimonium guar chloride,

[0333] Non-limiting examples of cationic starch include starch hydroxypropyltrimonium chloride, oxidized hydroxypropyltrimonium starch PGtrimonium chloride, and a mixture of the latter.

[0334] In various embodiments, the cationic conditioning polymer(s) are selected from polyquaterniums. Polyquaterniums include Polyquaternium-1 (ethanol, 2,2',2'' -nitrilotris-, polymer with 1,4-dichloro-2-butene and N,N,N',N'-tetramethyl-2-butene-1,4-diamine), Polyquaternium-2, (poly[bis(2-chloroethyl) ether-alt-1,3-bis[3-(dimethylamino)propyl]urea]), Poly-quaternium-4, (copolymer of hydroxyethylcellulose and diallylammonium chloride;Polyquaternium-5 (acrylamide-quaternized dimethyl-lammonium methacrylate copolymer), Polyquaternium-6 (poly(diallyldimethyl-lammonium chloride)), Polyquaternium-7 (acrylamide-diallyldimethylammonium chloride copolymer), Polyquaternium-8 (methacrylic acid methyl-stearyl dimethylaminoethyl ester copolymer, quaternized with dimethyl sulfate), Polyquaternium-9 (methacrylic acid N,N-(dimethylamino)ethyl ester homopolymer, quaternized with bromomethane), Polyquaternium-10 (quaternized hydroxyethylcellulose), Polyquaternium-11 (vinylpyrrolidone-methacrylate copolymer) quaternized dimethylaminoethyl), polyquaternium-12 (ethyl methacrylate / abietyl methacrylate / di- methacrylate copolymer; thylaminoethyl quaternized with dimethyl sulfate), polyquaternium-13 (ethyl methacrylate / oleyl methacrylate / diethylaminoethyl methacrylate quaternized with dimethyl sulfate copolymer), Polyquaternium-14 (trimethylaminoethyl methacrylate homopolymer), Polyquaternium-15 (acrylamide methyl chloride / dimethylaminoethyl methacrylate copolymer), Polyquaternium-16 (vinylpyrrolidone / vinylimidazole quaternized copolymer), Polyquaternium-17 (adipic acid / dimethylaminopropylamine / dichloroethyl ether copolymer), Polyquaternium-18 (azelanic acid / dimethylaminopropylamine / dichloroethyl ether copolymer), Polyquaternium-19 (poly(vinyl alcohol) copolymer and of 2,3-epoxypropylamine), Poly-quaternium-20 (copolymer of poly(vinyl octadecyl ether) and 2,3-epoxypropylamine), Polyquaternium-22 (copolymer of acrylic acid and diallyldimethylammonium chloride),Polyquaternium-24 (aquaternary ammonium salt of hydroxyethylcellulose reacted with a lauryl dimethylammonium substituted epoxide), Polyquaternium-27 (a sequenced copolymer of Polyquaternium-2 and Polyquaternium-17), Polyquaternium-28 (a copolymer of vinylpyrrolidone and metha-crylamidopropyl trimethylammonium), Polyquaternium-29 (chitosan modified with propylene oxide and quatemized with epichlorohydrin), Polyquaternium-30 (ethanaminium, N-, (carboxymethyl)-N,N-dimethyl-2-[(2-methyl-l-oxo-2-propen-l-yl)oxy]-, internal salt, polymer with methyl 2-methyl-2-propenoate), Polyquaternium-31 (N,N-dimethylaminopropyl-N-acrylamidine quaternized with diethyl sulfate linked to a polyacrylonitrile sequence), Polyquaternium-32 (poly(acrylamide chloride of 2-methacryloxyethyltrimethylammonium)), Polyquaternium-33 (copolymer of trimethylaminoethylacrylate salt and acrylamide), Polyquaternium-34 (copolymer of 1,3-dibromopropane and N,N-diethyl-N',N'-dimethyl-l,3-propanediamine), Poly-quaternium-35 (methosulfate of the copolymer of methacryloyloxyethyltrimethyl-lammonium and of methacryloyloxyethyldimethylacetylammonium), Polyquatemium-36 (copolymer of N,N-dimethylaminoethyl methacrylate and butyl methacrylate, quaternized with dimethyl sulfate), Polyquatemium-37 (poly(2-methacryloxyethyltrimethylammonium) chloride), Polyquaternium-39 (acrylic acid terpolymer,acrylamide and diallyldimethylammonium chloride), Poly-quatemium-42 (poly[oxyethylene(dimethylimino)ethylene (dimethylimino)ethylene] dichloride), Polyquatemium-43 (acrylamide, acrylamidopropyltrimonium chloride, 2-amidopropylacrylamide sulfonate and dimethylaminopropylamine copolymer), Polyquaternium-44 (methyl sulfate copolymer, 3-Methyl-1-vinylimidazolium-N-vinylpyrrolidone), Polyquatemium-45 (copolymer of (N-methyl-N-ethoxyglycine) and N,N- methacrylate dimethylaminoethyl, quatemized with dimethyl sulfate), Polyquaternium-46 (quamatemized vinylcaprolactam, vinylpyrrolidone and vinylimidazole terpolymer) and Polyquaternium-47 (acrylic acid, methacrylamidopropyl trimethylammonium chloride and methyl acrylate terpolymer) and / or Poly-quaternium-67.

[0335] In various embodiments, the cationic conditioning polymer(s) are selected from cationic cellulose derivatives, quatemized hydroxyethylcellulose (e.g., polyquaternium-10), cationic starch derivatives, cationic guar gum derivatives, acrylamide and dimethyldiallyammonium chloride copolymers (e.g., poly-quatemium-7), polyquaterniums, and a mixture of the latter. For example, the cationic polymer(s) can be chosen from among the polyquaterniums, for example, polyquaterniums selected from polyquatemium-4, polyquatemium-5, polyquaternium-6, polyquaternium-7, polyquaternium-10, polyquaternium-22, polyquaternium-37, polyquaternium-39, polyquaternium-47, polyquaternium-53, polyquaternium-67, and a mixture thereof. A combination of two or more polyquaterniums can be useful. A particularly preferred and useful cationic polymer is polyquaternium-10.

[0336] Les polymères cationiques peuvent être des polyquaterniums. Dans certains modes de réalisation, les tensioactifs cationiques peuvent être des polyquaterniums choisis parmi les polyquaternium-1, polyquaternium-2, polyquaternium-3, polyquaternium-4, polyquaternium-5, polyquaternium-6, polyquaternium-7, polyquaternium-8, poly-quatemium-9, polyquaternium-10, polyquaternium-11, polyquaternium-12, poly-quatemium-13, polyquaternium-14, polyquaternium-15, polyquaternium-16, poly-quatemium-17, polyquaternium-18, polyquaternium-19, polyquaternium-20, poly-quatemium-21, polyquaternium-22, polyquaternium-23, polyquaternium-24, poly-quatemium-25, polyquaternium-26, polyquaternium-27, polyquaternium-28, poly-quatemium-29, polyquaternium-30, polyquaternium-40, polyquaternium-41, poly-quatemium-42, polyquaternium-43, polyquaternium-44, polyquaternium-45, poly-quatemium-46, polyquaternium-47, polyquaternium-48, polyquaternium-49, poly-quatemium-50, polyquaternium-51, polyquaternium-52,polyquaternium-53, poly-quaternium-54, polyquaternium-55, polyquaternium-56, polyquaternium-57, poly-quaternium-58, polyquaternium-59, polyquaternium-60, polyquaternium-61, poly-quaternium-62, polyquaternium-63, polyquaternium-64, polyquaternium-65, poly-quatemium-66, polyquaternium-67, etc. In some cases, preferred poly-quatemium compounds include polyquaternium-10, polyquatemium-11, poly-quatemium-67, and a mixture thereof. ,

[0337] In certain embodiments, the conditioning polymer(s) ca tionics are chosen from cationic proteins and cationic protein hydrolysates (e.g., hydroxypropyltrimonium hydrolyzed wheat protein), quaternary diammonium polymers (e.g., hexadimethrin chloride), acrylamide and dimethyldiallyammonium chloride copolymers, and mixtures thereof.

[0338] Cationic conditioning polymers may be homopolymers or formed from two or more types of monomers. The molecular weight of the polymer may be between 5,000 and 10,000,000, typically at least 10,000, and preferably in the range of 100,000 to about 2,000,000. These polymers will typically have nitrogen-containing cationic groups such as quaternary or amino-protonated ammonium groups, or a mixture thereof.

[0339] The cationic charge density is suitably at least 0.1 meq / g, preferably greater than 0.8 or more. In some cases, the cationic charge density does not exceed 3 meq / g, or does not exceed 2 meq / g. The charge density can be measured by the Kjeldahl method and can be within the above limits at the desired pH of use, which will generally be between approximately 3 and 9 and preferably between 4 and 8.

[0340] The nitrogen-containing cationic group will generally be present as a substituent on a fraction of the total monomer units of the cationic conditioning polymer. Thus, when the polymer is not a homopolymer, it may contain non-cationic monomer spacer units.

[0341] Suitable cationic conditioning polymers include, for example, copolymers of vinyl monomers having cationic amine or quaternary ammonium functionalities with water-soluble spacer monomers such as (meth)acrylamide, alkyl and dialkyl (meth)acrylamides, alkyl (meth)acrylate, vinyl caprolactone, and vinyl pyrrolidine. The alkyl- and dialkyl-substituted monomers preferably have C1-C7 alkyl groups, or even better, C1-C3 alkyl groups. Other suitable spacers include vinyl esters, vinyl alcohol, maleic anhydride, propylene glycol, and ethylene glycol.

[0342] Cationic amines can be primary, secondary or tertiary amines, depending on the particular species and the pH of the composition.

[0343] Amine-substituted vinyl monomers and amines can be polymerized into amines and then converted into ammonium by quaternization.

[0344] Suitable quaternary amino and ammonium cationic monomers include, for example, vinyl compounds substituted with dialkylaminoalkyl acrylate, dialkylaminoalkyl methacrylate, monoalkylaminoalkyl acrylate, monoalkylaminoalkyl methacrylate, trialkylmethacryloxyalkylammonium salt, trialkylacryloxyalkylammonium salt, quaternary diallyl-ammonium salts, and Quaternary vinyl-ammonium monomers having cationic cyclic rings containing nitrogen, such as pyridinium, imidazolium, and quaternized pyrrolidine, for example, the salts of alkyl vinyl imidazolium and quaternized pyrrolidine, for example, the salts of alkyl vinyl imidazolium, alkyl vinyl pyridinium, and alkyl vinyl pyrrolidine. The alkyl portions of these monomers are preferably lower alkyls such as C1-C3 alkyls, or even better, C1-C2 alkyls.

[0345] Suitable amine-substituted vinyl monomers include dialkylaminoalkyl acrylate, dialkylaminoalkyl methacrylate, dialkylaminoalkyl acrylamide and dialkylaminoalkyl methacrylamide, wherein the alkyl groups are preferably Ci-C7 hydrocarbyls, better still Ci-C3 hydrocarbyls.

[0346] Cationic conditioning polymers may include mixtures of monomer motifs derived from quaternary amine and / or ammonium substituted monomers and / or compatible spacer monomers.

[0347] Suitable cationic conditioning polymers include, for example: copolymers of l-vinyl-2-pyrrolidine and l-vinyl-3-methylimidazolium salt (e.g., chloride salt) (called Polyquaternium-16) such as those commercially available from BASF under the brand name LUVIQUAT (e.g., LUVIQUAT FC 370); copolymers of l-vinyl-2-pyrrolidine and dimethylaminoethyl methacrylate (called Polyquaternium-11) such as those marketed by Gar Corporation (Wayne, NJ, USA) under the brand name GAFQUAT (e.g., GAFQUAT 755N); and a cationic polymer containing quaternary diallyl ammonium including, for example, a homopolymer of dimethyldiallyammonium chloride and copolymers of acrylamide and dimethyldiallyammonium chloride (called Polyquatemium-6 and Polyquaternium-7).

[0348] Other cationic conditioning polymers that can be used include polysaccharide polymers, such as cationic cellulose derivatives and cationic starch derivatives. Cationic cellulose is available from Amerchol Corp. (Edison, NJ, USA) in their Polymer JR (registered trademark) and LR (registered trademark) polymer lines, in the form of hydroxyethylcellulose salts that have reacted with a trimethylammonium substituted epoxide (called Polyquaternium-10). Another type of cationic cellulose includes polymeric quaternary ammonium salts of hydroxyethylcellulose that have reacted with a lauryl dimethyl ammonium substituted epoxide (called Polyquaternium-24). These materials are available from Amerchol Corp. (Edison, NJ, USA) under the trade name Polymer LM-200.

[0349] Other cationic conditioning polymers that can be used include cationic guar gum derivatives, such as hydroxypropyl guar chloride- trimonium.

[0350] Polyquaterniums include Polyquaternium-1 (ethanol, 2,2',2''-nitrilotris-, polymer with 1,4-dichloro-2-butene and N,N,N',N'-tetramethyl-2-butene-1,4-diamine), Polyquaternium-2, (poly[bis(2-chloroethyl) ether-alt-1,3-bis[3-(dimethylamino)propyl]urea]), Polyquaternium-4, (copolymer of hydroxyethylcellulose and diallylammonium chloride; copolymer of diallyldimethylammonium chloride-hydroxyethylcellulose), Polyquaterium-5 (copolymer of acrylamide and quaternized dimethylammonium methacrylate), Polyquaternium-6 (poly(diallyldimethylammonium chloride)), Polyquaternium-7 (copolymer of acrylamide and chloride of diallyldimethylammonium), Poly-quaternium-8 (methyl ester copolymer and stearyl dimethylaminoethyl methacrylic acid, quaternized with dimethyl sulfate), Polyquaternium-9 (homopolymer of N,N-(dimethylamino)ethyl methacrylic acid, quaternized with bromomethane), Polyquaternium-10 (quaternized hydroxyethylcellulose),polyquaternium-11 (copolymer of vinylpyrrolidone and quaternized dimethylaminoethyl methacrylate), polyquaterium-12 (copolymer of ethyl methacrylate / abietyl methacrylate / diethylaminoethyl methacrylate quaternized with dimethyl sulfate), polyquaterium-13 (copolymer of ethyl methacrylate / oleyl methacrylate / diethylaminoethyl methacrylate quaternized with dimethyl sulfate), Polyquaterium-14 (homopolymer of trimethylaminoethyl methacrylate), Polyquaterium-15 (copolymer of acrylamide methyl chloride and dimethylaminoethyl methacrylate), Polyquaterium-16 (copolymer of vinylpyrrolidone and quaternized vinylimidazole), Polyquaterium-17 (copolymer of adipic acid, dimethylaminopropylamine and dichloroethyl ether), Polyquatemium-18 (copolymer of azelanic acid, dimethylaminopropylamine and dichloroethyl ether), Polyquatemium-19 (copolymer of poly(vinyl alcohol) and 2,3-epoxypropylamine),Polyquatemium-20 (copolymer of poly(vinyl octadecyl ether) and 2,3-epoxypropylamine), Polyquaternium-22 (copolymer of acrylic acid and diallyldimethylammonium chloride), Polyquaternium-24 (aquaternary ammonium salt of hydroxyethylcellulose reacted with a lauryl dimethylammonium substituted epoxide), Polyquaternium-27 (sequenced copolymer of Polyquaternium-2 and Polyquaternium-17), Polyquaternium-28 (copolymer of vinylpyrrolidone and metha-crylamidopropyl trimethylammonium), Polyquatemium-29 (chitosan modified with propylene oxide and quaternized with epichlorohydrin), Polyquatemium-30 (ethanaminium, N-(carboxymethyl)-N,N-dimethyl-2-[(2-methyl-1-oxo-2-propen- l-yl)oxy]-, internal salt, polymer with methyl 2-methyl-2-propenoate), Polyquatemium-31 (N,N-dimethylaminopropyl-N-acrylamidine quaternized with diethyl sulfate linked to a , polyacrylonitrile sequence), Polyquaternium-32 (poly(acrylamide 2-methacryloxyethyltrimethylammonium chloride)), Polyquaternium-33 (copolymer of trimethylaminoethyl acrylate salt and acrylamide), Polyquaternium-34 (copolymer of 1,3-dibromopropane and N,N-diethyl-N',N'-dimethyl-1,3-propanediamine), Poly-quaternium-35 (methosulfate of the copolymer of methacryloyloxyethyltrimethyl-lammonium and methacryloyloxyethyldimethylacetylammonium), Polyquaternium-36 (copolymer of N,N-dimethylaminoethyl methacrylate and butyl methacrylate, quaternized with dimethyl sulfate), Polyquaternium-37 (poly(2-methacryloxyethyltrimethylammonium chloride)), Polyquaternium-39 (acrylic acid, acrylamide and diallyldimethylammonium chloride terpolymer), Poly-quatemium-42 (poly[oxyethylene(dimethylimino)ethylene (dimethylimino)ethylene] dichloride), Polyquatemium-43 (acrylamide, acrylamidopropyltrimonium chloride copolymer,2-amidopropylacrylamide and dimethylaminopropylamine sulfonate), Polyquaternium-44 (methyl sulfate copolymer of , 3-Methyl-1-vinylimidazolium-N-vinylpyrrolidone), Polyquaternium-45 (copolymer of (N-methyl-N-ethoxyglycine) methacrylate and N,N-dimethylaminoethyl methacrylate, quaternized with dimethyl sulfate), Polyquaternium-46 (terpolymer of vinylcaprolactam, vinylpyrrolidone and quaternized vinylimidazole) and Polyquaternium-47 (terpolymer of acrylic acid, methacrylamidopropyl trimethylammonium chloride and methyl acrylate). Thickening agents

[0351] Thickening agents that may be mentioned include the following:

[0352] a. Carboxylic acid or carboxylate-based homopolymer or copolymer, which may be linear or crosslinked: These polymers contain one or more monomers derived from acrylic acid, substituted acrylic acids, and salts and esters of these acrylic acids (acrylates) and substituted acrylic acids. Commercially available polymers include those sold under the trade names Carbopol, Acrysol, Polygel, Sokalan, CarbopolUltrez, and Polygel. Examples of commercially available carboxylic acid polymers include carbomers, which are acrylic acid homopolymers crosslinked with allyl ethers of sucrose or pentaerythritol. Carbomers are available in BF Goodrich's Carbopol 900 range (e.g., Carbopol 954). In addition, other suitable carboxylic acid polymer agents include Ultrez 10 (BFGoodrich) and C10-30 alkyl acrylate copolymers with one or more monomers of acrylic acid, methacrylic acid, or one of their short-chain esters (i.e., a Cl-4 alcohol), wherein the crosslinking agent is an allyl ether of sucrose or pentaerythritol. These copolymers are known as C10-C30 acrylate / alkyl acrylate crosslinked polymers and are available in . trade under the names Carbopol 1342, Carbopol 1382, Pemulen TR-1 and Pemulen TR-2, with BF Goodrich.

[0353] Other suitable carboxylic acid or carboxylate polymer agents include C5-C10 alkyl acrylic acid-acrylate copolymers, acrylic acid-maleic anhydride copolymers, and polyacrylate crosslinked-6 polymer. Polyacrylate crosslinked-6 polymer is available in the raw material known as Seppic's SEPIMAX ZEN.

[0354] Another suitable carboxylic acid or carboxylate polymeric agent includes acrylamidopropyltrimonium chloride / acrylates copolymer, a cationic acrylates copolymer (or a quaternary ammonium compound), available as a raw material known as Seppic's SIMULQUAT HC 305.

[0355] In some embodiments, the polymer thickeners of carboxylic acid or carboxylate useful in this document are those selected from carbomers, C10-C30 alkyl acrylate / acrylate crosslinked polymers, polyacrylate crosslinked polymer-6, acrylamidopropyltrimonium chloride / acrylates copolymer, and mixtures thereof.

[0356] b. Celluloses: Non-limiting examples of celluloses include cellulose, carboxymethyl hydroxyethylcellulose, cellulose acetate propionate carboxylate, hydroxyethylcellulose, hydroxyethyl ethylcellulose, hydroxypropylcellulose, hydroxypropyl methylcellulose, methyl hydroxyethylcellulose, microcrystalline cellulose, sodium cellulose sulfate, and mixtures thereof. In some cases, the cellulose is selected from water-soluble cellulose derivatives (e.g., carboxymethylcellulose, methylcellulose, methylhydroxypropylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, sodium salt of cellulose sulfate). In addition, in some cases, the cellulose is preferably hydroxypropylcellulose (HPC).

[0357] c. Polyvinylpyrrolidone (PVP) and copolymers: Non-limiting examples include polyvinylpyrrolidone (PVP), polyvinylpyrrolidone (PVP) / vinyl acetate copolymer (PVP / VA copolymer), polyvinylpyrrolidone (PVP) / eicosene copolymer, PVP / hexadecene copolymer, etc. Commercially available polyvinylpyrrolidone includes Luviskol K30, K85, K90, available from BASF. Commercially available vinylpyrrolidone and vinyl acetate copolymers include Luviskol VA37, VA64, available from BASF; vinylpyrrolidone, methacrylamide, and vinylimidazole copolymer (INCI: VP / Methacrylamide / Vinyl Imidazole Copolymer) is commercially available under the name Luviset from BASF. In some cases, PVP and PVP / VA copolymer are preferred.

[0358] d. Sucrose esters: Non-limiting examples include the following compounds; sucrose palmitate, sucrose cocoate, sucrose monooctanoate, sucrose monodecanoate, sucrose mono- or dilaurate, sucrose monomyristate, sucrose mono- or dipalmitate, sucrose mono- and distearate, sucrose mono-, di- or trioleate, sucrose mono- or dilinoleate, sucrose pentaoleate, sucrose hexaoleate, sucrose heptaoleate or sucrose octooleate, and mixed esters, such as sucrose palmitate / stearate and mixtures thereof.

[0359] e. Polyglyceryl esters: Non-limiting polyglycerol esters (polyglyceryl esters) of fatty acids include those of the following formula: GOLD 2 r^ochJch-chzO)^

[0360] in which n is between 2 and 20 or between 2 and 10 or between 2 and 5, or is equal to 2, 3, 4, 5, 6, 7, 8, 9 or 10, and R1, R2 and R3 can each independently be a fatty acid fraction or hydrogen, provided that at least one of R1, R2, and R3 is a fatty acid fraction. For example, R1, R2 and R3 can be saturated or unsaturated, linear or branched, and have a length in Ci-C40, Ci-C30, C1-C25, or CrC20, Ci-Ci6, or Ci-Ci0. In addition, non-limiting examples of non-ionic polyglycerol esters of fatty acids include the following: poly-glyceryl-4 caprylate / caprate, polyglyceryl-10 caprylate / caprate, polyglyceryl-4 caprate, polyglyceryl-10 caprate, polyglyceryl-4 laurate, polyglyceryl-5 laurate, polyglyceryl-6 laurate, polyglyceryl-10 laurate, polyglyceryl-10 cocoate, polyglyceryl-10 myristate, polyglyceryl-10 oleate, polyglyceryl-10 stearate, and mixtures thereof.

[0361] f. C8-24 hydroxyl-substituted aliphatic acid and C8-24 conjugated aliphatic acid: Non-limiting examples include conjugated linoleic acid, cis-parinaric acid, trans-7-octadecenoic acid, cis-5,8,11,14,17-eicosapentaenoic acid, cis-4,7,10,13,16,19-docosahexenoic acid, columbinic acid, linolene laidic acid, ricinolaic acid, stearidonic acid, 2-hydroxystearic acid, alpha-linolenic acid, arachidonic acid, cis-11,14-eicosadienoic acid, linolelaidic acid, monopetroselinic acid, petroselinic acid ricinoleic acid, trans-vaccenic acid, cis-ll,14,17-eicosatrienoic acid, cis-5-eicosenoic acid, cis-8,ll,14-eicosatrienoic acid, hexadecatrienoic acid, palmitoleic acid, petroselaidic acid, trans trans famesol, cis-13,16-docosadienoic acid, cis-vaccenic acid, cis-ll-eicosenoic acid, cis-13,16,19-docosatrienoic acid,cis-13-octadecanoic acid, cis-15-octadecanoic acid, cis-7,10,13,16-docosatetraenoic acid, elaidic acid, gamma-linolenic acid, geranoic acid, geranylgeranoic acid, linoleic acid, , oleic acid, pinolenic acid, trans-13-octadecenoic acid. Better still, aliphatic acid includes 12-hydroxystearic acid, conjugated linoleic acid or a mixture of these.

[0362] g. Gums: Non-limiting examples of gums include gum arabic, tragacanth gum, karaya gum, guar gum, gellan gum, tara gum, carob gum, tamarind gum, xanthan gum, carob gum, Seneca gum, sclerotium gum, gellan gum, etc. Viscosity

[0363] The viscosity of the base hair coloring composition is typically about 25 to about 150 cps at 25°C using a #1 spindle at 100 rpm.As an example only, the viscosity of basic hair coloring compositions can range from approximately 20 cps to approximately 150 cps, such as, for example, approximately 20 to approximately 125 cps, approximately 20 to approximately 100 cps, approximately 20 to approximately 85 cps, approximately 20 to approximately 70 cps, approximately 25 to approximately 125 cps, approximately 25 to approximately 100 cps, approximately 25 to approximately 85 cps, approximately 25 to approximately 70 cps, approximately 30 to approximately 125 cps, approximately 30 to approximately 100 cps, approximately 30 to approximately 85 cps, approximately 30 to approximately 70 cps, approximately 50 to approximately 100 cps, and approximately 60 to approximately 100 cps, from about 70 to about 100 cps, from about 50 to about 90 cps, from about 50 to about 80 cps, or from about 50 to about 75 cps, when measured at 25 °C using an M3 spindle at 100 rpm, for example, using a RheomatRM 180.

[0364] In some non-limiting embodiments where the developer composition is liquid, for example aqueous, the developer composition may have a viscosity in the range of about 250 to about 2,000 cps, such as, for example, about 500 to about 2,500 cps, about 500 to about 2,000 cps, about 500 to about 1,500 cps, about 600 to about 1,300 cps, or about 650 to about 1,200 cps when measured at 25 °C using a #4 spindle at 100 rpm, for example, using a Rheomat RM 180.

[0365] By way of example, the viscosity of the ready-to-use hair coloring composition may be in the range of about 250 cps to about 2,500 cps, such as, for example, from about 250 to about 2,000 cps, from about 250 to about 1,800 cps, from about 250 to about 1,600 cps, from about 300 to about 2,000 cps, from about 300 to about 1,800 cps, from about 300 to about 1,600 cps, from about 350 to about 2,000 cps, from about 350 to about 1,800 cps, from about 350 to about 1,600 cps, from about 400 to about 2,000 cps, from about 400 to approximately 1,800 cps, from approximately 400 to approximately 1,600 cps, from approximately 450 to approximately 2,000 cps, from approximately 450 to approximately 1,800 cps, from approximately 450 to approximately 1,600 cps, from approximately 500 to approximately 2,000 cps, from about 500 to about 1800 cps, or from about 500 to about 1600 cps when measured at 25 °C using an M3 spindle at 100 rpm, for example, using a RheomatRM 180. Processes

[0366] The compositions of this disclosure are useful in processes for preparing ready-to-use hair coloring compositions and in hair coloring processes. Processes for preparing ready-to-use hair coloring compositions include combining one or more hair coloring base compositions according to this disclosure with one or more developer compositions, including one or more developer compositions of this disclosure. However, the processes are not limited to the developer compositions of this disclosure. In various embodiments, a coloring base composition is combined with a developer composition to form a ready-to-use hair coloring composition having a pH of about 6 to about 8, preferably about 6.1 to about 7.9, or more preferably about 6.2 to about 7.8.One or more hair coloring base compositions can be combined with one or more developer compositions in a ratio of approximately 1:5 to approximately 5:1 (hair coloring base composition to developer composition). In some cases, the weight ratio is approximately 1:4 to approximately 4:1, approximately 1:3 to approximately 3:1, approximately 1:2 to approximately 2:1, or approximately 1:1 (hair coloring base composition to developer composition), provided that the pH of the ready-to-use hair coloring composition is at the desired pH.

[0367] Hair coloring processes, particularly for facial hair (beard and / or mustache), include the application of a ready-to-use hair coloring composition of this disclosure to the hair. The ready-to-use hair coloring composition can be prepared as described above, namely, by combining one or more hair coloring base compositions according to this disclosure with one or more developer compositions. The ready-to-use hair coloring composition is typically used (applied to the hair) shortly after formation, that is, shortly after the hair coloring base composition has been combined with the developer composition to form a ready-to-use hair coloring composition, the ready-to-use hair coloring composition is applied to the hair.In various embodiments, the ready-to-use hair coloring composition is applied to the hair within 1 hour of training. In other embodiments, the ready-to-use hair coloring composition is applied immediately after training up to approximately 1 hour after training, or up to approximately 45 minutes after. training, up to about 30 minutes after the training or up to about 15 minutes after the training.

[0368] The ready-to-use hair coloring composition can be applied to the hair on the head, body hair, facial hair (including beard and mustache hair), eyelashes, and / or eyebrows. In some embodiments, the ready-to-use hair coloring composition is applied to facial hair, preferably beard and mustache hair. In some embodiments, the hair to be treated (colored) has been previously chemically treated, for example, bleached, previously colored, previously permed, previously straightened, etc. In other embodiments, the hair to be treated (colored) includes naturally gray hair, i.e., hair that has developed a loss of natural pigmentation and / or melanin.

[0369] After application to the hair, the ready-to-use hair coloring composition is left to rest on the hair for a period of time, for example, a period of time sufficient to achieve a desired change in hair color.For example, the ready-to-use hair coloring composition can be left to rest on the hair for a period of time of up to 1 hour, such as from about 1 minute to about 45 minutes, from about 1 minute to about 30 minutes, from about 1 minute to about 15 minutes, from about 2 minutes to about 1 hour, from about 2 minutes to about 45 minutes, from about 2 minutes to about 30 minutes, from about 2 minutes to about 15 minutes, from about 2 minutes to about 10 minutes, from about 3 minutes to about 30 minutes, from about 3 minutes to about 25 minutes, from about 3 minutes to about 20 minutes, from about 3 minutes to about 15 minutes, from about 3 minutes to about 10 minutes, or from about 5 minutes to about 10 minutes.A person skilled in the art, considering various factors such as the initial and desired hair color, will be able to determine an appropriate duration for leaving the ready-to-use hair coloring composition on the hair to achieve the desired result. After the ready-to-use hair coloring composition has been left on the hair for a period of time, it can optionally be removed from the hair by rinsing or washing (for example, shampooing). Shapes

[0370] The hair coloring compositions of this disclosure (hair coloring base compositions, developer compositions, and / or ready-to-use hair coloring compositions) may be in a variety of forms. For example, in many cases, the compositions are in the form of a liquid, gel, lotion, cream, and / or spray. The compositions may be packaged in a variety of different containers. Examples not listed herein are not provided. Useful packaging options include tubes, jars, capsules, unit dose packs, and bottles, including squeezable tubes and bottles. Necessary

[0371] The hair coloring base compositions of this disclosure may be present in a kit. For example, in some implementations, such kits include: (i) one or more hair coloring base compositions according to this disclosure; and (ii) one or more developer compositions comprising one or more oxidizing agents in which the hair coloring base composition(s) of (i) and the developer composition(s) of (ii) are contained.

[0372] In some embodiments, the developer composition is aqueous or in the form of an emulsion. The developer composition may contain at least one solvent, selected from water, organic solvents, and mixtures thereof.

[0373] In various embodiments given by way of example, hydrogen peroxide is present in an amount of at least about 1% by weight, based on the total weight of the developer composition. In other embodiments, hydrogen peroxide is present in an amount ranging from about 0.1% to 80% by weight, such as about 1.0% to 75% by weight, or about 2% to 10% by weight, based on the total weight of the developer composition. In other embodiments given by way of example, hydrogen peroxide may be present in the developer composition in an amount ranging from about 2% to 25% by weight, such as about 4% to 20% by weight, about 6% to 15% by weight, or about 7% to 10%.

[0374] A cosmetically acceptable support for the developer composition may, for example, be present in an amount in the range of about 0.5% to about 99% by weight, such as about 5% to about 95% by weight, relative to the total weight of the developer composition.

[0375] In variant embodiments, the developer composition is substantially anhydrous. The term “substantially anhydrous” means that the developer composition is either completely free of water or does not contain an appreciable amount of water, for example, not more than 5% by weight, or not more than 2% by weight, or not more than 1% by weight, based on the weight of the developer composition. It should be noted that this refers, for example, to bound water, such as the water of crystallization of salts or traces of water absorbed by the starting materials used in the preparation of the compositions according to the disclosure embodiments.

[0376] When the developer composition is substantially anhydrous, the developer composition may include at least one solvent selected from organic solvents.

[0377]

[0378]

[0379]

[0380] Suitable organic solvents for use in developer formulations include ethanol, isopropyl alcohol, propanol, benzyl alcohol, phenylethyl alcohol, glycols and glycol ethers, such as propylene glycol, hexylene glycol, monomethyl, monoethyl, or monobutyl ethylene glycol ether, propylene glycol and its ethers, such as monomethyl propylene glycol ether, alkyl ethers of butylene glycol, dipropylene glycol, and diethylene glycol, such as monoethyl and monobutyl diethylene glycol ether, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, propane diol, glycerin, hydrocarbons such as linear-chain hydrocarbons, mineral oil, polybutene, hydrogenated polyisobutene, hydrogenated polylydecene, polydecene, squalane, petrolatum, isoparaffins, and mixtures thereof. The developer composition can be in the form of a powder, gel, liquid, foam, lotion, cream, mousse, and emulsion. The pH of the developer composition can be in a range of about 2 to about 12, such as about 3 to about 7, and it can be corrected to the desired value using acidifying / alkalizing agents that are well known in the art. EXAMPLES An implementation of this disclosure is provided through the following examples. These examples serve to illustrate the technology but are not exhaustive. EXAMPLE 1 (Basic compositions for hair coloring) ABCDEFGHI Oxidative Tint Precursor 2-METHOXYMETHYL-P-PH ENYLENEDIAMINE 0.8 1.9 3.2 2.7 3.1 3.1 3.1 3.1 3.0 2,3-DIAMINODIHYDRO-PY RAZOLO DIMETHOSULFONATE PYRAZOLONE 0.3 0.3 0.3 0.5 0.6 Calciuming Agent MONOETHANOLAMINE 0.93 5 1.0 6 1.0 2 0.6 6 qs pH 7.5 qs pH 8.7 qs pH 9.5 0.7 0.7 Reducing Agent AMMONIUM THIOLACTATE 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 Fatty Alcohol OLEYL ALCOHOL 1.1 1.1 1.1 1.1 1.1 1.1 1.1 1.1 1.1 Surfactant SEED AMIDE 24 24 24 24 24 24 24 24 24 24 Non-ionic RAPESEED PEG-4, DECETH-3, POLOXAMER 338, AND / OR GLYCERYL LAURYL ETHER Anionic surfactant LAURETH-5 CARBOXYLIC ACID 4.5 4.5 4.5 4.5 4.5 4.5 4.5 4.5 4.5 Water-soluble organic solvents DIPROPYLENE GLYCOL, HEXYLENE GLYCOL, PROPYLENE GLYCOL AND / OR ALCOHOL DENAT. 20.4 20.4 20.4 20.4 20.4 20.4 20.4 20.4 20.4 20.4 20.4 Couplers 2-AMINO-3-HYDROXYPYRIDIINE 0.0 3 0.2 0.1 0.1 0.1 0.1 0.1 HYDROXYBENZOMORPH OLINE 0.2 0.5 1.1 1.3 1.5 1.5 1.5 1.4 1.5 2-METHYL-5-HYDROXYETHYLAMINOPHENOL 0.08 0.2 0.8 0.8 0.8 0.8 1.0 0.8 2-METHYLRESORCINOL 0.5 0.9 1.0 2,4-DIAMINOPHENOXYETHANOL HCL 0.3 0.2 0.3 0.5 0.5 0.5 0.6 0.5 Miscellaneous FRAGRANCE, EDTA, ERYTHORBIC ACID (antioxidant) 1.3 1.3 1.3 1.3 1.3 1.3 1.3 1.3 1.3 Water WATER 45.5 43.4 41.4 42.2 41.0 41.0 41.0 40.7 40.8 pH 7.5 7.5 9 9 7.5 8.7 9.5 9 9 pH of the 1:1 mixture with the developer from Example 2 7.5 7.5 7.5 7.5 6.5 7.5 10 7.5 7.5 EXAMPLE 2 (Developer composition)

[0381] Developer 20 V % BY WEIGHT (a) Oxidizing agent HYDROGEN PEROXIDE 7 (c) Water-soluble solvent: Glycerin 0.5 (d) Fatty alcohol: Cetearyl alcohol 2.28 (e) Non-ionic surfactants: Trideceth-2 Carboxamide MEA 2 Ceteareth-25 0.57 (f) Miscellaneous: Sodium salicylate 0.035 Tetrasodium pyrophosphate 0.04 Tetrasodium etidronate 0.2 (b) Water: Water 83.525 EXAMPLE 3 (Tenacity study)

[0382] The hair coloring bases E, F, and G of Example 1 were mixed with the developer composition of Example 2 in a 1:1 ratio to form ready-to-use hair coloring compositions. The hair coloring bases E, F, and G of Example 1 are identical except for the amount of ethanolamine. The higher amounts of ethanolamine included in the hair coloring bases F and G resulted in these compositions having a higher pH than the hair coloring base E. The three ready-to-use hair coloring compositions are summarized in the table below.

[0383] [Tables] Ready-to-use color composition pH level #1 1:1 mixture of Base E and developer Composition E from Example 1 mixed with the developer from Example 2 in a 1:1 ratio 7.5 #2 1:1 mixture of Base F and developer Composition F from Example 1 mixed with the developer from Example 2 in a 1:1 ratio 6.3 #3 1:1 mixture of Base G and developer Composition G from Example 1 mixed with the developer from Example 2 in a 1:1 ratio 10

[0384] Each of the three hair dye compositions was mixed with International 20 V developer in a 1:1 mixing ratio. This mixture was applied The mixtures were applied to commercially available, 90% gray hair strands. They were left to sit on the hair (to be treated) for 5 minutes before being rinsed with water. The hair strands were then washed with a standard sulfate-based hair cleansing solution. This washing and rinsing procedure was repeated 15 times; that is, the hair strands were washed with the standard sulfate-based hair cleansing solution and then dried 15 consecutive times. Color measurements were taken, and images of the strands were captured before application, after the initial treatment with the ready-to-use hair coloring solutions, and after 5, 10, and 15 washes.

[0385] Color retention on the hair strands was evaluated as a function of washing using the CIE coordinates L*a*b*. AE represents a color difference, where a higher AE value represents increased color fading or reduced color retention. AE is defined by the following equation:

[0387] where L*, a* and b* represent the values ​​measured after a treatment, and LO*, aO* and bO* represent the values ​​measured before a treatment(s).

[0388] Hair color was analyzed before treatment with the ready-to-use hair coloring composition; immediately after the initial treatment with the ready-to-use hair coloring compositions; and after being washed 5, 10, and 15 times. The results are shown in [Fig. 1].

[0389] As illustrated by the data, the ready-to-use hair coloring compositions #1 and #2, having a pH of 7.5 and 6.3 respectively (prepared using the basic hair coloring compositions E and F), provided substantially better color retention on grey hair than the ready-to-use hair coloring composition #3 having a higher pH of 10 (prepared using the basic hair coloring composition G). EXAMPLE 4 (Tenacity study)

[0390] The procedure described above in Example 3 was repeated, except that the three ready-to-use colour compositions were applied to 90% permed hair strands (which are commercially available) instead of 90% bleached hair. The results are shown in [Fig. 2].

[0391] As illustrated by the data, the ready-to-use hair coloring compositions #1 and #2, having pH values ​​of 7.5 and 6.3 respectively (prepared using the base hair coloring compositions E and F), provided substantially better color retention on permed hair than the composition of co ready-to-use hair coloring #3 having a higher pH of 10 (prepared using the basic hair coloring composition G). Definitions

[0392] The term “hair” as used herein includes head hair, beard hair, moustache hair, eyebrows, eyelashes, and body hair, unless otherwise specified.

[0393] The term “beard hair” includes moustache hair, unless otherwise specified.

[0394] As used herein, the terms “comprising”, “having” and “including” are understood in their open, non-limiting sense.

[0395] A "hair coloring base composition" as used herein is a hair coloring composition containing one or more oxidative dye precursors and is mixed with a developer composition to form a ready-to-use hair coloring composition.

[0396] A "developer composition" as used herein is a composition containing one or more oxidizing agents, preferably a peroxide (hydrogen peroxide), and is mixed with a base hair coloring composition to form a ready-to-use hair coloring composition.

[0397] A "ready-to-use hair coloring composition" is an "active" composition that includes one or more oxidative dye precursors and one or more oxidizing agents; and is formed by combining a hair coloring base composition with a developer composition.

[0398] A "composition colorant" is a compound that colors the composition but has no appreciable coloring effect on the hair. In other words, the composition colorant is included to give color to the composition, for example, for aesthetic purposes. It is not included to give color to the hair. Hair gels, for example, may come in a variety of different colors (e.g., light blue, light pink, etc.), but applying the hair gel to the hair does not change the hair color.

[0399] The term "oil" is used here to refer to an organic compound that is insoluble in water at room temperature (25 °C) and atmospheric pressure (760 mmHg), namely, it has a water solubility of less than 5% by weight, or less than 1% by weight, or less than 0.1% by weight. The oils have in their structure a chain of at least two siloxane groups or at least one hydrocarbon chain comprising at least six carbon atoms. Furthermore, the oils are generally soluble in organic solvents under the same conditions of temperature and pressure, for example, in chloroform, ethanol, benzene, or decamethylcyclopentasiloxane. In addition, the oils are liquid at room temperature (25 °C) and atmospheric pressure (760 mmHg). The oils preferably do not contain carboxylic acid groups, namely, they do not contain -COOH or -COO- groups. As described throughout the disclosure, fatty alcohols are independent of fatty compounds and oils, i.e., even if a fatty alcohol is present in the compositions of this disclosure, the compositions may nevertheless be free or substantially free of fatty compounds of oils (since fatty alcohols are not included in the definition of fatty compounds and oils).

[0400] Throughout the disclosure, the phrase "a mixture of these" is used, following a list of items as shown in the following example where the letters A through F represent the items: "one or more items selected from the group consisting of A, B, C, D, E, F, and a mixture of these." The phrase "a mixture of these" does not require that the mixture include all of A, B, C, D, E, and F (although all of A, B, C, D, E, and F may be included). Rather, it indicates that a mixture of two or more of A, B, C, D, E, and F may be included. In other words, it is equivalent to the wording "one or more items selected from the group consisting of A, B, C, D, E, F, and a mixture of two or more of A, B, C, D, E, and F."

[0401] Similarly, the expression "a salt of it" also refers to "salts of it." Thus, when the disclosure refers to "a selected element from the group consisting of A, B, C, D, E, F, a salt of these, or a mixture of these," it indicates that one or more of A, B, C, D, and F may be included, one or more of a salt of A, a salt of B, a salt of C, a salt of D, a salt of E, and a salt of F may be included, or a mixture of any two of A, B, C, D, E, F, a salt of A, a salt of B, a salt of C, a salt of D, a salt of E, and a salt of F may be included.

[0402] The expression "one or more" means "at least one" and therefore includes individual components as well as mixtures / combinations.

[0403] Some of the various identified component categories may overlap. In cases where an overlap may exist and the composition includes both components (or the composition includes more than two overlapping components), an overlapping component does not represent more than one component. For example, a fatty acid may be considered both an emulsifier and a fatty compound. If a particular composition includes both an emulsifier and a fatty compound, a single fatty acid will serve only as an emulsifier or only as a fatty compound (the single fatty acid does not serve as both an emulsifier and a fatty compound).

[0404] The salts referred to throughout the disclosure may include salts containing a counterion such as an alkali metal, an alkaline earth metal, or an ammonium counterion. This list of counterions is not exhaustive.

[0405] The term "treat" (and its grammatical variations) is used here to do This refers to the application of the compositions of this disclosure to the surface of keratinous substrates such as hair. The term "treat" (and its grammatical variations) is also used here to refer to bringing keratinous substrates such as hair into contact with the compositions of this disclosure.

[0406] In this document, all ranges provided are intended to include each specific range within the given ranges, as well as a combination of intermediate subranges. Thus, a range from 1 to 5 specifically includes 1, 2, 3, 4, and 5, as well as subranges such as 2-5, 3-5, 2-3, 2-4, 1-4, etc. All ranges and values ​​disclosed herein are inclusive and combinable. For example, any value or point described in this document that falls within a range described in this document can serve as a minimum or maximum value to derive a subrange, etc.

[0407] The expression "substantially free" or "essentially free" as used in this document means that less than about 2% by weight of a specific material is added to a composition, relative to the total weight of the compositions. However, the compositions may include less than about 1% by weight, less than about 0.5% by weight, less than about 0.1% by weight, or none of the specified material. All components shown in this document may optionally be included or excluded from the compositions / processes / requirements. When excluded, the compositions / processes / requirements may be free or essentially free of the component. For example, a particular composition may be free or essentially free of alkoxylated compounds, e.g., ethoxylated thickeners and / or ethoxylated surfactants.Similarly, a particular composition may be free or essentially free of sulfates, such as sulfate surfactants.

Claims

Demands

1. A basic hair dye composition comprising: (a) 2-methoxymethyl-p-phenylenediamine, and one or more additional oxidative dye precursors selected from dimethylpiperazinium aminopyrazolopyridine, 2,3-diaminodihydropyrazolopyrazolone dimethosulfonate, salts thereof, and combinations thereof; (b) one or more couplers; and (c) 3% or less of one or more alkali-sausages; (d) 0.1 to 10% by weight of one or more fatty alcohols having 12 to 24 carbon atoms; (e) 5 to 40% by weight of one or more surfactants; (f) 10 to 40% by weight of one or more water-soluble organic solvents; (g) 25 to 60% by weight of water; in which (e), (f) and (g) are in quantities such that a combined quantity of (e), (f) and (g) constitutes at least 70% by weight of the basic hair coloring composition; and said basic composition being free from resorcinol and its derivatives;and the hair coloring base composition forms a ready-to-use hair coloring composition having a pH of 6 to 8 when mixed with a developer composition comprising hydrogen peroxide in a weight ratio of 1:5 to 5:1 (hair coloring base composition developer composition); and all weight percentages are based on the total weight of the hair coloring base composition.

2. Hair coloring base composition according to claim 1 having a pH of 7 to 10.

3. A basic hair coloring composition according to claim 1, wherein one or more alkalizing agents are selected from ammonia, ammonium hydroxide, ammonium carbonate, ammonium chloride, ammonium sulfate, ammonium nitrate, ammonium phosphate, ammonium acetate, ammonium hydrogen carbonate, ammonium carbamate, percarbonate salts, alkanolamines, alkali metal carbonates and a mixture thereof.

4. A basic hair coloring composition according to claim 3, wherein the alkanolamines are selected from monoeth- nolamine, diethanolamine, triethanolamine, monopropanolamine, dipropanolamine, tripropanolamine, 2-amino-2-methyl-l,3-propanediol, 2-amino-2-methyl-l-propanol and 2-amino-2-hydroxymethyl-l,3-propanediol, and a mixture of these.

5. A basic hair coloring composition according to claim 1, wherein one or more fatty alcohols are selected from cetyl alcohol, stearyl alcohol, cetearyl alcohol, behenyl alcohol, lauric alcohol, myristic or myristyl alcohol, arachidyl alcohol, lignoceryl alcohol, oleyl alcohol and mixtures thereof.

6. Hair coloring composition according to claim 1, wherein the water-soluble organic solvent(s) are selected from glycerin, mono-alcohols, polyols (polyhydric alcohols), glycols and a mixture thereof, preferably the water-soluble solvent(s) are selected from glycerin, propylene glycol, butylene glycol, pentylene glycol, dipropylene glycol, hexylene glycol, ethanol, isopropanol, t-butyl alcohol and a mixture thereof.

7. Necessary comprising: (i) one or more hair coloring base compositions according to claim 1; and (ii) one or more developer compositions comprising: (a) one or more oxidizing agents; and (b) water; wherein the hair coloring base composition(s) of (i) and the developer composition(s) of (ii) are contained separately.

8. Ready-to-use hair coloring composition comprising a mixture of: (i) the hair coloring base composition according to claim 1; and (ii) a developer composition comprising; (a) one or more oxidizing agents; and (b) water; wherein the ready-to-use hair coloring composition has a pH of 6 to 8, preferably 6.2 to 7.8, more preferably 6.5 to 7.

5.

9. A hair coloring process comprising: (i) obtaining the basic hair coloring composition according to claim 1; (ii) obtaining a developer composition comprising: (a) one or more oxidizing agents; and (b) water; (iii) mixing the base hair dye composition of (i) and the developer composition of (ii) in a weight ratio of 1:5 to 5:1 to form a ready-to-use hair dye composition having a pH of 6 to 8; and (iv) the application of the ready-to-use hair coloring composition to hair; (v) allowing the ready-to-use hair coloring composition to remain on the hair for a period of time, wherein the period of time is less than 30 minutes, preferably less than 15 minutes, more preferably less than 10 minutes; and (vi) after the time period has elapsed, rinse the ready-to-use hair coloring composition to remove it from the hair.