Composition for cleansing and / or caring for keratin material
A composition with alpha hydroxy acid, selenium sulfide, and cellulose enhances stability and efficacy against dandruff, addressing social incapacitation due to dandruff and itching.
Patent Information
- Application Number
- PCT/CN2024/082923
- Authority / Receiving Office
- WO · WO
- Patent Type
- Applications
- Current Assignee / Owner
- Filing Date
- 2024-03-21
- Publication Date
- 2025-09-25
AI Technical Summary
Cosmetic products comprising anti-dandruff agents face challenges with stability over time, especially at elevated temperatures, leading to social incapacitation due to visible dandruff and itching.
A composition comprising alpha hydroxy acid, selenium sulfide, and cellulose, which provides improved stability over time even at elevated temperatures.
The composition maintains stability at 50 ℃ for 5 days, effectively addressing dandruff and itching issues.
Smart Images

Figure PCTCN2024082923-FTAPPB-I100001 
Figure PCTCN2024082923-FTAPPB-I100002 
Figure PCTCN2024082923-FTAPPB-I100003
Abstract
Description
COMPOSITION FOR CLEANSING AND / OR CARING FOR KERATIN MATERIALTECHNICAL FIELD
[0001] The present invention relates to a composition for cleansing and / or caring for keratin material, preferably hairs and scalps. The present invention also relates to a process for cleansing and / or caring for scalp and hair.BACKGROUND ART
[0002] The scalp is an epidermis that undergoes continual renewal, like the rest of the cutaneous tissue, and that is rich in sebaceous glands. Normally, the scalp is renewed by imperceptible, non-visible elimination of the superficial skin cells. However, excessive renewal of the cells of the stratum corneum of the scalp, for various reasons, may result in the formation of large, thick patches of cells which are visible to the naked eye, known as “dandruff” .
[0003] Dandruff conditions are chronic, frequent, recurring conditions that are socially incapacitating owing to their obvious unattractive nature. These dandruffconditions of the scalps are reflected by an impairment of the barrier function of the epidermis. What is more, these conditions may give rise to sensations of itching or pruritus, resulting in scratching behavior which amplifies the phenomenon of appearance of the dandruff.
[0004] Many cosmetic products for cleansing and / or caring for keratin material have been developed to comprise at least one anti-dandruff agent to solve the above problems. However, often, there are challenges for the cosmetic products comprising an anti-dandruff agent to be stable over time, especially at an elevating temperature.
[0005] Therefore, there is a need for a composition for cleansing and / or caring for keratin material, which comprises at least one anti-dandruff agent, and can provide improved stability over time even at an elevating temperature.SUMMARY OF THE INVENTION
[0006] The inventors have found that such a need can be achieved by the composition according to the present invention.
[0007] According to a first aspect, the present invention provides a composition, preferably for cleansing and / or caring for keratin material, comprising:
[0008] a) 0.6 wt. %to 30 wt. %of at least one alpha hydroxy acid, relative to the total weight of the composition;
[0009] b) at least one selenium sulfide; and
[0010] c) at least one cellulose.
[0011] According to a second aspect, the present invention provides use of a cellulose for improving stability of a composition comprising at least one anti-dandruff agent, wherein the anti-dandruff agent comprises an alpha hydroxy acid and / or a selenium sulfide, and optionally a beta hydroxy acid and / or derivatives thereof.
[0012] According to a third aspect, the present invention provides a process for cleansing and / or caring for keratin material, preferably hairs and scalps, comprising the following steps:
[0013] a) applying the composition as described above onto wet keratin material;
[0014] b) massaging the keratin material for 2 seconds to 120 seconds; and
[0015] c) rinsing the keratin material with water.
[0016] The inventors found that the composition according to the present invention can provide improved stability over time even at an elevating temperature, e.g., 50 ℃ for 5 days.
[0017] Other subjects and characteristics, aspects and advantages of the present invention will emerge even more clearly on reading the detailed description and the examples that follow.DETAILED DESCRIPTION OF THE INVENTION
[0018] In that which follows and unless otherwise indicated, the limits of a range of values are included within this range, in particular in the expressions “of between” and “ranging from... to... ” .
[0019] The articles “a” and “an” , as used herein, mean one or more when applied to any feature in embodiments of the present invention described in the specification and claims. The use of “a” and “an” does not limit the meaning to a single feature unless such a limit is specifically stated. Moreover, the expression “at least one” used in the present description is equivalent to the expression “one or more” .
[0020] Throughout the present application, the expression “comprising” is to be interpreted as encompassing all specifically mentioned features as well optional, additional, unspecified ones. As used herein, the use of the term “comprising” also discloses the embodiment wherein no material features or even no features other than the specifically mentioned features are present (such as “consisting essentially of” and “consisting of” ) . In the case of “consisting essentially of, ” any additional compositions, materials, and / or components that materially affect the basic and novel characteristics are excluded from such an embodiment, but any compositions, materials and / or components that do not materially affect the basic and novel characteristics can be included in the embodiment.
[0021] Unless otherwise specified, all numerical values expressing amount of ingredients and the like used in the description and claims are to be understood as being modified by the term “about” . Accordingly, unless indicated to the contrary, the numerical values and parameters described herein are approximate values which are capable of being changed according to the desired performance obtained as required. The term “about” denoting a certain value is intended to denote a range within±5%of the value, e.g., ±3%, ±2%, ±1%, and±0.5%of the value.
[0022] As used herein, the term “keratin material (s) ” means at least one material chosen from the hair, the eyelashes, the eyebrows, the skin, the nails, mucous membranes, and the scalp, and preferably the hair and the scalp.
[0023] For the purposes of the present invention and unless otherwise indicated:
[0024] - an “alkyl” radical denotes a linear or branched saturated radical containing, for example, from 1 to 30 carbon atoms.
[0025] - an “alkenyl” radical denotes a hydrocarbon group formed when a hydrogen atom is removed from an alkene group.
[0026] - an “alkoxy” radical denotes an alkyl attached to the parent molecule through an oxygen atom (i.e., "-O-alkyl" ) , where "alkyl" is as defined above.
[0027] - a "heterocyclyl" radical denotes a monovalent group derived from a ring selected from 3-to 8-membered, preferably 4-to 6-membered, monocyclic, bicyclic, or polycyclic, saturated, partially unsaturated or fully unsaturated rings comprising at least one carbon atom in addition to 1, 2, 3, or 4 heteroatoms selected from oxygen, sulfur, and nitrogen.
[0028] - an "aryl" radical denotes a monovalent hydrocarbon radical derived from a monocyclic or fused bicyclic or polycyclic ring system (in which at least one ring contains a fully conjugated π-electron system) with known aromatic characteristics.
[0029] Alpha hydroxy acid
[0030] The composition according to the present invention comprises 0.6 wt. %to 30 wt. %of at least one alpha hydroxy acid, relative to the total weight of the composition.
[0031] The term “alpha hydroxy acid” is understood to mean, according to the present invention, a carboxylic acid having at least one hydroxyl functional group occupying an alpha-position on said acid (carbon adjacent to a carboxylic acid functional group) .
[0032] The alpha hydroxy acid present in the composition according to the present invention, includes, but is not limited to, glycolic acid, citric acid, lactic acid, methyllactic acid, glucuronic acid, 2-hydroxybutanoic acid, 2-hydroxypentanoic acid, 2-hydroxyhexanoic acid, 2-hydroxyheptanoic acid, 2-hydroxyoctanoic acid, 2-hydroxynonanoic acid, 2-hydroxydecanoic acid, 2-hydroxyundecanoic acid, 2-hydroxydodecanoic acid, 2-hydroxytetradecanoic acid, 2-hydroxyhexadecanoic acid, 2-hydroxyoctadecanoic acid, 2-hydroxytetracosanoic acid, 2-hydroxyeicosanoic acid, mandelic acid, phenyllactic acid, gluconic acid, galacturonic acid, ribonic acid, tartronic acid, tartaric acid, malic acid, fumaric acid, and mixtures thereof.
[0033] Preferably, the alpha hydroxy acid is a lower acid having 2-12 carbon atoms, more preferably 2-8 carbon atoms, even more preferably 2-6 carbon atoms.
[0034] Suitable alpha hydroxy acids include glycolic acid, lactic acid, tartaric acid, citric acid, gluconic acid, and combinations thereof.
[0035] Preferably, the alpha hydroxy acid is a mono-carboxylic acid.
[0036] More preferably, the alpha hydroxy acid is a lower mono-carboxylic acid having 2-8 carbon atoms, even more preferably 2-6 carbon atoms such as lactic acid.
[0037] The most preferable alpha hydroxy acid is lactic acid, for example, the one sold under the trade name L-LACTIC ACID (90%) (CRG) by the company MUSASHINO CHEMICAL LABORATORY, and the one sold under the trade name L (4) -LACTIC ACID 90%HEAT STABLE PERSONAL CARE by the company JUNGBUNZLAUER.
[0038] Advantageously, the alpha hydroxy acid is in an amount ranging from 0.6 wt. %to 20 wt. %, preferably from 0.6 wt. %to 10 wt. %, more preferably from 0.8 wt. %to 8 wt. %, and even more preferably from 1 wt. %to 6 wt. %, relative to the total weight of the composition.
[0039] Selenium sulfide
[0040] The composition according to the present invention comprises at least one selenium sulfide (or selenium sulphide or selenium disulfide or selenium disulphide) .
[0041] Selenium sulfide is a staple item of commerce. Selenium sulfide is generally regarded as a compound having one mole of selenium and two moles of sulfur. However, it may take the form of a cyclic structure, SexSy, wherein x+y=8. As sulfur and selenium form rings and chains readily, selenium sulfide is not a pure chemical compound but a mixture, e.g., a mixture of eight-membered-ring compounds where the overall Se: S ratio is 1: 2 (so is often abbreviated as SeS2) .
[0042] Selenium sulfide is used to treat dandruff and certain scalp infections (seborrhoeic dermatitis) . It reduces itching, irritation and redness of the scalp.
[0043] According to the present invention, the selenium sulfide is added as the raw material in the form of powder whose particle generally has a particle size (D90) of less than 200μm, preferably less than 100μm, preferably less than 150μm, preferably less than 100μm, preferably less than 50μm, and more preferably less than 25μm. For example, the selenium sulfide, as the raw material, may have a particle size (D90) ranging from 1μm to 24μm, preferably 3μm to 15 μm, and more preferably 5μm to 10μm, e.g., 24μm, 20μm, 18μm, 15μm, 10μm, 8μm, 7μm, 5μm, 3μm, 2μm or 1μm. For the purpose of the present invention, the particle size (D90) corresponds to the particle size defined such that 90%by volume of the particles have a size less than the particle size (D90) . The particle size can be measured by a forward laser light scattering device (e.g., a Malvern 3600 instrument) .
[0044] One especially preferable example of the selenium sulfide is the one sold under the trade name SELENIUM SULPHIDE EP / USP MICRONIZED by the company ESKAY FINE CHEMICALS.
[0045] Advantageously, the selenium sulfide is present in an amount ranging from 0.001 wt. %to 10 wt. %, preferably from 0.005 wt. %to 5 wt. %, and more preferably from 0.01 wt. %to 3 wt. %, and still more preferably 0.1 wt. %to 2 wt. %, relative to the total weight of the composition.
[0046] Cellulose
[0047] The composition according to the present invention comprises at least one cellulose.
[0048] As used herein, the term "cellulose" is intended to mean any polysaccharide compound having in its structure sequences of glucose residues linked together via beta-1, 4 bonds. The cellulose may be unsubstituted or substituted. Further, the cellulose may be anionic, cationic, amphoteric or non-ionic.
[0049] Preferably, the cellulose that used according to the invention is chosen from unsubstituted celluloses, including those in a microcrystalline form; cellulose esters; cellulose ethers; cellulose ester ethers; and mixtures thereof.
[0050] Among the cellulose esters are mineral esters of cellulose (cellulose nitrates, sulfates, phosphates, etc. ) , organic cellulose esters (cellulose monoacetates, triacetates, amidopropionates, acetatebutyrates, acetatepropionates and acetatetrimellitates, etc. ) , and mixed organic / mineral esters of cellulose, such as cellulose acetatebutyrate sulfates and cellulose acetatepropionate sulfates.
[0051] Cellulose ethers include non-ionic cellulose ethers, anionic cellulose ethers, and cationic cellulose ethers.
[0052] Among the non-ionic cellulose ethers, mention may be made of (C1-C4) alkylcelluloses, such as methylcelluloses and ethylcelluloses (for example, Ethocel standard 100 Premium from Dow Chemical) ; (poly) hydroxy (C1-C4) alkylcelluloses, such as hydroxymethylcelluloses, hydroxyethylcelluloses (for example, Natrosol 250 HHR provided by Ashland) and hydroxypropylcelluloses (for example, Klucel EF from Aqualon) ; mixed (poly) hydroxy (C1-C4) alkyl (C1-C4) alkylcelluloses, such as hydroxypropylmethylcelluloses (for example, Methocel E4M from Dow Chemical) , hydroxyethylmethylcelluloses, hydroxyethylethylcelluloses (for example, Bermocoll 20 E 481 FQ from Akzo Nobel) and hydroxybutylmethylcelluloses.
[0053] Among the anionic cellulose ethers, mention may be made of (poly) carboxy (C1-C4) alkylcelluloses and salts thereof. By way of example, mention may be made of carboxymethylcelluloses (for example Blanose 7M from the company Aqualon) and carboxymethylhydroxyethylcelluloses, and the sodium salts thereof.
[0054] Among the cationic cellulose ethers, mention may be made of cationic cellulose derivatives such as cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, and described in particular in patent US 4131576, such as (poly) hydroxy (C1-C4) alkyl celluloses, for instance hydroxymethyl-, hydroxyethyl-or hydroxypropylcelluloses grafted especially with a methacryloylethyltrimethylammonium, methacrylamidopropyltrimethylammonium or dimethyldiallylammonium salt.
[0055] Among the cellulose ester ethers, mention may be made of hydroxypropylmethylcellulose phthalates and ethylcellulose sulfates.
[0056] According to the present invention, the cellulose is preferably chosen from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, more preferably chosen from unsubstituted celluloses.
[0057] Advantageously, the cellulose is present in an amount ranging from 0.01 wt. %to 10 wt. %, preferably from 0.05 wt. %to 5 wt. %, and more preferably from 0.1 wt. %to 1 wt. %, relative to the total weight of the composition.
[0058] Beta hydroxy acid and / or derivatives thereof
[0059] According to the present invention, the composition may further comprise at least one beta hydroxy acid and / or derivatives thereof.
[0060] The term “beta hydroxy acid” is understood to mean, according to the present invention, a carboxylic acid having a hydroxyl functional group and a carboxylic functional group separated by two carbon atoms.
[0061] Preferably, the "derivative" in the term "beta hydroxy acid and / or derivatives thereof" means the hydroxyl functional group of beta hydroxy acid, rather than the carboxylic functional group, is derived and preferably acylated.
[0062] Preferably, the beta hydroxy acid and / or derivatives thereof is selected from salicylic acid, its acylated derivatives on hydroxyl group, and its derivative of the following formula (I) :
[0063] wherein R represents a linear, branched or cyclic saturated aliphatic group or an aliphatic unsaturated group containing one or a number of double bonds, which may or may not be conjugated, these groups containing from 2 to 22, preferably 3 to 11 carbon atoms and being optionally substituted by at least one substituent selected from (a) halogen atoms, (b) the trifluoromethyl group, (c) hydroxyl groups in the free form or esterified by an acid having from 1 to 6 carbon atoms or (d) a carboxyl functional group which is free or esterified by a lower alcohol having from 1 to 6 carbon atoms;
[0064] R' represents a hydroxyl group or an ester functional group of the following formula (II) :
[0065] wherein R1 is a linear or branched saturated or unsaturated aliphatic group having from 1 to 18 carbon atoms, preferably from 4 to 15 carbon atoms.
[0066] More preferably, the beta hydroxy acid and / or derivatives thereof is the one having a salicylic moiety, including salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, 5-n-decanoylsalicylic acid, 5-n-dodecanoylsalicylic acid, 5-propanoylsalicylic acid, 5-n-hexadecanoylsalicylic acid, 5-n-oleoylsalicylic acid, and mixtures thereof.
[0067] Non-limiting examples of other useful beta hydroxy acids and / or derivatives thereof include 5-n-octylsalicylic acid, 5-n-heptyloxysalicylic acid, 4-n-heptyloxysalicylic acid, 5-tert-octylsalicylic acid, 3-tert-butyl-5-methylsalicylic acid, 3-tert-butyl-6-methylsalicylic acid, 3, 5-diisopropylsalicylic acid, 5-butoxysalicylic acid, 5-octyloxysalicylic acid, 5-benzoylsalicylic acid, beta-hydroxypropionic acid, beta-hydroxybutyric acid, beta-hydroxy beta-methylbutyric acid, carnitine, lipohydroxy acid, 3-hydroxy valeric acid, and mixtures thereof.
[0068] According to the present invention, the beta hydroxy acid and / or derivatives thereof is particularly preferably chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof, and is more preferably salicylic acid.
[0069] One particularly preferable beta hydroxy acid and / or derivatives thereof is salicylic acid, for example, the one sold under the trade name AMIPRESERVE by the company ALBAN MULLER (CRODA) , and the one sold under the trade name SALICYLIC ACID USP by the company CELLMARK.
[0070] Advantageously, the beta hydroxy acid and / or derivatives thereof is in an amount ranging from 0.05 wt. %to 10 wt. %, preferably from 0.1 wt. %to 8 wt. %, more preferably from 0.2 wt. %to 6 wt. %, and still more preferably 0.2 wt. %to 3 wt. %, relative to the total weight of the composition.
[0071] Anionic surfactant
[0072] According to the present invention, the composition may comprise at least one anionic surfactant.
[0073] In the present description, a species is termed as being "anionic" when it bears at least one permanent negative charge or when it can be ionized as a negatively charged species, under the conditions of use of the composition of the invention (for example the medium or the pH) .
[0074] Preferably, the anionic surfactant is chosen from alkyl ether sulfates.
[0075] In some instances, the alkyl ether sulfates include those having the following formula (III) :
[0076] wherein, R represents hydrogen or alkyl chain having 6 to 24 carbon atoms, preferably alkyl chain having 8 to 18 carbon atoms, and more preferably alkyl chain having 12 to 18 carbon atoms, said alkyl chain being saturated or unsaturated, linear or branched, substituted or unsubstituted;
[0077] M represents a solubilizing cation such as alkali metal ions, e.g., sodium or potassium, ammonium or substituted ammonium ions, or alkanolammonium ions, e.g., monoethanolammonium or triethanolammonium ions; and
[0078] n is an integer from 0 to 3, preferably between 1 and 3, more preferably between 2 and 3.
[0079] Preferably, the anionic surfactant is Sodium Laureth Sulfate, for example, the one sold under the trade name EMAL 170S by the company KAO, or under the trade name KOPACOL N701 S RENU ULTRA / MB MASPHATE ES701M LD RSPO MB by the company KENSING PT MUSIM MAS.
[0080] Advantageously, the anionic surfactant is present in an amount ranging from 1 wt. %to 30 wt. %, preferably from 5 wt. %to 25 wt. %, and more preferably from 10 wt. %to 20 wt. %, relative to the total weight of the composition.
[0081] Fatty amine
[0082] According to the present invention, the composition may comprise at least one fatty amine as a conditioning agent. Two or more fatty amines may be used in combination. Thus, a single type of fatty amine or a combination of different types of fatty amines may be used.
[0083] The term “fatty amines” is understood to mean primary, secondary, or tertiary fatty amines, which are optionally (poly) oxyalkylenated, or salts thereof. The fatty amines generally comprise at least one C6-C30 hydrocarbon-based chain. Preferably, the fatty amines according to the present invention are not quaternized. Preferably, the fatty amines according to the present invention are not (poly) oxyalkylenated.
[0084] Preferably, the composition according to the present invention comprises at least one fatty amine comprising at least one C6-C30 hydrocarbon-based chain.
[0085] Preferably, the composition according to the present invention comprises at least one fatty amine chosen from tertiary fatty amines.
[0086] More preferably, the composition according to the present invention comprises one or more tertiary fatty amines chosen from amidoamines.
[0087] Amidoamines are a class of chemical compounds that are formed from fatty acids and diamines. Non-limiting examples of amidoamines include those of the following formula (IV) :
[0088] RCONHR'N (R") 2 (IV)
[0089] wherein R represents a hydrocarbon radical containing at least 6 carbon atoms. preferably from 6 to 30 carbon atoms, preferably from 8 to 24 carbon atoms, and in particular a linear or branched, saturated or unsaturated and substituted or unsubstituted C6-C30, preferably C8-C24, hydrocarbon radical, preferably a linear or branched C6-C30, preferably C8-C24, alkyl radical, or a linear or branched C6-C30, preferably C8-C24, alkenyl radical; and R' represents a divalent hydrocarbon radical containing less than 6 carbon atoms, preferably from 1 to 4 carbon atoms, which may be linear or branched, saturated or unsaturated, and substituted or unsubstituted; and R" which may be identical or different, represents hydrogen or a hydrocarbon radical containing less than 6 carbon atoms, preferably from 1 to 4 carbon atoms. In addition, R" may be linear or branched, acyclic or cyclic, saturated or unsaturated, substituted or unsubstituted. Preferably, R" is a linear or branched, acyclic alkyl or alkenyl group. More preferably, R" is hydrogen or a methyl group.
[0090] Non-limiting examples of amidoamines include, but not limit to oleamidopropyl dimethylamine, stearamidopropyl dimethylamine, isostearamidopropyl dimethylamine, stearamidoethyl dimethylamine, lauramidopropyl dimethylamine, myristamidopropyl dimethylamine, behenamidopropyl dimethylamine, dilinoleamidopropyl dimethylamine, palmitamidopropyl dimethylamine, ricinoleamindopropyl dimethylamine, soyamidopropyl dimethylamine, wheat germamidopropyl dimethylamine, sunflowerseedamidopropyl dimethylamine, almondamidopropyl dimethylamine, avocadoamidopropyl dimethylamine, babassuamidopropyl dimethylamine, cocamidopropyl dimethylamine, minkamidopropyl dimethylamine, oatamidopropyl dimethylamine, sesamidopropyl dimethylamine, tallamidopropyl dimethylamine, brassicamidopropyl dimethylamine, olivamidopropyl dimethylamine, stearamidoethyl diethylamine, stearamidopropyl diethylamine, palmitamidopropyl diethylamine, palmitamidoethyl diethylamine, palmitamidoethyldimethylamine, behenamidopropyl diethylamine, behenamidoethyl diethylamine, behenamidoethyl dimethylamine, arachidamidopropyl dimethylamine, arachidamidopropyl diethylamine, arachidamidoethyl diethylamine, arachidamidoethyl dimethylamine, diethylaminoethylstearamide, and mixtures thereof. Preferably, the fatty amine is brassicamidopropyl dimethylamine.
[0091] Other suitable fatty amines include, but are not limited to, octylamine, decylamine, dodecylamine, stearylamine, stearyl dimethyl amine, and mixtures thereof.
[0092] One especially preferable example of Brassicamidopropyl Dimethylamine is the one sold under the trade name PROCONDITION 2 by INOLEX CHEMICAL COMPANY.
[0093] Advantageously, the fatty amine is present in an amount ranging from 0.01 wt. %to 10 wt. %, preferably from 0.01 wt. %to 3 wt. %, more preferably from 0.05 wt. %to 2 wt. %, and even more preferably from 0.1 wt. %to 1 wt. %, relative to the total weight of the composition.
[0094] Nitrogen-containing compound
[0095] The composition according to the present invention may comprise at least one nitrogen-containing compound having the following formula (V)
[0096] wherein R1, R2, R3, R4 and R5, independently of each other, denotes a radical chosen from:
[0097] - a hydrogen atom,
[0098] - a carboxyl group, and
[0099] - a saturated or unsaturated linear C1-C6 or branched C3-C6 alkyl group, which is optionally interrupted by one or more heteroatoms chosen from O, S and N, and / or optionally substituted with one or more groups chosen from amino, imino, amidino, guanidino, hydroxyl, sulphydryl, carboxyl, amido, C1-C6 perfluoroalkyl, C1-C6 alkoxy, sulfate, phosphate, aryl, and heterocyclyl, and
[0100] wherein R1 and R4 optionally form a ring which contains 5 or 6 atoms chosen from carbon and nitrogen.
[0101] Preferably, R1, R2, R3, R4 and R5, independently of each other, denotes a radical chosen from:
[0102] - a hydrogen atom,
[0103] - a carboxyl group, and
[0104] - a saturated or unsaturated linear C1-C6 or branched C3-C6 alkyl group, which is optionally interrupted by one or more heteroatoms chosen from O, S and N, and / or optionally substituted with one or more groups chosen from amino, imino, amidino, guanidino, hydroxyl, sulphydryl, carboxyl, amido, C1-C6 alkoxy, phenyl, and heterocyclyl chosen from pyrimidyl, piperidyl, morpholinyl, pyranyl, furyl, piperazinyl, pyridyl, imidazolyl, and indolyl, and
[0105] wherein R1 and R4 optionally form a ring which contains 5 or 6 atoms chosen from carbon or nitrogen.
[0106] According to the present invention, the nitrogen-containing compound may have a molecular weight of less than 500, preferably less than 400, and more preferably less than 250.
[0107] Non-limiting examples of the nitrogen-containing compound include, but are not limited to, arginine, including L-arginine, trolamine, diethanolamine, L-alanine, L-asparagine, L-aspartate, L-cysteine, L-glutamate, L-glutamine, L-glycine, L-histidine, L-isoleucine, L-leucine, L-lysine, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, L-valine, tris (hydroxymethyl) aminomethane, ethanolamine, diethanolamine, monoisopropanolamine, diisopropanolamine, N-dimethylaminoethanolamine, triisopropanolamine, 3-isopropoxypropylamine, 3-methoxypropylamine (3-MPA) , 3-ethoxypropylamine, 3- (2-ethylhexyloxy) -propylamine, 2- (2-aminoethoxy) ethanol (2-2AEE) , 3-butoxypropylamine (3-BPA) , and monoethanolamine (MEA) , and mixtures thereof.
[0108] Preferably, the nitrogen-containing compound is selected from the group consisting of L-arginine, trolamine, tris (hydroxymethyl) aminomethane, ethanolamine, diethanolamine, and mixtures thereof, more preferably L-arginine.
[0109] Preferably, the composition comprises at least 1 wt. %to 10 wt. %of the nitrogen-containing compound selected from the group consisting of L-arginine, trolamine, tris (hydroxymethyl) aminomethane, ethanolamine, diethanolamine, and mixtures thereof, more preferably L-arginine.
[0110] One particularly preferable of the nitrogen-containing compound is the L-arginine sold under the trade name L ARGININE by the company KYOWA HAKKO.
[0111] Advantageously, the nitrogen-containing compound is present in an amount ranging from 1 wt. %to 10 wt. %, preferably from 1.2 wt. %to 8 wt. %, more preferably from 1.5 wt. %to 5 wt. %, and even more preferably from 1.8 wt. %to 5 wt. %, relative to the total weight of the composition..
[0112] Amphoteric surfactant
[0113] The composition according to the present invention may comprise at least one amphoteric surfactant.
[0114] The term "amphoteric surfactant" refers to a surfactant simultaneously carrying the anionic and cationic hydrophilic group with its structure containing simultaneously hermaphroditic ions which are able to form cation or anion according to the (such as pH changes) ambient conditions.
[0115] Useful amphoteric surfactants include betaines, sultaines (also referred to as sulfobetaines) , alkyl amphoacetates and alkyl amphodiacetates, alkyl amphopropionates, and mixtures thereof.
[0116] Preferably, the amphoteric surfactant is chosen from sultaines.
[0117] More preferably, the amphoteric surfactant is chosen from hydroxysultaine surfactants.
[0118] In some instances, the hydroxysultaine surfactant is chosen from alkyl (C8-C20) amidoalkyl (C1-C6) hydroxyl sulfobetaines.
[0119] Preferably, non-limiting examples of the hydroxysultaine surfactant include the hydroxysultaines of formula (VI) :
[0120] wherein R represents an alkyl group having 7-18 carbon atoms.
[0121] One particularly preferable of the hydroxysultaine surfactant is cocamidopropyl hydroxysultaine, for example, the one sold under the trade name TC-SHD 50 RSPO MB by the company GUANGZHOU TINCI MATERIALS, or those available from SEPPIC or KAO CHEMICAL.
[0122] Advantageously, the amphoteric surfactant is present in an amount ranging from 0.1 wt. %to 20 wt. %, preferably from 0.5 wt. %to 15 wt. %, and more preferably from 1 wt. %to 10 wt. %, relative to the total weight of the composition.
[0123] Cationic polymer
[0124] The composition according to the present invention may comprise at least one cationic polymer, other than celluloses.
[0125] Preferably, said cationic polymer is chosen from polyquaterniums, cationic guar gum derivatives and mixtures thereof.
[0126] In some instances, the cationic polymer can comprise monomer units derived from amine-and / or quaternary ammonium-substituted monomer and / or compatible spacer monomers.
[0127] Suitable cationic polymer includes, for example: copolymers of 1-vinyl-2-pyrrolidine and 1-vinyl-3-methyl-imidazolium salt (e.g., chloride salt) (referred to as Polyquaternium-16) such as those commercially available from BASF under the LUVIQUAT tradename (e.g., LUVIQUAT FC 370) ; copolymers of 1-vinyl-2-pyrrolidine and dimethylaminoethyl methacrylate (referred to as Polyquaternium-11) such as those commercially from Gar Corporation (Wayne, N.J., USA) under the GAFQUAT tradename (e.g., GAFQUAT 755N) ; and cationic diallyl quaternary ammonium-containing polymer including, for example, dimethyldiallyammonium chloride homopolymer and copolymers of acrylamide and dimethyldiallyammonium chloride (referred to as Polyquaternium-6 and Polyquaternium-7) .
[0128] Suitable cationic polymer may include other polyquaterniums, such as polyquaternium-1, polyquaternium-2, polyquaternium-3, polyquaternium-4, polyquaternium-5, polyquaternium-8, polyquaternium-9, polyquaternium-10, polyquaternium-12, polyquaternium-13, polyquaternium-14, polyquaternium-15, polyquaternium-17, polyquaternium-18, polyquaternium-19, polyquaternium-20, polyquaternium-21, polyquaternium-22, polyquaternium-23, polyquaternium-24, polyquaternium-25, polyquaternium-26, polyquaternium-27, polyquaternium-28, polyquaternium-29, polyquaternium-30, polyquaternium-40, polyquaternium-41, polyquaternium-42, polyquaternium-43, polyquaternium-44, polyquaternium-45, polyquaternium-46, polyquaternium-47, polyquaternium-48, polyquaternium-49, polyquaternium-50, polyquaternium-51, polyquaternium-52, polyquaternium-53, polyquaternium-54, polyquaternium-55, polyquaternium-56, polyquaternium-57, polyquaternium-58, polyquaternium-59, polyquaternium-60, polyquaternium-61, polyquaternium-62, polyquaternium-63, polyquaternium-64, polyquaternium-65, polyquaternium-66, polyquaternium-67, and combinations thereof.
[0129] Preferable cationic guar gum derivative may be guar hydroxypropyltrimonium chloride, and preferably hydroxypropyl guar hydroxypropyltrimonium chloride.
[0130] According to the present invention, the cationic polymer, other than celluloses, is preferably chosen from polyquaterniums, cationic guar gum derivatives and mixtures thereof, more preferably chosen from cationic guar gum derivatives, is still more preferably guar hydroxypropyltrimonium chloride, and most preferably hydroxypropyl guar hydroxypropyltrimonium chloride.
[0131] Advantageously, the cationic polymer is present in an amount ranging from 0.01 wt. %to 10 wt. %, preferably from 0.01 wt. %to 3 wt. %, more preferably from 0.05 wt. %to 2 wt. %, and even more preferably from 0.1 wt. %to 1 wt. %, relative to the total weight of the composition.
[0132] Aqueous solvent
[0133] The composition of the present invention may comprise at least one aqueous solvent.
[0134] Preferably, the aqueous solvent of the composition according to the present invention includes water and one or more water-miscible or at least partially water-miscible compounds, for instance C2-C8 polyols and monoalcohols.
[0135] The term “polyol” should be understood as meaning any organic molecule comprising at least two free hydroxyl groups.
[0136] More preferably, the composition according to the present invention comprises water.
[0137] Advantageously, water is present in an amount ranging from 30 wt. %to 95 wt. %, preferably from 40 wt. %to 90 wt. %, and more preferably from 50 wt. %to 85 wt. %, relative to the total weight of the composition.
[0138] Additional ingredients
[0139] The composition according to the present invention may comprise one or more additional ingredients, selected from those conventionally used in products for cleansing and / or caring for keratin material, e.g., hairs and scalps.
[0140] The composition in accordance with the present invention may comprise any of the following additives: pH adjusting agents, biological extracts, fragrances, preservatives and chelating agents.
[0141] According to the present invention, non-limiting examples of pH adjusting agent include potassium acetate, potassium hydroxide, sodium carbonate, sodium hydroxide, sodium hydrogen carbonate, ethanol amines, and mixtures thereof. One particularly preferable pH adjusting agent is sodium hydroxide.
[0142] A person skilled in the art can adjust the type and amount of the additional ingredients present in the compositions according to the present invention by means of routine operations, so that the desired properties of these compositions are not adversely affected by the additional ingredients.
[0143] Composition
[0144] According to the present invention, the composition comprising the above components is a composition for cleansing and / or caring for keratin material, preferably hairs and scalps.
[0145] According to the present invention, the composition comprising the above components is preferably in the form of fluid, e.g., lotion, emulsion, paste, cream and gel. In the context of the present disclosure, the term "fluid" means the composition can flow by means of external force.
[0146] According to the present invention, the composition preferably has a pH value of 2 to 6.5, preferably 2 to 6, more preferably 3.5 to 5.2.
[0147] By means of the above specific components, the composition according to the present invention can provide improved stability over time even at an elevating temperature, e.g., 50 ℃for 5 days, even at a lower pH value, e.g., a pH value of 2 to 6.5.
[0148] According to the present invention, the microorganisms include all of the microorganisms which can affect the skin, the nails and hairs&scalps and the mucous membranes. Examples of the microorganism include, but not limited to Nondermatophytes (the Candida species such as C. albicans, etc., the Scopulariopsis species such as S. brevicaulis, and Malassezia spp. ) . These are yeasts represented by the genus candida and by Malassezia furfur (formerly called pityrosporon) . Candida affects the skin, the nails and hairs&scalps and the mucous membranes. Malasseziafurfur, which is a frequent saprophyte of the skin, especially seborrheic skin, is the agent of pityriasis versicolor.
[0149] Moreover, by means of the specific fatty amine as defined above, the composition comprising the same can further improve smoothness sensation of the keratin material, even at a lower pH value, e.g., a pH value of 2 to 6.5.
[0150] By means of the specific arginine and / or cationic polymer as defined above, the composition comprising the same can improve smoothness and / or softness sensation (s) of the keratin material, even at a lower pH value, e.g., a pH value of 2 to 6.5.
[0151] By means of the specific hydroxysultaine surfactant as defined above, the foaming property of the composition comprising the same can be improved, even at a lower pH value, e.g., a pH value of 2 to 6.5.
[0152] By means of the relatively lower particle size of the raw material of selenium sulfide as defined above, the selenium sulfide can better disperse in the composition, and further provide improved smoothness and / or softness sensations for the composition comprising the same, even at a lower pH value, e.g., a pH value of 2 to 6.5.
[0153] In one preferred embodiment, the present invention relates to a composition for cleansing and / or caring for keratin material, relative to the total weight of the composition, comprising:
[0154] a) 0.8 wt. %to 8 wt. %of at least one alpha hydroxy acid being a lower acid having 2-12 carbon atoms, more preferably 2-8 carbon atoms, even more preferably 2-6 carbon atoms;
[0155] b) 0.005 wt. %to 5 wt. %of at least one selenium sulfide; and
[0156] c) 0.05 wt. %to 5 wt. %of at least one cellulose;
[0157] wherein the composition optionally has a pH value of 2 to 6.5.
[0158] In one more preferred embodiment, the present invention relates to a composition for cleansing and / or caring for keratin material, relative to the total weight of the composition, comprising:
[0159] a) 0.8 wt. %to 8 wt. %of at least one alpha hydroxy acid being a lower acid having 2-12 carbon atoms, more preferably 2-8 carbon atoms, even more preferably 2-6 carbon atoms;
[0160] b) 0.005 wt. %to 5 wt. %of at least one selenium sulfide;
[0161] c) 0.05 wt. %to 5 wt. %of at least one unsubstituted cellulose; and optionally at least one of the following components:
[0162] d) 0.1 wt. %to 8 wt. %of at least one beta hydroxy acid and / or derivatives thereof chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof;
[0163] e) 0.05 wt. %to 2 wt. %of at least one amidoamine;
[0164] f) 0.5 wt. %to 15 wt. %of at least one hydroxysultaine surfactant;
[0165] g) 1.2 wt. %to 8 wt. %of at least one nitrogen-containing compound selected from L-arginine, trolamine, tris (hydroxymethyl) aminomethane, ethanolamine, diethanolamine, and mixtures thereof; and
[0166] h) 0.05 wt. %to 2 wt. %of at least one cationic guar gum derivative,
[0167] wherein the composition optionally has a pH value of 2 to 6.5.
[0168] In one more preferred embodiment, the present invention relates to a composition for cleansing and / or caring for hairs and scalps, relative to the total weight of the composition, comprising:
[0169] a) 1 wt. %to 6 wt. %of at least one alpha hydroxy acid being a lower mono-carboxylic acid having 2-8 carbon atoms, even more preferably 2-6 carbon atoms, more preferably lactic acid;
[0170] b) 0.2 wt. %to 6 wt. %of at least one beta hydroxy acid and / or derivatives thereof chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof;
[0171] c) 0.01 wt. %to 3 wt. %of selenium sulfide;
[0172] d) 0.1 wt. %to 1 wt. %of at least one cellulose chosen from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, preferably unsubstituted celluloses; and optionally at least one of the following components:
[0173] e) 0.1 wt. %to 1 wt. %of brassicamidopropyl dimethylamine;
[0174] f) 1 wt. %to 10 wt. %of cocamidopropyl hydroxysultaine;
[0175] g) 1.5 wt. %to 5 wt. %of L-arginine; and
[0176] h) 0.1 wt. %to 1 wt. %of hydroxypropyl guar hydroxypropyltrimonium chloride,
[0177] wherein the composition optionally has a pH value of 3.5 to 5.2.
[0178] In one more preferred embodiment, the present invention relates to a composition for cleansing and / or caring for hairs and scalps, relative to the total weight of the composition, comprising:
[0179] a) 1 wt. %to 6 wt. %of lactic acid;
[0180] b) 0.2 wt. %to 6 wt. %of salicylic acid;
[0181] c) 0.01 wt. %to 3 wt. %of selenium sulfide; and
[0182] d) 0.1 wt. %to 1 wt. %of an unsubstituted cellulose;
[0183] wherein the composition optionally has a pH value of 3.5 to 5.2.
[0184] In one even more preferred embodiment, the present invention relates to a composition for cleansing and / or caring for hairs and scalps, relative to the total weight of the composition, comprising:
[0185] a) 1 wt. %to 6 wt. %of lactic acid;
[0186] b) 0.2 wt. %to 6 wt. %of salicylic acid;
[0187] c) 0.01 wt. %to 3 wt. %of selenium sulfide;
[0188] d) 0.1 wt. %to 1 wt. %of an unsubstituted cellulose; and optionally at least one of the following components:
[0189] e) 0.1 wt. %to 1 wt. %of brassicamidopropyl dimethylamine;
[0190] f) 1 wt. %to 10 wt. %of cocamidopropyl hydroxysultaine;
[0191] g) 1.5 wt. %to 5 wt. %of L-arginine; and
[0192] h) 0.1 wt. %to 1 wt. %of hydroxypropyl guar hydroxypropyltrimonium chloride, wherein the composition optionally has a pH value of 3.5 to 5.2.
[0193] Process and use
[0194] The composition according to the present invention can be used in a process for cleansing and / or caring for keratin material, preferably hairs and scalps, by being applied onto the keratin material.
[0195] It was found that the composition according to the present invention can provide improved stability over time even at an elevating temperature.
[0196] According to a second aspect, the present invention provides use of a cellulose for improving stability of a composition comprising at least one anti-dandruff agent, wherein the anti-dandruff agent comprises an alpha hydroxy acid and / or a selenium sulfide, and optionally a beta hydroxy acid and / or derivatives thereof, wherein the alpha hydroxy acid, beta hydroxy acid and / or derivatives thereof, selenium sulfide and cellulose are preferably defined above.
[0197] Preferably, the composition comprises a mixture of an alpha hydroxy acid, a beta hydroxy acid and / or derivatives thereof, and a selenium sulfide.
[0198] Preferably, the cellulose is chosen from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, preferably chosen from unsubstituted celluloses.
[0199] In some instances, the composition has a pH value of 2 to 6.5, preferably 2 to 6, more preferably 3.5 to 5.2.
[0200] According to a third aspect, the present invention provides a process for cleansing and / or caring for keratin material, preferably hairs and scalps, comprising the following steps:
[0201] a) applying the above composition onto wet keratin material;
[0202] b) massaging the keratin material for 2 seconds to 120 seconds; and
[0203] c) rinsing the keratin material with water.
[0204] Optionally, the process according to the present invention further comprises step d) drying the keratin material.
[0205] The present invention is illustrated in greater detail by the examples described below, which are given as non-limiting illustrations.
[0206] EXAMPLES
[0207] Main raw materials used, trade names and suppliers thereof were listed in Table 1, and materials without specification here were each commercially available.
[0208] Table 1
[0209] Comparative Examples 1-4 and Inventive Example 1-4
[0210] The compositions according to comparative examples (CE. ) 1-4 and inventive examples (Ex. ) 1-4 comprising the active ingredients shown in Table 2 were prepared, wherein all amounts were expressed by percentages by weight of active ingredients with regard to the total weight of each composition.
[0211] Preparation process
[0212] The composition was prepared from a process comprising the following steps:
[0213] 1) . mixing each component of Phase A till even to form Premix 1;
[0214] 2) . adding each component of Phase B into Premix 1 and mixing them well to transparent to form Premix 2;
[0215] 3) . adding each component of Phase C into Premix 2 to form Premix 3;
[0216] 4) . adding selenium sulfide of Phase D into Premix 3 and mixing them till even to form Mixture 1; and
[0217] 5) . adjusting pH value of Mixture 1 to 3.8 by adding sodium hydroxide to form the final composition.
[0218] Evaluation of compositions
[0219] The compositions as prepared were evaluated in terms of stability.
[0220] Test of stability
[0221] For each of the compositions of Inventive Example 1-4 and Comparative Examples 1-4, the stability was tested using the low-speed Centrifuge 5702 / 5702 R / 5702 RH from EPPENDORF, comprising the following steps:
[0222] 1) . adding each composition in a 15 ml centrifuge tube;
[0223] 2) . centrifuging each sample for 1 hour at a speed of 900 rpm, and
[0224] 3) . observing the samples to determine whether precipitation appeared.
[0225] Further, the stability was tested by storing each composition at a temperature of 50 ℃ for 5 days.
[0226] The results of stability of the compositions of Inventive Example 1-4 and Comparative Examples 1-4 were respectively shown in the following Table 3.
[0227] From Table 3, it can be seen that only the composition of Inventive Examples 1-4, comprising an amount of 0.6 wt. %or more of an alpha hydroxy acid, relative to the total weight of each composition, a selenium sulfide, and a cellulose, can bring desirable stability after centrifugation for 1 h at 900 rpm and after storing at an elevating temperature of 50℃ for 5 days.
[0228] By contrast, each of the compositions of Comparative Examples 1-4, which does not comprise the cellulose of the present invention, but comprises carbomer or xanthan gum instead, or comprises an amount out of the scope of the present invention of the alpha hydroxy acid, or does not comprise an alpha hydroxy acid, cannot bring desirable stability after centrifugation or after storing at 50 ℃ for 5 days.
[0229] In sum, the composition according to the present invention can bring improved stability over time at an elevating temperature.
Claims
1.A composition, preferably for cleansing and / or caring for keratin material, comprising:a) 0.6 wt. %to 30 wt. %of at least one alpha hydroxy acid, relative to the total weight of the composition;b) at least one selenium sulfide; andc) at least one cellulose.2.The composition according to claim 1, wherein the alpha hydroxy acid is a lower acid having 2-12 carbon atoms, preferably a lower mono-carboxylic acid having 2-8 carbon atoms, preferably 2-6 carbon atoms, and is more preferably lactic acid.3.The composition according to claim 1 or 2, wherein the alpha hydroxy acid is present in an amount ranging from 0.6 wt. %to 20 wt. %, preferably from 0.6 wt. %to 10 wt. %, more preferably from 0.8 wt. %to 8 wt. %, and even more preferably from 1 wt. %to 6 wt. %, relative to the total weight of the composition.4.The composition according to any one of the preceding claims, wherein the selenium sulfide is present in an amount ranging from 0.001 wt. %to 10 wt. %, preferably from 0.005 wt. %to 5 wt. %, more preferably from 0.01 wt. %to 3 wt. %, and still more preferably 0.1 wt. %to 2 wt. %, relative to the total weight of the composition.5.The composition according to any one of the preceding claims, wherein the cellulose is chosen from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, preferably chosen from unsubstituted celluloses.6.The composition according to any one of the preceding claims, wherein the cellulose is preferably present in an amount ranging from 0.01 wt. %to 10 wt. %, preferably from 0.05 wt. %to 5 wt. %, and more preferably from 0.1 wt. %to 1 wt. %, relative to the total weight of the composition.7.The composition according to any one of the preceding claims, further comprising at least one beta hydroxy acid and / or derivatives thereof, which is preferably chosen from salicylic acid, its acylated derivatives on hydroxyl group, and its derivatives of the formula (I) : wherein R represents a linear, branched or cyclic saturated aliphatic group or an aliphatic unsaturated group containing one or a number of double bonds, which may or may not be conjugated, these groups containing from 2 to 22, preferably 3 to 11 carbon atoms and being optionally substituted by at least one substituent selected from (a) halogen atoms, (b) the trifluoromethyl group, (c) hydroxyl groups in the free form or esterified by an acid having from 1 to 6 carbon atoms or (d) a carboxyl functional group which is free or esterified by a lower alcohol having from 1 to 6 carbon atoms;R' represents a hydroxyl group or an ester functional group of the following formula (II) :wherein R1 is a linear or branched saturated or unsaturated aliphatic group having from 1 to 18 carbon atoms, preferably from 4 to 15 carbon atoms; andis more preferably chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof, and more preferably salicylic acid, andwherein the beta hydroxy acid and / or derivatives thereof is preferably present in an amount ranging from 0.05 wt. %to 10 wt. %, preferably from 0.1 wt. %to 8 wt. %, more preferably from 0.2 wt. %to 6 wt. %, and still more preferably 0.2 wt. %to 3 wt. %, relative to the total weight of the composition.8.The composition according to any one of the preceding claims, further comprising at least one anionic surfactant, which is preferably chosen from alkyl ether sulfates having the formula (III) : wherein, R represents hydrogen or an alkyl chain having 6 to 24 carbon atoms, preferably 8 to 18 carbon atoms, and more preferably 12 to 18 carbon atoms;M is a solubilizing cation such as alkali metal ions, ammonium or substituted ammonium ions, or alkanolammonium ions; andn is an integer from 0 to 3, preferably between 1 and 3, more preferably between 2 and 3; and is most preferably Sodium Laureth Sulfate, andwherein the anionic surfactant is preferably present in an amount ranging from 1 wt. %to 30 wt. %, preferably from 5 wt. %to 25 wt. %, and more preferably from 10 wt. %to 20 wt. %, relative to the total weight of the composition.9.The composition according to any one of the preceding claims, further comprising at least one fatty amine, which is preferably chosen from amidoamines having the following formula (IV) : RCONHR'N (R") 2 (IV)wherein R represents a hydrocarbon radical containing at least 6 carbon atoms, R' represents a divalent hydrocarbon radical containing less than 6 carbon atoms, and R" which may be identical or different, represents hydrogen or a hydrocarbon radical containing less than 6 carbon atoms, andmore preferably, is selected from the group consisting of oleamidopropyl dimethylamine, stearamidopropyl dimethylamine, isostearamidopropyl dimethylamine, stearamidoethyl dimethylamine, lauramidopropyl dimethylamine, myristamidopropyl dimethylamine, behenamidopropyl dimethylamine, dilinoleamidopropyl dimethylamine, palmitamidopropyl dimethylamine, ricinoleamindopropyl dimethylamine, soyamidopropyl dimethylamine, wheat germamidopropyl dimethylamine, sunflowerseedamidopropyl dimethylamine, almondamidopropyl dimethylamine, avocadoamidopropyl dimethylamine, babassuamidopropyl dimethylamine, cocamidopropyl dimethylamine, minkamidopropyl dimethylamine, oatamidopropyl dimethylamine, sesamidopropyl dimethylamine, tallamidopropyl dimethylamine, brassicamidopropyl dimethylamine, olivamidopropyl dimethylamine, stearamidoethyl diethylamine, stearamidopropyl diethylamine, palmitamidopropyl diethylamine, palmitamidoethyl diethylamine, palmitamidoethyldimethylamine, behenamidopropyl diethylamine, behenamidoethyl diethylamine, behenamidoethyl dimethylamine, arachidamidopropyl dimethylamine, arachidamidopropyl diethylamine, arachidamidoethyl diethylamine, arachidamidoethyl dimethylamine, diethylaminoethylstearamide, and mixtures thereof; andmost preferably, is brassicamidopropyl dimethylamine, andwherein the fatty amine is preferably present in an amount ranging from 0.01 wt. %to 10 wt. %, preferably from 0.01 wt. %to 3 wt. %, more preferably from 0.05 wt. %to 2 wt. %, and even more preferably from 0.1 wt. %to 1 wt. %, relative to the total weight of the composition.10.The composition according to any one of the preceding claims, further comprising at least one amphoteric surfactant, which is preferably selected from betaines, sultaines, alkyl amphoacetates and alkyl amphodiacetates, alkyl amphopropionates, and mixtures thereof, more preferably chosen from sultaines, even more preferably chosen from hydroxysultaine surfactants, still more preferably chosen from alkyl (C8-C20) amidoalkyl (C1-C6) hydroxyl sulfobetaines, and is even more preferably a hydroxysultaine surfactant having the following formula (VI) : wherein R represents an alkyl group having 7-18 carbon atoms; and is most preferably cocamidopropyl hydroxysultaine, andwherein the hydroxysultaine surfactant is preferably present in an amount ranging from 0.1 wt. %to 20 wt. %, preferably from 0.5 wt. %to 15 wt. %, and more preferably from 1 wt. %to 10 wt. %, relative to the total weight of the composition.11.The composition according to any one of the preceding claims, further comprising at least one nitrogen-containing compound having the following formula (V) wherein R1, R2, R3, R4 and R5, independently of each other, denotes a radical chosen from:- a hydrogen atom,- a carboxyl group, and- a saturated or unsaturated linear C1-C6 or branched C3-C6 alkyl group, which is optionally interrupted by one or more heteroatoms chosen from O, S and N, and / or optionally substituted with one or more groups chosen from amino, imino, amidino, guanidino, hydroxyl, sulphydryl, carboxyl, amido, C1-C6 perfluoroalkyl, C1-C6 alkoxy, sulfate, phosphate, aryl (preferably phenyl) , and heterocyclyl which is preferably chosen from pyrimidyl, piperidyl, morpholinyl, pyranyl, furyl, piperazinyl, pyridyl, imidazolyl, and indolyl, andwherein R1 and R4 optionally form a ring which contains 5 or 6 atoms chosen from carbon and nitrogen,preferably, the nitrogen-containing compound is selected from arginine, including L-arginine, trolamine, diethanolamine, L-alanine, L-asparagine, L-aspartate, L-cysteine, L-glutamate, L-glutamine, L-glycine, L-histidine, L-isoleucine, L-leucine, L-lysine, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, L-valine, tris (hydroxymethyl) aminomethane, ethanolamine, diethanolamine, monoisopropanolamine, diisopropanolamine, N-dimethylaminoethanolamine, triisopropanolamine, 3-isopropoxypropylamine, 3-methoxypropylamine (3-MPA) , 3-ethoxypropylamine, 3- (2-ethylhexyloxy) -propylamine, 2- (2-aminoethoxy) ethanol (2-2AEE) , 3-butoxypropylamine (3-BPA) , and monoethanolamine (MEA) , and mixtures thereof,more preferably, is selected from L-arginine, trolamine, tris (hydroxymethyl) amino-methane, ethanolamine, diethanolamine, and mixtures thereof, andeven more preferably, is L-arginine; andwherein the nitrogen-containing compound is preferably present in an amount ranging from 1 wt. %to 10 wt. %, preferably from 1.2 wt. %to 8 wt. %, and more preferably from 1.5 wt. %to 5 wt. %, and even more preferably from 1.8 wt. %to 5 wt. %, relative to the total weight of the composition.12.The composition according to any one of the preceding claims, further comprising at least one cationic polymer, other than celluloses, which is preferably chosen from polyquaterniums, cationic guar gum derivatives and mixtures thereof, more preferably chosen from cationic guar gum derivatives, is still more preferably guar hydroxypropyltrimonium chloride, and most preferably hydroxypropyl guar hydroxypropyltrimonium chloride,wherein the cationic polymer is preferably present in an amount ranging from 0.01 wt. %to 10 wt. %, preferably from 0.01 wt. %to 3 wt. %, more preferably from 0.05 wt. %to 2 wt. %, and even more preferably from 0.1 wt. %to 1 wt. %, relative to the total weight of the composition.13.A composition for cleansing and / or caring for hairs and scalps, relative to the total weight of the composition, comprising:a) 1 wt. %to 6 wt. %of at least one alpha hydroxy acid being a lower mono-carboxylic acid having 2-8 carbon atoms, even more preferably 2-6 carbon atoms, more preferably lactic acid;b) 0.2 wt. %to 6 wt. %of at least one beta hydroxy acid and / or derivatives thereof chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof;c) 0.01 wt. %to 3 wt. %of selenium sulfide;d) 0.1 wt. %to 1 wt. %of at least one cellulose chosen from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, preferably unsubstituted celluloses; and optionally at least one of the following components:e) 0.1 wt. %to 1 wt. %of brassicamidopropyl dimethylamine;f) 1 wt. %to 10 wt. %of cocamidopropyl hydroxysultaine;g) 1.5 wt. %to 5 wt. %of L-arginine; andh) 0.1 wt. %to 1 wt. %of hydroxypropyl guar hydroxypropyltrimonium chloride,wherein the composition optionally has a pH value of 3.5 to 5.2.14.Use of a cellulose for improving stability of a composition comprising at least one anti-dandruff agent, wherein the anti-dandruff agent comprises an alpha hydroxy acid and / or a selenium sulfide, and optionally a beta hydroxy acid and / or derivatives thereof, and preferably comprises a mixture of an alpha hydroxy acid, a beta hydroxy acid and / or derivatives thereof, and a selenium sulfide; and wherein the composition is preferably defined according to any one of claims 1-13.15.A process for cleansing and / or caring for keratin material, more preferably hairs and scalps, comprising the following steps:a) applying the composition according to any one of claims 1 to 13 onto wet keratin material;b) massaging the keratin material for 2 seconds to 120 seconds; andc) rinsing the keratin material with water.
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