WASHING COMPOSITION FOR KERATINIC FIBERS COMPRISING AT LEAST ONE ANIONIC SURFACTANT, AT LEAST ONE AMPHOTERE OR ZWITTERIONIC SURFACTANT AND AT LEAST ONE GLUCAMIDE COMPOUND

A composition combining anionic surfactants, surfactant amphoteres or zwitteronics, and glucamide compounds addresses the challenges of existing hair washing compositions by enhancing washing power, cosmetic properties, and stability, resulting in clean, healthy-looking hair with improved foam generation.

FR3136977B1Active Publication Date: 2025-05-16LOREAL SA
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Patent Information

Application Number
FR2022006167
Authority / Receiving Office
FR · FR
Patent Type
Patents
Current Assignee / Owner
Filing Date
2022-06-22
Publication Date
2025-05-16
Estimated Expiration
2042-06-22

AI Technical Summary

Technical Problem

Existing washing compositions for keratinic fibers, such as hair, often have suboptimal environmental profiles due to the presence of silicones, inadequate foam generation, and rapid regrading of hair, leading to weighing down and undesirable cosmetic properties.

Method used

A composition comprising at least one anionic surfactant, at least one surfactant amphotere or zwitteronic, and at least one glucamide compound, with a specific weight ratio of anionic surfactants to total tensioactive zwitteronic content, designed to provide improved washing power, cosmetic properties, and stability.

Benefits of technology

The composition achieves excellent washing power, leaving hair particularly clean with good cosmetic properties, such as being light, soft, smooth, flexible, easy to detangle, and more disciplined, while also generating a good amount of foam and maintaining stability over time.

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Abstract

The present invention relates to a composition comprising at least one anionic surfactant, at least one amphoteric or zwitterionic surfactant, and at least one glucamide compound, with a particular weight ratio of the total anionic surfactant content (i) to the total amphoteric or zwitterionic surfactant content (ii). The invention also relates to a method for treating keratin fibers, comprising at least one step of applying a composition according to the invention to said keratin fibers.
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Description

Title of the invention: WASHING COMPOSITION FOR KERATIN FIBERS COMPRISING AT LEAST ONE ANIONIC SURFACTANT, AT LEAST ONE AMPHOTERIC OR ZWITTERIONIC SURFACTANT AND AT LEAST ONE GLUCAMIDE COMPOUND

[0001] The present invention relates to a composition comprising at least one anionic surfactant, at least one amphoteric or zwitterionic surfactant and at least one glucamide compound, with a particular weight ratio of the total content of anionic surfactant(s) (i), to the total content of amphoteric or zwitterionic surfactant(s) (ii).

[0002] The invention relates to a method for treating keratin fibers, comprising at least one step of applying to said keratin fibers a composition according to the invention.

[0003] For cleaning and / or washing keratin fibers such as hair, the use of detergent compositions (such as shampoos) based essentially on surfactants is common. These compositions are applied to wet hair and the foam generated by massage or friction with the hands allows, after rinsing with water, the elimination of various dirt initially present on the hair or skin.

[0004] Also, it is known to propose shampoos, in particular for hair sensitized or weakened to varying degrees following the action of atmospheric agents or repeated mechanical or chemical treatments, containing conditioning agents such as silicones, to give the keratin fibers conditioning properties, for example a better feel, more flexibility or even ease of detangling.

[0005] However, these washing compositions based on surfactants and silicones have several drawbacks: the environmental profile of the composition (biodegradability, water footprint) is not always optimal, due to the presence of silicone; the start of foam, the quality and more particularly the quantity of foam generated are considered insufficient; the rapid regreasing of keratin fibers accompanied by weighting.

[0006] Furthermore, repeated applications of these compositions often have the effect of inducing an unpleasant feel to the hair, a loss of volume and nervousness of the hair, and sometimes a lack of shine.

[0007] From these observations arose the interest in developing a natural cosmetic composition and biodegradable intended for the treatment of keratin fibers, advantageously silicone-free, having improved usage qualities and good cosmetic properties, and capable of washing keratin fibers without weighing them down so as to provide good conditioning properties to the keratin fibers.

[0008] At the same time, more and more users of cosmetic products are looking for more aesthetic, even more original, hair hygiene products.

[0009] There is therefore a real need to develop aesthetic compositions, stable over time, based on natural and / or biodegradable ingredients, preferably not comprising silicone, and making it possible to obtain excellent washing and usage properties, in particular in terms of foam initiation, quality and quantity of foam generated, and viscosity. It is also of interest that these compositions confer good conditioning properties to the keratin fibers, in particular in terms of feel, smoothness, flexibility and detangling.

[0010] These aims are achieved with the present invention which in particular relates to a composition, preferably cosmetic, comprising: i. at least one anionic surfactant, ii. at least one amphoteric or zwitterionic surfactant, and iii. at least one glucamide compound, and

[0011] in which the weight ratio of the total content of anionic surfactant(s) (i) to the total content of amphoteric or zwitterionic surfactant(s) (ii) is less than or equal to 4.5.

[0012] It has been found that the composition according to the invention has excellent washing power for keratin fibers.

[0013] In particular, the hair treated with the composition according to the invention is particularly clean, and has good cosmetic properties.

[0014] It has also been found that hair thus treated is particularly light, soft to the touch, smooth to the touch, supple, easy to detangle and more manageable.

[0015] Furthermore, it has been observed that the composition according to the invention has good qualities of use, in particular good foam start, good quality and quantity of foam. It has been particularly noted that the composition according to the invention makes it possible to generate a large quantity of foam.

[0016] The composition according to the invention has a viscosity suitable for use as a shampoo.

[0017] Furthermore, it has also been found that the composition according to the invention is particularly stable over time, at atmospheric pressure and at 25°C.

[0018] More particularly, when the composition according to the invention further comprises at least one opacifying agent, the composition remains homogeneous and no phenomenon of no phase shift in composition was observed.

[0019] According to an advantageous embodiment of the invention, the composition according to the invention further comprises one or more particles (e.g. opacifiers, pigments, glitter, etc.), in the form of a homogeneous and stable suspension.

[0020] The visually stable and homogeneous suspension of these particles significantly improves the aesthetics and originality of the composition according to the invention.

[0021] By "stable and homogeneous suspension", within the meaning of the invention, it is understood that said particles are dispersed homogeneously in the composition, that is to say distributed homogeneously within the composition, and that this homogeneous dispersion persists over time, that is to say that the particles do not float, do not sink, do not settle and / or do not form agglomerates in the composition over time, in particular after at least one week of storage.

[0022] The invention also relates to a method of treatment, in particular cosmetic treatment, of keratin fibers, in particular human keratin fibers such as hair, comprising at least one step of application to said keratin fibers of a composition according to the invention.

[0023] Other objects, characteristics, aspects and advantages of the invention will appear even more clearly on reading the description and the example which follows.

[0024] In this description, and unless otherwise indicated:

[0025] - the expression "at least one" is equivalent to the expression "one or more" and can be substituted for it;

[0026] - the expression "between... and..." is equivalent to the expression "ranging from... to..." and may be substituted therefor, and implies that the terminals are included;

[0027] - By the expression “greater than” and respectively the expression “less than” to the meaning of the present invention, it is understood to mean a strictly upper, respectively strictly lower open interval, and therefore that the limits are not included.

[0028] - By "keratin fibers" according to the present application, we mean more particularly mainly human keratin fibers, and more preferably hair.

[0029] - By "fatty acid" according to the present application, we mean an organic acid comprising in its structure a hydrocarbon chain, linear or branched, saturated or unsaturated comprising from 6 to 40 carbon atoms, preferably from 8 to 30 carbon atoms, more preferably from 10 to 22 carbon atoms.

[0030] - By "fatty alcohol" according to the present application, we mean an alcohol comprising in its structure a hydrocarbon chain, linear or branched, saturated or unsaturated comprising from 6 to 40 carbon atoms, preferably from 8 to 30 carbon atoms, more preferably from 10 to 22 carbon atoms.

[0031] Preferably, the composition according to the invention is free of silicone.

[0032] By the expression "silicone-free", it is meant that the composition according to the invention does not comprise silicone, or that the silicone(s) present in the composition according to the invention are comprised in a total content of less than or equal to 0.1% by weight, preferably less than or equal to 0.05% by weight, more preferably less than or equal to 0.01% by weight, relative to the total weight of the composition according to the invention, better still silicone-free (0% by weight).

[0033] By "silicone" is meant any organosilicon polymer or oligomer with a linear or cyclic, branched or crosslinked structure, of variable molecular weight, obtained for example by polymerization and / or by polycondensation of suitably functionalized silanes, and consisting essentially of a repetition of main units in which the silicon atoms are linked together by oxygen atoms (siloxane bond -Si-O-Si-), optionally substituted hydrocarbon radicals being directly linked via a carbon atom to said silicon atoms; and more particularly dialkylsiloxane polymers, amino silicones, dimethiconols.

[0034] The international standard ISO 16128-2 describes the methods for calculating the Natural, Natural Origin, Organic and Biological Origin Indices that apply to the categories of cosmetic ingredients and products defined in ISO 16128-1. ISO 16128-2 also provides a framework for determining the Natural, Natural Origin, Organic and Biological Origin Content of cosmetic products based on the characterization of the ingredients.

[0035] Preferably, the composition according to the invention has a percentage of natural origin within the meaning of international standard ISO 16128-2, greater than or equal to 90%; more preferably greater than or equal to 92%; more preferably still greater than or equal to 94%. Anionic surfactants

[0036] The composition according to the present invention comprises at least one anionic surfactant.

[0037] The term “anionic surfactant” means a surfactant, preferably non-silicone, comprising, as ionic or ionizable groups, only anionic groups.

[0038] In the present description, an entity is described as being "anionic" when it has at least one permanent negative charge or when it can be ionized into a negatively charged entity, under the conditions of use of the composition of the invention (medium, pH for example) and not comprising a cationic charge.

[0039] The anionic surfactants can be chosen from sulfate, sulfonate and carboxylic (or carboxylate) surfactants. It is obviously possible to use a mixture of these surfactants.

[0040] It is understood in this description that: - the carboxylate anionic surfactants comprise at least one carboxylic or carboxylate function (-COOH or -COO), and may optionally also comprise one or more sulfate and / or sulfonate functions; - the anionic sulfonate surfactants comprise at least one sulfonate function (-SO3H or -SO3), and may optionally further comprise one or more sulfate functions, but do not comprise a carboxylate function; and - anionic sulfate surfactants comprise at least one sulfate function but do not comprise a carboxylate or sulfonate function.

[0041] The carboxylate anionic surfactants that can be used therefore comprise at least one carboxylic or carboxylate function (-COOH or -COO).

[0042] The carboxylate anionic surfactants may be chosen from the following compounds: acylglycinates, acyllactylates, acylsarcosinates, acylglutamates; alkyl-D-galactoside-uronic acids, alkyl ether carboxylic acids, alkyl (C6-C30 aryl) ether carboxylic acids, alkyl amidoether carboxylic acids; as well as the salts of these compounds; and mixtures thereof; the alkyl and / or acyl groups of these compounds comprising from 6 to 30 carbon atoms, in particular from 12 to 28, even better from 14 to 24, or even from 16 to 22, carbon atoms; the aryl group preferably denoting a phenyl or benzyl group; these compounds may be polyoxyalkylenated, in particular polyoxyethylenated and then preferably comprising from 1 to 50 ethylene oxide units, better still from 2 to 10 ethylene oxide units.

[0043] Monoesters of C6-C24 alkyl and poly- Glycoside polycarboxylic acids such as C6-C24 alkyl polyglycoside citrates, C6-C24 alkyl polyglycoside tartrates and C6-C24 alkyl polyglycoside sulfosuccinates, and their salts.

[0044] Preferably, the carboxylate anionic surfactants are chosen from, alone or as a mixture: - acylglutamates, particularly C6-C24, or even C12-C20, such as stearoylglutamates, and in particular disodium stearoylglutamate; - acylsarcosinates, particularly C6-C24, or even C12-C20, such as palmitoyl sarcosinates, and in particular sodium palmitoyl sarcosinate; - acyllactylates, particularly Ci2-C28, or even Ci4-C24, such as behenoyl lactylates, and in particular sodium behenoyllactylate; - C6-C24 acylglycinates, especially C12-C20; - alkyl(C6-C24)ethercarboxylates, and in particular alkyl(C12-C20)ethercarboxylates; - polyoxyalkylenated alkyl(C6-C24) (amido) ether carboxylic acids, in particular those containing from 2 to 50 ethylene oxide groups; in particular in the form of salts of alkali or alkaline earth metals, ammonium, or amino alcohol.

[0045] Among the above carboxylic surfactants, mention may be made in particular of sarcosinate type surfactants, notably chosen from the alkyl(C6-C3o)sarcosinates of the following formula (I): RC(O)-N(CH3)-CH2-C(O)-OX (I) with - X denoting a hydrogen atom, an ammonium ion, an ion derived from an alkali or alkali-earth metal or an ion derived from an organic amine, preferably a hydrogen atom, and - R denoting a linear or branched alkyl group, with 5 to 29 carbon atoms. R preferably denotes a linear or branched alkyl group, with 8 to 24 carbon atoms, preferably with 12 to 20 carbon atoms.

[0046] Among the alkyl(C6-C3o)sarcosinates of formula (I) which can be used in the present composition, mention may be made of palmitoylsarcosinates, stearoylsarcosinates, myristoyl-sarcosinates, lauroylsarcosinates, and cocoylsarcosinates, in acid form or in salified form.

[0047] The anionic surfactant(s) of sarcosinate type are advantageously chosen from sodium lauroyl sarcosinate, stearoyl sarcosine, myristoyl sarcosine, and mixtures thereof, preferably from stearoyl sarcosine, myristoyl sarcosine, and mixtures thereof.

[0048] Among the above carboxylic surfactants, mention may also be made of polyoxyalkylenated alkyl(amido)ether carboxylic acids and their salts, in particular those comprising from 2 to 50 alkylene oxide groups, in particular ethylene oxide, such as the compounds proposed by the company KAO under the names AKYPO.

[0049] The polyoxyalkylenated alkyl(amido)ether carboxylic acids that can be used are preferably chosen from those of formula (II): Rl-(OC2H4)n-OCH2COOA (II) in which: - RI represents a linear or branched C6-C24 alkyl or alkenyl radical, an alkyl(C8-C9)phenyl radical, an R2CONH-CH2-CH2- radical with R2 denoting a linear or branched C9-C2i alkyl or alkenyl radical; preferably RI is a C8-C20, preferably C8-C18, alkyl radical, and aryl preferably denotes phenyl, - n is an integer or decimal number (average value) ranging from 2 to 24, preferably from 2 to 10, - A denotes H, ammonium, Na, K, Li, Mg or a monoethanolamine or triethanolamine residue.

[0050] Mixtures of compounds of formula (II) may also be used, in particular mixtures of compounds having different RI groups.

[0051] The particularly preferred polyoxyalkylenated alkyl(amido)ether carboxylic acids are those of formula (II) in which: - RI denotes a C12-C14 alkyl, cocoyl, oleyl, nonylphenyl or oc-tylphenyl radical, - A denotes a hydrogen or sodium atom, and - n varies from 2 to 20, preferably 2 to 10.

[0052] Even more preferably, compounds of formula (II) are used in which RI denotes a C12 alkyl radical, A denotes a hydrogen or sodium atom and n varies from 2 to 10.

[0053] The anionic sulfonate surfactants that can be used comprise at least one sulfonate function (-SO3H or -SO3).

[0054] The anionic sulfonate surfactants may be chosen from the following compounds: alkylsulfonates, alkylamidesulfonates, alkylarylsulfonates, alpha-olefin-sulfonates, paraffin-sulfonates, alkylsulfosuccinates, alkylethersulfosuccinates, alkylamidesulfosuccinates, alkylsulfoacetates, N-acyltaurates, acylisethionates, alkylsulfolaurates, as well as the salts of these compounds; the alkyl groups of these compounds comprising from 6 to 30 carbon atoms, in particular from 12 to 28, even better from 14 to 24, or even from 16 to 22, carbon atoms; the aryl group preferably denoting a phenyl or benzyl group; these compounds may be polyoxyalkylenated, in particular polyoxyethylenated and then preferably comprising from 1 to 50 ethylene oxide units, better still from 2 to 10 ethylene oxide units.

[0055] Preferably, the anionic sulfonate surfactants are chosen from, alone or as a mixture: - C6-C24 alkylsulfosuccinates, especially C12-C20, especially laurylsul-fosuccinates. - C6-C24 alkyl ether sulfosuccinates, in particular C12-C20; - N-acyltaurates in C6-C24, in particular in C12-C20 - (C6-C24)acylisethionates, preferably (Ci2-Ci8)acylisethionates, in particular in the form of alkali or alkaline earth metal, ammonium or amino alcohol salts.

[0056] Preferably, the anionic surfactant(s) of sulfonate type are chosen from C6-C24 N-acyltaurates, in particular C12-C20, and in particular N-acyl N- methyltaurates, C6-C24 acylisethionates, especially C12-C18, as well as their salts and mixtures.

[0057] More preferably, the anionic surfactant(s) of sulfonate type are chosen from C6-C24, in particular C12-C18, acyl isethionates, as well as their salts and their mixtures.

[0058] The anionic sulfate surfactants that can be used comprise at least one sulfate function (-OSO3H or -OSO3).

[0059] The anionic sulfate surfactants can be chosen from the following compounds: alkyl sulfates, alkyl ether sulfates, alkylamido ether sulfates, alkyl-laryl polyether sulfates, monoglyceride sulfates; as well as the salts of these compounds; the alkyl groups of these compounds comprising from 6 to 30 carbon atoms, in particular from 8 to 28, even better from 10 to 24, or even from 12 to 22, carbon atoms; the aryl group preferably denoting a phenyl or benzyl group; these compounds may be (poly)oxyalkylenated, in particular (poly)oxyethylenated and then preferably comprising from 1 to 50 ethylene oxide units, better still from 1 to 10 ethylene oxide units.

[0060] Preferably, the anionic sulfate surfactants are chosen from, alone or as a mixture: - alkyl sulfates, particularly C10-C24, or even C12-C22, - alkyl ether sulfates, in particular C10-C24, or even C12-C22, preferably comprising from 1 to 20 ethylene oxide units; in particular in the form of salts of alkali or alkaline earth metals, ammonium, or amino alcohol.

[0061] When the anionic surfactant is in salt form, said salt may be chosen from alkali metal salts such as the sodium or potassium salt, ammonium salts, amine salts and in particular amino alcohol salts, and alkaline earth metal salts such as the magnesium salt.

[0062] Examples of amino alcohol salts include mono-, di- and triethanolamine salts, mono-, di- or triisopropanolamine salts, 2-amino 2-methyl 1-propanol, 2-amino 2-methyl 1,3-propanediol and tris(hydroxymethyl)amino methane salts.

[0063] Preferably, salts of alkali or alkaline earth metals are used, and in particular sodium or magnesium salts.

[0064] Advantageously, the anionic surfactant(s) are chosen from sulfate anionic surfactants.

[0065] More preferably, the anionic surfactant(s) are chosen from alkyl sulfates, alkyl ether sulfates, alkylamidoether sulfates, alkylarylpolyether sulfates, monoglyceride sulfates, salts of these compounds, and mixtures thereof; the alkyl groups of these compounds preferably comprising from 6 to 30 carbon atoms, in particular from 8 to 28, even better from 10 to 24, or even from 12 to 22, carbon atoms; the aryl group preferably denoting a phenyl or benzyl group; these compounds can be (poly)oxyalkylenated, in particular (poly)oxyethylenated and then preferably comprising from 1 to 50 ethylene oxide units, better still from 1 to 10 ethylene oxide units.

[0066] More preferably still, the anionic surfactant(s) are chosen from: - C6-C30 alkyl sulfates, better still C8-C24, even better still C10-C24, or even C12-C22 - C6-C24 alkyl ether sulfates, better still C10-C24, or even C12-C22, preferably comprising from 1 to 20 ethylene oxide units, - the salts of these compounds and their mixtures; in particular in the form of salts of alkali or alkaline earth metals, ammonium, or amino alcohol.

[0067] More preferably still, the anionic surfactant(s) are chosen from C6-C30 alkyl sulfates, better still C8-C24, even better still C10-C24, or even C12-C22.

[0068] Preferably, the total content of anionic surfactant(s) present in the composition ranges from 0.1 to 25% by weight, more preferably from 1 to 20% by weight, even more preferably from 2 to 15% by weight, better still from 5 to 10% by weight, relative to the total weight of the composition.

[0069] Preferably, the total content of anionic sulfate surfactant(s) present in the composition ranges from 0.1 to 25% by weight, more preferably from 1 to 20% by weight, even more preferably from 2 to 15% by weight, better still from 5 to 10% by weight, relative to the total weight of the composition.

[0070] Preferably, the total content of C6-C30 alkyl sulfates present in the composition ranges from 0.1 to 25% by weight, more preferably from 1 to 20% by weight, even more preferably from 2 to 15% by weight, better still from 5 to 10% by weight, relative to the total weight of the composition. Amphoteric surfactants

[0071] The composition according to the present invention comprises at least one amphoteric or zwitterionic surfactant.

[0072] In particular, the amphoteric or zwitterionic surfactant(s), preferably non-silicone, used in the composition according to the present invention, may in particular be secondary or tertiary aliphatic amine derivatives, optionally quaternized, in which the aliphatic group is a linear or branched chain comprising from 8 to 22 carbon atoms, said amine derivatives containing at least one anionic group such as, for example, a carboxylate, sulfonate, sulfate, phosphate or phosphonate group.

[0073] Mention may in particular be made of alkyl(C8-C2o)betaines, alkyl(C8-C2o)sulfobetaines, alkyl(C8-C2o)amidoalkyl(Ci-C6)betaines, alkyl(C8-C20)-amidalkyl(Ci-C6)sulfobetaines, and mixtures thereof.

[0074] Among the derivatives of secondary or tertiary aliphatic amines, optionally quaternized, which can be used, as defined above, mention may also be made of the compounds of the following respective structures (III) and (IV): Ra-CONHCH2CH2-N+(Rb)(Rc)-CH2COO, M+, X (III) formula (III), in which: - Ra represents a C10 to C30 alkyl or alkenyl group derived from an acid RaCOOH, preferably present in hydrolyzed coconut oil, preferably Ra represents a heptyl, nonyl or undecyl group; - Rb represents a beta-hydroxyethyl group; - Rc represents a carboxymethyl group; - M+ represents a cationic counterion derived from an alkali metal, alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine; and - X represents an organic or inorganic anionic counterion, such as that chosen from halides, acetates, phosphates, nitrates, alkyl(Ci-C4)sulfates, alkyl(Ci-C4)- or alkyl(Ci-C4)aryl-sulfonates, in particular methylsulfate and ethylsulfate; or else M+ and X are absent; Ra'-CONHCH2CH2-N(B)(B') (IV) formula (IV), in which: - B represents the group -CH2CH2OX'; - B' represents the group -(CH2)ZY', with z = 1 or 2; - X' represents the group -CH2COOH, -CH2-COOZ', -CH2CH2COOH, CH2CH2 -COOZ', or a hydrogen atom; - Y' represents the group -COOH, -COOZ', -CH2CH(OH)SO3H or the group CH2 CH(OH)SO3-Z'; - Z' represents a cationic counterion derived from an alkali or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine; - Ra' represents a C10 to C30 alkyl or alkenyl group of an Ra'-COOH acid preferably present in coconut oil or in hydrolyzed linseed oil, preferably Ra' an alkyl group, in particular Cp and its iso form, an unsaturated Cp group.

[0075] These compounds are classified in the CTFA dictionary, 5th edition, 1993, under the names disodium cocoamphodiacetate, disodium lauroamphodiacetate, disodium caprylamphodiacetate, disodium capryloamphodiacetate, disodium cocoampho-dipropionate, disodium lauroamphodipropionate, disodium caprylampho-propionate, disodium capryloamphodipropionate, lauroamphodi- propionic, cocoamphodipropionic acid.

[0076] As an example, mention may be made of cocoamphodiacetate marketed by the company RHODIA under the trade name MIRANOL® C2M concentrate.

[0077] It is also possible to use compounds of formula (V): Ra”-NHCH(Y”)-(CH2)nCONH(CH2)nN(Rd)(Re) (V) formula (V), in which: - Y” represents the group -COOH, -COOZ”, -CH2-CH(OH)SO3H or the group CH2 CH(OH)SO3-Z”; - Rd and Re, independently of each other, represent a C1 to C4 alkyl or hydroxyalkyl radical; - Z” represents a cationic counterion derived from an alkali or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine; - Ra” represents a C10 to C30 alkyl or alkenyl group of an Ra”-COOH acid preferably present in coconut oil or in hydrolyzed linseed oil; and - n and n', independently of each other, denotes an integer ranging from 1 to 3.

[0078] Among the compounds of formula (V) we can cite the compound classified in the CTFA dictionary under the name sodium diethylaminopropyl cocoaspartamide and marketed by the company CHIMEX under the name CHIMEXANE HB.

[0079] These compounds can be used alone or in mixtures.

[0080] Among the amphoteric or zwitterionic surfactants mentioned above, advantageously used are alkyl(C8-C20)betaines, such as cocobetaine, alkyl(C8-C20)amidoalkyl(C3-C8)betaines, such as cocamidopropylbetaine, alkyl(C8-C20)amphoacetates, alkyl(C8-C20)amphodiacetates and mixtures thereof.

[0081] More preferably, the amphoteric or zwitterionic surfactant(s) are chosen from alkyl(C8-C20)betaines, alkyl(C8-C20)amidoalkyl(C3-C8)betaines and mixtures thereof; even more preferably from cocobetaine, cocamidopropylbetaine, and mixtures thereof.

[0082] Even better, the amphoteric or zwitterionic surfactant(s) are chosen from alkyl(C8-C2o)amidoalkyl(C3-C8)betaines, and very particularly cocamidopropylbetaine.

[0083] Preferably, the total content of amphoteric or zwitterionic surfactant(s) present in the composition ranges from 0.1 to 15% by weight, more preferably from 0.5 to 10% by weight, even more preferably from 1 to 5% by weight, relative to the total weight of the composition.

[0084] Preferably, the total content of alkyl(C8-C20)betaine(s) and alkyl(C8-C20)amidoalkyl(C3-C8)betaine(s) present in the composition ranges from 0.1 to 15% by weight, more preferably from 0.5 to 10% by weight, even more preferably from 1 to 5% by weight, relative to the total weight of the composition.

[0085] Preferably, the total content of alkyl(C8-C20)amidoalkyl(C3-C8)betaine(s), such as cocamidopropylbetaine, present in the composition ranges from 0.1 to 15% by weight, more preferably from 0.5 to 10% by weight, even more preferably from 1 to 5% by weight, relative to the total weight of the composition.

[0086] Advantageously, the total content of anionic surfactant(s) and amphoteric and zwitterionic surfactant(s) present in the composition is greater than or equal to 2% by weight, more preferably greater than or equal to 4% by weight, relative to the total weight of the composition.

[0087] Preferably, the total content of anionic surfactant(s) and amphoteric and zwitterionic surfactant(s) present in the composition ranges from 4 to 40% by weight, more preferably from 5 to 25% by weight, more preferably still from 6 to 20% by weight, better still from 7 to 15% by weight, better still from 7.5 to 12% by weight, relative to the total weight of the composition.

[0088] Preferably, the total content of anionic surfactant(s) sulfate(s) and amphoteric and zwitterionic surfactant(s) present in the composition ranges from 4 to 40% by weight, more preferably from 5 to 25% by weight, more preferably still from 6 to 20% by weight, better still from 7 to 15% by weight, better still from 7.5 to 12% by weight, relative to the total weight of the composition.

[0089] Preferably, the total content of C6-C3o alkyl sulfates and alkyl(C8-C2o)betaine(s) and alkyl(C8-C2o)amidoalkyl(C3-C8)betaine(s) present in the composition ranges from 4 to 40% by weight, more preferably from 5 to 25% by weight, more preferably still from 6 to 20% by weight, better still from 7 to 15% by weight, better still from 7.5 to 12% by weight, relative to the total weight of the composition.

[0090] According to the invention, the weight ratio of the total content of anionic surfactant(s) (i) to the total content of amphoteric or zwitterionic surfactant(s) (ii) is less than or equal to 4.5.

[0091] Preferably, the weight ratio of the total content of anionic surfactant(s) (i), to the total content of amphoteric and zwitterionic surfactant(s) (ii) is between 1 and 4.5; more preferably between 1.5 and 4.3; more preferably still between 2 and 4; better still between 2.1 and 3.9.

[0092] Preferably, the weight ratio of the total content of anionic sulfate surfactant(s) to the total content of amphoteric and zwitterionic surfactant(s) is between 1 and 4.5; more preferably between 1.5 and 4.3; more preferably still between 2 and 4; better still between 2.1 and 3.9.

[0093] Preferably, the weight ratio of the total content of C6-C30 alkyl sulfates to the total content of alkyl(C8-C20)betaine(s) and alkyl(C8-C20)amidoalkyl(C3-C8)betaine(s) is between 1 and 4.5; more preferably between 1.5 and 4.3; more preferably still between 2 and 4; better still between 2.1 and 3.9. Glucomide compounds

[0094] The composition according to the invention comprises at least one glucamide compound.

[0095] The glucamide compounds which can be used according to the invention are described in particular in patent applications WO 92 06154, US 5194639 and DE 44 43 645.

[0096] Preferably, the glucamide compounds are chosen from acyl-glucamides, more preferably those having a hydrocarbon chain comprising from 4 to 30 carbon atoms (counting the carbon atom of the carbonyl group -C(O)-), preferably from 6 to 22, better still from 6 to 20, even better still from 6 and 14.

[0097] More preferably, the glucamide compounds are chosen from those of the following general formula (A): in which: - The Gl-N group represents a glucamine, of which N is the nitrogen atom of glucamine, - Ri represents a C1-C2 alkyl radical, preferably a methyl, - R2 represents a linear or branched alkyl or alkenyl radical, C3-C29; preferably C5-C2i, more preferably C5-C19, better still C5-C13; and optionally substituted by one or more hydroxyl groups -OH.

[0098] More preferably still, in formula (A) above: - The Gl-N group represents a glucamine, of which N is the nitrogen atom of glucamine, - Ri represents a methyl, and - R2 represents a linear C3-C29 alkyl radical; preferably C5-C2i, more preferably C5-Ci9, better still C5-Ci3, better still C7-C9; and optionally substituted by one or more hydroxyl groups -OH.

[0099] Advantageously, the composition according to the invention may comprise at least two glucamide compounds; more preferably the composition according to the invention comprises two glucamide compounds.

[0100] For the purposes of the present invention, the terms “glucamide” and “glucamine” encompass all of their respective isomers.

[0101] Among the glucamide compounds which can be used according to the invention, mention may in particular be made, alone or as a mixture: - myristoyl methyl glucamide, lauroyl methyl glucamide, capryloyl methyl glucamide, caproyl methyl glucamide, cocoyl methyl glucamide, nonanoyl me- ethylglucamide, oleyl methyl glucamide, sunfloweroyl (sunfloweroyl) methyl glucamide, - methylglucamide oleoyl oleate, methylglucamide stearoyl stearate, methylglucamide tocopheryl succinate.

[0102] Particularly preferred are glucamide compounds chosen from, alone or as a mixture, myristoyl methyl glucamide, lauroyl methyl glucamide, capryloyl methyl glucamide, caproyl methyl glucamide, cocoyl methyl glucamide, nonanoyl methyl glucamide, oleyl methyl glucamide and sunfloweroyl (sunfloweroyl) methyl glucamide.

[0103] Among the mixtures of glucamide compounds, mention may be made of lauroyl / myristoyl methyl glucamide and capryloyl / caproyl methyl glucamide which are particularly preferred.

[0104] More preferably still, the composition according to the invention comprises at least capryloyl / caproyl methyl glucamide.

[0105] Preferably, the total content of glucamide compound(s) present in the composition ranges from 0.01 to 10% by weight, more preferably from 0.5 to 5% by weight, even more preferably from 0.8 to 3% by weight, relative to the total weight of the composition.

[0106] Preferably, the total content of acyl-glucamide compound(s) present in the composition ranges from 0.01 to 10% by weight, more preferably from 0.5 to 5% by weight, even more preferably from 0.8 to 3% by weight, relative to the total weight of the composition.

[0107] Preferably, the total content of acyl-glucamide compound(s) whose hydrocarbon chain comprises between 4 and 30 carbon atoms, present in the composition ranges from 0.01 to 10% by weight, more preferably from 0.5 to 5% by weight, even more preferably from 0.8 to 3% by weight, relative to the total weight of the composition.

[0108] Preferably, the total content of glucamide compound(s) of formula (A), present in the composition ranges from 0.01 to 10% by weight, more preferably from 0.5 to 5% by weight, even more preferably from 0.8 to 3% by weight, relative to the total weight of the composition.

[0109] Preferably, the total content of capryloyl / caproyl methyl glucamide in the composition ranges from 0.01 to 10% by weight, more preferably from 0.5 to 5% by weight, even more preferably from 0.8 to 3% by weight, relative to the total weight of the composition. Non-ionic surfactants

[0110] Preferably, the composition according to the present invention further comprises at least one non-ionic surfactant.

[0111] More preferably, the composition according to the present invention comprises in in addition to at least two non-ionic surfactants.

[0112] By way of examples, the non-ionic surfactants which can be used according to the invention can be chosen from: - alcohols, alpha-diols and alkyl(Ci-C2o)phenols, these compounds being polyethoxylated and / or polypropoxylated and / or polyglycerolated, the number of ethylene oxide and / or propylene oxide groups being able to range from 1 to 100, and the number of glycerol groups being able to range from 2 to 30; or these compounds comprising at least one fatty chain comprising from 8 to 40 carbon atoms, in particular from 16 to 30 carbon atoms; in particular alcohols comprising at least one C8 to C40 alkyl chain, saturated or unsaturated, linear or branched, oxyethylenated comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50, more particularly from 2 to 40 moles of ethylene oxide and comprising one or two fatty chains; - condensates of ethylene oxide and propylene oxide on fatty alcohols; - polyethoxylated fatty amides preferably having from 2 to 30 ethylene oxide units, polyglycerolated fatty amides comprising on average from 1 to 5 glycerol groups and in particular from 1.5 to 4; - ethoxylated sorbitan fatty acid esters preferably having from 2 to 40 ethylene oxide units; - sucrose fatty acid esters; - polyoxyalkylenated fatty acid esters, preferably polyoxyethylenated, having from 2 to 150 moles of ethylene oxide, including oxyethylenated vegetable oils; - N-(C6-C24 alkyl)glucamine derivatives, - amine oxides such as (Cio-Ci4 alkyl)amine oxides or N-(Cio-Ci4 acyl)aminopropylmorpholine oxides; - and their mixtures.

[0113] Preferably, the non-ionic surfactant(s) are chosen from monoesters of fatty acid and (poly)glycerol, alkyl(poly)glycosides, and mixtures thereof.

[0114] More preferably, the non-ionic surfactant(s) are chosen from C6-C40 fatty acid monoesters of (poly)glycerol, (C6-C30)alkyl(poly)glycosides, and mixtures thereof.

[0115] Among the monoesters of fatty acid and of (poly)glycerol which can be used according to the invention, mention may in particular be made of monoesters of fatty acid and of (poly)glycerol comprising on average from 1 to 30 moles of glycerol; more preferably from 1 to 10 moles of glycerol, better still from 1 to 5 moles of glycerol.

[0116] For the purposes of the present invention, the term “average” means a number average.

[0117] More preferably, the monoester(s) of fatty acid and of (poly)glycerol may be chosen from monoesters of C6-C40 fatty acid and of (poly)glycerol; more preferably still among the monoesters of C8-C30 fatty acid and (poly)glycerol.

[0118] According to a preferred embodiment of the invention, the monoester(s) of fatty acid and of (poly)glycerol are chosen from the compounds of the following formula (X): in which: - R represents a hydrocarbon chain, linear or branched, saturated or unsaturated, in C5-C39, preferably in C7-C29, better still in Cn-C2i; - m, p and r represent an integer between 0 and 30, and are such that the sum of the integers m, p and r is between 1 and 30, better between 1 and 10, and even better between 1 and 5.

[0119] Preferably according to this embodiment, p = r = 0, and m is an integer between 1 and 30, more preferably m is an integer between 1 and 10, or even between 1 and 5.

[0120] Even more preferably, the composition according to the present invention further comprises at least one monoester of fatty acid and (poly)glycerol; better still at least one monoester of fatty acid and glycerol (that is to say among the compounds of formula (X) for which p = r = 0 and m = 1); even better still at least one monoester of C6-C40 (or even C8-C30) fatty acid and glycerol.

[0121] According to a particularly preferred embodiment of the invention, the monoester(s) of fatty acid and of (poly)glycerol are chosen from the compounds of formula (XI) below: | (XI) FT TX OH in which: - R represents a hydrocarbon chain, linear or branched, saturated or unsaturated, in C5-C39, preferably in C7-C29, better in Cn-C2i, and even better in C14-C19.

[0122] Preferably according to this embodiment, the hydrocarbon chain R is unsaturated.

[0123] Most particularly preferably, the monoester(s) of fatty acid and of (poly)glycerol are chosen from monoesters of fatty acid and of glycerol (i.e. 1 mole of glycerol); preferably from monoesters of C6-C40 (even better C8-C30) fatty acid and of glycerol; and most particularly from the monoester of oleic acid and of glycerol, the monoester of sapienic acid and of glycerol, the monoester of palmitoleic acid and glycerol, monoester of linoleic acid and glycerol, monoester of lauric acid and glycerol, monoester of myristic acid and glycerol, monoester of stearic acid and glycerol, monoester of palmitic acid and glycerol, monoester of arachidic acid and glycerol, and mixtures thereof.

[0124] Better still, the monoester(s) of fatty acid and of (poly)glycerol are chosen from monoesters of oleic acid and of (poly)glycerol (such as glyceryl oleate, poly-glyceryl-2 oleate or polyglyceryl-5 oleate), and mixtures thereof.

[0125] Preferably, when they are present in the composition according to the invention, the total content of fatty acid monoester(s), preferably C6-C40 (even better C8-C30), and (poly)glycerol, is between 0.01 and 10% by weight, more preferably between 0.05 and 8% by weight, even more preferably between 0.1 and 5%, even better between 0.1 and 2% by weight, relative to the total weight of the composition.

[0126] Preferably, when they are present in the composition according to the invention, the total content of fatty acid monoester(s), preferably C6-C40 (even better C8-C30), and of glycerol present, is between 0.01 and 10% by weight, more preferably between 0.05 and 8% by weight, even more preferably between 0.1 and 5%, even better between 0.1 and 2% by weight, relative to the total weight of the composition.

[0127] Preferably, when they are present in the composition according to the invention, the total content of glyceryl oleate is between 0.01 and 10% by weight, more preferably between 0.05 and 8% by weight, more preferably still between 0.1 and 5%, even better still between 0.1 and 2% by weight, relative to the total weight of the composition.

[0128] Among the alkyl(poly)glycosides which can be used according to the invention, mention may in particular be made of the alkyl(poly)glycosides of the following general formula: R1O-(R2O)t-(G)v in which: - Ri represents a linear or branched alkyl or alkenyl radical containing 6 to 30 carbon atoms, in particular 8 to 24 carbon atoms, or an alkylphenyl radical whose linear or branched alkyl radical contains 6 to 30 carbon atoms, in particular 8 to 24 carbon atoms; - R2 represents an alkylene radical containing 2 to 4 carbon atoms, - G represents a sugar unit containing 5 to 6 carbon atoms, -1 denotes a value ranging from 0 to 10, preferably from 0 to 4, - v denotes a value ranging from 1 to 15, preferably from 1 to 4.

[0129] Preferably, the alkyl(poly)glycosides are compounds of formula described above in which: - Ri denotes a saturated or unsaturated, linear or branched alkyl radical containing from 8 to 24 carbon atoms, - R2 represents an alkylene radical containing 2 to 4 carbon atoms, -1 denotes a value ranging from 0 to 3, preferably equal to 0, - G denotes glucose, fructose or galactose, preferably glucose; - the degree of polymerization, that is to say the value of v, which can range from 1 to 15, preferably from 1 to 4; the average degree of polymerization being more particularly between 1 and 2.

[0130] The glucosidic bonds between the sugar units are generally of the 1-6 or 1-4 type, preferably of the 1-4 type.

[0131] Advantageously, the alkyl(poly)glycosides are alkyl(poly)glucosides, such as (C6-C30)alkyl(poly)glucosides. 1,4-(C8-C24)alkyl(poly)glucosides are particularly preferred, and in particular coco-glucosides, decylglucosides and caprylyl / capryl glucosides.

[0132] Among the commercial products, we can cite the products sold by the company COGNIS under the names PLANTAREN® (600 CS / U, 1200 and 2000) or PLANTACARE® (818, 1200 and 2000); the products sold by the company SEPPIC under the names ORAMIX CG 110 and ORAMIX® NS 10; the products sold by the company BASF under the name LUTENSOL GD 70 or the products sold by the company CHEM Y under the name AGIO LK.

[0133] More preferably still, the composition according to the present invention further comprises at least one alkyl(poly)glycoside; better still at least one alkyl(poly)glycoside chosen from (C6-C30)alkyl(poly)glycosides; even better still from (C8-C24)alkyl(poly)glycosides; or even from (C8-C18)alkyl(poly)glycosides such as coco-glucosides, decylglucosides, caprylyl / capryl glucosides, lauryl glucosides, and mixtures thereof.

[0134] According to a preferred embodiment of the invention, the composition comprises at least one alkyl(poly)glucoside; preferably chosen from (C6-C30)alkyl(poly)glucosides; more preferably still from (C8-C24)alkyl(poly)glucosides; even better from (C8-C18)alkyl(poly)glucosides such as coco-glucosides, decyl-glucosides, caprylyl / capryl-glucosides, lauryl glucosides, and mixtures thereof.

[0135] Preferably, when they are present in the composition according to the invention, the total content of alkyl(poly)glycoside(s) ranges from 0.01 to 10% by weight, more preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition.

[0136] Preferably, when they are present in the composition according to the invention, the total content of (C6-C3o)alkyl(poly)glycoside(s) ranges from 0.01 to 10% by weight, more preferably preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition.

[0137] Preferably, when they are present in the composition according to the invention, the total content of (C8-C24)alkyl(poly)glycoside(s) ranges from 0.01 to 10% by weight, more preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition.

[0138] Preferably, when they are present in the composition according to the invention, the total content of (C6-C30)alkyl(poly)glucoside(s) ranges from 0.01 to 10% by weight, more preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition.

[0139] Preferably, when they are present in the composition according to the invention, the total content of (C8-C24)alkyl(poly)glycoside(s) ranges from 0.01 to 10% by weight, more preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition.

[0140] In a very particularly preferred manner, the composition according to the invention further comprises: (iv) at least one monoester of fatty acid and (poly)glycerol; preferably chosen from monoesters of C6-C40 fatty acid and (poly)glycerol; more preferably from monoesters of C8-C30 fatty acid and (poly)glycerol; even more preferably from monoesters of C8-C30 fatty acid and glycerol, as described above; and (v) at least one alkyl(poly)glycoside; preferably chosen from (C6-C30)alkyl(poly)glycosides, more preferably from (C8-C24)alkyl(poly)glycosides; even more preferably from (C8-C18)alkyl(poly)glycosides; better still from coco-glucosides, decylglucosides, caprylyl / capryl glucosides, lauryl glucosides, and mixtures thereof, as described above.

[0141] Preferably, when they are present in the composition according to the invention, the weight ratio of the total content of alkyl(poly)glycoside(s) (v), to the total content of fatty acid monoester(s) and (poly)glycerol (iv) is less than or equal to 1, more preferably less than 1, more preferably still less than or equal to 0.9, better still between 0.01 and 0.9, even better still less than or equal to 0.8, or even between 0.05 and 0.8, particularly preferably less than or equal to 0.7, and very particularly preferably between 0.1 and 0.7.

[0142] Preferably, when they are present in the composition according to the invention, the weight ratio of the total content of (C6-C30)alkyl(poly)glycoside(s) (v), to the total content of monoester(s) of C6-C40 fatty acid (better still C8-C30) and of (poly)glycerol (iv) is less than or equal to 1, more preferably less than 1, more preferably particularly still less than or equal to 0.9, better still between 0.01 and 0.9, even better still less than or equal to 0.8, or even between 0.05 and 0.8, particularly preferred less than or equal to 0.7, and very particularly preferred between 0.1 and 0.7.

[0143] Preferably, when they are present in the composition according to the invention, the weight ratio of the total content of (C8-C24)alkyl(poly)glycoside(s) (v), to the total content of monoester(s) of C6-C40 fatty acid and of glycerol (iv) is less than or equal to 1, more preferably less than 1, more preferably still less than or equal to 0.9, better still between 0.01 and 0.9, even better still less than or equal to 0.8, or even between 0.05 and 0.8, particularly preferably less than or equal to 0.7, and very particularly preferably between 0.1 and 0.7.

[0144] Preferably, when they are present in the composition according to the invention, the weight ratio of the total content of (C6-C30)alkyl(poly)glucoside(s) (v), to the total content of monoester(s) of C6-C40 (better still C8-C30) fatty acid and of glycerol (iv) is less than or equal to 1, more preferably less than 1, more preferably still less than or equal to 0.9, better still between 0.01 and 0.9, even better still less than or equal to 0.8, or even between 0.05 and 0.8, particularly preferably less than or equal to 0.7, and very particularly preferably between 0.1 and 0.7. Cationic polymers

[0145] Preferably, the composition according to the present invention further comprises at least one cationic polymer.

[0146] For the purposes of the present invention, the expression "cationic polymer" designates any non-silicone polymer (not comprising a silicon atom) containing cationic groups and / or groups ionizable into cationic groups, and not containing anionic groups and / or groups ionizable into anionic groups.

[0147] Cationic polymers are not silicone (do not include a Si-O unit).

[0148] Cationic polymers may or may not be associative.

[0149] Preferably, the cationic polymer(s) are chosen from non-associative cationic polymers.

[0150] The cationic polymers that can be used preferably have a weight-average molar mass (Mw) of between 500 and 5.106 approximately, preferably of between 103 and 3.106 approximately.

[0151] Among the cationic polymers, we can cite more particularly:

[0152] (1) homopolymers or copolymers derived from acrylic esters or amides or methacrylic and comprising at least one of the units of the following formula: N R---N+....... formulas in which: - R3, identical or different, denote a hydrogen atom or a CH3 radical; - A, identical or different, represent a divalent alkyl group, linear or branched, of 1 to 6 carbon atoms, preferably 2 or 3 carbon atoms or a hydroxyalkyl group of 1 to 4 carbon atoms; - R4, R5 and R6, identical or different, represent an alkyl group having from 1 to 18 carbon atoms or a benzyl radical; preferably an alkyl group having from 1 to 6 carbon atoms; - R1 and R2, identical or different, represent a hydrogen atom or an alkyl group having from 1 to 6 carbon atoms, preferably methyl or ethyl; and - X denotes an anion derived from a mineral or organic acid such as a methosulfate anion or a halide such as chloride or bromide.

[0153] The copolymers of family (1) may also contain one or more units derived from comonomers which may be chosen from the family of acrylamides, methacrylamides, diacetone acrylamides, acrylamides and methacrylamides substituted on the nitrogen by lower alkyls (C1-C4), acrylic or methacrylic acids or their esters, vinyllactams such as vinylpyrrolidone or vinylcaprolactam, vinyl esters.

[0154] Among these copolymers of family (1), we can cite: - copolymers of acrylamide and dimethylaminoethyl methacrylate quaternized with dimethyl sulfate or with a dimethyl halide, such as that sold under the name HERCOFLOC by the company HERCULES, - copolymers of acrylamide and methacryloyloxyethyltrimethylammonium chloride, such as those sold under the name BINA QU AT P 100 by the company CIBA GEIGY, - the copolymer of acrylamide and methacryloyloxyethyltrimethylammonium methosulfate, such as that sold under the name RETEN by the company HERCULES, - vinylpyrrolidone / dialkylaminoalkyl acrylate or methacrylate copolymers, quaternized or not, such as the products sold under the name "GAFQUAT" by the company ISP such as for example "GAFQUAT 734" or "GAFQUAT 755" or the products called "COPOLYMER 845, 958 and 937". These polymers are described in detail in French patents 2,077,143 and 2,393,573, - dimethylaminoethyl methacrylate / vinylcaprolactam / vinyl-pyrrolidone terpolymers, such as the product sold under the name GAFFIX VC 713 by the company ISP, - vinylpyrrolidone / methacrylamidopropyldimethylamine copolymers, such as those marketed under the name STYLEZE CC 10 by ISP; - vinylpyrrolidone / quaternized dimethylaminopropyl methacrylamide copolymers, such as the product sold under the name "GAFQUAT HS 100" by the company ISP, - polymers, preferably crosslinked, of methacryloyloxyalkyl(Ci-C4)trialkyl(Ci-C4)ammonium salts such as polymers obtained by homopolymerization of dimethylaminoethylmethacrylate quaternized with methyl chloride, or by copolymerization of acrylamide with dimethylaminoethylmethacrylate quaternized with methyl chloride, the homo- or copolymerization being followed by crosslinking with an olefinically unsaturated compound, in particular methylene bisacrylamide. It is more particularly possible to use a crosslinked acrylamide / methacryloyloxyethyltrimethylammonium chloride copolymer (20 / 80 by weight) in the form of a dispersion comprising 50% by weight of said copolymer in mineral oil. This dispersion is marketed under the name "SALCARE® SC 92" by the company CIBA.A crosslinked homopolymer of methacryloyloxyethyl trimethylammonium chloride comprising about 50% by weight of the homopolymer in mineral oil or in a liquid ester can also be used. These dispersions are marketed under the names "SALCARE® SC 95" and "SALCARE® SC 96" by the company CIBA.

[0155] (2) Cationic polysaccharides, in particular celluloses and ga- Cationic lactomannans. Among the cationic polysaccharides, mention may be made more particularly of cellulose ether derivatives containing quaternary ammonium groups, cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer and cationic galactomannan gums.

[0156] Cellulose ether derivatives comprising quaternary ammonium groups are described in particular in FR1492597, and mention may be made of the polymers marketed under the name "UCARE POLYMER JR" (JR 400 LT, JR 125, JR 30M) or "LR" (LR 400, LR 30M) by the company AMERCHOL. These polymers are also defined in the CTFA dictionary as quaternary ammoniums of hydroxyethylcellulose having reacted with an epoxide substituted by a trimethylammonium group, such as for example polyquatemium-10.

[0157] Cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer are described in particular in patent US4131576, and mention may be made of hydroxyalkylcelluloses, such as hydroxymethyl-, hydroxyethyl- or hydroxypropyl celluloses grafted in particular with a salt of methacryloylethyl trimethylammonium, methacrylamidopropyl trimethylammonium, dimethyl-diallylammonium, such as for example polyquatemium-4. The marketed products meeting this definition are more particularly the products sold under the name "Celquat L 200" and "Celquat H 100" by the National Starch Company.

[0158] Among the cationic cellulose derivatives, it is also possible to use cationic associative celluloses, which can be chosen from quaternized cellulose derivatives, and in particular quaternized celluloses modified by groups comprising at least one fatty chain, such as linear or branched alkyl, linear or branched arylalkyl, linear or branched alkylaryl, preferably linear or branched alkyl, these groups comprising at least 8 carbon atoms, in particular from 8 to 30 carbon atoms, better still from 10 to 24, or even from 10 to 14, carbon atoms; or mixtures thereof.

[0159] Preferably, mention may be made of quaternized hydroxyethylcelluloses modified by groups comprising at least one fatty chain, such as linear or branched alkyl, linear or branched arylalkyl, linear or branched alkylaryl, preferably linear or branched alkyl, these groups comprising at least 8 carbon atoms, in particular from 8 to 30 carbon atoms, better still from 10 to 24, or even from 10 to 14, carbon atoms; or mixtures thereof.

[0160] Preferably, mention may be made of hydroxyethylcelluloses of formula (Ib):

[0161] in which:

[0162] - R represents an ammonium group RaRbRcN+-, Q in which Ra, Rb, Rc, identical or different represent a hydrogen atom or a linear or branched alkyl, C1 to C30, preferably an alkyl, and Q represents an anionic counterion such as a halide such as a chloride or bromide;

[0163] - R' represents an ammonium group R'aR'bR'cN+-, Q' in which R'a, R'b, R'c, identical or different, represent a hydrogen atom or a linear or branched alkyl, C1 to C30, preferably an alkyl, and Q' represents an anionic counterion such as a halide such as a chloride or bromide;

[0164] it being understood that at least one of the radicals Ra, Rb, Rc, R'a, R'b, R'c represents a linear or branched alkyl, C8 to C30;

[0165] - n, x and y, identical or different, represent an integer between 1 and 10,000.

[0166] Preferably, in formula (Ib), at least one of the radicals Ra, Rb, Rc, R'a, R'b, R'c represents a linear or branched alkyl, C8 to C30; better still C10 to C24, or even C10 to C50; mention may in particular be made of the dodecyl radical (C12). Preferably, the other radical(s) represent a linear or branched alkyl, C1 to C4, in particular methyl.

[0167] Preferably, in formula (Ib), only one of the radicals Ra, Rb, Rc, R'a, R'b, R'c represents a linear or branched alkyl, C8 to C30; better still C10 to C24, or even C10 to Cu; mention may in particular be made of the dodecyl radical (C12). Preferably, the other radicals represent a linear or branched alkyl, C1 to C4, in particular methyl.

[0168] Even better, R may be a group chosen from -N+(CH3)3, Q' and -N+(Ci2H25)(CH3)2, Q', preferably a group -N+(CH3)3, Q'.

[0169] Even better, R' can be a group -N+(Ci2H25)(CH3)2, Q'.

[0170] The aryl radicals preferably denote the phenyl, benzyl, naphthyl or anthryl groups.

[0171] We can notably cite the polymers with INCI names: - Polyquatemium-24, such as the product QUATRISOFT LM 200®, marketed by the company AMERCHOL / DOW CHEMICAL; - PG-Hydroxyethylcellulose Cocodimonium Chloride, such as the product CRODACEL QM®; - PG-Hydroxyethylcellulose Lauryldimonium Chloride (Ci2 alkyl), such as the product CRODACEL QL® and - PG-Hydroxyethylcellulose Stearyldimonium Chloride (C[8] alkyl) such as the product CRODACEL QS®, marketed by the company CRODA.

[0172] Mention may also be made of hydroxyethylcelluloses of formula (Ib) in which R represents trimethylammonium halide and R' represents dimethyldodecylammonium halide, preferably R represents trimethylammonium chloride Cl ,(CH3)3N+- and R' represents dimethyldodecylammonium chloride Cl ,(CH3)2(C12H25)N+-. This type of polymer is known under the INCI name Poly-quatemium-67; as commercial products, mention may be made of SOFTCAT POLYMER SL® polymers such as SL-100, SL-60, SL-30 and SL-5 from the company AMERCHOL / DOW CHEMICAL.

[0173] More particularly, the polymers of formula (Ib) are, for example, those whose viscosity is inclusively between 2000 and 3000 cPs, preferably between 2700 and 2800 cPs. Typically, SOFTCAT POLYMER SL-5 has a viscosity of 2500 cPs, SOFTCAT POLYMER SL-30 has a viscosity of 2700 cPs, SOFTCAT POLYMER SL-60 has a viscosity of 2700 cPs and SOFTCAT POLYMER SL-100 has a viscosity of 2800 cPs. SOFTCAT POLYMER SX-1300X with a viscosity of between 1000 and 2000 cPs can also be used.

[0174] Cationic galactomannan gums are described more particularly in patents US3589578 and US4031307, and mention may be made of guar gums comprising cationic trialkylammonium groups. For example, guar gums modified with a salt (for example a chloride) of 2,3-epoxypropyltrimethylammonium are used. Such products are marketed in particular under the names JAGUAR C13 S, JAGUAR C 15, JAGUAR C 17 or JAGUAR C162 or JAGUAR EXCEL by the company RHODIA. Such compounds have the INCI names guar hydroxypropyltrimonium chloride or hydroxypropyl guar hydroxypropyltrimonium chloride.

[0175] (3) polymers consisting of piperazinyl units and divalent alkylene radicals or hydroxyalkylene with linear or branched chains, optionally interrupted by oxygen, sulfur, nitrogen atoms or by aromatic or heterocyclic rings, as well as the oxidation and / or quaternization products of these polymers.

[0176] (4) water-soluble polyaminoamides, prepared in particular by polycon densification of an acidic compound with a polyamine; these polyaminoamides can be crosslinked by an epihalohydrin, a diepoxide, a dianhydride, an unsaturated dianhydride, a bis-unsaturated derivative, a bis-halohydrin, a bis-azetidinium, a bis-haloacyldiamine, an alkyl bis-halide or by an oligomer resulting from the reaction of a bifunctional compound reactive with respect to a bis-halohydrin, a bis- azetidinium, a bis-haloacyldiamine, an alkyl bis-halide, an epihalohydrin, a diepoxide or a bis-unsaturated derivative; the crosslinking agent being used in proportions ranging from 0.025 to 0.35 mole per amine group of the polyaminoamide; these polyaminoamides can be alkylated or, if they contain one or more tertiary amine functions, quaternized.

[0177] (5) polyaminoamide derivatives resulting from the condensation of polyalkylenes polyamines with polycarboxylic acids followed by alkylation by bifunctional agents. Examples include adipic acid-diacoylaminohydroxyalkyldialoylene triamine polymers in which the alkyl radical contains 1 to 4 carbon atoms and preferably denotes methyl, ethyl, propyl. Among these derivatives, mention may be made more particularly of the adipic acid / dimethylaminohydroxypropyl / diethylene triamine polymers sold under the name "Cartaretine F, F4 or F8" by the company Sandoz.

[0178] (6) polymers obtained by reaction of a polyalkylene polyamine comprising two primary amine groups and at least one secondary amine group with a dicarboxylic acid chosen from diglycolic acid and saturated aliphatic dicarboxylic acids having from 3 to 8 carbon atoms; the molar ratio between the polyalkylene polyamine and the dicarboxylic acid preferably being between 0.8:1 and 1.4:1; the resulting polyaminoamide being reacted with epichlorohydrin in a molar ratio of epichlorohydrin relative to the secondary amine group of the polyaminoamide preferably between 0.5:1 and 1.8:1. Polymers of this type are in particular marketed under the name "Hercosett 57" by the company Hercules Inc. or under the name "PD 170" or "Delsette 101" by the company Hercules in the case of the adipic acid / epoxypropyl / diethylene-triamine copolymer.

[0179] (7) alkyl diallyl amine or dialkyl diallyl ammonium cyclopolymers such as homopolymers or copolymers comprising as the main constituent of the chain units corresponding to formulas (VI) or (VII): ---- CR.. C(R^>CH2- -(CH.1F--CR~ ri ' ii H2c^ H 2 C , (VI) N+ y. (VII) H - Laughs formulas (VI) and (VII), in which: - k and t are equal to 0 or 1, the sum k + t being equal to 1; - Rn denotes a hydrogen atom or a methyl radical; - R10 and R11b, independently of each other, denote an alkyl group having from 1 to 6 carbon atoms, a hydroxyalkyl group in which the alkyl group has from 1 to 5 carbon atoms, a C1 to C4 amidoalkyl group; or R10 and Ru may denote, together with the nitrogen atom to which they are attached, heterocyclic groups, such as piperidinyl or morpholinyl; R10 and Ru, independently of each other, preferably denote an alkyl group having from 1 to 4 carbon atoms; and - Y is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate, phosphate.

[0180] Mention may be made more particularly of the homopolymer of salts (for example chloride) of dimethyldiallylammonium, for example sold under the name "MERQUAT 100" by the company NALCO (and their counterparts with low weight-average molar masses) and the copolymers of salts (for example chloride) of diallyldimethylammonium and acrylamide sold in particular under the name "MERQUAT 550" or "MERQUAT 7SPR".

[0181] (8) quaternary diammonium polymers comprising recurring units of formula: R13 R^ II ---N + - A, - N +- B -- ATII) ] : , t R^ x~ RtsX' formula (VIII), in which: - Rn, Ru, Rb and Ri6, identical or different, represent aliphatic, alicyclic, or arylaliphatic radicals comprising from 1 to 20 carbon atoms or lower hydroxyalkylaliphatic radicals (preferably C1 to C6), or Rn, R14, Ris and R16, together or separately, constitute with the nitrogen atoms to which they are attached heterocycles optionally comprising a second heteroatom other than nitrogen or R13, R14, R15 and R16 represent a linear or branched C1 to C6 alkyl radical substituted by a nitrile, ester, acyl, amide or -CO-OR i7-D or -CO-NH-Rp-D group where Rn is an alkylene and D a quaternary ammonium group; - Ai and Bi represent divalent polymethylene groups comprising from 2 to 20 carbon atoms which may be linear or branched, saturated or unsaturated, and which may contain, linked to or intercalated in the main chain, one or more aromatic rings, or one or more oxygen or sulfur atoms or sulfoxide, sulfone, disulfide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester groups, and - X denotes a union derived from a mineral or organic acid; it being understood that Ab Rn and Ri5 can form with the two nitrogen atoms to which they are attached a piperazine ring; furthermore, if Ai denotes a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene radical, Bi can also denote a group (CH2)n-CO-D-OC-(CH2)n- in which D denotes: (a) a glycol residue of formula -OZO-, where Z denotes a linear or branched hydrocarbon radical or a group corresponding to one of the following formulae: -(CH2 -CH2-O)X-CH2-CH2- and -[CH2-CH(CH3)-O]y-CH2-CH(CH3)- where x and y denote an integer from 1 to 4, representing a defined and unique degree of polymerization or any number from 1 to 4 representing an average degree of polymerization; (b) a bis-secondary diamine residue such as a piperazine derivative; c) a bis-primary diamine residue of formula: -NH-Y-NH-, where Y denotes a linear or branched hydrocarbon radical, or the divalent radical -CH2-CH2-SS-CH2-CH2-; Or d) a ureylene group of formula: -NH-CO-NH-.

[0182] Preferably, X is an anion such as chloride or bromide. These polymers have a number-average molar mass (Mn) generally between 1000 and 100000.

[0183] We can cite more particularly polymers which are made up of recurring units corresponding to the formula: R, R. U 11 -N (CHJ -N-(ŒA — RR ° sv--. formula (IX) in which Rh R2, R3 and R4, identical or different, denote an alkyl or hydroxyalkyl radical having from 1 to 4 carbon atoms approximately, n and p are whole numbers varying from 2 to 20 approximately and, X is an anion derived from a mineral or organic acid.

[0184] A particularly preferred compound of formula (IX) is that for which Rh R2, R3 and R4 represent a methyl radical, n=3, p=6 and X = Cl, called Hexadimethrine chloride according to the INCI nomenclature (CTFA).

[0185] (9) quaternary polyammonium polymers comprising units of formula (X): formula (X), in which: - R18, R19, R2o and R2i, identical or different, represent a hydrogen atom or a methyl, ethyl, propyl, [3-hydroxyethyl, [3-hydroxypropyl or -CH2CH2 (OCH2CH2)POH radical, where p is equal to 0 or to an integer between 1 and 6, provided that R[8, R[9, R20 and R2[ do not simultaneously represent a hydrogen atom, - r and s, identical or different, are whole numbers between 1 and 6, - q is equal to 0 or to an integer between 1 and 34, - X denotes an anion such as a halide, and - A denotes a radical of a dihalide or preferably represents -CH2-CH2-O-CH -CH2-,

[0186] Examples include the products "Mirapol® A 15", "Mirapol® ADI", "Mirapol® AZ1" and "Mirapol® 175" sold by the company Miranol.

[0187] (10) Quaternary polymers of vinylpyrrolidone and vinylimidazole such as for example, products marketed under the names Luviquat® FC 905, FC 550 and FC 370 by the company BASF

[0188] (11) Polyamines such as Polyquart® H sold by COGNIS, referenced under the name of "POLYETHYLENEGLYCOL (15) TALLOW POLYAMINE" in the CTFA dictionary.

[0189] (12) polymers comprising in their structure: (a) one or more patterns corresponding to the following formula (A): —CH z:— CH — ZI w M À A i k $ J i.-; (b) optionally one or more patterns corresponding to the following formula (B): —CH^—CH — | R HH—C~ H h O

[0190] In other words, these polymers can be chosen in particular from homo- or copolymers comprising one or more units derived from vinylamine and optionally one or more units derived from vinylformamide.

[0191] Preferably, these cationic polymers are chosen from polymers comprising, in their structure, from 5 to 100 mol% of units corresponding to the formula (A) and from 0 to 95 mol% of units corresponding to formula (B), preferably from 10 to 100 mol% of units corresponding to formula (A) and from 0 to 90 mol% of units corresponding to formula (B).

[0192] These polymers can be obtained for example by partial hydrolysis of polyvinylformamide. This hydrolysis can be carried out in an acidic or basic medium.

[0193] The weight-average molecular mass of said polymer, measured by light diffraction, may preferably vary from 1,000 to 3,000,000 g / mol, more preferably from 10,000 to 1,000,000 and more particularly still from 100,000 to 500,000 g / mol.

[0194] The cationic charge density of these polymers can preferably vary from 2 meq / g to 20 meq / g, more preferably from 2.5 to 15 and more particularly from 3.5 to 10 meq / g.

[0195] The polymers comprising units of formula (A) and optionally units of formula (B) are notably sold under the name LUPAMIN by the company BASF, such as, for example, and in a non-limiting manner, the products offered under the names LUPAMIN 9095, LUPAMIN 5095, LUPAMIN 1095, LUPAMIN 9030 (or LUVIQUAT 9030) and LUPAMIN 9010.

[0196] (13) and mixtures thereof.

[0197] Preferably, the cationic polymer(s) are chosen from cationic polysaccharides, in particular associative or non-associative cationic polysaccharides; more preferably non-associative cationic polysaccharides.

[0198] More preferably, the cationic polymer(s) are chosen from cellulose ether derivatives comprising quaternary ammonium groups, cationic cellulose copolymers, cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, cationic galactomannan gums, and mixtures thereof.

[0199] More preferably still, the cationic polymer(s) are chosen from cationic galactomannan gums.

[0200] In a very particularly preferred manner, the cationic polymer(s) are chosen from cationic guar gums.

[0201] Preferably, when they are present in the composition, the total content of cationic polymer(s) ranges from 0.01 to 10% by weight, more preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition.

[0202] Preferably, when they are present in the composition, the total content of cationic polysaccharide(s) ranges from 0.01 to 10% by weight, more preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition.

[0203] Preferably, when present in the composition, the total content of cationic galactomannan gum(s) ranges from 0.01 to 10% by weight, more preferably from 0.05 to 5% by weight, more preferably still from 0.1 to 3% by weight, even better still from 0.1 to 1% by weight, relative to the total weight of the composition. The particles

[0204] Preferably, the composition according to the present invention further comprises one or more particles.

[0205] By “particles” is meant small fractionated objects formed of solid particles aggregated together, of variable shapes and sizes. They may be of regular or irregular shape. They may in particular be spherical (such as granules, pellets, balls), square, rectangular, or elongated such as rods. Spherical particles are particularly preferred. The size of the particles may advantageously be, in its largest dimension, between 1 nm and 5 mm, preferably between 10 nm and 2 mm, more preferably between 100 nm and 100 pm and better still between 1 pm and 50 pm. These particle sizes may be measured with a laser granulometer (for example using the Brookhaven BI90).

[0206] Preferably, the particles according to the invention are chosen from opacifiers such as mica and glycol distearate, pigments such as titanium dioxide, fragments of one or more plants, and mixtures thereof.

[0207] For the purposes of the present invention, the term "fragment" means a piece or part of a plant, obtained for example by uprooting or grinding the plant, or by cutting said plant.

[0208] By "fragments of one or more plants" is meant, within the meaning of the present invention, that the composition comprises either several fragments of a single species of plant, or that the composition comprises several fragments of several different species of plants.

[0209] More particularly, the particles are visually suspended in a stable and homogeneous manner, in the medium, preferably cosmetic, of the composition according to the invention.

[0210] When the composition according to the invention comprises one or more particles, the suspensive properties of the composition according to the invention allow the particles to be maintained in stable and homogeneous suspension.

[0211] The viscosity of the composition according to the invention can be evaluated by determining at a temperature of 25°C, the flow time of a quantity of product (for example 90g of product flowed) through a calibrated orifice using a Ford cup viscosimeter, equipped with a Ford cup with an orifice diameter of 8 mm (cF8).

[0212] Preferably, the flow time of the composition according to the invention is greater than or equal to 30 seconds, in particular greater than or equal to 50 seconds; in particular particularly between 30 and 300 seconds, or even between 50 and 250 seconds, or even better between 50 and 120 seconds.

[0213] Preferably, the composition according to the invention further comprises at least one inorganic salt, and more preferably sodium chloride.

[0214] For the purposes of the present application, the inorganic salt(s) are different from the anionic surfactants (i) and the amphoteric or zwitterionic surfactants (ii), the particles, and more particularly from all the ingredients described above.

[0215] Preferably, the total content of inorganic salt(s) present in the composition according to the invention ranges from 0.01 to 5% by weight, more preferably from 0.05 to 3% by weight, and even more preferably from 0.1 to 2% by weight, relative to the total weight of the composition.

[0216] Preferably, the composition according to the invention comprises water, that is to say that the medium of the composition is aqueous or hydroalcoholic.

[0217] More preferably, the total water content of the composition according to the invention is between 20 and 98% by weight, more preferably between 50% and 96% by weight, even more preferably between 60 and 95% by weight, even better between 70 and 90% by weight, relative to the total weight of the composition.

[0218] The composition according to the invention may further comprise at least one organic solvent.

[0219] It is understood within the meaning of the invention that the organic solvents are liquid at 25°C and at atmospheric pressure.

[0220] As examples of organic solvents, it is possible in particular to use those which are water-soluble, such as C1-C7 alcohols, and in particular C1-C7 aliphatic or aromatic monoalcohols, C3-C7 polyols and C3-C7 polyol ethers, which can be used alone or in a mixture with water. Advantageously, the organic solvent(s) can be chosen from ethanol, isopropanol, propylene glycol, hexylene glycol, glycerin and mixtures thereof.

[0221] Preferably, the composition according to the invention comprises at least one C2-C7 polyol; more preferably C2-C6; and even more preferably propylene glycol.

[0222] Preferably, when the organic solvent(s) are present in the composition according to the invention, the total content of C2-C7 organic solvent(s) is between 0.01 and 10% by weight, more preferably between 0.05 and 5% by weight, even more preferably between 0.1 and 1% by weight, relative to the total weight of the composition.

[0223] Preferably, when the composition according to the invention comprises water, the pH of the composition is between 3.0 and 9.0, more preferably between 3.5 and 8.0, more preferably still between 4.0 and 7.0, even better between 4.5 and 6.5.

[0224] The pH of the composition according to the invention can be adjusted to the desired value by means of alkalizing agents (such as monoethanolamine) and / or acidifying agents (such as citric acid).

[0225] The composition according to the invention may optionally also contain one or more additives used in cosmetics, such as perfumes, thickeners, colorants.

[0226] These additives may be present in the composition according to the invention in an amount ranging from 0 to 20% by weight relative to the total weight of the composition.

[0227] A person skilled in the art will take care to choose these possible additives and their quantities so that they do not harm the properties of the compositions of the present invention.

[0228] The composition according to the invention can advantageously be presented in the form of a shampoo.

[0229] The invention also relates to a method for treating, in particular cosmetically, keratin fibers, in particular human keratin fibers such as hair, comprising at least one step of applying to said keratin fibers a composition as defined above.

[0230] Preferably, the process according to the invention is a process for washing and / or conditioning human keratin fibers, more particularly hair, comprising at least one step of applying to said human keratin fibers a composition as defined above.

[0231] According to a preferred embodiment of the invention, a step of rinsing the keratin fibers is carried out after the step(s) of applying to said fibers a composition according to the invention.

[0232] A step of drying the keratin fibers may be provided in the method according to the invention, in particular using a heating means such as a hair dryer, a straightening iron, a steam iron or a heating hood; the heating means being able to heat to a temperature ranging from 35°C to 230°C, preferably from 50°C to 120°C.

[0233] The invention further relates to the use of the composition according to the invention as described above for the treatment of keratin fibers, preferably for washing and / or conditioning keratin fibers.

[0234] The following examples serve to illustrate the invention without, however, being limiting in nature. Examples

[0235] Example 1: Compositions A1, A2 and A3 according to the invention are prepared from the ingredients indicated in the table below, the quantities of which are expressed in % by weight of active material (AM).

[0236] [Tables 1] Ingredients Al A2 A3 Sodium lauryl sulfate 6.7 6.5 6.7 Cocamidopropyl betaine 2.7 2.8 1.7 Coco-betaine 0.1 0.1 0.1 Capryloyl / caproyl methyl glucamide 1.0 1.4 1.0 Glyceryl oleate 0.4 0.4 0.4 Coco-glucoside 0.26 0.26 0.26 Hydroxypropyl guar hydroxy-propyltrimonium chloride 0.38 0.38 0.38 Sodium chloride 0.5 0.5 1.2 Glycol distearate 0.5 0.5 0.5 Carbomer 0.1 0.1 0.1 Preservatives qs qs qs Propylene glycol 0.1 0.2 0.1 pH agent Qsp pH = 4.8 Qsp pH = 4.8 Qsp pH = 5.3 Water Qsp 100 Qsp 100 Qsp 100 Weight ratio of the total content of anionic surfactant(s) (i), to the total content of amphoteric or zwitterionic surfactant(s) (ii) 2.4 2.2 3.7

[0237] It has been observed that hair treated with one of the compositions A1, A2 or A3 according to the invention is particularly clean, easy to detangle, supple and soft to the touch.

[0238] Furthermore, the compositions A1, A2 or A3 according to the invention generate a foam of good quality and in large quantity.

[0239] Example 2: Comparative composition B was prepared from the ingredients indicated in the table below, the quantities of which are expressed in % by weight of active ingredient (AI).

[0240] [Tables2] Ingredients B Comparative Sodium lauryl sulfate 5.90 Coco-betaine 1.61 Glyceryl oleate 0.53 Coco-glucoside 3.51 Hydroxypropyl guar hydroxy-propyltrimonium chloride 0.40 Sodium chloride 1.35 Glycol distearate 0.50 Preservatives Qs pH agent Qsp pH = 5.3 Water Qsp 100 Weight ratio of total anionic surfactant(s) content (i), to total amphoteric or zwitterionic surfactant(s) content (ii) 3.7

[0241] 2.1 Smoothing to the touch: The smoothness of the hair treated with compositions A1 and A2 of example 1 (invention) or composition B (comparative) were evaluated.

[0242] Compositions A1, A2 and B were respectively applied to strands of moderately sensitized Caucasian hair (SA20) weighing 1g and measuring 27cm in length, according to a ratio of 0.4 grams of composition / gram of hair.

[0243] The smoothness was then evaluated for each of the treated hair strands (dry or wet), by measuring the friction force (i.e. friction work in mJ) using a Lloyd Instrument (Ametek®) traction-compression machine.

[0244] More particularly, the friction force between the wick to be evaluated (dry or wet) and two rollers of the traction-compression machine which pass along the wick, from the root to the tips at constant speed, and which simulate the consumer's fingers, is measured in mJ.

[0245] The smoother the strand of hair is to the touch, the lower the measured friction force.

[0246] The results are grouped in the table below.

[0247] [Tables3] Compositions Rubbing work on wet hair (mj) Rubbing work on dry hair (mj) Al (invention) 96.9 ± 9.3 134.2 ± 11.3 A2 (invention) 92.5 ±10.4 131.99 ±7.72 B (comparative) 134.3 ±9.7 255.2 ± 18.6

[0248] It is observed that the hair treated with composition A1 or composition A2 according to the invention has better smoothness to the touch than the hair treated with comparative composition B.

[0249] 2.2 Stability: The stabilities of compositions A1 and A2 according to the invention and of comparative composition B were evaluated.

[0250] For this, compositions Al, A2 and B, white in color and with a homogeneous appearance, were placed for 2 months in an oven at a temperature of 45°C and in the dark.

[0251] After two months of storage at 45°C, it was found that the compositions A1 and A2 according to the invention remained homogeneous in appearance, white in color, and without any phase shift phenomenon.

[0252] After two months of storage at 45°C, it was found that comparative composition B is now phase-shifted and brown in color.

[0253] It appears that compositions A1 and A2 according to the invention exhibit better stability over time than comparative composition B.

[0254] Example 3: A sensory evaluation of the hair treated with compositions A1 and A2 (invention) of example 1 was carried out.

[0255] Compositions A1 and A2 according to the invention were respectively applied to locks of moderately sensitized Caucasian hair (SA20) according to a ratio of 0.4 grams of composition / gram of hair.

[0256] A sensory evaluation of the conditioning properties of each dry, then wet, treated strand was carried out by 3 experts. For this, each expert compares one of the treated strands (by Al or by A2) with a strand of hair treated with a commercial shampoo comprising a silicone and a cationic polymer and according to the same ratio of 0.4 grams of composition / gram of hair.

[0257] Each expert then rates the locks of hair treated according to the invention, according to the following notation: +3: much much better than with commercial shampoo, +2: much better than with commercial shampoo, + 1: better than with commercial shampoo, +0.5: a little better than with commercial shampoo, 0: similar to the strand treated with commercial shampoo, - 0.5: a little less good than with commercial shampoo, -1: less good than with commercial shampoo.

[0258] The results are grouped in the table below.

[0259] [Tables4] Properties Al A2 Wet hair Detangling +1 +3 Smooth +1 +1 Softness +1.5 +1 Coating +1 +2 Dry hair Smooth +1.5 +1 Softness +2 +0.5

[0260] It is found that the hair treated with the compositions A1 or A2 according to the invention has conditioning properties that are at least equivalent, and even better in certain respects, than the hair treated with the commercial shampoo based on silicone and cationic polymer.

[0261] Example 4: Compositions C1, C2 and C3 according to the invention, as well as comparative composition C', are prepared from the ingredients indicated in the table below, the quantities of which are expressed in % by weight of active material (AM).

[0262] [Tables5] Ingredients Cl invention C2 invention C3 invention C' comparative Sodium lauryl sulfate 6.6 5.4 6 7.8 Cocamidopropyl betaine 2.7 3.9 3.3 1.5 Coco-betaine 0.1 0.1 0.1 0.1 Capryloyl / caproyl methyl glucamide 1.0 1.0 1.0 1.0 Glyceryl oleate 0.4 0.4 0.4 0.4 Coco-glucoside 0.26 0.26 0.26 0.26 Hydroxypropyl guar hydroxypropyl-trimonium chloride 0.38 0.38 0.38 0.38 Sodium chloride 0.5 0.5 0.5 0.5 Glycol distearate 0.5 0.5 0.5 0.5 Carbomer 0.1 0.1 0.1 0.1 Preservatives qs qs qs qs Propylene glycol 0.1 0.1 0.1 0.1 pH agent Qsp pH = 4.8 Qsp pH = 4.8 Qsp pH = 4.8 Qsp pH = 4.8 Water Qsp 100 Qsp 100 Qsp 100 Qsp 100 Total content of anionic surfactant(s) and amphoteric and zwitterionic surfactant(s) 9.4 9.4 9.4 9.4 Weight ratio of total content of anionic surfactant(s) (i), to total content of amphoteric or zwitterionic surfactant(s) (ii) 2.4 1.3 1.8 4.9

[0263] 4.1 Smoothing to the touch and detangling: The above compositions are applied to moderately sensitized strands (alkaline solubility = 20%, SA 20) previously moistened in a standardized manner by kneading the strands for 15 seconds (6 passes between the fingers) at a rate of 1g / 2.7g of hair.

[0264] After a 1 minute pause, the hair is rinsed for 20 seconds (25 passes between the fingers).

[0265] The hair is then wrung out and assessed while still damp.

[0266] The impact of the invention on smooth feel performance was evaluated on damp hair by 5 experts, during a blind test, on a rating scale ranging from 0 (poor) to 8 (very good).

[0267] To assess smoothness, the expert grasps the strand between the thumb and index finger and slides his fingers along the strand from the top to the tips.

[0268] He assesses whether the hair is soft, whether it has no roughness, whether it does not catch the fingers, and whether it feels even.

[0269] The results are grouped in the table below.

[0270] [Tableauxô] Touch Smooth Cl invention C2 invention C3 invention C' comparative Expert 1 4 6 5 3 Expert 2 4 5 5 2 Expert 3 4 8 6 4 Expert 4 4 8 6 4 Expert 5 4 8 6 0 Average 4 7 5.6 2.6 Standard deviation 0 1.2 0.5 1.3

[0271] The experts judged that the smooth feel conferred by compositions C1, C2 and C3 according to the invention was improved compared to that of comparative composition C'.

[0272] The impact of the invention on detangling performance was evaluated on damp hair by 1 expert, during a blind test, on a rating scale ranging from 0 (poor) to 8 (very good).

[0273] To assess detangling, the expert evaluates how easily a fine comb can be passed through the hair, sliding it from root to tip.

[0274] The results are grouped in the table below.

[0275] [Tables?] Cl invention C2 invention C3 invention C' comparative 7 7 7 0

[0276] The hair treated with compositions C1, C2 and C3 according to the invention is easier to untangle compared to that treated with comparative composition C'.

Claims

Claims

1. Composition comprising: i. at least one anionic surfactant, ii. at least one amphoteric or zwitterionic surfactant, iii. at least one glucamide compound, and iv. at least one cationic galactomannan gum; wherein the weight ratio of the total content of anionic surfactant(s) (i), to the total content of amphoteric or zwitterionic surfactant(s) (ii) is between 1 and 4.

3.

2. Composition according to the preceding claim, characterized in that the anionic surfactant(s) are chosen from sulfate anionic surfactants; preferably from alkyl sulfates, alkyl ether sulfates, alkyl a-midoether sulfates, alkylarylpolyether sulfates, monoglyceride sulfates, salts of these compounds, and mixtures thereof; more preferably from C6-C30 alkyl sulfates, better still C8-C24, even better still C10-C24, or even C12-C22, C6-C24 alkyl ether sulfates, better still C10-C24, or even C12-C22, preferably comprising from 1 to 20 ethylene oxide units, salts of these compounds, and mixtures thereof; more preferably still among the C6-C30 alkyl sulfates, better still C8-C24, even better still C10-C24, or even C12-C22.

3. Composition according to any one of the preceding claims, characterized in that the amphoteric or zwitterionic surfactant(s) are chosen from alkyl(C8-C2o)betaines, alkyl(C8-C2o)amidoalkyl(C3-C8)betaines, alkyl(C8-C2o)amphoacetates, alkyl(C8-C2o)amphodiacetates and mixtures thereof; preferably from alkyl(C8-C2o)betaines, alkyl(C8-C2o)amidoalkyl(C3-C8)betaines and mixtures thereof.

4. Composition according to any one of the preceding claims, characterized in that the weight ratio of the total content of anionic surfactant(s) (i), to the total content of amphoteric or zwitterionic surfactant(s) (ii) is between 1.5 and 4.3; more preferably between 2 and 4; and better still between 2.1 and 3.

9.

5. A composition according to any preceding claim, ca- characterized in that the total content of anionic surfactant(s) and amphoteric and zwitterionic surfactant(s) ranges from 4 to 40% by weight, preferably from 5 to 25% by weight, more preferably from 6 to 20% by weight, more preferably still from 7 to 15% by weight, better still from 7.5 to 12% by weight, relative to the total weight of the composition.

6. Composition according to any one of the preceding claims, characterized in that the glucamide compound(s) are chosen from acyl-glucamides, preferably from acyl-glucamides having a hydrocarbon chain comprising from 4 to 30 carbon atoms, preferably from 6 to 22, better still from 6 to 20, even better still from 6 to 14 carbon atoms.

7. Composition according to any one of the preceding claims, characterized in that the total content of glucamide compound(s) ranges from 0.01 to 10% by weight, preferably from 0.5 to 5% by weight, more preferably from 0.8 to 3% by weight, relative to the total weight of the composition.

8. Composition according to any one of the preceding claims, characterized in that it further comprises at least one non-ionic surfactant; preferably at least one non-ionic surfactant chosen from monoesters of fatty acid and of (poly)glycerol, alkyl(poly)glycosides, and mixtures thereof; more preferably chosen from monoesters of C6-C40 fatty acid and of (poly)glycerol, (C6-C30)alkyl(poly)glycosides, and mixtures thereof.

9. Composition according to the preceding claim, characterized in that it further comprises: (iv) at least one monoester of fatty acid and of (poly)glycerol; preferably chosen from monoesters of C6-C40 fatty acid and of (poly)glycerol; more preferably from monoesters of C8-C30 fatty acid and of (poly)glycerol; more preferably still from monoesters of C8-C30 fatty acid and of glycerol; and (v) at least one alkyl(poly)glycoside; preferably chosen from (C6-C30)alkyl(poly)glycosides, more preferably from (C8-C24)alkyl(poly)glycosides; more preferably still from (C8-C18)alkyl(poly)glycosides; best among coco-glucosides, decyl-glucosides, caprylyl / capryl glucosides, lauryl glucosides, and mixtures thereof.

10. Composition according to any one of the preceding claims, characterized in that the cationic galactomannan gums are

11.

12.

13.

14. chosen from cationic guar gums. Composition according to any one of the preceding claims, characterized in that it is free from silicone. Composition according to any one of the preceding claims, characterized in that it further comprises one or more particles, preferably chosen from opacifiers, pigments, fragments of one or more plants, and mixtures thereof. Composition according to any one of the preceding claims, characterized in that it has a percentage of natural origin, within the meaning of international standard ISO 16128-2, greater than or equal to 90%; preferably greater than or equal to 92%; more preferably greater than or equal to 94%. Process for treating keratin fibers, preferably for washing and / or conditioning keratin fibers, comprising at least one step of applying to the keratin fibers a composition as defined in any one of claims 1 to 13.