MXPA00001033A - Aqueous composition for bleaching keratin fibers, especially hair, includes combination of water-soluble solvent and nonionic amphiphilic polymer with at least one fatty chain - Google Patents

Aqueous composition for bleaching keratin fibers, especially hair, includes combination of water-soluble solvent and nonionic amphiphilic polymer with at least one fatty chain

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Publication number
MXPA00001033A
MXPA00001033A MXPA/A/2000/001033A MXPA00001033A MXPA00001033A MX PA00001033 A MXPA00001033 A MX PA00001033A MX PA00001033 A MXPA00001033 A MX PA00001033A MX PA00001033 A MXPA00001033 A MX PA00001033A
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Mexico
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carbon atoms
composition according
group
alkyl
weight
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MXPA/A/2000/001033A
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Spanish (es)
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Legrand Frederic
Millequant Jean
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L'oreal
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Abstract

The composition comprises combination of water-soluble solvent and nonionic amphiphilic polymer with at least one fatty chain The composition comprises, in medium appropriate for bleaching, at least one alkaline agent A, at least one peroxy salt B, hydrogen peroxide, at least one water-soluble solvent C and also nonionic and/or anionic amphiphilic polymer D with at least one fatty chain. Composition may also contain water-soluble thickening polymer, substantive cationic or amphoteric polymer and additional auxiliary agents such as oxygen release control agents, surfactants, mineral and vegetable oils, waxes, binders, mineral fillers, opacity agents, colorants, sequestrants and perfumes. Composition preferably contains 2-20 (preferably 4-15) wt.%of B, 0.1-10 (preferably 0.5-8) wt.%of C, 0.01-10 (preferably 0.1-5) wt.%of D and 0.5-10 (preferably 1-8) wt.%of hydrogen peroxide. Independent claims are also included for:(1) process of bleaching of keratin fibers, especially hair, comprising stages of preparation, directly before use, of aqueous bleaching composition as claimed, application onto hair area to be bleached, leaving for a period necessary to produce desired bleaching effect, and removing bleaching mixture by rinsing with water followed by shampooing and drying;and (2) kit for bleaching keratin fibers, especially hair, containing at least three compartments of which one contains peroxy salt, second containing water-soluble solvent and alkaline agent as claimed, and the third containing aqueous composition of hydrogen peroxide;while polymer(s) D is (are) introduced to one or more of those compartments.

Description

AQUEOUS COMPOSITION OF DECOLORATION OF KERATINIC FIBERS READY TO USE, WHICH INCLUDES THE ASSOCIATION OF A HYDRO-SOLUBLE SOLVENT AND A NON-IONIC ANTIPHYLIC POLYMER OR ANIONIC THAT UNDERSTANDS WHEN AT LEAST A FATTY CHAIN DESCRIPTION OF THE INVENTION The present invention relates to ready-to-use aqueous compositions for the decolorization of keratin fibers, comprising the association of at least one water-soluble solvent and at least one non-ionic and / or anionic amphiphilic polymer comprising at least one chain fat, a keratin fiber discoloration process using these compositions and a package of containers containing such a composition. To discolor the hair, aqueous compositions resulting from the mixing, at the time of use, of an aqueous composition of hydrogen peroxide, an aqueous composition containing an alkaline agent and at least one water-soluble solvent and a powder containing a peroxygen reactant such as persulfate, perborate or ammonium or alkali metal percarbonate. In the domain of hair discoloration, bleaching compositions thick enough to allow an application are generally sought.
REF .: 32571 precise on certain areas of the hair and that does not run the risk of coloring over the rest or outside the areas that are intended to bleach. The thickener or gelling effect is conventionally obtained with conventional thickening agents such as cellulose derivatives, starch derivatives, alginates, thickener silicas or mixtures of judiciously selected surfactants. When these traditional thickeners are used, however, a significant decrease in the viscosity of the final decolorizing composition is observed over time. Thus, there is a need for a thickening system capable of ensuring the maintenance of a high viscosity for the time necessary to obtain the desired discoloration, generally comprised between ten minutes and one hour. The applicant has surprisingly discovered that it is possible to considerably improve the maintenance of the viscosity, as time passes, of the discoloration compositions described above, by associating with the initial system, a nonionic and / or anionic amphiphilic polymer comprising a fatty chain. In the same way, it is found that such a thickener system allows diluting, with the aqueous hydrogen peroxide compositions, clearly more important than the known thickener systems. The present invention, therefore, aims at an aqueous ready-to-use composition for the decolorization of keratin fibers, in particular human fibers, comprising, in a means suitable for decolorization, at least one alkaline agent, at least one water-soluble solvent , hydrogen peroxide, at least one peroxygenated salt and also at least one nonionic and / or anionic amphiphilic polymer comprising at least one fatty chain. Another objective is a process for decolorizing the keratin fibers, using the above-described aqueous discoloration composition, as well as a package of containers containing such a composition. Other objectives will appear after reading the description and Examples that follow. Nonionic amphiphilic polymers comprising at least one fatty chain useful in accordance with the present invention, include, for example, celluloses or hydroxyalkyl celluloses modified by groups comprising at least one fatty chain such as an alkyl, arylalkyl or alkylaryl group containing a alkyl group preferably of 8 to 22 carbon atoms, such as NATROSOL PLUS GRADO 330 CS products from AQUALON; BERMOCOLL EHM 100 of the company BEROL NOBEL; or POLYSURF 67 of the company HERCULES; or modified with polyalkoxylated alkylphenol groups such as the AMERCELL POLYMER HM-1500 product of the AMERCHOL company, the hydroxypropyl-sugars modified with groups comprising at least one fatty chain of 8 to 22 carbon atoms, such as the product ESAFLOR HM 22 (alkyl chain of 22 carbon atoms) from the company LAMBERTI; MIRACARE XC95-3 (alkyl chain of 14 carbon atoms) and RE205-1 (alkyl chain of 20 carbon atoms) of the company RHONE PLULENC, polyurethanes comprising at least one fatty chain of the alkyl or alkenyl type of 8 at 30 carbon atoms, such as the SER-AD FX 1100 product from the SERVODELBEN company, or the SMDI (saturated methylenediphenyl diisocyanate) polyethylene glycol copolymer (s) with decyl termination, the SMDI copolymer (Diisocyanate Saturated Methylenediphenyl) polyethylene glycol (s) with alkyl (methyl / 18 carbon atoms) termination, associated with a matrix of maltodextrin, and - the diurethane HMDI (Hexamethylene Diisocyanate) of oxyethylenated C 10 -C 18 alcohols (66 OE) and oxypropylenates (14 OP), marketed under the name ELFACOS T 212 by the company AKZO, the copolymers of vinylpyrrolidone and hydrophobic monomers with fatty chain as the products ANTARON V216 or GANEX V216 (poly- (vinylpyrrolidone / hexadecene)), ANTARON V220 or GANEX V220 (poly- (vinylpyrrolidone / eicosene)) from the company I.S.O .; copolymers of alkyl (meth) acrylates of 1 to 6 carbon atoms and amphiphilic monomers comprising at least one fatty chain; the copolymers of hydrophilic (meth) acrylates and hydrophobic monomers comprising at least one fatty chain, for example a poly (polyethylene glycol methacrylate / lauryl methacrylate). In particular, polyurethanes comprising at least one fatty chain of the alkyl type are preferred. to 20 carbon atoms and the hydroxyethylcelluloses modified with groups comprising at least one alkyl chain of 8 to 22 carbon atoms. Anionic amphiphilic polymers comprising at least one fatty chain useful in accordance with the present invention are copolymers, crosslinked or non-crosslinked, comprising hydrophilic units derived from one or a plurality of ethylenically unsaturated monomers carrying a carboxylic acid function free, and hydrophobic units derived from one or a plurality of ethylenically unsaturated monomers bearing a hydrophobic side chain, and optionally crosslinking units derived from one or a plurality of polyunsaturated monomers. The monomer (s) with ethylenic unsaturation carrying a carboxylic acid function are selected from the group consisting of ethacrylic acid, methacrylic acid and acrylic acid, preferably methacrylic acid, acrylic acid and mixtures thereof. The monomer (s) with ethylenic unsaturation bearing a hydrophobic side chain can be (i) esters of unsaturated carboxylic acids and fatty alcohols, or (ii) esters of allyl and fatty alcohols. (i) The esters of unsaturated carboxylic acids and fatty alcohols are selected from the group consisting of alkyl ethacrylates, methacrylates and / or acrylates of 10 to 30 carbon atoms, preferably 12 to 22 carbon atoms. They include, for example, lauryl acrylate, stearyl acrylate, decyl acrylate, isodecyl acrylate, dodecyl acrylate, as well as the corresponding methacrylates, namely, lauryl methacrylate, stearyl methacrylate, decyl methacrylate, methacrylate, isodecyl and dodecyl methacrylate. (ii) The allylic ethers of fatty alcohols forming the hydrophobic units of the anionic amphiphilic polymers of the present invention correspond to Formula (I) CH2 = CR 'CH2-0-Bn-R wherein R' represents an atom of hydrogen or a methyl group, B represents an ethyleneoxy group, n is an integer between 0 and 100, R represents a group. hydrocarbon which is selected from the group consisting of alkyl, arylalkyl, aryl, alkylaryl or cycloalkyl radicals of 8 to 30 carbon atoms, preferably 10 to 24 carbon atoms and more preferably 12 to 18 carbon atoms. A unit of the preferred Formula (I) according to the present invention is a unit in which R 'designates a hydrogen atom, n is equal to 10 and R represents a stearyl radical (of 18 carbon atoms). The crosslinking monomer is a compound comprising at least two polymerizable double bonds non-conjugated with respect to each other. Examples which may be mentioned are diallyl phthalate, allyl (meth) acrylate, divinylbenzene, (poly) ethylene glycol dimethacrylate, methylene-bis-acrylamide, polyallylsucrose or polyallyl pentaerythritol. Anionic amphiphilic polymers of the type described above are described, for example, in US Pat., 915,921 and US-4,509,949 (copolymers of (et / meth) acrylic acid and (et / et) alkyl acrylates of 10 to 30 carbon atoms), or in European Patent EP-0,216,479 B2 (copolymers of acid (et / met) acrylic and allyl ethers of fatty alcohols). Examples of the preferred polymers are: crosslinked polymers of acrylic acid and alkyl acrylate of 10 to 30 carbon atoms, such as the polymers marketed under the names PEMULEN TR1, PEMULEN TR2 and CARBOPOL 1382 by the company GOODRICH , - the crosslinked polymer of acrylic acid and alkyl methacrylate of 10 to 30 carbon atoms, such as CARBOPOL ETD 2020 marketed by GOODRICH, the terpolymer of methacrylic acid / ethyl acrylate / oxyethylenated stearyl methacrylate (55/35 / 10), the terpolymer of (meth) acrylic acid / ethyl acrylate / oxyethylenated behenyl-methacrylate (25 EO), and the terpolymer of methacrylic acid / ethyl acrylate / crosslinked stearyl allyl ether. These nonionic and / or anionic amphiphilic polymers comprising at least one fatty chain are used in a proportion of 0.01 to 10% by weight, preferably of 0. 1 to 5% by weight, with respect to the aqueous decolorizing composition. As indicated above, the aqueous decolorizing composition also contains at least one alkaline agent, at least one peroxygenated salt, at least one water-soluble solvent and hydrogen peroxide. The alkaline agent is selected from the group consisting of ammonia and organic amines such as monoethanolamine, diethanolamine or triethanolamine, 2-amino-2-methyl-1-propanol, diaminopropane, hydroxyalkylamines and oxyethylenated and / or oxypropylenated ethylenediamines. The peroxygenated salts are selected from the group consisting of persulfates, percarbonates and ammonium or alkali metal perborates. Preferably, persulfates are used, mainly sodium persulphate and potassium persulfate.
The compositions of the present invention comprise from 2 to 20% by weight and preferably from 4 to 15% by weight of the peroxygenated salt. For the purposes of the present invention, the term "water-soluble solvents" refers to solvents soluble in more than 5% by weight in water, at 25 ° C. The water-soluble solvents of the present invention are preferably selected from the group consisting of straight or branched chain aliphatic monoalcohols of 1 to 6 carbon atoms, straight or branched chain aliphatic polyols of 3 to 20 carbon atoms, polyol ethers which may be monoethers or aliphatic diethers of 1 to 6 carbon atoms of polyols of 2 to 9 carbon atoms and aromatic ethers of 6 to 9 carbon atoms of polyols of 2 to 9 carbon atoms. The compositions of the present invention contain from 0.1 to 10% by weight, preferably from 0.5 to 8% by weight, of the water-soluble solvent. They also contain between 0.5 and 10% by weight, preferably between 1 and 8% by weight, of hydrogen peroxide. The aqueous bleaching compositions according to the present invention may also contain any kind of bleaching aids capable of facilitating handling and application, of improving the preservation or efficacy of the compositions and of improving the cosmetic properties of the treated hair. These adjuvants, for example, are agents for controlling oxygen evolution such as magnesium carbonate and magnesia, anionic, nonionic, cationic, amphoteric surfactants or their terryiyos and mixtures thereof, mineral or vegetable oils, waxes, binders, mineral fillers such as silica and argyl, opacifiers such as titanium oxide, dyes, sequestrants, perfumes and polymers. The compositions of the present invention may contain in particular at least one water-soluble thickener, natural or synthetic polymer and / or at least one cationic and / or amphoteric substantive polymer. The compositions according to the present invention preferably comprise at least one surfactant agent. Suitable surfactants for the practice of the present invention are, in particular, the following: (i) Anionic surfactants: As an example of useful anionic surfactants alone or in combination, for the purposes of the present invention, mention may be made, in particular, of anionic surfactants. the salts (in particular alkali salts, mainly sodium, ammonium salts, salts of amines, salts of aminoalcohols or magnesium salts) of the following compounds: alkyl sulphates, alkyl ether sulphates, alkylamidoethers sulfates, alkylaryl polyether sulfates, sulphates of monoglycerides; alkylsulfonates, alkyl phosphates, alkylamidosulfonates, alkylarylsulfonates, α-olefin sulfonates, paraffin sulfonates; (C6-C24) alkyl sulfosuccinates, (C-C4) alkyl ether sulfosuccinates, (C6-C24) alkyl amidosulfosuccinates; alkyl (C6-C2) sulphoacetates; acyl (C6-C2) sarcocinates and acyl (C6-C2) glutamates. In the same way, carboxylic alkyl polyglycoside esters such as alkyl glucoside citrates, alkyl polyglycoside tartrate and alkyl polyglycoside sulfosuccinates, alkylsulfosuccinamates can be used to use carboxylic alkyl (C6-C24) esters.; acyl isothionates and N-acyltaurates, wherein the alkyl or acyl radical of all these different compounds comprises from 12 to 20 carbon atoms, and the aryl radical preferably designates a phenyl or benzyl group. Among the also useful anionic surfactants, fatty acid salts such as salts of oleic, ricinoleic, palmitic, stearic acids, copra oil acids or hydrogenated copra oil; acylacrylates whose acyl radical comprises from 8 to 20 carbon atoms. In the same manner, alkyl-D-galactoside uronic acids and their salts, polyoxyalkylenated alkyl (C6-C24) alkylcarboxylic acids, polyoxyalkylenated aryl ethercarboxylic alkyl (C6-C24) acids, polyoxyalkylenated alkyl (C6-C2) amidoethercarboxylic acids and their salts, in particular those comprising 2 to 50 alkylene oxide groups, in particular ethylene, and mixtures thereof, (ii) Nonionic surfactants: Nonionic surfactants are also known compounds (see mainly in this respect the "Handbook of Surfactants" by MR PORTER, editions Blackie &Son (Glasgow and London), 1991, pp. 116-178) and its nature, within the framework of the present invention, is not critical. Thus, they can be selected mainly from alcohols, alpha-diols, alkylphenols or polyethoxylated fatty acids, polypropoxylated with a fatty chain comprising, for example, between 8 and 18 carbon atoms, wherein the number of ethylene oxide or propylene oxide groups can be selected. it is mainly from 2 to 50. In the same way, mention may be made of copolymers of ethylene oxide and propylene oxide, condensates of ethylene oxide and propylene oxide on fatty alcohols; the polyethoxylated fatty amides preferably having from 2 to 30 moles of ethylene oxide, the polyglycerolated fatty amides comprising on average from 1 to 5 glycerol groups and in particular from 1.5 to 4; the polyethoxylated fatty amines preferably having 2 to 30 moles of ethylene oxide; the esters of oxyethylenated sorbitan fatty acids having from 2 to 30 moles of ethylene oxide; sucrose fatty acid esters, polyethylene glycol fatty acid esters, alkyl polyglucosides, N-alkylglucamine derivatives, amine oxides such as alkyl (C 10 -C 14) amines or N-acylaminopropylmorpholine oxides. It will be appreciated that the alkyl polyglucosides constitute nonionic surfactants that fit particularly well within the scope of the present invention. (iii) Amphoteric or suteionic surfactants: Amphoteric or suteionic surfactants whose nature is not of a critical nature within the scope of the present invention, may be mainly aliphatic secondary or tertiary amine derivatives, wherein the aliphatic radical is a straight chain or branched comprising from 8 to 18 carbon atoms and containing at least one water-solubilizing anionic group (for example carboxylate, sulfonate, sulfate, phosphate or phosphonate),. Mention may be made of (C 8 -C 20) alkyl betaines, sulfobetaines, (C 8 -C 20) alkyl, amidoalkyl (Ci-Cβ) betaines or alkyl (Ce-C 2o) amidoalkyl (Ci-Ce) sulfobetaines.
Among the derivatives of amines, mention may be made of the products described in US Pat. Nos. 2,528,378 and 2,781,354 and classified in the CTFA dictionary, 3rd edition, 1982, with the names Amphocarboxyglycinates and Amphocarboxypropionates of respective structures: Rl-CONHCH2CH2-N ( R2) (R3) (CH2COO-) wherein R2 designates an alkyl radical of a Ri-COOH acid present in the hydrolysed copra oil, a heptyl, nonyl or undecyl radical, R2 denotes a beta-hydroxyethyl group and R3 a carboxymethyl group; and Rl'-CONHCH2CH2-N (B) (C) wherein: B represents a group -CH2CH20X ', C represents a group - (CH2) Z-Y', where z is 1 or 2, X 'denotes the group -CH2CH2-COOH or a hydrogen atom, Y 'designates a group -COOH or the radical -CH2-CHOH-S03H, Ri' designates an alkyl radical of an acid R-COOH present in the copra oil or in the oil of hydrolysed linseed, an alkyl radical mainly of 7, 9, 11 or 13 carbon atoms, an alkyl radical of 17 carbon atoms and its iso form, a radical of 17 unsaturated carbon atoms. These compounds are classified in the CTFA dictionary, 5th edition, 1993, under the names cocoamphodiacetate disodium, disodium lauroamphodiacetate, disodium caprylampheracetate, disodium capryloamphodiacetate, disodium cocoamphodipropionate, disodium lauroamphopropionate, disodium caprylamodipropionate, disodium capryloamphodipropionate, lauroamphodipropionic acid, cocoamphodipropionic acid. (iv) Cationic surfactants: Among the cationic surfactants, mention may be made in particular of the salts of primary, secondary or tertiary fatty amines, optionally polyoxyalkylenated, the quaternary ammonium salts such as tetraalkylammonium chlorides or bromides, alkylamidoalkyltrialkylammonium bromides, trialkylbenzylammonium salts, trialkylhydroxyalkylammonium salts. or alkylpyridinium; the imidazoline derivatives; or the amine oxides of cationic character. The amounts of surfactants present in the composition according to the present invention can vary between 0.01 to 40% and preferably from 0.1 to 30%, with respect to the total weight of the composition.
The cationic substantive polymers useful in accordance with the present invention can be selected from any of those known to improve the cosmetic properties of hair, namely, those described in the Requests EP-A-337354 and EP-A -557203 and in French Patents FR-2,270,846; 1,383,660; 2,598,611; 2,470,596 and 2,519,863. Preferred cationic and amphoteric polymers are selected from those which contain units comprising primary, secondary, tertiary and / or quaternary amine groups and can either be part of the polymer backbone, or be carried by. a lateral substituent directly linked to it. The cationic polymers used generally have an average molecular mass of between about 500 and 5 x 10 and preferably between about 10 and 3 x 10. Among the cationic polymers, mention may be made more particularly of polymers of the polyamine, polyaminoamide and polyammonium quaternary type. These are known products. They are described mainly in French Patent Nos. 2,505,348 or 2,542,997. Among said polymers there may be mentioned: (1) homopolymers or copolymers derived from esters or from acrylic or methacrylic amides and comprising at least one of the units of Formulas (II), (III), (IV) or (V) following: wherein: Rβ are identical or different radicals denoting a hydrogen atom or a CH3 radical; A, are identical or different groups representing an alkyl group, straight or branched chain of 1 to 6 carbon atoms, preferably 2 to 3 carbon atoms or a hydroxyalkyl group of 1 to 4 carbon atoms; R "7, R °, P. ° are identical or different groups which represent a group which is a v_? A ± &v_? Carbon or a benzyl radical and preferably a alkyl group of 1 to 6 carbon atoms, R 4 and 5 are identical or different groups that T i X designates an anion derived from a mineral or organic acid such as a methosulfate anion or a halide such as chloride or bromide. The polymers of the family íl. they may also contain one or a plurality of units which are derived from comonomers which can be derived from the family of acrylamides, methacrylamides, diocesan acrylamides, acrylamides and methacrylamides substituted on the nitrogen with lower alkyl radicals (from 1 to 4 carbon atoms) Acrylic or methacrylic acids or their steres, vinyllactams such as vinylpyrrolidone or vi or 1 caproate and vinyl esters, Thus, among these family polymers (1 ^), one can cite: acrylamide sees dimethylaminoethylmethacrylate quaternized with dimethyl sulfate or with a dimethyl halide, the copolymers of acrylamide and methacryloxyethyltrimethylammonium chloride described for example in Patent Application EP-A-080976, the copolymer of acrylamide and methacryloxyethyltrimethylammonium methosulfate, the copolymers of vinylpyrrolidone / dialkylaminoalkyl acrylate or methacrylate quaternized or not.These polymers are describe in detail in French Patents 2,077,143 and 2,393,573, the terpolymers of dimethylaminoethyl methacrylate, vinyl caprolactam, vinylpyrrolidone, the copolymer of vinylpyrrolidone / methacrylamidopropyldimethylamine, and quaternized dimethylaminopropyl vinylpyrrolidone / methacrylamide copolymers. (2) The cellulose ether derivatives comprising quaternary ammonium groups described in French Patent 1,492,597. These polymers are also defined in the CTFA dictionary as ammonium quaternaries of hydroxyethylcellulose which have reacted with an epoxide substituted with a trimethylammonium group. (3) Cationic cellulose derivatives such as cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, and which are described primarily in US Pat. No. 4,131,576, such as hydroxyalkylcelluloses, such as hydroxymethyl-, hydroxyethyl- or hydroxypropyl celluloses grafted mainly with a methacrylethyltrimethylammonium, methacrylamidopropyltrimethylammonium and dimethyldiallylammonium salt. (4) The cationic polysaccharides described more particularly in U.S. Patent Nos. 3,589,578 and 4,031,307 such as guara gums containing cationic trialkylammonium groups. For example, guara gums modified by a salt (for example chloride) of 2,3-epoxypropyltrimethylammonium are used. (5) Polymers consisting of piperazinyl units and divalent straight or branched chain alkylene or hydroxyalkylene radicals, optionally interrupted by oxygen, sulfur, nitrogen or aromatic or heterocyclic rings, as well as oxidation products and / or Quaternization of these polymers. Such polymers are described mainly in French Patents 2,162,025 and 2,280,361. (6) Water-soluble polyaminoamides prepared in particular by polycondensation of an acid compound with a polyamine; these polyaminoamides being crosslinked by an epihalohydrin, a diepoxide, a dianhydride, an unsaturated dianhydride, a bis-unsaturated derivative, a bis-halohydrin, a bis-acetidinium, a bis-haloacylthiamine, an alkyl bis-halide or a an oligomer resulting from the reaction of a bifunctional compound reactive towards a bis-halohydrin, a bis-acetidinium, a bis-haloacildiamine, an alkyl bis-halide, an epihalohydrin, a diepoxide or a bis-unsaturated derivative; the crosslinked agent being used in proportions between 0.025 and 0.35 moles per amino group of the polyaminoamide; wherein these polyaminoamides may be alkylated or may comprise one or a plurality of tertiary, quaternized amine functions. Such polymers are described mainly in French Patents 2,252,840 and 2,368,508. (7) The polyaminoamide derivatives resulting from the condensation of polyalkylene polyamines with polycarboxylic acids, followed by an alkylation with bifunctional agents. Mention may be made, for example, of the polymers of adipic acid-dialkylaminohydroxyalkyldialkylenetriamine polymers in which the alkyl radical comprises from 1 to 4 carbon atoms, preferably a methyl, ethyl or propyl group. Such polymers are described mainly in French Patent 1,583,363. Among these derivatives, mention may be made more particularly of the adipic acid / dimethylaminohydroxypropyl / diethylenetriamine polymers sold under the name "Cartaretine F, F4 or F8" by the company Sandoz. (8) The polymers obtained by the reaction of a polyalkylene polyamine comprising two primary amine groups and at least one secondary amine group, with a dicarboxylic acid selected from the group consisting of diglycolic acid and the saturated aliphatic dicarboxylic acids having from 3 to 8 carbon atoms. The molar ratio of the polyalkylene polyamine to the dicarboxylic acid is between 0.8: 1 and 1.4: 1.; wherein the resulting polyaminoamide is reacted with an epichlorohydrin in a molar ratio of epichlorohydrin to the secondary amino group of the polyaminoamide comprised between 0.5: 1 and 1.8: 1. Such polymers are described primarily in U.S. Patents 3,227,615 and 2,961,347. (9) The cyclopolymers of alkyldiallylamine or dialkyldiallylammonium such as the homopolymers or copolymers comprising, as the main component of the chain, units having the Formulas (VI) or (VII): - (CH2> t) where k and t are equal to 0 or 1, the sum of k + t being equal to 1; R 12 denotes a hydrogen atom or a methyl radical; Rio and R 11, independently of one another, designate an alkyl group of 1 to 22 carbon atoms, a hydroxyalkyl group wherein the alkyl group preferably has 1 to 5 carbon atoms, a lower amidoalkyl group (1 to 4 atoms) carbon) or Rio and Rn may designate together with the nitrogen atom to which they are linked, a heterocyclic group such as piperidinyl or morpholinyl; Y ~ is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate, phosphate. These polymers are described mainly in French Patent 2,080,759 and in their certificate of addition 2,190,406. (10) The quaternary diammonium polymer containing recurring units, responds to the Formula: wherein R13, R14, R15 and Rie are identical or different radicals, represent aliphatic, alicyclic or arylaliphatic radicals containing from 1 to 20 carbon atoms or lower hydroxyalkylaiphatic radicals, or, R3, R1, R15 and Rie, together or separately, together with the nitrogen atoms to which they are bound, they constitute heterocyclic rings optionally containing a second heteroatom different from nitrogen, or else R13, R14, R15 and Ri6 represent an alkyl radical of 1 to 6 carbon atoms of chain linear or branched, substituted with a nitrile, ester, acyl, amide or -CO-O-R17-D or -CO-NH-R17-D group, wherein R17 is an alkylene radical and D is a quaternary ammonium group; i and Bi represent polymethylene groups containing from 2 to 20 carbon atoms, which may be straight or branched chain, saturated or unsaturated and may contain, linked or interspersed in the main chain, one or a plurality of aromatic rings or one or a plurality of oxygen atoms, sulfur or sulfoxide, sulfone, disulfide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester groups, and X- designates an anion derived from a mineral or organic acid; Ai, R13 and R15 can form, together with the two nitrogen atoms to which they are bonded, a cyclopiperazine; In addition, if Ai denotes a straight or branched chain, saturated or unsaturated alkylene or hydroxyalkylene radical, Bi can also designate a group - (CH2) n -CO-D-OC- (CH2) n- where D denotes: a) a glycol radical of the formula: -0-Z-0-, wherein Z designates a straight or branched chain hydrocarbon radical or a group that responds to one of the following formulas: - (CH2-CH2-0) X-CH2- CH2- - [CH2-CH (CH3) -0] y-CH2-CH (CH3) - where xyy 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 radical such as a piperazine derivative; c) a bis-primary diamine radical of the formula: -NH-Y-NH-, wherein Y denotes a straight or branched chain hydrocarbon radical, or the bivalent radical -CH2-CH2-S-CH2-CH2-; ri - TvJT-T- • Preferably, X is an anion such as chloride or bromide. These polymers have an average molecular mass generally comprised between 1000 and 100000. Polymers of this type are described mainly in French Patent 2,320,330; 2,270,846; 2,316,271; 2,336,434 and 2,413,907 and in US Patents 2,273,780; 2,375,853 2,188,614; 2,454,547; 3,206.46 ?; •?, 261, 002; 2,271,378 3,874,870; 4,001,432; 3,929,990; 3,966,904; 4,005,193 4.0? 5,617; 4,025,627; 4.0? 5.653; 4,026,945 and 4,027,020. More particularly, polymers which are constituted by recurring units corresponding to the following formula (IX) can be used: wherein R, R19, Ro and R21 are identical or different radicals and designate an alkyl or hydroxyalkyl radical of from 1 to 4 carbon atoms, n and p are integers from 2 to 20 approximately and X ~ is an anion derived from a mineral acid or organic (11) The polynalmonium quaternary polymers constituted by units of the Formula (X): wherein: R22, R23, R24 and R25 are identical or different radicals and represent a hydrogen atom or a methyl, ethyl, propyl, ß-hydroxyethyl, ß-hydroxypropyl or -CH2CH2 (OCH2CH2) pOH, where p is equal to 0 or is an integer between 1 and 6, provided that R22, R23, R24 and R25 do not simultaneously represent a hydrogen atom, r and s are identical or different and are integers between 1 and 6, q is equal to 0 or an integer between 1 and 34, X denotes a halogen atom, A designates a dihalide radical or preferably represents a group -CH2-CH2-O-CH2- CH2-. Such compounds are described primarily in Patent Application EP-A-122, 32. > (12) The quaternary polymers of vinylpyrrolidone and vinylimidazole. (13) Polyamines such as the product referred to under the name POLYETHYLENEGLYCOL (15) STEM POLYAMINE in the CTFA dictionary. (14) Cross-linked polymers of methacryloxyalkyl (1 to 4 carbon atoms) -trialkyl salts (from 1 to 4 carbon atoms) ammonium such as the polymers obtained by the homopolymerization of the dimethylaminoethyl methacrylate quaternized with methyl chloride, or by the copolymerization of acrylamide with dimethylaminoethyl methacrylate quaternized with methyl chloride, the homopolymerization or the copolymerization being followed by a crosslinking by a compound with olefinic unsaturations, in particular methylene-bis-acrylamide. In addition, in particular a crosslinked copolymer of acrylamide / methacryloxyethyltrimethylammonium chloride (20/80 by weight) in the form of a dispersion containing 50% by weight of said copolymer in mineral oil can be used. This dispersion is marketed under the name "SALCARRE® SC92" by the company ALLIED COLLOIDS.
In the same manner, a cross-linked homopolymer of methacryloxyethyltrimethylammonium chloride containing about 50% by weight of the homopolymer in a mineral oil or in a liquid ester can be used. These dispersions are marketed under the names SALCARE © SC95 and SALCARE® SC96 by the company ALLIED COLLOIDS. Other cationic substantive polymers useful in the context of the present invention are polyalkyleneimines, in particular polyethyleneimines, polymers containing vinylpyridine or vinylpyridinium units, condensates of polyamines and epichlorohydrin, quaternary polyureylenes and chitin derivatives. The amphoteric substantive polymers useful in accordance with the present invention may be selected from polymers comprising units K and M statistically distributed in the polymer chain, wherein K denotes a unit derived from a monomer comprising at least one basic nitrogen atom. and M designates a unit derived from an acid monomer comprising one or a plurality of carboxylic or sulphonic groups, or, K and M may designate groups derived from sutereionic monomers of carboxybetaines or sulfobetaines; in the same manner, K and M can designate a cationic polymer chain comprising primary, secondary, tertiary or quaternary amine groups, wherein at least one of the amine groups carries a carboxylic or sulfonic group linked by the intermediary of a hydrocarbon radical, or else, K and M form part of a chain of a polymer with an α, β-dicarboxylic ethylene unit, wherein one of the carboxylic groups is ready to react with a polyamine comprising one or a plurality of amine groups primary or secondary Amphoteric fumonogenic polymers which meet the above-described, more particularly preferred definition are selected from the group consisting of the following polymers: (1) Polymers resulting from the copolymerization of a monomer derived from a vinyl compound carrying a group carboxylic such as more particularly acrylic acid, methacrylic acid, maleic acid, alpha-chloroacrylic acid, with a basic monomer derived from a substituted vinyl compound containing at least one basic atom such as more particularly dialkylaminoalkyl methacrylates and acrylates, dialkylaminoalkylmethacrylamide and acrylamide. Such compounds are described in U.S. Patent No. 3,836,537. In the same way, mention may be made of the sodium acrylate / acrylamidopropyltrimethylammonium chloride copolymer. The vinyl compound can also be a dialkylalkylammonium salt such as diethyldiallylammonium chloride. (2) Polymers comprising units derived from: a) at least one monomer selected from the group consisting of acrylamides or methacrylamides substituted on the nitrogen with an alkyl radical, JLO b) at least one acid comonomer containing one or more plurality of reactive carboxylic groups, and c) at least one basic comonomer such as esters with primary, secondary amine substituents, tertiary and quaternary, acrylic and methacrylic acids and the quaternization product of dimethylaminoethyl methacrylate with dimethyl sulfate or diethyl sulfate. The N-substituted acrylamides or methacrylamides more particularly preferred according to the present invention, the groups whose alkyl radicals contain from 2 to 12 carbon atoms and more particularly N-ethylacrylamide, N-tert-butylacrylamide, N-tert-octylacrylamide , N-octylacrylamide, N-decylacrylamide, N-dodecyl acrylamide, as well as the corresponding methacrylamides.
The acidic comonomers are selected more particularly from acrylic, methacrylic, crotonic, itaconic, maleic, fumaric acids, as well as the alkyl monoesters of 1 to 4 carbon atoms of maleic or fumaric acids or anhydrides. Preferred basic comonomers are aminoethyl, butylaminoethyl, N, N'-dimethylaminoethyl, N-tert-butylaminoethyl methacrylates. Particularly, copolymers whose JLO designation CTFA (4th edition, 1991) is octylacrylamide / acrylates / butylaminoethyl methacrylate copolymer are used. (3) Crosslinked and partially or fully alkylated polyaminoamides derived from polyaminoamides of the General Formula: -. CO R26 CO Z (XI) 15 wherein R26 represents a divalent radical derived from a saturated dicarboxylic acid, from an aliphatic acid monocarboxylic or dicarboxylic acid with an ethylenic double bond, from an ester of a lower alkanol from 1 to 20 6 carbon atoms of these acids or of a radical derived from the addition of any of said acids with a bis-primary or bis-secondary amine, and Z denotes a radical of a bis-primary, mono- or bis-secondary polyalkylenepolyamine and preferably represents: ) in proportions of 60 to 100 mol%, the radical: 'NH- £ (CH2)? - • NH- n (XII) where x = 2 and p = 2 6 3, or, x = 3 and p = 2, deriving this radical from diethylenetriamine, from triethylene tetraamine or from dipropylenetriamine; b) in proportions of 0 to 40 mol% the radical (XXII) above, where x = 2 and p = l and which is derived from ethylenediamine, or the radical is derived from piperazine: c) in proportions of 0 to 20 mol%, the radical -NH- (CH2) 6-NH- deriving from hexamethylenediamine, wherein these polyaminoamines are crosslinked by the addition of a bifunctional crosslinking agent which is selected from the group consisting of epihalohydrins , diepoxides, dianhydrides, bis-unsaturated derivatives, with an average of 0.025 to 0.35 moles of the crosslinking agent per amino group of the polyaminoamide and are alkylated by the action of acrylic acid, chloroacetic acid or an alkanesultone or its salts. The saturated carboxylic acids are preferably selected from the group consisting of acids of 6 to 10 carbon atoms such as adipic acid, trimethyl-2,2,4-adipic and trimethyl-2,4,4-adipic, terephthalic, acids with ethylenic double bond such as, for example, acrylic, methacrylic, itaconic acids. The alkanesultones used in the alkylation, preferably are the propanosultone or butanosultone, the salts of the alkylating agents are preferably sodium or potassium salts. (4) Polymers comprising suteryionic units of the Formula: wherein R27 designates a polymerizable unsaturated group, such as an acrylate, methacrylate, acrylamide or methacrylamide group, y and z represent an integer from 1 to 3, R 2 and R 29 represent a hydrogen atom, a methyl, ethyl or propyl radical, R 30 and R31 represent a hydrogen atom or an alkyl radical, such that the sum of the carbon atoms in R30 and R31 is not greater than 10. The polymers comprising such units may also comprise units derived from non-suteionic monomers such as dimethylaminoethyl or diethylaminoethyl acrylate or methacrylate, or alkyl acrylates or methacrylates, acrylamides or chloro methacrylamides or vinyl acetate. By way of example, mention may be made of the methyl methacrylate / methyl dimethylcarboxymethylaminoethyl methacrylate copolymer. (5) Polymers derived from chitosan comprise monomer units that respond to the following Formulas (XIV), (XV) and (XVI): With the unit of Formula XIV present in proportions comprised between 0 and 30%, the unit of Formula XV in proportions comprised between 5 and 50% and the unit of Formula XVI in proportions comprised between 30 and 90%, it being understood that in this unit F, R2g represents a radical of the formula: wherein if q = 0, R33, R34 and R35, which may be identical or different, each represent a hydrogen atom, a methyl, hydroxyl, acetoxy or amino radical, a monoalkylamine radical or a dialkylamine radical, optionally interrupted by one or a plurality of nitrogen atoms and / or optionally substituted with one or a plurality of amine, hydroxyl, carboxyl, thioalkyl, sulphonic groups, a thioalkyl radical whose alkyl group carries an amino radical, wherein at least one of the radicals R30, R31 and R32, in this case, is a hydrogen atom; or else, if 1 = 1, R33, R34 and R35 each represent a hydrogen atom, as well as the salts formed by these compounds with bases or with acids. (6) Polymers derived from N-carboxyalkylation of chitosan, such as N-carboxymethylchitosan or N-carboxybutylchitosan. (7) Polymers that respond to the General Formula (XVIII), such as those described for example in French Patent 1,400,366: wherein R36 represents a hydrogen atom, a radical CH3O, CH3CH20, phenyl, R37 designates a hydrogen atom or a lower alkyl radical such as methyl, ethyl, R38 designates a hydrogen atom or a lower alkyl radical such as methyl, ethyl , R39 designates a lower alkyl radical such as methyl, ethyl or a radical that responds to the formula: -R40 ~ N (R38) 2 wherein R40 represents a group -CH2-CH2-, -CH2-CH2-CH2-, - CH2-CH (CH3) - and R38 is as previously defined, as well as the higher homologs of these radicals and containing up to 6 carbon atoms. (8) Amphoteric polymers of the -DXDX type are selected from the group consisting of: a) polymers obtained by the action of chloroacetic acid or sodium chloroacetate, on the compounds comprising at least one unit of the Formula: -DXDXD - (XIX) where D designates a radical and X denotes the symbol E or E ', where E or E' are identical or different and designate a bivalent radical which is a straight or branched chain alkylene radical comprising up to 7 carbon atoms in the main chain, substituted or not substituted with hydroxyl groups and which may further comprise oxygen, nitrogen, sulfur atoms, from 1 to 3 aromatic rings and / or heterocycles; wherein the oxygen, nitrogen and sulfur atoms are present in the form of ether, thioether, sulfoxide, sulfone, sulfonium, alkylamine, alkenylamine, hydroxyl, benzylamine, amine oxide, quaternary ammonium, amide, imide, alcohol, ester groups and / or urethane; b) polymers of the formula: -D-X-D-X- (XX) where D denotes a radical and X designates the symbol E or E 'and at least once E'; wherein E is as previously described and E 'is a bivalent radical which is a straight or branched chain alkylene radical having up to 7 carbon atoms in the main chain, substituted or not with one or a plurality of hydroxyl radicals and which comprises one or a plurality of nitrogen atoms, wherein the nitrogen atom is substituted with an alkyl chain optionally interrupted by an oxygen atom and which necessarily comprises one or a plurality of carboxyl functions or one or a plurality of hydroxyl functions and which are converted to betaines by a reaction with chloroacetic acid or sodium chloroacetate. (9) The copolymers of alkyl (1 to 5 carbon atoms) -vinyl ether / maleic anhydride partially modified by semi -mination with an N, N-dialkylaminoalkylamine such as N, N-dimethylaminopropylamine or by semi-esterification with an N, N-dialkanolamine. These copolymers can also comprise other vinyl comonomers, such as vinylcaprolactam. Among the cationic or amphoteric substantive polymers useful in accordance with the present invention, the following are especially preferred: the dimethyldiallylammonium chloride homopolymer sold under the tradename MERQUAT 100 DRY by the company MERCK; the copolymers of dimethyldiallylammonium chloride and of acrylamide, sold under the trade name MERQUAT 2200 by the company CALGON; the poly (quaternary ammonium) polymers prepared and described in French Patent 2,270,846, consisting of recurring units corresponding to Formula (XXI) below: and mainly those whose weight-average molar mass, determined by gel permeation chromatography, is between 9500 and 9900; polymers of the poly (quaternary ammonium) type prepared and described in French Patent 2,270,846, constituted by recurring units corresponding to the following Formula (XXII): and mainly those whose weight-average molar mass, determined by gel permeation chromatography, is about 1200; the poly (quaternary ammonium) type polymers described in U.S. Patent Nos. 4,390,689; 4,702,906; 4,719,282 and that are constituted by recurring units that respond to the following Formula (XXIII): where p is an integer from 1 to 6, D represents a single bond or a group - (CH2) r-CO-, where r has a value of 4 or 7, and mainly those whose weight-average molar mass is less than 100000, preferably less than or equal to 50000; the following amphoteric copolymers: the diallyldimethylammonium chloride / acrylic acid copolymer (80/20) marketed under the name MERQUAT 280 DRY by the company CALGON (CTFA name: Polyquaternium-22); the dimethyldiallylammonium chloride / acrylic acid copolymer (95/5) sold under the name MERQUAT 295 DRY by the company CALGON (CTFA name: Polyquaternium-22); the copolymer of methacrylamidopropyltrimonium chloride, of acrylic acid and of methyl acrylate, marketed under the name MERQUAT 2001 by the company CALGON (CTFA name: Polyquaternium-47); and the acrylamide / dimethyldiallylammonium chloride / acrylic acid terpolymer, marketed under the name MERQUAT PLUS 3330 DRY by the company CALGON (CTFA name: Polyquaternium-39). In the list of the abovementioned substantive polymers, amphoteric copolymers Polyquaternium-22, Polyquaternium-39 and Polyquaternium-47 (CTFA designations) are particularly preferred. The amounts of cationic or amphoteric substantive polymers in the compositions according to the present invention are generally between 0.03 and 30% by weight, based on the total weight of the composition. The water-soluble thickener polymers useful in accordance with the present invention encompass any water-soluble synthetic or naturally-occurring polymer, conventionally used in the cosmetic domain. Examples of synthetic thickener polymers include polyvinylpyrrolidone, polyacrylic acid, polyacrylamide, polyacrylamidomethylpropanesulfonic acid or copolymers thereof, these polymers being crosslinked or non-crosslinked. Thickening polymers of natural origin useful in accordance with the present invention are polymers comprising at least one sugar unit, namely: (a) nonionic guarant gums; (b) biopolysaccharide gums of microbial origin such as scleroglucan and xanthan gums; (c) gums extracted from plant exudates such as gum arabic, gati gum, karaya gum or adraganto gum; (d) gums extracted from algae such as carrageenans or agar; (e) gums derived from plant extracts such as carubic gum or pectins extracted from fruit pulps; (f) alginates; (g) starches; and (h) hydroxyalkylcelluloses and carboxyalkylcelluloses. The term "sugar unit" as used in the present invention, refers to a portion of monosaccharide or a portion of oligosaccharide or polysaccharide constituted by the same type of saccharide units (oligo or polyholosides) or by various types of saccharide units different (oligo or polyheterosides). The saccharide units of all these polymers can carry one or a plurality of substituents, for example alkyl, hydroxyalkyl, alkoxy, acyl or carboxyl groups, wherein the alkyl radicals comprise from 1 to 4 carbon atoms. Nonionic guara gums may be modified or unmodified. The unmodified guara gums are, for example, products sold under the name VIDOGUM GH 175 by the company UNIPECTINE and with the name JAGUAR C by the company MAYHALL. According to the present invention, it is also possible to use modified non-ionic gum rubbers with hydroxyalkyl groups of 1 to 4 carbon atoms, for example hydroxymethyl, hydroxyethyl, hydroxypropyl and hydroxybutyl. These modified guara gums are known in the art and can be prepared by reducing the guara gum with the appropriate alkylene oxides. The hydroxylation index (with respect to the number of alkylene oxide molecules fixed to the initial number of free hydroxyl groups) is preferably between 0.4 and 1.2. Such modified nonionic guara gums are sold, for example, under the names JAGUAR HP8, JAGUAR HP60, JAGUAR HP120, JAGUAR DC293 and JAGUAR HP105 by the company THONE POULENC (MAYHALL) or with the name GALACTASOL 4H4FD2 by the company AQUALON. Biopolysaccharide gums of microbial origin such as scleroglucan or xanthan gums, gums obtained from vegetable exudates such as gum arabic, gati gum, karaya gum, gum of adraganto, extracts of algae such as carrageenans or agar, plant extracts such as carubic gum or pectins, alginates, starches, hydroxyalkylcelluloses and carboxyalkylcelluloses, are known to those sed in the art and are mainly described in "Hadbook of Water Soluble Gums and Resins" by Robert L. Davidson, edited by Me Graw Hill Book Company (1980). Among these gums, scleroglucans are represented by the products sold by the company SANOFI BIO INDUSTRIES under the name ACTIGUM CS and in particular with the name ACTIGUM CS 11, and by the company ALBAN MULLER INTERNATIONAL with the name AMIGEL. In the same way, other scleroglucans can be used, for example a scleroglucan treated with a glyoxal described in Patent Application FR-A-2,633,940. Xanthan gums useful as thickeners in the compositions of the present invention, are represented for example by the products sold under the names KELTROL, KELTROL T, KELTROL TF, KELTROL BT, KELTROL RD and KELTROL CG by the company NUTRASWEET KELCO, or with the names RHODICARE S or RHODICARE H by the company RHODIA CHIMIE. The hydroxyalkylcelluloses are generally hydroxy (alkyl of 1 to 4 carbon atoms) -celluloses and more particularly hydroxyethylcelluloses. These are available, for example, under the trade names CELLOSIZE QP3L, CELLOSIZE QP4400H, CELLOSIZE QP30000H, CELLOSIZE HEC30000A or CELLOSIZE POLYMER PCG10 by the company AMERCHOL, under the trade names NATROSOL 250HHR, NATROSOL 250MR, NATROSOL 250M, NATROSOL 250HHXR, NATROSOL 250HHX, NATROSOL 250HR, NATROSOL HX by the company HERCULES or even with the name TYLOSE H1000 by the company HOECHST. The hydroxyalkylcelluloses can also be hydroxypropylcelluloses sold under the trade names KLUCEL EF, KLUCEL H, KLUCEL LHF, KLUCEL MF, KLUCEL G by the company AQUALON. Among the carboxyalkylcelluloses, carboxymethylcellulose is preferably used, which is marketed, for example, under the brand names BLANOSE 7M8 / SF, BLANOSE RAFFINÉE 7M, BLANOSE 7LF, BLANOSE 7MF, BLANOSE 9M31F, BLANOSE 12M31XP, BLANOSE 12M31P, BLANOSE 9, 31XF, BLANOSE 7H, BLANOSE 7M31, BLANOSE 7H3SXF by the company AQUALON, or with the names AQUASORB A500 and AMBERGUM 1221 by the company HERCULES, with the names CELLOGEN HP810A and CELLOGEN HP6HS9 by the company MONTELLO, or even with the name PRIMELLOSE by the AVEBE company. Particularly preferred water-soluble thickener polymers useful as conventional thickening agents in the anhydrous decolorizing composition of the present invention are guara gums, guara gum derivatives or hydroxyalkyl celluloses. The water-soluble thickening agent (s) described above is generally used in a proportion of 0.03 to 30% by weight, preferably from 0.3 to 15% by weight, with respect to the anhydrous composition. The present invention also aims at a process for decolorizing keratin fibers, in particular human hair. This process comprises the following steps: preparing the ready-to-use composition described above, applying the composition on the zone of the keratin fibers by decolouring, letting it stand for a sufficient time to obtain the intended discoloration, time generally comprised between 10 minutes and one hour , preferably between 10 and 45 minutes, and - removing the decolorization mixture by rinsing with water, followed by shampooing and then drying. Another object of the present invention is a multi-part packaging device, also called "package", comprising at least three compartments wherein the first contains a peroxygenated salt as defined above, the second contains a water-soluble solvent such as previously defined and the alkaline agent, and the third contains an aqueous composition of hydrogen peroxide, the nonionic and / or anionic amphiphilic poly (s) comprising at least one fatty chain, being introduced into one or a plurality of these compartments. The Examples presented below are purely illustrative and not limiting, and allow to better understand the present invention. EXAMPLE 1 Composition A Decyl alcohol ethoxylated with 3 moles of OE 30 g Ethoxylated decyl alcohol with 5 moles of OE 26 g Oleic acid 10 g- Oleic alcohol 3 g Propylene glycol 9 g Ethoxylated oleo-ethyl alcohol with 30 moles of OE 4.5 g Ethylene glycol monobutyl ether 3 g Ammonia at 20.5% in NH3 9 g Water c.b.p. 100 Composition B Sodium persulfate 26 g Potassium persulfate 40 g Sodium metasilicate 14 g Ammonium chloride 5 g AEDT 1 g Sodium lauryl sulfate 2 g Cetilhidroxietilcelulosa 2 g Silica c.b.p. 100 60 g of composition A, 20 g of composition B and 100 g of 6% by weight aqueous hydrogen peroxide solution are mixed. The viscosity of the mixture varies very little with respect to time and the mixture has a good decolouring power. EXAMPLE 2 The following decolorization composition was prepared (the amounts are given in% by weight): laureth-5-carboxylic acid 4 Ethanolamine 0.6 Deceth-3 4 Deceth-5 1.5 Miristiléter de PPG 2 Oleth-10 1.5 Oleic alcohol 1.5 Ethanol 5 Methoxyisopropanol 6.5 polyglyceryl 4-oleyl ether Merquat 100 1.5 Serad FX-1100 1 Hydrogen peroxide 3 Sequestrant 0.2 Perfume 1 Water c.b.p. 100 This composition, intended to be applied immediately on the hair by discoloration, is applied for 45 minutes under the cap. After rinsing and drying, a homogeneous discoloration is obtained. It is noted that in relation to this date, the best method known by the applicant to carry out the aforementioned invention, is the conventional one for the manufacture of the objects to which it relates.

Claims (25)

  1. CLAIMS Having described the invention as an antecedent, the content of the following claims is claimed as property: 1. A ready-to-use aqueous composition for the decolorization of keratin fibers, in particular human keratin fibers, comprising, in an appropriate medium for discoloration. , at least one alkaline agent, at least one peroxygenated salt, hydrogen peroxide and at least one water-soluble solvent, characterized in that it also contains at least one non-ionic and / or anionic amphiphilic polymer comprising at least one fatty chain.
  2. 2. The composition according to claim 1, characterized in that the nonionic amphiphilic polymer comprising at least one fatty chain, is selected from the group consisting of the celluloses or hydroxyalkylcelluloses modified with groups comprising at least one fatty chain of the alkyl type , arylalkyl or alkylaryl containing an alkyl group of 8 to 22 carbon atoms, or with polyalkoxylated alkylphenol groups; the modified hydroxypropyl-sugars with groups comprising at least one fatty chain of 8 to 22 carbon atoms; polyurethanes comprising at least one fatty chain of the alkyl or alkenyl type of 8 to 30 carbon atoms; vinylpyrrolidone copolymers and hydrophobic monomers with fatty chain; copolymers of alkyl (meth) acrylates of 1 to 6 carbon atoms and amphiphilic monomers comprising at least one fatty chain; the copolymers of hydrophilic (meth) acrylates and hydrophobic monomers comprising at least one fatty chain.
  3. 3. A composition according to any of claims 1 or 2, characterized in that the nonionic amphiphilic polymer is a modified hydroxyethylcellulose with groups comprising at least one alkyl radical of 8 to 22 carbon atoms or a polyurethane comprising at least one alkyl chain of 10 to 20 carbon atoms.
  4. 4. The composition according to claim 1, characterized in that the anionic amphiphilic polymer comprising at least one fatty chain is a copolymer comprising hydrophilic units derived from one or a plurality of ethylenically unsaturated monomers bearing a carboxylic acid function , and hydrophobic units derived from one or a plurality of monomers with ethylenic unsaturation, carrying a hydrophobic side chain.
  5. The composition according to claim 4, characterized in that the monomer (s) with ethylenic unsaturation carrying a carboxylic acid function are selected from the group consisting of ethacrylic acid, methacrylic acid and acrylic acid, preferably methacrylic acid, acid Acrylic and mixtures thereof.
  6. 6. A composition according to any of claims 4 and 5, characterized in that the monomer (s) with ethylenic unsaturation carrying a hydrophobic side chain are selected from the group consisting of alkyl ethacrylates, methacrylates and / or acrylates of 10 to 30 carbon atoms, preferably 12 to 22 carbon atoms.
  7. A composition according to any of claims 4 to 6, characterized in that the monomer (s) with ethylenic unsaturation bearing a hydrophobic side chain are selected from the group consisting of allyl ethers of fatty alcohols corresponding to Formula (I) CH2 = CR 'CH2-0-Bn-R wherein R' represents a hydrogen atom or a methyl group, B represents an ethyleneoxy group, n is an integer between 0 and 100, R represents a hydrocarbon group selected from A group consisting of alkyl, arylalkyl, aryl, alkylaryl or cycloalkyl radicals of 8 to 30 carbon atoms, preferably 10 to 24 carbon atoms.
  8. 8. A composition according to any of claims 4 to 7, characterized in that the amphiphilic anionic polymer comprising at least one fatty chain, it further comprises units derived from a crosslinking monomer containing two non-conjugated ethylenic double bonds.
  9. The composition according to claim 8, characterized in that the crosslinking monomer is selected from the group consisting of diallyl phthalate, allyl (meth) acrylate, divinylbenzene, (poly) ethylene glycol dimethacrylate, methylene-bis-acrylamide, polyallylsucrose or polyallyl pentaerythritol.
  10. 10. A composition according to any of claims 4 to 9, characterized in that the anionic amphiphilic polymer comprising at least one fatty chain is a crosslinked copolymer of acrylic acid and alkyl acrylate of 10 to 30 carbon atoms.
  11. 11. A composition according to any of the preceding claims, characterized in that the nonionic and / or anionic amphiphilic polymers comprising at least one fatty chain are present at a ratio of 0.01 to 10% by weight, preferably from 0.1 to 5% by weight, with respect to the total weight of the aqueous composition.
  12. 12. A composition according to any of the preceding claims, characterized in that the water-soluble solvent is selected from the group consisting of straight or branched chain aliphatic monoalcohols of 1 to 6 carbon atoms, straight or branched chain aliphatic polyols of 3 to 20 carbon atoms, ethers of polyols which can be monoethers or aliphatic diethers of 1 to 6 carbon atoms of polyols of 2 to 9 carbon atoms and aromatic ethers of 6 to 9 carbon atoms of polyols of 2 to 9 carbon atoms carbon.
  13. 13. A composition according to any of the preceding claims, characterized in that it contains from 0.1 to 10% by weight of water-soluble solvent and preferably from 0.5 to 8% by weight of water-soluble solvent, with respect to the total weight of the aqueous composition.
  14. A composition according to any of the preceding claims, characterized in that the alkaline agent is selected from the group consisting of ammonia and organic amines such as monoethanolamine, diethanolamine or triethanolamine, 2-amino-2-methyl-1-propanol, diaminopropane , oxyethylenated and / or oxypropylenated hydroxyalkylamines and ethylenediamines.
  15. 15. A composition according to any of the preceding claims, characterized in that the peroxygenated salt is selected from the group consisting of persulfates, percarbonates and perborates of ammonium and alkali metals, in particular sodium and potassium persulfates.
  16. 16. A composition according to any of the preceding claims, characterized in that it contains from 2 to 20% by weight and preferably from 4 to 15% by weight, of the peroxygenated salt.
  17. 17. A composition according to any of the preceding claims, characterized in that it contains from 0.5 to 10% by weight and preferably from 1 to 8% by weight, of hydrogen peroxide.
  18. 18. A composition according to any of the preceding claims, characterized in that it also contains bleaching aids that are selected from the group consisting of agents for controlling the evolution of oxygen, anionic, nonionic, cationic, amphoteric or suteionic surfactants and mixtures. of them, mineral and vegetable oils, waxes, binders, mineral fillers, opacifiers, dyes, sequestrants, perfumes and polymers.
  19. 19. The composition according to claim 18, characterized in that it contains at least one water-soluble natural and / or synthetic thickener polymer.
  20. The composition according to claim 19, characterized in that it contains from 0.03 to 30% by weight, preferably from 0.3 to 15% by weight of at least one water-soluble thickener polymer.
  21. 21. The composition according to claim 18, characterized in that it contains at least one cationic and / or amphoteric substantive polymer.
  22. 22. The composition according to claim 21, characterized in that it contains from 0.03 to 30% by weight of at least one cationic and / or amphoteric substantive polymer.
  23. 23. The composition according to claim 18, characterized in that it contains from 0.01 to 40% by weight and preferably from 0.1 to 30% by weight, of at least one surfactant.
  24. 24. A process for decolorizing keratin fibers, in particular human hair, characterized in that it comprises the steps of: preparing, immediately before use, an aqueous decolorizing composition according to any of claims 1 to 23, applying the composition on the zone of keratin fibers to be decolorized, let stand for a sufficient time to obtain the desired discoloration, and remove the decolorizing mixture by rinsing with water, followed by shampooing and then drying.
  25. 25. A device with several compartments or "package" for decolorizing keratin fibers and in particular human keratin fibers such as hair, characterized in that it comprises at least three compartments, of which the first contains a peroxygenated salt as defined in claim 15, the second contains a water-soluble solvent as defined in claim 12 and an alkaline agent as defined in claim 14 and the third contains an aqueous composition of hydrogen peroxide, the non-ionic amphiphilic polymer (s) and / or anionics comprising at least one fatty chain, being introduced into one or a plurality of the compartments.
MXPA/A/2000/001033A 1999-01-29 2000-01-28 Aqueous composition for bleaching keratin fibers, especially hair, includes combination of water-soluble solvent and nonionic amphiphilic polymer with at least one fatty chain MXPA00001033A (en)

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FR9901055 1999-01-29

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MXPA00001033A true MXPA00001033A (en) 2002-05-09

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