FR2942594A1 - Composition, useful for dyeing of human keratin fibers, preferably hair, comprises in a medium, one or more natural dyes e.g. lawsone, juglone, alizarin and purpurin, and 3-phenyl-1-propanol - Google Patents

Abstract

Dye composition (I) comprises in a medium, one or more natural dyes and 3-phenyl-1-propanol. An independent claim is included for a multi-compartment device comprising (I) and an oxidizing composition comprising one or more oxidizing agents.

Description

COMPOSITION COMPRISING A NATURAL COLOR AND 3-PHENYL-1-PROPANOL, COLORING OF KERATIN FIBERS

The subject of the present invention is compositions for staining human keratin fibers, comprising in a cosmetically acceptable medium at least one natural dye and 3-phenyl-1-propanol. It also relates to a process for staining human keratin fibers involving such a composition, as well as a multi-compartment device. Two major modes of staining human keratin fibers, and in particular the hair, are known. The first, called oxidation or permanent staining, consists in using one or more oxidation dye precursors, more particularly one or more oxidation bases optionally associated with one or more couplers. Usually, oxidation bases are chosen from ortho- or para-phenylenediamines, ortho- or para-aminophenols as well as heterocyclic compounds. These oxidation bases are colorless or weakly colored compounds which, combined with oxidizing products, make it possible to access, by a process of oxidative condensation, colored species which remain trapped inside the fiber. Very often, the shades obtained with these oxidation bases are varied by combining them with one or more couplers, the latter being chosen in particular from aromatic meta-diamines, meta-aminophenols, meta-diphenols and certain heterocyclic compounds, such as indole compounds. The variety of molecules involved in the oxidation bases and couplers makes it possible to obtain a rich palette of colors.

The second mode of staining, referred to as direct or semi-permanent staining, involves the application of direct dyes which are color and dye molecules having affinity for the fibers. Given the nature of the molecules used, these remain rather on the surface of the fiber and penetrate relatively little inside the fiber, compared to the small molecules of precursors of oxidation dyes. The direct dyes generally employed are chosen from nitrobenzene, anthraquinone, nitropyridine, azo, methine, azomethine, xanthene, acridine, azine or triarylmethane direct dyes. The chemical species used may be nonionic, anionic (acidic dyes) or cationic (basic dyes). Most of the direct dyes used have sufficient aqueous solubility and there are now many suitable dye supports for receiving them. The situation is different in the case of natural dyes.

Indeed, to effectively color the keratinous fibers, some of these dyes must be in most cases used in the presence of solvents whose role is to vectorize them in the fiber. Among the known cosmetic solvents for this purpose, aromatic solvents are frequently used. Mention may more particularly be made of benzyl alcohol, benzyloxyethanol or phenoxyethanol. Nevertheless, the presence of aromatic alcohols in these formulations amplifies the problem of staining of the scalp and the skin encountered in coloring. In addition, and this represents another disadvantage to the use of such dyes, the presence of aromatic solvents, very sparingly soluble in aqueous medium, requires the use of significant amounts of co-solvents (usually ethanol) to make them compatible with conventional dye formulations.

One of the objectives of the present invention is therefore to provide dye compositions comprising at least one natural dye and which have satisfactory dyeing properties, in particular in that they make it possible to obtain powerful, homogeneous colorings between the tip and the root of the same fiber and fiber to another, and chromatic, even on sensitized hair.

These and other objects are achieved by the present invention which relates to dye compositions comprising in a cosmetically acceptable medium, one or more natural dyes and 3-phenyl-1-propanol.

It also relates to a process for staining human keratinous fibers, and in particular the hair, of applying to said fibers, the composition according to the invention. It also has for another object a multi-compartment device or kit comprising at least one composition according to the invention devoid of oxidizing agent and an oxidizing composition comprising one or more oxidizing agents.

Other features and advantages of the invention will emerge more clearly on reading the description and examples.

It should be noted that in what follows, and unless otherwise indicated, the boundaries of a domain of values are included in this area.

As indicated above, the dyeing composition according to the invention comprises one or more natural dyes. By natural dyes is meant any dye or dye precursor having a natural occurrence and produced either by extraction (and optionally purification) from a plant matrix, or by chemical synthesis.

The natural dye or dyes suitable in particular for the implementation of the invention are preferably chosen from lawsone, juglone, alizarin, purpurine, carminic acid, kermesic acid, purpurogallin, anthragallol, protocatechaldehyde, indigo, isatin, curcumin, spinusoline, chlorophylls, chlorophyllins, orceins, haematein, hematoxylin, brazilin, braziline, safflower dyes (eg carthamine), flavonoids (with, for example, morine, apigenidine, sandalwood), anthocyanins (of the apigeninidine type), carotenoids, tannins, sorghum and cochineal carmine, or mixtures thereof. It is also possible to use the extracts or decoctions containing these natural dyes and in particular the henna extracts. Preferably, the natural dye (s) are chosen from lawsone, juglone, alizarin, purpurine, carminic acid, kermesic acid, purpurogalline, protocatechaldehyde, indigo, isatin, curcumin , spinulosin, apigenidine, chlorophyllin, sorghum, orceins, and cochineal carmine, or mixtures thereof.

The natural dye or dyes more particularly represent from 0.001 to 10% by weight, preferably from 0.01 to 8% by weight, more preferably from 0.1 to 5% by weight relative to the weight of the composition.

The content of 3-phenyl-1-propanol in the composition is more particularly from 0.05 to 50% by weight relative to the weight of said composition, and preferably from 0.1 to 30% by weight, relative to the weight of the composition.

The composition according to the invention may also comprise one or more additional dyes. In particular, this or these additional dyes may be chosen from synthetic direct dyes, oxidation dye precursors, or combinations thereof.

Thus, the composition may comprise one or more additional synthetic direct dyes chosen from ionic or nonionic, preferably cationic or nonionic, species. As examples of suitable additional synthetic direct dyes, mention may be made of azo direct dyes; methinic; carbonyls; azinic; nitro (hetero) aryl; tri- (hetero) aryl methanes; porphyrins and phthalocyanines, alone or in mixtures.

More particularly, the azo dyes comprise a function -N = N- whose two nitrogen atoms are not simultaneously engaged in a ring. However, it is not excluded that one of the two nitrogen atoms of the sequence -N = N- is engaged in a cycle.

The dyes of the family of methines are more particularly compounds comprising at least one sequence chosen from> C = C <and -N = C <whose two atoms are not simultaneously engaged in a ring. It is however specified that one of the nitrogen or carbon atoms of the chains can be engaged in a cycle. More particularly, the dyes of this family are derived from true methine-type compounds (comprising one or more -C = C- above-mentioned sequences); azomethine (comprising at least one or more -C = N- chains) with, for example, azacabocyanines and their isomers, diazacarbocyanines and their isomers, tetraazacarbocyanines; mono- and di-arylmethane; indoamines (or diphenylamines); indophenols; indoanilines. As regards the dyes of the carbonyl family, mention may be made, for example, of the dyes chosen from acridone, benzoquinone, anthraquinone, naphthoquinone, benzanthrone, anthranthrone, pyranthrone, pyrazolanthrone, pyrimidinoanthrone, flavanthrone, idanthrone, flavone, (iso) violanthrone, isoindolinone, benzimidazolone, isoquinolinone, anthrapyridone, pyrazoloquinazolone, perinone, quinacridone, quinophthalone, indigo, thioindigo, naphthalimide, anthrapyrimidine, diketopyrrolopyrrole, coumarin.

As regards the dyes of the family of azines, there may be mentioned in particular azine, xanthene, thioxanthene, fluorindine, acridine, (di) oxazine, (di) thiazine, pyronine. The nitro (hetero) aromatic dyes are more particularly nitrobenzene or nitro pyridinic direct dyes. With regard to porphyrin or phthalocyanine dyes, it is possible to use cationic or non-cationic compounds, optionally comprising one or more metals or metal ions, for example alkali and alkaline earth metals, zinc and silicon.

As examples of additional direct dyes of synthesis particularly suitable, mention may be made of the nitro dyes of the benzene series; azo direct dyes; methinic; azomethines with more particularly diazacarbocyanines and their isomers and tetraazacarbocyanines (tetraazapentamethines); quinone direct dyes and in particular anthraquinone, naphthoquinone or benzoquinone dyes; direct azine dyes; xanthenics; triarylmethanics; indoamines; indigoids; phthalocyanines and porphyrins; alone or in mixtures. Preferably, the direct dyes are chosen from nitro dyes of the benzene series; azo; azomethines with diazacarbocyanines and their isomers, tetraazacarbocyanines (tetraazapentamethines); anthraquinone direct dyes; triarylmethane direct dyes; alone or in mixtures.

Even more preferably, these additional direct dyes are chosen from nitro dyes of the benzene series; azo direct dyes; azomethines with diazacarbocyanines and their isomers, tetraazacarbocyanines (tetraazapentamethines); alone or in mixture.

These dyes may be monochromophoric dyes (that is to say comprising only one dye) or polychromophoric, preferably di- or tri-chromophoric dyes; the chromophores which may be identical or different, of the same chemical family or not. It should be noted that a polychromophoric dye comprises several radicals each derived from an absorbing molecule in the visible range between 400 and 800 nm. In addition, this absorbance of the dye does not require any prior oxidation thereof, or association with other (s) species (s) chemical (s). In the case of polychromophoric dyes, the chromophores are connected to each other by means of at least one linker which may or may not be cationic. Among the polychromophoric dyes, mention may be made more particularly of di- or tri-chromophoric, preferably dichromophoric, azo and / or azomethine dyes, symmetrical or otherwise, comprising on the one hand at least one aromatic heterocycle comprising 5 or 6 ring members, optionally condensed mixture, comprising at least one quaternized nitrogen atom engaged in said heterocycle and optionally at least one other heteroatom (such as nitrogen, sulfur, oxygen), and on the other hand, at least one phenyl or naphthyl group optionally substituted, optionally bearing at least one OR group with R representing a hydrogen atom, an optionally substituted C1-C6 alkyl radical, an optionally substituted phenyl ring, or at least one N (R ') group 2 with R 'identical or not, representing a hydrogen atom, an optionally substituted alkyl radical C1-C6, an optionally substituted phenyl ring; the radicals R 'which can form, with the nitrogen atom to which they are bonded, a saturated 5- or 6-membered heterocycle, or else one and / or both radicals R' may each form with the carbon atom of the aromatic ring placed in ortho of the nitrogen atom, a 5- or 6-membered saturated heterocycle. As aromatic cationic heterocycle, there may be mentioned, preferably, 5- or 6-membered rings comprising 1 to 3 nitrogen atoms, preferably 1 or 2 nitrogen atoms, one being quaternized; said heterocycle being optionally further fused to a benzene ring. It should also be noted that the heterocycle may optionally comprise another heteroatom different from nitrogen, such as sulfur or oxygen. If the heterocycles or phenyl or naphthyl groups are substituted, they are substituted, for example, with one or more C 1 -C 8 alkyl radicals optionally substituted with a hydroxyl, C 1 -C 2 alkoxy or C 2 -C 4 hydroxyalkoxy, acetylamino or substituted amino group. one or two C 1 -C 4 alkyl radicals, optionally carrying a hydroxyl group or both radicals which can form, with the nitrogen atom to which they are attached, a 5- or 6-membered heterocycle, optionally comprising another identical heteroatom or different from nitrogen; a halogen atom; a hydroxyl group; a C1-C2 alkoxy radical; a hydroxyalkoxy radical at 02-04; an amino radical; an amino radical substituted with one or two identical or different C 1 -C 4 alkyl radicals optionally bearing a hydroxyl group. Preferably, the linker is a linear, branched or cyclic C1-C20 alkyl chain; optionally interrupted by at least one heteroatom (such as nitrogen, oxygen) and / or at least one group comprising (CO, SO2); optionally interrupted by at least one phenyl or substituted or unsubstituted naphthyl group; Optionally interrupted by at least one saturated, unsaturated or aromatic heterocycle, condensed or not with a phenyl ring, said heterocycle comprising at least one quaternized nitrogen atom engaged in said ring and optionally at least one other heteroatom (such as oxygen , nitrogen or sulfur); optionally interrupted by at least one quaternary ammonium group substituted with two C 1 -C 15 alkyl groups; the linking arm does not comprise a nitro, nitroso or peroxo group. If the heterocycles or aromatic rings are substituted, they are, for example, substituted with one or more C 1 -C 8 alkyl radicals optionally substituted by a hydroxyl, C 1 -C 2 alkoxy or C 2 -C 4 hydroxyalkoxy or acetylamino or amino group substituted by a or two identical or different C 1 -C 4 alkyl radicals, optionally carrying a hydroxyl group, or the two radicals which can form, with the nitrogen atom to which they are attached, a 5- or 6-membered heterocycle, optionally comprising a another heteroatom that is the same or different from nitrogen; a halogen atom; a hydroxyl group; a C1-C2 alkoxy radical; a C2-C4 hydroxyalkoxy radical; an amino radical; an amino radical substituted with one or two identical or different C 1 -C 4 alkyl radicals optionally bearing a hydroxyl group. The link between the linker and each chromophore is generally by means of a heteroatom which substitutes the phenyl or naphthyl ring or by means of the quaternized nitrogen atom of the cationic heterocycle.

Among the azo, azomethine and methine monochromophoric direct dyes that may be used according to the invention, mention may be made of the cationic dyes described in patent applications WO 95/15144, WO 95/01772 and EP 714954; FR 2189006, FR 2285851, FR-2140205, EP 1378544, EP 1674073. Thus, mention may in particular be made of the cationic direct dyes corresponding to the following formulas: R1 AD = DWN x R2 R3 in which: D represents a nitrogen atom or the group -CH, R, and R2, which may be identical or different, represent a hydrogen atom; a C 1 -C 4 alkyl radical which may be substituted with a -CN, -OH or -NH 2 radical or form, with a carbon atom of the benzene ring, an optionally oxygenated or nitrogenous heterocycle, which may be substituted by one or more C 1 -C 4 alkyl radicals; C4; a 4'-aminophenyl radical, R3 and R'3, which may be identical or different, represent a hydrogen or halogen atom chosen from chlorine, bromine, iodine and fluorine, a cyano radical or a C1-alkyl radical; -C4, C1-C4 alkoxy or acetyloxy, X - represents an anion preferably selected from chloride, methyl sulfate and acetate, 7 A represents a group chosen by the following structures: R4 4 \ ~ N R4 nN N R4 N + R4 N + R4 R4 wherein R4 represents a C1-C4 alkyl radical which may be substituted with a hydroxyl radical; Wherein R5 represents a hydrogen atom, a C1-C4 alkoxy radical, a halogen atom such as bromine, chlorine, iodine or fluorine, R6 represents a hydrogen atom, a C1-C4 alkyl radical or forms, with a carbon atom of the benzene ring, an optionally oxygenated heterocycle and / or substituted with one or more C1-C4 alkyl groups, R7 represents a hydrogen atom or of halogen such as bromine, chlorine, iodine or fluorine, D, and D2, which are identical or different, represent a nitrogen atom or the group -CH, m = 0 or 1

X - represents a cosmetically acceptable anion and preferably selected from chloride, methyl sulfate and acetate, E represents a group chosen by the following structures: // R'-N + -N + N- R 'R' in which R 'represents a C1-C4 alkyl radical;

when m = 0 and that D, represents a nitrogen atom, then E can also designate a group of following structure: R 'N + R'

Wherein R 'represents a C1-C4 alkyl radical. Among the abovementioned compounds, the following compounds are especially used: CH 3 /H 3, -NN CH 3 N = N N -CH 3 X -N = NNX-N + H -N + CH 3 CH 3 CH 3 0 CH 3 NH 2 X -N = ## STR2 ## ## STR1 ## \ + '~ ~ N. N N N N X I N Y N, I N X I I OMe OMe OMe N + N * NNNN X I N + ~ N / N N, N X 1 I X N N 'NN N X NN * 1 \ 1N, N N OH OH X NN ~ NN. Embedded image X represents an anion preferably selected from chloride, iodide, methyl sulfate, and the like. ethyl sulfate, acetate.

Preferably, the direct dyes are chosen from monochromophoric direct dyes of nitrobenzene type; azo; azomethines with diazacarbocyanines and their isomers, tetraazacarbocyanines (tetraazapentamethines); anthraquinone direct dyes; triarylmethane direct dyes; and even more particularly among nitrobenzene dyes; azo; azomethines with diazacarbocyanines and their isomers, tetraazacarbocyanines (tetraazapentamethines); these dyes being present alone or in mixture. When present, the additional direct dye (s) of synthesis represent from 0.0001 to 10% by weight relative to the weight of the composition, and preferably from 0.005 to 5% by weight relative to the same reference. --- _ p r e _W S e i: xv. For example, the oxidation bases are chosen from para-phenylenediamines, bis-phenylalkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases and their salts. addition. Among the paraphenylenediamines, there may be mentioned, for example, para-phenylenediamine, paratoluylenediamine, 2-chloro-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,5-dimethyl-para-phenylenediamine, N, N-dimethyl-para-phenylenediamine, N, N-diethyl-para-phenylenediamine, N, N-dipropyl-para-phenylenediamine, 4-amino-N, N-diethyl-3-methylaniline, N, N- bis - ((3-hydroxyethyl) paraphenylenediamine, 4-N, N-bis - ((3-hydroxyethyl) amino-2-methylaniline, 4-N, N-bis - ((3-hydroxyethyl) amino 2-chloro aniline, 2-13-hydroxyethyl paraphenylenediamine, 2-fluoro-para-phenylenediamine, 2-isopropyl-para-phenylenediamine, N-O-hydroxy-propyl) paraphenylenediamine, 2-hydroxymethyl-para-phenylenediamine, N, N-dimethyl-3-methyl-para-phenylenediamine, N N- (ethyl, (3-hydroxyethyl) paraphenylenediamine, N-O 3, γ-dihydroxypropyl) p aphenylenediamine, N- (4'-aminophenyl) paraphenylenediamine, N-phenyl paraphenylenediamine, 2-13-hydroxyethyloxy para-phenylenediamine, 2-13-acetylaminoethyloxy para-phenylenediamine, N - ((3-methoxyethyl) paraphenylenediamine, 4 aminophenylpyrrolidine, 2-thienyl paraphenylenediamine, 2-hydroxyethylamino-5-amino toluene, 3-hydroxy-1- (4'-aminophenyl) pyrrolidine and their addition salts with an acid. Of the paraphenylenediamines mentioned above, paraphenylenediamine, paratoluylenediamine, 2-isopropyl paraphenylenediamine, 2-hydroxy-3-hydroxyethyl paraphenylenediamine, 2-hydroxy-hydroxyethyloxy-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6 ethyl paraphenylenediamine, 2,3-dimethyl paraphenylenediamine, N, N-bis - ((3-hydroxyethyl) paraphenylenediamine, 2-chloro-para-phenylenediamine, 2-13-acetylaminoethyloxy-para-phenylenediamine, and their addition salts with an acid Particularly preferred bis-phenylalkylenediamines include, for example, N, N'-bis - ((3-hydroxyethyl) N, N'-bis (4'-aminophenyl) -1,3 diamino propanol, N, N'-bis - ((3-hydroxyethyl) N, N'-bis- (4'-aminophenyl) ethylenediamine, N, N'-bis (4-aminophenyl) tetramethylenediamine, N, N'-bis- (8-hydroxyethyl) N, N'-bis (4-aminophenyl) tetramethylenediamine, N, N'-bis- (4-methylaminophenyl) tetramethyl N, N'-bis (ethyl) N, N'-bis (4'-amino, 3'-methylphenyl) ethylenediamine, 1,8-bis (2,5-diamino phenoxy) -3-ylenediamine , 6-dioxaoctane, and their addition salts.

Among para-aminophenols, para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluoro phenol, 4-amino-3-chlorophenol, 4- amino 3-hydroxymethyl phenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol, 4-amino-2 - ([ 3-hydroxyethylaminomethyl) phenol, 4-amino-2-fluoro phenol, and their addition salts with an acid. Among the ortho-aminophenols, mention may be made, for example, of 2-amino phenol, 2-amino-5-methylphenol, 2-amino-6-methylphenol and 5-acetamido-2-aminophenol, and their addition salts. Among the heterocyclic bases that may be mentioned by way of example are pyridine derivatives, pyrimidine derivatives and pyrazole derivatives. Among the pyridine derivatives, mention may be made of the compounds described for example in patents GB 1 026 978 and GB 1 153 196, such as 2,5-diamino pyridine, 2- (4-methoxyphenyl) amino-3-amino pyridine, 3,4-diamino pyridine, and their addition salts. Other pyridinic oxidation bases useful in the present invention are the 3-amino pyrazolo [1,5-a] pyridines oxidation bases or their addition salts described for example in the patent application FR 2801308. By way of example, mention may be made of pyrazolo [1,5-a] pyridin-3-ylamine; 2-acetylamino pyrazolo [1,5-a] pyridin-3-ylamine; 2-morpholin-4-yl-pyrazolo [1,5-a] pyridin-3-ylamine; 3-amino-pyrazolo [1,5-a] pyridin-2-carboxylic acid; 2-methoxy-pyrazolo [1,5-a] pyridin-3-ylamino; (3-Amino-pyrazolo [1,5-a] pyridin-7-yl) -methanol; 2- (3-Amino-pyrazolo [1,5-a] pyridin-5-yl) -ethanol; 2- (3-aminopyrazolo [1,5-a] pyridin-7-yl) -ethanol; (3-Amino-pyrazolo [1,5-a] pyridin-2-yl) -methanol; 3,6-diamino-pyrazolo [1,5-a] pyridine; 3,4-diamino-pyrazolo [1,5-a] pyridine; pyrazolo [1,5-a] pyridine-3,7-diamine; 7-morpholin-4-yl-pyrazolo [1,5-a] pyridin-3-ylamine; pyrazolo [1,5-a] pyridine-3,5-diamine; 5-morpholin-4-yl-pyrazolo [1,5-a] pyridin-3-ylamine; 2 - [(3-amino-pyrazolo [1,5-a] pyridin-5-yl) - (2-hydroxyethyl) amino] ethanol; 2 - [(3-aminopyrazolo [1,5-a] pyridin-7-yl) - (2-hydroxyethyl) amino] ethanol; 3-amino-pyrazolo [1,5-a] pyridin-5-ol; 3-amino-pyrazolo [1,5-a] pyridin-4-ol; 3-amino-pyrazolo [1,5-a] pyridin-6-ol; 3-amino-pyrazolo [1,5-a] pyridin-7-ol; as well as their addition salts. Among the pyrimidine derivatives, mention may be made of the compounds described, for example, in DE 2359399; JP 88-169571; JP 05-63124; EP 0770375 or patent application WO 96/15765 such as 2,4,5,6-tetraaminopyrimidine, 4-hydroxy 2,5,6-triaminopyrimidine, 2-hydroxy 4,5,6-triaminopyrimidine, 2 , 4-dihydroxy-5,6-diaminopyrimidine, 2,5,6-triaminopyrimidine and their addition salts and tautomeric forms, when tautomeric equilibrium exists.

Among the pyrazole derivatives, mention may be made of the compounds described in DE 3843892, DE 4133957 and patent applications WO 94/08969, WO 94/08970, FR-A-2 733 749 and DE 195 43 988 as the 4.5 1-methyl pyrazole, 4,5-diamino-1-yl-hydroxyethyl) pyrazole, 3,4-diamino pyrazole, 4,5-diamino-1- (4'-chlorobenzyl) pyrazole, diamino 1,3-dimethyl pyrazole, 4,5-diamino-3-methyl-1-phenyl pyrazole, 4,5-diamino-1-methyl-3-phenylpyrazole, 4-amino-1,3-dimethyl-5-hydrazino pyrazole, 1-Benzyl-4,5-diamino-3-methyl-pyrazole, 4,5-diamino-3-tert-butyl-1-methyl-pyrazole, 4,5-diamino-1-tert-butyl-3-methyl-pyrazole, 4,5 1 - ([3-hydroxyethyl) 3-methylpyrazole, 4,5-diamino-1-ethyl-3-methylpyrazole, 4,5-diamino-1-ethyl-3- (4'-methoxyphenyl) pyrazole, 5-diamino-1-ethyl-3-hydroxymethyl-pyrazole, 4,5-diamino-3-hydroxymethyl-1-methyl-pyrazole, 4,5-diamino-3-hydroxymethyl-1-isopropyl pyrazole, 4,5-diamino-3-methyl 1-isopropyl pyrazole, 4-amino-5- (2'-aminoethyl) amino-1,3-dimethyl pyrazole, 3,4,5-triamino pyrazole, 1-methyl-3,4,5-triamino pyrazole, 3,5-diamino-1-methyl-4-methylamino pyrazole, 3,5-diamino 4 - ([3-hydroxyethyl) amino-1-methyl pyrazole, and their addition salts. It is also possible to use 4-5-diamino-1 - ([3-methoxyethyl) pyrazole. As pyrazole derivatives, mention may also be made of diamino N, N-dihydropyrazolopyrazolones and in particular those described in patent application FR 2886136, such as the following compounds and their addition salts: 2,3-Diamino-6,7-dihydro-1 H, 5H-pyrazolo [1,2-a] pyrazol-1-one, 2-amino-3-ethylamino-6,7-dihydro-1H, 5H-pyrazolo [1,2-a] pyrazol-1-one 2-Amino-3-isopropylamino-6,7-dihydro-1H, 5H-pyrazolo [1,2-a] pyrazol-1-one, 2-amino-3- (pyrrolidin-1-yl) -6, 7-Dihydro-1H, 5H-pyrazolo [1,2-a] pyrazol-1-one, 4,5-diamino-1,2-dimethyl-1,2-dihydro-pyrazol-3-one, 4,5 -Diamino-1,2-diethyl-1,2-dihydro-pyrazol-3-one, 4,5-diamino-1,2-di- (2-hydroxyethyl) -1,2-dihydro-pyrazol-3-one 2-amino-3- (2-hydroxyethyl) amino-6,7-dihydro-1H, 5H-pyrazolo [1,2-a] pyrazol-1-one, 2-amino-3-dimethylamino-6,7 1-Dihydro-1H, 5H-pyrazolo [1,2-a] pyrazol-1-one, 2,3-diamino-5,6,7,8-tetrahydro-1H, 6H-pyridazino [1,2-a] ] pyrazol-1-one, 4-amino-1,2-diethyl-5- (pyrrolidin-1-yl) -1,2-dihydro-pyrazol-3-one, 4-amino-5- (3-dime) thylamino-pyrrolidin-1-yl) -1,2-diethyl-1,2-dihydro-pyrazol-3-one, 2,3-diamino-6-hydroxy-6,7-dihydro-1H, 5H-pyrazolo [ 1,2-a] pyrazol-1-one. As heterocyclic bases, it is preferable to use 4,5-diamino-1-yl-hydroxyethyl) pyrazole and / or 2,3-diamino-6,7-dihydro-1H, 5H-pyrazolo [1,2, A] pyrazol. -l-one and their addition salts.

The composition according to the invention may optionally comprise one or more couplers advantageously chosen from those conventionally used for dyeing keratinous fibers. Among these couplers, there may be mentioned meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalenic couplers, heterocyclic couplers and their addition salts. By way of example, mention may be made of 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 4-chloro-1,3-dihydroxybenzene and 2,4-diamino-1- (B- hydroxyethyloxy) benzene, 2-amino 4- (B-hydroxyethylamino) 1-methoxybenzene, 1,3-diamino benzene, 1,3-bis (2,4-diaminophenoxy) propane, 3-ureido aniline, 3-ureido 1-dimethylamino benzene, sesamol, 1-β-hydroxyethylamino-3,4-methylenedioxybenzene, α-naphthol, 2-methyl-1-naphthol, 6-hydroxyindole, 4-hydroxyindole, 4-hydroxy N-methylindole, 2-amino-3-hydroxypyridine, 6-hydroxybenzomorpholine 3,5-diamino-2,6-dimethoxypyridine, 1-N- (B-hydroxyethyl) amino-3 , 4-methylene dioxybenzene, 2,6-bis- (β-hydroxyethylamino) toluene, 6-hydroxy indoline, 2,6-dihydroxy 4-methyl pyridine, 1-H 3 -methyl pyrazole 5-one, 1-phenyl-3-methyl-pyrazole-5-one, 2,6-dimethyl-pyrazolo [1,5-b] -1,2,4-triazole, 2,6-dimethyl [3,2-c] -1, 2,4-triazole, 6-methyl pyrazolo [1,5 -a] -benzimidazole, their addition salts with an acid, and mixtures thereof.

In general, the addition salts of the oxidation bases and couplers that can be used in the context of the invention are chosen especially from the addition salts with an acid such as hydrochlorides, hydrobromides, sulphates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, phosphates and acetates.

The oxidation base or bases, when they are present in the composition, advantageously represent from 0.0001 to 10% by weight relative to the weight of the composition, and preferably from 0.005 to 5% by weight relative to the weight of the composition. the composition. The coupler or couplers, if present, advantageously represent from 0.0001 to 10% by weight relative to the weight of the composition, and preferably from 0.005 to 5% by weight relative to the weight of the composition.

The dyeing composition according to the invention may also comprise one or more conditioning agents. By way of example, mention may be made of linear, cyclic, branched or unbranched, volatile or non-volatile silicones. These silicones can be in the form of oils, resins or gums, they can in particular be polyorganosiloxanes insoluble in the cosmetically acceptable medium. Organopolysiloxanes are further defined in Walter Noll's "Chemistry and Technology of Silicones" (1968) Academic Press. They can be volatile or non-volatile. When they are volatile, the silicones are more particularly chosen from those having a boiling point of between 60 ° C. and 260 ° C. As a conditioning agent, it is also possible to use cationic polymers such as polyquaterniums. 22, 6, 10, 11, 35 and 37 and hexadimethrin chloride.

The concentration of conditioning agent (s) in the composition (s) useful in the invention may vary from 0.01% to 10% by weight relative to the total weight of the composition, preferably from 0.05% to 5% and more. preferentially still from 0.1 to 3%.

The compositions according to the invention may also contain one or more organic thickeners.

The organic thickening agents may be chosen from fatty acid amides (diethanol or coconut monoethanol amide, oxyethylenated alkyl ether carboxylic acid monoethanolamide), polymeric thickeners such as cellulosic thickeners (hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose), guar gum and its derivatives (hydroxypropylguar), gums of microbial origin (xanthan gum, scleroglucan gum), crosslinked homopolymers of acrylic acid or acrylamidopropanesulfonic acid and associative polymers (amphiphilic polymers comprising hydrophilic zones and hydrophobic fatty-chain zones capable, in an aqueous medium, of reversibly associating with each other or with other molecules.) According to one particular embodiment, the thickener is polymeric and chosen from cellulose thickeners (hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose), guar gum and its derivatives (hydroxypropylguar), gums of microbial origin (xanthan gum, gum scleroglucan), crosslinked homopolymers of acrylic acid or acrylamidopropanesulfonic acid.

With regard to the associative thickeners, it is possible to use one or more polymers of nonionic or ionic nature, preferably anionic or cationic.

Their chemical structure more particularly comprises at least one hydrophilic zone and at least one hydrophobic zone. Hydrophobic group is understood to mean a linear or branched, saturated or unsaturated hydrocarbon-based radical or polymer comprising at least 8 carbon atoms, preferably from 10 to 30 carbon atoms, in particular from 12 to 30 carbon atoms, and more preferably from 18 to 30 carbon atoms.

Preferably, the hydrocarbon group comes from a monofunctional compound. By way of example, the hydrophobic group may be derived from a fatty alcohol such as stearyl alcohol, dodecyl alcohol or decyl alcohol. It can also denote a hydrocarbon polymer such as for example polybutadiene.

Among the anionic amphiphilic polymers comprising at least one fatty chain (hydrophobic), mention may be made of:

(I) polymers comprising at least one hydrophilic unit, and at least one fatty-chain allyl ether unit, more particularly those whose hydrophilic unit consists of an ethylenic unsaturated anionic monomer, advantageously a vinyl carboxylic acid and any particularly with an acrylic acid or a methacrylic acid or mixtures thereof, and whose fatty-chain allyl ether unit corresponds to the following monomer of formula (A): CH 2 = CR 'CH 2 O Bn R (A) in which R 'denotes H or CH3, B denotes the ethyleneoxy radical, n is zero or denotes an integer ranging from 1 to 100, R denotes a hydrocarbon radical chosen from alkyl, arylalkyl, aryl, alkylaryl and cycloalkyl radicals, comprising from 8 to 30; carbon atoms, preferably 10 to 24, and more particularly 12 to 18 carbon atoms. A unit of formula (A) more particularly preferred is a unit in which R 'denotes H, n is equal to 10, and R denotes a stearyl (C18) radical.

Of these anionic fatty-chain polymers, polymers formed from 20 to 60% by weight of acrylic acid and / or methacrylic acid, from 5 to 60% by weight of lower alkyl (meth) acrylates are preferred. from 2 to 50% by weight of fatty-chain allyl ether of formula (A), and from 0 to 1% by weight of a crosslinking agent which is a well-known copolymerizable polyethylenic unsaturated monomer, such as sodium phthalate; diallyl, allyl (meth) acrylate, divinylbenzene, (poly) ethylene glycol dimethacrylate, and methylenebisacrylamide.

Among these, the crosslinked terpolymers of methacrylic acid, ethyl acrylate, polyethylene glycol (10 OE) and stearyl alcohol ether (Steareth 10) are particularly preferred, in particular those sold by the company ALLIED COLLOIDS under the names SALCARE SC 80 and SALCARE SC90 which are 30% aqueous emulsions of a crosslinked terpolymer of methacrylic acid, ethyl acrylate and steareth-10-allyl ether (40/50/10). (II) polymers comprising at least one hydrophilic unit of unsaturated olefinic carboxylic acid type, and at least one hydrophobic unit of the (C 10 -C 30) alkyl ester of unsaturated carboxylic acid type.

Preferably, these polymers are chosen from those whose hydrophilic unit of olefinic unsaturated carboxylic acid type corresponds to the following monomer of formula (B): ## STR2 ## wherein R 1 denotes H or CH 3 or C 2 H 5; that is to say, acrylic acid, methacrylic acid or ethacrylic acid units, and whose hydrophobic unit of unsaturated carboxylic acid (C 10 -C 30) alkyl ester type corresponds to the following monomer of formula (C): ## STR2 ## I II R2 O (C)

in which, R2 denotes H or CH3 or C2H5 (that is to say acrylate, methacrylate or ethacrylate units) and preferably H (acrylate units) or CH3 (methacrylate units), R3 denotes a C10-C30 alkyl radical; and preferably C12-C22.

The (C 10 -C 30) alkyl esters of unsaturated carboxylic acids are, for example, lauryl acrylate, stearyl acrylate, decyl acrylate, isodecyl acrylate and dodecyl acrylate. and corresponding methacrylates, lauryl methacrylate, stearyl methacrylate, decyl methacrylate, isodecyl methacrylate, and dodecyl methacrylate.

Among this type of fatty-chain anionic polymers, there will be used more particularly polymers formed from a monomer mixture comprising: (i) essentially acrylic acid, (ii) an ester of formula (C) described above. and wherein R2 is H or CH3, wherein R3 is an alkyl radical having 12 to 22 carbon atoms, and iii) a crosslinking agent which is a well-known copolymerizable polyethylenically unsaturated monomer, such as diallyl phthalate, allyl meth) acrylate, divinylbenzene, (poly) ethylene glycol dimethacrylate, and methylene-bis-acrylamide. Among this type of fatty-chain anionic polymers, use will more particularly be made of 95 to 60% by weight of acrylic acid (hydrophilic unit), 4 to 40% by weight of C 10 -C 30 alkyl acrylate (unit hydrophobic), and 0 to 6% by weight of polymerizable crosslinking monomer, or those consisting of 98 to 96% by weight of acrylic acid (hydrophilic unit), 1 to 4% by weight of C 10 alkyl acrylate. C30 (hydrophobic unit), and 0.1 to 0.6% by weight of crosslinking polymerizable monomer such as those described above. Among said polymers above, the products sold by the company Goodrich under the trade names Pemulen Tri, Pemulen TR2, Carbopol 1382, and even more preferentially Pemulen Tri, and the product sold by the company, are particularly preferred according to the present invention. SEPPIC company under the name COATEX SX.

(III) terpolymers of maleic anhydride / α-olefin C30-C38 / alkyl maleate such as the product (maleic anhydride copolymer / C30-C38 α-olefin / isopropyl maleate) sold under the name PERFORMA V 1608 by the company NEWPHASE TECHNOLOGIES. (IV) acrylic terpolymers comprising: (a) 20% to 70% by weight of a carboxylic acid having α, 13-monoethylenic unsaturation, (b) 20 to 80% by weight of α-unsaturated monomer, 13 -monoethylenic non-surfactant other than (a), (c) 0.5 to 60% by weight of a nonionic mono-urethane which is the reaction product of a monohydric surfactant with a monoisocyanate at monoethylenic unsaturation, such as those described in the patent application EP-A-0173109 and more particularly a methacrylic acid / methyl acrylate / dimethyl metaisopropenyl benzyl isocyanate terpolymer of ethoxylated behenyl alcohol (400E) in aqueous dispersion at 25%.

(V) copolymers comprising among their monomers an α, β-monoethylenically unsaturated carboxylic acid and an α, β-monoethylenically unsaturated carboxylic acid ester and an oxyalkylenated (C 8 -C 30) fatty alcohol.

Preferentially, these compounds also comprise, as monomer, a carboxylic acid ester with a, 13-monoethylenic unsaturation and a C1-C4 alcohol. By way of example of this type of compound, mention may be made of Aculyn 22 sold by Rohm and Haas, which is a methacrylic acid / ethyl acrylate / stearyl methacrylate oxyalkylenated terpolymer.

The fatty-chain (hydrophobic) nonionic amphiphilic polymers are preferably chosen from: (1) celluloses modified with groups comprising at least one fatty chain, such as in particular; hydroxyethylcelluloses modified with groups comprising at least one fatty chain such as alkyl, arylalkyl or alkylaryl groups, or mixtures thereof, and in which the alkyl groups are preferably C8-C22, such as the product NATROSOL PLUS GRADE 330 CS ( C16 alkyls) sold by the company AQUALON, or the BERMOCOLL EHM 100 product sold by the company BEROL NOBEL, - those modified with polyalkylene glycol ether alkyl phenol groups, such as the product AMERCELL POLYMER HM-1500 (polyethylene glycol ( 15) nonylphenol ether) sold by the company Amerchol. (2) hydroxypropyl guars modified with groups comprising at least one fatty chain such as the product ESAFLOR HM 22 (C22 alkyl chain) sold by LAMBERTI, the products RE210-18 (C14 alkyl chain) and RE205-1 (C20 alkyl chain) sold by the company Rhone Poulenc. (3) copolymers of vinyl pyrrolidone and hydrophobic fatty-chain monomers, with for example: ANTARON V216 or GANEX V216 products (vinylpyrrolidone / hexadecene copolymer) sold by I.S.P. products ANTARON V220 or GANEX V220 (vinylpyrrolidone / eicosene copolymer) sold by the company I.S.P.

(4) copolymers of methacrylates or of C1-C6 alkyl acrylates and of amphiphilic monomers comprising at least one fatty chain, such as, for example, the oxyethylenated methyl acrylate / stearyl acrylate copolymer sold by GOLDSCHMIDT under the name denomination ANTIL 208.

(5) copolymers of hydrophilic methacrylates or acrylates and of hydrophobic monomers comprising at least one fatty chain, such as, for example, polyethylene glycol methacrylate / lauryl methacrylate copolymer. (6) polymers having an aminoplast ether skeleton having at least one fatty chain, such as the PURE THIX compounds proposed by the company SUD-CHEMIE. (7) polyether polyurethanes comprising in their chain, both hydrophilic sequences of mostly polyoxyethylenated nature and hydrophobic sequences which may be aliphatic sequences alone and / or cycloaliphatic and / or aromatic sequences. Preferably, the polyether polyurethanes comprise at least two hydrocarbonaceous fatty chains, having from 8 to 30 carbon atoms, separated by a hydrophilic sequence, the hydrocarbon chains possibly being pendant chains or end chains of hydrophilic sequence. As examples of nonionic fatty-chain polyurethane polyethers that may be used in the invention, use may be made of the urea-functional Rheolate 205 sold by Rheox or else the Rheolates 208, 204 or 212, as well as Acrysol RM 184. Aculyn or Acrysol 44 and Aculyn or Acrysol 46 from the company Rohm & Haas [Aculyn 46 is a polycondensate of polyethylene glycol with 150 or 180 moles of ethylene oxide, stearyl alcohol and methylene bis (4-cyclohexyl isocyanate) (SMDI), 15% by weight in a matrix of maltodextrin (4%) and water (81%); ACULYN 44 is a polycondensate of polyethylene glycol with 150 or 180 moles of ethylene oxide, decyl alcohol and methylenebis (4-cyclohexylisocyanate) (SMDI), at 35% by weight in a propylene glycol mixture (39). %) and water (26%)]. Mention may also be made of the product ELFACOS T210 with a C12-C14 alkyl chain and the product ELFACOS T212 with a C4 alkyl chain from AKZO, as well as the product DW 1206B from ROHM & HAAS with a C20 alkyl chain and with urethane bond, proposed at 20% by dry matter in water. It is also possible to use solutions or dispersions of these polymers, especially in water or in an aqueous-alcoholic medium. By way of example, such polymers include, for example, Rheolate 255, Rheolate 278 and Rheolate 244 sold by Rheox. It is also possible to use the product DW 1206F and the DW 1206J proposed by the company Rohm & Haas. The polyether polyurethanes that can be used according to the invention are in particular those described in the article by G. Fonnum, J. Bakke and Fk. Hansen - Colloid Polym. Sci 271, 380, 389 (1993).

The cationic amphiphilic polymers comprising at least one fatty (hydrophobic) chain used may in particular be chosen from quaternized cellulose derivatives, cationic polyurethanes, cationic polyvinyllactams, and preferably from quaternized cellulose derivatives. Examples of polymers of this type include: quaternized celluloses modified with groups comprising at least one fatty chain, such as alkyl, arylalkyl or alkylaryl groups containing at least 8 carbon atoms, or mixtures thereof; quaternized hydroxyethylcelluloses modified with groups having at least one fatty chain, such as alkyl, arylalkyl, alkylaryl groups having at least 8 carbon atoms, or mixtures thereof. The alkyl radicals borne by the above-quaternized celluloses or hydroxyethylcelluloses preferably contain from 8 to 30 carbon atoms. The aryl radicals preferably denote phenyl, benzyl, naphthyl or anthryl groups. Examples of C8-C30 fatty chain quaternized alkylhydroxyethylcelluloses are QUATRISOFT LM 200, QUATRISOFT LM-X 529-18-A, QUATRISOFT LM-X 529-18B (C12 alkyl) and QUATRISOFT LM-X. 529-8 (alkyl of 018) marketed by Amerchol and the products CRODACEL QM, CRODACEL QL (C12 alkyl) and CRODACEL QS (C18 alkyl) marketed by CRODA.

The content of thickening polymers, if present, usually ranges from 0.05% to 5% by weight, based on the weight of the coloring composition.

According to a particularly advantageous embodiment, the dye composition comprises one or more surfactants. These can be indifferently chosen, alone or in mixtures, from anionic, amphoteric, nonionic, zwitterionic and cationic surfactants.

As regards the anionic surfactants, the salts, in particular the alkali metal salts such as the sodium salts, the ammonium salts, the amine salts, the aminoalcohol salts or the metal salts, are usually used. alkaline earth metals, for example magnesium, of the following compounds, alone or as a mixture: alkyl sulphates, alkyl ether sulphates, alkylamido ether sulphates, alkyl aryl polyether sulphates; alkylsulfonates, alkylamidesulfonates, alkylarylsulfonates; alkylsulfosuccinates, alkylethersulfosuccinates, alkylamide-sulfosuccinates; alkylsulfoacetates; acylsarconisates; and acylglutamates: alkyl and polyglycoside carboxylic acid esters such as alkyl glucoside citrates, alkyl polyglycoside tartrates, and alkyl polyglycoside sulfosuccinates; alkylsulfosuccinamates; acylisethionates, N-acyltaurates; acyllactylates; alkyl-D-galactoside uronic acids; polyoxyalkylenated alkyl ether carboxylic acids, polyoxyalkylenated alkylarylether carboxylic acids, polyoxyalkylenated alkylamidoether carboxylic acids; the alkyl or acyl group (RCO-) of these compounds having from 10 to 24 carbon atoms and the aryl group preferably denoting a phenyl or benzyl group; the number of oxyalkylenated groups, and preferably oxyethylenated, is between 2 and 50.

As regards the nonionic surfactants, the latter may advantageously be chosen from the following compounds, alone or as a mixture: polyethoxylated, polypropoxylated or polyglycerolated fatty alcohols, polyethoxylated, polypropoxylated or polyglycerolated alpha-diols, the number of ethylene or propylene oxide ranging from 2 to 50; the number of glycerol groups ranging from 2 to 30; condensates of ethylene oxide and propylene oxide on fatty alcohols; polyethoxylated fatty amides having from 2 to 30 moles of ethylene oxide; polyglycerolated fatty amides containing from 1 to 5 glycerol groups; polyethoxylated fatty amines having from 2 to 30 moles of ethylene oxide; ethoxylated fatty acid esters of sorbitan having from 2 to 30 moles of ethylene oxide, fatty acid esters of sucrose; alkylpolyglucosides, N-alkylglucamine derivatives; these compounds comprising at least one alkyl or alkenyl chain comprising 10 to 24 carbon atoms. copolymers of ethylene oxide and of propylene oxide.

The cationic surfactants used in the composition according to the invention may in particular be chosen from the following compounds, alone or as a mixture: primary, secondary or tertiary fatty amines optionally polyethoxylated (2 to 30 moles of ethylene oxide) and their salts the quaternary ammonium salts comprising or not one or more ester functions such as chlorides or bromides of tetraalkylammonium, alkylamidoalkyltrialkylammonium, trialkylbenzylammonium, trialkylhydroxyalkylammonium, alkylpyridinium, and quaternary diesters. alkyl imidazoline derivatives; these compounds comprising at least one alkyl chain comprising 10 to 24 carbon atoms.

Finally, the amphoteric surfactants may be chosen from the following compounds, alone or as a mixture: derivatives of secondary or tertiary aliphatic amines, in which the aliphatic group is a linear or branched chain containing 10 to 24 carbon atoms and comprising at least at least one anionic water-solubilising group such as, for example, a carboxylate, sulphonate, sulphate, phosphate or phosphonate group, alkylbetaines, sulphobetaines, (C.sub.6-C.sub.8) alkylamidoalkyl betaines, (C.sub.6-C.sub.8) alkylamidoalkylsulfobetaines; these compounds comprising at least one alkyl chain comprising from 10 to 24 carbon atoms.

Preferably, the surfactants are nonionic, anionic or amphoteric and even more preferably nonionic. Usually, the surfactants represent an amount of between 0.01 and 50% by weight, preferably between 0.1 and 25% by weight relative to the weight of the composition. The dye composition according to the invention may also contain various adjuvants conventionally used in hair dyeing compositions, such as, for example, anionic, nonionic, amphoteric or zwitterionic polymers other than the previously mentioned thickeners, or mixtures thereof; mineral thickeners such as clays; antioxidants such as, for example, ascorbic acid, erythorbic acid; reducing agents with inter alia sulphite, bisulphite or ammonium metabisulphite, ammonium thiolactate; penetrating agents, sequestering agents such as ethylenediamine tetraacetic or its salts; perfumes ; matting agents with, for example, titanium oxides; buffers; dispersants; film-forming agents; ceramides; carboxylic acids, especially aromatic acids such as benzoic acid; and preservatives. The adjuvants above are generally present in an amount for each of them between 0.01 and 20% by weight relative to the weight of the composition. The cosmetically acceptable medium of the composition, which is a suitable medium for dyeing human keratin fibers, preferably comprises water and optionally one or more additional solvents. As examples of such additional solvents, mention may be made, for example, linear or branched alkanols, 02-04, such as ethanol and isopropanol; polyols and polyol ethers such as 2-butoxyethanol, hexylene glycol, propylene glycol, dipropylene glycol, propylene glycol monomethyl ether, diethylene glycol monoethyl ether and monomethyl ether, glycerol and aromatic alcohols such as benzyl alcohol, benzyloxyethanol or phenoxyethanol, and mixtures thereof. The additional solvent or solvents may be present in proportions ranging preferably from 0.1 to 40% by weight relative to the total weight of the dyeing composition, and still more preferably from 5 to 30% by weight. It should be noted that the amount of water in the composition according to the invention is preferably greater than 10% by weight relative to the weight of the composition, and more preferably greater than or equal to 25% by weight. Preferably, the water content is between 25 and 98% by weight relative to the weight of the composition.

The pH of the composition according to the invention may be between 2 and 13. It is preferably between 2 and 11 and even more particularly it is less than 7 and better still between 2 and 6.

It can be adjusted to the desired value by means of one or more acidifying agents or one or more alkalinizing agents usually used in the field. Among the acidifying agents, mention may be made, for example, of mineral or organic acids such as hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids such as acetic acid, tartaric acid citric acid, lactic acid, sulphonic acids.

Among the alkalinizing agents that may be mentioned, for example, alkaline carbonates, alkanolamines such as mono-, di- and triethanolamines and their derivatives, hydroxides of sodium or potassium and compounds of the following formula: Rx Wherein W is a propylene residue optionally substituted with a hydroxyl group or a C1-C6 alkyl radical; Rx, Ry, Rz and Rt, identical or different, represent a hydrogen atom, a C1-C6 alkyl radical or C1-C6 hydroxyalkyl. The composition according to the invention may also comprise one or more oxidizing agents. In this case, we speak of ready-to-use compositions. In particular, the ready-to-use composition is obtained by extemporaneous mixing before application of a previously described composition with at least one composition comprising one or more oxidizing agents. The oxidizing agent is preferably chosen from hydrogen peroxide and peroxide.

Urea, alkali metal bromates or ferricyanides, peroxygenated salts such as for example persulfates, perborates and percarbonates of alkali or alkaline earth metals, such as sodium, potassium, magnesium. The use of hydrogen peroxide is particularly preferred. This oxidizing agent is advantageously constituted by hydrogen peroxide in aqueous solution (hydrogen peroxide) whose content may vary, more particularly, from 1 to 40 volumes, and even more preferably from 5 to 40 volumes. The compositions according to the invention may result from the extemporaneous mixing of several compositions.

Another object of the invention is therefore constituted by a process for dyeing keratinous fibers, which consists in applying the composition described above.

According to a first embodiment, the composition applied does not comprise an oxidizing agent. This embodiment is appropriate especially in the case where the composition does not comprise oxidation dye precursor (bases, coupler) According to a second embodiment, the composition is applied in the presence of at least one oxidizing agent. This embodiment can be implemented if the composition comprises, as dyestuffs, only natural dyes and optionally one or more additional direct dyes for synthesis, or even if the composition comprises one or more natural dyes, optionally one or additional direct synthetic dyes combined with one or more oxidation dye precursors (base / coupler).

According to a first variant of this embodiment, the ready-to-use composition which has just been detailed and which is obtained by extemporaneous mixing before application of a composition according to the invention without oxidizing agent with an oxidizing composition. According to a second variant of this embodiment, the composition according to the invention is applied without oxidizing agent, and an oxidizing composition, successively and without intermediate rinsing.

The oxidizing composition used comprises one or more oxidizing agents as defined above. Regarding the organic solvents possibly present in the oxidizing composition, reference may be made to the list indicated previously in the context of the description of the composition according to the invention. Note that the organic solvent may also be 3-phenyl-1-propanol. Usually, the pH of the oxidizing composition is less than 7. The oxidizing composition may be in the form of a solution, an emulsion or a gel.

It may optionally comprise one or more additives conventionally used in the field of human keratin fiber staining, depending on the desired dosage form. We can again refer to the list of additives given above.

Whatever the embodiment chosen (with or without an oxidant), the mixture applied to the fibers is left in place for a duration, in general, of the order of 1 minute to 1 hour, preferably of 10 minutes to 30 minutes. minutes.

The temperature during the process is conventionally between 10 and 200 ° C. and more particularly between room temperature (between 15 and 25 ° C.) and 80 ° C., preferably between room temperature and 60 ° C. At the end of the treatment, the human keratinous fibers are optionally rinsed with water, washed with shampoo, rinsed again with water and then dried or left to dry. Preferably human keratin fibers are hair.

Concrete but non-limiting examples of the invention will now be presented. EXAMPLES The following compositions A, B and C are prepared (the proportions are given in 0/0 by weight): ABC Comparative Comparative Comparative 3-phenyl-1-propanol 0 , 5% MA - - 2-phenyl-1-ethanol - 0.5% MA - Benzyl alcohol - - 0.5% MA Ethanol 15% pH agent qsp pH = 2.7 Perfume qs Water qs 100 Mix each of compositions A, B and C with orcein [NATURAL RED 28 / Cl 758600] such that each resulting mixture comprises 0.5% by weight of dye.

Each mixture is then applied to strands of hair with 90% natural white hair. The application time is 20 minutes at room temperature. At the end of this break time, the locks are dewatered, rinsed, shampooed and dried.

It is found that the composition according to the invention makes it possible to obtain a more intense coloration than in the case of comparative compositions. 10 15 20

Claims (10)

REVENDICATIONS1. Dye composition comprising in a cosmetically acceptable medium, one or more natural dyes and 3-phenyl-1-propanol. 2. Composition according to the preceding claim, characterized in that the natural dye or dyes are selected from lawsone, juglone, alizarin, purpurine, carminic acid, kermesic acid, purpurogallin, anthragallol the protocatechaldehyde, indigo, isatin, curcumin, spinusoline, chlorophylls, chloropyllines, orceins, haematein, hematoxylin, brazilin, braziline, safflower dyes, flavonoids, anthocyanins, carotenoids, tannins, sorghum and cochineal carmine, as well as extracts or decoctions containing these natural dyes and in particular henna extracts, or mixtures thereof. 3. Composition according to any one of the preceding claims, characterized in that the content of natural dye (s) varies from 0.001 to 10% by weight, preferably from 0.01 to 8% by weight, relative to the weight of the composition. 4. Composition according to any one of the preceding claims, characterized in that the content of 3-phenyl-1-propanol represents from 0.05 to 50%, preferably from 0.1 to 30% by weight, relative to weight of the composition. 5. Composition according to any one of the preceding claims, characterized in that it comprises at least one additional dye, selected from additional direct synthetic dyes, oxidation dye precursors, or combinations thereof. 6. Composition according to any one of the preceding claims, characterized in that it comprises water and optionally one or more additional organic solvents other than 3-phenyl-1-propanol. 7. Composition according to any one of the preceding claims, characterized in that it comprises one or more organic thickeners, preferably polymeric, and / or one or more surfactants. 8. Composition according to any one of the preceding claims, characterized in that it comprises one or more oxidizing agents. 9. Coloring process consisting in applying to the human keratin fibers a composition according to any one of the preceding claims. 10. Multi-compartment device comprising at least one composition according to any one of claims 1 to 7 and an oxidizing composition comprising one or more oxidizing agents.