FR3102359A1 - PROCESS FOR PREPARING A COLORING COMPOSITION CONSISTING OF THE MIXTURE OF SOLID PARTICLES WITH AN AQUEOUS COMPOSITION CONTAINING ARGININE, AND ITS USE - Google Patents

Abstract

The subject of the present application is a process for preparing a composition for dyeing keratin fibers, in particular human keratin fibers such as the hair, comprising the mixture of several identical or different solid particles comprising one or more dyes, preferably one or more oxidation dye precursors, with at least one aqueous composition comprising arginine, as well as a dyeing process and the use of the composition obtained for dyeing keratin fibers.

Description

METHOD FOR PREPARING A COLORING COMPOSITION COMPRISING THE MIXING OF SOLID PARTICLES WITH AN AQUEOUS COMPOSITION CONTAINING ARGININE, AND USE THEREOF

The subject of the present application is a process for preparing a composition for dyeing keratin fibres, in particular human keratin fibers such as the hair, comprising the mixture of several identical or different solid particles comprising one or more dyes, preferably one or more oxidation dye precursors, with at least one aqueous composition comprising arginine, as well as a dyeing process and the use of the composition obtained for dyeing keratin fibres.

It is known to dye keratin fibres, and in particular human hair, with dye compositions containing precursors of oxidation dyes, such as oxidation bases, in particular ortho- or para-phenylenediamines, ortho- or para- -aminophenols and heterocyclic compounds. These oxidation bases are colorless or weakly colored compounds which, associated with oxidizing products, can give rise to colored compounds by a process of oxidative condensation.

It is also known that the shades obtained with these oxidation bases can be varied by combining them with couplers or color modifiers, the latter being chosen in particular from aromatic meta-diaminobenzenes, meta-aminophenols, meta- diphenols and certain heterocyclic compounds such as indole compounds.

The variety of molecules involved in oxidation bases and couplers allows a rich palette of colors to be obtained.

Currently, the permanent coloring of keratin fibers is difficult to customize. Indeed, the user wishing to color his hair only has the choice from a catalog of predefined coloring compositions, each generally comprising a fixed mixture of base(s) and oxidation coupler(s) in predefined contents.

Thus, each of these coloring compositions only makes it possible to obtain a single shade of coloring and the user only has the choice among a limited number of shades preselected by the manufacturers, which do not always correspond to his wishes.

Moreover, the predefined coloring compositions do not always lead exactly to obtaining the corresponding preselected shade: depending on the natural shade (more or less light or dark) and the condition of the hair (more or less damaged, sensitized ) of the user, the final result in terms of coloring may vary significantly from one user to another.

Current coloring processes, in particular oxidation coloring processes, therefore do not make it possible to quickly obtain (for example during a user's appointment at the hairdressing salon) personalized colorings according to the pre-existing shade of the keratin fibers of the user, or according to his wishes.

There is therefore a real need to develop a process making it possible to prepare, just before coloring, a composition for coloring keratinous fibers making it possible to offer the user a very wide choice of possible shades, and allowing him to be able to choose , for example in a hairdressing salon, the shade he wants and not, failing that, the closest shade available.

The method should also make it possible to prepare, just before coloring, a composition for coloring keratin fibers making it possible to offer the user a tailor-made coloring, taking into account in particular its specificities such as the pre-existing shade and the nature of the fibers. keratins.

Furthermore, the process must also make it possible to obtain a composition capable of dyeing the keratin fibers in an intense, tenacious, not very selective, chromatic manner, with a good rise in color, and capable of leading to colorations resistant to the various attacks that can be subjected to fibers such as bad weather, washing and perspiration.

Efforts are also being made to develop processes to reduce unpleasant odors during use, in particular in the case of oxidation coloring, and to minimize damage to keratin fibres, while maintaining good dyeing properties.

These aims are achieved with the present invention, the subject of which is in particular a process for preparing a composition for dyeing keratin fibres, in particular human keratin fibers such as the hair, comprising the mixture:
a) several solid particles, identical or different, each containing one or more dyes chosen from direct dyes and/or oxidation dye precursors, preferably one or more oxidation dye precursors; with
b) at least one aqueous composition A comprising arginine.

It has been found that the preparation process according to the invention makes it possible to obtain a composition for coloring keratin fibers which is personalized and ready-to-use.

Indeed, the process according to the invention makes it possible to prepare, for each use, a specific coloring composition containing precise contents of dyes, in particular of oxidation dye precursors specifically chosen in order to obtain exactly the shade desired by the user.

It has in particular been found that the process according to the invention makes it possible to prepare compositions capable of combining a very large number of dyes, in particular of different oxidation precursors, at different respective contents, and thus of coloring the keratin fibers according to a very wide range of possible colors while taking into account the nature and condition of said fibers.

The composition obtained by the process according to the invention also makes it possible to dye the keratin fibers in a satisfactory manner, in particular by leading to powerful, tenacious, chromatic colorations, not very selective, and/or with a good rise in color.

Furthermore, the composition obtained by the process according to the invention leads to colorations which are resistant to the various attacks which the keratin fibers may undergo, such as bad weather, light, washing and/or perspiration.

The method according to the invention also makes it possible to reduce unpleasant odors during use, in particular in the case of oxidation coloring, and to minimize the alterations of keratin fibres, while maintaining good dyeing properties

On the other hand, the method according to the invention makes it possible to lead to a reproducible dyeing result from one time to another, in particular in the case where the solid particles contain a single dose of dye, in particular of dye precursor. oxidation with very good storage stability. In addition, the solid particles used in the process of the invention disintegrate quickly and lead easily and quickly to a homogeneous mixture with the aqueous composition(s) used in the process.

A subject of the invention is also a process for dyeing keratin fibres, in particular human keratin fibers such as the hair, comprising:
- the preparation of a composition for dyeing keratin fibers according to the preparation process of the invention; Then
- the application of said prepared composition to said keratin fibres.

A subject of the invention is also the use of the composition obtained by the preparation process according to the invention, for the coloring of keratin fibres, in particular human keratin fibers such as the hair.

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

In this description, and unless otherwise specified:

- the expression "at least one" is equivalent to the expression "one or more" and can be substituted therefor;

- the expression "included between" is equivalent to the expression "ranging from" and can be substituted therefor, and implies that the terminals are included;

- By "keratin fibers" according to the present application, is preferably meant human keratin fibers and more particularly the hair.

Solid particles

The preparation process according to the invention comprises mixing several solid particles, which are identical or different, each containing one or more dyes chosen from direct dyes and/or oxidation dye precursors, preferably from oxidation dye precursors. oxidation; with at least one aqueous composition A comprising arginine.
Said dyes can be identical or different from one solid particle to another.

Preferably, the colorant(s) represent(s) advantageously 0.001% to 50% by weight, more preferentially 0.1 to 50% by weight, more preferentially still 0.3% to 25% by weight, even better 0.4 to 22% by weight, relative to the total weight of the solid particle containing it(these).

Preferably, said solid particles comprise:
- one or more solid particles of a first type P1 containing a single dye C1; And
- one or more solid particles of a second type P2 containing a single dye C2;
it being understood that the dye C1 is different from the dye C2.

The process for preparing a composition for dyeing keratin fibers according to the invention therefore preferably comprises mixing:
- one or more solid particles of a first type P1 containing a single dye C1, more preferably a single oxidation dye precursor C1; And
- one or more solid particles of a second type P2 containing a single C2 dye, more preferably a single C2 oxidation dye precursor; with
- at least one aqueous composition A comprising arginine;
it being understood that the dye C1 is different from the dye C2.
Thus, according to this preferred embodiment, at least two types of solid particles used in the process according to the invention do not comprise the same dye, and more preferably the same oxidation dye precursor.

More preferably, each type of solid particle according to the invention comprises a single dye in a content of between 0.1 and 50% by weight relative to the total weight of the solid particle containing it.

According to a preferred embodiment, the method further comprises mixing with one or more solid particles of a third type P3, containing a C3 dye, in particular a single C3 oxidation dye precursor, more preferably in a content comprised between 0.1 and 50% by weight relative to the total weight of the solid particle(s) P3. It is thus possible to mix as much dye as necessary, and this in the respective proportions necessary, to achieve the desired shade.

Thus, according to another preferred embodiment, the method according to the invention comprises mixing n types of solid particles P1 to Pn (with n representing an integer greater than or equal to 3, and preferably between 3 and 20, more preferably between 3 and 15, and even more preferably between 4 and 10), each type of solid particle P1 to Pn containing at least one dye (respectively C1 to Cn), in particular a single dye, better still a single dye precursor d oxidation, more preferably in a content of between 0.1 and 50% by weight relative to the total weight of the solid particles P1 to Pn respectively, and it being understood that said dyes C1 to Cn are all different from each other.

According to a particular embodiment of the invention, the composition for dyeing keratin fibers additionally comprises the mixture of one or more solid particles of P'x type (with x representing an integer greater than 1, and preferably between 1 and 20, more preferably between 1 and 15, and even more preferably between 1 and 10) containing at least one Cx dye, in particular a single Cx dye, better still a single Cx oxidation dye precursor, more preferably in a content of between 0.1 and 50% by weight relative to the total weight of the solid particle(s) of P'x type; said solid particle of type P'x corresponding to the solid particle Px previously described, unlike the dye content Cx.

By way of example of this particular embodiment of the invention, the composition for dyeing keratin fibers may comprise the mixture:
(i) one or more solid particles of a first type P1 containing a single C1 dye, better still a single C1 oxidation dye precursor, preferably in a content of between 0.1 and 50% by weight relative to to the total weight of the solid particle(s) of type P1;
(ii) one or more solid particles of a second type P2 containing a single C2 dye, better still a single C2 oxidation dye precursor, preferably in a content of between 0.1 and 50% by weight relative to to the total weight of the solid particle(s) of type P2; And
(iii) one or more solid particles of type P'1 containing only said C1 dye, better still said C1 oxidation dye precursor, preferably in a content of between 0.1 and 50% by weight relative to the weight total of the solid particle(s) of type P'1; with
(iv) at least one aqueous composition A comprising arginine;
Being heard that :
- Dye C1, better oxidation dye precursor C1, is different from dye C2, better oxidation dye precursor C2;
- the content of dye C1, better of precursor of oxidation dye C1, contained in the solid particle(s) P1 is different from the content of dye C1, better of precursor of oxidation dye C1 contained in the solid particle(s) P'1.

Oxidation dye precursors
Advantageously, the dye or dyes are chosen from oxidation dye precursors.

Preferably, the oxidation dye precursors are selected from oxidation bases and oxidation couplers; more preferentially among the oxidation bases.

According to a preferred embodiment of the invention, the dye C1 as defined above is selected from oxidation bases and the dye C2 as defined above is selected from oxidation couplers (or vice versa).

Preferably, the total content of precursor(s) of oxidation coloration (for example C1, C2, and more generally C1 to Cn) advantageously represents 0.1 to 50% by weight, more preferably 0.3% to 25% by weight, more preferably still 0.4% to 22% by weight, relative to the total weight of each solid particle containing it(s) (for example solid particles of type P1, P2, and more generally P1 to Pn respectively) .

By way of example, the oxidation bases are chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases and the corresponding addition salts.

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

Among the para-phenylenediamines mentioned above, para-phenylenediamine, para-toluenediamine, 2-isopropyl-para-phenylenediamine, 2-β-hydroxyethyl-para-phenylenediamine, 2-β-hydroxyethyloxy-para- phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, N,N-bis(β-hydroxyethyl)-para-phenylenediamine , 2-chloro-para-phenylenediamine and 2-β-acetylaminoethyloxy-para-phenylenediamine and the corresponding acid addition salts.

Among the bis(phenyl)alkylenediamines which may be mentioned are, for example, N,N'-bis(β-hydroxyethyl)-N,N'-bis(4'-aminophenyl)-1,3-diaminopropanol, N ,N'-bis(β-hydroxyethyl)-N,N'-bis(4'-aminophenyl)ethylenediamine, N,N'-bis(4-aminophenyl)tetramethylenediamine, N,N'-bis(β-hydroxyethyl )-N,N'-bis(4-aminophenyl)tetramethylenediamine, N,N'-bis(4-methylaminophenyl)tetramethylenediamine, N,N'-bis(ethyl)-N,N'-bis(4'- amino-3'-methylphenyl)ethylenediamine and 1,8-bis(2,5-diaminophenoxy)-3,6-dioxaoctane and the corresponding addition salts.

Among the para-aminophenols which are mentioned are, for example, para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 4-amino-3-chlorophenol, 4-amino- 3-hydroxymethylphenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol, 4-amino-2-(β- hydroxyethylaminomethyl)phenol and 4-amino-2-fluorophenol and the corresponding acid addition salts.

Among the ortho-aminophenols which may be mentioned are, for example, 2-aminophenol, 2-amino-5-methylphenol, 2-amino-6-methylphenol and 5-acetamido-2-aminophenol and the salts of corresponding additions.

Among the heterocyclic bases which may be mentioned are, for example, pyridine, pyrimidine and pyrazole derivatives.

Among the pyridine derivatives which may be mentioned are the compounds described for example in patents GB 1,026,978 and GB 1,153,196, for example 2,5-diaminopyridine, 2-(4-methoxyphenyl)amino-3 -aminopyridine and 3,4-diaminopyridine and the corresponding addition salts.

Other pyridine oxidation bases which are useful in the present invention are the 3-aminopyrazolo[1,5-a]pyridine oxidation bases or the corresponding addition salts described, for example, in the application of patent FR 2 801 308. Examples which may be mentioned include pyrazolo[1,5-a]pyrid-3-ylamine, 2-acetylaminopyrazolo[1,5-a]pyrid-3-ylamine, 2-morpholin- 4-ylpyrazolo[1,5-a]pyrid-3-ylamine, 3-aminopyrazolo[1,5-a]pyridine-2-carboxylic acid, 2-methoxypyrazolo[1,5-a]pyrid-3- ylamine, (3-aminopyrazolo[1,5-a]pyrid-7-yl)methanol, 2-(3-aminopyrazolo[1,5-a]pyrid-5-yl)ethanol, 2-(3- aminopyrazolo[1,5-a]pyrid-7-yl)ethanol, (3-aminopyrazolo[1,5-a]pyrid-2-yl)methanol, 3,6-diaminopyrazolo[1,5-a]pyridine , 3,4-diaminopyrazolo[1,5-a]pyridine, pyrazolo[1,5-a]pyridine-3,7-diamine, 7-morpholin-4-ylpyrazolo[1,5-a]pyrid- 3-ylamine, pyrazolo[1,5-a]pyridine-3,5-diamine, 5-morpholin-4-ylpyrazolo[1,5-a]pyrid-3-ylamine, 2-[(3-aminopyrazolo [1,5-a]pyrid-5-yl)(2-hydroxyethyl)-amino]ethanol, 2-[(3-aminopyrazolo[1,5-a]pyrid-7-yl)(2-hydroxyethyl)amino ]ethanol, 3-aminopyrazolo[1,5-a]pyridin-5-ol, 3-aminopyrazolo[1,5-a]pyridin-4-ol, 3-aminopyrazolo[1,5-a]pyridin- 6-ol, 3-aminopyrazolo[1,5-a]pyridin-7-ol, 2-β-hydroxyethoxy-3-amino-pyrazolo[1,5-a]pyridine; 2-(4-dimethylpiperazinium-1-yl)-3-amino-pyrazolo[1,5-a]pyridine; and the corresponding addition salts.

More particularly, the oxidation bases which are useful in the present invention are chosen from 3-aminopyrazolo-[1,5-a]-pyridines and preferably substituted on the carbon atom 2 by:
a) a (di)(C ₁ -C ₆ )(alkyl)amino group, said alkyl group possibly being substituted by at least one hydroxy, amino or imidazolium group;
b) a heterocycloalkyl group containing 5 to 7 members and 1 to 3 heteroatoms, optionally cationic, optionally substituted by one or more (C ₁ -C ₆ )alkyl groups, such as a di(C ₁ -C ₄ )alkylpiperazinium group; Or
c) a (C ₁ -C ₆ )alkoxy group optionally substituted by one or more hydroxy groups such as a β-hydroxyalkoxy group and the corresponding addition salts.

Among the pyrimidine derivatives which may be mentioned are the compounds described, for example, in patents 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-triamino -pyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine, 2,5,6-triaminopyrimidine and their addition salts and their tautomeric forms, when a tautomeric equilibrium exists.

Among the pyrazole derivatives which may be mentioned are the compounds described in patents DE 3843892, DE 4133957 and patent applications WO 94/08969, WO 94/08970, FR A-2 733 749 and DE 195 43 988, such as 4,5-diamino-1-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)pyrazole, 3,4-diaminopyrazole, 4,5-diamino-1-(4'-chlorobenzyl )pyrazole, 4,5-diamino-1,3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyrazole, 4,5-diamino-1-methyl-3-phenylpyrazole, 4-amino -1,3-dimethyl-5-hydrazinopyrazole, 1-benzyl-4,5-diamino-3-methylpyrazole, 4,5-diamino-3- tert -butyl-1-methylpyrazole, 4,5-diamino- 1- tert -butyl-3-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)-3-methylpyrazole, 4,5-diamino-1-ethyl-3-methylpyrazole, 4,5-diamino -1-ethyl-3-(4'-methoxyphenyl)pyrazole, 4,5-diamino-1-ethyl-3-hydroxymethylpyrazole, 4,5-diamino-3-hydroxymethyl-1-methylpyrazole, 4,5- diamino-3-hydroxymethyl-1-isopropylpyrazole, 4,5-diamino-3-methyl-1-isopropylpyrazole, 4-amino-5-(2'-aminoethyl)amino-1,3-dimethylpyrazole, 3,4 ,5-triaminopyrazole, 1-methyl-3,4,5-triaminopyrazole, 3,5-diamino-1-methyl-4-methylaminopyrazole, 3,5-diamino-4-(β-hydroxyethyl)amino-1 -methylpyrazole and the corresponding addition salts. It is also possible to use 4,5-diamino-1-(β-methoxyethyl)pyrazole.

A 4,5-diaminopyrazole will preferably be used and even more preferably 4,5-diamino-1-(β-hydroxyethyl)pyrazole and/or a corresponding salt.

Pyrazole derivatives which may also be mentioned include diamino-N,N-dihydropyrazolopyrazolones and in particular those described in patent application FR-A-2 886 136, such as the following compounds and the corresponding addition salts: 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2-amino-3-ethylamino-6,7-dihydro-1H,5H-pyrazolo [1,2-a]pyrazol-1-one, 2-amino-3-isopropylamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2-amino -3-(pyrrolidin-1-yl)-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 4,5-diamino-1,2-dimethyl-1, 2-dihydropyrazol-3-one, 4,5-diamino-1,2-diethyl-1,2-dihydropyrazol-3-one, 4,5-diamino-1,2-di-(2-hydroxyethyl)- 1,2-dihydropyrazol-3-one, 2-amino-3-(2-hydroxyethyl)amino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2 -amino-3-dimethylamino-6,7-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-dihydropyrazol-3-one, 4- amino-5-(3-dimethylaminopyrrolidin-1-yl)-1,2-diethyl-1,2-dihydropyrazol-3-one, 2,3-diamino-6-hydroxy-6,7-dihydro-1H,5H -pyrazolo[1,2-a]pyrazol-1-one.

2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one and/or a corresponding salt will preferably be used.

Preferably, 4,5-diamino-1-(β-hydroxyethyl)pyrazole and/or 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1 will be used. -one and/or 2-β-hydroxyethoxy-3-amino-pyrazolo[1,5-a]pyridine and/or a corresponding salt as heterocyclic bases.

According to a preferred embodiment of the invention, the oxidation base(s) are chosen from para-phenylenediamine, para-toluenediamine, para-aminophenol, N,N-bis(β-hydroxyethyl)-para- phenylenediamine, 4,5-diamino-1-(β-hydroxyethyl)pyrazole, 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2-β-hydroxyethoxy-3-amino-pyrazolo[1,5-a]pyridine, and their addition salts.

Preferably, when the oxidation dye precursor is an oxidation base, the oxidation base advantageously represents 0.1% to 50% by weight, more preferentially 0.3% to 25% by weight, more preferentially still 0.4% to 22% by weight, relative to the total weight of the solid particle containing it.

By way of example, the oxidation couplers can be chosen from meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalene-based coupling agents and heterocyclic coupling agents, as well as their salts. addition corresponding or their solvates according to the invention.

Mention may be made, for example, of 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 4-chloro-1,3-dihydroxybenzene, 2,4-diamino-1-(β-hydroxyethyloxy)benzene, 2-amino-4-(ß-hydroxyethylamino)-1-methoxybenzene, 1,3-diaminobenzene, 1,3-bis(2,4-diaminophenoxy)propane, 3-ureidoaniline, 3-ureido-1 -dimethylaminobenzene, sesamol, 1-ß-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-(ß-hydroxyethyl)amino-3,4-methylenedioxybenzene, 2 ,6-bis(ß-hydroxyethylamino)toluene, 6-hydroxyindoline, 2,6-dihydroxy-4-methylpyridine, 1-H-3-methylpyrazol-5-one, 1-phenyl-3-methylpyrazol-5 -one, 2,6-dimethylpyrazolo[1,5-b]-1,2,4-triazole, 2,6-dimethyl[3,2-c]-1,2,4-triazole and 6- methylpyrazolo[1,5-a]benzimidazole, 2-methyl-5-aminophenol, 5-N-(ß-hydroxyethyl)amino-2-methylphenol, 3-aminophenol, 3-amino-2-chloro-6 -methylphenol, 2-[3-amino-4-methoxyphenyl]amino)ethanol the corresponding addition salts with an acid.

According to a preferred embodiment of the invention, the oxidation coupler(s) are chosen from meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalene-based coupling agents, heterocyclic coupling agents , and their corresponding addition salts or solvates, ; more preferably still 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 3-aminophenol, 6-hydroxybenzomorpholine, 5-N-(ß-hydroxyethyl)amino-2-methylphenol, 2, 4-diamino-1-(ß-hydroxyethyloxy)benzene, 2-methyl-5-aminophenol, 6-hydroxyindole, 4-chloro-1,3-dihydroxybenzene, 2-amino-3-hydroxypyridine, 3- amino-2-chloro-6-methylphenol, α-naphthol, 2-[3-amino-4-methoxyphenyl]amino)ethanol and their addition salts.

Preferably, when the oxidation dye precursor(s) is(are) an oxidation coupler(s), the oxidation coupler(s) advantageously represent(s) 0 1% to 50% by weight, more preferably 0.3% to 25% by weight, more preferably still 0.4% to 22% by weight, relative to the total weight of the solid particle containing it(s).

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

Direct dyes

Dyes (e.g. C1 and C2, and more generally C1 to Cn) can be selected from direct dyes; preferably selected from cationic, anionic, nonionic direct dyes, and mixtures thereof; more preferably from cationic and nonionic direct dyes and mixtures thereof.

Direct dyes can be synthetic or natural.

Examples of suitable direct dyes which may be mentioned are azo direct dyes; (poly)methine dyes such as cyanines, hemicyanines and styryls; carbonyl dyes; azine dyes; nitro(hetero)aryl dyes; tri(hetero)arylmethane dyes; porphyrin dyes; phthalocyanine dyes and natural direct dyes, alone or in the form of mixtures.

Mention may in particular be made, by way of example, of the dyes described in patent applications WO 95/15144, WO 95/01772 and EP-714954.

In particular, the useful direct dyes can be chosen from Basic Red 51, Basic Yellow 87 and Basic Orange 31 or corresponding derivatives:
, An ^- Basic Red 51

, An ^- Basic Orange 31

, An ^- Basic Yellow 87

Among the natural direct dyes which can be used according to the invention, mention may be made of hennotannic acid, juglone, alizarin, purpurin, carminic acid, kermesic acid, purpurogalline, protocatechaldehyde, indigo, isatin, curcumin, spinulosin, apigenidine and orcein. Extracts or decoctions containing these natural dyes and in particular henna-based poultices or extracts can also be used.

Preferably, when the direct dye(s) are present in the solid particles, the direct dye(s) advantageously represent(s) 0.001% to 10% by weight, more preferably 0.005% to 5% by weight , relative to the total weight of said solid particles.

Binding agents
The solid particles according to the invention (for example solid particles of type P1 and P2 and more generally P1 to Pn) preferably also comprise at least one binding agent.

By "binding agent" is meant in the sense of the invention a compound contributing to the cohesion of the solid particle. The binding agent allows in particular the agglomeration of the various components constituting the solid particle.

By way of example of binding agents, mention may in particular be made of proteins (such as gelatin); saccharides and their derivatives, oligosaccharides and their derivatives including disaccharides (such as sucrose and lactose) in particular in their anhydrous or hydrated forms, and sugar alcohols (such as xylitol, sorbitol and maltitol); polyvinyl alcohol (PVA); polysaccharides and their derivatives (for example, starches, cellulose and/or modified cellulose); alginate; and gums (eg, acacia gum, guar gum).

Examples of suitable modified cellulose include microcrystalline cellulose (MCC), especially in their anhydrous or hydrated forms, and cellulose ethers such as hydroxypropyl cellulose (HPC) and hydroxypropyl methyl cellulose (HPMC).

Preferably, the binding agent(s) are chosen from saccharides and their derivatives, oligosaccharides and their derivatives, polysaccharides and their derivatives, polyvinyl alcohol (PVA), and mixtures thereof; more preferably from lactose in particular in anhydrous or hydrated form, microcrystalline cellulose (MCC) in particular in anhydrous or hydrated form, polyvinyl alcohol (PVA), cellulose ethers such as hydroxypropyl cellulose (HPC) and hydroxypropylmethyl cellulose (HPMC), and mixtures thereof.

Preferably, when the binding agent(s) are present in the solid particles, the total content of binding agent(s) is greater than or equal to 30% by weight; more preferably greater than or equal to 50% by weight; more preferably still between 50% and 99.9% by weight, better still between 60% and 99.9% by weight, even better still between 70% and 99.9% by weight, relative to the total weight of each solid particle the (s) container.

Disintegrating agents
The solid particles according to the invention (for example solid particles of type P1 and P2 and more generally P1 to Pn) preferably also comprise at least one disintegrating agent.

Within the meaning of the present invention, the term "disintegrants" means a class of agents, preferably a class of polymers, particularly effective in inducing the disintegration of a solid particle (for example a tablet). A special class of disintegrating agents are called "superdisintegrants" because they are generally effective at low concentrations.

Disintegrating agents can be hygroscopic compounds that act by absorbing liquid from a medium when brought into contact with that medium (e.g. water from an aqueous medium). Such absorption may then induce disintegration by causing considerable swelling of the disintegrating agent and/or enhancing capillary action. The swelling pressure exerted by a disintegrating agent swollen in an outward or radial direction can cause a solid particle (eg a tablet) to burst.

By way of example of disintegrating agents, or even superdisintegrating agents, mention may in particular be made of crosslinked celluloses such as croscarmellose (or crosslinked carboxymethylcellulose, which is generally used in the form of the sodium salt) and its derivatives, marketed for example under the Ac-Di-Sol ^® , Explocel ^® , Nymcel ZSX ^® , Pharmacel ^® XL, Primellose ^® , Solutab ^® and Vivasol ^® references; crospovidone (or cross-linked polyvinylpyrrolidone) and its derivatives, marketed for example under the references Crospovidone ^M® , ^Kollidon® and ^{Polyplasdone®} ; cross-linked starch such as sodium starch glycolate, marketed for example under the references ^Explotab® , ^Explotab® CLV, ^Explosol® , ^Primojel® , ^Tablo® and ^Vivastar® ; cross-linked alginic acids, marketed for example under the reference ^Satialgine® ; crosslinked polyacrylic compounds such as ion exchange resins, marketed for example under the references Indion ^® 414, Tulsion ^® 339 and Amberlite ^® IRP; and certain polysaccharides, such as soy polysaccharide, marketed for example under the references ^Emcosoy® superdisintegrant.

Preferably, the disintegrating agent(s) are polymeric; more preferably each type of solid particle comprises at least one disintegrating polymer, more preferably at least one superdisintegrating polymer; more preferably still at least one superdisintegrating polymer chosen from cross-linked polymers of vinylpyrrolidone and its derivatives, and mixtures thereof; even better among crosslinked polyvinylpyrrolidones, crosslinked vinylpyrrolidone/vinyl acetate copolymers, and mixtures thereof.

Preferably, when the disintegrating agent(s) are present in the solid particles, the total content of disintegrating agent(s) is between 0.5 and 15% by weight; more preferably between 1 and 12% by weight, more preferably still between 2% and 10% by weight, relative to the total weight of each solid particle containing it(s).

Antioxidants
The solid particles according to the invention (for example solid particles of type P1 and P2 and more generally P1 to Pn) preferably also comprise at least one antioxidant agent.

By way of example of antioxidant agent(s), mention may in particular be made of ascorbic acid, its salts and its derivatives (such as sodium ascorbate, erythorbic acid, ascorbyl palmitate, ascorbyl laurate); salicylic acid, its salts and its derivatives (such as sodium salicylate); mercaptans and inorganic sulphites (such as sodium sulphite, sodium bisulphite, sodium metabisulphite, potassium sulphite and thioglycolic acid); 2,6-di-tert-butyl-4-methylphenol (BHT); butylated hydroxyanisole (BHA); sodium dithionite; and their mixtures.

Preferably, the antioxidant agent(s) are chosen from ascorbic acid, its salts and its derivatives (such as sodium ascorbate, erythorbic acid, ascorbyl palmitate, ascorbyl laurate); salicylic acid, its salts and its derivatives (such as sodium salicylate), mercaptans and inorganic sulphites (such as sodium sulphite, sodium bisulphite, sodium metabisulphite, potassium sulphite and thioglycolic acid), and mixtures thereof; more preferably from ascorbic acid, sodium sulphite, sodium bisulphite, sodium metabisulphite, sodium salicylate, and mixtures thereof.

Preferably, when the antioxidant agent(s) are present in the solid particles, the total content of antioxidant agent(s) is between 0.1 and 15% by weight; more preferably between 0.3 and 12% by weight, more preferably still between 0.4% and 10% by weight, better still between 0.5 and 5% by weight relative to the total weight of each solid particle containing the .

Lubricating and/or anti-adherent agents
The solid particles according to the invention (for example solid particles of type P1 and P2 and more generally P1 to Pn) preferably also comprise at least one lubricating and/or anti-adherent agent.

Within the meaning of the invention, the term "lubricating and/or anti-adherent agent" is understood to mean a compound making it possible to reduce, or even prevent, the agglomeration of the ingredients of the solid particles, to reduce adhesion (in particular during a compression step), and/or to improve the flow of the ingredients of the solid particles by reducing the friction and the cohesion between the ingredients.

Preferably, the lubricating and/or anti-adherent agent(s) are chosen from magnesium stearate, calcium silicate, magnesium silicate, magnesium carbonate, silicon dioxide, talc, silica, acid stearic acid, sodium stearoyl fumarate, and mixtures thereof; more preferably from silica, magnesium stearate, and mixtures thereof.

Preferably, when the lubricating and/or anti-adherent agent(s) are present in the solid particles, the total content of lubricating and/or anti-adherent agent(s) is between 0.1 and 10% by weight; more preferably between 0.3 and 8% by weight, more preferably still between 0.5% and 5% by weight, relative to the total weight of each solid particle containing it(these).

The top coating layer
The solid particles according to the invention (for example solid particles of type P1 and P2 and more generally P1 to Pn) preferably further comprise an upper coating layer (also called upper film-coating layer).

The upper coating layer according to the invention may optionally comprise cellulose ethers such as those described above.

The upper coating layer according to the invention may optionally comprise one or more other compounds such as polyethylene glycol (PEG); polyvinyl alcohol (PVA); polyvinylpyrrolidone (PVP); their copolymers (e.g. polyvinyl alcohol-polyethylene glycol PVA/PEG copolymer); sugars such as xanthan; and their mixtures.

Preferably, the upper coating layer comprises at least two different cellulose ethers.

According to a preferred embodiment of the invention, the upper coating layer comprises at least one cellulose ether as described above; more preferably a cellulose ether chosen from carboxymethylcellulose (CMC), ethylcellulose (CE), hydroxypropylcellulose (HPC), hydroxypropylmethylcellulose (HPMC), methylhydroxyethylcellulose (MHEC), and mixtures thereof, better still from hydroxypropylcellulose (HPC), hydroxypropyl methylcellulose (HPMC), and mixtures thereof.

More preferentially, the upper coating layer comprises hydroxypropylcellulose (HPC) and hydroxypropyl-methylcellulose (HPMC).

Preferably according to this embodiment of the invention, the total content of cellulose ether(s) present in the upper coating layer is between 30 and 99% by weight; more preferably between 40 and 90% by weight, more preferably still between 50 and 70% by weight, relative to the total weight of the upper coating layer.

According to another preferred embodiment according to the invention, the upper coating layer comprises at least one lubricating and/or anti-adherent agent such as those described previously; more preferably at least one lubricating and/or anti-adherent agent chosen from calcium silicate, magnesium silicate, magnesium carbonate, silicon dioxide, talc, silica, and mixtures thereof; more preferably, the lubricating and/or anti-adherent agent is talc.

Preferably according to this embodiment, the total content of lubricating agent(s) and/or anti-adherent agent(s) present in the upper coating layer is between 1 and 40% by weight; more preferably between 2 and 30% by weight, relative to the total weight of the upper coating layer.

Preferably, the upper coating layer according to the invention also comprises one or more pigments.

By way of example, the pigments can be white or colored, mineral and/or organic, coated or not. Mention may be made, among the mineral pigments, of metal oxides, in particular titanium dioxide, optionally surface-treated, zirconium, zinc or cerium oxides, as well as iron, titanium or chromium oxides, manganese violet, ultramarine blue, ultramarine pink, chromium hydrate and ferric blue, and mixtures thereof. Among the organic pigments, mention may be made of carbon black, D & C type pigments, and lakes based on cochineal carmine, barium, strontium, calcium, aluminum, and mixtures thereof.

According to a preferred embodiment of the invention, the upper coating layer according to the invention further comprises one or more pigments chosen from zirconium oxides, zinc oxides, cerium oxides, iron oxides, titanium oxides, chromium oxides, manganese violet, ultramarine blue, ultramarine pink, chromium hydrate and ferric blue, and mixtures thereof; more preferably one or more pigments chosen from titanium oxides such as titanium dioxide, iron oxides, chromium oxides, in particular green chromium oxide, and mixtures thereof.

When the upper coating layer comprises one or more pigments, the pigment(s) advantageously represents a total content ranging from 1% to 50% by weight, more preferably 5% to 40% by weight, by relative to the total weight of the upper coating layer.

Preferably, the solid particles according to the invention are anhydrous.
The term "anhydrous solid particle" means that the solid particle contains less than 2% by weight of water, preferably less than 1% by weight of water, and even more preferably less than 0.5% by weight of water relative to the total weight of the solid particle, and even said solid particle is free of water. In particular, any water present is not added during the preparation of the solid particle but corresponds to the residual water provided by the mixed ingredients.

The solid particles according to the invention can advantageously be in a spherical or spheroidal form; more preferably in a spherical shape, such as a ball shape.

Preferably, the solid particles according to the invention have an average volume of between 25 and 125 mm ³ ; more preferably between 30 and 90 mm ³ ; more preferably still between 45 and 65mm ³ .

The volume V of a solid particle in a substantially spherical or spheroidal form can in particular be calculated by the following equation:
V = (4/3).π.r ³
where r represents the radius of the solid particle.

Preferably, the solid particles have an average mass of between 30 and 120mg; more preferably between 40 and 80mg; more preferably still between 50 and 70 mg.

Preferably, the average hardness of the solid particles is between 2 and 15kPa; more preferably between 2 and 11 kPa.

The average hardness of solid particles can for example be measured using a semi-automatic tablet testing system commonly used in the pharmaceutical field, in particular using the Pharmatron ST50 device.

Preferably, the solid particles have an average disintegration time in 25 mL of hydrogen peroxide (at 6% by weight of H ₂ O ₂ ) at 25° C. and at atmospheric pressure of less than 60 seconds; more preferably less than 40 seconds; even better between 1 and 30 seconds.

For example, the average disintegration time can be measured using the following method:
1) in a 50mL beaker, 25mL of an oxidizing aqueous composition comprising 6% by weight of hydrogen peroxide are poured; Then
2) 10 identical solid coloring particles according to the invention are added all at once; the contents of the beaker are not mixed; Then
3) the stopwatch is started;
4) the stopwatch is stopped once all the solid particles have clearly disintegrated visually; that is to say once it is observed that the solid particles form a soft mass no longer containing a firm nucleus; and finally
5) the average disintegration time is noted on the chronometer.

The solid particles according to the invention are advantageously prepared according to the conventional methods for preparing tablets, optionally film-coated, such as the methods used in the pharmaceutical industry.

More particularly, the solid particles according to the invention can be prepared by the dry route according to the following steps:
- grinding of the ingredients of the solid particle; Then
- sieving the powder obtained; Then
- mixing said powder; Then
- direct compression of the mixture obtained in solid particles; and eventually
- coating of the solid particles obtained.

According to another particular method of preparation, the solid particles according to the invention can be prepared by wet granulation according to the following steps:
- premix of the binding agent(s) (for example lactose and microcrystalline cellulose, polyvinyl alcohol (PVA)), and of the colorant(s); Then
- spraying on the premix of the disintegrating agent(s) (for example a cross-linked polyvinylpyrrolidone) in solution in one or more solvents such as those described in the paragraph below for the coating composition, in particular in water, for obtaining the desired aggregate; Then
- drying of the aggregate; Then
- grinding of the other ingredients of the solid particle; Then
- sieving of the powder obtained by the grinding and of the aggregate; Then
- mixing of the powders obtained by sieving; Then
- direct compression of the mixture obtained in solid particles; and eventually
- coating of the solid particles obtained.

The coating composition, allowing the coating of the solid particles, comprises one or more cellulose ethers as previously described for the upper coating layer.

Preferably, said coating composition further comprises one or more of the preferred top coating layer ingredients as previously described; more preferentially in contents as previously described in the upper coating layer.

More preferably, said coating composition further comprises one or more solvents chosen from water, C ₁ -C ₆ alcohols, and mixtures thereof; more preferably still chosen from water, ethanol, and mixtures thereof.

By way of example, the coating composition can be prepared from one or more solvents, in particular as described above, and from a mixture containing hydroxypropylmethylcellulose and hydroxypropylcellulose. According to this example, the coating composition may optionally contain one or more fatty substances, preferably liquid at 25° C. and atmospheric pressure, such as one or more fatty alcohols, fatty esters and/or triglycerides, for example chosen from octyldodecanol, isopropyl mysistate vegetable oil and/or caprylic/capric acid triglyceride.

The composition may also optionally contain talc and/or pigments to color the coating, preferably talc and pigments such as titanium dioxide.

The grinding step can in particular be carried out using a grinder, for example of the U5 ^{Quadro® COMIL®} type.

The screening step can in particular be carried out using a granulator, for example of the ROTO P50 type (Zanchetta) or High Shear Mixer P/VAC-10 (Diosna).

The mixing step can in particular be carried out using a mixer, for example of the MB015 Blender type (Pharmatech).

The direct compression step of the mixture can in particular be carried out using a compression table, for example of the PR-1500 (PTK) type.

The step of coating said particles can in particular be carried out using a film-coating station, for example of the LDCS-Pilot HI- ^COATER® (Freund-vector) type.

Aqueous Composition A:

The process according to the present invention comprises the mixing of several solid particles as described above (for example solid particles of type P1 and P2, and more generally P1 to Pn) with at least one aqueous composition A comprising arginine.

Preferably, the total content of arginine present in the aqueous composition A is between 0.05 and 25% by weight, more preferably between 0.1 and 15% by weight, more preferably still between 0.5 and 10% by weight. , or even between 1 and 5% by weight, relative to the total weight of the aqueous composition A.

Advantageously, the aqueous composition A according to the invention comprises at least one additional alkaline agent other than arginine, and/or at least one oxidizing agent and/or at least one associative polymer.

Preferably, the water content of the aqueous composition A according to the invention is between 30 and 99% by weight; more preferably between 50 and 99% by weight, even better between 50 and 90% by weight, relative to the total weight of the aqueous composition A.

Additional alkaline agents
The aqueous composition A according to the invention preferably also comprises at least one additional alkaline agent other than arginine.

Preferably, the additional alkaline agent(s) can be chosen from organic alkaline agents and inorganic alkaline agents.

Preferably, the additional organic alkaline agent(s) are chosen from organic amines whose pK _b at 25° C. is less than 12, and more preferably less than 10, even more advantageously less than 6. It should be noted that it this is the pK _b corresponding to the highest basicity function. Furthermore, the organic amines do not comprise a fatty, alkyl or alkenyl chain comprising more than ten carbon atoms.

The additional organic alkaline agent(s) are preferably chosen from alkanolamines such as mono-, di- or tri-alkanolamines, comprising one to three C ₁ to C ₄ hydroxyalkyl radicals, identical or not.

By alkanolamine is meant an organic amine comprising a primary, secondary or tertiary amine function, and one or more alkyl groups, linear or branched, C ₁ to C ₈ carrying one or more hydroxy radicals.

The alkanolamines chosen from monoethanolamine (MEA), diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, N,N-dimethylethanolamine, 2-amino-2-methyl-1- propanol, triisopropanol-amine, 2-amino-2-methyl-1,3-propanediol, 3-amino-1,2-propanediol, 3-dimethylamino-1,2-propanediol, tris-hydroxymethylamino-methane . Among the alkanolamines, it is very particularly preferred to use monoethanolamine.

The amino acids different from arginine that can be used are of natural or synthetic origin, in their L, D, or racemic form and comprise at least one acid function chosen more particularly from carboxylic, sulphonic, phosphonic or phosphoric acid functions. Amino acids can be in neutral or ionic form.

As amino acids different from arginine which can be used in the present invention, mention may be made in particular of aspartic acid, glutamic acid, alanine, ornithine, citrulline, asparagine, carnitine, cysteine, glutamine, glycine, histidine, lysine, isoleucine, leucine, methionine, N-phenylalanine, proline, serine, taurine, threonine, tryptophan, tyrosine and valine.

Advantageously, the amino acids other than arginine are basic amino acids comprising an additional amine function optionally included in a cycle or in a ureido function.

The organic amine can also be chosen from organic amines of the heterocyclic type. Mention may in particular be made, in addition to the histidine already mentioned in the amino acids, of pyridine, piperidine, imidazole, triazole, tetrazole, benzimidazole.

The organic amine can also be chosen from amino acid dipeptides. As amino acid dipeptides that can be used in the present invention, mention may be made in particular of carnosine, anserine and balenine.

The organic amine can also be chosen from compounds comprising a guanidine function. As amines of this type which can be used in the present invention, mention may in particular be made, in addition to creatine, creatinine, 1,1-dimethylguanidine, 1,1-diethylguanidine, glycocyamine, metformin, agmatine, n -amidinoalanine, 3-guanidino-propionic acid, 4-guanidinobutyric acid and 2-([amino(imino)methyl]amino)-ethane-1-sulfonic acid.

Among the additional inorganic alkaline agents that can be used in the process according to the invention, mention may be made of mineral hydroxides.

The mineral hydroxides can be chosen from hydroxides of alkali metals or alkaline earth metals, of transition metals, of ammonium. As mineral hydroxides, mention may be made, for example, of ammonium hydroxide, sodium hydroxide, lithium hydroxide, calcium hydroxide, magnesium hydroxide, barium hydroxide, strontium, manganese hydroxide, zinc hydroxide.

Among the mineral hydroxides, ammonium hydroxide, also called ammonia, is preferred.

The additional inorganic alkaline agent(s) can also be chosen from urea, ammonium salts such as ammonium chloride, ammonium sulphate, ammonium phosphate or ammonium nitrate, silicates, phosphates or carbonates of alkali or alkaline-earth metals, such as lithium, sodium, potassium, magnesium, calcium, barium, and mixtures thereof, preferably from alkali or alkaline-earth metal silicates, in particular alkali or alkaline earth metal metasilicates such as sodium metasilicate

Preferably, the additional alkaline agent(s) other than arginine, useful in the invention, are chosen from ammonia, alkali or alkaline earth metal metasilicates, alkanolamines, amino acids in neutral or ionic form, in particular basic amino acids, compounds comprising a guanidine function, and preferably from ammonia, alkali metal or alkaline earth metal metasilicates and alkanolamines.

According to a preferred embodiment of the invention, the aqueous composition A comprises one or more additional alkaline agents other than arginine; more preferably chosen from ammonia, alkanolamines, alkali metal or alkaline earth metal metasilicates, and mixtures thereof; more preferably still from ammonia, monoethanolamine, sodium metasilicate, and mixtures thereof.

Preferably, when the additional alkaline agent(s) other than arginine are present in the aqueous composition A, the total content of additional alkaline agent(s) other than arginine is between 0.05 and 25% by weight, more preferably between 0.1 and 20% by weight, and even more preferably between 0.5 and 15% by weight, relative to the total weight of the aqueous composition A.

Advantageously, the pH of the aqueous composition A according to the invention generally varies from 8 to 13, preferably from 9 to 12.5, better still from 10 to 12.5.

Chemical oxidizing agents
The aqueous composition A according to the invention may optionally also comprise at least one chemical oxidizing agent.

By “ chemical oxidizing agent ”, is meant within the meaning of the present invention an oxidizing agent different from the oxygen in the air.

The chemical oxidizing agent(s) (or bleaching agents) that can be used in the present invention can be chosen from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulfates, in particular sodium persulphate, potassium persulphate and ammonium persulphate, peracids and oxidase enzymes (with their possible cofactors) among which mention may be made of peroxidases, 2-electron oxidoreductases such as uricases and 4-electron oxygenases such as laccases, and mixtures thereof; more preferably, the chemical oxidizing agent(s) are chosen from hydrogen peroxide, persalts, and mixtures thereof.

Preferably, when the chemical oxidizing agent(s) are present in the aqueous composition A, the total content of chemical oxidizing agent(s) is between 0.1 and 35% by weight, more preferably between 0 , 1 and 30% by weight, and even more preferably between 0.5 and 25% by weight, better still 2 to 12% by weight relative to the total weight of the aqueous composition A.

Associative polymers
The aqueous composition A according to the invention may optionally also comprise at least one associative polymer.

Preferably, the associative polymer(s) are chosen from anionic, nonionic, cationic, amphoteric associative polymers, and mixtures thereof.

It is recalled that “associative polymers” are polymers capable, in an aqueous medium, of combining reversibly with each other or with other molecules.

Their chemical structure more particularly comprises at least one hydrophilic zone and at least one hydrophobic zone.

By “hydrophobic zone”, is meant a radical or polymer with a hydrocarbon chain, saturated or not, linear or branched, comprising at least 8 carbon atoms, preferably from 10 to 30 carbon atoms, in particular from 12 to 30 carbon atoms. carbon 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 can come from a fatty alcohol such as stearyl alcohol, dodecyl alcohol, decyl alcohol. It can also designate a hydrocarbon-based polymer such as for example polybutadiene.

Among the associative polymers of the anionic type, mention may be made of:
- (a) those comprising at least one hydrophilic unit, and at least one fatty chain allyl ether unit, more particularly those whose hydrophilic unit consists of an ethylenically unsaturated anionic monomer, more particularly still of a vinyl carboxylic acid and most particularly by an acrylic acid or a methacrylic acid or mixtures thereof.
Among these anionic associative polymers, polymers formed from 20 to 60% by weight of acrylic acid and/or methacrylic acid, from 5 to 60% by weight of (meth)acrylates are particularly preferred according to the invention. of lower alkyls, from 2 to 50% by weight of fatty chain allyl ether, and from 0 to 1% by weight of a crosslinking agent which is a well-known copolymerizable polyethylenic unsaturated monomer, such as diallyl phthalate , allyl (meth)acrylate, divinylbenzene, (poly)ethylene glycol dimethacrylate, and methylene-bis-acrylamide.
Among the latter, the crosslinked terpolymers of methacrylic acid, ethyl acrylate, polyethylene glycol (10 EO) stearyl alcohol ether (Steareth 10) are very particularly preferred, in particular those sold by the company CIBA under the names SALCARE SC80® and SALCARE SC90® which are 30% aqueous emulsions of a cross-linked terpolymer of methacrylic acid, ethyl acrylate and steareth-10-allyl ether (40/50/10).
- (b) those comprising i) at least one hydrophilic unit of the olefinic unsaturated carboxylic acid type, and ii) at least one hydrophobic unit of the (C ₁₀ -C ₃₀ ) alkyl ester type of unsaturated carboxylic acid.
(C ₁₀ -C ₃₀ ) alkyl esters of unsaturated carboxylic acids useful in the invention include, for example, lauryl acrylate, stearyl acrylate, decyl acrylate, isodecyl acrylate , dodecyl acrylate, and the corresponding methacrylates, lauryl methacrylate, stearyl methacrylate, decyl methacrylate, isodecyl methacrylate, and dodecyl methacrylate.
Anionic polymers of this type are, for example, described and prepared according to US Pat. Nos. 3,915,921 and 4,509,949.
Among this type of anionic associative polymers, those consisting of 95 to 60% by weight of acrylic acid (hydrophilic unit), 4 to 40% by weight of C ₁₀ -C ₃₀ alkyl acrylate (hydrophilic unit) will be used more particularly. hydrophobic), and 0 to 6% by weight of crosslinking polymerizable 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 -C ₃₀ (hydrophobic unit), and 0.1 to 0.6% by weight of crosslinking polymerizable monomer such as those described above.
Among said above polymers, very particularly preferred according to the present invention are the products sold by the company GOODRICH under the trade names PEMULEN TR1®, PEMULEN TR2®, CARBOPOL 1382®, and even more preferably PEMULEN TR1®, and product sold by the company SEPPIC under the name COATEX SX®.
Mention may also be made of the acrylic acid/lauryl methacrylate/vinylpyrrolidone terpolymer sold under the name Acrylidone LM by the company ISP.
- (c) maleic anhydride/C ₃₀ -C ₃₈ α-olefin/alkyl maleate terpolymers such as the product (copolymer maleic anhydride/C ₃₀ -C ₃₈ α-olefin/isopropyl maleate) sold under the name PERFORMA V 1608® by the company NEWPHASE TECHNOLOGIES.
- (d) acrylic terpolymers comprising:
i) about 20 to 70% by weight of an α,β-monoethylenically unsaturated carboxylic acid [A],
ii) about 20 to 80% by weight of a non-surfactant α,β-monoethylenically unsaturated monomer different from [A],
iii) about 0.5 to 60% by weight of a nonionic monourethane which is the reaction product of a monohydric surfactant with a monoethylenically unsaturated monoisocyanate,
such as those described in patent application EP-A-0173109 and more particularly that described in example 3, namely, a terpolymer of methacrylic acid/methyl acrylate/dimethyl metaisopropenyl benzyl isocyanate of ethoxylated behenyl alcohol (40EO) in 25% aqueous dispersion.
- (e) copolymers comprising among their monomers an α,β-monoethylenically unsaturated carboxylic acid and an α,β-monoethylenically unsaturated carboxylic acid ester and an oxyalkylenated fatty alcohol.
Preferably, these compounds also comprise, as monomer, an ester of an α,β-monoethylenically unsaturated carboxylic acid and of a C ₁ -C ₄ alcohol.
As an example of this type of compound, mention may be made of ACULYN 22® (INCI name: Acrylates/Steareth-20 Methacrylate Copolymer) sold by the company ROHM and HAAS, which is a methacrylic acid/ethyl acrylate/ oxyalkylenated stearyl methacrylate as well as ACULYN 88 (INCI name: Acrylates/Steareth-20 Methacrylate Crosspolymer) or ACULYN 28 (INCI name: Acrylates/Beheneth-25 Methacrylate Copolymer) also sold by ROHM and HAAS.
- (f) Amphiphilic polymers comprising at least one ethylenically unsaturated monomer containing a sulphonic group, in free or partially or totally neutralized form and comprising at least one hydrophobic part. These polymers can be crosslinked or non-crosslinked. They are preferably cross-linked.
The ethylenically unsaturated monomers containing a sulfonic group are chosen in particular from vinylsulfonic acid, styrenesulfonic acid, (meth)acrylamido(C ₁ -C ₂₂ )alkylsulfonic acids, N-(C ₁ -C ₂₂ )alkyl( meth)acrylamido-(C ₁ -C ₂₂ )alkylsulphonics such as undecyl-acrylamido-methane-sulphonic acid as well as their partially or totally neutralized forms.
More preferably, (meth)acrylamido(C ₁ -C ₂₂ )alkylsulphonic acids such as for example acrylamido-methane-sulphonic acid, acrylamido-ethane-sulphonic acid, acrylamido-propane-sulphonic acid, 2-acrylamido-2-methylpropane-sulfonic acid, methacrylamido-2-methylpropane-sulfonic acid, 2-acrylamido-n-butane-sulfonic acid, 2-acrylamido-2,4,4- trimethylpentane-sulfonic, 2-methacrylamido-dodecyl-sulfonic acid, 2-acrylamido-2,6-dimethyl-3-heptane-sulfonic acid as well as their partially or totally neutralized forms.
More particularly, 2-acrylamido-2-methylpropanesulfonic acid (AMPS) as well as its partially or totally neutralized forms will be used.
The polymers of this family can in particular be chosen from random amphiphilic polymers of AMPS modified by reaction with an n-monoalkylamine or a di-n-alkylamine in C ₆ -C ₂₂ , and such as those described in patent application WO 00/31154 (forming an integral part of the content of the description). These polymers may also contain other ethylenically unsaturated hydrophilic monomers chosen, for example, from (meth)acrylic acids, their β-substituted alkyl derivatives or their esters obtained with monoalcohols or mono- or polyalkylene glycols, (meth)acrylamides , vinylpyrrolidone, maleic anhydride, itaconic acid or maleic acid or mixtures of these compounds.
The preferred polymers of this family are chosen from amphiphilic copolymers of AMPS and of at least one hydrophobic ethylenically unsaturated monomer.
These same copolymers may also contain one or more ethylenically unsaturated monomers not comprising a fatty chain such as (meth)acrylic acids, their β-substituted alkyl derivatives or their esters obtained with monoalcohols or mono- or poly-alkylene glycols, (meth)acrylamides, vinylpyrrolidone, maleic anhydride, itaconic acid or maleic acid or mixtures of these compounds.
These copolymers are described in particular in patent application EP-A-750899, US patent 5089578 and in the following publications by Yotaro Morishima:
- "Self-assembling amphiphilic polyelectrolytes and their nanostructures - Chinese Journal of Polymer Science Vol. 18, No. 40, (2000), 323-336. » ;
- “Miscelle formation of random copolymers of sodium 2-(acrylamido)-2-methylpropanesulfonate and a non-ionic surfactant macromonomer in water as studied by fluorescence and dynamic light scattering - Macromolecules, Vol. 33, No. 10 (2000), 3694-3704”;
- "Solution properties of miscelle networks formed by non-ionic moieties covalently bound to a polyelectrolyte: salt effects on rheological behavior - Langmuir, , Vol. 16, No. 12, (2000) 5324-5332”;
- “Stimuli responsive amphiphilic copolymers of sodium 2-(acrylamido)-2-methylpropanesulfonate and associative macromonomers - Polym. Preprint, Div. Polym. Chem., 40(2), (1999), 220-221”.

Among these polymers, we can mention:

- crosslinked or non-crosslinked copolymers, neutralized or not, comprising from 15 to 60% by weight of AMPS units and from 40 to 85% by weight of (C ₈ -C ₁₆ )alkyl (meth)acrylamide units or of (C ₈ -C ₁₆ )alkyl (meth)acrylate with respect to the polymer, such as those described in application EP-A750 899;

- terpolymers comprising from 10 to 90% by mole of acrylamide units, from 0.1 to 10% by mole of AMPS units and from 5 to 80% by mole of n-(C ₆ -C ₁₈ )alkylacrylamide units, such as those described in US-5089578.

Mention may also be made of copolymers of fully neutralized AMPS and of dodecyl methacrylate as well as non-crosslinked and crosslinked copolymers of AMPS and n-dodecylmethacrylamide, such as those described in the articles by Morishima cited above.

Among the cationic associative polymers, mention may be made of:
(a) cationic associative polyurethanes;
(b) the compound marketed by the company NOVEON under the name AQUA CC and which corresponds to the INCI name POLYACRYLATE-1 CROSSPOLYMER.
POLYACRYLATE-1 CROSSPOLYMER is the product of the polymerization of a mixture of monomers including:
- a di(C ₁ -C ₄ alkyl) amino(C ₁ -C ₆ alkyl) methacrylate,
- one or more C ₁ -C ₃₀ alkyl esters and (meth)acrylic acid,
- a polyethoxylated C ₁₀ -C ₃₀ alkyl methacrylate (20-25 moles of ethylene oxide unit),
- a 30/5 polyethylene glycol/polypropylene glycol allyl ether,
- a hydroxy(C ₂ -C ₆ alkyl) methacrylate, and
- an ethylene glycol dimethacrylate.
(c) quaternized (poly)hydroxyethylcelluloses modified with groups comprising at least one fatty chain, such as alkyl, arylalkyl, alkylaryl groups comprising at least 8 carbon atoms, or mixtures thereof. The alkyl radicals carried by the quaternized celluloses or hydroxyethylcelluloses above preferably contain from 8 to 30 carbon atoms. The aryl radicals preferably designate the phenyl, benzyl, naphthyl or anthryl groups. Mention may be made, as examples, of quaternized alkylhydroxyethyl celluloses with C ₈ -C ₃₀ fatty chains, such as the products QUATRISOFT LM 200®, QUATRISOFT LM-X 529-18-A®, QUATRISOFT LM-X 529-18-B ® (C ₁₂ alkyl) and QUATRISOFT LM-X 529-8® (C ₁₈ alkyl) sold by the company AQUALON, the products CRODACEL QM®, CRODACEL QL® (C ₁₂ alkyl) and CRODACEL QS® (C 12 alkyl) C ₁₈ ) sold by the company CRODA and the product SOFTCAT SL 100® sold by the company AQUALON.
(d) cationic polyvinyllactam polymers.

Such polymers are for example described in patent application WO-00/68282.

As cationic poly(vinyllactam) polymers according to the invention, use is made in particular of vinylpyrrolidone/dimethylaminopropylmethacrylamide/dodecyldimethylmethacrylamidopropylammonium tosylate terpolymers, vinylpyrrolidone/dimethylaminopropylmethacrylamide/cocoyldimethyl-methacrylamidopropylammonium tosylate terpolymers, vinylpyrrolidone/dimethylaminopropylmethacrylamidopropylammonium chloride or -propylammonium.

The amphoteric associative polymers are preferably chosen from those comprising at least one non-cyclic cationic unit. Even more particularly, those prepared from or comprising 1 to 20 mol% of monomer comprising a fatty chain, and preferably 1.5 to 15 mol% and even more particularly 1.5 to 6 mol%, relative to the number total moles of monomers.

Amphoteric associative polymers according to the invention are for example described and prepared in patent application WO 9844012.

Among the amphoteric associative polymers according to the invention, acrylic acid/(meth)acrylamidopropyl trimethyl ammonium chloride/stearyl methacrylate terpolymers are preferred.

The associative polymers of the nonionic type that can be used according to the invention are preferably chosen from:
(a) copolymers of vinyl pyrrolidone and fatty-chain hydrophobic monomers, which may be mentioned by way of example:
- ANTARON V216® or GANEX V216® products (vinylpyrrolidone/hexadecene copolymer) sold by ISP
- ANTARON V220® or GANEX V220® products (vinylpyrrolidone/eicosene copolymer) sold by ISP
(b) copolymers of C ₁ -C ₆ alkyl methacrylates or acrylates and amphiphilic monomers comprising at least one fatty chain such as, for example, the methyl acrylate/oxyethylenated stearyl acrylate copolymer sold by the company GOLDSCHMIDT under the name ANTIL 208®.
(c) copolymers of hydrophilic methacrylates or acrylates and hydrophobic monomers comprising at least one fatty chain such as, for example, the polyethylene glycol methacrylate/lauryl methacrylate copolymer.
(d) polyether polyurethanes comprising in their chain both hydrophilic sequences of a nature most often polyoxyethylenated and hydrophobic sequences which may be aliphatic sequences alone and/or cycloaliphatic and/or aromatic sequences.
(e) polymers with an ether aminoplast backbone possessing at least one fatty chain, such as the PURE THIX® compounds offered by the company SUD-CHEMIE.
(f) celluloses or their derivatives, modified with groups comprising at least one fatty chain such as alkyl, arylalkyl, alkylaryl groups or mixtures thereof where the alkyl groups are C ₈ -C ₃₀ and in particular:
* non-ionic alkylhydroxyethylcelluloses such as the products NATROSOL PLUS GRADE 330 CS and POLYSURF 67 (C ₁₆ alkyl) sold by the company AQUALON
* nonionic nonoxynylhydroxyethylcelluloses such as the product AMERCELL HM-1500 sold by the company AMERCHOL;
* non-ionic alkylcelluloses such as the product BERMOCOLL EHM 100 sold by the company BEROL NOBEL;
(g) associative guar derivatives such as hydroxypropylguars modified by a fatty chain such as the product ESAFLOR HM 22 (modified by a C ₂₂ alkyl chain) sold by the company LAMBERTI; the product MIRACARE XC 95-3 (modified by a C ₁₄ alkyl chain) and the product RE 205-146 (modified by a C ₂₀ alkyl chain) sold by RHODIA CHIMIE.

Preferably, the polyether polyurethanes comprise at least two lipophilic hydrocarbon chains, having from 6 to 30 carbon atoms, separated by a hydrophilic sequence, the hydrocarbon chains possibly being pendant chains or chains at the end of a hydrophilic sequence. In particular, it is possible that one or more hanging chains are provided. In addition, the polymer may comprise a hydrocarbon chain at one end or at both ends of a hydrophilic block.

Polyether polyurethanes can be multiblock, in particular in triblock form. The hydrophobic blocks can be at each end of the chain (for example: triblock copolymer with a hydrophilic central block) or distributed both at the ends and in the chain (multiblock copolymer for example). These same polymers can also be in grafts or in stars.

The nonionic polyurethane polyethers with a fatty chain can be triblock copolymers whose hydrophilic sequence is a polyoxyethylenated chain comprising from 50 to 1000 oxyethylenated groups. Non-ionic polyether polyurethanes have a urethane bond between the hydrophilic sequences, hence the origin of the name.

By extension, non-ionic polyurethane polyethers with a fatty chain also include those whose hydrophilic sequences are linked to the lipophilic sequences by other chemical bonds.

As examples of nonionic polyether polyurethanes with a fatty chain that can be used in the invention, it is also possible to use Rhéolate 205® with a urea function sold by the company RHEOX or else Rhéolates® 208, 204 or 212, as well as Acrysol RM 184®.

Mention may also be made of _the product ELFACOS T210® with a C _12-14 alkyl chain and the product ELFACOS T212® with a C ₁₈ alkyl chain from AKZO.

The DW 1206B® product from ROHM & HAAS with a C ₂₀ alkyl chain and urethane bond, offered at 20% dry matter in water, can also be used.

It is also possible to use solutions or dispersions of these polymers, in particular in water or in an aqueous-alcoholic medium. By way of example, such polymers include RHEOLATE® 255, RHEOLATE® 278 and RHEOLATE® 244 sold by the company RHEOX. It is also possible to use the DW 1206F and DW 1206J products offered by ROHM & HAAS.

The polyurethane polyethers which 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).

More particularly still, it is preferred to use a polyether polyurethane capable of being obtained by polycondensation of at least three compounds comprising (i) at least one polyethylene glycol comprising from 150 to 180 moles of ethylene oxide, (ii) stearyl alcohol or decyl alcohol and (iii) at least one diisocyanate.

Such polyether polyurethanes are sold in particular by the company ROHM & HAAS under the names ACULYN 46® and ACULYN 44® [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 containing 150 or 180 moles of ethylene oxide, decyl alcohol and methylene bis(4-cyclohexylisocyanate) (SMDI), at 35% by weight in a mixture of propylene glycol ( 39%) and water (26%)].

Preferably, the associative polymer(s) are chosen from nonionic associative polymers and anionic associative polymers.

More preferably, the nonionic associative polymers are chosen from celluloses or their derivatives, modified with groups comprising at least one fatty chain such as alkyl, arylalkyl, alkylaryl groups or their mixtures where the alkyl groups are C ₈ -C ₃₀ and in particular nonionic alkylhydroxyethylcelluloses.

More preferably, the anionic associative polymer(s) are chosen from associative polymers with acrylic and/or methacrylic units, polymers with 2-acrylamido-2-methyl-propanesulfonic acid units and/or their salified form.

According to one embodiment of the invention, the anionic associative polymer(s) are chosen from copolymers comprising among their monomers an α,β-monoethylenically unsaturated carboxylic acid and an α,β-monoethylenically unsaturated carboxylic acid ester and d an oxyalkylenated fatty alcohol.

According to a preferred embodiment of the invention, the aqueous composition A comprises one or more associative polymers chosen from anionic associative polymers, nonionic associative polymers, and mixtures thereof; more preferably from (i) copolymers comprising among their monomers an α,β-monoethylenically unsaturated carboxylic acid and an ester of an α,β-monoethylenically unsaturated carboxylic acid and an oxyalkylenated fatty alcohol, (ii) celluloses or derivatives thereof, modified with groups comprising at least one fatty chain such as alkyl, arylalkyl, alkylaryl groups or mixtures thereof where the alkyl groups are C ₈ -C ₃₀ and in particular nonionic alkylhydroxyethylcelluloses, and (iii) their mixtures; more preferably still from acrylates/beheneth-25 methacrylate copolymer, cetyl hydroxyethylcellulose, and mixtures thereof.

Preferably, when the associative polymer(s) are present in the aqueous composition A, the total content of associative polymer(s) is between 0.01 and 10% by weight, more preferably between 0.05 and 5% by weight, and even more preferably between 0.1 and 2% by weight, relative to the total weight of the aqueous composition A.

The aqueous composition A according to the invention may optionally also comprise at least one cationic polymer different from the associative polymers described previously.

Preferably, the cationic polymer(s) can be chosen from:
(1) alkyl diallyl amine or dialkyl diallyl ammonium cyclopolymers such as homopolymers or copolymers comprising, as main constituent of the chain, units corresponding to formulas (I) or (II):

in which
- k and t are equal to 0 or 1, the sum k + t being equal to 1;
-R₁₂denotes a hydrogen atom or a methyl radical;
-R₁₀and R₁₁, independently of each other, denote a C alkyl group₁-VS₆, a C hydroxyalkyl group₁-VS₅, a C amidoalkyl group₁-VS₄; or R₁₀and R₁₁may denote, together with the nitrogen atom to which they are attached, a heterocyclic group such as piperidinyl or morpholinyl; R₁₀and R₁₁, independently of one another, preferably denote a C alkyl group₁-VS₄;
- Y^-is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate, phosphate.
Mention may more particularly be made of the homopolymer of salts (for example chloride) of dimethyldiallylammonium, for example sold under the name "MERQUAT 100" by the company NALCO, and the copolymers of salts (for example chloride) of diallyldimethylammonium and of acrylamide marketed in particular under the name "MERQUAT 550" or "MERQUAT 7SPR".
(2) diquaternary ammonium polymers comprising recurring units of the following formula (III):

in which:
-R₁₃, R₁₄, R₁₅and R₁₆, identical or different, represent aliphatic, alicyclic or arylaliphatic radicals comprising from 1 to 20 carbon atoms or C hydroxyalkylaliphatic radicals₁-VS₁₂,
or R₁₃, R₁₄, R₁₅and R₁₆, together or separately, constitute with the nitrogen atoms to which they are attached heterocycles optionally comprising a second heteroatom other than nitrogen
or R₁₃, R₁₄, R₁₅and R₁₆represent a C alkyl radical₁-VS₆linear or branched substituted by a nitrile, ester, acyl, amide or -CO-O-R group₁₇-D or -CO-NH-R₁₇-D where R₁₇is an alkylene and D a quaternary ammonium group;
- AT₁and B₁represent divalent polymethylene groups comprising from 2 to 20 carbon atoms, linear or branched, saturated or unsaturated, and which may contain, linked to or intercalated in the main chain, one or more aromatic rings, or one or more oxygen atoms, sulfur or sulfoxide, sulfone, disulfide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester groups; And
-X^-denotes an anion derived from a mineral or organic acid;
it being understood that A₁, R₁₃and R₁₅can form with the two nitrogen atoms to which they are attached a piperazine ring;
furthermore if A₁denotes a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene radical, B₁can also designate a group (CH₂)n-CO-D-OC-(CH₂)_p-, with n and p, identical or different, being integers ranging from 2 to 20, and D denoting:
a) a glycol residue of formula -O-Z-O-, where Z denotes a linear or branched hydrocarbon radical or a group corresponding to one of the following formulas: -(CH₂CH₂O)_x-CH₂CH₂- and -[CH₂CH(CH₃)O]_there-CH₂CH(CH₃)- where x and y denote an integer from 1 to 4, representing a defined and unique degree of polymerization or any number from 1 to 4 representing an average degree of polymerization;
b) a bis-secondary diamine residue such as a piperazine derivative;
c) a bis-primary diamine residue of formula -NH-Y-NH- where Y denotes a linear or branched hydrocarbon radical, or else the divalent radical -CH₂-CH₂-S-S-CH₂-CH₂-;
d) a ureylene group of formula -NH-CO-NH-.

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

Mention may more particularly be made of polymers which consist of recurring units corresponding to the formula:
(IV)
in which R ₁ , R ₂ , R ₃ and R ₄ , which are identical or different, denote an alkyl or hydroxyalkyl radical having from 1 to 4 carbon atoms, n and p are integers ranging from 2 to 20, and X ^- is an anion derived from a mineral or organic acid.

A compound consisting of units of formula (IV) which is particularly preferred is that for which R ₁ , R ₂ , R ₃ and R ₄ represent a methyl radical, n=3, p=6 and X=Cl, called Hexadimethrine chloride according to the nomenclature INCI (CTFA).

More preferentially, the cationic polymer(s) can be chosen from polyquaternium-6, hexadimethrine chloride, and mixtures thereof.

Preferably, when the cationic polymer(s) different from the associative polymers described above are present in the aqueous composition A, the total content of cationic polymer(s) is between 0.01 and 15% by weight, more preferably between 0.05 and 10% by weight, and even more preferably between 0.1 and 5% by weight, or even between 0.5 and 2% by weight relative to the total weight of the aqueous composition A.

The aqueous composition A which can be used in the process according to the present invention may optionally also comprise one or more additives such as nacres; fatty substances; vitamins or provitamins; surfactants, especially nonionic surfactants; pH stabilizers; curators; perfumes.

A person skilled in the art will take care to choose the possible additives and their quantity so that they do not harm the properties of the methods and compositions of the present invention.

These additives, when present, are generally present in the aqueous composition A according to the invention in an amount ranging from 0 to 20% by weight relative to the total weight of the aqueous composition A.

The aqueous composition A used in the process according to the present invention may optionally also comprise one or more organic solvents.

By way of organic solvent, mention may be made, for example, of alkanols, linear or branched, C ₂ to C ₄ , such as ethanol and isopropanol; glycerol; polyols and polyol ethers such as 2-butoxyethanol, propylene glycol, hexylene glycol, dipropylene glycol, propylene glycol monomethyl ether, monoethyl ether and diethylene glycol monomethyl ether, as well as aromatic alcohols or ethers such as benzyl alcohol or phenoxyethanol, and mixtures thereof.

The process

Advantageously, the process according to the invention comprises the mixing of a number N of solid particles as described previously when these are identical, or of several numbers N _x , identical or different, when the solid particles are different.
N and N _x are whole numbers greater than or equal to 1, and x is an index varying from 1 to n with n the number of solid particles of different types.
N and N _x are defined before using the ready-to-use composition, depending on the shade desired by the user and/or the user's specificities such as the pre-existing shade and/or the nature keratin fibers.

Preferably, the numbers N and N _x are defined by means of computer software.

More preferably, the method according to the invention comprises mixing a number N ₁ of solid particle(s) of a first type P1 as described previously with a number N ₂ of solid particle(s) ) of a second type P2 as described previously, N ₁ and N ₂ being whole numbers greater than or equal to 1 defined before the use of the ready-to-use composition, depending on the shade desired by the user and/or specific features of the user such as the pre-existing shade and/or the nature of the keratin fibres.

More preferably still, the numbers N ₁ and N ₂ are defined by means of computer software.

Thus, according to a particular preferred embodiment, the method according to the invention comprises the mixture of numbers N ₁ to N _n of solid particle(s) respectively of type P1 to Pn (with n representing an integer greater than or equal to 3), the numbers N ₁ to N _n being whole numbers greater than or equal to 1 defined before the use of the ready-to-use composition, depending on the shade desired by the user and/or specificities of the user such as the pre-existing shade and/or the nature of the keratin fibres.

More preferably according to this embodiment, the numbers N ₁ to N _n are defined by means of computer software.

According to one particular embodiment of the invention, the process for preparing the composition for dyeing keratin fibers according to the invention further comprises mixing said particles P with one or more solid particles of P'x type (with x representing an integer greater than 1, and preferably between 1 and 20, more preferably between 1 and 15, and even more preferably between 1 and 10) containing at least one Cx dye, in particular a single Cx dye, better still a single Cx oxidation dye precursor, preferably in a content of between 0.1 and 50% by weight relative to the total weight of the solid particle(s) of P'x type; said solid particle of type P'x corresponding to the solid particle Px previously described, unlike the content of dye(s) Cx.

By way of example of this particular embodiment of the invention, the process for preparing the composition for dyeing keratin fibers according to the invention may comprise the mixture:
(i) a number N1 of solid particles of a first type P1 containing at least one C1 dye, in particular a single C1 dye, better still a single C1 oxidation dye precursor, preferably in a content of between 0.1 and 50% by weight relative to the total weight of the solid particle(s) of type P1; with
(ii) a number N2 of solid particles of a second type P2 containing at least one C2 dye, in particular a single C1 dye, better still a single C2 oxidation dye precursor, preferably in a content of between 0.1 and 50% by weight relative to the total weight of the solid particle(s) of type P2; with
(iii) a number N′1 of solid particles of type P′1 containing only the said dye(s) C1, preferably in a content of between 0.1 and 50% by weight relative to the total weight of the solid particle(s) of type P′1; And
(iv) at least one aqueous composition comprising arginine;
Being heard that :
- Dye C1 is different from Dye C2;
- the content of dye C1 contained in the solid particle(s) P1 is different from the content of dye C1 contained in the solid particle(s) P'1;
- The numbers N1, N2 and N'1 designating whole numbers greater than or equal to 1, identical or different.

Preferably, the process according to the invention is implemented less than two hours, more preferably less than one hour, more preferably still less than 30 minutes, before the application to the keratin fibers of the composition resulting from said mixture.

According to a preferred embodiment of the invention, the process for preparing the composition for dyeing keratin fibers according to the invention comprises mixing:
(i) several solid particles, identical or different, each containing one or more dyes, as previously described; with
(ii) the aqueous composition A as previously described; And
(iii) one or more additional aqueous compositions different from said composition A.

According to another preferred embodiment of the invention, the process for preparing the composition for dyeing keratin fibers according to the invention comprises mixing:
- several solid particles, identical or different, each containing one or more dyes, as previously described; with
- at least one aqueous composition A comprising arginine and optionally one or more additional alkaline agents other than arginine, as previously described; And
- at least one aqueous composition B distinct from composition A comprising at least one chemical oxidizing agent, preferably chosen from those as described above, more preferably from hydrogen peroxide, persalts and mixtures thereof; and or
- at least one aqueous composition C distinct from composition A and from composition B comprising at least one associative polymer, preferably chosen from those as described above, more preferably from anionic and nonionic associative polymers as described above.

Preferably according to this embodiment, the content of arginine present in the aqueous composition A is between 0.05 and 25% by weight, more preferably between 0.1 and 15% by weight, more preferably still between 0.5 and 10% by weight, and even better between 1 and 5% by weight, relative to the total weight of the aqueous composition A.

Preferably according to this embodiment, when the additional alkaline agent(s) other than arginine are present in the aqueous composition A, the total content of additional alkaline agent(s) different from l arginine is between 0.05 and 25% by weight, more preferably between 0.1 and 20% by weight, and even more preferably between 0.5 and 15% by weight, relative to the total weight of the aqueous composition A .

Preferably according to this embodiment, the total content of chemical oxidizing agent(s) present in the aqueous composition B is between 0.1 and 35% by weight, more preferably between 0. 1 and 30% by weight, and even more preferably between 0.5 and 25% by weight, better still between 2 and 12% by weight relative to the total weight of the aqueous composition B.

Preferably according to this embodiment, the total content of associative polymer(s) present in the aqueous composition C is between 0.01 and 10% by weight, more preferably between 0.05 and 5% by weight, and even more preferably between 0.1 and 2% by weight, relative to the total weight of the aqueous composition C.

According to yet another preferred embodiment of the invention, the process for preparing the composition for dyeing keratin fibers according to the invention comprises mixing:
- one or more solid particles of type P1 and one or more solid particles of type P2 (and more generally one or more particles of type P1 to Pn), as previously described; with
- at least one aqueous composition A comprising arginine and optionally one or more additional alkaline agents other than arginine, as previously described; And
- at least one distinct aqueous composition B comprising at least one chemical oxidizing agent, preferably chosen from those as described above, more preferably from hydrogen peroxide, persalts and mixtures thereof; and or
- at least one distinct aqueous composition C comprising at least one associative polymer, preferably chosen from those as described above, more preferably from anionic and nonionic associative polymers as described above.

Preferably according to this embodiment, the content of arginine present in the aqueous composition A is between 0.05 and 25% by weight, more preferably between 0.1 and 15% by weight, more preferably still between 0.5 and 10% by weight, and even better between 1 and 5% by weight, relative to the total weight of the aqueous composition A.

Preferably according to this embodiment, when the additional alkaline agent(s) other than arginine are present in the aqueous composition A, the total content of additional alkaline agent(s) different from l arginine is between 0.05 and 25% by weight, more preferably between 0.1 and 20% by weight, and even more preferably between 0.5 and 15% by weight, relative to the total weight of the aqueous composition A .

Preferably according to this embodiment, the total content of chemical oxidizing agent(s) present in the aqueous composition B is between 0.1 and 35% by weight, more preferably between 0. 1 and 30% by weight, and even more preferably between 0.5 and 25% by weight, better still between 2 and 12% by weight relative to the total weight of the aqueous composition B.

Preferably according to this embodiment, the total content of associative polymer(s) present in the aqueous composition C is between 0.01 and 10% by weight, more preferably between 0.05 and 5% by weight, and even more preferably between 0.1 and 2% by weight, relative to the total weight of the aqueous composition C.

According to a particularly preferred variant of the invention, the process for preparing the composition for dyeing keratin fibers according to the invention comprises mixing:
- several solid particles, identical or different, each containing one or more dyes, as previously described; with
- at least one aqueous composition A comprising arginine, at least one aqueous composition B and at least one aqueous composition C, as previously described.

According to another particularly preferred variant of the invention, the process for preparing the composition for dyeing keratin fibers according to the invention comprises mixing:
- one or more solid particles of type P1 and one or more solid particles of type P2 (and more generally one or more particles P1 to Pn), as previously described; with
- at least one aqueous composition A, at least one aqueous composition B and at least one aqueous composition C, as previously described.

According to a variant of the present invention, the process for preparing the composition for dyeing keratin fibers according to the invention comprises mixing:
- several solid particles, identical or different, each containing one or more dyes, as previously described; with
- at least one aqueous composition D comprising:
To. at least one chemical oxidizing agent, preferably chosen from those as described above, more preferably from hydrogen peroxide, persalts and mixtures thereof, and
b. arginine.

Preferably according to this variant, the total content of chemical oxidizing agent(s) present in the aqueous composition D is between 0.1 and 35% by weight, more preferably between 0.1 and 30% by weight, and even more preferably between 0.5 and 25% by weight, better still between 2 and 12% by weight relative to the total weight of the aqueous composition D.

Preferably according to this variant, the content of arginine present in composition D is between 0.05 and 25% by weight, more preferably between 0.1 and 15% by weight, more preferably still between 0.5 and 10% by weight. weight, or even between 1 and 5% by weight, relative to the total weight of the aqueous composition D.

According to this variant, said solid particles comprise one or more solid particles of type P1 and one or more solid particles of type P2 (and more generally one or more particles P1 to Pn), as previously described.

According to another variant of the present invention, the process for preparing the composition for dyeing keratin fibers according to the invention comprises mixing:
- several solid particles, identical or different, each containing one or more dyes, as previously described; with
- at least one aqueous composition E comprising:
To. at least one chemical oxidizing agent, preferably chosen from those as described above, more preferably from hydrogen peroxide, persalts and mixtures thereof, and
b. arginine, and
vs. at least one associative polymer, preferably chosen from those as described above, more preferably from anionic and nonionic associative polymers as described above.

Preferably according to this variant, the total content of chemical oxidizing agent(s) present in the aqueous composition E is between 0.1 and 35% by weight, more preferably between 0.1 and 30% by weight, and even more preferably between 0.5 and 25% by weight, better still between 2 and 12% by weight relative to the total weight of the aqueous composition E.

Preferably according to this variant, the content of arginine present in the aqueous composition E is between 0.05 and 25% by weight, more preferably between 0.1 and 15% by weight, more preferably still between 0.5 and 10% by weight, or even between 1 and 5% by weight, relative to the total weight of the aqueous composition E.

Preferably according to this variant, the total content of associative polymer(s) present in the aqueous composition E is between 0.01 and 10% by weight, more preferably between 0.05 and 5% by weight. , and even more preferably between 0.1 and 2% by weight, relative to the total weight of the aqueous composition E.

According to this variant, said solid particles comprise one or more solid particles of type P1 and one or more solid particles of type P2 (and more generally one or more particles P1 to Pn), as previously described.

According to another particular embodiment of the invention, the method for preparing the composition for dyeing keratin fibers can also use one or more solid particles free of dye.

The mixing of the solid particles with the aqueous composition or compositions can be carried out by means of a mechanical stirrer, a magnetic stirrer, and/or by hand using, for example, a coloring brush.

The ready-to-use composition

The ready-to-use composition, or final composition, is obtained after said mixing of the solid particles described above with at least the aqueous composition A as described above.

Preferably, the water content of said ready-to-use composition is between 30 and 99% by weight; more preferably between 50 and 99% by weight, even better between 50 and 90% by weight, relative to the total weight of said ready-to-use composition.

Preferably, the arginine content present in said ready-to-use composition ranges from 0.001 to 20% by weight, more preferably from 0.05 to 10% by weight, more preferably still from 0.1 to 5% by weight, even better from 0.5 to 3% by weight, relative to the total weight of said ready-to-use composition.

Preferably, the total content of alkaline agent(s) present in said ready-to-use composition ranges from 0.001 to 30% by weight, more preferably from 0.05 to 20% by weight, more preferably still from 0.5 to 10% by weight, even better still from 1 to 5% by weight, relative to the total weight of said ready-to-use composition .

Preferably, when said ready-to-use composition comprises one or more chemical oxidizing agents, these are advantageously present in a total content ranging from 0.001 to 30% by weight, more preferably from 0.05 to 20% by weight. weight, and even more preferably from 0.1 to 15% by weight, better still from 1 to 10% by weight relative to the total weight of said ready-to-use composition .

Preferably, when said ready-to-use composition comprises one or more associative polymers, these are advantageously present in a total content ranging from 0.001 to 8% by weight, more preferably from 0.005 to 4% by weight, and more preferably still from 0.01 to 1% by weight, relative to the total weight of said ready-to-use composition.

Preferably, the weight ratio of the total mass of the ready-to-use composition on the one hand, to the total mass of solid particles on the other hand, is between 1 and 22, more preferably between 2 and 15 ; more preferably still between 5 and 12.

The ready-to-use composition can be in various forms, such as in the form of liquids, creams, gels, or in any other form suitable for performing coloring of keratin fibres, and in particular of human hair.

A subject of the invention is also a process for dyeing, preferably oxidation dyeing, keratin fibres, in particular human keratin fibers such as the hair, comprising:
- the preparation of a composition for dyeing keratin fibers according to the preparation process described above; Then
- the application to said keratin fibers of said composition obtained by the preparation process as described previously.

Preferably, the preparation of said composition for dyeing keratin fibers is carried out less than two hours, more preferably less than one hour, more preferably still less than 30 minutes, before the application to the keratin fibers of said composition for coloring.

A subject of the invention is also the use of the composition obtained by the preparation process as described above, for the coloring, preferably for the oxidation coloring, of keratin fibers, in particular human keratin fibers such as hair.

More particularly, the invention relates to the use of the composition, obtained by the preparation process comprising the mixture:
- several solid particles, identical or different, each containing one or more dyes, preferably one or more oxidation dye precursors, as previously described; with
- at least one aqueous composition A comprising arginine and optionally one or more additional alkaline agents other than arginine, as previously described; And
- at least one distinct aqueous composition B comprising at least one chemical oxidizing agent, preferably chosen from those as described above, more preferably from hydrogen peroxide, persalts and mixtures thereof; And
- at least one distinct aqueous composition C comprising at least one associative polymer, preferably chosen from those as described above, more preferably from anionic and nonionic associative polymers as described above;
for coloring keratin fibres, in particular human keratin fibers such as the hair.

The following examples serve to illustrate the invention without however being limiting.

Examples

The solid particles and the compositions below according to the present invention were prepared from the ingredients whose contents are indicated, in mass percentage of active ingredient relative to the total weight of the solid particle or of the composition, in the tables below. -below.

Examples of particles
Solid particle without an upper coating layer
Ingredients Quantity MICROCRYSTALLINE CELLULOSE 56 LACTOSE 15 PVP 4.75 MAGNESIUM STEARATE 2 SILICA 1 TOLUENE-2,5-DIAMINE SULPHATE 20 SODIUM SULPHITE 1 WATER 0.25

Examples of top cover layer
Ingredients Quantity Hydroxypropylmethyl Cellulose (HPMC) 45 to 55 Hydroxypropyl cellulose (HPC) 5 to 20 Capric/Caprylic Triglyceride 1 to 10 Talc Qsp 100 Pigments 0 to 40

Examples of solid particle with top coating layer
Ingredients Quantity MICROCRYSTALLINE CELLULOSE 54.4 LACTOSE 14.6 PVP 4.6 MAGNESIUM STEARATE 1.94 SILICA 1.0 TOLUENE-2,5-DIAMINE SULPHATE 19.4 SODIUM SULPHITE 1.0 WATER 0.2 HYDROXYPROPYL METHYLCELLULOSE 1.46 HYDROXYPROPYLCELLULOSE 0.29 TALC 0.44 CAPRYLIC/CAPRIC TRIGLYCERIDE 0.15 PIGMENTS 0.51 ALUMINA 0.01

Ingredients Quantity MICROCRYSTALLINE CELLULOSE 77.2 LACTOSE 14.6 PVP 0.1 MAGNESIUM STEARATE 1 SILICA 0.54 RESORCINOL 0.85 HYDROXYPROPYL METHYLCELLULOSE 1.45 HYDROXYPROPYLCELLULOSE 0.30 TALC 0.4 CAPRYLIC/CAPRIC TRIGLYCERIDE 0.15 PIGMENTS 0.5 ALUMINA 0.01 VP/VA COPOLYMER 2.9

Ingredients Quantity MICROCRYSTALLINE CELLULOSE 63.5 LACTOSE 9.7 PVP 0.1 MAGNESIUM STEARATE 1 SILICA 0.5 RESORCINOL 16.5 ASCORBIC ACID 2.9 HYDROXYPROPYL METHYLCELLULOSE 1.5 HYDROXYPROPYLCELLULOSE 0.3 TALC 0.44 CAPRYLIC/CAPRIC TRIGLYCERIDE 0.15 PIGMENTS 0.5 ALUMINA 0.01 VP/VA COPOLYMER 2.9

Ingredients Quantity MICROCRYSTALLINE CELLULOSE 76.2 LACTOSE 15.5 PVP 0.5 MAGNESIUM STEARATE 1.0 SILICA 1.0 2,4-DIAMINOPHENOXYETHANOL HYDROCHLORIDE 1.0 SODIUM METABISULPHITE 1.94 WATER 0.02 HYDROXYPROPYL METHYLCELLULOSE 1.45 HYDROXYPROPYLCELLULOSE 0.29 TALC 0.44 CAPRYLIC/CAPRIC TRIGLYCERIDE 0.15 PIGMENTS 0.5 ALUMINA 0.01

Ingredients Quantity MICROCRYSTALLINE CELLULOSE 69.4 LACTOSE 11.6 PVP 2.8 MAGNESIUM STEARATE 1.0 SILICA 0.5 m-AMINOPHENOL 7.8 SODIUM METABISULPHITE 3.9 WATER 0.15 HYDROXYPROPYL METHYLCELLULOSE 1.46 HYDROXYPROPYLCELLULOSE 0.29 TALC 0.44 CAPRYLIC/CAPRIC TRIGLYCERIDE 0.15 PIGMENTS 0.5 ALUMINA 0.01

Oxidizing composition
Ingredients Quantity (g) Hydrogen peroxide 12 Stabilizer, sequestrant Q's Phosphoric acid Qs pH = 2.2 ± 0.2 Water Qs 100

Alkaline composition 1
Ingredients Quantity Arginine 3 Ammonium hydroxide 2 Monoethanolamine 5.8 sodium metasilicate 2 Polyquaternium-6 2 Hexadimethrine chloride 1.2 EDTA 0.2 Hydroxypropyl methyl cellulose (HPMC) 0.2 Cetyl hydroxyethyl cellulose 0.45 PEG-40 Stearate 1.8 Oleth-30 1.5 Oleic acid 3 C ₂₀ -C ₂₂ fatty alcohols 3 Stearamide MEA 4.8 Steareth-2 5.5 Water Qsp 100

Alkaline composition 2
Ingredients Quantity Arginine 3 Monoethanolamine 5.8 sodium metasilicate 2 Polyquaternium-6 2 Hexadimethrine chloride 1.2 EDTA 0.2 Hydroxypropyl methyl cellulose (HPMC) 1.2 Cetyl hydroxyethyl cellulose 0.45 PEG-40 Stearate 1.8 Oleth-30 1.5 Oleic acid 3 C ₂₀ -C ₂₂ fatty alcohols 3 Stearamide MEA 4.8 Steareth-2 5.5 Water Qsp 100

Thickening composition
Ingredients Quantity Hydrogen peroxide 12 Cetearyl alcohol 8 Acrylates/Beheneth-25 methacrylate copolymer, under the reference Aculyn 28 from ROHM and HAAS 0.4 Ceteareth-33 2 sequestrants, stabilizers Q's Phosphoric acid Qs pH = 2.2 ± 0.2 Water Qsp 100

Process for coloring keratin fibers
A composition (M) for coloring keratin fibers is prepared in a bowl according to the following steps:
(1) 100 coated solid particles (i.e. 6g) according to table 4 above, 58 coated solid particles (i.e. 3.48g) according to table 6 above, 22 coated solid particles (i.e. 1.32g) according to table 5 above, 21 coated solid particles (i.e. 1.26 g) according to Table 7 above, and 14 coated solid particles (i.e. 0.84 g) according to Table 8 above, are mixed with 12 g of oxidizing composition according to Table 9 above and 36 g of water stabilized and adjusted to pH 2.2; then after at least 30 seconds
(2) the mixture obtained in step (1) is mixed with 24 g of thickening composition according to Table 12 above, 28.8 g of alkaline composition 1 according to Table 10 above and 19.2 g of alkaline composition 2 according to Table 11 above.

An aqueous composition (M), homogeneous in which the coated solid particles have dispersed in the composition, is thus obtained.

The composition (M) obtained is then applied to locks of 90% white natural Caucasian hair (locks of BN hair) at the rate of 10 g of composition (M) per 1 g of hair. After leaving on for 30 minutes at 27° C., the locks are rinsed, washed with a standard shampoo, rinsed again and then dried.

Results L, a, b:
The colorimetric data of each of the locks are then measured in the CIELab system with a DATA COLOR SF600X spectrophotometer (illuminant D65, angle 10° and specular component included). In this L* a* b* system, L* represents the brightness, a* indicates the green/red color axis and b* the blue/yellow color axis. The higher the value of L*, the lighter or less intense the color. Conversely, the lower the value of L*, the darker or more intense the color. The higher the value of a* the more red the shade and the higher the value of b* the more yellow the shade.

The increase in color on the hair therefore corresponds to the variation in coloring between the locks of colored BN hair and the locks of uncolored (ie untreated) BN hair, is measured by the ∆E according to the following equation:

In this equation, L*, a* and b* represent the values measured after coloring the BN hair and L ₀ *, a ₀ * and b ₀ * represent the values measured for the locks of untreated BN hair. The higher the value of ∆E, the better the color rise.

The results are grouped in the table below:
I* To* b* ΔE Strand of untreated BN hair 57.78 1.40 13.97 - Strand of treated BN hair 23.57 2.39 5.25 35.32

It appears from the results of the table that the keratin fibers treated with the composition (M) prepared according to the preparation process of the invention are colored intensely and with a good rise in color.

It has also been found that composition (M) is easy to produce and to distribute over the locks of hair, in particular without dripping.

Claims (25)

Process for the preparation of a composition for the coloring of keratin fibers comprising the mixture:

1. several solid particles, identical or different, each containing one or more dyes chosen from direct dyes and/or oxidation dye precursors; with
2. at least one aqueous composition A comprising arginine.

Process according to the preceding claim, characterized in that the said solid particles a) comprise:
- one or more solid particles of a first type P1 containing a single dye C1; And
- one or more solid particles of a second type P2 containing a single dye C2;
it being understood that the dye C1 is different from the dye C2. Process according to any one of the preceding claims, characterized in that the dye(s) is (are) chosen from oxidation dye precursors; preferably from oxidation bases and oxidation couplers; more preferentially among the oxidation bases. Process according to Claim 3, characterized in that the dye C1 is chosen from oxidation bases and the dye C2 is chosen from oxidation couplers. Process according to any one of Claims 3 or 4, characterized in that the oxidation base(s) is (are) chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases, and the corresponding addition salts; more preferably from para-phenylenediamine, para-toluenediamine, para-aminophenol, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 4,5-diamino-1-(β-hydroxyethyl)pyrazole, 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2-β-hydroxyethoxy-3-amino-pyrazolo[1,5-a] pyridine, and their addition salts. Process according to either of Claims 3 and 4, characterized in that the oxidation coupler is chosen from meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalene-based coupling agents, heterocyclic coupling compounds, and their corresponding addition salts or solvates; more preferably from 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 3-aminophenol, 6-hydroxybenzomorpholine, 5-N-(ß-hydroxyethyl)amino-2-methylphenol, 2, 4-diamino-1-(ß-hydroxyethyloxy)benzene, 2-methyl-5-aminophenol, 6-hydroxyindole, 4-chloro-1,3-dihydroxybenzene, 2-amino-3-hydroxypyridine, 3- amino-2-chloro-6-methylphenol, α-naphthol, 2-[3-amino-4-methoxyphenyl]amino)ethanol and their addition salts. Process according to any one of the preceding claims, characterized in that the total content of colorant(s) represents 0.001 to 50% by weight; preferably 0.1 to 50% by weight, more preferably 0.3 to 25% by weight; more preferably still 0.4 to 22% by weight, relative to the total weight of each solid particle containing it(these). A method according to any preceding claim, characterized in that the solid particles comprise at least one binding agent; preferably selected from saccharides and their derivatives, oligosaccharides and their derivatives, polysaccharides and their derivatives, polyvinyl alcohol (PVA), and mixtures thereof; more preferentially from lactose in particular in anhydrous or hydrated form, polyvinyl alcohol (PVA), microcrystalline cellulose (MCC) in particular in anhydrous or hydrated form, cellulose ethers such as hydroxypropyl cellulose (HPC) and hydroxypropylmethyl cellulose (HPMC), and mixtures thereof. Process according to the preceding claim, characterized in that the total content of binding agent(s) is greater than or equal to 30% by weight; preferably greater than or equal to 50% by weight; more preferably between 50% and 99.9% by weight, more preferably still between 60% and 99.9% by weight, even better between 70% and 99.9% by weight, relative to the total weight of each solid particle the container(s). A method according to any preceding claim, characterized in that the solid particle or particles comprise at least one disintegrating agent; preferably polymeric; more preferably still at least one disintegrating polymer; more preferably at least one superdisintegrating polymer; even better at least one superdisintegrating polymer chosen from crosslinked vinylpyrrolidone polymers and derivatives thereof, and mixtures thereof, more preferably from crosslinked polyvinylpyrrolidones, crosslinked vinylpyrrolidone/vinyl acetate copolymers, and mixtures thereof. Process according to the preceding claim, characterized in that the total content of disintegrating agent(s) is between 0.5 and 15% by weight; preferably between 1 and 12% by weight, more preferably between 2% and 10% by weight, relative to the total weight of each solid particle containing it(s). A method according to any preceding claim, characterized in that the solid particle(s) comprises at least one antioxidant agent; preferably chosen from (a) ascorbic acid, its salts and its derivatives such as sodium ascorbate, erythorbic acid, ascorbyl palmitate, ascorbyl laurate, (b) salicylic acid, its salts and its derivatives such as sodium salicylate, (c) mercaptans and inorganic sulphites such as sodium sulphite, sodium bisulphite, sodium metabisulphite, potassium sulphite and thioglycolic acid , and mixtures thereof; more preferably selected from ascorbic acid, sodium sulfite, sodium bisulfite, sodium metabisulfite, sodium salicylate, and mixtures thereof; more preferably still in a total content of between 0.1 and 15% by weight, better still between 0.3 and 12% by weight, even better between 0.4% and 10% by weight, or even between 0.5 and 5% by weight, relative to the total weight of each solid particle containing it(these). A method according to any preceding claim, characterized in that the solid particles comprise a top coating layer comprising at least one cellulose ether; preferably a cellulose ether chosen from carboxymethylcellulose (CMC), ethylcellulose (CE), hydroxypropylcellulose (HPC), hydroxypropylmethylcellulose (HPMC), methylhydroxyethylcellulose (MHEC), and mixtures thereof, better still from hydroxypropylcellulose (HPC), hydroxypropyl methylcellulose (HPMC), and mixtures thereof. Process according to the preceding claim, characterized in that the upper coating layer comprises one or more pigments; more preferably one or more pigments chosen from zirconium oxides, zinc oxides, cerium oxides, iron oxides, titanium oxides, chromium oxides, manganese violet, ultramarine blue, ultramarine pink , chromium hydrate and ferric blue, and mixtures thereof; more preferably still one or more pigments chosen from titanium oxides such as titanium dioxide, iron oxides, chromium oxides, in particular green chromium oxide, and mixtures thereof. Process according to any one of the preceding claims, characterized in that the solid particles are anhydrous. Process according to any one of the preceding claims, characterized in that the solid particles have an average volume of between 25 and 125 mm ³ ; preferably between 30 and 90 mm ³ ; more preferably between 45 and 65mm ³ . Process according to any one of the preceding claims, characterized in that the arginine content is between 0.05 and 25% by weight, preferably between 0.1 and 15% by weight, more preferably between 0.5 and 10 % by weight, more preferably still between 1 and 5% by weight, relative to the total weight of the aqueous composition A. Process according to any one of the preceding claims, characterized in that composition A comprises one or more additional alkaline agents, preferably chosen from ammonia, alkanolamines, alkali or alkaline earth metal metasilicates, and mixtures thereof; more preferably still from ammonia, monoethanolamine, sodium metasilicate, and mixtures thereof A method according to any preceding claim, characterized in that said aqueous composition A further comprises at least one chemical oxidizing agent; preferably chosen from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulphates, in particular sodium persulphate, potassium persulphate and ammonium persulphate, peracids and oxidase enzymes such as peroxidases, 2-electron oxido-reductases such as uricases and 4-electron oxygenases such as laccases, and mixtures thereof; more preferably, the chemical oxidizing agent(s) are chosen from hydrogen peroxide, persalts, and mixtures thereof. Process according to any one of the preceding claims, characterized in that the said aqueous composition A also comprises at least one associative polymer; preferably chosen from anionic associative polymers, nonionic associative polymers, and mixtures thereof; more preferably from (i) copolymers comprising among their monomers an α,β-monoethylenically unsaturated carboxylic acid and an ester of an α,β-monoethylenically unsaturated carboxylic acid and an oxyalkylenated fatty alcohol, (ii) celluloses or derivatives thereof, modified with groups comprising at least one fatty chain such as alkyl, arylalkyl, alkylaryl groups or mixtures thereof where the alkyl groups are C ₈ -C ₃₀ and in particular nonionic alkylhydroxyethylcelluloses, and (iii) their mixtures; more preferably still from acrylates/beheneth-25 methacrylate copolymer, cetyl hydroxyethylcellulose, and mixtures thereof. Process according to any one of Claims 1 to 18, characterized in that it comprises mixing:
- solid particles as defined in any one of claims 1 to 16; with
- at least one aqueous composition A comprising arginine, as defined in claims 1, 17 and 18; And
- at least one oxidizing composition B distinct from composition A comprising at least one chemical oxidizing agent, preferably chosen from those as defined in claim 19, more preferably from hydrogen peroxide, persalts and mixtures thereof; and or
- at least one aqueous composition C distinct from composition A and from composition B comprising at least one associative polymer, preferably chosen from those as defined in claim 20, more preferably from anionic and nonionic associative polymers. Process according to the preceding claim, characterized in that it comprises mixing:
- several solid particles as defined according to any one of claims 1 to 16; with
- at least one aqueous composition A, at least one oxidizing composition B and at least one aqueous composition C, as defined according to claim 21. Process for dyeing keratin fibers comprising:
- the preparation of a composition for dyeing keratin fibers according to the process as defined in claims 1 to 22; Then
- the application of said composition to said keratin fibers. Process according to the preceding claim, characterized in that the preparation of the said composition for coloring keratin fibers is carried out less than two hours, preferably less than one hour, more preferably less than 30 minutes, before the application to the keratin fibers of said composition. Use of the composition obtained by the process as defined in any one of Claims 1 to 22, for dyeing keratin fibres.