• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a composition for oxidative dyeing of keratin fibers, in particular human keratin fibers, more particularly hair, containing at least one oxidizing dye in a medium suitable for dyeing, wherein the at least one polyoxyalkylenated carboxylic acid ether or salt thereof And at least one quaternized cellulose comprising at least one fatty chain. The invention also relates to a dyeing apparatus and method using the composition.
    公开号:KR20030053458A
    申请号:KR1020020082105
    申请日:2002-12-21
    公开日:2003-06-28
    发明作者:드센느빠트리시아；브보세실；로랑플로랑스
    申请人:로레알；
    IPC主号:
    专利说明:

    COMPOSITION FOR THE OXIDATION DYEING OF KERATIN FIBRES, COMPRISING AN OXYALKYLENATED CARBOXYLIC ACID ETHER AND A FATTY-CHAIN QUATERNIZED CELLULOSE}
    [1] The present invention relates to a composition for oxidative dyeing of keratin fibers, in particular human keratin fibers, more particularly hair, containing at least one oxidizing dye in a medium suitable for dyeing, wherein the at least one polyoxyalkylenated carboxylic acid ether or salt thereof And at least one quaternized cellulose comprising at least one fatty chain.
    [2] The invention also relates to a dyeing apparatus and method using the composition.
    [3] Dyeing keratin fibres, especially human hair, with dye compositions containing oxidative dye precursors, commonly referred to as "oxidation bases", in particular ortho- and para-phenylenediamines, ortho- or para-aminophenols, and heterocyclic bases It is a known practice to do so.
    [4] Oxidation dye precursors are initially uncolored or only weakly colored compounds that exert dying power on the hair in the presence of an oxidizing agent to form colored compounds. Coloring modifications generally present in oxidative condensation or "oxidation bases" and dye compositions used for oxidative dyeing, in particular represented by meta-phenylenediamines, meta-aminophenols and meta-diphenols and certain heterocyclic compounds Or by oxidative condensation of a "coupler".
    [5] The various molecules that make up the "oxidation base" on the one hand and the "coupler" on the other hand allow a very wide range of colors to be obtained.
    [6] These oxidation bases and couplers are mixed with oxidants and then formulated in a vehicle or support that allows them to be applied to keratin fibers.
    [7] The vehicle is generally aqueous and usually contains one or more surfactants.
    [8] Accordingly, it has already been recommended to use anionic surfactants in combination with fatty chain quaternized cellulose. With this combination, an oxidative dye composition is produced which produces a color tone with very good dyeability. However, studies are continued for a support that can further improve the properties of the obtained coloring.
    [9] Accordingly, the Applicant has made considerable research on this issue and now introduces one or more polyoxyalkylenated carboxylic acid ethers or salts thereof into the dye composition as a substitute for fatty acids, thereby making it even more powerful and more dyeable. It has been found that an oxidized dye composition can be obtained which produces a hue that is present.
    [10] This finding forms the basis of the present invention.
    [11] One subject of the present invention is therefore one or more polyoxyalkylenated carboxyls in a composition for oxidative dyeing of keratin fibers, in particular human keratin fibers, more particularly hair, containing at least one oxidizing dye in a medium suitable for dyeing. And an at least one quaternized cellulose derivative comprising an acid ether or salt thereof and at least one fatty chain (C 8 -C 30 ).
    [12] The dye composition also makes it possible to provide a more transparent appearance to formulations containing and liquid.
    [13] The color tone obtained also has good fastness.
    [14] Another subject of the invention relates to ready-to-use compositions for oxidative dyeing of keratin fibers, containing one or more compositions and one or more oxidants described above in a medium suitable for dyeing.
    [15] For the purposes of the present invention, the expression "available immediately" means a composition intended for immediate application to keratin fibres, ie it can be stored before use without further modification, or instantaneously containing two or more compositions It can be obtained by mixing.
    [16] The invention also comprises a method for oxidative dyeing of keratin fibers, in particular human keratin fibers, such as hair, comprising applying a dye composition containing at least one oxidizing dye to a fiber in a medium suitable for dyeing, the color being used for dyeing. It is developed at an alkaline, neutral or acidic pH using an oxidizing composition comprising at least one oxidant which is mixed with the dye composition when used in a suitable medium or applied sequentially without intermediate rinsing, and the dye composition and the oxidizing composition are between the two. At least one polyoxyalkylenated carboxylic acid ether or salt thereof, and at least one quaternized cellulose derivative comprising at least one fatty chain (C 8 -C 30 ), which is randomly distributed at.
    [17] In one variation of the above methods, the quaternized cellulose derivative (s) comprising polyoxyalkylenated carboxylic acid ether (s) or salts thereof, and at least one fatty chain (C 8 -C 30 ) are the same dye composition. Or in an oxidizing composition, more particularly in a dye composition.
    [18] The subject matter of the present invention also includes one compartment comprising a dye composition containing at least one oxidizing dye in a medium suitable for dyeing, and another compartment comprising an oxidizing composition containing an oxidizing agent in a medium suitable for dyeing, and The dye composition and the oxidizing composition may also comprise one or more polyoxyalkylenated carboxylic acid ethers or salts thereof, and one or more fatty chains (C 8 -C 30 ), which are randomly distributed between them. Keratin fibres, especially human keratin fibres, and more particularly multicompartment dyeing apparatus or "kits" for containing oxidized cellulose derivatives.
    [19] In one device variant, the quaternized cellulose derivative (s) comprising polyoxyalkylenated carboxylic acid ether (s) or salts thereof, and one or more fatty chains (C 8 -C 30 ) are the same dye composition or In oxidizing compositions, more particularly in dye compositions.
    [20] However, other features, aspects, subjects and advantages of the present invention will become more apparent from the following description and examples.
    [21] Oxyalkylenated carboxylic acid ethers and salts thereof
    [22] The expression "oxyalkylenated carboxylic acid ether" means any compound of formula
    [23]
    [24] (In the meal,
    [25] R is a linear or branched C 8 -C 22 alkyl or alkenyl radical, or a mixture of radicals, a (C 8 -C 9 ) alkylphenyl radical or a radical R'CONH-CH 2 -CH 2- (wherein R ' Represents a linear or branched C 11 -C 21 alkyl or alkenyl radical,
    [26] n is an integer or a fraction ranging from 2 to 24,
    [27] p is an integer or a fraction ranging from 0 to 6,
    [28] A represents a hydrogen atom or a Na, K, Li, 1/2 Mg or monoethanolamine, ammonium or triethanolamine residue).
    [29] Oxyalkylenated carboxylic acid ethers and salts thereof preferably used according to the invention are those wherein R is a (C 12 -C 14 ) alkyl, oleyl, cetyl or stearyl radical or mixture of radicals; Nonylphenyl or octylphenyl radicals, A represents a hydrogen or sodium atom, p = 0 and selected from those of formula 1 wherein n ranges from 2-20, preferably 2-10.
    [30] Even more preferred are compounds of formula (1) wherein R represents a (C 12 ) alkyl radical, A represents a hydrogen or sodium atom, p = 0 and n is in the range of 2 to 10.
    [31] Among commercially available products that can be preferably used, those sold by Chem Y under the following trade names:
    [32] Akypo NP 70 (R = nonylphenyl, n = 7, p = 0, A = H)
    [33] Akypo NP 40 (R = nonylphenyl, n = 4, p = 0, A = H)
    [34] Akypo OP 40 (R = octylphenyl, n = 4, p = 0, A = H)
    [35] Akypo OP 80 (R = octylphenyl, n = 8, p = 0, A = H)
    [36] Akypo OP 190 (R = octylphenyl, n = 19, p = 0, A = H)
    [37] Akypo RLM 38 (R = (C 12 -C 14 ) alkyl, n = 3.8, p = 0, A = H)
    [38] Akypo RLM 38 NV (R = (C 12 -C 14 ) alkyl, n = 4, p = 0, A = Na)
    [39] Akypo RLM 45 (R = (C 12 -C 14 ) alkyl, n = 4.5, p = 0, A = H)
    [40] Akypo RLM 45 NV (R = (C 12 -C 14 ) alkyl, n = 4.5, p = 0, A = Na)
    [41] Akypo RLM 100 (R = (C 12 -C 14 ) alkyl, n = 10, p = 0, A = H)
    [42] Akypo RLM 100 NV (R = (C 12 -C 14 ) alkyl, n = 10, p = 0, A = Na)
    [43] Akypo RLM 130 (R = (C 12 -C 14 ) alkyl, n = 13, p = 0, A = H)
    [44] Akypo RLM 160 NV (R = (C 12 -C 14 ) alkyl, n = 16, p = 0, A = Na)
    [45] Akypo RO 20 (R = oleyl, n = 2, p = 0, A = H)
    [46] Akypo RO 90 (R = oleyl, n = 9, p = 0, A = H)
    [47] Akypo RCS 60 (R = cetyl / stearyl, n = 6, p = 0, A = H)
    [48] Akypo RS 60 (R = stearyl, n = 6, p = 0, A = H)
    [49] Akypo RS 100 (R = stearyl, n = 10, p = 0, A = H)
    [50] Akypo RO 50 (R = oleyl, n = 5, p = 0, A = H),
    [51] Or products marketed by Sandoz under the following trade names:
    [52] Sandopan ACA-48 (R = cetyl / stearyl, n = 24, p = 0, A = H)
    [53] Sandopan DTC-Acid (R = (C 13 ) alkyl, n = 6, p = 0, A = H)
    [54] Sandopan DTC (R = (C 13 ) alkyl, n = 6, p = 0, A = Na)
    [55] Sandopan LS 24 (R = (C 12 -C 14 ) alkyl, n = 12, p = 0, A = Na)
    [56] Sandopan JA 36 (R = (C 13 ) alkyl, n = 18, p = 0, A = H),
    [57] And more particularly products sold under the following trade names:
    [58] Akypo NP 70
    [59] Akypo NP 40
    [60] Akypo OP 40
    [61] Akypo OP 80
    [62] Akypo RLM 25
    [63] Akypo RLM 45
    [64] Akypo RLM 100
    [65] Akypo RO 20
    [66] Akypo RO 50
    [67] Akypo RLM 38.
    [68] The oxyalkylenated carboxylic acid ether or salt thereof represents about 2% to 15%, preferably about 3% to 10% of the total weight of the dye composition, and the total of ready-to-use dye compositions (including oxidants) About 0.5% to 15% by weight, preferably about 0.7% to 10% by weight.
    [69] Quaternized cellulose derivatives containing one or more fatty chains
    [70] Fatty chain quaternized cellulose derivatives according to the invention are cationic types of associative polymers.
    [71] Associative polymers are water-soluble polymers that can reversibly associate with other molecules in an aqueous medium.
    [72] Its chemical structure includes a hydrophilic zone and a hydrophobic zone (characterized by one or more fatty chains).
    [73] According to the invention, mention may be made especially of the above:
    [74] Quaternized celluloses modified with groups or mixtures thereof containing at least one fatty chain, such as alkyl, arylalkyl and alkylaryl groups having 8 to 30 carbon atoms,
    [75] Quaternized hydroxyethyl cellulose modified with one or more fatty chains, such as groups comprising alkyl, arylalkyl and alkylaryl groups having 8 to 30 carbon atoms or mixtures thereof.
    [76] The aryl radicals preferably represent phenyl, benzyl, naphthyl or anthryl groups.
    [77] Examples of alkyl hydroxyethyl celluloses quaternized with C 8 -C 30 fatty chains that can be represented include Quatrisoft LM 200, a commercially available product from Amerchol. , Quatrisoft LM-X 529-18-A , Quatrisoft LM-X 529-18B (C 12 alkyl), and Quatrisoft LM-X 529-8 (C 18 alkyl) and Crodacel QM, commercially available from Croda. , Crodacel QL (C 12 alkyl), and Crodacel QS (C 18 alkyl) is included.
    [78] A particularly preferred quaternized alkylhydroxyethyl cellulose comprising C 8 -C 30 fatty chains according to the invention is quaternized laurylhydroxyethyl cellulose.
    [79] Its weight concentration in the dye composition may range from about 0.01% to 10% of the total weight of the composition, and in ready-to-use compositions (including oxidants) from about 0.0025% to 10% of the total weight of the composition. More preferably, the amount is about 0.1% to 5% by weight of the dye composition and about 0.025% to 10% by weight of the ready-to-use composition.
    [80] Oxide dye
    [81] Oxidation dyes which can be used according to the invention are selected from oxidation bases and / or couplers.
    [82] The composition according to the invention preferably contains at least one oxidation base.
    [83] Oxidation bases that can be used within the scope of the present invention are selected from those commonly used in oxidative dyeing, among which in particular ortho- and para-phenylenediamines, complex bases, ortho- and para-aminophenols, the following heterosi Click bases, also acid addition salts thereof, may be mentioned.
    [84] In particular, mention may be made of:
    [85] - (I) to the formula (2) para-phenylenediamine, and its acid addition salts:
    [86]
    [87] (In the meal,
    [88] R 1 is a hydrogen atom, a C 1 -C 4 alkyl radical, a C 1 -C 4 monohydroxyalkyl radical, a C 2 -C 4 polyhydroxyalkyl radical, (C 1 -C 4 ) alkoxy (C 1 -C 4 ) Alkyl radicals, or C 1 -C 4 alkyl radicals substituted with nitrogen-containing phenyl or 4′-aminophenyl groups;
    [89] R 2 is a hydrogen atom, a C 1 -C 4 alkyl radical, a C 1 -C 4 monohydroxyalkyl radical, a C 2 -C 4 polyhydroxyalkyl radical, (C 1 -C 4 ) alkoxy (C 1 -C 4 ) Alkyl radicals, or C 1 -C 4 alkyl radicals substituted with nitrogen-containing groups;
    [90] In addition, R 1 and R 2 , together with the nitrogen atoms they contain, may form a 5- or 6-membered nitrogen heterocycle optionally substituted with one or more alkyl, hydroxyl or ureido groups;
    [91] R 3 is hydrogen atom, halogen atom such as chlorine atom, C 1 -C 4 alkyl radical, sulfo radical, carboxyl radical, C 1 -C 4 monohydroxyalkyl radical, C 1 -C 4 hydroxyalkoxy radical, acetyl Amino (C 1 -C 4 ) alkoxy radicals, mesylamino (C 1 -C 4 ) alkoxy radicals or carbamoylamino (C 1 -C 4 ) alkoxy radicals,
    [92] R 4 represents hydrogen or a halogen atom or a C 1 -C 4 alkyl radical).
    [93] Among the nitrogen-containing groups of Formula 2, in particular, amino, mono (C 1 -C 4 ) alkylamino, di (C 1 -C 4 ) alkylamino, tri (C 1 -C 4 ) alkylamino, monohydroxy ( C 1 -C 4 ) alkylamino, imidazolinium and ammonium radicals may be mentioned.
    [94] Among the para-phenylenediamine of Chemical Formula 2, more particularly, para-phenylenediamine, para-tolylenediamine, 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-amino-N, N-bis (β-hydroxyethyl) -2-methylaniline, 4-amino-N, N-bis (β-hydroxyethyl) -2-chloro Aniline, 2-β-hydroxyethyl-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 and 2-β-hydroxyethyloxy-para-phenylenediamine, 2-β-acetylaminoethyloxy-para-phenylenediamine, N- (β-methoxyethyl) -Para-phenylenediamine, 2-methyl-1-N-β-hydroxyethyl-para-phenylenediamine and N- (4-aminophenyl) -3-hydroxypyrrolidine, and acid addition salts thereof May be mentioned.
    [95] Among the para-phenylenediamines of the above formula, para-phenylenediamine, para-tolylene-diamine, 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, Most particularly preferred are N, N-bis (β-hydroxyethyl) -para-phenylenediamine and 2-chloro-para-phenylenediamine, and acid addition salts thereof.
    [96] -(II) According to the invention, the term complex base means a compound comprising at least two aromatic nuclei with amino and / or hydroxyl groups.
    [97] Among the complex bases which can be used as the oxidation base in the dye compositions according to the invention, mention may be made in particular of the compounds corresponding to the following formula (3), and acid addition salts thereof:
    [98]
    [99] (In the meal,
    [100] Z 1 and Z 2 represent the hydroxyl or —NH 2 radicals which may be the same or different and may be substituted with a C 1 -C 4 alkyl radical or a linking branch Y;
    [101] The linking branch Y may be inserted or terminated with one or more nitrogen-containing groups and / or one or more heteroatoms (eg, oxygen, sulfur or nitrogen atoms), and comprises one or more hydroxyl or C 1 -C 6 alkoxy radicals Linear or branched alkylene chains having 1 to 14 carbon atoms which may be optionally substituted by;
    [102] R 5 and R 6 represent a hydrogen atom, a halogen atom, a C 1 -C 4 alkyl radical, a C 1 -C 4 monohydroxyalkyl radical, a C 2 -C 4 polyhydroxyalkyl radical, a C 1 -C 4 aminoalkyl A radical or a linking branch Y;
    [103] R 7 , R 8 , R 9 , R 10 , R 11 and R 12 may be the same or different and represent a hydrogen atom, a linking branch Y or a C 1 -C 4 alkyl radical;
    [104] Compounds of formula 3 are understood to contain only one linking branch Y per molecule).
    [105] Among the nitrogen-containing groups of formula 3, in particular amino, mono (C 1 -C 4 ) alkylamino, di (C 1 -C 4 ) alkylamino, tri (C 1 -C 4 ) alkylamino, monohydroxy (C Mention may be made of the 1- C 4 ) alkylamino, imidazolinium and ammonium radicals.
    [106] Among the complex bases of the general formula (3), more particularly, 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) -3,5-dioxaoctane, and its Acid addition salts may be mentioned.
    [107] In the complex base of Formula 3, N, N'-bis (β-hydroxyethyl) -N, N'-bis (4'-aminophenyl) -1,3-diaminopropanol and 1,8-bis ( Particularly preferred is 2,5-diaminophenoxy) -3,5-dioxaoctane, or one of its acid addition salts.
    [108] -(III) Para-aminophenols corresponding to Formula 4, and acid addition salts thereof:
    [109]
    [110] (In the meal,
    [111] R 13 is a hydrogen atom, a halogen atom such as fluorine, or C 1 -C 4 alkyl, C 1 -C 4 monohydroxyalkyl, (C 1 -C 4 ) alkoxy (C 1 -C 4 ) alkyl, C 1- C 4 aminoalkyl or hydroxy (C 1 -C 4 ) alkylamino (C 1 -C 4 ) alkyl radicals,
    [112] R 14 is a hydrogen atom, a halogen atom such as fluorine, or C 1 -C 4 -alkyl, C 1 -C 4 monohydroxyalkyl, C 2 -C 4 polyhydroxyalkyl, C 1 -C 4 aminoalkyl, C 1 -C 4 cyanoalkyl or (C 1 -C 4 ) alkoxy (C 1 -C 4 ) alkyl radical).
    [113] Among the para-aminophenols of the general formula (4), more particularly para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 4-amino-3-hydroxymethylphenol, 4- Amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol and 4-amino-2- (β-hydroxy Ethylaminomethyl) phenol, and acid addition salts thereof, may be mentioned.
    [114] -(IV) Ortho-aminophenols that can be used as the oxidizing base within the scope of the present invention are in particular 2-aminophenol, 2-amino-1-hydroxy-5-methylbenzene, 2-amino-1-hydroxy-6-methylbenzene And 5-acetamido-2-aminophenol, and acid addition salts thereof.
    [115] - (V) it may be mentioned among the heterocyclic base which can be used as oxidation base, more particularly pyridine derivatives, pyrimidine derivatives and pyrazole derivatives and their acid addition salts in the dye compositions according to the invention.
    [116] Among the pyridine derivatives, more particularly, the compounds described in, for example, the patents GB 1 026 978 and GB 1 153 196, such as 2,5-diaminopyridine, 2- (4-methoxyphenyl) amino-3-aminopyridine , 2,3-diamino-6-methoxypyridine, 2- (β-methoxyethyl) amino-3-amino-6-methoxypyridine and 3,4-diaminopyridine, and acid addition salts thereof can do.
    [117] Among the pyrimidine derivatives, more particularly compounds described in, for example, German patent DE'2'359'399 or Japanese patents JP'88-169'571 and JP 91-10659 or patent application WO 96/15765, such as 2,4,5,6 Tetraaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6- Diaminopyrimidines and 2,5,6-triaminopyrimidines may be mentioned and pyrazolopyrimidine derivatives such as those mentioned in patent application FR-A-2 750 048, among which pyrazolo [1,5- a] pyrimidine-3,7-diamine; 2,5-dimethylpyrazolo [1,5-a] pyrimidine-3,7-diamine; Pyrazolo [1,5-a] pyrimidine-3,5-diamine; 2,7-dimethylpyrazolo [1,5-a] pyrimidine-3,5-diamine; 3-aminopyrazolo [1,5-a] pyrimidin-7-ol; 3-aminopyrazolo [1,5-a] pyrimidin-5-ol; 2- (3-aminopyrazolo [1,5-a] pyrimidin-7-ylamino) ethanol; 2- (7-aminopyrazolo [1,5-a] pyrimidin-3-ylamino) ethanol; 2-[(3-aminopyrazolo [1,5-a] pyrimidin-7-yl) (2-hydroxyethyl) amino] ethanol, 2-[(7-aminopyrazolo [1,5-a] Pyrimidin-3-yl) (2-hydroxyethyl) amino] ethanol; 5,6-dimethylpyrazolo [1,5-a] pyrimidine-3,7-diamine; 2,6-dimethylpyrazolo [1,5-a] pyrimidine-3,7-diamine; 2,5, N7, N7-tetramethylpyrazolo [1,5-a] pyrimidine-3,7-diamine and 3-amino-5-methyl-7-imidazolylpropylamino-pyrazolo [1,5 -a] pyrimidine, and addition salts thereof, and tautomeric forms thereof and acid addition salts thereof, when tautomeric equilibrium is present.
    [118] Among the pyrazole derivatives, more particularly compounds described in patent DE 3 843 892, DE 4 133 957 and patent applications WO 94/08969, WO 94/08970, FR-A-2 733 749 and DE 및 195 43 988, such as 4 , 5-diamino-1-methylpyrazole, 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-methyl-pyrazole, 4,5-diamino -1-tert-butyl-3-methylpyrazole, 4,5-diamino-1- (β-hydroxyethyl) -3-methylpyrazole, 4,5-diamino-1- (β-hydroxy Ethyl) pyrazole, 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-diami -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 and 3 , 5-diamino-4- (β-hydroxyethyl) amino-1-methylpyrazole, and acid addition salts thereof may be mentioned.
    [119] According to the invention, the oxidizing base preferably represents approximately 0.0005% to 12% by weight relative to the total weight of the composition containing no oxidizing agent, even more preferably approximately 0.005% to 8% by weight relative to the weight. Indicates.
    [120] Couplers that can be used in the dye compositions according to the invention are those conventionally used in oxidative dye compositions, ie meta-aminophenol, meta-phenylenediamine and meta-diphenol, naphthol and heterocyclic couplers, for example Indole derivatives, indolin derivatives, sesamol and derivatives thereof, pyridine derivatives, pyrazolotriazole derivatives, pyrazolone, indazole, benzimidazole, benzothiazole, benzoxazole, 1,3-benzodioxol and quinoline, and Its acid addition salts.
    [121] The couplers are more particularly 2,4-diamino-1- (β-hydroxyethyloxy) benzene, 2-methyl-5-aminophenol, 5-N- (β-hydroxyethyl) amino-2-methyl Phenol, 3-aminophenol, 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 4-chloro-1,3-dihydroxybenzene, 2-amino-4- (β -Hydroxyethylamino) -1-methoxybenzene, 1,3-diaminobenzene, 1,3-bis (2,4-diaminophenoxy) propane, sesamol, 1-amino-2-methoxy- 4,5-methylenedioxybenzene, α-naphthol, 6-hydroxyindole, 4-hydroxyindole, 4-hydroxy-N-β-hydroxyethylindole, 6-hydroxyindolin, 2,6- Dihydroxy-4-methylpyridine, 1H-3-methylpyrazol-5-one, 1-phenyl-3-methylpyrazole-5-one, 2-amino-3-hydroxypyridine, 3,6-dimethyl Selected from pyrazolo [3,2-c] -1,2,4-triazole and 2,6-dimethylpyrazolo [1,5-b] -1,2,4-triazole, and acid addition salts thereof do.
    [122] If they are present, these couplers preferably represent from about 0.0001% to 10% by weight, even more preferably from about 0.005% to 5% by weight relative to the total weight of the composition containing no oxidizing agent.
    [123] In general, the acid addition salts of the oxidizing base and the coupler are especially chosen from hydrochloride, hydrobromide, sulphate, tartrate, lactate and acetate.
    [124] In addition, the dye compositions according to the invention may contain one or more direct dyes, in particular in order to modify the color tone or to enrich it with gloss. In particular, the direct dye is a neutral, cationic or anionic nitro dye, azo dye or anthraquinone dye which is commonly used in a weight ratio of about 0.001% to 20%, preferably 0.01% to 10% of the total weight of the composition. Or those described in patent applications FR-2 782 450, 2 782 451, 2 782 452 and EP-1 025 834.
    [125] Ready-to-use compositions according to the invention can be prepared in the dye compositions and / or oxidizing compositions for preparation of fluidity, such as any oxyethylenated fatty acid amides (coconut monoethanolamide or diethanolamide, oxyethylenated carboxylic acid alkyl ether mono). Ethanolamide), cellulose thickener (hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, etc.), guar gum and derivatives thereof (hydroxypropyl guar, etc.), gums of bacterial origin (xanthan gum, scleroglucan gum, etc.) ), Cross-linked homopolymers of acrylic acid or acrylamidopropanesulfonic acid, and other associative polymers of the anionic, nonionic, amphoteric or cationic type which are different from the fatty chain quaternized cellulose derivatives of the invention and described below. have.
    [126] Associative polymers of anionic type:
    [127] Among the above, mention may be made of:
    [128] (I) comprising at least one hydrophilic unit and at least one fatty chain allyl ether unit, more particularly the hydrophilic unit being an ethylenically unsaturated anionic monomer, more particularly vinylcarboxylic acid, most particularly acrylic acid or methacrylic acid or Consisting of a mixture of these, their fatty chain allyl ether units correspond to monomers of the formula
    [129] CH 2 = CR'CH 2 OB n R
    [130] (Wherein R 'represents H or CH 3 , B represents an ethyleneoxy radical, n represents 0 or an integer ranging from 1 to 100, R represents 8 to 30 carbon atoms, preferably 10 to 24, Even more particularly hydrocarbon-based radicals selected from 12 to 18 alkyl, arylalkyl, aryl, alkylaryl and cycloalkyl radicals). More particularly preferred units of formula (5) are those wherein R 'represents H, n is 10 and R represents a stearyl ( C18 ) radical.
    [131] Anionic associative polymers of this type are described and prepared according to the emulsion polymerization method in patent EP-0 216 479.
    [132] Among the anionic associative polymers particularly preferred according to the invention, from 20% to 60% by weight of acrylic acid and / or methacrylic acid, from 5% to 60% by weight of lower alkyl (meth) acrylate, from 2% by weight 50% by weight of fatty chain allyl ether of formula 5, and 0% by weight to 1% by weight of a crosslinking agent which is a well known copolymerizable unsaturated polyethylene based monomer such as diallyl phthalate, allyl (meth) acrylate, divinylbenzene, Polymers formed from (poly) ethylene glycol dimethacrylate or methylenebisacrylamide.
    [133] Of the latter polymers, most particularly preferred are crosslinked terpolymers of methacrylic acid, ethyl acrylate and polyethylene glycol (10 EO) stearyl ether (Steareth-10), in particular methacrylic acid, ethyl acrylate And Allied Colloids Saga trade name Salcare SC 80, which is a 30% aqueous emulsion of a crosslinked terpolymer of stearet-10 allyl ether (40/50/10) And Salcare SC 90 Are commercially available.
    [134] (II) at least one hydrophilic unit of the unsaturated olefinic carboxylic acid type and at least one hydrophobic unit of the (C 10 -C 30 ) alkyl ester of the unsaturated carboxylic acid type.
    [135] Preferably, the polymer is selected from those in which the hydrophilic units of the unsaturated olefinic carboxylic acid type correspond to monomers of the general formula:
    [136]
    [137] Wherein R 1 represents H or CH 3 or C 2 H 5 (ie, acrylic acid, methacrylic acid or ethacrylic acid units), wherein a (C 10 -C 30 ) alkyl ester of the unsaturated carboxylic acid type The hydrophobic unit of corresponds to the monomer of formula
    [138]
    [139] Wherein R 2 is H or CH 3 or C 2 H 5 (ie acrylate, methacrylate or acrylate units), preferably H (acrylate units) or CH 3 (methacrylate units) R 3 represents a C 10 -C 30 , preferably C 12 -C 22 alkyl radical).
    [140] (C 10 -C 30 ) alkyl esters of unsaturated carboxylic acids according to the invention include, for example, lauryl acrylate, stearyl acrylate, decyl acrylate, isodecyl acrylate and dodecyl acrylate, and corresponding Methacrylates, lauryl methacrylates, stearyl methacrylates, decyl methacrylates, isodecyl methacrylates and dodecyl methacrylates.
    [141] Anionic polymers of this type are described and prepared according to, for example, US Pat. Nos. 3 915 921 and 4 509 949.
    [142] More particularly among the above types of anionic associative polymers to be used are polymers formed from monomer mixtures comprising:
    [143] (i) essentially acrylic acid,
    [144] (ii) an ester of formula (7) wherein R 2 represents H or CH 3 and R 3 represents an alkyl radical having 12 to 22 carbon atoms; and
    [145] (iii) Crosslinking agents which are well known copolymerizable polyethylene-based unsaturated monomers such as diallyl phthalate, allyl (meth) acrylate, divinylbenzene, (poly) ethylene glycol dimethacrylate and methylenebisacrylamide.
    [146] More particularly among the anionic association polymers of this type to be used, 95% to 60% by weight of acrylic acid (hydrophilic units), 4% to 40% by weight of C 10 -C 30 alkyl acrylates (hydrophobic units) and 0% by weight Consisting of% to 6% by weight of crosslinkable polymerizable monomer, or alternatively 98% to 96% by weight of acrylic acid (hydrophilic unit), 1% to 4% by weight of C 10 -C 30 alkyl acrylate (hydrophobic unit) ) And 0.1% to 0.6% by weight of crosslinkable copolymerizable monomers such as those described above.
    [147] Among the above polymers, the most particularly preferred according to the invention is the Goodrich company under the trade name Pemulen TR1 , Pemulen TR2 And Carbopol 1382 , Even more preferably Pemulen TR1 Marketed by, and SEPPIC Corporation trade name Coatex SX It is a commercially available product.
    [148] (III) maleic anhydride / C 30 -C 38 α-olefin / alkyl maleate terpolymer, such as Newphase Technologies, Inc. tradename Performa V 1608 Commercially available product (maleic anhydride / C 30 -C 38 α-olefin / isopropyl maleate copolymer).
    [149] (IV) an acrylic terpolymer comprising:
    [150] (a) about 20% to 70% by weight of a carboxylic acid containing an α, β-monoethylenically unsaturated group,
    [151] (b) about 20% to 80% by weight of a non-surfactant monomer containing an α, β-monoethylenically unsaturated group other than (a),
    [152] (c) those described in patent EP-A-0 173 109, more particularly the terpolymers described in Example 3, ie methacrylic acid / methyl acrylate / behenyl dimethyl-meth-isopropenyl which is a 25% aqueous dispersion Nonionic monourethane, about 0.5% to 60% by weight, of a reaction product of a monoisocyanate containing monoethylenically unsaturated groups with a monovalent surfactant such as a benzyl isocyanate ethoxylated (40 EO) terpolymer.
    [153] (V) copolymers comprising, among monomers, carboxylic acids containing α, β-monoethylenically unsaturated groups and esters of carboxylic acids containing α, β-monoethylenically unsaturated groups with oxyalkylenated fatty alcohols .
    [154] Preferably, the compound also comprises esters of C 1 -C 4 alcohols with carboxylic acids containing α, β-monoethylenically unsaturated groups as monomers.
    [155] Examples of compounds of this type that may be mentioned include Aculyn 22 sold by Rohm & Haas, a methacrylic acid / ethyl acrylate / stearyl methacrylate oxyalkylenated terpolymer. There is this.
    [156] Associative Polymer of Cationic Type
    [157] Among the above, mention may be made of:
    [158] (I) the applicant's French patent application No. A cationic associative polyurethane belonging to the group described in 0 009 609 and represented by the following formula (8):
    [159] RX- (P) n- [L- (Y) m ] r -L '-(P') p -X'-R '(Ia)
    [160] (In the meal,
    [161] R and R 'may be the same or different and represent a hydrophobic group or a hydrogen atom;
    [162] X and X 'may be the same or different and represent an amine functional group-containing group optionally containing a hydrophobic group, or alternatively an L ″ group;
    [163] L, L 'and L "may be the same or different and represent a group derived from diisocyanate;
    [164] P and P 'may be the same or different and represent a group containing an amine functional group optionally containing a hydrophobic group;
    [165] Y represents a hydrophilic group;
    [166] r is an integer from 1 to 100, preferably from 1 to 50, in particular from 1 to 25;
    [167] n, m and p are each, independently of each other, in the range of 0 to 1000;
    [168] Molecules have one or more protonated or quaternized amine functional groups and one or more hydrophobic groups).
    [169] In one preferred embodiment of the polyurethane, the sole hydrophobic group is the R and R 'groups at the chain ends.
    [170] One preferred group of cationic associating polyurethanes corresponds to Formula 8 above:
    [171] R and R 'both independently represent a hydrophobic group,
    [172] X and X 'each represent an L "group,
    [173] n and p are from 1 to 1000,
    [174] L, L ', L ", P, P', Y and m have the same meaning as above.
    [175] Another preferred group of cationic associating polyurethanes corresponds to Formula 8 above:
    [176] R and R 'are both independently hydrophobic groups,
    [177] X and X 'are each L "groups,
    [178] n and p are 0,
    [179] L, L ', L ", Y and m have the same meaning as above.
    [180] The fact that n and p are zero means that the polymer does not comprise units derived from amine functional group containing monomers incorporated into the polymer during the polycondensation process. The protonated amine functional groups of the polyurethanes undergo hydrolysis of excess isocyanate functional groups at the chain ends, followed by alkylating agents containing hydrophobic groups, ie RQ or R'Q, wherein R and R 'are as defined above and , Q represents a leaving group such as halide, sulphate, etc.) is obtained from alkylation of a primary amine functional group formed of a group of compounds of the type.
    [181] However, another preferred group of cationic associating polyurethanes corresponds to the formula
    [182] R and R 'both independently represent a hydrophobic group,
    [183] X and X 'both independently represent a group containing a quaternary amine group,
    [184] n and p are 0,
    [185] L, L ', Y and m have the same meanings given above.
    [186] The number average molecular mass of the cationic associative polyurethane is preferably 400 to 500,000, in particular 1000 to 400,000, ideally 1000 to 300,000.
    [187] The expression “hydrophobic group” refers to a radical or polymer comprising a saturated or unsaturated, linear or branched hydrocarbon chain, or a perfluoro or silicone chain, which may comprise one or more heteroatoms such as P, O, N or S. It means the radical containing. When the hydrophobic group represents a hydrocarbon radical, it is 10 or more carbon atoms, preferably 10 to 30 carbon atoms, in particular 12 to 30 carbon atoms, more preferably 18 to 30 carbon atoms.
    [188] Preferably, the hydrocarbon-based group is derived from a monofunctional compound.
    [189] For example, hydrophobic groups can be derived from fatty alcohols such as stearyl alcohol, dodecyl alcohol or decyl alcohol. It may also represent hydrocarbon-based polymers such as polybutadiene.
    [190] When X and / or X 'represents a group comprising tertiary or quaternary amines, X and / or X' may represent one of the following formulas:
    [191] For X
    [192]
    [193] For X '
    [194]
    [195] (In the meal,
    [196] R 2 represents a linear or branched alkylene radical having 1 to 20 carbon atoms, or an arylene radical, optionally containing a saturated or unsaturated ring, wherein at least one of the carbon atoms is possibly from N, S, O and P May be replaced with a hetero atom selected;
    [197] R 1 and R 3 may be the same or different and represent a linear or branched C 1 -C 30 alkyl or alkenyl radical or an aryl radical, and at least one of the carbon atoms is possibly N, S, O and P Can be replaced with a hetero atom selected from;
    [198] A - is a physiologically acceptable counterion).
    [199] L, L 'and L "groups represent groups of the formula
    [200]
    [201] (In the meal,
    [202] Z represents -O-, -S- or -NH-;
    [203] R 4 represents a linear or branched alkylene radical having 1 to 20 carbon atoms, or an arylene radical, optionally containing a saturated or unsaturated ring, wherein at least one of the carbon atoms is possibly from N, S, O and P May be replaced with a hetero atom of choice).
    [204] P and P 'groups containing amine functional groups may represent one or more of the following formulas:
    [205]
    [206] (In the meal,
    [207] R 5 and R 7 have the same meanings as defined above for R 2 ;
    [208] R 6 , R 8 and R 9 have the same meanings as defined above for R 1 and R 3 ;
    [209] R 10 represents a linear or branched optionally unsaturated alkylene group, which may contain one or more hetero atoms selected from N, O, S and P,
    [210] A - is a physiologically acceptable counterion).
    [211] For the meaning of Y, the term "hydrophilic group" means a polymeric or nonpolymeric water soluble group.
    [212] For example, if it is not a polymer, mention may be made of ethylene glycol, diethylene glycol and propylene glycol.
    [213] If it is a hydrophilic polymer, mention may be made, for example, of polyethers, sulfonated polyesters, sulfonated polyamides or mixtures of these polymers, according to one preferred embodiment. Hydrophilic compounds are preferably polyethers, in particular poly (ethylene oxide) or poly (propylene oxide).
    [214] According to the present invention, cationic associative polyurethanes of formula (8) are formed from various compounds having diisocyanates and functional groups containing unstable hydrogen. The labile hydrogen-containing functional group may be an alcohol, primary or secondary amine or thiol functional group which, after reaction with the diisocyanate functional group, generates diisocyanate functional groups, polyurethanes and polyureas, respectively. The term "polyurethane" in the present invention encompasses three types of polymers: polyurethane itself, polyurea and polythiourea, and copolymers thereof.
    [215] Compounds of the first type which relate to the preparation of the polyurethanes of formula (8) are compounds comprising at least one unit with amine functionality. The compound may be multifunctional, but is preferably bifunctional, ie according to one preferred embodiment, the compound has two labile hydrogen atoms, which is for example hydroxyl, primary amine, secondary amine Or a thiol functional group. Mixtures of multifunctional and bifunctional compounds with low percentages of multifunctional compounds may also be used.
    [216] As mentioned above, the compound may comprise more than one unit containing an amine function. In this case, it is a polymer which repeats the unit containing an amine functional group.
    [217] Compounds of this type may be represented by one of the following formulas:
    [218] HZ- (P) n -ZH
    [219] or
    [220] HZ- (P ') p -ZH
    [221] Wherein Z, P, P ', n and p are as defined above.
    [222] Examples of compounds containing amine functional groups which may be mentioned include N-methyldiethanolamine, N-tert-butyldiethanolamine and N-sulfoethyldiethanolamine.
    [223] A second compound involved in the preparation of the polyurethane of formula 8 is a diisocyanate corresponding to the formula
    [224] O = C = NR 4 -N = C = O
    [225] Wherein R 4 is as defined above.
    [226] Methylenediphenyl diisocyanate, methylenecyclohexane diisocyanate, isophorone diisocyanate, toluene diisocyanate, naphthalene diisocyanate, butane diisocyanate and hexane diisocyanate may be mentioned.
    [227] The third compound involved in the preparation of the polyurethane of formula (8) is a hydrophobic compound for the purpose of forming terminal hydrophobic groups of the polymer of formula (8).
    [228] These compounds consist of hydrophobic groups and unstable hydrogen-containing functional groups such as hydroxyl, primary or secondary amines, or thiol functional groups.
    [229] For example, this compound may be a fatty alcohol such as in particular stearyl alcohol, dodecyl alcohol or decyl alcohol. If this compound comprises a polymeric chain, it may be for example α-hydroxylated hydrogenated polybutadiene.
    [230] Hydrophobic groups of the polyurethanes of formula 8 may also be obtained from quaternization of tertiary amines of compounds comprising at least one tertiary amine unit. Thus, hydrophobic groups are introduced via quaternization agents. The quaternization agent is a compound of the type RQ or R'Q, wherein R and R 'are as defined above and Q represents a leaving group such as halide, sulfate and the like.
    [231] Cationic associating polyurethanes may also include hydrophilic blocks. This block is provided by a fourth type of compound involved in the preparation of the polymer. This compound may be multifunctional. It is preferably bifunctional. It may also have a low percentage mixture of polyfunctional compounds.
    [232] The labile hydrogen containing functional group is an alcohol, primary or secondary amine or thiol functional group. This compound may be a polymer terminated at one of the above functional groups containing unstable hydrogen at the chain end.
    [233] For example, if it is not a polymer, mention may be made of ethylene glycol, diethylene glycol and propylene glycol.
    [234] If it is a hydrophilic polymer, mention may be made, for example, of polyethers, sulfonated polyesters and sulfonated polyamides, or mixtures of these polymers. Hydrophilic compounds are preferably polyethers, in particular poly (ethylene oxide) or poly (propyleneoxide).
    [235] In the formula (8), the hydrophilic group referred to as Y is optional. In particular, units containing protonated functional groups or quaternary amines may be sufficient to provide the solubility or water dispersity required for this type of polymer in aqueous solution. Although the presence of hydrophilic group Y is optional, cationic associative polyurethanes comprising such groups are preferred.
    [236] -(II) the applicant's French patent application No. Cationic polyvinyllactams belonging to the group described in 1 101 106.
    [237] The polymer includes the following:
    [238] a) at least one monomer of the vinyllactam or alkylvinyllactam type;
    [239] b) at least one monomer of formula 9 or 10:
    [240]
    [241]
    [242] (In the meal,
    [243] X represents an oxygen atom or radical NR 6 ,
    [244] R 1 and R 6 independently of one another represent a hydrogen atom or a linear or branched C 1 -C 5 alkyl radical,
    [245] R 2 represents a linear or branched C 1 -C 4 alkyl radical,
    [246] R 3 , R 4 and R 5 independently of one another represent a hydrogen atom, a linear or branched C 1 -C 30 alkyl radical or a radical of formula 11:
    [247]
    [248] (In the meal,
    [249] Y, Y 1 and Y 2 independently of one another represent a linear or branched C 2 -C 16 alkylene radical,
    [250] R 7 represents a hydrogen atom, a linear or branched C 1 -C 4 alkyl radical or a linear or branched C 1 -C 4 hydroxyalkyl radical,
    [251] R 8 represents a hydrogen atom or a linear or branched C 1 -C 30 alkyl radical,
    [252] p, q and r independently of each other represent either a value of 0 or a value of 1,
    [253] m and n independently of each other represent an integer ranging from 0 to 100,
    [254] x represents an integer ranging from 1 to 100,
    [255] Z represents an organic or inorganic acid anion,
    [256] only,
    [257] At least one of the substituents R 3 , R 4 , R 5 or R 8 represents a linear or branched C 9 -C 30 alkyl radical,
    [258] -if m or n is non-zero, q is 1,
    [259] if m or n is 0, p or q is 0).
    [260] The cationic poly (vinyllactam) polymers according to the invention can be crosslinked or uncrosslinked and can also be block polymers.
    [261] Preferably, the counterion Z − of the monomer of formula 9 is selected from halide ions, phosphate ions, metosulfate ions and tosylate ions.
    [262] Preferably, R 3 , R 4 and R 5 independently of one another represent a hydrogen atom or a linear or branched C 1 -C 30 alkyl radical).
    [263] More preferably, monomer b) is a monomer of formula (9), more preferably in the above formula, m and n are 0
    [264] The vinyllactam or alkyl vinyllactam monomer is preferably a compound having the formula
    [265]
    [266] (In the meal,
    [267] s represents an integer ranging from 3 to 6,
    [268] R 9 represents a hydrogen atom or a C 1 -C 5 alkyl radical,
    [269] R 10 represents a hydrogen atom or a C 1 -C 5 alkyl radical,
    [270] Provided that at least one of the radicals R 9 and R 10 represents a hydrogen atom).
    [271] Even more preferably, the monomer (IV) is vinylpyrrolidone.
    [272] The cationic poly (vinyllactam) polymers according to the invention may also contain one or more additional monomers, which are preferably cationic or nonionic.
    [273] As more particularly preferred compounds according to the invention, mention may be made of the following terpolymers comprising at least one of the following:
    [274] a)-monomer of formula 12,
    [275] b)-Formula 9, wherein p = 1, q = 0, R 3 and R 4 independently of one another represent a hydrogen atom or a C 1 -C 5 alkyl radical, and R 5 represents a C 9 -C 24 alkyl radical Monomers, and
    [276] c)-a monomer of formula 10 wherein R 3 and R 4 independently of one another represent a hydrogen atom or a C 1 -C 5 alkyl radical.
    [277] Even more preferably, ternary polymers containing 40% to 95% monomer (a), 0.1% to 55% monomer (c) and 0.25% to 50% monomer (b) by weight will be used. .
    [278] Such polymers are described in patent application WO 00/68282, the content of which forms an integral part of the invention.
    [279] Particularly used cationic poly (vinyllactam) polymers according to the invention include vinylpyrrolidone / dimethylaminopropylmethacrylamide / dodecyldimethylmethacrylamidopropylammonium tosylate terpolymer, vinylpyrrolidone / dimethyl Aminopropylmethacrylamide / cocoyldimethylmethacrylamidopropylammonium tosylate terpolymer and vinylpyrrolidone / dimethylaminopropylmethacrylamide / lauryldimethylmethacrylamidopropylammonium tosylate or chloride terpolymer Included.
    [280] The weight average molecular mass of the cationic poly (vinyllactam) polymer according to the invention is preferably 500 to 20,000,000. More particularly 200,000 to 2,000,000, even more preferably 400,000 to 800,000.
    [281] Amphoteric associative polymer
    [282] They are preferably selected from polymers comprising at least one noncyclic cationic unit. Even more particularly, it contains, or is prepared from, 1-20 mol%, preferably 1.5-15 mol%, even more particularly 1.5-6 mol%, of monomers comprising a fatty chain relative to the total moles of monomers. It is preferable.
    [283] Preferred amphoteric associating polymers according to the invention contain or are prepared by copolymerizing the at least one monomer of formula 13, 14 or 15 comprises at least one fatty chain:
    [284] 1) at least one monomer of formula 13 or 14:
    [285]
    [286]
    [287] (In the meal,
    [288] R 1 and R 2 may be the same or different and represent a hydrogen atom or a methyl radical,
    [289] R 3 , R 4 and R 5 may be the same or different and represent a linear or branched alkyl radical having 1 to 30 carbon atoms,
    [290] Z represents an NH group or an oxygen atom,
    [291] n is an integer from 2 to 5,
    [292] A − is an anion derived from an organic or inorganic acid, such as a methosulfate anion, or a halide such as chloride or bromide);
    [293] 2) at least one monomer of the formula
    [294] R 6 -CH = CR 7 -COOH
    [295] (Wherein R 6 and R 7 may be the same or different and represent a hydrogen atom or a methyl radical); And
    [296] 3) at least one monomer of formula 15:
    [297] R 6 -CH = CR 7 -COXR 8
    [298] (In the meal,
    [299] R 6 and R 7 may be the same or different and represent a hydrogen atom or a methyl radical;
    [300] X represents an oxygen or nitrogen atom;
    [301] R 8 represents a linear or branched alkyl radical having 1 to 30 carbon atoms).
    [302] Preferably, the monomers of Formulas 13 and 14 of the present invention are selected from the group consisting of:
    [303] Dimethylaminoethyl methacrylate, dimethylaminoethyl acrylate,
    [304] Diethylaminoethyl methacrylate, diethylaminoethyl acrylate,
    [305] Dimethylaminopropyl methacrylate, dimethylaminopropyl acrylate,
    [306] Dimethylaminopropylmethacrylamide, dimethylaminopropylacrylamide,
    [307] The monomers are optionally quaternized with, for example, C 1 -C 4 alkyl halides or C 1 -C 4 dialkyl sulfates.
    [308] More particularly, the monomer of formula 13 is selected from acrylamidopropyltrimethylammonium chloride and methacrylamidopropyltrimethylammonium chloride.
    [309] The monomer of the formula (16) of the present invention is preferably selected from the group consisting of acrylic acid, methacrylic acid, crotonic acid and 2-methylcrotonic acid. More particularly, the monomer of formula (II) is acrylic acid.
    [310] The monomer of formula 15 of the present invention is preferably selected from the group consisting of C 12 -C 22 , more particularly C 16 -C 18 alkyl acrylates or methacrylates.
    [311] It is preferred that the monomers composed of the fatty chain amphoteric polymers of the invention are already neutralized and / or quaternized.
    [312] The ratio of the cationic charge / anion charge number is preferably equal to about one.
    [313] The amphoteric associating polymer according to the invention preferably contains from 1 mol% to 10 mol%, preferably from 1.5 mol% to 6 mol% of monomers comprising a fatty chain (monomers of formula 13, 14 or 15).
    [314] The weight average molecular weight of the amphoteric associative polymer according to the invention may range from 500 to 50,000,000, preferably 10,000 to 5,000,000.
    [315] The amphoteric associating polymers according to the invention may also contain nonionic monomers, in particular other monomers such as C 1 -C 4 alkyl acrylates or methacrylates.
    [316] Amphoteric associative polymers according to the invention are described and prepared, for example, in patent application WO 98/44012.
    [317] Among the amphoteric associative polymers according to the invention, preferred are acrylic acid / (meth) acrylamidopropyltrimethylammonium chloride / stearyl methacrylate terpolymers.
    [318] Associative polymer of nonionic type
    [319] According to the invention, they are preferably selected from:
    [320] (1) cellulose modified with a group comprising at least one fatty chain;
    [321] Examples that may be mentioned include:
    [322] Hydroxyethylcellulose comprising one or more fatty chains, such as alkyl, arylalkyl or alkylaryl groups, wherein the alkyl groups are preferably modified with C 8 -C 22 groups, or mixtures thereof, for example the product Natrosol Plus Grade 330 CS (C 16 alkyl) (available from Aqualon) or product Bermocoll EHM 100 (Commercially available from Berol Nobel),
    [323] Modified with alkylphenyl polyalkylene glycol ether groups, such as the product Amercell Polymer HM-1500 (Nonylphenyl polyethylene glycol (15) ether) (commercially available from Amerchol).
    [324] (2) hydroxypropyl guar modified with a group comprising at least one fatty chain, such as the product Esaflor HM 22 (C 22 alkyl chain) (available from Lamberti), and product RE210-18 (C 14 alkyl chain) and RE205-1 (C 20 alkyl chain) (commercially available from Rhone-Poulenc).
    [325] (3) a copolymer of vinylpyrrolidone and a fatty chain hydrophobic monomer;
    [326] Examples that may be mentioned include:
    [327] -Products Antaron V216 Or Ganex V216 (Vinylpyrrolidone / hexadecene copolymer) (commercially available from ISP)
    [328] -Products Antaron V220 Or Ganex V220 (Vinylpyrrolidone / Eicosen Copolymer) (commercially available from ISP)
    [329] -(4) COne-C6 Copolymers of alkyl methacrylates or acrylates with amphiphilic monomers comprising at least one fatty chain, for example oxyethylenated methyl acrylate / stearyl acrylate copolymers (commercially available from Goldschmidt, trade name Antil 208).
    [330] (5) copolymers of hydrophilic methacrylates or acrylates with hydrophobic monomers comprising at least one fatty chain, such as polyethylene glycol methacrylate / lauryl methacrylate copolymers.
    [331] (6) Polyurethane polyethers containing both hydrophilic blocks of polyoxyethylenation properties in general and aliphatic sequences alone and / or hydrophobic blocks which may be alicyclic and / or aromatic sequences.
    [332] ( 7 ) polymers having an aminoplast ether backbone comprising at least one fatty chain, such as Pure Thix Compound (commercially available from Sud-Chemie).
    [333] Preferably, the polyurethane polyether contains at least two hydrocarbon based lipophilic chains having 6 to 30 carbon atoms separated by hydrophilic blocks, and the hydrocarbon based chains may be pendant chains or chains of hydrophilic block ends. In particular, one or more protruding chains may be included. In addition, the polymer may include a hydrocarbon based chain at one or both ends of the hydrophilic block.
    [334] The polyurethane polyethers may be in the form of multiblocks, in particular triple blocks. Hydrophobic blocks may be present at each end of the chain (eg: triple block copolymers having a hydrophilic central block) or may be distributed at both ends and in the chain (eg: multiblock copolymers). This same polymer may also be a graft polymer or a starburst polymer.
    [335] The nonionic fatty chain polyurethane polyether may be a triple block copolymer in which the hydrophilic block is a polyoxyethylenated chain comprising 50 to 1000 oxyethylene groups. Nonionic polyurethane polyethers include urethane linkages between hydrophilic blocks from which the name derives.
    [336] Expanding the scope, among the nonionic fatty chain polyurethane polyethers, those in which the hydrophilic block is connected to the lipophilic block through other chemical bonds are also included.
    [337] Examples of nonionic fatty chain polyurethane polyethers that may be used in the present invention include Rheolate 205 comprising urea functionality. (Commercially available from Rheox), or Rheolate 208, 204 or 212, and Acrysol RM 184 May also be mentioned.
    [338] In addition, products containing C 12-14 alkyl chain Elfacos T210 Mention may also be made of the product Elfacos T212 (Akzo) comprising a C 18 alkyl chain.
    [339] In addition, the product DW 1206B which contains a C 20 alkyl chain and a urethane linkage, and is commercially available in a solids content of 20% in water. (Rohm & Haas) can also be used.
    [340] It is also possible to use solutions or dispersions of the polymers, in particular in water or in aqueous-alcohol media. Examples of such polymers that may be mentioned are Rheolate 255, Rheolate 278 and Rheolate 244 (available from Rheox) may be mentioned. In addition, the products DW 1206F and DW 1206J (available from Rohm & Haas) can also be used.
    [341] Polyurethane polyethers which can be used according to the invention are described in particular in the paper [G. Fonnum, J. Bakke and Fk. Hansen-Colloid Polym. Sci 271, 380.389 (1993).
    [342] Even more particularly, according to the invention, 3 containing (i) at least one polyethylene glycol containing 150 to 180 moles of ethylene oxide, (ii) stearyl alcohol or decyl alcohol, and (iii) at least one diisocyanate Preference is given to using polyurethane polyethers which can be obtained by polycondensation of two or more compounds.
    [343] The polyurethane polyethers are, in particular, trade name Aculyn 46 And Aculyn 44 [Aculyn 46 15 weights in a matrix of maltodextrin (4%) and water (81%) of polyethylene glycol containing 150 or 180 moles of ethylene oxide, stearyl alcohol and methylenebis (4-cyclohexyl isocyanate) (SMDI) % Multicondensate; Aculyn 44 35% by weight in a mixture of propylene glycol (39%) and water (26%) of polyethylene glycol containing 150 or 180 moles of ethylene oxide, decyl alcohol and methylenebis (4-cyclohexylisocyanate) (SMDI) Is a polycondensate of Co., Ltd., available from Rohm & Haas.
    [344] The dye compositions according to the invention may also contain unsaturated fatty alcohols, such as oleyl alcohol, in a weight ratio ranging from 0.5% to 15% relative to the total weight of the dye composition.
    [345] Furthermore, more particularly other surfactants, including especially nonionic surfactants selected from oxyalkylenated fatty alcohols and mono- or polyglycerolated fatty alcohols, are contained in a weight ratio ranging from 2% to 40% relative to the total weight of the dye composition. can do.
    [346] In addition, ready-to-use compositions according to the invention may contain one or more cationic or amphoteric polymers in dye compositions and / or oxidizing compositions.
    [347] Cationic polymer
    [348] For the purposes of the present invention, the term "cationic polymer" means any polymer comprising a cationic group and / or a group that can be ionized with a cationic group.
    [349] Cationic polymers which can be used according to the invention are those already known per se as improving the cosmetic properties of hair, in particular patent application EP-A-337 354 and French patent FR-2 270 846, 2'383'660 , 2 598 611, 2 470 596 and 2 519 863.
    [350] Preferred cationic polymers are preferably selected from units comprising primary, secondary, tertiary and / or quaternary amine groups, which may form part of the polymer backbone or be included as side substituents directly attached thereto. Do.
    [351] Cationic polymers generally used have a number average molecular mass of approximately 500 to 5 x 10 6 , preferably approximately 10 3 to 3 x 10 6 .
    [352] More particularly, among the cationic polymers which may be mentioned, mention may be made of polymers of the polyamine, polyamino amide and poly quaternary ammonium types.
    [353] These are known products. These are described in particular in French patents 2 505 348 and 2 542 997. Among the above polymers, mention may be made of:
    [354] (1) homopolymers or copolymers derived from acrylic or methacryl esters or amides and comprising one or more units of the following formulas 17, 18, 19 or 20:
    [355]
    [356]
    [357]
    [358]
    [359] (In the meal,
    [360] R 3 may be the same or different and represents a hydrogen atom or a CH 3 radical;
    [361] A may be the same or different and represents a linear or branched alkyl group having 1 to 6 carbon atoms, preferably 2 or 3 carbon atoms, or a hydroxyalkyl group having 1 to 4 carbon atoms;
    [362] R 4 , R 5 and R 6 may be the same or different and represent an alkyl group having 1 to 18 carbon atoms, or a benzyl radical, preferably an alkyl group having 1 to 6 carbon atoms;
    [363] R 1 and R 2 may be the same or different and represent hydrogen or an alkyl group having 1 to 6 carbon atoms, preferably methyl or ethyl;
    [364] X represents an anion derived from an inorganic or organic acid such as a methosulfate anion or halide such as chloride or bromide).
    [365] The polymers of group (1) are also acrylamide, methacrylamide, diacetone acrylamide, acrylamide and methacrylamide substituted with lower (C 1 -C 4 ) alkyl on nitrogen, acrylic acid or methacrylic acid or And one or more units derived from comonomers thereof, which may be selected from the group thereof, vinyllactams such as vinylpyrrolidone or vinylcaprolactam, and vinyl esters.
    [366] Thus, among the polymers of the above group (1), the following may be mentioned:
    [367] Copolymers of dimethylaminoethyl methacrylate with acrylamide quaternized with dimethyl sulphate or dimethyl halide, such as tradename Hercofloc (Commercially available as Hercules)
    [368] -Described, for example, in patent application EP-A-080 976 and under the trade name Bina Quat P 100 A copolymer of methacryloyloxyethyltrimethylammonium chloride and acrylamide, sold by (Ciba Geigy),
    [369] -Trade name Reten A copolymer of methacryloyloxyethyltrimethylammonium methosulfate and acrylamide, sold by Hercules,
    [370] Quaternized or non-quaternized vinylpyrrolidone / dialkylaminoalkyl acrylate or methacrylate copolymers, eg the trade name "Gafquat (ISP), for example "Gafquat 734 "or" Gafquat Products marketed as 755 ", or otherwise" Copolymer 845, 958 and 937 ". The copolymers are described in detail in French patents 2 077 143 and 2 393 573.
    [371] Dimethylaminoethyl methacrylate / vinylcaprolactam / vinylpyrrolidone terpolymer, such as the trade name Gaffix Products marketed as VC 713 (ISP);
    [372] Especially the brand name Styleze Vinylpyrrolidone / methacrylamidopropyldimethylamine copolymer sold by CC 10 (ISP),
    [373] Quaternized vinylpyrrolidone / dimethylaminopropylmethacrylamide copolymer, such as the trade name “Gafquat Commercially available as HS 100 "(ISP).
    [374] (2) cellulose ether derivatives described in French patent 1 492 597 and comprising quaternary ammonium groups, in particular the trade name "JR "(JR 400, JR 125 and JR 30M) or" LR A polymer sold by "(LR 400 or LR 30M) (Union Carbide Corporation). The polymers are also defined in the CTFA dictionary as quaternary ammonium of hydroxyethylcellulose reacting with epoxides substituted with trimethylammonium groups.
    [375] (3) cationic cellulose derivatives, such as the cellulose derivatives or cellulose copolymers described in US Pat. No. 4,131,576, in particular grafted with water-soluble monomers of quaternary ammonium, such as hydroxyalkylcelluloses, for example methacryloyl Hydroxymethyl-, hydroxyethyl- or hydroxypropylcellulose, grafted with ethyltrimethylammonium, methacrylamidopropyltrimethylammonium or dimethyldiallylammonium salts.
    [376] Products falling within the above definition are more particularly referred to under the trade name "Celquat." L 200 "and" Celquat It is marketed as H 100 "(National Starch).
    [377] (4) more particularly guar gum comprising cationic polysaccharides such as cationic trialkylammonium groups described in US Pat. Nos. 3,589,578 and 4,031,307. For example, guar gum modified with salts of 2,3-epoxypropyltrimethylammonium (eg chloride) are used.
    [378] These products are specifically trade name Jaguar C13 S, Jaguar C 15, Jaguar C 17 or Jaguar Marketed as C162 (Meyhall).
    [379] (5) hydroxyalkylene radicals containing linear or branched chains and optionally substituted with oxygen, sulfur or nitrogen atoms, or aromatic or heterocyclic rings, or polymers composed of divalent alkylene and piperazinyl units, and Oxidation and / or quaternization product of the polymer. Such polymers are described in particular in French patents 2'162'025 and 2'280'361.
    [380] (6) water-soluble polyamino amides prepared, in particular, by polycondensation of acidic compounds and polyamines; The polyamino amide is epihalohydrin, diepoxide, dihydric anhydride, unsaturated dihydric anhydride, bis-unsaturated derivative, bis-halohydrin, bis-azetidinium, bis-haloacyldiamine, bis-alkyl Bifunctional compounds reactive with halides, or alternatively with bis-halohydrin, bis-azetidinium, bis-haloacyldiamine, bis-alkyl halides, epihalohydrin, diepoxides or bis-unsaturated derivatives May be crosslinked with oligomers resulting from the reaction of; Crosslinkers are used in proportions ranging from 0.025 to 0.35 moles per amine group of the polyamino amide; The polyamino amides can be alkylated or quaternized if they comprise one or more tertiary amine functionalities. Such polymers are described in particular in French patents 2 252 840 and 2 368 508.
    [381] (7) A polyamino amide derivative produced by alkylation of a polyalkylene polyamine with a polycarboxylic acid followed by alkylation with a bifunctional agent. For example, mention may be made of adipic acid / dialkylaminohydroxyalkyldialkylenetriamine polymers, wherein the alkyl radicals have 1 to 4 carbon atoms, preferably methyl, ethyl or propyl. Such polymers are described in particular in French patent 1 583 363.
    [382] Among the derivatives, more particularly from Sandoz, " Cartaretine Mention may be made of adipic acid / dimethylaminohydroxypropyl / diethylenetriamine polymer sold under the name F, F4 or F8 ″.
    [383] (8) reaction of a polyalkylene polyamine comprising two primary amine groups and at least one secondary amine group with a dicarboxylic acid selected from saturated aliphatic dicarboxylic acids and diglycolic acids having 3 to 8 carbon atoms; Polymer obtained. The molar ratio between polyalkylene polyamine and dicarboxylic acid is from 0.8: 1 to 1.4: 1; The resulting polyamino amide reacts with epichlorohydrin having a molar ratio of epichlorohydrin to the secondary amine groups of the polyamino amide in the range from 0.5: 1 to 1.8: 1. Such polymers are described in particular in US Pat. Nos. 3 227 615 and 2 961 347.
    [384] Polymers of this type are in particular Hercules Inc. From Herceett 57 "or alternatively, Hercules uses the" PD 170 "for adipic acid / epoxypropyl / diethylenetriamine copolymers. "Or" Delsette Commercially available under the name 101 ".
    [385] (9) cyclopolymers of alkyldiallylamine or dialkyldiallylammonium, such as homopolymers or copolymers comprising units corresponding to the general formula (21) or (22) as main components of the chain:
    [386]
    [387]
    [388] (Wherein k and t are equal to 0 or 1 and the sum k + t is 1; R 9 represents a hydrogen atom or a methyl radical; R 7 and R 8 independently of each other, an alkyl group having 1 to 6 carbon atoms, The alkyl group preferably represents a hydroxyalkyl group having 1 to 5 carbon atoms, a lower C 1 -C 4 amidoalkyl group, or R 7 and R 8 together with the nitrogen atom to which they are attached are heterocyclic groups such as piperidyl or Morpholinyl; R 7 and R 8 independently of one another, preferably alkyl groups of 1 to 4 carbon atoms; Y − an anion such as bromide, chloride, acetate, borate, citrate, tartrate, Bisulfate, bisulfite, sulfate or phosphate). Such polymers are described in particular in French patent 2 080 759 and its further certificate 2 190 406.
    [389] Among the polymers defined above, more particularly at the Calgon company "Merquat Dimethyldiallylammonium chloride homopolymer (and homologue of its low weight average molecular mass) sold under the name 100 ", and" Merquat Mention may be made of copolymers of diallyldimethylammonium chloride and acrylamide available under the name 550 ".
    [390] (10) quaternary diammonium polymers comprising repeating units corresponding to the formula:
    [391]
    [392] In Formula 23:
    [393] R 10 , R 11 , R 12 and R 13 may be the same or different and represent an aliphatic, cycloaliphatic or arylaliphatic radical or a lower hydroxyalkylaliphatic radical having 1 to 20 carbon atoms, or alternatively R 10 , R 11 , R 12 and R 13 together or separately together with the nitrogen atom to which they are attached, form a heterocycle optionally comprising a second hetero atom other than nitrogen, or alternatively R 10 , R 11 , R 12 and R 13 are Linear, substituted with a nitrile, ester, acyl or amide group, or group -CO-OR 14 -D or -CO-NH-R 14 -D wherein R 14 is alkylene and D is a quaternary ammonium group Or branched C 1 -C 6 alkyl radicals;
    [394] A 1 and B 1 may be linear or branched, saturated or unsaturated, having 2 to 20 carbon atoms, and have one or more aromatic rings or one or more oxygen or sulfur atoms or sulfoxides, sulfones, disulfides connected or inserted into the main chain A polymethylene group which may include a feed, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester group, and
    [395] X − represents an anion derived from an inorganic acid or an organic acid;
    [396] A 1 , R 10 and R 12 together with the two nitrogen atoms to which they are attached may form a piperazine ring; In addition, when A 1 represents a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene radical, B 1 also represents a group — (CH 2 ) n —CO—D—OC— (CH 2 ) n − (Wherein D represents:
    [397] a) Formula: -O-Z-O-, wherein Z represents a linear or branched hydrocarbon based radical or a group corresponding to one of the formulas:
    [398] -(CH 2 -CH 2 -O) x -CH 2 -CH 2-
    [399] -[CH 2 -CH (CH 3 ) -O] y -CH 2 -CH (CH 3 )-
    [400] A glycol residue of (wherein x and y represent an integer of 1 to 4 representing a defined intrinsic polymerization degree, or any number of 1 to 4 representing an average degree of polymerization);
    [401] b) bis-secondary diamine residues such as piperazine derivatives;
    [402] c) of the formula: -NH-Y-NH-, wherein Y represents a linear or branched hydrocarbon based radical, or alternatively a divalent radical -CH 2 -CH 2 -SS-CH 2 -CH 2- Bis-primary diamine residues;
    [403] d) ureylene groups of the formula: -NH-CO-NH-)).
    [404] Preferably, X − is an anion such as chloride or bromide.
    [405] The polymers generally have a number average molecular mass of 1000 to 100,000.
    [406] Polymers of this type are in particular French patents 2 320 330, 2 270 846, 2 316 271, 2 336 434 and 2 413 907 and US patents 2 273 780, 2 375 853, 2 388 614, 2 454 547, 3 206 462, 2 261 002, 2 271 378, 3 874 870, 4 001 432, 3 929 990, 3 966 904, 4 005 193, 4 025 617, 4 025 627, 4 025 653, 4 026 945 and 4 027 020 have.
    [407] More particularly, it is possible to use polymers composed of repeating units corresponding to formula (24):
    [408]
    [409] Wherein R 10 , R 11 , R 12 and R 13 may be the same or different and represent an alkyl or hydroxyalkyl radical having approximately 1 to 4 carbon atoms, n and p are integers in the range of approximately 2 to 20 carbon atoms And X − is an anion derived from an inorganic acid or an organic acid).
    [410] (11) a poly quaternary ammonium polymer composed of repeat units of formula
    [411]
    [412] (Wherein p represents an integer ranging from approximately 1 to 6, D may be nothing or represent a group (CH 2 ) r -CO- (where r represents a number of 4 or 7), X - is an anion).
    [413] Such polymers can be prepared according to the processes described in US Pat. Nos. 4,157, 388, 4, 702, 906 and 4, 719, 282. These are described in particular in patent application EP-A-122,324.
    [414] Among the above products, for example, "Mirapol commercially available from Miranol". A 15 "," Mirapol AD1 "," Mirapol AZ1 "and" Mirapol 175 ".
    [415] (12) quaternary polymers of vinylpyrrolidone and vinylimidazole, such as Luviquat from BASF Available under the names FC 905, FC 550 and FC 370.
    [416] (13) Polyamines given by the reference "polyethylene glycol (15) tallow polyamine" in the CTFA Dictionary, such as Polyquart sold by Henkel H.
    [417] (14) homopolymerization of crosslinked methacryloyloxy (C 1 -C 4 ) alkyltri (C 1 -C 4 ) alkylammonium salt polymers, such as dimethylaminoethyl methacrylate quaternized with methyl chloride, or methyl A polymer obtained by copolymerization of acrylamide with dimethylaminoethyl methacrylate quaternized with chloride, which is crosslinked with a compound comprising an olefinically unsaturated portion, in particular methylenebisacrylamide, after homo- or copolymerization. More particularly, crosslinked acrylamide / methacryloyloxyethyltrimethylammonium chloride copolymer (20/80 weight) in the form of a dispersion containing 50% by weight of the copolymer in mineral oil can be used. The dispersion was obtained from Allied Colloids, Inc. Commercially available under the name SC 92 ". Crosslinked methacryloyloxyethyltrimethylammonium chloride homopolymers containing about 50% by weight homopolymers in mineral oil or liquid esters can also be used. The dispersions are Allied Colloids. 4 "Salcare SC 95 "and" Salcare Commercially available under the name SC 96 ".
    [418] Other cationic polymers that may be used in connection with the present invention are polyalkyleneimines, in particular polymers comprising polyethyleneimine, vinylpyridine or vinylpyridinium units, condensates of polyamines and epichlorohydrin, quaternary polyureylenes and Chitin derivatives.
    [419] Of all cationic polymers that can be used in connection with the present invention, it is preferable to use polymers of the groups (1), (9), (10), (11), (12) and (14), And even more preferred are polymers composed of repeating units of 27:
    [420]
    [421] (Particularly those having a molecular weight of 9500 to 9900 as determined by gel permeation chromatography);
    [422]
    [423] (Especially those whose molecular weight is about 1200 as determined by gel permeation chromatography).
    [424] The concentration of cationic polymer in the composition according to the invention ranges from 0.01% to 10% by weight, preferably from 0.05% to 5% by weight, even more preferably from 0.1% to 3% by weight relative to the total weight of the composition. Can be.
    [425] Amphoteric polymer
    [426] Amphoteric polymers that can be used according to the invention can be selected from polymers comprising units K and M which are randomly dispersed in the polymer chain, where K is a unit derived from a monomer comprising at least one basic nitrogen atom. And M represents a unit derived from an acidic monomer comprising at least one carboxylic or sulfonic group, or alternatively K and M can represent a group derived from a zwitterionic carboxybetaine or sulfovebetain monomer and ;
    [427] K and M also denote cationic polymer chains comprising primary, secondary, tertiary or quaternary amine groups, wherein at least one amine group has a carboxylic or sulfonic group linked via a hydrocarbon based radical. Or, alternatively, K and M may form part of a polymer chain comprising α, β-dicarboxylic ethylene units, where one carboxylic group is one or more primary or secondary amine groups Made to react with the containing polyamine).
    [428] More particularly preferred amphoteric polymers corresponding to the above definitions are selected from the following polymers:
    [429] (1) monomers derived from vinyl compounds having carboxylic groups, such as, more particularly, basic monomers derived from substituted vinyl compounds comprising acrylic acid, methacrylic acid, maleic acid, α-chloroacrylic acid, and one or more basic atoms For example, more particularly, polymers produced by copolymerization of dialkylaminoalkyl methacrylates and acrylates, dialkylaminoalkylmethacrylamides and -acrylamides. Such compounds are described in US Pat. No. 3,836,537.
    [430] Also Polyquart from Henkel Mention may be made of the sodium acrylate / acrylamidopropyltrimethylammonium chloride copolymer sold under the name KE 3033.
    [431] The vinyl compound may also be a dialkyldiallylammonium salt, such as dimethyldiallylammonium chloride. Copolymers of acrylic acid and the latter monomers were obtained from Merquat from Calgon. 280, Merquat 295 and Merquat Available under the name Plus 3330.
    [432] (2) a polymer comprising units derived from:
    [433] a) at least one monomer selected from acrylamide and methacrylamide substituted with alkyl radicals on nitrogen,
    [434] b) at least one acidic comonomer comprising at least one reactive carboxylic group, and
    [435] c) quaternization of one or more basic comonomers, such as esters containing primary, secondary, tertiary and quaternary amine substituents of acrylic acid and methacrylic acid, dimethylaminoethyl methacrylate with dimethyl or diethyl sulfate product.
    [436] More particularly preferred N-substituted acrylamides or methacrylamides according to the invention are groups having an alkyl radical of 2 to 12 carbon atoms, more particularly N-ethylacrylamide, N-tert-butylacrylamide, N-tert-octylacryl Amide, N-octylacrylamide, N-decylacrylamide, N-dodecylacrylamide and the corresponding methacrylamide.
    [437] The acidic comonomers are more particularly selected from acrylic acid, methacrylic acid, crotonic acid, itaconic acid, maleic acid and fumaric acid, and alkyl monoesters or anhydrides having 1 to 4 carbon atoms of maleic or fumaric acid.
    [438] Preferred basic comonomers are aminoethyl, butylaminoethyl, N, N'-dimethylaminoethyl and N-tert-butylaminoethyl methacrylate.
    [439] A copolymer whose CTFA (4th edition, 1991) is octylacrylamide / acrylate / butylaminoethyl methacrylate copolymer, such as Amphomer from National Starch Or Lovocryl A product commercially available under the name 47 is especially used.
    [440] (3) crosslinked and alkylated polyamino amides partially or wholly derived from polyamino amides of the formula:
    [441]
    [442] Wherein R 19 is a divalent radical derived from an ester of a saturated dicarboxylic acid, a mono- or dicarboxylic aliphatic acid containing an ethylenic double bond, a lower alkanol having 1 to 6 carbon atoms of the acid or Represents a radical derived from the addition of a bis (primary) or bis (secondary) amine to any one of said acids, Z is a bis (primary), mono- or bis (secondary) polyalkylene-polyamine radical and Preferably the following is represented:
    [443] a) the following radicals in a ratio of 60 to 100 mole%, derived from diethylenetriamine, triethylenetetraamine or dipropylenetriamine:
    [444]
    [445] (Wherein x = 2 and p = 2 or 3, or alternatively x = 3 and p = 2);
    [446] b) 0 to 40 mole% of said radicals (wherein x = 2 and p = 1) derived from ethylenediamine or radicals derived from piperazine:
    [447]
    [448] c) 0 to 20 mole percent -NH- (CH 2 ) 6 -NH- radicals derived from hexamethylenediamine (the polyamino amines are epihalohydrin, diepoxide, divalent anhydride and bis-unsaturated); By addition of a bifunctional crosslinking agent selected from derivatives, crosslinked using 0.025 to 0.35 mole of crosslinking agent per amine group of the polyamino amide and alkylated by the action of acrylic acid, chloroacetic acid or alkane sultone, or salts thereof) ).
    [449] The saturated carboxylic acid preferably comprises an acid having 6 to 10 carbon atoms, such as adipic acid, 2,2,4-trimethyladipic acid and 2,4,4-trimethyladipic acid, terephthalic acid and ethylene-based double bonds. Acids such as acrylic acid, methacrylic acid and itaconic acid.
    [450] The alkane sultone used for alkylation is preferably propane sultone or butane sultone, and the salt of the alkylating agent is preferably the sodium or potassium salt.
    [451] (4) a polymer comprising a zwitterionic unit of the formula:
    [452]
    [453] Wherein R 20 represents a polymerizable unsaturated group such as an acrylate, methacrylate, acrylamide or methacrylamide group, y and z represent an integer of 1 to 3, and R 21 and R 22 represent a hydrogen atom , Methyl, ethyl or propyl, and R 23 and R 24 represent a hydrogen atom or an alkyl radical in which the sum of the carbon number of R 23 and R 24 does not exceed 10).
    [454] Polymers comprising such units are also derived from non-zwitterionic monomers such as dimethyl or diethylaminoethyl acrylate or methacrylate, or alkyl acrylate or methacrylate, acrylamide or methacrylamide, or vinyl acetate It may include a unit to be.
    [455] For example, Diaformer from Sandoz Mention may be made of copolymers of methyl methacrylate / dimethyl carboxymethylammonio ethyl methacrylate, such as the product sold under the name Z301.
    [456] (5) a polymer derived from chitosan comprising monomer units corresponding to the following formulas (31), (32) and (33):
    [457]
    [458]
    [459]
    [460] Unit 31 is present at a rate of 0 to 30%, unit 32 is present at a rate of 5 to 50%, and unit 33 is present at a rate of 30 and 90%, and in unit 33, R 25 is understood to represent a radical of the formula:
    [461]
    [462] Wherein q represents 0 or 1;
    [463] If q = 0, then R 26 , R 27 and R 28 may be the same or different and are each optionally interrupted with a hydrogen atom, methyl, hydroxyl, acetoxy or amino moiety, one or more nitrogen atoms and / or one or more amines , Monoalkylamine residues or dialkylamine residues optionally substituted with hydroxyl, carboxyl, alkylthio or sulfonic groups, alkylthio residues, wherein the alkyl groups have amino residues, in which case the radicals R 26 , R 27 and R At least one of 28 is a hydrogen atom;
    [464] if q = 1, R 26 , R 27 and R 28 each represent a hydrogen atom as well as a salt formed by said compound and a base or an acid).
    [465] (6) polymers derived from the N-carboxyalkylation of chitosans, such as those available from Jan Dekker. N-carboxymethylchitosan or N-carboxybutylchitosan available under the name ".
    [466] (7) a polymer corresponding to formula 34 as described, for example, in French patent 1 400 366:
    [467]
    [468] Wherein R 29 represents a hydrogen atom, CH 3 O, CH 3 CH 2 O or a phenyl radical, R 30 represents hydrogen or a lower alkyl radical such as methyl or ethyl, R 31 represents a hydrogen or lower alkyl radical, Eg methyl or ethyl, R 32 is a lower alkyl radical such as methyl or ethyl or the formula: -R 33 -N (R 31 ) 2 (R 33 is -CH 2 -CH 2- , -CH 2 -CH 2- Group represents a CH 2 -or -CH 2 -CH (CH 3 )-group, R 31 represents the same meaning as mentioned above, as well as the higher homologues of said radicals having up to 6 carbon atoms, r is the molecular weight Is 500 to 6,000,000, preferably 1000 to 1,000,000).
    [469] (8) amphoteric polymers of the type -D-X-D-X- selected from:
    [470] a) a polymer obtained by the action of chloroacetic acid or sodium chloroacetate on a compound comprising at least one unit of the formula:
    [471] -D-X-D-X-D-
    [472] Wherein D represents the following radical
    [473]
    [474] X represents the symbol E or E ', E or E' may be the same or different and is an alkylene radical having a linear or branched chain containing up to 7 carbon atoms in the main chain, and is unsubstituted or hydroxyl group Substituted and substituted with oxygen, nitrogen and sulfur atoms and may have 1 to 3 aromatic and / or heterocyclic rings; Oxygen, nitrogen and sulfur atoms are ether, thioether, sulfoxide, sulfone, sulfonium, alkylamine or alkenylamine groups, hydroxyl, benzylamine, amine oxide, quaternary ammonium, amide, imide, alcohol, ester And / or in the form of urethane groups);
    [475] b) a polymer of the formula:
    [476] -D-X-D-X-
    [477] Wherein D represents the following radical
    [478]
    [479] X represents the symbol E or E 'and one or more times E'; E has the meanings indicated above, E 'is a linear or branched alkylene radical having up to 7 carbon atoms in the main chain, unsubstituted or substituted with one or more hydroxyl radicals, and contains one or more nitrogen atoms , The nitrogen atom is substituted with an alkyl chain optionally interrupted by an oxygen atom and necessarily comprises at least one carboxyl function or at least one hydroxyl function and betained by reaction with chloroacetic acid or sodium chloroacetate) .
    [480] (9) partially modified by semiamidation with N, N-dialkylaminoalkylamines, such as N, N-dimethylaminopropylamine, or semiesterification with N, N-dialkanolamine (C 1 -C 5 ) alkyl vinyl ether / maleic anhydride copolymers. The copolymer may also include other vinyl comonomers such as vinylcaprolactam.
    [481] Particularly preferred ampholytic polymers according to the invention are those of group (1).
    [482] According to the invention, the amphoteric polymer (s) comprises from 0.01% to 10% by weight, preferably from 0.05% to 5% by weight and even more preferably from 0.1% to 3% by weight relative to the total weight of the composition. Can be represented.
    [483] medium
    [484] Suitable media for dye compositions for dyeing are preferably more particularly alcohols or diols such as ethyl alcohol, isopropyl alcohol, hexylene glycol (2-methyl 2,4-pentanediol), neopentylglycol, 3-methyl-1 , 5-pentanediol, benzyl alcohol and phenylethyl alcohol, or glycols or glycol ethers such as ethylene glycol monomethyl, monoethyl and monobutyl ether, propylene glycol or ethers thereof such as propylene glycol monomethyl ether, butylene glycol, di Is an aqueous medium consisting of propylene glycol, and also water, which can advantageously comprise a cosmetically acceptable organic solvent including diethylene glycol alkyl ethers such as diethylene glycol monoethyl ether or monobutyl ether. The solvent may then be present at concentrations of about 0.5% to 20%, preferably about 2% and 10% by weight relative to the total weight of the composition, respectively.
    [485] The composition according to the invention may also contain other surfactants, more particularly oxyalkylenated nonionic surfactants well known to those skilled in the art. By way of example, for example, oxyalkylenated alkylphenols having a chain of 8 to 22 carbon atoms and the number of ethylene oxide and / or propylene oxide groups possibly in particular range from 1 to 50; Oxyalkylenated alcohols having 8 to 30 carbon atoms, linear or branched, saturated or unsaturated, and in which the number of ethylene oxide and / or propylene oxide groups may possibly range from 1 to 50 in particular; Polyoxyethylenated fatty amides with 2 to 30 moles of ethylene oxide; Polyoxyethylenated fatty acid esters of sorbitol with 2 to 30 moles of ethylene oxide; Oxyethylenated, saturated or unsaturated vegetable oils; Mention may be made of single or mixed condensates of ethylene oxide and propylene oxide with fatty alcohols.
    [486] More particularly preferred oxyalkylenated nonionic surfactants are fatty alcohols oxyethylated with 1 to 10 moles of ethylene oxide, having 8 to 22 carbon atoms. Among these, mention may be made in particular of lauryl alcohol 2 EO, lauryl alcohol 3 EO decyl alcohol 3 EO and decyl alcohol 5 EO.
    [487] Other reinforcing agents
    [488] The dye compositions according to the invention can also be used in an effective amount of other agents previously known otherwise in oxidative dyeing, such as various general adjuvant such as sequestering agents such as EDTA and etidronic acid, UV screening agents, waxes, optionally organomodified Volatile or nonvolatile (particularly with amine groups), cyclic or linear or branched silicones, preservatives, ceramides, pseudoceramides, vegetable, mineral or synthetic oils, vitamins or provitamins such as panthenol, opacifying agents, etc. have.
    [489] The composition may also include a reducing agent or an antioxidant. Said preparations can in particular be selected from sodium sulfite, thioglycolic acid, thioractic acid, sodium bisulfite, dehydroascorbic acid, hydroquinone, 2-methylhydroquinone, tert-butylhydroquinone and homogentisic acid, in which case they are generally It is present in an amount ranging from about 0.05% to 3% by weight relative to the total weight of the composition.
    [490] Needless to say, those skilled in the art will appreciate that the above-mentioned optional additional compound (s) are not adversely affected or substantially disadvantaged by the additive (s) incorporating advantageous properties inherently associated with the compositions directly usable according to the invention. Attention will be given to the choice so that it is not affected.
    [491] Oxidant
    [492] In the oxidizing composition, the oxidizing agent is preferably selected from hydrogen peroxide, urea peroxide, alkali metal bromate or ferricyanide, and perchlorates such as perborate and persulfate. In particular, it is preferable to use hydrogen peroxide. The oxidant is advantageously composed of an aqueous hydrogen peroxide solution whose titer may more particularly be in the range of about 1 to 40 times, even more preferably about 5 to 40 times.
    [493] Oxidants that may also be used are one or more oxidoreductases such as laccases, peroxidases and 2-electron oxidoreductases (such as freecases) in the presence of their respective appropriate donor or recognizer.
    [494] The pH of ready-to-use compositions applied to keratinous fibers (compositions produced by mixing together dye compositions and oxidizing compositions) is generally 3 to 12, inclusive. Preferably it is 8.5-11 (including a boundary), and can be adjusted to a desired value using the oxidizing agent or basic agent well known in the prior art in dyeing keratin fibers.
    [495] Among the basicizing agents which may be mentioned are, for example, aqueous ammonia, alkali metal carbonates, alkanolamines such as monoethanolamine, diethanolamine and triethanolamine and derivatives thereof, oxyethylenated and / or oxypropyleneated hydroxides. Oxyalkylamines and ethylenediamines, sodium hydroxide, potassium hydroxide and compounds of the formula:
    [496]
    [497] Wherein R is a propylene moiety optionally substituted with a hydroxyl group or a C 1 -C 4 alkyl radical; R 38 , R 39 , R 40 and R 41 may be the same or different and represent a hydrogen atom, C 1- C 4 alkyl radicals or C 1 -C 4 hydroxyalkyl radicals).
    [498] The oxidizing agent is typically, for example, mineral acid or organic acid such as hydrochloric acid, orthophosphoric acid, carboxylic acid such as tartaric acid, citric acid or lactic acid, or sulfonic acid.
    [499] The dyeing process according to the invention preferably applies a ready-to-use composition prepared on-the-fly from the dye composition and the oxidizing composition described above to the wet or dry keratin fibers, the composition preferably in the range of about 1 to 60 minutes, More preferably it is allowed to work for an exposure time ranging from approximately 10 to 45 minutes, rinsing the fibers, optionally washing them with shampoo and then rinsing again and drying them.
    [500] Specific examples illustrating the invention are shown below without limiting properties.
    [501] Example
    [502] The following dye compositions were prepared:
    [503] Dye composition :
    [504] (Expressed in grams of active substance)
    [505] Carboxylic Lauryl Ether Acid 4.5 EO (Akypo, commercially available from Chem Y) RLM 45)7 Lauryl Alcohol 2 EO (Dehydol, commercially available from Cognis LS-2-DEO-N)4 Decyl alcohol 5 EO (Empilan, marketed by Albright & Wilson) KA-5 / 90-FL)8 Oleyl alcohol3 Carboxylic (C13 / C15) Alkyl Ether Acid Monoethanolamide Containing 2 Moles of Ethylene Oxide5 Cationic Association Polymer (Quarsoft LM 200, available from Amerchol )One Monoethanolamine2 Polyquaternium 6 (merquat sold by Calgon) 100)1.5 ethanol11 Propylene glycol5 Dipropylene glycol5 1,3-dihydroxybenzene (resorcinol)0.3 para-phenylenediamine0.3 Reducing agent, antioxidantQuantity IsolationQuantity air freshenerQuantity Aqueous ammonia (with 20.5% ammonia)1.6 Demineralized water quantity100
    [506] The dye composition was mixed for two minutes in a plastic container at the rate of one part of the dye composition with 20 times aqueous hydrogen peroxide titer and 1.5 parts of the oxidation composition in use.
    [507] The resulting mixture was applied to hair comprising 90% of white hair and left to work for 30 minutes.
    [508] The hair was then rinsed with water, washed with shampoo, rinsed again with water, dried and combed.
    [509] In this way, a greenish brown tint was obtained.
    [510] Through the present invention it is possible to obtain an oxidative dye composition which produces a more dyeable color tone.
    权利要求:
    Claims (44)
    [1" claim-type="Currently amended] A composition for the oxidative staining of keratin fibers, such as human keratin fibers, such as hair, containing at least one oxidizing dye in a medium suitable for dyeing, comprising at least one polyoxyalkylenated carboxylic acid ether or salt thereof, and at least one And at least one quaternized cellulose derivative comprising a fatty chain (C 8 -C 30 ).
    [2" claim-type="Currently amended] The composition of claim 1, wherein the polyoxyalkylenated carboxylic acid ethers and salts thereof are of formula (I):
    [Formula 1]
    (In the meal:
    R is a linear or branched C 8 -C 22 alkyl or alkenyl radical, or a mixture of radicals, a (C 8 -C 9 ) alkylphenyl radical or radical R'CONH-CH 2 -CH 2- (wherein R ' Represents a linear or branched C 11 -C 21 alkyl or alkenyl radical,
    n is an integer or fraction from 2 to 24,
    p is an integer or fraction from 0 to 6,
    A represents a hydrogen atom or a Na, K, Li, 1/2 Mg or monoethanolamine, ammonium or triethanolamine residue).
    [3" claim-type="Currently amended] 3. A composition according to claim 2, wherein in formula (1) R represents a ( C12 ) alkyl radical, A represents a hydrogen or sodium atom, p = 0 and n is in the range of 2 to 10.
    [4" claim-type="Currently amended] The quaternized cellulose derivative comprising at least one fatty chain (C 8 -C 30 ) is formed by cellulose and hydroxyethyl cellulose, and is quaternized to give alkyl, arylalkyl or Composition selected from alkylaryl groups or groups modified with mixtures thereof.
    [5" claim-type="Currently amended] The composition of claim 4 wherein the quaternized cellulose derivative comprising at least one fatty chain is selected from quaternized (C 8 -C 30 ) alkylhydroxyethylcelluloses.
    [6" claim-type="Currently amended] A composition according to claim 5, wherein the quaternized cellulose derivative comprising at least one fatty chain (C 8 -C 30 ) is quaternized laurylhydroxyethylcellulose.
    [7" claim-type="Currently amended] 7. Composition according to any of the preceding claims, characterized in that the oxyalkylenated carboxylic acid ethers or salts thereof represent from 2% to 15% by weight relative to the total weight of the composition.
    [8" claim-type="Currently amended] 8. A composition according to claim 7, wherein the oxyalkylenated carboxylic acid ether or salt thereof represents 3% to 10% by weight relative to the total weight of the composition.
    [9" claim-type="Currently amended] The quaternized cellulose derivative comprising at least one fatty chain (C 8 -C 30 ) is present in an amount of from 0.01% to 10% by weight, based on the total weight of the composition. The composition characterized by the above-mentioned.
    [10" claim-type="Currently amended] 10. The composition of claim 9, wherein the quaternized cellulose derivative comprising at least one fatty chain (C 8 -C 30 ) represents 0.1% to 5% by weight relative to the total weight of the composition on a weight basis.
    [11" claim-type="Currently amended] 7. A composition according to any one of the preceding claims wherein the oxidizing dye is selected from an oxidizing base and a coupler.
    [12" claim-type="Currently amended] 12. The composition of claim 11, which contains at least one oxidation base.
    [13" claim-type="Currently amended] 12. The process according to claim 11, wherein the oxidation base is selected from ortho- or para-phenylenediamines, complex bases, ortho- or para-aminophenols and heterocyclic bases, and also addition salts of said compounds and acids. Composition.
    [14" claim-type="Currently amended] The composition of claim 13, wherein the para-phenylenediamine is selected from compounds of the formula:
    [Formula 2]
    (In the meal,
    R 1 is a hydrogen atom, a C 1 -C 4 alkyl radical, a C 1 -C 4 monohydroxyalkyl radical, a C 2 -C 4 polyhydroxyalkyl radical, (C 1 -C 4 ) alkoxy (C 1 -C 4 ) Alkyl radicals, or C 1 -C 4 alkyl radicals substituted with nitrogen-containing phenyl or 4′-aminophenyl groups;
    R 2 is a hydrogen atom, a C 1 -C 4 alkyl radical, a C 1 -C 4 monohydroxyalkyl radical, a C 2 -C 4 polyhydroxyalkyl radical, (C 1 -C 4 ) alkoxy (C 1 -C 4 ) Alkyl radicals, or C 1 -C 4 alkyl radicals substituted with nitrogen-containing groups;
    In addition, R 1 and R 2 together with the nitrogen atoms they contain may form a 5- or 6-membered nitrogen heterocycle which may be substituted with one or more alkyl, hydroxyl or ureido groups;
    R 3 is hydrogen atom, halogen atom, C 1 -C 4 alkyl radical, sulfo radical, carboxyl radical, C 1 -C 4 monohydroxyalkyl radical, C 1 -C 4 hydroxyalkoxy radical, acetylamino (C 1 -C 4 ) alkoxy radical, mesylamino (C 1 -C 4 ) alkoxy radical or carbamoylamino (C 1 -C 4 ) alkoxy radical,
    R 4 represents hydrogen or a halogen atom or a C 1 -C 4 alkyl radical).
    [15" claim-type="Currently amended] The composition of claim 13, wherein the complex base is selected from compounds of formula
    [Formula 3]
    (In the meal:
    Z 1 and Z 2 represent the hydroxyl or —NH 2 radicals which may be the same or different and may be substituted with a C 1 -C 4 alkyl radical or a linking branch Y;
    The linking branch Y is inserted or terminated with at least one nitrogen containing group, at least one hetero atom such as oxygen, sulfur or nitrogen atom, or at least one nitrogen containing group and at least one hetero atom such as oxygen, sulfur or nitrogen atom A linear or branched alkylene chain having 1 to 14 carbon atoms, which may be substituted with one or more hydroxyl or C 1 -C 6 alkoxy radicals;
    R 5 and R 6 represent a hydrogen or halogen atom, a C 1 -C 4 alkyl radical, a C 1 -C 4 monohydroxyalkyl radical, a C 2 -C 4 polyhydroxyalkyl radical, a C 1 -C 4 aminoalkyl radical Or a linking branch Y;
    R 7 , R 8 , R 9 , R 10 , R 11 and R 12 may be the same or different and represent a hydrogen atom, a linking branch Y or a C 1 -C 4 alkyl radical;
    Compounds of formula 3 are understood to contain only one linking branch Y per molecule).
    [16" claim-type="Currently amended] The method of claim 14, wherein the nitrogen-containing group is amino, mono (C 1 -C 4 ) alkylamino, di (C 1 -C 4 ) alkylamino, tri (C 1 -C 4 ) alkylamino, monohydroxy (C 1 -C 4 ) alkylamino, imidazolinium and ammonium radicals.
    [17" claim-type="Currently amended] 14. A composition according to claim 13 wherein the para-aminophenol is selected from compounds of the formula
    [Formula 4]
    (In the meal,
    R 13 is a hydrogen atom, a halogen atom, or C 1 -C 4 alkyl, C 1 -C 4 monohydroxyalkyl, (C 1 -C 4 ) alkoxy (C 1 -C 4 ) alkyl, C 1 -C 4 amino Alkyl or hydroxy (C 1 -C 4 ) alkylamino (C 1 -C 4 ) alkyl radicals,
    R 14 is a hydrogen atom, a halogen atom, or C 1 -C 4 -alkyl, C 1 -C 4 monohydroxyalkyl, C 2 -C 4 polyhydroxyalkyl, C 1 -C 4 aminoalkyl, C 1 -C 4 cyanoalkyl or a (C 1 -C 4 ) alkoxy (C 1 -C 4 ) alkyl radical).
    [18" claim-type="Currently amended] 14. The composition of claim 13, wherein the heterocyclic base is selected from pyridine derivatives, pyrimidine derivatives including pyrazolopyrimidines and pyrazole derivatives.
    [19" claim-type="Currently amended] 12. The composition of claim 11, wherein the oxidation base is present at a concentration ranging from 0.0005% to 12% by weight relative to the total weight of the composition.
    [20" claim-type="Currently amended] 20. The composition of claim 19, wherein the oxidation base is present at a concentration ranging from 0.005% to 8% by weight relative to the total weight of the composition.
    [21" claim-type="Currently amended] 12. The composition of claim 11, wherein the coupler is selected from meta-phenylenediamine, meta-aminophenol, meta-diphenol and heterocyclic couplers, and addition salts of the compound and acid.
    [22" claim-type="Currently amended] 12. The composition of claim 11, wherein the coupler is present at a concentration ranging from 0.0001% to 10% by weight relative to the total weight of the composition.
    [23" claim-type="Currently amended] 23. The composition of claim 22, wherein the coupler is present at a concentration ranging from 0.005% to 5% by weight relative to the total weight of the composition.
    [24" claim-type="Currently amended] 14. The composition of claim 13, wherein the acid addition salts of the oxidizing base and the coupler are selected from hydrochloride, hydrobromide, sulfate, tartrate, lactate and acetate.
    [25" claim-type="Currently amended] The composition according to any one of claims 1 to 6, which also contains a direct dye.
    [26" claim-type="Currently amended] The composition according to claim 1, further comprising at least one reducing agent in an amount in the range of 0.05% to 3% by weight relative to the total weight.
    [27" claim-type="Currently amended] 7. A composition according to any one of the preceding claims, characterized in that it contains at least one oxyalkylenated or mono- or polyglycerolated nonionic surfactant in a ratio in the range of 2% to 40% by weight of the total weight. Composition.
    [28" claim-type="Currently amended] The composition according to any one of claims 1 to 6, which contains one or more unsaturated fatty alcohols in proportions ranging from 0.5% to 15% by weight of the total weight of the dye composition.
    [29" claim-type="Currently amended] 7. A composition according to any one of claims 1 to 6, containing at least one cationic or amphoteric polymer in a ratio in the range of 0.01% to 10% by weight.
    [30" claim-type="Currently amended] In a ready-to-use composition for the oxidative staining of keratin fibers, such as human keratin fibers, such as hair, a dye composition as defined in claim 1, and an oxidizing composition containing at least one oxidant Composition obtained by mixing.
    [31" claim-type="Currently amended] 31. The laccase, peroxidase and 2-electron oxidoreductase according to claim 30, wherein the oxidizing agent may be in the presence of hydrogen peroxide, urea peroxide, alkali metal bromate or ferricyanide, perchlorate, appropriate respective donor or official. A composition, characterized in that selected from oxidoreductases such as.
    [32" claim-type="Currently amended] 32. The composition of claim 31 wherein the oxidant is hydrogen peroxide.
    [33" claim-type="Currently amended] 33. The composition of claim 32 wherein the oxidant is an aqueous hydrogen peroxide solution in an appropriate range of 1 to 40 times.
    [34" claim-type="Currently amended] 7. A composition according to any one of claims 1 to 6, having a pH in the range of 3 to 12.
    [35" claim-type="Currently amended] 31. The composition of claim 30, wherein the oxyalkylenated carboxylic acid ether or salt thereof represents 0.5% to 15% by weight relative to the total weight of the composition.
    [36" claim-type="Currently amended] 36. The composition of claim 35, wherein the oxyalkylenated carboxylic acid ether or salt thereof represents 0.7% to 10% by weight relative to the total weight of the composition.
    [37" claim-type="Currently amended] 31. The composition of claim 30, wherein the fatty chain quaternized cellulose derivative represents 0.0025% to 10% by weight relative to the total weight of the composition on a weight basis.
    [38" claim-type="Currently amended] 38. The composition of claim 37, wherein the fatty chain quaternized cellulose derivative represents from 0.025% to 10% by weight relative to the total weight of the composition on a weight basis.
    [39" claim-type="Currently amended] A method for dyeing keratin fibers, such as human keratin fibers comprising hair, comprising applying a dye composition containing at least one oxidizing dye to a fiber in a medium suitable for dyeing, the color being used in a medium suitable for dyeing Color is developed at an alkaline, neutral or acidic pH using an oxidizing composition comprising at least one oxidant mixed with the dye composition or applied sequentially without intermediate rinsing, and the dye composition and the oxidizing composition are randomly distributed between the two. At least one polyoxyalkylenated carboxylic acid ether or salt thereof, and at least one quaternized cellulose derivative comprising at least one fatty chain (C 8 -C 30 ).
    [40" claim-type="Currently amended] A method for dyeing keratin fibers, such as human keratin fibers comprising hair, comprising applying a dye composition containing at least one oxidizing dye to a fiber in a medium suitable for dyeing, the color being used in a medium suitable for dyeing One that is mixed at an alkaline, neutral or acidic pH using an oxidizing composition comprising at least one oxidant mixed with the dye composition or applied sequentially without intermediate rinsing, and wherein the dye composition or oxidizing composition is combined in the same composition At least one polyoxyalkylenated carboxylic acid ether or salt thereof, and at least one quaternized cellulose derivative comprising at least one fatty chain (C 8 -C 30 ).
    [41" claim-type="Currently amended] 41. The wet or dry keratinous fiber of claim 40, wherein the ready-to-use composition, which is prepared immediately when used from the dye composition and the oxidizing composition, is left to allow the composition to function for an exposure time in the range of approximately 1 to 60 minutes, and the fibers are rinsed. After which they are possibly washed with shampoo and then rinsed and dried again.
    [42" claim-type="Currently amended] 42. The method of claim 41, wherein the exposure time of allowing the composition to act is in the range of 10 to 45 minutes.
    [43" claim-type="Currently amended] In a multi-compartment apparatus or "kit" for dyeing human keratin fibers, such as hair, one or more compartments comprise a dye composition containing one or more oxidizing dyes in a medium suitable for dyeing, and another compartment in a medium suitable for dyeing. An oxidizing composition containing an oxidizing agent, wherein the dye composition and the oxidizing composition also comprise one or more polyoxyalkylenated carboxylic acid ethers or salts thereof, and one or more fatty chains (C 8- C 30 ) A multi-compartment device or "kit" characterized in that it contains one or more quaternized cellulose derivatives.
    [44" claim-type="Currently amended] A multi-compartment apparatus or "kit" for dyeing human keratin fibers, such as hair, comprising an oxidizing agent in a compartment suitable for dyeing, including a dye composition containing one or more oxidizing dyes, and in a medium suitable for dyeing. Consisting of another compartment comprising an oxidizing composition, the dye composition and the oxidizing composition also comprising one or more polyoxyalkylenated carboxylic acid ethers or salts thereof, one or more associative polymers, and one or more fats Multicompartment dyeing apparatus or "kits" containing at least one quaternized cellulose derivative comprising a chain (C 8 -C 30 ).
    类似技术:
    公开号 | 公开日 | 专利标题
    JP3202025B2|2001-08-27|Composition for oxidative dyeing of keratin fibers containing nonionic amphiphilic polymer
    RU2246930C2|2005-02-27|Dyeing composition containing aminosilicone of particular structure for keratin fibers
    US7550015B2|2009-06-23|Dye composition with a reduced content of starting materials, and process for dyeing keratin fibers using the same
    DE60225304T2|2009-02-26|Cosmetic composition with sulphinic acid derivatives
    DE60208337T2|2006-08-17|Agent for the oxidative staining of keratin fibers containing a cationic polyvinyl lactam
    AU749404B2|2002-06-27|Composition for the oxidation dyeing of keratinous fibres comprising a fatty alcohol having more than twenty carbon atoms and an oxyalkylenated nonionic surfactant with an HLB greater than 5
    ES2316465T5|2017-02-17|Discoloration composition of stained keratin fibers
    AU749655B2|2002-06-27|Composition for the oxidation dyeing of keratinous fibres comprising a thickening polymer comprising at least one fatty chain and a fatty alcohol having more than twenty carbon atoms
    DE60125391T3|2015-08-27|Cosmetic composition containing sulfinic acid derivatives
    ES2309002T3|2008-12-16|Composition of oxidation staining of the keratin fibers containing a thicken polymer with aminoplastic eter skeleton.
    RU2176908C2|2001-12-20|Cosmetic composition for treatment of keratin fibers, method of their treatment, method of their coloring, set package for keratin fiber coloring
    AU751648B2|2002-08-22|Composition for the oxidation dyeing of keratinous fibres comprising a thickening polymer comprising at least one fatty chain and a mono-or polyglycerolated fatty alcohol
    ES2300424T3|2008-06-16|Composition of oxidation staining of keratin fibers containing a mono-or polyglycerolate fat spirit and a particular polyol.
    ES2300383T3|2008-06-16|Composition of oxidation staining of the queratinic fibers based on amphifily polymers that leads at least a monomero with ethylene insaturation with sulfonic group and also a hydrophobic part.
    ES2313938T3|2009-03-16|Composition for oxidation staining of querantinic fibers containing a cationic amphifyly polymer, a oxialquilated or glicerolated fatty alcohol and a hydroxylated solvent.
    DE60130790T2|2008-07-17|Composition for dying of keratin fibers containing an associative polymer and a polymer comprising acrylate, dialkyl diallylammonium halogeride and vinyl cabinic acid units
    DE60222682T2|2008-07-17|Cosmetic composition with sulfur acid derivatives
    DE60126976T2|2007-11-08|Composition for the oxidative dyeing of keratin fibers with glycerol and a polyol other than glycerine in a predetermined ratio
    US20030152534A1|2003-08-14|Composition for dyeing keratin fibers comprising a particular aminosilicone
    RU2242213C2|2004-12-20|Composition for oxidizing dyeing keratin fibers containing oxyalkylenic derivatives of oxycarbonic acid and quarternized cellulose with fatty chain
    AU2002325405B2|2005-08-18|Composition for the oxidation dyeing of keratin fibres, comprising an oxyalkylenated carboxylic acid ether, a nonionic surfactant and a particular polymer
    ES2272819T3|2007-05-01|Composition for oxidation staining of keratin fibers containing an amid of oxyethylated frazy acid.
    JP2010532341A|2010-10-07|Method and kit for permanently coloring hair
    AU2002223758B2|2004-09-02|Oxidation dyeing composition for keratinous fibres comprising a cationic associative polyurethane
    RU2240775C2|2004-11-27|Composition for oxidative staining kertin fiber comprising polyoxyalkylene carboxylic acid, associative polymer and unsaturated aliphatic alcohol
    同族专利:
    公开号 | 公开日
    PL357925A1|2003-06-30|
    CA2415259A1|2003-06-21|
    PL206074B1|2010-06-30|
    US7204858B2|2007-04-17|
    JP2003192550A|2003-07-09|
    DE60212053T2|2006-11-30|
    FR2833836A1|2003-06-27|
    DK1323409T3|2006-07-10|
    ES2266433T3|2007-03-01|
    KR100570946B1|2006-04-13|
    BR0205598A|2004-08-03|
    RU2242213C2|2004-12-20|
    AU2002323798B2|2005-08-18|
    PT1323409E|2006-10-31|
    FR2833836B1|2004-01-30|
    AT328575T|2006-06-15|
    EP1323409A3|2003-09-03|
    DE60212053D1|2006-07-20|
    CN1426775A|2003-07-02|
    CN1250199C|2006-04-12|
    MXPA02012934A|2004-09-03|
    EP1323409A2|2003-07-02|
    US20030182734A1|2003-10-02|
    AR038038A1|2004-12-22|
    JP3875631B2|2007-01-31|
    ZA200210198B|2003-07-03|
    EP1323409B1|2006-06-07|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2001-12-21|Priority to FR0116743A
    2001-12-21|Priority to FR0116743
    2002-12-21|Application filed by 로레알
    2003-06-28|Publication of KR20030053458A
    2006-04-13|Application granted
    2006-04-13|Publication of KR100570946B1
    优先权:
    申请号 | 申请日 | 专利标题
    FR0116743A|FR2833836B1|2001-12-21|2001-12-21|Composition for oxidation dyeing of keratinic fibers comprising an oxyalkylene carboxylic ether acid and a quaternized fatty chain cellulose|
    FR0116743|2001-12-21|
    [返回顶部]