Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/10—Preparations for permanently dyeing the hair
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds

Definitions

• the subject of the invention is a composition for the oxidation dyeing of keratin fibers, in particular human keratin fibers such as the hair, containing as coupler at least one pyrazolo- [3,4-d] - thiazole compound and at least one oxidation base.
• oxidation dye precursors in particular ortho or paraphenylenediamines, ortho or paraaminophenols, heterocyclic compounds, generally called oxidation bases.
• oxidation bases are colorless or weakly colored compounds which, associated with oxidizing products, can give rise, through an oxidative condensation process, to colored and coloring compounds.
• couplers or color modifiers the latter being chosen in particular from aromatic metadiamines, metaaminophenols, metadiphenols and certain heterocyclic compounds such as as indole compounds.
• the dyes must also make it possible to cover white hair, and finally be the least selective possible, that is to say allow to obtain the smallest possible color differences throughout the same keratin fiber, which can be in fact, differently sensitized (ie damaged) between its tip and its root.
• the subject of the invention is a composition for the oxidation dyeing of keratin fibers and in particular human keratin fibers such as the hair, characterized in that it comprises, in a medium suitable for dyeing:
• - R represents a hydrogen atom, a halogen atom such as bromine, chlorine or fluorine; an alkoxy radical (such as for example: methoxy, ethoxy, propyloxy, benzyloxy, methoxyethoxy, phenoxyethoxy, 2-cyanoethoxy, phenethyloxy, p-chlorobenzyloxy, methoxyethylcarbamoylmethoxy); an aryloxy radical (such as for example: phenoxy,
• a pyrazolyl radical an imidazolyl radical; a triazolyl radical; a tetrazolyl radical; a benzimidazolyl radical; a radical 1-benzyl 5-ethoxy 3-hydanto ' ⁇ nyle; a 1-benzyl 3-hydantoinyl radical; 5,5-dimethyl 2,4-dioxo 3-oxazolidinyl; a 2-oxy 1,2,2-dihydro 1-pyridinyl radical; an alkylamido radical; an arylamido radical; a radical NR "R IV with R" and R ', identical or different, an alkyl DC 4 hydroxyalkyl CC 4, a carboxyl radical, an alkoxycarboxyl radical, an alkyloxycarbonylamino radical, a aryloxycarbonylamino group, a sulfonyloxy such as methanesul
• R 2 can also denote a halogen atom (such as bromine, chlorine or fluorine); an acyl radical; a sulfonyl radical; a sulfinyl radical; a phosphonyl radical, a carbamoyl radical; a sulfamoyl radical; a cyano radical; a siloxy radical; an amino radical; an acylamino radical; an acyloxy radical; a carbamoyloxy radical; a sulfonamide radical; an imide radical; a ureido radical; a sulfamoylamino radical; an alkoxycarbonylamino radical; an aryloxycarbonylami ⁇ o radical; an alkoxycarbonyl radical; an aryloxycarbonyl radical; a carboxyl radical.
• a halogen atom such as bromine, chlorine or fluorine
• the addition salts with an acid of the compounds of the invention can be chosen in particular from hydrochlorides, hydrobromides, tartrates, tosylates, benzenesulfonates, sulfates, lactates and acetates.
• radicals R of the formula (I) defined above, preferred are the radicals chosen from the group consisting of a hydrogen atom; a C r C 4 alkoxy radical; phenoxy; phenoxy substituted with a halogen atom, a C 4 -C 4 alkyl, a carboxyl or a trifluoromethyl group; an acyloxy radical; benzyloxy; C r C 4 alkylthio; phenylthio; phenylthio substituted by a halogen atom, a C 4 -C 4 alkyl, a carboxyl or a trifluoromethyl group; a C 1 -C 4 alkylamido; phenylamido; a radical NR '"R I with R'" and R ⁇ v representing, identical or different, a C r C 4 alkyl or a CC 4 hydroxyalkyl; a carboxyl; a C 1 -C 4 alkoxycarboxyl
• radicals R are chosen, chosen from the group consisting of hydrogen, chlorine; ethoxy; phenoxy; benzyloxy; acyloxy; acetamido and dimethylamino.
• radicals R 2 of the formula (I) defined above preferred are the radicals chosen from the group consisting of a hydrogen atom; linear or branched C 1 -C 4 alkyl; phenyl; phenyl substituted with a halogen atom, a C, -C 4l alkoxy C, -C 4 alkyl, nitro, amino, trifluoromethyl or alkylamino C r C 4; a benzyl radical; benzyl substituted by a halogen radical, a C r C 4 alkoxy, C r C 4, a nitro group, an amino group, a trifluoromethyl group; a CC 4 alkylamino; a heterocycle chosen from thiophene, furan or pyridine; a trifluoromethyl radical; a radical (CH 2 ) p -X- (CH 2 ) q -OR 'where p and q are integers, identical or different, comprised between 1 and 3,
• R 2 radicals chosen from the group consisting of hydrogen are preferred; an alkyl chosen from methyl, ethyl, isopropyl, tert-butyl; a halogen chosen from fluorine and chlorine; phenyl; toluyle; 4-chlorophenyl; 4-methoxyphenyl; 3-methoxyphenyl; 2-methoxyphenyl; benzyl; a heterocycle chosen from pyridyl, furyl or thienyl; trifluoromethyl; hydroxymethyl; aminomethyl, methoxy or ethoxy; methylamino or ethylamino or dimethylamino; carboxyl; methoxycarbonyl or ethoxycarbonyl; cyano.
• radicals R 2 chosen from the group consisting of a hydrogen atom are preferred; a methyl radical; ethyl phenyl; toluyle; 4-chlorophenyl; 4-methoxyphenyl; benzyl trifluoromethyl; chloro; a methoxy or ethoxy radical; a methylamino or dimethylamino carboxyl radical; cyano.
• R. represents a hydrogen or chlorine atom and in which R 2 represents a hydrogen atom, a methyl, ethyl, isopropyl, phenyl, ethoxy, trifluoromethyl or methylthio radical.
• the compound or compounds of formula (I) in accordance with the invention preferably represent from 0.0005 to 12% by weight approximately of the total weight of the dye composition, and even more preferably from 0.005 to 6% by weight approximately of this weight .
• oxidation base or bases which can be used in the dye composition according to the invention is not critical.
• This or these oxidation bases are preferably chosen from paraphenylenediamines, bis-phenylalkylenediamines, paraaminophenols, ortho-aminophenols, heterocyclic bases, and their addition salts with an acid.
• R 3 represents a hydrogen atom, an alkyl radical DC 4 DC 4 monohydroxyalkyl, polyhydroxyalkyl, C 2 -C 4 alkoxy or (C r C 4) alkyl (C r C 4), - R 4 represents hydrogen, an alkyl radical in C r -C 4 monohydroxyalkyl, C r -C 4 polyhydroxyalkyl or C 2 -C 4,
• - R 5 represents a hydrogen atom, a halogen atom such as a chlorine atom, a C r C 4 alkyl radical, sulfo, carboxy, C r C 4 monohydroxyalkyl or CC 4 hydroxyalkoxy
• - R 6 represents a hydrogen atom or a C r C 4 alkyl radical.
• R 3 and R 4 preferably represent a hydrogen atom and R 5 is preferably identical to R 6 , and when R 5 represents a halogen atom, then R 3 , R 4 and R 6 preferably represent a hydrogen atom.
• paraphenylenediamines of formula (II) above there may be mentioned more particularly paraphenylenediamine, paratoluylenediamine, 2-isopropyl paraphenylen ⁇ e-diamine, 2- ⁇ -hydroxyethyl paraphenylenediamine, 2- ⁇ -hydroxyethyloxy para-phenylenediamine, 2,6-dimethyl paraphenylenediamine, 2,6-diethyl paraphenylene diamine, 2,3-dimethyl paraphenylenediamine, N, N-bis- ( ⁇ -hydroxyethyl) para-phenylenediamine, 4-amino 1- ( ⁇ - methoxyethyl) amino benzene, 2-chloro para-phenylenediamine, and their addition salts with an acid.
• - Q, and Q 2 identical or different, represent a hydroxyl radical or NHR 10 in which R 10 represents a hydrogen atom or a C-rC alkyl radical,
• R 7 represents a hydrogen atom, an alkyl radical in C, -C 4l monohydroxyalkyl, C r -C 4 polyhydroxyalkyl, C 2 -C 4 aminoalkyl or C, -C 4 alkyl which remains the amino may be substituted,
• R 8 and R 9 identical or different, represent a hydrogen or halogen atom or a CC 4 alkyl radical
• - W represents a radical taken from the group consisting of the following radicals:
• n is an integer between 0 and 8 inclusive and m is an integer between 0 and 4 inclusive.
• N N'-bis- ( ⁇ -hydroxyethyl) N, N'-bis- (4'-aminophenyl) 1, 3-diamino 2-propanol
• N, N'-bis- (4-methylaminophenyl) tetramethylenediamine N.N'-bis- (ethyl) N, N'-bis- (4'-amino, 3'-methylphenyl) ethylenediamine, and their acid addition salts.
• N, N'-bis- ( ⁇ - hydroxyethyl) N, N'-bis- (4'-aminophenyl) 1, 3-diamino propanol or one of its salts addition with an acid are particularly preferred.
• - R represents a hydrogen atom, an alkyl radical CC 4 monohydroxyalkyl, C r C 4 alkoxy (C r C 4) alkyl (C, -C 4) alkylamino or C
• -C 4 - R 12 represents a hydrogen or fluorine atom, an alkyl radical in C r -C 4 monohydroxyalkyl, C r -C 4 polyhydroxyalkyl, C 2 -C 4 aminoalkyl, C r -C 4 cyanoalkyl or CC 4 alkoxy ( C 1 -C 4 ) (C 1 -C 4 ) alkyl, it being understood that at least one of the radicals R 1 or R 12 represents a hydrogen atom.
• paraaminophenols of formula (IV) above mention may more particularly be made of paraaminophenol, 4-amino 3-methyl phenol, 4-amino 3-fluoro phenol, 4-amino 3-hydroxymethyl phenol, 4- amino 2-methyl phenol, 4-amino 2-hydroxymethyl phenol, 4-amino 2-methoxymethyl phenol, 4-amino 2-aminomethyl phenol, 4-amino 2- ( ⁇ -hydroxyethyl aminomethyl) phenol, and their salts addition with an acid.
• ortho-aminophenols which can be used as oxidation bases in the dye composition according to the invention, mention may be made in particular of 2-amino phenol, 2-amino 1-hydroxy 5-methyl benzene, 2-ami ⁇ o 1- hydroxy 6-methyl benzene, 5-acetamido 2-amino phenol, and their addition salts with an acid.
• heterocyclic bases which can be used as oxidation bases in the dye composition according to the invention, mention may in particular be made of pyridine derivatives, pyrimidine derivatives, pyrazole derivatives, and their addition salts with an acid.
• pyridine derivatives mention may more particularly be made of the compounds described for example in patents GB 1 026 978 and GB 1 153 196, such as 2,5-diaminopyridine, and their addition salts with an acid.
• pyrimidine derivatives mention may more particularly be made of the compounds described for example in the German patents DE 2 359 399 or Japanese JP 88-169 571 and JP 91-333 495, such as 2,4,5,6-tetra-aminopyrimidine , 4-hydroxy 2,5,6-triamino-pyrimidine, and their acid addition salts.
• pyrazole derivatives mention may more particularly be made of the compounds described in the patents DE 3 843 892, DE 4 133 957 and patent applications WO 94/08969 and WO 94/08970 such as 4,5-diamino 1-methyl pyrazole, 3,4-diamino pyrazole and 1- (4'-chiorobenzyl) -4.5-diaminopyrazole, and their addition salts with an acid.
• the oxidation base (s) preferably represent from 0.0005 to 12% by weight approximately of the total weight of the dye composition, and even more preferably from 0.005 to 6% by weight approximately of this weight.
• the dye composition according to the invention may also contain one or more additional couplers different from the compounds of formula (I) and / or one or more direct dyes so as to vary or enhance the shades obtained with the oxidation bases in reflections.
• the additional couplers which can be used in the composition according to the invention can be chosen from the couplers conventionally used in oxidation dyeing and among which there may be mentioned in particular metaphenylenediamines, meta-aminophenols, metadiphenols and heterocyclic couplers such as by example indole derivatives, indoline derivatives, and their addition salts with an acid
• couplers can in particular be chosen from 2-methyl 5-am ⁇ no phenol, 5-N- ( ⁇ -hydroxyethyl) am ⁇ no 2-methyl phenol, 3-am ⁇ no phenol, 1, 3-d ⁇ hydroxybenzène, 1, 3- d ⁇ hydroxy 2-methyl benzene, 4-chloro 1, 3-d ⁇ hydroxy benzene, 2,4-d ⁇ am ⁇ no l- ( ⁇ -hydroxyethyloxy) benzene, 2-am ⁇ no 4- ( ⁇ -hydroxyethylam ⁇ no) 1-methoxy benzene , 3-d ⁇ am ⁇ no benzene, 1, 3-b ⁇ s- (2,4-d ⁇ am ⁇ nophenoxy) propane, sesamol, ⁇ -naphthol, 6-hydroxy indole, 4-hydroxy indole, 4-hydroxy N-methyl indole, 6-hydroxy indoline, and their acid addition salts
• these additional couplers preferably represent from 0.0005 to 5% by weight approximately of the total weight of the dye composition, and even more preferably from 0.005 to 3% by weight approximately of this weight
• the addition salts with an acid of the oxidation base (s) and / or additional couplers which can be used in the dye composition of the invention are in particular chosen from hydrochlorides, hydrobromides, sulphates and tartrates, lactates and acetates
• the medium suitable for dyeing (or support) generally consists of water or of a mixture of water and at least one organic solvent to dissolve the compounds which are not sufficiently soluble in water.
• lower alcohols C 4 -C 4
• glycerol such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, monoethyl ether and diethylene glycol monomethyl ether
• aromatic alcohols such as benzyl alcohol or phenoxyethanol, analogues and mixtures thereof.
• the solvents may be present in proportions preferably of between 1 and 40% by weight approximately relative to the total weight of the dye composition, and even more preferably between 5 and 30% by weight approximately.
• the pH of the dye composition according to the invention is generally between 3 and 12. It can be adjusted to the desired value by means of acidifying or basifying agents usually used in dyeing keratin fibers.
• acidifying agents there may be mentioned, by way of example, mineral or organic acids such as hydrochloric acid, orthophosphoric acid, carboxylic acids such as tartaric acid, citric acid, lactic acid, sulfonic acids.
• mineral or organic acids such as hydrochloric acid, orthophosphoric acid, carboxylic acids such as tartaric acid, citric acid, lactic acid, sulfonic acids.
• basifying agents there may be mentioned, by way of example, ammonia, alkali carbonates, alkanolamines such as mono-, di- and triethanolamines as well as their derivatives, sodium or potassium hydroxides and compounds of following formula (V):
• R is a propylene residue optionally substituted by a hydroxyl group or a C r C 4 alkyl radical
• R 13, R t4, R 15 and R 16, identical or different, represent a hydrogen atom, an alkyl radical in C -.- C 4 hydroxyalkyl or C r C 4.
• the dye composition according to the invention may also contain various adjuvants conventionally used in compositions for dyeing the hair, such as anionic, cationic, nonionic, amphoteric, zwitterionic surfactants or mixtures thereof, anionic, cationic polymers , nonionic, amphoteric, zwitterionic or their mixtures, mineral or organic thickening agents, antioxidant agents, penetration agents, sequestering agents, perfumes, buffers, dispersing agents, conditioning agents such as for example silicones, film-forming agents, preserving agents, opacifying agents.
• adjuvants conventionally used in compositions for dyeing the hair, such as anionic, cationic, nonionic, amphoteric, zwitterionic surfactants or mixtures thereof, anionic, cationic polymers , nonionic, amphoteric, zwitterionic or their mixtures, mineral or organic thickening agents, antioxidant agents, penetration agents, sequestering agents, perfumes, buffers, dispersing agents, conditioning agents such
• the dye composition according to the invention can be in various forms, such as in the form of liquids, creams, gels, or in any other form suitable for dyeing keratin fibers, and in particular human hair.
• a subject of the invention is also the use of the compounds of formula (I) above, as a coupler, in combination with at least one oxidation base for the oxidation dyeing of keratin fibers and in particular of keratin fibers human such as hair.
• Another subject of the invention is a process for the oxidation dyeing of keratin fibers and in particular human keratin fibers such as the hair, using the dye composition as defined above.
• At least one dye composition as defined above is applied to the fibers, the color being revealed at acidic, neutral or alkaline pH using an oxidizing agent which is added just at the time of use. the dye composition or which is present in an oxidizing composition applied simultaneously or sequentially separately.
• the dye composition described above is mixed at the time of use with an oxidizing composition containing, in a medium suitable for dyeing, minus an oxidizing agent present in an amount sufficient to develop coloring.
• the mixture obtained is then applied to the keratin fibers and left to stand for 3 to 50 minutes approximately, preferably 5 to 30 minutes approximately, after which it is rinsed, washed with shampoo, rinsed again and dried.
• the oxidizing agent present in the oxidizing composition as defined above can be chosen from the oxidizing agents conventionally used for the oxidation dyeing of keratin fibers, and among which mention may be made of hydrogen peroxide, urea, alkali metal bromates, persalts such as perborates and persulfates. Hydrogen peroxide is particularly preferred.
• the pH of the oxidizing composition containing the oxidizing agent as defined above is such that after mixing with the dye composition, the pH of the resulting composition applied to the keratin fibers preferably varies between 3 and 12 approximately and even more preferably between 5 and 11. It is adjusted to the desired value by means of acidifying or basifying agents usually used in dyeing keratin fibers and as defined above.
• the oxidizing composition as defined above may also contain various adjuvants conventionally used in compositions for dyeing the hair and as defined above.
• composition which is finally applied to the keratin fibers can be in various forms, such as in the form of liquids, creams, gels, or in any other form suitable for dyeing keratin fibers, and in particular human hair. .
• Another object of the invention is a device with several compartments or "kit” for dyeing or any other packaging system with several compartments, a first compartment of which contains the dye composition as defined above and a second compartment of which contains the oxidizing composition. as defined above.
• the dye composition was mixed with an equal amount by weight of an aqueous solution of ammonium persulfate to 6.10- 3 mole%.
• the dye composition was mixed with an equal amount by weight of an aqueous solution of hydrogen peroxide at 20 volumes.
• the mixture obtained was applied for 30 minutes to locks of natural gray hair containing 90% white hairs, permanent or not, at a rate of 10 g per 1 g of hair. After rinsing, washing with a standard shampoo and drying the locks, powerful colors are obtained, which are not very selective in the range of reds.
• the dye composition was mixed with an equal amount by weight of an aqueous solution of ammonium persulfate at 6.10 '3 mole%.
• the mixture obtained was applied for 30 minutes to locks of natural gray hair containing 90% white hairs, permanent or not, at a rate of 10 g per 1 g of hair. After rinsing, washing with a standard shampoo and drying the locks, powerful colors are obtained, which are not very selective in the range of reds.
• the dye composition was mixed with an equal amount by weight of an aqueous solution of hydrogen peroxide at 20 volumes.
• the mixture obtained was applied for 30 minutes to locks of natural gray hair containing 90% white hairs, permanent or not, at a rate of 10 g per 1 g of hair. After rinsing, washing with a standard shampoo and drying the locks, powerful colors are obtained, which are not very selective in the range of reds.

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Birds (AREA)
• Epidemiology (AREA)
• Cosmetics (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=9495206

Family Applications (1)

Country Status (6)

Families Citing this family (11)

Family Cites Families (17)

• 1996
  • 1996-08-26 FR FR9610448A patent/FR2752523B1/fr not_active Expired - Fee Related
• 1997
  • 1997-08-22 WO PCT/FR1997/001521 patent/WO1998008486A2/fr not_active Application Discontinuation
  • 1997-08-22 JP JP51133498A patent/JP3288388B2/ja not_active Expired - Fee Related
  • 1997-08-22 US US09/242,902 patent/US6139589A/en not_active Expired - Fee Related
  • 1997-08-22 AU AU41210/97A patent/AU4121097A/en not_active Abandoned
  • 1997-08-22 EP EP97938945A patent/EP0927021A2/de not_active Withdrawn

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events