RU97122261A - COMPOSITION FOR OXIDATIVE COLORING KERATIN FIBERS, COLORING METHOD USING THIS COMPOSITION AND SET FOR COLORING - Google Patents
COMPOSITION FOR OXIDATIVE COLORING KERATIN FIBERS, COLORING METHOD USING THIS COMPOSITION AND SET FOR COLORINGInfo
- Publication number
- RU97122261A RU97122261A RU97122261/14A RU97122261A RU97122261A RU 97122261 A RU97122261 A RU 97122261A RU 97122261/14 A RU97122261/14 A RU 97122261/14A RU 97122261 A RU97122261 A RU 97122261A RU 97122261 A RU97122261 A RU 97122261A
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- Prior art keywords
- amino
- composition
- para
- alkyl
- composition according
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- 239000000203 mixture Substances 0.000 title claims 41
- 230000001590 oxidative Effects 0.000 title claims 11
- 239000000835 fiber Substances 0.000 title claims 8
- 102000011782 Keratins Human genes 0.000 title claims 7
- 108010076876 Keratins Proteins 0.000 title claims 7
- 238000004040 coloring Methods 0.000 title claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 15
- 238000004043 dyeing Methods 0.000 claims 13
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 13
- 239000011780 sodium chloride Substances 0.000 claims 13
- 239000002253 acid Substances 0.000 claims 11
- 239000002585 base Substances 0.000 claims 11
- CBCKQZAAMUWICA-UHFFFAOYSA-N P-Phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 10
- 239000000975 dye Substances 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- KEEQZNSCYCPKOJ-UHFFFAOYSA-N 2,6-diethylbenzene-1,4-diamine Chemical compound CCC1=CC(N)=CC(CC)=C1N KEEQZNSCYCPKOJ-UHFFFAOYSA-N 0.000 claims 7
- -1 2-chloroparaphenylene diamine Chemical class 0.000 claims 6
- 125000002091 cationic group Chemical group 0.000 claims 6
- BWAPJIHJXDYDPW-UHFFFAOYSA-N 2,5-dimethyl-p-phenylenediamine Chemical compound CC1=CC(N)=C(C)C=C1N BWAPJIHJXDYDPW-UHFFFAOYSA-N 0.000 claims 5
- 239000000654 additive Substances 0.000 claims 5
- 230000000996 additive Effects 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 229910052731 fluorine Inorganic materials 0.000 claims 5
- 125000004103 aminoalkyl group Chemical group 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 239000007800 oxidant agent Substances 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- MJAVQHPPPBDYAN-UHFFFAOYSA-N 2,6-dimethylbenzene-1,4-diamine Chemical compound CC1=CC(N)=CC(C)=C1N MJAVQHPPPBDYAN-UHFFFAOYSA-N 0.000 claims 2
- JLNOVDKXKXTKPN-UHFFFAOYSA-N 2-(1,6-diaminocyclohexa-2,4-dien-1-yl)oxyethanol Chemical compound NC1C=CC=CC1(N)OCCO JLNOVDKXKXTKPN-UHFFFAOYSA-N 0.000 claims 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-Aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-Aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 230000000875 corresponding Effects 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 2
- YZCKVEUIGOORGS-UHFFFAOYSA-N hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 claims 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- JVNHXFFLNMXWNX-UHFFFAOYSA-N 1,3-bis(4-aminoanilino)propan-1-ol Chemical compound C1=CC(N)=CC=C1NCCC(O)NC1=CC=C(N)C=C1 JVNHXFFLNMXWNX-UHFFFAOYSA-N 0.000 claims 1
- KQGOJGSMIRVVJL-UHFFFAOYSA-N 1-N-methyl-4-N-[4-[4-(methylamino)anilino]butyl]benzene-1,4-diamine Chemical compound C1=CC(NC)=CC=C1NCCCCNC1=CC=C(NC)C=C1 KQGOJGSMIRVVJL-UHFFFAOYSA-N 0.000 claims 1
- GZVVXXLYQIFVCA-UHFFFAOYSA-N 2,3-dimethylbenzene-1,4-diamine Chemical compound CC1=C(C)C(N)=CC=C1N GZVVXXLYQIFVCA-UHFFFAOYSA-N 0.000 claims 1
- ZFIKVYNBYPFDNY-UHFFFAOYSA-N 2-(2-aminoanilino)oxyethanol Chemical compound NC1=CC=CC=C1NOCCO ZFIKVYNBYPFDNY-UHFFFAOYSA-N 0.000 claims 1
- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 claims 1
- ALQKEYVDQYGZDN-UHFFFAOYSA-N 2-amino-6-methylphenol Chemical compound CC1=CC=CC(N)=C1O ALQKEYVDQYGZDN-UHFFFAOYSA-N 0.000 claims 1
- DSGHWUWQVNMCKK-UHFFFAOYSA-N 3-amino-4-methoxy-2-methylphenol Chemical compound COC1=CC=C(O)C(C)=C1N DSGHWUWQVNMCKK-UHFFFAOYSA-N 0.000 claims 1
- QNGVNLMMEQUVQK-UHFFFAOYSA-N 4-N,4-N-diethylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C=C1 QNGVNLMMEQUVQK-UHFFFAOYSA-N 0.000 claims 1
- WUWFSMNYUIGVBK-UHFFFAOYSA-N 4-N-(4-aminobutyl)-4-N-(4-aminophenyl)benzene-1,4-diamine Chemical compound C=1C=C(N)C=CC=1N(CCCCN)C1=CC=C(N)C=C1 WUWFSMNYUIGVBK-UHFFFAOYSA-N 0.000 claims 1
- OAQDBKQAJRFJIY-UHFFFAOYSA-N 4-N-[2-(4-amino-N-ethyl-3-methylanilino)ethyl]-4-N-ethyl-2-methylbenzene-1,4-diamine Chemical compound C=1C=C(N)C(C)=CC=1N(CC)CCN(CC)C1=CC=C(N)C(C)=C1 OAQDBKQAJRFJIY-UHFFFAOYSA-N 0.000 claims 1
- BOPZDXATCGECMU-UHFFFAOYSA-N 4-N-[2-(4-aminoanilino)ethyl]benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NCCNC1=CC=C(N)C=C1 BOPZDXATCGECMU-UHFFFAOYSA-N 0.000 claims 1
- OOPWJBCZQDTTNE-UHFFFAOYSA-N 4-N-[4-(4-aminoanilino)butyl]benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NCCCCNC1=CC=C(N)C=C1 OOPWJBCZQDTTNE-UHFFFAOYSA-N 0.000 claims 1
- PZKNKZNLQYKXFV-UHFFFAOYSA-N 4-amino-2-(aminomethyl)phenol Chemical compound NCC1=CC(N)=CC=C1O PZKNKZNLQYKXFV-UHFFFAOYSA-N 0.000 claims 1
- WSEFOZIMAJPJHW-UHFFFAOYSA-N 4-amino-2-(hydroxymethyl)phenol Chemical compound NC1=CC=C(O)C(CO)=C1 WSEFOZIMAJPJHW-UHFFFAOYSA-N 0.000 claims 1
- RGKJLNMYCNSVKZ-UHFFFAOYSA-N 4-amino-2-(methoxymethyl)phenol Chemical compound COCC1=CC(N)=CC=C1O RGKJLNMYCNSVKZ-UHFFFAOYSA-N 0.000 claims 1
- MXJQJURZHQZLNN-UHFFFAOYSA-N 4-amino-2-fluorophenol Chemical compound NC1=CC=C(O)C(F)=C1 MXJQJURZHQZLNN-UHFFFAOYSA-N 0.000 claims 1
- HDGMAACKJSBLMW-UHFFFAOYSA-N 4-amino-2-methylphenol Chemical compound CC1=CC(N)=CC=C1O HDGMAACKJSBLMW-UHFFFAOYSA-N 0.000 claims 1
- DHKIYDNMIXSKQP-UHFFFAOYSA-N 4-amino-3-(hydroxymethyl)phenol Chemical compound NC1=CC=C(O)C=C1CO DHKIYDNMIXSKQP-UHFFFAOYSA-N 0.000 claims 1
- MNPLTKHJEAFOCA-UHFFFAOYSA-N 4-amino-3-fluorophenol Chemical compound NC1=CC=C(O)C=C1F MNPLTKHJEAFOCA-UHFFFAOYSA-N 0.000 claims 1
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 claims 1
- XOVBEQRPIHPGPO-UHFFFAOYSA-N 5-(3-hydroxypropylamino)-2-methylphenol Chemical compound CC1=CC=C(NCCCO)C=C1O XOVBEQRPIHPGPO-UHFFFAOYSA-N 0.000 claims 1
- CQPLGGXOAHSQBD-UHFFFAOYSA-N 5-amino-2,4-dimethoxyphenol Chemical compound COC1=CC(OC)=C(O)C=C1N CQPLGGXOAHSQBD-UHFFFAOYSA-N 0.000 claims 1
- CNEHJJGZSQRWRR-UHFFFAOYSA-N 5-amino-2-(2-hydroxyethoxy)phenol Chemical compound NC1=CC=C(OCCO)C(O)=C1 CNEHJJGZSQRWRR-UHFFFAOYSA-N 0.000 claims 1
- BLQFHJKRTDIZLX-UHFFFAOYSA-N 5-amino-2-methoxyphenol Chemical compound COC1=CC=C(N)C=C1O BLQFHJKRTDIZLX-UHFFFAOYSA-N 0.000 claims 1
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 claims 1
- WDQMXRWYXILWPT-UHFFFAOYSA-N 5-amino-4-chloro-2-methylphenol Chemical compound CC1=CC(Cl)=C(N)C=C1O WDQMXRWYXILWPT-UHFFFAOYSA-N 0.000 claims 1
- MUHQJMUYRYHUIW-UHFFFAOYSA-N 5-amino-4-methoxy-2-methylphenol Chemical compound COC1=CC(C)=C(O)C=C1N MUHQJMUYRYHUIW-UHFFFAOYSA-N 0.000 claims 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N Hydrogen peroxide - urea Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 claims 1
- BKEFUBHXUTWQED-UHFFFAOYSA-N N-(4-amino-3-hydroxyphenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C(O)=C1 BKEFUBHXUTWQED-UHFFFAOYSA-N 0.000 claims 1
- 229940083082 Pyrimidine derivatives acting on arteriolar smooth muscle Drugs 0.000 claims 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001412 amines Chemical group 0.000 claims 1
- 150000001450 anions Chemical group 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 1
- 150000004985 diamines Chemical class 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N iodine atom Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims 1
- 150000002829 nitrogen Chemical group 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 239000003973 paint Substances 0.000 claims 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 1
- 150000003217 pyrazoles Chemical class 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- 150000003230 pyrimidines Chemical class 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 150000003892 tartrate salts Chemical class 0.000 claims 1
Claims (27)
где R1 является атомом водорода, алкилом с C1-C4, моногидроксиалкилом с C1-C4 или полигидроксиалкилом с C2-C4;
R2 является атомом водорода, алкилом с C1-C4, алкоксилом с C1-C4 или атомом галогена, выбираемого среди хлора, брома или фтора,
R3 является алкилом с C1-C4, алкоксилом с C1-C4, моногидроксиалкилом с C1-C4, полигидроксиалкилом с C2-C4, моногидроксиалкоксилом с C1-C4 или полигидроксиалкоксилом с C2-C4,
по меньшей мере один прямой катионный краситель, выбираемый среди соединений следующей формулы II:
где D является атомом азота или группой -СН;
R4 и R5, одинаковые или различные, являются атомом водорода; алкилом с C1-C4, который может быть замещен радикалом -CN, -ОН или NH2, или образуют с атомом углерода бензольного цикла гетероцикл, возможно содержащий кислород или азот, который может быть замещен одним или несколькими алкилами с C1-C4; радикал 4'-аминофенил;
R6 является атомом водорода или галогена, выбираемого среди хлора, брома, иода или фтора, алкоксилом с C1-C4 или ацетилоксилом;
Х является анионом, предпочтительно выбираемым среди хлорида, метилсульфата и ацетата;
А является группой, выбираемой среди следующих структур:
где R7 является алкилом с C1-C4, который может быть замещен гвдроксилом, a R8 является алкоксилом с C1-C4, при условии что, когда D является -СН, А является А4 или А13 и R6 не является алкоксилом, тогда R4 и R5 не обозначают одновременно атом водорода;
и по меньшей мере один окислитель.1. Ink dyeing composition for oxidative dyeing by oxidation of keratin fibers and, in particular, human keratin fibers, such as ready-to-use hair, characterized in that it contains at least one oxidative base in an environment suitable for dyeing, at least one paint-producing component selected among metaminophenol following formula I and their additive salts with acid:
where R 1 is a hydrogen atom, alkyl with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 or polyhydroxyalkyl with C 2 -C 4 ;
R 2 is a hydrogen atom, alkyl with C 1 -C 4 , alkoxy with C 1 -C 4 or halogen atom selected among chlorine, bromine or fluorine,
R 3 is alkyl with C 1 -C 4 , alkoxy with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 , polyhydroxyalkyl with C 2 -C 4 , monohydroxyalkoxy with C 1 -C 4 or polyhydroxyalkoxy with C 2 -C 4 ,
at least one direct cationic dye selected among compounds of the following formula II:
where D is a nitrogen atom or a —CH group;
R 4 and R 5 , the same or different, are a hydrogen atom; alkyl with C 1 -C 4 , which may be substituted by a -CN, -OH or NH 2 radical, or form a heterocycle with a carbon atom of the benzene ring, possibly containing oxygen or nitrogen, which may be substituted with one or more C 1 -C alkyl; 4 ; 4'-aminophenyl radical;
R 6 is a hydrogen or halogen atom selected from chlorine, bromine, iodine or fluorine, alkoxy with C 1 -C 4 or acetyloxy;
X is an anion, preferably selected among chloride, methyl sulfate and acetate;
A is a group selected among the following structures:
where R 7 is alkyl with C 1 -C 4 that may be substituted with hydroxy, and R 8 is alkoxy with C 1 -C 4 , provided that when D is -CH, A is A 4 or A 13 and R 6 is not alkoxy, then R 4 and R 5 do not simultaneously denote a hydrogen atom;
and at least one oxidizing agent.
где R9 является атомом водорода, алкилом с C1-C4, моногиароксиалкилом с C1-C4, полигидроксиалкилом с C2-C4, фенилом, 4'-аминофенилом или алкокси(C1-C4)алкилом с C1-C4;
R10 является атомом водорода, алкилом с C1-C4, моногидроксиалкилом с C1-C4, полигидроксиалкилом с C2-C4;
R11 является атомом водорода, атомом галогена, таким как атом хлора, брома, иода или фтора, алкилом с C1-C4, моногидроксиалкилом с C1-C4, гидроксиалкоксилом с C1-C4 ацетиламиноалкоксилом с C1-C4, мезиламиноалкоксилом с C1-C4 или карбомоиламиноалкоксилом с C1-C4;
R1 является атомом водорода или алкилом с C1-C4.4. The composition according to p. 2 or 3, characterized in that the paraphenylenediamine selected among the compounds of the following formula III and their additive salts with acid:
where R 9 is a hydrogen atom, alkyl with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 , polyhydroxyalkyl with C 2 -C 4 , phenyl, 4'-aminophenyl or alkoxy (C 1 -C 4 ) alkyl with C 1 -C 4 ;
R 10 is a hydrogen atom, alkyl with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 , polyhydroxyalkyl with C 2 -C 4 ;
R 11 is a hydrogen atom, a halogen atom such as a chlorine, bromine, iodine or fluorine atom, alkyl with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 , hydroxyalkoxy with C 1 -C 4 acetylaminoalkoxy with C 1 -C 4 , mesylaminoalkoxy with C 1 -C 4 or carbamoylaminoalkoxy with C 1 -C 4 ;
R 1 is a hydrogen atom or alkyl with C 1 -C 4 .
где Z1 и Z2, одинаковые или различные, являются гидроксилом или NHR16, в котором R16 является атомом водорода или алкилом с C1-C4,
R13 является атомом водорода, алкилом с C1-C4, моногидроксиалкилом с C1-C4, полигидроксиалкилом с C2-C4 или аминоалкилом с C1-C4, аминный остаток которого может быть замещен,
R14 и R15, одинаковые или различные, являются атомом водорода или галогена или алкилом с C1-C4,
Y является радикалом, взятым из группы, образованной следующими радикалами:
-(СН2)n; -(СН2)m-O-(СН2)m; -(СН2)m-СНОН-(СН2)m и
где n - целое число от 0 до 8 включительно;
m - целое число от 0 до 4 включительно.
where Z 1 and Z 2 , identical or different, are hydroxyl or NHR 16 , in which R 16 is a hydrogen atom or alkyl with C 1 -C 4 ,
R 13 is a hydrogen atom, alkyl with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 , polyhydroxyalkyl with C 2 -C 4 or aminoalkyl with C 1 -C 4 , the amine residue of which may be substituted,
R 14 and R 15 , the same or different, are a hydrogen or halogen atom or alkyl with C 1 -C 4 ,
Y is a radical taken from the group formed by the following radicals:
- (CH 2 ) n ; - (CH 2 ) m —O- (CH 2 ) m ; - (CH 2 ) m -CHOH- (CH 2 ) m and
where n is an integer from 0 to 8 inclusive;
m is an integer from 0 to 4 inclusive.
где R17 является атомом водорода или фтора, алкилом с C1-C4, моногидроксиалкилом с C1-C4, алкокси(C1-C4)алкил(C1-C4), аминоалкилом с C1-C4 или гидроксиалкил(C1-C4)аминоалкилом с C1-C4,
R18 является атомом водорода или фтора, алкилом с C1-C4, моногидроксиалкилом с C1-C4, полигидроксиалкилом с C2-C4, аминоалкилом с C1-C4, цианоалкилом с C1-C4 или алкокси(C1-C4)алкил (C1-C4),
при условии, что по меньшей мере один из радикалов R1 или R18 является атомом водорода.8. The composition according to p. 2 or 3, characterized in that the para-aminophenol selected among the compounds of the following formula V and their added salts with acid
where R 17 is a hydrogen or fluorine atom, alkyl with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 , alkoxy (C 1 -C 4 ) alkyl (C 1 -C 4 ), aminoalkyl with C 1 -C 4 or hydroxyalkyl (C 1 -C 4 ) aminoalkyl with C 1 -C 4 ,
R 18 is a hydrogen or fluorine atom, alkyl with C 1 -C 4 , monohydroxyalkyl with C 1 -C 4 , polyhydroxyalkyl with C 2 -C 4 , aminoalkyl with C 1 -C 4 , cyanoalkyl with C 1 -C 4 or alkoxy ( C 1 -C 4 ) alkyl (C 1 -C 4 ),
provided that at least one of the radicals R 1 or R 18 is a hydrogen atom.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9615892A FR2757385B1 (en) | 1996-12-23 | 1996-12-23 | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
FR9615892 | 1996-12-23 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU97122261A true RU97122261A (en) | 1999-08-27 |
RU2160086C2 RU2160086C2 (en) | 2000-12-10 |
Family
ID=9499035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU97122261/14A RU2160086C2 (en) | 1996-12-23 | 1997-12-22 | Composition for oxidative dyeing of keratin fibers, method of dyeing using this composition, and dyeing kit |
Country Status (21)
Country | Link |
---|---|
US (1) | US5919273A (en) |
EP (1) | EP0850636B2 (en) |
JP (1) | JP2968243B2 (en) |
KR (1) | KR100260453B1 (en) |
CN (1) | CN1145473C (en) |
AR (1) | AR009667A1 (en) |
AT (1) | ATE179592T1 (en) |
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DE (1) | DE69700210T3 (en) |
DK (1) | DK0850636T3 (en) |
ES (1) | ES2134055T5 (en) |
FR (1) | FR2757385B1 (en) |
GR (1) | GR3030473T3 (en) |
HU (1) | HU224430B1 (en) |
MX (1) | MX222898B (en) |
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FR3130569B1 (en) | 2021-12-16 | 2024-06-28 | Oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3130572A1 (en) | 2021-12-16 | 2023-06-23 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3130571B1 (en) | 2021-12-16 | 2024-02-16 | Oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3130567B1 (en) | 2021-12-16 | 2024-02-16 | Oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3130568B1 (en) | 2021-12-16 | 2024-02-16 | Oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3130570A1 (en) | 2021-12-16 | 2023-06-23 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3130610A1 (en) | 2021-12-20 | 2023-06-23 | L'oreal | Composition comprising a polyhydroxyalkanoate copolymer with a long hydrocarbon chain containing ionic group(s), process for treating keratin materials using the composition |
FR3136967A1 (en) | 2022-06-22 | 2023-12-29 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3136975A1 (en) | 2022-06-22 | 2023-12-29 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3136972A1 (en) | 2022-06-22 | 2023-12-29 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3136968A1 (en) | 2022-06-22 | 2023-12-29 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3136976A1 (en) | 2022-06-22 | 2023-12-29 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3136966A1 (en) | 2022-06-22 | 2023-12-29 | L'oreal | Composition for lightening keratin fibers and process for lightening keratin fibers using this composition |
FR3144510A1 (en) | 2022-12-29 | 2024-07-05 | L'oreal | Composition comprising at least N,N-dicarboxymethyl glutamic acid, at least one direct dye, at least one cationic polysaccharide, and at least one non-cationic polysaccharide |
FR3144513A1 (en) | 2022-12-29 | 2024-07-05 | L'oreal | Composition comprising at least N,N-dicarboxymethyl glutamic acid, at least one direct dye, and at least one associative polymer |
FR3144511A1 (en) | 2022-12-29 | 2024-07-05 | L'oreal | Composition comprising at least one direct dye, at least N,N-dicarboxymethyl glutamic acid, at least one cationic surfactant and at least one non-silicone fatty substance in a particular content |
FR3144512A1 (en) | 2022-12-29 | 2024-07-05 | L'oreal | Composition comprising at least N,N-dicarboxymethyl glutamic acid, at least one coloring agent, and at least one fatty amine |
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1997
- 1997-11-25 DE DE69700210.1T patent/DE69700210T3/en not_active Expired - Lifetime
- 1997-11-25 AT AT97402834T patent/ATE179592T1/en active
- 1997-11-25 EP EP97402834.2A patent/EP0850636B2/en not_active Expired - Lifetime
- 1997-11-25 DK DK97402834T patent/DK0850636T3/en active
- 1997-11-25 ES ES97402834.2T patent/ES2134055T5/en not_active Expired - Lifetime
- 1997-12-09 AU AU47629/97A patent/AU694398B2/en not_active Ceased
- 1997-12-11 MX MX9710072A patent/MX222898B/en active IP Right Grant
- 1997-12-15 ZA ZA9711240A patent/ZA9711240B/en unknown
- 1997-12-17 CZ CZ19974077A patent/CZ291838B6/en not_active IP Right Cessation
- 1997-12-17 AR ARP970105931A patent/AR009667A1/en active IP Right Grant
- 1997-12-18 BR BRPI9706295-2A patent/BR9706295B1/en not_active IP Right Cessation
- 1997-12-19 HU HU9702512A patent/HU224430B1/en not_active IP Right Cessation
- 1997-12-19 US US08/994,127 patent/US5919273A/en not_active Expired - Lifetime
- 1997-12-22 JP JP9353833A patent/JP2968243B2/en not_active Expired - Lifetime
- 1997-12-22 RU RU97122261/14A patent/RU2160086C2/en not_active IP Right Cessation
- 1997-12-22 CN CNB971208832A patent/CN1145473C/en not_active Expired - Fee Related
- 1997-12-22 KR KR1019970071967A patent/KR100260453B1/en not_active IP Right Cessation
- 1997-12-22 CA CA002223726A patent/CA2223726C/en not_active Expired - Fee Related
- 1997-12-22 PL PL97323987A patent/PL188695B1/en not_active IP Right Cessation
-
1999
- 1999-06-09 GR GR990401546T patent/GR3030473T3/en unknown
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