RU2000121060A - COLORING COMPOSITION AND METHODS OF PAINTING KERATIN FIBERS WITH WHICH ITS USE IT - Google Patents
COLORING COMPOSITION AND METHODS OF PAINTING KERATIN FIBERS WITH WHICH ITS USE ITInfo
- Publication number
- RU2000121060A RU2000121060A RU2000121060/14A RU2000121060A RU2000121060A RU 2000121060 A RU2000121060 A RU 2000121060A RU 2000121060/14 A RU2000121060/14 A RU 2000121060/14A RU 2000121060 A RU2000121060 A RU 2000121060A RU 2000121060 A RU2000121060 A RU 2000121060A
- Authority
- RU
- Russia
- Prior art keywords
- composition according
- composition
- paragraphs
- laccases
- keratin fibers
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 39
- 239000000835 fiber Substances 0.000 title claims 10
- 102000011782 Keratins Human genes 0.000 title claims 9
- 108010076876 Keratins Proteins 0.000 title claims 9
- 238000004040 coloring Methods 0.000 title claims 4
- 229920001577 copolymer Polymers 0.000 claims 13
- 229920000642 polymer Polymers 0.000 claims 13
- 108010029541 Laccase Proteins 0.000 claims 12
- 125000002091 cationic group Chemical group 0.000 claims 6
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinylpyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 5
- -1 methacryloyloxyethyl trimethyl ammonium halide Chemical class 0.000 claims 5
- 239000002253 acid Substances 0.000 claims 4
- 239000000975 dye Substances 0.000 claims 4
- 230000003647 oxidation Effects 0.000 claims 4
- 238000007254 oxidation reaction Methods 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 239000011780 sodium chloride Substances 0.000 claims 4
- 108090000790 Enzymes Proteins 0.000 claims 3
- 102000004190 Enzymes Human genes 0.000 claims 3
- 230000000875 corresponding Effects 0.000 claims 3
- 229920001519 homopolymer Polymers 0.000 claims 3
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-Aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims 2
- 241000196324 Embryophyta Species 0.000 claims 2
- 229940088598 Enzyme Drugs 0.000 claims 2
- 241000813090 Rhizoctonia solani Species 0.000 claims 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 2
- 239000000969 carrier Substances 0.000 claims 2
- 239000000306 component Substances 0.000 claims 2
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 claims 2
- 239000006185 dispersion Substances 0.000 claims 2
- 238000004043 dyeing Methods 0.000 claims 2
- 150000004820 halides Chemical class 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 239000002480 mineral oil Substances 0.000 claims 2
- 235000010446 mineral oil Nutrition 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- 229920001296 polysiloxane Polymers 0.000 claims 2
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-Naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims 1
- WSMJTXVQAZYLAV-UHFFFAOYSA-N 1-methylindol-4-ol Chemical compound C1=CC=C2N(C)C=CC2=C1O WSMJTXVQAZYLAV-UHFFFAOYSA-N 0.000 claims 1
- XAWPKHNOFIWWNZ-UHFFFAOYSA-N 1H-indol-6-ol Chemical compound OC1=CC=C2C=CNC2=C1 XAWPKHNOFIWWNZ-UHFFFAOYSA-N 0.000 claims 1
- JWLQULBRUJIEHY-UHFFFAOYSA-N 2,3-dihydro-1H-indol-6-ol Chemical compound OC1=CC=C2CCNC2=C1 JWLQULBRUJIEHY-UHFFFAOYSA-N 0.000 claims 1
- WCPGNFONICRLCL-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)ethanol Chemical compound NC1=CC=C(OCCO)C(N)=C1 WCPGNFONICRLCL-UHFFFAOYSA-N 0.000 claims 1
- SBUMIGFDXJIPLE-UHFFFAOYSA-N 2-(3-amino-4-methoxyanilino)ethanol Chemical compound COC1=CC=C(NCCO)C=C1N SBUMIGFDXJIPLE-UHFFFAOYSA-N 0.000 claims 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical group CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims 1
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 claims 1
- FLROJJGKUKLCAE-UHFFFAOYSA-N 3-amino-2-methylphenol Chemical compound CC1=C(N)C=CC=C1O FLROJJGKUKLCAE-UHFFFAOYSA-N 0.000 claims 1
- 229940018563 3-aminophenol Drugs 0.000 claims 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-Aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 1
- MWKPYVXITDAZLL-UHFFFAOYSA-N 4-[3-(2,4-diaminophenoxy)propoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCOC1=CC=C(N)C=C1N MWKPYVXITDAZLL-UHFFFAOYSA-N 0.000 claims 1
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims 1
- NLMQHXUGJIAKTH-UHFFFAOYSA-N 4-hydroxyindole Chemical compound OC1=CC=CC2=C1C=CN2 NLMQHXUGJIAKTH-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
- JJHVYGVVMBYCMQ-UHFFFAOYSA-N 6-hydroxy-4-methyl-1H-pyridin-2-one Chemical compound CC=1C=C(O)NC(=O)C=1 JJHVYGVVMBYCMQ-UHFFFAOYSA-N 0.000 claims 1
- 240000004731 Acer pseudoplatanus Species 0.000 claims 1
- 235000002754 Acer pseudoplatanus Nutrition 0.000 claims 1
- 241000157282 Aesculus Species 0.000 claims 1
- 244000144730 Amygdalus persica Species 0.000 claims 1
- 235000011446 Amygdalus persica Nutrition 0.000 claims 1
- 240000001407 Anacardium occidentale Species 0.000 claims 1
- 235000001274 Anacardium occidentale Nutrition 0.000 claims 1
- JYZIHLWOWKMNNX-UHFFFAOYSA-N Benzimidazole Chemical compound C1=C[CH]C2=NC=NC2=C1 JYZIHLWOWKMNNX-UHFFFAOYSA-N 0.000 claims 1
- KNMXNVMDTOAYBU-UHFFFAOYSA-N C(C(=C)C)(=O)OCC[N+](C(C)(C)C)(C)C Chemical compound C(C(=C)C)(=O)OCC[N+](C(C)(C)C)(C)C KNMXNVMDTOAYBU-UHFFFAOYSA-N 0.000 claims 1
- IGJVJJYVRVZWBP-UHFFFAOYSA-O C(C(=C)C)(=O)OCC[NH2+]C(C(C)C)=O Chemical compound C(C(=C)C)(=O)OCC[NH2+]C(C(C)C)=O IGJVJJYVRVZWBP-UHFFFAOYSA-O 0.000 claims 1
- HQLVRJJDJGNYQW-UHFFFAOYSA-O CC=C[NH+]1C=NC=C1 Chemical group CC=C[NH+]1C=NC=C1 HQLVRJJDJGNYQW-UHFFFAOYSA-O 0.000 claims 1
- 241000723377 Coffea Species 0.000 claims 1
- 244000251987 Coprinus macrorhizus Species 0.000 claims 1
- 235000001673 Coprinus macrorhizus Nutrition 0.000 claims 1
- 241000208175 Daucus Species 0.000 claims 1
- KZQYIMCESJLPQH-UHFFFAOYSA-N Demethylated antipyrine Chemical compound N1C(C)=CC(=O)N1C1=CC=CC=C1 KZQYIMCESJLPQH-UHFFFAOYSA-N 0.000 claims 1
- UIOFUWFRIANQPC-JKIFEVAISA-N Floxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=C(F)C=CC=C1Cl UIOFUWFRIANQPC-JKIFEVAISA-N 0.000 claims 1
- 241000146398 Gelatoporia subvermispora Species 0.000 claims 1
- 240000002883 Ginkgo biloba Species 0.000 claims 1
- 210000000554 Iris Anatomy 0.000 claims 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N M-Phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims 1
- 241001330975 Magnaporthe oryzae Species 0.000 claims 1
- 240000007119 Malus pumila Species 0.000 claims 1
- 235000011430 Malus pumila Nutrition 0.000 claims 1
- 235000015103 Malus silvestris Nutrition 0.000 claims 1
- 241000751065 Monotropa hypopitys Species 0.000 claims 1
- 241000204931 Musa sp. Species 0.000 claims 1
- 108090000854 Oxidoreductases Proteins 0.000 claims 1
- 102000004316 Oxidoreductases Human genes 0.000 claims 1
- 241000310787 Panaeolus papilionaceus Species 0.000 claims 1
- 241001156632 Panaeolus sphinctrinus Species 0.000 claims 1
- 229940072417 Peroxidase Drugs 0.000 claims 1
- 108090000437 Peroxidases Proteins 0.000 claims 1
- 102000003992 Peroxidases Human genes 0.000 claims 1
- 235000008092 Pistacia terebinthus subsp palaestina Nutrition 0.000 claims 1
- 241000058012 Pistacia terebinthus subsp. palaestina Species 0.000 claims 1
- 241000789035 Polyporus pinsitus Species 0.000 claims 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N Resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 1
- 241001072909 Salvia Species 0.000 claims 1
- 241000222480 Schizophyllum Species 0.000 claims 1
- 241000223255 Scytalidium Species 0.000 claims 1
- LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Natural products OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 claims 1
- 240000001016 Solanum tuberosum Species 0.000 claims 1
- 235000002595 Solanum tuberosum Nutrition 0.000 claims 1
- 240000002302 Toxicodendron succedaneum Species 0.000 claims 1
- 241000222355 Trametes versicolor Species 0.000 claims 1
- 229940029983 VITAMINS Drugs 0.000 claims 1
- 241000863486 Vinca minor Species 0.000 claims 1
- 229940021016 Vitamin IV solution additives Drugs 0.000 claims 1
- 150000001242 acetic acid derivatives Chemical class 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 230000000111 anti-oxidant Effects 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 claims 1
- 230000001580 bacterial Effects 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M buffer Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims 1
- 235000020226 cashew Nutrition 0.000 claims 1
- 235000019804 chlorophyll Nutrition 0.000 claims 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 claims 1
- 229930002875 chlorophylls Natural products 0.000 claims 1
- 239000008139 complexing agent Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000000490 cosmetic additive Substances 0.000 claims 1
- 239000000982 direct dye Substances 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 239000003205 fragrance Substances 0.000 claims 1
- 230000002538 fungal Effects 0.000 claims 1
- 230000037308 hair color Effects 0.000 claims 1
- 150000003840 hydrochlorides Chemical class 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- 150000003893 lactate salts Chemical class 0.000 claims 1
- 150000004988 m-phenylenediamines Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 150000004987 o-phenylenediamines Chemical class 0.000 claims 1
- 150000004989 p-phenylenediamines Chemical class 0.000 claims 1
- 238000010422 painting Methods 0.000 claims 1
- 230000035515 penetration Effects 0.000 claims 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims 1
- 230000002335 preservative Effects 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 230000002194 synthesizing Effects 0.000 claims 1
- 150000003892 tartrate salts Chemical class 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- VZTGWJFIMGVKSN-UHFFFAOYSA-O trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium Chemical group CC(=C)C(=O)NCCC[N+](C)(C)C VZTGWJFIMGVKSN-UHFFFAOYSA-O 0.000 claims 1
- 239000011782 vitamin Substances 0.000 claims 1
- 235000013343 vitamin Nutrition 0.000 claims 1
- 229930003231 vitamins Natural products 0.000 claims 1
Claims (1)
(а) по крайней мере, один фермент типа лакказы;
(б) по крайней мере, один катионный или амфотерный субстантивный полимер, выбираемый из группы, состоящей из:
(i) Polyquaternium-24;
(ii) сополимеров диметилдиаллиламмонийгалогенида;
(iii) гомополимеров и сополимеров метакрилоилоксиэтилтриметиламмонийгалогенида;
(iv) четвертичных полиаммониевых полимеров, выбираемых из полимеров, отвечающих следующим формулам (I), (II) и (III):
полимеры, образованные повторяющимися звеньями, отвечающими следующей формуле (I)
полимеры, образованные повторяющимися звеньями, отвечающими следующей формуле (II)
полимеры, образованные повторяющимися звеньями, отвечающими следующей формуле (III)
в которой р означает целое число, составляющее примерно 1 - 6; D может отсутствовать или может представлять собой группу -(СН2)r-СО-, в которой г означает число, равное 4 или 7;
(v) сополимеров винилпирролидона с катионными звеньями;
(vi) катионных полисилоксанов;
(в) по крайней мере, один фиксирующийся при окислении краситель.1. Ready-to-use composition for dyeing keratin fibers, in particular, human keratin fibers, and predominantly human hair, comprising, in a carrier suitable for keratin fibers:
(a) at least one laccase-type enzyme;
(b) at least one cationic or amphoteric substantive polymer selected from the group consisting of:
(i) Polyquaternium-24;
(ii) copolymers of dimethyldiallylammonium halide;
(iii) homopolymers and copolymers of methacryloyloxyethyl trimethyl ammonium halide;
(iv) Quaternary polyammonium polymers selected from polymers that meet the following formulas (I), (II) and (III):
polymers formed by repeating units corresponding to the following formula (I)
polymers formed by repeating units corresponding to the following formula (II)
polymers formed by repeating units corresponding to the following formula (III)
in which p is an integer of about 1 to 6; D may be absent or may be a group - (CH 2 ) r —CO—, in which g is a number equal to 4 or 7;
(v) copolymers of vinylpyrrolidone with cationic units;
(vi) cationic polysiloxanes;
(c) at least one dye that is fixed during oxidation.
11. Композиция по любому из пп. 1-10, отличающаяся тем, что концентрация субстантивного полимера может составлять примерно 0,01 - 10%, и предпочтительно 0,1 - 5%, по отношению к общей массе композиции.10. The composition according to claim 1, characterized in that the substantive polymers of the cationic polysiloxane type are selected from products comprising amodimethicone of the following formula (IV)
11. Composition according to any one of paragraphs. 1-10, characterized in that the concentration of the substantive polymer can be about 0.01 to 10%, and preferably 0.1 to 5%, relative to the total weight of the composition.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR98/00254 | 1998-01-13 | ||
FR9800254A FR2773477B1 (en) | 1998-01-13 | 1998-01-13 | TINCTORIAL COMPOSITION AND METHODS FOR DYEING KERATINIC FIBERS USING THE SAME |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000121060A true RU2000121060A (en) | 2002-07-27 |
RU2204377C2 RU2204377C2 (en) | 2003-05-20 |
Family
ID=9521705
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000121060/14A RU2204377C2 (en) | 1998-01-13 | 1998-12-18 | Composition for dyeing keratin fibers, method for their dyeing, kit for dyeing keratin fibers |
Country Status (18)
Country | Link |
---|---|
US (1) | US6471730B1 (en) |
EP (1) | EP1047377B1 (en) |
JP (1) | JP2002509087A (en) |
KR (1) | KR100388693B1 (en) |
CN (1) | CN1210011C (en) |
AT (1) | ATE202469T1 (en) |
AU (1) | AU729022B2 (en) |
BR (1) | BR9814740A (en) |
CA (1) | CA2318321A1 (en) |
DE (1) | DE69801009T2 (en) |
DK (1) | DK1047377T3 (en) |
ES (1) | ES2161074T3 (en) |
FR (1) | FR2773477B1 (en) |
GR (1) | GR3036644T3 (en) |
PL (1) | PL341594A1 (en) |
PT (1) | PT1047377E (en) |
RU (1) | RU2204377C2 (en) |
WO (1) | WO1999036035A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7060112B2 (en) * | 1998-01-13 | 2006-06-13 | L'oreal | Composition for the oxidation dyeing of keratinous fibers containing a laccase and dyeing method using this composition |
FR2773471B1 (en) * | 1998-01-13 | 2001-04-13 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
PL195678B1 (en) * | 1998-03-06 | 2007-10-31 | Oreal | Method of and cationic amphophilic polymer containing compositions for oxidisingly dyeing creatine fibre |
DE60029783T2 (en) | 1999-06-22 | 2007-10-31 | Lion Corp. | HAIR COLORING AGENT INDOLIN AND / OR AN INDOLIN COMPOUND AND LACCASE CONTAINING |
WO2002039966A2 (en) * | 2000-11-20 | 2002-05-23 | Henkel Kommanditgesellschaft Auf Aktien | Enzymatic coloring agents |
FR2833836B1 (en) * | 2001-12-21 | 2004-01-30 | Oreal | COMPOSITION FOR OXIDATION DYEING OF KERATINIC FIBERS COMPRISING AN OXYALKYLENE CARBOXYLIC ETHER ACID AND A QUATERNIZED FATTY CHAIN CELLULOSE |
FR2833833B1 (en) * | 2001-12-21 | 2004-01-30 | Oreal | COMPOSITION FOR KERATIN FIBER OXIDATION DYE COMPRISING OXYALKYLENE CARBOXYLIC ETHER ACID, ASSOCIATIVE POLYMER, AND UNSATURATED FATTY ALCOHOL |
US7591860B2 (en) * | 2004-02-27 | 2009-09-22 | L'oreal, S.A. | N-alkylpolyhydroxylated secondary para-phenylenediamines, dye compositions comprising them, processes, and uses thereof |
EP3067041B1 (en) * | 2013-10-17 | 2019-12-04 | Shisei Chemical Co., Ltd. | Method for dyeing keratin fibers, keratin fiber dye |
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JP2526099B2 (en) | 1988-07-07 | 1996-08-21 | 花王株式会社 | Keratin fiber dyeing composition |
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FR2687570A1 (en) * | 1992-02-21 | 1993-08-27 | Oreal | COSMETIC COMPOSITION BASED ON NON-IONIC SURFACTANT AGENTS AND CATIONIC OR AMPHOTERIC SUBSTANTIVE POLYMERS AND ITS USE AS A DYE OR DECOLORATION SUPPORT. |
FR2694018B1 (en) * | 1992-07-23 | 1994-09-16 | Oreal | Use of laccases of plant origin as oxidizing agents in cosmetics, cosmetic compositions containing them, process for cosmetic treatment using them and process for obtaining these enzymes. |
DE4234887A1 (en) | 1992-10-16 | 1994-04-21 | Wella Ag | Oxidation hair dye containing 4,5-diaminopyrazole derivatives as well as new 4,5-diaminopyrazole derivatives and process for their preparation |
DE4234885A1 (en) | 1992-10-16 | 1994-04-21 | Wella Ag | Process for the preparation of 4,5-diaminopyrazole derivatives, their use for dyeing hair and new pyrazole derivatives |
FR2699816B1 (en) * | 1992-12-30 | 1995-03-03 | Oreal | Dyeing compositions for keratin fibers based on paraphenylenediamines, metaphenylenediamines and benzimidazole derivatives, and dyeing process using them. |
EP0628559B1 (en) | 1993-06-10 | 2002-04-03 | Beiersdorf-Lilly GmbH | Pyrimidine compounds and their use as pharmaceuticals |
US5480801A (en) | 1993-09-17 | 1996-01-02 | Novo Nordisk A/S | Purified PH neutral Rhizoctonia laccases and nucleic acids encoding same |
FR2717383B1 (en) * | 1994-03-21 | 1996-04-19 | Oreal | Composition for dyeing oxidation of keratin fibers comprising a derivative of paraphenylenediamine and a cationic or amphoteric substantive polymer and use. |
AU694954B2 (en) | 1994-06-03 | 1998-08-06 | Novo Nordisk A/S | Purified myceliophthora laccases and nucleic acids encoding same |
PT763115E (en) | 1994-06-03 | 2001-03-30 | Novo Nordisk Biotech Inc | SCYTALIDIUM PURIFIED LACASES AND NUCLEIC ACIDS THAT ENCODES THEM |
MX9606726A (en) | 1994-06-24 | 1997-03-29 | Novo Nordisk Bitoech Inc | Purified polyporus laccases and nucleic acids encoding same. |
DE4440957A1 (en) | 1994-11-17 | 1996-05-23 | Henkel Kgaa | Oxidation dye |
FR2733749B1 (en) | 1995-05-05 | 1997-06-13 | Oreal | COMPOSITIONS FOR DYEING KERATINIC FIBERS CONTAINING DIAMINO PYRAZOLES, DYEING PROCESS, NOVEL DIAMINO PYRAZOLES, AND PREPARATION METHOD THEREOF |
FR2739282B1 (en) * | 1995-09-29 | 1997-10-31 | Oreal | TOPICAL COMPOSITION CONTAINING A POLYSILOXANE SKELETON POLYMER WITH NON-SILICON GRAFTS AND AN AMPHIPHILIC FATTY CHAIN POLYMER |
DE19543988A1 (en) | 1995-11-25 | 1997-05-28 | Wella Ag | Oxidative hair dye composition |
CN1084357C (en) | 1995-11-30 | 2002-05-08 | 诺沃奇梅兹有限公司 | Laccases with improved dyeing properties |
JP2000503042A (en) | 1995-11-30 | 2000-03-14 | ノボ ノルディスク アクティーゼルスカブ | Enzymes for dyeing keratin fibers |
-
1998
- 1998-01-13 FR FR9800254A patent/FR2773477B1/en not_active Expired - Fee Related
- 1998-12-18 AU AU17666/99A patent/AU729022B2/en not_active Ceased
- 1998-12-18 ES ES98962518T patent/ES2161074T3/en not_active Expired - Lifetime
- 1998-12-18 BR BR9814740-4A patent/BR9814740A/en not_active IP Right Cessation
- 1998-12-18 DK DK98962518T patent/DK1047377T3/en active
- 1998-12-18 DE DE69801009T patent/DE69801009T2/en not_active Revoked
- 1998-12-18 PT PT81105587T patent/PT1047377E/en unknown
- 1998-12-18 KR KR10-2000-7007598A patent/KR100388693B1/en not_active IP Right Cessation
- 1998-12-18 CN CNB988138654A patent/CN1210011C/en not_active Expired - Fee Related
- 1998-12-18 AT AT98962518T patent/ATE202469T1/en not_active IP Right Cessation
- 1998-12-18 JP JP2000539811A patent/JP2002509087A/en active Pending
- 1998-12-18 EP EP98962518A patent/EP1047377B1/en not_active Revoked
- 1998-12-18 PL PL98341594A patent/PL341594A1/en not_active Application Discontinuation
- 1998-12-18 WO PCT/FR1998/002794 patent/WO1999036035A1/en not_active Application Discontinuation
- 1998-12-18 CA CA002318321A patent/CA2318321A1/en not_active Abandoned
- 1998-12-18 RU RU2000121060/14A patent/RU2204377C2/en not_active IP Right Cessation
-
2000
- 2000-09-11 US US09/600,135 patent/US6471730B1/en not_active Expired - Fee Related
-
2001
- 2001-09-18 GR GR20010401502T patent/GR3036644T3/en not_active IP Right Cessation
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