RU2000121053A - CONTAINING PAINT COLORING COMPOSITION AND METHOD OF PAINTING KERATIN FIBERS - Google Patents
CONTAINING PAINT COLORING COMPOSITION AND METHOD OF PAINTING KERATIN FIBERSInfo
- Publication number
- RU2000121053A RU2000121053A RU2000121053/14A RU2000121053A RU2000121053A RU 2000121053 A RU2000121053 A RU 2000121053A RU 2000121053/14 A RU2000121053/14 A RU 2000121053/14A RU 2000121053 A RU2000121053 A RU 2000121053A RU 2000121053 A RU2000121053 A RU 2000121053A
- Authority
- RU
- Russia
- Prior art keywords
- composition according
- paragraphs
- composition
- alkyl
- laccases
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 35
- 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 2
- 239000003973 paint Substances 0.000 title 1
- 108010029541 Laccase Proteins 0.000 claims 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 7
- 239000000975 dye Substances 0.000 claims 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 5
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 5
- 230000003647 oxidation Effects 0.000 claims 5
- 238000007254 oxidation reaction Methods 0.000 claims 5
- 238000004043 dyeing Methods 0.000 claims 4
- 108090000790 Enzymes Proteins 0.000 claims 3
- 102000004190 Enzymes Human genes 0.000 claims 3
- 125000004432 carbon atoms Chemical group C* 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 239000011780 sodium chloride Substances 0.000 claims 3
- 241000196324 Embryophyta Species 0.000 claims 2
- 241001361634 Rhizoctonia Species 0.000 claims 2
- 241000813090 Rhizoctonia solani Species 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 230000003113 alkalizing Effects 0.000 claims 2
- 150000001413 amino acids Chemical class 0.000 claims 2
- 239000000969 carrier Substances 0.000 claims 2
- 239000000306 component Substances 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- LVTYICIALWPMFW-UHFFFAOYSA-N 1-(2-hydroxypropylamino)propan-2-ol Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 claims 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-Amino-2-propanol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims 1
- KODLUXHSIZOKTG-UHFFFAOYSA-N 1-aminobutan-2-ol Chemical compound CCC(O)CN KODLUXHSIZOKTG-UHFFFAOYSA-N 0.000 claims 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims 1
- IOAOAKDONABGPZ-UHFFFAOYSA-N 2-amino-2-ethylpropane-1,3-diol Chemical compound CCC(N)(CO)CO IOAOAKDONABGPZ-UHFFFAOYSA-N 0.000 claims 1
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 claims 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 claims 1
- LTACQVCHVAUOKN-UHFFFAOYSA-N 3-(diethylamino)propane-1,2-diol Chemical compound CCN(CC)CC(O)CO LTACQVCHVAUOKN-UHFFFAOYSA-N 0.000 claims 1
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-Aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-Aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-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
- 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
- ZBCBWPMODOFKDW-UHFFFAOYSA-N Diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-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
- 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
- 241000310787 Panaeolus papilionaceus Species 0.000 claims 1
- 241001156632 Panaeolus sphinctrinus Species 0.000 claims 1
- 240000008426 Persea americana Species 0.000 claims 1
- 235000008673 Persea americana Nutrition 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
- 241001072909 Salvia Species 0.000 claims 1
- 241000222481 Schizophyllum commune Species 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
- 230000000111 anti-oxidant Effects 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 claims 1
- 230000001580 bacterial Effects 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
- 239000000490 cosmetic additive Substances 0.000 claims 1
- 229940043276 diisopropanolamine Drugs 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 150000003893 lactate salts Chemical class 0.000 claims 1
- 150000004988 m-phenylenediamines Chemical class 0.000 claims 1
- 150000004987 o-phenylenediamines Chemical class 0.000 claims 1
- 230000001590 oxidative Effects 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
- 235000005426 persea americana Nutrition 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 230000002335 preservative Effects 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 150000003892 tartrate salts Chemical class 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- -1 triisopropanolamine Chemical compound 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 подщелачивающий компонент, выбираемый из группы, состоящей из
(i) основной аминокислоты,
(ii) соединения следующей формулы (А)
Х(ОН)n (А),
в которой Х означает К, Li, когда n= 1; Х означает Мg, Са, когда n= 2;
Х означает N+R1R2R3R4, где R1, R2, R3, R4, одинаковые или разные, означают (C1-C4)-алкил, моногидрокси-(C1-C4)-алкил или полигидрокси-(C2-C4)-алкил, когда n = 1;
(iii) соединения следующей формулы (В)
в которой R5 означает (C1-C6)-алкил, моногидрокси-(C1-C6)-алкил или полигидрокси-(С2-С6)-алкил;
R6, R7, одинаковые или разные, означают атом водорода, (C1-C6)-алкил, моногидрокси-(C1-С6)-алкил или полигидрокси-(С2-С6)-алкил,
при условии, что R5, R6, R7 не означают одновременно β-гидроксиалкильный радикал с 2 атомами углерода;
если R6 и R7 означают одновременно атом водорода, тогда R5 не означает моногидроксиалкильный радикал с 2 атомами углерода или разветвленный моногидроксиалкильный радикал с 4 атомами углерода;
если R5 означает атом водорода или (C1-С6)-алкил и в то же самое время R6 означает (C1-С6)-алкил, тогда R7 не означает атом водорода или (C1-С6)-алкил;
(iv) соединения следующей формулы (С)
в которой W означает пропиленовый остаток, возможно замещенный гидроксильной группой или (C1-C4)-алкилом;
R8, R9, R10 и R11 одинаковые или разные, означают атом водорода, (C1-C4)-алкил или гидрокси-(С1-С4)-алкил;
(в) по крайней мере один фиксирующийся при окислении краситель, за исключением самоокисляющихся индольных красителей.1. Ready-to-use composition for oxidative dyeing of keratin fibers, in particular, human keratin fibers, mainly human hair, including, in a carrier suitable for dyeing keratin fibers
(a) at least one laccase type enzyme,
(b) at least one alkalizing component selected from the group consisting of
(i) a basic amino acid,
(ii) compounds of the following formula (A)
X (OH) n (A),
in which X means K, Li, when n = 1; X means Mg, Sa, when n = 2;
X means N + R 1 R 2 R 3 R 4 , where R 1 , R 2 , R 3 , R 4 , identical or different, mean (C 1 -C 4 ) -alkyl, mono-hydroxy- (C 1 -C 4 ) -alkyl or polyhydroxy- (C 2 -C 4 ) -alkyl, when n = 1;
(iii) compounds of the following formula (B)
in which R 5 means (C 1 -C 6 ) -alkyl, monohydroxy- (C 1 -C 6 ) -alkyl or polyhydroxy- (C 2 -C 6 ) -alkyl;
R 6 , R 7 , the same or different, represent a hydrogen atom, (C 1 -C 6 ) -alkyl, mono-hydroxy- (C 1 -C 6 ) -alkyl or polyhydroxy- (C 2 -C 6 ) -alkyl,
provided that R 5 , R 6 , R 7 does not simultaneously mean a β-hydroxyalkyl radical with 2 carbon atoms;
if R 6 and R 7 mean simultaneously a hydrogen atom, then R 5 does not mean a monohydroxyalkyl radical with 2 carbon atoms or a branched monohydroxyalkyl radical with 4 carbon atoms;
if R 5 means a hydrogen atom or (C 1 -C 6 ) -alkyl and at the same time R 6 means (C 1 -C 6 ) -alkyl, then R 7 does not mean a hydrogen atom or (C 1 -C 6 ) -alkyl;
(iv) compounds of the following formula (C)
in which W denotes a propylene residue, possibly substituted by a hydroxyl group or (C 1 -C 4 ) -alkyl;
R 8 , R 9 , R 10 and R 11 are the same or different, represent a hydrogen atom, (C 1 -C 4 ) -alkyl or hydroxy- (C 1 -C 4 ) -alkyl;
(c) at least one dye which is fixed during oxidation, with the exception of self-oxidizing indole dyes.
где R12 означает группу, выбираемую из следующих групп
-(CH2)3NH2;
-(CH2)2NH2;
-(CH2)2NHCONH2;
8. Композиция по любому из пп. 1-6, отличающаяся тем, что соединения формулы (В) выбирают из группы, состоящей из диэтаноламина, моноизопропаноламина, диизопропаноламина, триизопропаноламина, 2-амино-2-метилпропан-1,3-диола, 2-амино-2-этилпропан-1,3-диола, 2-амино-н-бутан-1-ола, 1-диэтиламинопропан-2,3-диола, трис(гидроксиметил)-аминометана, этилмоноэтаноламина.7. Composition according to any one of paragraphs. 1-6, characterized in that the basic amino acids correspond to the following formula (D)
where R 12 means a group selected from the following groups
- (CH 2 ) 3 NH 2 ;
- (CH 2 ) 2 NH 2 ;
- (CH 2 ) 2 NHCONH 2 ;
8. Composition according to any one of paragraphs. 1-6, characterized in that the compounds of formula (B) are selected from the group consisting of diethanolamine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, 2-amino-2-methylpropan-1,3-diol, 2-amino-2-ethylpropan-1 , 3-diol, 2-amino-n-butan-1-ol, 1-diethylaminopropane-2,3-diol, tris (hydroxymethyl) -aminomethane, ethyl monoethanolamine.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9800250A FR2773473B1 (en) | 1998-01-13 | 1998-01-13 | TINCTORIAL COMPOSITION AND METHODS FOR DYEING KERATINIC FIBERS |
FR9800250 | 1998-01-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000121053A true RU2000121053A (en) | 2002-07-27 |
RU2202332C2 RU2202332C2 (en) | 2003-04-20 |
Family
ID=9521701
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000121053/14A RU2202332C2 (en) | 1998-01-13 | 1998-12-21 | Composition and method for staining keratin fibers in oxidation mode |
Country Status (17)
Country | Link |
---|---|
US (1) | US20060021155A1 (en) |
EP (1) | EP1047378B2 (en) |
JP (1) | JP2002509088A (en) |
KR (1) | KR100387151B1 (en) |
CN (1) | CN1203835C (en) |
AT (1) | ATE208606T1 (en) |
AU (1) | AU728757B2 (en) |
BR (1) | BR9814733A (en) |
CA (1) | CA2317953A1 (en) |
DE (1) | DE69802566T3 (en) |
DK (1) | DK1047378T3 (en) |
ES (1) | ES2168158T3 (en) |
FR (1) | FR2773473B1 (en) |
PL (1) | PL341704A1 (en) |
PT (1) | PT1047378E (en) |
RU (1) | RU2202332C2 (en) |
WO (1) | WO1999036036A1 (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60029783T2 (en) | 1999-06-22 | 2007-10-31 | Lion Corp. | HAIR COLORING AGENT INDOLIN AND / OR AN INDOLIN COMPOUND AND LACCASE CONTAINING |
US8771153B2 (en) | 2010-11-08 | 2014-07-08 | Icon Ip, Inc. | Exercise weight bar with rotating handle and cam selection device |
WO2014153158A1 (en) | 2013-03-14 | 2014-09-25 | Icon Health & Fitness, Inc. | Strength training apparatus with flywheel and related methods |
EP3974036B1 (en) | 2013-12-26 | 2024-06-19 | iFIT Inc. | Magnetic resistance mechanism in a cable machine |
CN106470739B (en) | 2014-06-09 | 2019-06-21 | 爱康保健健身有限公司 | It is incorporated to the funicular system of treadmill |
TWI644702B (en) | 2015-08-26 | 2018-12-21 | 美商愛康運動與健康公司 | Strength exercise mechanisms |
US10940360B2 (en) | 2015-08-26 | 2021-03-09 | Icon Health & Fitness, Inc. | Strength exercise mechanisms |
US10293211B2 (en) | 2016-03-18 | 2019-05-21 | Icon Health & Fitness, Inc. | Coordinated weight selection |
US10441840B2 (en) | 2016-03-18 | 2019-10-15 | Icon Health & Fitness, Inc. | Collapsible strength exercise machine |
US10252109B2 (en) | 2016-05-13 | 2019-04-09 | Icon Health & Fitness, Inc. | Weight platform treadmill |
US10661114B2 (en) | 2016-11-01 | 2020-05-26 | Icon Health & Fitness, Inc. | Body weight lift mechanism on treadmill |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3251742A (en) * | 1962-05-14 | 1966-05-17 | Revlon | Method for coloring human hair with polyhydric aromatic compound, aromatic amine andan oxidation enzyme |
US3907799A (en) * | 1971-08-16 | 1975-09-23 | Icn Pharmaceuticals | Xanthine oxidase inhibitors |
US4003699A (en) * | 1974-11-22 | 1977-01-18 | Henkel & Cie G.M.B.H. | Oxidation hair dyes based upon tetraaminopyrimidine developers |
FR2586913B1 (en) * | 1985-09-10 | 1990-08-03 | Oreal | PROCESS FOR FORMING IN SITU A COMPOSITION CONSISTING OF TWO SEPARATELY PACKED PARTS AND DISPENSING ASSEMBLY FOR THE IMPLEMENTATION OF THIS PROCESS |
FR2596985B1 (en) * | 1986-04-10 | 1990-08-24 | Oreal | COSMETIC COMPOSITIONS FOR DYEING OR COLORING HAIR |
DE3843892A1 (en) * | 1988-12-24 | 1990-06-28 | Wella Ag | OXIDATION HAIR AGENTS CONTAINING DIAMINOPYRAZOL DERIVATIVES AND NEW DIAMINOPYRAZOLE DERIVATIVES |
FR2673534B1 (en) * | 1991-03-08 | 1995-03-03 | Perma | COMPOSITION FOR THE ENZYMATIC COLORING OF KERATINIC FIBERS, ESPECIALLY HAIR, AND ITS APPLICATION IN A COLORING PROCESS. |
DE4133957A1 (en) * | 1991-10-14 | 1993-04-15 | Wella Ag | HAIR DYE CONTAINING AMINOPYRAZOLE DERIVATIVES AND NEW PYRAZOLE DERIVATIVES |
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. |
DE4440955A1 (en) * | 1994-11-17 | 1996-05-23 | Henkel Kgaa | An oxidation |
FR2730923B1 (en) * | 1995-02-27 | 1997-04-04 | Oreal | COMPOSITION FOR OXIDATION DYEING OF KERATINIC FIBERS COMPRISING AN OXIDATION BASE, AN INDOLIC COUPLER AND AN ADDITIONAL HETEROCYCLIC COUPLER, AND DYEING METHOD |
FR2740035B1 (en) * | 1995-10-20 | 1997-11-28 | Oreal | KERATINIC FIBER DYEING PROCESS AND COMPOSITION IMPLEMENTED DURING THIS PROCESS |
DE19543988A1 (en) * | 1995-11-25 | 1997-05-28 | Wella Ag | Oxidative hair dye composition |
JP2000501130A (en) * | 1995-11-30 | 2000-02-02 | ノボ ノルディスク アクティーゼルスカブ | Laccase with improved dyeability |
FR2751218B1 (en) * | 1996-07-19 | 1998-08-28 | Oreal | COMPOSITIONS FOR OXIDATION DYEING OF KERATINIC FIBERS AND DYEING METHOD USING THE SAME |
-
1998
- 1998-01-13 FR FR9800250A patent/FR2773473B1/en not_active Expired - Fee Related
- 1998-12-21 PT PT98962529T patent/PT1047378E/en unknown
- 1998-12-21 WO PCT/FR1998/002805 patent/WO1999036036A1/en active IP Right Grant
- 1998-12-21 CA CA002317953A patent/CA2317953A1/en not_active Abandoned
- 1998-12-21 KR KR10-2000-7007534A patent/KR100387151B1/en not_active IP Right Cessation
- 1998-12-21 AT AT98962529T patent/ATE208606T1/en not_active IP Right Cessation
- 1998-12-21 JP JP2000539812A patent/JP2002509088A/en active Pending
- 1998-12-21 EP EP98962529A patent/EP1047378B2/en not_active Expired - Lifetime
- 1998-12-21 DK DK98962529T patent/DK1047378T3/en active
- 1998-12-21 CN CNB988130955A patent/CN1203835C/en not_active Expired - Fee Related
- 1998-12-21 RU RU2000121053/14A patent/RU2202332C2/en not_active IP Right Cessation
- 1998-12-21 PL PL98341704A patent/PL341704A1/en not_active Application Discontinuation
- 1998-12-21 BR BR9814733-1A patent/BR9814733A/en not_active IP Right Cessation
- 1998-12-21 AU AU17676/99A patent/AU728757B2/en not_active Ceased
- 1998-12-21 DE DE69802566T patent/DE69802566T3/en not_active Expired - Lifetime
- 1998-12-21 ES ES98962529T patent/ES2168158T3/en not_active Expired - Lifetime
-
2004
- 2004-11-19 US US10/992,474 patent/US20060021155A1/en not_active Abandoned
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