RU96100839A - COMPOSITION FOR OXIDATIVE PAINTING OF KERATIN FIBERS, PAINTING METHOD AND DEVICE - Google Patents
COMPOSITION FOR OXIDATIVE PAINTING OF KERATIN FIBERS, PAINTING METHOD AND DEVICEInfo
- Publication number
- RU96100839A RU96100839A RU96100839/04A RU96100839A RU96100839A RU 96100839 A RU96100839 A RU 96100839A RU 96100839/04 A RU96100839/04 A RU 96100839/04A RU 96100839 A RU96100839 A RU 96100839A RU 96100839 A RU96100839 A RU 96100839A
- Authority
- RU
- Russia
- Prior art keywords
- atoms
- phenylene
- diamine
- radical
- composition
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 28
- 230000001590 oxidative Effects 0.000 title claims 7
- 239000000835 fiber Substances 0.000 title claims 6
- 102000011782 Keratins Human genes 0.000 title claims 5
- 108010076876 Keratins Proteins 0.000 title claims 5
- 238000010422 painting Methods 0.000 title claims 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims 17
- CBCKQZAAMUWICA-UHFFFAOYSA-N P-Phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 12
- 239000011780 sodium chloride Substances 0.000 claims 12
- 150000003839 salts Chemical class 0.000 claims 11
- -1 2,4-diamino-phenoxy Chemical group 0.000 claims 9
- 239000002253 acid Substances 0.000 claims 9
- 238000004040 coloring Methods 0.000 claims 8
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 5
- 150000004988 m-phenylenediamines Chemical class 0.000 claims 5
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims 4
- 239000002585 base Substances 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 239000007800 oxidant agent Substances 0.000 claims 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 238000004043 dyeing Methods 0.000 claims 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- ZFFAFXDAFACVBX-UHFFFAOYSA-N 2-(2,4-diamino-5-methylphenoxy)ethanol Chemical compound CC1=CC(OCCO)=C(N)C=C1N ZFFAFXDAFACVBX-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
- BGGGDHXHMQFBGA-UHFFFAOYSA-N 4-[(2,4-diaminophenoxy)methoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCOC1=CC=C(N)C=C1N BGGGDHXHMQFBGA-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
- AYAKPRUPZTWPLK-UHFFFAOYSA-N 4-ethoxy-6-methylbenzene-1,3-diamine Chemical compound CCOC1=CC(C)=C(N)C=C1N AYAKPRUPZTWPLK-UHFFFAOYSA-N 0.000 claims 1
- NQHVJMJEWQQXBS-UHFFFAOYSA-N 4-ethoxybenzene-1,3-diamine Chemical compound CCOC1=CC=C(N)C=C1N NQHVJMJEWQQXBS-UHFFFAOYSA-N 0.000 claims 1
- WERSDZKEJFOKJJ-UHFFFAOYSA-N 4-methoxy-5-methylbenzene-1,3-diamine Chemical compound COC1=C(C)C=C(N)C=C1N WERSDZKEJFOKJJ-UHFFFAOYSA-N 0.000 claims 1
- PSPYAOSEFGPDOA-UHFFFAOYSA-N 5-ethyl-4-methoxybenzene-1,3-diamine Chemical compound CCC1=CC(N)=CC(N)=C1OC PSPYAOSEFGPDOA-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
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-Methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims 1
- VMPITZXILSNTON-UHFFFAOYSA-N O-Anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 claims 1
- 230000002378 acidificating Effects 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 239000000982 direct dye Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 1
- 230000001264 neutralization Effects 0.000 claims 1
- 239000003960 organic solvent 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
Claims (16)
в которой R1 обозначает атом водорода, алкильный радикал с 1 - 4 С-атомами, моногидроксиалкильный радикал с 1 - 4 С-атомами или полигидроксиалкильный радикал с 2 - 4 С-атомами;
R2 и R3, одинаковые или разные, обозначают атом водорода, алкильный радикал с 1 - 4 С-атомами или гидроксиалкоксильный радикал с 1 - 4 С-атомами;
R4 обозначает алкоксильный радикал с 1 - 4 С-атомами, аминоалкоксильный радикал с 1 - 4 С-атомами, моногидроксиалкоксильный радикал с 1 - 4 С-атомами, полигидроксиалкоксильный радикал с 2 - 4 С-атомами или 2,4-диамино-фенокси алкоксильный радикал, при условии, что когда R1 обозначает атом водорода, тогда R2 и R4 одновременно не обозначают β-гидроксиэтилоксирадикал, и когда R1, R2 и R3 одновременно обозначают атом водорода, тогда R4 является отличным от метоксирадикала,
и их солей присоединения кислоты и по крайней мере одно второе окисляющееся основание, выбираемое среди производных третичного п-фенилен-диамина следующей формулы II
в которой R5 обозначает алкильный радикал с 1 - 4 С-атомами, моногидроксиалкильный радикал с 1 - 4 С-атомами, или полигидроксиалькильный радикал с 2 - 4 С-атомами;
R6 обозначает моногидроксиалкильный радикал с 1 - 4 С-атомами или полигидроксиалкильный радикал с 2 - 4 С-атомами;
R7 обозначает атом водорода, алкильный радикал с 1 - 4 С-атомами, алкоксильный радикал с 1 - 4 С-атомами или атом галогена,
и их солей присоединения кислоты.1. Composition for oxidative dyeing of keratin fibers and in particular human keratin fibers, such as hair, characterized in that it contains at least one first oxidizing base selected among p-phenylene diamine, 2-methyl -p-phenylene-diamine and their acid addition salts; at least one paint-forming component selected among the derivatives of m-phenylene-diamine of the following formula I
in which R 1 denotes a hydrogen atom, an alkyl radical with 1-4 C-atoms, a mono-hydroxyalkyl radical with 1-4 C-atoms or a polyhydroxyalkyl radical with 2-4 C-atoms;
R 2 and R 3 , which are the same or different, represent a hydrogen atom, an alkyl radical with 1-4 C-atoms or a hydroxyalkoxy radical with 1-4 C-atoms;
R 4 denotes an alkoxy radical with 1-4 C-atoms, an amino alkoxy radical with 1-4 C-atoms, a monohydroxyalkoxy radical with 1-4 C-atoms, a polyhydroxyalkoxy radical with 2-4 C-atoms or 2,4-diamino-phenoxy an alkoxy radical, provided that when R 1 represents a hydrogen atom, then R 2 and R 4 do not simultaneously mean a β-hydroxyethyloxy radical, and when R 1 , R 2 and R 3 simultaneously denote a hydrogen atom, then R 4 is different from the methoxy radical,
and their acid addition salts and at least one second oxidizable base selected among the tertiary p-phenylene diamine derivatives of the following formula II
in which R 5 denotes an alkyl radical with 1 to 4 C-atoms, a monohydroxyalkyl radical with 1 to 4 C-atoms, or a polyhydroxyalkyl radical with 2 to 4 C-atoms;
R 6 denotes a monohydroxyalkyl radical with 1 to 4 C atoms or a polyhydroxyalkyl radical with 2 to 4 C atoms;
R 7 denotes a hydrogen atom, an alkyl radical with 1-4 C-atoms, an alkoxy radical with 1-4 C-atoms or a halogen atom,
and their acid addition salts.
3,5-диамино-1-этил 2-метокси бензола,
3,5-диамино-2-метокси-1-метил бензола,
2,4-диамино-1-этокси бензола,
1,3-бис-(2,4-диаминофенокси)пропана,
бис-(2,4-диамино-фенокси)метана,
1-(β- аминоэтилокси)-2,4-диамино безола,
2-амино-1-(β- гидроксиэтилокси)-4) метиламино-бензола,
2,4-диамино-1-этокси-5-метил бензола,
2,4-диамино-5-(β- гидроксиэтилокси)-1 метилбензола,
2,4-диамино-1-(β,γ- дигидроксипропилокси)бензола,
2,4-диамино-1(β-гидроксиэтилокси)бензола,
2-амино-4-N-(β-гидроксиэтил)амино-1-метокси-бензола
и их солей присоединения кислоты.3. The composition according to claim 1 or 2, characterized in that the m-phenylene-diamine derivatives of the formula I are chosen among
3,5-diamino-1-ethyl 2-methoxy benzene,
3,5-diamino-2-methoxy-1-methyl benzene,
2,4-diamino-1-ethoxy benzene,
1,3-bis- (2,4-diaminophenoxy) propane,
bis (2,4-diamino-phenoxy) methane,
1- (β-aminoethyloxy) -2,4-diamino bezol,
2-amino-1- (β-hydroxyethyloxy) -4) methylamino-benzene,
2,4-diamino-1-ethoxy-5-methyl benzene,
2,4-diamino-5- (β-hydroxyethyloxy) -1 methylbenzene,
2,4-diamino-1- (β, γ-dihydroxypropyloxy) benzene,
2,4-diamino-1 (β-hydroxyethyloxy) benzene,
2-amino-4-N- (β-hydroxyethyl) amino-1-methoxy-benzene
and their acid addition salts.
1-(N-этил-N'-β-гидроксиэтил)амино 4-амино бензола,
1-N,N'-бис-(β- гидроксиэтил)амино 4-амино бензола,
1-N,N'-бис-(β,γ- дигидроксипропил)амино 4-амино бензола и их солей присоединения кислоты.4. Composition according to any one of paragraphs.1 to 3, characterized in that the derivatives of the tertiary p-phenylene-diamine of formula II is chosen among
1- (N-ethyl-N'-β-hydroxyethyl) amino 4-amino benzene,
1-N, N'-bis- (β-hydroxyethyl) amino 4-amino benzene,
1-N, N'-bis- (β, γ-dihydroxypropyl) amino 4-amino benzene and their acid addition salts.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9500587A FR2729564B1 (en) | 1995-01-19 | 1995-01-19 | COMPOSITION OF OXIDIZING DYE FOR KERATINIC FIBERS AND DYE PROCESS USING THIS COMPOSITION |
FR9500587 | 1995-01-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU96100839A true RU96100839A (en) | 1998-03-27 |
RU2135664C1 RU2135664C1 (en) | 1999-08-27 |
Family
ID=9475286
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU96100839A RU2135664C1 (en) | 1995-01-19 | 1996-01-18 | Composition for oxidative dyeing of keratin fibers |
Country Status (17)
Country | Link |
---|---|
US (1) | US5690696A (en) |
EP (1) | EP0722713B1 (en) |
JP (1) | JP2880110B2 (en) |
KR (1) | KR0178627B1 (en) |
CN (1) | CN1065425C (en) |
AR (1) | AR000709A1 (en) |
AT (1) | ATE156348T1 (en) |
AU (1) | AU674638B2 (en) |
BR (1) | BR9600457A (en) |
CA (1) | CA2167650C (en) |
DE (1) | DE69600046T2 (en) |
ES (1) | ES2109108T3 (en) |
FR (1) | FR2729564B1 (en) |
HU (1) | HU221065B1 (en) |
MX (1) | MX9600164A (en) |
PL (1) | PL183387B1 (en) |
RU (1) | RU2135664C1 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2684296B1 (en) * | 1991-12-03 | 1995-04-21 | Oreal | PROCESS FOR DYEING KERATINIC FIBERS WITH AN ACID PH ALCOXYMETAPHENYLENEDIAMINE AND COMPOSITIONS IMPLEMENTED. |
FR2730922B1 (en) * | 1995-02-27 | 1997-04-04 | Oreal | COMPOSITION FOR OXIDATION DYEING OF KERATINIC FIBERS COMPRISING AT LEAST TWO OXIDATION BASES AND AN INDOLIC COUPLER, AND DYEING METHOD |
FR2751219B1 (en) * | 1996-07-19 | 1998-08-21 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
US6406502B1 (en) | 1996-07-19 | 2002-06-18 | L'oreal | Compositions for the oxidation dyeing of keratin fibres and dyeing process |
FR2769210B1 (en) * | 1997-10-03 | 2000-02-11 | Oreal | KERATIN FIBER DYEING COMPOSITION AND DYEING METHOD USING THE SAME |
FR2769215B1 (en) * | 1997-10-03 | 1999-12-24 | Oreal | KERATIN FIBER DYEING COMPOSITION AND DYEING METHOD USING THE SAME |
FR2776288B1 (en) * | 1998-03-20 | 2001-04-06 | Oreal | NOVEL CATIONIC COUPLERS, THEIR USE FOR OXIDATION DYEING OF KERATINIC FIBERS, TINCTORIAL COMPOSITIONS AND DYEING METHODS |
DE19959320A1 (en) * | 1999-12-09 | 2001-06-13 | Henkel Kgaa | New dye combination |
FR2806299B1 (en) * | 2000-03-14 | 2002-12-20 | Oreal | COMPOSITIONS FOR DYEING KERATINIC FIBERS CONTAINING PYRROLIDINYL GROUPED PARAPHENYLENEDIAMINE DERIVATIVES |
FR2817474B1 (en) * | 2000-12-06 | 2003-01-03 | Oreal | OXIDATION DYE COMPOSITION BASED ON 1- (4-AMINOPHENYL) PYRROLIDINES SUBSTITUTED IN POSITION 2 AND METHOD OF IMPLEMENTING DYEING |
FR2817471B1 (en) * | 2000-12-06 | 2005-06-10 | Oreal | OXIDATION DYEING COMPOSITION BASED ON 1- (4-AMINOPHENYL) PYRROLIDINES SUBSTITUTED IN POSITION 3 AND 4 AND METHOD OF DYING THEREFOR |
FR2817470B1 (en) * | 2000-12-06 | 2003-01-03 | Oreal | OXIDATION DYE COMPOSITION BASED ON 1- (AMINOPHENYL) PYRROLIDINES SUBSTITUTED IN POSITION 2 AND 5 AND DYEING METHOD THEREOF |
FR2817473B1 (en) * | 2000-12-06 | 2003-01-03 | Oreal | OXIDATION DYE COMPOSITION BASED ON 1-4 (-AMINOPHENYL) PYRROLIDINES SUBSTITUTED IN POSITION 2 AND 4 AND DYEING METHOD THEREOF |
US7132534B2 (en) * | 2002-07-05 | 2006-11-07 | L'oreal | Para-phenylenediamine derivatives containing a pyrrolidyl group, and use of these derivatives for coloring keratin fibers |
FR2879922B1 (en) * | 2004-12-23 | 2007-03-02 | Oreal | NOVEL METHOD FOR WASHING COLORED KERATINOUS FIBERS WITH A COMPOSITION COMPRISING A PARTICULAR NON-IONIC SURFACTANT AND USE FOR PROTECTING COLOR |
EP1820488A3 (en) * | 2006-02-16 | 2010-09-01 | The Procter & Gamble Company | Hair colouring compositions |
FR2945736B1 (en) * | 2009-05-19 | 2011-06-10 | Oreal | TINCTORIAL COMPOSITION COMPRISING A SECONDARY PARA-PHENYLENE DIAMINE OXIDATION BASE AND A SELECTED PARA-PHENYLENE DIAMINE OXIDATION BASE |
WO2010133639A1 (en) * | 2009-05-19 | 2010-11-25 | L'oreal | Dyeing composition comprising a secondary para-phenylenediamine oxidation base and a selected para-phenylenediamine or para-aminophenol oxidation base |
FR2984089B1 (en) * | 2011-12-20 | 2014-01-10 | Oreal | APPLICATION DEVICE COMPRISING A COMPOSITION BASED ON HYDROPHOBIC FILMOGENIC POLYMER AND A VOLATILE SOLVENT, PROCESS FOR TREATING KERATINOUS FIBERS USING THE SAME |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3970423A (en) * | 1971-10-04 | 1976-07-20 | Clairol Incorporated | Oxidative hair dye compositions |
BE786710A (en) * | 1971-10-04 | 1973-01-25 | Bristol Myers Co | COMPOSITION FOR HAIR DYE WITH |
FR2362116A1 (en) * | 1976-08-20 | 1978-03-17 | Oreal | METAPHENYLENEDIAMINES AND TINCTORIAL COMPOSITIONS CONTAINING THEM |
DE2758735A1 (en) * | 1977-10-06 | 1979-04-19 | Bristol Myers Co | OXIDIZING COMPOSITION FOR DYE KERATINOESE FIBERS, ESPECIALLY HUMAN HAIR |
FR2430932A1 (en) * | 1978-07-12 | 1980-02-08 | Oreal | METAPHENYLENEDIAMINES AND TINCTORIAL COMPOSITIONS CONTAINING THEM |
FR2455030A1 (en) * | 1979-04-26 | 1980-11-21 | Oreal | METAPHENYLENEDIAMINES AND TINCTORIAL COMPOSITIONS CONTAINING THEM |
FR2460663A1 (en) * | 1979-07-10 | 1981-01-30 | Oreal | TINCTORIAL COMPOSITION FOR HAIR BASED ON PARAPHENYLENE DIAMINES |
FR2486075A1 (en) * | 1980-07-01 | 1982-01-08 | Oreal | METHAPHENYLENEDIAMINES AND METHOD FOR THE PRODUCTION THEREOF, TINCTORIAL COMPOSITIONS CONTAINING SAME, AND METHOD FOR DYING THE SAME |
FR2513418A1 (en) * | 1981-09-22 | 1983-03-25 | Mitsubishi Electric Corp | DISPLAY DEVICE WITH TIME DELAY COMPENSATION |
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 |
DE3622784A1 (en) * | 1986-07-07 | 1988-01-21 | Wella Ag | NEW 5-ALKOXY-2,4-DIAMINO-ALKYLBENZOLES AND HAIR-COLORING AGENTS WITH 5-ALKOXY-2,4-DIAMINO-ALKYL-BENZOLES |
FR2684296B1 (en) * | 1991-12-03 | 1995-04-21 | Oreal | PROCESS FOR DYEING KERATINIC FIBERS WITH AN ACID PH ALCOXYMETAPHENYLENEDIAMINE AND COMPOSITIONS IMPLEMENTED. |
-
1995
- 1995-01-19 FR FR9500587A patent/FR2729564B1/en not_active Expired - Fee Related
-
1996
- 1996-01-03 AU AU40775/96A patent/AU674638B2/en not_active Ceased
- 1996-01-09 MX MX9600164A patent/MX9600164A/en unknown
- 1996-01-12 AR ARP960100974A patent/AR000709A1/en active IP Right Grant
- 1996-01-16 BR BR9600457A patent/BR9600457A/en not_active Application Discontinuation
- 1996-01-17 AT AT96400115T patent/ATE156348T1/en not_active IP Right Cessation
- 1996-01-17 DE DE69600046T patent/DE69600046T2/en not_active Revoked
- 1996-01-17 EP EP96400115A patent/EP0722713B1/en not_active Revoked
- 1996-01-17 ES ES96400115T patent/ES2109108T3/en not_active Expired - Lifetime
- 1996-01-18 HU HU9600105A patent/HU221065B1/en not_active IP Right Cessation
- 1996-01-18 JP JP8006832A patent/JP2880110B2/en not_active Ceased
- 1996-01-18 CN CN96101011A patent/CN1065425C/en not_active Expired - Lifetime
- 1996-01-18 RU RU96100839A patent/RU2135664C1/en not_active IP Right Cessation
- 1996-01-18 PL PL96312376A patent/PL183387B1/en unknown
- 1996-01-19 KR KR1019960001123A patent/KR0178627B1/en not_active IP Right Cessation
- 1996-01-19 CA CA002167650A patent/CA2167650C/en not_active Expired - Fee Related
- 1996-01-19 US US08/588,726 patent/US5690696A/en not_active Expired - Lifetime
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