ZA200806461B - Hair composition comprising at least one disulphide direct dye and at least one alkaline hydroxide agent and simultaneous hair shaping and dyeing process - Google Patents
Hair composition comprising at least one disulphide direct dye and at least one alkaline hydroxide agent and simultaneous hair shaping and dyeing process Download PDFInfo
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- ZA200806461B ZA200806461B ZA200806461A ZA200806461A ZA200806461B ZA 200806461 B ZA200806461 B ZA 200806461B ZA 200806461 A ZA200806461 A ZA 200806461A ZA 200806461 A ZA200806461 A ZA 200806461A ZA 200806461 B ZA200806461 B ZA 200806461B
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- South Africa
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- different
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- 239000000982 direct dye Substances 0.000 title claims description 32
- 238000004043 dyeing Methods 0.000 title claims description 21
- 238000000034 method Methods 0.000 title claims description 19
- 239000003795 chemical substances by application Substances 0.000 title claims description 17
- 238000007493 shaping process Methods 0.000 title claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 title claims description 10
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- 125000005842 heteroatom Chemical group 0.000 claims description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims description 24
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- 108010076876 Keratins Proteins 0.000 claims description 21
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 20
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- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
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- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000001295 dansyl group Chemical group [H]C1=C([H])C(N(C([H])([H])[H])C([H])([H])[H])=C2C([H])=C([H])C([H])=C(C2=C1[H])S(*)(=O)=O 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000005056 dihydrothiazolyl group Chemical group S1C(NC=C1)* 0.000 description 1
- 238000009967 direct dyeing Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 229930003944 flavone Natural products 0.000 description 1
- 150000002213 flavones Chemical class 0.000 description 1
- 235000011949 flavones Nutrition 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- BLNWTAHYTCHDJH-UHFFFAOYSA-O hydroxy(oxo)azanium Chemical compound O[NH+]=O BLNWTAHYTCHDJH-UHFFFAOYSA-O 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 description 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical class C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 125000005956 isoquinolyl group Chemical group 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- LLLILZLFKGJCCV-UHFFFAOYSA-M n-methyl-n-[(1-methylpyridin-1-ium-4-yl)methylideneamino]aniline;methyl sulfate Chemical compound COS([O-])(=O)=O.C=1C=CC=CC=1N(C)\N=C\C1=CC=[N+](C)C=C1 LLLILZLFKGJCCV-UHFFFAOYSA-M 0.000 description 1
- 150000005002 naphthylamines Chemical class 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-M oxidooxomethyl Chemical compound [O-][C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-M 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 125000006684 polyhaloalkyl group Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 235000012756 tartrazine Nutrition 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 150000003732 xanthenes Chemical class 0.000 description 1
Classifications
-
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- 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
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
-
- 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
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
-
- 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
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4966—Triazines or their condensed derivatives
-
- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0756706A FR2919179B1 (fr) | 2007-07-24 | 2007-07-24 | Composition capillaire comprenant au moins un colorant direct disulfure et au moins un agent alcalin hydroxyde et procede de mise en forme et de coloration simultanees. |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200806461B true ZA200806461B (en) | 2009-08-26 |
Family
ID=39154165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200806461A ZA200806461B (en) | 2007-07-24 | 2008-07-24 | Hair composition comprising at least one disulphide direct dye and at least one alkaline hydroxide agent and simultaneous hair shaping and dyeing process |
Country Status (7)
Country | Link |
---|---|
US (1) | US8097044B2 (pt) |
EP (1) | EP2018847B1 (pt) |
BR (1) | BRPI0806648B1 (pt) |
ES (1) | ES2525944T3 (pt) |
FR (1) | FR2919179B1 (pt) |
MX (1) | MX2008009509A (pt) |
ZA (1) | ZA200806461B (pt) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007110537A2 (fr) * | 2006-03-24 | 2007-10-04 | L'oréal | Composition de teinture comprenant un colorant fluorescent thiol/disulfure a groupes amines et a charge cationique interne, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
US7780743B2 (en) | 2006-03-24 | 2010-08-24 | L'oreal S.A. | Fluorescent entity, dyeing composition containing at least one fluorescent entity, and method for lightening keratin materials using said at least one fluorescent entity |
US8070830B2 (en) | 2006-03-24 | 2011-12-06 | L'oreal S.A. | Fluorescent entity, dyeing composition containing at least one fluorescent entity comprising at least one heterocycle, with at least one internal cationic charge, and method for lightening keratin materials using said at least one fluorescent entity |
FR2898903B1 (fr) | 2006-03-24 | 2012-08-31 | Oreal | Composition de teinture comprenant un colorant disulfure fluorescent, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
FR2921377B1 (fr) * | 2007-09-21 | 2009-10-30 | Oreal | Compose styryl a motif hydroxy(cyclo)alkylamino thiol/disulfure, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
FR2921381B1 (fr) | 2007-09-21 | 2009-10-30 | Oreal | Colorant hemicyanine styryle thiol/disulfure, composition tinctoriale comprenant ce colorant, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
FR2921373B1 (fr) | 2007-09-21 | 2009-10-30 | Oreal | Colorant derive d'indole styryle a linker alkylene, composition tinctoriale comprenant ce colorant, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
FR2921376B1 (fr) * | 2007-09-21 | 2009-10-30 | Oreal | Compose styryl tetrahydroquinolinium thiol/disulfure, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
US20110015669A1 (en) * | 2007-11-08 | 2011-01-20 | Corcosteugi Borja F | Forceps |
CN101649128B (zh) * | 2008-08-15 | 2013-08-07 | 明德国际仓储贸易(上海)有限公司 | 具有n,n-二烷胺基桥基的反应性染料 |
EP2359804A3 (fr) * | 2010-01-28 | 2015-08-05 | L'Oréal | Composition comprenant un colorant d'oxydation et un derive d'hydroxyde d'ammonium ou de phosphonuim, coloration de fibres keratiniques et dispositif |
KR102052423B1 (ko) * | 2011-05-03 | 2019-12-05 | 바스프 에스이 | 디술피드 염료 |
US9358201B2 (en) * | 2013-08-23 | 2016-06-07 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
BR112017019798A2 (pt) * | 2015-03-19 | 2018-05-29 | Basf Se | compostos |
JP2017218396A (ja) | 2016-06-03 | 2017-12-14 | 花王株式会社 | 毛髪化粧料 |
US20190240133A1 (en) | 2018-02-02 | 2019-08-08 | Kao Usa Inc. | Hair coloring compositions and methods thereof |
JP7292837B2 (ja) * | 2018-08-29 | 2023-06-19 | ロレアル | ケラチン繊維を着色するための方法及び組成物 |
EP4013375A1 (en) * | 2019-08-14 | 2022-06-22 | Kao Corporation | Kit-of-parts and composition for dyeing of keratin fibers, method, and use thereof |
CN114507267B (zh) * | 2020-11-16 | 2023-06-27 | 北京医院 | 一种靶向肿瘤微环境的两亲性小分子纳米药物及其制备方法 |
CN115141297B (zh) * | 2022-07-07 | 2024-02-20 | 广东蓝海包装新技术有限公司 | 一种基于硝基苄二硫醚和吡啶鎓酯嵌段大分子偶氮引发剂的可降解聚苯乙烯合成方法 |
Family Cites Families (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB738585A (en) | 1952-07-17 | 1955-10-19 | May & Baker Ltd | Improvements in or relating to tetrazolium compounds |
BE559219A (pt) * | 1956-07-17 | |||
DE1078081B (de) | 1958-02-25 | 1960-03-24 | Thera Chemie Chemisch Therapeu | Mittel zum Faerben von Haaren oder Pelzen |
FR1516943A (fr) | 1966-01-10 | 1968-02-05 | Oreal | Colorants basiques utilisables pour la teinture des cheveux |
FR1530369A (fr) | 1966-07-07 | 1968-06-21 | Dow Corning | Compositions de traitement des cheveux |
FR1540423A (fr) | 1966-07-25 | 1968-09-27 | Oreal | Nouveaux colorants, leurs procédés de fabrication et leurs applications |
CH469060A (de) | 1966-08-05 | 1969-02-28 | Durand & Huguenin Ag | Verfahren zur Herstellung von wasserlöslichen, kationischen Monoazofarbstoffen und Verwendung derselben |
LU53050A1 (pt) | 1967-02-22 | 1968-08-27 | ||
LU53095A1 (pt) | 1967-03-01 | 1968-11-29 | ||
US3524842A (en) | 1967-08-04 | 1970-08-18 | Durand & Huguenin Ag | Water-soluble cationic phenylazo-naphthol dyestuffs containing a quaternary ammonium group |
LU70835A1 (pt) | 1974-08-30 | 1976-08-19 | ||
LU65539A1 (pt) | 1972-06-19 | 1973-12-21 | ||
LU67178A1 (pt) * | 1973-03-08 | 1974-10-09 | ||
GB1514466A (en) | 1974-06-21 | 1978-06-14 | Ici Ltd | Preparation of bipyridilium compounds |
LU71015A1 (pt) | 1974-09-27 | 1976-08-19 | ||
FR2472382A1 (fr) | 1979-12-28 | 1981-07-03 | Oreal | Procede de deformation permanente des cheveux |
FR2495931A2 (fr) | 1980-12-12 | 1982-06-18 | Oreal | Procede de defrisage des cheveux, et composition destinee a la mise en oeuvre de ce procede |
LU83703A1 (fr) | 1981-10-20 | 1983-06-08 | Oreal | Nouvelle composition cosmetique et son application a la deformation permanente des cheveux |
LU84463A1 (fr) | 1982-11-10 | 1984-06-13 | Oreal | Polymeres polysiloxanes polyquaternaires |
LU85564A1 (fr) | 1984-10-01 | 1986-06-11 | Oreal | Nouvelles compositions de teinture des fibres keratiniques contenant un colorant azoique,procede de preparation de ce colorant et mise en oeuvre desdites compositions pour la teinture des fibres keratiniques |
FR2586913B1 (fr) | 1985-09-10 | 1990-08-03 | Oreal | Procede pour former in situ une composition constituee de deux parties conditionnees separement et ensemble distributeur pour la mise en oeuvre de ce procede |
US4798722A (en) | 1986-11-12 | 1989-01-17 | Zotos International, Inc. | Permanent waving composition |
US4749732A (en) | 1987-01-02 | 1988-06-07 | Dow Corning Corporation | Hair care composition containing modified aminoalkyl substituted polydiorganosiloxane |
GB8713879D0 (en) | 1987-06-13 | 1987-07-15 | Dow Corning Ltd | Treating hair |
US5097662A (en) * | 1989-11-20 | 1992-03-24 | The Boeing Company | Apparatus for influencing the flow of air through a passageway |
US5094662A (en) * | 1990-11-13 | 1992-03-10 | Shiseido Co. Ltd. | Product for improved permanent waving of hair and simultaneously coloring and permanently waving hair and method therefor |
DE4137005A1 (de) | 1991-11-11 | 1993-05-13 | Bitterfeld Wolfen Chemie | Mittel zum faerben von haaren |
DE4220388A1 (de) | 1992-06-22 | 1993-12-23 | Bitterfeld Wolfen Chemie | Kationische Azofarbstoffe zum Färben von Keratinmaterialien |
TW311089B (pt) | 1993-07-05 | 1997-07-21 | Ciba Sc Holding Ag | |
TW325998B (en) | 1993-11-30 | 1998-02-01 | Ciba Sc Holding Ag | Dyeing keratin-containing fibers |
US5888252A (en) | 1993-11-30 | 1999-03-30 | Ciba Specialty Chemicals Corporation | Processes for dyeing keratin-containing fibres with cationicazo dyes |
ES2181761T3 (es) | 1994-11-03 | 2003-03-01 | Ciba Geigy Ag | Colorantes azoicos cationicos de imidazol. |
FR2748932B1 (fr) | 1996-05-23 | 1998-07-03 | Oreal | Composition de teinture directe capillaire comprenant un polymere reticule a motifs acryliques et acrylates d'akyles en c10-c30 |
GB9624590D0 (en) | 1996-11-27 | 1997-01-15 | Warner Jenkinson Europ Limited | Dyes |
FR2757385B1 (fr) | 1996-12-23 | 1999-01-29 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
FR2757384B1 (fr) | 1996-12-23 | 1999-01-15 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
FR2771409B1 (fr) | 1997-11-21 | 2000-01-14 | Oreal | Nouveaux composes azoiques, utilisation pour la teinture, compositions les contenant et procedes de teinture |
ATE258420T1 (de) | 1997-12-05 | 2004-02-15 | Oreal | Verfahren zur direkt-färbung von keratin-fasern in zwei stufen mit hilfe von direct basic färbungsmitteln |
ATE449591T1 (de) | 1998-02-10 | 2009-12-15 | Schwarzkopf & Henkel K K | Dauerwellzusammensetzung mit färbendem effekt und verfahren zur haarfärbung unter verwendung derselben |
FR2776186B1 (fr) | 1998-03-20 | 2001-01-26 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
FR2788433B1 (fr) | 1999-01-19 | 2003-04-04 | Oreal | Utilisation de composes phenyl-azo-benzeniques cationiques en teinture des fibres keratiniques, compositions tinctoriales et procedes de teinture |
DE60102904T2 (de) | 2000-03-09 | 2005-03-31 | Ciba Specialty Chemicals Holding Inc. | Verfahren zur färbung von haaren unter verwendung von kationischen farbstoffen |
EP1133975B1 (en) | 2000-03-17 | 2008-02-13 | Kao Corporation | Use of a compound for dyeing hair |
JP2001261535A (ja) | 2000-03-17 | 2001-09-26 | Kao Corp | 毛髪用染色剤組成物 |
US20020192175A1 (en) * | 2001-04-18 | 2002-12-19 | Manilal Patel | Hair relaxer and coloring system |
BR0212987A (pt) | 2001-09-24 | 2004-08-17 | Ciba Sc Holding Ag | Corantes reativos catiÈnicos |
FR2830189B1 (fr) | 2001-09-28 | 2004-10-01 | Oreal | Composition de teinture a effet eclaircissant pour fibres keratiniques humaines |
FR2853237B1 (fr) | 2003-04-01 | 2006-07-14 | Oreal | Procede de coloration avec effet eclaircissant de fibres keratiniques humaines ayant subi une deformation permanente, au moyen d'une composition comprenant un colorant fluorescent |
BRPI0508391B1 (pt) * | 2004-04-08 | 2017-10-10 | Ciba Specialty Chemicals Holding Inc | Method of dyeing fibers containing keratin, and composition |
FR2876576B1 (fr) * | 2004-10-14 | 2006-12-08 | Oreal | Composition de teinture comprenant un colorant disulfure particulier et procede de coloration des fibres keratiniques humaines a partir de ce colorant |
US7488354B2 (en) * | 2004-10-14 | 2009-02-10 | L'oreal S.A. | Dyeing composition comprising at least one disulphide dye and method of dyeing human keratin fibers using this dye |
ES2602089T3 (es) | 2005-06-15 | 2017-02-17 | Basf Se | Colorantes azoicos oligoméricos catiónicos |
ATE437205T1 (de) | 2005-06-16 | 2009-08-15 | Ciba Holding Inc | Styrylsulfidfarbstoffe |
US7550016B2 (en) | 2005-06-23 | 2009-06-23 | Ciba Specialty Chemicals Corp. | Sulfide dyes |
MX2007016551A (es) | 2005-06-23 | 2008-03-04 | Ciba Sc Holding Ag | Tintes de nitrosulfuro. |
US7799092B2 (en) * | 2005-06-29 | 2010-09-21 | L'oreal S.A. | Composition for simultaneously bleaching and dyeing keratin fibers, comprising at least one anionic or nonionic direct dye and at least one associative polymer |
CN101326246B (zh) | 2005-10-11 | 2012-09-05 | 西巴控股公司 | 硫化物染料混合物 |
FR2898903B1 (fr) * | 2006-03-24 | 2012-08-31 | Oreal | Composition de teinture comprenant un colorant disulfure fluorescent, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
-
2007
- 2007-07-24 FR FR0756706A patent/FR2919179B1/fr not_active Expired - Fee Related
-
2008
- 2008-07-24 MX MX2008009509A patent/MX2008009509A/es active IP Right Grant
- 2008-07-24 ES ES08161083.4T patent/ES2525944T3/es active Active
- 2008-07-24 BR BRPI0806648A patent/BRPI0806648B1/pt not_active IP Right Cessation
- 2008-07-24 US US12/219,616 patent/US8097044B2/en not_active Expired - Fee Related
- 2008-07-24 EP EP08161083.4A patent/EP2018847B1/fr not_active Not-in-force
- 2008-07-24 ZA ZA200806461A patent/ZA200806461B/en unknown
Also Published As
Publication number | Publication date |
---|---|
FR2919179A1 (fr) | 2009-01-30 |
EP2018847B1 (fr) | 2014-09-17 |
US20090126755A1 (en) | 2009-05-21 |
FR2919179B1 (fr) | 2010-02-19 |
BRPI0806648A2 (pt) | 2011-08-16 |
EP2018847A1 (fr) | 2009-01-28 |
ES2525944T3 (es) | 2015-01-02 |
BRPI0806648B1 (pt) | 2016-08-09 |
US8097044B2 (en) | 2012-01-17 |
MX2008009509A (es) | 2009-02-26 |
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