BE1000074A4 - Procede de teinture des fibres keratiniques avec le 5,6-dihydroxyindole et du peroxyde d'hydrogene, precede ou suivi d'un traitement par un iodure. - Google Patents
Procede de teinture des fibres keratiniques avec le 5,6-dihydroxyindole et du peroxyde d'hydrogene, precede ou suivi d'un traitement par un iodure. Download PDFInfo
- Publication number
- BE1000074A4 BE1000074A4 BE8700021A BE8700021A BE1000074A4 BE 1000074 A4 BE1000074 A4 BE 1000074A4 BE 8700021 A BE8700021 A BE 8700021A BE 8700021 A BE8700021 A BE 8700021A BE 1000074 A4 BE1000074 A4 BE 1000074A4
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- composition
- agents
- dihydroxyindole
- dyeing
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 39
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 title claims abstract description 33
- 238000004043 dyeing Methods 0.000 title claims abstract description 27
- SGNZYJXNUURYCH-UHFFFAOYSA-N 5,6-dihydroxyindole Chemical compound C1=C(O)C(O)=CC2=C1NC=C2 SGNZYJXNUURYCH-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 239000000835 fiber Substances 0.000 title claims abstract description 18
- 102000011782 Keratins Human genes 0.000 title claims abstract description 7
- 108010076876 Keratins Proteins 0.000 title claims abstract description 7
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 title claims description 8
- 239000000203 mixture Substances 0.000 claims abstract description 90
- -1 ions iodide Chemical class 0.000 claims abstract description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 22
- 210000004209 hair Anatomy 0.000 claims description 22
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 235000019441 ethanol Nutrition 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- 239000002562 thickening agent Substances 0.000 claims description 4
- 239000002535 acidifier Substances 0.000 claims description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical class COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 150000002193 fatty amides Chemical class 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 claims description 2
- 229940006461 iodide ion Drugs 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 3
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims 1
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 230000003750 conditioning effect Effects 0.000 claims 1
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 claims 1
- 150000004694 iodide salts Chemical class 0.000 claims 1
- 229940057867 methyl lactate Drugs 0.000 claims 1
- 238000007747 plating Methods 0.000 claims 1
- 230000008961 swelling Effects 0.000 claims 1
- 239000011701 zinc Substances 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- 239000002609 medium Substances 0.000 description 14
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 238000004040 coloring Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920013683 Celanese Polymers 0.000 description 3
- 244000303965 Cyamopsis psoralioides Species 0.000 description 3
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 3
- 241000282372 Panthera onca Species 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 229930182470 glycoside Natural products 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 239000002610 basifying agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 150000002338 glycosides Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 230000002269 spontaneous effect Effects 0.000 description 2
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920013806 TRITON CG-110 Polymers 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- PRKQVKDSMLBJBJ-UHFFFAOYSA-N ammonium carbonate Chemical class N.N.OC(O)=O PRKQVKDSMLBJBJ-UHFFFAOYSA-N 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000011162 ammonium carbonates Nutrition 0.000 description 1
- 229940107816 ammonium iodide Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229920001222 biopolymer Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- REOJLIXKJWXUGB-UHFFFAOYSA-N mofebutazone Chemical group O=C1C(CCCC)C(=O)NN1C1=CC=CC=C1 REOJLIXKJWXUGB-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/30—Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/08—Material containing basic nitrogen containing amide groups using oxidation dyes
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/20—Halogens; Compounds thereof
-
- 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
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
-
- 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
- A61Q5/10—Preparations for permanently dyeing the hair
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Textile Engineering (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU86256A LU86256A1 (fr) | 1986-01-20 | 1986-01-20 | Procede de teinture des fibres keratiniques avec du 5,6-dihydroxyindole associe avec un iodure |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE1000074A4 true BE1000074A4 (fr) | 1988-02-02 |
Family
ID=19730617
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE8700021A BE1000074A4 (fr) | 1986-01-20 | 1987-01-16 | Procede de teinture des fibres keratiniques avec le 5,6-dihydroxyindole et du peroxyde d'hydrogene, precede ou suivi d'un traitement par un iodure. |
| BE8700020A BE1000073A4 (fr) | 1986-01-20 | 1987-01-16 | Procede de teinture des fibres keratiniques avec le 5-6-dihydroxyindole associe a un iodure et composition tinctoriale mise en oeuvre. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE8700020A BE1000073A4 (fr) | 1986-01-20 | 1987-01-16 | Procede de teinture des fibres keratiniques avec le 5-6-dihydroxyindole associe a un iodure et composition tinctoriale mise en oeuvre. |
Country Status (19)
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5492541A (en) * | 1985-08-02 | 1996-02-20 | Clairol Incorporated | Dye compositions containing 5,6-dihydroxy indoles and a foam generator |
| DE3628397C2 (de) * | 1986-08-21 | 1994-06-09 | Goldwell Ag | Mittel zum oxidativen Färben von Haaren, Verfahren zu seiner Herstellung und Verwendung des Mittels |
| CH679150A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1986-11-07 | 1991-12-31 | Oreal | |
| LU86668A1 (fr) * | 1986-11-17 | 1988-06-13 | Oreal | Procede de teinture des fibres keratiniques avec des derives d'indole associes avec un iodure |
| LU86833A1 (fr) * | 1987-04-02 | 1988-12-13 | Oreal | Procede de teinture des fibres keratiniques avec le 5,6-dihydroxyindole associe a un iodure et une composition de peroxyde d'hydrogene a ph alcalin |
| DE3714775A1 (de) * | 1987-05-04 | 1988-11-24 | Wella Ag | Verwendung von 2,6-dinitro-anilinderivaten in haarfaerbemitteln und neue 2,6-dinitro-anilinderivate |
| LU86899A1 (fr) * | 1987-05-25 | 1989-01-19 | Oreal | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre |
| US5180399A (en) * | 1987-05-25 | 1993-01-19 | L'oreal | Process for dyeing keratinous fibres with oxidation bases combined with an iodide and dyeing composition employed |
| US5180397A (en) * | 1987-05-25 | 1993-01-19 | L'oreal | Process for dyeing keratinous fibres with couplers and/or "rapid" oxidation dyes combined with an iodide and dyeing composition employed |
| LU86947A1 (fr) * | 1987-07-17 | 1989-03-08 | Oreal | Procede de teinture des fibres keratiniques,en particulier humaines,avec le 5-(hydroxy ou-methoxy)6-hydroxyindole |
| LU87086A1 (fr) * | 1987-12-18 | 1989-07-07 | Oreal | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes au 5,6-dihydroxyindole et a un iodure et composition tinctoriale mise en oeuvre |
| US5180396A (en) * | 1987-12-18 | 1993-01-19 | L'oreal | Process for dyeing keratinous fibres with oxidation dyes combined with indole derivatives and dyeing composition employed |
| LU87097A1 (fr) * | 1987-12-30 | 1989-07-07 | Oreal | Procede de teinture des fibres keratiniques et composition de teinture mettant en oeuvre du 5,6-dihydroxyindole,un colorant direct nitre et un iodure |
| LU87113A1 (fr) * | 1988-01-26 | 1989-08-30 | Oreal | Procede de teinture des fibres keratiniques et composition de teinture mettant en oeuvre du 5,6-dihydroxyindole,un colorant quinonique et iodure |
| LU87128A1 (fr) * | 1988-02-08 | 1989-09-20 | Oreal | Composition de teinture des fibres keratiniques mettant en oeuvre du 5,6-dihydroxyindole et au moins une paraphenylenediamine disubstituee sur l'un des groupements amino et procede de mise en oeuvre |
| LU87196A1 (fr) | 1988-04-12 | 1989-11-14 | Oreal | Procede de conservation du pouvoir tinctorial du 5,6-dihydroxyindole en milieu aqueux,composition et procede de teinture |
| LU87256A1 (fr) * | 1988-06-21 | 1990-02-28 | Oreal | Procedes de teinture de fibres keratiniques a base de 5,6-dihydroxyindole et d'au moins un sel de terre rare et compositions de mise en oeuvre |
| LU87270A1 (fr) * | 1988-07-08 | 1990-02-07 | Oreal | Procede de teinture des fibres keratiniques avec du 5,6-dihydroxyindole associe a un nitrite et composition de mise en oeuvre |
| LU87336A1 (fr) * | 1988-09-12 | 1990-04-06 | Oreal | Procede de teinture des fibres keratiniques avec un monohydroxyindole associe a un iodure et compositions mises en oeuvre |
| US5354870A (en) * | 1988-09-12 | 1994-10-11 | L'oreal | Indole derivatives for dyeing keratin materials |
| LU87338A1 (fr) * | 1988-09-12 | 1990-04-06 | Oreal | Utilisation de derives d'indole pour la teinture de matieres keratiniques,compositions tinctoriales,composes nouveaux et procede de teinture |
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| KR101877238B1 (ko) * | 2011-10-14 | 2018-07-11 | (주)아모레퍼시픽 | 모발 염색용 화장료 조성물 및 이를 이용한 염색방법 |
| FR2994091B1 (fr) | 2012-08-02 | 2014-08-01 | Oreal | Composition de coloration comprenant de la gomme de guar non ionique ou l'un de ses derives non ionique, procede et dispositif |
| RU2015106932A (ru) | 2012-08-02 | 2016-09-20 | Л'Ореаль | Композиция для окрашивания, содержащая жировое вещество, неионную гуаровую камедь, амфотерное поверхностно-активное вещество и неионное или анионное поверхностно-активное вещество и окислитель, способ окрашивания и подходящее устройство |
| EP2879649B2 (en) | 2012-08-02 | 2022-08-24 | L'oreal | Dyeing composition comprising at least one fatty substance, at least one oxidizing agent and at least one non-ionic, anionic and amphoteric surfactant |
| FR2994084B1 (fr) | 2012-08-02 | 2014-10-31 | Oreal | Composition de coloration sous forme de creme comprenant au moins une huile, pas ou peu d'alcool gras solide, procede de coloration et dispositif approprie |
| FR3000675B1 (fr) * | 2013-01-09 | 2014-12-26 | Oreal | Composition de coloration exempte d'agent oxydant chimique comprenant un colorant d'oxydation, un alkylsulfate, un alkylpolyglycoside, un corps gras et de la gomme de guar non ionique |
| CN110200823A (zh) * | 2019-06-12 | 2019-09-06 | 四川大学 | 一种基于苯硼酸的染发剂及其制备和使用方法 |
| CN116687770A (zh) * | 2023-07-14 | 2023-09-05 | 珠海市丝域生物科技有限公司 | 一种含有碘化钾的护发组合物及其制备方法 |
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| FR1166172A (fr) * | 1957-02-02 | 1958-11-04 | Oreal | Procédé pour teindre les cheveux et substances analogues, composition utilisée et produits teints obtenus |
| GB2132642A (en) * | 1982-12-07 | 1984-07-11 | Bristol Myers Co | Hair dyeing process and kit |
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| FR1365276A (fr) * | 1961-08-04 | 1964-07-03 | Gillette Co | Perfectionnements aux compositions de teinture pour cheveux |
| DE1469739A1 (de) * | 1965-10-08 | 1969-01-02 | Bayer Ag | Verfahren zum Faerben von Polyolefinen und Polysiloxanen |
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| GB2078804B (en) * | 1980-06-16 | 1984-03-07 | Gureisu Kagaku Kk | Permanent hair-waving solution |
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1987
- 1987-01-15 DE DE3701044A patent/DE3701044C2/de not_active Expired - Fee Related
- 1987-01-15 DE DE3701026A patent/DE3701026C2/de not_active Expired - Fee Related
- 1987-01-16 BE BE8700021A patent/BE1000074A4/fr not_active IP Right Cessation
- 1987-01-16 PT PT84121A patent/PT84121B/pt not_active IP Right Cessation
- 1987-01-16 PT PT84122A patent/PT84122B/pt not_active IP Right Cessation
- 1987-01-16 BR BR8700188A patent/BR8700188A/pt not_active Application Discontinuation
- 1987-01-16 BE BE8700020A patent/BE1000073A4/fr not_active IP Right Cessation
- 1987-01-16 GR GR870065A patent/GR870065B/el unknown
- 1987-01-16 BR BR8700189A patent/BR8700189A/pt unknown
- 1987-01-17 KR KR870000351A patent/KR870007324A/ko not_active Ceased
- 1987-01-17 KR KR870000352A patent/KR870007325A/ko not_active Ceased
- 1987-01-19 NL NL8700116A patent/NL8700116A/nl not_active Application Discontinuation
- 1987-01-19 FR FR8700527A patent/FR2593061B1/fr not_active Expired
- 1987-01-19 NL NL8700115A patent/NL8700115A/nl not_active Application Discontinuation
- 1987-01-19 ES ES8700112A patent/ES2004060A6/es not_active Expired
- 1987-01-19 IT IT8767029A patent/IT1206851B/it active
- 1987-01-19 FR FR8700528A patent/FR2593062B1/fr not_active Expired
- 1987-01-19 CH CH173/87A patent/CH672728A5/fr not_active IP Right Cessation
- 1987-01-19 IT IT8767030A patent/IT1206852B/it active
- 1987-01-19 CH CH174/87A patent/CH671512A5/fr not_active IP Right Cessation
- 1987-01-19 ES ES8700111A patent/ES2003660A6/es not_active Expired
- 1987-01-20 ZA ZA87402A patent/ZA87402B/xx unknown
- 1987-01-20 JP JP62009175A patent/JPS62238878A/ja active Granted
- 1987-01-20 AU AU67811/87A patent/AU607880B2/en not_active Ceased
- 1987-01-20 CA CA000527703A patent/CA1298444C/fr not_active Expired - Lifetime
- 1987-01-20 AU AU67812/87A patent/AU602827B2/en not_active Ceased
- 1987-01-20 CN CN87100806A patent/CN1014022B/zh not_active Expired
- 1987-01-20 CN CN87100820A patent/CN1014023B/zh not_active Expired
- 1987-01-20 ZA ZA87401A patent/ZA87401B/xx unknown
- 1987-01-20 CA CA000527702A patent/CA1298443C/fr not_active Expired - Lifetime
- 1987-01-20 JP JP62009174A patent/JPH0663182B2/ja not_active Expired - Lifetime
- 1987-01-20 GB GB8701140A patent/GB2186891B/en not_active Expired - Lifetime
- 1987-01-20 GB GB8701141A patent/GB2185498B/en not_active Expired - Lifetime
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| FR1166172A (fr) * | 1957-02-02 | 1958-11-04 | Oreal | Procédé pour teindre les cheveux et substances analogues, composition utilisée et produits teints obtenus |
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Legal Events
| Date | Code | Title | Description |
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| RE | Patent lapsed |
Owner name: S.A. L OREAL Effective date: 19930131 |