BE1000115A3 - Procede de teinture des fibres keratiniques avec le 5,6-dihydroxyindole ou ses derives et un anion metallique. - Google Patents
Procede de teinture des fibres keratiniques avec le 5,6-dihydroxyindole ou ses derives et un anion metallique. Download PDFInfo
- Publication number
- BE1000115A3 BE1000115A3 BE8700145A BE8700145A BE1000115A3 BE 1000115 A3 BE1000115 A3 BE 1000115A3 BE 8700145 A BE8700145 A BE 8700145A BE 8700145 A BE8700145 A BE 8700145A BE 1000115 A3 BE1000115 A3 BE 1000115A3
- Authority
- BE
- Belgium
- Prior art keywords
- dihydroxyindole
- sep
- dyeing
- composition containing
- anion
- Prior art date
Links
- 238000004043 dyeing Methods 0.000 title claims abstract description 28
- 238000000034 method 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 26
- 150000001450 anions Chemical class 0.000 title claims abstract description 25
- 239000000835 fiber Substances 0.000 title claims abstract description 19
- 102000011782 Keratins Human genes 0.000 title claims abstract description 17
- 108010076876 Keratins Proteins 0.000 title claims abstract description 17
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 10
- 239000002184 metal Substances 0.000 title claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 37
- 230000008569 process Effects 0.000 claims abstract description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims abstract 2
- 210000004209 hair Anatomy 0.000 claims description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 30
- 239000000243 solution Substances 0.000 claims description 26
- 239000000975 dye Substances 0.000 claims description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 14
- 239000002609 medium Substances 0.000 claims description 11
- 239000012286 potassium permanganate Substances 0.000 claims description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000002671 adjuvant Substances 0.000 claims description 5
- 239000012736 aqueous medium Substances 0.000 claims description 5
- -1 sequestering them Substances 0.000 claims description 4
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 claims description 3
- ZUTZCXDHPIACCR-UHFFFAOYSA-N 3-methyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2C(C)=CNC2=C1 ZUTZCXDHPIACCR-UHFFFAOYSA-N 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 239000002562 thickening agent Substances 0.000 claims description 3
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
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- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000000872 buffer Substances 0.000 claims description 2
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 claims description 2
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 claims description 2
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- 229940057867 methyl lactate Drugs 0.000 claims description 2
- 150000007522 mineralic acids Chemical class 0.000 claims description 2
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- REOJLIXKJWXUGB-UHFFFAOYSA-N mofebutazone Chemical group O=C1C(CCCC)C(=O)NN1C1=CC=CC=C1 REOJLIXKJWXUGB-UHFFFAOYSA-N 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
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- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
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- 239000010413 mother solution Substances 0.000 description 4
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
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- 235000019270 ammonium chloride Nutrition 0.000 description 3
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- 210000002268 wool Anatomy 0.000 description 3
- QGJCWKNNWOVPTJ-UHFFFAOYSA-N 2-methyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2NC(C)=CC2=C1 QGJCWKNNWOVPTJ-UHFFFAOYSA-N 0.000 description 2
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 2
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- 241000557626 Corvus corax Species 0.000 description 2
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- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
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- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 229910017974 NH40H Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000002610 basifying agent Substances 0.000 description 2
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- 150000001768 cations Chemical class 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
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- 238000004898 kneading Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
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- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- 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
- HMTUVSJLXALWIU-UHFFFAOYSA-N 2,3-dimethyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2C(C)=C(C)NC2=C1 HMTUVSJLXALWIU-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical class COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
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- 239000005995 Aluminium silicate Substances 0.000 description 1
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- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 1
- 229920001503 Glucan Polymers 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 241000282372 Panthera onca Species 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
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- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
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- 230000003113 alkalizing effect Effects 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
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- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
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- 229910052793 cadmium Inorganic materials 0.000 description 1
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- 229910001431 copper ion Inorganic materials 0.000 description 1
- KGOIAFZMMLWXLM-UHFFFAOYSA-N dialuminum trioxido(trioxidosilyloxy)silane dihydrate Chemical compound O.O.[Al+3].[Al+3].[O-][Si]([O-])([O-])O[Si]([O-])([O-])[O-] KGOIAFZMMLWXLM-UHFFFAOYSA-N 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
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- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical compound [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
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- 150000002338 glycosides Chemical class 0.000 description 1
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- 239000010931 gold Substances 0.000 description 1
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- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
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- 229910052759 nickel Inorganic materials 0.000 description 1
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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
- D06P3/08—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
-
- 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)
- Inorganic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Engineering & Computer Science (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU86314A LU86314A1 (fr) | 1986-02-20 | 1986-02-20 | Procede de teinture des fibres keratiniques humaines avec le 5,6-dihydroxyindole et un anion metallique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE1000115A3 true BE1000115A3 (fr) | 1988-04-05 |
Family
ID=19730641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE8700145A BE1000115A3 (fr) | 1986-02-20 | 1987-02-19 | Procede de teinture des fibres keratiniques avec le 5,6-dihydroxyindole ou ses derives et un anion metallique. |
Country Status (10)
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH679150A5 (enrdf_load_stackoverflow) * | 1986-11-07 | 1991-12-31 | Oreal | |
| 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 |
| 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 |
| DE4323123A1 (de) * | 1993-07-10 | 1995-01-12 | Hoechst Ag | Verfahren zum Färben von Pelzfellen mit Oxidationsfarbstoffen |
| FR2757386B1 (fr) * | 1996-12-23 | 1999-01-29 | Oreal | Procede de teinture d'oxydation en deux temps des fibres keratiniques avec un sel ou un complexe de manganese et un 1-naphtol 4-substitue et kit de teinture |
| DE19713510A1 (de) * | 1997-04-01 | 1998-10-08 | Henkel Kgaa | Haarfärbemittel |
| DE102006031502A1 (de) * | 2006-07-06 | 2008-01-17 | Henkel Kgaa | Oxidationsfärbemittel zur Färbung keratinhaltiger Fasern mit Luftsauerstoff als einzigem Oxidationsmittel |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2101696A (en) * | 1934-12-15 | 1937-12-07 | Gen Aniline Works Inc | Process for producing two-color effects on skins or furs |
| DE694310C (de) * | 1937-08-15 | 1940-07-29 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung von Oxydationsfaerbungenls Beize |
| FR860591A (fr) * | 1939-08-09 | 1941-01-18 | Perfectionnements apportés aux procédés de teinture de poils, cheveux et matières textiles | |
| FR1166172A (fr) * | 1957-02-02 | 1958-11-04 | Oreal | Procédé pour teindre les cheveux et substances analogues, composition utilisée et produits teints obtenus |
| FR2390158A1 (fr) * | 1977-05-10 | 1978-12-08 | Oreal | Compositions liquides de colorants de la famille des indoles destinees a la teinture des cheveux |
| EP0133129A2 (fr) * | 1983-07-28 | 1985-02-13 | Secta-Laboratoires De Cosmetologie Yves Rocher | Procédé et compositions pour la coloration des phanères |
-
1986
- 1986-02-20 LU LU86314A patent/LU86314A1/fr unknown
-
1987
- 1987-02-19 GB GB8703842A patent/GB2187210B/en not_active Expired - Lifetime
- 1987-02-19 BE BE8700145A patent/BE1000115A3/fr not_active IP Right Cessation
- 1987-02-19 CH CH630/87A patent/CH672729A5/fr not_active IP Right Cessation
- 1987-02-19 IT IT8767119A patent/IT1207356B/it active
- 1987-02-19 FR FR878702162A patent/FR2594331B1/fr not_active Expired - Lifetime
- 1987-02-19 CA CA000530134A patent/CA1298042C/fr not_active Expired - Lifetime
- 1987-02-19 ES ES8700417A patent/ES2003225A6/es not_active Expired
- 1987-02-20 JP JP62035985A patent/JPS62246510A/ja active Pending
- 1987-02-20 DE DE19873705453 patent/DE3705453A1/de not_active Withdrawn
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2101696A (en) * | 1934-12-15 | 1937-12-07 | Gen Aniline Works Inc | Process for producing two-color effects on skins or furs |
| DE694310C (de) * | 1937-08-15 | 1940-07-29 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung von Oxydationsfaerbungenls Beize |
| FR860591A (fr) * | 1939-08-09 | 1941-01-18 | Perfectionnements apportés aux procédés de teinture de poils, cheveux et matières textiles | |
| FR1166172A (fr) * | 1957-02-02 | 1958-11-04 | Oreal | Procédé pour teindre les cheveux et substances analogues, composition utilisée et produits teints obtenus |
| FR2390158A1 (fr) * | 1977-05-10 | 1978-12-08 | Oreal | Compositions liquides de colorants de la famille des indoles destinees a la teinture des cheveux |
| EP0133129A2 (fr) * | 1983-07-28 | 1985-02-13 | Secta-Laboratoires De Cosmetologie Yves Rocher | Procédé et compositions pour la coloration des phanères |
Non-Patent Citations (2)
| Title |
|---|
| CHEMICAL ABSTRACTS, vol. 43, 1949, colonne 7689 f,g, Columbus, Ohio, US; A. GINZEL: "The dyeing of rabbit fur", & MELLIAND TEXTILBER, 28, 359(1947) * |
| R\MPPS CHEMIE LEXIKON, vol. 4, 7ième édition, 1974, pages 2468-2469, Stuttgart, DE; "Oxidimetrie", "Chromatometrie", "Manganometrie" * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1298042C (fr) | 1992-03-31 |
| FR2594331A1 (fr) | 1987-08-21 |
| ES2003225A6 (es) | 1988-10-16 |
| IT1207356B (it) | 1989-05-17 |
| DE3705453A1 (de) | 1987-08-27 |
| LU86314A1 (fr) | 1987-09-10 |
| IT8767119A0 (it) | 1987-02-19 |
| GB2187210B (en) | 1990-03-28 |
| GB2187210A (en) | 1987-09-03 |
| GB8703842D0 (en) | 1987-03-25 |
| FR2594331B1 (fr) | 1990-10-05 |
| CH672729A5 (enrdf_load_stackoverflow) | 1989-12-29 |
| JPS62246510A (ja) | 1987-10-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RE | Patent lapsed |
Owner name: S.A. L' OREAL Effective date: 19930228 |