LU84122A1 - Composition a base de colorants quinoniques destinee a etre utilisee pour la teinture des cheveux,procede de conservation de colorants quinoniques et utilisation pour la teinture des cheveux - Google Patents
Composition a base de colorants quinoniques destinee a etre utilisee pour la teinture des cheveux,procede de conservation de colorants quinoniques et utilisation pour la teinture des cheveux Download PDFInfo
- Publication number
- LU84122A1 LU84122A1 LU84122A LU84122A LU84122A1 LU 84122 A1 LU84122 A1 LU 84122A1 LU 84122 A LU84122 A LU 84122A LU 84122 A LU84122 A LU 84122A LU 84122 A1 LU84122 A1 LU 84122A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- dyes
- och3
- composition
- hair
- composition according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 87
- 239000000975 dye Substances 0.000 title claims description 52
- 238000004043 dyeing Methods 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 15
- -1 alkylene glycols Chemical class 0.000 claims description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 11
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000010790 dilution Methods 0.000 claims description 5
- 239000012895 dilution Substances 0.000 claims description 5
- 239000000982 direct dye Substances 0.000 claims description 5
- 150000002191 fatty alcohols Chemical class 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000002535 acidifier Substances 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 230000003113 alkalizing effect Effects 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- 239000000344 soap Substances 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- 235000013311 vegetables Nutrition 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 20
- 239000007788 liquid Substances 0.000 description 13
- 235000019441 ethanol Nutrition 0.000 description 12
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 10
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 10
- CSFWPUWCSPOLJW-UHFFFAOYSA-N lawsone Chemical compound C1=CC=C2C(=O)C(O)=CC(=O)C2=C1 CSFWPUWCSPOLJW-UHFFFAOYSA-N 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 150000004054 benzoquinones Chemical class 0.000 description 5
- 229960000541 cetyl alcohol Drugs 0.000 description 5
- 239000006071 cream Substances 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 4
- JNBVXNSWFXSRGS-UHFFFAOYSA-N 2-hydroxy-3-methoxynaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(OC)=C(O)C(=O)C2=C1 JNBVXNSWFXSRGS-UHFFFAOYSA-N 0.000 description 4
- BVQUETZBXIMAFZ-UHFFFAOYSA-N chembl1328567 Chemical compound C1=CC=C2C(=O)C(O)=C(O)C(=O)C2=C1 BVQUETZBXIMAFZ-UHFFFAOYSA-N 0.000 description 4
- 229960004106 citric acid Drugs 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CXRFDZFCGOPDTD-UHFFFAOYSA-M Cetrimide Chemical compound [Br-].CCCCCCCCCCCCCC[N+](C)(C)C CXRFDZFCGOPDTD-UHFFFAOYSA-M 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- GFAZBXKENDSJEB-UHFFFAOYSA-N Spinulosin Natural products COC1=C(O)C(=O)C(C)=C(O)C1=O GFAZBXKENDSJEB-UHFFFAOYSA-N 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 229960002887 deanol Drugs 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- GCDBEYOJCZLKMC-UHFFFAOYSA-N 2-hydroxyanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(O)=CC=C3C(=O)C2=C1 GCDBEYOJCZLKMC-UHFFFAOYSA-N 0.000 description 2
- WQASGOZUYRFMDF-UHFFFAOYSA-N 2-hydroxyjuglone Natural products C1=CC=C2C(=O)C(O)=CC(=O)C2=C1O WQASGOZUYRFMDF-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- WZUVPPKBWHMQCE-UHFFFAOYSA-N Haematoxylin Chemical compound C12=CC(O)=C(O)C=C2CC2(O)C1C1=CC=C(O)C(O)=C1OC2 WZUVPPKBWHMQCE-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 102000011782 Keratins Human genes 0.000 description 2
- 108010076876 Keratins Proteins 0.000 description 2
- 244000208060 Lawsonia inermis Species 0.000 description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
- 229930192627 Naphthoquinone Chemical class 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 244000186561 Swietenia macrophylla Species 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 150000002791 naphthoquinones Chemical class 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005063 solubilization Methods 0.000 description 2
- 230000007928 solubilization Effects 0.000 description 2
- VTARWSSIBFRCMF-UHFFFAOYSA-N 2,5-dihydroxy-3-methylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=C(O)C(=O)C=C(O)C1=O VTARWSSIBFRCMF-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 1
- RTZZCYNQPHTPPL-UHFFFAOYSA-N 3-nitrophenol Chemical compound OC1=CC=CC([N+]([O-])=O)=C1 RTZZCYNQPHTPPL-UHFFFAOYSA-N 0.000 description 1
- AQMHLTLDUPBBEF-UHFFFAOYSA-N 4,5-dihydroxynaphthalene-1,2-dione Chemical compound C1=CC(O)=C2C(O)=CC(=O)C(=O)C2=C1 AQMHLTLDUPBBEF-UHFFFAOYSA-N 0.000 description 1
- AXJPXJATWIBOQG-UHFFFAOYSA-N 4,7-dihydroxynaphthalene-1,2-dione Chemical compound OC1=CC=C2C(O)=CC(=O)C(=O)C2=C1 AXJPXJATWIBOQG-UHFFFAOYSA-N 0.000 description 1
- 244000017106 Bixa orellana Species 0.000 description 1
- 235000003392 Curcuma domestica Nutrition 0.000 description 1
- 244000008991 Curcuma longa Species 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 240000007829 Haematoxylum campechianum Species 0.000 description 1
- QXKHYNVANLEOEG-UHFFFAOYSA-N Methoxsalen Chemical group C1=CC(=O)OC2=C1C=C1C=COC1=C2OC QXKHYNVANLEOEG-UHFFFAOYSA-N 0.000 description 1
- 241000123069 Ocyurus chrysurus Species 0.000 description 1
- OOKBSCGBRWBGFL-UHFFFAOYSA-N Pseudopurpurin Chemical compound C1=CC=C2C(=O)C3=C(O)C(C(=O)O)=C(O)C(O)=C3C(=O)C2=C1 OOKBSCGBRWBGFL-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 229960004543 anhydrous citric acid Drugs 0.000 description 1
- 235000012665 annatto Nutrition 0.000 description 1
- 239000010362 annatto Substances 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- UWHUTZOCTZJUKC-CVEARBPZSA-N brazilin Natural products C12=CC(O)=C(O)C=C2C[C@@]2(O)[C@@H]1C1=CC=C(O)C=C1OC2 UWHUTZOCTZJUKC-CVEARBPZSA-N 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 235000003373 curcuma longa Nutrition 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000009967 direct dyeing Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000004338 hydroxy anthraquinones Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229960000448 lactic acid Drugs 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- AYLBVKUPVXVTSO-UHFFFAOYSA-N n,n-diphenylnitramide Chemical class C=1C=CC=CC=1N([N+](=O)[O-])C1=CC=CC=C1 AYLBVKUPVXVTSO-UHFFFAOYSA-N 0.000 description 1
- FYTRVVJHEWUARG-UHFFFAOYSA-N n-(2-aminophenyl)nitramide Chemical class NC1=CC=CC=C1N[N+]([O-])=O FYTRVVJHEWUARG-UHFFFAOYSA-N 0.000 description 1
- DZQXQAXLDXJEAG-UHFFFAOYSA-N n-(2-hydroxyphenyl)nitramide Chemical class OC1=CC=CC=C1N[N+]([O-])=O DZQXQAXLDXJEAG-UHFFFAOYSA-N 0.000 description 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 239000001003 triarylmethane dye Substances 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 235000013976 turmeric Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000002023 wood Substances 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
- A61K8/355—Quinones
-
- 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)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU84122A LU84122A1 (fr) | 1982-04-29 | 1982-04-29 | Composition a base de colorants quinoniques destinee a etre utilisee pour la teinture des cheveux,procede de conservation de colorants quinoniques et utilisation pour la teinture des cheveux |
| GB08311649A GB2119411B (en) | 1982-04-29 | 1983-04-28 | Composition based on quinone dyestuffs for use in hair dyeing and process for the preservation of quinone dyestuffs |
| FR8307045A FR2526031B1 (fr) | 1982-04-29 | 1983-04-28 | Composition a base de colorants quinoniques destinee a etre utilisee pour la teinture des cheveux, procede de conservation de colorants quinoniques et utilisation pour la teinture des cheveux |
| DE19833315522 DE3315522A1 (de) | 1982-04-29 | 1983-04-29 | Mittel auf der basis von chinonfarbstoffen, verfahren zur konservierung und verwendung derselben bei der haarfaerbung |
| US07/896,573 US5259849A (en) | 1982-04-29 | 1992-06-10 | Composition based on quinone dyestuffs for use in hair dyeing and process for the preservation of quinone dyestuffs |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU84122 | 1982-04-29 | ||
| LU84122A LU84122A1 (fr) | 1982-04-29 | 1982-04-29 | Composition a base de colorants quinoniques destinee a etre utilisee pour la teinture des cheveux,procede de conservation de colorants quinoniques et utilisation pour la teinture des cheveux |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU84122A1 true LU84122A1 (fr) | 1983-12-16 |
Family
ID=19729870
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU84122A LU84122A1 (fr) | 1982-04-29 | 1982-04-29 | Composition a base de colorants quinoniques destinee a etre utilisee pour la teinture des cheveux,procede de conservation de colorants quinoniques et utilisation pour la teinture des cheveux |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE3315522A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2526031B1 (enrdf_load_stackoverflow) |
| GB (1) | GB2119411B (enrdf_load_stackoverflow) |
| LU (1) | LU84122A1 (enrdf_load_stackoverflow) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU84511A1 (fr) * | 1982-12-08 | 1984-10-22 | Oreal | Utilisation de 5-hydroxynaphtoquinones pour la teinture des fibres keratiniques humaines,procede de teinture les mettant en oeuvre et composition tinctoriale utilisee |
| FR2588473B1 (fr) * | 1985-10-16 | 1988-06-10 | Oreal | Utilisation de la 2,3-indolinedione pour la coloration des fibres keratiniques |
| LU86521A1 (fr) * | 1986-07-18 | 1988-02-02 | Oreal | Procede de teinture des cheveux avec des colorants hydroxyquinoniques et des sels metalliques |
| FR2672211B1 (fr) * | 1991-02-04 | 1993-05-21 | Oreal | Procede de teinture des fibres keratiniques avec un mono- ou dihydroxyindole et un derive carbonyle aromatique non-oxydant et agent de teinture. |
| FR2724560B1 (fr) | 1994-09-21 | 1996-12-20 | Oreal | Procede de coloration directe des fibres keratiniques a l'aide de colorants directs cationiques et de vapeur d'eau |
| DE19713510A1 (de) * | 1997-04-01 | 1998-10-08 | Henkel Kgaa | Haarfärbemittel |
| WO2018087203A1 (en) * | 2016-11-11 | 2018-05-17 | Kao Germany Gmbh | Liquid composition comprising hair direct dyes and one or more diols |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE517244A (enrdf_load_stackoverflow) * | ||||
| NL36651C (enrdf_load_stackoverflow) * | 1932-12-10 | |||
| US2695259A (en) * | 1949-01-03 | 1954-11-23 | Union Francaise Commerciale Et Industrielle Sa | Dermatologically harmless hair dyeing creams |
| US3677691A (en) * | 1968-09-24 | 1972-07-18 | Kohnstamm & Co Inc H | Nontoxic dyes in polyglycerol fatty acid ester and glycol or glycerine and its mixture therein |
| FR2473310A1 (fr) * | 1980-01-15 | 1981-07-17 | Fabre Sa Pierre | Extrait stable de lawsonia inermis et son procede de preparation |
| LU83807A1 (fr) * | 1981-12-02 | 1983-09-01 | Oreal | Utilisation de benzoquinones pour la coloration directe des fibres keratiniques |
| LU83806A1 (fr) * | 1981-12-02 | 1983-09-01 | Oreal | Utilisation d'hydroxynaphtoquinones pour la teinture des fibres keratiniques humaines,procede de teinture les mettant en oeuvre et composition tinctoriale utilisee |
-
1982
- 1982-04-29 LU LU84122A patent/LU84122A1/fr unknown
-
1983
- 1983-04-28 FR FR8307045A patent/FR2526031B1/fr not_active Expired
- 1983-04-28 GB GB08311649A patent/GB2119411B/en not_active Expired
- 1983-04-29 DE DE19833315522 patent/DE3315522A1/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| GB2119411B (en) | 1985-10-23 |
| FR2526031B1 (fr) | 1987-01-30 |
| GB2119411A (en) | 1983-11-16 |
| DE3315522A1 (de) | 1983-11-03 |
| GB8311649D0 (en) | 1983-06-02 |
| FR2526031A1 (fr) | 1983-11-04 |
| DE3315522C2 (enrdf_load_stackoverflow) | 1992-02-27 |
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