LU83807A1 - Utilisation de benzoquinones pour la coloration directe des fibres keratiniques - Google Patents
Utilisation de benzoquinones pour la coloration directe des fibres keratiniques Download PDFInfo
- Publication number
- LU83807A1 LU83807A1 LU83807A LU83807A LU83807A1 LU 83807 A1 LU83807 A1 LU 83807A1 LU 83807 A LU83807 A LU 83807A LU 83807 A LU83807 A LU 83807A LU 83807 A1 LU83807 A1 LU 83807A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- benzoquinone
- methyl
- dihydroxy
- hair
- dyes
- Prior art date
Links
- 239000000835 fiber Substances 0.000 title claims description 14
- 238000004040 coloring Methods 0.000 title description 6
- 150000004054 benzoquinones Chemical class 0.000 title description 5
- 239000000203 mixture Substances 0.000 claims description 55
- 239000000975 dye Substances 0.000 claims description 38
- 238000004043 dyeing Methods 0.000 claims description 15
- 150000004057 1,4-benzoquinones Chemical class 0.000 claims description 14
- 102000011782 Keratins Human genes 0.000 claims description 13
- 108010076876 Keratins Proteins 0.000 claims description 13
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000006071 cream Substances 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- BFOTXRXRHJHTDX-UHFFFAOYSA-N 2-hydroxy-3-methyl-6-methoxybenzoquinone Natural products COC1=CC(=O)C(C)=C(O)C1=O BFOTXRXRHJHTDX-UHFFFAOYSA-N 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 229940005561 1,4-benzoquinone Drugs 0.000 claims description 3
- 239000000982 direct dye Substances 0.000 claims description 3
- 239000000284 extract Substances 0.000 claims description 3
- 239000003921 oil Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- DGQOCLATAPFASR-UHFFFAOYSA-N tetrahydroxy-1,4-benzoquinone Chemical compound OC1=C(O)C(=O)C(O)=C(O)C1=O DGQOCLATAPFASR-UHFFFAOYSA-N 0.000 claims description 3
- ZJKWJHONFFKJHG-UHFFFAOYSA-N 2-Methoxy-1,4-benzoquinone Chemical compound COC1=CC(=O)C=CC1=O ZJKWJHONFFKJHG-UHFFFAOYSA-N 0.000 claims description 2
- 235000013312 flour Nutrition 0.000 claims description 2
- 239000000499 gel Substances 0.000 claims description 2
- VTWDKFNVVLAELH-UHFFFAOYSA-N 2-methylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=CC(=O)C=CC1=O VTWDKFNVVLAELH-UHFFFAOYSA-N 0.000 claims 3
- RRSIQEMLRDKPLK-UHFFFAOYSA-N 2,3-dihydroxy-5,6-dimethylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=C(C)C(=O)C(O)=C(O)C1=O RRSIQEMLRDKPLK-UHFFFAOYSA-N 0.000 claims 2
- DUPLFIFGNDSGBB-UHFFFAOYSA-N 2,3-dihydroxy-5-methyl-1,4-benzoquinone Chemical compound CC1=CC(=O)C(O)=C(O)C1=O DUPLFIFGNDSGBB-UHFFFAOYSA-N 0.000 claims 2
- QFSYADJLNBHAKO-UHFFFAOYSA-N 2,5-dihydroxy-1,4-benzoquinone Chemical compound OC1=CC(=O)C(O)=CC1=O QFSYADJLNBHAKO-UHFFFAOYSA-N 0.000 claims 2
- HZKFHDXTSAYOSN-UHFFFAOYSA-N Polyporic acid Chemical compound O=C1C(O)=C(C=2C=CC=CC=2)C(=O)C(O)=C1C1=CC=CC=C1 HZKFHDXTSAYOSN-UHFFFAOYSA-N 0.000 claims 2
- GFAZBXKENDSJEB-UHFFFAOYSA-N Spinulosin Natural products COC1=C(O)C(=O)C(C)=C(O)C1=O GFAZBXKENDSJEB-UHFFFAOYSA-N 0.000 claims 2
- KEQHJBNSCLWCAE-UHFFFAOYSA-N thymoquinone Chemical compound CC(C)C1=CC(=O)C(C)=CC1=O KEQHJBNSCLWCAE-UHFFFAOYSA-N 0.000 claims 2
- SENUUPBBLQWHMF-UHFFFAOYSA-N 2,6-dimethylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=CC(=O)C=C(C)C1=O SENUUPBBLQWHMF-UHFFFAOYSA-N 0.000 claims 1
- ZIHGHGAQMRGZKY-UHFFFAOYSA-N 2-hydroxy-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione Chemical compound COC1=C(OC)C(=O)C(O)=C(C)C1=O ZIHGHGAQMRGZKY-UHFFFAOYSA-N 0.000 claims 1
- OUSQDTMHWCQLAU-UHFFFAOYSA-N 2-hydroxy-6-methylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=CC(=O)C=C(O)C1=O OUSQDTMHWCQLAU-UHFFFAOYSA-N 0.000 claims 1
- FKQQKMGWCJGUCS-UHFFFAOYSA-N atromentin Chemical compound O=C1C(O)=C(C=2C=CC(O)=CC=2)C(=O)C(O)=C1C1=CC=C(O)C=C1 FKQQKMGWCJGUCS-UHFFFAOYSA-N 0.000 claims 1
- AAEDGQBSNHENEM-UHFFFAOYSA-N atromentin Natural products OCC1(O)C2=C(C(=O)C(=C(C2=O)c3ccc(O)cc3)O)c4ccc(O)cc14 AAEDGQBSNHENEM-UHFFFAOYSA-N 0.000 claims 1
- GSNBWTFAGXSQCO-UHFFFAOYSA-N fumigatin Chemical compound COC1=C(O)C(=O)C(C)=CC1=O GSNBWTFAGXSQCO-UHFFFAOYSA-N 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 30
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000012153 distilled water Substances 0.000 description 9
- -1 2-methyl 1,4-benzoquinone 2.5-dihydroxy 1,4-benzoquinone 2 , 3,5,6-tetrahydroxy 1,4-benzoquinone 2-hydroxy 3-methyl 6-methoxy 1,4-benzoquinone 2.5- dihydroxy 3-methyl 6-methoxy 1,4-benzoquinone Chemical compound 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 229960000541 cetyl alcohol Drugs 0.000 description 6
- ALSTYHKOOCGGFT-UHFFFAOYSA-N cis-oleyl alcohol Natural products CCCCCCCCC=CCCCCCCCCO ALSTYHKOOCGGFT-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- CSFWPUWCSPOLJW-UHFFFAOYSA-N lawsone Chemical compound C1=CC=C2C(=O)C(O)=CC(=O)C2=C1 CSFWPUWCSPOLJW-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- PTIMJXRLFTZAOV-UHFFFAOYSA-N tetrahydroxy-1,4-benzoquinone hydrate Chemical compound O.O.OC1=C(O)C(=O)C(O)=C(O)C1=O PTIMJXRLFTZAOV-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000000987 azo dye Substances 0.000 description 2
- 150000001555 benzenes Chemical class 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000009967 direct dyeing Methods 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- KQPYUDDGWXQXHS-UHFFFAOYSA-N juglone Chemical compound O=C1C=CC(=O)C2=C1C=CC=C2O KQPYUDDGWXQXHS-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 150000002828 nitro derivatives Chemical class 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000004059 quinone derivatives Chemical class 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 2
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-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
- KUCWUAFNGCMZDB-UHFFFAOYSA-N 2-amino-3-nitrophenol Chemical compound NC1=C(O)C=CC=C1[N+]([O-])=O KUCWUAFNGCMZDB-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- DVIUQKDUMVBHKT-UHFFFAOYSA-N COC=1C(C=CC(C1)=O)=O.C1(C=CC(C=C1)=O)=O Chemical compound COC=1C(C=CC(C1)=O)=O.C1(C=CC(C=C1)=O)=O DVIUQKDUMVBHKT-UHFFFAOYSA-N 0.000 description 1
- 244000007835 Cyamopsis tetragonoloba Species 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
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 241000784726 Lycaena thetis Species 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 229930182559 Natural dye Natural products 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 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
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000001785 acacia senegal l. willd gum Substances 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 239000003963 antioxidant agent 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
- 150000003935 benzaldehydes Chemical class 0.000 description 1
- VYTBDSUNRJYVHL-UHFFFAOYSA-N beta-Hydrojuglone Natural products O=C1CCC(=O)C2=C1C=CC=C2O VYTBDSUNRJYVHL-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- QRJOYPHTNNOAOJ-UHFFFAOYSA-N copper gold Chemical compound [Cu].[Au] QRJOYPHTNNOAOJ-UHFFFAOYSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 239000000978 natural dye Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 125000004151 quinonyl group Chemical group 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000344 soap Substances 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
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- 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
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
- A61K2800/432—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 (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU83807A LU83807A1 (fr) | 1981-12-02 | 1981-12-02 | Utilisation de benzoquinones pour la coloration directe des fibres keratiniques |
| FR8220009A FR2517200B1 (en, 2012) | 1981-12-02 | 1982-11-29 | |
| GB08234178A GB2110722B (en) | 1981-12-02 | 1982-12-01 | Use of benzoquinones for the direct dyeing of keratin fibres |
| DE19823244454 DE3244454A1 (de) | 1981-12-02 | 1982-12-01 | Verwendung von benzochinonderivaten zum faerben von menschlichen keratinfasern, faerbeverfahren und faerbemittel, die diese verbindungen enthalten |
| JP57211212A JPS58109406A (ja) | 1981-12-02 | 1982-12-01 | 染毛組成物 |
| CH699282A CH655439B (en, 2012) | 1981-12-02 | 1982-12-01 | |
| IT68404/82A IT1156389B (it) | 1981-12-02 | 1982-12-01 | Composizione tintoria benzochinonica per fibre cheramiche particolarmente per capelli umani |
| CA000416878A CA1180283A (fr) | 1981-12-02 | 1982-12-02 | Utilisation de benzoquinones pour la coloration directe des fibres keratiniques |
| BE0/209630A BE895224A (fr) | 1981-12-02 | 1982-12-02 | Utilisation de benzoquinones pour la coloration directe des fibres keratiniques |
| US06/682,475 US4867751A (en) | 1981-12-02 | 1984-12-17 | Use of benzoquinones for the direct dyeing of keratin fibres |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU83807A LU83807A1 (fr) | 1981-12-02 | 1981-12-02 | Utilisation de benzoquinones pour la coloration directe des fibres keratiniques |
| LU83807 | 1981-12-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU83807A1 true LU83807A1 (fr) | 1983-09-01 |
Family
ID=19729775
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU83807A LU83807A1 (fr) | 1981-12-02 | 1981-12-02 | Utilisation de benzoquinones pour la coloration directe des fibres keratiniques |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4867751A (en, 2012) |
| JP (1) | JPS58109406A (en, 2012) |
| BE (1) | BE895224A (en, 2012) |
| CA (1) | CA1180283A (en, 2012) |
| CH (1) | CH655439B (en, 2012) |
| DE (1) | DE3244454A1 (en, 2012) |
| FR (1) | FR2517200B1 (en, 2012) |
| GB (1) | GB2110722B (en, 2012) |
| IT (1) | IT1156389B (en, 2012) |
| LU (1) | LU83807A1 (en, 2012) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5259849A (en) * | 1982-04-29 | 1993-11-09 | L'oreal | Composition based on quinone dyestuffs for use in hair dyeing and process for the preservation of quinone dyestuffs |
| LU84122A1 (fr) * | 1982-04-29 | 1983-12-16 | Oreal | 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 |
| GB2159828B (en) * | 1984-04-20 | 1987-10-21 | Shiseido Co Ltd | Naphthalene derivatives and hair dye compositions containing them |
| GB2168082B (en) * | 1984-07-31 | 1988-09-14 | Beecham Group Plc | Dye compositions |
| LU86521A1 (fr) * | 1986-07-18 | 1988-02-02 | Oreal | Procede de teinture des cheveux avec des colorants hydroxyquinoniques et des sels metalliques |
| 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 |
| LU87403A1 (fr) * | 1988-12-06 | 1990-07-10 | Oreal | Procede de teinture de fibres keratiniques avec un hydroxyindole,associe a un derive quinonique |
| FR2667788B1 (fr) * | 1990-10-12 | 1994-12-02 | Oreal | Utilisation d'hydroxyalkylamino-9,10-anthraquinones pour la teinture de fibres keratiniques humaines, composition cosmetique les contenant en association avec des colorants azouiques et nitres. |
| DE19653292C1 (de) * | 1996-12-20 | 1998-04-09 | Wella Ag | Mittel und Verfahren zum Färben von Keratinfasern |
| DE19931271A1 (de) * | 1999-07-07 | 2001-01-18 | Goldwell Gmbh | Pulverförmige Wirkstoffzusammensetzung, Verfahren zu deren Herstellung und Verwendung derselben |
| US9358201B2 (en) * | 2013-08-23 | 2016-06-07 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
| JP7695191B2 (ja) * | 2018-12-20 | 2025-06-18 | エコラボ ユーエスエー インコーポレイティド | ヒドロキシル化キノン重合防止剤および使用方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2086337A (en) * | 1937-07-06 | Process for the manufacture of | ||
| US1691500A (en) * | 1926-11-26 | 1928-11-13 | Shaw Cecil | Dyeing of wool and/or silk |
| DE490768C (de) * | 1926-11-26 | 1930-02-06 | Cecil Shaw | Verfahren zum Faerben von Wolle und Seide |
| GB277833A (en) * | 1926-11-26 | 1927-09-29 | Holliday Co Ltd L B | Improvements relating to the dyeing of wool and/or silk |
| US2183997A (en) * | 1937-02-20 | 1939-12-19 | Eastman Kodak Co | Azo compounds and process for coloring therewith |
| US2695259A (en) * | 1949-01-03 | 1954-11-23 | Union Francaise Commerciale Et Industrielle Sa | Dermatologically harmless hair dyeing creams |
| US2745788A (en) * | 1954-04-30 | 1956-05-15 | Gillette Co | Dyeing with quinones or hydroquinones and borohydrides and compositions therefor |
| GB773794A (en) * | 1954-04-30 | 1957-05-01 | Gillette Industries Ltd | Improvements in or relating to the production and/or stabilisation of hydroquinones |
| US3041244A (en) * | 1957-09-17 | 1962-06-26 | Jerome A Feit | Quinone hair dye compositions |
| US3272713A (en) * | 1961-07-26 | 1966-09-13 | Univ Minnesota | Actinic radiation protection by compositions comprising quinones and carbonyl containing compounds |
| LU59063A1 (en, 2012) * | 1969-07-08 | 1971-03-09 | ||
| US3981676A (en) * | 1970-03-03 | 1976-09-21 | L'oreal | Lyophilized dyes and the use thereof to color keratinic fibers |
| US4023926A (en) * | 1972-06-21 | 1977-05-17 | Societe Anonyme Dite: L'oreal | Diaminobenzoquinones in hair dye compositions |
| US3919265A (en) * | 1972-06-21 | 1975-11-11 | Oreal | Diaminobenzoquinones, the method of producing the same and hair dye compositions containing the same |
| JPS5157839A (ja) * | 1974-11-13 | 1976-05-20 | Yamashita Noriko | Keshoryo |
| JPS5157838A (ja) * | 1974-11-13 | 1976-05-20 | Yamashita Noriko | Keshoryo |
| US4104021A (en) * | 1976-05-28 | 1978-08-01 | Combe Incorporated | Process for dyeing hair in which the depth of shade is gradually increased in successive treatments |
| FR2385390A1 (fr) * | 1977-04-01 | 1978-10-27 | Marechal Raymond | Compositions topiques a base de composes aromatiques contenant au moins un groupe quinonique ou phenolique, utilisables sur le cuir chevelu |
| FR2472934A1 (fr) * | 1980-01-04 | 1981-07-10 | Oreal | Compositions cosmetiques a base d'une poudre d'origine vegetale |
-
1981
- 1981-12-02 LU LU83807A patent/LU83807A1/fr unknown
-
1982
- 1982-11-29 FR FR8220009A patent/FR2517200B1/fr not_active Expired
- 1982-12-01 DE DE19823244454 patent/DE3244454A1/de active Granted
- 1982-12-01 IT IT68404/82A patent/IT1156389B/it active
- 1982-12-01 CH CH699282A patent/CH655439B/fr unknown
- 1982-12-01 JP JP57211212A patent/JPS58109406A/ja active Granted
- 1982-12-01 GB GB08234178A patent/GB2110722B/en not_active Expired
- 1982-12-02 CA CA000416878A patent/CA1180283A/fr not_active Expired
- 1982-12-02 BE BE0/209630A patent/BE895224A/fr not_active IP Right Cessation
-
1984
- 1984-12-17 US US06/682,475 patent/US4867751A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| IT1156389B (it) | 1987-02-04 |
| GB2110722A (en) | 1983-06-22 |
| IT8268404A0 (it) | 1982-12-01 |
| GB2110722B (en) | 1985-08-07 |
| DE3244454C2 (en, 2012) | 1990-02-01 |
| CA1180283A (fr) | 1985-01-02 |
| BE895224A (fr) | 1983-06-02 |
| JPS58109406A (ja) | 1983-06-29 |
| FR2517200A1 (en, 2012) | 1983-06-03 |
| CH655439B (en, 2012) | 1986-04-30 |
| US4867751A (en) | 1989-09-19 |
| DE3244454A1 (de) | 1983-06-09 |
| FR2517200B1 (en, 2012) | 1985-04-12 |
| JPH026324B2 (en, 2012) | 1990-02-08 |
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