LU86899A1 - Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre - Google Patents
Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre Download PDFInfo
- Publication number
- LU86899A1 LU86899A1 LU86899A LU86899A LU86899A1 LU 86899 A1 LU86899 A1 LU 86899A1 LU 86899 A LU86899 A LU 86899A LU 86899 A LU86899 A LU 86899A LU 86899 A1 LU86899 A1 LU 86899A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- composition
- aminophenol
- amino
- dyeing
- hair
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 120
- 239000000975 dye Substances 0.000 title claims description 74
- 230000003647 oxidation Effects 0.000 title claims description 52
- 238000007254 oxidation reaction Methods 0.000 title claims description 52
- 238000000034 method Methods 0.000 title claims description 50
- 238000004043 dyeing Methods 0.000 title claims description 34
- 239000000835 fiber Substances 0.000 title claims description 27
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 title claims description 10
- 210000004209 hair Anatomy 0.000 claims description 115
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 95
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 64
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 49
- 235000019441 ethanol Nutrition 0.000 claims description 43
- -1 iodide ions Chemical class 0.000 claims description 28
- 239000002609 medium Substances 0.000 claims description 26
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 18
- 102000011782 Keratins Human genes 0.000 claims description 18
- 108010076876 Keratins Proteins 0.000 claims description 18
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
- 239000002243 precursor Substances 0.000 claims description 12
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 7
- QAOUFMMMANSOSS-UHFFFAOYSA-N 2-amino-3-(2-hydroxyethyl)phenol Chemical compound NC1=C(O)C=CC=C1CCO QAOUFMMMANSOSS-UHFFFAOYSA-N 0.000 claims description 6
- LPYUENQFPVNPHY-UHFFFAOYSA-N 3-methoxycatechol Chemical compound COC1=CC=CC(O)=C1O LPYUENQFPVNPHY-UHFFFAOYSA-N 0.000 claims description 6
- SXJQUUPSLJTKKT-UHFFFAOYSA-N 4-hydroxy-2-methoxyaniline Natural products COC1=CC(O)=CC=C1N SXJQUUPSLJTKKT-UHFFFAOYSA-N 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 239000002562 thickening agent Substances 0.000 claims description 5
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims description 4
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 239000012736 aqueous medium Substances 0.000 claims description 4
- 239000002585 base Substances 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- 239000011707 mineral Substances 0.000 claims description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 claims description 3
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 3
- URNPJAGSKRJTAK-UHFFFAOYSA-N 4-amino-3-methylsulfanylphenol Chemical compound CSC1=CC(O)=CC=C1N URNPJAGSKRJTAK-UHFFFAOYSA-N 0.000 claims description 3
- ROCVGJLXIARCAC-UHFFFAOYSA-N 4-aminobenzene-1,3-diol Chemical compound NC1=CC=C(O)C=C1O ROCVGJLXIARCAC-UHFFFAOYSA-N 0.000 claims description 3
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 3
- VVYWUQOTMZEJRJ-UHFFFAOYSA-N 4-n-methylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C=C1 VVYWUQOTMZEJRJ-UHFFFAOYSA-N 0.000 claims description 3
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 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 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 150000004694 iodide salts Chemical class 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- 239000011877 solvent mixture Substances 0.000 claims description 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 2
- YKYIFUROKBDHCY-ONEGZZNKSA-N (e)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one Chemical group CCO\C=C\C(=O)C(F)(F)F YKYIFUROKBDHCY-ONEGZZNKSA-N 0.000 claims description 2
- XGNXYCFREOZBOL-UHFFFAOYSA-N 1,3-benzodioxol-5-amine Chemical compound NC1=CC=C2OCOC2=C1 XGNXYCFREOZBOL-UHFFFAOYSA-N 0.000 claims description 2
- MJMRSGYLARBUDK-UHFFFAOYSA-N 2,4-dimethoxybenzene-1,3-diamine Chemical compound COC1=CC=C(N)C(OC)=C1N MJMRSGYLARBUDK-UHFFFAOYSA-N 0.000 claims description 2
- PTBHRJOTANEONS-UHFFFAOYSA-N 2,6-dimethoxypyridin-3-amine Chemical compound COC1=CC=C(N)C(OC)=N1 PTBHRJOTANEONS-UHFFFAOYSA-N 0.000 claims description 2
- MDKWXZDIFPHNPS-UHFFFAOYSA-N 2-(2,3-diaminophenyl)ethanol Chemical compound NC1=CC=CC(CCO)=C1N MDKWXZDIFPHNPS-UHFFFAOYSA-N 0.000 claims description 2
- KFJAXIIDYGWHFD-UHFFFAOYSA-N 2-(3,5-diaminopyridin-2-yl)ethanol Chemical compound OCCC1=NC=C(C=C1N)N KFJAXIIDYGWHFD-UHFFFAOYSA-N 0.000 claims description 2
- FZCQMIRJCGWWCL-UHFFFAOYSA-N 2-amino-5-chlorophenol Chemical compound NC1=CC=C(Cl)C=C1O FZCQMIRJCGWWCL-UHFFFAOYSA-N 0.000 claims description 2
- XCGOCWBIFFICFZ-UHFFFAOYSA-N 2-chloro-1-n-methylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C=C1Cl XCGOCWBIFFICFZ-UHFFFAOYSA-N 0.000 claims description 2
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 2
- UVUGDGRIYQQKIT-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-amine Chemical compound O1CCNC2=CC(N)=CC=C21 UVUGDGRIYQQKIT-UHFFFAOYSA-N 0.000 claims description 2
- RRIMNXYWOCQLCF-UHFFFAOYSA-N 4,6-dimethoxybenzene-1,3-diamine Chemical compound COC1=CC(OC)=C(N)C=C1N RRIMNXYWOCQLCF-UHFFFAOYSA-N 0.000 claims description 2
- UBKPLLYABUUFCE-UHFFFAOYSA-N 4-amino-2,3-dimethylphenol Chemical compound CC1=C(C)C(O)=CC=C1N UBKPLLYABUUFCE-UHFFFAOYSA-N 0.000 claims description 2
- OMVFXCQLSCPJNR-UHFFFAOYSA-N 4-amino-2,6-dimethylphenol Chemical compound CC1=CC(N)=CC(C)=C1O OMVFXCQLSCPJNR-UHFFFAOYSA-N 0.000 claims description 2
- ZYZQSCWSPFLAFM-UHFFFAOYSA-N 4-amino-2-chlorophenol Chemical compound NC1=CC=C(O)C(Cl)=C1 ZYZQSCWSPFLAFM-UHFFFAOYSA-N 0.000 claims description 2
- HDGMAACKJSBLMW-UHFFFAOYSA-N 4-amino-2-methylphenol Chemical compound CC1=CC(N)=CC=C1O HDGMAACKJSBLMW-UHFFFAOYSA-N 0.000 claims description 2
- ZBCATMYQYDCTIZ-UHFFFAOYSA-N 4-methylcatechol Chemical compound CC1=CC=C(O)C(O)=C1 ZBCATMYQYDCTIZ-UHFFFAOYSA-N 0.000 claims description 2
- CQPLGGXOAHSQBD-UHFFFAOYSA-N 5-amino-2,4-dimethoxyphenol Chemical compound COC1=CC(OC)=C(O)C=C1N CQPLGGXOAHSQBD-UHFFFAOYSA-N 0.000 claims description 2
- BLQFHJKRTDIZLX-UHFFFAOYSA-N 5-amino-2-methoxyphenol Chemical compound COC1=CC=C(N)C=C1O BLQFHJKRTDIZLX-UHFFFAOYSA-N 0.000 claims description 2
- KVHHMYZBFBSVDI-UHFFFAOYSA-N 8-aminonaphthalen-2-ol Chemical compound C1=C(O)C=C2C(N)=CC=CC2=C1 KVHHMYZBFBSVDI-UHFFFAOYSA-N 0.000 claims description 2
- 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
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical class COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims description 2
- SBXKRBZKPQBLOD-UHFFFAOYSA-N aminohydroquinone Chemical compound NC1=CC(O)=CC=C1O SBXKRBZKPQBLOD-UHFFFAOYSA-N 0.000 claims description 2
- 239000002280 amphoteric surfactant Substances 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 230000003750 conditioning effect Effects 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
- 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 150000002193 fatty amides Chemical class 0.000 claims description 2
- 125000002425 furfuryl group Chemical group C(C1=CC=CO1)* 0.000 claims description 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- 229940057867 methyl lactate Drugs 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 229960005323 phenoxyethanol Drugs 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- ILDXSRFKXABMHH-UHFFFAOYSA-N 2-(2-aminophenyl)ethanol Chemical compound NC1=CC=CC=C1CCO ILDXSRFKXABMHH-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 2
- RHDYQUZYHZWTCI-UHFFFAOYSA-N 1-methoxy-4-phenylbenzene Chemical compound C1=CC(OC)=CC=C1C1=CC=CC=C1 RHDYQUZYHZWTCI-UHFFFAOYSA-N 0.000 claims 1
- TUADYTFWZPZZTP-UHFFFAOYSA-N 2-amino-4-methoxyphenol Chemical compound COC1=CC=C(O)C(N)=C1 TUADYTFWZPZZTP-UHFFFAOYSA-N 0.000 claims 1
- MGLZGLAFFOMWPB-UHFFFAOYSA-N 2-chloro-1,4-phenylenediamine Chemical compound NC1=CC=C(N)C(Cl)=C1 MGLZGLAFFOMWPB-UHFFFAOYSA-N 0.000 claims 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 claims 1
- HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 claims 1
- XSBKXUJEVYHSNO-UHFFFAOYSA-N 3-amino-2,6-dimethylphenol Chemical compound CC1=CC=C(N)C(C)=C1O XSBKXUJEVYHSNO-UHFFFAOYSA-N 0.000 claims 1
- HEAHXMOKYXTEID-UHFFFAOYSA-N 3-amino-4-methoxyphenol Chemical compound COC1=CC=C(O)C=C1N HEAHXMOKYXTEID-UHFFFAOYSA-N 0.000 claims 1
- WEPOCTWSRWLQLL-UHFFFAOYSA-N 6-methoxypyridine-2,3-diamine Chemical compound COC1=CC=C(N)C(N)=N1 WEPOCTWSRWLQLL-UHFFFAOYSA-N 0.000 claims 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 1
- 150000004996 alkyl benzenes Chemical class 0.000 claims 1
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- REOJLIXKJWXUGB-UHFFFAOYSA-N mofebutazone Chemical group O=C1C(CCCC)C(=O)NN1C1=CC=CC=C1 REOJLIXKJWXUGB-UHFFFAOYSA-N 0.000 claims 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 claims 1
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 71
- 238000004040 coloring Methods 0.000 description 66
- 239000000243 solution Substances 0.000 description 62
- 238000001035 drying Methods 0.000 description 39
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Inorganic materials [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 11
- 229930182470 glycoside Natural products 0.000 description 10
- 239000000230 xanthan gum Substances 0.000 description 10
- 235000010493 xanthan gum Nutrition 0.000 description 10
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- 229940082509 xanthan gum Drugs 0.000 description 10
- 229920013806 TRITON CG-110 Polymers 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 7
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 229940107816 ammonium iodide Drugs 0.000 description 6
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 5
- 229940006461 iodide ion Drugs 0.000 description 5
- 230000001590 oxidative effect Effects 0.000 description 5
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 5
- 235000009518 sodium iodide Nutrition 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
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- 150000002338 glycosides Chemical class 0.000 description 4
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
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- 238000010168 coupling process Methods 0.000 description 2
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- 229920000642 polymer Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 description 1
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-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
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- PCAXITAPTVOLGL-UHFFFAOYSA-N 2,3-diaminophenol Chemical class NC1=CC=CC(O)=C1N PCAXITAPTVOLGL-UHFFFAOYSA-N 0.000 description 1
- GZVVXXLYQIFVCA-UHFFFAOYSA-N 2,3-dimethylbenzene-1,4-diamine Chemical compound CC1=C(C)C(N)=CC=C1N GZVVXXLYQIFVCA-UHFFFAOYSA-N 0.000 description 1
- PBDBPADWXQFEIN-UHFFFAOYSA-N 2,5-diamino-4-methoxyphenol Chemical compound COC1=CC(N)=C(O)C=C1N PBDBPADWXQFEIN-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
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-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
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- HWWIVWKTKZAORO-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-ol Chemical compound O1CCNC2=CC(O)=CC=C21 HWWIVWKTKZAORO-UHFFFAOYSA-N 0.000 description 1
- YRLORWPBJZEGBX-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazine Chemical class C1=CC=C2NCCOC2=C1 YRLORWPBJZEGBX-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- UWFNOURYAXAXSB-UHFFFAOYSA-N 4-n-(furan-2-ylmethyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NCC1=CC=CO1 UWFNOURYAXAXSB-UHFFFAOYSA-N 0.000 description 1
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 1
- WTFUTSCZYYCBAY-SXBRIOAWSA-N 6-[(E)-C-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-N-hydroxycarbonimidoyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C/C(=N/O)/C1=CC2=C(NC(O2)=O)C=C1 WTFUTSCZYYCBAY-SXBRIOAWSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 241000928106 Alain Species 0.000 description 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- IIPSZNGWPHACER-UHFFFAOYSA-N Cl.Cl.OCCC=1C(=C(C=CC1)N)N Chemical compound Cl.Cl.OCCC=1C(=C(C=CC1)N)N IIPSZNGWPHACER-UHFFFAOYSA-N 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 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
- 229920000084 Gum arabic Polymers 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 125000002066 L-histidyl group Chemical group [H]N1C([H])=NC(C([H])([H])[C@](C(=O)[*])([H])N([H])[H])=C1[H] 0.000 description 1
- 241000784726 Lycaena thetis Species 0.000 description 1
- 241000282372 Panthera onca Species 0.000 description 1
- 229920002305 Schizophyllan Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 244000186561 Swietenia macrophylla Species 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
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000002535 acidifier 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
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 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
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000002610 basifying 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
- 229920001222 biopolymer Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- IFDFMWBBLAUYIW-UHFFFAOYSA-N ethane-1,2-diol;ethyl acetate Chemical compound OCCO.CCOC(C)=O IFDFMWBBLAUYIW-UHFFFAOYSA-N 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 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
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 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
- SFMJNHNUOVADRW-UHFFFAOYSA-N n-[5-[9-[4-(methanesulfonamido)phenyl]-2-oxobenzo[h][1,6]naphthyridin-1-yl]-2-methylphenyl]prop-2-enamide Chemical compound C1=C(NC(=O)C=C)C(C)=CC=C1N1C(=O)C=CC2=C1C1=CC(C=3C=CC(NS(C)(=O)=O)=CC=3)=CC=C1N=C2 SFMJNHNUOVADRW-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 101150093826 par1 gene Proteins 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 230000029305 taxis Effects 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-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
- D06P3/08—Material containing basic nitrogen containing amide groups using oxidation dyes
-
- 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
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/347—Phenols
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/415—Aminophenols
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Priority Applications (29)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU86899A LU86899A1 (fr) | 1987-05-25 | 1987-05-25 | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre |
| NL8801318A NL8801318A (nl) | 1987-05-25 | 1988-05-20 | Werkwijze voor het verven van keratinevezels met koppelingsmiddelen en/of "snelle" oxydatie-kleurstoffen, geassocieerd met een jodide en verfsamenstelling voor deze toepassing. |
| PT87559A PT87559B (pt) | 1987-05-25 | 1988-05-23 | Processo para a coloracao de fibras ceratinicas com acopladores e/ou corantes de oxidacao rapida associados a um iodeto e de composicoes tintoriais ai utilizadas |
| GR880100347A GR880100347A (el) | 1987-05-25 | 1988-05-24 | Μεθοδος βαφης κερατινικων ινων με μεσα συζευξεως η/και χρωστικεσταχειας οξειδωσεως συνδυαζομενα με ιωδιουχο αλας & βαφικη συνθε ση που χρησιμοποιειται. |
| BR8802536A BR8802536A (pt) | 1987-05-25 | 1988-05-24 | Processo para a tintura das fibras queratinicas,composicao tintorial das fibras queratinicas,e dispositivo com varios compartimentos ou estojo de tintura |
| GR880100346A GR880100346A (el) | 1987-05-25 | 1988-05-24 | Μεθοδος βαφης κερατινικων ινων με βασεις οξειδωσεως συνδιαζομενες με ιωδιουχο αλας, βαφικη συνθεση & διαταξη που χρησιμοποιειται |
| ES8801622A ES2006953A6 (es) | 1987-05-25 | 1988-05-24 | Procedimiento de tincion de fibras queratinicas, composicion tintorea y estuche de varios compartimentos. |
| ES8801623A ES2006954A6 (es) | 1987-05-25 | 1988-05-24 | Procedimiento de tincion de fibras queratinicas, composicion tintorea y dispositivo de varios compartimentos. |
| KR1019880006127A KR880014190A (ko) | 1987-05-25 | 1988-05-24 | 발색단 및/또는 옥화물과 결합된 "신속" 산화염료로서 케라틴섬유의 염색방법 그리고 사용된 염색조성물 |
| JP63128139A JPH01110613A (ja) | 1987-05-25 | 1988-05-25 | ケラチン性繊維を染色するのに適当な組成物 |
| US07/198,806 US4985955A (en) | 1987-05-25 | 1988-05-25 | Process for dyeing keratinous fibres with couplers and/or "rapid" oxidation dyes combined with an iodide and dyeing composition employed |
| GB8812348A GB2205329B (en) | 1987-05-25 | 1988-05-25 | Process for dyeing keratinous fibres with oxidation bases combined with an iodide and dyeing composition employed |
| FR888806917A FR2615731B1 (fr) | 1987-05-25 | 1988-05-25 | Procede de teinture des fibres keratiniques avec des bases d'oxydation associees a un iodure, composition tinctoriale et dispositif mis en oeuvre |
| FR888806916A FR2615730B1 (fr) | 1987-05-25 | 1988-05-25 | Procede de teinture des fibres keratiniques avec des coupleurs et/ou des colorants d'oxydation " rapide " associes a un iodure et composition tinctoriale mise en oeuvre |
| DE3817687A DE3817687C3 (de) | 1987-05-25 | 1988-05-25 | Verfahren zum Färben keratinischer Fasern mit Oxidationsbasen in Kombination mit einem Jodid |
| IT67481/88A IT1224337B (it) | 1987-05-25 | 1988-05-25 | Procedimento di tintura di fibre cheratiniche con coloranti d'ossidazione associati a uno ioduro composizione tintoria messa in opera e dispositivo per la tintura |
| BE8800570A BE1001114A3 (fr) | 1987-05-25 | 1988-05-25 | Procede de teinture des fibres keratiniques avec des coupleurs et/ou des colorants d'oxydation ''rapide'' associes a un iodure et composition tinctoriale mise en oeuvre. |
| GB8812349A GB2205111B (en) | 1987-05-25 | 1988-05-25 | Upatentsfor dyeing keratinous fibres with couplers and/or "rapid" oxidation dyes combined with an iodide and dyeing composition employed |
| AU16606/88A AU618735B2 (en) | 1987-05-25 | 1988-05-25 | Process for dyeing keratinous fibres with couplers and/or `rapid' oxidation dyes combined with an iodide and dyeing composition employed |
| BE8800569A BE1001113A3 (fr) | 1987-05-25 | 1988-05-25 | Procede de teinture des fibres keratiniques avec des bases d'oxydation associees a un iodure, composition tinctoriale et dispositif mis en oeuvre. |
| ZA883727A ZA883727B (en) | 1987-05-25 | 1988-05-25 | Process for dyeing keratinous fibres with couplers and/or"rapid"oxidation dyes combined with an iodide and dyeing composition employed |
| IT67482/88A IT1219328B (it) | 1987-05-25 | 1988-05-25 | Procedimento di tintura di fibre cheratiniche con accoppianti e o coloranti di ossidazione rapida associati a uno ioduro composizione tintoria messa in opera e dispositivo per la tintura |
| DE3817710A DE3817710A1 (de) | 1987-05-25 | 1988-05-25 | Verfahren zur faerbung keratinischer fasern mit kupplungsstoffen und/oder "schnell"-oxidationsfarbstoffen in kombination mit einem jodid, verwendete faerbemittel und vorrichtungen |
| JP63-128140A JPH013111A (ja) | 1987-05-25 | 1988-05-25 | 染色組成物および装置 |
| AR310929A AR240013A1 (es) | 1987-05-25 | 1989-05-23 | Una composicion tintorea de fibras queratinicas y dispositivo que la contiene. |
| CH213/89A CH672731A5 (es) | 1987-05-25 | 1989-05-24 | |
| CH214/89A CH672732A5 (es) | 1987-05-25 | 1989-05-25 | |
| US07/599,113 US5180397A (en) | 1987-05-25 | 1990-10-17 | Process for dyeing keratinous fibres with couplers and/or "rapid" oxidation dyes combined with an iodide and dyeing composition employed |
| US07/717,253 US5180399A (en) | 1987-05-25 | 1991-06-18 | Process for dyeing keratinous fibres with oxidation bases combined with an iodide and dyeing composition employed |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU86899 | 1987-05-25 | ||
| LU86899A LU86899A1 (fr) | 1987-05-25 | 1987-05-25 | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU86899A1 true LU86899A1 (fr) | 1989-01-19 |
Family
ID=19730929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU86899A LU86899A1 (fr) | 1987-05-25 | 1987-05-25 | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4985955A (es) |
| JP (1) | JPH01110613A (es) |
| KR (1) | KR880014190A (es) |
| AR (1) | AR240013A1 (es) |
| AU (1) | AU618735B2 (es) |
| BE (2) | BE1001114A3 (es) |
| BR (1) | BR8802536A (es) |
| CH (2) | CH672731A5 (es) |
| DE (2) | DE3817687C3 (es) |
| ES (2) | ES2006954A6 (es) |
| FR (2) | FR2615730B1 (es) |
| GB (2) | GB2205329B (es) |
| GR (2) | GR880100346A (es) |
| IT (2) | IT1219328B (es) |
| LU (1) | LU86899A1 (es) |
| NL (1) | NL8801318A (es) |
| PT (1) | PT87559B (es) |
| ZA (1) | ZA883727B (es) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| LU86903A1 (fr) * | 1987-05-29 | 1989-01-19 | Oreal | Utilisation comme coupleur du 2,4-diamino-1,3-dimethoxybenzene ou l'un de ses sels,en association avec des precurseurs de colorants d'oxydation,pour la teinture des cheveux humains,composition de teinture capillaire contenant ledit coupleur et procede de preparation dudit coupleur |
| 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 |
| 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 |
| US5344464A (en) * | 1988-09-08 | 1994-09-06 | L'oreal | Oxidation dye composition containing at least one double base in combination with at least one single base and dyeing process making use of it |
| FR2635976B1 (fr) * | 1988-09-08 | 1994-01-21 | Oreal | Composition tinctoriale d'oxydation contenant au moins une base double associee a au moins une base simple et procede de teinture la mettant en oeuvre |
| FR2649886B1 (fr) * | 1989-07-21 | 1991-10-11 | Oreal | Composition de teinture des fibres keratiniques mettant en oeuvre un colorant indolique et au moins une paraphenylenediamine comportant un groupement amino secondaire et procede de mise en oeuvre |
| DE4003907A1 (de) * | 1990-02-09 | 1991-08-14 | Schwarzkopf Gmbh Hans | Neue substituierte 1,3-diaminobenzole, verfahren zu ihrer herstellung sowie faerbemittel fuer keratinische fasern, die diese enthalten |
| FR2659228B1 (fr) * | 1990-03-08 | 1994-10-14 | Oreal | Procede de teinture des fibres keratiniques avec des 6 ou 7-monohydroxy-indoles a ph acide et compositions mises en óoeuvre. |
| FR2662714B1 (fr) * | 1990-05-31 | 1994-04-08 | Oreal | Procede de teinture des fibres keratiniques avec le 2,4-diamino 1,3-dimethoxybenzene a ph acide et compositions mises en óoeuvre. |
| DE4017516A1 (de) * | 1990-05-31 | 1991-12-05 | Wella Ag | Oxidationshaarfaerbemittel mit einem gehalt an 3-aminophenol-derivaten, verfahren zum oxidativen faerben von haaren sowie neue 3-aminophenol-derivate |
| FR2662715B1 (fr) * | 1990-05-31 | 1994-04-08 | Oreal | Procede de teinture des fibres keratiniques avec le 2,6-dimethyl 1,4-diamino benzene et/ou le 2,3-dimethyl 1,4-diamino benzene et un agent oxydant en milieu acide et compositions mises en óoeuvre . |
| US5279619A (en) * | 1990-05-31 | 1994-01-18 | L'oreal | Process for dyeing keratinous fibers with 2,4-diamino-1,3-dimethoxybenzene at an acid ph and compositions employed |
| FR2675380A1 (fr) * | 1991-04-18 | 1992-10-23 | Oreal | Procede de teinture des fibres keratiniques avec des aminoindoles, a ph basique, compositions mises en óoeuvre et nouveaux composes. |
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| US7074244B2 (en) | 2003-07-03 | 2006-07-11 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Hair dyeing method including an aligning step |
| US7060111B2 (en) | 2003-07-03 | 2006-06-13 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Method for providing more vibrant, natural and long-lasting color to hair |
| CN102060713A (zh) * | 2010-12-09 | 2011-05-18 | 中华人民共和国嘉兴出入境检验检疫局 | 用于检测偶氮类染料的芳香胺半抗原及其制备方法 |
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| MX364254B (es) | 2012-03-27 | 2019-04-17 | Noxell Corp | Composiciones colorantes de cabello que comprenden 3-amino-2,6-dimetilfenol, métodos y estuches que comprenden las composiciones. |
| JP7104954B2 (ja) * | 2016-04-28 | 2022-07-22 | ホーユー株式会社 | 酸化染毛剤組成物 |
| CN115990116A (zh) * | 2016-04-28 | 2023-04-21 | 朋友株式会社 | 氧化染发剂组合物 |
| JP6792767B2 (ja) * | 2016-04-28 | 2020-12-02 | ホーユー株式会社 | 酸化染毛剤組成物 |
| TW202118477A (zh) * | 2019-10-31 | 2021-05-16 | 日商朋友股份有限公司 | 氧化染髮劑 |
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| US1677508A (en) * | 1925-07-11 | 1928-07-17 | Inecto Inc | Art of dyeing fibers |
| FR2045991A7 (en) * | 1969-06-11 | 1971-03-05 | Gillette Co | Hair tinting preparations with reduced - amounts of peroxide |
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| BE876985A (fr) * | 1978-06-15 | 1979-12-14 | Oreal | Supports de teinture ou de decoloration pour cheveux |
| US4096243A (en) * | 1976-02-09 | 1978-06-20 | Clairol Incorporated | Composition for lightening hair containing an oxidizing agent and certain quaternary amines |
| JPS5372836A (en) * | 1976-12-07 | 1978-06-28 | Toshio Yoshida | Hair dyeing method |
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| 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 |
-
1987
- 1987-05-25 LU LU86899A patent/LU86899A1/fr unknown
-
1988
- 1988-05-20 NL NL8801318A patent/NL8801318A/nl not_active Application Discontinuation
- 1988-05-23 PT PT87559A patent/PT87559B/pt not_active IP Right Cessation
- 1988-05-24 GR GR880100346A patent/GR880100346A/el unknown
- 1988-05-24 ES ES8801623A patent/ES2006954A6/es not_active Expired
- 1988-05-24 ES ES8801622A patent/ES2006953A6/es not_active Expired
- 1988-05-24 GR GR880100347A patent/GR880100347A/el unknown
- 1988-05-24 BR BR8802536A patent/BR8802536A/pt unknown
- 1988-05-24 KR KR1019880006127A patent/KR880014190A/ko not_active Application Discontinuation
- 1988-05-25 BE BE8800570A patent/BE1001114A3/fr not_active IP Right Cessation
- 1988-05-25 IT IT67482/88A patent/IT1219328B/it active
- 1988-05-25 GB GB8812348A patent/GB2205329B/en not_active Expired - Fee Related
- 1988-05-25 DE DE3817687A patent/DE3817687C3/de not_active Expired - Lifetime
- 1988-05-25 AU AU16606/88A patent/AU618735B2/en not_active Expired - Fee Related
- 1988-05-25 BE BE8800569A patent/BE1001113A3/fr not_active IP Right Cessation
- 1988-05-25 IT IT67481/88A patent/IT1224337B/it active
- 1988-05-25 FR FR888806916A patent/FR2615730B1/fr not_active Expired - Fee Related
- 1988-05-25 ZA ZA883727A patent/ZA883727B/xx unknown
- 1988-05-25 FR FR888806917A patent/FR2615731B1/fr not_active Expired - Lifetime
- 1988-05-25 DE DE3817710A patent/DE3817710A1/de active Granted
- 1988-05-25 US US07/198,806 patent/US4985955A/en not_active Expired - Fee Related
- 1988-05-25 JP JP63128139A patent/JPH01110613A/ja active Granted
- 1988-05-25 GB GB8812349A patent/GB2205111B/en not_active Expired - Fee Related
-
1989
- 1989-05-23 AR AR310929A patent/AR240013A1/es active
- 1989-05-24 CH CH213/89A patent/CH672731A5/fr not_active IP Right Cessation
- 1989-05-25 CH CH214/89A patent/CH672732A5/fr not_active IP Right Cessation
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