MXPA02008645A - Metodo para te°ir cabello usando tintes cationicos. - Google Patents
Metodo para te°ir cabello usando tintes cationicos.Info
- Publication number
- MXPA02008645A MXPA02008645A MXPA02008645A MXPA02008645A MXPA02008645A MX PA02008645 A MXPA02008645 A MX PA02008645A MX PA02008645 A MXPA02008645 A MX PA02008645A MX PA02008645 A MXPA02008645 A MX PA02008645A MX PA02008645 A MXPA02008645 A MX PA02008645A
- Authority
- MX
- Mexico
- Prior art keywords
- carbon atoms
- hydrogen
- formula
- alkyl
- dye
- Prior art date
Links
- 238000004040 coloring Methods 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims description 17
- 239000000975 dye Substances 0.000 title abstract description 66
- 210000004209 hair Anatomy 0.000 title abstract description 33
- 125000002091 cationic group Chemical group 0.000 title abstract description 10
- 102000011782 Keratins Human genes 0.000 claims abstract description 12
- 108010076876 Keratins Proteins 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 49
- -1 methoxy, methyl Chemical group 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 24
- 239000001257 hydrogen Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 21
- 125000003545 alkoxy group Chemical group 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 150000001450 anions Chemical class 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 150000003254 radicals Chemical class 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 claims 1
- 238000004043 dyeing Methods 0.000 description 27
- 239000000243 solution Substances 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 12
- 238000007254 oxidation reaction Methods 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 229920001577 copolymer Polymers 0.000 description 11
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 238000001914 filtration Methods 0.000 description 9
- 238000005406 washing Methods 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 8
- 239000002736 nonionic surfactant Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 125000002252 acyl group Chemical group 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 239000003945 anionic surfactant Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- 239000000982 direct dye Substances 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 150000002191 fatty alcohols Chemical class 0.000 description 5
- 239000012065 filter cake Substances 0.000 description 5
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000001043 yellow dye Substances 0.000 description 5
- 239000002888 zwitterionic surfactant Substances 0.000 description 5
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 4
- 108010009736 Protein Hydrolysates Proteins 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 239000003093 cationic surfactant Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 244000208060 Lawsonia inermis Species 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000003750 conditioning effect Effects 0.000 description 3
- 239000003581 cosmetic carrier Substances 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 239000002563 ionic surfactant Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000001048 orange dye Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- GKKCIDNWFBPDBW-UHFFFAOYSA-M potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 3
- 239000003531 protein hydrolysate Substances 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical group C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- RFQSMLBZXQOMKK-UHFFFAOYSA-N [3-[(4,8-diamino-6-bromo-1,5-dioxonaphthalen-2-yl)amino]phenyl]-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)C1=CC=CC(NC=2C(C3=C(N)C=C(Br)C(=O)C3=C(N)C=2)=O)=C1 RFQSMLBZXQOMKK-UHFFFAOYSA-N 0.000 description 2
- HSWXSHNPRUMJKI-UHFFFAOYSA-N [8-[(2-methoxyphenyl)hydrazinylidene]-7-oxonaphthalen-2-yl]-trimethylazanium;chloride Chemical compound [Cl-].COC1=CC=CC=C1N\N=C/1C2=CC([N+](C)(C)C)=CC=C2C=CC\1=O HSWXSHNPRUMJKI-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000001045 blue dye Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000005528 methosulfate group Chemical group 0.000 description 2
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000001044 red dye Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- MJYQFWSXKFLTAY-OVEQLNGDSA-N (2r,3r)-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl]butane-1,4-diol;(2r,3r,4s,5s,6r)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O.C1=C(O)C(OC)=CC(C[C@@H](CO)[C@H](CO)CC=2C=C(OC)C(O)=CC=2)=C1 MJYQFWSXKFLTAY-OVEQLNGDSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 description 1
- NOFPXGWBWIPSHI-UHFFFAOYSA-N 2,7,9-trimethylacridine-3,6-diamine;hydrochloride Chemical compound Cl.CC1=C(N)C=C2N=C(C=C(C(C)=C3)N)C3=C(C)C2=C1 NOFPXGWBWIPSHI-UHFFFAOYSA-N 0.000 description 1
- LGZSBRSLVPLNTM-UHFFFAOYSA-N 2-(4-amino-2-methyl-5-nitroanilino)ethanol Chemical compound CC1=CC(N)=C([N+]([O-])=O)C=C1NCCO LGZSBRSLVPLNTM-UHFFFAOYSA-N 0.000 description 1
- YESOPQNVGIQNEV-UHFFFAOYSA-N 2-(4-amino-2-nitroanilino)benzoic acid Chemical compound [O-][N+](=O)C1=CC(N)=CC=C1NC1=CC=CC=C1C(O)=O YESOPQNVGIQNEV-UHFFFAOYSA-N 0.000 description 1
- BEWCNXNIQCLWHP-UHFFFAOYSA-N 2-(tert-butylamino)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(C)(C)C BEWCNXNIQCLWHP-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
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- ZKYCLDTVJCJYIB-UHFFFAOYSA-N 2-methylidenedecanamide Chemical compound CCCCCCCCC(=C)C(N)=O ZKYCLDTVJCJYIB-UHFFFAOYSA-N 0.000 description 1
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- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
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- ZVDCYZVYRXZJQF-UHFFFAOYSA-N 6-nitro-1,2,3,4-tetrahydroquinoxaline Chemical compound N1CCNC2=CC([N+](=O)[O-])=CC=C21 ZVDCYZVYRXZJQF-UHFFFAOYSA-N 0.000 description 1
- TWLMSPNQBKSXOP-UHFFFAOYSA-N 6358-09-4 Chemical compound NC1=CC([N+]([O-])=O)=CC(Cl)=C1O TWLMSPNQBKSXOP-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 229920000945 Amylopectin Polymers 0.000 description 1
- 235000017847 Anchusa officinalis Nutrition 0.000 description 1
- 235000003261 Artemisia vulgaris Nutrition 0.000 description 1
- 240000006891 Artemisia vulgaris Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
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- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
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- 150000003904 phospholipids Chemical class 0.000 description 1
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- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
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- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- XDLVYYYGCNMREZ-UHFFFAOYSA-N propane-1,2-diol;sulfuric acid Chemical class CC(O)CO.OS(O)(=O)=O XDLVYYYGCNMREZ-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
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- 238000000746 purification Methods 0.000 description 1
- DQAKJEWZWDQURW-UHFFFAOYSA-N pyrrolidonecarboxylic acid Chemical class OC(=O)N1CCCC1=O DQAKJEWZWDQURW-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
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- 238000010992 reflux Methods 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- SOUHUMACVWVDME-UHFFFAOYSA-N safranin O Chemical compound [Cl-].C12=CC(N)=CC=C2N=C2C=CC(N)=CC2=[N+]1C1=CC=CC=C1 SOUHUMACVWVDME-UHFFFAOYSA-N 0.000 description 1
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- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- STZCRXQWRGQSJD-UHFFFAOYSA-N sodium;4-[[4-(dimethylamino)phenyl]diazenyl]benzenesulfonic acid Chemical compound [Na+].C1=CC(N(C)C)=CC=C1N=NC1=CC=C(S(O)(=O)=O)C=C1 STZCRXQWRGQSJD-UHFFFAOYSA-N 0.000 description 1
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- 125000001424 substituent group Chemical group 0.000 description 1
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- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
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- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
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- LLWJPGAKXJBKKA-UHFFFAOYSA-N victoria blue B Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)C)=C(C=C1)C2=CC=CC=C2C1=[NH+]C1=CC=CC=C1 LLWJPGAKXJBKKA-UHFFFAOYSA-N 0.000 description 1
- ROVRRJSRRSGUOL-UHFFFAOYSA-N victoria blue bo Chemical compound [Cl-].C12=CC=CC=C2C(NCC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 ROVRRJSRRSGUOL-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B44/00—Azo dyes containing onium groups
- C09B44/10—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system
- C09B44/16—1,3-Diazoles or hydrogenated 1,3-diazoles ; (Benz)imidazolium
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
-
- 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
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00810197 | 2000-03-09 | ||
| PCT/EP2001/002316 WO2001066646A1 (en) | 2000-03-09 | 2001-03-01 | A method of colouring hair using cationic dyes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA02008645A true MXPA02008645A (es) | 2003-02-24 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA02008645A MXPA02008645A (es) | 2000-03-09 | 2001-03-01 | Metodo para te°ir cabello usando tintes cationicos. |
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|---|---|
| US (2) | US6843256B2 (enExample) |
| EP (1) | EP1261666B1 (enExample) |
| JP (1) | JP2003525949A (enExample) |
| CN (1) | CN1217995C (enExample) |
| AT (1) | ATE264891T1 (enExample) |
| AU (1) | AU781845B2 (enExample) |
| BR (1) | BR0109060A (enExample) |
| CA (1) | CA2400337A1 (enExample) |
| DE (1) | DE60102904T2 (enExample) |
| ES (1) | ES2217131T3 (enExample) |
| MX (1) | MXPA02008645A (enExample) |
| WO (1) | WO2001066646A1 (enExample) |
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| AU781845B2 (en) * | 2000-03-09 | 2005-06-16 | Ciba Specialty Chemicals Holding Inc. | A method of colouring hair using cationic dyes |
| CA2427817C (en) * | 2000-11-03 | 2009-04-14 | Washington University | Estrone-derivatives having cytoprotective activity |
| EP1365732A1 (en) | 2001-03-08 | 2003-12-03 | Ciba SC Holding AG | Method of colouring porous material |
| FR2822693B1 (fr) | 2001-04-02 | 2003-06-27 | Oreal | Nouvelle composition tinctoriale pour la teinture des fibres keratiniques comprenant un colorant azoique cationique particulier |
| WO2003006554A1 (en) | 2001-07-11 | 2003-01-23 | Ciba Specialty Chemicals Holding Inc. | A method of coloring hair using cationic dyes |
| CN1556839A (zh) * | 2001-09-24 | 2004-12-22 | 西巴特殊化学品控股有限公司 | 阳离子反应性染料 |
| ATE371432T1 (de) * | 2001-10-10 | 2007-09-15 | Ciba Sc Holding Ag | Verfahren zur färbung von keratinhaltigen fasern |
| WO2003032939A1 (en) * | 2001-10-15 | 2003-04-24 | Ciba Specialty Chemicals Holding Inc. | Method of colouring keratin-containing fibres using diazonium salts |
| MX248524B (es) * | 2002-02-28 | 2007-08-30 | Ciba Sc Holding Ag | Proceso para la preparacion de compuestos azocationicos. |
| FR2844269B1 (fr) * | 2002-09-10 | 2004-10-15 | Oreal | Composition pour la teinture des fibres keratiniques humaines comprenant un colorant monoazoique monocationique |
| US7077873B2 (en) | 2002-09-10 | 2006-07-18 | L'Oréal, SA | Composition for the dyeing of human keratinous fibres comprising a monocationic monoazo dye |
| US7169194B2 (en) | 2002-12-23 | 2007-01-30 | L'oreal S.A. | Dye composition comprising at least one particular tricationic direct dye, dyeing process, use and multi-compartment devices |
| US7186276B2 (en) | 2002-12-23 | 2007-03-06 | L'oreal | Dye composition comprising at least one direct dye, dyeing processes, uses and multi-compartment devices |
| US7217297B2 (en) | 2002-12-30 | 2007-05-15 | L'oreal S.A. | Composition for dyeing keratin fibers comprising a defined diheteroylarylmethane direct dye or a leuco precursor of this dye and dyeing method using it |
| US7211118B2 (en) | 2002-12-30 | 2007-05-01 | L'oreal S.A. | Composition for dyeing keratin fibers comprising a defined triheteroylmethane direct dye or leuco precursor of this dye and dyeing method using it |
| US7211117B2 (en) * | 2002-12-30 | 2007-05-01 | L'oreal S.A. | Composition for dyeing keratin fibers comprising at least one dye chosen from monoheteroyldiarylmethane direct dyes and the leuco precursors thereof and dyeing method using it |
| BRPI0408436A (pt) * | 2003-03-18 | 2006-04-04 | Ciba Sc Holding Ag | corantes diméricos catiÈnicos |
| FR2855406B1 (fr) * | 2003-06-02 | 2006-08-04 | Oreal | Nouveaux composes imidazoles et utilisation de ces composes pour la teinture de fibres keratiniques |
| US7238212B2 (en) | 2003-06-02 | 2007-07-03 | L'oreal, S.A. | Imidazole compounds and use of these compounds for dyeing keratinous fibers |
| FR2855966B1 (fr) * | 2003-06-16 | 2005-09-02 | Oreal | Composition tinctoriale comprenant au moins un colorant direct a chromophores mixtes |
| US7201779B2 (en) | 2003-06-16 | 2007-04-10 | L'oreal S.A. | Dye composition comprising at least one direct dye containing mixed chromophores |
| US7172633B2 (en) | 2003-06-16 | 2007-02-06 | L'ORéAL S.A. | Lightening dye composition comprising at least one cationic direct dye containing mixed chromophores |
| MXPA06006855A (es) * | 2003-12-19 | 2006-08-23 | Ciba Sc Holding Ag | Metodo de coloracion con compuesto diazotizado coronado y componente de acoplamiento. |
| US7300471B2 (en) | 2004-02-27 | 2007-11-27 | L'oreal S.A. | Composition comprising at least one mixed dye based on at least one chromophore of azo or tri(hetero) arylmethane type, dyeing process and mixed dyes. |
| ES2373043T3 (es) * | 2004-04-02 | 2012-01-30 | Basf Se | Tintes catiónicos de azoimidazol que contienen una unidad estructural 2,5-diaminofenilo. |
| CN1997340B (zh) | 2004-04-08 | 2013-07-17 | 西巴特殊化学制品控股公司 | 二硫化物染料，包含它们的组合物以及染色的方法 |
| US7191834B2 (en) * | 2004-09-22 | 2007-03-20 | Halliburton Energy Services, Inc. | Foamed cement compositions and associated methods of use |
| US7488354B2 (en) | 2004-10-14 | 2009-02-10 | L'oreal S.A. | Dyeing composition comprising at least one disulphide dye and method of dyeing human keratin fibers using this dye |
| FR2882520B1 (fr) | 2005-02-25 | 2007-05-25 | Oreal | Composition de teinture des fibres keratiniques comprenant un colorant direct sulfonamidoxanthenique et procede de teinture la mettant en oeuvre |
| US7374581B2 (en) | 2005-04-29 | 2008-05-20 | L'oreal, S.A. | Dye composition containing a particular cationic hydrazone direct dye, dyeing process, use and multi-compartment devices |
| FR2889954B1 (fr) * | 2005-08-26 | 2007-10-19 | Oreal | Colorants mixtes cationiques comprenant un chromophore anthraquinone et leur utilisation en colorant capillaire |
| US7771490B2 (en) | 2005-08-30 | 2010-08-10 | Ciba Corporation | Dyes containing a thiol group |
| FR2898903B1 (fr) | 2006-03-24 | 2012-08-31 | Oreal | Composition de teinture comprenant un colorant disulfure fluorescent, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
| EP2029674B1 (en) | 2006-06-13 | 2013-05-22 | Basf Se | Tricationic dyes |
| FR2919179B1 (fr) | 2007-07-24 | 2010-02-19 | Oreal | Composition capillaire comprenant au moins un colorant direct disulfure et au moins un agent alcalin hydroxyde et procede de mise en forme et de coloration simultanees. |
| FR2921256B1 (fr) | 2007-09-24 | 2009-12-04 | Oreal | Composition pour la coloration de fibres keratiniques comprenant au moins un colorant direct a fonction disulfure/thiol et au moins un polymere a fonction thiol et procede utilisant la composition |
| MX2012000557A (es) | 2009-07-15 | 2012-03-07 | Basf Se | Tintes para el cabello polimeros. |
| ES2612475T3 (es) | 2010-08-17 | 2017-05-17 | Basf Se | Tintes capilares poliméricos de disulfuro o tiol |
| FR2968954B1 (fr) | 2010-12-15 | 2012-12-21 | Oreal | Procede de coloration de fibres keratiniques mettant en oeuvre un colorant direct a fonction disulfure/thiol/thiol protege et de la vapeur d'eau |
| FR2971935B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un polymere epaississant, un tensioactif non ionique, un agent alcalin, et un agent reducteur |
| FR2971937B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un polymere epaississant non cellulosique, un agent alcalin, et un agent reducteur |
| FR2971936B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un tensioactif non ionique, un tensioactif amphotere, un alcool gras ethoxyle, un agent alcalin, et un agent reducteur |
| FR2971939B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un corps gras, un agent alcalin, et un agent reducteur |
| FR2971938B1 (fr) | 2011-02-25 | 2013-08-02 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un alcool gras faiblement ou non ethoxyle, un tensioactif cationique, un agent alcalin, et un agent reducteur |
| BR112013021580B1 (pt) | 2011-02-25 | 2019-01-29 | L'oreal | composição cosmética, método para a tintura das fibras queratínicas, método para a tintura e clareamento das fibras queratínicas escuras e dispositivo ou kit de tintura com múltiplos compartimentos |
| BR112013028030B1 (pt) | 2011-05-03 | 2021-01-05 | Basf Se | composto, método para tingir fibras de queratina humanas, e, composição de tingimento |
| US9060944B2 (en) | 2011-07-05 | 2015-06-23 | L'oreal | Cosmetic composition rich in fatty substances comprising a polyoxyalkylenated fatty alcohol ether and a direct dye and/or an oxidation dye, the dyeing method and the device |
| FR2977482B1 (fr) | 2011-07-05 | 2013-11-08 | Oreal | Composition de coloration mettant en oeuvre un ether a longue chaine d'un alcool gras alcoxyle et un polymere cationique, procedes et dispositifs |
| WO2013004772A2 (en) | 2011-07-05 | 2013-01-10 | L'oreal | Dye composition comprising an alkoxylated fatty alcohol ether and a fatty alcohol |
| FR2980675B1 (fr) | 2011-09-30 | 2013-11-01 | Oreal | Procede de mise en forme coloree temporaire des fibres keratiniques |
| RU2015106908A (ru) | 2012-08-02 | 2016-09-20 | Л'Ореаль | Красящая композиция, содержащая по меньшей мере одно жирное вещество, по меньшей мере один окисляющий агент и по меньшей мере одно неионное, анионное и амфотерное поверхностно-активное вещество |
| FR2994084B1 (fr) | 2012-08-02 | 2014-10-31 | Oreal | Composition de coloration sous forme de creme comprenant au moins une huile, pas ou peu d'alcool gras solide, procede de coloration et dispositif approprie |
| CN109199922A (zh) | 2012-08-02 | 2019-01-15 | 莱雅公司 | 染色组合物、染色方法和合适的装置 |
| FR2994091B1 (fr) | 2012-08-02 | 2014-08-01 | Oreal | Composition de coloration comprenant de la gomme de guar non ionique ou l'un de ses derives non ionique, procede et dispositif |
| KR102244166B1 (ko) | 2013-09-02 | 2021-04-26 | 로레알 | 양이온성 스티릴 디술파이드 염료를 사용하는 케라틴 섬유 염색 방법, 및 상기 염료를 포함하는 조성물 |
| FR3016288B1 (fr) | 2013-12-23 | 2016-09-09 | Oreal | Article de conditionnement comportant une enveloppe et une composition anhydre comprenant un agent oxydant |
| FR3015231B1 (fr) | 2013-12-23 | 2017-02-24 | Oreal | Article de conditionnement comportant un enveloppe une composition colorante anhydre comprenant un colorant direct, utilisation et procede pour colorer les fibres keratiniques |
| FR3015232B1 (fr) | 2013-12-23 | 2016-01-08 | Oreal | Article de conditionnement comportant un enveloppe une composition colorante anhydre comprenant un colorant d'oxydation, utilisation et procede pour colorer les fibres keratiniques |
| FR3043551B1 (fr) | 2015-11-12 | 2017-11-24 | Oreal | Colorant direct cationique a chaine aliphatique et a fonction disulfure/thiol/thiol protege pour colorer les fibres keratiniques |
| FR3060990B1 (fr) | 2016-12-22 | 2019-11-01 | L'oreal | Procede de coloration et detente de boucles des fibres keratiniques, mettant en oeuvre des agents reducteurs et des colorants capillaires, et kit associe |
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| FR3083106B1 (fr) | 2018-06-29 | 2020-10-02 | Oreal | Procede de coloration des fibres keratiniques mettant en oeuvre un monosaccharide, un polysaccharide a groupes amines et une matiere colorante |
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| FR3097755B1 (fr) | 2019-06-28 | 2021-07-16 | Oreal | Procédé de coloration des fibres kératiniques comprenant une étape de traitement par plasma froid desdites fibres |
| FR3097760B1 (fr) | 2019-06-28 | 2022-04-01 | Oreal | Procédé de coloration des fibres kératiniques comprenant l’application d’un mélange extemporané d’un colorant direct etd’une composition comprenant un corps gras liquide, un corps gras solide et un tensioactif. |
| FR3098116B1 (fr) | 2019-07-05 | 2021-06-18 | Oreal | Composition comprenant un colorant naturel, un colorant direct triarylméthane et un composé aromatique |
| FR3098114B1 (fr) | 2019-07-05 | 2022-11-11 | Oreal | Composition comprenant un colorant naturel, un colorant direct synthétique cationique hydrazono et/ou azoïque et un composé aromatique |
| FR3103090B1 (fr) | 2019-11-20 | 2024-08-09 | Oreal | Procédé de coloration ou d’éclaircissement mettant en œuvre un appareil de coiffure à main et un substrat |
| FR3104952B1 (fr) | 2019-12-20 | 2022-08-26 | Oreal | Procédé de traitement cosmétique des fibres kératiniques mettant en œuvre une composition de coloration et une composition à base de terres rares |
| FR3104983B1 (fr) | 2019-12-20 | 2023-11-24 | Oreal | Composition de coloration capillaire comprenant un colorant direct, une gomme de scléroglucane et un polymère associatif non ionique. |
| FR3109313B1 (fr) | 2020-04-15 | 2022-11-25 | Oreal | Procede de traitement de matieres keratiniques mettant en oeuvre un polymere acrylique d’anhydride en dispersion huileuse et d’un compose hydroxyle et/ou thiole |
| FR3111553A1 (fr) | 2020-06-22 | 2021-12-24 | L'oreal | Procédé de coloration des fibres kératiniques mettant en œuvre un colorant direct et un sel de saccharinate et composition les comprenant |
| FR3111557B1 (fr) | 2020-06-23 | 2022-11-25 | Oreal | Composition cosmétique comprenant un copolymère polyhydroxyalcanoate comprenant au moins deux unités polymériques différentes à chaine hydrocarbonée (in)saturée dans un milieu gras |
| FR3111552B1 (fr) | 2020-06-23 | 2024-04-05 | Oreal | Composition pour la décoloration et la coloration simultanées des fibres kératiniques comprenant un sel hétérocyclique particulier et procédé mettant en œuvre cette composition |
| FR3111812B1 (fr) | 2020-06-24 | 2023-02-10 | Oreal | Composition cosmétique comprenant un copolymère polyhydroxyalcanoate greffé dans un milieu gras |
| FR3117806B1 (fr) | 2020-12-18 | 2024-03-01 | Oreal | Composition pour la décoloration et la coloration simultanées des fibres kératiniques et procédé mettant en œuvre cette composition |
| WO2022129345A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Process for lightening keratin fibres |
| FR3117807B1 (fr) | 2020-12-18 | 2024-03-01 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3117809B1 (fr) | 2020-12-18 | 2024-02-16 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3117808B1 (fr) | 2020-12-18 | 2024-03-01 | Oreal | Composition pour la décoloration et la coloration simultanées des fibres kératiniques et procédé mettant en œuvre cette composition |
| FR3117805B1 (fr) | 2020-12-18 | 2024-02-16 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3130567B1 (fr) | 2021-12-16 | 2024-02-16 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3130572B1 (fr) | 2021-12-16 | 2024-08-23 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3130568B1 (fr) | 2021-12-16 | 2024-02-16 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3130571B1 (fr) | 2021-12-16 | 2024-02-16 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3130570B1 (fr) | 2021-12-16 | 2024-11-01 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3130569B1 (fr) | 2021-12-16 | 2024-06-28 | Oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3130610B1 (fr) | 2021-12-20 | 2025-11-21 | Oreal | Composition comprenant un copolymère polyhydroxyalcanoate à longue chaine hydrocarbonnée à groupe(s) ionique(s), procédé de traitement des matières kératiniques mettant en œuvre la composition |
| FR3136966A1 (fr) | 2022-06-22 | 2023-12-29 | L'oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3136976A1 (fr) | 2022-06-22 | 2023-12-29 | L'oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3136967A1 (fr) | 2022-06-22 | 2023-12-29 | L'oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3136968A1 (fr) | 2022-06-22 | 2023-12-29 | L'oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3136972A1 (fr) | 2022-06-22 | 2023-12-29 | L'oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3136975A1 (fr) | 2022-06-22 | 2023-12-29 | L'oreal | Composition d’éclaircissement des fibres kératiniques et procédé d’éclaircissement des fibres kératiniques mettant en œuvre cette composition |
| FR3144510B1 (fr) | 2022-12-29 | 2025-11-28 | Oreal | Composition comprenant au moins l’acide N,N-dicarboxyméthyl glutamique, au moins un colorant direct, au moins un polysaccharide cationique, et au moins un polysaccharide non cationique |
| FR3144513A1 (fr) | 2022-12-29 | 2024-07-05 | L'oreal | Composition comprenant au moins l’acide N,N-dicarboxyméthyl glutamique, au moins un colorant direct, et au moins un polymère associatif |
| FR3144512B1 (fr) | 2022-12-29 | 2025-11-28 | Oreal | Composition comprenant au moins l’acide N,N-dicarboxyméthyl glutamique, au moins un agent colorant, et au moins une amine grasse |
| FR3144511B1 (fr) | 2022-12-29 | 2025-12-05 | Oreal | Composition comprenant au moins un colorant direct, au moins l’acide N,N-dicarboxyméthyl glutamique, au moins un tensioactif cationique et au moins un corps gras non siliconé dans une teneur particulière |
| FR3157133B1 (fr) | 2023-12-20 | 2026-06-26 | Oreal | Procédé de coloration des cheveux mettant en œuvre une composition éclaircissante et une composition de coloration comprenant un colorant direct, un composé aromatique et un solvant aliphatique hydroxylé. |
| FR3163261A1 (fr) | 2024-06-13 | 2025-12-19 | L'oreal | Procédé de coloration des fibres kératiniques mettant en œuvre un composé à fonctions acétoacétates, un composé (poly)aminé et un colorant direct |
| FR3163260A1 (fr) | 2024-06-13 | 2025-12-19 | L'oreal | Procédé de coloration des fibres kératiniques mettant en œuvre un composé à fonctions acétoacétates, un composé (poly)aminé et un colorant direct |
| FR3163844A1 (fr) | 2024-06-27 | 2026-01-02 | L'oreal | Procédé de coloration des cheveux mettant en œuvre une composition comprenant un colorant direct que l’on fait recirculer sur les cheveux |
| FR3169082A1 (fr) | 2024-12-03 | 2026-06-05 | L'oreal | Procédé de coloration des cheveux mettant en œuvre une composition alcaline et une composition de coloration comprenant un colorant direct. |
| FR3170270A1 (fr) | 2024-12-19 | 2026-06-26 | L'oreal | Composition comprenant un colorant direct, un polysaccharide non associatif, un acide polycarboxylique particulier, et un composé hydroxylé. |
| FR3170271A1 (fr) | 2024-12-19 | 2026-06-26 | L'oreal | Procédé de coloration des cheveux mettant en œuvre une composition comprenant un agent alcalin, une composition de coloration comprenant un colorant direct et une composition comprenant un composé à fonctions acétoacétates |
| FR3170297A1 (fr) | 2024-12-23 | 2026-06-26 | L'oreal | Composition comprenant un colorant direct, un polysaccharide cationique, un ester gras et des tensioactifs cationiques |
| FR3170286A1 (fr) | 2024-12-23 | 2026-06-26 | L'oreal | Procede de traitement des fibres keratiniques comprenant les applications d’une premiere composition oxydante et d’une seconde composition a base de colorants directs |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB885046A (en) * | 1958-06-25 | 1961-12-20 | Basf Ag | New cationic azo dyestuffs derived from imidazole and methods for their production and their use |
| DE1137815B (de) | 1958-09-30 | 1962-10-11 | Basf Ag | Verfahren zur Herstellung basischer Azofarbstoffe |
| DE1157324B (de) | 1959-10-29 | 1963-11-14 | Basf Ag | Verfahren zur Herstellung basischer Azofarbstoffe |
| EP0714954B1 (de) | 1994-11-03 | 2002-09-25 | Ciba SC Holding AG | Kationische Imidazolazofarbstoffe |
| AU781845B2 (en) * | 2000-03-09 | 2005-06-16 | Ciba Specialty Chemicals Holding Inc. | A method of colouring hair using cationic dyes |
-
2001
- 2001-03-01 AU AU46491/01A patent/AU781845B2/en not_active Ceased
- 2001-03-01 DE DE60102904T patent/DE60102904T2/de not_active Expired - Lifetime
- 2001-03-01 BR BR0109060-7A patent/BR0109060A/pt not_active Application Discontinuation
- 2001-03-01 WO PCT/EP2001/002316 patent/WO2001066646A1/en not_active Ceased
- 2001-03-01 ES ES01919361T patent/ES2217131T3/es not_active Expired - Lifetime
- 2001-03-01 EP EP01919361A patent/EP1261666B1/en not_active Expired - Lifetime
- 2001-03-01 JP JP2001565809A patent/JP2003525949A/ja active Pending
- 2001-03-01 AT AT01919361T patent/ATE264891T1/de not_active IP Right Cessation
- 2001-03-01 MX MXPA02008645A patent/MXPA02008645A/es active IP Right Grant
- 2001-03-01 CN CN01806132.XA patent/CN1217995C/zh not_active Expired - Fee Related
- 2001-03-01 CA CA002400337A patent/CA2400337A1/en not_active Abandoned
- 2001-03-01 US US10/220,863 patent/US6843256B2/en not_active Expired - Fee Related
-
2004
- 2004-12-08 US US11/007,450 patent/US7060806B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US6843256B2 (en) | 2005-01-18 |
| ATE264891T1 (de) | 2004-05-15 |
| EP1261666A1 (en) | 2002-12-04 |
| JP2003525949A (ja) | 2003-09-02 |
| US20050091764A1 (en) | 2005-05-05 |
| DE60102904D1 (de) | 2004-05-27 |
| CA2400337A1 (en) | 2001-09-13 |
| AU781845B2 (en) | 2005-06-16 |
| CN1411493A (zh) | 2003-04-16 |
| DE60102904T2 (de) | 2005-03-31 |
| AU4649101A (en) | 2001-09-17 |
| EP1261666B1 (en) | 2004-04-21 |
| CN1217995C (zh) | 2005-09-07 |
| ES2217131T3 (es) | 2004-11-01 |
| US7060806B2 (en) | 2006-06-13 |
| BR0109060A (pt) | 2003-06-03 |
| US20030066143A1 (en) | 2003-04-10 |
| WO2001066646A1 (en) | 2001-09-13 |
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| FG | Grant or registration |