AU2002215016A1 - Method of dyeing keratin-containing fibres - Google Patents

Method of dyeing keratin-containing fibres

Info

Publication number: AU2002215016A1
Authority: AU; Australia
Prior art keywords: sub; alkyl; phenyl; substituted; hydrogen
Prior art date: 2000-10-12
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Abandoned

Application number

AU2002215016A

Other languages

English (en)

Inventor

Peter Mockli

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF Schweiz AG

Original Assignee

Ciba Spezialitaetenchemie Holding AG

Ciba SC Holding AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-10-12

Filing date

2001-10-10

Publication date

2002-04-22

2001-10-10 Application filed by Ciba Spezialitaetenchemie Holding AG, Ciba SC Holding AG filed Critical Ciba Spezialitaetenchemie Holding AG

2002-04-22 Publication of AU2002215016A1 publication Critical patent/AU2002215016A1/en

Status Abandoned legal-status Critical Current

Links

238000004043 dyeing Methods 0.000 title claims abstract description 47
238000000034 method Methods 0.000 title claims abstract description 20
102000011782 Keratins Human genes 0.000 title claims abstract description 10
108010076876 Keratins Proteins 0.000 title claims abstract description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 32
125000000217 alkyl group Chemical group 0.000 claims abstract description 24
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 23
239000001257 hydrogen Substances 0.000 claims abstract description 23
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 22
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 22
229910052736 halogen Inorganic materials 0.000 claims abstract description 21
150000002367 halogens Chemical class 0.000 claims abstract description 21
125000004193 piperazinyl group Chemical group 0.000 claims abstract description 11
150000001450 anions Chemical class 0.000 claims abstract description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 8
125000003545 alkoxy group Chemical group 0.000 claims abstract description 8
125000001424 substituent group Chemical group 0.000 claims abstract description 6
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
150000002431 hydrogen Chemical class 0.000 claims abstract 5
-1 methoxy, methyl Chemical group 0.000 claims description 43
239000000203 mixture Substances 0.000 claims description 38
210000004209 hair Anatomy 0.000 claims description 30
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
239000000460 chlorine Chemical group 0.000 claims description 4
229910052801 chlorine Chemical group 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
125000005466 alkylenyl group Chemical group 0.000 claims description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 abstract description 3
239000000975 dye Substances 0.000 description 55
125000004432 carbon atom Chemical group C* 0.000 description 23
150000001875 compounds Chemical class 0.000 description 22
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 18
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 16
238000002360 preparation method Methods 0.000 description 14
239000000047 product Substances 0.000 description 14
229920001577 copolymer Polymers 0.000 description 12
235000014113 dietary fatty acids Nutrition 0.000 description 10
239000000194 fatty acid Substances 0.000 description 10
229930195729 fatty acid Natural products 0.000 description 10
230000003647 oxidation Effects 0.000 description 10
238000007254 oxidation reaction Methods 0.000 description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 9
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
125000002091 cationic group Chemical group 0.000 description 7
239000000126 substance Substances 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
150000007513 acids Chemical class 0.000 description 6
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
239000000982 direct dye Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
150000004665 fatty acids Chemical class 0.000 description 6
229940032007 methylethyl ketone Drugs 0.000 description 6
229920005862 polyol Polymers 0.000 description 6
125000000129 anionic group Chemical group 0.000 description 5
239000003945 anionic surfactant Substances 0.000 description 5
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
238000009826 distribution Methods 0.000 description 5
150000002191 fatty alcohols Chemical class 0.000 description 5
239000002736 nonionic surfactant Substances 0.000 description 5
150000003254 radicals Chemical class 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
238000005406 washing Methods 0.000 description 5
239000002888 zwitterionic surfactant Substances 0.000 description 5
108010009736 Protein Hydrolysates Proteins 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
125000002252 acyl group Chemical group 0.000 description 4
239000003093 cationic surfactant Substances 0.000 description 4
239000002563 ionic surfactant Substances 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
229920000642 polymer Polymers 0.000 description 4
150000003077 polyols Chemical class 0.000 description 4
229920001296 polysiloxane Polymers 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000002243 precursor Substances 0.000 description 4
239000003531 protein hydrolysate Substances 0.000 description 4
DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 3
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
244000208060 Lawsonia inermis Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
229910019142 PO4 Inorganic materials 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
239000002671 adjuvant Substances 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000000987 azo dye Substances 0.000 description 3
239000003581 cosmetic carrier Substances 0.000 description 3
239000013078 crystal Substances 0.000 description 3
238000002425 crystallisation Methods 0.000 description 3
230000008025 crystallization Effects 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
238000001914 filtration Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
235000021317 phosphate Nutrition 0.000 description 3
239000000725 suspension Substances 0.000 description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
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
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-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
229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
239000004372 Polyvinyl alcohol Substances 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical group C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
229910006069 SO3H Inorganic materials 0.000 description 2
229920002125 Sokalan® Polymers 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001340 alkali metals 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
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
239000001768 carboxy methyl cellulose Substances 0.000 description 2
235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
239000008112 carboxymethyl-cellulose Substances 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
150000001805 chlorine compounds Chemical class 0.000 description 2
230000003750 conditioning effect Effects 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
125000001033 ether group Chemical group 0.000 description 2
238000009472 formulation Methods 0.000 description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 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
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
125000005528 methosulfate group Chemical group 0.000 description 2
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 2
VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 2
239000001048 orange dye Substances 0.000 description 2
239000007800 oxidant agent Substances 0.000 description 2
150000003904 phospholipids Chemical class 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
229920002451 polyvinyl alcohol Polymers 0.000 description 2
239000001044 red dye Substances 0.000 description 2
239000002453 shampoo Substances 0.000 description 2
229920002545 silicone oil Polymers 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003860 storage Methods 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
239000001043 yellow dye Substances 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
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NLXFWUZKOOWWFD-UHFFFAOYSA-N 1-(2-hydroxyethylamino)-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(NCCO)=CC=C2NC NLXFWUZKOOWWFD-UHFFFAOYSA-N 0.000 description 1
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JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-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
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-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
JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-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
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229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
ZKYCLDTVJCJYIB-UHFFFAOYSA-N 2-methylidenedecanamide Chemical compound CCCCCCCCC(=C)C(N)=O ZKYCLDTVJCJYIB-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
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VTXBLQLZQLHDIL-UHFFFAOYSA-N 4-(3-hydroxypropylamino)-3-nitrophenol Chemical compound OCCCNC1=CC=C(O)C=C1[N+]([O-])=O VTXBLQLZQLHDIL-UHFFFAOYSA-N 0.000 description 1
UNBOSJFEZZJZLR-UHFFFAOYSA-N 4-(4-nitrophenylazo)aniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=C([N+]([O-])=O)C=C1 UNBOSJFEZZJZLR-UHFFFAOYSA-N 0.000 description 1
AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
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235000017847 Anchusa officinalis Nutrition 0.000 description 1
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BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
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CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
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BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
240000008886 Ceratonia siliqua Species 0.000 description 1
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GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
102000008186 Collagen Human genes 0.000 description 1
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239000002798 polar solvent Substances 0.000 description 1
229920001521 polyalkylene glycol ether Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 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
238000001556 precipitation Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000008569 process Effects 0.000 description 1
239000003380 propellant Substances 0.000 description 1
235000018102 proteins Nutrition 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 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
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000002994 raw material Substances 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
235000002020 sage Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
239000000344 soap Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000008347 soybean phospholipid Substances 0.000 description 1
239000012177 spermaceti Substances 0.000 description 1
229940084106 spermaceti Drugs 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
230000008961 swelling Effects 0.000 description 1
229920001864 tannin Chemical group 0.000 description 1
239000001648 tannin Chemical group 0.000 description 1
235000018553 tannin Nutrition 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
230000008719 thickening Effects 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
FAGMGMRSURYROS-UHFFFAOYSA-M trihexadecyl(methyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC FAGMGMRSURYROS-UHFFFAOYSA-M 0.000 description 1
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
DWKARHJHPSUOBW-UHFFFAOYSA-N trimethyl-[3-[(2e)-2-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)hydrazinyl]phenyl]azanium;chloride Chemical compound [Cl-].CC1=NN(C=2C=CC=CC=2)C(O)=C1N=NC1=CC=CC([N+](C)(C)C)=C1 DWKARHJHPSUOBW-UHFFFAOYSA-N 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
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
239000011782 vitamin Substances 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
239000001993 wax Substances 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- 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
- A61K8/49—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
- A61K8/4946—Imidazoles or their condensed derivatives, e.g. benzimidazoles
- 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
- 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

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Birds (AREA)
Epidemiology (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Cosmetics (AREA)
Coloring (AREA)
Paper (AREA)
Polymerization Catalysts (AREA)
Silicon Polymers (AREA)
Pyridine Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Hydrogenated Pyridines (AREA)

AU2002215016A 2000-10-12 2001-10-10 Method of dyeing keratin-containing fibres Abandoned AU2002215016A1 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CH20062000		2000-10-12
CH2006/00		2000-10-12
PCT/EP2001/011706 WO2002030374A1 (fr)	2000-10-12	2001-10-10	Procede de coloration de fibres contenant de la keratine

Publications (1)

Publication Number	Publication Date
AU2002215016A1 true AU2002215016A1 (en)	2002-04-22

Family

ID=4567095

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
AU2002215016A Abandoned AU2002215016A1 (en)	2000-10-12	2001-10-10	Method of dyeing keratin-containing fibres
AU2002215936A Abandoned AU2002215936A1 (en)	2000-10-12	2001-10-10	Cationic imidazole azo dyes

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
AU2002215936A Abandoned AU2002215936A1 (en)	2000-10-12	2001-10-10	Cationic imidazole azo dyes

Country Status (12)

Country	Link
US (3)	US20030177591A1 (fr)
EP (2)	EP1325085A1 (fr)
JP (2)	JP2004510799A (fr)
KR (2)	KR100843113B1 (fr)
AT (1)	ATE337049T1 (fr)
AU (2)	AU2002215016A1 (fr)
BR (2)	BR0114585A (fr)
DE (1)	DE60122545T2 (fr)
ES (1)	ES2269481T3 (fr)
MX (2)	MXPA03002559A (fr)
TW (1)	TWI280147B (fr)
WO (2)	WO2002031056A1 (fr)

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US7326259B2 (en) *	2004-06-23	2008-02-05	L'oreal S.A.	Use of polycationic compounds in the dyeing of keratinous fibres
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US7396368B2 (en)	2004-12-15	2008-07-08	L'oreal S.A.	Symmetrical diazo compounds comprising 4-pyridinium groups and a cationic or non-cationic linker, compositions comprising them, method for coloring, and device
US7438728B2 (en)	2004-12-15	2008-10-21	L'oreal S.A.	Dissymmetrical diazo compounds comprising 2-pyridinium group and a cationic or non-cationic linker, compositions comprising them, method for coloring, and device
FR2879196B1 (fr) *	2004-12-15	2007-03-02	Oreal	Composes diaz0iques symetriques a groupements 2-imidazolium et bras de liaison non cationique, compositions les comprenant, procede de coloration et dispositif
US7288639B2 (en)	2004-12-15	2007-10-30	L'oreal S.A.	Dyssymmetrical diazo compounds having at least one 4-pyridinium unit and a cationic or non-cationic linker, compositions comprising them, method of coloring, and device
FR2889954B1 (fr)	2005-08-26	2007-10-19	Oreal	Colorants mixtes cationiques comprenant un chromophore anthraquinone et leur utilisation en colorant capillaire
JP2009507944A (ja)	2005-08-30	2009-02-26	チバホールディングインコーポレーテッド	チオール基を含む染料
BRPI0712992A2 (pt)	2006-06-13	2012-04-17	Ciba Holding Inc	tinturas tricatiÈnicas
US7731761B2 (en) *	2006-07-18	2010-06-08	Ciba Corporation	Polymeric hair dyes
KR100851614B1 (ko) *	2007-02-28	2008-08-12	로레알	줄롤리딘 유닛을 가지는 양이온성 아조 염료, 그를포함하는 염색용 조성물, 및 염색 방법
ES2645629T3 (es) *	2008-01-17	2017-12-07	Basf Se	Tintes poliméricos para el cabello
MX2011005938A (es) *	2008-12-05	2011-06-27	Unilever Nv	Coloracion de fibras queratinosas usando un pretratamiento comprendiendo una sal de hierro y un revelador de color comprendiendo tanino hidrolizable.
WO2011006946A2 (fr)	2009-07-15	2011-01-20	Basf Se	Colorants capillaires polymères
US8641783B2 (en)	2010-08-17	2014-02-04	Basf Se	Disulfide or thiol polymeric hair dyes
GB201201536D0 (en) *	2012-01-30	2012-03-14	Sheedy Paul D	Method and apparatus for communicating messages to individuals
KR102244166B1 (ko)	2013-09-02	2021-04-26	로레알	양이온성 스티릴 디술파이드 염료를 사용하는 케라틴 섬유 염색 방법, 및 상기 염료를 포함하는 조성물
EP3271027A1 (fr)	2015-03-19	2018-01-24	Noxell Corporation	Compositions pour coloration capillaire avec colorants directs cationiques
WO2016149495A1 (fr)	2015-03-19	2016-09-22	The Procter & Gamble Company	Composés fluorescents résistant à la transpiration acide pour coloration des cheveux
WO2016149429A1 (fr) *	2015-03-19	2016-09-22	The Procter & Gamble Company	Compositions pour coloration capillaire avec colorants directs cationiques
EP3271025A1 (fr)	2015-03-19	2018-01-24	Noxell Corporation	Procédé de coloration des cheveux avec composés colorants directs
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WO2016149490A1 (fr)	2015-03-19	2016-09-22	The Procter & Gamble Company	Procédé permettant d'améliorer la résistance à la perspiration acide de composés fluorescents sur les cheveux
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2001
- 2001-10-10 MX MXPA03002559A patent/MXPA03002559A/es active IP Right Grant
- 2001-10-10 DE DE60122545T patent/DE60122545T2/de not_active Expired - Lifetime
- 2001-10-10 AU AU2002215016A patent/AU2002215016A1/en not_active Abandoned
- 2001-10-10 AU AU2002215936A patent/AU2002215936A1/en not_active Abandoned
- 2001-10-10 AT AT01983540T patent/ATE337049T1/de not_active IP Right Cessation
- 2001-10-10 EP EP01986706A patent/EP1325085A1/fr not_active Withdrawn
- 2001-10-10 JP JP2002533819A patent/JP2004510799A/ja active Pending
- 2001-10-10 MX MXPA03003042 patent/MX239064B/es active IP Right Grant
- 2001-10-10 WO PCT/EP2001/011708 patent/WO2002031056A1/fr not_active Ceased
- 2001-10-10 KR KR1020037005161A patent/KR100843113B1/ko not_active Expired - Fee Related
- 2001-10-10 ES ES01983540T patent/ES2269481T3/es not_active Expired - Lifetime
- 2001-10-10 WO PCT/EP2001/011706 patent/WO2002030374A1/fr not_active Ceased
- 2001-10-10 JP JP2002534430A patent/JP2004511609A/ja active Pending
- 2001-10-10 BR BR0114585-1A patent/BR0114585A/pt not_active Application Discontinuation
- 2001-10-10 US US10/398,825 patent/US20030177591A1/en not_active Abandoned
- 2001-10-10 EP EP01983540A patent/EP1324741B1/fr not_active Expired - Lifetime
- 2001-10-10 KR KR1020037005067A patent/KR100832255B1/ko not_active Expired - Fee Related
- 2001-10-10 BR BR0114586-0A patent/BR0114586A/pt not_active Application Discontinuation
- 2001-10-10 US US10/398,823 patent/US6762287B2/en not_active Expired - Fee Related
- 2001-10-11 TW TW090125069A patent/TWI280147B/zh not_active IP Right Cessation
2005
- 2005-09-27 US US11/235,912 patent/US7189268B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
WO2002030374A1 (fr)	2002-04-18
MXPA03002559A (es)	2003-06-30
TWI280147B (en)	2007-05-01
MXPA03003042A (es)	2003-07-14
US20060026776A1 (en)	2006-02-09
US20030177591A1 (en)	2003-09-25
EP1324741B1 (fr)	2006-08-23
EP1325085A1 (fr)	2003-07-09
DE60122545T2 (de)	2007-10-04
US6762287B2 (en)	2004-07-13
KR100843113B1 (ko)	2008-07-02
KR100832255B1 (ko)	2008-05-28
MX239064B (es)	2006-07-31
BR0114586A (pt)	2003-08-26
KR20030041163A (ko)	2003-05-23
US20040049020A1 (en)	2004-03-11
ES2269481T3 (es)	2007-04-01
JP2004510799A (ja)	2004-04-08
JP2004511609A (ja)	2004-04-15
WO2002031056A1 (fr)	2002-04-18
ATE337049T1 (de)	2006-09-15
EP1324741A1 (fr)	2003-07-09
AU2002215936A1 (en)	2002-04-22
KR20030036914A (ko)	2003-05-09
DE60122545D1 (de)	2006-10-05
BR0114585A (pt)	2003-08-26
US7189268B2 (en)	2007-03-13

Publication	Publication Date	Title
EP1324741B1 (fr)	2006-08-23	Procede de coloration de fibres contenant de la keratine
EP1261666B1 (fr)	2004-04-21	Procede servant a teindre des cheveux au moyen de colorants cationiques
EP1622686B1 (fr)	2010-01-13	Colorants cationiques a base de dimeres
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