JPS6348844B2 - - Google Patents
Info
- Publication number
- JPS6348844B2 JPS6348844B2 JP54041521A JP4152179A JPS6348844B2 JP S6348844 B2 JPS6348844 B2 JP S6348844B2 JP 54041521 A JP54041521 A JP 54041521A JP 4152179 A JP4152179 A JP 4152179A JP S6348844 B2 JPS6348844 B2 JP S6348844B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- composition according
- aminophenol
- hair
- composition
- Prior art date
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 claims description 150
- 239000000975 dye Substances 0.000 claims description 74
- 238000004043 dyeing Methods 0.000 claims description 63
- -1 alkali metal salts Chemical class 0.000 claims description 57
- 230000001590 oxidative effect Effects 0.000 claims description 44
- 125000000217 alkyl group Chemical group 0.000 claims description 40
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 39
- 229910052757 nitrogen Inorganic materials 0.000 claims description 34
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 26
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 24
- 239000007800 oxidant agent Substances 0.000 claims description 23
- 239000001257 hydrogen Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 21
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 18
- 239000002243 precursor Substances 0.000 claims description 18
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 16
- 230000003647 oxidation Effects 0.000 claims description 15
- 238000007254 oxidation reaction Methods 0.000 claims description 15
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 14
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 13
- 125000003277 amino group Chemical group 0.000 claims description 13
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 claims description 12
- 229910052736 halogen Inorganic materials 0.000 claims description 11
- 150000002367 halogens Chemical class 0.000 claims description 11
- 239000006071 cream Substances 0.000 claims description 10
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical group NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 9
- 239000002585 base Substances 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 9
- 239000000194 fatty acid Substances 0.000 claims description 9
- 229930195729 fatty acid Natural products 0.000 claims description 9
- 150000004665 fatty acids Chemical class 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 125000001424 substituent group Chemical group 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000000982 direct dye Substances 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 7
- 239000003995 emulsifying agent Substances 0.000 claims description 7
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 claims description 7
- QIJRTFXNRTXDIP-UHFFFAOYSA-N (1-carboxy-2-sulfanylethyl)azanium;chloride;hydrate Chemical compound O.Cl.SCC(N)C(O)=O QIJRTFXNRTXDIP-UHFFFAOYSA-N 0.000 claims description 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 229960001305 cysteine hydrochloride Drugs 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 150000004985 diamines Chemical class 0.000 claims description 5
- 150000002191 fatty alcohols Chemical class 0.000 claims description 5
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 5
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 5
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 150000007522 mineralic acids Chemical class 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- ZYZQSCWSPFLAFM-UHFFFAOYSA-N 4-amino-2-chlorophenol Chemical compound NC1=CC=C(O)C(Cl)=C1 ZYZQSCWSPFLAFM-UHFFFAOYSA-N 0.000 claims description 3
- 125000004442 acylamino group Chemical group 0.000 claims description 3
- 125000004945 acylaminoalkyl group Chemical group 0.000 claims description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 3
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 claims description 3
- DOGJSOZYUGJVKS-UHFFFAOYSA-N glyceryl monothioglycolate Chemical compound OCC(O)COC(=O)CS DOGJSOZYUGJVKS-UHFFFAOYSA-N 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- 239000002562 thickening agent Substances 0.000 claims description 3
- GYXHHICIFZSKKZ-UHFFFAOYSA-N 2-sulfanylacetamide Chemical compound NC(=O)CS GYXHHICIFZSKKZ-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
- JSWVCUXQICMATE-UHFFFAOYSA-N 4-amino-2,5-dimethylphenol Chemical compound CC1=CC(O)=C(C)C=C1N JSWVCUXQICMATE-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
- HDGMAACKJSBLMW-UHFFFAOYSA-N 4-amino-2-methylphenol Chemical compound CC1=CC(N)=CC=C1O HDGMAACKJSBLMW-UHFFFAOYSA-N 0.000 claims description 2
- GCWYXRHXGLFVFE-UHFFFAOYSA-N 4-hydroxy-2,6-dimethylaniline Chemical compound CC1=CC(O)=CC(C)=C1N GCWYXRHXGLFVFE-UHFFFAOYSA-N 0.000 claims description 2
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 claims description 2
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 2
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical group C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 2
- 239000002738 chelating agent Substances 0.000 claims description 2
- 229960002433 cysteine Drugs 0.000 claims description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims description 2
- 235000018417 cysteine Nutrition 0.000 claims description 2
- 150000002193 fatty amides Chemical class 0.000 claims description 2
- 239000003205 fragrance Substances 0.000 claims description 2
- 125000002425 furfuryl group Chemical group C(C1=CC=CO1)* 0.000 claims description 2
- 150000002334 glycols Chemical class 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- 230000000475 sunscreen effect Effects 0.000 claims description 2
- 239000000516 sunscreening agent Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 3
- UIKMRLLJORKSJL-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-2-amine Chemical compound C1=CC=C2OC(N)CNC2=C1 UIKMRLLJORKSJL-UHFFFAOYSA-N 0.000 claims 1
- YRUPBAWWCPVHFT-UHFFFAOYSA-N 4-(4-hydroxyanilino)phenol Chemical compound C1=CC(O)=CC=C1NC1=CC=C(O)C=C1 YRUPBAWWCPVHFT-UHFFFAOYSA-N 0.000 claims 1
- PNLPXABQLXSICH-UHFFFAOYSA-N 4-amino-3-chlorophenol Chemical compound NC1=CC=C(O)C=C1Cl PNLPXABQLXSICH-UHFFFAOYSA-N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 239000000443 aerosol Substances 0.000 claims 1
- 150000001412 amines Chemical group 0.000 claims 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 claims 1
- 125000005594 diketone group Chemical group 0.000 claims 1
- 239000000284 extract Substances 0.000 claims 1
- 150000004780 naphthols Chemical class 0.000 claims 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 58
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 53
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 29
- 229910021529 ammonia Inorganic materials 0.000 description 25
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 24
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 23
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 22
- 235000019441 ethanol Nutrition 0.000 description 22
- 238000000034 method Methods 0.000 description 22
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 19
- 235000011121 sodium hydroxide Nutrition 0.000 description 17
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 15
- 239000002453 shampoo Substances 0.000 description 14
- 235000017557 sodium bicarbonate Nutrition 0.000 description 14
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 14
- 229960001755 resorcinol Drugs 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 12
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 12
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 12
- YGRFRBUGAPOJDU-UHFFFAOYSA-N 5-(2-hydroxyethylamino)-2-methylphenol Chemical compound CC1=CC=C(NCCO)C=C1O YGRFRBUGAPOJDU-UHFFFAOYSA-N 0.000 description 11
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 11
- 239000000835 fiber Substances 0.000 description 11
- 238000011282 treatment Methods 0.000 description 11
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 10
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 10
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 10
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 10
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 10
- 239000005642 Oleic acid Substances 0.000 description 10
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 10
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 10
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 10
- 230000008569 process Effects 0.000 description 10
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 229940055577 oleyl alcohol Drugs 0.000 description 7
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 6
- 241001070941 Castanea Species 0.000 description 6
- 235000014036 Castanea Nutrition 0.000 description 6
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 6
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 6
- 229960000541 cetyl alcohol Drugs 0.000 description 6
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 6
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 6
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 6
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 5
- WYMDDFRYORANCC-UHFFFAOYSA-N 2-[[3-[bis(carboxymethyl)amino]-2-hydroxypropyl]-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)CN(CC(O)=O)CC(O)=O WYMDDFRYORANCC-UHFFFAOYSA-N 0.000 description 5
- 244000060011 Cocos nucifera Species 0.000 description 5
- 235000013162 Cocos nucifera Nutrition 0.000 description 5
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 5
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- LPMBTLLQQJBUOO-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCO)CCO LPMBTLLQQJBUOO-KTKRTIGZSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- BMJXMAAIWXBKBD-UHFFFAOYSA-N aniline;dihydrochloride Chemical compound Cl.Cl.NC1=CC=CC=C1 BMJXMAAIWXBKBD-UHFFFAOYSA-N 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 4
- MJAVQHPPPBDYAN-UHFFFAOYSA-N 2,6-dimethylbenzene-1,4-diamine Chemical compound CC1=CC(N)=CC(C)=C1N MJAVQHPPPBDYAN-UHFFFAOYSA-N 0.000 description 3
- JBESLYPTBIFSNQ-UHFFFAOYSA-N 2-methoxy-3,5-dimethylbenzene-1,4-diamine;dihydrochloride Chemical compound Cl.Cl.COC1=C(C)C(N)=C(C)C=C1N JBESLYPTBIFSNQ-UHFFFAOYSA-N 0.000 description 3
- WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 3
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 3
- RPNFVYFNLJCRRJ-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-amine;dihydrochloride Chemical compound Cl.Cl.O1CCNC2=CC(N)=CC=C21 RPNFVYFNLJCRRJ-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
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- 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
- 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
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/88—Two- or multipart kits
- A61K2800/884—Sequential application
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)
- Cosmetics (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7810276A FR2421606A1 (fr) | 1978-04-06 | 1978-04-06 | Procede de teinture de fibres keratiniques en deux temps |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS556570A JPS556570A (en) | 1980-01-18 |
| JPS6348844B2 true JPS6348844B2 (US20080094685A1-20080424-C00004.png) | 1988-09-30 |
Family
ID=9206799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4152179A Granted JPS556570A (en) | 1978-04-06 | 1979-04-05 | Dyeing of keratin fiber |
Country Status (9)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0586279U (ja) * | 1991-07-30 | 1993-11-22 | 年久 吉本 | 繰出位牌 |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU82860A1 (fr) * | 1980-10-16 | 1982-05-10 | Oreal | Compositions tinctoriales a base de precurseurs de colorants d'oxydation et de colorants nitres benzeniques stables en milieu alcalin reducteur et leur utilisation pour la teinture des fibres keratiniques |
| DE3047105A1 (de) * | 1980-12-13 | 1982-07-29 | Henkel KGaA, 4000 Düsseldorf | Haarfaerbemittel |
| DE3500877A1 (de) * | 1985-01-12 | 1986-07-17 | Henkel KGaA, 4000 Düsseldorf | Haarfaerbemittel-zubereitung |
| DE3543345A1 (de) * | 1985-12-07 | 1987-06-11 | Wella Ag | Oxidationshaarfaerbemittel auf der basis von 4-amino-2-aminomethyl-phenolen |
| US5161553A (en) * | 1986-09-19 | 1992-11-10 | Clairol Incorporated | Process for simultaneously waving and coloring hair |
| DE3711579A1 (de) * | 1987-04-06 | 1988-10-20 | Henkel Kgaa | Aminophenylalkylendiamine und deren verwendung in oxidationshaarfaerbemitteln |
| US5180399A (en) * | 1987-05-25 | 1993-01-19 | L'oreal | Process for dyeing keratinous fibres with oxidation bases combined with an iodide and dyeing composition employed |
| LU86899A1 (fr) * | 1987-05-25 | 1989-01-19 | Oreal | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre |
| 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 |
| EP0352375B1 (en) * | 1988-07-26 | 1994-11-02 | Teh-Shan Chang | Preparation for dyeing and setting hair |
| 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 |
| 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 |
| LU87611A1 (fr) * | 1989-10-20 | 1991-05-07 | Oreal | Composition tinctoriale pour fibres keratiniques contenant des precurseurs de colorants par oxydation et des coupleurs amino indoliques,procedes de teinture mettant en oeuvre ces compositions et composes nouveaux |
| DE4005008C2 (de) * | 1990-02-19 | 1995-01-05 | Wella Ag | Oxidationshaarfärbemittel aus einer flüssigen Farbträgermasse und einer emulsionsförmigen, oxidationsmittelhaltigen Zusammensetzung und Verfahren zum oxidativen Färben von Haaren |
| 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 . |
| FR2672210B1 (fr) * | 1991-02-01 | 1993-05-21 | Oreal | Procede de teinture des fibres keratiniques, associant l'isatine ou ses derives a un amino indole ou une amino indoline, compositions mises en óoeuvre. |
| FR2673533B1 (fr) * | 1991-03-05 | 1993-06-11 | Oreal | Procede de teinture des fibres keratiniques associant l'isatine ou ses derives a une aniline tri-, tetra- ou pentasubstituee, et agents de teinture. |
| DE4123941A1 (de) * | 1991-07-19 | 1993-01-21 | Wella Ag | Verfahren zur oxidativen faerbung von haaren |
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| US5376146A (en) * | 1993-08-26 | 1994-12-27 | Bristol-Myers Squibb Company | Two-part aqueous composition for coloring hair, which forms a gel on mixing of the two parts |
| FR2715297B1 (fr) * | 1994-01-24 | 1996-02-23 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et un dérivé de métaaminophénol, et procédé de teinture utilisant une telle composition. |
| DE4402363C2 (de) * | 1994-01-27 | 1995-08-17 | Kunststoff Maschinen Handelsge | Verfahren zur chromatotropischen LASER-Beschriftung von Kunststoffen |
| FR2717383B1 (fr) * | 1994-03-21 | 1996-04-19 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et un polymère substantif cationique ou amphotère et utilisation. |
| FR2719469B1 (fr) * | 1994-05-09 | 1996-06-14 | Oreal | Composition de teinture d'oxydation des fibres kératiniques et procédé de teinture mettant en Óoeuvre cette composition. |
| FR2720275B1 (fr) * | 1994-05-26 | 1996-07-05 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et une 6-hydroxy 1,4-benzoxazine, et procédé de teinture utilisant une telle composition . |
| FR2720633B1 (fr) * | 1994-06-06 | 1996-07-05 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant la 2-(BETHA-hydroxyéthyl) paraphénylènediamine, la 2-méthylrésorcine et le 3-aminophénol, et procédé de teinture utilisant une telle composition. |
| DE4421397A1 (de) * | 1994-06-18 | 1995-12-21 | Wella Ag | Mittel zur oxidativen Färbung von Haaren und neue 2-Alkylamino-4-amino-1-alkylbenzole |
| DE4438129A1 (de) * | 1994-10-27 | 1996-05-02 | Schwarzkopf Gmbh Hans | Neue substituierte 2,4-Diaminophenole, Verfahren zu ihrer Herstellung und Haarfärbemittel |
| DE19619071A1 (de) * | 1996-05-13 | 1997-11-20 | Henkel Kgaa | Mittel und Verfahren zum Färben und Tönen keratinischer Fasern |
| EP0912160A2 (de) * | 1996-07-03 | 1999-05-06 | Hans Schwarzkopf GmbH & Co. KG | Oxidationsfärbemittel |
| FR2751533B1 (fr) * | 1996-07-23 | 2003-08-15 | Oreal | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique |
| FR2753093B1 (fr) | 1996-09-06 | 1998-10-16 | Oreal | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile anionique |
| US5942009A (en) * | 1997-03-28 | 1999-08-24 | Brg, Ltd. | Same-day waving and coloring of hair |
| CA2295762A1 (en) | 1997-07-02 | 1999-01-14 | Ravi Shanker Garigipati | Novel cycloalkyl substituted imidazoles |
| US6074438A (en) * | 1998-03-03 | 2000-06-13 | Bristol-Myers Squibb Co. | Hair dyeing compositions containing 2-chloro- and 2,6-dichloro-4-aminophenol and phenylpyrazolones |
| JP2000086471A (ja) * | 1998-09-14 | 2000-03-28 | Hoyu Co Ltd | 染毛剤組成物 |
| DE10020731C2 (de) * | 2000-04-27 | 2002-03-07 | Goldwell Gmbh | Haarfärbemittel |
| WO2002069921A1 (en) * | 2001-03-07 | 2002-09-12 | Unilever Plc | Hair colouring compositions |
| DE10143293A1 (de) * | 2001-09-04 | 2003-03-20 | Wella Ag | Verfahren zum gleichzeitigen Färben und dauerhaften Verformen von Haaren |
| US7273058B2 (en) * | 2001-09-04 | 2007-09-25 | Wella Ag | Method for simultaneously dyeing and permanent shaping of hair |
| KR20030043210A (ko) * | 2001-11-27 | 2003-06-02 | 동성제약주식회사 | 페닐메칠피라졸론을 함유하는 모발염모제 조성물 및 그제조방법 |
| EP1484048B1 (en) * | 2003-06-02 | 2019-01-02 | Noxell Corporation | Hair colouring compositions |
| 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 |
| DE102004037105A1 (de) | 2004-07-30 | 2005-01-13 | Wella Ag | Mehrkomponenten-Kit und Verfahren zum Färben von Keratinfasern |
| JP2008521833A (ja) * | 2004-12-02 | 2008-06-26 | ザ プロクター アンド ギャンブル カンパニー | 毛髪染色組成物 |
| CN101068600A (zh) * | 2004-12-02 | 2007-11-07 | 宝洁公司 | 毛发染色组合物 |
| AU2005311860A1 (en) * | 2004-12-02 | 2006-06-08 | The Procter & Gamble Company | Polymer thickened hair colouring and bleaching compositions |
| JP5318418B2 (ja) | 2004-12-02 | 2013-10-16 | ザ プロクター アンド ギャンブル カンパニー | 増粘毛髪染色剤及び脱色組成物 |
| DE102005048183A1 (de) * | 2005-10-06 | 2007-04-12 | Henkel Kgaa | Verfahren zur oxidativen Färbung keratinhaltiger Fasern |
| US7566348B2 (en) * | 2006-01-26 | 2009-07-28 | Revlon Consumer Products Corporation | Method for coloring hair |
| DE602006016590D1 (de) * | 2006-07-12 | 2010-10-14 | Procter & Gamble | Auf Gelnetzwerk-Emulgatoren basierende Verdickersysteme für Haarfärbe und Haaraufhellungszusammensetzungen |
| JP5183049B2 (ja) * | 2006-09-20 | 2013-04-17 | 高砂香料工業株式会社 | 染毛剤用安定化剤 |
| DE102013203229A1 (de) | 2013-02-27 | 2014-08-28 | Henkel Ag & Co. Kgaa | Multionale Einschritt-Färbungen II |
| JP6787539B2 (ja) * | 2015-01-22 | 2020-11-18 | ホーユー株式会社 | 染毛剤組成物及び染毛剤組成物の色調安定化方法 |
| BR112019006332B1 (pt) * | 2016-09-30 | 2021-09-28 | L'oreal | Composição cosmética capilar, método para mascarar o efeito de amarelamento de produtos de descoloração ou clareamento nos cabelos e método para proporcionar aos cabelos um ou mais efeitos de cuidados capilares |
| BR112021025534A2 (pt) * | 2019-06-28 | 2022-03-03 | L´Oreal | Composição cosmética para o tingimento oxidativo de fibras de queratina |
| WO2021186917A1 (ja) * | 2020-03-17 | 2021-09-23 | 株式会社Ｎｉｌ | 染毛剤 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2610941A (en) * | 1946-12-14 | 1952-09-16 | L Oreal Soc | Hair-dye compositions |
| US2904385A (en) * | 1956-07-17 | 1959-09-15 | Oreal | Dyeing animal fibres and compositions therefor |
| DE1149497B (de) * | 1961-10-26 | 1963-05-30 | Interpal S A | Mittel zum Faerben menschlicher Haare |
| GB1077758A (en) * | 1964-12-11 | 1967-08-02 | Hoyu Kabushiki Kaisha | Dyeing and permanent weaving of keratinous substances |
| DE2119231A1 (de) * | 1971-04-21 | 1972-10-26 | Therachemie chemisch therapeutische Ges mbH, 4000 Dusseldorf | Verfahren und Mittel zum Farben menschlicher Haare |
| JPS4868750A (US20080094685A1-20080424-C00004.png) * | 1971-12-21 | 1973-09-19 | ||
| JPS509852A (US20080094685A1-20080424-C00004.png) * | 1973-06-01 | 1975-01-31 | ||
| JPS5064443A (US20080094685A1-20080424-C00004.png) * | 1973-10-15 | 1975-05-31 | ||
| JPS5218258A (en) * | 1975-08-01 | 1977-02-10 | Daiei Denki Seisakusho:Kk | Magnetism sellection control gear |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT71060B (de) | 1915-03-31 | 1916-01-25 | Anton Pogany | Sattelgurtspanner. |
| US2101696A (en) * | 1934-12-15 | 1937-12-07 | Gen Aniline Works Inc | Process for producing two-color effects on skins or furs |
| DE1003402B (de) * | 1951-04-19 | 1957-02-28 | Union Francaise Commerciale Et | Verfahren zum Faerben von Haaren |
| NL163269B (nl) * | 1951-07-20 | Airco Inc | Werkwijze voor het bereiden van ferritische staal- legeringen, alsmede hieruit geheel of grotendeels vervaardigde, gevormde voortbrengselen. | |
| FR65506E (fr) * | 1954-02-26 | 1956-02-28 | Union Francaise Commerciale Et Industrielle Sa | Composition nouvelle et son procédé d'application pour la teinture inoffensive des cheveux |
| AT217033B (de) * | 1959-01-30 | 1961-09-11 | American Cyanamid Co | Verfahren zur Umwandlung von 1,2,3,4-Tetrahydronaphthalinverbindungen in neue 1,2,3,4,4 a,9,9 a,10-Octahydroanthrazenverbindungen bzw. von 1,2,3,4-Tetrahydroanthrazenverbindungen in neue 1,2,3,4,4 a,5,12,12 a-Octahydronaphthazenverbindungen |
| AT222277B (de) * | 1959-07-24 | 1962-07-10 | Oreal | Verfahren und Mittel zum Färben menschlichen Haares |
| FR1257394A (fr) * | 1960-01-26 | 1961-03-31 | Braskamp W H Nv | Liquide pour la teinture et éventuellement la frisure permanente des cheveux |
| US3215605A (en) * | 1962-04-25 | 1965-11-02 | Revlon | Method for coloring hair and other keratinaceous fibers with metal salts |
| LU59265A1 (US20080094685A1-20080424-C00004.png) * | 1969-08-11 | 1971-06-21 | Oreal | |
| AT320160B (de) * | 1971-04-21 | 1975-01-27 | Therachemie Chem Therapeut | Verfahren und Mittel zum Färben menschlicher Haare |
| DE2349050C2 (de) * | 1973-09-29 | 1985-06-05 | Wella Ag, 6100 Darmstadt | Verfahren und Mittel zur Herabsetzung der Wirkstoffkonzentration in kosmetischen Präparaten |
| JPS5147778B2 (US20080094685A1-20080424-C00004.png) * | 1973-12-01 | 1976-12-16 |
-
1978
- 1978-04-06 FR FR7810276A patent/FR2421606A1/fr active Granted
-
1979
- 1979-04-05 CH CH321579A patent/CH641952A5/fr not_active IP Right Cessation
- 1979-04-05 GB GB7911899A patent/GB2018836B/en not_active Expired
- 1979-04-05 BE BE0/194419A patent/BE875341A/xx not_active IP Right Cessation
- 1979-04-05 IT IT67722/79A patent/IT1118455B/it active
- 1979-04-05 DE DE19792913808 patent/DE2913808A1/de active Granted
- 1979-04-05 US US06/027,400 patent/US4566875A/en not_active Expired - Lifetime
- 1979-04-05 CA CA000324999A patent/CA1141665A/fr not_active Expired
- 1979-04-05 JP JP4152179A patent/JPS556570A/ja active Granted
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2610941A (en) * | 1946-12-14 | 1952-09-16 | L Oreal Soc | Hair-dye compositions |
| US2904385A (en) * | 1956-07-17 | 1959-09-15 | Oreal | Dyeing animal fibres and compositions therefor |
| DE1149497B (de) * | 1961-10-26 | 1963-05-30 | Interpal S A | Mittel zum Faerben menschlicher Haare |
| GB1077758A (en) * | 1964-12-11 | 1967-08-02 | Hoyu Kabushiki Kaisha | Dyeing and permanent weaving of keratinous substances |
| DE2119231A1 (de) * | 1971-04-21 | 1972-10-26 | Therachemie chemisch therapeutische Ges mbH, 4000 Dusseldorf | Verfahren und Mittel zum Farben menschlicher Haare |
| JPS4868750A (US20080094685A1-20080424-C00004.png) * | 1971-12-21 | 1973-09-19 | ||
| JPS509852A (US20080094685A1-20080424-C00004.png) * | 1973-06-01 | 1975-01-31 | ||
| JPS5064443A (US20080094685A1-20080424-C00004.png) * | 1973-10-15 | 1975-05-31 | ||
| JPS5218258A (en) * | 1975-08-01 | 1977-02-10 | Daiei Denki Seisakusho:Kk | Magnetism sellection control gear |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0586279U (ja) * | 1991-07-30 | 1993-11-22 | 年久 吉本 | 繰出位牌 |
Also Published As
| Publication number | Publication date |
|---|---|
| IT1118455B (it) | 1986-03-03 |
| JPS556570A (en) | 1980-01-18 |
| DE2913808C2 (US20080094685A1-20080424-C00004.png) | 1992-11-19 |
| GB2018836B (en) | 1982-09-02 |
| BE875341A (fr) | 1979-10-05 |
| FR2421606B1 (US20080094685A1-20080424-C00004.png) | 1982-12-03 |
| US4566875A (en) | 1986-01-28 |
| CA1141665A (fr) | 1983-02-22 |
| IT7967722A0 (it) | 1979-04-05 |
| CH641952A5 (fr) | 1984-03-30 |
| GB2018836A (en) | 1979-10-24 |
| FR2421606A1 (fr) | 1979-11-02 |
| DE2913808A1 (de) | 1979-10-11 |
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