JPH04505459A - Oxidative hair dye comprising a liquid coloring agent and an emulsified oxidizing agent-containing composition, and a hair oxidative dyeing method - Google Patents
Oxidative hair dye comprising a liquid coloring agent and an emulsified oxidizing agent-containing composition, and a hair oxidative dyeing methodInfo
- Publication number
- JPH04505459A JPH04505459A JP3503700A JP50370091A JPH04505459A JP H04505459 A JPH04505459 A JP H04505459A JP 3503700 A JP3503700 A JP 3503700A JP 50370091 A JP50370091 A JP 50370091A JP H04505459 A JPH04505459 A JP H04505459A
- Authority
- JP
- Japan
- Prior art keywords
- component
- hair
- weight
- oxidative
- agent
- 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.)
- Granted
Links
- 210000004209 hair Anatomy 0.000 title claims description 50
- 239000000203 mixture Substances 0.000 title claims description 36
- 230000001590 oxidative effect Effects 0.000 title claims description 36
- 239000007788 liquid Substances 0.000 title claims description 30
- 238000004043 dyeing Methods 0.000 title claims description 21
- 239000003086 colorant Substances 0.000 title claims description 20
- 239000007800 oxidant agent Substances 0.000 title claims description 15
- 238000000034 method Methods 0.000 title claims description 9
- 239000000118 hair dye Substances 0.000 title description 43
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 41
- 239000003814 drug Substances 0.000 claims description 21
- 239000000975 dye Substances 0.000 claims description 18
- 229940079593 drug Drugs 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 238000010168 coupling process Methods 0.000 claims description 14
- 238000005859 coupling reaction Methods 0.000 claims description 14
- -1 C24 saturated fatty acid Chemical class 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 230000008878 coupling Effects 0.000 claims description 10
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000004615 ingredient Substances 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- 239000012875 nonionic emulsifier Substances 0.000 claims description 4
- 239000002243 precursor Substances 0.000 claims description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 2
- 125000005233 alkylalcohol group Chemical group 0.000 claims 1
- 239000006103 coloring component Substances 0.000 claims 1
- 239000000982 direct dye Substances 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 33
- 229910021529 ammonia Inorganic materials 0.000 description 16
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 12
- 210000003128 head Anatomy 0.000 description 11
- 239000002253 acid Substances 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 6
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 210000004761 scalp Anatomy 0.000 description 5
- VOQAOTALYZIMDB-UHFFFAOYSA-N 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl hydrogen sulfate Chemical compound OCCOCCOCCOCCOS(O)(=O)=O VOQAOTALYZIMDB-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- OJLOUXPPKZRTHK-UHFFFAOYSA-N dodecan-1-ol;sodium Chemical compound [Na].CCCCCCCCCCCCO OJLOUXPPKZRTHK-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 3
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 3
- 125000006353 oxyethylene group Chemical group 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- 229940075142 2,5-diaminotoluene Drugs 0.000 description 2
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 2
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
- 229940018563 3-aminophenol Drugs 0.000 description 2
- HVYWMOMLDIMFJA-UHFFFAOYSA-N 3-cholesterol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 HVYWMOMLDIMFJA-UHFFFAOYSA-N 0.000 description 2
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 description 2
- GPJJASIJVRXZFI-UHFFFAOYSA-N 4-methoxybenzene-1,3-diol Chemical compound COC1=CC=C(O)C=C1O GPJJASIJVRXZFI-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 206010000496 acne Diseases 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000002496 gastric effect Effects 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
- NKNCGBHPGCHYCQ-UHFFFAOYSA-N (2,5-diaminophenyl)methanol Chemical compound NC1=CC=C(N)C(CO)=C1 NKNCGBHPGCHYCQ-UHFFFAOYSA-N 0.000 description 1
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 1
- HHVMYUPMJJDVPG-UHFFFAOYSA-N 1-(2,5-diaminophenyl)ethanol Chemical compound CC(O)C1=CC(N)=CC=C1N HHVMYUPMJJDVPG-UHFFFAOYSA-N 0.000 description 1
- AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 description 1
- NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
- KWSVXCAQFTWTEF-UHFFFAOYSA-N 2-(2,5-diaminophenyl)ethanol Chemical compound NC1=CC=C(N)C(CCO)=C1 KWSVXCAQFTWTEF-UHFFFAOYSA-N 0.000 description 1
- DAGCJJZWDAVKRE-UHFFFAOYSA-N 2-(4-amino-3-nitroanilino)ethanol Chemical compound NC1=CC=C(NCCO)C=C1[N+]([O-])=O DAGCJJZWDAVKRE-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- IXQGCWUGDFDQMF-UHFFFAOYSA-N 2-Ethylphenol Chemical class CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 1
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- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 description 1
- ALQKEYVDQYGZDN-UHFFFAOYSA-N 2-amino-6-methylphenol Chemical compound CC1=CC=CC(N)=C1O ALQKEYVDQYGZDN-UHFFFAOYSA-N 0.000 description 1
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- HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 description 1
- XRMTWJAJYBZYLZ-UHFFFAOYSA-N 4-(1-hydroxyethoxy)benzene-1,3-diol Chemical compound CC(O)OC1=CC=C(O)C=C1O XRMTWJAJYBZYLZ-UHFFFAOYSA-N 0.000 description 1
- BOTGCZBEERTTDQ-UHFFFAOYSA-N 4-Methoxy-1-naphthol Chemical compound C1=CC=C2C(OC)=CC=C(O)C2=C1 BOTGCZBEERTTDQ-UHFFFAOYSA-N 0.000 description 1
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 description 1
- NLMQHXUGJIAKTH-UHFFFAOYSA-N 4-hydroxyindole Chemical compound OC1=CC=CC2=C1C=CN2 NLMQHXUGJIAKTH-UHFFFAOYSA-N 0.000 description 1
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 description 1
- BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- JSFUMBWFPQSADC-UHFFFAOYSA-N Disperse Blue 1 Chemical compound O=C1C2=C(N)C=CC(N)=C2C(=O)C2=C1C(N)=CC=C2N JSFUMBWFPQSADC-UHFFFAOYSA-N 0.000 description 1
- 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 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 206010019049 Hair texture abnormal Diseases 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241001072332 Monia Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Chemical compound OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
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- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
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- ZBWXLMQZILBRLB-UHFFFAOYSA-N anthracene-9,10-dione 1,4-diaminoanthracene-9,10-dione Chemical compound C1=CC=CC=2C(C3=CC=CC=C3C(C12)=O)=O.NC1=CC=C(C=2C(C3=CC=CC=C3C(C12)=O)=O)N ZBWXLMQZILBRLB-UHFFFAOYSA-N 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
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- 239000000987 azo dye Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
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- 238000005516 engineering process Methods 0.000 description 1
- PMNYTGAGAKEGJE-UHFFFAOYSA-N ethane-1,2-diamine;sodium Chemical compound [Na].[Na].NCCN PMNYTGAGAKEGJE-UHFFFAOYSA-N 0.000 description 1
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- GGNQRNBDZQJCCN-UHFFFAOYSA-N hydroxyhydroquinone Natural products OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000001005 nitro dye Substances 0.000 description 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
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- 150000007524 organic acids Chemical class 0.000 description 1
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- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
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- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- GUQPDKHHVFLXHS-UHFFFAOYSA-M sodium;2-(2-dodecoxyethoxy)ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOS([O-])(=O)=O GUQPDKHHVFLXHS-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000007447 staining method Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
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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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
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Abstract
(57)【要約】本公報は電子出願前の出願データであるため要約のデータは記録されません。 (57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 液状発色剤と乳化状の酸化剤含有組成物から成る酸化染毛剤、並びに毛髪の酸化 染色法 本発明は、液状発色剤、およびC1゜ないしC24の天然あるいは合成脂肪族ア ルコールの少なくとも一種2.5ないし12重量パーセントと酸化剤とを含有す る乳化状組成物を、それぞれ1:1.5ないし1:4の割合で、混合することに よって得られる毛髪の酸化染色剤、並びに毛髪の酸化染色法に関する。[Detailed description of the invention] Oxidizing hair dye consisting of a liquid coloring agent and an emulsified oxidizing agent-containing composition, and hair oxidation staining method The present invention provides a liquid coloring agent and a C1 to C24 natural or synthetic aliphatic aliphatic aliphatic acid. containing 2.5 to 12 weight percent of at least one alcohol and an oxidizing agent. The emulsified compositions are mixed in a ratio of 1:1.5 to 1:4, respectively. The present invention relates to an oxidative dyeing agent for hair obtained thereby, and a method for oxidative dyeing hair.
毛髪の酸化染色剤は従来と同様今日においても毛髪処理分野において非常に重要 な構成要素である。これは二つの成分からなっている。これらの成分は使用直前 に混合して、被処理毛髪に塗布される。Hair oxidation dyes are as important today as ever in the field of hair treatment. It is a component. It consists of two components. These ingredients should be prepared immediately before use. It is mixed with and applied to the hair to be treated.
第一成分、すなわち発色剤は発色作用を有する物質を含有する。これは液体、ゲ ルあるいはエマルジ1ンの形態で提供されている。第二成分は適当な酸化剤を含 有し、水溶液、クリームあるいは粉末の形態で提供されている。The first component, ie, the coloring agent, contains a substance that has a coloring effect. This is a liquid, It is available in the form of a bottle or an emulsion. The second component contains a suitable oxidizing agent. It is available in the form of an aqueous solution, cream or powder.
この場合染色は適当な酸化剤、たとえば過酸化水素の存在下に特定の顕色成分と 特定のカップリング成分を反応させることによって行われる。顕色成分としてお もに1.4−ジアミノベンゼン、2.5−ジアミノトルエン、2.5−ジアミノ フェニルエタノール、4−アミノフェノールおよび4−アミノ−3−メチルフェ ノールが用いられている。カップリング成分に対しては、たとえばレゾルシン、 4−クロルレゾルシン、ごま油、2−メチルレゾルシン、3−アミノフェノール 、4− (2’−ヒドロキシエチル)アミノ−1,2−メチレンジオキシベンゼ ンおよび2−アミノ−4−(2°−ヒドロキシエチルアミノ)−アニソールが一 般的に用いられている。In this case, the dyeing is carried out using a specific developer component in the presence of a suitable oxidizing agent, for example hydrogen peroxide. This is done by reacting specific coupling components. As a color developing component 1,4-diaminobenzene, 2,5-diaminotoluene, 2,5-diamino Phenylethanol, 4-aminophenol and 4-amino-3-methylphenol Nord is used. For coupling components, for example, resorcinol, 4-chlorresorcin, sesame oil, 2-methylresorcin, 3-aminophenol , 4-(2'-hydroxyethyl)amino-1,2-methylenedioxybenze and 2-amino-4-(2°-hydroxyethylamino)-anisole are Commonly used.
発色剤は、若干の国において、たとえば米国において、液状のものが主体的に用 いられている。出版物の中においても液状の発色剤がかなり重要視されている。In some countries, for example in the United States, liquid coloring agents are mainly used. I'm tired. Liquid coloring agents are given considerable importance in publications.
これは、これに含まれる原料物質が価格的に手にいれやすいという利点、および 液状物は技術的に製造しやすいという利点を持っている。This is due to the advantages that the raw materials contained in this product are easily available in terms of price, and Liquid materials have the advantage of being technically easy to manufacture.
染色を実施するに当たって液状発色剤は通常過酸化水素水溶液と、たとえば1: 1あるいはl:2の割合で、混合して用いられる。発色剤と過酸化水素水溶液の 混合物は、たとえば塗布用のびんに注入して製造され、製造後直ちに被染色毛髪 に塗布される。In carrying out dyeing, the liquid coloring agent is usually a hydrogen peroxide aqueous solution and, for example, 1: They are used as a mixture at a ratio of 1:1 or 1:2. Color former and hydrogen peroxide solution The mixture is prepared, for example, by pouring it into an application bottle and immediately applied to the hair to be dyed. is applied to.
しかし液状発色剤は大きな欠点を持っている。すなわち液状発色剤は過酸化水素 溶液と混合するとたちまちのうちに黒ずんでしまう。また、この酸化染毛剤の塗 布された毛髪は、染毛剤と接触しながら、非常にゆっくりと染色される。しかし 酸化染毛剤がすでに黒色化されているために、染毛剤は早すぎる時点で洗い流さ れてしまいがちであり、その結果毛髪上における作用時間が短すぎ、所望の濃度 に染色されないという欠陥が生じる。However, liquid color formers have major drawbacks. In other words, the liquid coloring agent is hydrogen peroxide. When mixed with a solution, it quickly turns black. Also, the application of this oxidative hair dye The clothed hair is dyed very slowly while in contact with the hair dye. but The hair dye may be washed out too early because the oxidative hair dye is already blackened. As a result, the action time on the hair is too short and the desired concentration is not achieved. A defect occurs in that the dye is not dyed.
さらに一般的に使用されている液状発色剤は、含有されているアンモニアをきわ めて容易に放出するために、不快な臭いに悩まされるという難点もある。そのほ かにも液状染毛剤は、特に明るい色調のものは、頭皮に望ましくない刺激を与え ることが知られている。そこで本発明は、毛髪の酸化染色において、公知の液状 発色剤における上記のような欠点を示さない液状発色剤を基本とする酸化染毛剤 を提供すること、並びにその酸化染毛剤による毛髪の酸化染色法を提供すること を課題として出発した。Furthermore, commonly used liquid coloring agents contain ammonia that is extremely strong. It also has the disadvantage of producing an unpleasant odor because it is easily released. That way Liquid hair dyes, especially those in light shades, can cause unwanted irritation to the scalp. It is known that Therefore, the present invention utilizes a known liquid method for oxidative hair dyeing. An oxidative hair dye based on a liquid color former that does not exhibit the above-mentioned drawbacks of color formers. and a method for oxidative dyeing hair using the oxidative hair dye. I set out with this as a challenge.
そしてここに、液状発色剤に酸化剤含有乳化状組成物を混合することによって得 られる酸化染毛剤が、頭皮に対して全く問題がなく、また酸化剤混合後早い段階 において染色結果に悪影響を及ぼすような黒ずみを呈することがなく、さらに公 知の染毛剤に比べて放出アンモニアによる不快臭が格段に少ないことが見い出さ れた。Here, the liquid color former is obtained by mixing an oxidizing agent-containing emulsified composition. The oxidizing hair dye that is used in this product does not cause any problems to the scalp, and it can be used at an early stage after mixing the oxidizing agent. It does not cause any darkening that would adversely affect the staining results, and it is It was found that the unpleasant odor caused by released ammonia was significantly lower than that of Chino's hair dye. It was.
すなわち本発明は、成分(A)、すなわち摂氏30度において100mPa、s 以下の粘度を示す液状発色剤、および成分(B)、すなわちCIOないL−Ct −の天然あるいは合成脂肪族アルコールの少なくとも一種2.5ないし12重量 パーセントと酸化剤を含有する乳化状組成物を、成分(A):成分(B) −1 :1.5ないし1:4の重量割合で、混合することによって得られる毛髪の酸化 染色剤を特徴とする 特に本発明による染色剤の望ましい実施形態は成分(A):成分(B)の重量割 合が1:2ないしに3のものである。液状発色剤の粘度はハーケ粘度計を用いて (ロッドII、5グラム)、摂氏30度において測定されたものである。That is, the present invention provides component (A), that is, 100 mPa, s at 30 degrees Celsius. A liquid coloring agent having a viscosity of - from 2.5 to 12% by weight of at least one natural or synthetic aliphatic alcohol; Component (A): Component (B)-1 : Hair oxidation obtained by mixing in a weight ratio of 1.5 to 1:4. Features a dye In particular, a preferred embodiment of the dyeing agent according to the present invention is a component (A):component (B) weight ratio. The ratio is 1:2 to 3. The viscosity of the liquid coloring agent is measured using a Haake viscometer. (Rod II, 5 grams), measured at 30 degrees Celsius.
乳化状の酸化剤含有成分(B)に含まれる天然あるいは合成脂肪族アルコールは CI4ないしC2゜の脂肪族アルコールであることが望ましい。成分(B)中に 含み得る脂肪族アルコールとして、たとえばセチルアルコールおよびステアリル アルコールおよびこれらの混合物を挙げることができる。The natural or synthetic aliphatic alcohol contained in the emulsified oxidizing agent-containing component (B) is Preferably, it is an aliphatic alcohol of CI4 to C2°. In component (B) Aliphatic alcohols which may include, for example, cetyl alcohol and stearyl Mention may be made of alcohols and mixtures thereof.
成分(B)は酸化剤を1ないし18重量パーセント、特に好ましくは4ないし1 4重量パーセント含有する。毛髪染色の顕色用の酸化剤としては、特に過酸化水 素、あるいは、その尿素、メラニンおよびほう酸ナトリウムに対する付加化合物 を挙げることができる。成分(B)は、中でも特に過酸化水素を1ないし18重 量パーセント含有することが望ましい。Component (B) contains oxidizing agent in an amount of 1 to 18% by weight, particularly preferably 4 to 1% by weight. Contains 4% by weight. As an oxidizing agent for color development in hair dyeing, peroxide water is especially recommended. or its adducts to urea, melanin and sodium borate can be mentioned. Component (B) especially contains 1 to 18 hydrogen peroxide. It is desirable to contain the amount percent.
成分(A)は、2ないし30重量パーセント、特に望ましくは8ないし16重量 パーセントの、天然あるいは合成の、CIOないしcga、特に望ましくはCI 6ないしC22の飽和あるいは不飽和の脂肪酸を、単独あるいは混合で、含有す る。成分(A)中に含み得るこのような脂肪酸として、たとえばエルカ酸、ミリ スチン酸、リシノール酸、ラウリン酸、バルミチン酸、およびオレイン酸を挙げ ることができる。これらの脂肪酸は、アンモニアを添加することによってアンモ ニエウム塩の形で本発明による染毛剤に溶解させることが望ましい。しかしアン モニアの代わりに、脂肪族アミン、たとえばモノエタノールアミンを使用するこ ともできる。Component (A) is present in an amount of 2 to 30% by weight, particularly preferably 8 to 16% by weight. percentage of natural or synthetic CIO or cga, particularly preferably CI 6 to C22 saturated or unsaturated fatty acids, singly or in combination. Ru. Such fatty acids that may be included in component (A) include, for example, erucic acid, Lists stinic acid, ricinoleic acid, lauric acid, valmitic acid, and oleic acid. can be done. These fatty acids can be converted to ammonia by adding ammonia. It is advisable to dissolve it in the hair dye according to the invention in the form of a nieum salt. But Ann Instead of monia, aliphatic amines such as monoethanolamine can be used. Can also be done.
成分(A)は、この他に低分子量の、CIないしC6のアルコール、Czないし C6のグリコール、たとえばエタノール、プロパツール、イソプロパツール、エ チレングリコール、1.2−プロピレングリコールあるいはブチルグリコール、 あるいはこれらの混合物を、2ないし30重量パーセント、望ましくは12ない し28重量パーセント含有し得る。In addition to this, component (A) also includes low molecular weight alcohols of CI or C6, Cz or C6 glycols, such as ethanol, propatool, isopropateol, tylene glycol, 1,2-propylene glycol or butyl glycol, Alternatively, the mixture may contain 2 to 30 weight percent, preferably 12 to 30 percent by weight. It may contain up to 28 weight percent.
成分(A)は、この他に更に非イオン系乳化剤を0.1ないし25重量パーセン ト含有し得る。特に望ましくは、本発明の染毛剤は非イオン系乳化剤を10ない し20重量パーセント含有する。用いることのできる非イオン系乳化剤として、 特にオキシエチル化したC0゜ないしC2゜の脂肪族アルコールあるいはCbな いしCI4のアルキル基を有するオキシエチル化アルキルフェノールあるいはこ れらの混合物を挙げることができる。成分(A)中に含有される脂肪族アルコー ルおよびアルキルフェノールは1ないし8個の、望ましくは1ないし6個のエチ レンオキサイド単位によってオキシエチル化されている。Component (A) further contains 0.1 to 25% by weight of a nonionic emulsifier. It may contain Particularly preferably, the hair dye of the present invention contains less than 10% of a nonionic emulsifier. Contains 20% by weight. Nonionic emulsifiers that can be used include In particular, oxyethylated C0° to C2° aliphatic alcohols or Cb Oxyethylated alkylphenol having an alkyl group of CI4 or this Mention may be made of mixtures thereof. Aliphatic alcohol contained in component (A) and alkylphenols contain 1 to 8, preferably 1 to 6 ethylphenols. Oxyethylated by ren oxide units.
成分(A)は、少な(とも一種類のカップリング成分と少なくとも一種類の顕色 成分、並びに必要に応じて補助的に自己カップリングし得る染料前駆体および毛 髪に直接染着し得る染料を含有する。カップリング成分および顕色成分は、染毛 剤中に、そのままの形態で、あるいは生理学上問題のない無機酸あるいは有機酸 との塩の形態で、たとえば塩化物、硫酸塩、燐酸塩、酢酸塩、プロピオン酸塩、 乳酸塩、あるいはクエン酸塩の形態で、用いられる。Component (A) contains a small amount (one kind of coupling component and at least one kind of color developing component). components and optionally auxiliary self-coupling dye precursors and hairs. Contains dyes that can be applied directly to hair. The coupling component and color developing component are used for hair dyeing. Contains inorganic or organic acids in their original form or without physiological problems. in the form of salts such as chlorides, sulfates, phosphates, acetates, propionates, It is used in the form of lactate or citrate.
カップリング成分は通常顕色成分に関してほぼ等モル量使用される。等モル量使 用することが明らかに合目的であるが、かりにカップリング成分がある程度過剰 であっても、あるいは過少であっても全く問題はない。またカップリング成分お よび顕色成分は単一製品である必要はなく、顕色成分が公知の顕色成分の混合物 であり、さらにカップリング成分が公知のカンプリング成分の混合物であっても 差し支えない。The coupling component is usually used in approximately equimolar amounts with respect to the color developing component. equimolar amount Although it is clearly a good idea to use There is no problem even if it is more or less than that. Also, the coupling component The color developer and color developer do not need to be a single product, and the color developer may be a mixture of known color developer components. and furthermore, even if the coupling component is a mixture of known camping components. No problem.
液状発色剤、すなわち成分(A)は、たとえば公知のカンプリング成分のなかで 、特に1−ナフトール、4−メトキシ−1−ナフトール、レゾルシン、4−クロ ルレゾルシン、4.6−ジクロルレゾルシン、2−メチルレゾルシン、3−アミ ノフェノール、4−ヒドロキシ−1,2−メチレンジオキシベンゼン、4−アミ ノ−1,2−メチレンジオキシベンゼン、4−(β〜ヒドロキシエチルアミノ) −1,2−メチレンジオキシベンゼン、4−ヒドロキシインドール、5−ヒドロ キシ−ベンゾジオキソール−(1,3”)、5−アミノ−ベンゾジオキソール− (1,3) 、 5− ((2−ヒドロキシエチル)アミノ)ベンゾジオキソー ル−(1,3)、および5−アミノ−2−メチルフェノールを、単独あるいは組 み合わせて含有する。この他に適するカップリング成分として、たとえば2,4 −ジヒドロキシアニソールおよび2.4−ジヒドロキシフェノキシエタノールの ような2.4−ジヒドロキシフェノールエーテルを挙げることができる。The liquid coloring agent, that is, component (A), is, for example, one of the known camping ingredients. , especially 1-naphthol, 4-methoxy-1-naphthol, resorcinol, 4-chloro Luresorcin, 4.6-dichlorresorcin, 2-methylresorcin, 3-ami Nophenol, 4-hydroxy-1,2-methylenedioxybenzene, 4-aminophenol No-1,2-methylenedioxybenzene, 4-(β~hydroxyethylamino) -1,2-methylenedioxybenzene, 4-hydroxyindole, 5-hydro xy-benzodioxole-(1,3”), 5-amino-benzodioxole- (1,3), 5-((2-hydroxyethyl)amino)benzodioxo (1,3) and 5-amino-2-methylphenol, singly or in combination. Contains both. Other suitable coupling components include, for example, 2,4 -dihydroxyanisole and 2,4-dihydroxyphenoxyethanol Examples include 2,4-dihydroxyphenol ethers such as
公知の顕色成分のなかで本発明の染毛剤成分として、特に1.4−ジアミノベン ゼン、2.5−ジアミノトルエン、2.5−ジアミノアニソール、2,5−ジア ミノベンジルアルコール、3−メチル−4−アミノフェノール、2−(β−ヒド ロキシエチル) −1,4−ジアミノベンゼン、テトラアミノピリミジン、2− (2’、5’−ジアミノフェニル)−エタノール、および4−アミノフェノー ルを挙げることができる。Among known color developing components, 1,4-diaminoben is particularly suitable as a hair dye component of the present invention. zene, 2,5-diaminotoluene, 2,5-diaminoanisole, 2,5-dia Minobenzyl alcohol, 3-methyl-4-aminophenol, 2-(β-hydro (oxyethyl) -1,4-diaminobenzene, tetraminopyrimidine, 2- (2',5'-diaminophenyl)-ethanol, and 4-aminophenol can be mentioned.
公知の毛髪染色用酸化剤の中で、成分(A)に適用することのできるものとして 、特にイー、ザガリンの1嘗“化粧品、科学と技術”、インチ−サイエンス・パ ブリッシャー・インコーホレイテッド、ニューヨーク(1957) 、503− 504 K、並びにエフチー ジャニスチンの1嘗“化粧品および香料ハンドブ ック” (1973)、338−339頁に記載のものを挙げることができる。Among the known oxidizing agents for hair dyeing, those that can be applied to component (A) include: , especially the first volume of Yi Zagarin's "Cosmetics, Science and Technology", Inch-Science Pa. Brisher Incorporated, New York (1957), 503- 504K and F.C. Janistine's 1st edition "Cosmetic and Fragrance Handbags" (1973), pp. 338-339.
成分(A)中に含有される顕色成分とカップリング成分の合計量は0.01ない し12.0重量パーセント、特に望ましくは0.2ないし4.0重量パーセント である所望の色合いを1′lるために上記の他にさらに一般に用いられているt i接染料、たとえばダイアモンド・ツクシン(C,1,42510) #よびレ ザー・ルビーHF(C。The total amount of color developing component and coupling component contained in component (A) is less than 0.01. 12.0% by weight, particularly preferably 0.2 to 4.0% by weight In addition to the above, t is commonly used to obtain a desired shade of 1'l. i-address dyes, such as diamond tuxin (C, 1, 42510) # and The Ruby HF (C.
1.42520)のようなトリフェニルメタン染料、2−アミノ−4,6−シニ トローフエノール、2−ニトロ−4−(β−ヒドロキシエチルアミノ)アニリン 、2−N−β−ジヒドロキシプロピルアミノ−5−(N−メチル、N−ヒドロキ シエチル)アミノ−ニトロベンゼンおよび2−アミノ−4−ニトロフェ・ノール のような芳香族ニトロ染料、アシッド・ブラウン4 (C,1,14805)お よびアシッド・ブルー135 (C,1,13385)のようなアゾ染料、ディ スパース・バイオレット4 (C,1,61105) 、ディスパース・ブルー 1 (C,!、64500) 、ディスパース・レッド15 (C,1,607 10) 、ディスパース・バイオレット1 (C,161100) 、さらに1 .4,5.8−テトラアミノアンスラキノンおよび1.4−ジアミノアンスラキ ノンのようなアンスラキノン染料を成分(A)に添加して用いることができる。triphenylmethane dyes such as 1.42520), 2-amino-4,6-cin Trophenol, 2-nitro-4-(β-hydroxyethylamino)aniline , 2-N-β-dihydroxypropylamino-5-(N-methyl, N-hydroxy ethyl)amino-nitrobenzene and 2-amino-4-nitrophenol Aromatic nitro dyes such as Acid Brown 4 (C, 1, 14805) and and azo dyes such as Acid Blue 135 (C, 1, 13385). Sparse Violet 4 (C, 1, 61105), Disperse Blue 1 (C,!, 64500), Disperse Red 15 (C, 1,607 10), Disperse Violet 1 (C, 161100), and 1 .. 4,5.8-tetraaminoanthraquinone and 1,4-diaminoanthraquinone Anthraquinone dyes such as NON can be added to component (A).
成分(A)はこの他にさらに自己カップリングてきる染料前駆体、たとえば2− アミノ−5−メチルフェノール、2−アミノ−6−メチルフェノール、2−アミ ノ−5−エトキシフェノール、さらには2−プロピルアミノ−5−アミノピリジ ンを含有しI5る。成分(八)中における!L接染料および自己カップリング染 料の合計量は0.Olないし7.0重量パーセント、望ましくは0.2ないし4 .0!l量パーセントである。Component (A) may also contain a dye precursor capable of self-coupling, such as 2- Amino-5-methylphenol, 2-amino-6-methylphenol, 2-amino Nor-5-ethoxyphenol and also 2-propylamino-5-aminopyridi Contains I5. Ingredient (8) in! L-attached dyes and self-coupling dyes The total amount of fees is 0. Ol to 7.0 weight percent, preferably 0.2 to 4 .. 0! 1 amount percent.
さらに成分(A)には、アスコルビン酸、レゾルシンあるいは亜硫酸ナトリウム のような酸化防止剤、およびエチレンジアミンテトラアセテートあるいはニトリ ロ酢酸のような重金属に対する錯化合物形成物質が、0.5重量パーセント以下 の割合で含有され1脣る。香油は本発明による染毛剤中にl[fパーセント以下 の量において含イfされ)!lる。成分(A)はこの他、湿潤剤、乳化剤、保護 剤、カチオン性樹脂、さらには一般に用いられている添加剤を含有し得る。In addition, component (A) includes ascorbic acid, resorcinol, or sodium sulfite. antioxidants such as ethylenediaminetetraacetate or nitride Contains less than 0.5 percent by weight of complex-forming substances for heavy metals, such as acetic acid. It is contained in a proportion of 1. The perfume oil may be present in the hair dye according to the invention in an amount of not more than 1[f%]. (contained in the amount of )! Ill. Ingredient (A) also contains wetting agents, emulsifiers, and protectants. agents, cationic resins, and even commonly used additives.
ここにおいて採用しているmuバーセン)Iは完成品中における数値ではなく、 それぞれ成分(A)ないしは成分(B)に関する数値である。The mu base) I adopted here is not the numerical value in the finished product, Each is a numerical value related to component (A) or component (B).
成分(八)および成分(B)を本発明による混合割合で混合することによって得 られる完成品は、毛髪を酸化染色するに当たって、酸性、中性あるいはアルカリ 性に調整され得る0毛髪の酸化染色に適用するに当たって、本発明による薬剤の PI[け7.5ないし12.0の範囲にあることが望ましい。obtained by mixing component (8) and component (B) in the mixing ratio according to the present invention. The finished product is suitable for acid, neutral or alkaline dyeing when hair is oxidized. The use of the agent according to the invention in its application to the oxidative dyeing of naturally adjustable hair It is desirable that the PI is in the range of 7.5 to 12.0.
上に述べた酸化染毛剤は本発明の方法に従って使用する。すなわちまず使用直前 に液状発色III(成分A)と過酸化水素乳化物(成分B)を本発明による!1 置温合割合、すなわち1:1.5ないし1:4の割合で混合し、ついでこの混合 物を被染色毛髪に対して充分な菫、毛髪の多少に応じて通常90ないし160g を塗布する。混合物は毛髪に対して摂氏15ないし50度において約5ないし6 0分間、望ましく1よ30分間作用させる。その復水で洗い流し、必要に応じて ジャンプおよびリンスを行い、乾燥する。The oxidative hair dyes mentioned above are used according to the method of the invention. In other words, immediately before use Liquid coloring III (component A) and hydrogen peroxide emulsion (component B) according to the present invention! 1 Mix at an incubation ratio of 1:1.5 to 1:4, and then Add enough violet to the hair to be dyed, usually 90 to 160g depending on the amount of hair. Apply. The mixture is applied to the hair at a temperature of about 5 to 6 degrees Celsius. Allow to act for 0 minutes, preferably 1 to 30 minutes. Rinse with condensate water and use as necessary. Jump, rinse and dry.
次に実施例に従って本発明の対象をさらに詳しく説明する。Next, the object of the present invention will be explained in more detail according to examples.
実施例 実施例1:明色染色用酸化染毛剤 液状発色剤(成分A) エルカ酸 12.0 g エチレンオキサイド4モルで オキシエチル化したノニルフェノール i5.o gパラ−フェニレンジアミン 0.05 t<レゾルシン 0.07 g ナトリウムラウリルアルコールー ジグリコールエーテルサルフヱートの28%水溶液5.0gエチレンジアミンテ トラ@酸のジナトリウム塩 1.0gエタノール 25.0 g 水 23.43 g 25%のアンモニア −■」−L ioo、o g 過酸化水素乳化物(成分B) セチルステアリルアルコール 10.0 gコレステリン 1.5g ナトリウムラウリルアルコール− ジグリコールエーテルサルフヱートの28%水溶液 4.0g35%の過酸化水 素 35.0 g 香料 0.3g 使用直前に上記の液状発色剤40gと過酸化水素乳化物80gを混合する(この 場合混合割合は1:2である)、この混合物120gを中褐色の入毛に塗布し、 室温において20分間作用させる0次いで染毛剤を水で洗い流し、乾燥させる、 この処理によって毛髪は根元から毛先まで均一に明るい褐色に染色される0本発 明による毛髪の酸化染色用薬剤は、二つの成分を混ぜ合わせた後においてもほと んど黒ずむことがなく、アンモニア臭も極わずかであり、さらに皮膚に対して全 く問題を示さない。Example Example 1: Oxidized hair dye for bright color dyeing Liquid coloring agent (component A) Erucic acid 12.0g 4 moles of ethylene oxide Oxyethylated nonylphenol i5. o g para-phenylenediamine 0.05 t<Resorcinol 0.07 g sodium lauryl alcohol 5.0 g of 28% aqueous solution of diglycol ether sulfate Disodium salt of tra@acid 1.0g Ethanol 25.0g Water 23.43g 25% ammonia -■"-L ioo, o g Hydrogen peroxide emulsion (component B) Cetylstearyl alcohol 10.0g Cholesterin 1.5g Sodium lauryl alcohol 28% aqueous solution of diglycol ether sulfate 4.0g 35% peroxide water Bare 35.0g Fragrance 0.3g Immediately before use, mix 40 g of the above liquid color former and 80 g of hydrogen peroxide emulsion (this (mixing ratio is 1:2), apply 120g of this mixture to medium brown hair, Leave to act for 20 minutes at room temperature. Then rinse the hair dye with water and dry. This process dyes the hair uniformly bright brown from root to tip. The agent for oxidative dyeing of hair by light remains almost unchanged even after the two ingredients are mixed together. It does not darken the skin, has very little ammonia odor, and is totally harmless to the skin. Does not show any problems.
実施例2:酸化染′r:、削 液状発色剤(成分式) エルカ酸 12.0 g エチレンオキサイド4モルで オキシエチル化したノニルフェノール 15.0 gナトリウムラウリルアルコ ールー ジグリコールエーテルサルフヱートの28%水熔WI3.Ogエチレンジアミン テトラ酊酸0・1g アスコルビン醇 0.3g 2.5−ジアミノトルエン硫酸塩 2.8gレゾルシン 1.OR −アミノフェノール 0.4g 2−アミノ−4=(2°−ヒドロキシ−エチルアミノ)アニソールW酸塩 0. 2゜25%のアンモニア 10・2g エタノール 16.0 g 過酸化水素乳化物(B) セチルステアリルアルコール 10.0 gコレステリン 1.5 g ナトリウムラウリルアルコールー ジグリコールエーテルサルフヱートの28%水tsWI 4.0g35%の過酸 化水素 17.0 g 香料 0.3g 使用直前に上記の液状発色剤40gと過酸化水素乳化物80gを混合する(この 場合混合割合は1:2である)、この混合物120gを灰色の入毛に塗布し、室 温において20分間作用させる0次いで染毛剤を水で洗い流し、毛髪を乾燥させ る0本発明による毛髪の酸化染色用!li剤は、はとんどアンモニア臭を呈する ことがなく、また酸化剤を混合した後も黒ずみをほとんど示さず、さらに皮膚に 対して全く問題がない、上記の処理によって毛髪はIlf掲色に均一に染色され る。Example 2: Oxidation dyeing Liquid coloring agent (component formula) Erucic acid 12.0g 4 moles of ethylene oxide Oxyethylated nonylphenol 15.0g sodium lauryl alcohol -Lou Diglycol ether sulfate 28% water melt WI3. Og ethylene diamine Tetraxic acid 0.1g Ascorbic liquor 0.3g 2.5-diaminotoluene sulfate 2.8g resorcinol 1. OR -Aminophenol 0.4g 2-amino-4=(2°-hydroxy-ethylamino)anisole W salt 0. 2.25% ammonia 10.2g Ethanol 16.0g Hydrogen peroxide emulsion (B) Cetylstearyl alcohol 10.0 g Cholesterin 1.5 g sodium lauryl alcohol Diglycol ether sulfate 28% water tsWI 4.0g 35% peracid Hydrogen chloride 17.0g Fragrance 0.3g Immediately before use, mix 40 g of the above liquid color former and 80 g of hydrogen peroxide emulsion (this (mixing ratio is 1:2), apply 120g of this mixture to gray hair and leave it indoors. Let it work for 20 minutes at a warm temperature.Then wash off the hair dye with water and let the hair dry. For oxidative dyeing of hair according to the present invention! Lime agents usually have an ammonia odor. There is no darkening, and there is almost no darkening even after mixing with oxidizing agents, and it does not irritate the skin. With the above treatment, the hair is uniformly dyed in Ilf color without any problem. Ru.
′X施例3二酸化染毛剤 液状発色剤($、分八へ オレイン酸 12.00 g エチレンオキサイF4モルで オキシエチル化したノニルフェノール 15.00 g純エタノール 16.0 0 g ナトリウムラウリルアルコール− ジグリコールエーテルサルフェートの28%水i液5.00 gエチレンジアミ ンテトラ酢酸の二ナトリウム塩 0.10gアスコルビン酸 0.30 g 2.5−ジアミノトルエン硫酸塩 0.60 gレゾルシン 0.30 g −アミノフェノール 0.02 g 25%アンモニア 12.00 g 水 −団り四Lt 100.00 g 使用直前に上記の液状発色剤40gと実施例2に記載の過酸化水素乳化物(成分 B)80gを混合する(この場合混合割合は1:2である)、この混合物120 gを灰色の入毛に塗布し、室温において20分間作用させる。次いで染毛剤を水 で洗い流し、毛髪を乾燥させる。本発明による毛髪の酸化染色用の薬剤は、はと んどアンモニア臭を呈することがな(、また酸化剤を混合した後も黒ずみをほと んど示さず、さらに皮膚に対して全く問題がない、上記の処理によって灰色の毛 髪は明るいブロンド色に均一に染色される。'X Example 3 Dioxide hair dye Liquid coloring agent ($, 80%) Oleic acid 12.00g 4 moles of ethylene oxy F Oxyethylated nonylphenol 15.00g Pure ethanol 16.0 0g Sodium lauryl alcohol 28% aqueous solution of diglycol ether sulfate 5.00 g ethylenediamine Disodium salt of tetraacetic acid 0.10g Ascorbic acid 0.30g 2.5-diaminotoluene sulfate 0.60 g Resorcinol 0.30 g -Aminophenol 0.02g 25% ammonia 12.00g Wed - Group 4 Lt 100.00g Immediately before use, add 40 g of the above liquid color former and the hydrogen peroxide emulsion (components) described in Example 2. B) Mix 80 g (in this case the mixing ratio is 1:2), 120 g of this mixture g is applied to gray hair and left to act for 20 minutes at room temperature. Then add the hair dye to water. Rinse and dry hair. The agent for oxidative dyeing of hair according to the present invention is No ammonia odor (and no blackheads even after mixing with oxidizing agent) The above treatment removes gray hair, which does not show any signs of aging and also has no problem with the skin. The hair is uniformly dyed a light blonde color.
比較実験A:明色染色における皮膚への影響本発明による酸化染毛剤と従来公知 の酸化染毛剤の皮膚への影響を比較するために実験を行った。まず中温色の毛髪 を有する10人の被験者のそれぞれの左頭部の毛髪に対して、実施例1に記載の 液状発色剤20gと一般に用いられている下記組成の過酸化水素組成物40gを 混合することによって製造される従来公知の普通の酸化染毛剤を、塗布する。Comparative experiment A: Effect on the skin during bright color dyeing Oxidized hair dye according to the present invention and conventionally known hair dye An experiment was conducted to compare the effects of oxidative hair dyes on the skin. First, medium-tone hair The method described in Example 1 was applied to the hair on the left side of each of the 10 subjects with 20g of liquid color former and 40g of commonly used hydrogen peroxide composition with the following composition. A conventional oxidative hair dye prepared by mixing is applied.
一般に用いられている過酸化水素組成物35%の過酸化水素 35.0 g 水 62.0 g メタアクリル酸とポリエチレングリコールステアリルエーテルの共重合物、ただ しこれはアクリル酸、メタアクリル酸、あるいはこれらの単一エステルから成る 七ツマ−を一個以上含有し、さらにポリエチレングリコールステアリルエーテル は分岐オキシエチレン単位を含む −」副」 100.0 g 次ぎに上記の被験者の右頭部の毛髪に対してそれぞれ、実施例1によって得られ る本発明による酸化染毛剤60gを、塗布する。ここで胃薬剤を毛髪ないし頭皮 上において室温において20分間作用させる。次いで薬剤を水で洗い流し、毛髪 をジャンプし、すすぎ、乾燥させる。Commonly used hydrogen peroxide composition 35% hydrogen peroxide 35.0 g Water 62.0g Copolymer of methacrylic acid and polyethylene glycol stearyl ether, just This is composed of acrylic acid, methacrylic acid, or a single ester thereof. Contains one or more seven-terminals, and further contains polyethylene glycol stearyl ether contains a branched oxyethylene unit -"sub" 100.0g Next, each of the hairs on the right head of the above subject was obtained according to Example 1. 60 g of the oxidative hair dye according to the invention are applied. Here, the gastric drug is applied to the hair or scalp. Leave to act for 20 minutes at room temperature. Next, wash off the drug with water and apply it to your hair. Jump, rinse and dry.
両酸化染毛剤作用中皮験者達は、本発明による染毛剤で処理した右頭部の皮膚に 比べて、左頭部の皮膚にひりひりする非常に強い痛みを感じた。Effects of both oxidative hair dyesMesodermal testers found that the skin on the right side of the head treated with the hair dye according to the present invention In comparison, I felt a very strong tingling pain in the skin on the left side of my head.
胃酸化染毛剤を水洗後、30%の被験者の左頭皮が非常に赤くなり、異常が生じ ていることが認められた。本発明による薬剤によって頭皮が赤くなった被験者は 一人もいなかった。After washing the gastric oxidation hair dye with water, the left scalp of 30% of the subjects became extremely red and abnormalities occurred. It was recognized that Subjects whose scalp became red due to the drug according to the present invention There wasn't a single person.
比較実験の結果、本発明による酸化染毛剤が皮膚に対して問題がなく、非常に優 れていることが認められた。As a result of comparative experiments, the oxidative hair dye according to the present invention has no problems with the skin and is very good. It was recognized that
比較実験B:薬剤のアンモニア臭 本発明による酸化染毛剤によって生じるアンモニア臭による不快感と従来一般に 用いられている酸化染毛剤によって生じるアンモニア臭による不快感を比較する ために、比較実験を行った。Comparative experiment B: Ammonia odor of medicine Discomfort due to ammonia odor caused by the oxidative hair dye of the present invention and conventional Compare the discomfort caused by ammonia odor caused by the oxidative hair dyes used For this purpose, we conducted a comparative experiment.
まず実施例2に記載の液状発色剤20gを従来一般に用いられている下記組成の 過酸化水素組成物40gと混合することによって、従来一般に用いられている酸 化染毛剤を製造する。First, 20 g of the liquid coloring agent described in Example 2 was mixed with the following composition, which is commonly used in the past. By mixing with 40g of hydrogen peroxide composition, the commonly used acid Manufactures chemical hair dye.
一般に用いられている過酸化水素組成物35%の過酸化水素 17.0 g 水 81.5 g メタアクリル酸とポリエチレングリコールステアリルエーテルの共重合物、ただ しこれはアクリル酸、メタアクリル酸、あるいはこれらの単一エステルから成る 七ツマ−を一個以上含有し、さらにポリエチレングリコールステアリルエーテル は分校オキシエチレン単位を含む −」」」 100.0 g この酸化染毛剤60gを、白髪の頭髪を有する10人の被験者の左頭部にそれぞ れ塗布する。Commonly used hydrogen peroxide composition 35% hydrogen peroxide 17.0 g Water 81.5g Copolymer of methacrylic acid and polyethylene glycol stearyl ether, just This is composed of acrylic acid, methacrylic acid, or a single ester thereof. Contains one or more seven-terminals, and further contains polyethylene glycol stearyl ether contains branch oxyethylene units ””” 100.0g 60g of this oxidative hair dye was applied to the left side of the head of 10 subjects with gray hair. Apply it.
比較のために、実施例2によって得られる本発明による酸化染毛剤60gを、上 記の被験者の右頭部にそれぞれ塗布する。For comparison, 60 g of the oxidative hair dye according to the invention obtained according to Example 2 were Apply each to the right side of the head of the subject listed below.
次いで20分間作用させる。この作用時間の間に両薬剤におけるアンモニア臭に 対して評価を行う。It is then allowed to act for 20 minutes. During this period of action, the ammonia odor in both drugs Evaluate the results.
実験を実施した理容姉達の評価はすべて同じであった。すなわち本発明による酸 化染毛剤によって処理した右頭部はほとんどアンモニア臭がしなかったのに対し て、左頭部は放出アンモニアによって非常に強い刺激臭があった。The barber sisters who conducted the experiment all gave the same evaluation. i.e. the acid according to the invention Whereas the right side of the head treated with chemical hair dye had almost no ammonia odor. The left side of his head had a very strong pungent odor due to released ammonia.
比較実験C:二成分混合による黒ずみ さらに、本発明による実施例3によって得られる酸化染毛剤と従来一般に用いら れている酸化染毛剤において、二成分混合後における薬剤の黒ずみに関して、比 較実験を行った。Comparative experiment C: Darkening due to two-component mixture Furthermore, the oxidative hair dye obtained according to Example 3 according to the present invention and the conventionally commonly used Regarding the darkening of the drug after mixing the two components, there is a comparative A comparison experiment was conducted.
まず実施例3に記載の液状発色剤20gを従来一般に用いられている下記組成の 過酸化水素組成物40gと混合することによって、従来一般に用いられている酸 化染毛剤を製造する。First, 20 g of the liquid coloring agent described in Example 3 was mixed with the following composition, which is commonly used in the past. By mixing with 40g of hydrogen peroxide composition, the commonly used acid Manufactures chemical hair dye.
一般に用いられている過酸化水素組成物35%の過酸化水素 17.0 g 水 81.5g メタアクリル酸とポリエチレングリコールステアリルエーテルの共重合物、ただ しこれはアクリル酸、メタアクリル酸、あるいはこれらの単一エステルから成る 七ツマ−を一個以上含有し、さらにポリエチレングリコールステアリルエーテル は分校オキシエチレン単位を含む −」Jl loo、0 g 上記の混合物60gを、白髪の毛髪を有する10人の被験者の左頭部にそれぞれ 塗布する。他方有頭部に、実施例3によって得られる本発明による酸化染毛剤6 0gをそれぞれ塗布する。次いで室温において20分の作用時間を置(。この間 に両薬剤の黒ずみに関して理容師による評価を行う。Commonly used hydrogen peroxide composition 35% hydrogen peroxide 17.0 g Water 81.5g Copolymer of methacrylic acid and polyethylene glycol stearyl ether, just This is composed of acrylic acid, methacrylic acid, or a single ester thereof. Contains one or more seven-terminals, and further contains polyethylene glycol stearyl ether contains a branch oxyethylene unit -”Jl loo, 0g 60g of the above mixture was applied to the left head of each of 10 subjects with gray hair. Apply. On the other head, the oxidative hair dye 6 according to the invention obtained according to Example 3 Apply 0g each. Then leave the action for 20 minutes at room temperature (during this time The darkening caused by both drugs will be evaluated by a barber.
比較実験の結果、左頭部に塗布した従来一般に用いられている酸化染毛剤と遣っ て、右頭部に塗布した本発明による酸化染毛剤は実質的にほとんど黒ずみを示さ なかった。このように本発明による酸化染毛剤はほとん゛ど黒ずみを示さないの で、確実に望み通りの染色結果を得ることができる。これに対して従来一般に用 いられている酸化染毛剤の場合、二成分混合後急速に黒ずみが生じるために、染 色進行度合の判定に狂いが生じ、望み通りの染色濃度を得ることができないこと がしばしばであった。本発明による薬剤によればこのような間違いを避けること ができる。As a result of a comparative experiment, it was found that the conventional oxidative hair dye applied to the left side of the head and the Therefore, the oxidative hair dye according to the present invention applied to the right side of the head showed virtually no darkening. There wasn't. In this way, the oxidative hair dye according to the present invention hardly causes any darkening. This will ensure that you get the desired staining result. In contrast, conventionally In the case of conventional oxidative hair dyes, darkening occurs rapidly after mixing the two components, so the dye Failure to obtain the desired dye density due to errors in determining the degree of color progression was often the case. With the drug according to the invention such mistakes can be avoided Can be done.
本明細書に記載のパーセント数はすべて重量パーセント数である。All percentages herein are weight percentages.
要約書 本発明の対象は、摂氏30度において100mPa、s以下の粘度を示す液状発 色剤と、CIGないしCzaの天然あるいは合成脂肪族アルコールの少なくとも 一種2゜5ないし12重量パーセントと酸化剤とを含有する乳化状組成物を、1 :1.5ないし1:4の割合で、混合することによって得られる毛髪の酸化染色 剤、並びに1.この薬剤を使用して毛髪を酸化染色する方法である。abstract The object of the present invention is a liquid vapor having a viscosity of 100 mPa, s or less at 30 degrees Celsius. At least a coloring agent and a natural or synthetic aliphatic alcohol such as CIG or Cza. An emulsified composition containing 2.5 to 12 weight percent of one species and an oxidizing agent, : Oxidative dyeing of hair obtained by mixing in a ratio of 1.5 to 1:4 agent, and 1. This is a method of oxidatively dyeing hair using this chemical.
この新規な薬剤は、液状発色剤、特に酸化染毛剤において起こりがちな染色効果 を低下する黒ずみやアンモニア放出による臭いの問題を防止し、しかも良好な皮 膚適合性を示す。This new agent eliminates the dyeing effects that tend to occur with liquid coloring agents, especially oxidative hair dyes. Reduces blackheads and prevents odor problems caused by ammonia release, while maintaining good skin Shows skin compatibility.
国際調査報告international search report
Claims (13)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4005008.4 | 1990-02-19 | ||
DE19904005008 DE4005008C2 (en) | 1990-02-19 | 1990-02-19 | Oxidative hair colorant from a liquid color carrier mass and an emulsion-type, oxidant-containing composition and method for the oxidative dyeing of hair |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04505459A true JPH04505459A (en) | 1992-09-24 |
JPH0662395B2 JPH0662395B2 (en) | 1994-08-17 |
Family
ID=6400392
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3503700A Expired - Lifetime JPH0662395B2 (en) | 1990-02-19 | 1991-02-04 | Oxidative hair dye comprising liquid colorant and emulsified oxidant-containing composition, and oxidative hair dyeing method |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPH0662395B2 (en) |
DE (1) | DE4005008C2 (en) |
WO (1) | WO1991011985A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09110658A (en) * | 1995-09-19 | 1997-04-28 | L'oreal Sa | Composition for dyeing keratin fiber containing substance p antagonist |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
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DE4332965A1 (en) * | 1993-09-28 | 1995-03-30 | Wella Ag | An oxidation hair dye comprising a cream-colored dye carrier mass and a preparation containing a polymer and an oxidizing agent, and a process for the oxidative dyeing of hair |
DE19604932A1 (en) * | 1996-02-10 | 1997-08-14 | Wella Ag | Oxidation hair dye |
FR2751533B1 (en) | 1996-07-23 | 2003-08-15 | Oreal | COMPOSITION OF OXIDIZING DYE FOR KERATINIC FIBERS CONTAINING A NON-IONIC AMPHIPHILIC POLYMER |
FR2753093B1 (en) * | 1996-09-06 | 1998-10-16 | Oreal | COMPOSITION OF OXIDIZING DYE FOR KERATINIC FIBERS CONTAINING AN ANIONIC AMPHIPHILIC POLYMER |
DE19827434C2 (en) * | 1998-06-19 | 2000-08-17 | Goldwell Gmbh | Hair dyes and processes for their preparation |
DE19847224C2 (en) * | 1998-10-14 | 2001-02-08 | Goldwell Gmbh | Process for the preparation of stable hair coloring emulsions |
FR2788975B1 (en) | 1999-01-29 | 2002-08-09 | Oreal | AQUEOUS READY-TO-USE KERATIN FIBER DECOLORING COMPOSITION COMPRISING THE ASSOCIATION OF A WATER-SOLUBLE SOLVENT AND A NON-IONIC OR ANIONIC AMPHIPHILIC POLYMER COMPRISING AT LEAST ONE FAT CHAIN |
ATE270088T1 (en) * | 1999-12-17 | 2004-07-15 | Unilever Nv | HAIR BLEACHING AND HAIR DYEING PREPARATION WITH A PH GREATER THAN PH 10 AND CONTAINING CHOLESTEROL |
FR2817468B1 (en) * | 2000-12-04 | 2005-05-06 | Oreal | COMPOSITION FOR THE OXIDATION DYE OF KERATIN FIBERS COMPRISING GYLCERIN AND POLYOL DIFFERENT FROM GLYCERIN IN A GIVEN REPORT |
KR100850223B1 (en) * | 2002-07-31 | 2008-08-04 | 가부시키가이샤 아리미노 | Emulsified compositions for bleaching or dyeing the hair and methods of bleaching or dyeing the hair using these emulsified compositions |
US7608116B2 (en) | 2002-12-24 | 2009-10-27 | L'oreal S.A. | Oxidation dye composition comprising at least one mesomorphic phase, process for preparing it and ready-to-use composition for dyeing keratin materials |
FR2848841B1 (en) * | 2002-12-24 | 2005-03-11 | Oreal | COLORING COMPOSITION CONTAINING A MESOMORPHIC PHASE AND PROCESS FOR PREPARING THE SAME, COMPOSITION READY FOR USE IN DYING KERATINIC MATERIALS |
ITTN20050005A1 (en) * | 2005-04-05 | 2006-10-06 | Antonio Arcelli | CHEMICAL PROCEDURE FOR THE REDUCTION OF TOXIC AND IRRITANT VAPORS CAUSED BY AMMONIA BY THE USE OF COLORING CREAMS OR DECOLORING HAIR. |
FR2925311B1 (en) | 2007-12-21 | 2009-12-18 | Oreal | PROCESS FOR LIGHTENING HUMAN KERATINOUS FIBERS USING ANHYDROUS COMPOSITION AND A PARTICULAR ORGANIC AMINE AND APPROPRIATE DEVICE |
FR2940090B1 (en) | 2008-12-19 | 2011-02-25 | Oreal | OXIDIZING COMPOSITION FOR THE TREATMENT OF KERATIN FIBERS COMPRISING OIL, FATTY ALCOHOL AND OXYALKYLENE FATTY ALCOHOL |
FR2940107B1 (en) | 2008-12-19 | 2011-03-18 | Oreal | PROCESS FOR LIGHTENING KERATINIC MATERIALS USING AN EMULSION COMPRISING AN ALKALI AGENT AND AN OXIDIZING COMPOSITION |
FR2940067B1 (en) | 2008-12-19 | 2011-02-25 | Oreal | OXIDIZING COMPOSITION FOR THE TREATMENT OF KERATIN FIBERS COMPRISING A CATIONIC POLYMER, A FATTY AMIDE AND AN OXYGEN AGENT |
FR2942704B1 (en) * | 2009-03-04 | 2011-09-02 | Oreal | DEVICE FOR DISPENSING A TINCTORIAL COMPOSITION FOR KERATIN FIBERS AND ASSOCIATED METHOD. |
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JPS61130209A (en) * | 1984-11-30 | 1986-06-18 | Sunstar Inc | Hair dye |
JPH01213220A (en) * | 1988-02-22 | 1989-08-28 | Hoou Kk | Hair dye composition |
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FR2421606A1 (en) * | 1978-04-06 | 1979-11-02 | Oreal | TWO-STAGE KERATINIC FIBER DYING PROCESS |
ZA836137B (en) * | 1982-08-30 | 1984-12-24 | Bristol Myers Co | Oxidative hair dye composition |
DE3423589A1 (en) * | 1984-06-27 | 1986-01-09 | Wella Ag, 6100 Darmstadt | OXIDATION HAIR COLORING AGENT BASED ON A LOW-VISCOSE WEIGHT |
DE3508309A1 (en) * | 1985-03-08 | 1986-09-11 | Henkel KGaA, 4000 Düsseldorf | Hair colouring compositions |
US4776855A (en) * | 1986-03-19 | 1988-10-11 | Clairol Inc. | Hair dyeing process and composition |
DE3625916A1 (en) * | 1986-07-31 | 1988-02-04 | Wella Ag | OXIDATION HAIR COLORING AGENT BASED ON A GEL-SHAPED WEIGHT AND METHOD FOR COLORING HAIR |
DE3732147A1 (en) * | 1987-09-24 | 1989-04-06 | Henkel Kgaa | EMULSION-SHAPED HYDROGEN PEROXIDE PREPARATIONS FOR BLONDING AND OXIDATIVE COLORING OF THE HAIR |
DE3834142A1 (en) * | 1988-10-07 | 1990-04-12 | Wella Ag | Storage-stable oxidation hair dye in cream form with high dye/electrolyte content |
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1990
- 1990-02-19 DE DE19904005008 patent/DE4005008C2/en not_active Revoked
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1991
- 1991-02-04 JP JP3503700A patent/JPH0662395B2/en not_active Expired - Lifetime
- 1991-02-04 WO PCT/EP1991/000204 patent/WO1991011985A1/en unknown
Patent Citations (2)
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JPS61130209A (en) * | 1984-11-30 | 1986-06-18 | Sunstar Inc | Hair dye |
JPH01213220A (en) * | 1988-02-22 | 1989-08-28 | Hoou Kk | Hair dye composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09110658A (en) * | 1995-09-19 | 1997-04-28 | L'oreal Sa | Composition for dyeing keratin fiber containing substance p antagonist |
Also Published As
Publication number | Publication date |
---|---|
DE4005008A1 (en) | 1991-08-22 |
DE4005008C2 (en) | 1995-01-05 |
WO1991011985A1 (en) | 1991-08-22 |
JPH0662395B2 (en) | 1994-08-17 |
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