JP5214079B2 - Hair dye composition - Google Patents
Hair dye composition Download PDFInfo
- Publication number
- JP5214079B2 JP5214079B2 JP2000397218A JP2000397218A JP5214079B2 JP 5214079 B2 JP5214079 B2 JP 5214079B2 JP 2000397218 A JP2000397218 A JP 2000397218A JP 2000397218 A JP2000397218 A JP 2000397218A JP 5214079 B2 JP5214079 B2 JP 5214079B2
- Authority
- JP
- Japan
- Prior art keywords
- hair
- hair dye
- weight
- dye
- 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.)
- Expired - Fee Related
Links
- 239000000118 hair dye Substances 0.000 title claims description 31
- 239000000203 mixture Substances 0.000 title claims description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 229920001577 copolymer Polymers 0.000 claims description 16
- -1 polyoxyethylene Polymers 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 9
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- 150000005215 alkyl ethers Chemical class 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- 229920006318 anionic polymer Polymers 0.000 claims description 5
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 3
- 125000005907 alkyl ester group Chemical group 0.000 claims description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims 1
- 238000004043 dyeing Methods 0.000 description 17
- 239000000975 dye Substances 0.000 description 16
- 230000001590 oxidative effect Effects 0.000 description 16
- 230000000694 effects Effects 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 8
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 238000002156 mixing Methods 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000000982 direct dye Substances 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- NLMKTBGFQGKQEV-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hexadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO NLMKTBGFQGKQEV-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
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 2
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 2
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 229940106010 beheneth-25 Drugs 0.000 description 2
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 229940056318 ceteth-20 Drugs 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000013583 drug formulation Substances 0.000 description 2
- VFPFQHQNJCMNBZ-UHFFFAOYSA-N ethyl gallate Chemical compound CCOC(=O)C1=CC(O)=C(O)C(O)=C1 VFPFQHQNJCMNBZ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 239000003051 hair bleaching agent Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- FBSFWRHWHYMIOG-UHFFFAOYSA-N methyl 3,4,5-trihydroxybenzoate Chemical compound COC(=O)C1=CC(O)=C(O)C(O)=C1 FBSFWRHWHYMIOG-UHFFFAOYSA-N 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 239000001026 semi permanent hair color Substances 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZBTRTXLGWIKSMO-UHFFFAOYSA-N (4-aminophenyl)sulfamic acid Chemical compound NC1=CC=C(NS(O)(=O)=O)C=C1 ZBTRTXLGWIKSMO-UHFFFAOYSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 1
- OQWWMUWGSBRNMA-UHFFFAOYSA-N 1-(2,4-diaminophenoxy)ethanol Chemical compound CC(O)OC1=CC=C(N)C=C1N OQWWMUWGSBRNMA-UHFFFAOYSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- 229940113489 2,4-diaminophenoxyethanol Drugs 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- HQCHAOKWWKLXQH-UHFFFAOYSA-N 2,6-Dichloro-para-phenylenediamine Chemical compound NC1=CC(Cl)=C(N)C(Cl)=C1 HQCHAOKWWKLXQH-UHFFFAOYSA-N 0.000 description 1
- OJXKOMJUERKEHW-UHFFFAOYSA-N 2-(2,3-diamino-4-methoxyphenyl)ethanol Chemical compound COC1=CC=C(CCO)C(N)=C1N OJXKOMJUERKEHW-UHFFFAOYSA-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
- WFXLRLQSHRNHCE-UHFFFAOYSA-N 2-(4-amino-n-ethylanilino)ethanol Chemical compound OCCN(CC)C1=CC=C(N)C=C1 WFXLRLQSHRNHCE-UHFFFAOYSA-N 0.000 description 1
- VLZVIIYRNMWPSN-UHFFFAOYSA-N 2-Amino-4-nitrophenol Chemical compound NC1=CC([N+]([O-])=O)=CC=C1O VLZVIIYRNMWPSN-UHFFFAOYSA-N 0.000 description 1
- DOPJTDJKZNWLRB-UHFFFAOYSA-N 2-Amino-5-nitrophenol Chemical compound NC1=CC=C([N+]([O-])=O)C=C1O DOPJTDJKZNWLRB-UHFFFAOYSA-N 0.000 description 1
- ISCYHXYLVTWDJT-UHFFFAOYSA-N 2-[4-amino-n-(2-hydroxyethyl)anilino]ethanol Chemical compound NC1=CC=C(N(CCO)CCO)C=C1 ISCYHXYLVTWDJT-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- MGLZGLAFFOMWPB-UHFFFAOYSA-N 2-chloro-1,4-phenylenediamine Chemical compound NC1=CC=C(N)C(Cl)=C1 MGLZGLAFFOMWPB-UHFFFAOYSA-N 0.000 description 1
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 1
- HVHNMNGARPCGGD-UHFFFAOYSA-N 2-nitro-p-phenylenediamine Chemical compound NC1=CC=C(N)C([N+]([O-])=O)=C1 HVHNMNGARPCGGD-UHFFFAOYSA-N 0.000 description 1
- ICIDSZQHPUZUHC-UHFFFAOYSA-N 2-octadecoxyethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCO ICIDSZQHPUZUHC-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- DGRGLKZMKWPMOH-UHFFFAOYSA-N 4-methylbenzene-1,2-diamine Chemical compound CC1=CC=C(N)C(N)=C1 DGRGLKZMKWPMOH-UHFFFAOYSA-N 0.000 description 1
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 1
- RAUWPNXIALNKQM-UHFFFAOYSA-N 4-nitro-1,2-phenylenediamine Chemical compound NC1=CC=C([N+]([O-])=O)C=C1N RAUWPNXIALNKQM-UHFFFAOYSA-N 0.000 description 1
- DPIZKMGPXNXSGL-UHFFFAOYSA-N 4-nitro-1,3-phenylenediamine Chemical compound NC1=CC=C([N+]([O-])=O)C(N)=C1 DPIZKMGPXNXSGL-UHFFFAOYSA-N 0.000 description 1
- YGRFRBUGAPOJDU-UHFFFAOYSA-N 5-(2-hydroxyethylamino)-2-methylphenol Chemical compound CC1=CC=C(NCCO)C=C1O YGRFRBUGAPOJDU-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
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000004262 Ethyl gallate Substances 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- WACJWPASJLIZCD-UHFFFAOYSA-M [Cl-].OCCC[N+](C)(C)CCCO Chemical compound [Cl-].OCCC[N+](C)(C)CCCO WACJWPASJLIZCD-UHFFFAOYSA-M 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- 235000019277 ethyl gallate Nutrition 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- LRBQNJMCXXYXIU-QWKBTXIPSA-N gallotannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@H]2[C@@H]([C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-QWKBTXIPSA-N 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 229940040102 levulinic acid Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- IBKQQKPQRYUGBJ-UHFFFAOYSA-N methyl gallate Natural products CC(=O)C1=CC(O)=C(O)C(O)=C1 IBKQQKPQRYUGBJ-UHFFFAOYSA-N 0.000 description 1
- 239000001005 nitro dye Substances 0.000 description 1
- 239000001006 nitroso dye Substances 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- 239000001024 permanent hair color Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 1
- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 description 1
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940100459 steareth-20 Drugs 0.000 description 1
- 229940073743 steareth-20 methacrylate Drugs 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 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
- 229960004418 trolamine Drugs 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229940075420 xanthine Drugs 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Coloring (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は染毛剤に関するもので、詳しくは、毛髪の柔軟性、しっとり感あるいは滑らかさを向上させ、かつ染色堅牢性に優れる染毛剤組成物に関するものである。 The present invention relates to a hair dye, and more particularly to a hair dye composition that improves the flexibility, moist feeling or smoothness of hair and is excellent in dyeing fastness.
従来より、染毛剤としては酸化染料中間体を含有する第1剤と、酸化剤を含有する第2剤よりなる二剤型の酸化染毛剤が広く利用されている。この酸化染毛剤は、無色の低分子の酸化染料中間体を毛髪中に浸透させ、毛髪内部で酸化重合を行わせることにより色素を生成させて染着させるものである。これらの酸化染毛剤は要望に応じた種々の色調に毛髪を染色することができ、しかもその染毛力も優れているので非常に便利なものである。 Conventionally, two-component oxidative hair dyes comprising a first agent containing an oxidative dye intermediate and a second agent containing an oxidant have been widely used as hair dyes. In this oxidative hair dye, a colorless low molecular weight oxidative dye intermediate is infiltrated into hair, and oxidative polymerization is performed inside the hair to produce a dye and dye it. These oxidation hair dyes are very convenient because they can dye hair in various colors according to demands, and also have excellent hair dyeing power.
しかしながら、従来の酸化染毛剤では、染毛処理によって毛髪が損傷しがちであったため、毛髪のつややうるおいがなくなったり、染め上がりが不自然な色となり第三者に違和感を与えたり、また、櫛通りが悪く、髪のしなやかさがなくなるといった課題があった。これらの課題を解決するために、しばしば、カチオン性ポリマーが用いられることがあるが、カチオン性ポリマーのみを配合した場合、毛髪との親和性が高いため、過剰に作用して毛髪にゴワつきやパサつきが生じることもあり、十分な解決には至っていない。 However, with conventional oxidative hair dyes, the hair tends to be damaged by the hair dyeing treatment, so that the gloss and moisture of the hair disappears, the dyed color becomes unnatural and gives a strange feeling to a third party, There was a problem that the comb was bad and the hair was not supple. In order to solve these problems, a cationic polymer is often used. However, when only a cationic polymer is blended, it has a high affinity with hair, so it acts excessively and becomes irritating to the hair. It may not be enough to solve the problem.
従って、毛髪のつやや柔軟性を向上させ、さらに自然な染め上がりと十分な堅牢性が得られる染毛剤の開発が望まれていた。 Accordingly, there has been a demand for the development of a hair dye that improves the gloss and flexibility of the hair and that provides a natural dyeing and sufficient fastness.
【課題を解決するための手段】本発明者は、上記実状を鑑み鋭意研究を重ねた結果、両性高分子化合物であるアクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体と、特定のアニオン性高分子化合物とを組み合わせることにより、上記課題が解決されることを見出し、本発明を完成するに至った。以下、本発明についてさらに詳細に説明する。 Means for Solving the Problems The present inventor has made extensive studies in view of the above-mentioned circumstances, and as a result, has found that an amphoteric polymer acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer and a specific anionic high The present inventors have found that the above problems can be solved by combining with a molecular compound, and have completed the present invention. Hereinafter, the present invention will be described in more detail.
【発明の実施の形態】本発明の染毛剤組成物は、両性高分子化合物であるアクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体と、特定のアニオン性高分子化合物を必須とする。さらに酸化染料と酸化剤を配合した組成物が酸化染毛剤組成物であり、酸化染料を配合しなければ毛髪脱色剤となる。また直接染料のみを用いた半永久染毛剤として利用することもできる。 BEST MODE FOR CARRYING OUT THE INVENTION The hair dye composition of the present invention essentially comprises an amphoteric polymer acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer and a specific anionic polymer compound. Further, a composition containing an oxidative dye and an oxidant is an oxidative hair dye composition, and if no oxidative dye is added, it becomes a hair bleaching agent. It can also be used as a semi-permanent hair dye using only a direct dye.
本発明の染毛剤組成物は、両性高分子化合物を必須とするが、両性高分子化合物としては、両性ターポリマーであるアクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体が好ましく、具体的には、ポリクォータニウム39(Polyquaternium-39)として知られ、マーコートプラス3330,3331(カルゴン社製)として市販されている化合物が挙げられる。 Although the amphoteric polymer compound is essential for the hair dye composition of the present invention, the amphoteric polymer compound is preferably an amphoteric terpolymer acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer. Is known as Polyquaternium-39 and is commercially available as Marquat Plus 3330, 3331 (Calgon).
その配合量は0.05〜10重量%、好ましくは0.1〜5重量%である。0.05重量%未満であると十分な効果が得られず、10重量%を超えてもそれ以上効果が上がらない。 The amount of that from 0.05 to 10% by weight, preferably 0.1 to 5 wt%. If it is less than 0.05% by weight, a sufficient effect cannot be obtained, and if it exceeds 10% by weight, the effect is not further improved.
アニオン性高分子化合物は、(a)イタコン酸とポリオキシエチレンアルキルエーテルとの半エステルまたはメタクリル酸とポリオキシエチレンアルキルエーテルとのエステル、及び(b)アクリル酸、メタクリル酸およびそれらのアルキルエステルから選ばれる少なくとも一つのモノマーから成る共重合体から選ばれる1種以上である。これらの化合物は、具体的には例えばAcrylates/Ceteth−20 Itaconate Copolymer、Acrylates/Steareth−20 Itaconate Copolymer、Acrylates/Beheneth−25 Itaconate Copolymer、Acrylates/Ceteth−20Methacrylate Copolymer、Acrylates/Steareth−20 Methacrylate CopolymerあるいはAcrylates/Beheneth−25 Methacrylate Copolymerという名称で知られる。 The anionic polymer compound comprises : ( a) a half ester of itaconic acid and polyoxyethylene alkyl ether or an ester of methacrylic acid and polyoxyethylene alkyl ether; and (b) acrylic acid, methacrylic acid and their alkyl esters. It is at least one selected from a copolymer comprising at least one monomer selected. These compounds, specifically, for example Acrylates / Ceteth-20 Itaconate Copolymer, Acrylates / Steareth-20 Itaconate Copolymer, Acrylates / Beheneth-25 Itaconate Copolymer, Acrylates / Ceteth-20Methacrylate Copolymer, Acrylates / Steareth-20 Methacrylate Copolymer or Acrylates / Beheneth-25 is known under the name of Methacrylate Copolymer.
その配合量は、過酸化水素の安定性に支障のない範囲で配合ができ、好ましくは、0.05〜20重量%であり、経済面から0.1〜10重量%が特に望ましい。 The blending amount can be blended within a range that does not hinder the stability of hydrogen peroxide, preferably 0.05 to 20% by weight, and particularly preferably 0.1 to 10% by weight from the economical aspect.
本発明の染毛剤組物を永久染毛剤とする場合、通常、酸化染料とアルカリ剤を配合した第1剤と、酸化剤を配合した第2剤からなる多剤型の酸化染毛剤組成物となる。そして第1剤に酸化染料を配合しなければ毛髪脱色剤として機能する。 When the hair dye assembly of the present invention is used as a permanent hair dye, it is usually a multi-component oxidative hair dye comprising a first agent containing an oxidizing dye and an alkaline agent and a second agent containing an oxidizing agent. It becomes a composition. And if an oxidation dye is not mix | blended with a 1st agent, it will function as a hair bleaching agent.
第1剤に配合する酸化染料は、通常、主要中間体とカプラーに分けられる。主要中間体としては、フェニレンジアミン類、アミノフェノール類、ジアミノピリジン類等及びそれらの塩類の1種又は2種以上が挙げられる。塩類としては塩酸塩、硫酸塩、酢酸塩等が挙げられる。これらの中でもp−フェニレンジアミン、トルエン−2,5−ジアミン、N,N−ビス(β−ヒドロキシエチル)−p−フェニレンジアミン、2−β−ヒドロキシエチル−p−フェニレンジアミン、N−β−ヒドロキシエチル−N−エチル−p−フェニレンジアミン、N−フェニル−p−フェニレンジアミン、4,4’−ジアミノジフェニルアミン、2−クロロ−p−フェニレンジアミン、N,N−ジメチル−p−フェニレンジアミン、p−アミノフェノール、o−アミノフェノール、p−メチルアミノフェノール、2,6−ジクロロ−p−フェニレンジアミン、p−アミノフェニルスルファミン酸、2,5−ジアミノピリジン及びそれらの塩類が効果および染毛力の点から好ましい。その配合量は染毛用第1剤の全重量に対して0.01〜15重量%であり、0.01重量%よりも少ないと十分な染毛効果が得られず、15重量%を超えても、その効果は変わらず経済的ではない。さらには0.1重量%〜10重量%が好ましく、0.1重量%以上配合することにより、より優れた染毛効果が得られる。一方、10重量%を超えた場合は染毛効果の上昇は少なくなる。 The oxidation dye blended in the first agent is usually divided into a main intermediate and a coupler. Examples of the main intermediate include one or more of phenylenediamines, aminophenols, diaminopyridines, and the like and salts thereof. Examples of the salt include hydrochloride, sulfate, acetate and the like. Among these, p-phenylenediamine, toluene-2,5-diamine, N, N-bis (β-hydroxyethyl) -p-phenylenediamine, 2-β-hydroxyethyl-p-phenylenediamine, N-β-hydroxy Ethyl-N-ethyl-p-phenylenediamine, N-phenyl-p-phenylenediamine, 4,4'-diaminodiphenylamine, 2-chloro-p-phenylenediamine, N, N-dimethyl-p-phenylenediamine, p- Aminophenol, o-aminophenol, p-methylaminophenol, 2,6-dichloro-p-phenylenediamine, p-aminophenylsulfamic acid, 2,5-diaminopyridine and salts thereof are effective and hair dyeing power To preferred. The blending amount is 0.01 to 15% by weight with respect to the total weight of the first agent for hair dyeing, and if it is less than 0.01% by weight, sufficient hair dyeing effect cannot be obtained and exceeds 15% by weight. However, the effect remains the same and is not economical. Furthermore, 0.1 weight%-10 weight% are preferable, and the more superior hair dyeing effect is acquired by mix | blending 0.1 weight% or more. On the other hand, when it exceeds 10% by weight, the increase in the hair dyeing effect is reduced.
また、カプラーとしては、レゾルシン、ピロガロール、カテコール、m−アミノフェノール、m−フェニレンジアミン、2,4−ジアミノフェノール、1,2,4−ベンゼントリオール、トルエン−3,4−ジアミン、トルエン−2,4−ジアミン、ハイドロキノン、α−ナフトール、2,6−ジアミノピリジン、1,5−ジヒドロキシナフタレン、5−アミノ−o−クレゾール、ジフェニルアミン、p−メチルアミノフェノール、フロログルシン、2,4−ジアミノフェノキシエタノール、没食子酸、タンニン酸、没食子酸エチル、没食子酸メチル、没食子酸プロピル、五倍子、1−メトキシ−2−アミノ−4−(2−ヒドロキシエチル)アミノベンゼン、5−(2−ヒドロキシエチルアミノ)−2−メチルフェノ−ル等及びそれらの塩を配合することができる。この配合量は0.01〜10重量%であり、0.01重量%よりも少ないと十分な染色性が得られず、10重量%を超えても、その効果は変わらず経済的ではない。さらには、0.1重量%〜5重量%が好ましく、0.1重量%以上配合することにより、より優れた染色性が得られる。一方、5重量%を超えた場合は染色性の上昇は少なくなる。その他、「医薬部外品原料規格」(1991年6月発行,薬事日報社)に収載されたものも適宜、用いることができる。 As couplers, resorcin, pyrogallol, catechol, m-aminophenol, m-phenylenediamine, 2,4-diaminophenol, 1,2,4-benzenetriol, toluene-3,4-diamine, toluene-2, 4-diamine, hydroquinone, α-naphthol, 2,6-diaminopyridine, 1,5-dihydroxynaphthalene, 5-amino-o-cresol, diphenylamine, p-methylaminophenol, phloroglucin, 2,4-diaminophenoxyethanol, gallic acid Acid, tannic acid, ethyl gallate, methyl gallate, propyl gallate, pentaploid, 1-methoxy-2-amino-4- (2-hydroxyethyl) aminobenzene, 5- (2-hydroxyethylamino) -2- Methylphenol etc. and their salts It is possible to focus. The blending amount is 0.01 to 10% by weight, and if it is less than 0.01% by weight, sufficient dyeability cannot be obtained, and even if it exceeds 10% by weight, the effect is not changed and it is not economical. Furthermore, 0.1 weight%-5 weight% is preferable, and the more outstanding dyeability is obtained by mix | blending 0.1 weight% or more. On the other hand, when it exceeds 5% by weight, the increase in dyeability is reduced. In addition, those listed in "Quasi-drug raw material standards" (issued in June 1991, Yakuji Nippo) can be used as appropriate.
さらに、本発明の染毛剤には調色剤として直接染料が配合でき、タール系色素や天然色素などの公知のものを1種又は2種以上併用できる。その中でも、ニトロ系染料、アゾ染料、ニトロソ染料、トリフェニルメタン染料、キサンチン染料、キノリン染料、アントラキノン染料又はインジゴ染料が、良好な染毛効果を得られ好ましく、また、これらの染料を染毛剤組成物中に0.01〜10重量%配合するのが最も良い。0.01重量%より少ない場合、染毛効果は不十分であり、逆に10重量%より多い場合には、染毛力が向上しないばかりか頭皮、手指への染着が著しくなり望ましくない。 Furthermore, the hair dye of the present invention can be blended with a direct dye as a toning agent, and one or more known ones such as tar-based pigments and natural pigments can be used in combination. Among them, nitro dyes, azo dyes, nitroso dyes, triphenylmethane dyes, xanthine dyes, quinoline dyes, anthraquinone dyes or indigo dyes are preferable because they give a good hair dyeing effect, and these dyes are used as hair dyes. It is best to blend 0.01 to 10% by weight in the composition. When the amount is less than 0.01% by weight, the hair dyeing effect is insufficient. On the other hand, when the amount is more than 10% by weight, not only the hair dyeing power is not improved, but also the dyeing to the scalp and fingers is remarkable.
直接染料の具体例としては、ニトロ−p−フェニレンジアミン、p−ニトロ−O−フェニレンジアミン、p−ニトロ−m−フェニレンジアミン、2−アミノ−4−ニトロフェノ−ル、2−アミノ−5−ニトロフェノ−ル、ピクラミン酸、それらの塩および「医薬品等に使用することができるタール色素を定める省令」(昭和41年告示、厚生省)により定められた染料が挙げられる。 Specific examples of the direct dye include nitro-p-phenylenediamine, p-nitro-O-phenylenediamine, p-nitro-m-phenylenediamine, 2-amino-4-nitrophenol, and 2-amino-5-nitrophenol. -Dye specified by the ordinance for determining tar pigments that can be used for pharmaceuticals, etc. (announced in 1966, Ministry of Health and Welfare).
アルカリ剤としては、酸化染毛剤に通常使用されるものでよく、例えばエタノールアミン、ジエタノールアミン、トリエタノールアミン、イソプロパノールアミン及び2−アミノ−2−メチル−1−プロパノ−ル等のアルカノールアミン類やアンモニアが挙げられる。 Alkaline agents may be those usually used for oxidative hair dyes, such as alkanolamines such as ethanolamine, diethanolamine, triethanolamine, isopropanolamine and 2-amino-2-methyl-1-propanol. Ammonia is mentioned.
さらに、この第1剤には本発明の効果を妨げない範囲において、従来公知の成分を添加配合することができる。例えば、流動パラフィンやワセリン等の炭化水素類、高級アルコール、エステル油、脂肪酸、シリコーンおよびその誘導体、多価アルコール、紫外線吸収剤、防腐剤、界面活性剤、増粘剤、pH調整剤、アルカリ剤、香料、パール化剤などが挙げられる。 Furthermore, conventionally known components can be added and blended with the first agent within a range that does not hinder the effects of the present invention. For example, hydrocarbons such as liquid paraffin and petrolatum, higher alcohols, ester oils, fatty acids, silicones and derivatives thereof, polyhydric alcohols, ultraviolet absorbers, preservatives, surfactants, thickeners, pH adjusters, alkaline agents , Fragrance, pearlizing agent and the like.
一方、第2剤に配合する酸化剤は、通常、過酸化水素が用いられる。 On the other hand, hydrogen peroxide is usually used as the oxidizing agent to be blended with the second agent.
これらの他、必要に応じて高級アルコール、多価アルコール、界面活性剤、高分子物質、pH調整剤、金属封鎖剤、酸化防止剤、アミノ酸、香料、防腐剤、抗炎剤、着色料等を配合しても良く、それらは公知のものを広く使用できる。 In addition to these, higher alcohols, polyhydric alcohols, surfactants, polymer substances, pH adjusters, sequestering agents, antioxidants, amino acids, fragrances, preservatives, anti-flame agents, coloring agents, etc. You may mix | blend and they can use a well-known thing widely.
本発明の染毛剤組成物を、半永久染毛剤とする場合には、上述の直接染料のみが使用され、さらに染色促進剤としてエタノールなどの低級アルコール、ベンジルアルコールなどの芳香族アルコール、アルキレンカーボネート、N−メチルピロリドンあるいはレブリン酸等の各種溶剤が配合される。その他、必要に応じて高級アルコール、多価アルコール、界面活性剤、高分子物質、pH調整剤、金属封鎖剤、酸化防止剤、アミノ酸、香料、防腐剤、抗炎剤、着色料等を配合しても良く、それらは公知のものを広く使用できる。 When the hair dye composition of the present invention is used as a semi-permanent hair dye, only the above-mentioned direct dyes are used. Further, lower alcohols such as ethanol, aromatic alcohols such as benzyl alcohol, alkylene carbonates as dyeing accelerators. Various solvents such as N-methylpyrrolidone or levulinic acid are blended. In addition, higher alcohols, polyhydric alcohols, surfactants, polymer substances, pH adjusters, sequestering agents, antioxidants, amino acids, fragrances, preservatives, anti-flame agents, coloring agents, etc. These may be widely used.
本発明の染毛剤組成物の剤型としては、液状、乳液状、クリーム状、ゲル状あるいはエアゾール泡沫状など、通常知られている形態をとることができる。 As the dosage form of the hair dye composition of the present invention, it is possible to take a commonly known form such as liquid, emulsion, cream, gel or aerosol foam.
次に本発明を実施例を挙げて詳細に説明するが、本発明は以下の実施例により限定されるものではない。 EXAMPLES Next, although an Example is given and this invention is demonstrated in detail, this invention is not limited by a following example.
表1に酸化染毛剤組成物の第1剤及び第2剤の配合例を示す。また表2に、これら第1剤及び第2剤の組合せによる実施例1および比較例1〜5を示す。 Table 1 shows formulation examples of the first agent and the second agent of the oxidative hair dye composition. Table 2 shows Example 1 and Comparative Examples 1 to 5 based on a combination of these first and second agents.
<染毛試験>
各組成物を常法にて調製した。染毛試験は、比較例5を対照とし、パネラーを用いてハーフヘッドで染毛比較を行った。染毛剤第1剤と第2剤を重量比1:1で混合し、頭髪に塗布後、30分放置し、シャンプーで洗浄後、ドライヤーで乾燥した。仕上がりの感触は、毛髪の柔らかさ、しっとり感及び滑らかさなどを総合的に、また色持ちは1ヶ月後の状態を目視により、以下の基準で評価した。<Hair dyeing test>
Each composition was prepared in a conventional manner. In the hair dyeing test, Comparative Example 5 was used as a control, and a hair dye was compared with a half head using a panel. The first and second hair dyes were mixed at a weight ratio of 1: 1, applied to the hair, left for 30 minutes, washed with shampoo, and dried with a dryer. The feel of the finish was evaluated based on the following criteria by comprehensively evaluating the softness, moistness and smoothness of the hair, and the color retention was visually observed after one month.
<評価基準>
○:比較例5に比べ、非常に良い。
△:比較例5に比べ、やや良い。
×:比較例5と同等。
これらの結果を表2に示す。<Evaluation criteria>
○: Very good as compared with Comparative Example 5.
Δ: Slightly better than Comparative Example 5.
X: Equivalent to Comparative Example 5.
These results are shown in Table 2.
表2に示す結果から分かるように、実施例1はいずれの評価も良好であった。 As can be seen from the results shown in Table 2, Example 1 was good in all evaluations.
実施例2及び比較例6
実施例2(酸性染毛料組成物)
Example 2 and Comparative Example 6
Example 2 (acid hair dye composition)
※1:アクリルアミド・アクリル酸・塩化ジメチルジアリルアンモニウム共重合体(カルゴン社製) * 1: Acrylamide / acrylic acid / dimethyldiallylammonium chloride copolymer (Calgon)
上記実施例2から両性高分子化合物(マーコートプラス3331)及びアニオン性高分子化合物(Acrylates/Ceteth-20 Itaconate Copolymer)を除いただけの組成物を比較例6とし、各成分を室温にて精製水に順次溶解し、二剤式酸性染毛料を得た。そして第1剤を毛髪に塗布後、40℃程度に加温しながら10分間程度放置した後、第2剤を毛髪に塗布し、さらに45℃にて10分間程度放置した後、これを水で充分に洗い流すことにより、染毛を行った。その結果、仕上がりの感触と色持ちは、比較例6に比べ、非常に良好であった。 The composition obtained by removing the amphoteric polymer compound (Mercoat Plus 3331) and the anionic polymer compound (Acrylates / Ceteth-20 Itaconate Copolymer) from Example 2 was used as Comparative Example 6, and each component was added to purified water at room temperature. Dissolving sequentially, a two-component acidic hair dye was obtained. Then, after applying the first agent to the hair, let it stand for about 10 minutes while warming to about 40 ° C., then apply the second agent to the hair and leave it at 45 ° C. for about 10 minutes, and then wash it with water. The hair was dyed by washing thoroughly. As a result, the finished feel and color were very good as compared with Comparative Example 6.
実施例3(エアゾール泡沫状酸化染毛剤)
Example 3 (aerosol foamy oxidative hair dye)
上記原液と噴射剤(LPG3.5)を96:4の比率でエアゾール缶に充填し、染毛剤組成物を得た。常法により染毛し、その結果、実施例1と同様に、良好な仕上がりの感触と色持ちが得られた。 The stock solution and the propellant (LPG3.5) were filled in an aerosol can at a ratio of 96: 4 to obtain a hair dye composition. The hair was dyed by a conventional method, and as a result, as in Example 1, a good finished feel and color persistence were obtained.
以下に本件発明の処方例を示す。
<第1剤処方>
※2:ヒドロキシエチルヒドロキシプロピルトリメチルアンモニウムクロリドエーテル(ライオン社製)The prescription example of this invention is shown below.
<First drug formulation>
* 2: Hydroxyethylhydroxypropyltrimethylammonium chloride ether (manufactured by Lion)
<第2剤処方>
<Second drug formulation>
上述の第1〜2剤を常法にて調製した。これら染毛剤組成物第1剤と第2剤を適宜組み合わせて、実施例1と同様に試験したところ、仕上がりの感触や色持ちに優れた効果を示した。 The above-mentioned first and second agents were prepared by a conventional method. When these hair dye composition 1st agent and 2nd agent were combined suitably and it tested similarly to Example 1, the effect excellent in the feel of a finish and color retention was shown.
毛髪の柔軟性、しっとり感あるいは滑らかさを向上させ、かつ染色堅牢性に優れる染毛剤組成物を提供することができる。 It is possible to provide a hair dye composition that improves the flexibility, moist feeling or smoothness of hair and is excellent in dyeing fastness.
Claims (2)
An acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer , (a) a half ester of itaconic acid and polyoxyethylene alkyl ether, or an ester of methacrylic acid and polyoxyethylene alkyl ether, and (b) acrylic acid, methacrylic acid A hair dye composition comprising at least one anionic polymer compound selected from a copolymer comprising at least one monomer selected from acids and alkyl esters thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000397218A JP5214079B2 (en) | 2000-12-27 | 2000-12-27 | Hair dye composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000397218A JP5214079B2 (en) | 2000-12-27 | 2000-12-27 | Hair dye composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002193772A JP2002193772A (en) | 2002-07-10 |
| JP5214079B2 true JP5214079B2 (en) | 2013-06-19 |
Family
ID=18862372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000397218A Expired - Fee Related JP5214079B2 (en) | 2000-12-27 | 2000-12-27 | Hair dye composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5214079B2 (en) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004091359A (en) * | 2002-08-30 | 2004-03-25 | Kanebo Ltd | Aerosol type creamy hair dye agent |
| JP2004091355A (en) * | 2002-08-30 | 2004-03-25 | Kanebo Ltd | Simultaneously spraying type creamy hair dye composition |
| JP3520078B1 (en) | 2003-02-26 | 2004-04-19 | ホーユー株式会社 | Depigmenting composition and hair coloring composition |
| DE102004018723A1 (en) * | 2004-04-17 | 2005-11-03 | Wella Ag | Itaconic acid monoester / acrylate copolymer and polystyrenesulfonate containing hair treatment agent |
| WO2006060568A1 (en) | 2004-12-02 | 2006-06-08 | The Procter & Gamble Company | Thickened hair colourant and bleaching compositions |
| CA2588373A1 (en) * | 2004-12-02 | 2006-06-08 | The Procter & Gamble Company | Polymer thickened hair colouring and bleaching compositions |
| JP4950749B2 (en) * | 2006-04-25 | 2012-06-13 | 花王株式会社 | Hair cosmetics |
| EP1878469B1 (en) | 2006-07-12 | 2010-09-01 | The Procter & Gamble Company | Gel network surfactant based thickening systems for hair colourant and bleaching compositions |
| JP5530588B2 (en) * | 2007-06-14 | 2014-06-25 | ホーユー株式会社 | Hair elasticity improver |
| TWI407973B (en) * | 2008-05-30 | 2013-09-11 | Kao Corp | Two-part foam hair dye |
| JP5824763B2 (en) * | 2010-11-18 | 2015-12-02 | 株式会社マンダム | Decoloring agent or oxidative hair dye, and method for decoloring or dyeing hair |
| JP5824764B2 (en) * | 2010-11-18 | 2015-12-02 | 株式会社マンダム | Decoloring agent or oxidative hair dye, and method for decoloring or dyeing hair |
| JP5875257B2 (en) * | 2011-06-15 | 2016-03-02 | 株式会社ミルボン | Method for producing oxidative hair dye |
| US9226879B2 (en) * | 2011-09-30 | 2016-01-05 | L'oreal | Foam dye composition comprising at least one particular oxyethylenated nonionic surfactant |
| JP5907608B2 (en) * | 2012-01-13 | 2016-04-26 | 株式会社ミルボン | Multi-agent hair treatment |
| JP6124660B2 (en) * | 2013-04-18 | 2017-05-10 | 株式会社ミルボン | Oxidizing hair treatment agent |
| BR112015030531B1 (en) | 2013-06-05 | 2020-10-06 | Kao Corporation | CAPILLARY COSMETICS AND ITS USE |
| EP3108872B2 (en) | 2014-02-17 | 2021-09-15 | Kao Corporation | Hair cosmetic |
| JP6410336B2 (en) * | 2014-02-17 | 2018-10-24 | 花王株式会社 | Decolorization or hair dye composition |
| EP2957324B1 (en) * | 2014-06-17 | 2017-09-27 | Noxell Corporation | A cosmetic composition comprising a thickening polymer having hydrophobic and hydrophilic portions |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3890161B2 (en) * | 1999-04-15 | 2007-03-07 | ホーユー株式会社 | Oxidative hair dye composition |
-
2000
- 2000-12-27 JP JP2000397218A patent/JP5214079B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002193772A (en) | 2002-07-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5214079B2 (en) | Hair dye composition | |
| JP6873994B2 (en) | Composition for treating hair | |
| CN103781465B (en) | Method for pigmented hair | |
| JP5296329B2 (en) | Oxidative hair dye or decolorant composition | |
| JP2000297019A (en) | Oxidation hair-dyeing agent composition | |
| WO2013136480A1 (en) | Hair dye and hair dyeing method | |
| CN102223872A (en) | Hair cosmetic composition | |
| JP2004075644A (en) | Hair dye composition | |
| JP4718063B2 (en) | Oxidizing agent composition, hair dyeing agent or hair bleaching agent | |
| JP2011102244A (en) | Hair treating agent | |
| JP4551545B2 (en) | Oxidative hair dye composition | |
| JP3992404B2 (en) | Foam hair dye composition | |
| JP2025185265A (en) | Hair dye composition | |
| JP5506285B2 (en) | Hair treatment agent | |
| JP2010018569A (en) | Hair cosmetic composition | |
| JP3926057B2 (en) | Oxidative hair dye composition and hair treatment composition for hair dyeing | |
| JP2007145783A (en) | Hair dye composition | |
| JP2005239627A (en) | Hair dye composition | |
| JP7396622B2 (en) | Oxidative hair dye composition and hair dyeing method | |
| JP2003119116A (en) | Method and kit for treating hair | |
| JP2011042584A (en) | Hair-treating method and hair-treating kit | |
| JP3932483B2 (en) | Oxidative hair dye for temporary hair color restoration and hair dyeing method | |
| JP5439090B2 (en) | Hair treatment agent | |
| JP5005276B2 (en) | Multi-agent hair treatment agent and method of using the same | |
| JP2016088891A (en) | Oxidative hair dye |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070803 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20081029 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20100413 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100614 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20101102 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130227 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 Ref document number: 5214079 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20160308 Year of fee payment: 3 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |