JP4113490B2 - 持続性保持ヘアスタイリング組成物およびその使用法 - Google Patents
持続性保持ヘアスタイリング組成物およびその使用法 Download PDFInfo
- Publication number
- JP4113490B2 JP4113490B2 JP2003386113A JP2003386113A JP4113490B2 JP 4113490 B2 JP4113490 B2 JP 4113490B2 JP 2003386113 A JP2003386113 A JP 2003386113A JP 2003386113 A JP2003386113 A JP 2003386113A JP 4113490 B2 JP4113490 B2 JP 4113490B2
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- Prior art keywords
- acid
- polymer
- pascals
- hair
- polymer mixture
- 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 - Lifetime
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- 239000000203 mixture Substances 0.000 title claims description 117
- 210000004209 hair Anatomy 0.000 title claims description 109
- 230000014759 maintenance of location Effects 0.000 title description 13
- 238000000034 method Methods 0.000 title description 13
- 230000002085 persistent effect Effects 0.000 title 1
- 229920000642 polymer Polymers 0.000 claims description 122
- 229920002959 polymer blend Polymers 0.000 claims description 37
- -1 methacrylate ester Chemical class 0.000 claims description 33
- 229920001577 copolymer Polymers 0.000 claims description 29
- 239000002904 solvent Substances 0.000 claims description 22
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 14
- 238000003860 storage Methods 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 13
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 12
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 12
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 10
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- 238000006116 polymerization reaction Methods 0.000 claims description 9
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 7
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 7
- 150000003926 acrylamides Chemical class 0.000 claims description 7
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- 150000003839 salts Chemical class 0.000 claims description 7
- 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 6
- CWNNYYIZGGDCHS-UHFFFAOYSA-N 2-methylideneglutaric acid Chemical compound OC(=O)CCC(=C)C(O)=O CWNNYYIZGGDCHS-UHFFFAOYSA-N 0.000 claims description 6
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 claims description 6
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 claims description 6
- 229940018557 citraconic acid Drugs 0.000 claims description 6
- OVHKECRARPYFQS-UHFFFAOYSA-N cyclohex-2-ene-1,1-dicarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCC=C1 OVHKECRARPYFQS-UHFFFAOYSA-N 0.000 claims description 6
- 239000001530 fumaric acid Substances 0.000 claims description 6
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 6
- 239000011976 maleic acid Substances 0.000 claims description 6
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 6
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 claims description 6
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 6
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 6
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 claims description 6
- UDXXYUDJOHIIDZ-UHFFFAOYSA-N 2-phosphonooxyethyl prop-2-enoate Chemical compound OP(O)(=O)OCCOC(=O)C=C UDXXYUDJOHIIDZ-UHFFFAOYSA-N 0.000 claims description 5
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 5
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- 102000004169 proteins and genes Human genes 0.000 claims description 5
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- 150000003440 styrenes Chemical class 0.000 claims description 5
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- 239000002280 amphoteric surfactant Substances 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 239000003945 anionic surfactant Substances 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000003093 cationic surfactant Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
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- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- QENRKQYUEGJNNZ-UHFFFAOYSA-N 2-methyl-1-(prop-2-enoylamino)propane-1-sulfonic acid Chemical compound CC(C)C(S(O)(=O)=O)NC(=O)C=C QENRKQYUEGJNNZ-UHFFFAOYSA-N 0.000 claims 3
- 229920002554 vinyl polymer Polymers 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 2
- DZSVIVLGBJKQAP-UHFFFAOYSA-N 1-(2-methyl-5-propan-2-ylcyclohex-2-en-1-yl)propan-1-one Chemical class CCC(=O)C1CC(C(C)C)CC=C1C DZSVIVLGBJKQAP-UHFFFAOYSA-N 0.000 claims 1
- 239000004872 foam stabilizing agent Substances 0.000 claims 1
- 235000008216 herbs Nutrition 0.000 claims 1
- QJWFJOSRSZOLKK-UHFFFAOYSA-N prop-2-enamide Chemical class NC(=O)C=C.NC(=O)C=C QJWFJOSRSZOLKK-UHFFFAOYSA-N 0.000 claims 1
- 239000010408 film Substances 0.000 description 24
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 11
- 150000002009 diols Chemical class 0.000 description 9
- 239000007921 spray Substances 0.000 description 9
- 229920000728 polyester Polymers 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 7
- 239000000499 gel Substances 0.000 description 7
- 239000008266 hair spray Substances 0.000 description 7
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000000834 fixative Substances 0.000 description 5
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 5
- 239000003380 propellant Substances 0.000 description 5
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 229920002396 Polyurea Polymers 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 4
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 4
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
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- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWAPMFBHEQZLGK-UHFFFAOYSA-N 5-(dimethylamino)-2-methylidenepentanamide Chemical compound CN(C)CCCC(=C)C(N)=O ZWAPMFBHEQZLGK-UHFFFAOYSA-N 0.000 description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
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- 239000004094 surface-active agent Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 2
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 2
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
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- 239000002585 base Substances 0.000 description 2
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- 102100026735 Coagulation factor VIII Human genes 0.000 description 1
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 description 1
- 206010019049 Hair texture abnormal Diseases 0.000 description 1
- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
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- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- HDFGOPSGAURCEO-UHFFFAOYSA-N N-ethylmaleimide Chemical compound CCN1C(=O)C=CC1=O HDFGOPSGAURCEO-UHFFFAOYSA-N 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 1
- IEVMHCBVNQZMKV-UHFFFAOYSA-K [Na+].[Na+].[Na+].[O-]C(=O)c1cccc(C([O-])=O)c1S([O-])(=O)=O Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)c1cccc(C([O-])=O)c1S([O-])(=O)=O IEVMHCBVNQZMKV-UHFFFAOYSA-K 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical class CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
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- 229920001400 block copolymer Polymers 0.000 description 1
- 229920005605 branched copolymer Polymers 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 210000001520 comb Anatomy 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000008406 cosmetic ingredient Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- VVTXSHLLIKXMPY-UHFFFAOYSA-L disodium;2-sulfobenzene-1,3-dicarboxylate Chemical compound [Na+].[Na+].OS(=O)(=O)C1=C(C([O-])=O)C=CC=C1C([O-])=O VVTXSHLLIKXMPY-UHFFFAOYSA-L 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- TVFJAZCVMOXQRK-UHFFFAOYSA-N ethenyl 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC(=O)OC=C TVFJAZCVMOXQRK-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- ZCTXEAQXZGPWFG-UHFFFAOYSA-N imidurea Chemical compound O=C1NC(=O)N(CO)C1NC(=O)NCNC(=O)NC1C(=O)NC(=O)N1CO ZCTXEAQXZGPWFG-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229940119545 isobornyl methacrylate Drugs 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000008258 liquid foam Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
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- 235000020957 pantothenol Nutrition 0.000 description 1
- 239000011619 pantothenol Substances 0.000 description 1
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- 229920002647 polyamide Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
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- 230000001012 protector Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229940073743 steareth-20 methacrylate Drugs 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- LINXHFKHZLOLEI-UHFFFAOYSA-N trimethyl-[phenyl-bis(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C1=CC=CC=C1 LINXHFKHZLOLEI-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Polymers 0.000 description 1
- 125000000391 vinyl group Chemical class [H]C([*])=C([H])[H] 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
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- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
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- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
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- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
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- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
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Landscapes
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Description
a)30℃から250℃のガラス転移温度(Tg」)を有する第一ポリマーまたはポリマー混合物;
b)−20℃から35℃のTgを有する第二ポリマーまたはポリマー混合物;
c)1以上の美容上許容される溶媒;
を含むポリマー組成物であって、
第一ポリマーまたはポリマー混合物と第二ポリマーまたはポリマー混合物のTgの差が10℃以上であり;
第一ポリマーまたはポリマー混合物および第二ポリマーまたはポリマー混合物を一緒にc)の溶媒と同じかまたは異なる美容上許容される溶媒中に溶解させ、乾燥させてフィルムを形成する場合に、該フィルムは、20℃で1×1010パスカル〜1×108パスカルの引張貯蔵弾性率を有し、70℃で1×109パスカル〜1×106パスカルの引張貯蔵弾性率を有するポリマー組成物を提供する。乾燥すると、本発明のポリマー組成物は、非粘着性、柔軟性の強靱な弾性フィルムを提供し、ここにおいて、フィルムは、それ以下では弾性挙動を示し、それ以上では延性挙動を示す降伏応力を有する。
a)i)30℃から250℃のガラス転移温度(Tg)を有する第一ポリマーまたはポリマー混合物;
ii)−20℃から35℃のガラス転移温度を有する第二ポリマーまたはポリマー混合物;および
iii)1以上の美容上許容される溶媒
(ここにおいて、第一ポリマーまたはポリマー混合物と第二ポリマーまたはポリマー混合物のTgにおける差は10℃以上であり;
第一ポリマーまたはポリマー混合物と第二ポリマーまたはポリマー混合物を美容上許容される溶媒中に一緒に溶解させ、乾燥させてフィルムを形成する場合に、フィルムが20℃で1×1010パスカル〜1×108パスカルの引張貯蔵弾性率を有し、70℃で1×109パスカル〜1×106パスカルの引張貯蔵弾性率を有する)
を含むヘアスタイリングに有効な量の組成物を髪に適用する工程;および
b)所望の形状に髪を固定する工程
を含む髪をスタイリングする方法である。いくつかの場合において、工程a)およびb)を逆にして、所望のスタイリング結果を得ることができる。「有効なスタイリング量」なる用語は、髪を所望のスタイルに保持する組成物の量を意味する。
表3〜5に詳細に記載された各物質を組み合わせ、アミノメチルプロパノールを用いてpH7.5に中和することにより、髪固定組成物を調製した。表3〜5のポリマーの量は活性固体の重量パーセントとして記載する。ブレンドにおいて用いられるポリマーは表1および2に記載する。
カールする前の頭髪(DeMeo Brothers,New Yorkから入手したEuropean Brown Virgin Hair)は、平均8インチの長さ、3.5±0.1グラムの重さであった。これらを使用前にマイルドシャンプー中で洗浄し、22ミリメートル(mm)×70mmカーラー上にボビーピンで固定して湿らせてカールさせた。カールさせた頭髪を実験室の作業台上で一夜空気乾燥した。
硬さの保持率(%)=(w5/wi)×100
(式中、wiは最初の圧縮の負荷、w5は連続した5番目の負荷でカールを圧縮するために必要な負荷である)。この試験において、良好な硬さの保持率は、髪に対する良好な耐久性の尺度であると見なされる。満足できる硬さの保持率は80%以上であり、好ましくは85%以上,さらに好ましくは90%以上である。
乾燥されたフィルムサンプルを、表3〜5の各ヘアスプレー組成物約16g(グラム)を直径63mmの平底PTFE(ポリテトラフルオロエチレン)蒸発皿中で乾燥することにより調製した。フィルムを室温で48時間乾燥させ、皿から取り出し、評価前少なくとも2時間、約22℃、相対湿度55%で調節した。評価基準は次の通りである:
前記のようにして調製された乾燥フィルムのレオロジー特性を、Rheometric Scientific’s Dynamic Mechanical Thermal Analyzer(DMTA)MarkIV型を用いて測定した。試験はフィルム取り付け器具を用いてテンションをかけて行った。実験を行う前に、装置に対する次のような校正を行った:エレクトロニクス、ダイナミックモード、位置、および力。これらの校正はRheometric Scientificガイドラインに従って行った。温度スイープ3℃/分で行い、振動周波数を1Hzに一定に維持することにより、物質の粘弾性を調べた。振幅は典型的には0.005%であり、物質の線形粘弾性領域内であった(線形粘弾性領域は、動的弾性率が所定の振動数で一定に維持されるひずみの範囲として定義される)。
TA装置2920型示差走査熱量計を用いて、通常(20℃/分昇温速度)の方法または調節昇温試験法のいずれかでガラス転移温度(Tg)を測定した。
ポリマーの分子量は、次の方法に従って、溶出溶媒としてTHFまたはDMFのいずれかを用いて測定することができる:
1)THF:測定は、Agilent1100シリーズHPLCポンプ、2カップルPolymer Lab20ミクロン混合床カラム、Water410RI検出器を含むシステムで35℃で行った。
2)DMF:測定は、60℃で、Waters150Cゲル透過クロマトグラフィーで行った。
次の略語を表および実施例において使用した:
BA=ブチルアクリレート
EA=エチルアクリレート
HEMA=ヒドロキシメタアクリレート
MAA=メタアクリル酸
VA=酢酸ビニル
PVP=ポリビニルピロリドン
DMAPA=ジメチルアミノプロピルアクリルアミド
PVM=ポリビニルメチルエーテル
MA=メチルアクリレート
CHDM=1,4−シクロヘキサンジメタノール
SIP=スルホイソフタル酸ナトリウム
HDI ヘキサメチレンジイソシアネート
2=National Starch and Chemical Company
3=BASF Corporation
4=International Specialty Products
5=Eastman Chemical Company
商品名は、製造業者の商標である。
Claims (4)
- a)75℃から130℃のガラス転移温度(Tg)を有する第一ポリマーまたはポリマー混合物;
b)20℃から35℃のTgを有する第二ポリマーまたはポリマー混合物;
c)1以上の美容上許容される溶媒;
を含むヘアスタイリング組成物であって、
第一ポリマーまたはポリマー混合物および第二ポリマーまたはポリマー混合物を一緒にc)の溶媒と同じかまたは異なる美容上許容される溶媒中に溶解させ、乾燥させてフィルムを形成する場合に、該フィルムは、20℃で1×1010パスカル〜1×108パスカルの引張貯蔵弾性率を有し、70℃で1×109パスカル〜1×106パスカルの引張貯蔵弾性率を有し、かつ
第一および第二ポリマーは多段重合プロセスを用いてブレンドで調製され、さらに第一および第二ポリマーは、メタアクリル酸;アクリル酸;メタアクリレートエステル、アクリレートエステル、スチレン、置換スチレン、有機酸のビニルエステル、N−ビニル化合物、アクリルアミド;メタアクリルアミド;置換アクリルアミド;アミン官能性アクリルアミド、置換メタアクリルアミド;ヒドロキシアルキルメタアクリレート、ヒドロキシアルキルアクリレート、ジエン、ビニルエーテル;マレイン酸、無水マレイン酸、フマル酸、α−メチレングルタル酸、イタコン酸、無水イタコン酸、シトラコン酸、メサコン酸、シクロヘキセンジカルボン酸、2−アクリルアミド−2−メチルプロパンスルホン酸、モノアクリルオキシエチルホスフェート、およびその水溶性塩:から選択される1種以上のモノマーから得られる、ブロック、グラフトおよび分岐ホモポリマー並びにコポリマーから独立して選択される、
ヘアスタイリング組成物。 - a)75℃から130℃のガラス転移温度(Tg)を有する第一ポリマーまたはポリマー混合物;
b)20℃から35℃のTgを有する第二ポリマーまたはポリマー混合物;
c)1以上の美容上許容される溶媒;および
d)香料、染料、保存料、金属イオン封鎖剤、増粘剤、シリコーン、柔軟剤、泡相乗剤、泡安定剤、太陽光フィルター、解膠剤、コンディショニング剤、光沢剤、タンパク質、ハーブ、植物性薬品、中和剤、可塑剤、および陰イオン性、非イオン性、陽イオン性、または両性界面活性剤、およびその混合物から選択される1以上の美容上許容される成分を含むヘアスタイリング組成物であって、
第一ポリマーまたはポリマー混合物と第二ポリマーまたはポリマー混合物をc)における溶媒と同一または異なる美容上許容される溶媒中に一緒に溶解させ、乾燥させてフィルムを形成する場合に、フィルムが20℃で1×1010パスカル〜1×108パスカルの引張貯蔵弾性率を有し、70℃で1×109パスカル〜1×106パスカルの引張貯蔵弾性率を有し、かつ
第一および第二ポリマーは多段重合プロセスを用いてブレンドで調製され、さらに第一および第二ポリマーは、メタアクリル酸;アクリル酸;メタアクリレートエステル、アクリレートエステル、スチレン、置換スチレン、有機酸のビニルエステル、N−ビニル化合物、アクリルアミド;メタアクリルアミド;置換アクリルアミド;アミン官能性アクリルアミド、置換メタアクリルアミド;ヒドロキシアルキルメタアクリレート、ヒドロキシアルキルアクリレート、ジエン、ビニルエーテル;マレイン酸、無水マレイン酸、フマル酸、α−メチレングルタル酸、イタコン酸、無水イタコン酸、シトラコン酸、メサコン酸、シクロヘキセンジカルボン酸、2−アクリルアミド−2−メチルプロパンスルホン酸、モノアクリルオキシエチルホスフェート、およびその水溶性塩:から選択される1種以上のモノマーから得られる、ブロック、グラフトおよび分岐ホモポリマー並びにコポリマーから独立して選択される、
ヘアスタイリング組成物。 - a)i)75℃から130℃のガラス転移温度(Tg)を有する第一ポリマーまたはポリマー混合物;
ii)20℃から35℃のTgを有する第二ポリマーまたはポリマー混合物;および
iii)1以上の美容上許容される溶媒
(ここにおいて、
第一ポリマーまたはポリマー混合物と第二ポリマーまたはポリマー混合物をiii)における溶媒と同一または異なる美容上許容される溶媒中に一緒に溶解させ、乾燥させてフィルムを形成する場合に、フィルムが20℃で1×1010パスカル〜1×108パスカルの引張貯蔵弾性率を有し、70℃で1×109パスカル〜1×106パスカルの引張貯蔵弾性率を有し、かつ
第一および第二ポリマーは多段重合プロセスを用いてブレンドで調製され、さらに第一および第二ポリマーは、メタアクリル酸;アクリル酸;メタアクリレートエステル、アクリレートエステル、スチレン、置換スチレン、有機酸のビニルエステル、N−ビニル化合物、アクリルアミド;メタアクリルアミド;置換アクリルアミド;アミン官能性アクリルアミド、置換メタアクリルアミド;ヒドロキシアルキルメタアクリレート、ヒドロキシアルキルアクリレート、ジエン、ビニルエーテル;マレイン酸、無水マレイン酸、フマル酸、α−メチレングルタル酸、イタコン酸、無水イタコン酸、シトラコン酸、メサコン酸、シクロヘキセンジカルボン酸、2−アクリルアミド−2−メチルプロパンスルホン酸、モノアクリルオキシエチルホスフェート、およびその水溶性塩:から選択される1種以上のモノマーから得られる、ブロック、グラフトおよび分岐ホモポリマー並びにコポリマーから独立して選択される)
を含むスタイリングに有効な量の組成物を髪に適用する工程;および
b)所望の形状に髪を固定する工程を含む、髪をスタイリングする方法。 - a)所望の形状に髪を固定する工程;および
b)i)75℃から130℃のガラス転移温度(Tg)を有する第一ポリマーまたはポリマー混合物;
ii)20℃から35℃のTgを有する第二ポリマーまたはポリマー混合物;および
iii)1以上の美容上許容される溶媒
(ここにおいて、
第一ポリマーまたはポリマー混合物と第二ポリマーまたはポリマー混合物をiii)における溶媒と同一または異なる美容上許容される溶媒中に一緒に溶解させ、乾燥させてフィルムを形成する場合に、フィルムが20℃で1×1010パスカル〜1×108パスカルの引張貯蔵弾性率を有し、70℃で1×109パスカル〜1×106パスカルの引張貯蔵弾性率を有し、かつ
第一および第二ポリマーは多段重合プロセスを用いてブレンドで調製され、さらに第一および第二ポリマーは、メタアクリル酸;アクリル酸;メタアクリレートエステル、アクリレートエステル、スチレン、置換スチレン、有機酸のビニルエステル、N−ビニル化合物、アクリルアミド;メタアクリルアミド;置換アクリルアミド;アミン官能性アクリルアミド、置換メタアクリルアミド;ヒドロキシアルキルメタアクリレート、ヒドロキシアルキルアクリレート、ジエン、ビニルエーテル;マレイン酸、無水マレイン酸、フマル酸、α−メチレングルタル酸、イタコン酸、無水イタコン酸、シトラコン酸、メサコン酸、シクロヘキセンジカルボン酸、2−アクリルアミド−2−メチルプロパンスルホン酸、モノアクリルオキシエチルホスフェート、およびその水溶性塩:から選択される1種以上のモノマーから得られる、ブロック、グラフトおよび分岐ホモポリマー並びにコポリマーから独立して選択される)
を含むスタイリングに有効な量の組成物を髪に適用する工程を含む、髪をスタイリングする方法。
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FR2744632B1 (fr) * | 1996-02-13 | 1998-03-27 | Oreal | Utilisation d'une suspension aqueuse de microfibrilles d'origine naturelle pour la preparation de compositions cosmetiques ou dermatologiques, compositions cosmetiques ou dermatologiques et applications |
JP3856477B2 (ja) * | 1996-10-24 | 2006-12-13 | マサチューセッツ・インスティテュート・オブ・テクノロジー | 患者監視指輪センサ |
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FR2779643B1 (fr) | 1998-06-11 | 2000-08-11 | Oreal | Composition cosmetique comprenant au moins un polymere collant et au moins un polymere fixant |
DE69934461T2 (de) * | 1998-09-11 | 2007-09-27 | Rohm And Haas Co. | Festigende Haarformungs-Zusammensetzungen |
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FR2798061A1 (fr) | 1999-09-07 | 2001-03-09 | Oreal | Composition cosmetique comprenant des dispersions de particules de polymeres dans une phase grasse liquide |
FR2809306B1 (fr) * | 2000-05-23 | 2004-02-06 | Oreal | Utilisation en cosmetique de copolymeres ethyleniques sequences a caractere elastique et compositions les contenant |
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US20030147833A1 (en) * | 2001-12-20 | 2003-08-07 | L'oreal | Reshapable hair styling non-rinse composition comprising (meth)acrylic copolymers |
US20040057923A9 (en) * | 2001-12-20 | 2004-03-25 | Isabelle Rollat | Reshapable hair styling rinse composition comprising (meth)acrylic copolymers |
-
2003
- 2003-11-05 EP EP03256982A patent/EP1419759B1/en not_active Revoked
- 2003-11-06 US US10/702,361 patent/US7651693B2/en active Active
- 2003-11-07 BR BR0304859-4A patent/BR0304859A/pt not_active Application Discontinuation
- 2003-11-12 AU AU2003262108A patent/AU2003262108B2/en not_active Ceased
- 2003-11-13 MX MXPA03010382A patent/MXPA03010382A/es active IP Right Grant
- 2003-11-17 JP JP2003386113A patent/JP4113490B2/ja not_active Expired - Lifetime
- 2003-11-17 KR KR1020030080974A patent/KR101038423B1/ko active IP Right Grant
Also Published As
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AU2003262108B2 (en) | 2009-07-23 |
JP2004168776A (ja) | 2004-06-17 |
MXPA03010382A (es) | 2004-05-20 |
BR0304859A (pt) | 2004-08-31 |
EP1419759B1 (en) | 2012-12-26 |
US7651693B2 (en) | 2010-01-26 |
KR101038423B1 (ko) | 2011-06-01 |
AU2003262108A1 (en) | 2004-06-03 |
EP1419759A3 (en) | 2004-12-08 |
KR20040044139A (ko) | 2004-05-27 |
EP1419759A2 (en) | 2004-05-19 |
US20040096474A1 (en) | 2004-05-20 |
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