JP2002322035A - Pretreatment agent for hair color, treatment agent for hair color and method for treating hair - Google Patents
Pretreatment agent for hair color, treatment agent for hair color and method for treating hairInfo
- Publication number
- JP2002322035A JP2002322035A JP2001294049A JP2001294049A JP2002322035A JP 2002322035 A JP2002322035 A JP 2002322035A JP 2001294049 A JP2001294049 A JP 2001294049A JP 2001294049 A JP2001294049 A JP 2001294049A JP 2002322035 A JP2002322035 A JP 2002322035A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- agent
- treatment
- color
- hair color
- 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.)
- Pending
Links
- 230000037308 hair color Effects 0.000 title claims abstract description 80
- 238000000034 method Methods 0.000 title claims abstract description 19
- 102000011782 Keratins Human genes 0.000 claims abstract description 25
- 108010076876 Keratins Proteins 0.000 claims abstract description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 161
- 239000003531 protein hydrolysate Substances 0.000 claims description 22
- 238000002203 pretreatment Methods 0.000 claims description 15
- 206010020649 Hyperkeratosis Diseases 0.000 claims description 9
- 235000021118 plant-derived protein Nutrition 0.000 claims description 9
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 claims description 7
- 102000002322 Egg Proteins Human genes 0.000 claims description 7
- 108010000912 Egg Proteins Proteins 0.000 claims description 7
- 235000014103 egg white Nutrition 0.000 claims description 7
- 210000000969 egg white Anatomy 0.000 claims description 7
- 150000003904 phospholipids Chemical class 0.000 claims description 7
- 229940106189 ceramide Drugs 0.000 claims description 5
- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 claims description 4
- CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical class CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 claims description 4
- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 claims description 4
- 150000001783 ceramides Chemical class 0.000 claims description 4
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 claims description 4
- 230000006378 damage Effects 0.000 abstract description 18
- 239000000975 dye Substances 0.000 description 36
- 239000000118 hair dye Substances 0.000 description 35
- 230000000694 effects Effects 0.000 description 26
- 230000001590 oxidative effect Effects 0.000 description 18
- 230000002378 acidificating effect Effects 0.000 description 15
- 239000007844 bleaching agent Substances 0.000 description 13
- -1 alkyl methacrylate Chemical compound 0.000 description 10
- 239000002453 shampoo Substances 0.000 description 10
- 238000002845 discoloration Methods 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 108010009736 Protein Hydrolysates Proteins 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 230000002265 prevention Effects 0.000 description 6
- 230000001953 sensory effect Effects 0.000 description 5
- LIFHMKCDDVTICL-UHFFFAOYSA-N 6-(chloromethyl)phenanthridine Chemical compound C1=CC=C2C(CCl)=NC3=CC=CC=C3C2=C1 LIFHMKCDDVTICL-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 238000004737 colorimetric analysis Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 230000003700 hair damage Effects 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 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
- 241001465754 Metazoa Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 230000003020 moisturizing effect Effects 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 235000013772 propylene glycol Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008347 soybean phospholipid Substances 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- 235000021357 Behenic acid Nutrition 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
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- AERBNCYCJBRYDG-UHFFFAOYSA-N D-ribo-phytosphingosine Natural products CCCCCCCCCCCCCCC(O)C(O)C(N)CO AERBNCYCJBRYDG-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- BBAFBDLICMHBNU-MFZOPHKMSA-N N-(2-hydroxyoctadecanoyl)-4-hydroxysphinganine Chemical compound CCCCCCCCCCCCCCCCC(O)C(=O)N[C@@H](CO)[C@H](O)[C@H](O)CCCCCCCCCCCCCC BBAFBDLICMHBNU-MFZOPHKMSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- IEZRNEGTKRQRFV-LFBNJJMOSA-N N-octadecanoyl-4-hydroxysphinganine Chemical compound CCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)[C@H](O)CCCCCCCCCCCCCC IEZRNEGTKRQRFV-LFBNJJMOSA-N 0.000 description 1
- VODZWWMEJITOND-NXCSZAMKSA-N N-octadecanoylsphingosine Chemical compound CCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)\C=C\CCCCCCCCCCCCC VODZWWMEJITOND-NXCSZAMKSA-N 0.000 description 1
- ATGQXSBKTQANOH-UWVGARPKSA-N N-oleoylphytosphingosine Chemical compound CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@H](CO)NC(=O)CCCCCCC\C=C/CCCCCCCC ATGQXSBKTQANOH-UWVGARPKSA-N 0.000 description 1
- 241000772415 Neovison vison Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 229920002385 Sodium hyaluronate Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- MIUIRGGKIICMBP-NFOZDHADSA-N [27-oxo-27-[[(2s,3s,4r)-1,3,4-trihydroxyoctadecan-2-yl]amino]heptacosyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)[C@H](O)CCCCCCCCCCCCCC MIUIRGGKIICMBP-NFOZDHADSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 239000010495 camellia oil Substances 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- WDDNSUVHFQMEDX-UHFFFAOYSA-N diethyl sulfate;5-(dimethylamino)-2-methylpent-2-enoic acid Chemical compound CCOS(=O)(=O)OCC.CN(C)CCC=C(C)C(O)=O WDDNSUVHFQMEDX-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000003719 hair strength Effects 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 229940001447 lactate Drugs 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- AERBNCYCJBRYDG-KSZLIROESA-N phytosphingosine Chemical compound CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@@H](N)CO AERBNCYCJBRYDG-KSZLIROESA-N 0.000 description 1
- 229940033329 phytosphingosine Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 235000013930 proline Nutrition 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 235000004400 serine Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229940010747 sodium hyaluronate Drugs 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 229940045920 sodium pyrrolidone carboxylate Drugs 0.000 description 1
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 description 1
- HYRLWUFWDYFEES-UHFFFAOYSA-M sodium;2-oxopyrrolidine-1-carboxylate Chemical compound [Na+].[O-]C(=O)N1CCCC1=O HYRLWUFWDYFEES-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ヘアカラー処理の
前に使用する前処理剤、およびヘアカラー処理の前後に
使用する前に使用する前処理剤と後に使用する後処理剤
からなるヘアカラー用処理剤、並びにこれらを用いた毛
髪処理方法に関するものである。本発明によれば、ヘア
カラー処理における毛髪の損傷を防止し、染料の定着を
良くし、ヘアカラー処理後のゴワツキ感を改善するのに
有効である。[0001] The present invention relates to a pretreatment agent used before hair color treatment, and a hair color comprising a pretreatment agent used before and after hair color treatment and a post-treatment agent used after. And a hair treatment method using the same. ADVANTAGE OF THE INVENTION According to this invention, it is effective in preventing damage to the hair at the time of a hair color process, improving the fixation of a dye, and improving the feeling of roughness after a hair color process.
【0002】[0002]
【従来の技術】白髪染めやおしゃれ染めなどの目的で、
従来から酸化染毛剤や酸性染毛料などが使用されてい
る。このうち一般的に使用されているのは、染毛作用と
ブリーチ作用を持つ酸化染毛剤であり、この染毛剤では
酸化染料と過酸化水素が毛髪内部に浸透し、酸化染料が
酸化重合して発色させるものである。また同時に過酸化
水素は、アルカリ存在下で毛髪中のメラニン色素を酸化
分解する。こうした酸化染毛剤では、毛髪が本来持つ色
より明るく染めることができることや色落ちを非常に少
なくする点で優れていると言われている。しかしなが
ら、酸化染毛剤では、毛髪のアルカリによる膨潤や過酸
化水素による毛髪組織の破壊により、毛髪のダメージが
増大して毛髪強度が低下し、毛髪のゴワツキ、パサツキ
などを生じさせるという問題があった。[Prior Art] For the purpose of dyeing gray hair or fashion,
Conventionally, oxidative hair dyes, acidic hair dyes, and the like have been used. Of these, commonly used are oxidative hair dyes that have a hair dyeing action and bleaching action. In this hair dye, the oxidation dye and hydrogen peroxide penetrate inside the hair, and the oxidation dye is oxidatively polymerized. The color is developed. At the same time, hydrogen peroxide oxidizes and decomposes melanin pigment in hair in the presence of alkali. It is said that such an oxidative hair dye is excellent in that it can be dyed brighter than the hair originally has, and that the color fading is extremely reduced. However, the oxidative hair dye has a problem that swelling of the hair by alkali or destruction of the hair tissue by hydrogen peroxide causes an increase in damage to the hair and a decrease in the strength of the hair. Was.
【0003】一方、酸性染毛料は、酸性下で酸性染料が
毛髪ケラチンのアミノ基とイオン結合して染着するメカ
ニズムを利用したものである。この酸性染毛剤では、ブ
リーチ作用がなく、pHが酸性であることから、酸化染
毛剤と比べると毛髪のダメージは少ない。しかしながら
酸性染毛料を用いると、施術を繰り返すことで毛髪が収
斂して硬くなる傾向にあり、また染料の浸透剤として配
合されている溶剤(例えばベンジルアルコールなど)
は、毛髪を脱脂するため、毛髪の手触りが悪化するとい
う問題があった。[0003] On the other hand, the acidic hair dye utilizes a mechanism in which an acid dye is dyed under acidic conditions by ionic bonding with an amino group of hair keratin. Since this acidic hair dye has no bleaching action and has an acidic pH, hair damage is less than that of an oxidative hair dye. However, when an acidic hair dye is used, the hair tends to converge and become harder by repeating the treatment, and a solvent (such as benzyl alcohol) incorporated as a penetrant for the dye
However, there is a problem that the feel of the hair deteriorates because the hair is degreased.
【0004】上記の問題を解決する毛髪処理剤として
は、動植物由来または微生物由来のタンパク質加水分解
物またはその誘導体を含有する処理剤(特開平10−2
26629号)、ケラチン加水分解物またはその誘導体
を含有する処理剤(特開平10−291919号)、ケ
ラチン加水分解物またはその誘導体とケラチン以外の動
植物由来または微生物由来のタンパク質加水分解物また
はその誘導体を含有する処理剤(特開平11−1399
40号)などが提案されている。しかしながら、これら
の処理剤は、ヘアカラー処理における毛髪の損傷はある
程度防止できるものの、染料の定着を良くし、ヘアカラ
ー処理後のゴワツキ感を改善するには不十分であった。As a hair treatment agent which solves the above-mentioned problems, a treatment agent containing a protein hydrolyzate derived from animals and plants or a microorganism or a derivative thereof (Japanese Patent Laid-Open No. 10-2)
No. 26629), a treating agent containing a keratin hydrolyzate or a derivative thereof (Japanese Patent Laid-Open No. 10-291919), a keratin hydrolyzate or a derivative thereof and a protein hydrolyzate or a microorganism-derived protein or a derivative thereof other than keratin. Processing agent contained (Japanese Unexamined Patent Application Publication No. 11-1399)
No. 40) has been proposed. However, although these treatment agents can prevent hair damage during hair color treatment to some extent, they are insufficient for improving the fixation of the dye and improving the feeling of crunch after the hair color treatment.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記の様な
従来技術における課題を解決するためになされたもので
あって、その目的は、ヘアカラー処理における毛髪の損
傷を防止し、染料の定着を良くし、ヘアカラー処理後の
ゴワツキ感を改善することのできるヘアカラー用前処理
剤およびヘアカラー用処理剤、並びにこれらを用いた毛
髪処理方法を提供することにある。SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems in the prior art, and an object of the present invention is to prevent hair from being damaged in a hair color treatment, An object of the present invention is to provide a hair color pretreatment agent and a hair color treatment agent capable of improving fixation and improving a feeling of stiffness after hair color treatment, and a hair treatment method using the same.
【0006】[0006]
【課題を解決するための手段】上記課題を解決し得た本
発明のヘアカラー用前処理剤とは、ヘアカラー処理の前
後に使用する前処理剤であって、ケラチン加水分解物お
よび/またはその誘導体を含有する点に要旨を有するも
のである。この前処理剤においては、pHが4〜8の範
囲であることが好ましく、前記ケラチン加水分解物とし
ては、α−ケラトースが好ましく用いられる。またこの
前処理剤を用いて毛髪を処理するに当たっては、この前
処理剤を毛髪に塗布した後、ヘアカラー処理を行う様に
すれば良い。Means for Solving the Problems The pretreatment agent for hair color of the present invention which can solve the above-mentioned problems is a pretreatment agent used before and after the hair color treatment, and includes a keratin hydrolyzate and / or It has a gist in containing its derivative. In this pretreatment agent, the pH is preferably in the range of 4 to 8, and α-keratose is preferably used as the keratin hydrolyzate. In treating hair with this pretreatment agent, the hair color treatment may be performed after applying this pretreatment agent to the hair.
【0007】一方、上記課題を解決し得た本発明のヘア
カラー用処理剤とは、ヘアカラー処理の前後に使用する
前処理剤と後処理剤からなるヘアカラー用処理剤であっ
て、前記前処理剤はケラチン加水分解物および/または
その誘導体を含有する点に要旨を有するものである。こ
の処理剤においては、前処理剤のpHが4〜8の範囲で
あることが好ましく、前処理剤に含有するケラチン加水
分解物としては、α−ケラトースが好ましく用いられ
る。On the other hand, the hair color treating agent of the present invention which can solve the above-mentioned problems is a hair color treating agent comprising a pre-treatment agent and a post-treatment agent used before and after the hair color treatment. The pretreatment agent has a gist in that it contains a keratin hydrolyzate and / or a derivative thereof. In this treatment agent, the pH of the pretreatment agent is preferably in the range of 4 to 8, and α-keratose is preferably used as the keratin hydrolyzate contained in the pretreatment agent.
【0008】この処理剤においては、前記後処理剤が、
セラミド、セラミドの誘導体、リン脂質およびリン脂質
の誘導体よりなる群から選ばれる1種以上を含有するも
のが好ましく、必要によって、更に植物由来のタンパク
質加水分解物、植物由来のタンパク質加水分解物の誘導
体、卵白由来のタンパク質加水分解物および卵白由来の
タンパク質加水分解物の誘導体よりなる群から選ばれる
1種以上を含有することも有効である。In this treating agent, the post-treating agent comprises:
Ceramides, ceramide derivatives, those containing one or more selected from the group consisting of phospholipids and phospholipid derivatives are preferred, and further, if necessary, further plant-derived protein hydrolysates, plant-derived protein hydrolysates It is also effective to contain at least one selected from the group consisting of a protein hydrolyzate derived from egg white and a protein hydrolyzate derived from egg white.
【0009】また、本発明のヘアカラー用処理剤を用い
て毛髪を処理するに当たっては、前処理剤を毛髪に塗布
した後、ヘアカラー処理を行い、その後後処理剤を塗布
する様にすれば良い。尚、この方法におけるより具体的
な手順としては、(1)前処理剤を塗布した後、ヘアカ
ラー処理を行い、その後後処理剤を塗布して洗い流す、
(2)前処理剤を塗布した後、ヘアカラー処理を行い、
その後後処理剤を塗布して洗い流さない、等の構成を挙
げることができる。In treating hair with the hair coloring treatment agent of the present invention, a hair treatment is performed after applying a pre-treatment agent to hair, and then a post-treatment agent is applied. good. In addition, as a more specific procedure in this method, (1) after applying a pre-treatment agent, performing a hair color treatment, then applying a post-treatment agent and washing away,
(2) After applying the pretreatment agent, perform hair color treatment,
Thereafter, a configuration in which a post-treatment agent is applied and not washed away can be used.
【0010】[0010]
【発明の実施の形態】本発明は上記の如く構成される
が、要するに、(1)ヘアカラー用前処理剤、または
(2)前処理剤と後処理剤からなるヘアカラー用処理剤
における前処理剤として、ケラチン加水分解物および/
またはその誘導体を含有するものを用いてヘアカラー処
理前に毛髪に処理することにより、ケラチンが毛髪に吸
着して、ヘアカラーによるダメージを防止するとともに
染料の定着を良くすることができたのである。BEST MODE FOR CARRYING OUT THE INVENTION The present invention is constituted as described above. In short, the present invention relates to (1) a pretreatment agent for hair color, or (2) a pretreatment agent for hair color comprising a pretreatment agent and a posttreatment agent. Keratin hydrolyzate and / or
Or, by treating the hair with a hair containing a derivative thereof before the hair color treatment, keratin was adsorbed to the hair, thereby preventing damage due to the hair color and improving fixation of the dye. .
【0011】本発明のヘアカラー用前処理剤、またはヘ
アカラー用処理剤で用いる前処理剤においては、前述の
如くケラチン加水分解物やその誘導体を含有する必要が
ある。毛髪の損傷が特に激しい部分は、親水性の性質が
強くなっているため、染料の定着が悪く退色しやすい。
このため疎水性の高いケラチン加水分解物またはその誘
導体を含有する前処理剤を毛髪に塗布して、毛髪自身の
疎水性を高めることは非常に有効である。The pretreatment agent for hair color of the present invention or the pretreatment agent used in the treatment agent for hair color must contain a keratin hydrolyzate or a derivative thereof as described above. The part where the hair is particularly severely damaged has a strong hydrophilic property, so that the dye is poorly fixed and is easily discolored.
Therefore, it is very effective to apply a pretreatment agent containing a highly hydrophobic keratin hydrolyzate or a derivative thereof to hair so as to increase the hydrophobicity of the hair itself.
【0012】上記ケラチン加水分解物(加水分解ケラチ
ン)としては、α−ケラトース(結晶性ケラチン)とγ
−ケラトース(非結晶性ケラチン)があるが、疎水性を
高めるにはα−ケラトースがより好ましい。またα−ケ
ラトースは、毛髪のすべりの改善効果にも優れている。
平均分子量の大きいケラチン加水分解物だけでは、手触
りが硬くなる傾向があるが、これを解消するためには、
平均分子量の小さいケラチン加水分解物またはその誘導
体と併用すること、或はこうした誘導体単独を使用する
ことで柔軟性を付与することができる。The keratin hydrolyzate (hydrolyzed keratin) includes α-keratose (crystalline keratin) and γ
-Keratose (amorphous keratin), but α-keratose is more preferred for increasing hydrophobicity. Α-Keratose is also excellent in improving the slippage of hair.
Keratin hydrolyzate with a large average molecular weight alone tends to have a hard feel, but in order to eliminate this,
Flexibility can be imparted by using in combination with a keratin hydrolyzate having a small average molecular weight or a derivative thereof, or by using such a derivative alone.
【0013】前処理剤は通常水溶液として調製される
が、溶媒としてアルコール類(例えばエタノール、プロ
ピレングリコールなど)を配合して疎水的環境を増すこ
とによって、ケラチン加水分解物またはその誘導体は、
親水基を内側、疎水基を外側にした構造を増加できるの
で、毛髪との疎水結合を向上させることができる。The pretreatment agent is usually prepared as an aqueous solution, but by adding an alcohol (eg, ethanol, propylene glycol, etc.) as a solvent to increase the hydrophobic environment, the keratin hydrolyzate or its derivative is
Since the structure having the hydrophilic group inside and the hydrophobic group outside can be increased, the hydrophobic bond with the hair can be improved.
【0014】本発明の前処理剤においては、ヘアカラー
による損傷の防止効果やヘアカラー処理時の変色防止を
考慮すると、そのpHは4〜8の範囲であることが好ま
しい。前処理剤のpHがこの範囲から外れると、十分な
損傷防止効果が発揮されず、また次に行うヘアカラーの
色味が変化し、予定していた色味と異なる場合がある。
尚、前処理剤のpHは,更に好ましい範囲は6〜7程度
であり、この範囲内では前処理による処理効果が最も有
効に発揮される。The pH of the pretreatment agent of the present invention is preferably in the range of 4 to 8 in consideration of the effect of preventing damage due to hair color and the prevention of discoloration during hair color treatment. If the pH of the pretreatment agent is out of this range, the effect of preventing damage is not sufficiently exhibited, and the color of a hair color to be performed next changes, which may be different from the expected color.
The pH of the pretreatment agent is more preferably in the range of about 6 to 7, and within this range, the treatment effect of the pretreatment is most effectively exhibited.
【0015】上記の様なヘアカラー用前処理剤を用い、
ヘアカラー処理の前に前処理だけを行っても上記の効果
が発揮されるが、こうしたヘアカラー処理後に後処理剤
を用いて処理することも更に効果的である。このとき用
いる後処理剤としては、一般的に使用されているもので
も良いが、セラミド、セラミドの誘導体、リン脂質およ
びリン脂質の誘導体よりなる群から選ばれる1種以上を
含有する後処理剤を用いることが好ましく、こうした後
処理剤を用いてヘアカラー処理後に毛髪に処理すること
により、毛髪の保湿性を高めて柔軟性を付与し、ヘアカ
ラー処理後のゴワツキ感を改善することができる。また
これらの成分は、保湿性が高いだけでなく、耐シャンプ
ー性にも優れており、手触りの改善効果の持続性にも優
れた効果を発揮する。このうち、セラミドまたはその誘
導体としては、N−ステアロイルオキシヘプタコサノイ
ルフィトスフィンゴシン、N−ステアロイルスフィンゴ
シン、N−ステアロイルフィトスフィンゴシン、N−オ
レオイルフィトスフィンゴシン、N−2−ヒドロキシス
テアロイルフィトスフィンゴシン、フィトスフィンゴシ
ン、コメヌカスフィンゴ糖脂質(植物セラミド)などが
挙げられる。またリン脂質またはその誘導体としては、
水素添加大豆リン脂質、水酸化大豆リン脂質、水素添加
大豆リゾリン脂質などが挙げられる。Using the above hair color pretreatment agent,
Although the above effects can be obtained by performing only the pre-treatment before the hair color treatment, treatment with a post-treatment agent after such hair color treatment is more effective. The post-treatment agent used at this time may be a commonly used post-treatment agent, but may be a post-treatment agent containing at least one selected from the group consisting of ceramide, ceramide derivatives, phospholipids and phospholipid derivatives. It is preferable to use such a post-treatment agent, and by treating the hair after the hair color treatment with the use of such a post-treatment agent, it is possible to enhance the moisturizing property of the hair, to impart flexibility, and to improve the feeling of crunch after the hair color treatment. These components not only have high moisturizing properties, but also have excellent shampoo resistance, and exhibit excellent effects of improving the feel of the touch. Among them, ceramide or a derivative thereof includes N-stearoyloxyheptacosanoylphytosphingosine, N-stearoylsphingosine, N-stearoylphytosphingosine, N-oleoylphytosphingosine, N-2-hydroxystearoylphytosphingosine, phytosphingosine, Glycosphingoglycolipid (plant ceramide) and the like. Further, as a phospholipid or a derivative thereof,
Examples include hydrogenated soybean phospholipids, hydroxylated soybean phospholipids, and hydrogenated soybean lysophospholipids.
【0016】本発明で用いる後処理剤には、必要によ
り、上記成分に加えて更に、植物由来のタンパク質加水
分解物、植物由来のタンパク質加水分解物の誘導体、卵
白由来のタンパク質加水分解物および卵白由来のタンパ
ク質加水分解物の誘導体よりなる群から選ばれる1種以
上を含有させることも有効である。これらの物質を含有
させることによって、毛髪の保湿性を高めるとともに、
毛髪への塗布時の引っかかりを改善することができる。
植物由来のタンパク質加水分解物またはその誘導体とし
ては、大豆、小麦、トウモロコシ、アーモンド、カラス
ムギなどを加水分解して得られるタンパク質加水分解
物、これらのタンパク加水分解物のエステル、カチオン
化物、アシル化物またはその塩、シリル化物などが挙げ
られる。毛髪への塗布時の引っかかり改善には、特にカ
チオン化物が有効である。The post-treatment agent used in the present invention may further comprise, if necessary, a plant-derived protein hydrolyzate, a plant-derived protein hydrolyzate, an egg white-derived protein hydrolyzate, and an egg white in addition to the above components. It is also effective to include one or more selected from the group consisting of derivatives of protein hydrolysates derived from the same. By containing these substances, while increasing the moisture retention of the hair,
The snagging at the time of application to hair can be improved.
As a plant-derived protein hydrolyzate or a derivative thereof, soybeans, wheat, corn, almond, oats and the like obtained by hydrolyzing protein hydrolysates, esters of these protein hydrolysates, cationized products, acylated products or And salts and silylated products thereof. A cationized product is particularly effective in improving the catch during application to hair.
【0017】本発明の後処理剤は、ヘアカラー処理後の
毛髪に残留したアルカリを除去するために酸、塩、ある
いは酸と塩を含有することが好ましい。ただし、酸によ
る急激な中和は、逆に毛髪強度の低下を引き起こし、ま
た変色する場合もあることから、塩を含有させて中和す
ることがより好ましい。こうした塩としては、クエン酸
塩、乳酸塩、グリコール酸塩などが挙げられる。The post-treatment agent of the present invention preferably contains an acid, a salt, or an acid and a salt in order to remove the alkali remaining on the hair after the hair color treatment. However, rapid neutralization with an acid causes a decrease in hair strength and may cause discoloration, and therefore, it is more preferable to neutralize by adding a salt. Such salts include citrate, lactate, glycolate and the like.
【0018】本発明の後処理剤のpHは、ヘアカラーの
変色を考慮するとpH4〜9の範囲であることが好まし
い。後処理剤のpHが、この範囲から外れると、後処理
剤塗布後にヘアカラーの色味を変化させてしまう場合が
ある。尚、後処理剤のpHは,更に好ましい範囲は5〜
8程度であり、この範囲内では後処理による処理効果が
最も有効に発揮される。The pH of the post-treatment agent of the present invention is preferably in the range of 4 to 9 in consideration of discoloration of the hair color. If the pH of the post-treatment agent is out of this range, the color of the hair color may change after the application of the post-treatment agent. The pH of the post-treatment agent is more preferably in the range of 5 to 5.
It is about 8, and within this range, the processing effect by the post-processing is most effectively exhibited.
【0019】後処理剤に塩を含有させて、毛髪に塗布し
やすいように増粘させる場合は、アクリル酸アルキル・
メタクリル酸アルキル・ポリオキシエチレンステアリル
エーテル共重合体エマルションなどにより増粘するのが
好ましい。一般的に増粘剤として使用されるカルボキシ
ビニルポリマーなどは、塩やタンパク質加水分解物など
を含有すると安定した粘性が得られない。When a salt is contained in the post-treatment agent to increase the viscosity so that it can be easily applied to the hair, use an alkyl acrylate.
The viscosity is preferably increased by an alkyl methacrylate / polyoxyethylene stearyl ether copolymer emulsion or the like. A carboxyvinyl polymer or the like generally used as a thickener cannot obtain a stable viscosity if it contains a salt or a protein hydrolyzate.
【0020】本発明の前処理剤と後処理剤からなるヘア
カラー用処理剤は、上記成分の他に、本発明の効果を損
なわない範囲で、各種成分を適宜選択して含有させるこ
とができる。即ち、ミリスチルアルコール、セチルアル
コール、ステアリルアルコールなどの高級アルコール、
流動パラフィン、ワセリン、スクワランなどの炭化水
素、ミリスチン酸イソプロピル、パルミチン酸イソプロ
ピル、オレイン酸デシルなどのエステル油、ツバキ油、
ホホバ油、オリーブ油、ミンク油などの動植物油、ミツ
ロウ、キャンデリラロウなどのロウ類、ジメチルポリシ
ロキサン、メチルフェニルポリシロキサンなどのシリコ
ーン油、パルミチン酸、ステアリン酸、べへニン酸など
の高級脂肪酸、エチレングリコール、プロピレングリコ
ール、1,3−ブチレングリコール、グリセリン、ソル
ビトールなどの多価アルコール、ヒアルロン酸ナトリウ
ム、ピロリドンカルボン酸ナトリウム、乳酸ナトリウム
などの保湿剤、ポリグリセリン脂肪酸エステル、ポリオ
キシエチレンソルビタン脂肪酸エステル、ポリオキシエ
チレンアルキルエーテルなどのノニオン性界面活性剤、
アルキル硫酸塩、ポリオキシエチレンアルキルエーテル
硫酸塩、アルキルスルホコハク酸塩、アルキルエーテル
カルボン酸塩、N−アシルグルタミン酸塩などのアニオ
ン性界面活性剤、アルキルベタイン、アルキルアミドプ
ロピルベタイン、イミダゾリニウムベタインなどの両性
界面活性剤、塩化アルキルトリメチルアンモニウム、塩
化ジアルキルジメチルアンモニウムなどのカチオン性界
面活性剤、上記以外のタンパク質加水分解物、グリシ
ン、プロリン、セリンなどのアミノ酸、キサンタンガ
ム、ヒドロキシエチルセルロース、ヒドロキシプロピル
セルロースなどの増粘剤、ポリビニルピロリドン、ビニ
ルピロリドン・酢酸ビニル共重合体、アクリル樹脂アル
カノールアミン液、N−メタクリロイルオキシエチル
N,N−ジメチルアンモニウム−α−N−メチルカルボ
キシベタイン・メタクリル酸アルキルエステル共重合
体、ビニルピロリドン・N,N−ジメチルアミノエチル
メタクリル酸共重合体ジエチル硫酸塩液などのセット樹
脂、金属イオン封鎖剤、pH調整剤、防腐剤、紫外線吸
収剤、酸化防止剤、色素、香料などを必要に応じて適宜
配合することができる。The hair color treating agent of the present invention comprising a pre-treatment agent and a post-treatment agent can contain various components in addition to the above-mentioned components, as long as the effects of the present invention are not impaired. . That is, higher alcohols such as myristyl alcohol, cetyl alcohol, stearyl alcohol,
Liquid paraffin, Vaseline, hydrocarbons such as squalane, isopropyl myristate, isopropyl palmitate, ester oils such as decyl oleate, camellia oil,
Animal and vegetable oils such as jojoba oil, olive oil and mink oil, waxes such as beeswax and candelilla wax, silicone oils such as dimethylpolysiloxane and methylphenylpolysiloxane, higher fatty acids such as palmitic acid, stearic acid and behenic acid, Polyhydric alcohols such as ethylene glycol, propylene glycol, 1,3-butylene glycol, glycerin and sorbitol; humectants such as sodium hyaluronate, sodium pyrrolidone carboxylate and sodium lactate; polyglycerin fatty acid esters; polyoxyethylene sorbitan fatty acid esters; Nonionic surfactants such as polyoxyethylene alkyl ethers,
Anionic surfactants such as alkyl sulfates, polyoxyethylene alkyl ether sulfates, alkyl sulfosuccinates, alkyl ether carboxylates, N-acyl glutamates, alkyl betaines, alkyl amidopropyl betaines, imidazolinium betaines, etc. Amphoteric surfactants, cationic surfactants such as alkyltrimethylammonium chloride, dialkyldimethylammonium chloride, protein hydrolysates other than the above, amino acids such as glycine, proline, serine, xanthan gum, hydroxyethylcellulose, hydroxypropylcellulose, etc. Viscous agent, polyvinylpyrrolidone, vinylpyrrolidone / vinyl acetate copolymer, acrylic resin alkanolamine solution, N-methacryloyloxyethyl N, N-dimethylammonium Set resins such as um-α-N-methylcarboxybetaine / alkyl methacrylate copolymer, vinylpyrrolidone / N, N-dimethylaminoethyl methacrylic acid diethyl sulfate solution, sequestering agent, pH adjuster , A preservative, an ultraviolet absorber, an antioxidant, a dye, a fragrance, and the like can be appropriately compounded as necessary.
【0021】本発明のヘアカラー用処理剤における前処
理剤及び後処理剤の剤型は、液状、ミスト状、クリーム
状、ゲル状、泡状、エアゾールなど種々のタイプが可能
で、特に限定されるものではない。The form of the pre-treatment agent and post-treatment agent in the hair color treatment agent of the present invention can be of various types such as liquid, mist, cream, gel, foam, and aerosol, and is particularly limited. Not something.
【0022】上記の様な本発明のヘアカラー用処理剤を
用いて毛髪を処理するにあたり、前処理剤を塗布した
後、ヘアカラー処理を行い、その後後処理剤を塗布する
ことによって本発明の効果が達成される。この方法にお
いて、前処理剤を塗布した後、乾燥させなくてもよい
し、ドライヤー、スチーマーなどで加温し乾燥させても
よい。前処理剤に含有させたケラチン加水分解物または
その誘導体は、毛髪が濡れた状態では浸透し、乾燥させ
ることで疎水結合により毛髪に強く吸着する。こうした
効果を有効に発揮させるためには、前処理剤を塗布後、
一定時間加温放置することが好ましい。カラー処理後の
後処理剤の塗布後は、洗い流してもよいし洗い流さなく
てもよいが、その効果をより向上させるためには後処理
剤を塗布後、一定時間加温放置することが好ましい。In treating hair using the hair color treatment agent of the present invention as described above, a hair color treatment is performed after applying a pre-treatment agent, and then a post-treatment agent is applied. The effect is achieved. In this method, after the pretreatment agent is applied, it may not be dried, or may be dried by heating with a drier, a steamer or the like. The keratin hydrolyzate or a derivative thereof contained in the pretreatment agent penetrates when the hair is wet, and is strongly adsorbed to the hair by hydrophobic bonding when dried. In order to exhibit these effects effectively, after applying the pretreatment agent,
It is preferable to leave for a certain period of time while heating. After the application of the post-treatment agent after the color treatment, it may or may not be washed away. However, in order to further improve the effect, it is preferable to leave the post-treatment agent heated for a certain period of time after the application of the post-treatment agent.
【0023】尚、本発明の後処理剤を、ヘアカラー処理
前に塗布することも可能であり、こうした使用方法によ
ってもヘアカラーによる損傷を防止することができる。
特に油分(例えばシリコーンなど)を含有させた後処理
剤を毛髪の傷みの激しい部分に塗布することで、ヘアカ
ラーの染まりを弱めることができるとともに損傷を防止
することができる。また本発明のヘアカラー用処理剤に
よって処理した後は、ヘアトリートメントやヘアクリー
ムなどを使用することで更に毛髪のコンディションを整
えることができる。It is to be noted that the post-treatment agent of the present invention can be applied before the hair color treatment, and such a method of use can also prevent the hair color from being damaged.
In particular, by applying a post-treatment agent containing an oil (for example, silicone) to a severely damaged portion of the hair, it is possible to reduce the staining of the hair color and to prevent damage. After the treatment with the hair color treating agent of the present invention, the condition of the hair can be further adjusted by using a hair treatment or a hair cream.
【0024】次に、実施例によって本発明の詳細を説明
するが、下記実施例は本発明を制限するものではなく、
前・後記の趣旨を逸脱しない範囲で変更実施すること
は、全て本発明の技術範囲に包含される。Next, the present invention will be described in detail with reference to examples, but the following examples do not limit the present invention.
Modifications and alterations without departing from the spirit of the preceding and the following are all included in the technical scope of the present invention.
【0025】[0025]
【実施例】(実施例1〜5、参考例1)下記表1に示す
組成で前処理剤を調製した。尚、表中の各成分の配合量
は質量%である。EXAMPLES (Examples 1 to 5, Reference Example 1) Pretreatment agents having the compositions shown in Table 1 below were prepared. In addition, the compounding quantity of each component in a table | surface is a mass%.
【0026】[0026]
【表1】 [Table 1]
【0027】上記前処理剤を用いて下記の通り処理し、
染料の定着性を評価した。その結果を表2に示す。Using the above pretreatment agent, the following treatment is carried out,
The fixability of the dye was evaluated. Table 2 shows the results.
【0028】(染料の定着性) (1)処理方法 毛束をハイブリーチ1回処理(ハイブリーチ剤:中野製
薬製)し、損傷毛を準備した。ハイブリーチ毛を各前処
理剤に40℃、30分浸漬し、脱水、40℃、30分ラ
ップで包み加温した後、すすぎ、自然乾燥させた。前処
理剤にて処理した毛束を酸化染毛剤(アッシュ:中野製
薬製)で染色し、更に毛束を2%ラウリル硫酸トリエタ
ノールアミン水溶液に60℃、1時間浸漬した。 (2)測色 上記処理を行った毛束のL*、a*、b*を色差計にて
測定し、b*値を比較することにより、酸化染毛剤(ア
ッシュ)の染料の定着性を評価した。b*値が小さいほ
ど青みが強く、染料の定着性に優れていることを示す。(Dye fixability) (1) Treatment method The hair bundle was treated once with a high bleach (a high bleaching agent: manufactured by Nakano Pharmaceutical Co., Ltd.) to prepare damaged hair. The high bleach hair was immersed in each pretreatment agent at 40 ° C. for 30 minutes, dehydrated, wrapped in wrap at 40 ° C. for 30 minutes, heated, rinsed, and air-dried. The hair bundle treated with the pretreatment agent was dyed with an oxidative hair dye (Ash: manufactured by Nakano Pharmaceutical), and the hair bundle was immersed in a 2% aqueous solution of triethanolamine lauryl sulfate at 60 ° C. for 1 hour. (2) Colorimetry L *, a *, and b * of the hair bundle subjected to the above treatment are measured by a color difference meter, and the b * values are compared to determine the fixability of the dye of the oxidative hair dye (ash). Was evaluated. The smaller the b * value, the stronger the bluish color and the better the fixability of the dye.
【0029】[0029]
【表2】 [Table 2]
【0030】この結果から明らかなように、本発明の前
処理剤を使用した実施例1〜5は、b*値が小さく、退
色しやすいアッシュの青みが残っており、染料の定着性
に優れていることがわかる。特にα−ケラトースを用い
た実施例1が、染料の定着性に優れていることがわか
る。これに対して本発明の前処理剤を使用していない参
考例1では、b*値が大きく、染料の定着が悪いことが
わかる。As is apparent from the results, Examples 1 to 5 using the pretreatment agent of the present invention have a small b * value, leave ash bluish easily discolored, and have excellent dye fixing properties. You can see that it is. In particular, it can be seen that Example 1 using α-keratose was excellent in dye fixability. On the other hand, in Reference Example 1 in which the pretreatment agent of the present invention was not used, the b * value was large, and it was found that the fixing of the dye was poor.
【0031】(実施例6〜11、参考例2)下記表3に
示す組成で前処理剤を調製した。表中の各成分の配合量
は質量%である。(Examples 6 to 11, Reference Example 2) Pretreatment agents having the compositions shown in Table 3 below were prepared. The amount of each component in the table is% by mass.
【0032】[0032]
【表3】 [Table 3]
【0033】上記前処理剤の染料の定着性を評価し、そ
の結果を表4に示した。評価方法は、実施例1〜5、参
考例1の方法と同様である。The dye fixability of the above pretreatment agent was evaluated, and the results are shown in Table 4. The evaluation method is the same as the methods of Examples 1 to 5 and Reference Example 1.
【0034】[0034]
【表4】 [Table 4]
【0035】この結果から明らかなように、本発明の前
処理剤を使用した実施例6〜11は、b*値が小さく、
退色しやすいアッシュの青みが残っており、染料の定着
性に優れていることがわかる。これに対して本発明の前
処理剤を使用していない参考例2では、b*値が大き
く、染料の定着が悪いことがわかる。As is clear from the results, Examples 6 to 11 using the pretreatment agent of the present invention have small b * values,
The bluish color of the ash which is easily discolored remains, indicating that the dye has excellent fixability. On the other hand, in Reference Example 2 in which the pretreatment agent of the present invention was not used, the b * value was large, indicating that the fixing of the dye was poor.
【0036】(実施例12、13、参考例3)前記表3
に示したNo.8の前処理剤に、毛束を浸漬する際の浸
漬時間を変えて、染料の定着性を評価した。その結果を
下記表5に示す。このときの評価方法は、前記実施例1
〜5、参考例1の方法と同様である。(Examples 12, 13 and Reference Example 3)
No. shown in FIG. The fixability of the dye was evaluated by changing the immersion time when the hair bundle was immersed in the pretreatment agent No. 8 described above. The results are shown in Table 5 below. The evaluation method at this time is as described in the first embodiment.
To 5, the same as the method of Reference Example 1.
【0037】[0037]
【表5】 [Table 5]
【0038】この結果から明らかなように、実施例12
と13のb*値の比較では、浸漬の時間の長い実施例1
2のb*値が小さく、退色しやすいアッシュの青みがよ
り残っていることがわかる。これにより、浸漬時間を長
くすると染料の定着性を向上させることができることが
わかる。As is apparent from the results, Example 12
Comparison between b * value of Example 1 and Example 13 shows that
It can be seen that the b * value of No. 2 is small and the bluish color of the ash that is easily discolored remains. Thus, it is understood that the fixing property of the dye can be improved by increasing the immersion time.
【0039】(実施例14〜18、参考例4〜6)前記
表3に示したNo.8のpHを変えた前処理剤を調製し
て、染料の定着性、損傷防止効果、変色について評価し
た。その結果を下記表6に示す。このときの評価方法
は、下記の通りである。(Examples 14 to 18, Reference Examples 4 to 6) A pretreatment agent having a pH of 8 was prepared, and the fixability, damage prevention effect, and discoloration of the dye were evaluated. The results are shown in Table 6 below. The evaluation method at this time is as follows.
【0040】(染料の定着性)実施例1〜5、参考例1
の方法と同様。(Dye fixability) Examples 1 to 5, Reference Example 1
The same way.
【0041】(損傷防止効果:官能評価)専門パネラー
10名により、実施例1〜5、参考例1と同様の方法で
処理した毛束の「手触り感」について、良い場合を5
点、悪い場合を1点とする5段階で官能評価し、評点の
平均値を求め、下記の基準で評価した。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Effect of Damage Prevention: Sensory Evaluation) Five expert panelists evaluated the "feeling feeling" of the hair bundles treated in the same manner as in Examples 1 to 5 and Reference Example 1 in 5 cases.
The sensory evaluation was performed on a scale of 1 to 5 in terms of points and bad cases, the average of the scores was obtained, and evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0042】(変色)専門パネラー10名により、実施
例1〜5、参考例1と同様の方法で処理した毛束の「変
色」について、変色のないものを5点、変色のきついも
のを1点とする5段階で目視評価し、評点の平均値を求
め、下記の基準で評価した。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Discoloration) As for "discoloration" of hair bundles treated in the same manner as in Examples 1 to 5 and Reference Example 1 by 10 expert panelists, 5 points without discoloration and 1 point with severe discoloration It was visually evaluated in five stages, and the average of the scores was obtained and evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0043】[0043]
【表6】 [Table 6]
【0044】この結果から明らかなように、本発明の前
処理剤を使用した実施例14〜18は染料の定着性、損
傷防止効果に優れ、また変色も少ないことがわかる。こ
れに対して、本発明から外れる参考例4、5及び本発明
の前処理剤を使用していない参考例6は、全ての項目を
満足させることはできなかった。参考例5は、b*値が
小さく、染料の染着性が優れているように思えるが、こ
れは色味が濃い方向へ変色しているものであって、設定
されていた酸化染毛剤の色味とは異なったものであり好
ましい結果ではない。As is apparent from the results, Examples 14 to 18 using the pretreatment agent of the present invention are excellent in the fixing property of the dye, the effect of preventing damage, and the discoloration is small. On the other hand, in Reference Examples 4 and 5 deviating from the present invention and Reference Example 6 in which the pretreatment agent of the present invention was not used, all items could not be satisfied. In Reference Example 5, although the b * value was small and the dyeing properties seemed to be excellent, the color was discolored in the darker direction and the oxidized hair dye was set. Is different from that of the color, and is not a preferable result.
【0045】(実施例19〜23、参考例7)下記表7
に示す組成で前処理剤を調製した。表中の各成分の配合
量は質量%である。(Examples 19 to 23, Reference Example 7)
A pretreatment agent was prepared with the composition shown in Table 1. The amount of each component in the table is% by mass.
【0046】[0046]
【表7】 [Table 7]
【0047】上記前処理剤を下記の通り処理し、引っ張
り強度を測定することにより損傷防止効果を評価した。
その結果を図1に示す。The pretreatment agent was treated as described below, and the tensile strength was measured to evaluate the effect of preventing damage.
The result is shown in FIG.
【0048】(損傷防止効果:引っ張り強度の測定) (1)処理方法 毛束をハイブリーチ3回処理(ハイブリーチ剤:中野製
薬製)し、損傷毛を準備した。ハイブリーチ毛を各前処
理剤に10秒浸漬した後、引き上げ、液が垂れない程度
まで放置した。40℃、10分ラップで包み加温した
後、ドライヤーにて乾燥させた。前処理剤にて処理した
毛束を酸化染毛剤(アッシュ:中野製薬製)で染色し、
ラウリル硫酸トリエタノーリアミン水溶液で洗浄後、ド
ライヤーにて乾燥させた。 (2)引っ張り強度測定 各毛束を恒温恒湿室(20℃、60%RH)に24時間
以上放置した後、テンシロンUTM−11−20(オリ
エンテック製)を用い、純水中にて引っ張り強度の測定
を行った。(Effect of Damage Prevention: Measurement of Tensile Strength) (1) Treatment Method The hair bundle was treated three times with a high bleach (a high bleach agent: manufactured by Nakano Pharmaceutical Co., Ltd.) to prepare damaged hair. The high bleached hair was immersed in each pretreatment agent for 10 seconds, pulled up, and left until the solution did not drip. After wrapping in a wrap at 40 ° C. for 10 minutes and heating, it was dried with a dryer. The hair bundle treated with the pretreatment agent is dyed with an oxidative hair dye (Ash: manufactured by Nakano Pharmaceutical),
After washing with a triethanolamine aqueous solution of lauryl sulfate, it was dried with a dryer. (2) Measurement of tensile strength Each hair bundle was left in a constant temperature and humidity chamber (20 ° C., 60% RH) for 24 hours or more, and then pulled in pure water using Tensilon UTM-11-20 (manufactured by Orientec). The strength was measured.
【0049】この結果から明らかなように、本発明の前
処理剤を使用した実施例19〜23は、酸化染毛剤によ
る引っ張り強度の低下を防止する効果があることがわか
る。これに対し、本発明の前処理剤を使用しない参考例
7は、酸化染毛剤による引っ張り強度の低下が大きいこ
とがわかる。As is apparent from the results, Examples 19 to 23 using the pretreatment agent of the present invention have an effect of preventing the oxidative hair dye from lowering the tensile strength. On the other hand, in Reference Example 7 in which the pretreatment agent of the present invention was not used, it was found that the tensile strength was significantly reduced by the oxidative hair dye.
【0050】(実施例24〜27、参考例8)下記表8
に示す組成で後処理剤を調製した。表中の各成分の配合
量は質量%である。(Examples 24 to 27, Reference Example 8) Table 8 below
Was prepared with the composition shown in Table 1. The amount of each component in the table is% by mass.
【0051】[0051]
【表8】 [Table 8]
【0052】前記表7のNo.11の前処理剤及び上記
後処理剤を下記の通り処理し、毛髪への塗布性、ヘアカ
ラー処理後のゴワツキ感のなさ、しっとり感の付与、耐
シャンプー性を評価した。その結果を、下記表9に示
す。In Table 7 above, No. Eleven pre-treatment agents and the above-mentioned post-treatment agents were treated as described below to evaluate the applicability to hair, the lack of stiffness after hair color treatment, the impartation of a moist feeling, and the shampooing resistance. The results are shown in Table 9 below.
【0053】(毛髪への塗布性)頭髪に前処理剤を塗布
し、ドライヤーにて乾燥後、酸化染毛剤(アッシュ:中
野製薬製)で染色した。その後後処理剤を塗布する際の
「毛髪への塗布性」について、専門パネラー10名によ
り、良い場合を5点、悪い場合を1点とする5段階で官
能評価し、評点の平均値を求め、下記の基準で評価し
た。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Applicability to Hair) The hair was coated with a pretreatment agent, dried with a drier, and dyed with an oxidative hair dye (Ash: manufactured by Nakano Pharmaceutical). Afterwards, the "applicability to hair" when applying the post-treatment agent was sensory-evaluated by 10 expert panelists on a 5-point scale with 5 points for good cases and 1 point for bad cases, and the average value of the scores was obtained. Was evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0054】(ヘアカラー後のゴワツキ感のなさ)頭髪
に前処理剤を塗布し、ドライヤーにて乾燥後、酸化染毛
剤(アッシュ:中野製薬製)で染色した。その後後処理
剤を塗布し、40℃で5分放置後、洗い流し、ドライヤ
ーで乾燥させて、「ヘアカラー処理後のゴワツキ感のな
さ」について専門パネラー10名により、良い場合を5
点、悪い場合を1点とする5段階で官能評価し、評点の
平均値を求め、下記の基準で評価した。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Lack of stiffness after hair coloring) A pretreatment agent was applied to the hair, dried with a drier, and dyed with an oxidative hair dye (Ash: manufactured by Nakano Pharmaceutical). After that, apply a post-treatment agent, leave it at 40 ° C for 5 minutes, wash it off, dry it with a drier, and give 10 good panelists about “no stiffness after hair color treatment”.
The sensory evaluation was performed on a scale of 1 to 5 in terms of points and bad cases, the average of the scores was obtained, and evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0055】(しっとり感の付与)頭髪に前処理剤を塗
布し、ドライヤーにて乾燥後、酸化染毛剤(アッシュ:
中野製薬製)で染色した。その後、後処理剤を塗布し、
40°Cで5分放置後、洗い流し、ドライヤーで乾燥さ
せて「しっとり感の付与」について専門パネラー10名
により、よい場合を5点、悪い場合を1点とする5段階
で官能評価し、評点の平均値を求め、下記の基準で評価
した。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Providing a moist feeling) A pretreatment agent is applied to the hair, dried with a dryer, and then oxidized hair dye (ash:
(Manufactured by Nakano Pharmaceutical Co., Ltd.). After that, apply a post-treatment agent,
After leaving it at 40 ° C for 5 minutes, it was rinsed off, dried with a drier, and given 10 moist feelings by a panel of 10 expert panelists for “giving a moist feeling”. Was determined and evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0056】(耐シャンプー性)頭髪に前処理剤を塗布
し、ドライヤーにて乾燥後、酸化染毛剤(アッシュ:中
野製薬製)で染色した。その後後処理剤を塗布し、40
℃で5分放置後、洗い流し、ドライヤーで乾燥させた。
次にシャンプーを3回行いドライヤーで乾燥させて、
「耐シャンプー性」について専門パネラー10名によ
り、良い場合を5点、悪い場合を1点とする5段階で官
能評価し、評点の平均値を求め、下記の基準で評価し
た。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Shampoo resistance) The hair was coated with a pretreatment agent, dried with a drier, and dyed with an oxidative hair dye (Ash: manufactured by Nakano Pharmaceutical). Thereafter, a post-treatment agent is applied, and 40
After leaving it at 5 ° C. for 5 minutes, it was washed off and dried with a dryer.
Next, shampoo three times and dry with a dryer,
"Shampoo resistance" was evaluated by a panel of 10 expert panelists in five stages, with 5 points for good cases and 1 point for bad cases, and the average of the scores was determined and evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0057】[0057]
【表9】 [Table 9]
【0058】この結果から明らかなように、本発明の前
処理剤で処理し、その後本発明の後処理剤で処理した実
施例24〜30は、ヘアカラー後のゴワツキ感が改善さ
れ、耐シャンプー性に優れていることがわかる。また植
物由来のタンパク質加水分解物および卵白由来のタンパ
ク質加水分解物を含有している実施例27〜29はしっ
とり感が付与され、植物由来のタンパク質加水分解物の
カチオン化物を含有している実施例27は毛髪への塗布
性が改善されることがわかる。尚、実施例30は、液状
のためトリガーに充填し、ミスト状に噴霧して使用し
た。これに対して前処理剤のみで仕上げた参考例8は、
ヘアカラー後のゴワツキ感が改善されていないことがわ
かる。As is apparent from the results, Examples 24 to 30 which were treated with the pre-treatment agent of the present invention and then treated with the post-treatment agent of the present invention showed improved stiffness after hair coloring and improved shampoo resistance. It turns out that it is excellent. Examples 27 to 29 containing a plant-derived protein hydrolyzate and an egg white-derived protein hydrolyzate are examples in which a moist feeling is imparted and the plant-derived protein hydrolyzate contains a cationized product. 27 indicates that the applicability to hair is improved. In addition, since Example 30 was liquid, it was filled in a trigger and sprayed in the form of a mist. On the other hand, Reference Example 8 finished only with the pretreatment agent,
It can be seen that the feeling of roughness after hair coloring is not improved.
【0059】(実施例31、32、参考例9)前記表7
のNo.11の前処理剤及び表8のNo.7の後処理剤
を前処理剤として下記の通り処理し、引っ張り強度を測
定することにより損傷防止効果を評価した。その結果を
図2に示す。(Examples 31 and 32, Reference Example 9)
No. 11 and No. 11 in Table 8. 7 was treated as a pretreatment agent as described below, and the damage prevention effect was evaluated by measuring the tensile strength. The result is shown in FIG.
【0060】(損傷防止効果:引っ張り強度の測定) (1)処理方法 毛束をハイブリーチ1回処理(ハイブリーチ剤:中野製
薬製)し、次にパーマ1回処理(チオ系パーマ剤:中野
製薬製)し、損傷毛を準備した。損傷毛を各処理剤に1
0秒浸漬した後、引き上げ、液が垂れない程度まで放置
した。40℃、10分ラップで包み加温した後、ドライ
ヤーにて乾燥させた。処理剤にて処理した毛束を酸化染
毛剤(アッシュ:中野製薬製)で染色し、ラウリル硫酸
トリエタノールアミン水溶液で洗浄後、ドライヤーにて
乾燥させた。尚、このテストでは、後処理剤No.7を
前処理剤として使用している。 (2)引っ張り強度測定 各毛束を恒温恒湿室(20℃、60%RH)に24時間
以上放置した後、テンシロンUTM−11−20(オリ
エンテック製)を用い、純水中にて引っ張り強度の測定
を行った。(Effect of Damage Prevention: Measurement of Tensile Strength) (1) Treatment Method The hair bundle is treated once with a high bleach (a high bleaching agent: manufactured by Nakano Pharmaceutical), and then once with a permanent (a thioperming agent: Nakano). Pharmaceutical) and damaged hair was prepared. Apply damaged hair to each treatment
After immersion for 0 seconds, it was pulled up and allowed to stand until the liquid did not drip. After wrapping in a wrap at 40 ° C. for 10 minutes and heating, it was dried with a dryer. The hair bundle treated with the treating agent was dyed with an oxidative hair dye (Ash: manufactured by Nakano Pharmaceutical), washed with an aqueous solution of triethanolamine lauryl sulfate, and dried with a dryer. In this test, the post-treatment agent No. 7 is used as a pretreatment agent. (2) Measurement of tensile strength Each hair bundle was left in a constant temperature and humidity chamber (20 ° C., 60% RH) for 24 hours or more, and then pulled in pure water using Tensilon UTM-11-20 (manufactured by Orientec). The strength was measured.
【0061】この結果から明らかなように、本発明の前
処理剤No.11を使用した実施例31は、酸化染毛剤
による引っ張り強度の低下を防止する効果があることが
わかる。また後処理剤No.7を前処理剤として使用し
た実施例32も同様の効果があることがわかる。これに
より、本発明の後処理剤は、前処理剤としても使用で
き、ヘアカラー処理における毛髪の損傷を防止する効果
を有することがわかる。これに対して本発明の前処理剤
を使用しない参考例9は、酸化染毛剤による引っ張り強
度の低下が大きいことがわかる。As is evident from the results, the pretreatment agent No. It can be seen that Example 31 using No. 11 has an effect of preventing a decrease in the tensile strength due to the oxidative hair dye. In addition, the post-treatment agent No. It can be seen that Example 32 in which No. 7 was used as a pretreatment had the same effect. This shows that the post-treatment agent of the present invention can also be used as a pre-treatment agent, and has an effect of preventing damage to hair in hair color treatment. On the other hand, in Reference Example 9 in which the pretreatment agent of the present invention was not used, it was found that the tensile strength was significantly reduced by the oxidative hair dye.
【0062】(実施例33、参考例10)前記表7のN
o.11の前処理剤を用いて下記の通り処理し、染料の
定着性を評価した。その結果を、下記表10に示す。
尚、実施例1〜32は、酸化染毛剤に対する効果を評価
したものであったが、本実施例以降は、酸性染毛料に対
する効果を評価したものである。(Example 33, Reference Example 10)
o. Using the 11 pretreatment agents, treatment was performed as described below, and the fixability of the dye was evaluated. The results are shown in Table 10 below.
In Examples 1 to 32, the effects on oxidative hair dyes were evaluated. From this Example, the effects on acid hair dyes were evaluated.
【0063】(染料の定着性) (1)処理方法 毛束をハイブリーチ3回処理(ハイブリーチ剤:中野製
薬製)し、損傷毛を準備した。ハイブリーチ毛を前処理
剤に10秒浸漬し、脱水後、ドライヤーで乾燥させた。
前処理剤にて処理した毛束を酸性染毛料(ブルー:中野
製薬製)で染色し、更に毛束を2%ラウリル硫酸トリエ
タノールアミン水溶液に50℃、30分浸漬した。 (2)測色 上記処理を行った毛束のL*、a*、b*を色差計にて
測定し、b*値を比較することにより、酸性染毛料(ブ
ルー)の染料の定着性を評価した。b*値が小さいほど
青みが強く、染料の定着性に優れていることを示す。(Dye fixability) (1) Treatment method The hair bundle was treated three times with a high bleach (a high bleaching agent: manufactured by Nakano Pharmaceutical Co., Ltd.) to prepare damaged hair. The high bleach hair was immersed in the pretreatment agent for 10 seconds, dehydrated, and then dried with a dryer.
The hair bundle treated with the pretreatment agent was dyed with an acidic hair dye (Blue: manufactured by Nakano Pharmaceutical), and the hair bundle was immersed in a 2% aqueous solution of triethanolamine lauryl sulfate at 50 ° C. for 30 minutes. (2) Colorimetry L *, a *, and b * of the hair bundle subjected to the above treatment are measured with a color difference meter, and the b * values are compared to determine the fixability of the dye of the acidic hair dye (blue). evaluated. The smaller the b * value, the stronger the bluish color and the better the fixability of the dye.
【0064】[0064]
【表10】 [Table 10]
【0065】この結果から明らかなように、本発明の前
処理剤を使用した実施例33は、b*値が小さく、酸性
染毛料(ブルー)の青みが残っており、染料の定着性に
優れていることがわかる。これに対して本発明の前処理
剤を使用していない参考例10では、b*値が大きく、
染料の定着が悪いことがわかる。実施例1〜32は、酸
化染毛剤に対する効果であったが、今回の結果から酸性
染毛料に対しても有効であることがわかる。As is clear from the results, in Example 33 using the pretreatment agent of the present invention, the b * value was small, the bluish color of the acidic hair dye (blue) remained, and the fixing property of the dye was excellent. You can see that it is. On the other hand, in Reference Example 10 in which the pretreatment agent of the present invention was not used, the b * value was large,
It can be seen that the fixing of the dye is poor. Examples 1 to 32 show the effect on the oxidative hair dye, but it is understood from the present results that they are also effective on the acidic hair dye.
【0066】(実施例34、参考例11)前記表7のN
o.11の前処理剤を用いて下記の通り処理し、染料の
定着性を評価した。その結果を、表11に示す。(Example 34, Reference Example 11)
o. Using the 11 pretreatment agents, treatment was performed as described below, and the fixability of the dye was evaluated. Table 11 shows the results.
【0067】(染料の定着性) (1)処理方法 毛束をハイブリーチ3回処理(ハイブリーチ剤:中野製
薬製)し、損傷毛を準備した。ハイブリーチ毛を前処理
剤に10秒浸漬し、脱水後、ドライヤーで乾燥させた。
前処理剤にて処理した毛束を酸性染毛料(レッド:中野
製薬製)で染色し、更に毛束を2%ラウリル硫酸トリエ
タノールアミン水溶液に50℃、1時間浸漬した。 (2)測色 上記処理を行った毛束のL*、a*、b*を色差計にて
測定し、a*値を比較することにより、酸性染毛料(レ
ッド)の染料の定着性を評価した。a*値が大きいほど
赤みが強く、染料の定着性に優れていることを示す。(Dye fixability) (1) Treatment method The hair bundle was treated three times with a high bleach (a high bleaching agent: manufactured by Nakano Pharmaceutical Co., Ltd.) to prepare damaged hair. The high bleach hair was immersed in the pretreatment agent for 10 seconds, dehydrated, and then dried with a dryer.
The hair bundle treated with the pretreatment agent was dyed with an acidic hair dye (Red: manufactured by Nakano Pharmaceutical), and the hair bundle was immersed in a 2% aqueous solution of triethanolamine lauryl sulfate at 50 ° C. for 1 hour. (2) Colorimetry L *, a *, and b * of the hair bundle subjected to the above treatment are measured with a color difference meter, and the a * values are compared to determine the fixability of the dye of the acidic hair dye (red). evaluated. The larger the a * value, the stronger the redness, indicating that the dye has excellent fixability.
【0068】[0068]
【表11】 [Table 11]
【0069】この結果から明らかなように、本発明の前
処理剤を使用した実施例34は、a*値が大きく、酸性
染毛料(レッド)の赤みが残っており、染料の定着性に
優れていることがわかる。これに対して本発明の前処理
剤を使用していない参考例11では、a*値が小さく、
染料の定着が悪いことがわかる。As is apparent from the results, Example 34 using the pretreatment agent of the present invention has a large a * value, the reddish color of the acidic hair dye (red) remains, and the dye has excellent fixability. You can see that it is. On the other hand, in Reference Example 11 in which the pretreatment agent of the present invention was not used, the a * value was small,
It can be seen that the fixing of the dye is poor.
【0070】(実施例35、参考例12)前記表7のN
o.11の前処理剤及び表8のNo.4の後処理剤を下
記の通り処理し、ヘアカラー処理後のゴワツキ感のな
さ、耐シャンプー性を評価した。その結果を、表12に
示す。(Example 35, Reference Example 12)
o. 11 and No. 11 in Table 8. The four post-treatment agents were treated as described below, and were evaluated for lack of stiffness and shampoo resistance after hair color treatment. Table 12 shows the results.
【0071】(ヘアカラー後のゴワツキ感のなさ)頭髪
に前処理剤を塗布し、ドライヤーにて乾燥後、酸性染毛
料(ブルー:中野製薬製)で染色した。その後後処理剤
を塗布し、40℃で5分放置後、洗い流し、ドライヤー
で乾燥させて、「ヘアカラー処理後のゴワツキ感のな
さ」について専門パネラー10名により、良い場合を5
点、悪い場合を1点とする5段階で官能評価し、評点の
平均値を求め、下記の基準で評価した。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Lack of stiffness after hair coloring) The hair was coated with a pretreatment agent, dried with a drier, and dyed with an acidic hair dye (Blue: manufactured by Nakano Pharmaceutical). After that, apply a post-treatment agent, leave it at 40 ° C for 5 minutes, wash it off, dry it with a drier, and give 10 good panelists about “no stiffness after hair color treatment”.
The sensory evaluation was performed on a scale of 1 to 5 in terms of points and bad cases, the average of the scores was obtained, and evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0072】(耐シャンプー性)頭髪に前処理剤を塗布
し、ドライヤーにて乾燥後、酸性染毛料(ブルー:中野
製薬製)で染色した。その後後処理剤を塗布し、40℃
で5分放置後、洗い流し、ドライヤーで乾燥させた。次
にシャンプーを3回行いドライヤーで乾燥させて、「耐
シャンプー性」について専門パネラー10名により、良
い場合を5点、悪い場合を1点とする5段階で官能評価
し、評点の平均値を求め、下記の基準で評価した。 ◎:4点以上 ○:3点以上4点未満 △:2点以上3点未満 ×:1点以上2点未満(Shampoo resistance) The hair was coated with a pretreatment agent, dried with a drier, and dyed with an acidic hair dye (blue: manufactured by Nakano Pharmaceutical). After that, a post-treatment agent is applied,
For 5 minutes, rinsed, and dried with a dryer. Next, shampoo three times and dry with a drier. Sensory evaluation of "shampoo resistance" was carried out by 10 expert panelists on a 5-point scale with 5 points for good cases and 1 point for bad cases. And evaluated according to the following criteria. :: 4 points or more ○: 3 points or more and less than 4 points Δ: 2 points or more and less than 3 points ×: 1 point or more and less than 2 points
【0073】[0073]
【表12】 [Table 12]
【0074】この結果から明らかなように、本発明の前
処理剤で処理し、その後本発明の後処理剤で処理した実
施例35は、ヘアカラー後のゴワツキ感はなく、耐シャ
ンプー性に優れていることがわかる。これに対して前処
理剤のみで仕上げた参考例12は、やや硬さがあり、手
触りが良好ではなかった。As is evident from the results, Example 35 treated with the pre-treatment agent of the present invention and then treated with the post-treatment agent of the present invention has no stiffness after hair coloring and has excellent shampoo resistance. You can see that it is. On the other hand, Reference Example 12, which was finished only with the pretreatment agent, was slightly hard and had a poor feel.
【0075】[0075]
【発明の効果】本発明は以上のように構成されており、
ヘアカラー処理における毛髪の損傷を防止し、染料の定
着を良くし、ヘアカラー処理後のゴワツキ感を改善する
のに有効であるため、損傷の激しい毛髪に対してもヘア
カラー処理後の手触りが良く、美しい色を長持ちさせる
ことが可能である。The present invention is configured as described above.
It is effective in preventing hair damage during hair color treatment, improving dye fixation, and improving the feeling of stiffness after hair color treatment, so that the touch after hair color treatment can be applied to severely damaged hair. It is possible to make good and beautiful colors last longer.
【図1】実施例19〜23、参考例7における前処理剤
の損傷防止効果を比較して示したグラフである。BRIEF DESCRIPTION OF DRAWINGS FIG. 1 is a graph showing a comparison between the effects of pretreatment agents in Examples 19 to 23 and Reference Example 7 for preventing damage.
【図2】実施例31、32、参考例9における前処理剤
の損傷防止効果を比較して示したグラフである。FIG. 2 is a graph showing a comparison between the effects of pretreatment agents in Examples 31, 32 and Reference Example 9 for preventing damage.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 田中 真一 滋賀県草津市南山田町63−1 中野製薬株 式会社内 Fターム(参考) 4C083 AC072 AC122 AC302 AC542 AC641 AC642 AD092 AD152 AD411 AD412 AD441 AD442 AD571 AD572 CC31 CC33 EE07 EE26 EE29 ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Shinichi Tanaka 63-1 Minamiyamadacho, Kusatsu-shi, Shiga F-term in Nakano Pharmaceutical Co., Ltd. (reference) 4C083 AC072 AC122 AC302 AC542 AC641 AC642 AD092 AD152 AD411 AD412 AD441 AD442 AD571 AD572 CC31 CC33 EE07 EE26 EE29
Claims (10)
ー用前処理剤であって、ケラチン加水分解物および/ま
たはその誘導体を含有することを特徴とするヘアカラー
用前処理剤。1. A pretreatment agent for a hair color used before a hair color treatment, characterized by containing a keratin hydrolyzate and / or a derivative thereof.
載のヘアカラー用前処理剤。2. The pretreatment agent for a hair color according to claim 1, wherein the pH is in the range of 4 to 8.
である請求項1または2に記載のヘアカラー用前処理
剤。3. The pretreatment agent for hair color according to claim 1, wherein the keratin hydrolyzate is α-keratose.
剤を毛髪に塗布した後、ヘアカラー処理を行うことを特
徴とする毛髪処理方法。4. A hair treatment method, comprising applying a pre-treatment agent according to claim 1 to hair and then performing a hair coloring treatment.
剤と後処理剤からなるヘアカラー用処理剤であって、前
記前処理剤はケラチン加水分解物および/またはその誘
導体を含有することを特徴とするヘアカラー用処理剤。5. A hair coloring treatment agent comprising a pre-treatment agent and a post-treatment agent used before and after the hair color treatment, wherein the pre-treatment agent contains a keratin hydrolyzate and / or a derivative thereof. Characteristic hair color treatment agent.
求項5に記載のヘアカラー用処理剤。6. The hair coloring treatment agent according to claim 5, wherein the pH of the pretreatment agent is in the range of 4 to 8.
が、α−ケラトースである請求項5または6に記載のヘ
アカラー用処理剤。7. The hair coloring treatment agent according to claim 5, wherein the keratin hydrolyzate contained in the pretreatment agent is α-keratose.
体、リン脂質およびリン脂質の誘導体よりなる群から選
ばれる1種以上を含有するものである請求項5〜7のい
ずれかに記載のヘアカラー用処理剤。8. The hair according to claim 5, wherein the post-treating agent contains at least one selected from the group consisting of ceramide, ceramide derivatives, phospholipids and phospholipid derivatives. Color treatment agent.
加水分解物、植物由来のタンパク質加水分解物の誘導
体、卵白由来のタンパク質加水分解物および卵白由来の
タンパク質加水分解物の誘導体よりなる群から選ばれる
1種以上を含有するものである請求項8に記載のヘアカ
ラー用処理剤。9. The post-treating agent is further selected from the group consisting of a plant-derived protein hydrolyzate, a plant-derived protein hydrolyzate, an egg white-derived protein hydrolyzate, and an egg white-derived protein hydrolyzate. The hair color treating agent according to claim 8, which contains one or more selected ones.
カラー処理剤を用いて毛髪を処理するにあたり、前処理
剤を毛髪に塗布した後、ヘアカラー処理を行い、その後
後処理剤を塗布することを特徴とする毛髪処理方法。10. In treating hair with the hair color treatment agent according to any one of claims 5 to 9, after applying a pre-treatment agent to the hair, performing a hair color treatment, and then applying a post-treatment agent. A hair treatment method characterized by applying.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001294049A JP2002322035A (en) | 2001-02-20 | 2001-09-26 | Pretreatment agent for hair color, treatment agent for hair color and method for treating hair |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001-43226 | 2001-02-20 | ||
| JP2001043226 | 2001-02-20 | ||
| JP2001294049A JP2002322035A (en) | 2001-02-20 | 2001-09-26 | Pretreatment agent for hair color, treatment agent for hair color and method for treating hair |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002322035A true JP2002322035A (en) | 2002-11-08 |
Family
ID=26609690
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001294049A Pending JP2002322035A (en) | 2001-02-20 | 2001-09-26 | Pretreatment agent for hair color, treatment agent for hair color and method for treating hair |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2002322035A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7110117B2 (en) | 2002-06-28 | 2006-09-19 | Seethrough Ltd. | Hair color measurement and treatment |
| JP2010105964A (en) * | 2008-10-30 | 2010-05-13 | Aderans Co Ltd | Aftertreatment agent for permanent wave and hair color |
| WO2011045840A1 (en) * | 2009-10-15 | 2011-04-21 | 株式会社アスター美容 | Hair cosmetic composition |
| JP2015511611A (en) * | 2012-03-26 | 2015-04-20 | オーテーツェー・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングOtc Gmbh | Hair conditioning composition for permanent and semi-permanent hair dyeing applications |
| JP2023503492A (en) * | 2019-11-26 | 2023-01-30 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | Method for improving the grip of dyed keratinous material, especially human hair |
Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07330556A (en) * | 1994-06-08 | 1995-12-19 | Kanebo Ltd | Hair pretreatment and hair cosmetic and hair dyeing method |
| JPH0853328A (en) * | 1994-04-22 | 1996-02-27 | L'oreal Sa | Composition for treating and protecting hair using ceramide and a polymer containing a cationic group |
| JPH10182371A (en) * | 1996-12-20 | 1998-07-07 | Seiwa Kasei:Kk | Hair dyeing agent |
| JPH10226629A (en) * | 1997-02-18 | 1998-08-25 | Seiwa Kasei:Kk | Pretreating agent for hair dyeing |
| JPH10291919A (en) * | 1997-02-18 | 1998-11-04 | Seiwa Kasei:Kk | Pretreatment for hair dye |
| JPH11139940A (en) * | 1997-10-31 | 1999-05-25 | Seiwa Kasei Kk | Preliminarily treating agent for dyeing hair |
| WO1999034768A2 (en) * | 1998-01-12 | 1999-07-15 | Unilever Plc | Hair conditioning composition |
| JPH11269045A (en) * | 1998-03-20 | 1999-10-05 | Seiwa Kasei Kk | Hair-protecting agent |
| JPH11322571A (en) * | 1998-05-15 | 1999-11-24 | Kurooda Japan Kk | Cosmetic composition |
| JP2000309513A (en) * | 1999-02-26 | 2000-11-07 | Shiseido Co Ltd | Hair cosmetic |
| JP2001302472A (en) * | 2000-04-21 | 2001-10-31 | Seiwa Kasei:Kk | Pretreatment agent for hair dyeing |
| JP2002114644A (en) * | 2000-10-02 | 2002-04-16 | Hoyu Co Ltd | Pre-treating agent for hair dyeing |
-
2001
- 2001-09-26 JP JP2001294049A patent/JP2002322035A/en active Pending
Patent Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0853328A (en) * | 1994-04-22 | 1996-02-27 | L'oreal Sa | Composition for treating and protecting hair using ceramide and a polymer containing a cationic group |
| JPH07330556A (en) * | 1994-06-08 | 1995-12-19 | Kanebo Ltd | Hair pretreatment and hair cosmetic and hair dyeing method |
| JPH10182371A (en) * | 1996-12-20 | 1998-07-07 | Seiwa Kasei:Kk | Hair dyeing agent |
| JPH10226629A (en) * | 1997-02-18 | 1998-08-25 | Seiwa Kasei:Kk | Pretreating agent for hair dyeing |
| JPH10291919A (en) * | 1997-02-18 | 1998-11-04 | Seiwa Kasei:Kk | Pretreatment for hair dye |
| JPH11139940A (en) * | 1997-10-31 | 1999-05-25 | Seiwa Kasei Kk | Preliminarily treating agent for dyeing hair |
| WO1999034768A2 (en) * | 1998-01-12 | 1999-07-15 | Unilever Plc | Hair conditioning composition |
| JP2002500173A (en) * | 1998-01-12 | 2002-01-08 | ユニリーバー・ナームローゼ・ベンノートシヤープ | Hair conditioning composition |
| JPH11269045A (en) * | 1998-03-20 | 1999-10-05 | Seiwa Kasei Kk | Hair-protecting agent |
| JPH11322571A (en) * | 1998-05-15 | 1999-11-24 | Kurooda Japan Kk | Cosmetic composition |
| JP2000309513A (en) * | 1999-02-26 | 2000-11-07 | Shiseido Co Ltd | Hair cosmetic |
| JP2001302472A (en) * | 2000-04-21 | 2001-10-31 | Seiwa Kasei:Kk | Pretreatment agent for hair dyeing |
| JP2002114644A (en) * | 2000-10-02 | 2002-04-16 | Hoyu Co Ltd | Pre-treating agent for hair dyeing |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7110117B2 (en) | 2002-06-28 | 2006-09-19 | Seethrough Ltd. | Hair color measurement and treatment |
| US7304739B2 (en) | 2002-06-28 | 2007-12-04 | Seethrough Ltd. | Hair color measurement and treatment |
| JP2010105964A (en) * | 2008-10-30 | 2010-05-13 | Aderans Co Ltd | Aftertreatment agent for permanent wave and hair color |
| WO2011045840A1 (en) * | 2009-10-15 | 2011-04-21 | 株式会社アスター美容 | Hair cosmetic composition |
| JP2015511611A (en) * | 2012-03-26 | 2015-04-20 | オーテーツェー・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングOtc Gmbh | Hair conditioning composition for permanent and semi-permanent hair dyeing applications |
| US10226416B2 (en) | 2012-03-26 | 2019-03-12 | Clariant International Ltd. | Hair conditioning composition for permanent and semi-permanent hair coloration applications |
| JP2023503492A (en) * | 2019-11-26 | 2023-01-30 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | Method for improving the grip of dyed keratinous material, especially human hair |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2022228183B2 (en) | Hair strengthening composition and method for strengthening hair | |
| KR101196280B1 (en) | Hair cosmetics | |
| EP1655056B1 (en) | Process to colour and permanently restructure hair | |
| JP2001525822A (en) | Hair treatment composition | |
| JP4170116B2 (en) | Hair dye composition | |
| EP1837010A2 (en) | Process for relaxing or straightening hair | |
| WO2004047777A1 (en) | Cosmetic hair preparation | |
| JP7213819B2 (en) | chemical composition | |
| JPH04308522A (en) | Two-pack hair-treating agent composition and hair-treating method | |
| JP2005170838A (en) | Pretreatment agent composition for hair dyeing | |
| JP2002322035A (en) | Pretreatment agent for hair color, treatment agent for hair color and method for treating hair | |
| US5591425A (en) | Two-package pretreatment and hair relaxer compositions | |
| JP7508189B2 (en) | Hair Strengthener | |
| JP2020117442A (en) | Fiber modifier and method for treating fiber | |
| JP7531795B2 (en) | Hair treatment products | |
| JP2005255570A (en) | Hair dye composition | |
| JP3781413B2 (en) | Pretreatment composition for hair dyeing | |
| JP6564440B2 (en) | Hair treatment method | |
| JP2003300836A (en) | Hair pretreatment agent and hair pretreatment method | |
| JP2886283B2 (en) | Hair treatment agent | |
| JP3542878B2 (en) | Two-part hair treatment composition | |
| JP4577961B2 (en) | Two-component hair cosmetic and hair treatment method using the same | |
| JP2003300843A (en) | Hair treatment agent and hair treatment method | |
| JP2023003921A (en) | Treatment agent for hair deformation | |
| JP3810921B2 (en) | Keratinous fiber treatment agent composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20040818 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20080714 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20101026 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20101102 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20101222 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20110125 |