JPH0920627A - Oxidative hair dye composition - Google Patents
Oxidative hair dye compositionInfo
- Publication number
- JPH0920627A JPH0920627A JP7187871A JP18787195A JPH0920627A JP H0920627 A JPH0920627 A JP H0920627A JP 7187871 A JP7187871 A JP 7187871A JP 18787195 A JP18787195 A JP 18787195A JP H0920627 A JPH0920627 A JP H0920627A
- Authority
- JP
- Japan
- Prior art keywords
- hair dye
- hair
- dye composition
- agent
- sugar
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 131
- 239000000118 hair dye Substances 0.000 title claims abstract description 80
- 230000001590 oxidative effect Effects 0.000 title claims abstract description 79
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 82
- 235000000346 sugar Nutrition 0.000 claims abstract description 59
- 238000002156 mixing Methods 0.000 claims abstract description 30
- 239000000975 dye Substances 0.000 claims abstract description 28
- 239000007800 oxidant agent Substances 0.000 claims abstract description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- -1 aliphatic glycoside Chemical class 0.000 claims description 65
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 22
- 239000003921 oil Substances 0.000 claims description 14
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 13
- 239000000194 fatty acid Substances 0.000 claims description 13
- 229930195729 fatty acid Natural products 0.000 claims description 13
- 239000000845 maltitol Substances 0.000 claims description 12
- 229940035436 maltitol Drugs 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 10
- 235000010449 maltitol Nutrition 0.000 claims description 10
- 150000004665 fatty acids Chemical class 0.000 claims description 9
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical group OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 claims description 9
- 229930182470 glycoside Natural products 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- LQXBZWFNAKZUNM-UHFFFAOYSA-N 16-methyl-1-(16-methylheptadecoxy)heptadecane Chemical compound CC(C)CCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC(C)C LQXBZWFNAKZUNM-UHFFFAOYSA-N 0.000 claims description 5
- 229930182558 Sterol Natural products 0.000 claims description 5
- 150000003432 sterols Chemical class 0.000 claims description 5
- 235000003702 sterols Nutrition 0.000 claims description 5
- 239000010696 ester oil Substances 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000003925 fat Substances 0.000 claims description 3
- 238000004043 dyeing Methods 0.000 abstract description 68
- 238000005406 washing Methods 0.000 abstract description 9
- 238000009472 formulation Methods 0.000 description 49
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 36
- 230000000052 comparative effect Effects 0.000 description 33
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 238000012360 testing method Methods 0.000 description 20
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 19
- 239000007788 liquid Substances 0.000 description 19
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 18
- 239000002211 L-ascorbic acid Substances 0.000 description 17
- 235000000069 L-ascorbic acid Nutrition 0.000 description 17
- 229960005070 ascorbic acid Drugs 0.000 description 17
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 239000003205 fragrance Substances 0.000 description 12
- 229960001755 resorcinol Drugs 0.000 description 12
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 11
- 239000000499 gel Substances 0.000 description 11
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 11
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 10
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 10
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 10
- 235000011114 ammonium hydroxide Nutrition 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000004094 surface-active agent Substances 0.000 description 9
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 8
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 8
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 8
- 229960002216 methylparaben Drugs 0.000 description 8
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 8
- 239000002562 thickening agent Substances 0.000 description 8
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 7
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 7
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 7
- 239000002304 perfume Substances 0.000 description 7
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 5
- ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 5
- 229940075861 ammonium thioglycolate Drugs 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 229920006317 cationic polymer Polymers 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000002453 shampoo Substances 0.000 description 5
- 230000002195 synergetic effect Effects 0.000 description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000004166 Lanolin Substances 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 229960000541 cetyl alcohol Drugs 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000005562 fading Methods 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 229940039717 lanolin Drugs 0.000 description 4
- 235000019388 lanolin Nutrition 0.000 description 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 4
- CPJSUEIXXCENMM-UHFFFAOYSA-N phenacetin Chemical compound CCOC1=CC=C(NC(C)=O)C=C1 CPJSUEIXXCENMM-UHFFFAOYSA-N 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 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 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000005215 alkyl ethers Chemical class 0.000 description 3
- 239000010495 camellia oil Substances 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 229940082500 cetostearyl alcohol Drugs 0.000 description 3
- 235000012000 cholesterol Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
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- SBXFGBBTYRHJFF-UHFFFAOYSA-N diamino sulfate Chemical compound NOS(=O)(=O)ON SBXFGBBTYRHJFF-UHFFFAOYSA-N 0.000 description 3
- TVQLLNFANZSCGY-UHFFFAOYSA-N disodium;dioxido(oxo)tin Chemical compound [Na+].[Na+].[O-][Sn]([O-])=O TVQLLNFANZSCGY-UHFFFAOYSA-N 0.000 description 3
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 3
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- 230000003993 interaction Effects 0.000 description 3
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- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
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- 229940032094 squalane Drugs 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- BORJONZPSTVSFP-UHFFFAOYSA-N tetradecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)O BORJONZPSTVSFP-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 229940071127 thioglycolate Drugs 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940118594 trimethylolpropane triisostearate Drugs 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 239000010497 wheat germ oil Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- FYGDTMLNYKFZSV-BYLHFPJWSA-N β-1,4-galactotrioside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@H](CO)O[C@@H](O[C@@H]2[C@@H](O[C@@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-BYLHFPJWSA-N 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、染毛剤組成物、特に酸
化染毛剤組成物の改良に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to improvements in hair dye compositions, especially oxidative hair dye compositions.
【0002】[0002]
【従来の技術】酸化染毛剤は永久染毛剤の中で最も広く
使用されているもので、染毛剤中の酸化染料が毛髪中に
浸透して酸化重合し、発色することにより毛髪を化学的
に染着するので染毛効果が持続することが特徴である。
酸化染毛剤の剤型としては、粉末剤で用時水と混合して
用いる1剤型や、3剤以上の多剤型もあるが、酸化染料
を含む第1剤と、酸化剤を含む第2剤とを用時混合して
用いる2剤型が最も多い。何れにしても、酸化染毛剤は
酸化重合反応によって化学的に毛髪を染毛する。この酸
化重合はかなり激しい反応であり、酸化染毛剤の毛髪へ
の塗布性が悪いと染色むら等を生じることがあった。こ
の染色むらをなくすためには毛髪に塗布した際にすばや
く、均一に塗布できることが重要であり、よって、酸化
染毛剤は、各種溶媒・分散媒等を配合して流動性の高い
液状で提供されていた。2. Description of the Related Art Oxidative hair dyes are the most widely used permanent hair dyes. The oxidation dye in the hair dye penetrates into the hair, undergoes oxidative polymerization, and develops color to cause hair to grow. The feature is that the hair dyeing effect lasts because it is chemically dyed.
As the dosage form of the oxidative hair dye, there are a one-part type that is a powder agent mixed with water at the time of use and a multi-part type of three or more agents. The most common type is the two-part type, which is used by mixing with the second part before use. In any case, the oxidative hair dye chemically dyes the hair by an oxidative polymerization reaction. This oxidative polymerization is a fairly vigorous reaction, and uneven application of the oxidative hair dye to the hair may cause uneven dyeing. In order to eliminate this uneven dyeing, it is important that it can be applied quickly and evenly when applied to the hair.Therefore, the oxidative hair dye is provided as a highly fluid liquid by blending various solvents, dispersion media, etc. It had been.
【0003】[0003]
【発明が解決しようとする課題】ところが、このような
流動性の高い液状では、染毛処理中や染毛処理後に染毛
剤が毛髪から垂れ落ち、皮膚や衣服に付着したり、顔面
を流れ落ちたりする等の問題があった。一方、増粘剤等
を用いて染毛剤が垂れ落ちしないように粘度を高くしよ
うとすると、従来の増粘剤では酸化染毛剤の毛髪への伸
展性、塗布性、均染性が悪くなったり、また、増粘剤が
酸化染料の毛髪への浸透性を阻害するために、染着性が
低下するという問題があった。However, in such a liquid having high fluidity, the hair dye drips from the hair during or after the hair dyeing treatment, and adheres to the skin or clothes or flows down the face. There was such a problem as On the other hand, if an attempt is made to increase the viscosity of the hair dye by using a thickener or the like so that the hair dye does not sag, the conventional thickener is poor in the spreadability, coatability, and levelness of the oxidative hair dye on the hair. Further, there is a problem that the dyeing property is deteriorated because the thickener inhibits the permeability of the oxidation dye into the hair.
【0004】また、酸化染毛剤による染毛後の髪はパサ
つきやすく、滑らかさに欠けるという問題点も有してい
た。本発明はこのような従来技術の課題に鑑み成された
ものであり、その目的は、染毛処理中に染毛剤の垂れ落
ちがないにもかかわらず、伸展性、塗布性等の使用性が
良好であり、染めむらがなく均染性に優れ、また、酸化
染料の染着性良好で、しかも、染毛後の使用感が良好な
酸化染毛剤組成物を提供することにある。Further, there is a problem that hair after dyeing with an oxidative hair dye is easily dry and lacks in smoothness. The present invention has been made in view of the problems of the prior art as described above, and an object thereof is usability such as extensibility and applicability in spite of no dripping of the hair dye during hair dyeing treatment. The object of the present invention is to provide an oxidative hair dye composition which has good dyeing property, has no uneven dyeing and is excellent in level dyeing property, has good dyeing property of an oxidative dye, and has a good feeling after use.
【0005】[0005]
【課題を解決するための手段】本発明者らは前記目的を
達成するため鋭意検討を行った結果、ある種の糖誘導体
と油性成分を酸化染料を含有する第1剤に配合すること
により、前記課題が解決されることを見出した。すなわ
ち、本発明の請求項1記載の酸化染毛剤組成物は、一般
式化4で表される糖誘導体と、油性成分と、酸化染料と
を含有する第1剤と、酸化剤を含有する、第1剤以外の
1剤もしくは2剤以上とを用時混合してなることを特徴
とする。Means for Solving the Problems As a result of intensive studies for achieving the above-mentioned object, the present inventors have found that a certain sugar derivative and an oily component are added to a first agent containing an oxidative dye, It has been found that the above problems can be solved. That is, the oxidative hair dye composition according to claim 1 of the present invention contains a sugar derivative represented by the general formula 4, a first agent containing an oily component and an oxidative dye, and an oxidant. , One agent or two or more agents other than the first agent are mixed before use.
【化4】 (但し、式中Aは糖からn個の水酸基を除いた残基、R
は総炭素数18〜32で、且つ、分岐鎖を有する脂肪
鎖、nは1以上を表す。)Embedded image (In the formula, A is a residue obtained by removing n hydroxyl groups from sugar, R is
Represents a fatty chain having a total carbon number of 18 to 32 and having a branched chain, and n represents 1 or more. )
【0006】請求項2記載の酸化染毛剤組成物は、請求
項1記載の酸化染毛剤組成物において、糖誘導体が一般
式化5で表される糖分岐脂肪族エーテルであることを特
徴とする。An oxidative hair dye composition according to claim 2 is characterized in that, in the oxidative hair dye composition according to claim 1, the sugar derivative is a sugar-branched aliphatic ether represented by the general formula 5. And
【化5】 (但し、式中Aは糖からn個の非ヘミアセタール性水酸
基を除いた残基、R及びnは前記化1に同じである。)Embedded image (However, in the formula, A is a residue obtained by removing n non-hemiacetal hydroxyl groups from a sugar, and R and n are the same as those in the above chemical formula 1.)
【0007】請求項3記載の酸化染毛剤組成物は、請求
項1記載の酸化染毛剤組成物において、糖誘導体が一般
式化6で表される分岐脂肪族グリコシドであることを特
徴とする。The oxidative hair dye composition according to claim 3 is characterized in that, in the oxidative hair dye composition according to claim 1, the sugar derivative is a branched aliphatic glycoside represented by the general formula (6). To do.
【化6】 (但し、式中Aは糖からヘミアセタール性水酸基を除い
た残基、Rは前記化1に同じである。)[Chemical 6] (However, in the formula, A is a residue obtained by removing a hemiacetal hydroxyl group from a sugar, and R is the same as the above chemical formula 1.)
【0008】請求項4記載の酸化染毛剤組成物は、請求
項1又は2記載の酸化染毛剤組成物において、糖誘導体
がマルチトールイソステアリルエーテルであることを特
徴とする。請求項5記載の酸化染毛剤組成物は、請求項
1又は3記載の酸化染毛剤組成物において、糖誘導体が
イソステアリルマルトシドであることを特徴とする。The oxidative hair dye composition according to claim 4 is the oxidative hair dye composition according to claim 1 or 2, wherein the sugar derivative is maltitol isostearyl ether. The oxidative hair dye composition according to claim 5 is the oxidative hair dye composition according to claim 1 or 3, wherein the sugar derivative is isostearyl maltoside.
【0009】請求項6記載の酸化染毛剤組成物は、請求
項1〜5記載の酸化染毛剤組成物において、油性成分と
して天然油脂、高級脂肪酸、ステロール類、エステル油
の中から選ばれた1種又は2種以上を含有することを特
徴とする。以下に本発明の構成を詳述する。The oxidative hair dye composition according to claim 6 is the oxidative hair dye composition according to any one of claims 1 to 5, wherein the oil component is selected from natural fats and oils, higher fatty acids, sterols and ester oils. It is characterized by containing one or more kinds. The constitution of the present invention will be described in detail below.
【0010】まず、本発明に係る糖誘導体は、糖の水酸
基と分岐脂肪族炭化水素基とのエーテル結合物であり、
特に、糖のヘミアセタール性水酸基以外の水酸基(非ヘ
ミアセタール性水酸基)と分岐脂肪族炭化水素基とのエ
ーテル結合物を糖分岐脂肪族エーテル、糖のヘミアセタ
ール性水酸基と分岐脂肪族炭化水素基とのエーテル結合
物(いわゆるグリコシド結合を形成している)を分岐脂
肪族グリコシドと呼ぶ。First, the sugar derivative according to the present invention is an ether bond product of a sugar hydroxyl group and a branched aliphatic hydrocarbon group,
In particular, an ether bond of a hydroxyl group other than hemiacetal hydroxyl groups of sugar (non-hemiacetal hydroxyl group) and a branched aliphatic hydrocarbon group is a sugar branched aliphatic ether, a hemiacetal hydroxyl group of sugar and a branched aliphatic hydrocarbon group. An ether bond with (which forms a so-called glycoside bond) is called a branched aliphatic glycoside.
【0011】本発明で用いられる糖誘導体は前記一般式
化4で表され、式中、Aは糖からn個の水酸基を除いた
残基であり、このような糖としては、グルコース、ガラ
クトース、キシロース、フルクトース、アルトロース、
タロース、マンノース、アラビノース、イドース、リキ
ソース、リボース、アロース等の単糖類及びその混合
物、マルトース、イソマルトース、ラクトース、キシロ
ビオース、ケンチオビオース、コージオビオース、セロ
ビオース、ソホロース、ニゲロース、スクロース、メリ
ビオース、ラミナリビオース、ルチノース等の二糖類及
びその混合物、マルトトリオース等の三糖類及びその混
合物、又はそれ以上の多糖類や、単糖の重合物、これら
糖類の混合物の他、マルチトール、ソルビトール、エリ
スリトール、マンニトール、ガラクチトール、グルシト
ール、イノシトール、マルトトリイトール、マルトテト
ライトール等の糖アルコール及びその混合物が挙げられ
る。尚、nは糖1分子に対して結合した分岐脂肪鎖の平
均結合数であり、糖誘導体が分岐脂肪族グリコシドの時
はnは1を表し、糖誘導体が糖分岐脂肪族エーテルの時
はnは1以上を表す。The sugar derivative used in the present invention is represented by the above general formula 4, wherein A is a residue obtained by removing n hydroxyl groups from the sugar, and such sugars include glucose, galactose, Xylose, fructose, altrose,
Monosaccharides such as talose, mannose, arabinose, idose, lyxose, ribose, and allose, and mixtures thereof, maltose, isomaltose, lactose, xylobiose, kentiobiose, cordiobiose, cellobiose, sophorose, nigerose, sucrose, melibiose, laminaribiose. Su, disaccharides and mixtures thereof such as rutinose, trisaccharides and mixtures thereof such as maltotriose, or a polysaccharide or more thereof, a polymer of monosaccharides, other mixtures of these sugars, maltitol, sorbitol, erythritol, Examples thereof include sugar alcohols such as mannitol, galactitol, glucitol, inositol, maltotriitol and maltotetriitol, and mixtures thereof. It should be noted that n is the average number of branched fatty chains bonded to one sugar molecule, and n is 1 when the sugar derivative is a branched aliphatic glycoside, and n when the sugar derivative is a sugar branched aliphatic ether. Represents 1 or more.
【0012】Rは分岐鎖を有する脂肪鎖で総炭素数18
〜32である。分岐鎖の具体例としては、例えばメチル
基、エチル基、プロピル基、イソプロピル基、ブチル
基、ペンチル基、ヘキシル基、ヘプチル基、オクチル
基、ノニル基、デシル基、ウンデシル基、ドデシル基、
トリデシル基、テトラデシル基、ヘプタデシル基、ヘキ
サデシル基、ヘプタデシル基、更にはそれ以上の高級脂
肪鎖が挙げられる。このような分岐鎖の位置ならびに数
は特に限定されない。Rの具体例としては、2−デシル
テトラデシル基、2−テトラデシルオクタデシル基、イ
ソステアリル基、2,7−ジメチルヘキサデシル基、テ
トラヒドラゲラニル基、2,7−ジメチルオクタデシル
基等が挙げられるが、分岐鎖を有し、総炭素数18〜3
2の脂肪鎖であれば特に限定されない。Rが直鎖状の脂
肪鎖であったり、Rの炭素数の合計が18より小さいと
増粘作用が十分に発揮されず、総炭素数が32より大き
い場合には疎水性が高くなって水に対する溶解度が悪く
なり、水系での使用が困難になる。R is a branched fatty chain having 18 carbon atoms in total.
~ 32. Specific examples of the branched chain include, for example, methyl group, ethyl group, propyl group, isopropyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group,
Examples thereof include a tridecyl group, a tetradecyl group, a heptadecyl group, a hexadecyl group, a heptadecyl group, and further higher fatty chains. The position and number of such branched chains are not particularly limited. Specific examples of R include 2-decyltetradecyl group, 2-tetradecyloctadecyl group, isostearyl group, 2,7-dimethylhexadecyl group, tetrahydrageranyl group, and 2,7-dimethyloctadecyl group. Has a branched chain and has a total carbon number of 18 to 3
It is not particularly limited as long as it has 2 fatty chains. When R is a linear fatty chain or the total number of carbon atoms of R is less than 18, the thickening effect is not sufficiently exhibited, and when the total number of carbon atoms is greater than 32, the hydrophobicity becomes high and water Solubility is poor and it becomes difficult to use in water.
【0013】本発明に係る糖誘導体は既知の物質であ
り、例えば特開平4−76082に記載の方法で製造す
ることができる。また、分岐脂肪族アルコールと糖の脱
水縮合反応でも得ることができる。本発明の酸化染毛剤
組成物においては、糖誘導体を2種以上用いることがで
きる。例えば、糖分岐脂肪族エーテル又は分岐脂肪族グ
リコシドの分岐脂肪鎖や糖の種類、糖分岐脂肪族エーテ
ルにおいては分岐脂肪鎖の結合数や結合位置等が異なる
糖誘導体の混合物を用いてもよい。もちろん、糖分岐脂
肪族エーテルと分岐脂肪族グリコシドの混合物でも構わ
ない。The sugar derivative according to the present invention is a known substance and can be produced, for example, by the method described in JP-A-4-76082. It can also be obtained by a dehydration condensation reaction of a branched aliphatic alcohol and sugar. Two or more sugar derivatives can be used in the oxidative hair dye composition of the present invention. For example, a mixture of sugar-branched aliphatic ether or a branched fatty chain of a branched aliphatic glycoside or a kind of sugar, and in the sugar-branched aliphatic ether, a mixture of sugar derivatives different in the number of bonded branched fatty chains or the bonding position may be used. Of course, a mixture of a sugar-branched aliphatic ether and a branched aliphatic glycoside may be used.
【0014】本発明の酸化染毛剤組成物において、糖誘
導体の配合量は本発明の効果が得られる範囲であれば別
段限定されず、配合量を適宜調整して用いることができ
るが、一般的には0.5〜60重量%、好ましくは1〜
15重量%である。。本発明において前記糖誘導体と併
用される油性成分としては、天然油脂、高級脂肪酸、ス
テロール類、エステル油、炭化水素油、高級アルコール
等が挙げられ、好ましくは天然油脂、高級脂肪酸、ステ
ロール類、エステル油である。天然油脂としては、例え
ばアボガド油、ツバキ油、マカデミアナッツ油、トウモ
ロコシ油、ミンク油、オリーブ油、ナタネ油、卵黄油、
ゴマ油、小麦胚芽油、ヒマシ油、アマニ油、サフラワー
油、綿実油、大豆油、落花生油、茶実油、コメヌカ油、
ホホバ油、胚芽油、トリグリセリン、トリオクタン酸グ
リセリン、トリイソパルミチン酸グリセリン等の液体油
脂が挙げられる。In the oxidative hair dye composition of the present invention, the blending amount of the sugar derivative is not particularly limited as long as the effects of the present invention can be obtained, and the blending amount can be appropriately adjusted and used. 0.5 to 60% by weight, preferably 1 to
15% by weight. . Examples of the oily component used in combination with the sugar derivative in the present invention include natural oils and fats, higher fatty acids, sterols, ester oils, hydrocarbon oils and higher alcohols, preferably natural oils and fats, higher fatty acids, sterols and esters. It is oil. Examples of natural oils and fats include avocado oil, camellia oil, macadamia nut oil, corn oil, mink oil, olive oil, rapeseed oil, egg yolk oil,
Sesame oil, wheat germ oil, castor oil, linseed oil, safflower oil, cottonseed oil, soybean oil, peanut oil, teaseed oil, rice bran oil,
Liquid fats and oils such as jojoba oil, germ oil, triglycerin, glyceryl trioctanoate, and glyceryl triisopalmitate are mentioned.
【0015】高級脂肪酸としては、例えば、ラウリン
酸、ミリスチン酸、パルミチン酸、ステアリン酸、ベヘ
ン(ベヘニン)酸、オレイン酸、12−ヒドロキシステ
アリン酸、ウンデシレン酸、トール酸、イソステアリン
酸、リノール酸、リノレイン酸、エイコサペンタエン酸
(EPA)、ドコサヘキサエン酸(DHA)等が挙げら
れる。ステロール類としては、例えば、コレステロー
ル、フィトステロール等が挙げられる。Examples of the higher fatty acid include lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, 12-hydroxystearic acid, undecylenic acid, tall acid, isostearic acid, linoleic acid and linolein. Acid, eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), and the like. Examples of sterols include cholesterol and phytosterol.
【0016】エステル油としては、ミリスチン酸イソプ
ロピル、オクタン酸セチル、ミリスチン酸オクチルドデ
シル、パルミチン酸イソプロピル、ステアリン酸ブチ
ル、ラウリン酸ヘキシル、ミリスチン酸ミリスチル、オ
レイン酸デシル、ジメチルオクタン酸ヘキシルデシル、
乳酸セチル、乳酸ミリスチル、酢酸ラノリン、ステアリ
ン酸イソセチル、イソステアリン酸イソセチル、12−
ヒドロキシステアリン酸コレステリル、ジ−2−エチル
ヘキシル酸エチレングリコール、ジペンタエリスリトー
ル脂肪酸エステル、モノイソステアリン酸N−アルキル
グリコール、ジカプリン酸ネオペンチルグリコール、リ
ンゴ酸ジイソステアリル、ジ−2−ヘプチルウンデカン
酸グリセリン、トリ−2−エチルヘキシル酸トリメチロ
ールプロパン、トリイソステアリン酸トリメチロールプ
ロパン、テトラ−2−エチルヘキシル酸ペンタエリスリ
トール、トリ−2−エチルヘキシル酸グリセリン、セチ
ル−2−エチルヘキサノエート、エチルヘキシルパルミ
テート等が挙げられる。As the ester oil, isopropyl myristate, cetyl octanoate, octyldodecyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, decyl oleate, hexyldecyl dimethyloctanoate,
Cetyl lactate, myristyl lactate, lanolin acetate, isocetyl stearate, isocetyl isostearate, 12-
Cholesteryl hydroxystearate, ethylene glycol di-2-ethylhexylate, dipentaerythritol fatty acid ester, N-alkyl glycol monoisostearate, neopentyl glycol dicaprate, diisostearyl malate, glycerin di-2-heptylundecanoate, tri Examples include 2-ethylhexyl trimethylolpropane, trimethylolpropane triisostearate, pentaerythritol tetra-2-ethylhexylate, glyceryl tri-2-ethylhexylate, cetyl-2-ethylhexanoate, ethylhexyl palmitate and the like.
【0017】炭化水素油としては、流動パラフィン、オ
ゾケライト、スクワレン、プリスタン、パラフィン、セ
レシン、ワセリン、マイクロクリスタリンワックス等が
挙げられる。高級アルコールとしては、ラウリルアルコ
ール、セチルアルコール、ステアリルアルコール、ベヘ
ニルアルコール、ミリスチルアルコール、オレイルアル
コール、セトステアリルアルコール等の直鎖高級アルコ
ール、モノステアリルグリセリンエーテル(バチルアル
コール)、2−デシルテトラデシノール、ラノリンアル
コール、ヘキシルドデカノール、イソステアリルアルコ
ール、オクチルドデカノール等の分岐鎖高級アルコール
が挙げられる。Examples of the hydrocarbon oil include liquid paraffin, ozokerite, squalene, pristane, paraffin, ceresin, petrolatum and microcrystalline wax. As higher alcohols, linear higher alcohols such as lauryl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol, myristyl alcohol, oleyl alcohol, cetostearyl alcohol, monostearyl glycerin ether (batyl alcohol), 2-decyl tetradecinol, lanolin alcohol And branched chain higher alcohols such as hexyldodecanol, isostearyl alcohol, and octyldodecanol.
【0018】本発明においては前記油性成分を一種又は
二種以上を任意に用いることができる。なお、前記油性
成分の配合量としては染毛剤組成物全量に対して0.0
1〜15.0重量%が好適である。油性成分の配合料が
0.01重量%未満では十分な効果は得られず、また、
15重量%を超えて配合した場合には均染性や、染着
性、耐洗浄性に悪影響が及ぼすとともに、べたつきを生
じて使用感が悪くなることがある。In the present invention, one kind or two or more kinds of the oily components can be optionally used. The blending amount of the oily component is 0.0 with respect to the total amount of the hair dye composition.
1 to 15.0% by weight is suitable. If the compounding amount of the oily component is less than 0.01% by weight, a sufficient effect cannot be obtained, and
When it is blended in an amount of more than 15% by weight, the level dyeing property, the dyeing property, and the washing resistance are adversely affected, and stickiness may occur to deteriorate the usability.
【0019】本発明の酸化染毛剤組成物に用いられる酸
化染料としては、例えば、フェニレンジアミン類、アミ
ノフェノール類、トルイレンジアミン類、アミノニトロ
フェノール類、ジフェニルアミン類、ジアミノフェニル
アミン類、N−フェニルフェニレンジアミン類、ジアミ
ノピリジン類、レゾルシン、ピロガロール、カテコー
ル、アミノクレゾール類及びこれらの塩等が挙げられ
る。酸化染料の配合量は通常酸化染毛剤に用いられる範
囲であれば特に限定されない。尚、本発明においては、
一般に主剤となる酸化染料と併用して色調を変化させる
色調調製剤も本発明の酸化染料として包含する。Examples of the oxidative dyes used in the oxidative hair dye composition of the present invention include phenylenediamines, aminophenols, toluylenediamines, aminonitrophenols, diphenylamines, diaminophenylamines and N-. Examples thereof include phenylphenylenediamines, diaminopyridines, resorcin, pyrogallol, catechol, aminocresols and salts thereof. The blending amount of the oxidative dye is not particularly limited as long as it is within the range generally used for oxidative hair dyes. In the present invention,
In general, a color tone adjusting agent that changes a color tone in combination with an oxidative dye as a main agent is also included in the oxidative dye of the present invention.
【0020】本発明で用いられる酸化剤としては、例え
ば、過酸化水素、過硫酸塩、過ホウ酸塩、臭素酸塩、過
ヨウ素酸塩、過酸化尿素等が挙げられる。酸化剤の配合
量は通常酸化染毛剤に用いられる範囲であれば特に限定
されない。本発明に係る酸化染毛剤組成物は垂れ落ちた
り、流れたりしない適度な粘度を有し、しかも、毛髪に
すばやく均一に塗布できて染上がりも均一であるという
特徴を有している。本発明に係る糖誘導体は酸化染料が
毛髪中に浸透し、染着するのを阻害せず油性成分と共に
作用して酸化染料を良好に染着し、しかも染毛後の毛髪
が滑らかに仕上がる。さらに、本発明の糖誘導体は酸、
アルカリ中でも分解することなく安定で、また、染毛剤
組成物に配合しても感作性、刺激性がなく、安全性にも
優れるという特徴も有する。Examples of the oxidizing agent used in the present invention include hydrogen peroxide, persulfate, perborate, bromate, periodate, urea peroxide and the like. The blending amount of the oxidizing agent is not particularly limited as long as it is within the range generally used for oxidizing hair dyes. The oxidative hair dye composition according to the present invention has an appropriate viscosity such that it does not drip or flow, and is characterized in that it can be applied to hair quickly and evenly and the dyeing is even. The sugar derivative according to the present invention does not prevent the oxidation dye from penetrating into the hair and dye it, and acts together with the oil component to satisfactorily dye the oxidation dye, and the hair after dyeing is smoothly finished. Furthermore, the sugar derivative of the present invention is an acid,
It also has the characteristics that it is stable without being decomposed even in alkali, has no sensitizing property or irritating property even when incorporated into a hair dye composition, and is excellent in safety.
【0021】また、染毛剤組成物にはエタノール、イソ
プロパノール等の低級アルコール類が配合されることが
あるが、このような系において界面活性剤を増粘剤とし
て用いると増粘効果が著しく低下するために界面活性剤
を多量に配合する必要があり、刺激性や染着性阻害等の
問題が生じやすい。本発明に係る糖誘導体を用いればこ
のような系においても少量で増粘効果を得ることができ
る。The hair dye composition may contain lower alcohols such as ethanol and isopropanol. When a surfactant is used as a thickener in such a system, the thickening effect is remarkably reduced. Therefore, it is necessary to add a large amount of a surfactant, and problems such as irritation and inhibition of dyeing property tend to occur. If the sugar derivative according to the present invention is used, a thickening effect can be obtained with a small amount even in such a system.
【0022】本発明の酸化染毛剤の剤型は2剤以上の多
剤型であり、特に、糖誘導体、油性成分を酸化染料を含
有する第1剤に配合し、酸化剤を含有する、前記第1剤
以外の1剤もしく2剤以上を用時混合してなることを特
徴とする。このように、糖誘導体、油性成分及び酸化染
料を第1剤に配合することにより、染毛後の毛髪が滑ら
かになる等の使用感が大幅に向上するとともに、酸化染
料の染着性や耐洗浄性が大幅に向上するという相乗効果
が発揮される。なお、この相乗効果は油性成分を糖誘導
体、酸化染料とともに第1剤に配合し、この第1剤と、
酸化染料を含有する他剤とを用時混合して得られる酸化
染料組成物において発揮されるもので、例えば糖誘導体
と酸化染料を含有する第1剤と、油性成分と酸化剤を含
有する第2剤を用時混合して得られる酸化組成物におい
てはこのような相乗効果は発揮されない。この原因につ
いては明らかではないが、あらかじめ油性成分を糖誘導
体及び酸化染料とともに第1剤に配合した場合には、油
性成分と糖誘導体、酸化染料の間に何らかの相互作用が
生じ、これが染着性や耐洗浄性の向上をもたらすことが
考えられる。これに対し、油性成分が予め糖誘導体及び
酸化染料と配合されていない場合には、前記のような相
互作用を予め生じることができず、用時混合された時に
もその他の成分の影響により前記のような相互作用を強
固に形成することが困難であるために、染着性等に相乗
効果が発揮されないのではないかと推察される。The dosage form of the oxidative hair dye of the present invention is a multi-part formulation of two or more agents. In particular, a sugar derivative and an oily component are mixed with the first agent containing an oxidative dye, and the oxidant is included. One or two or more agents other than the first agent are mixed at the time of use. In this way, by adding the sugar derivative, the oily component and the oxidative dye to the first agent, the feeling of use such as smoothing of the hair after dyeing is greatly improved, and the dyeing property and resistance of the oxidative dye are improved. The synergistic effect that the detergency is significantly improved is exhibited. The synergistic effect is that the oil component is mixed with the sugar derivative and the oxidation dye in the first agent,
What is exhibited in an oxidative dye composition obtained by mixing with another agent containing an oxidative dye at the time of use, for example, a first agent containing a sugar derivative and an oxidative dye, and a first agent containing an oily component and an oxidant. Such a synergistic effect is not exhibited in the oxidizing composition obtained by mixing the two agents at the time of use. The reason for this is not clear, but if an oily component was previously mixed with the sugar derivative and the oxidative dye in the first agent, some interaction occurred between the oily component, the sugar derivative and the oxidative dye, which caused the dyeing property. It is thought that this will bring about an improvement in cleaning resistance. On the other hand, when the oily component is not previously blended with the sugar derivative and the oxidative dye, the interaction as described above cannot occur in advance, and even when the oily component is mixed at the time of use, due to the influence of other components, Since it is difficult to strongly form such an interaction, it is presumed that a synergistic effect may not be exerted on the dyeing property and the like.
【0023】また、本発明のような多剤型染毛剤組成物
は製品安定性に優れ、また、特に乳化剤、分散剤、可溶
化剤等を配合しなくても糖誘導体が界面活性効果も有し
ているので油性成分を均一に乳化や分散することができ
るという特徴も有している。本発明の染毛剤組成物が例
えば2剤型組成物の場合には、第1剤と第2剤との混合
比は、通常重量比で第1剤:第2剤=1:1であること
が多いが、垂れ落ちや使用性、均染性、滑らかさ、染着
性、耐洗浄性等において不都合がない限り特に限定され
ない。Further, the multi-component hair dye composition of the present invention is excellent in product stability, and the sugar derivative also has a surfactant effect even if it does not contain an emulsifier, a dispersant, a solubilizer and the like. Since it has, it also has a feature that the oily component can be uniformly emulsified or dispersed. When the hair dye composition of the present invention is, for example, a two-component composition, the mixing ratio of the first agent and the second agent is usually 1: 1 by weight: 2 by 1: 1. Often, it is not particularly limited as long as there is no inconvenience in dripping, usability, level dyeing property, smoothness, dyeing property, cleaning resistance, and the like.
【0024】本発明の酸化染毛剤組成物は本発明の効果
が損なわれない範囲で通常染毛剤に用いられる他の成分
も配合することが可能である。例えば、通常第1剤に配
合される成分としては、グリセリン、プロピレングリコ
ール、ジプロピレングリコール、ポリエチレングリコー
ル、コンドロイチン硫酸塩、ヒアルロン酸塩、ジグリセ
リン、1,3−ブチレングリコール、ピロリドンカルボ
ン酸塩、ソルビトール、マルチトール、ラクトース、オ
リゴ糖等の保湿剤、メチルフェニルポリシロキサン、ジ
メチルシロキサン・メチル(ポリオキシエチレン)シロ
キサン共重合体、ゴム状シメチルポリシロキサン、アミ
ノ変性ポリシロキサン等のシリコーン類が挙げられる。The oxidative hair dye composition of the present invention may contain other components usually used in hair dyes as long as the effects of the present invention are not impaired. For example, as a component usually added to the first agent, glycerin, propylene glycol, dipropylene glycol, polyethylene glycol, chondroitin sulfate, hyaluronate, diglycerin, 1,3-butylene glycol, pyrrolidone carboxylate, sorbitol. , Moisturizers such as maltitol, lactose and oligosaccharides, silicones such as methylphenyl polysiloxane, dimethyl siloxane / methyl (polyoxyethylene) siloxane copolymer, rubbery dimethyl polysiloxane, amino modified polysiloxane. .
【0025】また、チオグリコール酸塩、L−アスコル
ビン酸塩、亜硫酸水素塩、ハイドロサルファイト塩、硫
酸水素塩等の酸化防止剤及び安定化剤、コラーゲン加水
分解物、ケラチン加水分解物、シルクプロテイン加水分
解物、エラスチン加水分解物、大豆蛋白加水分解物等の
蛋白質加水分解物及びこれらの四級化物、アンモニア
水、アルカノールアミン、炭酸アンモニウム、炭酸水素
ナトリウム、水酸化カリウム等のアルカリ剤を配合する
ことも可能である。また、乳化剤として、他の両親媒性
物質や、界面活性剤を用いることも可能である。In addition, antioxidants and stabilizers such as thioglycolate, L-ascorbate, bisulfite, hydrosulfite, bisulfate, collagen hydrolyzate, keratin hydrolyzate and silk protein. Protein hydrolyzate such as hydrolyzate, elastin hydrolyzate, soybean protein hydrolyzate and the like, and quaternary products thereof, ammonia water, alkanolamine, ammonium carbonate, sodium hydrogen carbonate, and an alkali agent such as potassium hydroxide are added. It is also possible. It is also possible to use other amphiphilic substances or surfactants as emulsifiers.
【0026】非イオン性界面活性剤としては、ポリオキ
シエチレンアルキルエーテル、ポリオキシエチレン脂肪
酸エステル、ポリオキシエチレン多価アルコール脂肪酸
部分エステル、ポリオキシエチレン硬化ヒマシ油誘導体
等のポリオキシエチレン系界面活性剤、オクチルポリグ
リコシド等のアルキルポリグリコシド類、ポリグリセリ
ン脂肪酸エステル、ポリグリセリンアルキルエーテル等
のポリグリセリン系界面活性剤、マルチトールヒドロキ
シアルキルエーテル等の糖アルコールヒドロキシアルキ
ルエーテル類、脂肪酸ジエタノールアミド等が挙げら
れ、高級脂肪酸塩類、アルキルベンゼンスルホン酸塩
類、リン酸エステル類、アルキル硫酸塩類、アルキル硫
酸エステル塩類、ポリオキシエチレンアルキル硫酸エス
テル塩類等のアニオン性界面活性剤、アミノ酸類、アル
キルトリメチルアンモニウム塩、ジアルキルジメチルア
ンモニウム塩、アルキルジメチルアミンオキサイド等の
カチオン性界面活性剤、その他の界面活性剤を適宜併用
できる。As the nonionic surfactant, polyoxyethylene-based surfactants such as polyoxyethylene alkyl ether, polyoxyethylene fatty acid ester, polyoxyethylene polyhydric alcohol fatty acid partial ester, and polyoxyethylene hydrogenated castor oil derivative. Examples include alkyl polyglycosides such as octyl polyglycoside, polyglycerin fatty acid esters, polyglycerin-based surfactants such as polyglycerin alkyl ether, sugar alcohol hydroxyalkyl ethers such as maltitol hydroxyalkyl ether, and fatty acid diethanolamide. Anions such as higher fatty acid salts, alkylbenzene sulfonates, phosphoric acid esters, alkyl sulfates, alkyl sulfate ester salts, and polyoxyethylene alkyl sulfate ester salts Surfactants, amino acids, alkyl trimethyl ammonium salt, dialkyl dimethyl ammonium salts, alkyl cationic surfactants dimethylamine oxide, and the like, other surfactants can be appropriately used in combination.
【0027】更に、例えば、エタノール、ブタノール、
プロパノール、イソプロパノール、ベンジルアルコール
等の低級アルコール類、2−エチルヘキシルアルコー
ル、2−ヘキシルデシルアルコール、2−デシルテトラ
デシルアルコール、イソステアリルアルコール、セトス
テアリルアルコール、ラウリルアルコール、ステアリル
アルコール、セチルアルコール等の高級アルコール類等
を配合することができる。 また、金属イオン封鎖剤及
び防腐剤として、ヒドロキシエタンジホスホン酸塩類、
フェナセチン、EDTA及びその塩、パラベン類、スズ
酸塩類等が挙げられ、高分子化合物としては、ポリ(ジ
メチルアリルアンモニウムハライド)型カチオン性高分
子、ポリエチレングリコール、エピクロルヒドリン、プ
ロピレンアミン及び牛脂脂肪酸より得られるタロイルア
ミンの縮合生成物型であるカチオン性高分子、ポリエチ
レングリコール、エピクロルヒドリン、プロピレンアミ
ン及びヤシ油脂肪酸より得られるココイルアミンの縮合
生成物型であるカチオン性高分子、ビニルピロリドン、
ジメチルアミノメタアクリレート共重合体型カチオン性
高分子、第4級窒素含有セルロースエーテル型カチオン
性高分子類等が挙げられる。Further, for example, ethanol, butanol,
Lower alcohols such as propanol, isopropanol and benzyl alcohol, higher alcohols such as 2-ethylhexyl alcohol, 2-hexyldecyl alcohol, 2-decyltetradecyl alcohol, isostearyl alcohol, cetostearyl alcohol, lauryl alcohol, stearyl alcohol and cetyl alcohol. It is possible to add a kind or the like. Further, as a sequestering agent and a preservative, hydroxyethane diphosphonates,
Phenacetin, EDTA and its salts, parabens, stannates and the like can be mentioned. As the polymer compound, poly (dimethylallylammonium halide) type cationic polymer, polyethylene glycol, epichlorohydrin, propyleneamine and tallow fatty acid can be obtained. Cationic polymer which is a condensation product type of taroylamine, polyethylene glycol, epichlorohydrin, cationic polymer which is a condensation product type of cocoylamine obtained from propyleneamine and coconut oil fatty acid, vinylpyrrolidone,
Examples thereof include dimethylaminomethacrylate copolymer type cationic polymers and quaternary nitrogen-containing cellulose ether type cationic polymers.
【0028】また、ラウリン酸ジエタノールアミド、カ
ルボキシメチルセルロース、カルボキシビニルポリマ
ー、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、メチルセルロース、キサンタンガム、カラ
ギーナン、アルギン酸塩、ペクチン、フェーセラン、ア
ラビアガム、ガツチガム、カラヤガム、トラガントガ
ム、カンテン末、ベントナイト、架橋性ポリアクリル酸
塩等の増粘剤も本発明の効果が損なわれない範囲で併用
することができる。Further, lauric acid diethanolamide, carboxymethyl cellulose, carboxy vinyl polymer, hydroxyethyl cellulose, hydroxypropyl cellulose, methyl cellulose, xanthan gum, carrageenan, alginate, pectin, phaceran, gum arabic, gutchi gum, karaya gum, tragacanth gum, agar powder, bentonite. Further, a thickener such as a crosslinkable polyacrylic acid salt can also be used in combination as long as the effect of the present invention is not impaired.
【0029】その他、pH調整剤、香料、薬剤、着色
剤、水等も適宜配合可能である。これらは、必要に応じ
適宜選択されて配合され、特にこれらに限定されるもの
ではない。第2剤に配合される成分としては、例えば、
フェナセチン、EDTA及びその塩、パラベン類、スズ
酸塩類等のパラフィン等の金属イオン封鎖剤及び防腐
剤、2−エチルヘキシルアルコール、2−ヘキシルデシ
ルアルコール、2−デシルテトラデシルアルコール、イ
ソステアリルアルコール、セトステアリルアルコール、
ラウリルアルコール、ステアリルアルコール、セチルア
ルコール等の高級アルコール類、ポリオキシエチレンア
ルキルエーテル類、アルキル硫酸エステル塩類、アシル
メチルタウリン類等の界面活性剤、クエン酸、リンゴ
酸、酢酸、乳酸、シュウ酸、酒石酸、ギ酸、レブリン酸
等の有機酸や、リン酸、塩酸等の無機酸等の酸、pH調
整剤、香料、薬剤、着色剤、水等が挙げられ、必要に応
じて適宜選択されるが、これらに特に限定されるもので
はない。In addition, a pH adjusting agent, a fragrance, a drug, a coloring agent, water and the like can be appropriately added. These are appropriately selected and blended as needed, and are not particularly limited thereto. Examples of components to be added to the second agent include, for example,
Phenacetin, EDTA and salts thereof, parabens such as parabens and stannates, sequestering agents and preservatives, 2-ethylhexyl alcohol, 2-hexyldecyl alcohol, 2-decyltetradecyl alcohol, isostearyl alcohol, cetostearyl alcohol,
Higher alcohols such as lauryl alcohol, stearyl alcohol, cetyl alcohol, polyoxyethylene alkyl ethers, alkyl sulfate salts, surfactants such as acylmethyl taurines, citric acid, malic acid, acetic acid, lactic acid, oxalic acid, tartaric acid , Organic acids such as formic acid and levulinic acid, acids such as phosphoric acid and inorganic acids such as hydrochloric acid, pH adjusters, fragrances, agents, colorants, water and the like, which are appropriately selected as necessary, It is not particularly limited to these.
【0030】[0030]
【実施例】以下、実施例を挙げて本発明を具体的に説明
するが、本発明はこれに限定されるものではない。実施
例に先立ち、各実施例で用いた試験法について説明す
る。 〔染毛試験〕各被験染毛剤組成物を用いて10人のパネ
ラーの頭髪を染毛処理し、染毛時の垂れ落ち、頭髪への
伸展性・塗布性、均染性ならびに染毛後の毛髪の滑らか
さを相対評価した。評価基準は以下の通り。EXAMPLES The present invention will now be described specifically with reference to examples, but the present invention is not limited to these examples. Prior to the examples, the test method used in each example will be described. [Hair dyeing test] The hair of 10 panelists was dyed with each of the test hair dye compositions, and drooped during hair dyeing, spreadability / applicability to hair, leveling and after hair dyeing. The relative smoothness of the hair was evaluated. The evaluation criteria are as follows.
【0031】〈垂れ落ちの評価〉 ◎:垂れ落ち、流れ落ちが全くない ○:垂れ落ち、流れ落ちが殆どない △:垂れ落ち、流れ落ちがある ×:垂れ落ち、流れ落ちがひどい 〈伸展性、塗布性の評価〉 ◎:非常に伸びがよく、塗布しやすい ○:まあまあ伸びがよく、塗布しやすい △:伸びがあまりよくなく、塗布しにくい ×:伸びが悪く、塗布にムラができる<Evaluation of dripping> ⊚: No dripping, no dripping ○: Almost no dripping, no dripping △: Dripping, dripping ×: Severe dripping, dripping <Extensibility, coating property Evaluation> ◎: Very good elongation and easy application ○: Fairly good elongation and easy application Δ: Not very good elongation and difficult application ×: Poor elongation and uneven application
【0032】〈均染性の評価〉 ◎:均一によく染った ○:殆ど均一に染った △:やや染めムラができた ×:染めムラができた 〈滑らかさの評価〉 ◎:非常に滑らか ○:滑らか △:やや滑らか ×:滑らかさに欠ける<Evaluation of Level Dyeability> ◎: Evenly dyed well ○: Almost uniformly dyed Δ: Some dyeing unevenness was formed ×: Dyeing unevenness was formed <Evaluation of smoothness> ◎: Very Very smooth ○: Smooth Δ: Slightly smooth ×: Lack of smoothness
【0033】〔染着性試験〕白髪の混じった人毛束2g
程度を市販のシャンプーで洗い、タオルで軽く拭いてア
ルミ盆に置く。染毛剤組成物5gをアルミ盆にとり、2
5〜30℃で人毛束の裏・表を歯ブラシでよく塗擦して
15分間放置する。その後微温湯で良く洗い、タオルで
拭き、次いで、ドライヤーで乾燥後、未処理の白髪の混
じった人毛との色の差を肉眼で判定した。 〈染着性の評価〉 ◎:非常に良好 ○:良好 △:やや悪い ×:悪い[Dyeing test] 2 g of a human hair bundle with white hair
Wash the area with commercially available shampoo, lightly wipe with a towel and place on an aluminum tray. Take 5g of hair dye composition in an aluminum tray and 2
Rub the back and front of the human hair bundle at 5 to 30 ° C with a toothbrush and leave for 15 minutes. Then, it was thoroughly washed with slightly warm water, wiped with a towel, then dried with a dryer, and the difference in color from that of human hair containing untreated white hair was visually judged. <Evaluation of dyeing property> ◎: Very good ○: Good Δ: Slightly bad ×: Bad
【0034】〔耐洗浄性試験〕前記染着性試験において
判定後、染毛された人毛束を2等分し、一方を市販シャ
ンプー液に含浸して10回手もみ洗いした後、乾燥し
た。これを10回繰り返し、シャンプー前の人毛束と、
シャンプー後の人毛束の色を肉眼で比較し、耐洗浄性
(耐シャンプー性)を調べた。 〈耐洗浄性の評価〉 ◎:非常に良好(全く退色しない) ○:良好(僅かに退色する) △:やや悪い(退色する) ×:悪い(退色が著しい)[Washing resistance test] After judgment in the dyeing test, the dyed human hair bundle is divided into two equal parts, one of them is impregnated with a commercial shampoo solution, hand-washed 10 times, and then dried. . Repeat this 10 times, with the human hair bundle before shampoo,
The color of human hair bundles after shampoo was visually compared to examine the wash resistance (shampoo resistance). <Evaluation of cleaning resistance> ◎: Very good (no fading at all) ○: Good (slightly fading) △: Slightly bad (fading) X: Bad (fading is remarkable)
【0035】配合例1〜2、比較例1〜2 まず、従来使用されている増粘剤であるエマレックスO
P−5を比較例とし、次のような染毛剤組成物を調製
し、試験を行った。 〔染毛剤組成物の調製〕1)第1剤の調製 表1に記載の試料を用いて、下記の処方により第1剤を
定法に従って調製した。 Formulation Examples 1-2, Comparative Examples 1-2 First, the conventionally used thickener, Emarex O.
Using P-5 as a comparative example, the following hair dye composition was prepared and tested. [Preparation of Hair Dye Composition] 1) Preparation of First Agent Using the samples shown in Table 1, a first agent was prepared according to a conventional method according to the following formulation.
【0036】 〈処方〉 第1剤 イソプロパノール 5.0wt% 試料(表1参照) 15.0〜35.0 チオグリコール酸アンモニウム 0.1 L−アスコルビン酸 0.5 EDTA 0.5 アンモニア水 6.0 パラフェニレンジアミン 1.0 レゾルシン 1.0 香料 適 量 イオン交換水 残 余<Formulation> First agent Isopropanol 5.0 wt% Sample (see Table 1) 15.0 to 35.0 Ammonium thioglycolate 0.1 L-Ascorbic acid 0.5 EDTA 0.5 Ammonia water 6.0 Paraphenylenediamine 1.0 Resorcin 1.0 Fragrance Suitable amount Ion-exchanged water Residual
【0037】[0037]
【表1】 試 料(配合量) 配合例1 マルチトールモノイソステアリルエーテル(5.0wt%)+ ミリスチン酸イソプロピル(10.0wt%) 配合例2 イソステアリルマルトシド(5.0wt%)+ ミリスチン酸イソプロピル(10.0wt%) 比較例1 エマレックスOP−5**(25.0wt%) 比較例2 エマレックスOP−5**(25.0wt%)+ ミリスチン酸イソプロピル(10.0wt%) *POE(5)オクチルフェニルエーテル、日本エマルジョン(株)製[Table 1] Reagents (blending amount) Blending example 1 Maltitol monoisostearyl ether (5.0 wt%) + isopropyl myristate (10.0 wt%) Blending example 2 Isostearyl maltoside (5.0 wt%) + Myristin Isopropylate (10.0 wt%) Comparative Example 1 Emarex OP-5 ** (25.0 wt%) Comparative Example 2 Emarex OP-5 ** (25.0 wt%) + Isopropyl myristate (10.0 wt%) * POE (5) octyl phenyl ether, manufactured by Nippon Emulsion Co., Ltd.
【0038】2)第2剤aの調製 次に、下記表2の処方で定法により透明液状の第2剤a
を調製した。 2) Preparation of Second Agent a Next, the second liquid a, which is a transparent liquid, is prepared according to the formula shown in Table 2 below.
Was prepared.
【表2】 成分 配合量 過酸化水素30% 15.0 リン酸緩衝液 pH3に調製 メチルパラベン 0.1 スズ酸ナトリウム 0.1 イオン交換水 残 余[Table 2] Ingredients Amount of hydrogen peroxide 30% 15.0 Phosphate buffer adjusted to pH 3 Methylparaben 0.1 Sodium stannate 0.1 Ion-exchanged water Residual
【0039】〔染毛試験〕前記配合例1〜2及び比較例
1〜2の各第1剤と、第2剤aを重量比1:1で混合
し、得られた酸化染毛剤組成物を用いて染毛試験を行っ
た。混合前後の性状及び染毛試験の結果を表3に示す。[Hair dyeing test] An oxidative hair dye composition obtained by mixing the respective first agents of the above-mentioned formulation examples 1 and 2 and comparative examples 1 and 2 with the second agent a in a weight ratio of 1: 1. Was used to carry out a hair dyeing test. Table 3 shows the properties before and after mixing and the results of the hair dyeing test.
【表3】 第1剤 性状 垂れ落ち 伸展性 均染性 滑らかさ 混合前 混合後 ・塗布性 配合例1 ゲル状 ゲル状 ◎ ◎ ◎ ◎ 配合例2 ゲル状 ゲル状 ◎ ◎ ◎ ◎ 比較例1 液状 液状 × ○ × × 比較例2 液状 液状 × ○ × △[Table 3] 1st Agent Properties Dripping Spreadability Leveling Smoothness Before mixing After mixing / Applicability Blending Example 1 Gel-like gel ◎ ◎ ◎ ◎ ◎ Blending example 2 Gel-like gel ◎ ◎ ◎ ◎ ◎ Comparative Example 1 Liquid Liquid × ○ × × Comparative Example 2 Liquid Liquid × × × ×
【0040】表3からも判るように、糖誘導体と油性成
分(ミリスチン酸イソプロピル)を併用した第1剤(配
合例1〜2)はゲル状で、第2剤aと混合後もゲル状を
呈していたのに対し、従来の増粘剤(エマレックスOP
−5)を用いた第1剤(比較例1)又はこれに油性成分
を併用した第1剤(比較例2)は液状で、第2剤aと混
合後も液状のままであり、混合しにくく不均一になりや
すかった。また、染毛試験においては、配合例1〜2の
第1剤を用いた酸化染毛剤組成物はいずれも垂れ落ち、
流れ落ちがなく、しかも、毛髪に対する伸展性・塗布性
が良好で、均染性及び染毛後の滑らかさに優れていた。
これに対し、従来の増粘剤を用いた比較例1〜2の混合
物は液状であるため垂れ落ちや流れ落ちがあり、均染
性、滑らかさに劣る等の問題が有った。As can be seen from Table 3, the first agent (formulation examples 1 and 2) in which the sugar derivative and the oily component (isopropyl myristate) were used in combination was in the form of gel, and even after mixing with the second agent a. Whereas the conventional thickener (Emarex OP
The first agent using (-5) (Comparative Example 1) or the first agent (Comparative Example 2) in which an oily component is used in combination is liquid and remains liquid after mixing with the second agent a. It was difficult and uneven. In addition, in the hair dyeing test, any of the oxidative hair dye compositions using the first agent of Formulation Examples 1 and 2 dripped,
There was no runoff, and the extensibility and application to hair were good, and the leveling properties and the smoothness after dyeing were excellent.
On the other hand, since the mixtures of Comparative Examples 1 and 2 using the conventional thickener were liquid, they had problems such as dripping and runoff, poor levelness and smoothness.
【0041】比較例3〜5 表4の試料を用いて前記配合例1〜2と同様の処方で糖
誘導体又は油性成分のみを配合した第1剤(比較例3〜
5)を調製し、前記第2剤aを重量比1:1で混合して
酸化染毛剤組成物を調製した。 Comparative Examples 3 to 5 Using the samples of Table 4, the first agent (Comparative Examples 3 to 3) in which only the sugar derivative or the oil component was blended in the same formulation as in the above Formulation Examples 1 and 2
5) was prepared, and the second agent a was mixed in a weight ratio of 1: 1 to prepare an oxidative hair dye composition.
【表4】 第1剤 試 料(第1剤中の配合量) 比較例3 マルチトールモノイソステアリルエーテル(5.0wt%) 比較例4 イソステアリルマルトシド(5.0wt%) 比較例5 ミリスチン酸イソプロピル(10.0wt%)[Table 4] First agent Reagent (content in the first agent) Comparative example 3 Maltitol monoisostearyl ether (5.0 wt%) Comparative example 4 Isostearyl maltoside (5.0 wt%) Comparative example 5 Myristin Isopropyl acid (10.0wt%)
【0042】比較例3〜5の第1剤を用いた染毛剤組成
物と、前記配合例1〜2を用いた染毛剤組成物の性状、
染毛試験、染着性試験、耐洗浄性試験結果の比較を表5
に示す。Properties of the hair dye compositions using the first agent of Comparative Examples 3 to 5 and the hair dye compositions using the above Formulation Examples 1 and 2,
Table 5 shows a comparison of the results of the hair dyeing test, the dyeing property test, and the wash resistance test.
Shown in
【表5】 第1剤 性状 垂れ落ち 伸展性 均染性 滑らかさ 染着性 耐洗浄性 (混合後) ・塗布性 配合例1 ケ゛ル状 ◎ ◎ ◎ ◎ ◎ ○ 配合例2 ケ゛ル状 ◎ ◎ ◎ ◎ ◎ ○ 比較例3 ケ゛ル状 ◎ ◎ ◎ △ ○ △ 比較例4 ケ゛ル状 ◎ ◎ ◎ △ ○ △ 比較例5 液状 × △ × △ × ×[Table 5] 1st agent Properties Dripping Spreadability Level dyeing Smoothness Dyeing resistance Washability (after mixing) -Coatability Blend example 1 gel ◎ ◎ ◎ ◎ ◎ ◎ ○ Blend example 2 gel ◎ ◎ ◎ ◎ ◎ ◎ ○ Comparative Example 3 gel shape ◎ ◎ ◎ △ ○ △ △ Comparative Example 4 gel shape ◎ ◎ ◎ ◎ △ ○ △ Comparative Example 5 Liquid × △ × △ × ×
【0043】表5から判るように、糖誘導体及び油性成
分(ミリスチン酸イソプロピル)を併用した場合(配合
例1〜2)にはゲル状の染毛剤組成物が得られ、垂れ落
ちがなく、毛髪への伸展性・塗布性、均染性が良好であ
る。また、染着性及び耐洗浄性にも優れていた。さら
に、染毛後の毛髪が非常に滑らかで使用感に優れてい
た。これに対し、糖誘導体のみを配合した場合(比較例
3〜4)には配合例1〜2と性状、垂れ落ち、伸展性・
塗布性、均染性は大差ないものの、染着性、耐洗浄性、
染毛後の滑らかさにおいて劣っていた。As can be seen from Table 5, when the sugar derivative and the oily component (isopropyl myristate) were used in combination (Formulation Examples 1 and 2), gel hair dye compositions were obtained and there was no dripping. Good spreadability / applicability to hair and level dyeability. It was also excellent in dyeing property and wash resistance. Furthermore, the hair after dyeing was very smooth and had an excellent feeling of use. On the other hand, when only the sugar derivative was blended (Comparative Examples 3-4), the properties, sagging, extensibility
Although there is not much difference in coating property and level dyeing property, dyeing property, washing resistance,
The smoothness after dyeing was poor.
【0044】また、油性成分のみを配合した場合(比較
例5)には、得られた染毛剤組成物が液状で、染毛試
験、染着性試験、耐洗浄性試験において何れの評価も著
しく劣っていた。以上のことから、本発明の効果は糖誘
導体と油性成分を併用した場合に相乗的に得られること
が理解される。When only the oily component was blended (Comparative Example 5), the obtained hair dye composition was in a liquid state and was evaluated in any of the hair dyeing test, the dyeing property test and the washing resistance test. It was extremely inferior. From the above, it is understood that the effects of the present invention are synergistically obtained when a sugar derivative and an oily component are used in combination.
【0045】配合例3〜6、比較例6〜7 表6の試料を用いて前記配合例1〜2と同様の処方で第
1剤を調製し、前記第2剤と重量比1:1で混合して酸
化染毛剤組成物を得た。 Formulation Examples 3 to 6 and Comparative Examples 6 to 7 Using the samples of Table 6, a first agent was prepared in the same formulation as in the formulation examples 1 and 2, and the weight ratio to the second agent was 1: 1. An oxidative hair dye composition was obtained by mixing.
【表6】 配合例 配合例 配合例 配合例 比較例 比較例 試料 3 4 5 6 6 7 イソステアリルマルトシト゛ 4.0 4.0 4.0 − 4.0 −マルチトールイソステアレート − − − 4.0 − 4.0ミリスチン 酸イソフ゜ロヒ゜ル 0.01 0.1 1.0 15.0 0.005 30.0 性状 ケ゛ル状 ケ゛ル状 ケ゛ル状 ケ゛ル状 ケ゛ル状 ケ゛ル状 垂れ落ち ◎ ◎ ◎ ◎ ◎ ◎ 伸展性・塗布性 ◎ ◎ ◎ ◎ ◎ ◎ 均染性 ◎ ◎ ◎ ◎ ◎ △ 滑らかさ ○ ◎ ◎ ◎ △ ◎ 染着性 ◎ ◎ ◎ ◎ ○ △ 耐洗浄性 ○ ○ ○ ○ △ △[Table 6] Formulation example Formulation example Formulation example Formulation example Comparative example Comparative example Sample 3 4 5 6 6 7 Isostearyl Maltositide 4.0 4.0 4.0-4.0-Maltitol Isostearate --- 4.0-4.0 Isophoryl myristate 0.01 0.1 1.0 15.0 0.005 30.0 Gell Gell Gell Gell Gell Gell Gell Dripping ◎ ◎ ◎ ◎ ◎ ◎ ◎ Extendability / applicability ◎ ◎ ◎ ◎ ◎ ◎ Level uniformity ◎ ◎ ◎ ◎ ◎ ◎ △ Smoothness ○ ◎ ◎ ◎ ◎ △ ◎ Dyeability ◎ ◎ ◎ ◎ ◎ ○ △ Wash resistance ○ ○ ○ ○ △ △
【0046】表6から判るように、油性成分が染毛剤組
成物に対して0.01重量%より少ない場合(比較例
7)には滑らかさ、染着性、耐洗浄性が十分でなく、1
5重量%を超える場合には、均染性、染着性、耐洗浄性
がかえって低下する傾向が認められ、使用感にもべたつ
きが感じられた。以上のことから、本発明の酸化染毛剤
組成物において油性成分の配合量は0.01〜15重量
%であることが好ましい。As can be seen from Table 6, when the oily component is less than 0.01% by weight with respect to the hair dye composition (Comparative Example 7), the smoothness, dyeing property and washing resistance are insufficient. 1
When it exceeds 5% by weight, the level dyeing property, the dyeing property, and the washing resistance tend to be rather deteriorated, and stickiness is felt in use. From the above, the blending amount of the oily component in the oxidative hair dye composition of the present invention is preferably 0.01 to 15% by weight.
【0047】配合例7〜9、比較例8〜10 表7の試料を用いて前記配合例1〜2と同様の処方で第
1剤を調製し、前記第2剤aと重量比1:1で混合して
酸化染毛剤組成物を得た。 Formulation Examples 7 to 9 and Comparative Examples 8 to 10 Using the samples of Table 7, a first agent was prepared in the same formulation as in the formulation examples 1 and 2, and the weight ratio to the second agent a was 1: 1. To obtain an oxidative hair dye composition.
【表7】 配合例 配合例 配合例 比較例 比較例 比較例 試料 7 8 9 8 9 10 イソステアリルマルトシト゛ 7.0 − − − − −マルチトールイソステアリルエーテル − 7.0 − − − − 2-テトラテ゛シルオクタテ゛シルマルトシト゛ − − 7.0 − − −ステアリルマルトシト゛ − − − 7.0 − − 2-ヘキシルテ゛シルマルトシト゛ − − − − 7.0 − 2-ヘキサテ゛シルオクタテ゛シルマルトシト゛ − − − − − 7.0ミリスチン 酸イソフ゜ロヒ゜ル 15.0 15.0 15.0 15.0 15.0 15.0 性状 混合前 ケ゛ル状 ケ゛ル状 ケ゛ル状 液状 液状 分離 混合後 ケ゛ル状 ケ゛ル状 ケ゛ル状 液状 液状 分離 染毛試験 垂れ落ち ◎ ◎ ◎ × × −* 伸展性・塗布性 ◎ ◎ ◎ ○ ○ −* 均染性 ◎ ◎ ◎ × × −* 滑らかさ ◎ ◎ ◎ △ △ −* * −:染毛試験を行わなかったことを示す。[Table 7] Formulation Example Formulation Example Formulation Example Comparative Example Comparative Example Comparative Example Sample 7 8 9 8 9 10 Isostearyl Maltositide 7.0 ---- Maltitol Isostearyl Ether-7.0 ---- 2-Tetradecyl Octadecyl Maltate Cid --- 7.0 ---- Stearyl maltoside --- 7.0 --- 2-Hexyl decyl maltoside --- --- 7.0 -2-Hexadecyl octa decyl maltoside --- --- 7.0 Properties Before mixing Gel-like gel-like gel-like liquid-liquid separation After mixing gel-like gel-like gel-like liquid liquid-separation Hair dyeing test Dripping ◎ ◎ ◎ × ×-* Extendability / coatability ◎ ◎ ◎ ○ ○-* Level dispersibility ◎ ◎ ◎ × × − * Smoothness ◎ ◎ ◎ △ △ − * * −: Indicates that the hair dyeing test was not performed.
【0048】表7から判るように、本発明の糖誘導体を
配合した配合例7〜9ではゲル状の酸化染毛剤組成物を
得ることができるが、脂肪鎖が直鎖である場合(比較例
8)や、分岐脂肪鎖の総炭素数が18より小さい場合
(比較例9)では染毛剤組成物が液状でゲル状にならな
かった。また、分岐脂肪鎖の総炭素数が32より大きい
場合(比較例10)には分離してしまい、均一な染毛剤
組成物が得られなかった。また、配合例7〜9を用いた
染毛剤組成物では染毛試験において何れの評価も優れて
いたが、比較例8〜9の第1剤を用いた染毛剤組成物で
は液状のために垂れ落ち等があり、また、伸展性・塗布
性、均染性、滑らかさにおいても本発明の配合例7〜9
に比して劣るものであった。As can be seen from Table 7, in the formulation examples 7 to 9 containing the sugar derivative of the present invention, gel-like oxidative hair dye compositions can be obtained, but when the fatty chain is linear (comparison In Example 8) or when the total number of carbon atoms in the branched fatty chain was less than 18 (Comparative Example 9), the hair dye composition was liquid and did not form a gel. Moreover, when the total number of carbon atoms in the branched fatty chain was greater than 32 (Comparative Example 10), the branched hair chains were separated and a uniform hair dye composition could not be obtained. Further, in the hair dye composition using Formulation Examples 7 to 9, any evaluation was excellent in the hair dyeing test, but the hair dye composition using the first agent of Comparative Examples 8 to 9 was liquid. In addition, the compounding examples 7 to 9 of the present invention are excellent in extensibility / applicability, levelness and smoothness.
It was inferior to.
【0049】配合例10〜16 表8に示す試料を用いて前記配合例1〜2と同様の処方
で各第1剤を調製後、前記第2剤aと重量比1:1で混
合し、各混合物について各種試験を行った。 Formulation Examples 10 to 16 Using the samples shown in Table 8, each first agent was prepared in the same formulation as in Formulation Examples 1 and 2, and then mixed with the second agent a in a weight ratio of 1: 1. Various tests were performed on each mixture.
【表8】 配 合 例 試料 10 11 12 13 14 15 16 イソステアリルマルトシト゛ 8.0 8.0 8.0 8.0 8.0 4.0 −マルチトールイソステアリルエーテル − − − − − 4.0 8.0アホ゛カ゛ト゛ 油 12.0 − − − 6.0 12.0 −ラウリン 酸 − 12.0 − − 6.0 − 6.0コレステロール − − 12.0 − − − 6.0ミリスチン 酸ミリスチル − − − 12.0 − − − 垂れ落ち ◎ ◎ ◎ ◎ ◎ ◎ ◎ 伸展性・塗布性 ◎ ◎ ◎ ◎ ◎ ◎ ◎ 均染性 ◎ ◎ ◎ ◎ ◎ ◎ ◎ 滑らかさ ◎ ◎ ◎ ◎ ◎ ◎ ◎ 染着性 ◎ ◎ ◎ ◎ ◎ ◎ ◎ 耐洗浄性 ○ ○ ○ ○ ○ ○ ○[Table 8] Composition Example Sample 10 11 12 13 14 15 15 16 Isostearyl Maltositide 8.0 8.0 8.0 8.0 8.0 4.0-Maltitol Isostearyl Ether ----- 4.0 8.0 Avocado Oil 12.0 --- 6.0 12.0-Lauric Acid- 12.0 − − 6.0 − 6.0 Cholesterol − − 12.0 − − − 6.0 Myristyl acid myristyl − − − 12.0 − − − Dripping ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ Extendability / applicability ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ Uniform dyeability ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ Smoothness ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ Dyeing property ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ Cleaning resistance ○ ○ ○ ○ ○ ○ ○ ○
【0050】以上のことから、本発明の酸化染毛剤組成
物は、ゲル状で、染毛性、染着性、耐洗浄性、及び染毛
後の毛髪の滑らかさに優れた酸化染毛剤組成物が得られ
ることが理解される。比較例11 下記に示す処方で調製した第1剤及び第2剤bを重量比
1:1で混合して酸化染毛剤組成物を調製し、同様に各
種試験を行った。その結果、この染毛剤組成物はゲル状
で、垂れ落ちや染めムラはなかったものの、滑らかさや
染着性、耐洗浄性が十分でなく、従って油性成分を第2
剤に配合した場合には本発明の効果である糖誘導体と油
性成分の相乗効果は発揮されないことが判明した。以上
のことから、油性成分は糖誘導体及び酸化染料と共に第
1剤に配合する必要があることが理解される。From the above, the oxidative hair dye composition of the present invention is a gel-like oxidative hair dye which is excellent in hair dyeability, dyeability, wash resistance, and smoothness of hair after dyeing. It is understood that an agent composition is obtained. Comparative Example 11 An oxidative hair dye composition was prepared by mixing a first agent and a second agent b prepared by the following formulation in a weight ratio of 1: 1 and various tests were conducted in the same manner. As a result, this hair dye composition was in the form of gel and did not have dripping or uneven dyeing, but the smoothness, dyeing property, and washing resistance were not sufficient, and therefore the oily component
It was found that the synergistic effect of the sugar derivative and the oily component, which is the effect of the present invention, is not exhibited when blended in the agent. From the above, it is understood that the oil component must be blended in the first agent together with the sugar derivative and the oxidation dye.
【0051】 <第1剤> イソプロパノール 5.0wt% イソステアリルマルトシド 5.0 チオグリコール酸アンモニウム 0.1 L−アスコルビン酸 0.5 EDTA 0.5 アンモニア水 6.0 パラフェニレンジアミン 1.0 レゾルシン 1.0 香料 適 量 イオン交換水 残 余<First agent> Isopropanol 5.0 wt% Isostearyl maltoside 5.0 Ammonium thioglycolate 0.1 L-Ascorbic acid 0.5 EDTA 0.5 Ammonia water 6.0 Paraphenylenediamine 1.0 Resorcinol 1.0 Fragrance Suitable amount Ion exchange water Residual
【0052】 <第2剤b>(クリーム液状) 過酸化水素30% 15.0 リン酸緩衝液 pH3に調製 メチルパラベン 0.1 スズ酸ナトリウム 0.1 ミリスチン酸イソプロピル 5.0 ステアリルアルコール 3.0 ラウリル硫酸ナトリウム 0.5 POE(20)セチルエーテル 0.5 イオン交換水 残 余<Second agent b> (Cream liquid) 30% hydrogen peroxide 15.0 Phosphate buffer adjusted to pH 3 Methylparaben 0.1 Sodium stannate 0.1 Isopropyl myristate 5.0 Stearyl alcohol 3.0 Lauryl Sodium sulfate 0.5 POE (20) cetyl ether 0.5 Ion-exchanged water Residual
【0053】配合例17 3剤型染毛剤 <第1剤> イソプロパノール 5.0 イソステアリルマルトシド 5.0 イソステアリン酸 5.0 ミリスチン酸イソプロピル 5.0 ピロリドンカルボン酸ナトリウム 1.0 チオグリコール酸アンモニウム 1.0 L−アスコルビン酸 0.5 EDTA 0.5 アンモニア水 7.0 パラフェニレンジアミン 1.0 香料 適 量 イオン交換水 残 余 <第2剤c> 過酸化水素水 30% 15.0 リン酸緩衝液 0.1 メチルパラベン 0.1 錫酸ナトリウム 0.1 イオン交換水 残 余 <第3剤> 硫酸アンモニウム 2.0 メタケイ酸ナトリウム 20.0 過硫酸アンモニウム 75.0 EDTA 1.0 カルボキシメチルセルロースナトリウム 2.0 Formulation Example 17 Three-part hair dye <First agent> Isopropanol 5.0 Isostearyl maltoside 5.0 Isostearic acid 5.0 Isopropyl myristate 5.0 Sodium pyrrolidonecarboxylate 1.0 Ammonium thioglycolate 1.0 L-ascorbic acid 0.5 EDTA 0.5 Ammonia water 7.0 Para-phenylenediamine 1.0 Fragrance appropriate amount Ion-exchanged water Residual <Second agent c> Hydrogen peroxide solution 30% 15.0 Phosphoric acid Buffer solution 0.1 Methylparaben 0.1 Sodium stannate 0.1 Ion-exchanged water Residual <Third agent> Ammonium sulfate 2.0 Sodium metasilicate 20.0 Ammonium persulfate 75.0 EDTA 1.0 Sodium carboxymethylcellulose 2.0
【0054】(製法)上記第1剤の処方をイオン交換水
に順次溶解して第1剤を得た。又、第2剤cも同様にし
て調製した。上記第3剤の各成分をよく粉砕、混合して
第3剤を得た。第3剤を第2剤cに溶解し、これに第1
剤を混合して3剤型染毛料組成物を得た。通常上記の順
序で混合するが、順序はこれに限定されない。上記の処
方で調製した第1剤、第2剤c及び第3剤を重量比1:
1:1で混合したところ、均一で適度な粘度を有するゲ
ル状組成物で、染毛処理の際に頭髪からの垂れ落ちもな
く、伸展性、塗布性、均染性、染着性、耐洗浄性が良好
で、処理後の毛髪の仕上がりが滑らかな酸化染毛剤組成
物が得られた。(Production Method) The formulation of the above-mentioned first agent was sequentially dissolved in ion-exchanged water to obtain a first agent. Also, the second agent c was prepared in the same manner. Each component of the third agent was well pulverized and mixed to obtain a third agent. Dissolve the third agent in the second agent c,
The agents were mixed to obtain a three-component hair dye composition. Usually, they are mixed in the above order, but the order is not limited to this. The weight ratio of the first agent, the second agent c and the third agent prepared by the above formulation is 1:
When mixed at a ratio of 1: 1, it is a gel composition having a uniform and appropriate viscosity, and does not drip from the hair during hair dyeing treatment, and it has spreadability, applicability, leveling property, dyeing property, resistance to dyeing. An oxidative hair dye composition having good detergency and a smooth hair finish after treatment was obtained.
【0055】下記の配合例18〜31の処方で調製した
第1剤を前記表3の第2剤aと重量比1:1で混合した
ところ、均一で適度な粘度を有するゲル状の酸化染毛剤
組成物が得られた。これらは何れも染毛処理の際に頭髪
からの垂れ落ちもなく、伸展性、塗布性、均染性、染着
性、耐洗浄性が良好で、しかも、染毛後の毛髪が滑らか
で使用感に優れた酸化染毛剤組成物が得られた。また、
何れの染毛剤組成物も頭皮に対して刺激のない安全な染
毛剤組成物であった。The first agent prepared by the formulation of the following formulation examples 18 to 31 was mixed with the second agent a in Table 3 in a weight ratio of 1: 1. As a result, a gel-like oxidative dyeing having a uniform and appropriate viscosity was obtained. A hair composition was obtained. All of these have no dripping from the hair during hair dyeing, have good spreadability, applicability, level dyeability, dyeability, and wash resistance, and the hair after dyeing is smooth and used. An oxidative hair dye composition having an excellent feeling was obtained. Also,
Each hair dye composition was a safe hair dye composition with no irritation to the scalp.
【0056】配合例18 イソプロパノール 5.0 イソステアリルマルトシド 3.0 前記一般式化3で表され、Aがグルコース単糖3個の重合物、 Rがイソステアリル基である化合物 1.0 前記一般式化3で表され、Aがグルコース単糖4個の重合物、 Rがイソステアリル基である化合物 1.0 ナトリウムハイドロサルファイト 0.1 L−アスコルビン酸 0.5 EDTA 0.5 モノエタノールアミン 0.5 パラトルエンジアミノサルフェート 1.0 レゾルシン 1.0 オルソアミノフェノール 0.1 パラアミノフェノール 0.01 パラアミノオルソクレゾール 0.05 ツバキ油 12.0 香料 適 量 イオン交換水 残 余 Formulation Example 18 Isopropanol 5.0 Isostearyl Maltoside 3.0 Compound represented by the above general formula 3, wherein A is a polymer of three glucose monosaccharides, and R is an isostearyl group 1.0 The above general A compound represented by Formula 3, in which A is a polymer of four glucose monosaccharides, and R is an isostearyl group 1.0 Sodium hydrosulfite 0.1 L-ascorbic acid 0.5 EDTA 0.5 monoethanolamine 0.5 paratoluene diaminosulfate 1.0 resorcin 1.0 orthoaminophenol 0.1 paraaminophenol 0.01 paraaminoorthocresol 0.05 camellia oil 12.0 perfume proper amount ion-exchanged water residual
【0057】配合例19 イソプロパノール 5.0 イソステアリルマルトシド 4.0 前記一般式化3で表され、Aがグルコース単糖3個の重合物、 Rがイソステアリル基である化合物 1.0 ピロ亜硫酸ナトリウム 0.1 L−アスコルビン酸 0.5 EDTA 0.5 モノエタノールアミン 0.5 パラトルエンジアミノサルフェート 1.0 レゾルシン 1.0 オルソアミノフェノール 0.1 メタフェニレンジアミン 0.01 パラアミノオルソクレゾール 0.05 ヒマシ油 3.0 香料 適 量 イオン交換水 残 余 Formulation Example 19 Isopropanol 5.0 Isostearyl Maltoside 4.0 Compound represented by the above general formula 3, wherein A is a polymer of three glucose monosaccharides, and R is an isostearyl group 1.0 Pyrosulfite Sodium 0.1 L-ascorbic acid 0.5 EDTA 0.5 monoethanolamine 0.5 paratoluene diaminosulfate 1.0 resorcin 1.0 1.0 orthoaminophenol 0.1 metaphenylenediamine 0.01 paraaminoorthocresol 0.05 Castor oil 3.0 Fragrance appropriate amount Ion-exchanged water residual
【0058】配合例20 イソプロパノール 5.0 イソステアリルマルトシド 5.0 ジメチルポリシロキサン(20cs) 2.0 ホホバ油 15.0 ナトリウムハイドロサルファイト 0.1 L−アスコルビン酸 0.5 ヒドロキシエタンジホスホン酸 0.5 アンモニア水 6.0 モノエタノールアミン 1.0 パラフェニレンジアミノサルフェート 1.0 レゾルシン 1.0 パラアミノフェノール 0.1 パラニトロオルソフェニレンジアミン 0.01 パラアミノオルソクレゾール 0.01 香料 適 量 イオン交換水 残 余 Formulation Example 20 Isopropanol 5.0 Isostearyl maltoside 5.0 Dimethylpolysiloxane (20cs) 2.0 Jojoba oil 15.0 Sodium hydrosulfite 0.1 L-Ascorbic acid 0.5 Hydroxyethanediphosphonic acid 0.5 Ammonia water 6.0 Monoethanolamine 1.0 Para-phenylenediaminosulfate 1.0 Resorcin 1.0 Para-aminophenol 0.1 Para-nitro-ortho-phenylenediamine 0.01 Para-amino-ortho-cresol 0.01 Fragrance Ion-exchanged water Remnant
【0059】配合例21 イソプロパノール 5.0 ワセリン 0.5 1,3−ブチレングリコール 5.0 イソステアリルマルトシド 5.0 チオグリコール酸アンモニウム 0.5 L−アスコルビン酸 0.5 EDTA 0.5 メチルパラベン 1.0 モノエタノールアミン 0.5 水酸化ナトリウム 0.2 パラフェニレンジアミン 1.0 パラアミノオルソクレゾール 1.0 オルソアミノフェノール 0.1 マイクロクリスタリンワックス 10.0 香料 適 量 イオン交換水 残 余 Formulation Example 21 Isopropanol 5.0 Vaseline 0.5 1,3-butylene glycol 5.0 Isostearyl maltoside 5.0 Ammonium thioglycolate 0.5 L-Ascorbic acid 0.5 EDTA 0.5 Methylparaben 1 0.0 monoethanolamine 0.5 sodium hydroxide 0.2 paraphenylenediamine 1.0 paraaminoorthocresol 1.0 orthoaminophenol 0.1 microcrystalline wax 10.0 perfume proper amount ion-exchanged water residual
【0060】配合例22 イソプロパノール 5.0 流動パラフィン 13.0 イソステアリルマルトシド 5.0 チオグリコール酸アンモニウム 0.1 L−アスコルビン酸 0.5 EDTA 0.5 モノエタノールアミン 0.5 炭酸水素ナトリウム 1.0 パラフェニレンジアミン 1.0 メタアミノフェノール 1.0 オルソアミノフェノール 0.1 メタフェニレンジアミン 0.01 パラアミノオルソクレゾール 0.01 香料 適 量 イオン交換水 残 余 Formulation Example 22 Isopropanol 5.0 Liquid paraffin 13.0 Isostearyl maltoside 5.0 Ammonium thioglycolate 0.1 L-Ascorbic acid 0.5 EDTA 0.5 Monoethanolamine 0.5 Sodium hydrogencarbonate 1 0.0 para-phenylenediamine 1.0 meta-aminophenol 1.0 ortho-aminophenol 0.1 meta-phenylenediamine 0.01 para-amino-ortho-cresol 0.01 perfume proper amount ion-exchanged water residual
【0061】配合例23 マルチトール水溶液 14.0 イソプロパノール 5.0 スクワラン 20.0 イソステアリルマルトシド 7.0 ナトリウムハイドロサルファイト 0.1 L−アスコルビン酸 0.5 EDTA 0.5 アンモニア水 6.0 炭酸アンモニウム 2.0 パラトルエンジアミノサルフェート 1.0 メタアミノフェノール 2.0 オルソアミノフェノール 0.3 香料 適 量 イオン交換水 残 余 Formulation Example 23 Maltitol Aqueous Solution 14.0 Isopropanol 5.0 Squalane 20.0 Isostearyl Maltoside 7.0 Sodium Hydrosulfite 0.1 L-Ascorbic Acid 0.5 EDTA 0.5 Ammonia Water 6.0 Ammonium carbonate 2.0 Paratoluene diaminosulfate 1.0 Metaaminophenol 2.0 Orthoaminophenol 0.3 Perfume Suitable amount Ion-exchanged water Residual
【0062】配合例24 ベンジルアルコール 2.0 イソステアリルマルトシド 8.0 ピロ亜硫酸ナトリウム 0.1 L−アスコルビン酸 0.5 EDTA 0.5 モノエタノールアミン 0.5 パラフェニレンジアミン 1.0 レゾルシン 1.0 オルソアミノフェノール 0.2 メタアミノフェノール 0.1 パラアミノオルソクレゾール 0.05 コレステロール 10.0 香料 適 量 イオン交換水 残 余 Formulation Example 24 Benzyl alcohol 2.0 Isostearyl maltoside 8.0 Sodium pyrosulfite 0.1 L-Ascorbic acid 0.5 EDTA 0.5 Monoethanolamine 0.5 Paraphenylenediamine 1.0 Resorcinol 1. 0 Orthoaminophenol 0.2 Metaaminophenol 0.1 Paraaminoorthocresol 0.05 Cholesterol 10.0 Fragrance Suitable amount Ion-exchanged water Residual
【0063】配合例25 イソプロパノール 5.0 イソステアリルマルトシド 5.0 ナトリウムハイドロサルファイト 0.5 L−アスコルビン酸 0.5 EDTA 0.5 モノエタノールアミン 2.0 パラトルエンジアミノサルフェート 1.0 レゾルシン 1.0 パラアミノフェノール 0.1 ミリスチルアルコール 12.0 香料 適 量 イオン交換水 残 余 Formulation Example 25 Isopropanol 5.0 Isostearyl Maltoside 5.0 Sodium Hydrosulfite 0.5 L-Ascorbic Acid 0.5 EDTA 0.5 Monoethanolamine 2.0 Paratoluenediaminosulfate 1.0 Resorcinol 1 0.0 Para aminophenol 0.1 Myristyl alcohol 12.0 Fragrance Suitable amount Ion-exchanged water Residual
【0064】配合例26 プロピレングリコール 10.0 イソプロパノール 5.0 イソステアリルマルトシド 5.0 セタノール 13.0 ケラチン加水分解物 0.5 ナトリウムハイドロサルファイト 0.1 L−アスコルビン酸 0.5 EDTA 0.5 アンモニア水 6.0 パラフェニレンジアミン 1.0 パラアミノフェノール 1.0 パラアミノオルトクレゾール 0.02 香料 適 量 イオン交換水 残 余 Formulation Example 26 Propylene Glycol 10.0 Isopropanol 5.0 Isostearyl Maltoside 5.0 Cetanol 13.0 Keratin Hydrolyzate 0.5 Sodium Hydrosulfite 0.1 L-Ascorbic Acid 0.5 EDTA 0.1. 5 Ammonia water 6.0 Para-phenylenediamine 1.0 Para-aminophenol 1.0 Para-aminoorthocresol 0.02 Fragrance Suitable amount Ion-exchanged water Residual
【0065】配合例27 流動パラフィン 2.0 イソプロパノール 5.0 イソステアリルマルトシド 5.0 イソステアリルアルコール 14.5 ナトリウムハイドロサルファイト 0.1 L−アスコルビン酸 0.5 EDTA 0.5 アンモニア水 6.0 パラフェニレンジアミン 1.0 メタアミノフェノール 1.0 パラニトロオルトフェニレンジアミン 0.02 香料 適 量 イオン交換水 残 余 Formulation Example 27 Liquid paraffin 2.0 Isopropanol 5.0 Isostearyl maltoside 5.0 Isostearyl alcohol 14.5 Sodium hydrosulfite 0.1 L-Ascorbic acid 0.5 EDTA 0.5 Ammonia water 6. 0 para-phenylenediamine 1.0 meta-aminophenol 1.0 para-nitro-ortho-phenylenediamine 0.02 perfume proper amount ion-exchanged water residual
【0066】配合例28 ラノリン 2.0 エタノール 5.0 イソステアリルマルトシド 10.0 ピロ亜硫酸ナトリウム 0.1 水酸化ナトリウム 0.3 L−アスコルビン酸 0.5 EDTA 0.5 メチルパラベン 1.0 アンモニア水 6.0 パラトルエンジアミノサルフェート 1.0 レゾルシン 1.0 パラアミノオルソクレゾール 0.5 ラウリン酸ヘキシル 10.0 香料 適 量 イオン交換水 残 余 Formulation Example 28 Lanolin 2.0 Ethanol 5.0 Isostearyl Maltoside 10.0 Sodium Pyrosulfite 0.1 Sodium Hydroxide 0.3 L-Ascorbic Acid 0.5 EDTA 0.5 Methylparaben 1.0 Ammonia Water 6.0 Paratoluenediaminosulfate 1.0 Resorcinol 1.0 Paraaminoorthocresol 0.5 Hexyl laurate 10.0 Fragrance Suitable amount Ion-exchanged water Residual
【0067】配合例29 プロピレングリコール 10.0 イソプロパノール 5.0 イソステアリルマルトシド 5.0 12−ヒドロキシステアリン酸コレステリル 11.5 ナトリウムハイドロサルファイト 0.1 L−アスコルビン酸 0.5 EDTA 0.5 メチルパラベン 1.0 モノエタノールアミン 2.0 アンモニア水 5.0 パラフェニレンジアミン 1.5 レゾルシン 1.0 パラアミノフェノール 0.2 メタアミノフェノール 0.1 香料 適 量 イオン交換水 残 余 Formulation Example 29 Propylene Glycol 10.0 Isopropanol 5.0 Isostearyl Maltoside 5.0 Cholesteryl 12-hydroxystearate 11.5 Sodium hydrosulfite 0.1 L-Ascorbic acid 0.5 EDTA 0.5 Methylparaben 1.0 Monoethanolamine 2.0 Ammonia water 5.0 Para-phenylenediamine 1.5 Resorcin 1.0 Para-aminophenol 0.2 Meta-aminophenol 0.1 Perfume Suitable amount Ion-exchanged water Residual
【0068】配合例30 ワセリン 2.0 エタノール 5.0 イソステアリルマルトシド 5.0 オクタン酸セチル 17.5 チオ硫酸ナトリウム 0.1 N−メチルピロリドン 0.5 L−アスコルビン酸 0.5 EDTA 0.5 メチルパラベン 0.1 モノエタノールアミン 3.0 水酸化カリウム 0.3 パラフェニレンジアミン 1.0 レゾルシン 1.0 メタアミノフェノール 0.1 パラアミノオルソクレゾール 0.05 香料 適 量 イオン交換水 残 余 Formulation Example 30 Vaseline 2.0 Ethanol 5.0 Isostearyl maltoside 5.0 Cetyl octanoate 17.5 Sodium thiosulfate 0.1 N-Methylpyrrolidone 0.5 L-Ascorbic acid 0.5 EDTA 0. 5 Methylparaben 0.1 Monoethanolamine 3.0 Potassium hydroxide 0.3 Paraphenylenediamine 1.0 Resorcinol 1.0 Metaaminophenol 0.1 Paraaminoorthocresol 0.05 Perfume Appropriate amount Ion-exchanged water Residual
【0069】配合例31 ラノリン 2.0 イソプロパノール 5.0 イソステアリルマルトシド 5.0 マルチトールヒドロキシ脂肪族エーテル 2.0 オレイルアルコール 18.0 ナトリウムハイドロサルファイト 0.1 L−アスコルビン酸 0.5 EDTA 0.5 メチルパラベン 0.1 モノエタノールアミン 0.5 パラフェニレンジアミン 1.0 パラアミノフェノール 1.0 レゾルシン 0.05 パラニトロオルトフェニレンジアミン 0.02 香料 適 量 イオン交換水 残 余 Formulation Example 31 Lanolin 2.0 Isopropanol 5.0 Isostearyl Maltoside 5.0 Maltitol hydroxyaliphatic ether 2.0 Oleyl alcohol 18.0 Sodium hydrosulfite 0.1 L-Ascorbic acid 0.5 EDTA 0.5 Methylparaben 0.1 Monoethanolamine 0.5 Paraphenylenediamine 1.0 Paraaminophenol 1.0 Resorcinol 0.05 Paranitroorthophenylenediamine 0.02 Fragrance Suitable amount Ion-exchanged water Residual
【0070】[0070]
【発明の効果】本発明に係る酸化染毛剤組成物は、油性
成分と糖誘導体を酸化染料と共に第1剤に配合すること
により、適度な粘度を有し、染毛処理の際に頭髪からの
垂れ落ちもなく、伸展性、塗布性、均染性に優れると共
に、滑らかさ、染着性、耐洗浄性が相乗的に向上すると
いういう特徴を有する。EFFECTS OF THE INVENTION The oxidative hair dye composition according to the present invention has an appropriate viscosity by blending an oily component and a sugar derivative together with an oxidative dye in the first agent, so that the hair can be removed from the hair during hair dyeing treatment. It has the characteristics that it does not droop down and is excellent in extensibility, coating property and level dyeing property, and that the smoothness, dyeing property and washing resistance are synergistically improved.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 植原 計一 神奈川県横浜市港北区新羽町1050番地 株 式会社資生堂第一リサーチセンター内 (72)発明者 奥村 昌和 兵庫県高砂市梅井5丁目1番1号 日本精 化株式会社研究所内 (72)発明者 楠本 隆文 東京都中央区小伝馬町4−9 小伝馬町第 一生命ビル 日本精化株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Keiichi Uehara 1050 Shinba-cho, Kohoku-ku, Yokohama-shi, Kanagawa Inside Shiseido Daiichi Research Center (72) Inventor Masakazu Okumura 5-1-1 Umei, Takasago, Hyogo No. 1 Inside the Nippon Seika Co., Ltd. (72) Inventor Takafumi Kusumoto 4-9 Kodenma-cho, Chuo-ku, Tokyo Kodenma-cho Daiichi Seimei Building Nihon Seika Co., Ltd.
Claims (6)
成分と、酸化染料とを含有する第1剤と、酸化剤を含有
する、第1剤以外の1剤もしくは2剤以上とを用時混合
してなることを特徴とする酸化染毛剤組成物。 【化1】 (但し、式中Aは糖からn個の水酸基を除いた残基、R
は総炭素数18〜32で、且つ、分岐鎖を有する脂肪
鎖、nは1以上を表す。)1. A first agent containing a sugar derivative represented by the general formula 1, an oily component and an oxidizing dye, and one or more agents other than the first agent containing an oxidizing agent. An oxidative hair dye composition, which is obtained by mixing when used. Embedded image (In the formula, A is a residue obtained by removing n hydroxyl groups from sugar, R is
Represents a fatty chain having a total carbon number of 18 to 32 and having a branched chain, and n represents 1 or more. )
て、糖誘導体が一般式化2で表される糖分岐脂肪族エー
テルであることを特徴とする酸化染毛剤組成物。 【化2】 (但し、式中Aは糖からn個の非ヘミアセタール性水酸
基を除いた残基、R及びnは前記化1に同じである。)2. The oxidative hair dye composition according to claim 1, wherein the sugar derivative is a sugar-branched aliphatic ether represented by the general formula 2. Embedded image (However, in the formula, A is a residue obtained by removing n non-hemiacetal hydroxyl groups from a sugar, and R and n are the same as those in the above chemical formula 1.)
て、糖誘導体が一般式化3で表される分岐脂肪族グリコ
シドであることを特徴とする酸化染毛剤組成物。 【化3】 (但し、式中Aは糖からヘミアセタール性水酸基を除い
た残基、Rは前記化1に同じである。)3. The oxidative hair dye composition according to claim 1, wherein the sugar derivative is a branched aliphatic glycoside represented by the general formula 3. Embedded image (However, in the formula, A is a residue obtained by removing a hemiacetal hydroxyl group from a sugar, and R is the same as the above chemical formula 1.)
において、糖誘導体がマルチトールイソステアリルエー
テルであることを特徴とする酸化染毛剤組成物。4. The oxidative hair dye composition according to claim 1, wherein the sugar derivative is maltitol isostearyl ether.
において、糖誘導体がイソステアリルマルトシドである
ことを特徴とする酸化染毛剤組成物。5. The oxidative hair dye composition according to claim 1 or 3, wherein the sugar derivative is isostearyl maltoside.
おいて、油性成分として天然油脂、高級脂肪酸、ステロ
ール類、エステル油の中から選ばれた1種又は2種以上
を含有することを特徴とする酸化染毛剤組成物。6. The oxidative hair dye composition according to any one of claims 1 to 5, which contains, as an oily component, one or more selected from natural fats and oils, higher fatty acids, sterols and ester oils. An oxidative hair dye composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7187871A JPH0920627A (en) | 1995-06-30 | 1995-06-30 | Oxidative hair dye composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7187871A JPH0920627A (en) | 1995-06-30 | 1995-06-30 | Oxidative hair dye composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0920627A true JPH0920627A (en) | 1997-01-21 |
Family
ID=16213678
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7187871A Withdrawn JPH0920627A (en) | 1995-06-30 | 1995-06-30 | Oxidative hair dye composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0920627A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003081790A (en) * | 2001-09-13 | 2003-03-19 | Hoyu Co Ltd | Decolorant composition and hair color composition |
| WO2008035500A1 (en) * | 2006-09-20 | 2008-03-27 | Takasago International Corporation | Hair dye stabilizer |
| JP2008533139A (en) * | 2005-03-15 | 2008-08-21 | ユニバーシティ マラヤ | Branched alkyl oligosaccharides for liquid crystals and other related applications |
| JP2009120527A (en) * | 2007-11-14 | 2009-06-04 | Shiseido Co Ltd | Skin care preparation for external use |
| JP2015525737A (en) * | 2012-06-29 | 2015-09-07 | ロレアル | Cosmetic composition for keratin fibers |
| JP2018168092A (en) * | 2017-03-30 | 2018-11-01 | 株式会社ナノエッグ | Hair dye composition |
-
1995
- 1995-06-30 JP JP7187871A patent/JPH0920627A/en not_active Withdrawn
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003081790A (en) * | 2001-09-13 | 2003-03-19 | Hoyu Co Ltd | Decolorant composition and hair color composition |
| JP2008533139A (en) * | 2005-03-15 | 2008-08-21 | ユニバーシティ マラヤ | Branched alkyl oligosaccharides for liquid crystals and other related applications |
| WO2008035500A1 (en) * | 2006-09-20 | 2008-03-27 | Takasago International Corporation | Hair dye stabilizer |
| JP2008074760A (en) * | 2006-09-20 | 2008-04-03 | Takasago Internatl Corp | Stabilizer for hair dye |
| US7753966B2 (en) | 2006-09-20 | 2010-07-13 | Takasago International Corporation | Hair dye stabilizer |
| JP2009120527A (en) * | 2007-11-14 | 2009-06-04 | Shiseido Co Ltd | Skin care preparation for external use |
| JP2015525737A (en) * | 2012-06-29 | 2015-09-07 | ロレアル | Cosmetic composition for keratin fibers |
| JP2018168092A (en) * | 2017-03-30 | 2018-11-01 | 株式会社ナノエッグ | Hair dye composition |
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