JP2013133320A - Hair dye - Google Patents
Hair dye Download PDFInfo
- Publication number
- JP2013133320A JP2013133320A JP2011285400A JP2011285400A JP2013133320A JP 2013133320 A JP2013133320 A JP 2013133320A JP 2011285400 A JP2011285400 A JP 2011285400A JP 2011285400 A JP2011285400 A JP 2011285400A JP 2013133320 A JP2013133320 A JP 2013133320A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- hair dye
- dye
- examples
- blended
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000118 hair dye Substances 0.000 title claims abstract description 105
- 239000000975 dye Substances 0.000 claims abstract description 48
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 37
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 35
- SEBIKDIMAPSUBY-ARYZWOCPSA-N Crocin Chemical compound C([C@H]1O[C@H]([C@@H]([C@@H](O)[C@@H]1O)O)OC(=O)C(C)=CC=CC(C)=C\C=C\C=C(/C)\C=C\C=C(C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)O1)O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SEBIKDIMAPSUBY-ARYZWOCPSA-N 0.000 claims abstract description 20
- VFLDPWHFBUODDF-FCXRPNKRSA-N curcumin Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)CC(=O)\C=C\C=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-FCXRPNKRSA-N 0.000 claims abstract description 20
- WZUVPPKBWHMQCE-UHFFFAOYSA-N Haematoxylin Chemical compound C12=CC(O)=C(O)C=C2CC2(O)C1C1=CC=C(O)C(O)=C1OC2 WZUVPPKBWHMQCE-UHFFFAOYSA-N 0.000 claims abstract description 18
- SEBIKDIMAPSUBY-JAUCNNNOSA-N Crocin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C(=O)OC1OC(COC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O)C=CC=C(/C)C(=O)OC3OC(COC4OC(CO)C(O)C(O)C4O)C(O)C(O)C3O SEBIKDIMAPSUBY-JAUCNNNOSA-N 0.000 claims abstract description 16
- 239000003513 alkali Substances 0.000 claims abstract description 15
- 125000003396 thiol group Chemical group [H]S* 0.000 claims abstract description 15
- 235000012730 carminic acid Nutrition 0.000 claims abstract description 12
- 239000004106 carminic acid Substances 0.000 claims abstract description 12
- 229940109262 curcumin Drugs 0.000 claims abstract description 10
- 235000012754 curcumin Nutrition 0.000 claims abstract description 10
- 239000004148 curcumin Substances 0.000 claims abstract description 10
- VFLDPWHFBUODDF-UHFFFAOYSA-N diferuloylmethane Natural products C1=C(O)C(OC)=CC(C=CC(=O)CC(=O)C=CC=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-UHFFFAOYSA-N 0.000 claims abstract description 10
- YBHILYKTIRIUTE-UHFFFAOYSA-N berberine Chemical compound C1=C2CC[N+]3=CC4=C(OC)C(OC)=CC=C4C=C3C2=CC2=C1OCO2 YBHILYKTIRIUTE-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229940093265 berberine Drugs 0.000 claims abstract description 9
- QISXPYZVZJBNDM-UHFFFAOYSA-N berberine Natural products COc1ccc2C=C3N(Cc2c1OC)C=Cc4cc5OCOc5cc34 QISXPYZVZJBNDM-UHFFFAOYSA-N 0.000 claims abstract description 9
- DGQLVPJVXFOQEV-NGOCYOHBSA-N carminic acid Chemical compound OC1=C2C(=O)C=3C(C)=C(C(O)=O)C(O)=CC=3C(=O)C2=C(O)C(O)=C1[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O DGQLVPJVXFOQEV-NGOCYOHBSA-N 0.000 claims abstract description 8
- 229940114118 carminic acid Drugs 0.000 claims abstract description 8
- 240000001972 Gardenia jasminoides Species 0.000 claims abstract 2
- 239000000049 pigment Substances 0.000 claims description 31
- 239000001055 blue pigment Substances 0.000 claims description 6
- 235000003373 curcuma longa Nutrition 0.000 claims description 6
- 235000003392 Curcuma domestica Nutrition 0.000 claims description 5
- 235000013976 turmeric Nutrition 0.000 claims description 5
- 241001222097 Xenocypris argentea Species 0.000 claims description 4
- 229940080423 cochineal Drugs 0.000 claims description 4
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 3
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 claims description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 3
- 239000009627 gardenia yellow Substances 0.000 claims description 3
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims description 3
- 240000005109 Cryptomeria japonica Species 0.000 claims description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims 2
- 244000008991 Curcuma longa Species 0.000 claims 1
- 238000004043 dyeing Methods 0.000 abstract description 46
- 241000196324 Embryophyta Species 0.000 abstract description 10
- 239000004615 ingredient Substances 0.000 abstract description 5
- UWHUTZOCTZJUKC-JKSUJKDBSA-N brazilin Chemical compound C12=CC(O)=C(O)C=C2C[C@]2(O)[C@H]1C1=CC=C(O)C=C1OC2 UWHUTZOCTZJUKC-JKSUJKDBSA-N 0.000 abstract 1
- UWHUTZOCTZJUKC-CVEARBPZSA-N brazilin Natural products C12=CC(O)=C(O)C=C2C[C@@]2(O)[C@@H]1C1=CC=C(O)C=C1OC2 UWHUTZOCTZJUKC-CVEARBPZSA-N 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 65
- 239000000203 mixture Substances 0.000 description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
- 239000013065 commercial product Substances 0.000 description 23
- 238000011156 evaluation Methods 0.000 description 17
- 239000000047 product Substances 0.000 description 11
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 10
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- 244000111489 Gardenia augusta Species 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 7
- 239000000284 extract Substances 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- UFULAYFCSOUIOV-UHFFFAOYSA-N cysteamine Chemical compound NCCS UFULAYFCSOUIOV-UHFFFAOYSA-N 0.000 description 6
- 229960003151 mercaptamine Drugs 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- PZASAAIJIFDWSB-CKPDSHCKSA-N 8-[(1S)-1-[8-(trifluoromethyl)-7-[4-(trifluoromethyl)cyclohexyl]oxynaphthalen-2-yl]ethyl]-8-azabicyclo[3.2.1]octane-3-carboxylic acid Chemical compound FC(F)(F)C=1C2=CC([C@@H](N3C4CCC3CC(C4)C(O)=O)C)=CC=C2C=CC=1OC1CCC(C(F)(F)F)CC1 PZASAAIJIFDWSB-CKPDSHCKSA-N 0.000 description 5
- 244000163122 Curcuma domestica Species 0.000 description 5
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 4
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 4
- 235000001453 Glycyrrhiza echinata Nutrition 0.000 description 4
- 235000006200 Glycyrrhiza glabra Nutrition 0.000 description 4
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 description 4
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 4
- 244000042664 Matricaria chamomilla Species 0.000 description 4
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 4
- 241000199919 Phaeophyceae Species 0.000 description 4
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 4
- 235000010418 carrageenan Nutrition 0.000 description 4
- 239000000679 carrageenan Substances 0.000 description 4
- 229920001525 carrageenan Polymers 0.000 description 4
- 229940113118 carrageenan Drugs 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 229940097275 indigo Drugs 0.000 description 4
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 4
- 229940010454 licorice Drugs 0.000 description 4
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 4
- 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 4
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 3
- 244000178231 Rosmarinus officinalis Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
- 244000306301 Caesalpinia sappan Species 0.000 description 2
- 235000015162 Caesalpinia sappan Nutrition 0.000 description 2
- 235000018958 Gardenia augusta Nutrition 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 241000202807 Glycyrrhiza Species 0.000 description 2
- 244000303040 Glycyrrhiza glabra Species 0.000 description 2
- 240000007829 Haematoxylum campechianum Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 description 2
- 244000113306 Monascus purpureus Species 0.000 description 2
- 235000002322 Monascus purpureus Nutrition 0.000 description 2
- 241000972673 Phellodendron amurense Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229940024606 amino acid Drugs 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 239000001099 ammonium carbonate Substances 0.000 description 2
- VEVZSMAEJFVWIL-UHFFFAOYSA-O cyanidin cation Chemical compound [O+]=1C2=CC(O)=CC(O)=C2C=C(O)C=1C1=CC=C(O)C(O)=C1 VEVZSMAEJFVWIL-UHFFFAOYSA-O 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229940057059 monascus purpureus Drugs 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 2
- QIJRTFXNRTXDIP-UHFFFAOYSA-N (1-carboxy-2-sulfanylethyl)azanium;chloride;hydrate Chemical compound O.Cl.SCC(N)C(O)=O QIJRTFXNRTXDIP-UHFFFAOYSA-N 0.000 description 1
- BNAZKIJXZHLHTG-WCCKRBBISA-N (2r)-2-acetamido-3-sulfanylpropanoic acid;hydrochloride Chemical compound Cl.CC(=O)N[C@@H](CS)C(O)=O BNAZKIJXZHLHTG-WCCKRBBISA-N 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- RECMXJOGNNTEBG-UHFFFAOYSA-N 1-phenylmethoxyethanol Chemical compound CC(O)OCC1=CC=CC=C1 RECMXJOGNNTEBG-UHFFFAOYSA-N 0.000 description 1
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 244000178937 Brassica oleracea var. capitata Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 240000000731 Fagus sylvatica Species 0.000 description 1
- 235000010099 Fagus sylvatica Nutrition 0.000 description 1
- 241000350160 Haematoxylum Species 0.000 description 1
- ZUKLFFYDSALIQW-MSUKCBDUSA-N Iridoid glycoside Chemical compound [H][C@]12CC[C@H](C(O)=O)[C@@]1([H])[C@H](OC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OC=C2 ZUKLFFYDSALIQW-MSUKCBDUSA-N 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000228347 Monascus <ascomycete fungus> Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241001282110 Pagrus major Species 0.000 description 1
- 241000485664 Protortonia cacti Species 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 241000580955 Sapindus mukorossi Species 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229960004308 acetylcysteine Drugs 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- -1 aromatic alcohols Chemical class 0.000 description 1
- 102000006995 beta-Glucosidase Human genes 0.000 description 1
- 108010047754 beta-Glucosidase Proteins 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 235000007336 cyanidin Nutrition 0.000 description 1
- 229960002433 cysteine Drugs 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 150000001944 cysteine derivatives Chemical class 0.000 description 1
- 229960001305 cysteine hydrochloride Drugs 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 239000003676 hair preparation Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229930182489 iridoid glycoside Natural products 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- HKUHOPQRJKPJCJ-UHFFFAOYSA-N pelargonidin Natural products OC1=Cc2c(O)cc(O)cc2OC1c1ccc(O)cc1 HKUHOPQRJKPJCJ-UHFFFAOYSA-N 0.000 description 1
- 235000006251 pelargonidin Nutrition 0.000 description 1
- YPVZJXMTXCOTJN-UHFFFAOYSA-N pelargonidin chloride Chemical compound [Cl-].C1=CC(O)=CC=C1C(C(=C1)O)=[O+]C2=C1C(O)=CC(O)=C2 YPVZJXMTXCOTJN-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- GNBVPFITFYNRCN-UHFFFAOYSA-M sodium thioglycolate Chemical compound [Na+].[O-]C(=O)CS GNBVPFITFYNRCN-UHFFFAOYSA-M 0.000 description 1
- 229940046307 sodium thioglycolate Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229940035024 thioglycerol Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
- A61K8/498—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9794—Liliopsida [monocotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
- A61K2800/432—Direct dyes
- A61K2800/4324—Direct dyes in preparations for permanently dyeing the hair
Abstract
Description
本発明は、特定の染料が配合された染毛剤に関するものである。 The present invention relates to a hair dye containing a specific dye.
毛髪を着色するために用いられる染毛剤の一種として、酸化染料を配合した第1剤と過酸化水素を配合した第2剤とを混合した酸化染毛剤が知られており、他の染毛剤として、ウコン、蘇芳、アカミノ木、黄檗、藍等の植物に由来する色素を配合したものが知られている。後者の染毛剤における植物由来色素には染料となる色素が含まれており、当該色素によって毛髪を着色する。そして、特許文献1には、蘇芳、黄檗などの植物に由来する天然草木染成分を含むものの開示があり(請求項1)、特許文献2には、藍のすくもなど及び亜硫酸ソーダを配合した染毛剤の開示がある(実施例1等)。 As one type of hair dye used for coloring hair, an oxidative hair dye in which a first agent containing an oxidative dye and a second agent containing hydrogen peroxide are mixed is known. As hair agents, those containing pigments derived from plants such as turmeric, Suho, Akamino trees, twilight and indigo are known. The plant-derived pigment in the latter hair dye contains a pigment that becomes a dye, and the hair is colored with the pigment. Patent Document 1 discloses a material containing a natural plant dye component derived from plants such as Suho and Huangpu (Claim 1), and Patent Document 2 discloses a hair dye containing indigo spider and sodium sulfite. There is a disclosure of the agent (Example 1).
上記のような植物由来成分と同じ染料を用いて毛髪を染色することは、自然派志向者にも好まれやすい。また、染毛剤による染まりを濃くすることは、望まれる場面が多い。 Dyeing hair using the same dyes as the plant-derived components as described above is also preferred by naturalists. Further, it is often desired to increase the dyeing by the hair dye.
本発明は、上記事情に鑑み、植物にも含まれている成分と同じ特定染料が配合され且つその染料による濃染性が高い染毛剤の提供を目的とする。 In view of the above circumstances, an object of the present invention is to provide a hair dye which contains the same specific dye as the component contained in plants and has high darkness with the dye.
本発明者が植物にも含まれている染料成分を配合した染毛剤について鋭意検討を行った結果、特定の染料と共にチオール基を有する還元剤及びアルカリ剤が配合された染毛剤であれば、濃染性が高いことを見出し、本発明を完成するに至った。 As a result of the present inventors diligently studying hair dyes containing dye components contained in plants, a hair dye containing a specific dye and a reducing agent having a thiol group and an alkali agent is used. As a result, the present inventors have found that the deep dyeing property is high and have completed the present invention.
すなわち、本発明に係る染毛剤は、ブラジリン、ヘマトキシリン、ベルベリン、クロシン、モナスコルブリン、キサントモナシン、カルミン酸、クルクミン、及びクチナシ青色素から選ばれた一種又は二種以上の染料、チオール基を有する還元剤、並びに、アルカリ剤が配合されたことを特徴とする。当該染毛剤には、ブラジリンを含有するスオウ色素、ヘマトキシリンを含有するアカミノキ色素、ベルベリンを含有するキハダ色素、クロシンを含有するクチナシ黄色素、モナスコルブリンを含有するベニコウジ色素、キサントモナシンを含有するベニコウジ色素、カルミン酸を含有するコチニール色素、及びクルクミンを含有するウコン色素から選ばれた一種又は二種以上が配合されていても良い。 That is, the hair dye according to the present invention is one or two or more dyes selected from bradylin, hematoxylin, berberine, crocin, monascorbulin, xanthmonacin, carmic acid, curcumin, and gardenia blue pigment, thiol group It is characterized in that a reducing agent having an alkaline agent and an alkaline agent are blended. The hair dye contains sugi pigment containing bradylin, acaminoki pigment containing hematoxylin, yellowfin pigment containing berberine, gardenia yellow pigment containing crocin, benichouji pigment containing monascorbline, and xanthomonasin 1 type or 2 types or more chosen from the beech mushroom pigment | dye to be used, the cochineal pigment | dye containing a carminic acid, and the turmeric pigment | dye containing curcumin may be mix | blended.
本発明に係る染毛剤のpHは、例えば8.0以上11.0以下である。 The pH of the hair dye according to the present invention is, for example, 8.0 or more and 11.0 or less.
前記アルカリ剤として、アルカノールアミンが配合されていると好適である。当該アルカノールアミンとして、モノエタノールアミン、ジエタノールアミン、トリエタノールアミン、モノプロパノールアミン、ジプロパノールアミン、トリプロパノールアミン、モノイソプロパノールアミン、2−アミノ−2−メチル−1,3−プロパンジオール、2−アミノ−2−メチル−1−プロパノール、又は2−アミノ−2−ヒドロキシメチル−1,3−プロパンジオールが配合されると良い。 It is preferable that alkanolamine is blended as the alkali agent. As the alkanolamine, monoethanolamine, diethanolamine, triethanolamine, monopropanolamine, dipropanolamine, tripropanolamine, monoisopropanolamine, 2-amino-2-methyl-1,3-propanediol, 2-amino- 2-Methyl-1-propanol or 2-amino-2-hydroxymethyl-1,3-propanediol is preferably blended.
チオール基を有する還元剤及びアルカリ剤が配合された本発明に係る染毛剤によれば、特定の染料による毛髪の濃染性が高い。 According to the hair dye according to the present invention in which a reducing agent having a thiol group and an alkali agent are blended, the hair is highly dyeable with a specific dye.
本発明の実施形態に係る染毛剤に基づき、本発明を以下に説明する。
本実施形態に係る染毛剤は、染料、還元剤、及びアルカリ剤を水と配合したものである(水の配合量は、例えば70質量%以上)。また、本実施形態に係る染毛剤には、更に公知の染毛剤用原料が任意原料として配合されていても良い。
Based on the hair dye which concerns on embodiment of this invention, this invention is demonstrated below.
The hair dye which concerns on this embodiment mix | blends dye, a reducing agent, and an alkaline agent with water (The compounding quantity of water is 70 mass% or more, for example). Moreover, the hair dye which concerns on this embodiment may further mix | blend the well-known raw material for hair dyes as an arbitrary raw material.
(染料)
本実施形態の染毛剤には、ブラジリン、ヘマトキシリン、ベルベリン、クロシン、モナスコルブリン、キサントモナシン、カルミン酸、クルクミン、及びクチナシ青色素から選ばれた一種又は二種以上が必須染料として配合される。
(dye)
In the hair dye of this embodiment, one or more selected from bradylin, hematoxylin, berberine, crocin, monascorbulin, xanthmonacin, carminic acid, curcumin, and gardenia blue pigment are blended as essential dyes. The
上記必須染料は植物由来色素とその構造が同じであり、その染料を使用した際の色などは次の通りである。ブラジリンは、スオウ(Caesalpinia sappan)の幹の芯材にも含まれている色素であり、ブラジリンのみを染料として配合した染毛剤で処理した白色ヤク毛の色は、赤色系である。ヘマトキシリンは、アカミノキ(Haematoxylum campechianum)の樹液に含まれている色素であり、ヘマトキシリンのみを染料として配合した染毛剤で処理した白色ヤク毛の色は、紫色系である。ベルベリンは、キハダ(Phellodendron amurense)の樹皮から水又はエタノールで抽出して得られるものに含まれる色素であり、ベルベリンのみを染料として配合した染毛剤で処理した白色ヤク毛の色は、黄色系である。クロシンは、クチナシ(Gardenia jasminoides)の果実から水又は含水エタノールで抽出して得られるものに含まれる色素であり、クロシンのみを染料として配合した染毛剤で処理した白色ヤク毛の色は、黄色系である。モナスコブリンは、ベニコウジカビ(Monascus purpureus)から含水エタノール又は含水プロピレングリコールで抽出して得られるものに含まれている色素であり、モナスコブリンのみを染料として配合した染毛剤で処理した白色ヤク毛の色は、赤色系である。キサントモナシンは、乾燥したベニコウジカビ(Monascus purpureus)の培養液を粉砕したものから弱塩酸酸性エタノールで抽出し、中和して得られる色素に含まれているものであり、キサントモナシンのみを染料として配合した染毛剤で処理した白色ヤク毛の色は、黄色系である。カルミン酸は、エンジムシ(Coccus cacti)の乾燥体から含水エタノールで抽出して得られるものに含まれている色素であり、カルミン酸のみを染料として配合した染毛剤で処理した白色ヤク毛の色は、紫色系である。クルクミンは、ウコン(Curcuma longa)の根茎の乾燥品からエタノールで抽出して得られるものに含まれている色素であり、クルクミンのみを染料として配合した染毛剤で処理した白色ヤク毛の色は、黄色系である。クチナシ青色素は、クチナシ(Gardenia jasminoides)の果実から水抽出して得られたイリドイド配糖体とタンパク質分解物の混合物に、β-グルコシダーゼを添加した後、分離して得られるものであり、クチナシ青色素のみを染料として配合した染毛剤で処理した白色ヤク毛の色は、青色系である。 The essential dye has the same structure as the plant-derived pigment, and the color when the dye is used is as follows. Bradylin is a pigment also contained in the core material of the trunk of Suesu (Caesalpinia sappan), and the color of white yak hair treated with a hair dye containing only bradylin as a dye is red. Hematoxylin is a pigment contained in the sap of red sea bream (Haematoxylum campechianum), and the color of white yak hair treated with a hair dye containing only hematoxylin as a dye is purple. Berberine is a pigment contained in water and ethanol extracted from the bark of yellowfin (Phellodendron amurense), and the color of white yak hair treated with a hair dye containing berberine alone as a dye is yellow. It is. Crocin is a pigment contained in the fruit of gardenia jasminoides, extracted with water or water-containing ethanol, and the color of white yak hair treated with a hair dye containing crocin alone as a dye is yellow. It is a system. Monascobrin is a pigment contained in a product obtained by extraction from Monascus purpureus with water-containing ethanol or water-containing propylene glycol, and white yak hair treated with a hair dye containing only monascobrin as a dye. The color of is red. Xanthomonasin is contained in the pigment obtained by extraction with neutral acid acid ethanol after neutralizing the dried culture liquid of Monascus purpureus and neutralizing it. The color of white yak hair treated with a hair dye formulated as a dye is yellow. Carminic acid is a pigment contained in a product obtained by extraction with water-containing ethanol from a dried body of Coccus cacti, and the color of white yak hair treated with a hair dye containing only carminic acid as a dye. Is purple. Curcumin is a pigment contained in a product obtained by extraction with ethanol from a dried turmeric (Curcuma longa) rhizome, and the color of white yak hair treated with a hair dye containing curcumin alone as a dye is It is yellowish. Gardenia blue pigment is obtained by adding β-glucosidase to a mixture of iridoid glycoside and proteolysate obtained by water extraction from gardenia (Gardenia jasminoides) fruit and separating it. The color of white yak hair treated with a hair dye containing only a blue pigment as a dye is blue.
本実施形態の染毛剤における必須染料の配合量は、特に限定されないが、例えば1質量%以上10質量%以下である。 Although the compounding quantity of the essential dye in the hair dye of this embodiment is not specifically limited, For example, they are 1 mass% or more and 10 mass% or less.
上記必須染料以外の公知の染毛剤に配合されている染料を、本実施形態の染毛剤の染料として配合しても良い。 You may mix | blend the dye mix | blended with well-known hair dyes other than the said essential dye as a dye of the hair dye of this embodiment.
(還元剤)
本実施形態の染毛剤には、チオール基を有する還元剤から選ばれた一種又は二種以上が必須還元剤として配合される。ここで、「還元剤」とは、毛髪のジスルフィド結合を還元切断可能な性質を有する化合物をいう。
(Reducing agent)
In the hair dye of this embodiment, 1 type, or 2 or more types chosen from the reducing agent which has a thiol group is mix | blended as an essential reducing agent. Here, the “reducing agent” refers to a compound having a property capable of reducing and cleaving a disulfide bond of hair.
チオール基を有する還元剤としては、例えば、チオグリコール酸、チオグリコール酸ナトリウムなどのチオグリコール酸の塩、システイン、システイン塩酸塩などのシステインの塩、N−アセチルシステイン、N−アセチルシステイン塩酸塩などのN−アセチルシステインの塩、システアミン、チオグリセロール、チオ乳酸、チオ乳酸の塩、チオリンゴ酸、チオリンゴ酸の塩が挙げられる。 Examples of the reducing agent having a thiol group include salts of thioglycolic acid such as thioglycolic acid and sodium thioglycolate, cysteine salts such as cysteine and cysteine hydrochloride, N-acetylcysteine, N-acetylcysteine hydrochloride, and the like. N-acetylcysteine salt, cysteamine, thioglycerol, thiolactic acid, thiolactic acid salt, thiomalic acid, thiomalic acid salt.
本実施形態の染毛剤におけるチオール基を有する還元剤の配合量は、特に限定されないが、0.1質量%以上1.0質量%以下が良い。この配合量範囲を外れる場合には、濃染性の向上が不十分な場合がある。 Although the compounding quantity of the reducing agent which has a thiol group in the hair dye of this embodiment is not specifically limited, 0.1 to 1.0 mass% is good. When the blending amount is out of the range, the deep dyeing may not be sufficiently improved.
上記のチオール基を有する還元剤以外の公知の還元剤を、本実施形態の染毛剤に配合する還元剤としても良い。 A known reducing agent other than the above-described reducing agent having a thiol group may be used as a reducing agent blended in the hair dye of the present embodiment.
(アルカリ剤)
本実施形態の染毛剤には、アルカリ剤から選ばれた一種又は二種以上が配合される。ここで、「アルカリ剤」とは、水溶液とした場合にpHをアルカリ性にする原料を意味する。
(Alkaline agent)
In the hair dye of this embodiment, 1 type, or 2 or more types chosen from the alkali agent are mix | blended. Here, the “alkali agent” means a raw material that makes the pH alkaline when an aqueous solution is used.
アルカリ剤としては、例えば、アンモニア、アルカノールアミン(モノエタノールアミン、ジエタノールアミン、トリエタノールアミン、モノプロパノールアミン、ジプロパノールアミン、トリプロパノールアミン、モノイソプロパノールアミン、2−アミノ−2−メチル−1,3−プロパンジオール、2−アミノ−2−メチル−1−プロパノール、2−アミノ−2−ヒドロキシメチル−1,3−プロパンジオールなど)、塩基性アミノ酸(アルギニンなど)、炭酸塩(炭酸アンモニウム、炭酸水素アンモニウム、炭酸ナトリウム、炭酸水素ナトリウムなど)、リン酸塩(リン酸一水素ナトリウムなど)、水酸化ナトリウムが挙げられる。濃染性を高めるためのアルカリ剤として好適なものとしては、例えばアルカノールアミンである。 Examples of the alkali agent include ammonia, alkanolamine (monoethanolamine, diethanolamine, triethanolamine, monopropanolamine, dipropanolamine, tripropanolamine, monoisopropanolamine, 2-amino-2-methyl-1,3- Propanediol, 2-amino-2-methyl-1-propanol, 2-amino-2-hydroxymethyl-1,3-propanediol, etc., basic amino acid (eg arginine), carbonate (ammonium carbonate, ammonium hydrogen carbonate) , Sodium carbonate, sodium hydrogen carbonate, etc.), phosphates (sodium monohydrogen phosphate, etc.), and sodium hydroxide. A suitable example of the alkali agent for enhancing the deep dyeability is alkanolamine.
本実施形態の染毛剤におけるアルカリ剤の配合量は、特に限定されないが、例えば染毛剤のpHを8.0以上11.0以下にする量である。 Although the compounding quantity of the alkaline agent in the hair dye of this embodiment is not specifically limited, For example, it is the quantity which makes pH of a hair dye 8.0 or more and 11.0 or less.
(任意原料)
本発明の染毛剤に配合される任意原料は、公知の染毛剤原料から適宜に選定される。染毛剤原料は、アニオン界面活性剤、カチオン界面活性剤、両性界面活性剤、アルコール、多価アルコール、糖類、エステル油、油脂、脂肪酸、炭化水素、ロウ、シリコーン、高分子化合物、アミノ酸、動植物抽出物、微生物由来物、無機化合物、香料、防腐剤、金属イオン封鎖剤、紫外線吸収剤などである。
(Optional raw material)
The arbitrary raw material mix | blended with the hair dye of this invention is suitably selected from a well-known hair dye raw material. Hair dye raw materials are anionic surfactants, cationic surfactants, amphoteric surfactants, alcohols, polyhydric alcohols, sugars, ester oils, fats and oils, fatty acids, hydrocarbons, waxes, silicones, polymer compounds, amino acids, animals and plants Extracts, microorganism-derived substances, inorganic compounds, fragrances, preservatives, sequestering agents, ultraviolet absorbers and the like.
エタノール、イソプロパノールなどの低級アルコール;プロピレングリコール、1,3−ブチレングリコール、イソプロピレングリコール、グリセリンなどの多価アルコール;及び、ベンジルアルコール、ベンジルオキシエタノールなどの芳香族アルコール;のいずれかを配合すれば、濃染性を高めるためには好ましい。 Any one of lower alcohols such as ethanol and isopropanol; polyhydric alcohols such as propylene glycol, 1,3-butylene glycol, isopropylene glycol and glycerine; and aromatic alcohols such as benzyl alcohol and benzyloxyethanol; In order to improve the deep dyeability, it is preferable.
(剤型)
染毛剤の使用時の剤型は、特に限定されず、例えば、液状、クリーム状、フォーム状(泡状)が挙げられる。所望の剤型にするために粘度を高める必要がある場合には、公知の染毛剤と同様、高分子化合物などを配合すれば良い。
(Form)
The dosage form at the time of use of a hair dye is not specifically limited, For example, liquid form, cream form, foam form (foam form) is mentioned. When it is necessary to increase the viscosity in order to obtain a desired dosage form, a polymer compound or the like may be blended in the same manner as known hair dyes.
(pH)
本実施形態の染毛剤のpHは、アルカリ性である。そのpHは、8.0以上11.0以下であると良い。なお、pHの調整が必要な場合には、上記のアルカリ剤の配合により行うと良い。
(PH)
The pH of the hair dye of this embodiment is alkaline. The pH is preferably 8.0 or more and 11.0 or less. In addition, when adjustment of pH is required, it is good to carry out by mix | blending said alkali agent.
以下、実施例に基づき本発明を詳述するが、本発明の趣旨を逸脱しない限り、この実施例の記載に基づいて本発明が限定的に解釈されるものではない。 EXAMPLES Hereinafter, although this invention is explained in full detail based on an Example, this invention is not interpreted limitedly based on description of this Example, unless it deviates from the meaning of this invention.
下記実施例及び比較例の染毛剤を製造し、この染毛剤を用いて白色毛束(ヤク毛の毛束)の染毛処理を行った。その染毛処理は、白色毛束に染毛剤を塗布して30分程度放置後に、シャンプーを用いて洗浄することにより行った。そして、温風乾燥させた後の毛束色を、目視により確認した。 The hair dye of the following Example and Comparative Example was manufactured, and the hair dyeing process of the white hair bundle (yak hair bundle) was performed using this hair dye. The hair dyeing treatment was performed by applying a hair dye to the white hair bundle and leaving it to stand for about 30 minutes, followed by washing with a shampoo. And the hair | bristle bundle color after making it dry with warm air was confirmed visually.
(実施例1a〜1e、比較例1a〜1c)
スオウ(Caesalpinia sappan)由来のブラジリンが配合された市販品(リアル化学社製「ボタニカルカラー・紅色」、全配合成分の表示名称:スオウ木、デキストリン、カラギーナン、褐藻エキス、アルギン酸Na、モナスカスエキス、ローズマリー、カミツレ、甘草)と温水を、市販品:温水=1:10の質量比で混合した。この混合物に、更に、表1に示す濃度となるように還元剤及びアルカリ剤を添加することで、pHが9.0〜10.0である実施例1a〜1e及び比較例1a〜1cの染毛剤を製造した。
(Examples 1a to 1e, Comparative Examples 1a to 1c)
Commercially available products containing brazirin derived from Caesalpinia sappan ("Botanical Color / Red" manufactured by Real Chemical Co., Ltd.) Names of all ingredients: Suougi, dextrin, carrageenan, brown algae extract, sodium alginate, monascus extract, rose Marie, chamomile, licorice) and warm water were mixed at a mass ratio of commercial product: warm water = 1: 10. By adding a reducing agent and an alkaline agent to the mixture so as to have the concentrations shown in Table 1, the dyes of Examples 1a to 1e and Comparative Examples 1a to 1c having a pH of 9.0 to 10.0 were added. A hair preparation was produced.
上記実施例1a〜1e及び比較例1a〜1cの染毛剤を用いて染毛処理を行った「濃染性の評価」結果を、下記表1に示す。「濃染性の評価」は、比較例1aによるものを基準として次の通り行った。
○○○:基準よりも非常に濃く染まっていた。
○○ :基準よりも濃く染まっていた。
○ :基準よりもやや濃く染まっていた。
― :基準(比較例1a)又は基準と同等。
× :基準よりも染まりが薄かった。
Table 1 below shows the results of “evaluation of deep dyeing” in which the hair dyeing treatment was performed using the hair dyes of Examples 1a to 1e and Comparative Examples 1a to 1c. “Evaluation of dark dyeing” was performed as follows based on the results of Comparative Example 1a.
OO: It was dyed very darker than the standard.
○○: It was dyed darker than the standard.
○: It was dyed slightly darker than the standard.
-: Standard (Comparative Example 1a) or equivalent to the standard.
X: Dyeing was lighter than the standard.
上記表1の濃染性評価においては、チオール基を有する還元剤とアルカリ剤が配合された実施例1a〜1eは、還元剤及びアルカリ剤が配合されなかった比較例1a、チオール基を有する還元剤が配合されなかった比較例1b、及びアルカリ剤が配合されなかった比較例1cのいずれよりも、濃染性の評価が良好であったことを確認できる。また、還元剤としてシステアミンを用いることが濃染性に有利であること(実施例1aと、実施例1d及び1eとの対比)、アルカリ剤としてアルカノールアミンを用いることが濃染性に有利であること(実施例1a及び1bと、実施例1cとの対比)を、確認できる。 In the dark dyeing evaluation in Table 1 above, Examples 1a to 1e in which a reducing agent having a thiol group and an alkali agent were blended were Comparative Examples 1a in which a reducing agent and an alkali agent were not blended, and a reduction having a thiol group. It can be confirmed that the evaluation of deep dyeing was better than those of Comparative Example 1b in which no agent was blended and Comparative Example 1c in which no alkali agent was blended. In addition, it is advantageous for deep dyeing to use cysteamine as a reducing agent (contrast between Example 1a and Examples 1d and 1e), and use of alkanolamine as an alkaline agent is advantageous for deep dyeing. (Contrast with Examples 1a and 1b and Example 1c) can be confirmed.
(実施例1f−1〜1f−2、実施例1g−1〜1g−2、実施例1h−1〜1h−2)
実施例1aと同様にして混合した市販品と温水の混合物に、更に、表2に示す濃度となるように還元剤及びアルカリ剤を添加することで、pH9.0〜10.0の実施例1f−1〜1f−2、実施例1g−1〜1g−2、及び実施例1h−1〜1h−2の染毛剤を製造した。
(Examples 1f-1 to 1f-2, Examples 1g-1 to 1g-2, Examples 1h-1 to 1h-2)
Example 1f having a pH of 9.0 to 10.0 was further added to a mixture of a commercial product and warm water mixed in the same manner as in Example 1a by adding a reducing agent and an alkaline agent so as to have the concentrations shown in Table 2. The hair dyes of -1 to 1f-2, Examples 1g-1 to 1g-2, and Examples 1h-1 to 1h-2 were produced.
上記実施例1f−1〜1f−2、実施例1g−1〜1g−2、及び実施例1h−1〜1h−2の染毛剤を用いて染毛処理を行った「濃染性の優劣」結果を、下記表2に示す。「濃染性の優劣」は、実施例1f−1と実施例1f−2との対比、実施例1g−1と実施例1g−2との対比、実施例1h−1と実施例1h−2との対比とし、対比の結果、濃く染まっている方の評価を「○」とし、薄く染まっている方又は両者同等の場合を「―」とした。 The hair dyeing treatment was performed using the hair dyes of Examples 1f-1 to 1f-2, Examples 1g-1 to 1g-2, and Examples 1h-1 to 1h-2. The results are shown in Table 2 below. “Superiority of dark dyeing” refers to the comparison between Example 1f-1 and Example 1f-2, the comparison between Example 1g-1 and Example 1g-2, Example 1h-1 and Example 1h-2. As a result of the comparison, the evaluation of the darkly stained one was “O”, and the case of being lightly dyed or equivalent to both was “-”.
上記表2は、還元剤の配合量を増加させることが、濃染性に必ず有利になるものではないことを示す。 Table 2 above shows that increasing the blending amount of the reducing agent is not necessarily advantageous to the deep dyeability.
(実施例2a〜2e、比較例2a〜2b)
温水と混合する市販品としてアカミノキ(Haematoxylum
campechianum)由来のヘマトキシリンが配合された市販品(リアル化学社製「ボタニカルカラー・アカミノキ色」、全配合成分の表示名称:アカミノ木、カラギーナン、褐藻エキス、ローズマリー、カミツレ、甘草)を用いた以外は実施例1aと同様にして、pHが9.0〜10.0である実施例2a〜2e及び比較例2a〜2bの染毛剤を製造した。
(Examples 2a to 2e, Comparative Examples 2a to 2b)
As a commercial product to be mixed with warm water, Haematoxylum
Other than using commercially available products containing hematoxylin derived from campechianum ("Botanical Color / Akaminoki Color" manufactured by Real Chemical Co., Ltd.), and the names of all ingredients included: Acamino Tree, Carrageenan, Brown Algae Extract, Rosemary, Chamomile, Licorice) Produced hair dyes of Examples 2a to 2e and Comparative Examples 2a to 2b having a pH of 9.0 to 10.0 in the same manner as Example 1a.
上記実施例2a〜2e及び比較例2a〜2bの染毛剤を用いて染毛処理を行った「濃染性の評価」結果を、下記表3に示す。「濃染性の評価」は、比較例2aによるものを基準として実施例1aと同様に行った。 Table 3 below shows the results of “evaluation of deep dyeing” in which the hair dyeing treatment was performed using the hair dyes of Examples 2a to 2e and Comparative Examples 2a to 2b. “Evaluation of deep dyeability” was carried out in the same manner as in Example 1a, with reference to Comparative Example 2a.
上記表3においては、表1と同様の濃染性評価が示されている。すなわち、チオール基を有する還元剤とアルカリ剤が配合された実施例2a〜2eは、還元剤及びアルカリ剤が配合されなかった比較例2a、及びチオール基を有する還元剤が配合されなかった比較例2bのいずれよりも、濃染性の評価が良好であった。また、還元剤としてシステアミンを用いることが濃染性に有利であること(実施例2aと、実施例2d及び2eとの対比)、アルカリ剤としてアルカノールアミンを用いることが濃染性に有利であること(実施例2a及び2bと、実施例2cとの対比)を、確認できる。 In Table 3 above, the same dark dyeing evaluation as in Table 1 is shown. That is, Examples 2a to 2e, in which a reducing agent having a thiol group and an alkaline agent were blended, Comparative Example 2a in which a reducing agent and an alkaline agent were not blended, and Comparative Example in which a reducing agent having a thiol group was not blended The evaluation of deep dyeing was better than any of 2b. In addition, it is advantageous for deep dyeing to use cysteamine as a reducing agent (contrast between Example 2a and Examples 2d and 2e), and alkanolamine as an alkaline agent is advantageous to deep dyeing. (Contrast with Examples 2a and 2b and Example 2c) can be confirmed.
(実施例2f−1〜2f−2、実施例2g−1〜2g−2、実施例2h−1〜2h−2)
実施例2aと同様にして混合した市販品と温水の混合物に、更に、表4に示す濃度となるように還元剤及びアルカリ剤を添加することで、pHが9.0〜10.0である実施例2f−1〜2f−2、実施例2g−1〜2g−2、及び実施例2h−1〜2h−2の染毛剤を製造した。
(Examples 2f-1 to 2f-2, Examples 2g-1 to 2g-2, Examples 2h-1 to 2h-2)
The pH is 9.0 to 10.0 by further adding a reducing agent and an alkaline agent to the mixture of a commercial product and warm water mixed in the same manner as in Example 2a so as to have the concentrations shown in Table 4. The hair dyes of Examples 2f-1 to 2f-2, Examples 2g-1 to 2g-2, and Examples 2h-1 to 2h-2 were produced.
上記実施例2f−1〜2f−2、実施例2g−1〜実施例2g−2、及び2h−1〜2h−2の染毛剤を用いて染毛処理を行った「濃染性の優劣」結果を、下記表4に示す。「濃染性の優劣」は、実施例2f−1と実施例2f−2との対比、実施例2g−1と実施例2g−2との対比、実施例2h−1と実施例2h−2との対比とし、対比の結果、濃く染まっている方の評価を「○」とし、薄く染まっている方又は同等の場合を「―」とした。 The hair dyeing treatment was performed using the hair dyes of Examples 2f-1 to 2f-2, Example 2g-1 to Example 2g-2, and 2h-1 to 2h-2. The results are shown in Table 4 below. “Superiority of dark dyeing” is a comparison between Example 2f-1 and Example 2f-2, a comparison between Example 2g-1 and Example 2g-2, Example 2h-1 and Example 2h-2. As a result of the comparison, the evaluation of the one that is darkly dyed as a result of the comparison is “◯”, and the one that is lightly dyed or the equivalent is “−”.
上記表4は、表2と同様、還元剤の配合量を増加させることが、濃染性に必ず有利になるものではないことを示す。 Table 4 shows that, as in Table 2, increasing the blending amount of the reducing agent is not necessarily advantageous for dark dyeing.
(実施例3a〜3e、比較例3a〜3b)
温水と混合する市販品としてキハダ(Phellodendron amurense)由来のベルベリンが配合された市販品(リアル化学社製「ボタニカルカラー・キハダ色」、全配合成分の表示名称:キハダ末、スクロース、褐藻エキス、カラギーナン、ローズマリー、カミツレ、甘草)を用いた以外は実施例1aと同様にして、pH9.0〜10.0の実施例3a〜3e及び比較例3a〜3bの染毛剤を製造した。
(Examples 3a to 3e, Comparative Examples 3a to 3b)
A commercial product that contains berberine derived from Phellodendron amurense as a commercial product to be mixed with warm water ("Botanical Color / Yellow Color" manufactured by Real Chemical Co., Ltd.), Name of all ingredients: Yellowfin powder, sucrose, brown algae extract, carrageenan , Rosemary, chamomile, licorice) In the same manner as in Example 1a, hair dyes of Examples 3a to 3e and Comparative Examples 3a to 3b having a pH of 9.0 to 10.0 were produced.
上記実施例3a〜3e及び比較例3a〜3bの染毛剤を用いて染毛処理を行った「濃染性の評価」結果を、下記表5に示す。「濃染性の評価」は、比較例3aによるものを基準として実施例1aと同様に行った。 Table 5 below shows the results of “evaluation of deep dyeing” in which the hair dyeing treatment was performed using the hair dyes of Examples 3a to 3e and Comparative Examples 3a to 3b. “Evaluation of dark dyeing” was carried out in the same manner as in Example 1a, with reference to Comparative Example 3a.
上記表5においては、表1と同様の濃染性評価が示されている。すなわち、チオール基を有する還元剤とアルカリ剤が配合された実施例3a〜3eは、還元剤及びアルカリ剤が配合されなかった比較例3a、及びチオール基を有する還元剤が配合されなかった比較例3bのいずれよりも、濃染性の評価が良好であった。また、還元剤としてシステアミンを用いることが濃染性に有利であること(実施例3aと、実施例3d及び3eとの対比)、アルカリ剤としてアルカノールアミンを用いることが濃染性に有利であること(実施例3a及び3bと、実施例3cとの対比)を、確認できる。 In Table 5 above, the same dark dyeing evaluation as in Table 1 is shown. That is, Examples 3a to 3e, in which a reducing agent having a thiol group and an alkaline agent were blended, Comparative Example 3a in which a reducing agent and an alkaline agent were not blended, and Comparative Example in which a reducing agent having a thiol group was not blended The evaluation of deep dyeing was better than any of 3b. In addition, it is advantageous for deep dyeing to use cysteamine as a reducing agent (contrast with Example 3a and Examples 3d and 3e), and alkanolamine as an alkaline agent is advantageous to deep dyeing. (Contrast between Examples 3a and 3b and Example 3c) can be confirmed.
(実施例4)
アルカリ剤及び還元剤を配合したpH10の組成物(2−アミノ−2−メチル−1−プロパノール2質量%、システアミン1質量%、ベンジルアルコール8質量%、エタノール16質量%との配合濃度となるように、それら全てを水と配合した組成物)10質量部と、クロシンを含む市販品(ダイワ化成株式会社製クチナシ黄色素含有品「クロシンP-1900」)1質量部とを混合して、実施例4の染毛剤を製造した。
Example 4
A composition having a pH of 10 containing an alkaline agent and a reducing agent (concentration concentration of 2-amino-2-methyl-1-propanol 2% by mass, cysteamine 1% by mass, benzyl alcohol 8% by mass, ethanol 16% by mass) And 10 parts by mass of a composition in which all of them are mixed with water) and 1 part by mass of a commercially available product containing crocin (Daiwa Kasei Co., Ltd. gardenia yellow pigment-containing product “Crosin P-1900”) The hair dye of Example 4 was produced.
(比較例4)
実施例4におけるpH10の組成物を水に変更した以外は実施例4と同様にして、比較例4の染毛剤を製造した。
(Comparative Example 4)
A hair dye of Comparative Example 4 was produced in the same manner as in Example 4 except that the pH 10 composition in Example 4 was changed to water.
実施例4の染毛剤で処理した毛束と比較例4の染毛剤で処理した毛束の濃染性を比較すると、実施例4の染毛剤で処理した毛束の方が濃く染まっていた。 Comparing the dark dyeing properties of the hair bundle treated with the hair dye of Example 4 and the hair bundle treated with the hair dye of Comparative Example 4, the hair bundle treated with the hair dye of Example 4 was dyed darker. It was.
(実施例5)
実施例4における「クロシンを含む市販品」を「クチナシ青色素を含む市販品(ダイワ化成株式会社製「ハイブルーGP−4A」)に変更した以外は実施例4と同様にして、実施例5の染毛剤を製造した。
(Example 5)
Example 5 was carried out in the same manner as in Example 4 except that “commercial product containing crocin” in Example 4 was changed to “commercial product containing gardenia blue pigment (“ High Blue GP-4A ”manufactured by Daiwa Kasei Co., Ltd.). A hair dye was produced.
(比較例5)
実施例5におけるpH10の組成物を水に変更した以外は実施例5と同様にして、比較例5の染毛剤を製造した。
(Comparative Example 5)
A hair dye of Comparative Example 5 was produced in the same manner as in Example 5 except that the pH 10 composition in Example 5 was changed to water.
実施例5の染毛剤で処理した毛束と比較例5の染毛剤で処理した毛束の濃染性を比較すると、実施例5の染毛剤で処理した毛束の方が濃く染まっていた。 When the dark dyeing properties of the hair bundle treated with the hair dye of Example 5 and the hair bundle treated with the hair dye of Comparative Example 5 are compared, the hair bundle treated with the hair dye of Example 5 dyes darker. It was.
(実施例6)
実施利4における「クロシンを含む市販品」を「モナスコルブリンを含む市販品(ダイワ化成株式会社製ベニコウジ色素含有品「ダイワモナスPH−3000」)」に変更した以外は実施例4と同様にして、実施例6の染毛剤を製造した。
(Example 6)
In the same manner as in Example 4 except that “commercial product containing crocin” in practical example 4 was changed to “commercial product containing Monascorbulin (Daiwa Chemical Co., Ltd. Benikouji dye-containing product“ Daiwamonas PH-3000 ”)”. The hair dye of Example 6 was produced.
(比較例6)
実施例6におけるpH10の組成物を水に変更した以外は実施例6と同様にして、比較例6の染毛剤を製造した。
(Comparative Example 6)
A hair dye of Comparative Example 6 was produced in the same manner as in Example 6 except that the pH 10 composition in Example 6 was changed to water.
実施例6の染毛剤で処理した毛束と比較例6の染毛剤で処理した毛束の濃染性を比較すると、実施例6の染毛剤で処理した毛束の方が濃く染まっていた。 When the dark dyeing properties of the hair bundle treated with the hair dye of Example 6 and the hair bundle treated with the hair dye of Comparative Example 6 were compared, the hair bundle treated with the hair dye of Example 6 dyed darker. It was.
(実施例7)
実施利4における「クロシンを含む市販品」を「キサントモナシンを含む市販品(ダイワ化成株式会社製ベニコウジ色素含有品「ダイワモナスイエローTK」)」に変更した以外は実施例4と同様にして、実施例7の染毛剤を製造した。
(Example 7)
In the same manner as in Example 4, except that “commercial product containing crocin” in practical example 4 was changed to “commercial product containing xanthmonacin (Daiwa Kasei Co., Ltd. Benikouji dye-containing product“ Daiwamonas Yellow TK ”)”. The hair dye of Example 7 was produced.
(比較例7)
実施例7におけるpH10の組成物を水に変更した以外は実施例7と同様にして、比較例7の染毛剤を製造した。
(Comparative Example 7)
A hair dye of Comparative Example 7 was produced in the same manner as in Example 7 except that the pH 10 composition in Example 7 was changed to water.
実施例7の染毛剤で処理した毛束と比較例7の染毛剤で処理した毛束の濃染性を比較すると、実施例7の染毛剤で処理した毛束の方が濃く染まっていた。 When the dark dyeing properties of the hair bundle treated with the hair dye of Example 7 and the hair bundle treated with the hair dye of Comparative Example 7 are compared, the hair bundle treated with the hair dye of Example 7 is more intensely dyed. It was.
(実施例8)
実施利4における「クロシンを含む市販品」を「カルミン酸を含む市販品(ダイワ化成株式会社製コチニール色素含有品「コチニールレッドP−900」)」に変更した以外は実施例4と同様にして、実施例8の染毛剤を製造した。
(Example 8)
In the same manner as in Example 4 except that “commercial product containing crocin” in practical example 4 was changed to “commercial product containing carminic acid (cochineal dye-containing product“ Cochineal Red P-900 ”manufactured by Daiwa Kasei Co., Ltd.)”. The hair dye of Example 8 was produced.
(比較例8)
実施例8におけるpH10の組成物を水に変更した以外は実施例8と同様にして、比較例8の染毛剤を製造した。
(Comparative Example 8)
A hair dye of Comparative Example 8 was produced in the same manner as in Example 8, except that the pH 10 composition in Example 8 was changed to water.
実施例8の染毛剤で処理した毛束と比較例8の染毛剤で処理した毛束の濃染性を比較すると、実施例8の染毛剤で処理した毛束の方が濃く染まっていた。 When the dark dyeing properties of the hair bundle treated with the hair dye of Example 8 and the hair bundle treated with the hair dye of Comparative Example 8 are compared, the hair bundle treated with the hair dye of Example 8 dyes darker. It was.
(実施例9)
実施利4における「クロシンを含む市販品」を「クルクミンを含む市販品(ダイワ化成株式会社製ウコン色素「クルクミン精製品」)」に変更した以外は実施例4と同様にして、実施例9の染毛剤を製造した。
Example 9
Example 9 is the same as Example 4 except that “commercial product containing crocin” in Example 4 was changed to “commercial product containing curcumin (turmeric pigment“ curcumin purified product ”manufactured by Daiwa Kasei Co., Ltd.)”. A hair dye was produced.
(比較例9)
実施例9におけるpH10の組成物を水に変更した以外は実施例9と同様にして、比較例9の染毛剤を製造した。
(Comparative Example 9)
A hair dye of Comparative Example 9 was produced in the same manner as in Example 9, except that the pH 10 composition in Example 9 was changed to water.
実施例9の染毛剤で処理した毛束と比較例9の染毛剤で処理した毛束の濃染性を比較すると、実施例9の染毛剤で処理した毛束の方が濃く染まっていた。 When the dark dyeing properties of the hair bundle treated with the hair dye of Example 9 and the hair bundle treated with the hair dye of Comparative Example 9 are compared, the hair bundle treated with the hair dye of Example 9 is dyed darker. It was.
(実施例10〜16)
アルカリ剤及び還元剤を配合したpH10の組成物(2−アミノ−2−メチル−1−プロパノール2質量%、システアミン0.5質量%、ベンジルアルコール8質量%、エタノール16質量%との配合濃度となるように、それら全てを水と配合した組成物)10質量部と、染料を含む市販品1質量部とを混合して、実施例10〜16の染毛剤を製造した。ここで用いた染料を含む市販品は、実施例10では、ダイワ化成株式会社製「ダイワモナスPH−3000」2質量部、ダイワ化成株式会社製「クロシンP-1900」2質量部、及びリアル化学社製「ボタニカルカラー・アカミノキ色」1質量部の混合物とし、実施例11では、リアル化学社製「ボタニカルカラー・アカミノキ色」とし、実施例12では、ダイワ化成株式会社製「ハイブルーGP−4A」とし、実施例13では、ダイワ化成株式会社製「クロシンP-1900」とし、実施例14では、ダイワ化成株式会社製「ダイワモナスPH−3000」1質量部、及びダイワ化成株式会社製「クロシンP-1900」1質量部の混合物とし、実施例15では、リアル化学社製「ボタニカルカラー・紅色」とし、実施例16では、リアル化学社製「ボタニカルカラー・紅色」1質量部、及びリアル化学社製「ボタニカルカラー・アカミノキ色」1質量部の混合物とした。
(Examples 10 to 16)
PH 10 composition containing alkali agent and reducing agent (2-amino-2-methyl-1-propanol 2% by mass, cysteamine 0.5% by mass, benzyl alcohol 8% by mass, ethanol 16% by mass, Thus, the hair dye of Examples 10-16 was manufactured by mixing 10 parts by mass of a composition prepared by mixing all of them with water and 1 part by mass of a commercial product containing a dye. In Example 10, commercially available products containing the dye used here were 2 parts by mass of “Daiwamonas PH-3000” manufactured by Daiwa Kasei Co., Ltd., 2 parts by mass of “Crosin P-1900” manufactured by Daiwa Kasei Co., Ltd., and Real Chemical Co., Ltd. “Botanical Color / Akaminoki Color” manufactured by Daiichi Kasei Co., Ltd. in Example 12 and “High Blue GP-4A” manufactured by Daiwa Kasei Co., Ltd. In Example 13, “Crocine P-1900” manufactured by Daiwa Kasei Co., Ltd., and in Example 14, 1 part by weight of “Daiwamonas PH-3000” manufactured by Daiwa Kasei Co., Ltd. 1900 "1 part by weight of the mixture, in Example 15," Botanical Color / Red "manufactured by Real Chemical Co., Ltd. Over-red "1 part by weight, and was real Kagaku" Botanical Color haematoxylum campechianum color "1 part by weight mixture.
上記実施例10の染毛剤で染色処理を行った毛束は、茶色系の色に染まっていた。また、実施例11〜16の染毛剤による処理を行った毛束は、実施例11の場合には紫色系の色に、実施例12の場合には青色系の色に、実施例13の場合には黄色系の色に、実施例14の場合には橙色系の色に、実施例15の場合には赤色系の色に、実施例16の場合には紫色系の色に、夫々染まっていた。 The hair bundle that was dyed with the hair dye of Example 10 was dyed a brown color. Moreover, the hair bundle which performed the process by the hair dye of Examples 11-16 is a purple color in the case of Example 11, the blue color in the case of Example 12, and the hair color of Example 13. In the case of Example 14, the color of orange in the case of Example 14, the color of red in the case of Example 15, and the color of purple in Example 16. It was.
(比較例10a〜10h)
温水と混合する市販品としてインジゴが配合された市販品(リアル化学社製「ボタニカルカラー・藍色」、全配合成分の表示名称:アイ、カラギーナン、セルロース、褐藻エキス、ムクロジエキス、ローズマリー、カミツレ、甘草)を用いた以外は実施例1aと同様にして、pH9.0〜10.0の比較例10〜10の染毛剤を製造した。
(Comparative Examples 10a to 10h)
Commercial product with indigo blended as a commercial product to be mixed with warm water ("Botanical Color / Indigo" manufactured by Real Chemical Co., Ltd., display name of all the ingredients: Eye, Carrageenan, Cellulose, Brown Algae Extract, Mukuroji Extract, Rosemary, Chamomile , Licorice) was used in the same manner as in Example 1a to prepare hair dyes of Comparative Examples 10 to 10 having a pH of 9.0 to 10.0.
上記比較例10a〜10hの染毛剤を用いて染毛処理を行った「濃染性の評価」結果を、下記表6に示す。「濃染性の評価」は、比較例10fによるものを基準として実施例1aと同様に行った。 Table 6 below shows the results of “evaluation of deep dyeing” in which the hair dyeing treatment was performed using the hair dyes of Comparative Examples 10a to 10h. “Evaluation of dark dyeing” was carried out in the same manner as in Example 1a, with reference to Comparative Example 10f.
上記表6においては、表1と異なる傾向の濃染性評価が示されている。すなわち、還元剤を配合しても染色性が悪くなり(比較例10fと、比較例10hとの対比)、還元剤とアルカリ剤の双方を配合しても染色性が悪くなった(比較例10fと、比較例10a〜10eとの対比)。なお、比較例10fの毛束のみが青色系の色に染まっていたが、他の毛束については、染まっていなかった。 In Table 6 above, darkness evaluation with a tendency different from Table 1 is shown. That is, even when a reducing agent was added, the dyeability deteriorated (comparative with Comparative Example 10f and Comparative Example 10h), and even when both the reducing agent and the alkali agent were added, the dyeability deteriorated (Comparative Example 10f). And comparison with Comparative Examples 10a to 10e). In addition, although only the hair | bristle bundle of the comparative example 10f was dye | stained by the blue color, it was not dye | stained about the other hair | bristle bundle.
(比較例11a)
実施例4における「クロシンを含む市販品」を「シアニジンアシルグリコシドを含むアカキャベツ色素含有市販品」に変更した以外は実施例4と同様にして、比較例11aの染毛剤を製造した。
(Comparative Example 11a)
A hair dye of Comparative Example 11a was produced in the same manner as in Example 4 except that “commercial product containing crocin” in Example 4 was changed to “commercial product containing red cabbage pigment containing cyanidin acylglycoside”.
(比較例11b)
比較例11aにおけるpH10の組成物を水に変更した以外は比較例11aと同様にして、比較例11bの染毛剤を製造した。
(Comparative Example 11b)
A hair dye of Comparative Example 11b was produced in the same manner as Comparative Example 11a, except that the pH 10 composition in Comparative Example 11a was changed to water.
比較例11aの染毛剤で処理した毛束と比較例11bの染毛剤で処理した毛束の濃染性を確認した結果、双方共に毛束の染まりを確認できなかった。 As a result of confirming the deep dyeing property of the hair bundle treated with the hair dye of Comparative Example 11a and the hair bundle treated with the hair dye of Comparative Example 11b, it was not possible to confirm the dyeing of the hair bundle in both cases.
(比較例12a)
実施例4における「クロシンを含む市販品」を「ペラルゴニジンアシルグリコシドを含むアカダイコン色素含有市販品」に変更した以外は実施例4と同様にして、比較例12aの染毛剤を製造した。
(Comparative Example 12a)
A hair dye of Comparative Example 12a was produced in the same manner as in Example 4 except that “commercial product containing crocin” in Example 4 was changed to “commercial product containing radish pigment containing pelargonidin acylglycoside”.
(比較例12b)
比較例12aにおけるpH10の組成物を水に変更した以外は比較例12aと同様にして、比較例12bの染毛剤を製造した。
(Comparative Example 12b)
A hair dye of Comparative Example 12b was produced in the same manner as Comparative Example 12a, except that the pH 10 composition in Comparative Example 12a was changed to water.
比較例12aの染毛剤で処理した毛束と比較例12bの染毛剤で処理した毛束の濃染性を確認した結果、双方共に毛束の染まりを確認できなかった。 As a result of confirming the deep dyeing property of the hair bundle treated with the hair dye of Comparative Example 12a and the hair bundle treated with the hair dye of Comparative Example 12b, it was not possible to confirm the dyeing of the hair bundle in both cases.
Claims (5)
Examples of the alkanolamine include monoethanolamine, diethanolamine, triethanolamine, monopropanolamine, dipropanolamine, tripropanolamine, monoisopropanolamine, 2-amino-2-methyl-1,3-propanediol, 2-amino- The hair dye according to claim 4, wherein 2-methyl-1-propanol or 2-amino-2-hydroxymethyl-1,3-propanediol is blended.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011285400A JP6235768B2 (en) | 2011-12-27 | 2011-12-27 | Hair dye |
KR1020120152011A KR20130075680A (en) | 2011-12-27 | 2012-12-24 | Hair dye |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011285400A JP6235768B2 (en) | 2011-12-27 | 2011-12-27 | Hair dye |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013133320A true JP2013133320A (en) | 2013-07-08 |
JP6235768B2 JP6235768B2 (en) | 2017-11-22 |
Family
ID=48910256
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011285400A Active JP6235768B2 (en) | 2011-12-27 | 2011-12-27 | Hair dye |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP6235768B2 (en) |
KR (1) | KR20130075680A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018162760A1 (en) * | 2017-03-10 | 2018-09-13 | Pierre Fabre Dermo-Cosmetique | Gardenia extract for keratin fibre dyeing |
WO2018181008A1 (en) * | 2017-03-27 | 2018-10-04 | グリコ栄養食品株式会社 | Hair coloring composition |
CN109758380A (en) * | 2019-03-26 | 2019-05-17 | 赵军 | A kind of hair-dyeing agent of pigment containing biomass or pigment precursor |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102196631B1 (en) * | 2019-01-24 | 2020-12-30 | 강원대학교산학협력단 | Composition for hair dye comprising polymer of cationic polymer and gardenia yellow pigment with increased hair permeability as effective component |
KR102366910B1 (en) * | 2020-09-29 | 2022-02-25 | 장혜영 | Composition for removing hair dye and method for preparing the same |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04342518A (en) * | 1991-05-16 | 1992-11-30 | Kishi Kasei Kk | Hair dyeing agent |
JPH0930940A (en) * | 1995-07-17 | 1997-02-04 | Lion Corp | Hair-dyeing composition and hair dyeing using the same |
JPH11158049A (en) * | 1997-12-01 | 1999-06-15 | Kimi Kasei Kk | Hair dye composition |
JPH11302139A (en) * | 1998-04-24 | 1999-11-02 | Seniru Laboratory:Kk | Hair-treating agent for permanent wave treatment or curly hair-correcting treatment, and treatment by using the hair-treating agent |
JP2001294768A (en) * | 2000-04-13 | 2001-10-23 | Nippon Shokuhin Kako Co Ltd | Fading inhibitor, fading inhibiting method of food and drink and coloring composition |
JP2002138024A (en) * | 2000-10-27 | 2002-05-14 | Riaru Kagaku Kk | Hair dyeing agent, hair dyeing set and hair dyeing method using the same |
JP2002322040A (en) * | 2001-04-27 | 2002-11-08 | Cosmo Beauty:Kk | Hair-coloring and -styling composition |
JP2004002475A (en) * | 2003-08-28 | 2004-01-08 | Riaru Kagaku Kk | Hair dye and hair-dyeing method using the dye |
JP2005053821A (en) * | 2003-08-01 | 2005-03-03 | Hoyu Co Ltd | Hair cosmetic and article for hair cosmetic |
JP2009136187A (en) * | 2007-12-05 | 2009-06-25 | Calpis Co Ltd | Method for preventing color deterioration of beverage |
JP2010248158A (en) * | 2009-04-20 | 2010-11-04 | Hoyu Co Ltd | Hair cosmetic composition |
JP2011084582A (en) * | 2004-04-19 | 2011-04-28 | Arimino Kagaku Kk | Hair transformation agent (design forming), hair softening agent and penetrating agent for hair of low cysteamine concentration, and a hair treating method using these agents |
-
2011
- 2011-12-27 JP JP2011285400A patent/JP6235768B2/en active Active
-
2012
- 2012-12-24 KR KR1020120152011A patent/KR20130075680A/en not_active Application Discontinuation
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04342518A (en) * | 1991-05-16 | 1992-11-30 | Kishi Kasei Kk | Hair dyeing agent |
JPH0930940A (en) * | 1995-07-17 | 1997-02-04 | Lion Corp | Hair-dyeing composition and hair dyeing using the same |
JPH11158049A (en) * | 1997-12-01 | 1999-06-15 | Kimi Kasei Kk | Hair dye composition |
JPH11302139A (en) * | 1998-04-24 | 1999-11-02 | Seniru Laboratory:Kk | Hair-treating agent for permanent wave treatment or curly hair-correcting treatment, and treatment by using the hair-treating agent |
JP2001294768A (en) * | 2000-04-13 | 2001-10-23 | Nippon Shokuhin Kako Co Ltd | Fading inhibitor, fading inhibiting method of food and drink and coloring composition |
JP2002138024A (en) * | 2000-10-27 | 2002-05-14 | Riaru Kagaku Kk | Hair dyeing agent, hair dyeing set and hair dyeing method using the same |
JP2002322040A (en) * | 2001-04-27 | 2002-11-08 | Cosmo Beauty:Kk | Hair-coloring and -styling composition |
JP2005053821A (en) * | 2003-08-01 | 2005-03-03 | Hoyu Co Ltd | Hair cosmetic and article for hair cosmetic |
JP2004002475A (en) * | 2003-08-28 | 2004-01-08 | Riaru Kagaku Kk | Hair dye and hair-dyeing method using the dye |
JP2011084582A (en) * | 2004-04-19 | 2011-04-28 | Arimino Kagaku Kk | Hair transformation agent (design forming), hair softening agent and penetrating agent for hair of low cysteamine concentration, and a hair treating method using these agents |
JP2009136187A (en) * | 2007-12-05 | 2009-06-25 | Calpis Co Ltd | Method for preventing color deterioration of beverage |
JP2010248158A (en) * | 2009-04-20 | 2010-11-04 | Hoyu Co Ltd | Hair cosmetic composition |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018162760A1 (en) * | 2017-03-10 | 2018-09-13 | Pierre Fabre Dermo-Cosmetique | Gardenia extract for keratin fibre dyeing |
FR3063639A1 (en) * | 2017-03-10 | 2018-09-14 | Pierre Fabre Dermo-Cosmetique | GARDENIA EXTRACT FOR COLORING KERATIN FIBERS |
JP2020510686A (en) * | 2017-03-10 | 2020-04-09 | ピエール、ファブレ、デルモ‐コスメティークPierre Fabre Dermo−Cosmetique | Gardenia extract for keratin fiber dyeing |
JP7301746B2 (en) | 2017-03-10 | 2023-07-03 | ピエール、ファブレ、デルモ‐コスメティーク | Gardenia extract for keratin fiber dyeing |
WO2018181008A1 (en) * | 2017-03-27 | 2018-10-04 | グリコ栄養食品株式会社 | Hair coloring composition |
CN109758380A (en) * | 2019-03-26 | 2019-05-17 | 赵军 | A kind of hair-dyeing agent of pigment containing biomass or pigment precursor |
CN109758380B (en) * | 2019-03-26 | 2022-02-11 | 赵军 | Hair coloring agent containing biomass pigment or pigment precursor |
Also Published As
Publication number | Publication date |
---|---|
JP6235768B2 (en) | 2017-11-22 |
KR20130075680A (en) | 2013-07-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6235768B2 (en) | Hair dye | |
EP2438900B1 (en) | Protective plant hair dye | |
KR101840743B1 (en) | Hair coloring product | |
US8034126B2 (en) | Henna and vegetable dye based compositions for coloring of human hair | |
KR20110104422A (en) | Hair treatment agent | |
BRPI0907293A2 (en) | keratin fiber coloring process, cosmetic composition and multi-compartment device | |
KR20120047914A (en) | Hair dye, dyeing hair product combination and its use method | |
CN105992583A (en) | Process for dyeing keratin materials using powder from indigo-producing plants and alkaline agent(s) | |
WO2012127502A1 (en) | Hair colouring composition using plant dyes | |
CN102198058A (en) | Herbal hair dye | |
CN114080218A (en) | Novel hair dyeing composition | |
CN105168016B (en) | A kind of hair dye | |
EP2833974A2 (en) | Hair treatment methods | |
CN108392433B (en) | Composite hair dye | |
KR101862330B1 (en) | Composition for hairdye comprising extract of henna and mulberry as effective component | |
KR101510486B1 (en) | Hair dye composition comprising catechin | |
JP2008290977A (en) | Hair protecting composition, hair cosmetic, and hair protection method | |
KR20140103136A (en) | Microbicidal composition and method for preparing the same | |
WO2010020587A2 (en) | Use of hydrophobin for non-permanent dyeing of keratin | |
GB2468016A (en) | Colouring material and its uses, in particular in the field of cosmetics, especially for making up the skin and superficial body growths | |
CN115252444A (en) | Hair dye and using method thereof, hair dye liquid, hair dye paste and hair dye comb | |
KR102502513B1 (en) | Composition for dyeing | |
TWI771134B (en) | Natural hair dye and its commercialized formula | |
KR20130143296A (en) | Hair dye composition containing gadenia yellow and pinus sylvestri leaf oil | |
KR20180000906A (en) | Hair dye composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20141127 |
|
RD03 | Notification of appointment of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7423 Effective date: 20150324 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20150811 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20150825 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20151023 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20151023 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20160405 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20160629 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20160629 |
|
A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20160725 |
|
A912 | Re-examination (zenchi) completed and case transferred to appeal board |
Free format text: JAPANESE INTERMEDIATE CODE: A912 Effective date: 20161007 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20171027 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6235768 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |