JPH0160447B2 - - Google Patents
Info
- Publication number
- JPH0160447B2 JPH0160447B2 JP27375085A JP27375085A JPH0160447B2 JP H0160447 B2 JPH0160447 B2 JP H0160447B2 JP 27375085 A JP27375085 A JP 27375085A JP 27375085 A JP27375085 A JP 27375085A JP H0160447 B2 JPH0160447 B2 JP H0160447B2
- Authority
- JP
- Japan
- Prior art keywords
- agent
- hair
- compounds
- iron
- copper
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 210000004209 hair Anatomy 0.000 claims description 166
- 239000003795 chemical substances by application Substances 0.000 claims description 114
- 238000011282 treatment Methods 0.000 claims description 55
- 238000000034 method Methods 0.000 claims description 50
- 238000004043 dyeing Methods 0.000 claims description 40
- 229910052751 metal Inorganic materials 0.000 claims description 39
- 239000002184 metal Substances 0.000 claims description 39
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 33
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 25
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 19
- 150000003839 salts Chemical class 0.000 claims description 19
- 239000010949 copper Substances 0.000 claims description 17
- 229910052802 copper Inorganic materials 0.000 claims description 17
- 229910052742 iron Inorganic materials 0.000 claims description 17
- 239000003638 chemical reducing agent Substances 0.000 claims description 16
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 14
- 238000005406 washing Methods 0.000 claims description 14
- 239000007800 oxidant agent Substances 0.000 claims description 12
- 239000003352 sequestering agent Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- -1 cysteine mercapto compounds Chemical class 0.000 claims description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 9
- 230000003699 hair surface Effects 0.000 claims description 8
- 239000003086 colorant Substances 0.000 claims description 7
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims description 5
- 235000018417 cysteine Nutrition 0.000 claims description 5
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical class OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 claims description 4
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims description 2
- 150000002085 enols Chemical class 0.000 claims description 2
- 238000007493 shaping process Methods 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 20
- 239000007788 liquid Substances 0.000 description 19
- 239000000118 hair dye Substances 0.000 description 16
- 230000000694 effects Effects 0.000 description 14
- 230000008569 process Effects 0.000 description 14
- 230000014759 maintenance of location Effects 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 235000019646 color tone Nutrition 0.000 description 9
- 229960003067 cystine Drugs 0.000 description 9
- 230000001590 oxidative effect Effects 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 229940079593 drug Drugs 0.000 description 7
- 239000003814 drug Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 102000011782 Keratins Human genes 0.000 description 6
- 108010076876 Keratins Proteins 0.000 description 6
- 230000009471 action Effects 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 5
- 235000013824 polyphenols Nutrition 0.000 description 5
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 4
- 238000005562 fading Methods 0.000 description 4
- 239000002075 main ingredient Substances 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 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
- 238000004040 coloring Methods 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000007794 irritation Effects 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- 238000002791 soaking Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- DOPJTDJKZNWLRB-UHFFFAOYSA-N 2-Amino-5-nitrophenol Chemical compound NC1=CC=C([N+]([O-])=O)C=C1O DOPJTDJKZNWLRB-UHFFFAOYSA-N 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- 206010012434 Dermatitis allergic Diseases 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- 206010070834 Sensitisation Diseases 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 241000244317 Tillandsia usneoides Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 201000008937 atopic dermatitis Diseases 0.000 description 2
- 208000010668 atopic eczema Diseases 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 2
- FUWUEFKEXZQKKA-UHFFFAOYSA-N beta-thujaplicin Chemical compound CC(C)C=1C=CC=C(O)C(=O)C=1 FUWUEFKEXZQKKA-UHFFFAOYSA-N 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000010504 bond cleavage reaction Methods 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- HLUCICHZHWJHLL-UHFFFAOYSA-N hematein Chemical compound C12=CC=C(O)C(O)=C2OCC2(O)C1=C1C=C(O)C(=O)C=C1C2 HLUCICHZHWJHLL-UHFFFAOYSA-N 0.000 description 2
- 150000002506 iron compounds Chemical group 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 230000008313 sensitization Effects 0.000 description 2
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical class [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229940071127 thioglycolate Drugs 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- GOAGYXMUVBZZQV-UHFFFAOYSA-N (5-amino-2-methylphenyl) hydrogen sulfate Chemical compound CC1=CC=C(N)C=C1OS(O)(=O)=O GOAGYXMUVBZZQV-UHFFFAOYSA-N 0.000 description 1
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 1
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- ICVRBKCRXNVOJC-UHFFFAOYSA-N 1-amino-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2NC ICVRBKCRXNVOJC-UHFFFAOYSA-N 0.000 description 1
- VPMMJSPGZSFEAH-UHFFFAOYSA-N 2,4-diaminophenol;hydrochloride Chemical compound [Cl-].NC1=CC=C(O)C([NH3+])=C1 VPMMJSPGZSFEAH-UHFFFAOYSA-N 0.000 description 1
- VLZVIIYRNMWPSN-UHFFFAOYSA-N 2-Amino-4-nitrophenol Chemical compound NC1=CC([N+]([O-])=O)=CC=C1O VLZVIIYRNMWPSN-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- DUAYDERMVQWIJD-UHFFFAOYSA-N 2-n,2-n,6-trimethyl-1,3,5-triazine-2,4-diamine Chemical compound CN(C)C1=NC(C)=NC(N)=N1 DUAYDERMVQWIJD-UHFFFAOYSA-N 0.000 description 1
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 1
- JSQGOXTYKZBABW-UHFFFAOYSA-N 3-(3-hydroxyanilino)phenol Chemical compound OC1=CC=CC(NC=2C=C(O)C=CC=2)=C1 JSQGOXTYKZBABW-UHFFFAOYSA-N 0.000 description 1
- WADQOGCINABPRT-UHFFFAOYSA-N 3-chloro-2-methylphenol Chemical compound CC1=C(O)C=CC=C1Cl WADQOGCINABPRT-UHFFFAOYSA-N 0.000 description 1
- XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- FEPBITJSIHRMRT-UHFFFAOYSA-N 4-hydroxybenzenesulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C=C1 FEPBITJSIHRMRT-UHFFFAOYSA-N 0.000 description 1
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 1
- ZVNPWFOVUDMGRP-UHFFFAOYSA-N 4-methylaminophenol sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 ZVNPWFOVUDMGRP-UHFFFAOYSA-N 0.000 description 1
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 description 1
- OJFZXRZZXBFEAP-UHFFFAOYSA-N 5-chloro-1,6-dimethylcyclohexa-2,4-dien-1-ol Chemical compound ClC=1C(C(C=CC1)(C)O)C OJFZXRZZXBFEAP-UHFFFAOYSA-N 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 1
- QZKRHPLGUJDVAR-UHFFFAOYSA-K EDTA trisodium salt Chemical compound [Na+].[Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O QZKRHPLGUJDVAR-UHFFFAOYSA-K 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 241000208690 Hamamelis Species 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- 244000208060 Lawsonia inermis Species 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 239000004153 Potassium bromate Substances 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical class CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000013566 allergen Substances 0.000 description 1
- TUFYVOCKVJOUIR-UHFFFAOYSA-N alpha-Thujaplicin Natural products CC(C)C=1C=CC=CC(=O)C=1O TUFYVOCKVJOUIR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 1
- 229940075861 ammonium thioglycolate Drugs 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 229940035674 anesthetics Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 1
- KYZHGEFMXZOSJN-UHFFFAOYSA-N benzoic acid isobutyl ester Natural products CC(C)COC(=O)C1=CC=CC=C1 KYZHGEFMXZOSJN-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 230000037029 cross reaction Effects 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- XJCRCPKBJWRZAX-UHFFFAOYSA-L disodium;dibenzoate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 XJCRCPKBJWRZAX-UHFFFAOYSA-L 0.000 description 1
- JZKFHQMONDVVNF-UHFFFAOYSA-N dodecyl sulfate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(O)(=O)=O JZKFHQMONDVVNF-UHFFFAOYSA-N 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 239000003193 general anesthetic agent Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000003700 hair damage Effects 0.000 description 1
- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 1
- 229960004068 hexachlorophene Drugs 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 239000004306 orthophenyl phenol Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229940090668 parachlorophenol Drugs 0.000 description 1
- QKNZNUNCDJZTCH-UHFFFAOYSA-N pentyl benzoate Chemical compound CCCCCOC(=O)C1=CC=CC=C1 QKNZNUNCDJZTCH-UHFFFAOYSA-N 0.000 description 1
- 239000001024 permanent hair color Substances 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 229940094037 potassium bromate Drugs 0.000 description 1
- 235000019396 potassium bromate Nutrition 0.000 description 1
- FRMWBRPWYBNAFB-UHFFFAOYSA-M potassium salicylate Chemical compound [K+].OC1=CC=CC=C1C([O-])=O FRMWBRPWYBNAFB-UHFFFAOYSA-M 0.000 description 1
- 229960003629 potassium salicylate Drugs 0.000 description 1
- HYTYHTSMCRDHIM-UHFFFAOYSA-M potassium;2-sulfanylacetate Chemical compound [K+].[O-]C(=O)CS HYTYHTSMCRDHIM-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 1
- 229960004172 pyridoxine hydrochloride Drugs 0.000 description 1
- 235000019171 pyridoxine hydrochloride Nutrition 0.000 description 1
- 239000011764 pyridoxine hydrochloride Substances 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- ZZPKZRHERLGEKA-UHFFFAOYSA-N resorcinol monoacetate Chemical compound CC(=O)OC1=CC=CC(O)=C1 ZZPKZRHERLGEKA-UHFFFAOYSA-N 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229960004025 sodium salicylate Drugs 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
- UENNEPPWFZYINW-UHFFFAOYSA-M sodium;2-amino-4,6-dinitrophenolate Chemical compound [Na+].NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1[O-] UENNEPPWFZYINW-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- KSYNLCYTMRMCGG-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;dihydrate Chemical compound O.O.[Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O KSYNLCYTMRMCGG-UHFFFAOYSA-J 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- 229960005066 trisodium edetate Drugs 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Classifications
-
- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
-
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
-
- 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
- A61Q5/04—Preparations for permanent waving or straightening 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
- A61K2800/51—Chelating agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Description
〔産業上の利用分野〕
本発明は、毛髪にパーマネントウエーブの形成
処理或いはくせ毛、巻毛等の縮毛矯正(本明細書
中においては「パーマネントウエーブ等の形成処
理」と言う)と染毛処理とを同時並行的に施術す
ることを目的とするものであり、パーマネントウ
エーブ液と金属性染毛剤とを組み合わせてなる毛
髪処理用薬剤及びこれを用いた毛髪処理方法に関
する。
〔従来の技術〕
衣服、装身具、化粧等と並び、パーマネントウ
エーブ及び染毛等の毛髪処理は現代的フアツシヨ
ンの重要な要素である。髪のおしやれとして、従
来より、パーマネントウエーブ等の形成と染毛と
が広く行われている。また、個性的なフアツシヨ
ンを目指す人が増えるにつれて、パーマネントウ
エーブと染毛処理の両方を施す人の数も多くなつ
ており、髪のおしやれに対する関心度は非常に高
いと言える。
まず、パーマネントウエーブ等の形成処理につ
いて説明する。従来のパーマネントウエーブ液
は、通常、第1液と第2液との組合せよりなつて
いる。第1液には、チオグリコール酸塩又はシス
テイン等の還元剤が含有され、第2液にはブロム
酸塩類、過ホウ酸塩類、過酸化水素水等の酸化剤
が含有される。
パーマネントウエーブ等の形成方法は、大別す
ると二種類ある。一つは加熱操作を必要とする加
温式ウエーブ法であり、もう一つは常温で施術す
るコールド式ウエーブ法である。コールド式ウエ
ーブ法によるパーマネントウエーブ等の形成手順
を説明すると、おおよそ次の通りである。
始めに、毛髪をロツドに巻くなどして所望ウエ
ーブ形状となるように整形し、次いで、前記第1
液をロツドに巻かれた毛髪に塗布し所要時間放置
する。或いは、前記第1液を塗布しながら毛髪を
ロツドに巻いてもよい。第1液中の還元剤は、ケ
ラチン側鎖のシスチン結合を切断して毛髪から復
元力を取り去る。こうして可塑性になつた毛髪に
水洗、リンス等を施した後、次いで、前記第2液
を塗布する。第2液中の酸化剤は、切断されたシ
スチン結合を再結合する作用を有している。従つ
て、毛髪はウエーブ等が形成された新たな状態に
固定される。このようにして所望のパーマネント
ウエーブ等が形成されたならば、髪からロツドを
はずし、水洗、リンス、乾燥等を行う。
加温式ウエーブ法は、上述のコールド式ウエー
ブ法において、ロツドに巻かれた毛髪に第1液を
塗布した後、60℃を越えない程度に加熱して化学
反応を促進させるという方法である。加温式ウエ
ーブ法は、コールド式に比べて還元剤、酸化剤等
の消費量が少なくて済むが、加熱するための加温
装置が必要である。
一方、染毛法を大きく分類すると、一時染毛法
と、シヤンプーによつても色落ちしない永久染毛
法とに分類される。
一時染毛法は、カラー・スプレー、カラー・ク
レヨン、カラー・リンス等の顔料を基剤に混合し
た染毛剤で一時的に毛髪の表面を被覆する方法で
ある。従つて、シヤンプーにより簡単に色落ち
し、染毛効果を失うという欠点がある。
そこで、堅牢な染毛効果を得ようとする場合に
は植物性染毛剤、酸化染毛剤、金属染毛剤等を使
用する永久染毛法に依ることになる。
上記染毛剤のうち、植物性染毛剤として代表的
なものは、ヘンナの葉を煮詰めた液又は乾燥粉末
を熱湯で練つた液にクエン酸等を加えて酸性溶液
としたものである。これを毛髪に塗布し、蒸しタ
オル等でパツクして染毛する。ただし、この染毛
法は色調が赤色系であるため、施術対象が一部の
者に限定される。即ち、髪のおしやれに対する多
様な嗜好を満足させることが難しく、実用的では
ない。
現在、多彩な色調を得ることのできる永久染毛
法として広く使用されているのは、酸化染毛法と
金属性染毛法である。
酸化染毛法に使用される染毛剤は、パラフエニ
レンジアミン、パラトルエンジアミン等の芳香族
アミノ化合物を主剤とする第1液と、過酸化水素
等の酸化剤を主成分とする第2液とからなる。上
記第1液には、色調に変化を与える修正剤として
アミン類、ポリフエノール類等が添加され、その
他に、アンモニア等が加えられアルカリ性に調整
されている。第1液を毛髪に塗布した後、続いて
第2液を塗布すると、第2液中の過酸化水素等の
酸化剤が第1液のアルカリによつて急速に分解さ
れ酸素を発生させる。第1液中の芳香族アミノ化
合物及び修正剤は、この酸素により酸化されて酸
化染料を形成しつつ毛髪内部に浸透する。それと
同時に、毛髪のメラニン色素が発生期の酸素によ
つて酸化分解される。このように、酸化染料の生
成によるケラチンの染着反応と、メラニン色素の
酸化分解による脱色反応とを平行して進行させる
ことにより、毛髪を様々な色調に染めることがで
きる。
他方、金属性染毛剤とは、主に鉄の化合物を主
剤とする金属塩液と、前記金属塩と呈色反応を示
す発色剤とからなる二液式(又は毛髪の前処理剤
等を加えた三液式)の薬剤である。前記金属塩液
を毛髪に塗布すると、鉄等の金属分子はケラチン
と結合して毛髪の表面に定着する。次いで、前記
発色剤を塗布すると、定着した金属との間で呈色
反応が生じ、毛髪を所定の色調に染毛する。
〔発明が解決しようとする課題〕
美容院、理容院等で髪にパーマネントウエーブ
等の形成処理と永久染毛処理の両方を施術する場
合には、それぞれの処理を順次別々に行う、つま
り、毛髪にパーマネントウエーブ等を形成した後
に染毛処理を施すか、或いは染毛処理を施した後
にパーマネントウエーブ等を形成するというのが
一般的な方法である。従つて、いずれの順序で施
術するとしても、かなりの手間と時間とを要する
ものであり、大変不経済であつた。
永久染毛法として広く用いられている酸化染毛
法は、色調が豊富であり、シヤンプーによる色落
ちが少ないという特長があるが、アレルギー性皮
膚炎の発生率が高いという欠点がある。主剤のパ
ラフエニレンジアミン、パラトルエンジアミン等
の芳香族アミノ化合物は香粧品に使用されている
化合物中で最も感作性の高いアレルゲンであるこ
とが知られており、そのため、酸化染毛剤の反復
使用によつて高率でアレルギー性皮膚炎が発生す
る。しかも、染毛の被施術者ばかりでなく、施術
を担当する美容師にも多くの発症例が観察されて
いる。その上、アレルギー反応の経験者は、サル
フア剤、麻酔剤等に含まれている上記パラフエニ
レンジアミン、パラトルエンジアミンと構造類似
の芳香族アミノ化合物によつて交叉反応を起こす
ことも明らかにされている。その他、第1液は強
アルカリ性であるため皮膚に対して一次刺激性を
有する。染毛反応は強アルカリ性の下に進行する
酸化反応が主体であるため毛髪の損傷が著しい。
シスチン結合が切断されるためパーマネントウエ
ーブが掛りにくくなる。さらに紫外線の照射や酸
性シヤンプー、酸性リンスによつて褪色する等、
多くの問題点があつた。
金属性染毛法は、金属とケラチンとの結合が強
固であるため染毛効果が堅牢であり、人体に対し
て一次刺激性も感作性もないので酸化染毛剤のよ
うなアレルギー反応を起こすことはない。しかし
ながら、金属染毛剤中の金属分子が、パーマネン
トウエーブ液中のチオグリコール酸塩又はシステ
イン等の還元剤と反応し易い。そのため、還元力
を低下させてパーマネントウエーブの強度を弱め
ると同時に染毛効率も悪くするという問題点を有
している。
〔課題を解決するための手段〕
本発明者は、安全で、且つ永久性の高いパーマ
ネントウエーブ等の形成処理と染毛処理とを同時
並行的に施術することを目的として鋭意工夫を重
ねた。その結果、以下に説明する毛髪処理用薬剤
及び処理方法を用いることにより、上記目的を満
足させるに至つた。
本発明に係る毛髪処理用薬剤の特徴は、下記の
第1剤乃至第4剤からなることである。
(1) 還元剤としてチオグリコール酸塩類又はシス
テインのメルカプト化合物類を含有すると共
に、鉄又は銅の金属封鎖剤としてフエノール性
水酸基、エノール型水酸基若しくはこれらに類
する水酸基を有する化合物又はカルボキシル基
を有する化合物又はこれらの誘導体を含有する
第1剤
(2) 鉄又は銅の金属塩を含有する第2剤
(3) 第2剤に含有される鉄又は銅と反応して呈色
する発色剤としてフエノール性水酸基、エノー
ル型水酸基若しくはこれらに類する水酸基を有
する化合物又はカルボキシル基を有する化合物
又はこれらの誘導体を含有する第3剤
(4) 酸化剤としてブロム酸塩類、過ホウ酸塩類又
は過酸化水素水を含有する第4剤
上記第1剤において、チオグリコール酸塩類と
は、チオグリコール酸、チオグリコール酸アンモ
ニウム、チオグリコール酸ナトリウム、チオグリ
コール酸カリウム等を言う。
また、第1剤及び第3剤におけるフエノール性
水酸基、エノール型水酸基若しくはこれらに類す
る水酸基又はカルボキシル基を有する化合物又は
これらの誘導体とは、没食子酸、没食子酸プロピ
ル等の没食子酸エステル類、サリチル酸、サリチ
ル酸ナトリウム・サリチル酸カリウム等のサリチ
ル酸塩類、サリチル酸メチル、サリチル酸フエニ
ル等のサリチル酸エステル類、タンニン酸及びそ
のエステル類、レゾルシン、酢酸レゾルシン、ピ
ロガロール、カテコール、ヒドロキノン、ヘマテ
イン、ハマメリス水、ノニル酸バニリド、2―ヒ
ドロキシ―5―ニトロ―2′,4′―ジアミノアゾベ
ンゼン―5′―スルホン酸ナトリウム、フエノー
ル・ニトロフエノール・オルトアミノフエノー
ル・メタアミノフエノール・硫酸メタアミノフエ
ノール・硫酸パラアミノフエノール・硫酸パラメ
チルアミノフエノール・硫酸オルトアミノフエノ
ール・パラクロルフエノール・2―アミノ―4―
ニトロフエノール・2―アミノ―5―ニトロフエ
ノール・3,3′―イミノジフエノール・硫酸2―
アミノ―5―ニトロフエノール・塩酸2,4―ジ
アミノフエノール・パラアミノフエノール・パラ
メチルアミノフエノール・オルトフエニルフエノ
ール等のフエノール類、塩酸ピリドキシン、ヘキ
サクロロフエン、ヒノキチオール、クレゾール、
5―アミノオルトクレゾール・硫酸5―アミノオ
ルトクレゾール・クロルクレゾール等のクレゾー
ル類、クロルキシレノール、1―アミノ―4―メ
チルアミノアントラキノン、ピクラミン酸ナトリ
ウム、1,4―ジアミノアントラキノン、1,5
―ジヒドロキシナフタレン、α―ナフトール、オ
イゲノール、イソオイゲノール、バニリン、パラ
フエノールスルホン酸亜塩、2―(2―ヒドロキ
シ―5―メチルフエニル)ベンゾトリアゾール、
アセト酢酸エチル等のアセト酢酸エステル類、ア
スコルビン酸、グルコン酸及びこの塩類、安息香
酸、安息香酸ナトリウム・安息香酸デナトリウム
等の安息香酸塩類、安息香酸アミル・安息香酸イ
ソブチル・安息香酸パントテニルエステル・安息
香酸シヨ糖エステル等の安息香酸エステル類、パ
ラアミノ安息香酸、パラアミノ安息香酸エチル・
パラアミノ安息香酸グリセリン等のパラアミノ安
息香酸エステル類、並びにこれらの誘導体を指
す。なお、第1剤には上記のもののほか、エデト
酸二ナトリウム・エデト酸三ナトリウム・エデト
酸四ナトリウム二水塩・エデト酸四ナトリウム四
水塩等のEDTA類を用いることができる。
上記第2剤における鉄又は銅の金属塩とは、硫
酸第一鉄、塩化第二鉄、四三酸化鉄、三二酸化
鉄、黄酸化鉄等の鉄化合物類、及び酢酸銅、硫酸
銅、グリシン銅等の銅化合物類を言う。
上記第4剤のブロム酸塩類、過ホウ酸塩類と
は、ブロム酸カリウム、ブロム酸ナトリウム等の
ブロム酸塩類、過ホウ酸ナトリウム等の過ホウ酸
塩類である。
次に、上記第1剤乃至第4剤を用いて毛髪にパ
ーマネントウエーブ等の所望形状の形成処理と染
毛処理とを同時並行的に施術する本発明方法を説
明する。
まず、前記第1剤を塗布しつつ又は塗布した後
にロツドに巻きつけるなどして毛髪を所望形状に
整形し、該整形状態を保持しながら所要時間放置
した後水洗するなどして毛髪表面に残存する前記
第1剤を除去する。次に、鉄又は銅の金属塩を含
有する第2剤を前記毛髪に塗布し、所要時間放置
した後、再び水洗するなどして毛髪表面に残存す
る前記第2剤を除去する。次いで、前記第2剤に
含有される鉄又は銅と呈色反応を示す第3剤を前
記毛髪に塗布した後、続いて酸化剤を含有する第
4剤を塗布して所要時間放置した後、毛髪の整形
保持状態を解除し、洗浄、乾燥等の適宜処理を施
せば、所望形状の形成処理と染毛処理とが施術さ
れた毛髪を得ることが出来る。
なお、上記の第1剤塗布後の水洗及び第2剤塗
布後の水洗に替えて、スポンジ等により毛髪表面
に残存する剰余の薬剤を吸い取るか又は拭き取る
等の方法を用いてもよい。また、第1剤塗布後の
水洗を省略することも出来る。この場合、第1剤
の還元力が反応の進行に従つて減衰するのみなら
ず、後述するように第2剤が第1剤の還元反応を
停止させるので、水洗を省略しても毛髪が傷つく
ことは殆どない。
本発明の毛髪処理方法は、第1剤乃至第4剤を
順次毛髪に塗布するばかりでなく、前記第2剤と
前記第3剤とを混合して毛髪に塗布し、所要時間
放置した後水洗するなどして毛髪表面に残存する
前記第2剤及び第3剤を除去し、しかる後に第4
剤を塗布する方法も可能であり、或いは前記第3
剤と前記第4剤とを混合して毛髪に塗布すること
もできる。更には、第1剤乃至第4剤を塗布する
順番を、第1,2,4,3剤の順、第1,3,
4,2剤の順、第1,4,2,3剤の順又は第
1,4,3,2剤の順のように変更することも可
能である。
〔作用〕
本発明に係る第1剤乃至第4剤の営む作用を以
下に説明する。
まず第1剤中の還元剤は、毛髪のシスチン結合
を切断して、所望形状に整形保持された状態で毛
髪を可塑性にする。また、第1剤の還元剤は、毛
髪を膨潤化させる作用があるので、後に塗布され
る第2剤中の金属分子と毛髪のケラチンとの結合
を促進する働きも有している。第1剤に配合する
金属封鎖剤の作用については後述する。
次に第2剤を塗布することにより、鉄又は銅の
金属分子がケラチンと強固に結合して毛髪に定着
する。ところで、金属塩には還元剤と反応し易い
という性質がある。従つて、第1剤塗布後、水洗
を省略して第2剤を塗布したときには、第2剤中
の金属塩によつて第1剤の還元反応を停止させる
ことができる。
第3剤に含まれているフエノール性水酸基、エ
ノール型水酸基若しくはこれに類する水酸基を有
する化合物又はカルボキシル基を有する化合物又
はこれらの誘導体(以下、「水酸基又はカルボキ
シル基を有する化合物類」と言う)は、前記金属
分子と結合して有色の分子を生成する。従つて第
3剤を塗布することにより、毛髪が所定の色調に
染められる。
第4剤中の酸化剤は、第1剤により切断された
シスチン結合を再結合する作用を有している。従
つて、第4剤を塗布すると、毛髪は整形されてい
た形状のままで新たなシスチン結合状態に固定さ
れる。また、第4剤は、前記有色分子を酸化して
呈色性により顕著にする作用、及び水酸基又はカ
ルボキシル基を有する化合物類を有色分子と酸化
重合させて該有色分子を成長させる作用を有して
いる。従つて、第4剤の塗布することによつて、
毛髪全体がむらなくかつ色濃く染め上げられ、し
かも染毛の堅牢性が高まる。なお上記酸化重合反
応に、金属分子は触媒的に関与しているものと推
測される。
次に、第1剤に配合した金属封鎖剤の作用につ
いて説明する。毛髪中に鉄又は銅の金属分子が存
在していると、還元剤のシスチン切断作用が阻害
され、パーマネントウエーブの形成力が弱められ
ることは前述した。ところで、水酸基又はカルボ
キシル基を有する化合物類は、鉄又は銅が還元剤
と反応するのを防止する作用を有している。従つ
て、水酸基又はカルボキシル基を有する化合物類
を金属封鎖剤として第1剤に配合しておけば、予
め金属性染毛剤によつて染められた毛髪を第1剤
で処理する場合にも、還元剤のシスチン切断作用
が阻害されることはない。むしろ、水酸基又はカ
ルボキシル基を有する化合物類も還元力を有して
いるから、シスチン結合の切断反応を助勢して、
毛髪の可塑化を促進する。
なお、第1剤乃至第4剤が営む作用は独立性が
強いから、塗布する順番を変更したからといつ
て、各薬剤が引き起こす化学反応そのものの程度
や内容に影響を受けることはほとんどない。それ
故、第1剤乃至第4剤を塗布する順番を、前述し
た如く適当に変更することができ、しかも、毛髪
処理の結果にさほどの相違が生ずることもない。
〔実施例〕
本発明により、パーマネントウエーブの形成処
理と染毛処理とを同時並行的に施術する具体的な
実施例を以下に説明する。
まず、第1剤をロツドに巻いた頭髪に塗布し、
又は第1剤を頭髪に塗布しながらロツドに巻き、
10〜20分間放置する。その後、水洗して毛髪及び
頭皮の表面に残存する第1剤を除去する。又は、
水洗せずにそのまま第2剤を万遍なくロツドに巻
かれた頭髪に塗布して10分間放置し、鉄又は銅の
金属を毛髪内に浸透させる。その後、再度水洗し
て毛髪表面に残存する第2剤を除去する。引き続
いて、第3剤、第4剤を順次毛髪に塗布するか、
或いは処理時間の節約のために使用直前に第3剤
と第4剤とを混合して塗布する。10〜15分間放置
した後ロツドを外し、水洗、乾燥等を行う。この
ようにして、所要時間がロツドを巻く時間(約20
分)を含め約1時間余りでパーマネントウエーブ
の形成と染毛とが完了する。但し、上記処理時間
は、被施術者の毛髪の状態、所望するパーマネン
トウエーブの形状やウエーブ度、染毛程度等に応
じて適宜変更することができる。
本発明により得られる毛髪のウエーブ度、ウエ
ーブ保持性、色調、褪色性及び金属性染毛処理が
施された毛髪に対する二回目のパーマネントウエ
ーブ形成力等の試験結果を、次の表1乃至表3に
示す。試験用毛髪には、長さ20cmの白髪又は脱色
処理毛の50本を一束とし、シヤンプー、水洗をし
て乾燥させたものを用いた。パーマネントウエー
ブを形成するために用いるウエーブ形成具は第1
図に示したように、板状材にA乃至Gの7本のピ
ンを所定間隔で平行二列に植立させたものであ
る。前記ピンの直径は3mm、各ピンの間隔は
AB,BC,…,EF各間が22.5mm、AC,CE各間及
びBD,DF,FG各間が20.0mmである。試験方法
は、水洗して軽く水気を取つ毛束の一端(毛根
側)を、第2図に示した如くウエーブ形成具のピ
ンAに固定し、ピンB乃至F及びGに渡つて千鳥
足状に装着した後、ピンAを上側、ピンGが下側
となるようにウエーブ形成具を垂立させて毛束の
下端に重錘を吊し、100gの荷重を付与する。張
架された状態で毛束をピンGに固定した後、荷重
を取り除き、ウエーブ形成具を水平にして、毛髪
処理を行う。
毛髪処理方法は、毛束に第1剤をスポイトで万
遍なく塗布し、10分間放置した後30秒間水洗す
る。次に、第2剤を第1剤と同様に塗布し、10分
間放置した後30秒間水洗する。続いて、第3剤と
第4剤を2:1の割合で混合したものを第1剤と
同様に塗布し、15分間放置後、毛束をウエーブ形
成具より取り外し、30秒間水洗し、綿布上で乾燥
させる。
各表におけるウエーブ度は次式により求めたも
のである。
ウエーブ度(%)=(X−Z)/(X−Y)×100
但し、
X:ピンCDE間に固定された毛髪の長さ
Y:ピンCE間の距離
Z:毛束がピンC,Eに接していた点間のウエ
ーブ形成具から取り外したときの距離(第
3図参照)
また、ウエーブ保持性は、上記処理を施した毛
束を洗剤液(0.5%ラウリル硫酸トリエタノール
アミン水溶液)に1分間浸した後、精製水の入つ
たビーカー10個に順に漬けて洗浄し、ハンドドラ
イヤーにて乾燥させる、という処理を5回繰り返
し(但し、5回目はハンドドライヤーを用いずに
綿布上で風乾させる)、前記式中のZの値を測定
して当該処理の前後におけるウエーブ度を求め、
次式により算出したものである。
ウエーブ保持性(%)
=処理後のウエーブ度/処理前のウエーブ度×100
上記ウエーブ保持性試験は、日常生活において
普通行われる洗髪等を連続して5回繰り返すのに
も匹敵する毛髪に対してかなり苛酷な試験であ
る。
色調の判定は、最初の毛髪処理が施された毛束
について、5人の判定者により500W昼光色スポ
ツトライト下で視覚評価を行つたものである。
そして、褪色性の判定は、前記ウエーブ保持性
試験の洗剤処理を行つた毛束について上記色調判
定と同様の視覚評価を行い、洗剤処理前の毛束と
比較して褪色の有無を判定したものである。
なお、試験に用いた第1剤乃至第4剤は全て精
製水で調整された水溶液であり、主剤以外の組成
は次の通りである。(単位は全て重量%である)
第1剤 エタノール 10.0%
脂肪酸ジエタノールアミド 1.2%
両性系界面活性剤 12.0%
第2剤 ノニオン系界面活性剤 10.0%
第3剤 エタノール 45.0%
第4剤 精製水のみ
〔試験1〕
試験1は、本発明により、毛髪にパーマネント
ウエーブの形成処理と染毛処理とを同時並行的に
施術できることを実証すると共に、第1剤に配合
される金属封鎖剤、第2剤に配合される金属塩、
第3剤に配合される発色剤及び第4剤に配合され
る酸化剤の種類及び濃度を変えることにより、
様々な色調、ウエーブ度を持つた毛髪が得られる
ことを確かめたものである。各試験における毛髪
処理に要した時間は約40分であつた。(但し、試
番4―1の試験において、第1剤塗布後の放置時
間は20分間とした。)
この結果を表1―1及び表1―2に示す。
なお、対照例として、第1剤に金属封鎖剤を配
合しないものであつて、第2剤以降は同様の処理
を行つたもの(C―1)、第3剤の発色剤を省略
したもの(C―2)、第2剤の金属塩及び第3剤
の発色剤を省略したもの(C―3)を挙げた。
[Industrial Application Field] The present invention relates to a treatment for forming permanent waves on hair or for straightening curly hair, curly hair, etc. (herein referred to as "a treatment for forming permanent waves, etc."), and a hair dyeing treatment. The present invention relates to a hair treatment agent comprising a combination of a permanent wave solution and a metallic hair dye, and a hair treatment method using the same. [Prior Art] Along with clothing, accessories, makeup, etc., hair treatments such as permanent waves and hair dyeing are important elements of modern fashion. 2. Description of the Related Art Formation of permanent waves and hair dyeing have been widely practiced to care for hair. Additionally, as more and more people aim to create unique hairstyles, more and more people are choosing both permanent waves and hair dyeing, and it can be said that interest in hair care is extremely high. First, a process for forming permanent waves and the like will be explained. Conventional permanent wave fluids typically consist of a combination of a first fluid and a second fluid. The first liquid contains a reducing agent such as a thioglycolate or cysteine, and the second liquid contains an oxidizing agent such as a bromate salt, a perborate salt, or a hydrogen peroxide solution. There are two types of methods for forming permanent waves. One is the heated wave method, which requires heating, and the other is the cold wave method, which is performed at room temperature. The procedure for forming permanent waves etc. by the cold wave method is roughly as follows. First, the hair is shaped into a desired wave shape by winding it into a rod, and then the first
Apply the solution to the hair wrapped in a rod and leave it for the required time. Alternatively, the hair may be rolled into a rod while applying the first liquid. The reducing agent in the first liquid cleaves the cystine bonds in the keratin side chains and removes the restoring power from the hair. After washing, rinsing, etc. the hair that has become plastic in this way, the second liquid is then applied. The oxidizing agent in the second liquid has the effect of recombining broken cystine bonds. Therefore, the hair is fixed in a new state in which waves and the like are formed. Once the desired permanent waves have been formed in this way, the rods are removed from the hair, washed with water, rinsed, dried, etc. The heated wave method is a method in which the first liquid is applied to the hair wound into a rod in the above-mentioned cold wave method, and then heated to a temperature not exceeding 60°C to accelerate the chemical reaction. The heated wave method consumes less reducing agent, oxidizing agent, etc. than the cold method, but requires a heating device for heating. On the other hand, hair dyeing methods are broadly classified into temporary hair dyeing methods and permanent hair dyeing methods that do not fade even with shampoo. The temporary hair dyeing method is a method in which the surface of the hair is temporarily coated with a hair dye such as color spray, color crayon, color rinse, etc. in which a pigment is mixed into a base. Therefore, there is a drawback that the color easily fades due to shampoo and the hair dyeing effect is lost. Therefore, in order to obtain a durable hair dyeing effect, permanent hair dyeing methods using vegetable hair dyes, oxidative hair dyes, metal hair dyes, etc. are resorted to. Among the hair dyes mentioned above, typical vegetable hair dyes are made by adding citric acid or the like to a liquid obtained by boiling down henna leaves or a liquid obtained by kneading dry powder with boiling water to form an acidic solution. Apply this to your hair, pack it with a steamed towel, etc., and dye your hair. However, since this hair dyeing method has a reddish tone, the treatment is limited to a limited number of people. That is, it is difficult to satisfy various preferences regarding hair care, and it is not practical. Currently, oxidative hair dyeing methods and metallic hair dyeing methods are widely used as permanent hair dyeing methods that can provide a wide variety of color tones. The hair dye used in the oxidative hair dyeing method consists of a first liquid whose main ingredient is an aromatic amino compound such as paraphenylene diamine or paratoluene diamine, and a second liquid whose main ingredient is an oxidizing agent such as hydrogen peroxide. Consists of liquid. To the first liquid, amines, polyphenols, etc. are added as modifiers that change the color tone, and ammonia etc. are also added to adjust the alkalinity. When the first liquid is applied to the hair and then the second liquid is applied, the oxidizing agent such as hydrogen peroxide in the second liquid is rapidly decomposed by the alkali of the first liquid and generates oxygen. The aromatic amino compound and the modifier in the first liquid are oxidized by this oxygen and penetrate into the hair while forming an oxidized dye. At the same time, the melanin pigment in the hair is oxidized and decomposed by the nascent oxygen. In this way, by allowing the dyeing reaction of keratin due to the production of oxidative dye and the decolorization reaction due to oxidative decomposition of melanin pigment to proceed in parallel, hair can be dyed in various tones. On the other hand, metallic hair dye is a two-component type (or a hair pre-treatment agent, etc.) consisting of a metal salt solution whose main ingredient is an iron compound and a coloring agent that exhibits a coloring reaction with the metal salt. It is a three-component drug. When the metal salt solution is applied to hair, metal molecules such as iron bond with keratin and become fixed on the hair surface. Next, when the coloring agent is applied, a coloring reaction occurs with the fixed metal, dyeing the hair to a predetermined color tone. [Problems to be Solved by the Invention] When hair is subjected to both permanent wave forming treatment such as permanent wave treatment and permanent hair dyeing treatment at a hair salon, barber salon, etc., each treatment is performed separately in sequence. A common method is to form a permanent wave or the like on the hair and then dye the hair, or to form a permanent wave or the like after the hair dye. Therefore, no matter which order the treatments are performed, a considerable amount of time and effort is required, which is very uneconomical. Oxidative hair dyeing, which is widely used as a permanent hair dyeing method, has the advantage of being rich in color and having little discoloration due to shampoo, but has the disadvantage of a high incidence of allergic dermatitis. Aromatic amino compounds such as para-phenylene diamine and para-toluene diamine, which are the main ingredients, are known to be the most sensitizing allergens among compounds used in cosmetics. Allergic dermatitis occurs at a high rate with repeated use. Moreover, many cases of the disease have been observed not only in hair dye recipients but also in the hairdressers who perform the treatments. Furthermore, it has been revealed that people who have experienced allergic reactions may experience cross-reactions with aromatic amino compounds with similar structures to the above-mentioned paraphenylene diamine and para-toluenediamine contained in sulfur drugs, anesthetics, etc. ing. In addition, since the first liquid is strongly alkaline, it has primary irritation to the skin. Since the hair dyeing reaction is mainly an oxidation reaction that proceeds under strong alkaline conditions, hair damage is significant.
Cystine bonds are broken, making it difficult for permanent waves to form. Furthermore, the color may fade due to UV irradiation, acid shampoo, acid rinse, etc.
There were many problems. Metallic hair dyeing has a strong bond between the metal and keratin, so the hair dyeing effect is robust, and it does not cause any allergic reactions like oxidative hair dyes because it does not cause primary irritation or sensitization to the human body. It won't happen. However, metal molecules in metal hair dyes tend to react with reducing agents such as thioglycolate or cysteine in permanent wave solutions. Therefore, there is a problem that the reducing power is reduced and the strength of the permanent wave is weakened, and at the same time, the hair dyeing efficiency is also deteriorated. [Means for Solving the Problems] The present inventor has made extensive efforts with the aim of simultaneously performing a safe and highly permanent permanent wave formation process and hair dyeing process. As a result, by using the hair treatment chemicals and hair treatment methods described below, the above objectives were achieved. The hair treatment agent according to the present invention is characterized by comprising the following first to fourth agents. (1) Compounds containing thioglycolates or cysteine mercapto compounds as reducing agents, and having phenolic hydroxyl groups, enol-type hydroxyl groups, or similar hydroxyl groups, or compounds having carboxyl groups as sequestering agents for iron or copper. or a derivative thereof (2) A second agent containing a metal salt of iron or copper (3) A phenolic coloring agent that reacts with the iron or copper contained in the second agent to develop a color A third agent containing a hydroxyl group, an enol-type hydroxyl group, or a compound having a similar hydroxyl group, or a compound having a carboxyl group, or a derivative thereof (4) Contains bromates, perborates, or hydrogen peroxide as an oxidizing agent Fourth Agent In the first agent, the thioglycolates include thioglycolic acid, ammonium thioglycolate, sodium thioglycolate, potassium thioglycolate, and the like. In addition, the compounds having a phenolic hydroxyl group, an enol type hydroxyl group, or a similar hydroxyl group or a carboxyl group in the first and third agents, or derivatives thereof include gallic acid, gallic acid esters such as propyl gallate, salicylic acid, Salicylates such as sodium salicylate and potassium salicylate, salicylic acid esters such as methyl salicylate and phenyl salicylate, tannic acid and its esters, resorcinol, resorcinol acetate, pyrogallol, catechol, hydroquinone, hematein, Hamamelis water, nonylic acid vanillide, 2- Sodium hydroxy-5-nitro-2',4'-diaminoazobenzene-5'-sulfonate, phenol, nitrophenol, ortho-aminophenol, meta-aminophenol, meta-aminophenol sulfate, para-aminophenol sulfate, para-methylaminophenol sulfate, Orthoaminophenol sulfate/parachlorophenol/2-amino-4-
Nitrophenol, 2-amino-5-nitrophenol, 3,3'-iminodiphenol, sulfuric acid 2-
Phenols such as amino-5-nitrophenol, 2,4-diaminophenol hydrochloride, para-aminophenol, para-methylaminophenol, orthophenylphenol, pyridoxine hydrochloride, hexachlorophene, hinokitiol, cresol,
Cresols such as 5-aminoorthocresol, 5-aminoorthocresol sulfate, and chlorcresol, chlorxylenol, 1-amino-4-methylaminoanthraquinone, sodium picramate, 1,4-diaminoanthraquinone, 1,5
-dihydroxynaphthalene, α-naphthol, eugenol, isoeugenol, vanillin, paraphenolsulfonic acid subsalt, 2-(2-hydroxy-5-methylphenyl)benzotriazole,
Acetoacetic acid esters such as ethyl acetoacetate, ascorbic acid, gluconic acid and their salts, benzoic acid, benzoates such as sodium benzoate and disodium benzoate, amyl benzoate, isobutyl benzoate, pantothenyl benzoate, Benzoic acid esters such as sucrose benzoic acid ester, para-aminobenzoic acid, ethyl para-aminobenzoate, etc.
Refers to para-aminobenzoic acid esters such as para-aminobenzoic acid glycerin, and derivatives thereof. In addition to the above, the first agent may include EDTAs such as disodium edetate, trisodium edetate, tetrasodium edetate dihydrate, and tetrasodium edetate tetrahydrate. The metal salts of iron or copper in the second agent mentioned above include iron compounds such as ferrous sulfate, ferric chloride, triferric tetroxide, iron sesquioxide, and yellow iron oxide, as well as copper acetate, copper sulfate, and glycine. Refers to copper compounds such as copper. The bromate salts and perborate salts of the fourth agent are bromate salts such as potassium bromate and sodium bromate, and perborate salts such as sodium perborate. Next, a method of the present invention will be described in which hair is simultaneously subjected to a hair dyeing process and a hair dyeing process using the first to fourth agents described above. First, the hair is shaped into a desired shape by winding it around a rod while or after applying the first agent, and the hair is left in the shaped state for a required period of time, and then washed with water so that it remains on the hair surface. The first agent is removed. Next, a second agent containing a metal salt of iron or copper is applied to the hair, left for a required period of time, and then washed with water again to remove the second agent remaining on the hair surface. Next, after applying to the hair a third agent that exhibits a coloring reaction with iron or copper contained in the second agent, a fourth agent containing an oxidizing agent is applied and left for a required period of time. By removing the hair from its shape-holding state and subjecting it to appropriate treatments such as washing and drying, it is possible to obtain hair that has been subjected to a desired shape forming process and hair dyeing process. Note that instead of washing with water after applying the first agent and washing with water after applying the second agent, a method such as absorbing or wiping off the excess agent remaining on the hair surface with a sponge or the like may be used. Furthermore, washing with water after applying the first agent can be omitted. In this case, not only the reducing power of the first agent decreases as the reaction progresses, but also the second agent stops the reducing reaction of the first agent as described later, so even if washing with water is omitted, the hair will be damaged. There are almost no such things. The hair treatment method of the present invention includes not only sequentially applying the first to fourth agents to the hair, but also mixing the second agent and the third agent, applying the mixture to the hair, leaving it for a required period of time, and then washing with water. The second and third agents remaining on the hair surface are removed by
A method of applying an agent is also possible, or the third method described above is also possible.
It is also possible to mix the agent and the fourth agent and apply the mixture to the hair. Furthermore, the order in which the first to fourth agents are applied is changed to 1st, 2nd, 4th, 3rd agents, 1st, 3rd, 3rd agents, etc.
It is also possible to change the order of the 4th and 2nd drugs, the 1st, 4th, 2nd and 3rd drugs, or the 1st, 4th, 3rd and 2nd drugs. [Function] The functions of the first to fourth agents according to the present invention will be explained below. First, the reducing agent in the first agent breaks the cystine bonds in the hair, making the hair plastic while maintaining it in a desired shape. Furthermore, since the reducing agent in the first agent has the effect of swelling the hair, it also has the function of promoting the bond between the metal molecules in the second agent applied later and the keratin of the hair. The action of the sequestering agent added to the first agent will be described later. Next, by applying the second agent, iron or copper metal molecules are firmly bonded to keratin and fixed to the hair. By the way, metal salts have the property of easily reacting with reducing agents. Therefore, when the second agent is applied without washing with water after applying the first agent, the reduction reaction of the first agent can be stopped by the metal salt in the second agent. Compounds having phenolic hydroxyl groups, enol-type hydroxyl groups, or similar hydroxyl groups, or compounds having carboxyl groups, or derivatives thereof (hereinafter referred to as "compounds having hydroxyl groups or carboxyl groups") contained in the third agent are , combine with the metal molecules to produce colored molecules. Therefore, by applying the third agent, the hair is dyed to a predetermined color tone. The oxidizing agent in the fourth agent has the effect of recombining the cystine bonds cleaved by the first agent. Therefore, when the fourth agent is applied, the hair is fixed in a new cystine bond state while maintaining its previously shaped shape. Further, the fourth agent has the effect of oxidizing the colored molecule to make it more noticeable in color development, and the effect of oxidatively polymerizing compounds having a hydroxyl group or carboxyl group with the colored molecule to grow the colored molecule. ing. Therefore, by applying the fourth agent,
The entire hair is dyed evenly and deeply, and the fastness of the dye is improved. It is assumed that metal molecules are catalytically involved in the above oxidative polymerization reaction. Next, the action of the metal sequestering agent blended into the first agent will be explained. As mentioned above, when metal molecules such as iron or copper are present in hair, the cystine-cleaving action of the reducing agent is inhibited, and the ability to form permanent waves is weakened. By the way, compounds having a hydroxyl group or a carboxyl group have the effect of preventing iron or copper from reacting with a reducing agent. Therefore, if a compound having a hydroxyl group or a carboxyl group is incorporated into the first agent as a sequestering agent, even when hair that has been previously dyed with a metallic hair dye is treated with the first agent, The cystine cleaving action of the reducing agent is not inhibited. Rather, since compounds having hydroxyl or carboxyl groups also have reducing power, they assist in the cystine bond cleavage reaction.
Promotes hair plasticization. The actions of the first to fourth agents are highly independent, so even if the order of application is changed, the extent and content of the chemical reactions themselves caused by each agent will hardly be affected. Therefore, the order in which the first to fourth agents are applied can be changed appropriately as described above, and there is no significant difference in the hair treatment results. [Example] A specific example in which permanent wave forming treatment and hair dyeing treatment are performed simultaneously in accordance with the present invention will be described below. First, apply the first agent to the hair wrapped in a rod,
Or, while applying the first agent to your hair, wrap it in a knot.
Leave for 10-20 minutes. Thereafter, the first agent remaining on the hair and scalp surfaces is removed by washing with water. Or
Apply the second agent evenly to the curly hair without washing with water and leave it for 10 minutes to allow the iron or copper metal to penetrate into the hair. Thereafter, the second agent remaining on the hair surface is removed by washing with water again. Subsequently, apply the third and fourth agents to the hair in sequence, or
Alternatively, to save processing time, the third and fourth agents may be mixed and applied immediately before use. After leaving it for 10 to 15 minutes, remove the rod, wash with water, and dry. In this way, the time required to wind the rod (approximately 20
Permanent wave formation and hair dyeing are completed in about 1 hour, including 1 minute). However, the above-mentioned treatment time can be changed as appropriate depending on the condition of the hair of the recipient, the desired shape and degree of permanent waves, the degree of hair dyeing, and the like. The test results of the degree of wave, wave retention, color tone, fading resistance, and second permanent wave formation ability for hair that has been subjected to metallic hair dyeing treatment are shown in Tables 1 to 3 below. Shown below. The hair for the test was a bundle of 50 white or bleached hairs with a length of 20 cm, shampooed, washed with water, and dried. The wave forming tool used to form permanent waves is the first one.
As shown in the figure, seven pins A through G are planted in two parallel rows at a predetermined interval on a plate-like material. The diameter of the pin is 3mm, and the interval between each pin is
The distance between AB, BC,..., EF is 22.5mm, and the distance between AC, CE, and BD, DF, and FG is 20.0mm. The test method is to fix one end (root side) of the hair bundle, which has been washed with water and lightly drained, to pin A of the wave former as shown in Fig. After attaching the hair bundle to the hair bundle, the wave former is vertically placed so that pin A is on the upper side and pin G is on the lower side, and a weight is suspended from the lower end of the hair bundle to apply a load of 100 g. After the hair bundle is fixed to the pin G in a stretched state, the load is removed, the wave former is held horizontally, and the hair is processed. To treat hair, apply the first agent evenly to the hair strands with a dropper, leave it for 10 minutes, and then rinse with water for 30 seconds. Next, apply the second part in the same manner as the first part, leave it for 10 minutes, and then wash with water for 30 seconds. Next, apply a mixture of the third and fourth agents at a ratio of 2:1 in the same manner as the first agent, leave it for 15 minutes, remove the hair from the wave former, wash it with water for 30 seconds, and apply it with a cotton cloth. Dry on top. The degree of wave in each table was determined using the following formula. Wave degree (%) = (X-Z) / (X-Y) x 100 However, X: Length of hair fixed between pins CDE Y: Distance between pins CE Z: Hair bundle is fixed between pins C and E The distance between the points that were in contact with each other when removed from the wave former (see Figure 3) Wave retention can also be determined by soaking the treated hair bundle in a detergent solution (0.5% lauryl sulfate triethanolamine aqueous solution). After soaking for 1 minute, soaking in 10 beakers of purified water, washing, and drying with a hand dryer, repeat the process 5 times (however, for the 5th time, air dry on a cotton cloth without using a hand dryer). ), measure the value of Z in the formula to determine the wave degree before and after the processing,
It was calculated using the following formula. Wave retention (%) = Degree of wave after treatment / Degree of wave before treatment × 100 The above wave retention test was conducted on hair, which is comparable to repeating hair washing five times in a row, which is a common practice in daily life. It's a pretty tough test. The color tone was visually evaluated by five judges under a 500W daylight color spotlight on the hair strands that had undergone the initial hair treatment. The fading property was determined by visually evaluating the detergent-treated hair strands in the wave retention test in the same way as the color tone assessment above, and comparing the hair strands with the detergent-treated hair strands to determine the presence or absence of fading. It is. The first to fourth agents used in the test were all aqueous solutions prepared with purified water, and their compositions other than the main agent were as follows. (All units are weight %) Part 1 Ethanol 10.0% Fatty acid diethanolamide 1.2% Amphoteric surfactant 12.0% Part 2 Nonionic surfactant 10.0% Part 3 Ethanol 45.0% Part 4 Purified water only [ Test 1] Test 1 demonstrated that according to the present invention, permanent wave formation treatment and hair dyeing treatment can be performed simultaneously on hair, and that the metal sequestering agent blended in the first agent and the second agent Metal salts to be mixed,
By changing the type and concentration of the coloring agent blended in the third part and the oxidizing agent blended in the fourth part,
It was confirmed that hair with various tones and waves can be obtained. The time required for hair treatment in each test was approximately 40 minutes. (However, in the test No. 4-1, the standing time after applying the first agent was 20 minutes.) The results are shown in Tables 1-1 and 1-2. As control examples, the first part did not contain a sequestering agent and the second part and subsequent parts were treated in the same manner (C-1), and the third part omitted the coloring agent (C-1). C-2), and (C-3) in which the metal salt of the second agent and the coloring agent of the third agent were omitted.
【表】【table】
【表】【table】
試験2は、本発明によつて、毛髪中に金属が残
存しているときにも、高いウエーブ度を得ること
ができ、ウエーブ保持性も低下しないことを示し
たものである。
試験方法は、毛束をウエーブ形成具に装着せず
に直毛状態のままで一回目の処理を行い、風乾
後、ウエーブ形成具に装着して二回目の処理を行
つて、ウエーブ度、ウエーブ保持性、色調、褪色
性を判定したものである。但し、上記一回目の毛
髪処理は、前掲の表1―1中の試番2―1の薬剤
組成によつて行い、表2には、二回目の処理条件
を示してある。
対照例は、試番2―1の薬剤組成において、第
1剤の金属封鎖剤を省略したものを用いて2回の
処理を行つたもの(C―4)、及び第1剤の金属
封鎖剤と第2剤の金属塩を省略したもので一回目
の処理を行つた後C―4と同じ組成の薬剤で二回
目の処理を行つたもの(C―5)である。つま
り、C―4は二回目の処理時に金属が毛髪に残存
している場合、C―5は毛髪に金属が残存してい
ない場合の対照例である。
この結果を表2―1〜3に示す。
Test 2 showed that according to the present invention, even when metal remains in the hair, a high degree of wave can be obtained and the wave retention does not deteriorate. The test method was to perform the first treatment with the hair bundle straight without attaching it to the wave former, and after air-drying, perform the second treatment with the hair bundle attached to the wave former. The retention, color tone, and fading resistance were evaluated. However, the above-mentioned first hair treatment was carried out using the chemical composition of Trial No. 2-1 in Table 1-1 above, and Table 2 shows the conditions for the second treatment. The control examples are a case in which the drug composition of Trial No. 2-1 was treated twice using the drug composition in which the metal sequestering agent of the first agent was omitted (C-4), and a case in which the metal sequestering agent of the first agent was treated twice. After the first treatment was performed with the metal salt of the second agent omitted, the second treatment was performed with a chemical having the same composition as C-4 (C-5). In other words, C-4 is a control example in which metal remains in the hair during the second treatment, and C-5 is a control example in which no metal remains in hair. The results are shown in Tables 2-1 to 2-3.
【表】【table】
【表】【table】
【表】
表2―1における対照例C―4から明らかなよ
うに、金属分子が残存する毛髪に対してパーマネ
ントウエーブ形成処理を施したときは、そのウエ
ーブ度が非常に低くなり(7.0%)、ウエーブ保持
性は全く失われる(0%)。これに対して、本発
明によれば、対照例に比べて非常に優れたウエー
ブ度、ウエーブ保持性を得ることができた。ま
た、金属分子の存在しない毛髪にパーマネントウ
エーブの形成処理と染毛処理とを施したもの(C
―5)と比較しても、本発明によれば、高いウエ
ーブ度及びウエーブ保持性を得ることができる。
これらの効果は第1剤に金属封鎖剤として配合し
た水酸基又はカルボキシル基を有する化合物類の
作用によるものである。そして、上記化合物類の
配合比率を変えることにより、毛髪のウエーブ度
及びウエーブ保持性に様々な変化を与えることも
可能である。
次の表2―4及び5は、上記試験を、金属塩が
銅塩の場合においても、また、還元剤を低濃度に
した場合においても同様の効果が得られることを
示したものである。C―6及びC―7はそれぞれ
対照例である。なお、表2―5の還元剤濃度を低
くした試験では、第1剤塗布後の放置時間を20分
間とした。[Table] As is clear from Control Example C-4 in Table 2-1, when the permanent wave forming treatment was applied to hair in which metal molecules remained, the degree of waving was extremely low (7.0%). , wave retention is completely lost (0%). On the other hand, according to the present invention, it was possible to obtain extremely excellent wave degree and wave retention compared to the control example. In addition, hair that does not contain metal molecules is subjected to permanent wave forming treatment and hair dyeing treatment (C
-5) According to the present invention, high wave degree and wave retention can be obtained.
These effects are due to the action of compounds having a hydroxyl group or a carboxyl group that are blended into the first agent as a metal sequestering agent. By changing the blending ratio of the above-mentioned compounds, it is also possible to give various changes to the degree of wave and wave retention of the hair. Tables 2-4 and 5 below show that similar effects can be obtained from the above test even when the metal salt is a copper salt and when the reducing agent is used at a low concentration. C-6 and C-7 are control examples, respectively. In addition, in the test in which the reducing agent concentration was lowered in Table 2-5, the standing time after applying the first agent was 20 minutes.
【表】【table】
試験1,2は白髪又は脱色毛に対して本発明を
実施した試験結果であるが、試験3は、通常の黒
髪に対しても本発明の効果が得られることを証明
したものである。この試験例では、第1剤塗布後
の放置時間及び第3剤と第4剤との混合塗布後の
放置時間を、それぞれ20分間にした。その結果を
表3に示す。
Tests 1 and 2 are test results in which the present invention was applied to gray hair or bleached hair, but Test 3 proves that the effects of the present invention can also be obtained on normal black hair. In this test example, the standing time after application of the first agent and the standing time after the mixed application of the third agent and the fourth agent were each 20 minutes. The results are shown in Table 3.
【表】【table】
本発明による効果を以下に述べる。
パーマネントウエーブの形成処理或いは縮毛
矯正等の所望形状の形成処理と染毛処理とを同
時並行的に行うことができる。従つて、従来、
別々に順次行つていたため、非常な手間と時間
とを要していたパーマネントウエーブ等の形成
処理と染毛処理とを、遥かに短縮された時間内
で簡単に施術することができる。
第1剤に配合した金属封鎖剤は、第1剤の還
元剤のシスチン結合切断反応が、毛髪中に残存
する鉄又は銅の金属塩によつて阻害されるのを
防止する。つまり、予め金属性染毛処理が施さ
れた毛髪に対しても、確実にパーマネントウエ
ーブ等が形成される。故に、本発明を用いれ
ば、何度でも繰り返してパーマネントウエーブ
等の形成処理と染毛処理とを同時並行的に施術
することができる。
染毛剤として金属性染毛剤を用いたので、堅
牢で永久性の高い染毛処理を施すことができ、
しかも、人体に対して感作性も一次刺激性も無
く、安全性に優れる。
毛髪処理剤の組成を変更することにより、豊
富な色調を得ることができ、白髪染ばかりでな
く、金髪、赤毛、栗毛等は勿論、黒髪にも染毛
処理を施すことが可能である。また、ウエーブ
度の変更も自在であるから、髪のおしやれに対
する多様な要望を満足させることができる。
以上を要するに、本発明は実用的価値の極めて
大なる毛髪処理用薬剤及び毛髪処理方法を提供す
るものである。
The effects of the present invention will be described below. A desired shape forming process such as permanent wave forming process or hair straightening process and hair dyeing process can be performed simultaneously. Therefore, conventionally,
The permanent wave formation process and hair dyeing process, which used to take a lot of time and effort to perform separately and sequentially, can now be easily performed in a much shorter time. The sequestering agent blended into the first agent prevents the cystine bond cleavage reaction of the reducing agent of the first agent from being inhibited by iron or copper metal salts remaining in the hair. In other words, permanent waves are reliably formed even on hair that has been previously subjected to metallic hair dyeing treatment. Therefore, by using the present invention, it is possible to repeatedly perform permanent wave formation treatment and hair dyeing treatment simultaneously and in parallel as many times as desired. Since metallic hair dye is used as the hair dye, it is possible to apply a strong and highly permanent hair dye treatment.
Moreover, it has no sensitization or primary irritation to the human body, and is excellent in safety. By changing the composition of the hair treatment agent, a wide range of color tones can be obtained, and it is possible to dye not only gray hair but also blonde, red, chestnut, etc., as well as black hair. In addition, since the degree of waving can be changed freely, it is possible to satisfy various demands for hair care. In summary, the present invention provides a hair treatment agent and a hair treatment method of extremely high practical value.
第1図は、本発明の試験のために用いるウエー
ブ形成具を示す斜視図、第2図は、ウエーブ形成
具へ毛束を装着した状況を示す正面図である。第
3図は、ウエーブ度を測定する毛束の個所を説明
する図である。
FIG. 1 is a perspective view showing a wave forming device used for testing the present invention, and FIG. 2 is a front view showing a state in which a hair bundle is attached to the wave forming device. FIG. 3 is a diagram illustrating the locations of the hair bundle where the degree of wave is measured.
Claims (1)
第3剤及び第4剤を組み合わせてなることを特徴
とする毛髪処理用薬剤。 (1) 還元剤としてチオグリコール酸塩類又はシス
テインのメルカプト化合物類を含有すると共
に、鉄又は銅の金属封鎖剤としてフエノール性
水酸基、エノール型水酸基若しくはこれらに類
する水酸基を有する化合物又はカルボキシル基
を有する化合物又はこれらの誘導体を含有する
第1剤 (2) 鉄又は銅の金属塩を含有する第2剤 (3) 前記第2剤に含有される鉄又は銅の金属塩と
反応して呈色する発色剤としてフエノール性水
酸基、エノール型水酸基若しくはこれらに類す
る水酸基を有する化合物又はカルボキシル基を
有する化合物又はこれらの誘導体を含有する第
3剤 (4) 酸化剤としてブロム酸塩類、過ホウ酸塩類又
は過酸化水素水を含有する第4剤 2 毛髪にパーマネントウエーブ等の形成処理と
染毛処理とを同時並行的に施す毛髪処理方法であ
つて、下記に列挙するA乃至Eの工程からなるこ
とを特徴とする毛髪処理方法。 A 還元剤としてチオグリコール酸塩類又はシス
テインのメルカプト化合物類を含有すると共
に、鉄又は銅の金属封鎖剤としてフエノール性
水酸基、エノール型水酸基若しくはこれらに類
する水酸基を有する化合物又はカルボキシル基
を有する化合物又はこれらの誘導体を含有する
第1剤を塗布しつつ又は塗布した後に毛髪を所
望形状に整形する工程 B 上記整形状態を保持しながら所要時間放置し
た後、水洗し又は水洗せずにそのまま鉄又は銅
の金属塩を含有する第2剤を前記毛髪に塗布す
る工程 C 所要時間放置した後、水洗するなどして毛髪
表面に残存する前記第2剤を除去し、次いで前
記第2剤に含有される鉄又は銅の金属塩と反応
して呈色する発色剤としてフエノール性水酸
基、エノール型水酸基若しくはこれらに類する
水酸基を有する化合物又はカルボキシル基を有
する化合物又はこれらの誘導体を含有する第3
剤を前記毛髪に塗布する工程 D 続いて、酸化剤としてブロム酸塩類、過ホウ
酸塩類又は過酸化水素水を含有する第4剤を塗
布する工程 E 所要時間放置した後、毛髪の整形保持状態を
解除し、洗髪、乾燥等の適宜処理を施す工程 3 前記第2剤と前記第3剤とを混合して毛髪に
塗布し、所要時間放置した後水洗するなどして毛
髪表面に残存する前記第2剤及び第3剤を除去
し、しかる後に第4剤を塗布することを特徴とす
る特許請求の範囲第2項記載の毛髪処理方法。 4 前記第3剤と前記第4剤とを混合して毛髪に
塗布することを特徴とする特許請求の範囲第2項
記載の毛髪処理方法。 5 毛髪を特定形状に成形せずに処理を行うこと
を特徴とする特許請求の範囲第2項乃至第4項記
載の毛髪処理方法。[Claims] 1. A first agent, a second agent listed in (1) to (4) below,
A hair treatment agent comprising a combination of a third agent and a fourth agent. (1) Compounds containing thioglycolates or cysteine mercapto compounds as reducing agents, and having phenolic hydroxyl groups, enol-type hydroxyl groups, or similar hydroxyl groups, or compounds having carboxyl groups as sequestering agents for iron or copper. or a first agent containing a derivative thereof (2) a second agent containing a metal salt of iron or copper (3) a color that develops by reacting with the metal salt of iron or copper contained in the second agent A third agent containing a phenolic hydroxyl group, an enol-type hydroxyl group, or a compound having a similar hydroxyl group, or a compound having a carboxyl group, or a derivative thereof as an oxidizing agent (4) Bromates, perborates, or peroxide as an oxidizing agent Fourth Agent 2 Containing Hydrogen Water A hair treatment method in which hair is simultaneously subjected to a forming treatment such as a permanent wave and a hair dyeing treatment, and is characterized by comprising steps A to E listed below. hair treatment method. A Compounds containing thioglycolates or cysteine mercapto compounds as reducing agents, and compounds having phenolic hydroxyl groups, enol-type hydroxyl groups, or similar hydroxyl groups, or compounds having carboxyl groups as sequestering agents for iron or copper. Step B of shaping the hair into a desired shape while or after applying the first agent containing a derivative of Step C of applying a second agent containing a metal salt to the hair: After leaving it for a required period of time, the second agent remaining on the hair surface is removed by washing with water, and then the iron contained in the second agent is removed. Or a third compound containing a compound having a phenolic hydroxyl group, an enol type hydroxyl group, or a similar hydroxyl group, or a compound having a carboxyl group, or a derivative thereof as a coloring agent that develops color by reacting with a copper metal salt.
Step D of applying the agent to the hair; Next, Step E of applying a fourth agent containing bromate salts, perborate salts, or hydrogen peroxide as an oxidizing agent; and After leaving it for the required time, the hair is kept in a shape-retaining state. Step 3: Mix the second agent and the third agent, apply the mixture to the hair, leave it for a required period of time, and then wash with water to remove the residual agent on the hair surface. The hair treatment method according to claim 2, characterized in that the second agent and the third agent are removed, and then the fourth agent is applied. 4. The hair treatment method according to claim 2, wherein the third agent and the fourth agent are mixed and applied to the hair. 5. The hair treatment method according to claims 2 to 4, characterized in that the hair treatment is performed without shaping the hair into a specific shape.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27375085A JPS62132813A (en) | 1985-12-05 | 1985-12-05 | Agent for hair treatment and method therefor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27375085A JPS62132813A (en) | 1985-12-05 | 1985-12-05 | Agent for hair treatment and method therefor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62132813A JPS62132813A (en) | 1987-06-16 |
| JPH0160447B2 true JPH0160447B2 (en) | 1989-12-22 |
Family
ID=17532052
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27375085A Granted JPS62132813A (en) | 1985-12-05 | 1985-12-05 | Agent for hair treatment and method therefor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62132813A (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6466109A (en) * | 1987-09-04 | 1989-03-13 | Sanshidou Seiyaku Kk | Method for treating hair |
| JPH01238516A (en) * | 1988-03-18 | 1989-09-22 | Sansho Seiyaku Co Ltd | Hair dye and method for dyeing hair |
| JPH01249713A (en) * | 1988-03-30 | 1989-10-05 | Sansho Seiyaku Co Ltd | Hair dye |
| KR19980077541A (en) * | 1997-04-21 | 1998-11-16 | 박종호 | Simultaneous perm dye using direct hair dye and perm solution and preparation method |
| US6428580B2 (en) | 1997-08-20 | 2002-08-06 | L'oreal | Use of ascorbic acid in permanent waving and hair coloring compositions |
| EP1292266B1 (en) | 2000-06-20 | 2005-11-16 | Henkel Kommanditgesellschaft auf Aktien | Pyridoxine as novel coupling component for oxidative hair dyes |
| DK1292263T3 (en) * | 2000-06-20 | 2006-03-06 | Henkel Kgaa | Vitamin B6 derivatives as care components in the oxidative hair treatment |
| EP1292264B1 (en) * | 2000-06-20 | 2007-01-03 | Henkel Kommanditgesellschaft auf Aktien | Agent for dyeing or coloring and simultaneously protecting hair |
| MX369683B (en) * | 2014-12-05 | 2019-10-02 | Procter & Gamble | Composition for hair frizz reduction. |
| JP7108455B2 (en) * | 2018-04-24 | 2022-07-28 | ヘンケルジャパン株式会社 | Non-oxidizing hair dye and hair dyeing method |
-
1985
- 1985-12-05 JP JP27375085A patent/JPS62132813A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62132813A (en) | 1987-06-16 |
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