CN1503657A - 用于氧化性染发的新型偶合剂 - Google Patents
用于氧化性染发的新型偶合剂 Download PDFInfo
- Publication number
- CN1503657A CN1503657A CNA018190286A CN01819028A CN1503657A CN 1503657 A CN1503657 A CN 1503657A CN A018190286 A CNA018190286 A CN A018190286A CN 01819028 A CN01819028 A CN 01819028A CN 1503657 A CN1503657 A CN 1503657A
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- CN
- China
- Prior art keywords
- amino
- hair
- methyl
- phenol
- ethanol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 230000001590 oxidative effect Effects 0.000 title claims abstract description 15
- 230000037308 hair color Effects 0.000 title description 35
- 239000000203 mixture Substances 0.000 claims abstract description 60
- 210000004209 hair Anatomy 0.000 claims abstract description 57
- 150000001875 compounds Chemical class 0.000 claims abstract description 42
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 19
- 239000007822 coupling agent Substances 0.000 claims abstract description 15
- 238000004043 dyeing Methods 0.000 claims abstract description 13
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 8
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 7
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 6
- 125000005843 halogen group Chemical group 0.000 claims abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 21
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 19
- 239000000975 dye Substances 0.000 claims description 17
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- 239000007800 oxidant agent Substances 0.000 claims description 15
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 229910052740 iodine Inorganic materials 0.000 claims description 8
- 238000004040 coloring Methods 0.000 claims description 7
- ISCYHXYLVTWDJT-UHFFFAOYSA-N 2-[4-amino-n-(2-hydroxyethyl)anilino]ethanol Chemical compound NC1=CC=C(N(CCO)CCO)C=C1 ISCYHXYLVTWDJT-UHFFFAOYSA-N 0.000 claims description 6
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 6
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 claims description 5
- ALQKEYVDQYGZDN-UHFFFAOYSA-N 2-amino-6-methylphenol Chemical compound CC1=CC=CC(N)=C1O ALQKEYVDQYGZDN-UHFFFAOYSA-N 0.000 claims description 5
- FLROJJGKUKLCAE-UHFFFAOYSA-N 3-amino-2-methylphenol Chemical compound CC1=C(N)C=CC=C1O FLROJJGKUKLCAE-UHFFFAOYSA-N 0.000 claims description 5
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 5
- YGRFRBUGAPOJDU-UHFFFAOYSA-N 5-(2-hydroxyethylamino)-2-methylphenol Chemical compound CC1=CC=C(NCCO)C=C1O YGRFRBUGAPOJDU-UHFFFAOYSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 5
- 239000003153 chemical reaction reagent Substances 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 239000012279 sodium borohydride Substances 0.000 claims 2
- 229910000033 sodium borohydride Inorganic materials 0.000 claims 2
- 206010019049 Hair texture abnormal Diseases 0.000 claims 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 claims 1
- 239000012346 acetyl chloride Substances 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 125000002636 imidazolinyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract description 3
- -1 haloacetyl chloride Chemical compound 0.000 description 22
- 239000000543 intermediate Substances 0.000 description 19
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 16
- 229920000642 polymer Polymers 0.000 description 11
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 11
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 9
- 239000000118 hair dye Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000002562 thickening agent Substances 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- 229960001755 resorcinol Drugs 0.000 description 7
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 6
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 125000000623 heterocyclic group Chemical group 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 5
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 4
- 229940018563 3-aminophenol Drugs 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 4
- BKEFUBHXUTWQED-UHFFFAOYSA-N n-(4-amino-3-hydroxyphenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C(O)=C1 BKEFUBHXUTWQED-UHFFFAOYSA-N 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- HHVMYUPMJJDVPG-UHFFFAOYSA-N 1-(2,5-diaminophenyl)ethanol Chemical compound CC(O)C1=CC(N)=CC=C1N HHVMYUPMJJDVPG-UHFFFAOYSA-N 0.000 description 3
- JDTDIZGWSVNMDX-UHFFFAOYSA-N 1-(5-amino-2-hydroxyphenyl)ethane-1,2-diol Chemical compound NC1=CC=C(O)C(C(O)CO)=C1 JDTDIZGWSVNMDX-UHFFFAOYSA-N 0.000 description 3
- WCPGNFONICRLCL-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)ethanol Chemical compound NC1=CC=C(OCCO)C(N)=C1 WCPGNFONICRLCL-UHFFFAOYSA-N 0.000 description 3
- KWSVXCAQFTWTEF-UHFFFAOYSA-N 2-(2,5-diaminophenyl)ethanol Chemical compound NC1=CC=C(N)C(CCO)=C1 KWSVXCAQFTWTEF-UHFFFAOYSA-N 0.000 description 3
- SBUMIGFDXJIPLE-UHFFFAOYSA-N 2-(3-amino-4-methoxyanilino)ethanol Chemical compound COC1=CC=C(NCCO)C=C1N SBUMIGFDXJIPLE-UHFFFAOYSA-N 0.000 description 3
- KDBUTNSQYYLYOY-UHFFFAOYSA-N 2-(4,5-diaminopyrazol-1-yl)ethanol Chemical compound NC=1C=NN(CCO)C=1N KDBUTNSQYYLYOY-UHFFFAOYSA-N 0.000 description 3
- PBBRFJWECSDSDZ-UHFFFAOYSA-N 2-[2,4-diamino-5-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound NC1=CC(N)=C(OCCO)C=C1OCCO PBBRFJWECSDSDZ-UHFFFAOYSA-N 0.000 description 3
- BMTSZVZQNMNPCT-UHFFFAOYSA-N 2-aminopyridin-3-ol Chemical compound NC1=NC=CC=C1O BMTSZVZQNMNPCT-UHFFFAOYSA-N 0.000 description 3
- URPJUMVYJFHGOR-UHFFFAOYSA-N 2-benzylpyrazole-3,4-diamine Chemical compound NC1=C(N)C=NN1CC1=CC=CC=C1 URPJUMVYJFHGOR-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
- HWWIVWKTKZAORO-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-ol Chemical compound O1CCNC2=CC(O)=CC=C21 HWWIVWKTKZAORO-UHFFFAOYSA-N 0.000 description 3
- URWKQPHSJZKEOB-UHFFFAOYSA-N 3-(2,4-diaminophenoxy)propan-1-ol Chemical compound NC1=CC=C(OCCCO)C(N)=C1 URWKQPHSJZKEOB-UHFFFAOYSA-N 0.000 description 3
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000490 cosmetic additive Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
- YCIMNLLNPGFGHC-UHFFFAOYSA-N o-dihydroxy-benzene Natural products OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 150000004989 p-phenylenediamines Chemical class 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
- XGNXYCFREOZBOL-UHFFFAOYSA-N 1,3-benzodioxol-5-amine Chemical compound NC1=CC=C2OCOC2=C1 XGNXYCFREOZBOL-UHFFFAOYSA-N 0.000 description 2
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 2
- IYNWDOLJDNUWPD-UHFFFAOYSA-N 1-(2,5-diaminophenyl)ethane-1,2-diol Chemical compound NC1=CC=C(N)C(C(O)CO)=C1 IYNWDOLJDNUWPD-UHFFFAOYSA-N 0.000 description 2
- XAWPKHNOFIWWNZ-UHFFFAOYSA-N 1h-indol-6-ol Chemical compound OC1=CC=C2C=CNC2=C1 XAWPKHNOFIWWNZ-UHFFFAOYSA-N 0.000 description 2
- ORVPXPKEZLTMNW-UHFFFAOYSA-N 1h-indol-7-ol Chemical compound OC1=CC=CC2=C1NC=C2 ORVPXPKEZLTMNW-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- BYYOWEYWJDNTBJ-UHFFFAOYSA-N 2-[(4-methylphenyl)methyl]pyrazole-3,4-diamine Chemical compound C1=CC(C)=CC=C1CN1C(N)=C(N)C=N1 BYYOWEYWJDNTBJ-UHFFFAOYSA-N 0.000 description 2
- ZMXYNJXDULEQCK-UHFFFAOYSA-N 2-amino-p-cresol Chemical compound CC1=CC=C(O)C(N)=C1 ZMXYNJXDULEQCK-UHFFFAOYSA-N 0.000 description 2
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 2
- SRJCJJKWVSSELL-UHFFFAOYSA-N 2-methylnaphthalen-1-ol Chemical compound C1=CC=CC2=C(O)C(C)=CC=C21 SRJCJJKWVSSELL-UHFFFAOYSA-N 0.000 description 2
- OBOSXEWFRARQPU-UHFFFAOYSA-N 2-n,2-n-dimethylpyridine-2,5-diamine Chemical compound CN(C)C1=CC=C(N)C=N1 OBOSXEWFRARQPU-UHFFFAOYSA-N 0.000 description 2
- RGKJLNMYCNSVKZ-UHFFFAOYSA-N 4-amino-2-(methoxymethyl)phenol Chemical compound COCC1=CC(N)=CC=C1O RGKJLNMYCNSVKZ-UHFFFAOYSA-N 0.000 description 2
- NLMQHXUGJIAKTH-UHFFFAOYSA-N 4-hydroxyindole Chemical compound OC1=CC=CC2=C1C=CN2 NLMQHXUGJIAKTH-UHFFFAOYSA-N 0.000 description 2
- XCJRRZLPXALCIP-UHFFFAOYSA-N 4-n-(2-methoxyethyl)benzene-1,4-diamine Chemical compound COCCNC1=CC=C(N)C=C1 XCJRRZLPXALCIP-UHFFFAOYSA-N 0.000 description 2
- LMIQERWZRIFWNZ-UHFFFAOYSA-N 5-hydroxyindole Chemical compound OC1=CC=C2NC=CC2=C1 LMIQERWZRIFWNZ-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
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- 239000004215 Carbon black (E152) Substances 0.000 description 2
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-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
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- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
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- 230000003113 alkalizing effect Effects 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
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- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
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- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
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- 229940008099 dimethicone Drugs 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
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- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- ZUVBIBLYOCVYJU-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21 ZUVBIBLYOCVYJU-UHFFFAOYSA-N 0.000 description 2
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229960004063 propylene glycol Drugs 0.000 description 2
- 235000013772 propylene glycol Nutrition 0.000 description 2
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000003384 small molecules Chemical class 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
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- WEPOCTWSRWLQLL-UHFFFAOYSA-N 6-methoxypyridine-2,3-diamine Chemical compound COC1=CC=C(N)C(N)=N1 WEPOCTWSRWLQLL-UHFFFAOYSA-N 0.000 description 1
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 244000144927 Aloe barbadensis Species 0.000 description 1
- 235000002961 Aloe barbadensis Nutrition 0.000 description 1
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- JRBRAWYBYWPDQZ-UHFFFAOYSA-N C1(=CC=CC=C1)O.CC1=C(O)C=CC=C1O Chemical compound C1(=CC=CC=C1)O.CC1=C(O)C=CC=C1O JRBRAWYBYWPDQZ-UHFFFAOYSA-N 0.000 description 1
- QZKVOTIRXPHRSS-UHFFFAOYSA-N C1(CCCC=C1)O.C1=CC=CC=C1 Chemical compound C1(CCCC=C1)O.C1=CC=CC=C1 QZKVOTIRXPHRSS-UHFFFAOYSA-N 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 244000208060 Lawsonia inermis Species 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 1
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920000289 Polyquaternium Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Chemical class 0.000 description 1
- OYDQPYUVQAHEJH-UHFFFAOYSA-N [3-(dimethylamino)phenyl]urea Chemical compound CN(C)C1=CC=CC(NC(N)=O)=C1 OYDQPYUVQAHEJH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- 235000011399 aloe vera Nutrition 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 229920006318 anionic polymer Polymers 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
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- FLNKWZNWHZDGRT-UHFFFAOYSA-N azane;dihydrochloride Chemical compound [NH4+].[NH4+].[Cl-].[Cl-] FLNKWZNWHZDGRT-UHFFFAOYSA-N 0.000 description 1
- WBOXZLRDVULSGV-UHFFFAOYSA-N azanium;ethyl sulfate Chemical compound [H+].N.CCOS([O-])(=O)=O WBOXZLRDVULSGV-UHFFFAOYSA-N 0.000 description 1
- 229940106010 beheneth-25 Drugs 0.000 description 1
- YSJGOMATDFSEED-UHFFFAOYSA-M behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 1
- 229960002233 benzalkonium bromide Drugs 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- KHSLHYAUZSPBIU-UHFFFAOYSA-M benzododecinium bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 KHSLHYAUZSPBIU-UHFFFAOYSA-M 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- OCBHHZMJRVXXQK-UHFFFAOYSA-M benzyl-dimethyl-tetradecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 OCBHHZMJRVXXQK-UHFFFAOYSA-M 0.000 description 1
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- UWTDFICHZKXYAC-UHFFFAOYSA-N boron;oxolane Chemical compound [B].C1CCOC1 UWTDFICHZKXYAC-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 229940096584 c12-15 pareth-3 Drugs 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 229940078916 carbamide peroxide Drugs 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- SXPWTBGAZSPLHA-UHFFFAOYSA-M cetalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SXPWTBGAZSPLHA-UHFFFAOYSA-M 0.000 description 1
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- 229960000541 cetyl alcohol Drugs 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- 230000008859 change Effects 0.000 description 1
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- BVQUETZBXIMAFZ-UHFFFAOYSA-N chembl1328567 Chemical compound C1=CC=C2C(=O)C(O)=C(O)C(=O)C2=C1 BVQUETZBXIMAFZ-UHFFFAOYSA-N 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 1
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- WLCFKPHMRNPAFZ-UHFFFAOYSA-M didodecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC WLCFKPHMRNPAFZ-UHFFFAOYSA-M 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 125000004990 dihydroxyalkyl group Chemical group 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- RHZNQEWFWUODFC-UHFFFAOYSA-N ethyl(dimethyl)azanium;ethyl sulfate Chemical compound CC[NH+](C)C.CCOS([O-])(=O)=O RHZNQEWFWUODFC-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 210000004919 hair shaft Anatomy 0.000 description 1
- CGFLXNWWUXLUIX-UHFFFAOYSA-M hexadecyl-(2-hydroxyethyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCO CGFLXNWWUXLUIX-UHFFFAOYSA-M 0.000 description 1
- KDNFLUWYIMPBSA-UHFFFAOYSA-N hydrogen peroxide;1,3,5-triazine-2,4,6-triamine Chemical compound OO.NC1=NC(N)=NC(N)=N1 KDNFLUWYIMPBSA-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 239000008206 lipophilic material Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 150000004988 m-phenylenediamines Chemical class 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 description 1
- 229960004963 mesalazine Drugs 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- MLKPMOZMNCKWGN-UHFFFAOYSA-N n-[2-(2,5-diaminophenoxy)ethyl]acetamide Chemical compound CC(=O)NCCOC1=CC(N)=CC=C1N MLKPMOZMNCKWGN-UHFFFAOYSA-N 0.000 description 1
- JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- TYRGSDXYMNTMML-UHFFFAOYSA-N propyl hydrogen sulfate Chemical compound CCCOS(O)(=O)=O TYRGSDXYMNTMML-UHFFFAOYSA-N 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 1
- UBUFOHLVTQZEQF-UHFFFAOYSA-N pyridine-2,3,4,6-tetramine Chemical compound NC1=CC(N)=C(N)C(N)=N1 UBUFOHLVTQZEQF-UHFFFAOYSA-N 0.000 description 1
- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- 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
- A61K8/416—Quaternary ammonium compounds
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/74—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C215/76—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton of the same non-condensed six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
用于氧化性染发的染发组合物的偶合剂为式(1)的化合物:如右式其中X选自卤素;R3选自C1-C2烷基和羟基乙基;R、R1和R2各自独立选自C1-C22烷基或C1-C22一或二烷基,或R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族基团或C3-C14芳族基团,该环脂族基团或芳族基团可任选地在其环上包含一个或多个选自O、S和N的杂原子。
Description
发明领域
本发明涉及用于与一种或多种氧化剂结合使用,包含一种或多种氧化性染发剂的染发组合物的新型偶合剂。本发明还涉及此类新型偶合剂的染发组合物,并涉及使用含有此类偶合物的组合物染发。
发明背景
染发是一种源于古代实践的、使用多种方法的过程。在现代,最为广泛使用的染发方法是通过一种氧化性染发方法进行染发,该方法是利用把一种或多种氧化性染发剂和一种或多种氧化剂结合使用的染发系统。
最为普遍的是一种过氧氧化剂与一种或多种氧化性染发剂结合使用,通常是能扩散到头发中的小分子并包含一种或多种主要中间体和一种或多种偶合剂。在这一过程中,一种过氧化物如过氧化氢用于活化主要中间体的小分子,以使其能与偶合剂反应在发轴处形成更大尺寸的化合物,使得可以进行多种不同颜色、色彩深浅的染发。
在这种氧化性染发系统和组合物中可以使用多种主要中间体和偶合剂。在主要中间体中可以使用对苯二胺、对甲苯二胺、对氨基酚、4-氨基-3-甲基苯酚,偶合剂可以使用间苯二酚、2-甲基间苯二酚、3-氨基酚和5-氨基-2-甲基苯酚。使用基于对苯二胺的染料可产生大多数深浅不同的颜色。
为了能将头发染成橙色,2-甲基-5-氨基酚被广泛地与对氨基酚结合使用作为主要中间体。然而,头发上得到的橙色在暴露于光线或洗发时会发生很大变化。美国专利4,065,255和欧洲专利634165 Al和EP 667143 Al建议使用2-甲基-5-N-羟乙基氨基苯酚、2-甲基-5-烷基氨基苯酚和2-甲基-5-氨基酚作为偶合剂。因而,需要一种新的橙色偶合剂用于氧化性染发组合物和系统。
发明概述
本发明提供一种式(1)的新型偶合剂:
其中X选自卤素,此处卤素优选为Cl、Br或I;R3选自C1-C2烷基和羟基乙基;R、R1和R2各自独立选自C1-C22烷基或C1-C22一或二羟烷基或R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族或C3-C14芳族基团,该环脂族或芳族基团可任选地在其环上包含一个或多个选自O、S和N的杂原子。这些新型偶合剂用于提供一种毛发染色,对头发具有良好的着色性并提供能够在相对较长时间内稳定的颜色。该新型偶合剂提供一种染发方法使得染后的颜色具有良好的洗涤不褪色性,在暴露于光线或冲洗时不会象使用2-甲基-5-氨基酚一样产生明显的变化。
发明详述
本发明中优选的偶合剂化合物如式(1)所示:
其中X为Cl、Br或I;R3为甲基、乙基或羟基乙基;R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族或C3-C6芳族基团,该基团可任选地在其环上包含另外的N原子。
本发明中尤其优选的偶合剂为下列化合物:
1-[2-(3-羟基-4-甲基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
1-[2-(3-羟基-4-乙基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
1-[2-(3-羟基-4-羟基乙基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
1-[2-(3-羟基-4-甲基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓溴化物;
1-[2-(3-羟基-4-甲基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓碘化物;
1-[2-(3-羟基-4-乙基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓丙基硫酸化物;
N-[2-(3-羟基-4-甲基-苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-乙基-苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-羟基乙基-苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-甲基-苯氨基)-乙基-N′-甲基-哌啶鎓溴化物;和
N-[2-(3-羟基-4-甲基-苯氨基)-乙基-N′-甲基-哌啶鎓碘化物;
本发明中式(1)的化合物根据以下反应顺序很容易制备;
在反应顺序中,溶在四氢呋喃(THF)中的一种式(2)的氨基酚溶液加入到一种卤代乙酰氯的溶液中,生成一种式(5)的化合物。用一种硼烷-THF络合物处理式(5)的化合物生成一种式(6)的化合物,该化合物再与一种式N(R1)(R2)(R3)的季铵化试剂反应生成一种式(1)的化合物。
合成实例1-10
在上述的合成过程中,使用适宜的氨基酚、卤代乙酰氯和N(R1)(R2)(R3)季铵化试剂,可以制备本发明的下列偶合剂化合物。
1-[2-(3-羟基-4-甲基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
N-[2-(3-羟基-4-甲基-苯氨基)-乙基-N′-甲基-哌啶鎓基啶鎓氯化物;
1-[2-(3-羟基-4-乙基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
l-[2-(3-羟基-4-羟基乙基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
1-[2-(3-羟基-4-甲基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓溴化物;
1-[2-(3-羟基-4-甲基-苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓碘化物;
N-[2-(3-羟基-4-乙基-苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-羟基乙基-苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-甲基-苯氨基)-乙基-N′-甲基-哌啶鎓溴化物;和
N-[2-(3-羟基-4-甲基-苯氨基)-乙基-N′-甲基-哌啶鎓碘化物;
本发明中的染发组合物可包含将本发明的新型偶合剂作为唯一的偶合剂,或者也可包含其它的偶合剂与主要中间体结合。
为得到本发明中的染发组合物,可以把一种或多种适宜的主要中间体与本发明中的新型偶合剂结合使用。适宜的主要中间体包括,例如,
对苯二胺衍生物例如:苯-1,4-二胺(一般称为对苯二胺),2-甲基-苯-1,4-二胺,2-氯代-苯-1,4-二胺,N-苯基-苯-1,4-二胺,N-(2-乙氧基乙基)苯-1,4-二胺,2-[(4-氨基苯基)-(2-羟基乙基)-氨基]-乙醇(一般称为N,N-二(2-羟基乙基)-对苯二胺),(2,5-二氨基苯基)-甲醇,1-(2,5-二氨基苯基)-乙醇,2-(2,5-二氨基苯基)-乙醇,N-(4-氨基苯基)苯-1,4-二胺,2,6-二甲基-苯-1,4-二胺,2-异丙基-苯-1,4-二胺,1-[(4-氨基苯基)氨基]-丙烷-2-醇,2-丙基-苯-1,4-二胺,1,3-二[(4-氨基苯基)(2-羟基乙基)氨基]丙烷-2-醇,N4,N4,2-三甲基苯-1,4-二胺,2-甲氧基苯-1,4-二胺,1-(2,5-二氨基苯基)乙烷-1,2-二醇,2,3-二甲基-苯-1,4-二胺,N-(4-氨基-3-羟基苯基)-乙酰胺,2,6-二乙基苯-1,4-二胺,2,5-二甲基苯-1,4-二胺,2-噻吩-2-基苯-1,4-二胺,2-噻吩-3-基苯-1,4-二胺,2-吡啶-3-基苯-1,4-二胺,1,1′-联苯-2,5-二胺,2-(甲氧基甲基)苯-1,4-二胺,2-(氨基甲基)苯-1,4-二胺,2-(2,5-二氨基苯氧基)乙醇,N-[2-(2,5-二氨基苯氧基)乙基]-乙酰胺,N,N-二甲基苯-1,4-二胺,N,N-二乙基苯-1,4-二胺,N,N-二丙基苯-1,4-二胺,2-[(4-氨基苯基)(乙基)氨基]乙醇,2-[(4-氨基-3-甲基苯基)-(2-羟基乙基)-氨基]-乙醇,N-(2-甲氧基乙基)-苯-1,4-二胺,3-[(4-氨基苯基)氨基]丙烷-1-醇,3-[(4-氨基苯基)-氨基]丙烷-1,2-二醇,N-{4-[(4-氨基苯基)氨基]丁基}苯-1,4-二胺以及2-[2-(2-{2-[(2,5-二氨基苯基)-氧]乙氧基}乙氧基)乙氧基]苯-1,4-二胺;
氨基酚的衍生物如:4-氨基酚(一般称为对氨基酸),4-甲基氨基-苯酚,4-氨基-3-甲基苯酚,4-氨基-2-羟甲基苯酚,4-氨基-2-甲基苯酚,4-氨基-2-[(2-羟基-乙基氨基)-甲基]-苯酚,4-氨基-2-甲氧基甲基苯酚,5-氨基-2-羟基苯甲酸,1-(5-氨基-2-羟基苯基)-乙烷-1,2-二醇,4-氨基-2-(2-羟基乙基)-苯酚,4-氨基-3-(羟甲基)苯酚,4-氨基-3-氟代苯酚,4-氨基-2-(氨甲基)-苯酚,以及4-氨基-2-氟代苯酚;
邻氨基酚的衍生物如:2-氨基酚(一般称为邻氨基酚),2,4-二氨基苯酚,2-氨基-5-甲基苯酚,2-氨基-6-甲基苯酚,N-(4-氨基-3-羟基苯基)-乙酰胺,以及2-氨基-4-甲基苯酚;和
杂环衍生物如:嘧啶-2,4,5,6-四胺(一般称为2,4,5,6-四氨基吡啶),1-甲基-1H-吡唑-4,5-二胺,2-(4,5-二氨基-1H-吡唑-1-基)乙醇,N2,N2-二甲基-吡啶-2,5-二胺,2-[(3-氨基-6-甲氧基吡啶-2-基)氨基]乙醇,6-甲氧基-N2-甲基-吡啶-2,3-二胺,2,5,6-三氨基嘧啶-4(1H)-酮,吡啶-2,5-二胺,1-异丙基-1H-吡唑-4,5-二胺,1-(4-甲苄基)-1H-吡唑-4,5-二胺,1-(苄基)-1H-吡唑-4,5-二胺和1-(4-氯苄基)-1H-吡唑-4,5-二胺。
本发明中式(1)的偶合剂可以与本发明中染发组合物或系统中应用的其它任意适宜的偶合剂一起使用。
适宜的为人熟知的偶合剂包括,例如:
苯酚,间苯二酚和萘酚的衍生物例如:萘-1,7-二酚,苯-1,3-二酚,4-氯苯-1,3-二酚,萘-1-酚,2-甲基-萘-1-酚,萘-1,5-二酚,萘-2,7-二酚,苯-1,4-二酚,2-甲基-苯-1,3-二酚,7-氨基-4-羟基-萘-2-磺酸,2-异丙基-5-甲基苯酚,1,2,3,4-四氢-萘-1,5-二酚,2-氯苯-1,3-二酚,4-羟基-萘-1-磺酸,苯-1,2,3-三元酚,萘-2,3-二酚,5-二氯-2-甲苯-1,3-二酚,4,6-二氯苯-1,3-二酚,和2,3-二羟基-[1,4]萘醌;
间苯二胺如:2,4-二氨基苯酚,苯-1,3-二胺,2-(2,4-二氨基苯氧基)-乙醇,2-[(3-氨基苯基)-(2-羟基乙基)-氨基]-乙醇,2-甲基-苯-1,3-二胺,2-[[2-(2,4-二氨基苯氧基)-乙基]-(2-羟基乙基)-氨基]-乙醇,4-{3-[(2,4-二氨基苯酚)氧]丙氧基}苯-1,3-二胺,2-(2,4-二氨基-苯基)-乙醇,2-(3-氨基-4-甲氧基-苯氨基)-乙醇,4-(2-氨基-乙氧基)-苯-1,3-二胺,(2,4-二氨基苯氧基)-乙酸,2-[2,4-二氨基-5-(2-羟基乙氧基)-苯氧基]-乙醇,4-乙氧基-6-甲基-苯-1,3-二胺,2-(2,4-二氨基-5-甲基-苯氧基)-乙醇,4,6-二甲氧基-苯-1,3-二胺,2-[3-(2-羟基-乙氨基)-2-甲基-苯氨基]-乙醇,3-(2,4-二氨基苯氧基)-丙烷-1-醇,N-[3-(二甲基氨基)苯基]尿素,4-甲氧基-6-甲苯-1,3-二胺,4-氟代--6-甲苯-1,3-二胺,2-({3-[(2-羟基乙基)氨基]-4,6-二甲氧基苯酚}-氨基)乙醇,3-(2,4-二氨基苯氧基)-丙烷-1,2-二醇,2-[2-氨基-4-(甲氨基)-苯氧基]乙醇,2-[(5-氨基-2-乙氧基-苯基)-(2-羟基乙基)-氨基]-乙醇,2-[(3-氨基苯基)氨基]乙醇,N-(2-氨基乙基)苯-1,3-二胺,4-{[(2,4-二氨基-苯基)氧]甲氧基}-苯-1,3-二胺,以及2,4-二甲氧基苯-1,3-二胺;
间氨基酚如:3-氨基酚,2-(3-羟基-4-甲基-苯氨基)-乙酰胺,2-(3-羟基-苯氨基)-乙酰胺,5-氨基-2-甲基苯酚,5-(2-羟基-乙氨基)-2-甲基苯酚,5-氨基-2,4-二氯-苯酚,3-氨基-2-甲基苯酚,3-氨基-2-氯代-6-甲基苯酚,5-氨基-2-(2-羟基乙氧基)-苯酚,2-氯代-5-(2,2,2-三氟代-乙氨基)-苯酚,5-氨基-4-氯代-2-甲基苯酚,3-环戊氨基-苯酚,5-[(2-羟基乙基)氨基]-4-甲氧基-2-甲基苯酚,5-氨基-4-甲氧基-2-甲基苯酚,3-(二甲基氨基)苯酚,3-(二乙基氨基)苯酚,5-氨基-4-氟代-2-甲基苯酚,5-氨基-4-乙氧基-2-甲基苯酚,3-氨基-2,4-二氯代-苯酚,3-[(2-甲氧基乙基)氨基]苯酚,3-[(2-羟基乙基)氨基]苯酚,5-氨基-2-乙基-苯酚,5-氨基-2-甲氧基苯酚,5-[(3-羟丙基)氨基]-2-甲基苯酚,3-[(3-羟基-2-甲基苯基)-氨基]丙烷-1,2-二醇,以及3-[(2-羟基乙基)氨基]-2-甲基苯酚;和
杂环衍生物如:3,4-二氢-2H-1,4-苯并噁嗪-6-酚,4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮,6-甲氧基喹啉-8-胺,4-甲基吡啶-2,6-二酚,2,3-二氢-1,4-苯并二噁英-5-酚,1,3-苯并二噁茂-5-酚,2-(1,3-苯并二噁茂-5-基氨基)乙醇,3,4-二甲基吡啶-2,6-二酚,5-氯代吡啶-2,3-二酚,2,6-二甲氧基吡啶-3,5-二胺,1,3-苯并二噁茂-5-胺,2-{[3,5-二氨基-6-(2-羟基乙氧基)-吡啶-2-基]氧}-乙醇,1H-吲哚-4-酚,5-氨基-2,6-二甲氧基吡啶-3-酚,1H-吲哚-5,6-二酚,1H-吲哚-7-酚,1H-吲哚-5-酚,1 H-吲哚-6-酚,6-溴代-1,3-苯并二噁茂-5-酚,2-氨基吡啶-3-酚,吡啶-2,6-二胺,3-[(3,5-二氨基吡啶-2-基)氧]丙烷-1,2-二醇,5-[(3,5-二氨基吡啶-2-基)氧]戊烷-1,3-二醇,1H-吲哚-2,3-二酮,吲哚-5,6-二酚,3,5-二甲氧基吡啶-2,6-二胺,6-甲氧基吡啶-2,3-二胺,以及3,4-二氢-2H-1,4-苯并噁嗪-6-胺。
优选的主要中间体包括:
对苯二胺衍生物例如:2-甲苯-1,4-二胺,苯-1,4-二胺,1-(2,5-二氨基-苯基)-乙醇,2-(2,5-二氨基-苯基)-乙醇,N-(2-甲氧基乙基)苯-1,4-二胺,2-[(4-氨基苯基)-(2-羟基乙基)-氨基]-乙醇,以及1-(2,5-二氨基苯基)乙烷-1,2-二醇;
对氨基酚的衍生物如4-氨基酚,4-甲氨基-苯酚,4-氨基-3-甲基苯酚,4-氨基-2-甲氧基甲基苯酚,以及1-(5-氨基-2-羟基苯基)-乙烷-1,2-二醇;
邻氨基酚的衍生物如:2-氨基酚,2-氨基-5-甲基苯酚,2-氨基-6-甲基苯酚,N-(4-氨基-3-羟基苯基)-乙酰胺,以及2-氨基-4-甲基苯酚;
杂环衍生物如:嘧啶-2,4,5,6-四胺,1-甲基-1H-吡唑-4,5-二胺,2-(4,5-二氨基-1H-吡唑-1-基)乙醇,1-(4-甲基苄基)-1H-吡唑-4,5-二胺,1-(苄基)-1H-吡唑-4,5-二胺以及N2,N2-二甲基-吡啶-2,5-二胺。
优选的偶合剂包括:
苯酚,间苯二酚和萘酚的衍生物例如:萘-1,7-二酚,苯-1,3-二酚,4-氯苯-1,3-二酚,萘-1-酚,2-甲基-萘-1-酚,萘-1,5-二酚,萘-2,7-二酚,苯-1,4-二酚,2-甲苯-1,3-二酚,以及2-异丙基-5-甲基苯酚;
间苯二胺如:苯-1,3-二胺,2-(2,4-二氨基苯氧基)-乙醇,4-{3-[(2,4-二氨基苯基)氧]丙氧基}苯-1,3-二胺,2-(3-氨基-4-甲氧基-苯氨基)-乙醇,2-[2,4-二氨基-5-(2-羟基乙氧基)-苯氧基]-乙醇,以及3-(2,4-二氨基苯氧基)-丙烷-1-醇;
间氨基酚如:3-氨基酚,5-氨基-2-甲基苯酚,5-(2-羟基-乙氨基)-2-甲基苯酚,以及3-氨基-2-甲基苯酚;和
杂环衍生物如:3,4-二氢-2H-1,4-苯并噁嗪-6-酚,4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮,1,3-苯并二噁茂-5-酚,1,3-苯并二噁茂-5-胺,1H-吲哚-4-酚,1H-吲哚-5,6-二酚,1H-吲哚-7-酚,1H-吲哚-5-酚,1H-吲哚-6-酚,1H-吲哚-2,3-二酮,吡啶-2,6-二胺,以及2-氨基吡啶-3-酚。
最优选的主要中间体包括:
对苯二胺衍生物例如:2-甲苯-1,4-二胺,苯-1,4-二胺,2-(2,5-二氨基苯基)-乙醇,1-(2,5-二氨基苯基)-乙醇,以及2-[(4-氨基苯基)-(2-羟基乙基)-氨基]-乙醇;
对氨基酚的衍生物如:4-氨基酚,4-甲氨基-苯酚,4-氨基-3-甲基苯酚,以及1-(5-氨基-2-羟基苯基)-乙烷-1,2-二醇;
邻氨基酚如:2-氨基酚,2-氨基-5-甲基苯酚,2-氨基-6-甲基苯酚,以及N-(4-氨基-3-羟基苯基)-乙酰胺;和
杂环衍生物如:嘧啶-2,4,5,6-四胺,2-(4,5-二氨基-1H-吡唑-1-基)乙醇,1-(4-甲基苄基)-1H-吡唑-4,5-二胺,以及1-(苄基)-1H-吡唑-4,5-二胺。
最优选的偶合剂包括:
苯酚,间苯二酚和萘酚的衍生物例如:苯-1,3-二酚,4-氯苯-1,3-二酚,萘-1-酚,2-甲基-萘-1-酚,和2-甲苯-1,3-二酚;
间苯二胺如:2-(2,4-二氨基苯氧基)-乙醇,2-(3-氨基-4-甲氧基苯氨基)-乙醇,2-[2,4-二氨基-5-(2-羟基乙氧基)-苯氧基]-乙醇,以及3-(2,4-二氨基苯氧基)-丙烷-1-醇;
间氨基酚如:3-氨基酚,5-氨基-2-甲基苯酚,5-(2-羟基乙氨基)-2-甲基苯酚,以及3-氨基-2-甲基苯酚;和
杂环衍生物如:3,4-二氢-2H-1,4-苯并噁嗪-6-酚,4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮,1H-吲哚-6-酚以及2-氨基吡啶-3-酚。
可以理解,偶合剂化合物和主要中间体化合物以及其它染料化合物,就它们作为为碱而言,可以用以游离碱,或以与有机或无机酸如盐酸或硫酸生成的相应的盐的形式存在,或者,就它们具有芳香族羟基而言,可以以与碱反应生成的盐的形式,例如碱性酚盐的形式存在。
本发明中用在染发组合物或系统中的染料前体化合物(例如主要中间体和偶合剂化合物)的总量一般占染发组合物总重量的约0.001%至10%,优选约0.02%至10%,更优选为约0.2%至6.0%。主要中间体和偶合剂化合物一般等量使用。然而,也可能使用过量或不足的主要中间体化合物,即主要中间体与偶合剂的摩尔比一般在约5∶1至约1∶5的范围内。
本发明中的染发组合物包含有效染发剂量的偶合剂,一般在染发组合物中的量按重量计为约0.001%至约6%,优选为约0.01%至约3.5%。其它偶合剂,如果添加,通常的量为使得偶合剂在组合物中的总浓度按重量百分比计为约0.01%至6%。主要中间体以有效染发浓度存在,通常其量按重量计占染发组合物的约0.001%至约6.0%,优选为约0.01%至3.5%。可使用任何合适的载体或赋形剂,通常使用一种水溶液或水醇溶液,优选一种水溶液。载体或赋形剂所占的质量百分比通常可达约40%。
本发明中的染发组合物可包含一种或多种阳离子、阴离子或两性表面活性剂、香料、抗氧化剂、螯合剂、增稠剂、碱化或酸化剂以及其它染发试剂。
本发明的组合物通过与适宜的氧化剂混合来使用,氧化剂与毛发染料前体作用产生染发效果。任何适宜的过氧化物提供剂均可使用在本发明的染发组合物中,尤其是过氧化氢(H2O2)或其前体。同样适宜的有过氧化脲,过硼酸钠,过碳酸钠,以及过氧化三聚氰胺。
此外,通常用于染发组合物的化妆品添加剂成分也可用于本发明的染发组合物,例如抗氧化剂,如抗坏血酸、巯基乙酸或亚硫酸钠、香料油、成形络合物、润湿剂、乳化剂、增稠剂以及保养材料。
根据本发明的染发组合物的形态可以是,例如溶液,尤其是水溶液或水醇溶液。然而,特别优选的形态为霜膏、凝胶或乳液。该组合物为染料成分与适宜于特殊制备的常规的化妆品添加剂成分的混合物。
在溶液、霜膏、乳液或凝胶中的常规的化妆品用添加剂成分包括,例如:
溶剂:除了水,可以使用的溶剂为低级链烷醇(例如乙醇,丙醇,异丙醇);多元醇(例如,卡必醇,丙二醇,甘油)。在适宜的方法中,高级醇例如鲸蜡醇,在引入其它材料通常为亲脂材料之前,如果先将其在低温(50至80℃)下熔化液化,就适于作为有机溶剂。参见WO 98/27941(稀释剂部分),并入本文以供参考。
阴离子和非离子表面活性剂:这些材料可以在阴离子,阳离子,两性的或非离子表面活性剂化合物的种类中选择,例如硫酸脂肪醇,乙氧基化的硫酸脂肪醇,烷基磺酸盐,烷基苯磺酸盐,烷基三甲基铵盐,烷基三甲铵乙内酯,乙氧基化的脂肪醇,乙氧基化的壬基苯酚,脂肪酸链烷醇酰胺和乙氧基化的脂肪酸酯。包含这些活性剂的原因有多种,例如,辅助增厚,用于形成乳液,在使用染发组合物时助润湿头发,等。适宜的材料为烷基硫酸盐,乙氧基化的烷基硫酸盐,烷基甘油醚磺酸盐,甲酰基牛磺酸盐,酰基羟乙基磺酸盐,烷基乙氧基羧酸盐,脂肪酸一和二乙醇酰胺。参考文献见1998年11月26日公告的专利WO 98/52523,引入本文以供参考。
增稠剂:适宜的增稠剂包括如高级脂肪醇,淀粉,纤维素衍生物,凡士林,石蜡油,脂肪酸和基于聚丙烯酸和聚氨酯聚合物的阴离子及非离子聚合增稠剂。实例为羟乙基纤维素,羟甲基纤维素和其它纤维素衍生物,疏水改性的阴离子聚合物和非离子聚合物,尤其是同时具有亲水和疏水部分聚合物(例如两亲聚合物。可用的非离子聚合物包括聚氨酯衍生物如PEG-150/硬脂醇/SDMI共聚物和PEG-150/硬脂醇SDMI共聚物。其它可用的两亲聚合物如美国专利6010541中所述,引入本文以供参考。可以用作增稠剂的阴离子聚合物例子为丙烯酸盐共聚物,丙烯酸盐/十六烷基聚氧乙烯醚-20异丁烯酸盐共聚物,丙烯酸盐/十六烷基聚氧乙烯醚-20衣康酸盐共聚物和丙烯酸盐/二十二烷基聚氧乙烯醚-25丙烯酸盐共聚物。以及Rohm &Haas销售的Aculyn聚合物,以及毛发保养材料,例如阳离子树脂,羊毛脂衍生物,胆固醇,泛酸和内铵盐。
碱化剂:用于增加染发组合物的pH值的适宜的材料包括氨水,氨基甲基丙醇,甲基乙醇胺,三乙醇胺和胆胺。
调节剂:适宜的材料包括聚硅氧烷和聚硅氧烷衍生物;烃油脂;单体四价化合物和季铵化的聚合物。单体四价化合物是典型的阳离子化合物,但也可包括内铵盐和其它两性的和两性离子材料。适宜的单体四价化合物包括二十二烷基三烷基氯化铵,二十二烷基三甲基氯化铵,苄烷铵溴化物或氯化物,苄基三乙基氯化铵,双-羟基乙基牛油甲基氯化铵,C12-18二烷基二甲基氯化铵,十六烷基二甲基苄基氯化铵,十六烯基三甲铵溴化物和氯化物,十六烷基三甲铵地溴化物、氯化物和甲基硫酸化物,十六烷基吡啶氯化铵,椰油酰氨基丙基乙基二甲基乙基硫酸铵,椰油酰氨基丙基乙基硫酸铵,椰油乙基二甲基乙基硫酸铵,椰油三甲铵氯化物和乙基硫酸化物,二-二十二烷基二甲基氯化铵,二-十六烷基二甲基氯化铵,二椰油二甲基氯化铵,二月桂二甲基氯化铵,二大豆二甲基氯化铵,二牛油二甲基氯化铵,氢化牛油三甲基氯化铵,羟乙基鲸蜡基二甲基氯化铵,十四烷二甲基苄基氯化铵,油酸二甲基苄基氯化铵,大豆乙基甲基乙基硫酸铵,大豆三甲基氯化铵,硬脂基二甲基苄基氯化铵和许多其它化合物。参见WO 98/27941,引入本文以供参考。季铵化的聚合物典型的是阳离子聚合物,但也可包括两性和两性离子聚合物。可用的聚合物有例如聚季铵-4,聚季铵-6,聚季铵-7,聚季铵-8,聚季铵-9,聚季铵-10,聚季铵-22,聚季铵-32,聚季铵-39,聚季铵-44和聚季铵-47。适宜于护发的聚硅氧烷有二甲聚硅氧烷,氨代二甲聚硅氧烷,二甲聚硅氧烷多元醇共聚物和二甲聚硅氧烷醇。适宜的聚硅氧烷参见1999年7月15日公告的专利WO 99/34770,引入本文以供参考。适宜的烃类油包括矿物油。
天然成分:例如,蛋白质衍生物、芦荟汁、洋甘菊和散沫花叶粉提取物。
其它辅助剂包括降低pH值的酸化剂,缓冲剂,螯合抗氧化剂,多价螯合剂,等。上文提到的但并未特殊指出的此类和其它种类适宜的材料在由The Cosmetics,Toiletry,and Fragrance Association 出版的InternationalCosmetics Ingredient Dictionary and Handbook(第八版)中列出,引入本文以供参考。特别参考第3部分第2卷(化学类))和第4部分(功能),这些部分在确定可获得特殊或多种用途的具体的辅助剂/赋形剂时很有帮助。
上文提及的常规的化妆品成分均可以以适宜其用途的剂量使用。例如润湿剂和乳化剂的使用浓度按重量计为约0.5%至30%,增稠剂使用的剂量按重量计为约0.1%至25%,护发材料的浓度按重量计为约0.1%至5.0%。
本发明的染发组合物根据其成分可以是弱酸性、中性或碱性的。该组合物典型的pH值为6.8至11.5。组合物的pH值可以用氨水在一定的范围内调节。有机胺也可以用于该用途,包括一乙醇胺和三乙醇胺,或也可用无机碱,例如氢氧化钠和氢氧化钾。无机的或有机酸可用于在酸性范围内调节pH值,例如磷酸,乙酸,柠檬酸或酒石酸。
本发明中的染发组合物包含偶合剂,该偶合剂单独或和其它偶合剂结合以有效染发剂量使用,通常用量质量百分比为约0.01%至2.5%。如果还有其它偶合剂,那么用量质量百分比达到约2.5%。主要中间体的所用量质量百分比通常为大0.01%至约3.5%。主要中间体和偶合剂的摩尔比通常在约5∶1至约1∶5的范围内,并可在任意合适载体或赋形剂中使用,该载体或赋形剂通常为水溶液或水醇溶液,优选为水溶液。载体或赋形剂所占质量百分比通常可达约40%。
为了使用氧化性染发组合物染发,根据本发明需在使用前将上述的染发组合物与一种氧化剂立即混合,并根据头发的量将足量的混合物施用的头发上,一般为约60至200克。上面列出的一些辅助剂(例如,增稠剂,护发剂,等等)可以加入到染发组合物或显色剂中,或两个中都加入,这决定于成分的性质、可能的相互作用等等,正如本领域中为人所熟知的。
典型地,过氧化氢或是其与尿素、三聚氰胺、硼酸钠或碳酸钠的加成化合物可以以3%至12%,优选6%的水溶液使用作为氧化剂用于染发显色过程。氧气也可用作氧化剂。如果使用6%的过氧化氢溶液作为氧化剂,染发组合物与氧化剂的重量比为5∶1至1∶2,但优选1∶1。本发明的氧化剂和染发组合物的混合物要在约15至50℃条件下在头发上作用约10至45分钟,优选约30分钟,而后冲洗并干燥头发。如果需要,洗涤头发并最后用弱的有机酸如柠檬酸或酒石酸后漂洗头发。随后再干燥头发。
根据本发明以式(1)的化合物为偶合剂的染发组合物使得染后的头发具有优异的不褪色性,尤其是光不褪色性、洗涤不褪色性和摩擦不褪色性。
一般地,将主要中间体和偶合剂的第一种组合物制备出来,然后当使用时,将氧化剂如H2O2与之混合,直到得到一种均质的组合物,该组合物应用于待染的头发,并与头发保持接触有效的染发时间,一般要约2至45分钟,优选约2至30分钟,而后中洗头发、洗涤并干燥头发。可任选的,可以提供一种单独的调理产品。本发明中的染发组合物包含染发偶合剂(1)和含有氧化剂的显色剂共同形成了一种用于染发的系统。该系统可以成套的提供,包括在一个包装内的装有染发组合物、引发剂、可选择的调理剂或毛发处理产品的分装的瓶子以及使用说明。
实施例11
以下表1中所示的组合物可用于染前的头发。染发溶液与100克20体积的过氧化氢混合物。得到的混合物施用于头发并与头发保持接触30分钟。染后的头发随后洗涤、用水冲洗并干燥。
表1
染发组合物
成分 | 范围(重量百分比) | 重量百分比 |
椰油酰胺丙基内铵盐一乙醇胺1油酸柠檬酸28%氢氧化铵1二十二烷基三甲基氯化铵亚硫酸钠EDTA异抗坏血酸乙氧基二甘醇C11-15Pareth-9(Tergitol 15-S-9)C12-15Pareth-3(Neodol 25-3)异丙醇丙二醇对苯二胺2N,N-二(羟基乙基)-对苯二胺23-甲基-对氨基酚2对氨基酚2本发明的偶合剂5-氨基-2-甲基苯酚2,4-二氨基苯氧基乙醇水 | 0-250-152-220-30-151-50-10-10-11-100.5-50.25-52-101-120-50-50-50-50.5-50-50-5适量至100.00 | 17.002.000.750.105.000.500.100.100.403.501.000.504.002.002毫摩尔2毫摩尔1毫摩尔5毫摩尔5毫摩尔2毫摩尔2毫摩尔适量至100.00 |
1在聚集体中,这些成分浓度按重量计在2%至15%的范围内。
2通常这些染料前体中至少有一种存在。
使用了本发明中式(1)的偶合剂化合物的染发组分的示例性组合如表1和表A中的C1-C126所示。向下看表A中的列,Xes指定了一种染料化合物(包括本发明的新型偶合剂),该染料化合物根据本发明可以说明性地复配成染料的适宜的化合物。例如,在表A的No.C1组合中,本发明的新型偶合剂(表A的第1行)与X、R、R1、R2和R3同上文定义中所述,该偶合剂可与对甲苯二胺和2-氨基酚结合使用。在表A的C1-C126的组合中,本发明的尤其优选的式(1)的偶合剂为:
1-[2-(3-羟基-4-甲基苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
1-[2-(3-羟基-4-乙基苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
1-[2-(3-羟基-4-羟基乙基苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓氯化物;
1-[2-(3-羟基-4-甲基苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓溴化物;
1-[2-(3-羟基-4-甲基苯氨基)-乙基]-3甲基3-H-咪唑-1-鎓碘化物;
N-[2-(3-羟基-4-甲基苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-乙基苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-羟基乙基苯氨基)-乙基-N′-甲基-哌啶鎓氯化物;
N-[2-(3-羟基-4-甲基苯氨基)-乙基-N′-甲基-哌啶鎓溴化物;和
N-[2-(3-羟基-4-甲基苯氨基)-乙基-N′-甲基-哌啶鎓碘化物;
表A
表A
染料组合物
表A
染料组合物
表A
染料组合物
表A
染料组合物
表A
染料组合物
表A
染料组合物
表A
染料组合物
根据本发明的上述描述,在不背离本发明精神的前提下,本领域中的专业人员可以对发明进行一些改进。因此,本发明的范围并不限于说明和描述的具体实施方案。
Claims (22)
2.如权利要求1所述的化合物,其中X选自Cl、Br和I;R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族基团或C3-C6芳族基团,该基团可任选地在其环上包含另外的N原子。
3.如权利要求2所述的化合物,其中X为Cl。
4.如权利要求3所述的化合物,其中R3为甲基。
5.如权利要求4所述的化合物,其中R、R1和R2中的两个与它们所连接的N原子一起形成一个咪唑啉环。
6.如权利要求4所述的化合物,其中R、R1和R2中的两个与它们所连接的N原子一起形成一个哌嗪环。
8.如权利要求7所述的方法,其中X选自Cl、Br和I;R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族基团或C3-C6芳族基团,该基团可任选地在其环上包含另外的N原子。
9.如权利要求8所述的方法,其中X为Cl;R3为甲基;R、R1和R2中不形成环脂族基团或芳族基团的另一个基团为甲基。
10.如权利要求7所述的方法,其中还原剂选自硼氢化钠和三乙酸基硼氢化钠。
12.如权利要求11所述的染发系统,其中包含一种或多种氧化性染发剂的组合物还包含一种或多种选自下列物质的主要中间体:2-甲基-苯-1,4-二胺,苯-1,4-二胺,2-(2,5-二氨基苯基)-乙醇,1-(2,5-二氨基苯基)-乙醇,2-[(4-氨基苯基)-(2-羟基乙基)-氨基]-乙醇,4-氨基酚,4-甲氨基-苯酚,4-氨基-3-甲基苯酚,1-(5-氨基-2-羟基苯基)-乙烷-1,2-二醇,2-氨基酚,2-氨基-5-甲基苯酚,2-氨基-6-甲基苯酚,N-(4-氨基-3-羟基苯基)-乙酰胺,嘧啶-2,4,5,6-四胺,2-(4,5-二氨基-1H-吡唑-1-基)乙醇,1-(4-甲基苄基)-1H-吡唑-4,5-二胺以及1-(苄基)-1H-吡唑-4,5-二胺。
13.如权利要求12所述的染发系统,其中X选自Cl、Br和I;R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族基团或C3-C6芳族基团,该基团可任选地在其环上包含另外的N原子。
15.如权利要求14所述的染发系统,其中该系统还包含一种或多种选自下列物质的主要中间体:2-甲基-苯-1,4-二胺,苯-1,4-二胺,2-(2,5-二氨基-苯基)-乙醇,1-(2,5-二氨基苯基)-乙醇,2-[(4-氨基苯基)-(2-羟基乙基)-氨基]-乙醇,4-氨基酚,4-甲氨基-苯酚,4-氨基-3-甲基苯酚,1-(5-氨基-2-羟基苯基)-乙烷-1,2-二醇,2-氨基酚,2-氨基-5-甲基苯酚,2-氨基-6-甲基苯酚,N-(4-氨基-3-羟基苯基)-乙酰胺,嘧啶-2,4,5,6-四胺,2-(4,5-二氨基-1H-吡唑-1-基)乙醇,1-(4-甲基苄基)-1H-吡唑-4,5-二胺以及1-(苄基)-1H-吡唑-4,5-二胺。
16.如权利要求14所述的染发系统,其中该系统还包含一种或多种选自下列物质的偶合剂:苯-1,3-二酚,4-氯苯-1,3-二酚,萘-1-酚,2-甲基-萘-1-酚,2-甲基-苯-1,3-二酚,2-(2,4-二氨基苯氧基)-乙醇,2-(3-氨基-4-甲氧基苯氨基)-乙醇,2-[2,4-二氨基-5-(2-羟基乙氧基)-苯氧基]-乙醇,和3-(2,4-二氨基苯氧基)-丙烷-1-醇,3-氨基酚,5-氨基-2-甲基苯酚,5-(2-羟基乙氨基)-2-甲基苯酚,3-氨基-2-甲基苯酚,3,4-二氢-2H-1,4-苯并噁嗪-6-酚,4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮,1H-吲哚-6-酚和2-氨基吡啶-3-酚。
17.如权利要求15所述的染发系统,其中该系统包含一种或多种选自下列物质的偶合剂:苯-1,3-二酚,4-氯苯-1,3-二酚,萘-1-酚,2-甲基萘-1-酚,2-甲基-苯-1,3-二酚,2-(2,4-二氨基苯氧基)-乙醇,2-(3-氨基-4-甲氧基苯氨基)-乙醇,2-[2,4-二氨基-5-(2-羟基乙氧基)-苯氧基]-乙醇,和3-(2,4-二氨基-苯氧基)-丙烷-1-醇,3-氨基酚,5-氨基-2-甲基苯酚,5-(2-羟基-乙氨基)-2-甲基苯酚,3-氨基-2-甲基苯酚,3,4-二氢-2H-1,4-苯并噁嗪-6-酚,4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮,1H-吲哚-6-酚和2-氨基吡啶-3-酚。
18.如权利要求15所述的用于染发的系统,其中X选自Cl、Br和I;R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族基团或C3-C6芳族基团,该基团可任选地在其环上包含另外的N原子。
19.一种用于人发染色的染发组合物,其包括在一种合适的载体或赋形剂中的染色有效量的下列物质:
(a)至少一种主要中间体,
(b)至少一种含有式(1)的化合物的偶合剂:
其中X选自卤素;R3选自C1-C2烷基和羟基乙基;R、R1和R2各自独立选自C1-C22烷基或C1-C22一或二烷基基团,或R、R1和R2中的两个一起形成C3-C6环脂族基团或C3-C14芳族基团,该环脂族基团或芳族基团可任选地在其环上包含一个或多个选自O、S和N的杂原子;和
(c)至少一种氧化剂。
20.如权利要求19所述的染发组合物,其中X选自Cl、Br和I;R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族基团或C3-C6芳族基团,该基团可任选地在其环上包含另外的N原子。
21.一种用于人发染色的方法,其包括将权利要求19中所述的有效量的染发组合物施用于头发,并使组合物与头发接触对染发有效的时间段,然后冲洗、洗发、干燥头发。
22.如权利要求21所述的方法,其中X选自Cl、Br和I;R、R1和R2中的两个与它们所连接的氮原子一起形成C3-C6环脂族基团或C3-C6芳族基团,该基团可任选地在其环上包含另外的N原子。
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CN103764111A (zh) * | 2011-09-15 | 2014-04-30 | 莱雅公司 | 包含阳离子对氨基苯酚氧化显色碱的染料组合物 |
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BR0313991A (pt) | 2002-09-02 | 2005-07-19 | Ciba Sc Holding Ag | Método de tingimento de material poroso |
US7238212B2 (en) | 2003-06-02 | 2007-07-03 | L'oreal, S.A. | Imidazole compounds and use of these compounds for dyeing keratinous fibers |
FR2855406B1 (fr) * | 2003-06-02 | 2006-08-04 | Oreal | Nouveaux composes imidazoles et utilisation de ces composes pour la teinture de fibres keratiniques |
US12138330B2 (en) * | 2020-04-12 | 2024-11-12 | Pwai, Llc | Hair coloring modification additive and related methods |
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FR2315255A1 (fr) * | 1975-06-26 | 1977-01-21 | Oreal | Coupleurs glycoles |
FR2707490B1 (fr) | 1993-07-13 | 1995-09-22 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant un para-aminophénol, un méta-aminophénol et un para-aminophénol 2-substitué. |
FR2715296B1 (fr) | 1994-01-24 | 1996-04-12 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant une paraphénylènediamine, une métalphénylènediamine et un para-aminophénol ou un méta-aminophénol, et procédé de teinture utilisant une telle composition. |
FR2776289B1 (fr) * | 1998-03-20 | 2001-02-02 | Oreal | Composition de teinture d'oxydation contenant un coupleur cationique, procedes de teinture, nouveaux coupleurs cationiques |
FR2788769B1 (fr) * | 1999-01-21 | 2001-02-16 | Oreal | Nouveaux coupleurs cationiques, leur utilisation pour la teinture d'oxydation, compositions pour la teinture les comprenant, et procedes de teinture |
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AU1983502A (en) | 2002-05-27 |
US20020108187A1 (en) | 2002-08-15 |
JP2004513910A (ja) | 2004-05-13 |
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