FI69752C - Haorfaergningsmedel - Google Patents
Haorfaergningsmedel Download PDFInfo
- Publication number
- FI69752C FI69752C FI793469A FI793469A FI69752C FI 69752 C FI69752 C FI 69752C FI 793469 A FI793469 A FI 793469A FI 793469 A FI793469 A FI 793469A FI 69752 C FI69752 C FI 69752C
- Authority
- FI
- Finland
- Prior art keywords
- bis
- hair
- diaminophenoxy
- phenylenediamine
- blue
- Prior art date
Links
- -1 2,4-diaminophenoxy Chemical group 0.000 claims description 19
- 238000005859 coupling reaction Methods 0.000 claims description 16
- 230000008878 coupling Effects 0.000 claims description 15
- 238000010168 coupling process Methods 0.000 claims description 15
- 239000000118 hair dye Substances 0.000 claims description 14
- 230000001590 oxidative effect Effects 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 239000003086 colorant Substances 0.000 claims description 3
- 150000007522 mineralic acids Chemical class 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 239000000975 dye Substances 0.000 description 11
- 150000001335 aliphatic alkanes Chemical class 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 238000004040 coloring Methods 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 239000006071 cream Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000005691 oxidative coupling reaction Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 235000019646 color tone Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 239000007868 Raney catalyst Substances 0.000 description 3
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 3
- 229910000564 Raney nickel Inorganic materials 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000010626 work up procedure Methods 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
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 2
- HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 description 2
- WBRBBXFBDHGRBW-UHFFFAOYSA-N 4-[(2,4-diaminophenoxy)methoxy]benzene-1,3-diamine;tetrahydrochloride Chemical compound Cl.Cl.Cl.Cl.NC1=CC(N)=CC=C1OCOC1=CC=C(N)C=C1N WBRBBXFBDHGRBW-UHFFFAOYSA-N 0.000 description 2
- UPGGLFQQGHSFFG-UHFFFAOYSA-N 4-[2-(2,4-diaminophenoxy)ethoxy]benzene-1,3-diamine;tetrahydrochloride Chemical compound Cl.Cl.Cl.Cl.NC1=CC(N)=CC=C1OCCOC1=CC=C(N)C=C1N UPGGLFQQGHSFFG-UHFFFAOYSA-N 0.000 description 2
- UXPUOLAAWYPPLE-UHFFFAOYSA-N 4-[3-(2,4-diaminophenoxy)propoxy]benzene-1,3-diamine;tetrahydrochloride Chemical compound Cl.Cl.Cl.Cl.NC1=CC(N)=CC=C1OCCCOC1=CC=C(N)C=C1N UXPUOLAAWYPPLE-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- XSFKCGABINPZRK-UHFFFAOYSA-N 4-aminopyrazol-3-one Chemical class NC1=CN=NC1=O XSFKCGABINPZRK-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 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
- 239000007822 coupling agent Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 description 2
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical compound NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 230000002110 toxicologic effect Effects 0.000 description 2
- 231100000027 toxicology Toxicity 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
- NXVHEHXRZVQDCR-UHFFFAOYSA-N 1-n,1-n-diethyl-2-methylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C=C1C NXVHEHXRZVQDCR-UHFFFAOYSA-N 0.000 description 1
- MIMCDARZGRDCQA-UHFFFAOYSA-N 1-n,4-n-diethyl-2-methylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(NCC)C(C)=C1 MIMCDARZGRDCQA-UHFFFAOYSA-N 0.000 description 1
- HQCHAOKWWKLXQH-UHFFFAOYSA-N 2,6-Dichloro-para-phenylenediamine Chemical compound NC1=CC(Cl)=C(N)C(Cl)=C1 HQCHAOKWWKLXQH-UHFFFAOYSA-N 0.000 description 1
- SDBZMQLOUCARLE-UHFFFAOYSA-N 2-[(2-amino-4-nitrophenoxy)methoxy]-5-nitroaniline Chemical compound NC1=CC([N+]([O-])=O)=CC=C1OCOC1=CC=C([N+]([O-])=O)C=C1N SDBZMQLOUCARLE-UHFFFAOYSA-N 0.000 description 1
- BRYVNYREMPLLAS-UHFFFAOYSA-N 2-[2-(2-amino-4-nitrophenoxy)ethoxy]-5-nitroaniline Chemical compound NC1=CC([N+]([O-])=O)=CC=C1OCCOC1=CC=C([N+]([O-])=O)C=C1N BRYVNYREMPLLAS-UHFFFAOYSA-N 0.000 description 1
- YQPYJIJMQMCMAQ-UHFFFAOYSA-N 2-[2-(4-aminophenyl)-2-(2-hydroxyethylamino)hydrazinyl]ethanol Chemical compound NC1=CC=C(N(NCCO)NCCO)C=C1 YQPYJIJMQMCMAQ-UHFFFAOYSA-N 0.000 description 1
- COPPRTPTIJAZDK-UHFFFAOYSA-N 2-[3-(2-amino-4-nitrophenoxy)propoxy]-5-nitroaniline Chemical compound NC1=CC([N+]([O-])=O)=CC=C1OCCCOC1=CC=C([N+]([O-])=O)C=C1N COPPRTPTIJAZDK-UHFFFAOYSA-N 0.000 description 1
- JZPNTHCLRNZJFE-UHFFFAOYSA-N 2-[4-(2-amino-4-nitrophenoxy)butoxy]-5-nitroaniline Chemical compound NC1=CC([N+]([O-])=O)=CC=C1OCCCCOC1=CC=C([N+]([O-])=O)C=C1N JZPNTHCLRNZJFE-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- RCANFVUNFLBTJG-UHFFFAOYSA-N 2-bromo-6-chlorobenzene-1,4-diamine Chemical compound NC1=CC(Cl)=C(N)C(Br)=C1 RCANFVUNFLBTJG-UHFFFAOYSA-N 0.000 description 1
- MGLZGLAFFOMWPB-UHFFFAOYSA-N 2-chloro-1,4-phenylenediamine Chemical compound NC1=CC=C(N)C(Cl)=C1 MGLZGLAFFOMWPB-UHFFFAOYSA-N 0.000 description 1
- MPUYRZSQOVOWER-UHFFFAOYSA-N 2-chloro-6-methylbenzene-1,4-diamine Chemical compound CC1=CC(N)=CC(Cl)=C1N MPUYRZSQOVOWER-UHFFFAOYSA-N 0.000 description 1
- KNRVAYVZVIKHHL-UHFFFAOYSA-N 2-methoxy-5-methylbenzene-1,4-diamine Chemical compound COC1=CC(N)=C(C)C=C1N KNRVAYVZVIKHHL-UHFFFAOYSA-N 0.000 description 1
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 1
- HSVBSQWCIQIJNQ-UHFFFAOYSA-N 2-n,4-n-dimethylpyrimidine-2,4,5,6-tetramine Chemical compound CNC1=NC(N)=C(N)C(NC)=N1 HSVBSQWCIQIJNQ-UHFFFAOYSA-N 0.000 description 1
- FJNLCHNQVJVCPY-UHFFFAOYSA-N 2-n-methoxy-2-n-methyl-4-n,6-n-dipropyl-1,3,5-triazine-2,4,6-triamine Chemical compound CCCNC1=NC(NCCC)=NC(N(C)OC)=N1 FJNLCHNQVJVCPY-UHFFFAOYSA-N 0.000 description 1
- CSGNEKGWOJHKOI-UHFFFAOYSA-N 4-(4-azaniumyl-n-butylanilino)butane-1-sulfonate Chemical compound OS(=O)(=O)CCCCN(CCCC)C1=CC=C(N)C=C1 CSGNEKGWOJHKOI-UHFFFAOYSA-N 0.000 description 1
- BGGGDHXHMQFBGA-UHFFFAOYSA-N 4-[(2,4-diaminophenoxy)methoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCOC1=CC=C(N)C=C1N BGGGDHXHMQFBGA-UHFFFAOYSA-N 0.000 description 1
- UUUMOQCLNYFCJI-UHFFFAOYSA-N 4-[10-(2,4-diaminophenoxy)decoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCCCCCCCCOC1=CC=C(N)C=C1N UUUMOQCLNYFCJI-UHFFFAOYSA-N 0.000 description 1
- MGCRDDNVJMNSHP-UHFFFAOYSA-N 4-[12-(2,4-diaminophenoxy)dodecoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCCCCCCCCCCOC1=CC=C(N)C=C1N MGCRDDNVJMNSHP-UHFFFAOYSA-N 0.000 description 1
- SSCLOVXDBSTPRH-UHFFFAOYSA-N 4-[2-(2,4-diaminophenoxy)ethoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCOC1=CC=C(N)C=C1N SSCLOVXDBSTPRH-UHFFFAOYSA-N 0.000 description 1
- QBOMSLKKGQZEPS-UHFFFAOYSA-N 4-[2-(2,4-diaminophenoxy)propoxy]benzene-1,3-diamine Chemical compound C=1C=C(N)C=C(N)C=1OC(C)COC1=CC=C(N)C=C1N QBOMSLKKGQZEPS-UHFFFAOYSA-N 0.000 description 1
- MWKPYVXITDAZLL-UHFFFAOYSA-N 4-[3-(2,4-diaminophenoxy)propoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCOC1=CC=C(N)C=C1N MWKPYVXITDAZLL-UHFFFAOYSA-N 0.000 description 1
- OFVCSDCMBRABAA-UHFFFAOYSA-N 4-[4-(2,4-diaminophenoxy)butoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCCOC1=CC=C(N)C=C1N OFVCSDCMBRABAA-UHFFFAOYSA-N 0.000 description 1
- KVJSVTDVNZEXFP-UHFFFAOYSA-N 4-[4-(2,4-diaminophenoxy)butoxy]benzene-1,3-diamine;tetrahydrochloride Chemical compound Cl.Cl.Cl.Cl.NC1=CC(N)=CC=C1OCCCCOC1=CC=C(N)C=C1N KVJSVTDVNZEXFP-UHFFFAOYSA-N 0.000 description 1
- JTRXLTFHEJQXSG-UHFFFAOYSA-N 4-[5-(2,4-diaminophenoxy)pentoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCCCOC1=CC=C(N)C=C1N JTRXLTFHEJQXSG-UHFFFAOYSA-N 0.000 description 1
- TVHRAMOSOXKYOY-UHFFFAOYSA-N 4-[8-(2,4-diaminophenoxy)octoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCCCCCCOC1=CC=C(N)C=C1N TVHRAMOSOXKYOY-UHFFFAOYSA-N 0.000 description 1
- OZCJSIBGTRKJGX-UHFFFAOYSA-N 4-methylcyclohexa-1,5-diene-1,4-diamine Chemical compound CC1(N)CC=C(N)C=C1 OZCJSIBGTRKJGX-UHFFFAOYSA-N 0.000 description 1
- FWEQBUQMTDZOMM-UHFFFAOYSA-N 4-n,4-n-diethyl-6-methyl-2h-pyrimidine-1,2,4,5-tetramine Chemical compound CCN(CC)C1=NC(N)N(N)C(C)=C1N FWEQBUQMTDZOMM-UHFFFAOYSA-N 0.000 description 1
- BKIIRHXARCYZNY-UHFFFAOYSA-N 4-n,4-n-dimethylpyrimidine-2,4,5,6-tetramine Chemical compound CN(C)C1=NC(N)=NC(N)=C1N BKIIRHXARCYZNY-UHFFFAOYSA-N 0.000 description 1
- YOJKEVXNAVNUGW-UHFFFAOYSA-N 4-n-chlorobenzene-1,4-diamine Chemical compound NC1=CC=C(NCl)C=C1 YOJKEVXNAVNUGW-UHFFFAOYSA-N 0.000 description 1
- VVYWUQOTMZEJRJ-UHFFFAOYSA-N 4-n-methylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C=C1 VVYWUQOTMZEJRJ-UHFFFAOYSA-N 0.000 description 1
- SGWBUDIVEVIHND-UHFFFAOYSA-N 4-n-phenylpyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(NC=2C=CC=CC=2)=N1 SGWBUDIVEVIHND-UHFFFAOYSA-N 0.000 description 1
- NZRGVFBNMBPYLN-UHFFFAOYSA-N 5,6-diamino-2-anilino-1h-pyrimidin-4-one Chemical compound O=C1C(N)=C(N)NC(NC=2C=CC=CC=2)=N1 NZRGVFBNMBPYLN-UHFFFAOYSA-N 0.000 description 1
- DUHATDNXRFRRFH-UHFFFAOYSA-N 6-morpholin-4-ylpyrimidine-2,4,5-triamine Chemical compound NC1=NC(N)=C(N)C(N2CCOCC2)=N1 DUHATDNXRFRRFH-UHFFFAOYSA-N 0.000 description 1
- QKEUDMVNJHDWNZ-UHFFFAOYSA-N 6-piperidin-1-ylpyrimidine-2,4,5-triamine Chemical compound NC1=NC(N)=C(N)C(N2CCCCC2)=N1 QKEUDMVNJHDWNZ-UHFFFAOYSA-N 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
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols 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
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 125000000950 dibromo group Chemical group Br* 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 230000003700 hair damage Effects 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 150000004988 m-phenylenediamines Chemical class 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- ITTJPHUQMZDKHQ-UHFFFAOYSA-N n-(2-hydroxy-6-nitrophenyl)acetamide Chemical class CC(=O)NC1=C(O)C=CC=C1[N+]([O-])=O ITTJPHUQMZDKHQ-UHFFFAOYSA-N 0.000 description 1
- VXSYHZYBAVDVMH-UHFFFAOYSA-N n-ethyl-n-[4-(ethylamino)phenyl]hydroxylamine Chemical compound CCNC1=CC=C(N(O)CC)C=C1 VXSYHZYBAVDVMH-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 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
- 239000002304 perfume Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 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
- 239000010981 turquoise Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
-
- 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
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI842781A FI76068C (fi) | 1978-12-02 | 1984-07-11 | Foerfarande foer framstaellning av 1,3-bis-(2,4-diaminofenoxi)-propan. |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782852156 DE2852156C2 (de) | 1978-12-02 | 1978-12-02 | Haarfärbemittel auf der Basis von Oxidationsfarbstoffen und Bis-(2,4-diaminophenoxy)-alkane |
| DE2852156 | 1978-12-02 | ||
| DE19792932460 DE2932460C2 (de) | 1979-08-10 | 1979-08-10 | Verfahren zur Herstellung von 1,3-Bis-(2,4-diaminophenoxy)-propan; |
| DE2932460 | 1979-08-10 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI793469A7 FI793469A7 (fi) | 1980-06-03 |
| FI69752B FI69752B (fi) | 1985-12-31 |
| FI69752C true FI69752C (fi) | 1986-05-26 |
Family
ID=25776693
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI793469A FI69752C (fi) | 1978-12-02 | 1979-11-05 | Haorfaergningsmedel |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4314809A (da) |
| EP (1) | EP0011844B1 (da) |
| AR (1) | AR224256A1 (da) |
| AU (1) | AU530720B2 (da) |
| BR (1) | BR7907807A (da) |
| DK (1) | DK158441C (da) |
| FI (1) | FI69752C (da) |
| NO (1) | NO147302C (da) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3011191A1 (de) * | 1980-03-22 | 1981-10-01 | Henkel KGaA, 4000 Düsseldorf | Neue kupplerkomponenten fuer oxidationshaarfarben, deren herstellung und verwendung sowie diese enthaltende haarfaerbemittel |
| DE3235615A1 (de) * | 1982-09-25 | 1984-03-29 | Henkel KGaA, 4000 Düsseldorf | Haarfaerbemittel |
| DE3711579A1 (de) * | 1987-04-06 | 1988-10-20 | Henkel Kgaa | Aminophenylalkylendiamine und deren verwendung in oxidationshaarfaerbemitteln |
| FR2636062B1 (fr) * | 1988-09-06 | 1990-11-30 | Oreal | Procede de preparation d'(alpha), (omega)-diamines aliphatiques, compose nouveau et son utilisation en teinture capillaire |
| 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. |
| TW290558B (da) * | 1994-04-28 | 1996-11-11 | Nissan Chemical Ind Ltd | |
| US5865854A (en) * | 1997-11-21 | 1999-02-02 | Bristol-Myers Squibb Company | BIS-(2-4-diaminophenoxy) benzenes and their use as coupling components in oxidative hair coloring compositions and methods |
| FR2776290B1 (fr) * | 1998-03-20 | 2001-08-10 | Oreal | Nouveaux composes cationiques, leur utilisation comme coupleurs pour la teinture d'oxydation des fibres keratiniques, compositions tinctoriales et procedes de teinture |
| FR2786092B1 (fr) * | 1998-11-20 | 2002-11-29 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| DE10100928A1 (de) * | 2001-01-10 | 2002-09-26 | Henkel Kgaa | Kuppler/Entwickler- und Kuppler/Kuppler-Hybridfarbstoffe und -hybridfarbstoffvorprodukte |
| DE10351842A1 (de) * | 2003-11-06 | 2005-06-09 | Wella Ag | m-Diaminobenzole und deren Säureaddukte sowie deren Verwendung in Färbemitteln |
| EP2226065A3 (en) * | 2010-03-15 | 2010-09-29 | KPSS-Kao Professional Salon Services GmbH | Colouring composition for keratin fibres |
| CN104292118A (zh) * | 2013-07-18 | 2015-01-21 | 宜兴市新宇化工有限公司 | 一种1,3-二(2,4-二氨基苯氧基)丙烷盐酸盐的生产工艺 |
| US12479816B2 (en) | 2019-02-08 | 2025-11-25 | University of Pittsburgh—of the Commonwealth System of Higher Education | 20-HETE formation inhibitors |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1210751A (en) * | 1915-10-08 | 1917-01-02 | Chem Ind Basel | Substantive orthooxyazo dyestuffs and a process of making same. |
| US2204230A (en) * | 1939-03-29 | 1940-06-11 | Du Pont | Azo dyes |
| GB1081282A (en) * | 1964-08-14 | 1967-08-31 | Geigy Uk Ltd | Bis-benzotriazoles and compositions containing same |
| CH502418A (de) * | 1967-03-15 | 1971-01-31 | Ciba Geigy Ag | Verfahren zur Herstellung von Disazofarbstoffen |
| DE1809172C3 (de) * | 1968-11-15 | 1979-10-11 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyurethanelastomeren |
| US3862226A (en) * | 1972-02-28 | 1975-01-21 | Burroughs Wellcome Co | Bis-{8 beta-(4-N,N-diacetylaminophenoxy)ethyl{9 ether |
| FR2362116A1 (fr) * | 1976-08-20 | 1978-03-17 | Oreal | Metaphenylenediamines et compositions tinctoriales les contenant |
| DE2658329C2 (de) * | 1976-12-23 | 1983-01-13 | Hoechst Ag, 6000 Frankfurt | Nitroaminäther, Verfahren zu ihrer Herstellung und ihre Verwendung als Disazoverbindungen |
| US4161474A (en) * | 1977-11-25 | 1979-07-17 | Monsanto Company | Bis-(alkylaminophenoxy)alkanes as antidegradants for rubber |
-
1979
- 1979-11-05 FI FI793469A patent/FI69752C/fi not_active IP Right Cessation
- 1979-11-05 NO NO793554A patent/NO147302C/no unknown
- 1979-11-05 DK DK467079A patent/DK158441C/da not_active IP Right Cessation
- 1979-11-14 US US06/094,276 patent/US4314809A/en not_active Expired - Lifetime
- 1979-11-26 EP EP79104694A patent/EP0011844B1/de not_active Expired
- 1979-11-30 AU AU53366/79A patent/AU530720B2/en not_active Expired
- 1979-11-30 BR BR7907807A patent/BR7907807A/pt not_active IP Right Cessation
- 1979-12-03 AR AR279120A patent/AR224256A1/es active
Also Published As
| Publication number | Publication date |
|---|---|
| FI793469A7 (fi) | 1980-06-03 |
| BR7907807A (pt) | 1980-07-29 |
| AR224256A1 (es) | 1981-11-13 |
| NO147302B (no) | 1982-12-06 |
| DK467079A (da) | 1980-06-03 |
| FI69752B (fi) | 1985-12-31 |
| US4314809A (en) | 1982-02-09 |
| AU5336679A (en) | 1980-06-05 |
| AU530720B2 (en) | 1983-07-28 |
| NO793554L (no) | 1980-06-03 |
| DK158441B (da) | 1990-05-21 |
| NO147302C (no) | 1983-03-16 |
| EP0011844A1 (de) | 1980-06-11 |
| EP0011844B1 (de) | 1982-05-26 |
| DK158441C (da) | 1990-10-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MA | Patent expired |
Owner name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN |