FI69055C - Som oxidationsfaergers nya kopplingskomponenter anvaendbara m-enylendiaminderivat framstaellning av dem samt dessa inne hallande haorfaergaemnen - Google Patents
Som oxidationsfaergers nya kopplingskomponenter anvaendbara m-enylendiaminderivat framstaellning av dem samt dessa inne hallande haorfaergaemnen Download PDFInfo
- Publication number
- FI69055C FI69055C FI811007A FI811007A FI69055C FI 69055 C FI69055 C FI 69055C FI 811007 A FI811007 A FI 811007A FI 811007 A FI811007 A FI 811007A FI 69055 C FI69055 C FI 69055C
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- Finland
- Prior art keywords
- formula
- acid
- coupling
- hair
- compounds
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- 101100148710 Clarkia breweri SAMT gene Proteins 0.000 title 1
- 238000010168 coupling process Methods 0.000 claims abstract description 17
- 238000005859 coupling reaction Methods 0.000 claims abstract description 17
- 230000008878 coupling Effects 0.000 claims abstract description 16
- 239000000975 dye Substances 0.000 claims abstract description 14
- 150000004988 m-phenylenediamines Chemical class 0.000 claims abstract description 9
- 238000002360 preparation method Methods 0.000 claims description 17
- 239000000118 hair dye Substances 0.000 claims description 16
- 230000001590 oxidative effect Effects 0.000 claims description 15
- -1 alkaline earth metal salts Chemical class 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 6
- 230000003647 oxidation Effects 0.000 abstract description 4
- 238000007254 oxidation reaction Methods 0.000 abstract description 4
- 238000004043 dyeing Methods 0.000 abstract description 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 159000000000 sodium salts Chemical class 0.000 description 15
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 239000011734 sodium Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000007822 coupling agent Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000002329 infrared spectrum Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- UEANEAODIZOETQ-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)acetic acid Chemical compound NC1=CC=C(OCC(O)=O)C(N)=C1 UEANEAODIZOETQ-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- KHZHJGIOIIUHOO-UHFFFAOYSA-N 2-(2,4-diaminophenyl)acetic acid Chemical compound NC1=CC=C(CC(O)=O)C(N)=C1 KHZHJGIOIIUHOO-UHFFFAOYSA-N 0.000 description 3
- WCCVPONMFCESFL-UHFFFAOYSA-N 2-(2,4-dinitrophenoxy)butanoic acid Chemical compound CCC(C(O)=O)OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O WCCVPONMFCESFL-UHFFFAOYSA-N 0.000 description 3
- QMPRSWQOPAUVSY-UHFFFAOYSA-N 3-(2,4-diaminophenyl)propanoic acid Chemical compound NC1=CC=C(CCC(O)=O)C(N)=C1 QMPRSWQOPAUVSY-UHFFFAOYSA-N 0.000 description 3
- NJGXPGVYYHJEBT-UHFFFAOYSA-N 3-(2,4-dinitrophenyl)propanoic acid Chemical compound OC(=O)CCC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O NJGXPGVYYHJEBT-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000007942 carboxylates Chemical class 0.000 description 3
- 235000019646 color tone Nutrition 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 239000010981 turquoise Substances 0.000 description 3
- KAJALVWKFPQZOO-UHFFFAOYSA-N (4-azaniumylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C=C1 KAJALVWKFPQZOO-UHFFFAOYSA-N 0.000 description 2
- 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
- PFWOPESNYPKSLN-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(N)C=C1N PFWOPESNYPKSLN-UHFFFAOYSA-N 0.000 description 2
- TZXQHDWGPRDQHL-UHFFFAOYSA-N 2-(2,4-dinitrophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O TZXQHDWGPRDQHL-UHFFFAOYSA-N 0.000 description 2
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-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
- QISFOZFBRWGNCP-UHFFFAOYSA-N 4-methylcyclohexa-1,5-diene-1,4-diamine;sulfuric acid Chemical compound OS(O)(=O)=O.CC1(N)CC=C(N)C=C1 QISFOZFBRWGNCP-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
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 240000007817 Olea europaea Species 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 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
- 239000003086 colorant Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 2
- MQEFDQWUCTUJCP-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine;sulfuric acid Chemical compound OS(O)(=O)=O.NC1=NC(N)=C(N)C(N)=N1 MQEFDQWUCTUJCP-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- NZTCRHBIQWZHEY-UHFFFAOYSA-N (4-azaniumylphenyl)-methylazanium;sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(N)C=C1 NZTCRHBIQWZHEY-UHFFFAOYSA-N 0.000 description 1
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
- 125000001917 2,4-dinitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1*)[N+]([O-])=O)[N+]([O-])=O 0.000 description 1
- KCNISYPADDTFDO-UHFFFAOYSA-N 2,4-dinitrophenylacetic acid Chemical compound OC(=O)CC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O KCNISYPADDTFDO-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
- NUWNDYIGUKOVGU-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)butanoic acid Chemical compound CCC(C(O)=O)OC1=CC=C(N)C=C1N NUWNDYIGUKOVGU-UHFFFAOYSA-N 0.000 description 1
- UZZSCQDTKXKIDN-UHFFFAOYSA-N 2-(2,4-diaminophenyl)butanoic acid Chemical compound NC1=C(C=CC(=C1)N)C(C(=O)O)CC UZZSCQDTKXKIDN-UHFFFAOYSA-N 0.000 description 1
- OWEDBRWCJFWVFZ-UHFFFAOYSA-N 2-(2,4-dinitrophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O OWEDBRWCJFWVFZ-UHFFFAOYSA-N 0.000 description 1
- WFXLRLQSHRNHCE-UHFFFAOYSA-N 2-(4-amino-n-ethylanilino)ethanol Chemical compound OCCN(CC)C1=CC=C(N)C=C1 WFXLRLQSHRNHCE-UHFFFAOYSA-N 0.000 description 1
- SXERGJJQSKIUIC-UHFFFAOYSA-N 2-Phenoxypropionic acid Chemical compound OC(=O)C(C)OC1=CC=CC=C1 SXERGJJQSKIUIC-UHFFFAOYSA-N 0.000 description 1
- WRPDHMGXFGCCPT-UHFFFAOYSA-N 2-[(2,5,6-triaminopyrimidin-4-yl)amino]ethanol Chemical compound NC1=NC(N)=C(N)C(NCCO)=N1 WRPDHMGXFGCCPT-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
- 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
- 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
- HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 description 1
- KTFJGRIGYYVFKN-UHFFFAOYSA-N 2-methyl-4H-pyrimidine-4,5,5,6-tetramine Chemical compound CC=1N=C(C(C(N=1)N)(N)N)N KTFJGRIGYYVFKN-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
- TVSPPYGAFOVROT-UHFFFAOYSA-N 2-phenoxybutanoic acid Chemical compound CCC(C(O)=O)OC1=CC=CC=C1 TVSPPYGAFOVROT-UHFFFAOYSA-N 0.000 description 1
- INHMUHMBARWGRW-UHFFFAOYSA-N 3-(2,4-diaminophenoxy)propanoic acid Chemical compound NC1=CC=C(OCCC(O)=O)C(N)=C1 INHMUHMBARWGRW-UHFFFAOYSA-N 0.000 description 1
- HWUQAEQZNRXQTL-UHFFFAOYSA-N 4-(2,4-diaminophenoxy)butanoic acid Chemical compound NC1=CC=C(OCCCC(O)=O)C(N)=C1 HWUQAEQZNRXQTL-UHFFFAOYSA-N 0.000 description 1
- IRMVTXMIPLBURL-UHFFFAOYSA-N 4-(2,4-diaminophenyl)butanoic acid Chemical compound NC1=CC=C(CCCC(O)=O)C(N)=C1 IRMVTXMIPLBURL-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
- 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
- XBTWVJKPQPQTDW-UHFFFAOYSA-N 4-n,4-n-diethyl-2-methylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C(C)=C1 XBTWVJKPQPQTDW-UHFFFAOYSA-N 0.000 description 1
- RDURCWNWCVUFEG-UHFFFAOYSA-N 4-n,4-n-diethyl-6-n-methylpyrimidine-2,4,5,6-tetramine Chemical compound CCN(CC)C1=NC(N)=NC(NC)=C1N RDURCWNWCVUFEG-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
- 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
- QLBARDOZHACNNY-UHFFFAOYSA-M CCC(C([O-])=O)OC(C=CC(N)=C1)=C1N.[Na+] Chemical compound CCC(C([O-])=O)OC(C=CC(N)=C1)=C1N.[Na+] QLBARDOZHACNNY-UHFFFAOYSA-M 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
- 229920000877 Melamine resin Polymers 0.000 description 1
- YCIZVSSJFSPZFS-UHFFFAOYSA-N O.S(=O)(=O)(O)O.CS(=O)(=O)N.S(=O)(=O)(O)O.S(=O)(=O)(O)O.CS(=O)(=O)N.O Chemical compound O.S(=O)(=O)(O)O.CS(=O)(=O)N.S(=O)(=O)(O)O.S(=O)(=O)(O)O.CS(=O)(=O)N.O YCIZVSSJFSPZFS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 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
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 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
- 230000037308 hair color Effects 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 239000003973 paint 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
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- KXXXUIKPSVVSAW-UHFFFAOYSA-K pyranine Chemical compound [Na+].[Na+].[Na+].C1=C2C(O)=CC(S([O-])(=O)=O)=C(C=C3)C2=C2C3=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C2=C1 KXXXUIKPSVVSAW-UHFFFAOYSA-K 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000002562 thickening agent Substances 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
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
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- 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
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/56—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lift-Guide Devices, And Elevator Ropes And Cables (AREA)
- Load-Engaging Elements For Cranes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3016881 | 1980-05-02 | ||
| DE19803016881 DE3016881A1 (de) | 1980-05-02 | 1980-05-02 | Neue kupplerkomponenten fuer oxidationshaarfarben, deren herstellung sowie diese enthaltende haarfaerbemittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI811007L FI811007L (fi) | 1981-11-03 |
| FI69055B FI69055B (fi) | 1985-08-30 |
| FI69055C true FI69055C (fi) | 1985-12-10 |
Family
ID=6101470
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI811007A FI69055C (fi) | 1980-05-02 | 1981-04-01 | Som oxidationsfaergers nya kopplingskomponenter anvaendbara m-enylendiaminderivat framstaellning av dem samt dessa inne hallande haorfaergaemnen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4684371A (da) |
| EP (1) | EP0039455B1 (da) |
| JP (1) | JPS56169655A (da) |
| AT (1) | ATE8250T1 (da) |
| DE (2) | DE3016881A1 (da) |
| DK (1) | DK150503C (da) |
| FI (1) | FI69055C (da) |
| NO (1) | NO152004C (da) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3309913A1 (de) * | 1983-03-19 | 1984-09-27 | Henkel KGaA, 4000 Düsseldorf | Neue 2,4-diaminobenzolderivate als kuppler fuer oxidationshaarfaerbemittel |
| US5310682A (en) * | 1992-06-17 | 1994-05-10 | Indiana University Foundation | Fluorogenic reagents for detection of glycoconjugates, α-ketoacids and diketones |
| DE4417546A1 (de) * | 1994-05-19 | 1995-11-23 | Henkel Kgaa | 2-Oxoessigsäurederivate zum Färben keratinhaltiger Fasern |
| FR3001386B1 (fr) | 2013-01-29 | 2015-06-05 | Oreal | Composition de teinture mettant en oeuvre au moins un coupleur de type meta-phenylenediamine substituee en position 4 dans un milieu comprenant un corps gras, procedes et dispositif |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2181057A (en) * | 1937-05-24 | 1939-11-21 | Gen Aniline Works Inc | Azo dyestuffs |
| US2603659A (en) * | 1950-06-16 | 1952-07-15 | Du Pont | Photographic developers |
| US3861868A (en) * | 1971-03-30 | 1975-01-21 | Procter & Gamble | Dyeing human hair with oxidation dyes and arginine or a protamine protein |
| FR2362116A1 (fr) * | 1976-08-20 | 1978-03-17 | Oreal | Metaphenylenediamines et compositions tinctoriales les contenant |
| LU77995A1 (fr) * | 1977-08-19 | 1979-05-23 | Oreal | Compositions tinctoriales a base de colorants directs contenant un acide(2,5-dihydroxyphenyl)carboxylique ou l'un de ses sels et procede de preparation |
| DE2758735A1 (de) * | 1977-10-06 | 1979-04-19 | Bristol Myers Co | Oxidationsfaerbemittelzusammensetzung fuer das einfaerben keratinoeser fasern, insbesondere menschlichen haaren |
| FR2430932A1 (fr) * | 1978-07-12 | 1980-02-08 | Oreal | Metaphenylenediamines et compositions tinctoriales les contenant |
| DE2855917A1 (de) * | 1978-12-23 | 1980-07-10 | Wella Ag | Mittel und verfahren zur faerbung von haaren |
| FR2459042A1 (fr) * | 1979-06-18 | 1981-01-09 | Oreal | Nouvelles compositions tinctoriales pour cheveux contenant, comme coupleur le diamino-2,4 butoxybenzene et/ou ses sels |
| FR2461494A1 (fr) * | 1979-07-24 | 1981-02-06 | Oreal | Compositions tinctoriales pour cheveux contenant, en tant que coupleur, au moins un diamino-2,4 alkylbenzene |
| DE2948093A1 (de) * | 1979-11-29 | 1981-06-11 | Henkel KGaA, 4000 Düsseldorf | Neue kupplerkomponenten fuer oxidationshaarfarben, deren herstellung und verwendung sowie diese enthaltende haarfaerbemittel |
| US4452603A (en) * | 1980-07-17 | 1984-06-05 | Wella Aktiengesellschaft | Process for dyeing hair and composition therefor |
| US4286989A (en) * | 1980-09-30 | 1981-09-01 | International Business Machines Corporation | Formulations for ink jet printing |
| US4566876A (en) * | 1983-03-10 | 1986-01-28 | Clairol Incorporated | Meta-phenylenediamine coupler compounds and oxidative hair dye compositions and methods using same |
-
1980
- 1980-05-02 DE DE19803016881 patent/DE3016881A1/de not_active Withdrawn
-
1981
- 1981-04-01 DK DK148081A patent/DK150503C/da not_active IP Right Cessation
- 1981-04-01 FI FI811007A patent/FI69055C/fi not_active IP Right Cessation
- 1981-04-01 NO NO811123A patent/NO152004C/no unknown
- 1981-04-24 DE DE8181103090T patent/DE3164542D1/de not_active Expired
- 1981-04-24 EP EP81103090A patent/EP0039455B1/de not_active Expired
- 1981-04-24 AT AT81103090T patent/ATE8250T1/de not_active IP Right Cessation
- 1981-04-30 JP JP6433581A patent/JPS56169655A/ja active Pending
-
1985
- 1985-12-19 US US06/814,062 patent/US4684371A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0039455B1 (de) | 1984-07-04 |
| NO811123L (no) | 1981-11-03 |
| DE3164542D1 (en) | 1984-08-09 |
| DK148081A (da) | 1981-11-03 |
| US4684371A (en) | 1987-08-04 |
| ATE8250T1 (de) | 1984-07-15 |
| JPS56169655A (en) | 1981-12-26 |
| NO152004C (no) | 1985-07-17 |
| DK150503C (da) | 1987-12-14 |
| FI69055B (fi) | 1985-08-30 |
| DK150503B (da) | 1987-03-16 |
| NO152004B (no) | 1985-04-09 |
| FI811007L (fi) | 1981-11-03 |
| DE3016881A1 (de) | 1981-11-19 |
| EP0039455A1 (de) | 1981-11-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN |