BRPI0005896B1 - derivados de 1,4 - diaminobenzeno e agentes de tingimento contendo esses compostos - Google Patents
derivados de 1,4 - diaminobenzeno e agentes de tingimento contendo esses compostos Download PDFInfo
- Publication number
- BRPI0005896B1 BRPI0005896B1 BRPI0005896A BR0005896A BRPI0005896B1 BR PI0005896 B1 BRPI0005896 B1 BR PI0005896B1 BR PI0005896 A BRPI0005896 A BR PI0005896A BR 0005896 A BR0005896 A BR 0005896A BR PI0005896 B1 BRPI0005896 B1 BR PI0005896B1
- Authority
- BR
- Brazil
- Prior art keywords
- amino
- diamino
- methyl
- benzene
- phenyl
- Prior art date
Links
- 239000000975 dye Substances 0.000 title claims abstract description 36
- 150000001875 compounds Chemical class 0.000 title abstract description 17
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical class NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 title abstract description 5
- YATFNFXGMVOFKB-UHFFFAOYSA-N 2-(aminomethyl)benzene-1,4-diamine Chemical class NCC1=CC(N)=CC=C1N YATFNFXGMVOFKB-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000835 fiber Substances 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 150000003839 salts Chemical class 0.000 claims abstract description 6
- -1 (4-amino-phenyl-amino) -methyl Chemical group 0.000 claims description 103
- 239000000126 substance Substances 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 230000008878 coupling Effects 0.000 claims description 9
- 238000010168 coupling process Methods 0.000 claims description 9
- 238000005859 coupling reaction Methods 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 102000011782 Keratins Human genes 0.000 claims description 7
- 108010076876 Keratins Proteins 0.000 claims description 7
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 6
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 6
- 150000003254 radicals Chemical class 0.000 claims description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- MLMWBZJIVMYEEK-UHFFFAOYSA-N 2-[3,6-diamino-2-[(4-aminoanilino)methyl]phenyl]ethanol Chemical compound C1=CC(N)=CC=C1NCC1=C(N)C=CC(N)=C1CCO MLMWBZJIVMYEEK-UHFFFAOYSA-N 0.000 claims description 5
- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- YTNOHUXCYTWDTB-UHFFFAOYSA-N 2-[(4-aminoanilino)methyl]benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NCC1=CC(N)=CC=C1N YTNOHUXCYTWDTB-UHFFFAOYSA-N 0.000 claims description 4
- PYBTVDBDKFUKNK-UHFFFAOYSA-N 2-[3,6-diamino-2-[(3-aminoanilino)methyl]phenyl]ethanol Chemical compound NC1=CC=CC(NCC=2C(=C(N)C=CC=2N)CCO)=C1 PYBTVDBDKFUKNK-UHFFFAOYSA-N 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- HDBUEGDDRXDTRP-UHFFFAOYSA-N 2-[(2-aminoanilino)methyl]benzene-1,4-diamine Chemical compound NC1=CC=C(N)C(CNC=2C(=CC=CC=2)N)=C1 HDBUEGDDRXDTRP-UHFFFAOYSA-N 0.000 claims description 3
- ZZLXSXBKAACFES-UHFFFAOYSA-N 2-[(2-pyrrolidin-1-ylanilino)methyl]benzene-1,4-diamine Chemical compound NC1=CC=C(N)C(CNC=2C(=CC=CC=2)N2CCCC2)=C1 ZZLXSXBKAACFES-UHFFFAOYSA-N 0.000 claims description 3
- RSYQMABMCQPGHU-UHFFFAOYSA-N 2-[(3-aminoanilino)methyl]benzene-1,4-diamine Chemical compound NC1=CC=CC(NCC=2C(=CC=C(N)C=2)N)=C1 RSYQMABMCQPGHU-UHFFFAOYSA-N 0.000 claims description 3
- WNQMPGJFGKMMJQ-UHFFFAOYSA-N 2-[2-amino-4-[(2,5-diaminophenyl)methylamino]phenoxy]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=C(N)C(OCCO)=CC=2)=C1 WNQMPGJFGKMMJQ-UHFFFAOYSA-N 0.000 claims description 3
- OAYHZHTYJVLGES-UHFFFAOYSA-N 2-[2-amino-4-[(2,5-diaminophenyl)methylamino]phenyl]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=C(N)C(CCO)=CC=2)=C1 OAYHZHTYJVLGES-UHFFFAOYSA-N 0.000 claims description 3
- MWKIEHWDVSGOIW-UHFFFAOYSA-N 2-[2-amino-5-[(2,5-diaminophenyl)methylamino]phenyl]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=C(CCO)C(N)=CC=2)=C1 MWKIEHWDVSGOIW-UHFFFAOYSA-N 0.000 claims description 3
- MPXVFHGOEKSFPZ-UHFFFAOYSA-N 2-[3,6-diamino-2-[[4-[bis(2-hydroxyethyl)amino]anilino]methyl]phenyl]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=CC(=CC=2)N(CCO)CCO)=C1CCO MPXVFHGOEKSFPZ-UHFFFAOYSA-N 0.000 claims description 3
- ZJQBLNFEBYWTBJ-UHFFFAOYSA-N 2-[4-[(2,5-diaminophenyl)methylamino]-n-(2-hydroxyethyl)anilino]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=CC(=CC=2)N(CCO)CCO)=C1 ZJQBLNFEBYWTBJ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 2
- YKYAIMOLGYRBRR-UHFFFAOYSA-N 2-[(4-amino-3-chloroanilino)methyl]benzene-1,4-diamine Chemical compound NC1=CC=C(N)C(CNC=2C=C(Cl)C(N)=CC=2)=C1 YKYAIMOLGYRBRR-UHFFFAOYSA-N 0.000 claims description 2
- WVFJACHSZYWJCU-UHFFFAOYSA-N 2-[(4-amino-3-methoxyanilino)methyl]benzene-1,4-diamine Chemical compound C1=C(N)C(OC)=CC(NCC=2C(=CC=C(N)C=2)N)=C1 WVFJACHSZYWJCU-UHFFFAOYSA-N 0.000 claims description 2
- CZRWNFWHBZNHTD-UHFFFAOYSA-N 2-[(4-amino-3-methylanilino)methyl]benzene-1,4-diamine Chemical compound C1=C(N)C(C)=CC(NCC=2C(=CC=C(N)C=2)N)=C1 CZRWNFWHBZNHTD-UHFFFAOYSA-N 0.000 claims description 2
- PGMRVWMHJCMXGJ-UHFFFAOYSA-N 2-[2-[(2,5-diaminophenyl)methylamino]anilino]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C(=CC=CC=2)NCCO)=C1 PGMRVWMHJCMXGJ-UHFFFAOYSA-N 0.000 claims description 2
- RFDTWLQBUDNQSQ-UHFFFAOYSA-N 2-[2-[bis(2-hydroxyethyl)amino]-4-[(2,5-diaminophenyl)methylamino]phenyl]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=C(C(CCO)=CC=2)N(CCO)CCO)=C1 RFDTWLQBUDNQSQ-UHFFFAOYSA-N 0.000 claims description 2
- SCXLBFCBFAMOOK-UHFFFAOYSA-N 2-[2-[bis(2-hydroxyethyl)amino]-5-[(2,5-diaminophenyl)methylamino]phenyl]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=C(CCO)C(N(CCO)CCO)=CC=2)=C1 SCXLBFCBFAMOOK-UHFFFAOYSA-N 0.000 claims description 2
- ZBZWUKWLIZWFAK-UHFFFAOYSA-N 2-[3-[(2,5-diaminophenyl)methylamino]anilino]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=C(NCCO)C=CC=2)=C1 ZBZWUKWLIZWFAK-UHFFFAOYSA-N 0.000 claims description 2
- RYNVYDFPUNYZJR-UHFFFAOYSA-N 2-[4-[(2,5-diaminophenyl)methylamino]-n-(2-hydroxyethyl)-2-methylanilino]ethanol Chemical compound C1=C(N(CCO)CCO)C(C)=CC(NCC=2C(=CC=C(N)C=2)N)=C1 RYNVYDFPUNYZJR-UHFFFAOYSA-N 0.000 claims description 2
- JPTGTSULXNOSFN-UHFFFAOYSA-N 2-[5-[(2,5-diaminophenyl)methylamino]-2-(2-hydroxyethoxy)-n-(2-hydroxyethyl)anilino]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=C(C(OCCO)=CC=2)N(CCO)CCO)=C1 JPTGTSULXNOSFN-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- UFLPKRRUNPNZMA-UHFFFAOYSA-N 2-[(4-amino-2-methoxyanilino)methyl]benzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1NCC1=CC(N)=CC=C1N UFLPKRRUNPNZMA-UHFFFAOYSA-N 0.000 claims 1
- HFTBGPVZWDWZEY-UHFFFAOYSA-N 2-[4-[(2,5-diaminophenyl)methylamino]-n-(2-hydroxyethyl)-2-methoxyanilino]ethanol Chemical compound C1=C(N(CCO)CCO)C(OC)=CC(NCC=2C(=CC=C(N)C=2)N)=C1 HFTBGPVZWDWZEY-UHFFFAOYSA-N 0.000 claims 1
- WDBOPYZNISSMDR-UHFFFAOYSA-N 2-[4-[(2,5-diaminophenyl)methylamino]-n-(2-hydroxyethyl)-3-methoxyanilino]ethanol Chemical compound COC1=CC(N(CCO)CCO)=CC=C1NCC1=CC(N)=CC=C1N WDBOPYZNISSMDR-UHFFFAOYSA-N 0.000 claims 1
- LROUNJHBTQNDBJ-UHFFFAOYSA-N 2-[4-[(2,5-diaminophenyl)methylamino]anilino]ethanol Chemical compound NC1=CC=C(N)C(CNC=2C=CC(NCCO)=CC=2)=C1 LROUNJHBTQNDBJ-UHFFFAOYSA-N 0.000 claims 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims 1
- SERASDFIHHDDRZ-UHFFFAOYSA-N 4-pyrrolidin-1-ylbenzamide Chemical compound C1=CC(C(=O)N)=CC=C1N1CCCC1 SERASDFIHHDDRZ-UHFFFAOYSA-N 0.000 claims 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000004043 dyeing Methods 0.000 abstract description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 15
- 230000001590 oxidative effect Effects 0.000 abstract description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 18
- 239000000203 mixture Substances 0.000 description 12
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 238000003786 synthesis reaction Methods 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 7
- 239000007800 oxidant agent Substances 0.000 description 7
- IFPGBDJPISQJJZ-UHFFFAOYSA-N 6-methylbenzene-1,2,4-triamine Chemical class CC1=CC(N)=CC(N)=C1N IFPGBDJPISQJJZ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- 229910021529 ammonia Inorganic materials 0.000 description 5
- 235000010323 ascorbic acid Nutrition 0.000 description 5
- 229960005070 ascorbic acid Drugs 0.000 description 5
- 239000011668 ascorbic acid Substances 0.000 description 5
- 238000001819 mass spectrum Methods 0.000 description 5
- 239000002453 shampoo Substances 0.000 description 5
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 229940096992 potassium oleate Drugs 0.000 description 4
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- LGGKGPQFSCBUOR-UHFFFAOYSA-N 2-(4-chloro-2-nitroanilino)ethanol Chemical compound OCCNC1=CC=C(Cl)C=C1[N+]([O-])=O LGGKGPQFSCBUOR-UHFFFAOYSA-N 0.000 description 3
- CDFNUSAXZDSXKF-UHFFFAOYSA-N 2-chloro-6-(ethylamino)-4-nitrophenol Chemical compound CCNC1=CC([N+]([O-])=O)=CC(Cl)=C1O CDFNUSAXZDSXKF-UHFFFAOYSA-N 0.000 description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 description 3
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 3
- 229940018563 3-aminophenol Drugs 0.000 description 3
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 description 3
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
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- 239000002253 acid Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 235000019646 color tone Nutrition 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
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- 150000007522 mineralic acids Chemical class 0.000 description 3
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
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- 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
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 2
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- LASIYSKAWSELOM-UHFFFAOYSA-N 2-[3,6-diamino-2-[[4-(dimethylamino)anilino]methyl]phenyl]ethanol Chemical compound C1=CC(N(C)C)=CC=C1NCC1=C(N)C=CC(N)=C1CCO LASIYSKAWSELOM-UHFFFAOYSA-N 0.000 description 2
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- 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
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- 239000000654 additive Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 150000001555 benzenes Chemical class 0.000 description 2
- 239000001049 brown dye Substances 0.000 description 2
- YAGCIXJCAUGCGI-UHFFFAOYSA-N butoxycarbonyl butyl carbonate Chemical compound CCCCOC(=O)OC(=O)OCCCC YAGCIXJCAUGCGI-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 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
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- GYXGCRBOQGOWEI-UHFFFAOYSA-N NC1=C(C=C(C=C1N)CCO)[N+](=O)[O-] Chemical compound NC1=C(C=C(C=C1N)CCO)[N+](=O)[O-] GYXGCRBOQGOWEI-UHFFFAOYSA-N 0.000 description 1
- 101800000399 Neurokinin A Proteins 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 102100024304 Protachykinin-1 Human genes 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Chemical class 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- WGQKYBSKWIADBV-UHFFFAOYSA-N aminomethyl benzene Natural products NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- ZTCJMKUOBMZFDN-UHFFFAOYSA-N butyl 4-hydrazinylbenzoate Chemical compound CCCCOC(=O)C1=CC=C(NN)C=C1 ZTCJMKUOBMZFDN-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001913 cellulose Chemical class 0.000 description 1
- 229920002678 cellulose Chemical class 0.000 description 1
- 229940107161 cholesterol Drugs 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 239000000490 cosmetic additive Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- VGSVNUGKHOVSPK-UHFFFAOYSA-N leukoaminochrome Chemical compound C1=C(O)C(O)=CC2=C1NCC2 VGSVNUGKHOVSPK-UHFFFAOYSA-N 0.000 description 1
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 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
- 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
- 238000000034 method Methods 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- WMZGLOVOJHEQQX-UHFFFAOYSA-N n-[2-(2,5-diaminophenoxy)ethyl]acetamide;dihydrochloride Chemical compound Cl.Cl.CC(=O)NCCOC1=CC(N)=CC=C1N WMZGLOVOJHEQQX-UHFFFAOYSA-N 0.000 description 1
- ZUVBIBLYOCVYJU-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21 ZUVBIBLYOCVYJU-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
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 239000001005 nitro dye Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010979 pH adjustment Methods 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
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229950006768 phenylethanolamine Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 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
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-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
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- LZTRCELOJRDYMQ-UHFFFAOYSA-N triphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C1=CC=CC=C1 LZTRCELOJRDYMQ-UHFFFAOYSA-N 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
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/44—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring
- C07C211/49—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring having at least two amino groups bound to the carbon skeleton
- C07C211/50—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring having at least two amino groups bound to the carbon skeleton with at least two amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/51—Phenylenediamines
-
- 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
- C07C215/68—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings and hydroxy groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/78—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C217/80—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
- C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
- C07C217/84—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
Description
Claims (9)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19961274A DE19961274C1 (de) | 1999-12-18 | 1999-12-18 | Neue 1,4-Diaminobenzol-Derivate und diese Verbindungen enthaltende Färbemittel für keratinische Fasern, insbesondere Haarfärbemittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR0005896A BR0005896A (pt) | 2001-07-17 |
| BRPI0005896B1 true BRPI0005896B1 (pt) | 2016-08-30 |
Family
ID=7933295
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0005896A BRPI0005896B1 (pt) | 1999-12-18 | 2000-12-15 | derivados de 1,4 - diaminobenzeno e agentes de tingimento contendo esses compostos |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US6602302B1 (pt) |
| EP (1) | EP1108708B1 (pt) |
| JP (1) | JP4424574B2 (pt) |
| AT (1) | ATE230719T1 (pt) |
| BR (1) | BRPI0005896B1 (pt) |
| DE (2) | DE19961274C1 (pt) |
| ES (1) | ES2189717T3 (pt) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6800097B2 (en) * | 1999-12-18 | 2004-10-05 | Wella Aktiengesellschaft | Substituted 2-aminoalkyl-1,4-Diaminobenzene compounds and oxidation dye precursor compositions containing same |
| ATE312808T1 (de) * | 1999-12-18 | 2005-12-15 | Wella Ag | 2-aminoalkyl-1,4-diaminobenzol-derivate und diese verbindungen enthaltende färbemittel |
| DE10014855C2 (de) * | 2000-03-24 | 2002-05-16 | Wella Ag | p-Diaminobenzol-Derivate und diese Verbindungen enthaltende Färbemittel |
| DE10048733A1 (de) * | 2000-09-29 | 2002-04-18 | Henkel Kgaa | Oxidationsfärbemittel mit 2-Amino-5-methylphenol |
| DE10112506B4 (de) * | 2001-03-15 | 2013-06-27 | Wella GmbH | 1,4-Diamino-2-(2-aminoethyl)-benzol-Derivate und diese Verbindungen enthaltende Färbemittel |
| DE10114084A1 (de) * | 2001-03-22 | 2002-09-26 | Wella Ag | 1,3-Diamino-4-(aminomethyl)-benzol-Derivate und diese Verbindungen enthaltende Färbemittel |
| DE10125451A1 (de) * | 2001-05-25 | 2002-11-28 | Wella Ag | N-Benzyl-m-phenylendiamin-Derivate und diese Verbindungen enthaltende Färbemittel |
| US8028299B2 (en) * | 2005-04-21 | 2011-09-27 | Waratek Pty, Ltd. | Computer architecture and method of operation for multi-computer distributed processing with finalization of objects |
| EP2863877B1 (en) * | 2012-06-25 | 2019-11-27 | Noxell Corporation | Hair colorant compositions comprising 2-methoxymethyl-1,4-diaminobenzene and 2,6-diaminopyridine, methods, and kits comprising the compositions |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE47349C (de) | Dr. H. ERDMANN, Dozent der Chemie an der Universität in Halle a. d. Saale, Sophienstr. 12 | Verfahren zum Färben von Haaren und Federn | ||
| US3743509A (en) * | 1967-03-31 | 1973-07-03 | Addressograph Multigraph | O-aminomethyl-p-phenylenediamines and diazonium salts thereof |
| DE3432214A1 (de) * | 1984-09-01 | 1986-03-13 | Henkel KGaA, 4000 Düsseldorf | Haarfaerbemittel |
| DE3510039A1 (de) * | 1985-03-20 | 1986-09-25 | Henkel KGaA, 4000 Düsseldorf | Haarfaerbemittel |
| DE3741236A1 (de) * | 1987-12-05 | 1989-06-15 | Henkel Kgaa | Phenylamino- und phenylaminomethyl-pyridine und diese enthaltende haarfaerbemittel |
| DE19822041A1 (de) * | 1998-05-16 | 1999-12-23 | Wella Ag | 2,5-Diamino-1-phenylbenzol-Derivate enthaltende Oxidationshaarfärbemittel sowie neue 2,5-Diamino-1-phenylbenzol-Derivate |
-
1999
- 1999-12-18 DE DE19961274A patent/DE19961274C1/de not_active Expired - Fee Related
-
2000
- 2000-10-07 ES ES00121908T patent/ES2189717T3/es not_active Expired - Lifetime
- 2000-10-07 DE DE50001037T patent/DE50001037D1/de not_active Expired - Lifetime
- 2000-10-07 AT AT00121908T patent/ATE230719T1/de not_active IP Right Cessation
- 2000-10-07 EP EP00121908A patent/EP1108708B1/de not_active Expired - Lifetime
- 2000-11-03 US US09/706,000 patent/US6602302B1/en not_active Expired - Lifetime
- 2000-11-24 JP JP2000357603A patent/JP4424574B2/ja not_active Expired - Fee Related
- 2000-12-15 BR BRPI0005896A patent/BRPI0005896B1/pt not_active IP Right Cessation
-
2002
- 2002-09-20 US US10/251,765 patent/US6685751B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US6685751B2 (en) | 2004-02-03 |
| DE50001037D1 (de) | 2003-02-13 |
| ES2189717T3 (es) | 2003-07-16 |
| DE19961274C1 (de) | 2001-02-15 |
| EP1108708B1 (de) | 2003-01-08 |
| US20030110578A1 (en) | 2003-06-19 |
| JP2001199942A (ja) | 2001-07-24 |
| BR0005896A (pt) | 2001-07-17 |
| US6602302B1 (en) | 2003-08-05 |
| ATE230719T1 (de) | 2003-01-15 |
| JP4424574B2 (ja) | 2010-03-03 |
| EP1108708A1 (de) | 2001-06-20 |
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| B07A | Application suspended after technical examination (opinion) [chapter 7.1 patent gazette] | ||
| B15K | Others concerning applications: alteration of classification |
Free format text: ALTERADA DA INT.CL: C07C 211/55, A61K 8/41, A61Q 5/10 Ipc: C07C 211/55 (2009.01), A61K 7/13 (00000007) |
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| B09B | Patent application refused [chapter 9.2 patent gazette] |
Free format text: INDEFERIDO O PEDIDO COM BASE NOS ARTIGOS 8O E 13 DA LPI. |
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| B12B | Appeal against refusal [chapter 12.2 patent gazette] | ||
| B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
| B25D | Requested change of name of applicant approved |
Owner name: WELLA GMBH (DE) |
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| B25G | Requested change of headquarter approved |
Owner name: WELLA GMBH (DE) |
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| B16A | Patent or certificate of addition of invention granted [chapter 16.1 patent gazette] |
Free format text: PRAZO DE VALIDADE: 10 (DEZ) ANOS CONTADOS A PARTIR DE 30/08/2016, OBSERVADAS AS CONDICOES LEGAIS. |
|
| B25A | Requested transfer of rights approved | ||
| B15K | Others concerning applications: alteration of classification |
Ipc: A61Q 5/10 (2006.01), A61K 8/41 (2006.01), C07C 211 |
|
| B21F | Lapse acc. art. 78, item iv - on non-payment of the annual fees in time |
Free format text: REFERENTE A 19A ANUIDADE. |
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| B24J | Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12) |
Free format text: EM VIRTUDE DA EXTINCAO PUBLICADA NA RPI 2544 DE 08-10-2019 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDA A EXTINCAO DA PATENTE E SEUS CERTIFICADOS, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |