CH660016A5 - Reaktivfarbstoffe und deren herstellung. - Google Patents
Reaktivfarbstoffe und deren herstellung. Download PDFInfo
- Publication number
- CH660016A5 CH660016A5 CH6035/83A CH603583A CH660016A5 CH 660016 A5 CH660016 A5 CH 660016A5 CH 6035/83 A CH6035/83 A CH 6035/83A CH 603583 A CH603583 A CH 603583A CH 660016 A5 CH660016 A5 CH 660016A5
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- sulfonic acid
- acid
- parts
- dye
- Prior art date
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- 239000000985 reactive dye Substances 0.000 title claims description 39
- 238000004519 manufacturing process Methods 0.000 title description 6
- 239000000975 dye Substances 0.000 claims description 211
- -1 alkyl radical Chemical class 0.000 claims description 114
- 238000005859 coupling reaction Methods 0.000 claims description 58
- 230000008878 coupling Effects 0.000 claims description 54
- 238000010168 coupling process Methods 0.000 claims description 54
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 51
- 150000001412 amines Chemical class 0.000 claims description 39
- 125000004432 carbon atom Chemical group C* 0.000 claims description 39
- 150000003254 radicals Chemical class 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 27
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 23
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 20
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 20
- 239000000460 chlorine Chemical group 0.000 claims description 17
- 238000002360 preparation method Methods 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 125000005843 halogen group Chemical group 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 12
- 230000008569 process Effects 0.000 claims description 11
- 125000001424 substituent group Chemical group 0.000 claims description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 8
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 8
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 8
- 150000004056 anthraquinones Chemical class 0.000 claims description 8
- 239000010949 copper Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
- 125000005236 alkanoylamino group Chemical group 0.000 claims description 6
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
- WLFXSECCHULRRO-UHFFFAOYSA-N pyridine-2,6-diol Chemical compound OC1=CC=CC(O)=N1 WLFXSECCHULRRO-UHFFFAOYSA-N 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 5
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 5
- 239000001007 phthalocyanine dye Substances 0.000 claims description 5
- XRIGHGYEGNDPEU-UHFFFAOYSA-N 1-anilinoanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1NC1=CC=CC=C1 XRIGHGYEGNDPEU-UHFFFAOYSA-N 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
- 239000001000 anthraquinone dye Substances 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 150000002790 naphthalenes Chemical class 0.000 claims description 4
- 125000004999 nitroaryl group Chemical group 0.000 claims description 4
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical group O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 claims description 3
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 3
- 229910006069 SO3H Inorganic materials 0.000 claims description 3
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 3
- 150000004696 coordination complex Chemical class 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical group 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 claims description 2
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 claims description 2
- WDJHALXBUFZDSR-UHFFFAOYSA-N Acetoacetic acid Natural products CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 claims description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 229910004727 OSO3H Inorganic materials 0.000 claims description 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims description 2
- WDEQGLDWZMIMJM-UHFFFAOYSA-N benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate Chemical compound OCC1CC(O)CN1C(=O)OCC1=CC=CC=C1 WDEQGLDWZMIMJM-UHFFFAOYSA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000003363 1,3,5-triazinyl group Chemical class N1=C(N=CN=C1)* 0.000 claims 1
- 241001104043 Syringa Species 0.000 claims 1
- 235000004338 Syringa vulgaris Nutrition 0.000 claims 1
- 235000013351 cheese Nutrition 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- 239000002253 acid Substances 0.000 description 115
- 239000000243 solution Substances 0.000 description 84
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 81
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 48
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 40
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 38
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 34
- PYNUOAIJIQGACY-UHFFFAOYSA-N propylazanium;chloride Chemical compound Cl.CCCN PYNUOAIJIQGACY-UHFFFAOYSA-N 0.000 description 34
- 238000006243 chemical reaction Methods 0.000 description 33
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 32
- XWBDWHCCBGMXKG-UHFFFAOYSA-N ethanamine;hydron;chloride Chemical compound Cl.CCN XWBDWHCCBGMXKG-UHFFFAOYSA-N 0.000 description 29
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 28
- 150000004699 copper complex Chemical class 0.000 description 28
- 239000000203 mixture Substances 0.000 description 25
- 230000007935 neutral effect Effects 0.000 description 25
- 239000011780 sodium chloride Substances 0.000 description 17
- 239000002002 slurry Substances 0.000 description 15
- 238000004043 dyeing Methods 0.000 description 14
- 150000000182 1,3,5-triazines Chemical class 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 12
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 12
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 10
- 229920000742 Cotton Polymers 0.000 description 10
- 235000017550 sodium carbonate Nutrition 0.000 description 10
- 229910000029 sodium carbonate Inorganic materials 0.000 description 10
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 9
- VMKJWLXVLHBJNK-UHFFFAOYSA-N cyanuric fluoride Chemical compound FC1=NC(F)=NC(F)=N1 VMKJWLXVLHBJNK-UHFFFAOYSA-N 0.000 description 9
- 150000008049 diazo compounds Chemical class 0.000 description 9
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 9
- WMPOWTWJFGZRIG-UHFFFAOYSA-N 4,5,6-tribromotriazine Chemical compound BrC1=NN=NC(Br)=C1Br WMPOWTWJFGZRIG-UHFFFAOYSA-N 0.000 description 8
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 230000002378 acidificating effect Effects 0.000 description 8
- 125000002252 acyl group Chemical group 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- JVMSQRAXNZPDHF-UHFFFAOYSA-N 2,4-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(N)=C1 JVMSQRAXNZPDHF-UHFFFAOYSA-N 0.000 description 7
- HPIITGUWGFPYGJ-UHFFFAOYSA-N 4,5,6-tris(ethylsulfonyl)triazine Chemical compound CCS(=O)(=O)C1=NN=NC(S(=O)(=O)CC)=C1S(=O)(=O)CC HPIITGUWGFPYGJ-UHFFFAOYSA-N 0.000 description 7
- YYTRUFPLZKSNDK-UHFFFAOYSA-N 4,5-dichloro-6-fluorotriazine Chemical compound FC1=NN=NC(Cl)=C1Cl YYTRUFPLZKSNDK-UHFFFAOYSA-N 0.000 description 7
- 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 7
- SMXUXPDUMQUWGI-UHFFFAOYSA-N ClC=1C(=NN=NC1S(=O)(=O)C)S(=O)(=O)C Chemical compound ClC=1C(=NN=NC1S(=O)(=O)C)S(=O)(=O)C SMXUXPDUMQUWGI-UHFFFAOYSA-N 0.000 description 7
- ZIEZSHKUKVICHE-UHFFFAOYSA-N ClC=1C(=NN=NC1S(=O)(=O)O)S(=O)(=O)O Chemical compound ClC=1C(=NN=NC1S(=O)(=O)O)S(=O)(=O)O ZIEZSHKUKVICHE-UHFFFAOYSA-N 0.000 description 7
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 7
- 125000003277 amino group Chemical group 0.000 description 7
- 239000000987 azo dye Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 6
- MRYIKYDDYVEWAW-UHFFFAOYSA-N 4,5,6-tris(benzenesulfonyl)triazine Chemical compound N=1N=NC(S(=O)(=O)C=2C=CC=CC=2)=C(S(=O)(=O)C=2C=CC=CC=2)C=1S(=O)(=O)C1=CC=CC=C1 MRYIKYDDYVEWAW-UHFFFAOYSA-N 0.000 description 6
- QZMNTLVGYUZLQF-UHFFFAOYSA-N 4,5,6-tris(methylsulfonyl)triazine Chemical compound CS(=O)(=O)C1=NN=NC(S(C)(=O)=O)=C1S(C)(=O)=O QZMNTLVGYUZLQF-UHFFFAOYSA-N 0.000 description 6
- HBZVNWNSRNTWPS-UHFFFAOYSA-N 6-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N)=CC=C21 HBZVNWNSRNTWPS-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000007859 condensation product Substances 0.000 description 6
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 6
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
- HEAHMJLHQCESBZ-UHFFFAOYSA-N 2,5-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(N)C(S(O)(=O)=O)=C1 HEAHMJLHQCESBZ-UHFFFAOYSA-N 0.000 description 5
- ZMCHBSMFKQYNKA-UHFFFAOYSA-N 2-aminobenzenesulfonic acid Chemical compound NC1=CC=CC=C1S(O)(=O)=O ZMCHBSMFKQYNKA-UHFFFAOYSA-N 0.000 description 5
- FOINSAWEWXUXPQ-UHFFFAOYSA-N 4-acetamido-2-aminobenzenesulfonic acid Chemical compound CC(=O)NC1=CC=C(S(O)(=O)=O)C(N)=C1 FOINSAWEWXUXPQ-UHFFFAOYSA-N 0.000 description 5
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 5
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 5
- 229910052804 chromium Inorganic materials 0.000 description 5
- 239000011651 chromium Substances 0.000 description 5
- 150000004985 diamines Chemical class 0.000 description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- YAIKCRUPEVOINQ-UHFFFAOYSA-N 2-aminonaphthalene-1,5-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC2=C(S(O)(=O)=O)C(N)=CC=C21 YAIKCRUPEVOINQ-UHFFFAOYSA-N 0.000 description 4
- ZUQOBHTUMCEQBG-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-1,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC=C(S(O)(=O)=O)C2=C1 ZUQOBHTUMCEQBG-UHFFFAOYSA-N 0.000 description 4
- KZCSUEYBKAPKNH-UHFFFAOYSA-N 6-aminonaphthalene-1,3-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KZCSUEYBKAPKNH-UHFFFAOYSA-N 0.000 description 4
- GFPQSWFFPRQEHH-UHFFFAOYSA-N 7-aminonaphthalene-1,3,6-trisulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C=C(S(O)(=O)=O)C(N)=CC2=C1S(O)(=O)=O GFPQSWFFPRQEHH-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000005917 acylation reaction Methods 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
- 150000004982 aromatic amines Chemical class 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 238000004108 freeze drying Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000001103 potassium chloride Substances 0.000 description 4
- 235000011164 potassium chloride Nutrition 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 238000005185 salting out Methods 0.000 description 4
- 238000007127 saponification reaction Methods 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 238000001694 spray drying Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 229950000244 sulfanilic acid Drugs 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- ZNXSFVXZQBETRJ-UHFFFAOYSA-N (3-aminophenyl)urea Chemical compound NC(=O)NC1=CC=CC(N)=C1 ZNXSFVXZQBETRJ-UHFFFAOYSA-N 0.000 description 3
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
- OPBOOIFXQHPAPJ-UHFFFAOYSA-N 1-amino-4-anilino-9,10-dioxoanthracene-2-sulfonic acid Chemical class C1=C(S(O)(=O)=O)C(N)=C2C(=O)C3=CC=CC=C3C(=O)C2=C1NC1=CC=CC=C1 OPBOOIFXQHPAPJ-UHFFFAOYSA-N 0.000 description 3
- ZAKYBQTZZHWXOB-UHFFFAOYSA-N 2-amino-3,4-dimethylbenzenesulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C(N)=C1C ZAKYBQTZZHWXOB-UHFFFAOYSA-N 0.000 description 3
- VJHJWHAIOWSVCP-UHFFFAOYSA-N 2-amino-5-chloro-3-methylbenzenesulfonic acid Chemical compound CC1=CC(Cl)=CC(S(O)(=O)=O)=C1N VJHJWHAIOWSVCP-UHFFFAOYSA-N 0.000 description 3
- KTFUNVBAGAPLLC-UHFFFAOYSA-N 2-amino-5-ethoxybenzenesulfonic acid Chemical compound CCOC1=CC=C(N)C(S(O)(=O)=O)=C1 KTFUNVBAGAPLLC-UHFFFAOYSA-N 0.000 description 3
- LTPSRQRIPCVMKQ-UHFFFAOYSA-N 2-amino-5-methylbenzenesulfonic acid Chemical compound CC1=CC=C(N)C(S(O)(=O)=O)=C1 LTPSRQRIPCVMKQ-UHFFFAOYSA-N 0.000 description 3
- LTASFWDWBYFZQQ-UHFFFAOYSA-N 2-amino-5-nitrobenzenesulfonic acid Chemical compound NC1=CC=C([N+]([O-])=O)C=C1S(O)(=O)=O LTASFWDWBYFZQQ-UHFFFAOYSA-N 0.000 description 3
- ACHUDPKPXIEHAD-UHFFFAOYSA-N 2-amino-6-chlorobenzenesulfonic acid Chemical compound NC1=CC=CC(Cl)=C1S(O)(=O)=O ACHUDPKPXIEHAD-UHFFFAOYSA-N 0.000 description 3
- GWIAAIUASRVOIA-UHFFFAOYSA-N 2-aminonaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(N)=CC=C21 GWIAAIUASRVOIA-UHFFFAOYSA-N 0.000 description 3
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 238000003032 molecular docking Methods 0.000 description 1
- SJWQCBCAGCEWCV-UHFFFAOYSA-N n-(3-amino-4-methoxyphenyl)acetamide Chemical compound COC1=CC=C(NC(C)=O)C=C1N SJWQCBCAGCEWCV-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 1
- 239000001048 orange dye Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 235000011149 sulphuric acid Nutrition 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
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical compound C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/4401—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system
- C09B62/4403—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system the heterocyclic system being a triazine ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH6035/83A CH660016A5 (de) | 1983-11-09 | 1983-11-09 | Reaktivfarbstoffe und deren herstellung. |
| EP84113351A EP0144766B1 (de) | 1983-11-09 | 1984-11-06 | Reaktivfarbstoffe, deren Herstellung und Verwendung |
| DE8484113351T DE3474457D1 (en) | 1983-11-09 | 1984-11-06 | Reactive dyes, their preparation and their use |
| JP59235349A JPS60118752A (ja) | 1983-11-09 | 1984-11-09 | 反応染料およびその製造法と使用法 |
| US06/821,213 US4754023A (en) | 1983-11-09 | 1986-01-23 | Reactive dyestuffs comprising a triazine moiety and a vinylsulfonyl moiety both being linked by a substituted alkylene bridge member |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH6035/83A CH660016A5 (de) | 1983-11-09 | 1983-11-09 | Reaktivfarbstoffe und deren herstellung. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH660016A5 true CH660016A5 (de) | 1987-03-13 |
Family
ID=4303170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH6035/83A CH660016A5 (de) | 1983-11-09 | 1983-11-09 | Reaktivfarbstoffe und deren herstellung. |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4754023A (OSRAM) |
| EP (1) | EP0144766B1 (OSRAM) |
| JP (1) | JPS60118752A (OSRAM) |
| CH (1) | CH660016A5 (OSRAM) |
| DE (1) | DE3474457D1 (OSRAM) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3561325D1 (en) * | 1984-04-05 | 1988-02-11 | Ciba Geigy Ag | Reactive dyes, their preparation and their use |
| DE3669323D1 (de) * | 1985-07-12 | 1990-04-12 | Ciba Geigy Ag | Reaktivfarbstoffe, deren herstellung und verwendung. |
| US5023325A (en) * | 1985-07-12 | 1991-06-11 | Ciba-Geigy Corporation | Fibre-reactive dyes containing a substituted aminocarbonyl-phenylamino or naphthylamino reactive moiety |
| BR8606825A (pt) * | 1985-08-14 | 1987-10-27 | Ciba Geigy Ag | Corantes reativos,sua preparacao e emprego |
| US4766206A (en) * | 1985-10-03 | 1988-08-23 | Ciba-Geigy Corporation | Reactive dyestuffs comprising a vinylsulfonylalkylaminocarbonyl moiety |
| EP0233139B1 (de) * | 1986-01-10 | 1991-01-16 | Ciba-Geigy Ag | Reaktivfarbstoffe, deren Herstellung und Verwendung |
| US4845203A (en) * | 1986-09-12 | 1989-07-04 | Ciba-Geigy Corporation | Fibre-reaction disazo dyes with a bi-reaction moiety comprising a halotriazine and vinylsulfonyl type radical |
| DE3862766D1 (de) * | 1987-02-06 | 1991-06-20 | Ciba Geigy Ag | Reaktivfarbstoffe, deren herstellung und verwendung. |
| DE3868104D1 (de) * | 1987-03-27 | 1992-03-12 | Ciba Geigy Ag | Reaktivfarbstoffe, deren herstellung und verwendung. |
| EP0285571B1 (de) * | 1987-04-02 | 1992-02-05 | Ciba-Geigy Ag | Reaktivfarbstoffe, deren Herstellung und Verwendung |
| US4900813A (en) * | 1987-07-02 | 1990-02-13 | Ciba-Geigy Corporation | Fiber-reactive azo dyes having a 4,6-diaminopyridine coupling component |
| DE3868300D1 (de) * | 1987-07-03 | 1992-03-19 | Ciba Geigy Ag | Reaktivfarbstoffe, verfahren zu deren herstellung und deren verwendung. |
| US4880434A (en) * | 1987-07-23 | 1989-11-14 | Sumitomo Chemical Company, Limited | Method of obtaining dyed and finished cellulose fiber materials using reactive metallized formazan dye with no color change |
| US4918169A (en) * | 1987-08-27 | 1990-04-17 | Ciba-Geigy Corporation | Fiber-reactive dyestuffs comprising a 5-formylpyrimidine moiety |
| ES2042796T5 (es) * | 1987-09-24 | 2000-10-16 | Ciba Sc Holding Ag | Colorantes reactivos, su obtencion y empleo. |
| US4925928A (en) * | 1988-06-23 | 1990-05-15 | Ciba-Geigy Corporation | Reactive dyes containing vinylsulfonylalkylamino bound to a bis-(triazinylamino)-benzene group |
| US5243034A (en) * | 1988-12-21 | 1993-09-07 | Hoechst Aktiengesellschaft | Disazo dyestuffs having a triazine moiety and a fiberreactive group of vinylsulfone series |
| DE59004457D1 (de) * | 1989-03-22 | 1994-03-17 | Hoechst Ag | Wasserlösliche faserreaktive Farbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung. |
| US5274083A (en) * | 1989-05-03 | 1993-12-28 | Bayer Aktiengesellschaft | Polyfunctional fibre-reactive dyestuffs |
| DE3914628A1 (de) * | 1989-05-03 | 1990-11-15 | Bayer Ag | Polyfunktionelle faserreaktive farbstoffe |
| DE4206040A1 (de) * | 1992-02-27 | 1993-09-02 | Bayer Ag | Neue reaktivfarbstoffe |
| DE4214740A1 (de) * | 1992-05-04 | 1993-11-11 | Bayer Ag | Reaktivfarbstoffe, deren Herstellung und Verwendung |
| EP0568876B1 (de) * | 1992-05-04 | 1996-08-28 | Bayer Ag | Reaktivfarbstoffe, deren Herstellung und Verwendung |
| ES2133375T3 (es) * | 1992-07-23 | 1999-09-16 | Ciba Sc Holding Ag | Colorantes reactivos, procedimiento para su obtencion y utilizacion de los mismos. |
| DE4417719A1 (de) * | 1994-05-20 | 1995-11-23 | Hoechst Ag | Reaktivfarbstoffe mit hydrolysestabilen Reaktivgruppen |
| EP0719840A1 (en) * | 1994-12-26 | 1996-07-03 | Sumitomo Chemical Company, Limited | Monoazo compounds and method for dyeing or printing fiber materials using the same |
| JPH09137074A (ja) * | 1995-11-14 | 1997-05-27 | Sumitomo Chem Co Ltd | モノアゾ化合物及びそれを用いる繊維材料の染色又は捺染方法 |
| EP0775730B1 (de) * | 1995-11-23 | 2000-05-03 | Ciba SC Holding AG | Reaktivfarbstoffe, Verfahren zu deren Herstellung und deren Verwendung |
| EP0775731B1 (de) * | 1995-11-23 | 1999-12-29 | Ciba SC Holding AG | Reaktivfarbstoffe, Verfahren zu deren Herstellung und deren Verwendung |
| EP1247842B1 (de) * | 1995-11-23 | 2008-05-21 | Huntsman Advanced Materials (Switzerland) GmbH | Faserreaktive Anthrachinonfarbstoffe, deren Herstellung und deren Verwendung |
| JPH09324130A (ja) * | 1996-06-05 | 1997-12-16 | Sumitomo Chem Co Ltd | モノアゾ化合物及びそれを用いる繊維材料の染色又は捺染方法 |
| GB2315493B (en) * | 1996-07-24 | 2001-01-03 | Lexmark Int Inc | Ink jet ink dyes |
| DE10014654A1 (de) | 1999-04-07 | 2000-11-02 | Sumitomo Chemical Co | Bisazoverbindungen und Verfahren zum Färben oder Bedrucken unter deren Verwendung |
| JP2001002952A (ja) * | 1999-04-19 | 2001-01-09 | Sumitomo Chem Co Ltd | ビスアゾ化合物又はその塩及びそれらの繊維材料への適用 |
| TWI260334B (en) * | 1999-11-01 | 2006-08-21 | Clariant Int Ltd | Azo dyestuffs |
| US6177552B1 (en) | 1999-12-28 | 2001-01-23 | Dystartextilfarben Gmbh & Co. Deutschland Kg | Fiber-reactive azo compounds, processes for their preparation and their use as dyes |
| US6391066B1 (en) * | 2000-02-23 | 2002-05-21 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Dye mixture comprising water-soluble fiber-reactive dyes, preparation thereof and use thereof |
| AU2001258273A1 (en) * | 2000-03-22 | 2001-10-03 | Ciba Specialty Chemicals Holding Inc. | Fibre reactive naphthylazonaphthyl triazinyl dyes |
| KR101785258B1 (ko) | 2010-02-18 | 2017-10-16 | 훈츠만 어드밴스트 머티리얼스(스위처랜드) 게엠베하 | 섬유-반응성 염료들의 혼합물, 및 2색성 또는 3색성 염색 또는 프린팅 방법에 있어서의 이의 용도 |
| CN107532008A (zh) | 2015-05-12 | 2018-01-02 | 亨斯迈先进材料（瑞士）有限公司 | 反应性染料的混合物及其用于纺织纤维材料的染色或印刷的用途 |
| WO2017129297A1 (en) | 2016-01-29 | 2017-08-03 | Huntsman Advanced Materials (Switzerland) Gmbh | Fibre reactive formazan dyes, their preparation and their use |
| EP3336148A1 (en) * | 2016-12-15 | 2018-06-20 | DyStar Colours Distribution GmbH | Blue and navy fibre reactive dye mixtures |
| BR112022019692A8 (pt) | 2020-04-27 | 2023-05-09 | Huntsman Adv Mat Switzerland | Misturas de corantes reativos e seu uso para tingimento ou impressão de materiais de fibra têxteis |
| MX2024008952A (es) | 2022-01-25 | 2024-08-28 | Archroma Switzerland Gmbh | Mezcla isomerica de colorantes reactivos y su uso para el te?ido o estampado de materiales de fibra textil. |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1644155B2 (de) * | 1965-09-07 | 1977-04-07 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von disazofarbstoffen und deren metallkomplexverbindungen |
| CH463650A (de) * | 1958-01-28 | 1968-10-15 | Bayer Ag | Verfahren zur Herstellung von Farbstoffen |
| DE1265698C2 (de) * | 1961-05-06 | 1968-11-07 | Hoechst Ag | Verfahren zur Erzeugung von nassechten Faerbungen und Drucken |
| DE1262475B (de) * | 1962-02-08 | 1968-03-07 | Hoechst Ag | Verfahren zur Herstellung von organischen Farbstoffen |
| DE1644164B2 (de) * | 1966-06-24 | 1976-04-29 | Hoechst Ag, 6000 Frankfurt | 2 zu 1-chromkomplex-monoazofarbstoffe, verfahren zu ihrer herstellung und ihre verwendung |
| GB1151936A (en) * | 1966-08-15 | 1969-05-14 | Ici Ltd | Water-Soluble Reactive Metal Complex Monoazo Dyestuffs |
| AR207988A1 (es) * | 1974-07-16 | 1976-11-22 | Ciba Geigy Ag | Complejos de cobre niquel cromo y cobalto de colorantes azoicos y azometinicos y procedimiento para su obtencion |
| DE2614550C3 (de) * | 1976-04-03 | 1981-06-25 | Cassella Ag, 6000 Frankfurt | Neue Reaktivfarbstoffe, ihre Herstellung und Verwendung zum Färben und Bedrucken von Cellulose sowie natürlichen und synthetischen Polyamidsubstraten |
| US4378313B1 (en) * | 1979-06-01 | 1994-05-03 | Sumitomo Chemical Co | Reactive yellow dye having both monochlorotriazinyl and vinylsulfone type reactive groups |
| US4341699A (en) * | 1979-07-13 | 1982-07-27 | Sumitomo Chemical Company, Limited | Reactive red dye having both monochlorotriazinyl- and vinylsulfone-type reactive groups |
| DE3272886D1 (en) * | 1981-07-21 | 1986-10-02 | Ciba Geigy Ag | Reactive dyestuffs, their preparation and their use |
| EP0074928A3 (de) * | 1981-09-16 | 1983-04-20 | Ciba-Geigy Ag | Reaktivfarbstoffe, deren Herstellung und Verwendung |
| EP0085025B1 (de) * | 1982-01-21 | 1986-10-15 | Ciba-Geigy Ag | Reaktivfarbstoffe, deren Herstellung und Verwendung |
| DE3373110D1 (en) * | 1982-01-29 | 1987-09-24 | Ciba Geigy Ag | Reactive dyes, their preparation and their use |
-
1983
- 1983-11-09 CH CH6035/83A patent/CH660016A5/de not_active IP Right Cessation
-
1984
- 1984-11-06 EP EP84113351A patent/EP0144766B1/de not_active Expired
- 1984-11-06 DE DE8484113351T patent/DE3474457D1/de not_active Expired
- 1984-11-09 JP JP59235349A patent/JPS60118752A/ja active Granted
-
1986
- 1986-01-23 US US06/821,213 patent/US4754023A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0144766A3 (en) | 1985-12-18 |
| JPS60118752A (ja) | 1985-06-26 |
| DE3474457D1 (en) | 1988-11-10 |
| JPH0225386B2 (OSRAM) | 1990-06-01 |
| EP0144766A2 (de) | 1985-06-19 |
| EP0144766B1 (de) | 1988-10-05 |
| US4754023A (en) | 1988-06-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUE | Assignment |
Owner name: CIBA-GEIGY AG TRANSFER- CIBA SC HOLDING AG |
|
| PFA | Name/firm changed |
Owner name: CIBA SC HOLDING AG TRANSFER- CIBA SPECIALTY CHEMIC |
|
| PL | Patent ceased |