TW213944B - - Google Patents
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- Publication number
- TW213944B TW213944B TW080106130A TW80106130A TW213944B TW 213944 B TW213944 B TW 213944B TW 080106130 A TW080106130 A TW 080106130A TW 80106130 A TW80106130 A TW 80106130A TW 213944 B TW213944 B TW 213944B
- Authority
- TW
- Taiwan
- Prior art keywords
- alkyl
- group
- dyes
- patent application
- formula
- Prior art date
Links
- 239000000975 dye Substances 0.000 claims abstract description 40
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 13
- 238000011049 filling Methods 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 8
- 150000002431 hydrogen Chemical group 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 229930014669 anthocyanidin Natural products 0.000 claims 1
- 150000001452 anthocyanidin derivatives Chemical class 0.000 claims 1
- 235000008758 anthocyanidins Nutrition 0.000 claims 1
- 229910052786 argon Inorganic materials 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- -1 phenylene, substituted phenylene Chemical group 0.000 abstract description 8
- 229910052736 halogen Inorganic materials 0.000 abstract description 6
- 150000002367 halogens Chemical class 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 3
- 125000001424 substituent group Chemical group 0.000 abstract description 3
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 2
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 239000000126 substance Substances 0.000 description 22
- 239000000203 mixture Substances 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical group 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 description 7
- 239000000047 product Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 6
- 239000010985 leather Substances 0.000 description 6
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- 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 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 125000006239 protecting group Chemical group 0.000 description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 2
- 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 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 2
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 125000000743 hydrocarbylene group Chemical group 0.000 description 2
- TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical compound OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000012038 nucleophile Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- UWTAAGCNRMXMMZ-UHFFFAOYSA-N 1-(2-chlorophenyl)-5-methylpyrazol-3-amine Chemical compound CC1=CC(N)=NN1C1=CC=CC=C1Cl UWTAAGCNRMXMMZ-UHFFFAOYSA-N 0.000 description 1
- FMKMKBLHMONXJM-UHFFFAOYSA-N 5-methyl-2-phenylpyrazol-3-amine Chemical compound N1=C(C)C=C(N)N1C1=CC=CC=C1 FMKMKBLHMONXJM-UHFFFAOYSA-N 0.000 description 1
- PWSZRRFDVPMZGM-UHFFFAOYSA-N 5-phenyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C=C1C1=CC=CC=C1 PWSZRRFDVPMZGM-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 101100080278 Caenorhabditis elegans ncr-2 gene Proteins 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical group 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000003851 azoles Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 229940061607 dibasic sodium phosphate Drugs 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- 101150009274 nhr-1 gene Proteins 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 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
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
- C09B62/08—Azo dyes
- C09B62/082—Azo dyes dyes containing in the molecule at least one azo group and at least one other chromophore group
-
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Coloring (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Photoreceptors In Electrophotography (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Plural Heterocyclic Compounds (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB909017863A GB9017863D0 (en) | 1990-08-15 | 1990-08-15 | Dyes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW213944B true TW213944B (en, 2012) | 1993-10-01 |
Family
ID=10680668
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW080106130A TW213944B (en, 2012) | 1990-08-15 | 1991-08-05 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US6271355B1 (en, 2012) |
| EP (1) | EP0471456B1 (en, 2012) |
| JP (1) | JP2927578B2 (en, 2012) |
| KR (1) | KR100188290B1 (en, 2012) |
| AT (1) | ATE128166T1 (en, 2012) |
| AU (1) | AU641531B2 (en, 2012) |
| CA (1) | CA2048742A1 (en, 2012) |
| DE (1) | DE69113175T2 (en, 2012) |
| ES (1) | ES2076475T3 (en, 2012) |
| FI (1) | FI913793L (en, 2012) |
| GB (2) | GB9017863D0 (en, 2012) |
| ID (1) | ID864B (en, 2012) |
| IN (1) | IN184823B (en, 2012) |
| NO (1) | NO175315C (en, 2012) |
| PT (1) | PT98672B (en, 2012) |
| TR (1) | TR25190A (en, 2012) |
| TW (1) | TW213944B (en, 2012) |
| ZA (1) | ZA915908B (en, 2012) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107760060A (zh) * | 2017-11-16 | 2018-03-06 | 上海俪源科技有限公司 | 一种高日晒翠绿色活性染料化合物的制备工艺 |
| CN107760059A (zh) * | 2017-11-16 | 2018-03-06 | 上海俪源科技有限公司 | 一种高日晒翠绿色吡啶酮活性染料化合物及其制备方法和应用 |
| CN107936614A (zh) * | 2017-11-16 | 2018-04-20 | 上海俪源科技有限公司 | 一种高日晒翠绿色吡唑啉酮活性染料化合物及其制备方法和应用 |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9016451D0 (en) * | 1990-07-26 | 1990-09-12 | Ici Plc | Anionic compounds |
| JPH08134365A (ja) * | 1994-11-04 | 1996-05-28 | Sumitomo Chem Co Ltd | フタロシアニンモノアゾ化合物 |
| US5717077A (en) * | 1994-12-14 | 1998-02-10 | Sumitomo Chemical Company, Limited | Fiber reactive phthalocyanine monoazo compounds having improved dyeing properties |
| GB0005299D0 (en) * | 2000-03-07 | 2000-04-26 | Avecia Ltd | Compound, compositions and use |
| ATE512201T1 (de) * | 2007-11-26 | 2011-06-15 | Procter & Gamble | Verbessertes schattierungsverfahren |
| CN107828241A (zh) * | 2017-11-16 | 2018-03-23 | 上海俪源科技有限公司 | 一种耐晒翠绿色吡唑啉酮结构活性染料化合物及其制备方法和应用 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3082201A (en) * | 1956-08-17 | 1963-03-19 | Ciba Ltd | New phthalocyanine dyestuffs containing halogenated triazine nuclei |
| CH387195A (de) * | 1959-01-13 | 1965-01-31 | Ciba Geigy | Verfahren zur Herstellung von Phthalocyaninfarbstoffen |
| US3123594A (en) * | 1959-07-16 | 1964-03-03 | -sojnh- | |
| CH553843A (de) * | 1961-02-10 | 1974-09-13 | Sandoz Ag | Verfahren zur herstellung metallhaltiger reaktivfarbstoffe. |
| ES275004A2 (es) | 1961-02-28 | 1962-07-16 | Ciba Geigy | Procedimiento para la preparaciën de colorantes de ftalocianina |
| DE1569827A1 (de) * | 1962-03-09 | 1969-08-14 | Sandoz Ag | Verfahren zur Herstellung wasserloeslicher Reaktivfarbstoffe der Phthalocyaninreihe |
| CH489582A (de) * | 1967-08-21 | 1970-04-30 | J R Geigy Ag Chemische Fabrike | Verfahren zur Herstellung von wasserlöslichen Disazofarbstoffen |
| DE1795162C3 (de) * | 1968-08-17 | 1978-11-16 | Bayer Ag, 5090 Leverkusen | Reaktivazofarbstoffe und ihre Verwendung zum Färben und Bedrucken von natürlichen und synthetischen Cellulose- oder Polyamidmaterialien |
| DE3019960A1 (de) * | 1980-05-24 | 1981-12-03 | Hoechst Ag, 6000 Frankfurt | Verfahren zum faerben und bedrucken von hydroxy- und/oder carbonamidgruppen enthaltenden fasermaterialien |
| JPS59152958A (ja) * | 1983-02-17 | 1984-08-31 | Sumitomo Chem Co Ltd | フタロシアニン化合物およびそれを用いて染色または捺染する方法 |
| GB9016451D0 (en) * | 1990-07-26 | 1990-09-12 | Ici Plc | Anionic compounds |
-
1990
- 1990-08-15 GB GB909017863A patent/GB9017863D0/en active Pending
-
1991
- 1991-07-22 DE DE69113175T patent/DE69113175T2/de not_active Expired - Fee Related
- 1991-07-22 ES ES91306641T patent/ES2076475T3/es not_active Expired - Lifetime
- 1991-07-22 GB GB919115762A patent/GB9115762D0/en active Pending
- 1991-07-22 EP EP91306641A patent/EP0471456B1/en not_active Expired - Lifetime
- 1991-07-22 AT AT91306641T patent/ATE128166T1/de not_active IP Right Cessation
- 1991-07-26 ZA ZA915908A patent/ZA915908B/xx unknown
- 1991-07-29 IN IN682DE1991 patent/IN184823B/en unknown
- 1991-07-29 AU AU81420/91A patent/AU641531B2/en not_active Ceased
- 1991-08-05 TW TW080106130A patent/TW213944B/zh active
- 1991-08-08 CA CA002048742A patent/CA2048742A1/en not_active Abandoned
- 1991-08-09 FI FI913793A patent/FI913793L/fi unknown
- 1991-08-14 PT PT98672A patent/PT98672B/pt not_active IP Right Cessation
- 1991-08-14 TR TR91/0789A patent/TR25190A/xx unknown
- 1991-08-14 NO NO913170A patent/NO175315C/no unknown
- 1991-08-14 KR KR1019910013983A patent/KR100188290B1/ko not_active Expired - Fee Related
- 1991-08-15 JP JP3205131A patent/JP2927578B2/ja not_active Expired - Fee Related
- 1991-11-19 ID IDP93891A patent/ID864B/id unknown
-
1993
- 1993-08-17 US US08/107,146 patent/US6271355B1/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107760060A (zh) * | 2017-11-16 | 2018-03-06 | 上海俪源科技有限公司 | 一种高日晒翠绿色活性染料化合物的制备工艺 |
| CN107760059A (zh) * | 2017-11-16 | 2018-03-06 | 上海俪源科技有限公司 | 一种高日晒翠绿色吡啶酮活性染料化合物及其制备方法和应用 |
| CN107936614A (zh) * | 2017-11-16 | 2018-04-20 | 上海俪源科技有限公司 | 一种高日晒翠绿色吡唑啉酮活性染料化合物及其制备方法和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| NO175315C (no) | 1994-09-28 |
| EP0471456B1 (en) | 1995-09-20 |
| FI913793A7 (fi) | 1992-02-16 |
| TR25190A (tr) | 1993-01-01 |
| EP0471456A1 (en) | 1992-02-19 |
| US6271355B1 (en) | 2001-08-07 |
| FI913793L (fi) | 1992-02-16 |
| IN184823B (en, 2012) | 2000-09-30 |
| NO913170D0 (no) | 1991-08-14 |
| ATE128166T1 (de) | 1995-10-15 |
| DE69113175D1 (de) | 1995-10-26 |
| DE69113175T2 (de) | 1996-03-21 |
| PT98672A (pt) | 1992-07-31 |
| KR100188290B1 (ko) | 1999-06-01 |
| JP2927578B2 (ja) | 1999-07-28 |
| AU8142091A (en) | 1992-02-20 |
| ID864B (id) | 1996-08-08 |
| KR920004518A (ko) | 1992-03-27 |
| ZA915908B (en) | 1992-04-29 |
| PT98672B (pt) | 1999-01-29 |
| CA2048742A1 (en) | 1992-02-16 |
| GB9115762D0 (en) | 1991-09-04 |
| NO913170L (no) | 1992-02-17 |
| AU641531B2 (en) | 1993-09-23 |
| NO175315B (no) | 1994-06-20 |
| JPH04261470A (ja) | 1992-09-17 |
| GB9017863D0 (en) | 1990-09-26 |
| ES2076475T3 (es) | 1995-11-01 |
| FI913793A0 (fi) | 1991-08-09 |
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