TW473516B - Mixtures of reactive disazo dyes, reactive disazo dyes and their use - Google Patents
Mixtures of reactive disazo dyes, reactive disazo dyes and their use Download PDFInfo
- Publication number
- TW473516B TW473516B TW087105129A TW87105129A TW473516B TW 473516 B TW473516 B TW 473516B TW 087105129 A TW087105129 A TW 087105129A TW 87105129 A TW87105129 A TW 87105129A TW 473516 B TW473516 B TW 473516B
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- TW
- Taiwan
- Prior art keywords
- formula
- dye
- scope
- patent application
- hal
- Prior art date
Links
- 239000000975 dye Substances 0.000 title claims abstract description 122
- 239000000203 mixture Substances 0.000 title claims abstract description 54
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title description 3
- 238000004043 dyeing Methods 0.000 claims abstract description 52
- 239000000985 reactive dye Substances 0.000 claims abstract description 46
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000011049 filling Methods 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 18
- 239000002657 fibrous material Substances 0.000 claims description 16
- 239000004952 Polyamide Substances 0.000 claims description 13
- 230000002079 cooperative effect Effects 0.000 claims description 13
- 229920002647 polyamide Polymers 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000001246 bromo group Chemical group Br* 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 229920003043 Cellulose fiber Polymers 0.000 claims description 3
- 150000003254 radicals Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 229910004727 OSO3H Inorganic materials 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 17
- 239000000835 fiber Substances 0.000 abstract description 6
- 239000000243 solution Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000001048 orange dye Substances 0.000 description 16
- 210000002268 wool Anatomy 0.000 description 16
- 239000001045 blue dye Substances 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 229920000742 Cotton Polymers 0.000 description 11
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- -1 amine Salts Chemical class 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000004744 fabric Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 239000004753 textile Substances 0.000 description 6
- 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 5
- 238000001816 cooling Methods 0.000 description 5
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000001044 red dye Substances 0.000 description 4
- 230000002940 repellent Effects 0.000 description 4
- 239000005871 repellent Substances 0.000 description 4
- 239000001632 sodium acetate Substances 0.000 description 4
- 235000017281 sodium acetate Nutrition 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 238000009980 pad dyeing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910006069 SO3H Inorganic materials 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 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 1
- IALORYHODRVWKZ-UHFFFAOYSA-N 2-(4-aminophenyl)sulfonylethyl sulfate;hydron Chemical compound NC1=CC=C(S(=O)(=O)CCOS(O)(=O)=O)C=C1 IALORYHODRVWKZ-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 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
- 244000205754 Colocasia esculenta Species 0.000 description 1
- 235000006481 Colocasia esculenta Nutrition 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
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- AOJDZKCUAATBGE-UHFFFAOYSA-N bromomethane Chemical compound Br[CH2] AOJDZKCUAATBGE-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-N sodium;sulfuric acid Chemical compound [H+].[H+].[Na+].[O-]S([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-N 0.000 description 1
- 239000012192 staining solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical class OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material 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
- C09B62/44—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
- C09B62/465—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 the reactive group being an acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
- C09B62/47—Azo dyes
- C09B62/475—Disazo or polyazo dyes
-
- 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
- C09B62/443—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 the reactive group being alternatively specified
- C09B62/447—Azo dyes
- C09B62/453—Disazo or polyazo dyes
-
- 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
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0046—Mixtures of two or more azo dyes
- C09B67/0055—Mixtures of two or more disazo dyes
- C09B67/0057—Mixtures of two or more reactive disazo dyes
- C09B67/0059—Mixtures of two or more reactive disazo dyes all the reactive groups are not directly attached to a heterocyclic system
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/38—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes
- D06P1/384—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes reactive group not directly attached to heterocyclic group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH80697 | 1997-04-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW473516B true TW473516B (en) | 2002-01-21 |
Family
ID=4195626
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW087105129A TW473516B (en) | 1997-04-07 | 1998-04-04 | Mixtures of reactive disazo dyes, reactive disazo dyes and their use |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US5849887A (enExample) |
| EP (1) | EP0870807B1 (enExample) |
| JP (1) | JP4244076B2 (enExample) |
| KR (1) | KR100533181B1 (enExample) |
| CN (1) | CN1084769C (enExample) |
| DE (1) | DE59800980D1 (enExample) |
| ES (1) | ES2159929T3 (enExample) |
| ID (1) | ID20526A (enExample) |
| MY (1) | MY116247A (enExample) |
| PT (1) | PT870807E (enExample) |
| SG (1) | SG68660A1 (enExample) |
| TW (1) | TW473516B (enExample) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0969051B1 (de) * | 1998-06-30 | 2002-11-27 | Ciba SC Holding AG | Mischungen von Reaktivfarbstoffen und deren Verwendung |
| DE69903599T2 (de) | 1998-07-21 | 2003-06-12 | Dystar Textilfarben Gmbh & Co Deutschland Kg | Marineblaue Mischungen von faserreaktiven Azofarbstoffen |
| TW466263B (en) * | 1998-07-28 | 2001-12-01 | Dystar Textilfarben Gmbh & Amp | Fiber-reactive black dye mixtures and use thereof for dyeing hydroxy-and/or carboxamido-containing fiber material |
| US6086639A (en) * | 1999-03-09 | 2000-07-11 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Black dye mixtures of fiber-reactive azo dyes and use thereof for dyeing hydroxy- and/or carboxamido-containing fiber material |
| US6036732A (en) * | 1999-04-30 | 2000-03-14 | Dystar Textilfarben Gmbh & Co. Deuschland Kg | Black dye mixtures of fiber-reactive azo dyes, methods for their preparation and use thereof for dyeing hydroxy-and/or carboxamido-cont |
| EP1196502A2 (en) | 1999-06-24 | 2002-04-17 | DyStar Textilfarben GmbH & Co. Deutschland KG | Reactive dye mixtures |
| JP2001139835A (ja) | 1999-09-16 | 2001-05-22 | Ciba Specialty Chem Holding Inc | アクリロイルアミノ置換染料の付加生成物、その調製法及び用途 |
| US6159251A (en) * | 1999-10-05 | 2000-12-12 | Dystar Textilfarbon Gmbh & Co. Deutschland Kg | Dye mixtures of fiber-reactive azo dyes and use thereof for dyeing material containing hydroxy-and/or carboxamido groups |
| US6585782B2 (en) * | 2001-02-27 | 2003-07-01 | Everlight Usa, Inc. | Mixtures of reactive dyes and their use |
| US6623534B2 (en) * | 2000-12-29 | 2003-09-23 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Black dye mixtures of fiber-reactive azo dyes, methods for their preparation and use thereof for dyeing hydroxy-and/or carboxamido-containing fiber material |
| DE10127062A1 (de) * | 2001-06-02 | 2002-12-12 | Dystar Textilfarben Gmbh & Co | Farbstoffmischungen von faserreaktiven Azofarbstoffen und ihre Verwendung |
| DE10212769A1 (de) | 2002-03-22 | 2003-10-02 | Dystar Textilfarben Gmbh & Co | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
| US20050223508A1 (en) * | 2002-03-22 | 2005-10-13 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Dye mixtures of fiber reactive azo dyes, production and use |
| KR101181250B1 (ko) * | 2003-11-18 | 2012-09-11 | 시바 홀딩 인크 | 반응성 염료 혼합물 및 이를 포함하는 수성 잉크 |
| TWI434896B (zh) * | 2004-02-13 | 2014-04-21 | Ciba Sc Holding Ag | 活性染料混合物及其用途 |
| CN1317336C (zh) * | 2004-09-16 | 2007-05-23 | 明德国际仓储贸易(上海)有限公司 | 季铵盐双偶氮反应性染料及其应用 |
| CN1322066C (zh) * | 2004-09-22 | 2007-06-20 | 上海科华染料工业有限公司 | 一种复合活性黑染料 |
| CN1312226C (zh) * | 2004-09-22 | 2007-04-25 | 上海科华染料工业有限公司 | 一种复合活性黑染料 |
| CN100368483C (zh) * | 2004-11-29 | 2008-02-13 | 明德国际仓储贸易(上海)有限公司 | 染料组成物及其应用 |
| CN100413930C (zh) * | 2005-08-31 | 2008-08-27 | 明德国际仓储贸易(上海)有限公司 | 反应性染料组成物及其应用 |
| DE102005047391A1 (de) * | 2005-10-05 | 2007-04-12 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbstoffe und Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
| MX2008012702A (es) | 2006-04-07 | 2008-10-15 | Clariant Finance Bvi Ltd | Colorantes acidos. |
| KR100686977B1 (ko) | 2006-04-14 | 2007-02-26 | (주)경인양행 | 반응성 염료 화합물 및 그 제조방법 |
| JP5165880B2 (ja) * | 2006-11-06 | 2013-03-21 | ユニチカトレーディング株式会社 | 涼感性獣毛繊維布帛及びそれを用いてなるフォーマル衣料 |
| CN101235219B (zh) * | 2007-02-01 | 2010-09-08 | 明德国际仓储贸易(上海)有限公司 | 应用于纺织品数字印染的黑色染料组成物及墨水组成物 |
| CN101117449B (zh) * | 2007-09-04 | 2012-05-16 | 大连理工大学 | 一种高浓度复合活性染料 |
| DE102008054404A1 (de) * | 2008-12-09 | 2010-06-10 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Faserreaktive Azofarbstoffe und Farbstoffmischungen, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US8349029B2 (en) | 2008-12-09 | 2013-01-08 | Dystar Colours Deutschland Gmbh | Fiber-reactive azo dyes and dye mixtures, preparation thereof and use thereof |
| CN102115614B (zh) * | 2009-12-30 | 2013-05-29 | 上海雅运纺织化工股份有限公司 | 藏青色活性染料组合物及其在纤维上的染色应用 |
| TWI444437B (zh) * | 2010-06-18 | 2014-07-11 | Everlight Chem Ind Corp | 藍色、紅色及黃色染料化合物及所組成之黑色墨水組成物 |
| CN103044960A (zh) * | 2010-08-27 | 2013-04-17 | 天津德凯化工股份有限公司 | 一种染料活性兰及其制备方法 |
| JP5805416B2 (ja) * | 2011-03-29 | 2015-11-04 | オー・ジー長瀬カラーケミカル株式会社 | セルロース繊維用染料組成物、及びセルロース繊維を含む染色物を製造する方法 |
| WO2013021352A2 (en) | 2011-08-10 | 2013-02-14 | Colourtex Industries Limited | Black mixtures of fibre reactive azo reactive dyestuffs |
| CN102504577A (zh) * | 2011-09-29 | 2012-06-20 | 天津德凯化工股份有限公司 | 一种黑色活性染料 |
| IN2014DN02370A (enExample) * | 2011-12-14 | 2015-05-15 | Huntsman Adv Mat Switzerland | |
| MX380268B (es) | 2012-10-25 | 2025-03-12 | Dystar Colours Distrib Gmbh | Mezclas de tinturas azoicas reactivas con fibras, su preparación y su uso. |
| EP2725068A1 (en) | 2012-10-25 | 2014-04-30 | DyStar Colours Distribution GmbH | Mixtures of fiber-reactive azo dyes, their preparation and their use |
| EP2725069A1 (en) * | 2012-10-25 | 2014-04-30 | DyStar Colours Distribution GmbH | Mixtures of fiber-reactive azo dyes, their preparation and their use |
| EP2725070A1 (en) | 2012-10-25 | 2014-04-30 | DyStar Colours Distribution GmbH | Mixtures of fiber-reactive azo dyes, their preparation and their use |
| CN104755561A (zh) * | 2012-10-25 | 2015-07-01 | 德司达染料分销有限公司 | 纤维活性偶氮染料的混合物,及其制备方法和应用 |
| CN103013176B (zh) * | 2013-01-05 | 2014-12-10 | 江苏德美科化工有限公司 | 一种高性能绿色活性染料混合物及其应用 |
| CN104119693A (zh) * | 2013-04-28 | 2014-10-29 | 浙江科永化工有限公司 | 一种橙色活性染料化合物及其应用 |
| EP2862902A1 (en) * | 2013-08-29 | 2015-04-22 | DyStar Colours Distribution GmbH | Dye mixtures of metal free reactive dyes, production and use |
| CN104513497A (zh) * | 2013-09-27 | 2015-04-15 | 浙江科永化工有限公司 | 一种活性黑染料组合物 |
| CN103571231A (zh) * | 2013-11-07 | 2014-02-12 | 褚平忠 | 具有高固色率的深黑色活性染料 |
| CN104263007B (zh) * | 2014-08-20 | 2016-04-06 | 张家港市振新印染有限公司 | 一种高日晒牢度活性染料 |
| CN105566946A (zh) * | 2015-12-22 | 2016-05-11 | 浙江亿得化工有限公司 | 复合毛用活性蓝染料及其制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2032927C3 (de) * | 1970-07-03 | 1979-06-13 | Hoechst Ag, 6000 Frankfurt | Wasserlösliche Metallkomplex-Disazofarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung zum Färben oder Bedrucken von Wolle, Seide, Leder, Polyamidoder Polyurethanfasern oder nativen oder regenerierten Cellulosefasern |
| TW268967B (enExample) * | 1992-11-28 | 1996-01-21 | Hoechst Ag | |
| TW279889B (enExample) * | 1993-10-07 | 1996-07-01 | Ciba Geigy Ag | |
| DE19511688C2 (de) * | 1995-03-30 | 1999-07-22 | Dystar Textilfarben Gmbh & Co | Farbstoffmischungen von faserreaktiven Azofarbstoffen und ihre Verwendung zum Färben von hydroxy- und/oder carbonamidgruppenhaltigem Fasermaterial |
| US5611821A (en) * | 1995-09-16 | 1997-03-18 | Everlight Usa, Inc. | Black reactive dye composition |
| MY117759A (en) * | 1996-01-19 | 2004-08-30 | Ciba Sc Holding Ag | Reactive dyes their preparation and use. |
-
1998
- 1998-03-27 SG SG1998000641A patent/SG68660A1/en unknown
- 1998-03-30 US US09/050,280 patent/US5849887A/en not_active Expired - Lifetime
- 1998-03-30 EP EP98810272A patent/EP0870807B1/de not_active Expired - Lifetime
- 1998-03-30 PT PT98810272T patent/PT870807E/pt unknown
- 1998-03-30 DE DE59800980T patent/DE59800980D1/de not_active Expired - Lifetime
- 1998-03-30 ES ES98810272T patent/ES2159929T3/es not_active Expired - Lifetime
- 1998-03-30 MY MYPI98001391A patent/MY116247A/en unknown
- 1998-04-03 ID IDP980505A patent/ID20526A/id unknown
- 1998-04-03 JP JP09049198A patent/JP4244076B2/ja not_active Expired - Fee Related
- 1998-04-04 TW TW087105129A patent/TW473516B/zh not_active IP Right Cessation
- 1998-04-06 CN CN98106332A patent/CN1084769C/zh not_active Expired - Fee Related
- 1998-04-07 KR KR1019980012197A patent/KR100533181B1/ko not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| ID20526A (id) | 1999-01-07 |
| JPH10279827A (ja) | 1998-10-20 |
| JP4244076B2 (ja) | 2009-03-25 |
| EP0870807B1 (de) | 2001-07-11 |
| KR100533181B1 (ko) | 2006-03-22 |
| HK1015812A1 (en) | 1999-10-22 |
| EP0870807A1 (de) | 1998-10-14 |
| ES2159929T3 (es) | 2001-10-16 |
| KR19980081141A (ko) | 1998-11-25 |
| US5849887A (en) | 1998-12-15 |
| CN1084769C (zh) | 2002-05-15 |
| SG68660A1 (en) | 1999-11-16 |
| PT870807E (pt) | 2001-12-28 |
| DE59800980D1 (de) | 2001-08-16 |
| CN1195678A (zh) | 1998-10-14 |
| MY116247A (en) | 2003-12-31 |
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