ZA200406383B - Dye mixtures of fiber-reactive azo dyes, their production and use - Google Patents
Dye mixtures of fiber-reactive azo dyes, their production and use Download PDFInfo
- Publication number
- ZA200406383B ZA200406383B ZA200406383A ZA200406383A ZA200406383B ZA 200406383 B ZA200406383 B ZA 200406383B ZA 200406383 A ZA200406383 A ZA 200406383A ZA 200406383 A ZA200406383 A ZA 200406383A ZA 200406383 B ZA200406383 B ZA 200406383B
- Authority
- ZA
- South Africa
- Prior art keywords
- general formula
- dyes
- alkyl
- hydrogen
- independently
- Prior art date
Links
- 239000000975 dye Substances 0.000 title claims abstract description 80
- 239000000203 mixture Substances 0.000 title claims abstract description 48
- 239000000987 azo dye Substances 0.000 title description 3
- -1 carbamoylphenyl Chemical group 0.000 claims abstract description 84
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 43
- 239000000985 reactive dye Substances 0.000 claims abstract description 20
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 4
- 238000002360 preparation method Methods 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims abstract 5
- 239000007788 liquid Substances 0.000 claims abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 50
- 239000001257 hydrogen Substances 0.000 claims description 50
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 35
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 33
- 229910052736 halogen Inorganic materials 0.000 claims description 30
- 150000002367 halogens Chemical class 0.000 claims description 30
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 25
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 21
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 17
- 125000003368 amide group Chemical group 0.000 claims description 16
- 125000001153 fluoro group Chemical group F* 0.000 claims description 13
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- 238000004043 dyeing Methods 0.000 claims description 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 8
- 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 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 6
- 239000011593 sulfur Chemical group 0.000 claims description 6
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 125000001246 bromo group Chemical group Br* 0.000 claims description 5
- 125000004957 naphthylene group Chemical group 0.000 claims description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- 125000005518 carboxamido group Chemical group 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 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
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 230000008878 coupling Effects 0.000 claims 10
- 238000010168 coupling process Methods 0.000 claims 10
- 238000005859 coupling reaction Methods 0.000 claims 10
- 150000001412 amines Chemical class 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000011737 fluorine Substances 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 239000007900 aqueous suspension Substances 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 150000001989 diazonium salts Chemical class 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000000980 acid dye Substances 0.000 abstract 4
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229920000742 Cotton Polymers 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
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 150000002790 naphthalenes Chemical class 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
- 125000004959 2,6-naphthylene group Chemical group [H]C1=C([H])C2=C([H])C([*:1])=C([H])C([H])=C2C([H])=C1[*:2] 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241001024304 Mino Species 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
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 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
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 125000006308 propyl amino group Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical group 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
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 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
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
- 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
-
- 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
-
- 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
- C09B67/0047—Mixtures of two or more reactive azo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2002112770 DE10212770A1 (de) | 2002-03-22 | 2002-03-22 | Farbstoffmischungen von faserreaktiven Azofarbstoffen und ihre Verwendung |
DE10212769A DE10212769A1 (de) | 2002-03-22 | 2002-03-22 | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
DE2002117478 DE10217478A1 (de) | 2002-04-19 | 2002-04-19 | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
DE2002117476 DE10217476A1 (de) | 2002-04-19 | 2002-04-19 | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
DE2003109406 DE10309406A1 (de) | 2003-03-05 | 2003-03-05 | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
PCT/EP2003/002836 WO2003080739A1 (de) | 2002-03-22 | 2003-03-18 | Farbstoffmischungen von faserreaktiven azofarbstoffen, ihre herstellung und ihre verwendung |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200406383B true ZA200406383B (en) | 2006-05-31 |
Family
ID=28457949
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200406383A ZA200406383B (en) | 2002-03-22 | 2004-08-12 | Dye mixtures of fiber-reactive azo dyes, their production and use |
Country Status (16)
Country | Link |
---|---|
US (2) | US7455699B2 (ko) |
EP (1) | EP1490441B2 (ko) |
JP (1) | JP4534093B2 (ko) |
KR (1) | KR100890687B1 (ko) |
CN (1) | CN100434483C (ko) |
AT (1) | ATE407978T1 (ko) |
AU (1) | AU2003222770A1 (ko) |
BR (1) | BRPI0308755B1 (ko) |
CA (1) | CA2477718C (ko) |
DE (2) | DE10212769A1 (ko) |
HK (1) | HK1075267A1 (ko) |
MX (1) | MXPA04009131A (ko) |
PT (1) | PT1490441E (ko) |
TW (1) | TWI289587B (ko) |
WO (1) | WO2003080739A1 (ko) |
ZA (1) | ZA200406383B (ko) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10217477A1 (de) * | 2002-04-19 | 2003-11-06 | Dystar Textilfarben Gmbh & Co | Faserreaktive Azofarbstoffe, deren Herstellung und ihre Verwendung |
JP4486810B2 (ja) | 2003-01-08 | 2010-06-23 | 富士フイルム株式会社 | 着色組成物及びインクジェット記録方法 |
MY158815A (en) * | 2003-04-01 | 2016-11-15 | Ciba Specialty Chemicals Holding Inc | Mixture of reactive dyes and their use |
DE10337636A1 (de) | 2003-08-16 | 2005-03-17 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
CN1871308A (zh) * | 2003-10-20 | 2006-11-29 | 西巴特殊化学品控股有限公司 | 活性染料混合物和其用途 |
EP1713865B1 (en) * | 2004-02-13 | 2012-11-28 | Huntsman Advanced Materials (Switzerland) GmbH | Mixtures of reactive dyes and their use |
GB0411589D0 (en) * | 2004-05-24 | 2004-06-23 | Dystar Textilfarben Gmbh & Co | Mixtures of fibre reactive azo dyes |
DE102004042521A1 (de) * | 2004-09-02 | 2006-03-09 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
CH695613A5 (de) * | 2005-06-08 | 2006-07-14 | Bezema Ag | Mischungen von schwermetallfreien faserreaktiven Farbstoffen auf der Basis von Triazo-Verbindungen, deren Herstellung und Verwendung. |
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 |
CN101440227B (zh) * | 2007-11-22 | 2012-10-03 | 上海雅运精细化工有限公司 | 黄色活性染料组合物及其应用 |
CN102250491B (zh) * | 2010-05-17 | 2013-04-10 | 中国中化股份有限公司 | 双偶氮活性染料 |
CN103031004B (zh) * | 2010-08-27 | 2015-07-15 | 天津德凯化工股份有限公司 | 一种活性兰染料及其制备方法 |
WO2013021352A2 (en) | 2011-08-10 | 2013-02-14 | Colourtex Industries Limited | Black mixtures of fibre reactive azo reactive dyestuffs |
CN102504584B (zh) * | 2011-09-28 | 2016-04-27 | 天津德凯化工股份有限公司 | 一种偶氮型蓝色活性蓝染料、制备方法及其应用 |
CN102504586A (zh) * | 2011-09-28 | 2012-06-20 | 天津德凯化工股份有限公司 | 一种蓝色活性染料及其制备方法 |
CN102433029B (zh) * | 2011-09-28 | 2013-08-07 | 吴江桃源染料有限公司 | 一种活性黑色染料混合物 |
CN103087549A (zh) * | 2012-12-31 | 2013-05-08 | 浙江瑞华化工有限公司 | 一种新型活性藏青染料及其制备方法 |
CN103073917B (zh) * | 2012-12-31 | 2014-09-03 | 浙江瑞华化工有限公司 | 一种黑色活性染料组合物 |
GB201317952D0 (en) | 2013-10-10 | 2013-11-27 | Guest John Int Ltd | A connector for connecting to a tube |
CN104327543A (zh) * | 2014-10-13 | 2015-02-04 | 天津德凯化工股份有限公司 | 一种藏青色尼龙活性染料 |
CN104861739A (zh) * | 2015-04-29 | 2015-08-26 | 浙江亿得化工有限公司 | 红色活性染料及其制备方法 |
TWI683863B (zh) | 2015-09-22 | 2020-02-01 | 德商德司達染料分銷有限公司 | 纖維活性染料之混合物 |
NL2018826B1 (en) * | 2017-05-02 | 2018-11-09 | Spgprints B V | One-pot synthesis of reactive deep black |
CN107987555B (zh) * | 2017-09-08 | 2019-12-31 | 浙江科永化工有限公司 | 一种活性蓝至黑染料组合物及染料制品 |
CN107987556B (zh) * | 2017-12-04 | 2020-01-21 | 湖北华丽染料工业有限公司 | 一种复合活性黑染料 |
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JPS58160362A (ja) | 1982-03-17 | 1983-09-22 | Sumitomo Chem Co Ltd | 反応染料組成物、その製法およびそれを用いる繊維の染色方法 |
JPH0812887B2 (ja) * | 1985-04-13 | 1996-02-07 | 富士通株式会社 | 高速集積回路パツケ−ジ |
JPH0662874B2 (ja) * | 1988-05-17 | 1994-08-17 | 紀和化学工業株式会社 | ジスアゾ染料とその製法及び黒色反応染料混合物 |
TW222298B (en) | 1991-10-23 | 1994-04-11 | Hoechst Ag | Fiber reactive dyes which contain a sulfonamido-triazinyl group and one or two groups or the vinyl sulfone series |
TW268967B (ko) * | 1992-11-28 | 1996-01-21 | Hoechst Ag | |
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DE4422864A1 (de) | 1994-06-30 | 1996-01-04 | Hoechst Ag | Mit polymeren Aminverbindungen modifizierte synthetische cellulosische Fasern |
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US5611821A (en) | 1995-09-16 | 1997-03-18 | Everlight Usa, Inc. | Black reactive dye composition |
DE19600765A1 (de) | 1996-01-11 | 1997-07-17 | Basf Ag | Reaktive Azofarbstoffe mit einer Kupplungskomponente aus der Reihe der Aminonaphthalinsulfonsäuren sowie deren Zwischenprodukte |
SG68660A1 (en) | 1997-04-07 | 1999-11-16 | Ciba Sc Holding Ag | Mixtures of reactive dyes and their use |
US6011995A (en) | 1997-12-29 | 2000-01-04 | The Regents Of The University Of California | Endovascular device for hyperthermia and angioplasty and method for using the same |
WO2000006652A2 (de) * | 1998-07-27 | 2000-02-10 | Ciba Specialty Chemicals Holding Inc. | Reaktivfarbstoffe, mischungen von reaktivfarbstoffen, deren herstellung und deren verwendung |
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 |
US6171349B1 (en) * | 1999-01-20 | 2001-01-09 | Everlight Usa, Inc. | Reactive dye composition |
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 |
WO2002098988A2 (en) * | 2001-06-01 | 2002-12-12 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Black dye mixtures of fiber-reactive azo dyes and use thereof for dyeing material containing hydroxy-and/or carboxamido groups |
JP2005520910A (ja) | 2002-03-22 | 2005-07-14 | ダイスター・テクスティルファルベン・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング・ウント・コンパニー・ドイッチュラント・コマンデイトゲゼルシャフト | 繊維反応性アゾ染料の染料混合物及びその調製及び使用 |
KR100942560B1 (ko) | 2009-05-04 | 2010-02-12 | 김관정 | 자체 구동형 케이지 엘리베이터 |
-
2002
- 2002-03-22 DE DE10212769A patent/DE10212769A1/de not_active Withdrawn
-
2003
- 2003-03-18 AT AT03718695T patent/ATE407978T1/de not_active IP Right Cessation
- 2003-03-18 MX MXPA04009131A patent/MXPA04009131A/es active IP Right Grant
- 2003-03-18 EP EP03718695A patent/EP1490441B2/de not_active Expired - Lifetime
- 2003-03-18 PT PT03718695T patent/PT1490441E/pt unknown
- 2003-03-18 AU AU2003222770A patent/AU2003222770A1/en not_active Abandoned
- 2003-03-18 JP JP2003578477A patent/JP4534093B2/ja not_active Expired - Fee Related
- 2003-03-18 US US10/508,630 patent/US7455699B2/en not_active Expired - Lifetime
- 2003-03-18 BR BRPI0308755A patent/BRPI0308755B1/pt not_active IP Right Cessation
- 2003-03-18 KR KR1020047014948A patent/KR100890687B1/ko not_active IP Right Cessation
- 2003-03-18 CA CA2477718A patent/CA2477718C/en not_active Expired - Fee Related
- 2003-03-18 DE DE50310472T patent/DE50310472D1/de not_active Expired - Lifetime
- 2003-03-18 WO PCT/EP2003/002836 patent/WO2003080739A1/de active IP Right Grant
- 2003-03-18 CN CNB038065843A patent/CN100434483C/zh not_active Expired - Fee Related
- 2003-03-20 TW TW092106213A patent/TWI289587B/zh not_active IP Right Cessation
-
2004
- 2004-08-12 ZA ZA200406383A patent/ZA200406383B/en unknown
-
2005
- 2005-08-26 HK HK05107504.9A patent/HK1075267A1/xx not_active IP Right Cessation
-
2008
- 2008-06-27 US US12/163,236 patent/US7708786B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
BRPI0308755B1 (pt) | 2015-09-15 |
JP2005520909A (ja) | 2005-07-14 |
US7708786B2 (en) | 2010-05-04 |
CN1643079A (zh) | 2005-07-20 |
HK1075267A1 (en) | 2005-12-09 |
CN100434483C (zh) | 2008-11-19 |
EP1490441B2 (de) | 2012-12-26 |
TW200306335A (en) | 2003-11-16 |
US20090025152A1 (en) | 2009-01-29 |
US7455699B2 (en) | 2008-11-25 |
WO2003080739A1 (de) | 2003-10-02 |
MXPA04009131A (es) | 2004-12-07 |
KR100890687B1 (ko) | 2009-03-26 |
DE10212769A1 (de) | 2003-10-02 |
KR20050019066A (ko) | 2005-02-28 |
ATE407978T1 (de) | 2008-09-15 |
EP1490441B1 (de) | 2008-09-10 |
JP4534093B2 (ja) | 2010-09-01 |
PT1490441E (pt) | 2008-11-03 |
DE50310472D1 (de) | 2008-10-23 |
CA2477718A1 (en) | 2003-10-02 |
CA2477718C (en) | 2010-07-13 |
EP1490441A1 (de) | 2004-12-29 |
US20050166339A1 (en) | 2005-08-04 |
BR0308755A (pt) | 2005-01-11 |
TWI289587B (en) | 2007-11-11 |
AU2003222770A1 (en) | 2003-10-08 |
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