TWI338021B - Phthalimidyl-azo dyes, process for their preparation and their use - Google Patents
Phthalimidyl-azo dyes, process for their preparation and their use Download PDFInfo
- Publication number
- TWI338021B TWI338021B TW092131377A TW92131377A TWI338021B TW I338021 B TWI338021 B TW I338021B TW 092131377 A TW092131377 A TW 092131377A TW 92131377 A TW92131377 A TW 92131377A TW I338021 B TWI338021 B TW I338021B
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- Prior art keywords
- dye
- formula
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- ethyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 19
- 239000000987 azo dye Substances 0.000 title description 6
- 239000000975 dye Substances 0.000 claims description 62
- 239000000203 mixture Substances 0.000 claims description 25
- 239000002657 fibrous material Substances 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 16
- 238000004043 dyeing Methods 0.000 claims description 15
- 230000002209 hydrophobic effect Effects 0.000 claims description 13
- 238000007639 printing Methods 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- -1 Ethyl ethoxy Chemical group 0.000 claims description 7
- 239000004753 textile Substances 0.000 claims description 6
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 238000003786 synthesis reaction Methods 0.000 claims description 5
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 238000006396 nitration reaction Methods 0.000 claims description 2
- 150000002828 nitro derivatives Chemical class 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 230000002152 alkylating effect Effects 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000002466 imines Chemical class 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 229910052739 hydrogen Inorganic materials 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 238000006243 chemical reaction 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
- 238000006193 diazotization reaction Methods 0.000 description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 3
- 235000019260 propionic acid Nutrition 0.000 description 3
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
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- 239000000986 disperse dye Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
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- 150000002431 hydrogen Chemical class 0.000 description 2
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- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
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- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 1
- RXQNKKRGJJRMKD-UHFFFAOYSA-N 5-bromo-2-methylaniline Chemical compound CC1=CC=C(Br)C=C1N RXQNKKRGJJRMKD-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 240000008886 Ceratonia siliqua Species 0.000 description 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920001612 Hydroxyethyl starch Polymers 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229910052936 alkali metal sulfate Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229940105329 carboxymethylcellulose Drugs 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229940125758 compound 15 Drugs 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- BEQZMQXCOWIHRY-UHFFFAOYSA-H dibismuth;trisulfate Chemical compound [Bi+3].[Bi+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BEQZMQXCOWIHRY-UHFFFAOYSA-H 0.000 description 1
- 238000010018 discharge printing Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 229940050526 hydroxyethylstarch Drugs 0.000 description 1
- 238000007654 immersion Methods 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
- ZDGGJQMSELMHLK-UHFFFAOYSA-N m-Trifluoromethylhippuric acid Chemical compound OC(=O)CNC(=O)C1=CC=CC(C(F)(F)F)=C1 ZDGGJQMSELMHLK-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
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 150000004060 quinone imines Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000008961 swelling Effects 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
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing 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
- C09B29/0003—Monoazo dyes prepared by diazotising and coupling from diazotized anilines
-
- 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
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0029—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing only nitrogen as heteroatom
- C09B29/0033—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing only nitrogen as heteroatom containing a five-membered heterocyclic ring with one nitrogen atom
-
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
-
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
- C09B29/0805—Amino benzenes free of acid groups
- C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
- C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/40—Preparation of azo dyes from other azo compounds by substituting hetero atoms by radicals containing other hetero atoms
- C09B43/42—Preparation of azo dyes from other azo compounds by substituting hetero atoms by radicals containing other hetero atoms by substituting radicals containing hetero atoms for —CN radicals
-
- 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
- C09B67/0051—Mixtures of two or more azo dyes mixture of two or more monoazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring (AREA)
Description
Ί338021 玟、發明說明: 【發明所屬之技術領域】’ 本發明係關於具有N-甲基-酞醯亞胺-重氮組分及一苯 胺偶合組分之分散染料,製備此種染料之方法及其於染色 或印花半合成及尤其是合成疏水性纖維材料,尤其是紡織 材料之用途。 【先前技術】 茲對於具有N-烷基-駄醯亞胺·重氮組分及一苯胺偶合 組分之分散偶氮染料已有一段長時間的瞭解且其被使用於 木色疏水性纖維材料中。然而,茲已被發現使用目前習知 木料所獲得之染色或印花並非在所有例子中皆能滿足現在 的需求,尤其是在耐洗牢度及耐汗清牢度上。因此,有一 種對於尤其是具有良好耐洗牢度性質之新穎染料的需求。 令人驚t牙地’目前已發現根據本發明之染料符合前述 之標準而達到一值得考慮的程度。 【發明内容】 ^因此’本發明係關於可產生具有高度耐洗牢度及耐汗 此外 在盡染(exhaust)法及熱溶(thermosol)法及 在織物印花-去φ θ -t- a , ^ 化一者中具有良好提昇特性之染色的分散染料。 該等染料亦適合用於拔染印花。 根據本發明之染料相當於下式 1338021
⑴, 其中匕是2-甲氧基乙基、2-乙氧基乙基或2-(2-乙氧 基乙氧基)乙基, h是未經取代或經一或更多氫氧基基團、函素原子、 h-C4院氧基基團' q-C8烷氧基烷氧基基困、院基一 COO-基團或(^-(:4烷基-0C0-基團所取代的CrCe烷基, 尺3是甲基 '氫氧基、齒素、-NH-S02-R5 或-NH-CO-R, lv 6 其中是曱基或乙基以及Re是甲基、乙基、甲氧基甲基 或2-甲氧基乙基,和 h是乙基或正-丙基。 做為R2之Ci_Ce烷基可以是(例如)甲基、乙基、正丙 基、異丙基、正—丁基、異丁基、第二-丁基、第三_ 丁基、 正_戊基、新戊基或正_己基。 做為Rg的鹵素可以是氟、演或較佳的為氣。
Ri及R2較佳的具有相同的意義。
Ri較佳的為2-曱氧基乙基。 R3較佳的為—NH-C0-R6。
Re較佳的為甲基。 h較佳的為乙基。 尤其較佳的是染料具有式(la)、(lb)及(ic)
(lb)· (la)’
(lc). 本發明亦關於製備式(1)染料的方法,其中狀醢亞胺 為式 Ο
Ο (2), 其中I是如上所定義, 係如(例如)Organic Synthesis,Collective Volume (年卷X_XIX之修正版)J. Wiley & Sons第459頁所述 ,於酸性範圍中抽 祀®1干被硝化,所4到的硝基化合物接著被烷基 1338021 化(例如根據 Journal of 〇rganic chemistry 32. (1967)第 1923頁第3段所述的方法),然後(例如藉由如Bull s〇c Chim. de France 1-9.57 _% 569頁所述的還原處理)轉換成 下式的中間物
(3), 式(3 )中間物是根據一般所知的方法於酸性介質中單函 化,然後被重氮化(diazotised)及偶合成式(4)化合物
R. 其中I?i、Rz及R;}係如上所定義,然後函素取代基被氛 所置換。 鹵化的進行是藉由(例如)將式(3)化合物先在醋酸令與 醋酸鈉反應’然後在同一介質中與溴反應生成相關的單溴 化合物。 重氮化也是以其本質已知的方式進行,例如,於一酸 性(例如含氫氣酸或含硫酸)之水性介質中與亞硝酸鈉反應 °然而’該重氮化亦可使用其他重氮化劑,例如使用亞石肖 基硫酸。在該重氮化中,一額外的酸可存在於反應介質中 ^38021 ,例如,填酸、硫酸、醋酸、丙酸、氩氣酸或此種酸類之 現合物,例如,丙酸及醋酸之混合物《該重氮化係有利地 在-10至3 0 °C之溫度下(例如-10 °C至室溫)進行。 經重氮化之化合物的偶合至式(4)偶合成分係同樣地以 習知方式,例如,於一酸性、水性或水性-有機介質中,有 利地在-10至3CTC之溫度下,尤其是在1(rc以下之溫度下 進行。所使用Ssc類之實例為氫氣酸、醋酸、丙酸、硫酸及 磷醆。 該形成最終染料之反應的進行係藉由其本質已知的方 法在單函素化合物中做氰置換,例如於一溶劑中(例如二甲 基曱酿胺、二甲亞楓、三甲基乙酿胺、N_甲基咖略院綱、 環丁碾或毗啶)使用⑽或CUCN及鹼金屬氛化物之混合 物。 該重氮化合物及該式⑷之偶合成分為習知的或可以其 本質已知之方式製備。 本發明亦關於染料混合物,其含有至少兩個結構上不 同的式(1)偶氮染料。 含有兩個結構上不同之式m 飞(1)偶氮杂料的染料混合物是 3有至少兩個結構上不同 明 備 式)偶氮染料的根據本, 之杂科混合物可以(例如)藉 。 ^褙田間單的混合個別染料而: 1338021 從70:30至30:70重量份,更尤其是含有兩種偶氮染料之 根據本發明染料混合物中個別染料的從55:45至45:55重 量份。 根據本發明的染料及染料混合物可以用於染色或印花 之半合成及(尤其是)合成的疏水性纖維材料,尤其是紡織 材料。包括此種半合成或合成疏水性纖維材料之由混紡織 材料所組成之紡織材料亦可使用根據本發明之染料或染料 混合物染色或印花。 合適的半合成纖維材料尤其是纖維素2lv醋酸酯及纖 維素三醋酸酯。 合成的疏水性纖維材料尤其是由線型、芳香聚酯類所 組成’例’對苯二甲酸及乙二醇的聚酯,尤其是乙二醇 ’或對苯二甲酸及14_雙(經曱基)環己烷之縮合產物;聚 碳酸醋類所組成者’例如,一甲基-4,4-二經基_二苯基 曱烷及光氣的聚碳酸酯類’及基於聚氣乙烯與基於聚醯胺 之纖維所組成者。 根據本發明之染料及染料混合物對纖維材料之應用係 依照習知染色方法眘 法實施。例如,聚酯纖維材料係於盡染法 中於習常陰離子或非離子分散劑及,可選擇地,習常溶脹 劑『色載體)之存在下,在自8〇至航之溫度下自水性
刀政液中染色。纖維素2l/2-醋酸酿係較佳地於65至85°C 之溫度下染色且纖維素三醋_係於65至U5t之溫度下 染色。 根據本發明之染料 及染料渴*合物將不會於染浴中著色 12 1338021 同時存在之羊毛及棉,或僅輕微地著色此種材料(非常良好 之防染)’所以它們亦可被滿意地使用於聚醋/羊毛及聚醋/ 纖維素纖維混纺織物之染色中。 根據本發明之染料及染料混合物適合用於依照熱溶法 、盡染法及印花法之染色中。 在此種方法中,該纖維材料可為不同的處理形式,例 如,以纖維、紗或不織布的形式、以織布或針織物之形式。 在使用前將根據本發明之染料或染料混合物轉化成染 料製劑是較有佳的。為此㈣,該染料被研磨,使其粒徑 為平均〇·丨至10微米。研磨可在分散劑之存在下進行。例 如,該經乾燥之染料係與分散劑一起研磨,或與分散劑一 起捏和成糊狀形式,然後在真空下或藉由喷霧作用乾燥。 在加水後,該生成的製劑可被使用來製備印花漿及染液。 為了印花,將使用習常印花漿料,例如’經修飾或未 經修飾的天然產物,例如,海藻酸鹽、印染膠 '阿拉伯樹 膠、結晶樹膠、刺槐豆粉狀物質、黃箸膠、羧甲基纖維素 、羥乙基纖維素、澱粉或合成的產物,例如,$丙烯醯胺 類 '聚丙烯酸或其共聚物或聚乙烯醇類。 根據本發明之染料及染料混合物給予該材料,尤其是 給予聚酯材料,具有非常良好的使用牢度性質如,尤其是 ,良好耐日光牢度、耐熱定形牢度、耐褶牢度、耐氣牢度 、及耐溼牢度,例&,耐水浸牢度、耐汗漬牢度及耐洗牢 度之均勻顏色色澤;該經整理染料之進一步特徵在於具有 非常良好之耐摩擦牢度β對於所獲得染料之良好牢度性質 13 1338021 所給予之特別強調的是耐汗潰 .度及尤其是,耐洗牢度。 生產與其他:/月之染料及染料混合物亦可被滿意地使用於 生產與其他染料—起之混合色澤。 超臨Π,:據本發明之染料及染料混合物亦充分適合於 超6»界co2中染色疏水性纖維材料。 本發明亦關於根據本發明之染料及染料混合物之前述 爵於#半合成或合成疏水性纖維材料(尤其是紡
織材料)之染色咬gp X 方法,在該方法中,根據本發明之染 料係被施用至該材料哎併人I 士 次併入其中。該疏水性纖維材料係較 佳地為纺織聚酷材料β可被根據本發明方法處理之另外的 被染物及較佳處理條件可見前述根據本發明染料之用途的 更詳細描述。 本發明亦關於藉由該方法染色或印花之疏水性纖維材 料,較佳地為聚㈣織材料。根據本發明之染料也適合現 代再生產方法,例如熱轉移印花。 °其中除非特別指出, 「百分比J係為「重量 量份及體積份之關聯係 下列實施例將作為說明本發明 否則「部份」係為「重量份」,及 百分比」。溫度係為攝氏度。該重 同公克及立方公分。 【實施方式】 I ·製劑實施例 實施例 1. 1 : Α.將5,5毫升96 %的硫酸放入實驗室反應儀器中β逐 1338021 滴加入1 _ 3毫升的冰水並搜拌及以冰浴冷卻之。然後,在 内部溫度為25°C時,·導入2.7克下式化合物
將如此得到的懸浮液攪拌1 〇分鐘。然後在1 〇分鐘期 間裡逐滴加入1.85毫升40 %的亞硝基硫酸,於i8-20oC 下冷卻’且在該溫度下進行攪拌2小時。 將1毫升32 %的氫氣酸(於60毫升冰水中)導入25〇 毫升的實驗室反應儀器中。攪拌加入以25毫升醋酸稀釋 之6.5克48 %的式(4a)化合物水性溶液 Γ=\ ch2ch2och3
<\ />—N /~/ CH2CH2OCH3 (4a)。 nhcoch3 然後在1 0分鐘期間裡添加重偶氮鹽溶液;同時,導入 約50克的冰,使得内部溫度為〇_5〇c。 於0-5°C搜拌如此得到的紅色懸浮液1小時,以抽。 過攄,以去離子水清洗並乾燥之。 獲得4. 8克(理論產量的88 %)下式化合物 15 1338021
熔點:175-178°C 外觀:帶黃色的紅褐色 B.將2.23克式(6a)化合物及10毫升二曱亞楓置於 100毫升的實驗室反應儀器中,及在室溫(RT)攪拌1〇分 鐘。導入0.17克氰化鈉及0.30克氰化亞銅,且在室溫下 攪拌混合物10分鐘。然後升高溫度至70-75。(:,在該溫 度攪拌反應混合物2小時。在冷卻到6〇°C及逐滴添加5毫 升水之後,抽吸過濾懸浮液,以溫水(5〇。〇洗滌並乾燥之 〇 獲得1.8克(理論產量的73 %)下式偶氣染料
熔點:200-203°C 外觀:紫色 1338021 下面同樣適合染色半合成或合成疏水性纖維材料的染 料(表1)可以類似實施例1. 1製備:
R, R, R, -CH’CH’OCH, -CH,CH,OCH, -CH, -C,H, -CH,CH,CH, -CH’COOCH, -CH,COOC,H, -CH(CH,)-COOCH, -CH(CH3)-COOC2H, -CH^H^COOCH, -CH,CH,COOC,H, -CH,CH,0-C0-CH, -CH,CH,0-CO-C7Hs 笨甲基 -C,H, -NH-CO-CH, -CH,CH,CH, -CH,COOCH, -CH,COOC,H, -CH(CH,)-COOCH, -CH(CH,)-COOC,Hs -CH,CH,COOCH, -CH7CH,COOC,H, -CH,CH,0-C0-CH, -CH,CH,0-C0-C,Hs 苯甲基 -ch7ch,och, -NH-CO-C,H, -c2h5 -CH,CH,CH, -CH,COOCH, -CH,COOC,H, -CHiCHO-COOCH, -CH(CH〇-COOC,H, -CH,CH,COOCH, 17 ^38021
R, r2 R, Μ -CH,CH,COOC,H, II fl -ch7ch,o-co-ch, ” -CH,CH,0-C0-C,H, 笨甲基 ” -CH2CH2OCH, -nh-so2-ch, -c7h, ” -CH,CH,CH, II II -CH’COOCH, II 曹曹 -CH,COOC,Hs ft " -CH(CH,)-COOCH, II ” -CH(CH〇-COOC,HS ” -CH,CH,COOCH, -CH,CH,COOC,H, " -CH^CH^O-CO-CH, If -CH,CH,0-C0-C,H, It 笨甲基 ” " -CH,CH,OCH, -NH-SO^CH, Μ C,H, " -CH7CH7CH, Μ -CH,COOCH, ” ft -CH,COOC,H, II ” -CH(CH,)-COOCH, ft It -CH(CH,)-COOC,H, " -CH,CH?COOCH, -CH?CH,COOC,H, " -CH,CH,0-C0-CH, Μ -CH,CH,0-C0-C,Hs (曹 苯曱基 ft Μ -ch,ch7och, -NH-CO-CH,OCH, It -C,H, tf -CH,CH,CH, " -CH,COOCH, If It -CH,COOC,Hs " -CH(CH,)-C〇OCH' -CH(CH,)-COOC,H, It -CH^^COOCH, ft M -CH,CH,COOC,H, II " -CH,CH,0-C0-CH, -CH7CH70-C0-C,H, If 笨甲基 11 II -ΟΗ,ΟΗ,ΟΟΗ, -OH It -C,H, fl -CH,CH,CH, " -CH^OOCH, II M -CH,COOC,H, II If -CHiCHO-COOCH, II II -CH(CH〇-COOC,H, M 18 1338021
11.應用實施例 實施例11.1 : 1重量份的下式染料
(la) 2於一研砂機中與17重量份之水及2重量份之商業上 可獲得之二蔡基甲烧二續酸鹽形式之分散液-起研磨,並 轉化成5%水性分散液。 使用該調配物,藉由高溫盡染法在13(TCT於織物聚 酉曰織上產生1%染色(基於染料及被染物)及被還原地清潔 。該以此方式獲得之紫色染色具有非常良好的使用牢度性 質’尤其是優良的耐洗牢度。 當織物聚醋織品以熱溶法(10克/升染料,溶液吸液 50% ’固著溫度210。(:)染色時,可達到相同的良好牢度性 質。 19
Claims (1)
- I#38021I、申請專利範圍: 1 · 一種下式染料基乙氧基)乙基, h是未經取代的或經一或更多氫氧基基團、鹵素原子 、q-c;4燒氧基基團、q-c:8烷氧基烷氧基基團、Cl-c4燒基_ C00_基團或CrC4烷基-0C0-基團取代的CrCe烷基, R3是曱基、氫氧基、函素、_NH_S〇2-R5或―NH_c〇〜R&, 其中h是曱基或乙基及Re是甲基、乙基、甲氧基甲基或 2 -甲軋基乙基,以及 h是乙基或正-丙基。 2. 根據申請專利範圍第1項的染料,其中R!及R2是相 同的® 3. 根據申請專利範圍第1或2項的染料,其中&是2_ 甲氧基乙基。 4. 根據前述申請專利範圍中任一項的染料,其中r3是 -NH-CO-R6 。 5. 根據申請專利範圍第4項的染料,其中是甲基。 根據⑴述申清專利範圍中任一項的染料,其中尺 是乙基。 ' ί 7.根據申請專利範圍第1項的式(la)、(lb)或(1C)染料 20 1338021 P-CH,•〜積製備根據申請專利範圍第1項之式(1)染料的方法 於該方法中,將下式之酞酿亞胺於—酸性範圍中硝化’然後將該生成之硝基化合物烷 基化且藉由還原處理轉化成下式之中間物 0將該式(3)中間物於一酸介質中單卤化,然後重氮化偶 21 (4),1338021 合成式(4)化合物 R其中Ri、R2及h係如申請專利範圍第J項所定義然 後該函素取代基被氛取代。 9. 一種包含至少兩種結構上不同的根據申請專利範圍 第1項式(1)染料的染料混合物。 1〇·種染色或印花半合成或合成疏水性纖維材料的方 :’其中根據中請專利範圍第1項的A (1)染料或根據申 二專利範圍第9項的染料混合物係施用至該材料或混合至 料 u ·—種根據申請專利範圍第 其係用於染色或印花半合成及 ’尤其是紡織材料。 1項之式(1)染料之用途 尤其是合成疏水性纖維材 12·—種半合成或尤其是合成 万織材料’其係藉由根據申請專 色或印花。 疏水性纖維材料,尤其是 利範圍第10項之方法染 拾壹、明式: 無。 22
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CN (1) | CN100379825C (zh) |
AU (1) | AU2003276247A1 (zh) |
TW (1) | TWI338021B (zh) |
WO (1) | WO2004044058A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US6619793B2 (en) | 2000-07-04 | 2003-09-16 | Seiko Epson Corporation | Recording method |
Families Citing this family (17)
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CN1317337C (zh) * | 2004-12-28 | 2007-05-23 | 浙江龙盛集团股份有限公司 | 一种红色单偶氮染料组合物 |
EP2337820B1 (en) * | 2008-10-21 | 2013-05-15 | Huntsman Advanced Materials (Switzerland) GmbH | Azo dyes, a process for the preparation thereof and the use thereof |
PT2513229E (pt) | 2009-12-16 | 2014-07-14 | Huntsman Adv Mat Switzerland | Corantes azo dispersos, um processo para o seu fabrico e o seu uso |
EP2754696A1 (en) | 2013-01-15 | 2014-07-16 | DyStar Colours Distribution GmbH | AOX-free navy and black disperse dye mixtures |
PT2943537T (pt) | 2013-01-14 | 2019-02-15 | Dystar Colours Distrib Gmbh | Misturas de corantes com humidade elevada e dispersão rápida |
CN103965094B (zh) * | 2013-01-31 | 2016-07-06 | 江苏道博化工有限公司 | N-甲基-4-氨基-5-溴-邻苯二甲酰亚胺的合成方法 |
CN104448894B (zh) * | 2014-11-18 | 2016-08-24 | 昌邑福莱蒽特精细化工有限公司 | 高水洗牢度和升华牢度的分散绿光蓝染料及其制备方法 |
CN104403348B (zh) * | 2014-11-18 | 2016-09-07 | 李百春 | 一种高水洗牢度和升华牢度的紫色分散染料及其制备方法 |
CN104448893B (zh) * | 2014-11-18 | 2017-04-05 | 杭州福莱蒽特精细化工有限公司 | 一种高水洗牢度和升华牢度的红色分散染料及其制备方法 |
CN104448892B (zh) * | 2014-11-18 | 2017-04-05 | 李百春 | 一种高水洗牢度和升华牢度的宝蓝分散染料及其制备方法 |
CN105647224A (zh) * | 2016-01-28 | 2016-06-08 | 俞杏英 | 一种邻苯二甲酰亚胺-偶氮分散染料单体化合物及其制备方法和应用 |
CN105602278B (zh) * | 2016-01-28 | 2018-02-16 | 俞杏英 | 一种蓝色分散染料单体化合物及其制备方法和应用 |
TWI707002B (zh) * | 2016-05-25 | 2020-10-11 | 瑞士商杭斯曼高級材料公司 | 分散偶氮染料、其製備方法及其用途 |
EP3461861B1 (en) | 2017-10-02 | 2020-07-15 | DyStar Colours Distribution GmbH | High wet fast disperse dye mixtures |
CN107722663A (zh) * | 2017-10-10 | 2018-02-23 | 浙江万丰化工有限公司 | 一种偶氮染料化合物及其制备方法和应用 |
CN108864732B (zh) * | 2018-07-06 | 2020-05-05 | 浙江万丰化工股份有限公司 | 一种含甲磺酰胺基团的偶氮染料化合物及其制备方法和应用 |
CN109054429B (zh) * | 2018-07-06 | 2020-06-09 | 浙江万丰化工股份有限公司 | 一种含乙酰胺基团的偶氮染料化合物及其制备方法和应用 |
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US3980634A (en) * | 1973-07-02 | 1976-09-14 | Eastman Kodak Company | Phthalimidyl-azo aniline type compounds and polyester fibers dyed therewith |
JPS5818470B2 (ja) * | 1974-09-06 | 1983-04-13 | 三菱化学株式会社 | ゴウセイセンイルイ ノ センシヨクホウホウ |
EP0051563B1 (de) * | 1980-10-30 | 1985-04-24 | Ciba-Geigy Ag | Monoazoverbindungen |
DE59104277D1 (de) * | 1990-02-19 | 1995-03-02 | Ciba Geigy Ag | Phthalimidyl-Azofarbstoffe. |
JPH06329930A (ja) * | 1993-05-06 | 1994-11-29 | Ciba Geigy Ag | アゾ染料 |
US6008332A (en) * | 1994-02-11 | 1999-12-28 | Ciba Specialty Chemicals Corporation | Phthalimidylazo dyes, process for their preparation and the use thereof |
TW328094B (en) | 1994-02-11 | 1998-03-11 | Ciba Sc Holding Ag | Phthalimidylazo dyes, process for their preparation and the use thereof |
TWI243192B (en) * | 1998-12-31 | 2005-11-11 | Ciba Sc Holding Ag | Phthalimidyl azo pigments, method for producing same and utilization thereof |
PT1358274E (pt) | 2001-02-07 | 2011-04-05 | Huntsman Adv Mat Switzerland | Corante à base de ftalimidilo azo, processo para a sua preparação e uso do mesmo |
CZ20032382A3 (cs) * | 2001-02-07 | 2003-11-12 | Ciba Specialty Chemicals Holding Inc. | Ftalimidylová azobarviva, způsob jejich přípravy a jejich použití |
-
2003
- 2003-11-04 AU AU2003276247A patent/AU2003276247A1/en not_active Abandoned
- 2003-11-04 WO PCT/EP2003/012282 patent/WO2004044058A1/en active Application Filing
- 2003-11-04 US US10/533,010 patent/US20060101594A1/en not_active Abandoned
- 2003-11-04 KR KR1020057008394A patent/KR101035841B1/ko not_active IP Right Cessation
- 2003-11-04 EP EP03810962.5A patent/EP1560883B1/en not_active Expired - Lifetime
- 2003-11-04 CN CNB2003801029505A patent/CN100379825C/zh not_active Expired - Lifetime
- 2003-11-04 JP JP2004550922A patent/JP4589726B2/ja not_active Expired - Lifetime
- 2003-11-10 TW TW092131377A patent/TWI338021B/zh not_active IP Right Cessation
-
2008
- 2008-03-31 US US12/059,344 patent/US20080184499A1/en not_active Abandoned
-
2010
- 2010-12-09 US US12/964,053 patent/US20110078863A1/en not_active Abandoned
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2014
- 2014-03-18 US US14/217,903 patent/US20140196224A1/en not_active Abandoned
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6619793B2 (en) | 2000-07-04 | 2003-09-16 | Seiko Epson Corporation | Recording method |
US6808257B2 (en) | 2000-07-04 | 2004-10-26 | Seiko Epson Corporation | Recording method |
US6969167B2 (en) | 2000-07-04 | 2005-11-29 | Seiko Epson Corporation | Recording method |
Also Published As
Publication number | Publication date |
---|---|
US20060101594A1 (en) | 2006-05-18 |
EP1560883B1 (en) | 2013-07-10 |
WO2004044058A1 (en) | 2004-05-27 |
US20140196224A1 (en) | 2014-07-17 |
KR20050075390A (ko) | 2005-07-20 |
CN100379825C (zh) | 2008-04-09 |
JP2006505662A (ja) | 2006-02-16 |
KR101035841B1 (ko) | 2011-05-20 |
US20110078863A1 (en) | 2011-04-07 |
US20080184499A1 (en) | 2008-08-07 |
EP1560883A1 (en) | 2005-08-10 |
AU2003276247A1 (en) | 2004-06-03 |
TW200420672A (en) | 2004-10-16 |
JP4589726B2 (ja) | 2010-12-01 |
CN1711319A (zh) | 2005-12-21 |
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