ES2205850T3 - Colorantes reactivos, mezclas de colorantes reactivos6 obtencion y utilizacion de los mismos. - Google Patents
Colorantes reactivos, mezclas de colorantes reactivos6 obtencion y utilizacion de los mismos.Info
- Publication number
- ES2205850T3 ES2205850T3 ES99932887T ES99932887T ES2205850T3 ES 2205850 T3 ES2205850 T3 ES 2205850T3 ES 99932887 T ES99932887 T ES 99932887T ES 99932887 T ES99932887 T ES 99932887T ES 2205850 T3 ES2205850 T3 ES 2205850T3
- Authority
- ES
- Spain
- Prior art keywords
- formula
- hal
- alkyl
- halogen
- sulfo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003153 chemical reaction reagent Substances 0.000 title description 6
- 239000003086 colorant Substances 0.000 title description 2
- 239000000975 dye Substances 0.000 claims abstract description 93
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 26
- 150000002367 halogens Chemical class 0.000 claims abstract description 25
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims abstract description 25
- 125000001424 substituent group Chemical group 0.000 claims abstract description 15
- 239000002657 fibrous material Substances 0.000 claims abstract description 13
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 13
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 13
- 239000001257 hydrogen Substances 0.000 claims abstract description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000004043 dyeing Methods 0.000 claims abstract description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
- -1 hydroxy, carboxy Chemical group 0.000 claims description 54
- 239000000203 mixture Substances 0.000 claims description 38
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 150000001875 compounds Chemical class 0.000 claims description 23
- 239000000835 fiber Substances 0.000 claims description 23
- 125000003545 alkoxy group Chemical group 0.000 claims description 20
- 150000001412 amines Chemical class 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 20
- 229920000742 Cotton Polymers 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 6
- 125000004414 alkyl thio group Chemical group 0.000 claims description 6
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 6
- 125000005184 naphthylamino group Chemical group C1(=CC=CC2=CC=CC=C12)N* 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- XSXHWVKGUXMUQE-UHFFFAOYSA-N osmium dioxide Inorganic materials O=[Os]=O XSXHWVKGUXMUQE-UHFFFAOYSA-N 0.000 claims description 4
- 229920003043 Cellulose fiber Polymers 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000004744 fabric Substances 0.000 description 16
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 11
- 239000000985 reactive dye Substances 0.000 description 11
- 150000008049 diazo compounds Chemical class 0.000 description 10
- 230000008878 coupling Effects 0.000 description 9
- 238000010168 coupling process Methods 0.000 description 9
- 238000005859 coupling reaction Methods 0.000 description 9
- 229940098465 tincture Drugs 0.000 description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 8
- 229910052801 chlorine Inorganic materials 0.000 description 8
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 230000002378 acidificating effect Effects 0.000 description 7
- 229920002678 cellulose Polymers 0.000 description 7
- 239000001913 cellulose Substances 0.000 description 7
- 239000003599 detergent Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 235000017557 sodium bicarbonate Nutrition 0.000 description 6
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 6
- 235000002639 sodium chloride Nutrition 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
- 229910052794 bromium Inorganic materials 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000000344 soap Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 235000010288 sodium nitrite Nutrition 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 235000011167 hydrochloric acid Nutrition 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- LJRGBERXYNQPJI-UHFFFAOYSA-M sodium;3-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC(S([O-])(=O)=O)=C1 LJRGBERXYNQPJI-UHFFFAOYSA-M 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- 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 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 229940072056 alginate Drugs 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- POJOORKDYOPQLS-UHFFFAOYSA-L barium(2+) 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonate Chemical compound [Ba+2].C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O.C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O POJOORKDYOPQLS-UHFFFAOYSA-L 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 230000027326 copulation Effects 0.000 description 2
- 238000000502 dialysis Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 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
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- VNMGVBPCESRCOG-UHFFFAOYSA-N OC(=O)ClS(O)(=O)=O Chemical compound OC(=O)ClS(O)(=O)=O VNMGVBPCESRCOG-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
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 235000019646 color tone Nutrition 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 238000010409 ironing 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
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([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
- 239000010985 leather Substances 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
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 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
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 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
- C09B62/503—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 esterified or non-esterified hydroxyalkyl sulfonyl or mercaptoalkyl sulfonyl group, a quaternised or non-quaternised aminoalkyl sulfonyl group, a heterylmercapto alkyl sulfonyl group, a vinyl sulfonyl or a substituted vinyl sulfonyl group, or a thiophene-dioxide group
- C09B62/507—Azo dyes
- C09B62/513—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
- C09B62/02—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
- C09B62/09—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
- C09B62/4401—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system
- C09B62/4403—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system the heterocyclic system being a triazine ring
- C09B62/4411—Azo dyes
- C09B62/4415—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
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/924—Polyamide fiber
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Detergent Compositions (AREA)
- Luminescent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98810722 | 1998-07-27 | ||
| EP98810722 | 1998-07-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2205850T3 true ES2205850T3 (es) | 2004-05-01 |
Family
ID=8236214
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99932887T Expired - Lifetime ES2205850T3 (es) | 1998-07-27 | 1999-07-15 | Colorantes reactivos, mezclas de colorantes reactivos6 obtencion y utilizacion de los mismos. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6537332B1 (enExample) |
| EP (1) | EP1137716B1 (enExample) |
| JP (1) | JP4322427B2 (enExample) |
| AT (1) | ATE247694T1 (enExample) |
| AU (1) | AU4911099A (enExample) |
| DE (1) | DE59906709D1 (enExample) |
| ES (1) | ES2205850T3 (enExample) |
| PT (1) | PT1137716E (enExample) |
| WO (1) | WO2000006652A2 (enExample) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10212769A1 (de) * | 2002-03-22 | 2003-10-02 | Dystar Textilfarben Gmbh & Co | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
| DE10217477A1 (de) * | 2002-04-19 | 2003-11-06 | Dystar Textilfarben Gmbh & Co | Faserreaktive Azofarbstoffe, deren Herstellung und ihre Verwendung |
| MY136589A (en) * | 2003-02-05 | 2008-10-31 | Ciba Sc Holding Ag | Mixtures of reactive dyes and their use |
| MY158815A (en) | 2003-04-01 | 2016-11-15 | Ciba Specialty Chemicals Holding Inc | Mixture of reactive dyes and their use |
| CN100335561C (zh) * | 2003-04-01 | 2007-09-05 | 西巴特殊化学品控股有限公司 | 活性染料混合物以及其应用 |
| DE10337636A1 (de) | 2003-08-16 | 2005-03-17 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbstoffmischungen von faserreaktiven Azofarbstoffen, ihre Herstellung und ihre Verwendung |
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| BRPI0508957B1 (pt) * | 2004-03-19 | 2015-08-11 | Huntsman Adv Mat Switzerland | Tintura reativa, seu uso e seu processo de preparação, tinta aquosa, e processo para imprimir material de fibra têxtil, papel ou filme plastico |
| CN100344707C (zh) * | 2005-08-30 | 2007-10-24 | 大连理工大学 | 适于冷轧堆染色的耐碱型黑色活性染料 |
| 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 |
| CN100590152C (zh) * | 2006-04-26 | 2010-02-17 | 明德国际仓储贸易(上海)有限公司 | 季铵盐双偶氮红色反应性染料化合物 |
| CN101463569B (zh) * | 2007-12-21 | 2011-06-01 | 上海安诺其纺织化工股份有限公司 | 纤维素纤维用耐后丝光的活性黑染料 |
| CN102115613B (zh) * | 2009-12-30 | 2014-01-15 | 上海雅运纺织化工股份有限公司 | 蓝色活性染料组合物及其在纤维材料上的染色应用 |
| 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 |
| CN102115612B (zh) * | 2009-12-30 | 2014-01-15 | 上海雅运纺织化工股份有限公司 | 深蓝色活性染料组合物及其在纤维上的染色应用 |
| TW201307417A (zh) * | 2011-04-07 | 2013-02-16 | Bayer Materialscience Ag | 熱塑性聚胺基甲酸酯於轉換機械能為電能的用途 |
| MX354037B (es) * | 2011-04-07 | 2018-02-06 | Huntsman Adv Mat Switzerland | Tintes reactivos con fibras, su preparacion y su uso. |
| WO2013018057A2 (en) | 2011-08-04 | 2013-02-07 | Colourtex Industries Limited | Fibre reactive bisazo reactive colorants, mixtures of reactive colorants, production and use thereof |
| KR20140052004A (ko) | 2011-08-04 | 2014-05-02 | 훈츠만 어드밴스트 머티리얼스(스위처랜드) 게엠베하 | 반응성 염료의 혼합물 및 이의 용도 |
| IN2014MN00383A (enExample) | 2011-08-10 | 2015-06-19 | Colourtex Ind Ltd | |
| CN102585548B (zh) * | 2011-12-30 | 2014-02-26 | 浙江科永化工有限公司 | 一种红色活性染料组合物 |
| CN102977632A (zh) * | 2012-11-27 | 2013-03-20 | 江苏德旺化工工业有限公司 | 一种复合活性红染料 |
| CN104119691A (zh) * | 2013-04-28 | 2014-10-29 | 浙江龙盛集团股份有限公司 | 一种橙红色活性染料化合物及其应用 |
| 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 |
| CN104804470B (zh) * | 2014-01-24 | 2019-06-04 | 浙江科永化工有限公司 | 一种活性黑染料组合物 |
| CN104479403A (zh) * | 2014-12-11 | 2015-04-01 | 吴江桃源染料有限公司 | 一种环保型活性红色双偶氮染料及其制备方法 |
| CN104530755B (zh) * | 2014-12-19 | 2017-02-08 | 浙江亿得化工有限公司 | 一种复合型活性黑染料 |
| CN105400234B (zh) * | 2015-11-20 | 2018-02-13 | 浙江龙盛集团股份有限公司 | 一种多偶氮活性黑染料组合物和染料制品及其应用 |
| CN106833013A (zh) * | 2016-12-05 | 2017-06-13 | 泰兴锦云染料有限公司 | 一种活性深红染料及其制备和应用 |
| MX2020008576A (es) | 2018-02-16 | 2020-09-21 | Huntsman Adv Mat Switzerland | Proceso para el curtido y teñido simultáneo de material fibroso que contiene colágeno. |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0713200B2 (ja) * | 1987-02-13 | 1995-02-15 | 日本化薬株式会社 | トリスアゾ化合物及びそれを用いる染色法 |
| 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 |
| JP2729402B2 (ja) * | 1989-07-26 | 1998-03-18 | ダイスタージャパン株式会社 | 水溶性トリスアゾ色素 |
| MY116477A (en) | 1993-05-17 | 2004-02-28 | Ciba Sc Holding Ag | Reactive dyes, processes for their preparation and their use |
| JPH07252786A (ja) * | 1994-03-11 | 1995-10-03 | Nippon Kayaku Co Ltd | 銅後処理型反応染料染色法 |
| JPH07258983A (ja) * | 1994-03-16 | 1995-10-09 | Nippon Kayaku Co Ltd | 銅後処理型反応染料による吸尽染色法及び染色物の後処理法 |
| JPH0860017A (ja) * | 1994-08-23 | 1996-03-05 | Sumitomo Chem Co Ltd | ビスアゾ化合物およびそれを用いて繊維材料を染色または捺染する方法 |
| JPH08127730A (ja) * | 1994-10-31 | 1996-05-21 | Taoka Chem Co Ltd | インクジェット捺染用フルブラックインク及びそれを用いる布帛の捺染方法 |
| DE19600765A1 (de) | 1996-01-11 | 1997-07-17 | Basf Ag | Reaktive Azofarbstoffe mit einer Kupplungskomponente aus der Reihe der Aminonaphthalinsulfonsäuren sowie deren Zwischenprodukte |
| DE19640189A1 (de) * | 1996-09-30 | 1998-04-02 | Basf Ag | Reaktivfarbstoffe mit einem heterocyclischen Anker |
-
1999
- 1999-07-15 AU AU49110/99A patent/AU4911099A/en not_active Abandoned
- 1999-07-15 JP JP2000562440A patent/JP4322427B2/ja not_active Expired - Fee Related
- 1999-07-15 WO PCT/EP1999/005020 patent/WO2000006652A2/de not_active Ceased
- 1999-07-15 US US09/744,487 patent/US6537332B1/en not_active Expired - Fee Related
- 1999-07-15 ES ES99932887T patent/ES2205850T3/es not_active Expired - Lifetime
- 1999-07-15 EP EP99932887A patent/EP1137716B1/de not_active Revoked
- 1999-07-15 DE DE59906709T patent/DE59906709D1/de not_active Revoked
- 1999-07-15 PT PT99932887T patent/PT1137716E/pt unknown
- 1999-07-15 AT AT99932887T patent/ATE247694T1/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1137716B1 (de) | 2003-08-20 |
| ATE247694T1 (de) | 2003-09-15 |
| AU4911099A (en) | 2000-02-21 |
| JP4322427B2 (ja) | 2009-09-02 |
| US6537332B1 (en) | 2003-03-25 |
| JP2002521548A (ja) | 2002-07-16 |
| EP1137716A2 (de) | 2001-10-04 |
| DE59906709D1 (de) | 2003-09-25 |
| WO2000006652A3 (de) | 2001-07-26 |
| WO2000006652A2 (de) | 2000-02-10 |
| PT1137716E (pt) | 2004-01-30 |
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