CH589703A5 - Fibre-reactive tetrazo dyes contg. halotriazine ring - for dyeing and printing cotton, and nitrogenous materials greenish-blue shades - Google Patents

Fibre-reactive tetrazo dyes contg. halotriazine ring - for dyeing and printing cotton, and nitrogenous materials greenish-blue shades

Info

Publication number: CH589703A5
Authority: CH; Switzerland
Prior art keywords: acid; formula; reactive; amino; parts
Prior art date: 1974-01-04

Application number

CH6174A

Other languages

German (de)

English (en)

Original Assignee

Ciba Geigy Ag

Priority date (The priority date 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 date listed.)

1974-01-04

Filing date

1974-01-04

Publication date

1977-07-15

1974-01-04 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1974-01-04 Priority to CH6174A priority Critical patent/CH589703A5/de

1974-12-12 Priority to US05/532,420 priority patent/US3966705A/en

1974-12-24 Priority to AU76831/74A priority patent/AU492637B2/en

1974-12-28 Priority to JP49149298A priority patent/JPS5850265B2/ja

1974-12-30 Priority to FR7443328A priority patent/FR2256950B1/fr

1974-12-30 Priority to IT54816/74A priority patent/IT1026200B/it

1975-01-02 Priority to BR10/75A priority patent/BR7500010A/pt

1975-01-02 Priority to CS7537A priority patent/CS187454B2/cs

1975-01-02 Priority to DE2500062A priority patent/DE2500062C2/de

1975-01-03 Priority to GB297/75A priority patent/GB1488952A/en

1975-01-03 Priority to BE152125A priority patent/BE824076A/fr

1976-01-01 Priority to AR20473376D priority patent/AR204733A1/es

1977-07-15 Publication of CH589703A5 publication Critical patent/CH589703A5/de

Links

239000000975 dye Substances 0.000 title abstract description 45
238000004043 dyeing Methods 0.000 title abstract description 13
238000007639 printing Methods 0.000 title abstract description 8
229920000742 Cotton Polymers 0.000 title abstract description 7
241000974482 Aricia saepiolus Species 0.000 title abstract 2
239000000463 material Substances 0.000 title description 4
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 title 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 22
125000005843 halogen group Chemical group 0.000 claims abstract description 5
230000008878 coupling Effects 0.000 claims description 23
238000010168 coupling process Methods 0.000 claims description 23
238000005859 coupling reaction Methods 0.000 claims description 23
APRRQJCCBSJQOQ-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S(O)(=O)=O)=CC2=C1 APRRQJCCBSJQOQ-UHFFFAOYSA-N 0.000 claims description 12
238000000034 method Methods 0.000 claims description 11
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 claims description 10
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims description 9
UGEHFOSBNBEWMP-UHFFFAOYSA-N 2,3-diaminobenzenesulfonic acid Chemical compound NC1=CC=CC(S(O)(=O)=O)=C1N UGEHFOSBNBEWMP-UHFFFAOYSA-N 0.000 claims description 9
238000002360 preparation method Methods 0.000 claims description 9
ZAJAQTYSTDTMCU-UHFFFAOYSA-N 3-aminobenzenesulfonic acid Chemical compound NC1=CC=CC(S(O)(=O)=O)=C1 ZAJAQTYSTDTMCU-UHFFFAOYSA-N 0.000 claims description 8
230000010933 acylation Effects 0.000 claims description 8
238000005917 acylation reaction Methods 0.000 claims description 8
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 7
HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
238000009833 condensation Methods 0.000 claims description 7
230000005494 condensation Effects 0.000 claims description 7
150000008049 diazo compounds Chemical class 0.000 claims description 7
125000000542 sulfonic acid group Chemical group 0.000 claims description 7
125000001424 substituent group Chemical group 0.000 claims description 6
229950000244 sulfanilic acid Drugs 0.000 claims description 4
JVMSQRAXNZPDHF-UHFFFAOYSA-N 2,4-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(N)=C1 JVMSQRAXNZPDHF-UHFFFAOYSA-N 0.000 claims description 3
-1 linen Polymers 0.000 abstract description 13
210000002268 wool Anatomy 0.000 abstract description 5
229920002678 cellulose Polymers 0.000 abstract description 4
239000001913 cellulose Substances 0.000 abstract description 4
239000004952 Polyamide Substances 0.000 abstract description 2
239000010985 leather Substances 0.000 abstract description 2
229920002647 polyamide Polymers 0.000 abstract description 2
229920002635 polyurethane Polymers 0.000 abstract description 2
239000004814 polyurethane Substances 0.000 abstract description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
239000000243 solution Substances 0.000 description 19
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
239000000203 mixture Substances 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 8
239000003929 acidic solution Substances 0.000 description 7
239000004744 fabric Substances 0.000 description 7
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
239000011780 sodium chloride Substances 0.000 description 6
239000002253 acid Substances 0.000 description 5
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 5
150000003254 radicals Chemical class 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
229920003043 Cellulose fiber Polymers 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 4
239000012670 alkaline solution Substances 0.000 description 4
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
ZMCHBSMFKQYNKA-UHFFFAOYSA-N 2-aminobenzenesulfonic acid Chemical class NC1=CC=CC=C1S(O)(=O)=O ZMCHBSMFKQYNKA-UHFFFAOYSA-N 0.000 description 3
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
239000003513 alkali Substances 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000000835 fiber Substances 0.000 description 3
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 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
239000001488 sodium phosphate Substances 0.000 description 3
ODIGIKRIUKFKHP-UHFFFAOYSA-N (n-propan-2-yloxycarbonylanilino) acetate Chemical compound CC(C)OC(=O)N(OC(C)=O)C1=CC=CC=C1 ODIGIKRIUKFKHP-UHFFFAOYSA-N 0.000 description 2
125000003363 1,3,5-triazinyl group Chemical group N1=C(N=CN=C1)* 0.000 description 2
VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 2
UEUIKXVPXLWUDU-UHFFFAOYSA-N 4-diazoniobenzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=C([N+]#N)C=C1 UEUIKXVPXLWUDU-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
VMKJWLXVLHBJNK-UHFFFAOYSA-N cyanuric fluoride Chemical compound FC1=NC(F)=NC(F)=N1 VMKJWLXVLHBJNK-UHFFFAOYSA-N 0.000 description 2
239000003599 detergent Substances 0.000 description 2
239000013067 intermediate product Substances 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
238000005185 salting out Methods 0.000 description 2
235000010288 sodium nitrite Nutrition 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
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 2
239000007858 starting material Substances 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 1
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
VHYBUUMUUNCHCK-UHFFFAOYSA-N 2,4,6-tribromo-1,3,5-triazine Chemical compound BrC1=NC(Br)=NC(Br)=N1 VHYBUUMUUNCHCK-UHFFFAOYSA-N 0.000 description 1
QGNJPFLIBOTDKU-UHFFFAOYSA-N 2,5-diaminobenzene-1,3-disulfonic acid Chemical compound NC1=CC(S(O)(=O)=O)=C(N)C(S(O)(=O)=O)=C1 QGNJPFLIBOTDKU-UHFFFAOYSA-N 0.000 description 1
VOPSFYWMOIKYEM-UHFFFAOYSA-N 2,5-diaminobenzene-1,4-disulfonic acid Chemical compound NC1=CC(S(O)(=O)=O)=C(N)C=C1S(O)(=O)=O VOPSFYWMOIKYEM-UHFFFAOYSA-N 0.000 description 1
HEAHMJLHQCESBZ-UHFFFAOYSA-N 2,5-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(N)C(S(O)(=O)=O)=C1 HEAHMJLHQCESBZ-UHFFFAOYSA-N 0.000 description 1
ZCGVPUAAMCMLTM-UHFFFAOYSA-N 2-amino-5-chlorobenzenesulfonic acid Chemical compound NC1=CC=C(Cl)C=C1S(O)(=O)=O ZCGVPUAAMCMLTM-UHFFFAOYSA-N 0.000 description 1
KZKGEEGADAWJFS-UHFFFAOYSA-N 2-amino-5-methoxybenzenesulfonic acid Chemical compound COC1=CC=C(N)C(S(O)(=O)=O)=C1 KZKGEEGADAWJFS-UHFFFAOYSA-N 0.000 description 1
LTPSRQRIPCVMKQ-UHFFFAOYSA-N 2-amino-5-methylbenzenesulfonic acid Chemical compound CC1=CC=C(N)C(S(O)(=O)=O)=C1 LTPSRQRIPCVMKQ-UHFFFAOYSA-N 0.000 description 1
LTASFWDWBYFZQQ-UHFFFAOYSA-N 2-amino-5-nitrobenzenesulfonic acid Chemical compound NC1=CC=C([N+]([O-])=O)C=C1S(O)(=O)=O LTASFWDWBYFZQQ-UHFFFAOYSA-N 0.000 description 1
LDCCBULMAFILCT-UHFFFAOYSA-N 2-aminobenzene-1,4-disulfonic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1S(O)(=O)=O LDCCBULMAFILCT-UHFFFAOYSA-N 0.000 description 1
VZLLZDZTQPBHAZ-UHFFFAOYSA-N 2-nitroaniline-4-sulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1[N+]([O-])=O VZLLZDZTQPBHAZ-UHFFFAOYSA-N 0.000 description 1
YADSWTKOIHUSDX-UHFFFAOYSA-N 4,6-diaminobenzene-1,3-disulfonic acid Chemical compound NC1=CC(N)=C(S(O)(=O)=O)C=C1S(O)(=O)=O YADSWTKOIHUSDX-UHFFFAOYSA-N 0.000 description 1
ZWUBBMDHSZDNTA-UHFFFAOYSA-N 4-Chloro-meta-phenylenediamine Chemical compound NC1=CC=C(Cl)C(N)=C1 ZWUBBMDHSZDNTA-UHFFFAOYSA-N 0.000 description 1
FOINSAWEWXUXPQ-UHFFFAOYSA-N 4-acetamido-2-aminobenzenesulfonic acid Chemical compound CC(=O)NC1=CC=C(S(O)(=O)=O)C(N)=C1 FOINSAWEWXUXPQ-UHFFFAOYSA-N 0.000 description 1
YPECXEWEXWBMNK-UHFFFAOYSA-N 4-amino-2-chlorobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(Cl)=C1 YPECXEWEXWBMNK-UHFFFAOYSA-N 0.000 description 1
NQHVJMJEWQQXBS-UHFFFAOYSA-N 4-ethoxybenzene-1,3-diamine Chemical compound CCOC1=CC=C(N)C=C1N NQHVJMJEWQQXBS-UHFFFAOYSA-N 0.000 description 1
PTMVFRKAMOUORT-UHFFFAOYSA-N 4-ethylbenzene-1,3-diamine Chemical compound CCC1=CC=C(N)C=C1N PTMVFRKAMOUORT-UHFFFAOYSA-N 0.000 description 1
TZBROGJRQUABOK-UHFFFAOYSA-N 4-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=C2C(O)=CC(S(O)(=O)=O)=CC2=C1 TZBROGJRQUABOK-UHFFFAOYSA-N 0.000 description 1
PHRVJZNHPVJYOM-UHFFFAOYSA-N 5-acetamido-2-aminobenzenesulfonic acid Chemical compound CC(=O)NC1=CC=C(N)C(S(O)(=O)=O)=C1 PHRVJZNHPVJYOM-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
125000004442 acylamino group Chemical group 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
125000004448 alkyl carbonyl group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000005129 aryl carbonyl group Chemical group 0.000 description 1
125000004391 aryl sulfonyl group Chemical group 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000006172 buffering agent Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000000460 chlorine Chemical group 0.000 description 1
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Substances ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
238000006193 diazotization reaction Methods 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
229910000397 disodium phosphate Inorganic materials 0.000 description 1
235000019800 disodium phosphate Nutrition 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000009413 insulation Methods 0.000 description 1
238000002955 isolation Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
229910000403 monosodium phosphate Inorganic materials 0.000 description 1
235000019799 monosodium phosphate Nutrition 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
239000000047 product Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
239000004627 regenerated cellulose Substances 0.000 description 1
238000010020 roller printing Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 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

Classifications

- 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
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
- D06P3/66—Natural or regenerated cellulose using reactive 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
- 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
- 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
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/24—Polyamides; Polyurethanes

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)

CH6174A 1974-01-04 1974-01-04 Fibre-reactive tetrazo dyes contg. halotriazine ring - for dyeing and printing cotton, and nitrogenous materials greenish-blue shades CH589703A5 (en)

Priority Applications (12)

Application Number	Priority Date	Filing Date	Title
CH6174A CH589703A5 (en)	1974-01-04	1974-01-04	Fibre-reactive tetrazo dyes contg. halotriazine ring - for dyeing and printing cotton, and nitrogenous materials greenish-blue shades
US05/532,420 US3966705A (en)	1974-01-04	1974-12-12	Disulfo naphthalene containing fiber-reactive tetrazo dyes
AU76831/74A AU492637B2 (en)	1974-01-04	1974-12-24	Fibre-reactive tetrazo dyes their manufacture and use
JP49149298A JPS5850265B2 (ja)	1974-01-04	1974-12-28	センイハンノウセイテトラゾセンリヨウノセイホウ
FR7443328A FR2256950B1 (fr)	1974-01-04	1974-12-30
IT54816/74A IT1026200B (it)	1974-01-04	1974-12-30	Coloranti tetrazoici reattivi per le fibre e procedimento per la loro produzione e applicazione
BR10/75A BR7500010A (pt)	1974-01-04	1975-01-02	Processo para a preparacao de tetrazocorantes reativos de fibra
CS7537A CS187454B2 (en)	1974-01-04	1975-01-02	Process for preparing tetrazodyes reactive with fiber
DE2500062A DE2500062C2 (de)	1974-01-04	1975-01-02	Faserreaktive Tetrazofarbstoffe und ihre Verwendung
GB297/75A GB1488952A (en)	1974-01-04	1975-01-03	Fibre-reactive tetrazo dyes their manufacture and use
BE152125A BE824076A (fr)	1974-01-04	1975-01-03	Colorants tetrazoiques reagissant sur les fibres textiles
AR20473376D AR204733A1 (es)	1974-01-04	1976-01-01	Colorantes tetrazoicos reactivos con las fibras y un procedimiento para su preparacion

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH6174A CH589703A5 (en)	1974-01-04	1974-01-04	Fibre-reactive tetrazo dyes contg. halotriazine ring - for dyeing and printing cotton, and nitrogenous materials greenish-blue shades

Publications (1)

Publication Number	Publication Date
CH589703A5 true CH589703A5 (en)	1977-07-15

Family

ID=4178419

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH6174A CH589703A5 (en)	1974-01-04	1974-01-04	Fibre-reactive tetrazo dyes contg. halotriazine ring - for dyeing and printing cotton, and nitrogenous materials greenish-blue shades

Country Status (2)

Country	Link
BE (1)	BE824076A (fr)
CH (1)	CH589703A5 (fr)

1974
- 1974-01-04 CH CH6174A patent/CH589703A5/de not_active IP Right Cessation
1975
- 1975-01-03 BE BE152125A patent/BE824076A/fr unknown

Also Published As

Publication number	Publication date
BE824076A (fr)	1975-07-03

Legal Events

Date	Code	Title	Description
1990-09-28	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0040806B1 (fr)	1984-09-19	Composés colorés solubles dans l'eau, procédé pour leur préparation et leur utilisation comme colorants
EP0076782B1 (fr)	1986-03-05	Colorants réactifs, leur préparation et leur utilisation
EP0134193B1 (fr)	1988-01-13	Colorants réactifs, leur préparation et leur emploi
DE2500062C2 (de)	1986-02-20	Faserreaktive Tetrazofarbstoffe und ihre Verwendung
DE2001960B2 (de)	1976-07-01	Azotriazinyl-reaktivfarbstoffe und deren verwendung zum faerben von cellulose-textilstoffen
EP0074928A2 (fr)	1983-03-23	Colorants réactifs, leur préparation et leur utilisation
DE1644203B2 (de)	1977-11-17	Reaktivfarbstoffe
DE2601043A1 (de)	1976-07-22	Tetrareaktive disazofarbstoffe, deren herstellung und verwendung
EP0141776B1 (fr)	1987-07-08	Colorants réactifs, leur préparation et leur utilisation
DE3045789A1 (de)	1982-07-22	Faseraktive azofarbstoffe, verfahren zu ihrer herstellung und ihre verwendung zum faerben und bedrucken von hydroxylgruppen- und/oder stickstoffhaltigen fasermaterialien
EP0170612B1 (fr)	1989-05-24	Colorants réactifs, leur préparation et leur utilisation
EP0096659B1 (fr)	1987-04-01	Procédé de teinture ou d'impression de matières fibreuses textiles avec des colorants réactifs
DE3217388A1 (de)	1983-11-17	Wasserloesliche disazoverbindungen, verfahren zu ihrer herstellung und ihre verwendung als farbstoffe
EP0112797A1 (fr)	1984-07-04	Procédé de teinture ou d'impression, avec des colorants réactifs, de matières fibreuses contenant de la cellulose
CH589703A5 (en)	1977-07-15	Fibre-reactive tetrazo dyes contg. halotriazine ring - for dyeing and printing cotton, and nitrogenous materials greenish-blue shades
EP0134197B1 (fr)	1988-06-01	Colorants réactifs disazoiques, leur préparation et leur utilisation
CH606345A5 (en)	1978-10-31	Tetrakis:azo dyes contg. two fibre-reactive triazinyl gps.
EP0122881B1 (fr)	1986-08-13	Colorants réactifs, leur préparation et leur utilisation
CH599316A5 (en)	1978-05-31	Fibre-reactive azo dyes prepn.
EP0105027B1 (fr)	1987-05-06	Colorants réactifs, leur préparation et leur emploi
EP0134192B1 (fr)	1987-09-30	Colorants réactifs, leur préparation et leur utilisation
DE3132724A1 (de)	1983-03-03	Wasserloesliche azoverbindungen, verfahren zu ihrer herstellung und ihre verwendung als farbstoffe
DE2927718A1 (de)	1980-01-24	Faserreaktive azofarbstoffe, deren herstellung und verwendung
DE3517755A1 (de)	1987-01-15	Wasserloesliche mono- und disazoverbindungen, verfahren zu deren herstellung und ihre verwendung als farbstoffe
DE1644206C3 (de)	1978-06-01	Wasserlösliche Reaktivfarbstoffe, deren Herstellung und Verwendung zum Färben von Cellulosematerialien, Wolle, Seide, Polyamid- und Polyurethanfasern