CH655734A5 - Chlortriazinyl-monoazoverbindungen. - Google Patents
Chlortriazinyl-monoazoverbindungen. Download PDFInfo
- Publication number
- CH655734A5 CH655734A5 CH4799/83A CH479983A CH655734A5 CH 655734 A5 CH655734 A5 CH 655734A5 CH 4799/83 A CH4799/83 A CH 4799/83A CH 479983 A CH479983 A CH 479983A CH 655734 A5 CH655734 A5 CH 655734A5
- Authority
- CH
- Switzerland
- Prior art keywords
- formula
- compound
- mixture
- compounds
- hydrogen
- Prior art date
Links
- -1 CHLORTRIAZINYL MONOAZO COMPOUNDS Chemical class 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 22
- 238000004043 dyeing Methods 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 12
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 7
- 238000009833 condensation Methods 0.000 claims description 6
- 230000005494 condensation Effects 0.000 claims description 6
- 230000008878 coupling Effects 0.000 claims description 6
- 238000010168 coupling process Methods 0.000 claims description 6
- 238000005859 coupling reaction Methods 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 229940126062 Compound A Drugs 0.000 claims description 3
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 3
- 239000004753 textile Substances 0.000 claims description 3
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 2
- 239000010985 leather Substances 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000000975 dye Substances 0.000 description 22
- 229920000742 Cotton Polymers 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 6
- 150000001768 cations Chemical class 0.000 description 6
- 239000000985 reactive dye Substances 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000010446 mirabilite Substances 0.000 description 4
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- AIRRELHUAAZTTL-UHFFFAOYSA-N 3-nitrobenzenesulfonic acid;sodium Chemical compound [Na].OS(=O)(=O)C1=CC=CC([N+]([O-])=O)=C1 AIRRELHUAAZTTL-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 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
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 229910001413 alkali metal ion Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000005185 salting out Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- DMLFFHKJTSNRDT-UHFFFAOYSA-N ClN=NC1=CC=NN=N1 Chemical group ClN=NC1=CC=NN=N1 DMLFFHKJTSNRDT-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000010016 exhaust dyeing Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 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 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- WXWCDTXEKCVRRO-UHFFFAOYSA-N para-Cresidine Chemical compound COC1=CC=C(C)C=C1N WXWCDTXEKCVRRO-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 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
- C09B62/02—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
- C09B62/085—Monoazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8226002 | 1982-09-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH655734A5 true CH655734A5 (de) | 1986-05-15 |
Family
ID=10532864
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH4799/83A CH655734A5 (de) | 1982-09-13 | 1983-09-01 | Chlortriazinyl-monoazoverbindungen. |
Country Status (11)
| Country | Link |
|---|---|
| JP (1) | JPS5966459A (en, 2012) |
| BE (1) | BE904411Q (en, 2012) |
| CH (1) | CH655734A5 (en, 2012) |
| DE (1) | DE3331861A1 (en, 2012) |
| FR (1) | FR2532943B1 (en, 2012) |
| GB (1) | GB2127840B (en, 2012) |
| HK (1) | HK91686A (en, 2012) |
| IT (1) | IT1170482B (en, 2012) |
| KE (1) | KE3886A (en, 2012) |
| MY (1) | MY8700164A (en, 2012) |
| SG (1) | SG30789G (en, 2012) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2640988B1 (en, 2012) * | 1988-12-22 | 1993-02-19 | Sandoz Sa |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB869279A (en) * | 1956-09-14 | 1961-05-31 | Ciba Ltd | New azodyestuffs derived from cyanuric halides and processes for their manufacture and application |
| US2945022A (en) * | 1956-09-14 | 1960-07-12 | Ciba Ltd | Monoazo and disazo triazine dyes |
| DE2152511A1 (de) * | 1970-10-27 | 1972-05-04 | Ciba Geigy Ag | Azoverbindungen,deren Herstellung und Verwendung |
| DE2816937C2 (de) * | 1978-04-19 | 1982-07-15 | Basf Ag, 6700 Ludwigshafen | Verwendung von Reaktivfarbstoffen zum Färben von cellulosehaltigem Textilmaterial oder Leder |
| DE2842687A1 (de) * | 1978-09-30 | 1980-04-10 | Bayer Ag | Faserreaktive azofarbstoffe |
| GB2031932B (en) * | 1978-09-16 | 1982-11-10 | Bayer Ag | Fibre-reactive azo dyestuffs |
| DE2840380C2 (de) * | 1978-09-16 | 1985-05-30 | Bayer Ag, 5090 Leverkusen | Faserreaktive Azofarbstoffe |
| DE2945058A1 (de) * | 1979-11-08 | 1981-06-04 | Bayer Ag, 5090 Leverkusen | Faserreaktive monoazofarbstoffe, deren herstellung und verwendung |
| DE3045789A1 (de) * | 1980-12-04 | 1982-07-22 | Bayer Ag, 5090 Leverkusen | Faseraktive azofarbstoffe, verfahren zu ihrer herstellung und ihre verwendung zum faerben und bedrucken von hydroxylgruppen- und/oder stickstoffhaltigen fasermaterialien |
| DE3102287A1 (de) * | 1981-01-24 | 1982-09-02 | Hoechst Ag, 6000 Frankfurt | Wasserloesliche monoazoverbindungen, verfahren zu ihrer herstellung und ihre verwendung als farbstoffe |
-
1983
- 1983-09-01 CH CH4799/83A patent/CH655734A5/de not_active IP Right Cessation
- 1983-09-03 DE DE19833331861 patent/DE3331861A1/de active Granted
- 1983-09-09 FR FR8314504A patent/FR2532943B1/fr not_active Expired
- 1983-09-09 GB GB08324170A patent/GB2127840B/en not_active Expired
- 1983-09-12 IT IT48959/83A patent/IT1170482B/it active
- 1983-09-12 JP JP58166807A patent/JPS5966459A/ja active Granted
-
1986
- 1986-03-13 BE BE1/011454A patent/BE904411Q/fr not_active IP Right Cessation
- 1986-11-27 HK HK916/86A patent/HK91686A/xx not_active IP Right Cessation
-
1987
- 1987-12-30 MY MY164/87A patent/MY8700164A/xx unknown
-
1989
- 1989-05-11 SG SG307/89A patent/SG30789G/en unknown
- 1989-05-24 KE KE3886A patent/KE3886A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IT8348959A0 (it) | 1983-09-12 |
| GB8324170D0 (en) | 1983-10-12 |
| JPH0522738B2 (en, 2012) | 1993-03-30 |
| MY8700164A (en) | 1987-12-31 |
| KE3886A (en) | 1989-08-11 |
| FR2532943B1 (fr) | 1985-06-14 |
| DE3331861C2 (en, 2012) | 1987-06-11 |
| DE3331861A1 (de) | 1984-03-15 |
| SG30789G (en) | 1989-08-11 |
| HK91686A (en) | 1986-12-05 |
| JPS5966459A (ja) | 1984-04-14 |
| GB2127840B (en) | 1986-06-25 |
| GB2127840A (en) | 1984-04-18 |
| FR2532943A1 (fr) | 1984-03-16 |
| IT1170482B (it) | 1987-06-03 |
| BE904411Q (fr) | 1986-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE4209261B4 (de) | Anionische Disazoverbindungen | |
| DE3043915A1 (de) | Halo-triazinyl verbindungen | |
| CH675126A5 (en, 2012) | ||
| AT390441B (de) | Verfahren zur herstellung von reaktiven disazoverbindungen und ihre verwendung | |
| DE3046452C2 (en, 2012) | ||
| CH655735A5 (de) | Reaktive monoazoverbindungen. | |
| DE2854517A1 (de) | Azo reaktivfarbstoffverbindungen | |
| CH674849A5 (en, 2012) | ||
| DE3320972C2 (en, 2012) | ||
| DE3331861C2 (en, 2012) | ||
| DE2944624C2 (en, 2012) | ||
| CH667279A5 (de) | Metallisierte disazoverbindungen. | |
| DE2706417A1 (de) | Monoazoverbindungen enthaltend einen pyrimidinrest | |
| CH671232A5 (en, 2012) | ||
| DE3443962A1 (de) | Reaktive disazoverbindungen | |
| DE3332212C2 (en, 2012) | ||
| DE19515251B4 (de) | Faserreaktive Disazofarbstoffe | |
| DE3835724A1 (de) | Faserreaktive metallisierte monoazoverbindungen | |
| DE2839429A1 (de) | Anthrachinon-reaktivfarbstoffverbindungen | |
| DE3923483A1 (de) | Faserreaktive disazofarbstoffe | |
| DE4327006B4 (de) | Faserreaktive Monoazofarbstoffe | |
| CH639121A5 (en) | Monoazo compounds having a fibre-reactive radical, preparation thereof and use thereof in dyeing and printing leather | |
| DE3046451A1 (de) | "halo-triazinyl-verbindungen, deren herstellung und verwendung" | |
| DE4331386B4 (de) | Faserreaktive Monoazofarbstoffe | |
| AT220742B (de) | Verfahren zur Herstellung von neuen Azofarbstoffen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NV | New agent |
Representative=s name: SANDOZ TECHNOLOGIE AG |
|
| PUE | Assignment |
Owner name: SANDOZ AG TRANSFER- CLARIANT FINANCE (BVI) LIMITED |
|
| NV | New agent |
Representative=s name: CLARIANT INTERNATIONAL LTD. |
|
| PL | Patent ceased |