BE631379A - - Google Patents
Info
- Publication number
- BE631379A BE631379A BE631379DA BE631379A BE 631379 A BE631379 A BE 631379A BE 631379D A BE631379D A BE 631379DA BE 631379 A BE631379 A BE 631379A
- Authority
- BE
- Belgium
- Prior art keywords
- parts
- water
- soluble
- solutions
- dye
- Prior art date
Links
- 239000000975 dye Substances 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 7
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Tris Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 5
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000011780 sodium chloride Substances 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 238000004090 dissolution Methods 0.000 claims 1
- 239000000243 solution Substances 0.000 description 25
- 238000002360 preparation method Methods 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- 229960004418 Trolamine Drugs 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229940029612 triethanolamine Drugs 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N ethanolamine Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229940051142 Metanil yellow Drugs 0.000 description 2
- 239000000980 acid dye Substances 0.000 description 2
- -1 aliphatic diamines Chemical class 0.000 description 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical compound [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 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N 1,2-ethanediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N 2-(2-Ethoxyethoxy)ethanol Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N Hexamethylenediamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene (PE) Substances 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N Xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 235000012970 cakes Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000006103 coloring component Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N n-methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000001187 sodium carbonate Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000126 substance 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
- 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
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0072—Preparations with anionic dyes or reactive dyes
- C09B67/0073—Preparations of acid or reactive dyes in liquid form
-
- 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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/02—Dyestuff salts, e.g. salts of acid dyes with basic dyes
- C09B69/04—Dyestuff salts, e.g. salts of acid dyes with basic dyes of anionic dyes with nitrogen containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE631379A true BE631379A (es) |
Family
ID=199881
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE631379D BE631379A (es) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE631379A (es) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2311073A1 (de) * | 1972-03-17 | 1973-09-27 | Sandoz Ag | Sulfonsaeuregruppenhaltige stilbenazofarbstoffe und/oder stilben-azoxyfarbstoffe |
| DE2341293A1 (de) * | 1973-08-16 | 1975-03-13 | Bayer Ag | Konzentrierte loesungen anionischer farbstoffe |
| FR2332310A1 (fr) * | 1975-11-20 | 1977-06-17 | Ici Ltd | Solution aqueuse concentree de colorants azoiques et son utlisation pour la coloration de la pate a papier |
| EP0033719A2 (de) * | 1980-02-05 | 1981-08-12 | Ciba-Geigy Ag | Flüssigformulierung eines anionischen Farbstoffes der Disazoreihe, Verfahren zur Herstellung und Verwendung |
| FR2478658A1 (fr) * | 1980-03-21 | 1981-09-25 | Ugine Kuhlmann | Procede de preparation de colorant jaune direct 11 sous forme de solutions concentrees stables, solutions obtenues et applications |
| FR2484431A1 (fr) * | 1980-06-13 | 1981-12-18 | Ugine Kuhlmann | Procede pour la preparation de solutions concentrees de colorants azoiques et solutions ainsi obtenues |
| JPS61296069A (ja) * | 1985-06-25 | 1986-12-26 | Nippon Kagaku Kogyosho:Kk | 水性濃厚染料溶液組成物 |
| EP0810264A2 (de) * | 1996-05-31 | 1997-12-03 | Basf Aktiengesellschaft | Verfahren zur Herstellung von Phenylazonaphthalinen |
| EP0926209A1 (de) * | 1997-12-10 | 1999-06-30 | Ciba SC Holding AG | Wässrige Farbstofflösungen und deren Verwendung |
| US6033445A (en) * | 1997-02-10 | 2000-03-07 | Ciba Specialty Chemicals Corporation | Dye mixtures and their use |
| WO2004048478A1 (de) * | 2002-11-28 | 2004-06-10 | Basf Aktiengesellschaft | Verfahren zur herstellung einer flüssigformulierung von salzen sulfonsaurer azofarbstoffe |
-
0
- BE BE631379D patent/BE631379A/fr unknown
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2311073A1 (de) * | 1972-03-17 | 1973-09-27 | Sandoz Ag | Sulfonsaeuregruppenhaltige stilbenazofarbstoffe und/oder stilben-azoxyfarbstoffe |
| DE2341293A1 (de) * | 1973-08-16 | 1975-03-13 | Bayer Ag | Konzentrierte loesungen anionischer farbstoffe |
| FR2332310A1 (fr) * | 1975-11-20 | 1977-06-17 | Ici Ltd | Solution aqueuse concentree de colorants azoiques et son utlisation pour la coloration de la pate a papier |
| EP0033719A2 (de) * | 1980-02-05 | 1981-08-12 | Ciba-Geigy Ag | Flüssigformulierung eines anionischen Farbstoffes der Disazoreihe, Verfahren zur Herstellung und Verwendung |
| EP0033719A3 (en) * | 1980-02-05 | 1982-05-19 | Ciba-Geigy Ag | Liquid preparation of an anionic disazo dyestuff, process for its preparation, and use |
| FR2478658A1 (fr) * | 1980-03-21 | 1981-09-25 | Ugine Kuhlmann | Procede de preparation de colorant jaune direct 11 sous forme de solutions concentrees stables, solutions obtenues et applications |
| FR2484431A1 (fr) * | 1980-06-13 | 1981-12-18 | Ugine Kuhlmann | Procede pour la preparation de solutions concentrees de colorants azoiques et solutions ainsi obtenues |
| JPH07748B2 (ja) | 1985-06-25 | 1995-01-11 | 株式会社日本化学工業所 | 水性濃厚染料溶液組成物 |
| JPS61296069A (ja) * | 1985-06-25 | 1986-12-26 | Nippon Kagaku Kogyosho:Kk | 水性濃厚染料溶液組成物 |
| EP0810264A2 (de) * | 1996-05-31 | 1997-12-03 | Basf Aktiengesellschaft | Verfahren zur Herstellung von Phenylazonaphthalinen |
| EP0810264A3 (de) * | 1996-05-31 | 1999-01-27 | Basf Aktiengesellschaft | Verfahren zur Herstellung von Phenylazonaphthalinen |
| US6033445A (en) * | 1997-02-10 | 2000-03-07 | Ciba Specialty Chemicals Corporation | Dye mixtures and their use |
| EP0926209A1 (de) * | 1997-12-10 | 1999-06-30 | Ciba SC Holding AG | Wässrige Farbstofflösungen und deren Verwendung |
| WO2004048478A1 (de) * | 2002-11-28 | 2004-06-10 | Basf Aktiengesellschaft | Verfahren zur herstellung einer flüssigformulierung von salzen sulfonsaurer azofarbstoffe |
| CN100345910C (zh) * | 2002-11-28 | 2007-10-31 | 巴斯福股份公司 | 制备磺化偶氮染料盐的液体制剂的方法 |
| US7488810B2 (en) | 2002-11-28 | 2009-02-10 | Basf Aktiengesellschaft | Method for producing a liquid formulation of salts of sulfoacidic azo dyes |
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