GB849772A - s-triazine derivatives - Google Patents
s-triazine derivativesInfo
- Publication number
- GB849772A GB849772A GB3897356A GB3897356A GB849772A GB 849772 A GB849772 A GB 849772A GB 3897356 A GB3897356 A GB 3897356A GB 3897356 A GB3897356 A GB 3897356A GB 849772 A GB849772 A GB 849772A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphonate
- acid
- benzene
- salt
- sodium
- 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
Links
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
- D06P3/663—Natural or regenerated cellulose using reactive dyes reactive group directly attached to heterocyclic 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
- C09B43/02—Preparation of azo dyes from other azo compounds by sulfonation
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
The invention comprises compounds containing at least one s-triazine nucleus to at least one carbon atom of which is attached a sulphonic acid group in the form of its alkali metal or alkaline earth metal (including magnesium) salt. They may be prepared by reacting the corresponding halogen derivatives with a metal salt of sulphurous acid, preferably in aqueous solution. All or part of the halogen may be replaced. It is also possible to replace one halogen atom by sulphonate and a second by hydroxyl. The reaction medium is preferably neutralised to pH 6-8 before isolating the product which may be effected by adding an alkali or alkaline earth metal salt to precipitate the corresponding sulphonate. Heating the products with acid liberates sulphur dioxide while with aqueous alkalis or alkali/hypochlorite mixtures, all or part of the sulphonate is replaced by hydroxyl. The halogenated starting materials may contain organic substituents attached to triazine ring carbon through nitrogen, oxygen or sulphur. Such compounds may be p obtained by treating a halogenated triaziane with an amine, alcohol, phenol or mercaptan. Starting materials prepared in Examples are: (10) the sodium salt of (4, 6-dichloro-s-triazinylamino)-benzene-3-sulphonic acid; from metanilic acid and cyanuric chloride; in (19) this is converted with sodium hydrogen sulphide to the disodium salt of (4, 6-dimercapto-s-trazinylamino)-benzene-3-sulphonic acid, which is further reacted with sodium hydroxide/sodium hypochlorite mixture to give the trisodium salt of (4-sulpho-6-hydroxy-s-triazinylamino)- benzene-3-sulphonic acid; in (18) the reaction product of cyanauric chloride and sodium sulphite is reacted with sodium metanilate to give (4, 6-disulpho-s-triazinylamino)-benzene-3-sulphonic acid trisodium salt. Specification 707,557 is referred to.ALSO:The invention comprises dyestuffs containing at least one s-triazine nucleus to at least one carbon atom of which is attached a sulphonic acid group in the form of its alkali metal or alkaline-earth metal (including magnesium) salt. They may be prepared by reacting the corresponding halogen compounds with a metal salt of sulphurous acid, preferably in aqueous solution. All or part of the halogen may be replaced. It is also possible to replace one halogen atom by sulphonate and a second by hydroxyl and to convert the sulphonate group to a hydroxyl group. The reaction medium is preferably neutralized to pH 6-8 before isolating the product, which may be effected by adding an alkali or alkaline-earth metal salt to precipitate the corresponding sulphonate. Heating the products with acid liberates SO2, while with aqueous alkalis or alkali/hypochlorite mixtures, all or part of the sulphonate is replaced by hydroxyl. The halogenated starting materials may contain organic substituents attached to triazine ring carbon through nitrogen, oxygen or sulphur. Such compounds may be obtained by treating a halogenated triazine with an amine, alcohol, phenol or mercaptan. The products may contain anthraquinone, azo, nitro, naphthalene and phthalocyanine residues, examples being provided. The preparation of some of the starting materials is also described. In examples, the dyes are applied by padding or printing to cotton, viscose rayon, nylon and silk. An acid-binding agent is preferably used before, with or after the dye. The dyed fabric may be steamed. Compounds of the invention containing two or more sulphonate groups attached to the triazine ring may be used to attach to cellulose products chemically related thereto, such as starch. In Example 46 cotton limbric is impregnated with a starch solution, dried and treated with an aqueous sodium bicarbonate solution of trisodium (4, 6-disulpho-s-triazinylamino)-benzene-3-sulphonate, dried and baked to give a stiffened fabric resistant to boiling soap treatment. In Example 47, the starch, bicarbonate and sulphonate are applied together to the cotton. In Example 50 a cotton cloth is impregnated with a sodium bicarbonate solution of trisodium (4, 6-disulpho-s-triazinylamino)-benzene-3-sulphonate, baked, washed and dried to give a fabric resistant to soiling. The products may be used to treat textiles dyed or printed with dyes containing amino- or mono-substituted amino groups to increase fastness to washing. In Example 45 silk, wool or polyacrylonitrile fabric dyed with tetramino anthraquinone is padded with an aqueous solution containing trisodium (4, 6-disulpho -striazinylamino) -benzene -3- sulphonate, dried and acid-steamed; viscose rayon and cotton dyed with a direct dye are treated similarly. In Example 49 a viscose rayon fabric is impregnated with a sodium carbonate solution of trisodium (4, 6-disulpho -striazinylamino)-benzene -3- sulphonate, dried, printed with a thickened paste comprising the dyestuff composition of Example 2 of Specification 707,557, lactic acid and di(2, 21-hydroxyethyl) sulphide, steamed, acetic acid rinsed, water rinsed, boiled in aqueous soap solution and dried.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3897356A GB849772A (en) | 1956-12-21 | 1956-12-21 | s-triazine derivatives |
CH5405057A CH366050A (en) | 1956-12-21 | 1957-12-20 | Process for the production of new organic compounds |
DEJ14148A DE1234892B (en) | 1956-12-21 | 1957-12-21 | Process for the production of dyes |
FR1195350D FR1195350A (en) | 1956-12-21 | 1957-12-21 | Process for the manufacture of water-soluble organic compounds containing triazine nuclei |
GB2891659A GB942796A (en) | 1956-12-21 | 1959-08-24 | New pyrimidine dyestuffs |
DE19601419858 DE1419858A1 (en) | 1956-12-21 | 1960-08-04 | Process for the production of dyes |
FR836639A FR79115E (en) | 1956-12-21 | 1960-08-24 | Process for the manufacture of water-soluble organic compounds containing triazine nuclei |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3897356A GB849772A (en) | 1956-12-21 | 1956-12-21 | s-triazine derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB849772A true GB849772A (en) | 1960-09-28 |
Family
ID=10406837
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3897356A Expired GB849772A (en) | 1956-12-21 | 1956-12-21 | s-triazine derivatives |
Country Status (4)
Country | Link |
---|---|
CH (1) | CH366050A (en) |
DE (1) | DE1234892B (en) |
FR (1) | FR1195350A (en) |
GB (1) | GB849772A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105399857A (en) * | 2015-11-26 | 2016-03-16 | 浙江理工大学 | Method for modifying sodium alginate by utilizing monochlorotriazine arylamine sulfoacid |
CN105399856A (en) * | 2015-11-26 | 2016-03-16 | 浙江理工大学 | Preparation method of dichloro sym-triazine type active group modified sodium alginate |
CN113599990A (en) * | 2021-07-13 | 2021-11-05 | 克拉玛依市杰德科技有限责任公司 | Anhydrous desulfurizer and application thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3054793A (en) * | 1956-06-15 | 1962-09-18 | Ici Ltd | New water soluble nitro dyestuffs containing a mono- or di-halogeno-1:3:5-triazinyl-(2)-amino group |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2733976A (en) * | 1956-02-07 | Sulfonateds-acylamino | ||
BE543213A (en) * | ||||
US2377145A (en) * | 1940-12-13 | 1945-05-29 | Sandoz Ag | Dyestuffs of the anthraquinone series and a process for their manufacture |
US2412790A (en) * | 1943-07-16 | 1946-12-17 | Sandoz Ltd | Dyestuffs of the anthraquinone series and a process of making same |
US2685581A (en) * | 1952-10-08 | 1954-08-03 | Eastman Kodak Co | Organic phosphorus compounds |
FR1128353A (en) * | 1954-07-30 | 1957-01-04 | Ciba Geigy | New monoazo dyes, their preparation and use |
-
1956
- 1956-12-21 GB GB3897356A patent/GB849772A/en not_active Expired
-
1957
- 1957-12-20 CH CH5405057A patent/CH366050A/en unknown
- 1957-12-21 FR FR1195350D patent/FR1195350A/en not_active Expired
- 1957-12-21 DE DEJ14148A patent/DE1234892B/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105399857A (en) * | 2015-11-26 | 2016-03-16 | 浙江理工大学 | Method for modifying sodium alginate by utilizing monochlorotriazine arylamine sulfoacid |
CN105399856A (en) * | 2015-11-26 | 2016-03-16 | 浙江理工大学 | Preparation method of dichloro sym-triazine type active group modified sodium alginate |
CN105399856B (en) * | 2015-11-26 | 2017-08-15 | 浙江理工大学 | A kind of preparation method of dichloro s-triazine type active group modified sodium alginate |
CN105399857B (en) * | 2015-11-26 | 2017-08-15 | 浙江理工大学 | A kind of method using a chloro-s-triazine arylamine sulfonic acid modified sodium alginate |
CN113599990A (en) * | 2021-07-13 | 2021-11-05 | 克拉玛依市杰德科技有限责任公司 | Anhydrous desulfurizer and application thereof |
CN113599990B (en) * | 2021-07-13 | 2024-02-27 | 克拉玛依市杰德科技有限责任公司 | Anhydrous desulfurizing agent and application thereof |
Also Published As
Publication number | Publication date |
---|---|
FR1195350A (en) | 1959-11-17 |
CH366050A (en) | 1962-12-15 |
DE1234892B (en) | 1967-02-23 |
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