GB849772A - s-triazine derivatives - Google Patents

s-triazine derivatives

Info

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
Application number
GB3897356A
Inventor
John Reginald Atkinson
Frank Hall
William Elliot Stephen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB3897356A priority Critical patent/GB849772A/en
Priority to CH5405057A priority patent/CH366050A/en
Priority to DEJ14148A priority patent/DE1234892B/en
Priority to FR1195350D priority patent/FR1195350A/en
Priority to GB2891659A priority patent/GB942796A/en
Priority to DE19601419858 priority patent/DE1419858A1/en
Priority to FR836639A priority patent/FR79115E/en
Publication of GB849772A publication Critical patent/GB849772A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/66Natural or regenerated cellulose using reactive dyes
    • D06P3/663Natural or regenerated cellulose using reactive dyes reactive group directly attached to heterocyclic group
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/02Preparation of azo dyes from other azo compounds by sulfonation
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/02Reactive 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
    • C09B62/04Reactive 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.
GB3897356A 1956-12-21 1956-12-21 s-triazine derivatives Expired GB849772A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Cited By (6)

* Cited by examiner, † Cited by third party
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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