GB421971A - Manufacture of insoluble azo-dyestuffs on the fibre - Google Patents

Manufacture of insoluble azo-dyestuffs on the fibre

Info

Publication number
GB421971A
GB421971A GB17811/33A GB1781133A GB421971A GB 421971 A GB421971 A GB 421971A GB 17811/33 A GB17811/33 A GB 17811/33A GB 1781133 A GB1781133 A GB 1781133A GB 421971 A GB421971 A GB 421971A
Authority
GB
United Kingdom
Prior art keywords
acid
amino
class
sodium
iii
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
GB17811/33A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB421971A publication Critical patent/GB421971A/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
    • D06P3/68Preparing azo dyes on the material

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Insoluble azo-dyestuffs are made on the fibre by applying a mixture containing an alkali salt of a diazo-sulphonic acid of the general formula <FORM:0421971/IV/1> wherein R=an alkyl, aralkyl or alicyclic radical and wherein the aromatic nuclei may contain substituents, and an alkali salt of an o-coupling hydroxylated component, provided that neither of the dyestuff components contain a group producing solubility in water, and then subjecting the goods thus treated to a steaming operation. The free coupling component and sufficient alkali may also be used instead of the alkali salt. Dyeing assistants may be added. In examples: (1) cotton is printed with a paste containing the sodium salt of 4-benzylamino-2 : 5-dimethoxybenzene-1-diazosulphonic acid, 2 : 3 - oxynaphthoylaminobenzene, caustic soda, thiodiglycol, sodium chromate and starch tragacanth, dried, steamed, rinsed in an acid solution, soaped and rinsed (greenish blue); (2) the potassium salt of 4 - mono - n - butylamino - 3 - chlorobenzene - 1 - diazosulphonic acid and 2 : 3 - oxynaphthoyl - (1 - amino - 2 - methyl - 5 - chlorobenzene) is used as in (1); (3) the sodium salt of 2 : 5 - dimethoxy - 4 - (2<1> : 6<1> - dichlorbenzylamino)-benzene - 1 - diazosulphonic acid and the p-chloranilide of 2 : 3 - oxynaphthoic acid are ground with sodium acetate and then with caustic soda; (4) the sodium salt of 4-methylamino - 3 - chlorobenzene - 1 - diazosulphonic acid, the disodium salt of the o-toluidide of 2 : 3 - oxynaphthoic acid are ground with sodium acetate. Other components specified are the 2 : 3 - oxynaphthoyl derivatives of o-anisidine and 1-amino-4-methoxy-2-methylbenzene, diacetoacetyl-o-tolidine, 2-hydroxycarbazole - 3 - carboyl - (1 - amino - 4 - chlorbenzene); the diazosulphonate of 1-amino-4-cyclohexylaminobenzene - 3 - sulphonyldiethylamine. The process may be applied to viscose or silk. The Specification as open to inspection under Sect. 91 comprises the use of the following components: b -naphthol and its derivatives e.g. aroylaminonaphthols, arylides of 2 : 3-oxynaphthoic acid (Specification 23732/13, [Class 2 (iii)]), arylides of 6-halogen or 6-arylamino - 2 : 3 - oxynaphthoic acid (Specification 330,349, [Class 2 (iii)]), 1 - naphthol - 4 - carboxylic acid derivatives (Specification 211,223, [Class 2 (iii)]), e.g. 1 - naphthol - 4 - phenylketone, pyrazol nes and b -ketone-aldehyde derivatives (Specifications 211,814 and 211,772, [both in Class 2 (iii)]); dioxyquinolines (Specification 332,940, [Class 2 (iii)]), arylides of 6- or 7-hydroxy - 2 : 1 - and 1 : 2 - naphthocarbazolecarboxylic acids (Specification 330,643, [Class 2 (iii)]) and arylides of 2-oxyanthracene-3-carboxylic acid (Specification 367,907). In the examples the components of (1) and (2) above are ground with sodium acetate before incorporation into the printing paste. In a further example the sodium salt of 2 : 5-dimethoxy - 4 - (2<1> : 4<1> - dichlorobenzylamino) - benzene - 1 - diazosulphonic acid, the m-chloranilide of 2 : 3-oxynaphthoic acid, sulphur and sodium sulphite are ground to a powder, made into a paste with caustic soda, thiodiglycol, sodium chromate and starch tragacanth and printed as above. The following additional components are specified in a table: diazosulphonates of 1 - amino - 4 - benzylamino - 2 - methylbenzene and 1 - amino - 4 - (2<1> : 4<1> - dichlorbenzylamino) - 2 : 5 - dimethoxybenzene; the a - naphthylamide, the 2 : 5 - dimethoxyanilide, the 2 : 5 - dimethoxy - 4 - bromoanilide, the 4 - methoxy - 3 - methylanilide, the m-nitranilide of 2 : 3-oxynaphthoic acid, 1-phenyl-3-methyl - 5 - pyrazolone, the o - toluidide of 2-oxyanthracene - 3 - carboxylic acid and the 2 : 4 - dimethoxyanilide of 6 - bromo - 2 : 3 - oxynaphthoic acid. This subject-matter does not appear in the Specification as accepted. 1 - Amino - 4 - benzylamino - 2 : 5 - dimethoxybenzene and 1 - amino - 4 - (2<1> : 6<1> - dichlorobenzyl) - amino - 2 p : 5 - dimethoxybenzene are made by causing benzyl chloride or the appropriate substitution product thereof to react on the appropriate nitroamino compound in presence of sodium acetate and reducing. 1 - Amino - 4 - methyl - or n - butylamino - 3 - chlorobenzene are made by condensing methylamine and n-butylamine respectively with 3 : 4 - dichloronitrobenzene and reducing. 1 - Amino - 4 - cyclohexylaminobenzene - 3 - sulphonyldiethylamine is made by condensing cyclohexylamine with 1-chloro-4-nitrobenzene-2-sulphonic acid, converting into the sulphochloride, condensing with diethylamine and reducing.
GB17811/33A 1932-06-22 1933-06-22 Manufacture of insoluble azo-dyestuffs on the fibre Expired GB421971A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE421971X 1932-06-22

Publications (1)

Publication Number Publication Date
GB421971A true GB421971A (en) 1934-12-24

Family

ID=6461135

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17811/33A Expired GB421971A (en) 1932-06-22 1933-06-22 Manufacture of insoluble azo-dyestuffs on the fibre

Country Status (1)

Country Link
GB (1) GB421971A (en)

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