GB533364A - Manufacture of azo-dyestuffs - Google Patents

Manufacture of azo-dyestuffs

Info

Publication number
GB533364A
GB533364A GB23196/39A GB2319639A GB533364A GB 533364 A GB533364 A GB 533364A GB 23196/39 A GB23196/39 A GB 23196/39A GB 2319639 A GB2319639 A GB 2319639A GB 533364 A GB533364 A GB 533364A
Authority
GB
United Kingdom
Prior art keywords
acid
hydroxyquinoline
cotton
yielding
components
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
GB23196/39A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB533364A publication Critical patent/GB533364A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C09B39/00Other azo dyes prepared by diazotising and coupling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

533,364. Azo dyes. SOC. OF CHEMICAL INDUSTRY IN BASLE. Aug. 11, 1939, Nos. 23196 and 23197. Convention dates, Aug. 16, 1938 and July 28, 1939. [Classes 2 (iii). and 15 (ii)] Triazo or polyazo dyes are prepared by coupling diazo compounds with coupling components and/or by linking azo dyestuffs with one another or with suitable compounds, the components being so selected that the finished dyestuff contains at least once the grouping =C-C<SP>11</SP>-N=C<SP>1</SP>-H as part of the tins I OH condensed nuclei of 8-hydroxyquinaline and is sufficiently soluble for application in an aqueous medium. The products may be used for dyeing or printing wool, silk, leather, cotton, linen or regenerated cellulose fibres and as pigments ; they yield metal complex compounds on treatment in substance or on the fibre with agents yielding metal, e.g., iron, chromium, nickel, cobalt or copper and the components may be so chosen as to impart an enhanced affinity for vegetable fibres, various components suitable for this purpose being specified. Examples (1) to (9) relate to the production of the following dyestuffs :- (1) 4 - - aminophenol - 2 - carboxylic acid # 1 : 7 - aminonaphthalenesulphonic acid # 1 : 7 or 1 : 6 - aminonaphthalenesulphonic acid # 8-hydroxyquinoline, yielding on vegetable or regenerated cellulose fibres blue dyeings which become fast to washing and to light on after-treatment with a copper salt ; (2) salicylic acid # benzidine # 1 : 6 - aminonaphthalenesulphonic acid # 8-hydroxyquinoline, yielding on cotton brown dyeings which may be aftercoppered ; (3) benzidine - 3 : 3<SP>1</SP> - dicarboxylic acid <SP>#</SP> # 1 : 6 - aminonaphthalenesulphonic acid (2 mols) <SP>#</SP> # 1 : 7 - aminonaphthalenesulphonic acid (2 mols.)<SP>#</SP> # 8 - hydroxyquinoline (2 mols.), yielding on cotton grey dyeings which may be after-coppered ; (4) the product obtained by reduction with glucose, as described in Specification 491,551, of the nitro groups of the dyestuff, 5 - nitro - 2 - aminophenol # (alkaline) 2 : 5 : 7 - aminonaphtholsulphonic acid # 8 - hydroxyquinoline, yielding on cotton, on aftercoppering, blue-grey dyeings fast to washing and to light; (5) the product obtained by similar reduction of the corresponding dyestuff in which the end componet is 8-hydroxyquinoline - 7 - sulphonic acid, yielding on cotton grey dyeings which may be after-coppered ; (6) salicylic acid # benzidine - 3 : 3<SP>1</SP> - dicarboxylic acid # (alkaline) 2 : 5 : 7 - aminonaphtholsulphonic acid # 8 - hydroxyquinoline, yielding on cotton, on after-coppering, violet-blue dyeings ; (7) salicylic acid # benzidine # 1 - amino - 2 - methoxynaphthalene - 6 - sulphonic acid - 8 - hydroxyquinoline, yielding on cotton, on after-coppering, blackish-brown dyeings ; (8) and (9) salicylic acid # benzidine # 1 : 6 - aminonaphthalenesulphonic acid # 8 - hydroxyquinoline - 7- and 5 - sulphonic acids respectively, yielding on cotton, on aftercoppering, red-brown dyeings. Examples are also given of the coppering in substance and on cotton fibre in a fresh bath of the dyestuff of Example 3 and on cotton fibre in the dyebath of the dyestuff of Example (1).Additional specified components are (a) diazo components, aminosulphonic acids of the benzene series, anthranilic acid, 1 : 4 - and 1 : 5 - aminonaphthalenesulphonic acids, 2 : 4 : 8 - and 2 : 6 : 8 - aminonaphthalenedisulphonicacids, O-esters of 1 : 8 - aminonaphtholsulphonic acids, dehydrothiotoluidine and such as contain an 8-hydroxyquinoline residue, (b) tetrazo components, tolidine, dianisidine, 4-nitraniline or its 2- sulphonic acid, (nitro groups reduced) 4- acetylaminoaniline or 1 - amino - 4 - acetylaminonaphthalene - 6 - sulphonic acid (acetylamino groups saponified), diaminostilbenedisulphonic acid and 4 : 4<SP>1</SP> - diaminodiphenylurea, (c) middle components, aniline (as the #- methanesulphonic acid), m-toluidine, cresidine, 2 : 5 - dialkoxyanilines, 5 - amino - 8 - hydroxyquinoline, 1 - aminonaphthalene, 1 - amino - 2 - methoxy - or ethoxy-naphthalene and their 6- or 7-sulphonic acids and 2 : 8 : 6 - aminonaphtholsulphonic acid, (d) end component, 2 : 8 : 6 - aminonaphtholsulphonic acid and halogen-substituted 8-hydroxyquinolines. The linking of components by means of phosgene or halogenated triazines is also specified. Specifications 455,274, 458,501, 468,362 and 497,350 also are referred to.
GB23196/39A 1938-08-16 1939-08-11 Manufacture of azo-dyestuffs Expired GB533364A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH533364X 1938-08-16

Publications (1)

Publication Number Publication Date
GB533364A true GB533364A (en) 1941-02-12

Family

ID=4518609

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23196/39A Expired GB533364A (en) 1938-08-16 1939-08-11 Manufacture of azo-dyestuffs

Country Status (1)

Country Link
GB (1) GB533364A (en)

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