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GB710797A - Improvements relating to copper-containing disazo dyestuffs - Google Patents

Improvements relating to copper-containing disazo dyestuffs

Info

Publication number
GB710797A
GB710797A GB3124/52A GB312452A GB710797A GB 710797 A GB710797 A GB 710797A GB 3124/52 A GB3124/52 A GB 3124/52A GB 312452 A GB312452 A GB 312452A GB 710797 A GB710797 A GB 710797A
Authority
GB
United Kingdom
Prior art keywords
radical
copper
acid
complex
salts
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
GB3124/52A
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.)
Novartis AG
Original Assignee
JR Geigy 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 JR Geigy AG filed Critical JR Geigy AG
Publication of GB710797A publication Critical patent/GB710797A/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
    • 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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds
    • C09B45/18Monoazo compounds containing copper
    • 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
    • C09B62/44Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/4401Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system
    • C09B62/4403Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system the heterocyclic system being a triazine ring
    • C09B62/4411Azo dyes
    • 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
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/38General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Abstract

The invention comprises complex copper compounds from disazo dyestuffs of the general formula:- <FORM:0710797/IV(c)/1> (wherein one X represents hydrogen and the other a sulphonic acid group, Y represents a 1 : 4-phenyl or 4 : 4\sv-diphenyl radical, and Z an acylamino radical), and the preparation thereof by coupling tetrazotized o-dianisidine with the appropriate coupling components in either order and treating the resulting disazo dyestuff with an agent yielding copper. Z may be an aroylamino radical or preferably an alkoylamino radical of not more than 8 carbon atoms or an alkoxycarbonylamino radical in which the alkyl group contains not more than 9 carbon atoms. The two couplings preferably take place in an alkaline medium, the naphtholdisulphonic acid being advantageously coupled first, whilst the coppering may be effected in an aqueous solution or suspension at a raised temperature, if desired in the presence of additives such as wetting or dispersing agents or salts such as sodium phosphates or sodium chloride, the agents yielding copper being normal or complex salts of copper with inorganic or organic anions. The products, in the form of their alkali metal salts, are suitable for dyeing natural and regenerated cellulose fibres. Examples describe the use of derivatives of 2 : 5 : 7-aminonaphtholsulphonic acid in which Y is a 1 : 4-phenyl radical and Z is acetylamino, benzoylamino salicoylamino, p-toluylamino or -NHCOOR (where R is -CH3, -C2H5, -C2H4OCH3, -CH (CH2)-CH2OCH3, -C3H6OC3H6OCH3, -CH (CH9)- CH2OC2H5, -C2H4OC2H5 or -C3H6OC3 H6OC2H5), and in which Y is a 3\sv-sulpho-4 : 4\sv-diphenyl radical and Z is acetylamino. In a further example, cotton is dyed blue with the copper complex of the dyestuff 1\sv-naphthol-3 : 8- disulphonic acid \sM o-dianisidine --> 2-(4\sv-acetylaminophenylamino)-5-naphthol-7-sulphonic acid from a bath containing Glauber salt and sodium carbonate. Specification 352,956 and German Specification 196,924 are referred to.
GB3124/52A 1951-02-07 1952-02-06 Improvements relating to copper-containing disazo dyestuffs Expired GB710797A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH710797X 1951-02-07

Publications (1)

Publication Number Publication Date
GB710797A true GB710797A (en) 1954-06-16

Family

ID=4530754

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3124/52A Expired GB710797A (en) 1951-02-07 1952-02-06 Improvements relating to copper-containing disazo dyestuffs

Country Status (1)

Country Link
GB (1) GB710797A (en)

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