GB806050A - Cupriferous dis-azo-dyestuffs of the benzthiazole series - Google Patents

Cupriferous dis-azo-dyestuffs of the benzthiazole series

Info

Publication number
GB806050A
GB806050A GB7736/55A GB773655A GB806050A GB 806050 A GB806050 A GB 806050A GB 7736/55 A GB7736/55 A GB 7736/55A GB 773655 A GB773655 A GB 773655A GB 806050 A GB806050 A GB 806050A
Authority
GB
United Kingdom
Prior art keywords
dyestuffs
methoxy
group
methyl
benzene
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
GB7736/55A
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
Ciba 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 Ciba AG filed Critical Ciba AG
Publication of GB806050A publication Critical patent/GB806050A/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
    • 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
    • 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
    • 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
    • C09B45/24Disazo or polyazo compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/30Inkjet printing inks
    • C09D11/32Inkjet printing inks characterised by colouring agents
    • C09D11/328Inkjet printing inks characterised by colouring agents characterised by 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
    • 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

Abstract

The invention comprises dyestuffs of formula <FORM:0806050/IV (c)/1> where R is a benzene residue fused to the thiazole ring as indicated, R1 is a benzene residue bound to the azo link in p-position to the thiazole ring, R2 and R3 are benzene or naphthalene residues and at least one of R and R1 contains a sulphonic acid group and groups R1-N=N-, -O-Cu- and -N=N- are in the 1-, 3-, 4-positions of R2. They may be made by treating dyestuffs of formul\mg <FORM:0806050/IV (c)/2> and <FORM:0806050/IV (c)/3> in conventional fashion with copper-yielding agents so that the desired dyestuffs are obtained The unmetallized dyestuffs are also made by conventional methods from appropriate components. Residues R and Rl may contain substituents such as chlorine atoms, methoxy or ethoxy groups and especially methyl and/or sulphonic acid groups. Preferred initial components are mono- and di-sulphonic acids of 2-(41 - aminophenyl) - 6 - methyl - benzthiazole. Middle components corresponding to R2 are preferably of the benzene series, the alkoxy group being advantageously a methoxy group. Specified components corresponding to R2 are 1-amino-2-methoxy-5-methyl- and -2,5-dimethoxy- and -diethoxy-benzenes, 1-amino-2-methoxy- and -ethoxy-naphthalenes and their 6-and 7-sulphonic acids and preferably 1-amino-2-methoxybenzene. Residue R3 advantageously contains a group imparting solubility in water such as a sulphonamide or carboxyl group and especially a sulphonic acid group. Specified components corresponding to R3 are aniline and its 2-methoxy, 2- and 4-carboxy, 3- and 4-sulpho- and sulphonamido- and 3-sulpho-4-methyl-derivatives and 2-aminonaphthalene-6-mono- and -4,8-sulphonic acids. The dyestuffs dye wool, silk and leather and especially cotton, linen and also regenerated cellulose and artificial silk. In examples illustrative of the preparation of the dyestuffs and their use in dyeing cotton in greenish or grey shades components used are selected from those listed above with the addition of 2-(41-aminophenyl)-benzthiazole-x-sulphonic acid as an initial component and aniline-3-carboxylic acid as a component corresponding to R3. Specification 719,363 is referred to.
GB7736/55A 1954-03-16 1955-03-16 Cupriferous dis-azo-dyestuffs of the benzthiazole series Expired GB806050A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH806050X 1954-03-16

Publications (1)

Publication Number Publication Date
GB806050A true GB806050A (en) 1958-12-17

Family

ID=4538066

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7736/55A Expired GB806050A (en) 1954-03-16 1955-03-16 Cupriferous dis-azo-dyestuffs of the benzthiazole series

Country Status (1)

Country Link
GB (1) GB806050A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2458584A2 (en) 2008-02-21 2012-05-30 Snell Limited Audio visual signature, method of deriving a signature, and method of comparing audio-visual data

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2458584A2 (en) 2008-02-21 2012-05-30 Snell Limited Audio visual signature, method of deriving a signature, and method of comparing audio-visual data

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