GB859899A - New monoazo dyestuffs derived from benzthiazole - Google Patents

New monoazo dyestuffs derived from benzthiazole

Info

Publication number
GB859899A
GB859899A GB3518958A GB3518958A GB859899A GB 859899 A GB859899 A GB 859899A GB 3518958 A GB3518958 A GB 3518958A GB 3518958 A GB3518958 A GB 3518958A GB 859899 A GB859899 A GB 859899A
Authority
GB
United Kingdom
Prior art keywords
substituted
groups
alkyl radical
fibres
sulphonic
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
GB3518958A
Inventor
Brian Ribbons Fishwick
Eric Leslie Johnson
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 GB3518958A priority Critical patent/GB859899A/en
Priority to CH8018359A priority patent/CH410231A/en
Priority to CH556659A priority patent/CH411178A/en
Publication of GB859899A publication Critical patent/GB859899A/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/0025Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds

Landscapes

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

Abstract

The invention comprises water-insoluble dyes of formula: <FORM:0859899/IV (c)/1> where A is a substituted or unsubstituted 1, 4-phenylene or -naphthylene nucleus which is free from sulphonic or carboxylic acid groups, R is H or a lower alkyl radical which may be substituted or an aralkyl radical, R1 is a lower alkyl radical which may be substituted, X is CN or SCN and B may contain substituents other than sulphonic and carboxylic groups, provided that R and R1, when substituted, are free from sulphonic and carboxylic acid groups and that when R is a b - cyanolower alkyl radical R1 is neither a b -cyanonor a b - acyloxylower alkyl radical. Lower alkyl and alkoxy groups contain 1 to 4 carbon atoms. The dyes are made by diazotising appropriate aminobenzothiazoles and coupling with the desired azo components. Specified substituents for A are methyl, methoxy, chlorine, bromine, trifluoromethyl and acetylamino groups. Specified substituents for B are methyl, chlorine and bromine groups. Representative of values specified for R and R1 are: methyl, hydroxybutyl, ethoxyethyl, cyanopropyl, acetoxyethyl, bromoethyl, carbethoxymethyl, methylsulphonylethyl, ethylcarbonylethyl, aminocarbonylethyl, g - chloro -b - hydroxypropyl, b , g - epoxypropyl and b - (4, 6- diamino -s-triazin -2- yl) ethyl groups. R is also specified as a benzyl group. The dyes dye textiles comprising artificial fibres such as cellulose ester fibres e.g. acetate and triacetate, polyamide fibres, e.g. polyhexamethyleneadipamides and polycaprolactams, polyvinyl fibres, e.g. polyacrylonitriles which may be modified, and aromatic polyester fibres e.g. polyethyleneterephthalates. Dispersed dyeing processes are preferred. Orange to greenishblue shades are obtained. Examples are provided of the preparation of the dyes and their use in dyeing processes. In the Provisional Specification A is described as any substituted or unsubstituted benzene or naphthalene nucleus which is free from sulphonic and carboxylic acid groups and R and R1 are H or a substituted or unsubstituted alkyl radical or a cycloalkyl or aralkyl radical. Specifications 440,113 and 787,369 are referred to.
GB3518958A 1958-11-03 1958-11-03 New monoazo dyestuffs derived from benzthiazole Expired GB859899A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB3518958A GB859899A (en) 1958-11-03 1958-11-03 New monoazo dyestuffs derived from benzthiazole
CH8018359A CH410231A (en) 1958-11-03 1959-11-02 Process for the production of new azo dyes
CH556659A CH411178A (en) 1958-11-03 1959-11-02 Process for the production of new azo dyes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3518958A GB859899A (en) 1958-11-03 1958-11-03 New monoazo dyestuffs derived from benzthiazole

Publications (1)

Publication Number Publication Date
GB859899A true GB859899A (en) 1961-01-25

Family

ID=10374875

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3518958A Expired GB859899A (en) 1958-11-03 1958-11-03 New monoazo dyestuffs derived from benzthiazole

Country Status (2)

Country Link
CH (2) CH410231A (en)
GB (1) GB859899A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2046913A1 (en) * 1969-06-19 1971-03-12 Ciba Geigy
FR2578850A1 (en) * 1985-03-18 1986-09-19 Sandoz Sa NOVEL MONOAZOIC COMPOUNDS, THEIR PREPARATION AND THEIR USE AS COLORANTS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2046913A1 (en) * 1969-06-19 1971-03-12 Ciba Geigy
FR2578850A1 (en) * 1985-03-18 1986-09-19 Sandoz Sa NOVEL MONOAZOIC COMPOUNDS, THEIR PREPARATION AND THEIR USE AS COLORANTS

Also Published As

Publication number Publication date
CH410231A (en) 1966-03-31
CH411178A (en) 1966-04-15

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