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GB1057065A - Disazo dyes, their production and application - Google Patents

Disazo dyes, their production and application

Info

Publication number
GB1057065A
GB1057065A GB4086263A GB4086263A GB1057065A GB 1057065 A GB1057065 A GB 1057065A GB 4086263 A GB4086263 A GB 4086263A GB 4086263 A GB4086263 A GB 4086263A GB 1057065 A GB1057065 A GB 1057065A
Authority
GB
United Kingdom
Prior art keywords
alkyl
formula
coupling
disazo dyes
acetoacetylamino
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
GB4086263A
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.)
Sandoz Patent Ltd
Sandoz AG
Original Assignee
Sandoz Patent Ltd
Sandoz 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
Priority claimed from CH1257462A external-priority patent/CH400419A/en
Priority claimed from CH1501262A external-priority patent/CH416662A/en
Application filed by Sandoz Patent Ltd, Sandoz AG filed Critical Sandoz Patent Ltd
Publication of GB1057065A publication Critical patent/GB1057065A/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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/08Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
    • C09B35/10Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type
    • C09B35/105Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type from two coupling components with reactive methylene groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/58Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton

Landscapes

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

Abstract

The invention comprises the disazo dyes produced by coupling a tetrazotized 4,41-diaminodiphenyl which may be further substituted, e.g. by Cl, Br or NO2 with compounds of formula <FORM:1057065/C4-C5/1> wherein R and "alkyl" each represet C1-C4 alkyl radicals. The dyes are water-insoluble and may be used as pigments in the colouring of paper, natural and synthetic resins, rubber and cellulose lacquers (see Division C3) in yellow, orange or brown shades.ALSO:Compounds of formula <FORM:1057065/C2/1> wherein R and "alkyl" are C1-C4 alkyl groups are prepared by brominating the corresponding 1 - acylacetylamino - 2,5 - dialkoxy - benzenes. Thus 1 - acetoacetylamino - 2,5 - dimethoxy benzene is reacted with bromine in glacial acetic acid solution to give 1-acetoacetylamino-2,5-dimethoxy-4-bromobenzene.ALSO:In examples polyvinyl chloride films and nitrocellulose lacquers are coloured in yellow and brown shades by the incorporation of disazo dyes obtained by coupling tetrazotized 4,41-diaminodiphenyls with coupling components of formula <FORM:1057065/C3/1> wherein R and "alkyl" are C1-C4 alkyl groups.
GB4086263A 1962-10-29 1963-10-16 Disazo dyes, their production and application Expired GB1057065A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH1257462A CH400419A (en) 1962-10-29 1962-10-29 Process for the preparation of disazo dyes
CH1501262A CH416662A (en) 1962-12-21 1962-12-21 Process for the preparation of 1-acylacetylamino-2,5-dialkoxy-4-bromobenzenes

Publications (1)

Publication Number Publication Date
GB1057065A true GB1057065A (en) 1967-02-01

Family

ID=25710557

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4086263A Expired GB1057065A (en) 1962-10-29 1963-10-16 Disazo dyes, their production and application

Country Status (1)

Country Link
GB (1) GB1057065A (en)

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