GB913604A - Water-insoluble disazo-dyestuffs derived from diamino-tetrachloro-diphenyl and process for their manufacture - Google Patents

Water-insoluble disazo-dyestuffs derived from diamino-tetrachloro-diphenyl and process for their manufacture

Info

Publication number
GB913604A
GB913604A GB1246161A GB1246161A GB913604A GB 913604 A GB913604 A GB 913604A GB 1246161 A GB1246161 A GB 1246161A GB 1246161 A GB1246161 A GB 1246161A GB 913604 A GB913604 A GB 913604A
Authority
GB
United Kingdom
Prior art keywords
dyes
colour
polyvinyl chloride
nitrocellulose
coupling 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
GB1246161A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst 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 DEF30956A external-priority patent/DE1153844B/en
Application filed by Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB913604A publication Critical patent/GB913604A/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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Paints Or Removers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Water-insoluble dyes of the formula <FORM:0913604/IV(a)/1> where Z is a polycyclic aryl radical, are used to colour nitrocellulose and polyvinyl chloride resins. Values indicated for Z are of the naphthalene, anthracene, acenaphthene, pyrene, chrysene and phenanthrene series, naphthalenic residues being preferred. In Example (1) the dye 4,41-diamino-2,21,5,51-dichlorodiphenyl \sQ 1-acetoacetylaminonaphthalene is used to colour, in greenish-yellow shades, a nitrocellulose lacquer and a polyvinyl chloride composition consisting of the dye, P.V.C., dioctyl- and dibutyl-phthalates and titanium dioxide.ALSO:The invention comprises water-insoluble dyes of formula <FORM:0913604/IV (b)/1> where Z is a polycyclic aryl radical. The dyes are made in conventional fashion from appropriate diaminodiphenyl tetrazo and acetoacetyl coupling components. Coupling is preferably effected in the presence of a dispersing agent. The dyes may be made in substance, on the fibre or on another substratum. Coupling components indicated are of the naphthalene, anthracene, acenaphthene, pyrene, chrysene or phenanthrene series and they may contain substituents. e.g. halogen, alkyl, alkoxy, nitro, cyano or acylamino groups. Naphthalenic coupling components are preferred. Yellow dyeings are obtained on vegetable fibres, e.g. of regenerated cellulose, and rayon and viscose or cellulose ethers or esters, polyamides or polyurethanes may also be coloured. They also colour lacquers and solutions of acetylcellulose, nitrocellulose, natural and synthetic resins, e.g. amino- and pheno-plasts, polystyrene, polypropylene, polyacrylic compounds, polyvinyl chloride and acetate, caoutchouc, casein and silicone resins and are used in lake formation. Examples are provided of the preparation of the dyes and their use in colouring processes.
GB1246161A 1960-04-08 1961-04-06 Water-insoluble disazo-dyestuffs derived from diamino-tetrachloro-diphenyl and process for their manufacture Expired GB913604A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF30956A DE1153844B (en) 1960-04-08 1960-04-08 Process for the preparation of water-insoluble disazo dyes

Publications (1)

Publication Number Publication Date
GB913604A true GB913604A (en) 1962-12-19

Family

ID=7093993

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1246161A Expired GB913604A (en) 1960-04-08 1961-04-06 Water-insoluble disazo-dyestuffs derived from diamino-tetrachloro-diphenyl and process for their manufacture

Country Status (2)

Country Link
BE (1) BE602384R (en)
GB (1) GB913604A (en)

Also Published As

Publication number Publication date
BE602384R (en) 1961-07-17

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