GB365759A - Preparation of new stable tetrazomonoazo compounds - Google Patents

Preparation of new stable tetrazomonoazo compounds

Info

Publication number
GB365759A
GB365759A GB498/31A GB49831A GB365759A GB 365759 A GB365759 A GB 365759A GB 498/31 A GB498/31 A GB 498/31A GB 49831 A GB49831 A GB 49831A GB 365759 A GB365759 A GB 365759A
Authority
GB
United Kingdom
Prior art keywords
precipitated
tetrazotized
naphthylamine
tetrazo compound
compounds
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
GB498/31A
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 AG
Original Assignee
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
Application filed by Sandoz AG filed Critical Sandoz AG
Publication of GB365759A publication Critical patent/GB365759A/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
    • C09B35/36Trisazo dyes of the type
    • 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
    • C09B35/04Disazo dyes characterised by the tetrazo component the tetrazo component being a benzene derivative
    • 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
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films

Landscapes

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

Abstract

Stable tetrazomonoazo compounds are obtained by adding a suitable metal salt and/or an arylsulphonate to a solution of a tetrazo compound of the formula <FORM:0365759/IV/1> where R = a benzene or naphthalene nucleus, Y = an inorganic acid residue, and X = hydrogen, an alkyl, alkoxy or nitro group or a halogen, separating the precipitate and drying it. Diluents, e.g. salts, may be added. They are useful for producing black shades on the fibre and in substance by coupling with 2 : 3-oxynaphthoic acid arylides. In examples: (1) tetrazotized benzidine is coupled with a -naphthylamine (1 mol.), again diazotized and the tetrazo compound precipitated with aqueous zinc chloride and sodium chloride; o-anisidine or p-cresidine may be used instead of a -naphthylamine; (2) the tetrazo compound in (1) is precipitated with naphthalene-1 : 3 : 6-trisulphonic acid; (3) tetrazotized dianisidine is coupled with 3-amino-4-methoxy-1-methyl-benzene, again diazotized and precipitated as in (1); (4) tetrazotized m-mononitrobenzene is coupled with a -naphthylamine, again diazotized and the tetrazo compound precipitated as in (1). The p-aminodiaryl-p<1>-azoaryl-p-amino compounds of Specification 275,147, [Class 2 (iii), Dyes &c.], may also be tetrazotized and precipitated in a similar manner.
GB498/31A 1930-01-07 1931-01-06 Preparation of new stable tetrazomonoazo compounds Expired GB365759A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE365759X 1930-01-07

Publications (1)

Publication Number Publication Date
GB365759A true GB365759A (en) 1932-01-28

Family

ID=6317648

Family Applications (1)

Application Number Title Priority Date Filing Date
GB498/31A Expired GB365759A (en) 1930-01-07 1931-01-06 Preparation of new stable tetrazomonoazo compounds

Country Status (4)

Country Link
DE (1) DE573180C (en)
ES (1) ES121191A1 (en)
FR (1) FR708822A (en)
GB (1) GB365759A (en)

Also Published As

Publication number Publication date
ES121191A1 (en) 1931-01-16
DE573180C (en)
FR708822A (en) 1931-07-29

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