GB409451A - Improvements in colouring rubber - Google Patents

Improvements in colouring rubber

Info

Publication number
GB409451A
GB409451A GB3645332A GB3645332A GB409451A GB 409451 A GB409451 A GB 409451A GB 3645332 A GB3645332 A GB 3645332A GB 3645332 A GB3645332 A GB 3645332A GB 409451 A GB409451 A GB 409451A
Authority
GB
United Kingdom
Prior art keywords
hydroxynaphthoic acid
acid
hydroxynaphthoic
chloranilide
mols
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
GB3645332A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB3645332A priority Critical patent/GB409451A/en
Publication of GB409451A publication Critical patent/GB409451A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/22Compounds containing nitrogen bound to another nitrogen atom
    • C08K5/23Azo-compounds
    • C08K5/235Diazo and polyazo compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Rubber is coloured by the addition to the mix of compounds of the general formula <FORM:0409451/IV/1> in which X represents hydrogen, halogen, alkyl, alkoxyl or aralkyl, and R represents the radicle of a hydroxynaphthoic acid amide. The dyestuffs are free from nitro, sulpho, and further p carboxylic acid groups and from metals. Compounds mentioned are:--tetrazotized benzidine, tolidine, dianisidine or 3 : 3<1> dichlorbenzidine coupled with 2 mols. of 2 : 3 hydroxynaphthoic acid anilide, together with tetrazotizeddianisidine coupled with two mols. of 2 : 3 hydroxynaphthoic acid - p - chloranilide, or 2 : 3 - hydroxynaphthoic acid - m - chloranilide, or 2 : 3 - hydroxynaphthoic acid 5 - chlor - 2 - toluidide, or 2 : 3 - hydroxynaphthoic acid - m - anisidide, or 2 : 3 hydroxynaphthoic acid 2 : 4 - dimethoxy - 5 - chloranilide or 2 : 3 hydroxynaphthoic acid amide, and tetrazotized 3 : 3<1> dichlorbenzidine coupled with two mols. of 2 : 3 - hydroxynaphthoic acid amide, or 2 : 3 - hydroxynaphthoic acid - o - anisidide. Further compounds mentioned as coupling components are the 2 : 6 - hydroxynaphthoic acid arylides, and the compounds obtained by condensing ortho meta or paranitrobenzoic acid or a halide thereof with aniline or a nuclear alkoxyl, alkyl or halogen substituted aniline, reducing the nitro group in the resulting product and condensing the amino aroylamino compound with 2 : 3 hydroxy - naphthoic acid. Other coupling components which may be used are those referred to in Specification 374,548.ALSO:Rubber is coloured by the addition to the mix of compounds of the general formula <FORM:0409451/V/1> in which X represents hydrogen, halogen, alkyl, alkoxyl or aralkyl, and R represents the radicle of a hydroxynaphthoic acid amide. The dyestuffs are free from nitro, sulpho, and further carboxylic acid groups, and from metals. Compounds mentioned are: tetrazotized benzidine tolidine, dianisidine, or 3.31-dichlorbenzidine coupled with 2 mols. of 2 : 3 hydroxynaphthoic-acid-anilide, together with tetrazotized dianisidine coupled with two mols. of 2 : 3 hydroxynaphthoic acid-p-chloranilide, or 2 : 3-hydroxynaphthoic acid m-chloranilide, or 2 : 3-hydroxynaphthoic acid 5-chlor-2-toluidide, or 2 : 3 hydroxynaphthoic acid-m-anisidide, or 2 : 3 hydroxynaphthoic acid-2 : 4-dimethoxy-5-chloranilide, or 2 : 3-hydroxynaphthoic acid amide, and tetrazotized 3 : 31 dichlorbenzidine coupled with two mols. of 2 : 3 hydroxynaphthoic acid amide, or 2 : 3-hydroxynaphthoic acid-o-anisidide Further compounds mentioned as coupling components are the 2 : 6 hydroxynaphthoic acid arylides, and the compounds obtained by condensing ortho, meta or paranitrobenzoic acid or a halide thereof with aniline, or a nuclear alkoxyl-alkyl or halogen substituted aniline reducing the nitro group in the resulting product and condensing the amine aroylamino compound with 2 : 3 hydroxynaphthoic acid. Other coupling components which may be used are those referred to in Specification 374,548, [Group IV].
GB3645332A 1932-12-23 1932-12-23 Improvements in colouring rubber Expired GB409451A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3645332A GB409451A (en) 1932-12-23 1932-12-23 Improvements in colouring rubber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3645332A GB409451A (en) 1932-12-23 1932-12-23 Improvements in colouring rubber

Publications (1)

Publication Number Publication Date
GB409451A true GB409451A (en) 1934-05-03

Family

ID=10388275

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3645332A Expired GB409451A (en) 1932-12-23 1932-12-23 Improvements in colouring rubber

Country Status (1)

Country Link
GB (1) GB409451A (en)

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