GB409451A - Improvements in colouring rubber - Google Patents
Improvements in colouring rubberInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/23—Azo-compounds
- C08K5/235—Diazo 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].
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) |
-
1932
- 1932-12-23 GB GB3645332A patent/GB409451A/en not_active Expired
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