GB323792A - Improvements in or relating to the colouration of cellulose derivatives - Google Patents
Improvements in or relating to the colouration of cellulose derivativesInfo
- Publication number
- GB323792A GB323792A GB2864628A GB2864628A GB323792A GB 323792 A GB323792 A GB 323792A GB 2864628 A GB2864628 A GB 2864628A GB 2864628 A GB2864628 A GB 2864628A GB 323792 A GB323792 A GB 323792A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitro
- amino
- diamino
- dinitro
- alpha
- 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
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Cosmetics (AREA)
Abstract
323,792. British Celanese, Ltd., and Ellis, G. H. Oct. 5, 1928. Azo dyes suitable for dyeing cellulose esters and ethers are made by coupling 1, 2, 3 or more molecular parts of the same or different coupling components with diazotized aminonitro compounds containing two or more aryl residues linked in any desired manner. Diazo compounds specified are 2-nitrobenzidine, 2 : 2'- or 3 : 3<1>-dinitrobenzidine, 5-nitro-o-tolidine, 5 : 5<1>-dinitro-o-tolidine, 6: 6<1>- dinitro-o-dianisidine, 4-nitro-4<1>-aminodiphenyl ; 3-nitro-4-amino- and 5-nitro-2-aminodiphenylether; 4 : 4<1>-diamino-3 : 3<1>-dinitrodiphenylsulphone; 2 :4-dinitro-3'- (or 4') amino, 4-chlor-2- nitro-4<1>-amino-, 2- (or 4) nitro-4'-amino-, 2-nitro- 4-amino or 2-nitro-4-amino-4<1>-methyldiphenylamine (the latter from 3-nitro-4-chloracetanilide and p-toluidine and hydrolysis) ; 5-nitro-2- amino-, 3-nitro-4-amino-, 2-nitro-2<1>-amino or 4 : 4<1>-diamino-3 : 3<1>-dinitrobenzophenone, 4 : 4<1>- diamino-2-nitro-, 4 : 4<1>-diamino-2 : 2<1>-dinitro- or 4 :4<1>-diamino-3 :3<1>-dinitrodiphenylmethane and tri-(2-nitro-4-aminophenyl)-methane; 2-amino-5- nitrobenzanilide, 4<1>-nitrobenzyl-2-amino-5-nitroaniline, 4-nitrobenzoyl-p-phenylenediamine and 4 : 4<1>-diamino-2 : 2<1>-dinitrodiphenylurea. Specified coupling components are xylidines, cresidines, anisidines, phenetidines, m-toluidine, mphenylenediamine, p-nitro-m-phenylenediamine, alkyl-, aryl- or aralkylanilines, phenols, cresols, resorcinol, aminophenols, or alkylaminophenols as dimethyl-m-aminophenol, alpha- or #-naphthylamines or alkyl derivatives thereof, naphthylamine ethers, #-oxyethyl-alpha-naphthylamine, alpha-chlor-#- oxypropyl-alpha-naphthylamine, aminonaphthoic acids, aminonaphthols or N-acidyl compounds of the above coupling components. The azo dyestuffs may contain any other desired additional substituents e.g. nitro, amino, alkylamino, acidylamino, alkyl, alkoxy, hydroxy, carboxy, halogen and mercapto groups. Compositions containing the insoluble azo dyes_ and dispersing agents and/or protective colloids are referred to. The following dyestuffs are specified : (1) 2 :4-dinitro- 4<1>- (or 3<1>) aminodiphenylamine # phenol, mtoluidine, dimethylaniline, m-phenylenediamine or resorcinol, (2) 3-nitro-4-amimodiphenylether # alpha-naphthylamine, (3) 2 : 2<1>-dinitrobenzidine # toluidine or cresidine (CH3 :NH2 :OCH3 =1 : 3 : 4). The azo dyestuffs obtainable from 4- nitro-4<1>-aminodiphenylsulphide and compositions containing these dyestuffs and Specifications 310,779 [Class 15 (ii), Dyeing, Processes &c. for], and 310,827 are disclaimed. Specifications 219,349, 222,001, 224,925, 237,943; 239,470, [Class 15 (ii), Dyeing, Processes &c. for], 242,393, 242,711, 269,960, 273,819, 273,820, 283,081, and 283,253 also are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2864628A GB323792A (en) | 1928-10-05 | 1928-10-05 | Improvements in or relating to the colouration of cellulose derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2864628A GB323792A (en) | 1928-10-05 | 1928-10-05 | Improvements in or relating to the colouration of cellulose derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB323792A true GB323792A (en) | 1930-01-06 |
Family
ID=10278876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2864628A Expired GB323792A (en) | 1928-10-05 | 1928-10-05 | Improvements in or relating to the colouration of cellulose derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB323792A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2357683A1 (en) * | 1976-07-09 | 1978-02-03 | Bayer Ag | PROCESS FOR DYING HYDROPHOBIC FIBER MATERIALS |
-
1928
- 1928-10-05 GB GB2864628A patent/GB323792A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2357683A1 (en) * | 1976-07-09 | 1978-02-03 | Bayer Ag | PROCESS FOR DYING HYDROPHOBIC FIBER MATERIALS |
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