GB323792A - Improvements in or relating to the colouration of cellulose derivatives - Google Patents

Improvements in or relating to the colouration of cellulose derivatives

Info

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
Application number
GB2864628A
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.)
Acordis UK Ltd
Original Assignee
British Celanese Ltd
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 British Celanese Ltd filed Critical British Celanese Ltd
Priority to GB2864628A priority Critical patent/GB323792A/en
Publication of GB323792A publication Critical patent/GB323792A/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

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.
GB2864628A 1928-10-05 1928-10-05 Improvements in or relating to the colouration of cellulose derivatives Expired GB323792A (en)

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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2357683A1 (en) * 1976-07-09 1978-02-03 Bayer Ag PROCESS FOR DYING HYDROPHOBIC FIBER MATERIALS

Cited By (1)

* Cited by examiner, † Cited by third party
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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