GB445266A - Process for the improvement of dyeings on cellulosic fibres with substantive dyestuffs - Google Patents

Process for the improvement of dyeings on cellulosic fibres with substantive dyestuffs

Info

Publication number
GB445266A
GB445266A GB2257634A GB2257634A GB445266A GB 445266 A GB445266 A GB 445266A GB 2257634 A GB2257634 A GB 2257634A GB 2257634 A GB2257634 A GB 2257634A GB 445266 A GB445266 A GB 445266A
Authority
GB
United Kingdom
Prior art keywords
pyrazolone
carboxylic acid
diazotized
phenyl
treated
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
GB2257634A
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 GB2257634A priority Critical patent/GB445266A/en
Publication of GB445266A publication Critical patent/GB445266A/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
    • C09B39/00Other azo dyes prepared by diazotising and coupling

Landscapes

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

Abstract

Azo dyes, forming on the material; printing.--Dyeing on cellulosic fibres with azo dyestuffs of the general formula R[--NH--CO--R<1>--N = N--Py]n wherein R represents the residue of an aromatic amine or of an aminoazo compound not containing the residue Py, R<1> represents a residue of the benzene series, Py represents the residue of a 1-aminoaryl - 5 - pyrazolone - 3 - carboxylic acid (or ester) coupling component, and n is 1 or 2, the whole dyestuff being so constituted that only the aminoarylpyrazolone residue is capable of further coupling with a diazo component, are after-treated with a diazotized base free from water-solubilizing groups, e.g. diazotized m- or p-nitraniline or 4- or 5-nitro-2-anisidine, to improve the fastness to washing. Compared with the dyeings similarly produced from the dyestuffs specifically referred to in Specifications 14315/09 and 7303/13, [both in Class 2(iii)] the resulting dyeings are of an improved dischargeability to a pure white. The following examples are specified: (1) Cotton, dyed from a Glauber's salt-soda bath with the reduced dyestuff from tetrazotized di - (4<11> - aminobenzoyl) - 4 : 4<1> - diaminodiphenylurea - 3 : 3<1> - disulphonic acid (1 mol.) and 1-(3<1>-nitro)phenyl-5-pyrazolone-3-carboxylic acid (2 mols.), is after-treated with diazotized p-nitraniline to obtain a dyeing of good fastness to light and dischargeable to a pure white. (2) Cotton, similarly dyed with the dyestuff obtainable by reducing the nitro group of p-nitrobenzoyl-p-phenylene diamine --> 1-phenyl-5-pyrazolone-3-carboxylic acid, diazotizing, coupling with 1 - (m-nitro)phenyl - 5 - pyrazolone - 3 - carboxylic acid and reducing the nitro group, is after-treated with diazotized p-nitraniline. (3) Cotton, similarly dyed with the dyestuff obtainable by saponifying the acetylamino group of acetyl - p - phenylenediamine --> salicylic acid, condensing with p-nitrobenzoyl chloride, reducing the nitro group, diazotizing and coupling with 1 - (m - or p - amino)phenyl - 5 - pyrazolone - 3 - carboxylic acid, is after-treated with diazotized p-nitraniline or 4- or 5-nitro-2-anisidine. (4) Cotton, similarly dyed with the dyestuff, 2-aminobenzoic acid --> (alkaline) p - aminobenzoyl - 2 - amino - 5 - naphthol - 7 - sulphonic acid --> 1-(m-amino)phenyl-5-pyrazolone-3-carboxylic acid, is after-treated with diazotized p-nitraniline. (5) Cotton, similarly dyed with the dyestuff, m-aminobenzoyldehydrothiotoluidinesulphonic acid --> 1-(m-amino)phenyl - 5 - pyrazolone - 3 - carboxylic acid, is similarly after-treated.
GB2257634A 1934-08-02 1934-08-02 Process for the improvement of dyeings on cellulosic fibres with substantive dyestuffs Expired GB445266A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2257634A GB445266A (en) 1934-08-02 1934-08-02 Process for the improvement of dyeings on cellulosic fibres with substantive dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2257634A GB445266A (en) 1934-08-02 1934-08-02 Process for the improvement of dyeings on cellulosic fibres with substantive dyestuffs

Publications (1)

Publication Number Publication Date
GB445266A true GB445266A (en) 1936-04-02

Family

ID=10181637

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2257634A Expired GB445266A (en) 1934-08-02 1934-08-02 Process for the improvement of dyeings on cellulosic fibres with substantive dyestuffs

Country Status (1)

Country Link
GB (1) GB445266A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0072508A2 (en) * 1981-08-18 1983-02-23 Bayer Ag Pyrazolone derivatives, their preparation and use as coupling components

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0072508A2 (en) * 1981-08-18 1983-02-23 Bayer Ag Pyrazolone derivatives, their preparation and use as coupling components
EP0072508A3 (en) * 1981-08-18 1983-03-16 Bayer Ag Pyrazolone derivatives, their preparation and use as coupling components

Similar Documents

Publication Publication Date Title
GB209723A (en) Manufacture of new azo-dyestuffs
GB609299A (en) Manufacture of disazo-dyestuffs
GB445266A (en) Process for the improvement of dyeings on cellulosic fibres with substantive dyestuffs
US2192153A (en) Azo dyestuffs
US2666757A (en) Azo dyes for cellulosic fibers
GB252957A (en) Manufacture of diazotizable azo-dyestuffs and intermediate products therefor
GB286717A (en) Process for the manufacture of substantive azo dyestuffs
US2155685A (en) Azo dyes
US2286392A (en) Azo dye
GB595181A (en) Manufacture of new azo-dyestuffs
GB536159A (en) Manufacture of brown polyazo dyestuffs, especially suitable for dyeing leather
US1686947A (en) Diazotizable azodyestuffs
GB237739A (en) Improvements in dyeing acetyl silk
GB763064A (en) Manufacture of polyazo-dyestuffs
GB331822A (en) Improvements in the dyeing of regenerated cellulose materials
GB397879A (en) Azo dyestuffs
GB555791A (en) Manufacture of new azo dyestuffs
GB1002648A (en) New dyestuffs containing ring-condensed halopyridazinyl residues
GB551982A (en) Manufacture of trisazo dyestuffs and copper complex compounds thereof
GB191100488A (en) Improvements in Dyestuffs.
GB333243A (en) Improvements in the dyeing of regenerated cellulose materials
GB815737A (en) New polyazo-dyestuffs derived from 3,3-dihydroxydiphenylamine and processes for their manufacture
GB542449A (en) Manufacture of trisazo dyestuffs and copper complex compounds thereof
GB583849A (en) Manufacture of azo-dyestuffs
GB733361A (en) Manufacture of new trisazo-dyestuffs