Water-soluble disazo dyestuff derived from 4,4-diaminobenzanilide

Information

  • Patent Grant
  • 4250091
  • Patent Number
    4,250,091
  • Date Filed
    Monday, May 7, 1979
    45 years ago
  • Date Issued
    Tuesday, February 10, 1981
    43 years ago
Abstract
The sulfonated disazo dyestuff of the formula: ##STR1## is useful in dyeing cotton and other cellulosic fibers.
Description

DESCRIPTION OF THE INVENTION
The present invention relates to a new sulfonated disazo dyestuff which is well suited for the direct dyeing of cotton and other cellulosic fibers such as linen, regenerated cellulose fibers, hemp, jute and the like.
The invention provides a new water-soluble disazo dyestuff of the formula: ##STR2##
This direct dyestuff has application characteristics which are similar to those of conventional direct dyestuffs, for example, dyestuffs of the benzidine series, but the process for its manufacture does not involve any toxicological risks. Actually, benzidine, and its derivatives which are used for preparing conventional dyestuffs having characteristics which are similar to those according to the invention, are hazardous substances i.e., they are carcinogenic and therefore require strict and carefully controlled conditions.
On cellulosic fibers, the dyestuff of the invention produces orange shades. Dyeing of fibers with the dyestuff of the invention is carried out using the same methods as are used with conventional direct dyestuffs, i.e., at a temperature ordinarily ranging from 50.degree. to 100.degree. C., using a water-bath containing adequate quantities e.g.- from 0,01 g of 2-3% about or according to the user's exigence of dyestuff and from 5 to 20% (with respect to the weight of the fiber) of anhydrous Na.sub.2 SO.sub.4 or NaCl.





The following example is given to illustrate the invention, all parts being understood as parts by weight unless otherwise stated.
EXAMPLE
22.7 parts of 4-4'-diamino-benzanilide suspended in 50 parts of water and 52 parts of 20.degree. Be hydrochloric acid were tetra-azotized, after cooling with 150 parts of ice, by adding dropwise at 0.degree.-5.degree. C., in 30 minutes a solution of 14 parts of NaNO.sub.2 in 60 parts of H.sub.2 O. After 60 minutes stirring, the excess nitrous acid was removed with sulfamic acid. 50.8 parts of 1-N-parasulfophenyl-3-methyl-5-pyrazolone were dissolved in 300 parts H.sub.2 O at 60.degree. C. and 40 parts Na.sub.2 CO.sub.3 at a pH of 8.5-9. After cooling to below 5.degree. C., by adding 150 parts of ice, the tetra-azotization mass was rapidly poured in over a period of 5 minutes at a pH of 7.5-8. The whole was kept under stirring overnight, while allowing the temperature to rise to room temperature, i.e., about 20.degree. C. The following morning the mass was completely solubilized by addition of 20 parts of 36.degree. Be NaOH and heating to 70.degree.-80.degree. C. The dyestuff was precipitated by salting with 110 parts about of rock salt. To complete the precipitation, the whole mass was acidified to Congo red with 40 parts of 20.degree. Be HCl. The mass was filtered under vacuum and squeezed dry.
The obtained product, dried at 70.degree.-80.degree. C., dyes cellulose fibers with orange shades and excellent uniformity.
Modifications and variations can, of course, be made without departing from the spirit and scope of the invention.
Claims
  • 1. The sulfonated disazo dyestuff of the formula: ##STR3##
Priority Claims (1)
Number Date Country Kind
19963 A/74 Jan 1974 ITX
CROSS REFERENCE TO RELATED APPLICATIONS:

This is a continuation of application Ser. No. 828,310, filed Aug. 29, 1977, which is in turn a continuation of application Ser. No. 702,871, filed July 6, 1976, which is in turn a continuation of application Ser. No. 542,938, filed Jan. 22, 1975 all now abandoned.

US Referenced Citations (3)
Number Name Date Kind
936367 Schedler Jul 1909
2571990 Stratton Oct 1951
3467645 Keller et al. Sep 1969
Foreign Referenced Citations (1)
Number Date Country
957336 May 1961 GBX
Non-Patent Literature Citations (2)
Entry
Szadowski et al., "Chem. Abs.," 79, No. 4, 7/30/73, No. 20278f.
"Chem. Abs.," 79, Formula Index, C.sub.33 H.sub.28 N.sub.10 O.sub.9 S.sub.2, 1973.
Continuations (3)
Number Date Country
Parent 828310 Aug 1977
Parent 702871 Jul 1976
Parent 542938 Jan 1975