GB541730A - Improvements relating to dyestuff preparations - Google Patents

Improvements relating to dyestuff preparations

Info

Publication number
GB541730A
GB541730A GB9963/40A GB996340A GB541730A GB 541730 A GB541730 A GB 541730A GB 9963/40 A GB9963/40 A GB 9963/40A GB 996340 A GB996340 A GB 996340A GB 541730 A GB541730 A GB 541730A
Authority
GB
United Kingdom
Prior art keywords
hydroxyethyl
dyestuffs
methyl
aniline
methoxy
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
GB9963/40A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB541730A publication Critical patent/GB541730A/en
Expired legal-status Critical Current

Links

Abstract

541,730. Dye preparations ; dyeing textiles. SOC. OF CHEMICAL INDUSTRY IN BASLE. June 7, 1940, Nos. 9963 and 9964. Convention dates, June 8, 1939, and May 9, 1940. [Classes 2 (iii) and 15 (ii)] Preparations for use in producing strong blue dyeings on cellulose acetate artificial silk comprise a mixture of two or more blue-dyeing dyestuffs of the general formula wherein X represents -CN, halogen or -SO 2 - alkyl, Y represents halogen or NO 2 , R 1 represents the residue of a benzene nucleus, which may be substituted, R 2 represents H or hydroxyalkyl and the hydroxyethylamino group is in pposition to the azo group. Such preparations may be obtained by (a) using mixtures of appropriate intermediate products for the manufacture of the dyestuffs, (b) precipitation from a solution of the dyestuffs in a common solvent, (c) finely grinding the dyestuffs together or (d) adding the previously dispersed dyestuffs to the same dyebath. Suitable dyestuffs are described in Specifications 447,561, 451,970 and 505,854. Specified diazo components are the 4-nitro- 2-cyano-6-chloro-, 2:4-dinitro-6-methylsulphone-, 2:4- dinitro-6-chloro- and 2:4- dinitro-6-cyanoderivatives of aniline and specified coupling components are the 3-methyl-N-di- (hydroxyethyl)-, 3-methyl-N-hydroxyethyl-, 3- methyl-6-methoxy-N-di- (hydroxyethyl)-, 3- methyl-6-methoxy-N-hydroxyethyl-, 3 : 6- dimethoxy-N-di-(hydroxyethyl)-, 3 : 6-diethoxy- N-di-(hydroxyethyl)- and 3-acetylamino-6-methoxy-N-di- (hydroxyethyl)- derivatives of aniline. In examples, (1) equal weights of the dyestuffs, 2 :4-dinitroaniline- 6-methylsulphone# 3- methyl-N-di-(hydroxyethyl)-aniline and 2 : 4- dinitroaniline -6-methylsulphone # 3-methyl-6- methoxy -N-hydroxyethyl-aniline, are ground together with sulphite cellulose lye or other dispersing agent ; the paste obtained may be dried and ground ; (2) equal weights of 10 per cent aqueous pastes of the dyestuffs in (1) are stirred into a solution at 50‹C. of soap or a soaplike material, such as the sodium salt of the acid sulphuric ester of oleyl alcohol or sodium Á-heptadecyl - N - benzyl - benzimidazole - diulphonate, and the mixture is diluted with warm water; cellulose acetate artificial silk is introduced into this solution and dyed a deep blue at 75-80‹C. A table is also given specifying various mixtures of the dyestuffs. Specification 219,349, [Class 2 (iii)], also is referred to. 3 : 6 -Diethoxy-N-di-(hydroxyethyl)-aniline is obtained by the action of ethylene chlorhydrin on 3 : 6- diethoxyaniline in presence of magnesia. The Specification as open to inspection under Sect. 91 comprises also the similar preparation and use of mixtures of two or more dyestuffs of the above general formula all dyeing blue or all dyeing brown tints in which R 2 may additionally be alkyl. Additional specified diazo components are the 4-nitro-2 : 6-dichloro-, and 4-nitro-2-chloro-6-bromoderivatives of aniline and additional coupling components are the 3-methyl-N-ethyl-or butyl-N-hydroxyethyl-, 3-methyl-6-methoxy-N-methyl- or ethyl-N- hydroxyethyl- and 3-methylsulphone-N-ethyl- N-hydroxyethylderivatives of aniline. This subject-matter does not appear in the Specification as accepted.
GB9963/40A 1939-06-08 1940-06-07 Improvements relating to dyestuff preparations Expired GB541730A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH541730X 1939-06-08

Publications (1)

Publication Number Publication Date
GB541730A true GB541730A (en) 1941-12-09

Family

ID=4519098

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9963/40A Expired GB541730A (en) 1939-06-08 1940-06-07 Improvements relating to dyestuff preparations

Country Status (1)

Country Link
GB (1) GB541730A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3413075A (en) * 1966-02-08 1968-11-26 American Aniline Prod Azo dyestuff mixtures and aromatic polyester fibers colored therewith
GB2002408A (en) * 1977-07-25 1979-02-21 Ciba Geigy Ag Transfer printing dyes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3413075A (en) * 1966-02-08 1968-11-26 American Aniline Prod Azo dyestuff mixtures and aromatic polyester fibers colored therewith
GB2002408A (en) * 1977-07-25 1979-02-21 Ciba Geigy Ag Transfer printing dyes

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