GB751997A - Triazine dyes for cotton containing carbamyl hydrazide and its imido and thio analogues - Google Patents
Triazine dyes for cotton containing carbamyl hydrazide and its imido and thio analoguesInfo
- Publication number
- GB751997A GB751997A GB9124/54A GB912454A GB751997A GB 751997 A GB751997 A GB 751997A GB 9124/54 A GB9124/54 A GB 9124/54A GB 912454 A GB912454 A GB 912454A GB 751997 A GB751997 A GB 751997A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- mol
- acid
- mols
- guanylhydrazine
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
- C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises dyes of the formulae:-<FORM:0751997/IV(c)/1> and <FORM:0751997/IV(c)/2> wherein R represents either O, S, or NH, R1 represents a sulphonated or carboxylated azo radical or metallised complex thereof linked to the triazine ring by a NH- group, and R2 represents a sulphonated or carboxylated diamino aromatic linking component radical which is linked to the two cyanuric nuclei at the nitrogen atoms of the two amino groups. In examples, (1) 1 mol. 4.41-diamino-2.21-disulphostilbene is reacted with 2 mols. cyanuric chloride and the product so obtained is reacted with 2 mols. of the reduction product from the dye 5-nitroanthranilic acid --> 3-methyl-5-pyrazolone, and with 1 mol. guanylhydrazine, semicarbazide, or thiosemicarbazide; (2) 1 mol. cyanuric chloride is condensed with 1 mol. each of 4-amino - 41 - hydroxy-azobenzene - 31 - carboxylic acid, 1-amino-8-hydroxynaphthalene-3.6-disulphonic acid and either guanylhydrazine or thiosemicarbazide and the product reacted with the diazotised dyestuff 1-amino-8-hydroxynaphthalene-3.6-disulphonic acid-->3-amino-4-cresol methyl ether; (3) cyanuric chloride is condensed with 2 mols. 2-amino-5-hydroxynaphthalene-7-sulphonic acid (J acid) and 1 mol. semicarbazide or guanylhydrazine, followed by coupling with 2 mols. diazotised 2-aminophenol-4-sulphonic acid. The products may be after-treated with copper sulphate and partially polymerised cyano guanidene-formaldehyde. Values of R1 specified are those having the formulae:- <FORM:0751997/IV(c)/3> <FORM:0751997/IV(c)/4> <FORM:0751997/IV(c)/5> <FORM:0751997/IV(c)/6> <FORM:0751997/IV(c)/7> <FORM:0751997/IV(c)/8> and <FORM:0751997/IV(c)/9> and values of R2 specified are those having the formulae:- <FORM:0751997/IV(c)/100> <FORM:0751997/IV(c)/111> <FORM:0751997/IV(c)/122> <FORM:0751997/IV(c)/133> <FORM:0751997/IV(c)/144> <FORM:0751997/IV(c)/155> <FORM:0751997/IV(c)/166> <FORM:0751997/IV(c)/17
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US751997XA | 1953-03-30 | 1953-03-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB751997A true GB751997A (en) | 1956-07-04 |
Family
ID=22124194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9124/54A Expired GB751997A (en) | 1953-03-30 | 1954-03-29 | Triazine dyes for cotton containing carbamyl hydrazide and its imido and thio analogues |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB751997A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002070609A1 (en) * | 2001-03-03 | 2002-09-12 | Avecia Limited | Ink jet printing composition comprising a dye containing hydrazine or hydrazide |
US7141106B2 (en) | 2001-03-03 | 2006-11-28 | Fujifilm Imaging Colorants Limited | Ink jet printing composition comprising a dye containing hydrazine or hydrazide |
US7166564B2 (en) * | 2003-08-21 | 2007-01-23 | Ciba Specialty Chemicals Corp. | Optical brighteners |
-
1954
- 1954-03-29 GB GB9124/54A patent/GB751997A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002070609A1 (en) * | 2001-03-03 | 2002-09-12 | Avecia Limited | Ink jet printing composition comprising a dye containing hydrazine or hydrazide |
GB2389588A (en) * | 2001-03-03 | 2003-12-17 | Avecia Ltd | Ink jet printing composition comprising a dye containing hydrazine or hydrazide |
GB2389588B (en) * | 2001-03-03 | 2005-03-23 | Avecia Ltd | Ink jet printing composition comprising a dye containing hydrazide groups |
US7141106B2 (en) | 2001-03-03 | 2006-11-28 | Fujifilm Imaging Colorants Limited | Ink jet printing composition comprising a dye containing hydrazine or hydrazide |
US7166564B2 (en) * | 2003-08-21 | 2007-01-23 | Ciba Specialty Chemicals Corp. | Optical brighteners |
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