GB859990A - New monoazo triazine dyestuffs - Google Patents
New monoazo triazine dyestuffsInfo
- Publication number
- GB859990A GB859990A GB687459A GB687459A GB859990A GB 859990 A GB859990 A GB 859990A GB 687459 A GB687459 A GB 687459A GB 687459 A GB687459 A GB 687459A GB 859990 A GB859990 A GB 859990A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthol
- dyes
- mono
- triazine
- acid
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
- C09B62/08—Azo dyes
- C09B62/085—Monoazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises dyes, which in their free acid form, are of formula: <FORM:0859990/IV (c)/1> where A is a 1- sulpho -2- naphthyl group which may contain additional SO3H groups, X is H, Hlg or SO3H one Y is H or SO3H and the other: <FORM:0859990/IV (c)/2> where Z is Hlg, n is an integer and Q is a substituent of at most 13 C atoms bound to the triazine nucleus via a C, N, O or S atom. The dyes may be made by coupling an appropriate diazotised naphthylaminesulphonic acid with the required triazine component or by condensing appropriate triazine halides and azo dyes. Compounds containing Q bound to the triazine nucleus via N may be made by treating appropriate azo-triazine dyes, where Q is Hlg, with the required amine or ammonia. Indicated for A are 1- mono-, 1, 5- di- and 1, 5, 7- trisulphonaphthyl groups. Preferably n is 2 to 5, especially 2 and Q is a lower alkyl group or a sulphonated phenyl group. Representative of specified components corresponding to the naphthol sulphonic acid moiety of the dye molecule are 2- amino -5- naphthol -7- mono-and 1, 7 -di-, 2- amino -1- chloro -8- naphthol -6-mono-, 2- b - hydroxyethyl- and -butylamino -8-naphthol -6- mono- and 2- methylamino -5-naphthol -7- mono- and -8- naphthol -6- mono-sulphonic acids the last two compounds being especially preferred. Representative of specified triazine components are 2- methyl-, -cyclohexyl-, -dodecyl-, -21- methoxyphenyl- and -benzyl- 4, 6-dichloro -striazines and compounds obtained by treating cyanuric chloride with methyl-, di- (b -hydroxyethyl)-, benzyl- and dodecylamines, #s-toluidene, aniline -psulphonic acid, pamino-acetanilide, N- ethylaniline, piperidine, m-aminobenzotrifluoride, 2- naphthylamine, m-aminobenzoic acid, thio -b - naphthol, pthiocresol, pnitrophenol and propanol- 2. The dyes dye cellulose textile materials in conjunction with treatment by an acid-binding agent, see e.g. Specification 797,946 red to orange shades being obtained. Examples are provided of the preparation of the dyes and their use in dyeing cellulosic materials. The Provisional Specification relates to dyes, which in their free acid form contain at least 2 SO3H groups, and are of the above formula where A is an aryl residue free from hydroxyl or amino groups. A is indicated to be a benzene or naphthalene residue and may contain substituents such as bromine, nitro, benzamido, methyl, ethoxy, phenoxy, carboxy and sulphonic acid groups. Specifications 837,990 and 838,340 also are referred to. p
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB687459A GB859990A (en) | 1958-03-26 | 1958-03-26 | New monoazo triazine dyestuffs |
CH7125959A CH380265A (en) | 1958-03-26 | 1959-03-25 | Process for the preparation of new monoazo dyes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB687459A GB859990A (en) | 1958-03-26 | 1958-03-26 | New monoazo triazine dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB859990A true GB859990A (en) | 1961-01-25 |
Family
ID=9822361
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB687459A Expired GB859990A (en) | 1958-03-26 | 1958-03-26 | New monoazo triazine dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB859990A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3261826A (en) * | 1962-05-28 | 1966-07-19 | Ici Ltd | Monoazo triazine containing dyestuffs |
CN102433021A (en) * | 2011-08-23 | 2012-05-02 | 湖北华丽染料工业有限公司 | Orange active dye and preparation method thereof |
-
1958
- 1958-03-26 GB GB687459A patent/GB859990A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3261826A (en) * | 1962-05-28 | 1966-07-19 | Ici Ltd | Monoazo triazine containing dyestuffs |
CN102433021A (en) * | 2011-08-23 | 2012-05-02 | 湖北华丽染料工业有限公司 | Orange active dye and preparation method thereof |
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