GB923887A - New monoazo triazine dyestuffs - Google Patents
New monoazo triazine dyestuffsInfo
- Publication number
- GB923887A GB923887A GB1012859A GB1012859A GB923887A GB 923887 A GB923887 A GB 923887A GB 1012859 A GB1012859 A GB 1012859A GB 1012859 A GB1012859 A GB 1012859A GB 923887 A GB923887 A GB 923887A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyes
- substituted
- so3h
- formula
- residue
- 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, as free acids, are of formula <FORM:0923887/IV(a)/1> where D is a phenylene or sulphophenylene residue, X is Cl or Br, Y is Cl or Br, OAIK or aryloxy or an amino group which may be substituted, A is a phenylene residue, Z is So3H or COOH and m is 1 or 2 provided that the number of So3H and COOH groups in the dye is at least 3. The dyes are made by conventional diazotization and coupling processes, the diazo component being an aminophenylaminotriazine, by condensing appropriate dyes and halotriazines, or by treating appropriate dihalotriazine dyes with a compound TQ, where T is H, or alkali metal, and Q is an alkoxy, aryloxy, amino or substituted amino group. Representative of specified values for Y are methoxy, methylphenoxy, nitrosulphophenoxy, ethyl-di-(b -hydroxyethyl) and N-methyl-N-propyl-amino, di-sulphoanilino, carboxyanilino and naphthylamino. The dyes colour cellulosic materials, e.g. cotton, viscose rayon and linen textiles, in reddish- or yellowish-brown shades, and are preferably used in conjunction with an acid-binding agent. Preferred dyes are those of formula <FORM:0923887/IV(a)/2> where D1 is sulphophenylene and of formula Examples are provided of the preparation of the dyes and their use in colouring cellulosic textile materials. In the Provisional Specification dyes are described of formula <FORM:0923887/IV(a)/3> where D is a benzene, diphenyl, stilbene, diphenylamine, benzanilide or naphthalene residue, which may be substituted, P is H or SO3H, R is H or alkyl, X is Cl or Br, Y is Cl or Br, alkyl, alkoxy, aryl, aryloxy, thioaryl, thiocyano or substituted or unsubstituted amino, Z is H, alkyl, alkoxy or SO3H o to the azo link, m is 1-3, n is 1-5 and A is a benzene or naphthalene residue which may be substituted. Specifications 797,946, 838,337, 842,933, 851,537 and 876,923 are referred to.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1012859A GB923887A (en) | 1959-03-24 | 1959-03-24 | New monoazo triazine dyestuffs |
| CH325560A CH405540A (en) | 1959-03-24 | 1960-03-23 | Process for the production of new azo dyes |
| CH191265A CH486539A (en) | 1959-03-24 | 1960-03-23 | Process for the production of new azo dyes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1012859A GB923887A (en) | 1959-03-24 | 1959-03-24 | New monoazo triazine dyestuffs |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB923887A true GB923887A (en) | 1963-04-18 |
Family
ID=9962026
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1012859A Expired GB923887A (en) | 1959-03-24 | 1959-03-24 | New monoazo triazine dyestuffs |
Country Status (2)
| Country | Link |
|---|---|
| CH (1) | CH405540A (en) |
| GB (1) | GB923887A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0636665A1 (en) * | 1993-07-31 | 1995-02-01 | Hoechst Aktiengesellschaft | Water-soluble azo-compounds, process of their production and their use as dyestuffs |
| CN103030997A (en) * | 2010-08-30 | 2013-04-10 | 天津德凯化工股份有限公司 | Reactive red dye |
-
1959
- 1959-03-24 GB GB1012859A patent/GB923887A/en not_active Expired
-
1960
- 1960-03-23 CH CH325560A patent/CH405540A/en unknown
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0636665A1 (en) * | 1993-07-31 | 1995-02-01 | Hoechst Aktiengesellschaft | Water-soluble azo-compounds, process of their production and their use as dyestuffs |
| US5569748A (en) * | 1993-07-31 | 1996-10-29 | Hoechst Aktiengesellschaft | 2-amino-8-hydroxy-6-sulfonaphtalene-containing monoazo reactive dyes |
| CN103030997A (en) * | 2010-08-30 | 2013-04-10 | 天津德凯化工股份有限公司 | Reactive red dye |
| CN103030997B (en) * | 2010-08-30 | 2014-04-30 | 天津德凯化工股份有限公司 | Reactive red dye |
Also Published As
| Publication number | Publication date |
|---|---|
| CH405540A (en) | 1966-01-15 |
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