GB691507A - Triazine vat dyes - Google Patents
Triazine vat dyesInfo
- Publication number
- GB691507A GB691507A GB18699/51A GB1869951A GB691507A GB 691507 A GB691507 A GB 691507A GB 18699/51 A GB18699/51 A GB 18699/51A GB 1869951 A GB1869951 A GB 1869951A GB 691507 A GB691507 A GB 691507A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methoxyphenyl
- triazine
- dicyandiamide
- methoxybenzoyl
- methoxybenzoylbiuret
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/36—Dyes with acylated amino groups
- C09B1/46—Dyes with acylated amino groups the acyl groups being residues of cyanuric acid or an analogous heterocyclic compound
- C09B1/467—Dyes with acylated amino groups the acyl groups being residues of cyanuric acid or an analogous heterocyclic compound attached to two or more anthraquinone rings
Abstract
2 - (o - Methoxyphenyl) - 4,6 - dichlortriazine is obtained from the 4,6-dihydroxy body by reaction with phosphorus oxychloride and pentachloride. 2 - (o - Methoxyphenyl) - 4,6 - dihydroxy - triazine is obtained by treating o-methoxybenzoylbiuret with aqueous caustic potash. o-Methoxybenzoylbiuret is obtained by heating o-methoxybenzoyl dicyandiamide with aqueous hydrochloric acid. o - Methoxybenzoyl dicyandiamide is obtained by treating dicyandiamide in acetone with caustic potash to its potassium salt, and reacting this with o-methoxybenzoyl chloride.ALSO:The invention comprises 2 - (o - methoxyphenyl) - 4,6 - di - (41 - methoxyanthraquinonyl-amino)-triazine, which is a red vat dye and is prepared by heating 2-(o-methoxyphenyl)-4,6-dichlortriazine (see Group IV (b)), with 1-amino-4-methoxyanthraquinone. An example of the condensation is given wherein the reactants are heated in nitrobenzene.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US691507XA | 1951-05-23 | 1951-05-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB691507A true GB691507A (en) | 1953-05-13 |
Family
ID=22087075
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18699/51A Expired GB691507A (en) | 1951-05-23 | 1951-08-08 | Triazine vat dyes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB691507A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2832779A (en) * | 1955-03-30 | 1958-04-29 | Basf Ag | Production of 4-aryl-2.6-dihydroxy-1.3.5-triazines |
DE1110403B (en) * | 1957-05-08 | 1961-07-06 | Ciba Geigy | The coloring of high molecular weight organic products with pigments |
-
1951
- 1951-08-08 GB GB18699/51A patent/GB691507A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2832779A (en) * | 1955-03-30 | 1958-04-29 | Basf Ag | Production of 4-aryl-2.6-dihydroxy-1.3.5-triazines |
DE1110403B (en) * | 1957-05-08 | 1961-07-06 | Ciba Geigy | The coloring of high molecular weight organic products with pigments |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB576361A (en) | Hydrazino-1,3,5-triazino derivatives of substituted phenylarsenic compounds | |
GB646348A (en) | Improvements in magenta colored phenazonium dyestuff photographic images by color development | |
GB691507A (en) | Triazine vat dyes | |
GB1215387A (en) | Process for the preparation of 2-chloropyridine and its derivatives | |
GB537690A (en) | Process for the manufacture of derivatives of [1,3,5-triazinyl-(6)]-aminophenyl-arsonic acids | |
GB1328709A (en) | Chlorination of cyanuric acid | |
US2314356A (en) | Compounds of the anthraquinone series | |
GB1388936A (en) | Chloroisocyanuric acids | |
GB595065A (en) | Process for the production of water-soluble condensation products, and the resulting products | |
GB992558A (en) | New monoazo dyestuffs and processes for their manufacture and use | |
GB593659A (en) | Improvements relating to the manufacture of heterocyclic amines | |
GB1023218A (en) | Substituted pyrido [2,3-e]-triazine 1-oxides | |
GB730949A (en) | Manufacture of new amino-benzene-sulphonamides | |
GB887753A (en) | New anthraquinone vat dyestuffs | |
GB611417A (en) | Preparation of guanidine | |
GB897488A (en) | New anthraquinone dyestuffs and process for their manufacture | |
US2476642A (en) | Amino anthraquinone dyestuffs containing an amino stilbene group | |
GB1274092A (en) | New basic naphtholactam dyes | |
SU66302A1 (en) | Method for producing intermediates for vat dyes | |
GB560094A (en) | Improvement in sulfauro compounds and processes for their production | |
GB487261A (en) | Improvements in the manufacture and production of dyestuffs of the phthalocyanine series | |
GB599738A (en) | Improvements in or relating to the preparation of 2-sulfanilamidopyrazine | |
GB709400A (en) | Vat grey to black dyestuffs comprising polyamino dibenzanthrones and isodibenzanthrones | |
GB683334A (en) | Manufacture of a new quinazoline derivative | |
GB807620A (en) | Manufacture of indole derivatives |