GB373160A - The manufacture of new basic dyestuffs - Google Patents
The manufacture of new basic dyestuffsInfo
- Publication number
- GB373160A GB373160A GB503231A GB503231A GB373160A GB 373160 A GB373160 A GB 373160A GB 503231 A GB503231 A GB 503231A GB 503231 A GB503231 A GB 503231A GB 373160 A GB373160 A GB 373160A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyes
- heated
- violet
- carbon tetrachloride
- base
- 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/26—Triarylmethane dyes in which at least one of the aromatic nuclei is heterocyclic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Cyclammoniumpolymethine dyes.--Basic dyes are obtained by causing a carbon tetrahalogenide to react upon a base derived from a heterocyclic ammonium salt containing a reactive methyl group in the a -position with respect to the nitrogen. The products contain three molecules of the starting material combined to form a carbocyanine, and dye tannin-mordanted cotton clear red to blue shades. In examples (1) 1 : 3-3-trimethyl-2-methylene indoline base is heated with carbon tetrachloride or tetrabromide (dyes red-violet shades): (2) 6-acetylamino-1 : 3 : 3-trimethyl-2-methylene indoline (prepared by reducing the 6-nitro-1 : 3 : 3-trimethylmethyleneindoline and adding the theoretical quantity of acetic anhydride to the amino base in ether) is heated with carbon tetrachloride (dyes blueish-violet): (3) N-methyl-2-methylenebenzthiazoline is heated with carbon tetrachloride (dyes brownish-violet): (4) the base from N-ethylquinaldine iodide is heated with carbon tetrachloride (dyes blueish-violet).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB503231A GB373160A (en) | 1931-02-17 | 1931-02-17 | The manufacture of new basic dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB503231A GB373160A (en) | 1931-02-17 | 1931-02-17 | The manufacture of new basic dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB373160A true GB373160A (en) | 1932-05-17 |
Family
ID=9788447
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB503231A Expired GB373160A (en) | 1931-02-17 | 1931-02-17 | The manufacture of new basic dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB373160A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4026884A (en) * | 1973-07-02 | 1977-05-31 | Eastman Kodak Company | Methyne dyes and photographic elements |
US4080496A (en) * | 1975-04-14 | 1978-03-21 | Eastman Kodak Company | Methyne dyes and photographic elements |
-
1931
- 1931-02-17 GB GB503231A patent/GB373160A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4026884A (en) * | 1973-07-02 | 1977-05-31 | Eastman Kodak Company | Methyne dyes and photographic elements |
US4080496A (en) * | 1975-04-14 | 1978-03-21 | Eastman Kodak Company | Methyne dyes and photographic elements |
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