CH100188A - Process for the preparation of an acridine dye. - Google Patents
Process for the preparation of an acridine dye.Info
- Publication number
- CH100188A CH100188A CH100188DA CH100188A CH 100188 A CH100188 A CH 100188A CH 100188D A CH100188D A CH 100188DA CH 100188 A CH100188 A CH 100188A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- golden yellow
- formic acid
- dye
- acridine dye
- Prior art date
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
- C09B15/00—Acridine dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Description
Verfahren zur Darstellung eines Aeridinfarbstoffes. Es wurde die Beobachtung gemacht, dass sich 2,7-Dimethyl-3,6-diamino-10-methylacri- diniumchlorid, darstellbar nach deutschem Patent Nr. 143893, Beispiel 1, durch Kochen mit starker Ameisensäure in einen neuen wertvollen Farbstoff überführen lässt, der sich vom Ausgangsmaterial durch reinere und rötere Nuancen und grössere Echtheit seiner Färbungen vorteilhaft unterscheidet.
Beispiel: 45 kg 2,7-Dimethyl-3,6-diamino-10-me- thylacridiniumchlorid werden mit 180 kg Ameisensäure von 85 % und 20 kg wasser freiem Natriumformiat 4 bis 5 Stunden un ter Rückfluss gekocht und dann die über schüssige Ameisensäure abdestilliert unter vermindertem Druck. Der Rückstand wird mit zirka 200 Liter heissem Wasser verrührt, mit Salzsäure kongosauer gestellt und nach dem Erkalten filtriert und getrocknet. Der neue Farbstoff bildet ein goldgelbes Pulver, das sich in heissem Wasser mit der gleichen Farbe löst und tannierte Baumwolle in gold gelber Nuance färbt.
Die Lösung in konzen- trierter Schwefelsäure ist grünlichgelb mit blaugrüner Fluorescenz.
Process for the preparation of an aeridine dye. It was observed that 2,7-dimethyl-3,6-diamino-10-methylacridiniumchlorid, which can be prepared according to German patent no. 143893, example 1, can be converted into a new valuable dye by boiling with strong formic acid, which advantageously differs from the starting material by purer and redder nuances and greater authenticity of its colorations.
Example: 45 kg of 2,7-dimethyl-3,6-diamino-10-methylacridinium chloride are refluxed for 4 to 5 hours with 180 kg of formic acid of 85% and 20 kg of anhydrous sodium formate and then the excess formic acid is distilled off under reduced pressure. The residue is stirred with about 200 liters of hot water, acidified to Congo with hydrochloric acid and, after cooling, filtered and dried. The new dye forms a golden yellow powder, which dissolves in hot water with the same color and dyes tannic cotton in a golden yellow shade.
The solution in concentrated sulfuric acid is greenish yellow with blue-green fluorescence.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100188T | 1922-04-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH100188A true CH100188A (en) | 1923-07-02 |
Family
ID=4358462
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH100188D CH100188A (en) | 1922-04-13 | 1922-04-13 | Process for the preparation of an acridine dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH100188A (en) |
-
1922
- 1922-04-13 CH CH100188D patent/CH100188A/en unknown
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