CH128166A - Process for the preparation of a dye of the phenonaphtosafranine series. - Google Patents
Process for the preparation of a dye of the phenonaphtosafranine series.Info
- Publication number
- CH128166A CH128166A CH128166DA CH128166A CH 128166 A CH128166 A CH 128166A CH 128166D A CH128166D A CH 128166DA CH 128166 A CH128166 A CH 128166A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- preparation
- dye
- phenonaphtosafranine
- series
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes der Phenonaphtosafraninreihe. Es wurde gefunden, daB ein wertvoller, neuer Farbstoff en .steht, wenn man 1- Amino -5- methyl -4- monoäthylanilin -2- sulf o- säure mit 3-Dimethylisorosindulin-1.6.13- trisulfosäure der Formel
EMI0001.0014
kondensiert.
Die entstandene Phenonaphto- safranintrisulfosäure enthält eine Sulfo- gruppe in Orthostellung zum Safraninstick- stoff (-16-Stellung), wodurch die vorzüg liche Alkaliechtheit der Färbungen bedingt wird.
Der neue Farbstoff ist ein dunkles Pul ver, das in Wasser mit blauer Farbe, in konzentrierter Schwefelsäure grasgrün lös lich ist- <I>Beispiel:</I> 400 Teile einer wässerigen Lösung, ent haltend 30 Teile (1/ Moleküle) des Mono natriumsalzes der 3-Dimethylisorosindulin- 1. 6. 13 - trisulfosäure und 20 Teile Na triumazetat kristallisiert werden zusam men mit einer Lösung von 12 Teilen 1 Amino-5-methyl-4-monoäthylanilin-2-sulfo säure in 80 Teilen Wasser und 3 Teilen Soda so lange gekocht, bis eine Probe, in konzen trierter Schwefelsäure gelöst, eine rein grüne Farbe zeigt.
Der mit Kochsalz ausgeschiedene Farbstoff färbt die animalische Faser aus saurem Bade licht- und alkaliecht blau. Seine Konstitution ist folgende:
EMI0001.0034
Process for the preparation of a dye of the phenonaphtosafranine series. It has been found that a valuable, new dye is produced if 1-amino -5-methyl -4- monoethylaniline -2-sulfonic acid is mixed with 3-dimethylisorosindulin-1.6.13-trisulfonic acid of the formula
EMI0001.0014
condensed.
The resulting phenonaphthosafranin trisulphonic acid contains a sulpho group in the ortho position to the safranine nitrogen (-16 position), which means that the dyeings are particularly fast to alkali.
The new dye is a dark powder that is green in water and soluble in concentrated sulfuric acid - <I> Example: </I> 400 parts of an aqueous solution containing 30 parts (1 / molecule) of the mono sodium salt of 3-dimethylisorosindulin- 1. 6. 13 - trisulfonic acid and 20 parts of sodium acetate are crystallized together with a solution of 12 parts of 1 amino-5-methyl-4-monoethylaniline-2-sulfo acid in 80 parts of water and 3 parts Soda is boiled until a sample, dissolved in concentrated sulfuric acid, shows a pure green color.
The dyestuff excreted with common salt dyes the animal fibers from acidic bath light and alkaline light blue. Its constitution is as follows:
EMI0001.0034
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128166X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128166A true CH128166A (en) | 1928-10-16 |
Family
ID=25710338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128166D CH128166A (en) | 1926-02-13 | 1927-02-08 | Process for the preparation of a dye of the phenonaphtosafranine series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128166A (en) |
-
1927
- 1927-02-08 CH CH128166D patent/CH128166A/en unknown
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