CH128168A - 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
- CH128168A CH128168A CH128168DA CH128168A CH 128168 A CH128168 A CH 128168A CH 128168D A CH128168D A CH 128168DA CH 128168 A CH128168 A CH 128168A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- acid
- phenonaphtosafranine
- series
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes der Phenonaphtosafraninreihe. Es wurde gefunden, dass ein neuer, wertvoller Farbstoff entsteht, wenn man 1 Amino-5-methyl-4-monomethylanilin-2-sulfo- säure mit 3-Dimethylisorosindulin-2. 6. 13 trisulfosäure der Formel:
EMI0001.0007
kondensiert.
Die entstandene Phenönaphto- 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. Beispiel 200 Teile einer wässerigen Lösung, enthaltend 30 Teile des Mononatrium salzes der 3-Dimethylisorosindulin-2. 6. 13 trisulfosäure und 20 Teile Natriumazetat kristallisiert werden zusammen mit einer Lösung von 1-Amino-5-methyl-4-mono- methylanilin-2-sulfosäure in 80 Teilen Was ser und 3 Teilen Soda so lange gekocht, bis eine Probe, in konzentrierter Schwefel säure gelöst, eine rein grüne Farbe zeigt.
Der mit Kochsalz ausgeschiedene Farbstoff färbt die animalische Faser aus saurem Bade licht- und alkaliecht blau. Seine Konstitu tion ist folgende:
EMI0001.0026
Process for the preparation of a dye of the phenonaphtosafranine series. It has been found that a new, valuable dye is produced if 1-amino-5-methyl-4-monomethylaniline-2-sulfonic acid is mixed with 3-dimethylisorosindulin-2. 6. 13 trisulfonic acid of the formula:
EMI0001.0007
condensed.
The phenoenaphthosafranin trisulphonic acid formed 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 blue in water and grass-green in concentrated sulfuric acid. Example 200 parts of an aqueous solution containing 30 parts of the monosodium salt of 3-dimethylisorosindulin-2. 6. 13 trisulfonic acid and 20 parts of sodium acetate are crystallized together with a solution of 1-amino-5-methyl-4-monomethylaniline-2-sulfonic acid in 80 parts of water and 3 parts of soda boiled until a sample is in concentrated sulfuric acid dissolved, 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:
EMI0001.0026
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128168X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128168A true CH128168A (en) | 1928-10-16 |
Family
ID=25710340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128168D CH128168A (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) | CH128168A (en) |
-
1927
- 1927-02-08 CH CH128168D patent/CH128168A/en unknown
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