CH128167A - 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
- CH128167A CH128167A CH128167DA CH128167A CH 128167 A CH128167 A CH 128167A CH 128167D A CH128167D A CH 128167DA CH 128167 A CH128167 A CH 128167A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- acid
- series
- phenonaphtosafranine
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes der Phenonaphtocafraninreihe. Es wurde gefunden, dass ein neuer, wertvoller Farbstoff entsteht, wenn man 1 Amino-4-dimethylanilin-2-suUosäure mit 3- Dimethylisorosindulin-1. 6.13 -trisulf osäure der Formel:
EMI0001.0008
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.
Beispiel: 400 Teile einer wässerigen Lösung, ent haltend 30 Teile (i/ Moleküle) des Mono natriumsalzes der 3-Dimethylisorosindulin- 1 . 6. 13-trisulfosäure und 20 Teile Natrium azetat kristallisiert werden zusammen mit einer Lösung von 12 Teilen 1-Amino-4-di- methylanilin-2-sulfosäure in 80 Teilen Was ser und 3,1 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:
EMI0001.0030
Process for the preparation of a dye of the phenonaphtocafranine series. It has been found that a new, valuable dye is produced if 1-amino-4-dimethylaniline-2-suUoic acid is mixed with 3-dimethylisorosindulin-1. 6.13 -trisulfonic acid of the formula:
EMI0001.0008
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 blue in water and grass-green in concentrated sulfuric acid.
Example: 400 parts of an aqueous solution containing 30 parts (i / molecules) of the monosodium 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-4-dimethylaniline-2-sulfonic acid in 80 parts of water and 3.1 parts of soda 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:
EMI0001.0030
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128167X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128167A true CH128167A (en) | 1928-10-16 |
Family
ID=25710339
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128167D CH128167A (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) | CH128167A (en) |
-
1927
- 1927-02-08 CH CH128167D patent/CH128167A/en unknown
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