CH128162A - 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
- CH128162A CH128162A CH128162DA CH128162A CH 128162 A CH128162 A CH 128162A CH 128162D A CH128162D A CH 128162DA CH 128162 A CH128162 A CH 128162A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- acid
- preparation
- phenonaphtosafranine
- series
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes der Phenonaphtosafraninreihe. Es wurde gefunden, dass ein. neuer, wertvol ler Farbstoff entsteht, wenn man 1-Amino- 5 - methyl - 4 - monomethylanilin- 2 - sulf osäure mit 3-Dimethylisorosindulin-1 # 6 # 12-trisulfo- säure der Formel
EMI0001.0016
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 Pulver, das in Wasser mit blauer Farbe, in konzen trierter Schwefelsäure grasgrün löslich ist. <I>Beispiel:</I> 400 Teile einer wässerigen Lösung, ent haltend 30 Teile (1/z Molekül) des Mono natriumsalzes der 3-Dimethylisorosindulin- 1 # 6 # 12-trisulfosäure und 20 Teile Natrium azetat kristallisiert werden zusammen mit einer Lösung von 11 Teilen 1-Amino-5-methyl- 4-rizonomethylanilin-2-sulfosäure in 80 Teilen Wasser 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 Konstitution ist folgende
EMI0001.0041
Process for the preparation of a dye of the phenonaphtosafranine series. It was found that a. New, valuable dye is created when 1-amino-5-methyl-4-monomethylaniline-2-sulfonic acid is mixed with 3-dimethylisorosindulin-1 # 6 # 12-trisulfonic acid of the formula
EMI0001.0016
condensed. The
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 soluble in water with a blue color, and in concentrated sulfuric acid it is grass-green. <I> Example: </I> 400 parts of an aqueous solution containing 30 parts (1 / z molecule) of the monosodium salt of 3-dimethylisorosindulin- 1 # 6 # 12-trisulfonic acid and 20 parts of sodium acetate are crystallized together with a Solution of 11 parts of 1-amino-5-methyl-4-rizonomethylaniline-2-sulfonic acid in 80 parts of water and 3 parts of soda boiled until a sample is 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
EMI0001.0041
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128162X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128162A true CH128162A (en) | 1928-10-16 |
Family
ID=25710334
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128162D CH128162A (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) | CH128162A (en) |
-
1927
- 1927-02-08 CH CH128162D patent/CH128162A/en unknown
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