CH128144A - 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
- CH128144A CH128144A CH128144DA CH128144A CH 128144 A CH128144 A CH 128144A CH 128144D A CH128144D A CH 128144DA CH 128144 A CH128144 A CH 128144A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- dye
- phenonaphtosafranine
- preparation
- series
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes der Phenonaphtosafraninreihe. Es wurde gefunden, dass ein wertvoller, neuer Farbstoff entsteht, wenn man 1-Amino- 4-dimethylanilin-2-sulfosäure mit 3-Dimethyl- isorosindulin-1.6-disulfosäure der Formel:
EMI0001.0008
kondensiert.
Die entstandene Phenonaphto- safranindisulfosäure enthält eine Sulfo- gruppe in Orthostellung'zum Safraninstick- stoff (-I6-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 kon zentrierter Schwefelsäure grasgrün löslich ist. <I>Beispiel:</I> 11 Teile 1-Amino-4-dimethylanilin-2- sulfosäure werden mit 3 Teilen Soda in 80 Teilen Wasser gelöst und 26 Teile Mono natriumsalz der 3-Dimethylisorosindulin- 1.6-disulfosäure, sowie 20 Teile Natrium- azetat kristallisiert in 200 Teilen. Wasser beigefügt. Man kocht so lange unter Rück fluss, bis eine gezogene Probe, in konzentrier ter Schwefelsäure gelöst, eine rein grüne Farbe zeigt, Man macht mit Soda alkalisch und salzt den Farbstoff aus.
Er färbt die animalische Faser aus saurem Bade alkali- und lichtecht blau.
Der Farbstoff hat folgende Konstitution:
EMI0001.0027
Process for the preparation of a dye of the phenonaphtosafranine series. It has been found that a valuable, new dye is created when 1-amino-4-dimethylaniline-2-sulfonic acid is mixed with 3-dimethyl-isorosindulin-1,6-disulfonic acid of the formula:
EMI0001.0008
condensed.
The resulting phenonaphthosafranine disulphonic acid contains a sulpho group in the ortho position to the safranine nitrogen (-I6 position), which is the reason for the excellent alkali fastness of the dyeings.
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> 11 parts of 1-amino-4-dimethylaniline-2-sulfonic acid are dissolved with 3 parts of soda in 80 parts of water and 26 parts of the monosodium salt of 3-dimethylisorosindulin-1,6-disulfonic acid, and 20 parts of sodium - Acetate crystallizes in 200 parts. Water attached. It is boiled under reflux until a sample drawn, dissolved in concentrated sulfuric acid, shows a pure green color. It is made alkaline with soda and the dye is salted out.
It dyes the animal fibers from acidic baths, alkali and lightfast blue.
The dye has the following constitution:
EMI0001.0027
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128144X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128144A true CH128144A (en) | 1928-10-16 |
Family
ID=25710316
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128144D CH128144A (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) | CH128144A (en) |
-
1927
- 1927-02-08 CH CH128144D patent/CH128144A/en unknown
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