CH128159A - 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
- CH128159A CH128159A CH128159DA CH128159A CH 128159 A CH128159 A CH 128159A CH 128159D A CH128159D A CH 128159DA CH 128159 A CH128159 A CH 128159A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- dye
- preparation
- phenonaphtosafranine
- series
- Prior art date
Links
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- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes der Phenonaphtosafr aninreihe. Es wurde gefunden, dass ein neuer, wert voller Farbstoff entsteht, wenn man 1-Amino- 5-methyl-4-monoäthylanilin-2-sulfosäure mit 3 -Diäthylisorosindulin-1 . 6. 13 -trisulf osäure der Formel
EMI0001.0010
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 dunkelbron- ziges Pulver, das in Wasser mit blauer Farbe, in konzentrierter Schwefelsäure grasgrün löslich ist. <I>Beispiel:</I> 400 Teile einer wässerigen Lösung, ent haltend 31,5 Teile (i/2 Mol.) des Mono- natriumsalzes der 3-Diäthylisorosindulin- 1. 6.
13-trisulfosäure und 20 Teile Natrium azetat kristallisiert werden zusammen mit einer Lösung von 12 Teilen 1-Amino-5-me- thyl-4-monoäthylanilin-2-sulfosäure in 80 Teilen Wasser und 3 Teilen Soda so lange gekocht, bis eine Probe, in konzentrierter Schwefelsäure gelöst, eine rein grüne Farbe zeigt. Auf Zusatz von Kochsalz fällt der Farbstoff als kupferiges Pulver aus. Er färbt die animalische Faser aus saurem Bade licht- und alkaliecht reinblau. Seine Konsti tution ist folgende:
EMI0001.0037
Process for the preparation of a dye of the phenonaphtosafranine series. It has been found that a new, valuable dye is formed if 1-amino-5-methyl-4-monoethylaniline-2-sulfonic acid is mixed with 3-diethylisorosindulin-1. 6. 13 -trisulfonic acid of the formula
EMI0001.0010
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 bronze 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 31.5 parts (i / 2 mol.) Of the monosodium salt of 3-diethylisorosindulin-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-sulfonic acid in 80 parts of water and 3 parts of soda boiled until a sample dissolved in concentrated sulfuric acid, shows a pure green color. Upon addition of table salt, the dye precipitates as a coppery powder. It dyes the animal fibers from acidic baths light and alkali-like pure blue. Its constitution is as follows:
EMI0001.0037
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128159X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128159A true CH128159A (en) | 1928-10-16 |
Family
ID=25710331
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128159D CH128159A (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) | CH128159A (en) |
-
1927
- 1927-02-08 CH CH128159D patent/CH128159A/en unknown
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