CH128143A - 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
- CH128143A CH128143A CH128143DA CH128143A CH 128143 A CH128143 A CH 128143A CH 128143D A CH128143D A CH 128143DA CH 128143 A CH128143 A CH 128143A
- 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- 5-methyl-4-monoäthylanilin-2-sulfosäure mit 3 -Dimethylisorosindulin-1. 6-disulfosäure der Formel
EMI0001.0008
kondensiert. Die entstandene Phenonaphto- safranindisulfosäure 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 kupferiges Pul ver, das in Wasser mit blauer Farbe, in konzentrierter Schwefelsäure grasgrün lös lich ist. <I>Beispiel</I> 11,5 Teile 1-Amino-5-methyl-4-mono- äthvlanilin-2-sulfosäure werden mit 3 Tei len ySoda in 80 Teilen Wasser siedend gelöst und 26 Teile Mononatriumsalz der 3-Di- methylisorosindulin-1.6-disulfosäure, sowie 20 Teile Natriumazetat kristallisiert in 200 Teilen Wasser beigefügt.
Man kocht so lange unter Rückfluss, bis eine gezogene Probe, in konzentrierter Schwefelsäure gelöst, eine rein grüne Farbe zeigt. Nach dem Verdünnen der Lösung auf 1500 Teile und Alkalisch machen mit Soda wird der Farbstoff mit Kochsalz ausgeschieden. Er färbt Wolle und Seide aus saurem Bade in alkali- und licht echten Blautönen. Der Farbstoff entspricht der Konstitution:
EMI0001.0037
Process for the preparation of a dye of the phenonaphtosafranine series. It has been found that a valuable, new dye is produced if 1-amino-5-methyl-4-monoethylaniline-2-sulfonic acid is mixed with 3-dimethylisorosindulin-1. 6-disulfonic acid of the formula
EMI0001.0008
condensed. The resulting phenonaphthosafranine disulfonic acid contains a sulfo group in the ortho position to the
Safranine nitrogen (-16 position), which determines the excellent alkali fastness of the dyeings.
The new dye is a coppery powder that is blue-colored in water and grass-green in concentrated sulfuric acid. <I> Example </I> 11.5 parts of 1-amino-5-methyl-4-mono- äthvlanilin-2-sulfonic acid are dissolved with 3 parts of soda in 80 parts of boiling water and 26 parts of the monosodium salt of the 3-di- methylisorosindulin-1,6-disulfonic acid and 20 parts of sodium acetate crystallized in 200 parts of water were added.
It is refluxed until a drawn sample, dissolved in concentrated sulfuric acid, shows a pure green color. After diluting the solution to 1500 parts and making it alkaline with soda, the dye is eliminated with common salt. He dyes wool and silk from acid bath in alkaline and light blue tones. The dye corresponds to the constitution:
EMI0001.0037
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128143X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128143A true CH128143A (en) | 1928-10-16 |
Family
ID=25710315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128143D CH128143A (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) | CH128143A (en) |
-
1927
- 1927-02-08 CH CH128143D patent/CH128143A/en unknown
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