CH128149A - 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
- CH128149A CH128149A CH128149DA CH128149A CH 128149 A CH128149 A CH 128149A CH 128149D A CH128149D A CH 128149DA CH 128149 A CH128149 A CH 128149A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- dye
- preparation
- phenonaphtosafranine
- series
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur ]Darstellung eines Farbstoffes der Pheiionaphtosafrauliireilie. Es wurde gefunden, dass ein wertvoller, neuer Farbstoff entsteht, wenn man 1-Ami- no-4-dimethylanilin-2-suliosäure mit 3-Di- äthylisorosindulin-2. 6-disuliosäure der For mel
EMI0001.0009
kondensiert.
Die entstandene Phenonaplito- safranindisulioso,ure enthält eine Sulfo- gruppe in Orthostellung zum Safraninstick- stoff (-16-Stellung), wodurch die vorzüglielte Alkaliechtheit der Färbungen bedingt wird.
Der neue Farbstoff ist ein dunkles Pül- ver, löslich in Wasser mit blauer Farbe und in konzentrierter Schwefelsäure grasgrün. Beis.piel: <B>11</B> Teile 1-Amino-4-dimetliylanilin-2-sul- fosäure werden mit 3. Teilen Soda in<B>80</B> Teilen Wasser gelöst und<B>27,5</B> Teile Mono- natriumsalz der 3-Diäthylisorosindulin-2.6- disulfosäure, sowie 20 Teile Natriumacetat kristallisiert in 20Ü Teilen Wasser beige fügt.
Es muss mehrere Stunden gekocht wer den, bis eine gezogene Probe, in konzen trierter Schwefelsäure gelöst, eine rein grune Farbe zeigt. Der Farbstoff wird sodaalka- liseli ausgeschieden, und zwar durch Zu gabe von Kochsalz. Er färbt die animalische Faser aus saurem Bade licht- und alkalieellt blau. Seine Konstitution ist folgende:
EMI0001.0037
Process for the preparation of a dye of the Pheiionaphtosafrauliireilie. It has been found that a valuable, new dye is produced when 1-amino-4-dimethylaniline-2-sulioic acid is mixed with 3-diethylisorosindulin-2. 6-disulioic acid of the formula
EMI0001.0009
condensed.
The phenonaplitosafranin disulioso, ure that is formed contains a sulfo group in the ortho position to the safranin nitrogen (-16 position), which gives the dyeings excellent alkali fastness.
The new dye is a dark powder, soluble in water with a blue color and grass green in concentrated sulfuric acid. Example: <B> 11 </B> parts of 1-amino-4-dimethylaniline-2-sulphonic acid are dissolved in <B> 80 </B> parts of water with 3rd parts of soda and <B> 27, 5 parts of the monosodium salt of 3-diethylisorosindulin-2,6-disulfonic acid and 20 parts of sodium acetate crystallized in 20 parts of water are added.
It has to be boiled for several hours until a sample taken, dissolved in concentrated sulfuric acid, turns a pure green color. The dye is excreted in soda alkali by adding table salt. It dyes the animal fibers from acidic baths light and alkaline blue. Its constitution is as follows:
EMI0001.0037
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128149X | 1926-02-13 | ||
CH124764T | 1928-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128149A true CH128149A (en) | 1928-10-01 |
Family
ID=25710321
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128149D CH128149A (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) | CH128149A (en) |
-
1927
- 1927-02-08 CH CH128149D patent/CH128149A/en unknown
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