CH192036A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH192036A CH192036A CH192036DA CH192036A CH 192036 A CH192036 A CH 192036A CH 192036D A CH192036D A CH 192036DA CH 192036 A CH192036 A CH 192036A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- new
- dye
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
- C09B29/28—Amino naphthols
- C09B29/30—Amino naphtholsulfonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 190423. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man die Diazover- bindung des 1-Aminobenzol-2,4-diäthyldisul- fons in saurer Lösung mit 1-Amii)o-5-oxy- riaphthalin-7-stilfonsäure vereinigt. Der neue Farbstoff bildet ein dunkles Pulver, das sich in Wasser mit violetter Farbe löst und Wolle aus essigsaurem Bade in echten blauen Tönen färbt.
<I>Beispiel:</I> <B>277</B> Teile 1-Aminobenzol-2,4-diätbyldistil- fon werden in verdünnter Essigsäure mit<B>250</B> Teilen Salzsäure vom spezifischen Gewicht <B>1,15</B> verrührt und langsam mit einer kon zentrierten Lösung von<B>69</B> Teilen Natrium- nitrit versetzt. In diese durch Zusatz von Eis gekühlte Diazolösung lässt man nun eine schwach essigsauer gestellte Lösung von<B>239</B> Teilen 1-Amino-5-oxynaphthalin-7-sulfonsäure zutropfen. Die Farbstoffbildung kann durch Zusatz neutralisierender Mittel, wie z. B.
Natriumacetat oder Natriumformiat, beschleu nigt werden. Der entstandene Farbstoff wird abfiltriert, durch Lösen in heissem Wasser und Zugabe eines Alkalis, Aussalzen und Filtrieren und Trocknen isoliert.
Additional patent to main patent no. 190423. Process for the production of a new azo dye. It has been found that a new azo dye is obtained if the diazo compound of 1-aminobenzene-2,4-diethyl disulfone is combined in acidic solution with 1-amii) o-5-oxyriaphthalene-7-stilfonic acid. The new dye forms a dark powder that dissolves in water with a purple color and dyes wool from an acetic acid bath in true blue tones.
<I> Example: </I> <B> 277 </B> parts of 1-aminobenzene-2,4-dietbyldistil- fon are in dilute acetic acid with <B> 250 </B> parts of hydrochloric acid with a specific gravity <B> 1.15 </B> and slowly mixed with a concentrated solution of <B> 69 </B> parts of sodium nitrite. A solution of 239 parts of 1-amino-5-oxynaphthalene-7-sulfonic acid, which has been made weakly acidic in acetic acid, is now added dropwise to this diazo solution, which has been cooled by adding ice. The dye formation can be achieved by adding neutralizing agents, such as. B.
Sodium acetate or sodium formate, can be accelerated. The resulting dye is filtered off, isolated by dissolving in hot water and adding an alkali, salting out and filtering and drying.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH192036T | 1935-09-07 | ||
CH190423T | 1935-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH192036A true CH192036A (en) | 1937-07-15 |
Family
ID=25721976
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH192036D CH192036A (en) | 1935-09-07 | 1935-09-07 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH192036A (en) |
-
1935
- 1935-09-07 CH CH192036D patent/CH192036A/en unknown
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