CH192037A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH192037A CH192037A CH192037DA CH192037A CH 192037 A CH192037 A CH 192037A CH 192037D A CH192037D A CH 192037DA CH 192037 A CH192037 A CH 192037A
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man die Diazo- verbindung des 1-Aminobenzol-2.4-dibutyldi- sulfons in saurer Lösung mit 1-Amino-5-ogy- naphthalin-2-sulfonsäure vereinigt. Der neue Farbstoff bildet ein dunkles Pulver, das sich in Wasser mit blauer Farbe löst und Wolle aus sauren Bade in echten blauen Tönen färbt.
<I>Beispiel:</I> 333 Teile 1-Aminobenzol-2.4-dibutyldi- sulfon werden in verdünnter Essigsäure mit 250 Teilen Salzsäure vom spezifischen Ge wicht 1,15 verrührt und langsam mit einer konzentrierten Lösung von 69 Teilen Natrium nitrit versetzt. In diese durch Zusatz von Eis gekühlte Diazolösung lässt man eine neu tralisierte Lösung von 239 Teilen 1-Amino- 5-ogynaphthalin-2-sulfonsäure zutropfen. Die Farbstoffbildung kann durch Zusatz neutrali sierender Mittel, wie z. B. Natriumacetat oder Natriumformiat beschleunigt werden.
Man kann die Umsetzung auch bei mässig erhöhter Temperatur. -durchführen. Der ent standene Farbstoff. wird abfiltriert, durch Lösen in heissem Wasser und Zugabe eines Alkalis, Aussalzen und Filtrieren und Trocknen isoliert.
Process for the production of a new azo dye. It has been found that a new azo dye is obtained when the diazo compound of 1-aminobenzene-2,4-dibutyl disulfone is combined in acidic solution with 1-amino-5-ogynaphthalene-2-sulfonic acid. The new dye forms a dark powder that dissolves in water with a blue color and dyes wool from acid baths in true blue tones.
<I> Example: </I> 333 parts of 1-aminobenzene-2,4-dibutyl disulfone are stirred in dilute acetic acid with 250 parts of hydrochloric acid with a specific weight of 1.15 and slowly mixed with a concentrated solution of 69 parts of sodium nitrite. A neutralized solution of 239 parts of 1-amino-5-ogynaphthalene-2-sulfonic acid is added dropwise to this diazo solution, which has been cooled by adding ice. The dye formation can be neutralized by adding agents such. B. sodium acetate or sodium formate can be accelerated.
The reaction can also be carried out at a moderately elevated temperature. -carry out. 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 |
---|---|---|---|
CH192037T | 1935-09-07 | ||
CH190423T | 1935-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH192037A true CH192037A (en) | 1937-07-15 |
Family
ID=25721977
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH192037D CH192037A (en) | 1935-09-07 | 1935-09-07 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH192037A (en) |
-
1935
- 1935-09-07 CH CH192037D patent/CH192037A/en unknown
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