CH234945A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH234945A CH234945A CH234945DA CH234945A CH 234945 A CH234945 A CH 234945A CH 234945D A CH234945D A CH 234945DA CH 234945 A CH234945 A CH 234945A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- red
- production
- new azo
- new
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Terfahren zur Herstellung eines neuen Azofarbstoifes. Es wurde .gefunden, dass man einen neuen Azofarbstoff erhält, wenn man diazotiertes 2-Aminodiphenyl mit 1-Benzoylamino-8-oxy- naphthalin-4,6-disulfonsäure vereinigt.
Der getrocknete neue Farbstoff bildet ein rotes Pulver, -das sich in konzentrierter Schwefelsäure zunächst mit rotvioletter Farbe löst, welche nach kurzer Zeit in grün um schlägt und Wolle aus. saurem Bade in sehr reinen blaustichig-roten Tönen färbt.
<I>Beispiel:</I> 16.,9 Teile 2-Aminodiphenyl werden mit Salzsäure und 6,9 Teilen Natriumnitrit diazo- tiert. Die erhaltene Diazolösung lässt man unter Kühlung in eine überschüssiges Na- triumcarbonat enthaltende Lösung von 42,6 Teilen 1-Benzoylamino-8-oxynaphthalin-4,6- dieulfonsäure unter Rühren einlaufen.
Die Kupplung erfolgt rasch. Nach Beendigung der Kupplung wird der zum Teil ausgeschie dene Farbstoff durch Zusatz von Natrium chlorid vollständig abgeschieden und filtriert.
Terfahren for the production of a new azo dye. It was found that a new azo dye is obtained when diazotized 2-aminodiphenyl is combined with 1-benzoylamino-8-oxynaphthalene-4,6-disulfonic acid.
The dried new dye forms a red powder, which initially dissolves in concentrated sulfuric acid with a red-violet color, which after a short time turns green and wool becomes out. acidic bath colors in very pure bluish-red tones.
<I> Example: </I> 16..9 parts of 2-aminodiphenyl are diazotized with hydrochloric acid and 6.9 parts of sodium nitrite. The diazo solution obtained is allowed to run, while cooling, into a solution of 42.6 parts of 1-benzoylamino-8-oxynaphthalene-4,6-dieulfonic acid containing excess sodium carbonate, while stirring.
The coupling is quick. After the coupling has ended, the dye, which has partly been eliminated, is completely separated off by adding sodium chloride and filtered.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH234945T | 1940-10-17 | ||
CH233185T | 1940-10-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH234945A true CH234945A (en) | 1944-10-31 |
Family
ID=25727784
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH234945D CH234945A (en) | 1940-10-17 | 1940-10-17 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH234945A (en) |
-
1940
- 1940-10-17 CH CH234945D patent/CH234945A/en unknown
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