CH197279A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH197279A CH197279A CH197279DA CH197279A CH 197279 A CH197279 A CH 197279A CH 197279D A CH197279D A CH 197279DA CH 197279 A CH197279 A CH 197279A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- acid
- amino
- baths
- azo 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/08—Disazo dyes in which the coupling component is a hydroxy-amino compound
- C09B33/10—Disazo dyes in which the coupling component is a hydroxy-amino compound in which the coupling component is an amino naphthol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen wert vollen Azofarbstoff erhält, wenn man die Diazoverbindung des 1-Amino-4-nitrobenzols in saurem Medium mit 1-Amino-8-oxynaph- thalin-3.6-disulfonsäure vereinigt und die sen so erhältlichen Farbstoff in alkalischem Medium mit der Diazoverbindung des 4- Chlor-2-aminodiphenyläthers umsetzt.
Der neue Farbstoff bildet ein dunkles Pulver, das sich in Wasser mit blauer Farbe löst und Wolle aus saurem Bade, Naturseide oder be schwerte Seide aus saurem oder seifenhalti- gem Bade in grünstichigblauen Tönen von guten Echtheitseigenschaften färbt.
<I>Beispiel:</I> 152 Teile 1-Amino-4-nitrobenzol werden nach bekannten Methoden diazotiert. Diese Diazolösung gibt man unter Rühren zu 319 Teilen frisch gefällter 1-Amino-8-oxy- naphthalin-3. 6-distilfonsäure und rührt einige Stunden bei Aussentemperatur. Dieser Mono- azofarbstoff wird nun durch Zusatz von Na- triumchlorid und Filtrieren isoliert, ohne zu trocknen in Wasser angerührt und durch Zu gabe von Natriumcarbonat neutralisiert.
Man versetzt diese Farbstoffsuspension mit 350Tei- len kristallisiertem Natriumacetat und trägt unter gutem Rühren die Diazolösung, die man durch Diazotieren von 220 Teilen 4- Chor - 2 - aminodiphenyläther auf übliche Weise erhält, ein. Man rührt bis die Farb- stoffbildung beendet ist und filtriert ab. Der Farbstoff kann gegebenenfalls durch Lösen in heissem Wasser und Ausfällen mit Chlor natrium gereinigt werden.
Nach dem Trock nen bildet er ein dunkles Pulver, das sich in Wasser mit blauer Farbe löst und Wolle aus saurem Bade, Naturseide oder beschwerte Seide aus saurem oder seifenhaltigem Bade in grünstichig blauen Tönen von guten Echt heitseigenschaften färbt.
Process for the preparation of an azo dye. It has been found that a valuable azo dye is obtained if the diazo compound of 1-amino-4-nitrobenzene is combined in an acidic medium with 1-amino-8-oxynaphthalene-3,6-disulfonic acid and this dye obtainable in this way is combined in an alkaline one Reacts medium with the diazo compound of 4-chloro-2-aminodiphenyl ether.
The new dye forms a dark powder that dissolves in water with a blue color and dyes wool from acidic baths, natural silk or weighted silk from acidic or soapy baths in greenish-blue shades with good fastness properties.
<I> Example: </I> 152 parts of 1-amino-4-nitrobenzene are diazotized using known methods. This diazo solution is added to 319 parts of freshly precipitated 1-amino-8-oxynaphthalene-3 with stirring. 6-distilfonic acid and stir for a few hours at outside temperature. This monoazo dye is then isolated by adding sodium chloride and filtering, stirred in water without drying, and neutralized by adding sodium carbonate.
350 parts of crystallized sodium acetate are added to this dye suspension and the diazo solution obtained by diazotizing 220 parts of 4-chloro-2-aminodiphenyl ether in the usual way is introduced with thorough stirring. The mixture is stirred until the formation of color has ended and the mixture is filtered off. The dye can optionally be purified by dissolving it in hot water and precipitating it with sodium chloride.
After drying, it forms a dark powder that dissolves in water with a blue color and dyes wool from acid baths, natural silk or weighted silk from acid or soap baths in greenish blue tones with good fastness properties.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH197279T | 1937-02-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH197279A true CH197279A (en) | 1938-04-30 |
Family
ID=4440797
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH197279D CH197279A (en) | 1937-02-09 | 1937-02-09 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH197279A (en) |
-
1937
- 1937-02-09 CH CH197279D patent/CH197279A/en unknown
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