CH181716A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH181716A CH181716A CH181716DA CH181716A CH 181716 A CH181716 A CH 181716A CH 181716D A CH181716D A CH 181716DA CH 181716 A CH181716 A CH 181716A
- Authority
- CH
- Switzerland
- Prior art keywords
- brown
- azo dye
- production
- new
- yellow
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
-
- 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
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/12—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the benzene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>178818.</B> Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen, en wertvollen, eliromierbaren Monoazofarbstoff erhält, wenn man die Diazoverbindung von 4-Nitro-2-aminophenol-6-sulfünsäure mit p- 4(,rtiärem Amyl-phenol kuppelt.
Der neue Farbstoff ist ein braunes Pul ver-. er färbt Wolle aus saurem Bade in gelb braunen Tönen. Durch Chromieren entstellen wertvolle, satte und gedeckte Brauntöne, die vorzügliche Echtheitseigenschaften besitzen. Der Farbstoff kann gegebenenfalls vor der V(,rwendung im Färbeprozess in Chromkom plexe übergeführt werden.
<I>Beispiel:</I> 23,4<B>kg</B> 4-Nitro-92-aminophenol-6-sulion- säure werden nach bekannten Methoden diazo- tiert. Mit Bikarbonat wird die überschüssige Mineralsäure abgestumpft und die Diazo- niumlösung unter Rühren zu einer Lösung von<B>16,5 kg</B> p-tertiärem Amyl-phenol in<B>6 kg</B> Nalilauge 100%ig und<B>50</B> Liter Wasser ge- <B>C</B> ter Kupplung wird aus- "eben. Nach beende gesalzen,
filtriert und getrocknet. Die Farb- stoffbildung verläuft etwas rascher in Gegen wart von Pyridin.
Der Farbstoff bildet ein braunes Pulver, das sich in Wasser und konzentrierter Schwe felsäure mit gelbbrauner Farbe löst.
Additional patent to main patent no. <B> 178818. </B> Process for the production of a new azo dye. It has been found that a new, valuable, eliromizable monoazo dye is obtained if the diazo compound of 4-nitro-2-aminophenol-6-sulphuric acid is coupled with p-4 (, tertiary amylphenol.
The new dye is a brown powder. he dyes wool from an acid bath in yellow-brown tones. Chromating disfigures valuable, rich and muted brown tones that have excellent fastness properties. The dye can optionally be converted into chromium complexes prior to use in the dyeing process.
<I> Example: </I> 23.4 <B> kg </B> 4-nitro-92-aminophenol-6-sulionic acid are diazotized according to known methods. The excess mineral acid is blunted with bicarbonate and the diazonium solution is converted into a solution of <B> 16.5 kg </B> p-tertiary amylphenol in <B> 6 kg </B> 100% sodium hydroxide solution while stirring <B> 50 </B> liters of water <B> C </B> the clutch is evened out. When finished, salted,
filtered and dried. The formation of color takes place somewhat faster in the presence of pyridine.
The dye forms a brown powder that dissolves in water and concentrated sulfuric acid with a yellow-brown color.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH181716T | 1934-11-05 | ||
CH178818T | 1935-07-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH181716A true CH181716A (en) | 1935-12-31 |
Family
ID=25720206
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH181716D CH181716A (en) | 1934-11-05 | 1934-11-05 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH181716A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2612523A1 (en) * | 1987-03-19 | 1988-09-23 | Ciba Geigy Ag | PROCESS FOR THE PREPARATION OF METALLABLE MONOAZOIC DYES |
-
1934
- 1934-11-05 CH CH181716D patent/CH181716A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2612523A1 (en) * | 1987-03-19 | 1988-09-23 | Ciba Geigy Ag | PROCESS FOR THE PREPARATION OF METALLABLE MONOAZOIC DYES |
BE1000630A5 (en) * | 1987-03-19 | 1989-02-21 | Ciba Geigy Ag | PROCESS FOR THE PREPARATION OF METALLIC MONOAZOIC DYES. |
CH677303GA3 (en) * | 1987-03-19 | 1991-05-15 |
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