CH240617A - Process for the preparation of a new monoazo dye. - Google Patents
Process for the preparation of a new monoazo dye.Info
- Publication number
- CH240617A CH240617A CH240617DA CH240617A CH 240617 A CH240617 A CH 240617A CH 240617D A CH240617D A CH 240617DA CH 240617 A CH240617 A CH 240617A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- preparation
- dye
- monoazo dye
- parts
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen 11Zonoazofarbstoffes. Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung eines neuen ehro- mierbaren Monoazowollfarbstoffes, indem di- azotierte 6 - Nitro - 2 - aminophenol - 4 - sulf on- säure mit 1- (p - 4' - Chlorphenoxyphenyl) - 3 - inethyl-5-pyrazolon gekuppelt wird.
<I>Beispiel:</I> 4,68 Teile 6-Nitro-2-aminophenol-4-sulfon- säure werden mit 60 Teilen Wasser und 5 Teilen 36%iger Salzsäure gerührt. Dann versetzt man mit einer Lösung von 1,4 Teilen Natriumnitrit in 10 Teilen Wasser, wobei die Temperatur auf 5 C gehalten wird. Die so erhaltene Diazolösung lässt man innerhalb 10 Minuten in eine Lösung von 6,01 Teilen 1- (p - 4'- Chlorphenoxyphenyl) - 3 - methyl - 5 - pyrazolon einfliessen.
Diese Pyrazolonlösung wurde durch Lösen des Pyrazolons in 100 Teilen Wasser unter Zugabe einer solchen Menge Natronlauge, bis die Lösung eben auf gelbes Claytonpapier alkalisch reagiert, und nachfolgende Zugabe von 8 Teilen was- serfreiem Natriumcarbonat hergestellt. Nach dem Rühren während 15 Stunden wird der neue Farbstoff abfiltriert und bei 50 C ge trocknet.
Der neue Farbstoff färbt Wolle nach dem Metachromverfahren in orangebraunen Farb tönen von ausgezeichneter Wasch-, Walk-., Potting- und Lichtechtheit.
Process for the preparation of a new 11-zonoazo dye. The present invention relates to a process for the production of a new earmouldable monoazo wool dye by mixing diacotated 6-nitro-2-aminophenol-4-sulfonic acid with 1- (p-4'-chlorophenoxyphenyl) -3-ynethyl-5 -pyrazolon is coupled.
<I> Example: </I> 4.68 parts of 6-nitro-2-aminophenol-4-sulfonic acid are stirred with 60 parts of water and 5 parts of 36% strength hydrochloric acid. A solution of 1.4 parts of sodium nitrite in 10 parts of water is then added, the temperature being maintained at 5 ° C. The diazo solution thus obtained is allowed to flow into a solution of 6.01 parts of 1- (p-4'-chlorophenoxyphenyl) -3-methyl-5-pyrazolone within 10 minutes.
This pyrazolone solution was prepared by dissolving the pyrazolone in 100 parts of water with the addition of such an amount of sodium hydroxide solution until the solution just reacts alkaline on yellow clay paper, and then adding 8 parts of anhydrous sodium carbonate. After stirring for 15 hours, the new dye is filtered off and dried at 50.degree.
The new dye dyes wool using the metachrome process in orange-brown shades of excellent wash, milled, potting and lightfastness.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB240617X | 1942-09-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH240617A true CH240617A (en) | 1946-01-15 |
Family
ID=10205745
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH240617D CH240617A (en) | 1942-09-18 | 1943-09-17 | Process for the preparation of a new monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH240617A (en) |
-
1943
- 1943-09-17 CH CH240617D patent/CH240617A/en unknown
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