CH257039A - Process for the preparation of a nitro dye. - Google Patents
Process for the preparation of a nitro dye.Info
- Publication number
- CH257039A CH257039A CH257039DA CH257039A CH 257039 A CH257039 A CH 257039A CH 257039D A CH257039D A CH 257039DA CH 257039 A CH257039 A CH 257039A
- Authority
- CH
- Switzerland
- Prior art keywords
- nitro
- preparation
- brown
- nitro dye
- 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
- C09B51/00—Nitro or nitroso dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 240226. Verfahren zur Herstellung eines Nitrofarbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines Nitrofarb- stoffes. Das Verfahren ist dadurch gekenn zeichnet, dass man 3'-Nitro-4'-chlor-benzo- phenon-2-carbonsäure mit 4-Amino-diphenyl- amin-2-sulfonsäure umsetzt.
Der so erhaltene Farbstoff ist ein dunkel braunes Pulver, das sich in Wasser mit braun- oranger Farbe löst und Wolle aus saurem Bade in braunorangen Tönen von guter Licht echtheit färbt.
<I>Beispiel:</I> 61,1 Teile 3'-Nitro-4'-chlor-benzophenon- 2-carbonsäure werden mit Soda in 500 Teilen Wasser neutral gelöst. Anderseits werden 52,8 Teile 4-Amino-diphenylamin-2-sulfon- säure ebenfalls mit Soda in 500 Teilen Was- ser neutral gelöst. Beide Lösungen werden vereinigt und nach Zugabe von 15 Teilen calc. Soda :etwa 20 Stunden am Rückfluss gekocht. Dann wird,der gebildete Farbstoff durch Zu gabe von Kochsalz abgeschieden.
Additional patent to main patent no. 240226. Process for the production of a nitro dye. The subject of the present patent is a process for the production of a nitro dye. The process is characterized in that 3'-nitro-4'-chlorobenzophenone-2-carboxylic acid is reacted with 4-aminodiphenylamine-2-sulfonic acid.
The dye obtained in this way is a dark brown powder which dissolves in water with a brown-orange color and dyes wool from an acid bath in brown-orange shades with good lightfastness.
<I> Example: </I> 61.1 parts of 3'-nitro-4'-chloro-benzophenone-2-carboxylic acid are dissolved neutrally in 500 parts of water with soda. On the other hand, 52.8 parts of 4-aminodiphenylamine-2-sulfonic acid are also dissolved in 500 parts of water in a neutral manner using soda. Both solutions are combined and, after adding 15 parts of calc. Soda: refluxed for about 20 hours. Then the dye formed is deposited by adding sodium chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH240226T | 1943-10-11 | ||
CH257039T | 1943-10-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH257039A true CH257039A (en) | 1948-09-15 |
Family
ID=25728500
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH257039D CH257039A (en) | 1943-10-11 | 1943-10-11 | Process for the preparation of a nitro dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH257039A (en) |
-
1943
- 1943-10-11 CH CH257039D patent/CH257039A/en unknown
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