CH257041A - Process for the preparation of a nitro dye. - Google Patents
Process for the preparation of a nitro dye.Info
- Publication number
- CH257041A CH257041A CH257041DA CH257041A CH 257041 A CH257041 A CH 257041A CH 257041D A CH257041D A CH 257041DA CH 257041 A CH257041 A CH 257041A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dye
- nitro dye
- brown
- acid
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (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',5'-Dinitro-4'-chlor-benzo- phenon-2-carbonsäure mit 4-Amino-diphenyl- amin-2-sulfonsäure umsetzt.
Der so erhaltene Farbstoff ist ein braunes Pulver, das sich in Wasser mit brauner Farbe löst und Wolle aus saurem Bade in orange braunen Tönen von guter Lichtechtheit färbt. Beispiel: 70,1 Teile 3',5'-Dinitro-4'-chlor-benzo- phenon-2-carbonsäure werden mit Soda in 500 Teilen Wasser neutral gelöst. Anderseits wer den 52,8 Teile 4-Amino-diphenylamin-2-sul- fonsäure ebenfalls mit Soda in 500 Teilen Wasser neutral gelöst. Beide Lösungen wer den vereinigt und nach Zugabe von 15 Teilen calc. Soda etwa 20 Stunden am Rüekfluss gekocht.
Dann wird der gebildete Farbstoff durch Zugabe 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 ', 5'-dinitro-4'-chloro-benzophenone-2-carboxylic acid is reacted with 4-aminodiphenylamine-2-sulfonic acid.
The dye thus obtained is a brown powder which dissolves in water with a brown color and dyes wool from an acid bath in orange-brown shades of good lightfastness. Example: 70.1 parts of 3 ', 5'-dinitro-4'-chlorobenzophenone-2-carboxylic acid are dissolved neutrally in 500 parts of water with soda. On the other hand, the 52.8 parts of 4-aminodiphenylamine-2-sulphonic acid are also dissolved neutrally with soda in 500 parts of water. Both solutions who combined and calc after the addition of 15 parts. Soda boiled on the backflow for about 20 hours.
Then the dye formed is deposited by adding common salt.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH257041T | 1943-10-11 | ||
CH240226T | 1943-10-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH257041A true CH257041A (en) | 1948-09-15 |
Family
ID=25728502
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH257041D CH257041A (en) | 1943-10-11 | 1943-10-11 | Process for the preparation of a nitro dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH257041A (en) |
-
1943
- 1943-10-11 CH CH257041D patent/CH257041A/en unknown
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