CH257040A - Process for the preparation of a nitro dye. - Google Patents
Process for the preparation of a nitro dye.Info
- Publication number
- CH257040A CH257040A CH257040DA CH257040A CH 257040 A CH257040 A CH 257040A CH 257040D A CH257040D A CH 257040DA CH 257040 A CH257040 A CH 257040A
- Authority
- CH
- Switzerland
- Prior art keywords
- nitro
- dye
- preparation
- nitro dye
- orange
- 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'-Nitro-4'-chlor-benzo- phenon-2-carbonsäure mit 4-Amino-4'-methyl- rliphenylamin-2-sulfonsäure umsetzt.
Der so erhaltene Farbstoff ist ein dunkel braunes Pulver, das sich in Wasser mit orangebrauner Farbe löst und Wolle aus sau rem Bade in orangebraunen Tönen von guter Lichtechtheit färbt.
Beispiel: 61,1 Teile 3'-Nitro-4'-chlor-benzophenon- 2-carbonsäure werden in 500 Teilen Wasser mit Soda neutral gelöst und mit einer neu tralen Lösung von 55,5 Teilen 4-Amino-4'- methyl-diphenylamin-2-sulfonsäure in 500 Teilen Wasser vereinigt, nach Zugabe von 15 Teilen calc. Soda wird etwa 15 Stunden am Rückfluss gekocht. Durch Zugabe von Kochsalz wird dann der gebildete Farbstoff 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'-chloro-benzophenone-2-carboxylic acid is reacted with 4-amino-4'-methylrliphenylamine-2-sulfonic acid.
The dye thus obtained is a dark brown powder which dissolves in water with an orange-brown color and dyes wool from an acid bath in orange-brown shades of good lightfastness.
Example: 61.1 parts of 3'-nitro-4'-chlorobenzophenone-2-carboxylic acid are dissolved in 500 parts of water with neutral soda and treated with a neutral solution of 55.5 parts of 4-amino-4'-methyl- diphenylamine-2-sulfonic acid combined in 500 parts of water, after the addition of 15 parts of calc. Soda is refluxed for about 15 hours. The dye formed is then deposited by adding common salt.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH257040T | 1943-10-11 | ||
CH240226T | 1943-10-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH257040A true CH257040A (en) | 1948-09-15 |
Family
ID=25728501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH257040D CH257040A (en) | 1943-10-11 | 1943-10-11 | Process for the preparation of a nitro dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH257040A (en) |
-
1943
- 1943-10-11 CH CH257040D patent/CH257040A/en unknown
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