CH202741A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH202741A CH202741A CH202741DA CH202741A CH 202741 A CH202741 A CH 202741A CH 202741D A CH202741D A CH 202741DA CH 202741 A CH202741 A CH 202741A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- acid
- amino
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur flerstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen Azo- farbstoff erhält, wenn man die Diazoverbin- clung des 1-Amino-4-nitrobenzol-2-metliylsul- fons mit (2-Äthoxy-5-methyl-2'-sulfonsäure- 4'-acetylamino)-diplienylamin der Formel
EMI0001.0012
vereinigt.
Der neue Farbstoff bildet ein dunkles Pulver, das sich in Wasser mit -violet ter Farbe löst und das Wolle und Seide aus saurem Bade in violettblauen Tönen färbt.
<I>Beispiel:</I> <B>216</B> Teile 1-Amino-4-nitrobenzol-2-methyl- sulion werden diazotiert und in die mineral saure Lösung dieser Diazoverbindung die Lö sung des Natriumsalzes aus 364 Teilen (2- Äthoxy <B>- 5 -</B> methyl <B>-</B> 2'- sulionsäure <B>-</B> 4'- acetyl - amino)-d-iphenylamin eingetragen.
Nachdem die Farbstoffbilduno- beendet ist, wird abfil- triert, der Farbstoff in Wasser suspendiert und durch Verrühren mit einem Alkali neu tral gestellt. Der Farbstoff wird eventuell durch Zusatz eines Salzes ausgeschieden, ab- filtriert und getrocknet.
Process for the production of an azo dye. It has been found that an azo dye is obtained when the diazo compound of 1-amino-4-nitrobenzene-2-methylsulfone is used with (2-ethoxy-5-methyl-2'-sulfonic acid-4'- acetylamino) -diplienylamine of the formula
EMI0001.0012
united.
The new dye forms a dark powder that dissolves in water with a violet color and dyes the wool and silk from acid baths in violet-blue tones.
<I> Example: </I> <B> 216 </B> parts of 1-amino-4-nitrobenzene-2-methylsulion are diazotized and the solution of the sodium salt of 364 parts in the mineral acid solution of this diazo compound ( 2- Ethoxy <B> - 5 - </B> methyl <B> - </B> 2'-sulionic acid <B> - </B> 4'-acetyl-amino) -d-iphenylamine.
After the dye formation has ended, it is filtered off, the dye is suspended in water and neutralized by stirring with an alkali. The dye is possibly precipitated by adding a salt, filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH202741T | 1937-03-15 | ||
| CH200063T | 1938-11-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH202741A true CH202741A (en) | 1939-01-31 |
Family
ID=25723414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH202741D CH202741A (en) | 1937-03-15 | 1937-03-15 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH202741A (en) |
-
1937
- 1937-03-15 CH CH202741D patent/CH202741A/en unknown
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