CH191757A - Process for the preparation of an acidic chromating dye of the anthraquinone series. - Google Patents
Process for the preparation of an acidic chromating dye of the anthraquinone series.Info
- Publication number
- CH191757A CH191757A CH191757DA CH191757A CH 191757 A CH191757 A CH 191757A CH 191757D A CH191757D A CH 191757DA CH 191757 A CH191757 A CH 191757A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- acidic
- anthraquinone series
- chromating
- Prior art date
Links
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Chemical Treatment Of Metals (AREA)
Description
Verfahren zur Darstellung eines sauren Chromierungsfarbstoffes der Anthrachinonreihe. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung eines sauren Chro- mierungsfarbstoffes der Anthrachinonreihe, ,welches dadurch gekennzeichnet ist, daB man 1-amino-4-bromanthra.chinon-2-sulfosau- res Natrium mit 4-Amino-4'-oxyazobenzol-3'- earbonsäure kondensiert.
<I>Beispiel:</I> 16 Gewichtsteile 1-a-mino-4-bromantlira- ehinon-2-sulfosaures Natrium, 13: Gewichts- teile 4-Amino-4'-oxyazobenzol-3'-carbonsäure, 10 Gewichtsteile Soda oalciniert, 1 Gewichts teil Kupferehlorür werden in 2;50 Gewichts- teilen Wasser bis zur Beendigung der Um setzung zum Sieden erhitzt.
Man säuert :dann das Reaktionsprodukt mit verdünnter Salz säure an, erwärmt kurze Zeit auf<B>80'</B> C, saugt ab und wäscht :den Filterkuchen mit verdünnter Salzsäure nach. Beim Lösen in verdünnter Sodalösung oder Ammoniak er hält man eine grüne Lösung, aus welcher,der Farbstoff durch Aussalzen isoliert wird. Das Produkt färbt Wolle aus saurer Flotte in grünen Tönen, welche in ihren Echtheiten durch Nachchromieren verbessert werden.
Process for the preparation of an acidic chromating dye of the anthraquinone series. The subject of this additional patent is a process for the preparation of an acidic chromating dye of the anthraquinone series, which is characterized in that 1-amino-4-bromoanthraquinone-2-sulfoacid is sodium with 4-amino-4'-oxyazobenzene 3'-carbonic acid condensed.
<I> Example: </I> 16 parts by weight of 1-a-mino-4-bromantlira-ehinon-2-sulfonic acid sodium, 13: parts by weight of 4-amino-4'-oxyazobenzene-3'-carboxylic acid, 10 parts by weight of soda Calcined, 1 part by weight of copper chlorine is heated to boiling in 2; 50 parts by weight of water until the reaction has ended.
It is acidified: then the reaction product is acidified with dilute hydrochloric acid, heated to <B> 80 '</B> C for a short time, filtered off with suction and washed: the filter cake with dilute hydrochloric acid. When dissolving in dilute soda solution or ammonia, you get a green solution, from which the dye is isolated by salting out. The product dyes wool from acidic liquor in green tones, the fastness of which is improved by post-chrome plating.
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE191757X | 1934-12-22 | ||
DE231035X | 1935-10-23 | ||
CH188888T | 1935-12-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH191757A true CH191757A (en) | 1937-06-30 |
Family
ID=27177773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH191757D CH191757A (en) | 1934-12-22 | 1935-12-19 | Process for the preparation of an acidic chromating dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH191757A (en) |
-
1935
- 1935-12-19 CH CH191757D patent/CH191757A/en unknown
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