CH180694A - Process for the preparation of a chromable azo dye. - Google Patents
Process for the preparation of a chromable azo dye.Info
- Publication number
- CH180694A CH180694A CH180694DA CH180694A CH 180694 A CH180694 A CH 180694A CH 180694D A CH180694D A CH 180694DA CH 180694 A CH180694 A CH 180694A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- chromium
- preparation
- chromable
- colorations
- Prior art date
Links
Landscapes
- Paper (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines ehromierbaren Azofarbstoffes. Es wurde gefunden, dass man einen wert vollen chromierbaren Azofarbstoff erhält, wenn man diazotiertes 1-Oxy-2-amino-5- nitro-4-chlorbenzol mit 1-Oxynaphthalin-4,8- disulfonsäure kuppelt.
Der so erhältliche Azofarbstoff färbt tierische Fasern bordorot; beim Na.chchromie- ren entstehen tiefblaue Färbungen mit sehr guten Echtheitseigenschaften. Durch Behan deln des neuen Azofarbstoffes in Substanz mit chromabgebenden Mitteln erhält man die komplexe Chromverbindung, welche tief marineblaue, sehr egale Färbungen von aus gezeichneter Echtheit liefert.
Als chromab gebende Mittel eignen sich Chromsalze or- ;;anischer Säuren, zum Beispiel Chromsalze von Naphthalinsulfonsäuren oder Chrom- Lormiat, ferner Chromsalze anorganischer Säuren, zum Beispiel Chromsulfat, sowie Ge- misclie soleher Chromsalze.
<I>Beispiel:</I> <B>18,9</B> Teile 1-Oxy-2-amino-5-nitro-4-chlor- benzol werden diazotiert und dann in soda- alkalischer Lösung mit 33 Teilen 1-Oxynaph- thalin - 4,8 - disulfonsäure gekuppelt. Die Kupplung ist in ein bis zwei Stunden be endet. Der mit Kochsalz ausgesalzene Farb stoff färbt Wolle in bordoroten Tönen; durch Nachchromieren entsteht eine tiefblaue Fär bung.
Zur Herstellung der komplexen Chrom verbindung behandelt man den Farbstoff etwa drei Stunden lang bei 130 C mit einer Lösung von Chromsulfat, die 12 Teile Chrom oxyd enthält. Die ausgesalzene Chromver bindung ergibt auf Wolle tief marineblaue, sehr egale Färbungen von ausgezeichneter Lichtechtheit und guter Abendfarbe.
Process for the production of an honorable azo dye. It has been found that a valuable chromable azo dye is obtained if diazotized 1-oxy-2-amino-5-nitro-4-chlorobenzene is coupled with 1-oxynaphthalene-4,8-disulfonic acid.
The azo dye obtainable in this way dyes animal fibers Bordeaux red; Na.chroming produces deep blue colorations with very good fastness properties. By treating the new azo dye in substance with chromium-releasing agents, the complex chromium compound is obtained, which provides deep navy blue, very level colorations of excellent authenticity.
Chromium salts of organic acids, for example chromium salts of naphthalenesulfonic acids or chromium lormate, furthermore chromium salts of inorganic acids, for example chromium sulfate, and mixtures of such chromium salts are suitable as chromium donating agents.
<I> Example: </I> <B> 18.9 </B> parts of 1-oxy-2-amino-5-nitro-4-chlorobenzene are diazotized and then in a soda-alkaline solution with 33 parts of 1 -Oxynaphthalene - 4.8 - disulfonic acid coupled. The coupling is finished in one to two hours. The dye, salted out with table salt, dyes wool in bordeaux red tones; chrome plating creates a deep blue color.
To produce the complex chromium compound, the dye is treated for about three hours at 130 C with a solution of chromium sulfate containing 12 parts of chromium oxide. The salted-out chromium compound produces deep navy blue, very level dyeings of excellent lightfastness and good evening color on wool.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE180694X | 1934-04-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH180694A true CH180694A (en) | 1935-11-15 |
Family
ID=5712349
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH180694D CH180694A (en) | 1934-04-19 | 1935-02-22 | Process for the preparation of a chromable azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH180694A (en) |
-
1935
- 1935-02-22 CH CH180694D patent/CH180694A/en unknown
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