CH164547A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH164547A CH164547A CH164547DA CH164547A CH 164547 A CH164547 A CH 164547A CH 164547D A CH164547D A CH 164547DA CH 164547 A CH164547 A CH 164547A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- sulfonic acid
- leather
- dye
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoffes. Durch Kombination von Amidoalphyloxy- naphthyltriazolsulfosäuren mit Diazoverbin- dungen werden, wie bekannt, Azofarbstoffe erhalten, die besondere Affinität zur Baum wollfaser haben und sich auf ihr diazotieren und entwickeln lassen.
Es wurde nun gefunden, dass man zu wertvollen Farbstoffen gelangt, die im Ge gensatz zu den erwähnten keine Affinität zur Baumwollfaser besitzen, sondern den Cha rakter vorn Säurefarbstoffen haben, die in hervorragendem blasse befähigt sind, Leder aus saurem Bade gleichmässig anzufärben, wenn man eine Aryloxynaphthyl-1.2-triazol- sulfosKure, die im Arylkern eine Nitrogruppe trägt, als Azokomponente wählt.
Beispiel: 27,7 Teile 4-Aminoazobenzol-4'-sulfosäure werden in bekannter Weise dianotiert und mit einer kalten sodaalkalisch gehaltenen Lösung von 40,8 Teilen 4'-nitrophenyl-5-oxy- rraphthyi-1.2-triazol-7-sulfosaurem Natrium der Formel
EMI0001.0021
vereinigt. Nach beendeter Kupplung wird mit Koch salz abgeschieden und der Farbstoff in übli cher Weise aufgearbeitet. Er färbt Chrom leder und vegetabilisch gegerbtes Leder in schönen rotbraunen Tönen von guter Licht echtheit an.
Process for the preparation of an azo dye. By combining amidoalphyloxynaphthyltriazole sulfonic acids with diazo compounds, as is known, azo dyes are obtained which have a particular affinity for cotton fibers and which can be diazotized and developed on it.
It has now been found that valuable dyes are obtained which, in contrast to those mentioned, have no affinity for cotton fibers, but rather have the character of acid dyes, which are extremely pale capable of evenly staining leather from acidic baths if one Chooses aryloxynaphthyl-1,2-triazol-sulfosKure, which has a nitro group in the aryl nucleus, as the azo component.
Example: 27.7 parts of 4-aminoazobenzene-4'-sulfonic acid are dianotized in a known manner and treated with a cold solution of 40.8 parts of 4'-nitrophenyl-5-oxyrraphthyi-1,2-triazole-7-sulfonic acid sodium the formula
EMI0001.0021
united. When the coupling is complete, it is deposited with sodium chloride and the dye is worked up in a customary manner. It stains chrome leather and vegetable-tanned leather in beautiful red-brown tones with good lightfastness.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE164547X | 1932-02-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH164547A true CH164547A (en) | 1933-10-15 |
Family
ID=5684527
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH164547D CH164547A (en) | 1932-02-15 | 1932-11-04 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH164547A (en) |
-
1932
- 1932-11-04 CH CH164547D patent/CH164547A/en unknown
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