CH131503A - Process for the production of a new chromium-containing azo dye. - Google Patents
Process for the production of a new chromium-containing azo dye.Info
- Publication number
- CH131503A CH131503A CH131503DA CH131503A CH 131503 A CH131503 A CH 131503A CH 131503D A CH131503D A CH 131503DA CH 131503 A CH131503 A CH 131503A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- chromium
- blue
- gray
- production
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen chromhaltigen Azofarbstoffes. Es wurde gefunden, dass man einen neuen, wertvollen ehromhaltigen Azofarb- =toff erhält, wenn man den Farbstoff aus rliazotiertem 5-Nitro-2-amino-l-phenol und 2 - Acetylamino - 5 - oxyn.aphtalin - 7 - sulf osäure mit chromabgebenden Mitteln behandelt.
Der neue chromhaltige Farbstoff stellt trok- ken ein dunkelblaues Pulver dar, welches sich in Wasser mit blaugrauer und in ver dünnter Sodalösung mit rotstichig grauer Farbe löst. Der Farbstoff färbt Wolle aus sehwefelsaurem Bade in reinen blaugrauen, alkali- und wa.lkechten Tönen an. Baum wolle wird aus neutralem Bade ebenfalls in echten blaugrauen Tönen gefärbt.
<I>Beispiel:</I> 4,46 Gewichtsteile .des Farbstoffes aus diazotiertem 5-Nitro-2-amino-l-phenol und 2 -Acetylamino - 5 -oxynaphtalin - 7 - sulfosäure werden in 400 Teilen Wasser gelöst und mit einer 1,52 Gewichtsteilen Cr20.- entsprechen den Menge Fluorchrom 24 Stunden zum Sie- den erhitzt; die gebildete Chromverbindung wird hierauf mit Kochsalz abgeschieden, ausgewaschen und bei mässiger Temperatur getrocknet.
Process for the production of a new chromium-containing azo dye. It has been found that a new, valuable Ehrom-containing azo dye is obtained if the dye is made from rliazotized 5-nitro-2-amino-1-phenol and 2 - acetylamino - 5 - oxyn.aphthalene - 7 - sulfonic acid treated chromium-releasing agents.
The new chromium-containing dye is a dry, dark blue powder that dissolves in water with a blue-gray color and in diluted soda solution with a reddish gray color. The dye stains wool from a sulfuric acid bath in pure blue-gray, alkaline and water-resistant shades. Cotton from neutral bath is also dyed in real blue-gray tones.
<I> Example: </I> 4.46 parts by weight of the dye from diazotized 5-nitro-2-amino-1-phenol and 2-acetylamino-5-oxynaphthalene-7-sulfonic acid are dissolved in 400 parts of water and treated with a 1.52 parts by weight of Cr20.- correspond to the amount of fluorochrome heated to boiling for 24 hours; the chromium compound formed is then deposited with common salt, washed out and dried at a moderate temperature.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH128006T | 1927-08-19 | ||
CH131503T | 1927-08-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH131503A true CH131503A (en) | 1929-02-15 |
Family
ID=25711022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH131503D CH131503A (en) | 1927-08-19 | 1927-08-19 | Process for the production of a new chromium-containing azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH131503A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5123930A (en) * | 1984-04-27 | 1992-06-23 | Sandoz Ltd. | 1:2 chromium and cobalt complexes of monoazo compounds for drying porous oxide layers on aluminum and aluminum alloy substrates |
US5283325A (en) * | 1984-04-27 | 1994-02-01 | Sandoz Ltd. | 1:2 chromium and cobalt complexes of monoazo compounds having further unsubstituted or substituted nitro-2-hydroxyphenyl diazo component radicals and 6- or 7-acyl-amino-1-hydroxy-3-sulfonaphthalene coupling component radicals |
-
1927
- 1927-08-19 CH CH131503D patent/CH131503A/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5123930A (en) * | 1984-04-27 | 1992-06-23 | Sandoz Ltd. | 1:2 chromium and cobalt complexes of monoazo compounds for drying porous oxide layers on aluminum and aluminum alloy substrates |
US5283325A (en) * | 1984-04-27 | 1994-02-01 | Sandoz Ltd. | 1:2 chromium and cobalt complexes of monoazo compounds having further unsubstituted or substituted nitro-2-hydroxyphenyl diazo component radicals and 6- or 7-acyl-amino-1-hydroxy-3-sulfonaphthalene coupling component radicals |
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