CH141877A - Process for the preparation of a stain-coloring disazo dye. - Google Patents
Process for the preparation of a stain-coloring disazo dye.Info
- Publication number
- CH141877A CH141877A CH141877DA CH141877A CH 141877 A CH141877 A CH 141877A CH 141877D A CH141877D A CH 141877DA CH 141877 A CH141877 A CH 141877A
- Authority
- CH
- Switzerland
- Prior art keywords
- parts
- stain
- preparation
- coloring
- brown
- Prior art date
Links
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
Verfahren zur Darstellung eines beizenfärbenden Disazofar bstoffes. Es wurde gefunden, .dass man einen wert vollen, beizenfärbenden Disazofarbstoff er hält, wenn man 1-Aminona.phtalin-5-sulfo- säure .dia.zotiert, mit 1-AminonaphtaIin-6- sulfosä,ure kombiniert.
erneut diazotiert und mit 1-OxS.-benzbl-2-carbonsäure kuppelt.
<I>Beispiel.:</I> 22,3 Teile 1-Aminonaphtalin-5-sulfosäure in 10%iger Ansehlämmung werden nach Zu- -;atz von 12 Teilen Salzsäure 30%ig mit 6,9 Teilen Natriumnitrit aiazotiert, worauf eine Lösung von 22.3 Teilen 1-Aminonaph- talin-6-sulfosäure in 250 Teilen Wasser zu- sefü"t wird.
Nach beendeter Kupplung und nach Zusatz; von d Teilen Natronhydrat wer den 7 Teile Natriumnitrit zugegeben und in 35 Teile Sa'lzsä'ure M i- i- verdünnt mit 200 Teilen Wasser .bei 15 einlaufen gelassen. Die Diazoverbindung wird mit Kochsalz aus gefällt und gepresst.
Der Presskuchen wird darauf mit 150 Teilen Wasser und 150 Tei len Eis angeteir;t, mit 1.1 Teilen 1-Oxyben- zol-2-carbonsäure als Natronsalz versetzt und 30 Teile Natronlauge 20%ig langsam zuf@lie- ssen gelassen. Nach beendeter Kupplung wird mit 10 Teilen Essigsäure 80%ig neutralisiert und der Farbstoff mit Kochsalz gefällt.
Der Farbstoff bildet ein braunes Pulver, löslich in Wasser mit gelbbrauner, in kon zentrierter Schwefelsäure mit lalaugrüner Farbe. Er erzeugt im Chromdruck ein Braun von grosser Seifen-, Wasch- und Lichtecht heit.
Process for the preparation of a stain-dyeing disazo dye. It has been found that a valuable, stain-staining disazo dye is obtained if 1-aminona.phtalin-5-sulfoic acid is dia.zotiert, combined with 1-aminonaphthalen-6-sulfoic acid.
diazotized again and coupled with 1-OxS.-benzbl-2-carboxylic acid.
<I> Example: </I> 22.3 parts of 1-aminonaphthalene-5-sulfonic acid in 10% slurry are after addition of 12 parts of 30% hydrochloric acid aiazotized with 6.9 parts of sodium nitrite, whereupon a Solution of 22.3 parts of 1-aminonaphthalene-6-sulfonic acid in 250 parts of water is added.
After coupling is complete and after addition; 7 parts of sodium nitrite of d parts of sodium hydrate are added and diluted with 200 parts of water in 35 parts of Sa'lzsä'ure M i-i-allowed to run. The diazo compound is precipitated with table salt and pressed.
The press cake is then mixed with 150 parts of water and 150 parts of ice, 1.1 parts of 1-oxybenzene-2-carboxylic acid as sodium salt are added, and 30 parts of 20% sodium hydroxide solution are allowed to slowly add. After the coupling has ended, the mixture is neutralized with 10 parts of 80% strength acetic acid and the dye is precipitated with sodium chloride.
The dye forms a brown powder, soluble in water with yellow-brown, in concentrated sulfuric acid with a lala green color. With chrome printing, it creates a brown that is extremely fast to soap, washing and light.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE141877X | 1928-02-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH141877A true CH141877A (en) | 1930-08-31 |
Family
ID=5668911
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH141877D CH141877A (en) | 1928-02-20 | 1929-02-18 | Process for the preparation of a stain-coloring disazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH141877A (en) |
-
1929
- 1929-02-18 CH CH141877D patent/CH141877A/en unknown
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