CH143590A - 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
- CH143590A CH143590A CH143590DA CH143590A CH 143590 A CH143590 A CH 143590A CH 143590D A CH143590D A CH 143590DA CH 143590 A CH143590 A CH 143590A
- Authority
- CH
- Switzerland
- Prior art keywords
- coloring
- preparation
- parts
- stain
- brown
- Prior art date
Links
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
Verfahren zur Darstellung eines beizenfärbenden Disazofarbstoffes. Es wurde gefunden, dass man einen wert- vollen,beizenfärbendenDisazofarbstoft erhält, wenn man 2-Aminonaplitalin-6,8-disulfo- säure diazotiert, mit 1-Aminonaplitalin-7- sulfosäure kombiniert, erneut diazotiert und mit 1-Oxybenzol-2-carbonsäure kuppelt.
<I>Beispiel:</I> 30,3 Teile 2-Aminonapl-italin-6,8-disulfo- säure in 10%iger Anschlämmung werden nach Zusatz von 12 Teilen Salzsäure 30%ig mit 6,9 Teilen Natriumnitrit diazotiert, worauf eine Lösung von 22,3 Teilen 1- Aminonaphtalin-7-sulfosäure in 250 Teilen Wasser zugefügt wird.
Nach beendeter Kupplung wird mit 4 Teilen Natronhydrat neutralisiert, 7 Teile Natriumnitrit zugegeben und bei<B>10'</B> durch Zusatz von 35 Teilen Salzsäure 30%ig rasch diazotiert. Die Di- azoverbindung wird mit Chlorkalium aus gefällt und gepresst. Der Presskuchen wird darauf mit 150 Teilen Wasser und 1.50 Tei len Eis angeteigt, mit 14 Teilen 1-Oxy- benzol-2-carbonsäure als Natronsalz versetzt und 30 Teile Natronlauge 20%ig langsam zufliessen gelassen.
Nach beendeter Kupp lung wird der Farbstoff mit Kochsalz ge fällt.
Der Farbstoff bildet ein braunes Pulver, löslich in Wasser mit gelbbrauner, in konz. Schwefelsäure mit blaugrüner Farbe. Er er zeugt im Chromdruck ein Braun von grosser Seifen-, Wasch- und Lichtechtheit.
Process for the preparation of a stain-coloring disazo dye. It has been found that a valuable, stain-coloring disazo dye is obtained if 2-aminonaplitalin-6,8-disulfonic acid is diazotized, combined with 1-aminonaplitalin-7-sulfonic acid, diazotized again and with 1-oxybenzene-2-carboxylic acid clutch.
<I> Example: </I> 30.3 parts of 2-aminonapl-italin-6,8-disulphonic acid in 10% suspension are diazotized with 6.9 parts of sodium nitrite after addition of 12 parts of 30% hydrochloric acid, whereupon a solution of 22.3 parts of 1-aminonaphthalene-7-sulfonic acid in 250 parts of water is added.
After coupling has ended, the mixture is neutralized with 4 parts of sodium hydrate, 7 parts of sodium nitrite are added and, at 10%, the mixture is rapidly diazotized by adding 35 parts of 30% hydrochloric acid. The diazo compound is precipitated with potassium chloride and pressed. The press cake is then made into a paste with 150 parts of water and 1.50 parts of ice, 14 parts of 1-oxybenzene-2-carboxylic acid as sodium salt are added and 30 parts of 20% sodium hydroxide solution are allowed to slowly flow in.
After coupling is complete, the dye is precipitated with common salt.
The dye forms a brown powder, soluble in water with yellow-brown, in conc. Sulfuric acid with a blue-green color. With chrome printing, it creates a brown that is extremely fast to soap, washing and light.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE143590X | 1928-02-20 | ||
CH141877T | 1929-04-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH143590A true CH143590A (en) | 1930-11-15 |
Family
ID=25713944
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH143590D CH143590A (en) | 1928-02-20 | 1929-02-18 | Process for the preparation of a stain-coloring disazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH143590A (en) |
-
1929
- 1929-02-18 CH CH143590D patent/CH143590A/en unknown
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