AT47156B - Process for the preparation of a purple disazo dye. - Google Patents
Process for the preparation of a purple disazo dye.Info
- Publication number
- AT47156B AT47156B AT47156DA AT47156B AT 47156 B AT47156 B AT 47156B AT 47156D A AT47156D A AT 47156DA AT 47156 B AT47156 B AT 47156B
- Authority
- AT
- Austria
- Prior art keywords
- preparation
- purple
- disazo dye
- dye
- parts
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung eines violetten Disazofarbstoffes. Es wurde gefunden, dass die Tetrazoverbindung des Dichlordianisidins der Formel :
EMI1.1
welches aus Chlornitrophenoläther (OCjHg : VOg : Cl = 1 : 2 : 4) leicht dargestellt werden kann, bei Kombination mit 2 Mol. 2-Naphtol-3 : 6-disulfosäure einen rötlich violetten Farbstoff liefert, welcher sowohl zum Färben von Wolle als auch zur Darstellung von Pigmentfarben dienen kann. Diese letzteren sind vorzüglich kalk-, wasser-und ölecht wegen ihrer guten Lichtechtheit und reinen rötlich violetten Nuance von besonderem Werte.
Die Darstellung des Farbstoffes kann wie folgt ausgeführt werden : 15#6 Teile Dichlordianisidin werden mit 6#9 Teilen Natriumnitrit und der nötigen Menge Salzsäure diazotiert und die, wenn nötig filtrierte Lösung in eine bis zum Schlusse der Kombination sodaalkalisch gehaltene und mit Eis gekühlte Lösung von 36 Teilen 2-Naphtol-3 : 6-disulfosäure (Dinatriumsalz) einfliessen gelassen. Nach Vollendung der Farb-
EMI1.2
getrocknet. Seine Überführung in Pigmontfarben kann nach den üblichen Methoden erfolgen.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for the preparation of a purple disazo dye. It was found that the tetrazo compound of dichlorodianisidine of the formula:
EMI1.1
which can easily be prepared from chloronitrophenol ether (OCjHg: VOg: Cl = 1: 2: 4), when combined with 2 mol. 2-naphthol-3: 6-disulfonic acid provides a reddish violet dye, which is used both for dyeing wool and can be used to represent pigment colors. These latter are especially lime, water and oil because of their good lightfastness and pure reddish violet nuances of particular value.
The preparation of the dye can be carried out as follows: 15 # 6 parts of dichlorodianisidine are diazotized with 6 # 9 parts of sodium nitrite and the necessary amount of hydrochloric acid and the solution, filtered if necessary, into a solution of soda-alkaline until the end of the combination and cooled with ice 36 parts of 2-naphthol-3: 6-disulfonic acid (disodium salt) were allowed to flow in. After completing the color
EMI1.2
dried. It can be converted into Pigmont colors by the usual methods.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE47156X | 1909-08-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT47156B true AT47156B (en) | 1911-03-27 |
Family
ID=5625541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT47156D AT47156B (en) | 1909-08-10 | 1910-04-23 | Process for the preparation of a purple disazo dye. |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT47156B (en) |
-
1910
- 1910-04-23 AT AT47156D patent/AT47156B/en active
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