CH198058A - Process for the preparation of a polyazo dye. - Google Patents
Process for the preparation of a polyazo dye.Info
- Publication number
- CH198058A CH198058A CH198058DA CH198058A CH 198058 A CH198058 A CH 198058A CH 198058D A CH198058D A CH 198058DA CH 198058 A CH198058 A CH 198058A
- Authority
- CH
- Switzerland
- Prior art keywords
- molecule
- dye
- preparation
- combined
- acid
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/38—Trisazo dyes ot the type
- C09B35/44—Trisazo dyes ot the type the component K being a hydroxy amine
- C09B35/46—Trisazo dyes ot the type the component K being a hydroxy amine the component K being an amino naphthol
- C09B35/463—D being derived from diaminodiphenyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 194457. Verfahren zur Darstellung eines Polyazofarbstoffes. Das vorliegende Patent betrifft ein Ver fahren zur Darstellung eines blauen Polyazo- farbstoffes und ist dadurch gekennzeichnet, dass man ein Molekül Tetrazobenzidin in saurer Lösung mit einem Molekül 1,8-Amino- naphthol - 3,6 - dis ulfonsäure kombiniert, das Zwischenprodukt mit einem Molekül Diazo- benzolparasulfonsäure in -alkalischer Lösung kuppelt,
hierauf mit einem Molekül 1,8- Aminonaphtol - 3,6 - disulfonsäure alkalisch vereinigt und. den erhaltenen Farbstoff mit Phosgengas behandelt. <I>Beispiel:</I> 18,4 Teile Benzidin werden in der üblichen Weise tetrazotiert und mit 34,1 Teilen 1,8 Aminonaphtol.3,6.disulforrsäure(Mononatrium- salz) mineralsauer gekuppelt.
Ist die Bildung des Zwischenproduktes beendet, so wird es mit der Diazoverbindung aus 17,3 Teilen Amino- benzolpärasulfonsäure sodaalkalisch vereinigt. Zu dem entstandenen Disazofarbstoff lässt man eine sodaalkalische Lösung von 31,9 Teilen 1,8-Aminonaphtol-3,6-disulfonsäure zufliessen. 'Nach erfolgter Kupplung fügt man zu der Flüssigkeit 5,5 Teile Soda, erwärmt auf<B>700</B> und leitet bei dieser Temperatur so lange Phosgengas durch die Flüssigkeit, bis dieselbe schwach sauer reagiert.
Durch Versetzen der sauer gewordenen Lösung mit Kochsalz wird der Farbstoff gefällt; er wird abgenutscht, mit etwas Wasser angerührt, reit Soda neutral gestellt und zur Trockne verdampft.
Der neue Farbstoff stellt ein in kaltem Wasser leicht lösliches, graues, bronzierendes Pulver dar. In der Lichtechtheit übertrifft er den nicht mit Phosgen behandelten, rotstichig- blauen -Farbstoff; der am Licht stark nach Grün verschiesst, sehr wesentlich. Er färbt Leder verschiedenster Gerbungsart in schönen blauen Tönen an.
Additional patent to main patent No. 194457. Process for the preparation of a polyazo dye. The present patent relates to a method for the preparation of a blue polyazo dye and is characterized in that one molecule of tetrazobenzidine in acidic solution is combined with one molecule of 1,8-amino naphthol - 3,6 - disulfonic acid, the intermediate product with a Molecule of diazo-benzenesulfonic acid in alkaline solution couples,
then combined with a molecule of 1,8-aminonaphthol-3,6-disulfonic acid and alkaline. treated the dye obtained with phosgene gas. <I> Example: </I> 18.4 parts of benzidine are tetrazotized in the usual way and coupled with 34.1 parts of 1.8 aminonaphthol.3,6.disulforric acid (monosodium salt) with mineral acid.
When the formation of the intermediate product has ended, it is combined with the diazo compound from 17.3 parts of aminobenzene para-sulfonic acid in an alkaline-soda manner. A soda-alkaline solution of 31.9 parts of 1,8-aminonaphthol-3,6-disulfonic acid is allowed to flow into the disazo dye formed. After coupling has taken place, 5.5 parts of soda are added to the liquid, heated to 700 and phosgene gas is passed through the liquid at this temperature until the liquid reacts slightly acidic.
The dye is precipitated by adding common salt to the acidic solution; it is sucked off, mixed with a little water, made neutral with soda and evaporated to dryness.
The new dye is a gray, bronzing powder that is easily soluble in cold water. In terms of lightfastness, it exceeds the reddish-blue dye that has not been treated with phosgene; which shoots strongly towards green in the light, very essential. He dyes leather of various types of tanning in beautiful blue tones.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH198058T | 1937-03-13 | ||
US1170174XA | 1955-09-14 | 1955-09-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH198058A true CH198058A (en) | 1938-05-31 |
Family
ID=25723057
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH198058D CH198058A (en) | 1937-03-13 | 1937-03-13 | Process for the preparation of a polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH198058A (en) |
-
1937
- 1937-03-13 CH CH198058D patent/CH198058A/en unknown
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