CH143570A - Process for the preparation of a polyazo dye. - Google Patents
Process for the preparation of a polyazo dye.Info
- Publication number
- CH143570A CH143570A CH143570DA CH143570A CH 143570 A CH143570 A CH 143570A CH 143570D A CH143570D A CH 143570DA CH 143570 A CH143570 A CH 143570A
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- green
- preparation
- acid
- dye
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Polyazofarbstoffes. T s wurde gefunden, da.ss man einen grü- n(1n wertvollen Direktfarbstoff erhält, wenn man die diazotierte Aminoazoverbindung aus diazotierter 1- Aminobenzol-2 .
5-disulio- s <B><U>41</U></B> und 1-Amino-2-metliylmereaptonaph- aure talin mit dem Kondensationsprodukt aus inolaren Mengen Cyanurchlorid. 1-(4'-Amino- benzoyl)- Amiiio-8-osy naphtalin-4 .
6-disulf o- säure, 4-Amino-4'-oxy-azo-benzol-3'-earbon- siiure und -l.-Aminobenzoesäure kuppelt.
<I>Beispiel:</I> Die in üblicher Weise aus .t53 Gewichts teilen der Aminoazoverbindung aus diazo- tierter 1-Aminobenzol-2.5-disulfosäure und 1- Amino-?-methylmerca.ptonaphtalin
EMI0001.0034
hergestellte, abgeschiedene und mit Eiswas ser verrührte Diazoverbindung fliesst.bei 5 bis<B>10 '</B> zu einer gut gerührten, zweckmässig mit Pyridin versetzten Lösung von 1052 Ge- v,
ichtsteilen des Kondensationsproduktes aus molaren Mengen Cyanurchlorid, 1-(4'-Amino- bL,nzoyl)-Amino-8-oxynaphtalin-4 . 6-disulf o- säure, 4-Amino-4'-oxy-azo-benzol-3'-carbon- säure und 4-Aminobenzoesäure. Die Kupp lung setzt sofort unter Tiefgrünfärbung der Lösung ein und ist bald beendig.-t.
Der Farbstoff stellt in getrocknetem Zu stand ein dunkles, bronzeglänzendes Pulver dar, das sich mit grüner Farbe in Wasser löst und aus dem Glaubersalz-Sodabad in leuchtenden. gelbstichig grünen Tönen auf die pflanzliche Faser zieht. Die Färbung be sitzt eine bemerkenswerte Lichtechtheit.
Process for the preparation of a polyazo dye. It has been found that a green (1n valuable direct dye is obtained if the diazotized aminoazo compound is obtained from diazotized 1-aminobenzene-2.
5-disulio- s <B><U>41</U> </B> and 1-amino-2-methylmereaptonaph- aure talin with the condensation product of molar amounts of cyanuric chloride. 1- (4'-Amino-benzoyl) - Amiiio-8-osy naphthalene-4.
6-disulfonic acid, 4-amino-4'-oxy-azo-benzene-3'-earbonic acid and -l-aminobenzoic acid are coupled.
<I> Example: </I> The usual way of dividing .t53 weight of the aminoazo compound from diazo- tated 1-aminobenzene-2,5-disulfonic acid and 1-amino -? - methylmerca.ptonaphthalene
EMI0001.0034
The diazo compound produced, separated and mixed with ice water flows at 5 to <B> 10 '</B> to form a well-stirred solution of 1052 wt.
Not part of the condensation product from molar amounts of cyanuric chloride, 1- (4'-amino-bL, nzoyl) -amino-8-oxynaphthalene-4. 6-disulfonic acid, 4-amino-4'-oxy-azo-benzene-3'-carboxylic acid and 4-aminobenzoic acid. The coupling sets in immediately, the solution turns deep green and will soon be over.
When dry, the dye is a dark, bronze-shimmering powder that dissolves in water with a green color and turns into glowing from the Glauber's salt soda bath. yellowish green tones on the vegetable fibers. The coloring has a remarkable lightfastness.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE143570X | 1927-11-22 | ||
| CH140415T | 1928-11-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH143570A true CH143570A (en) | 1930-11-15 |
Family
ID=25713520
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH143570D CH143570A (en) | 1927-11-22 | 1928-11-14 | Process for the preparation of a polyazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH143570A (en) |
-
1928
- 1928-11-14 CH CH143570D patent/CH143570A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH238453A (en) | Process for the preparation of a copper-compatible polyazo dye. | |
| CH143570A (en) | Process for the preparation of a polyazo dye. | |
| CH143581A (en) | Process for the preparation of a polyazo dye. | |
| CH143580A (en) | Process for the preparation of a polyazo dye. | |
| CH140415A (en) | Process for the preparation of a polyazo dye. | |
| CH143579A (en) | Process for the preparation of a polyazo dye. | |
| CH141879A (en) | Process for the preparation of a polyazo dye. | |
| CH143578A (en) | Process for the preparation of a polyazo dye. | |
| CH143582A (en) | Process for the preparation of a polyazo dye. | |
| CH143572A (en) | Process for the preparation of a polyazo dye. | |
| CH141541A (en) | Process for the preparation of a polyazo dye. | |
| CH143577A (en) | Process for the preparation of a polyazo dye. | |
| CH143566A (en) | Process for the preparation of a polyazo dye. | |
| CH143568A (en) | Process for the preparation of a polyazo dye. | |
| CH143571A (en) | Process for the preparation of a polyazo dye. | |
| CH142347A (en) | Process for the preparation of an azo dye. | |
| DE728886C (en) | Process for the preparation of copper complex compounds of substantive azo dyes | |
| CH143569A (en) | Process for the preparation of a polyazo dye. | |
| CH217944A (en) | Process for the preparation of a substantive trisazo dye. | |
| CH135219A (en) | Process for the production of a new chromium-containing dye. | |
| CH191149A (en) | Process for the preparation of a monoazo dye. | |
| CH143574A (en) | Process for the preparation of a polyazo dye. | |
| CH182594A (en) | Process for the preparation of a monoazo dye. | |
| CH208541A (en) | Process for the preparation of a disazo dye. | |
| CH136386A (en) | Process for the preparation of a polyazo dye. |