CH302024A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH302024A CH302024A CH302024DA CH302024A CH 302024 A CH302024 A CH 302024A CH 302024D A CH302024D A CH 302024DA CH 302024 A CH302024 A CH 302024A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- parts
- amino
- sulfonic 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. (legenstand des vorliegenden Zusatzpaten- tes ist ein Verfahren zur Herstellung eines Azofarbstoffes, welches dadurch gekennzeich net ist, dass man die Diazoniumverbindung aus 1-Aminobenzol-3-(ss-chloräthylsulfon) mit 2- Amino - 8 - oxynaphthalin - 6 - sulfonsäur e verei nigt.
<I>Beispiel:</I> 12,3 Gewiehtsteile 2-Amino-8-oxyna,phtha- liti-6-sulfonsäure (97,10/aig) werden in 375 Volumteilen Wasser und 50 Volumteilen ln- Natronlauge gelöst.
Die filtrierte Lösung wird in eine -Mischung aus 75 Volumteilen ln-Salz- .I I *i Lire -und 175 Volumteilen Wasser eingerührt, @vobei die 2-Amino-8-oxvnaphthalin-6-sulfon- säure in feinverteilter Form ausfällt.
In diese saure Suspension lässt man bei 5-10 C die aus 11 Gewichtsteilen 1-Aminobenzol-3-(ss- ehloräthylsulfon) in üblicher Weise herge stellte Diazolösung einfliessen. Nach beendeter Kupplung wird der Azofarbstoff der folgen den Formel:
EMI0001.0039
mit Kaliumchlorid ausgesalzen, abgesaugt, mit <B>10</B> 1/o irrer Kaliumchloridlösung gewaschen und getrocknet.
Das so erhaltene Produkt stellt ein dunkel rotes Pulver dar, das Wolle in roten Tönen von guten Echtheitseigenschaften färbt.
Process for the preparation of an azo dye. (The status of the present additional patent is a process for the production of an azo dye, which is characterized in that the diazonium compound from 1-aminobenzene-3- (ss-chloroethylsulfone) with 2-amino-8-oxynaphthalene-6-sulfonic acid united.
<I> Example: </I> 12.3 parts by weight of 2-amino-8-oxyna, phthalite-6-sulfonic acid (97.10 / aig) are dissolved in 375 parts by volume of water and 50 parts by volume of sodium hydroxide solution.
The filtered solution is stirred into a mixture of 75 parts by volume of ln salt and 175 parts by volume of water, with the 2-amino-8-oxynaphthalene-6-sulfonic acid precipitating in finely divided form.
The diazo solution prepared in the usual manner from 11 parts by weight of 1-aminobenzene-3- (ss-ehloräthylsulfon) is allowed to flow into this acidic suspension at 5-10 ° C. After the coupling is complete, the azo dye will have the following formula:
EMI0001.0039
Salted out with potassium chloride, filtered off with suction, washed with <B> 10 </B> 1 / o crazy potassium chloride solution and dried.
The product thus obtained is a dark red powder which dyes wool in red shades with good fastness properties.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE302024X | 1950-07-03 | ||
| CH296340T | 1954-01-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH302024A true CH302024A (en) | 1954-09-30 |
Family
ID=25733681
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH302024D CH302024A (en) | 1950-07-03 | 1951-06-29 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH302024A (en) |
-
1951
- 1951-06-29 CH CH302024D patent/CH302024A/en unknown
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