CH215830A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH215830A CH215830A CH215830DA CH215830A CH 215830 A CH215830 A CH 215830A CH 215830D A CH215830D A CH 215830DA CH 215830 A CH215830 A CH 215830A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- color
- preparation
- blue
- tinged
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- 239000000975 dye Substances 0.000 claims description 5
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 claims description 3
- WASQBNCGNUTVNI-UHFFFAOYSA-N 2-amino-4,6-dichlorophenol Chemical compound NC1=CC(Cl)=CC(Cl)=C1O WASQBNCGNUTVNI-UHFFFAOYSA-N 0.000 claims description 3
- 150000008049 diazo compounds Chemical class 0.000 claims description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Azofarbstoffes, dadurch gekennzeichnet, dass man die Diazo- verbindung von 4,6-Dichlor-2-aminophenol mit dem N-Phenylharnstoff der 1-Amino-7-oxy- naphthalin-3-sulfonsäure vereinigt.
Der so erhaltene Farbstoff ist getrocknet ein dunkles Pulver, das sich in Na.trium- carbonatlösung mit blauer, in konzentrierter Schwefelsäure mit blaustichigroter Farbe löst. Er färbt Wolle aus saurem Bade in violetten Tönen, die beim Chromieren in ein grün- stichiges Blaugrau von ausgezeichneten Echt heitseigenschaften und schöner Abendfarbe übergehen.
<I>Beispiel:</I> 17,8 Teile 4,6-Dichlor-2-aminophenol wer den diazotiert und die Diazoverbindung ab geschieden. Die so erhaltene Paste trägt man in eine mit überschüssigem Natriumcarbonat versetzte Lösung von 35,8 Teilen N-Phenyl- harnstoff der 1 - Amino -7- oxynaphthalin - 3 - sulfonsäure ein und rührt, bis die Kupplung beendet ist. Der Farbstoff wird abgeschieden und getrocknet.
Process for the preparation of an azo dye. The present patent relates to a process for the production of an azo dye, characterized in that the diazo compound of 4,6-dichloro-2-aminophenol with the N-phenylurea of 1-amino-7-oxynaphthalene-3-sulfonic acid united.
The dye obtained in this way is dried, a dark powder which dissolves in sodium carbonate solution with a blue color and in concentrated sulfuric acid with a bluish-tinted red color. It dyes wool from an acid bath in violet tones, which when chromed turn into a green-tinged blue-gray with excellent fastness properties and a beautiful evening color.
<I> Example: </I> 17.8 parts of 4,6-dichloro-2-aminophenol are diazotized and the diazo compound is separated off. The paste obtained in this way is introduced into a solution of 35.8 parts of N-phenylurea of 1-amino-7-oxynaphthalene-3-sulfonic acid, to which excess sodium carbonate has been added, and the mixture is stirred until the coupling has ended. The dye is deposited and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE215830X | 1939-02-18 | ||
| CH211927T | 1939-03-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH215830A true CH215830A (en) | 1941-07-15 |
Family
ID=25725120
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH215830D CH215830A (en) | 1939-02-18 | 1939-03-23 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH215830A (en) |
-
1939
- 1939-03-23 CH CH215830D patent/CH215830A/en unknown
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