CH202742A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH202742A CH202742A CH202742DA CH202742A CH 202742 A CH202742 A CH 202742A CH 202742D A CH202742D A CH 202742DA CH 202742 A CH202742 A CH 202742A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- purple
- diphenylamine
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 6
- DMBHHRLKUKUOEG-UHFFFAOYSA-N N-phenyl aniline Natural products C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 150000008049 diazo compounds Chemical class 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims 1
- 239000003513 alkali Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003457 sulfones Chemical class 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen Azo- farbstoff erhält, wenn man die Diazoverbin- dung des 1-Amino-4-nitrobenzol-2-methylsul- fons mit (2-Äthogy-5-methyl-2'-sulfonsäure- 4' - o - chlorbenzoylamino) - diphenylamin der Formel
EMI0001.0012
vereinigt. Der neue Farbstoff bildet ein dunkles Pulver,
das sich in Wasser mit violet ter Farbe löst und das Wolle und Seide aus saurem Bade in violettblauen Tönen färbt.
Beispiel: 216 Teile 1.-Amino-4-nitrobenzol-2-metbyl-. sulfon werden diazotiert und in die mineral saure Lösung dieser Diazoverbindung die Lö sung des Natriumsalzes aus 460 Teilen (2- Äthoxy- 5 -methyl- 2'- sulfonsäure- 4'- o -Chlor- benzoylamino) - diphenylamin eingetragen.
Nachdem die Farbstoffbildung beendet ist, wird abfiltriert, der Farbstoff in Wasser sus- pendiert und durch Verrühren mit einem Alkali neutral gestellt. Der Farbstoff wird eventuell durch Zusatz eines Salzes ausge schieden, abfiltriert und getrocknet.
Process for the preparation of an azo dye. It has been found that an azo dye is obtained if the diazo compound of 1-amino-4-nitrobenzene-2-methylsulfone is used with (2-ethogy-5-methyl-2'-sulfonic acid-4 '- o - chlorobenzoylamino) - diphenylamine of the formula
EMI0001.0012
united. The new dye forms a dark powder,
which dissolves in water with a violet color and dyes the wool and silk from acid baths in violet-blue tones.
Example: 216 parts of 1.-amino-4-nitrobenzene-2-metbyl-. sulfone are diazotized and the solution of the sodium salt of 460 parts (2-ethoxy-5-methyl-2'-sulfonic acid-4'- o -chlorobenzoylamino) - diphenylamine entered into the mineral acid solution of this diazo compound.
After the formation of the dye has ended, it is filtered off, the dye is suspended in water and neutralized by stirring with an alkali. The dye is possibly separated out by adding a salt, filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH202742T | 1937-03-15 | ||
| CH200063T | 1938-11-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH202742A true CH202742A (en) | 1939-01-31 |
Family
ID=25723415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH202742D CH202742A (en) | 1937-03-15 | 1937-03-15 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH202742A (en) |
-
1937
- 1937-03-15 CH CH202742D patent/CH202742A/en unknown
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