CH196345A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH196345A CH196345A CH196345DA CH196345A CH 196345 A CH196345 A CH 196345A CH 196345D A CH196345D A CH 196345DA CH 196345 A CH196345 A CH 196345A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- amino
- preparation
- dye
- cyanobenzene
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- 239000000975 dye Substances 0.000 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 159000000000 sodium salts Chemical class 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- WFZFMHDDZRBTFH-CZEFNJPISA-N 2-[(e)-2-(5-carbamimidoyl-1-benzofuran-2-yl)ethenyl]-1-benzofuran-5-carboximidamide;dihydrochloride Chemical compound Cl.Cl.NC(=N)C1=CC=C2OC(/C=C/C=3OC4=CC=C(C=C4C=3)C(=N)N)=CC2=C1 WFZFMHDDZRBTFH-CZEFNJPISA-N 0.000 description 1
- YBAZINRZQSAIAY-UHFFFAOYSA-N 4-aminobenzonitrile Chemical compound NC1=CC=C(C#N)C=C1 YBAZINRZQSAIAY-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000009938 salting Methods 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
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/16—Naphthol-sulfonic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Azofar bstoffes. Es wurde gefunden, dass man einen Azo- färbstoff erhält, wenn man diazotiertes 1- Amino - 4 - cyanbenzol - 2 - methylsulfon in saurem Medium mit 1-Amino-5-oxynaphtha- lin-2-sulfonsäure vereinigt.
Der demgemäss erhaltene Farbstoff bildet in Form seines Natriumsalzes in trockenem Zustand ein dunkles Pulver, das sich in Wasser mit blauer Farbe löst und Wolle aus saurem Bade in echten blauen Tönen färbt. Beispiel: <B>19,6</B> Teile 1-Amino - 4 - cyanbenzol - 2 - me- thylsulfon werden nach gebräuchlichen Me thoden diazotiert und die saure Diazolösung mit einer neutralen Lösung des Natriumsalzes aus 28,
9- Teilen 1-Amino-5-Qxynaphthalin-2-- sulfonsäure versetzt. Der Farbstoff, fällt aus oder kann durch Zugabe von neutralisieren den und aussalzenden Mitteln abgeschieden werden.
Process for the production of an azo dye. It has been found that an azo dye is obtained when diazotized 1-amino-4-cyanobenzene-2-methylsulfone is combined with 1-amino-5-oxynaphthalin-2-sulfonic acid in an acidic medium.
The dyestuff thus obtained forms, in the dry state, a dark powder in the form of its sodium salt, which dissolves in water with a blue color and dyes wool from an acid bath in true blue tones. Example: <B> 19.6 </B> parts of 1-amino - 4 - cyanobenzene - 2 - methylsulfone are diazotized according to customary methods and the acidic diazo solution with a neutral solution of the sodium salt from 28,
9 parts of 1-amino-5-xynaphthalene-2-sulfonic acid are added. The dye precipitates or can be deposited by adding neutralizing and salting agents.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH196345T | 1936-12-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH196345A true CH196345A (en) | 1938-03-15 |
Family
ID=4440330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH196345D CH196345A (en) | 1936-12-31 | 1936-12-31 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH196345A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4618674A (en) * | 1983-12-30 | 1986-10-21 | Dellian Kurt A | Red-1-(cyanophenylazo- or cyano, halophenylazo)-2-amino-8-hydroxynaphthalene-6 sulfonic acid dyestuffs |
-
1936
- 1936-12-31 CH CH196345D patent/CH196345A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4618674A (en) * | 1983-12-30 | 1986-10-21 | Dellian Kurt A | Red-1-(cyanophenylazo- or cyano, halophenylazo)-2-amino-8-hydroxynaphthalene-6 sulfonic acid dyestuffs |
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