CH204451A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH204451A CH204451A CH204451DA CH204451A CH 204451 A CH204451 A CH 204451A CH 204451D A CH204451D A CH 204451DA CH 204451 A CH204451 A CH 204451A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new dye
- dye
- new
- pyridine
- Prior art date
Links
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 8
- 239000000975 dye Substances 0.000 claims description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 239000005711 Benzoic acid Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/325—Dyes with no other substituents than the amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 200368. Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen lös lichen Farbstoff erhält, wenn man auf 1.4- Di-(p-amiriophenyl)-aminoanthraohinon in Ge genwart von Pyridin 2 Mol Benzoesäure-3- sulfochlorid einwirken lässt. Das neue Pro dukt bildet ein dunkles Pulver, das sich in Wasser mit blauer Farbe löst und Wolle aus saurein Bade grünblau färbt.
<I>Beispiel;</I> 21 Teile 1.4-Di-(p-aminophenyl)-amino- antbrachinon, 66 Teile Benzoesäure-3-sulfo- ohlorid und 300 Teile Pyridin werden so lange bei 90-100 verrührt, bis eine Probe des Produktes in angesäuertem Wasser löslich wird. Nach dem Abdestillieren des Pyridins wird der Rückstand in Wasser gelöst; die Lösung mit Natriumearbonat alkalisch ge stellt, kurze Zeit erwärmt und der Farbstoff mit Natriumchlorid gefällt.
Additional patent to main patent no. 200368. Process for the production of a new dye. It has been found that a soluble dye is obtained if 2 moles of benzoic acid-3-sulfochloride are allowed to act on 1,4-di- (p-amiriophenyl) -aminoanthraohinone in the presence of pyridine. The new product forms a dark powder that dissolves in water with a blue color and dyes wool from acidic baths green-blue.
<I> Example; </I> 21 parts of 1,4-di- (p-aminophenyl) -amino-antbrachinone, 66 parts of benzoic acid-3-sulfochloride and 300 parts of pyridine are stirred at 90-100 until a sample is obtained of the product becomes soluble in acidified water. After the pyridine has been distilled off, the residue is dissolved in water; the solution is made alkaline with sodium carbonate, warmed for a short time and the dye is precipitated with sodium chloride.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH204451T | 1936-12-16 | ||
| CH200368T | 1936-12-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH204451A true CH204451A (en) | 1939-04-30 |
Family
ID=25723470
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH204451D CH204451A (en) | 1936-12-16 | 1936-12-16 | Process for the production of a new dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH204451A (en) |
-
1936
- 1936-12-16 CH CH204451D patent/CH204451A/en unknown
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