CH118968A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH118968A CH118968A CH118968DA CH118968A CH 118968 A CH118968 A CH 118968A CH 118968D A CH118968D A CH 118968DA CH 118968 A CH118968 A CH 118968A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- new
- oxyazo
- formaldehyde
- violet
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 claims description 4
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- 238000005859 coupling reaction Methods 0.000 claims description 3
- 241000974482 Aricia saepiolus Species 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000008049 diazo compounds Chemical class 0.000 claims description 2
- DXRFSTNITSDOKK-UHFFFAOYSA-N formaldehyde;sulfurous acid Chemical compound O=C.OS(O)=O DXRFSTNITSDOKK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/08—Preparation of azo dyes from other azo compounds by reduction
-
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man den o-Oxyazo- farbstoff, der erhalten wird durch Reduzie ren des Kupplungsproduktes der nitrierten Diazoverbindung der 1-Amino-2-oxynaph- thalin-4-sulfosäure mit f8-Naphthol in des sen co-Methansulfosäurederivat überführt,
zum Beispiel durch Behandeln mit Formal dehyd und Bisulfit oder formaldehydschwef- liger Säure bezw. deren Salzen. Der neue Farbstoff bildet ein schwarzes Pulver, das sich in Wasser mit violettbrauner, in ver dünnter Natronlauge mit schwärzlich vio- lettbrauner und in Sololösung mit grünlich blauer Farbe löst. Im Gegensatz zum Aus gangsfarbstoff ist das neue Produkt schon in kaltem Wasser löslich und bleibt auch nach -Versetzen seiner Lösungen xnit Mine ralsäure gelöst.
Beispiel 450 Teile des o-Oxyazofarbstoffes, der erhalten wird durch Reduzieren des Kupp lungsproduktes der nitrierten Diazoverbin- Jung der 1-Amino-2-oxynaphthalin-4-sulfo- säure mit ss-Naphthol, zweckmässig in Form des frisch hergestellten Reduktionsansatzes, werden mittelst 45 Teilen Ätznatron in zirka 8000 Teilen Wasser bei<B>50'</B> gelöst, worauf man eine Mischung von 100 Teilen 35 %iges Formaldehyd und 28,5 Teilen 40 %iger Natriumbisulfitlauge beifügt.
Man rührt einige Zeit und versetzt hierauf mit so viel 10 %iger Essigsäure, bis die intensiv blaue Farbe der Lösung nach violett umge schlagen ist, salzt aus und filtriert.
Process for the production of a new dye. It has been found that a new dye is obtained if the o-oxyazo dye, which is obtained by reducing the coupling product of the nitrated diazo compound of 1-amino-2-oxynaphthalene-4-sulfonic acid with f8-naphthol in the sen co-methanesulfonic acid derivative transferred,
for example, by treatment with formaldehyde and bisulfite or formaldehyde-sulphurous acid respectively. their salts. The new dye forms a black powder that dissolves in water with a violet-brown color, in diluted sodium hydroxide solution with a blackish violet-brown color, and in a solo solution with a greenish-blue color. In contrast to the starting dye, the new product is already soluble in cold water and remains dissolved even after its solutions have been mixed with mineral acid.
Example 450 parts of the o-oxyazo dye, which is obtained by reducing the coupling product of the nitrated Diazoverbin- Jung of 1-amino-2-oxynaphthalene-4-sulfonic acid with β-naphthol, expediently in the form of the freshly prepared reduction mixture, are averaged 45 parts of caustic soda are dissolved in about 8000 parts of water at <B> 50 '</B>, whereupon a mixture of 100 parts of 35% formaldehyde and 28.5 parts of 40% sodium bisulphite liquor is added.
The mixture is stirred for some time and then mixed with 10% acetic acid until the intense blue color of the solution has turned violet, salted out and filtered.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH118968T | 1927-02-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH118968A true CH118968A (en) | 1927-02-16 |
Family
ID=4377942
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH118968D CH118968A (en) | 1927-02-16 | 1925-09-24 | Process for the production of a new dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH118968A (en) |
-
1925
- 1925-09-24 CH CH118968D patent/CH118968A/en unknown
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