CH249010A - Process for the preparation of a metallizable trisazo dye. - Google Patents
Process for the preparation of a metallizable trisazo dye.Info
- Publication number
- CH249010A CH249010A CH249010DA CH249010A CH 249010 A CH249010 A CH 249010A CH 249010D A CH249010D A CH 249010DA CH 249010 A CH249010 A CH 249010A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- mol
- metallizable
- copper
- preparation
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 4
- 239000000975 dye Substances 0.000 claims description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 150000004699 copper complex Chemical class 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- 229920000297 Rayon Polymers 0.000 claims description 2
- 150000001844 chromium Chemical class 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 239000002964 rayon Substances 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical group C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 238000009835 boiling 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/36—Trisazo dyes of the type
- C09B35/366—D is diphenyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 243336. Verfahren zur Herstellung eines metallisierbaren Trisazofarbstoffes: Das vorliegende Patent betrifft ein Ver fahren zur Herstellung eines neuen metalli- sierbaren Trisazofarbstoffes und ist dadurch gekennzeichnet, dass man den Kupfer komplex des Trisazofarbstoffes, aus.
1 Mol 3,3'-Dimethoxy-4,4'-,diaminodiphenyl alka lisch mit 1 Mol 2-Amino-8-oxynaphthalin-6- sulfonsäure kombiniert, weiterdiazotiert und mit 2 Mol 1,8-Dioxynaphthalin-4-sulfonsäure gekuppelt mit konzentrierter Salzsäure ent- kupfert.
<I>Beispiel:</I> 1 Teil des Kupferkomplexes des Trisazo- fa,rbstoffes aus 1 Mol 3,3'-Dimethoxy-4,4'-di- aminodiphenyl alkalisch mit 1 Mol 2-Amino- 8-oxynaphthalin-6-sulfonsäure kombiniert, weiterdiazotiert und mit 2M01 1,8-Dioxy- na.phtha_lin-4-.sulfonsäure gekuppelt, wird in 6 Teilen Wasser aufgeschlämmt,
bei Siede temperatur langsam mit 10 Teilen konzen trierter Salzsäure versetzt und 3/4 Stunden am Rührwerk rückfliessend gekocht und dann filtriert. Der kupferfreie Farbstoff wird in das Na-Salz umgewandelt und getrocknet. Er stellt so ein schwarzes Pulver dar, das sich in Wasser und in konzentrierter Schwe felsäure mit blauer Farbe löst. Der Farb stoff färbt Zellwolle dunkelblau, mit Kup fer- und Chromsalzen nachbehandelt licht- und waschecht grau.
<B> Additional patent </B> to main patent no. 243336. Process for the production of a metallizable trisazo dye: The present patent relates to a process for the production of a new metallizable trisazo dye and is characterized in that the copper complex of the trisazo dye is made .
1 mole of 3,3'-dimethoxy-4,4 '-, diaminodiphenyl alka cally combined with 1 mole of 2-amino-8-oxynaphthalene-6-sulfonic acid, further diazotized and coupled with 2 moles of 1,8-dioxynaphthalene-4-sulfonic acid concentrated hydrochloric acid decoppered.
<I> Example: </I> 1 part of the copper complex of Trisazofa, dye from 1 mol of 3,3'-dimethoxy-4,4'-di-aminodiphenyl alkaline with 1 mol of 2-amino-8-oxynaphthalene-6 -sulfonic acid combined, further diazotized and coupled with 2M01 1,8-Dioxy- na.phtha_lin-4-.sulfonic acid, is suspended in 6 parts of water,
slowly mixed with 10 parts of concentrated hydrochloric acid at boiling temperature and refluxed for 3/4 hours on a stirrer and then filtered. The copper-free dye is converted into the sodium salt and dried. It is a black powder that dissolves in water and concentrated sulfuric acid with a blue color. The dye dyes rayon staple dark blue, treated with copper and chromium salts, lightfast and washable gray.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH249010T | 1945-02-12 | ||
| CH243336T | 1945-02-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH249010A true CH249010A (en) | 1947-05-31 |
Family
ID=25728816
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH249010D CH249010A (en) | 1945-02-12 | 1945-02-12 | Process for the preparation of a metallizable trisazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH249010A (en) |
-
1945
- 1945-02-12 CH CH249010D patent/CH249010A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE734240C (en) | Process for the production of chromable dyes of the phthalein series | |
| DE445729C (en) | Process for the preparation of Bz-2-oxybenzanthrone | |
| CH260860A (en) | Process for the production of a new azo dye. | |
| CH308405A (en) | Process for the preparation of a monoazo dye. | |
| CH221174A (en) | Process for the preparation of a stilbene dye. | |
| CH293362A (en) | Process for the preparation of a substantive azo dye. | |
| CH202747A (en) | Process for the preparation of an azo dye. | |
| CH263506A (en) | Process for the preparation of an azo dye. | |
| CH311042A (en) | Process for the preparation of a yellow monoazo dye. | |
| CH275080A (en) | Process for the preparation of a stilbene dye. | |
| CH131253A (en) | Process for the production of a new azo dye. | |
| CH237130A (en) | Process for the production of a new azo dye. | |
| CH292653A (en) | Process for the preparation of a substantive azo dye. | |
| CH202741A (en) | Process for the preparation of an azo dye. | |
| CH241145A (en) | Process for the preparation of a new disazo dye. | |
| CH220748A (en) | Process for the preparation of a new pyrazolone derivative. | |
| CH197279A (en) | Process for the preparation of an azo dye. | |
| CH266278A (en) | Process for the preparation of an o, o'-dioxyazo dye. | |
| CH292654A (en) | Process for the preparation of a substantive azo dye. | |
| CH238336A (en) | Process for the preparation of a new disazo dye. | |
| CH199371A (en) | Process for the preparation of an azo dye. | |
| CH239330A (en) | Process for the preparation of a disazo dye. | |
| CH169693A (en) | Process for the preparation of a chromium-containing azo dye. | |
| CH199368A (en) | Process for the preparation of an azo dye. | |
| CH202749A (en) | Process for the preparation of an azo dye. |