CH292303A - Process for the production of an acid milled dye of the anthraquinone series. - Google Patents
Process for the production of an acid milled dye of the anthraquinone series.Info
- Publication number
- CH292303A CH292303A CH292303DA CH292303A CH 292303 A CH292303 A CH 292303A CH 292303D A CH292303D A CH 292303DA CH 292303 A CH292303 A CH 292303A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- anthraquinone series
- brominating agent
- production
- treatment
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 7
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 title claims description 4
- 150000004056 anthraquinones Chemical class 0.000 title claims description 4
- 238000004519 manufacturing process Methods 0.000 title description 2
- 239000002253 acid Substances 0.000 title 1
- 239000000975 dye Substances 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 239000004677 Nylon Substances 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- 229920001778 nylon Polymers 0.000 claims description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- 230000031709 bromination Effects 0.000 claims 1
- 238000005893 bromination reaction Methods 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- 210000002268 wool Anatomy 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
- C09B1/343—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in the anthracene nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 287563. Verfahren zur Herstellung eines sauren Walkfarbstoffes der Anthrachinonreihe. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines sauren Wallfarbstoffes der Anthrachinonreihe, wel ches darin besteht, dass man 1-Amino-4 (4'-benzoylamino)-phenylaminoanthraehinon- 2-sulfonsällre durch Behandeln mit einem bromfierenden Mittel in den dibromierten Ab kömmling überführt.
Beispiel: 53,5 Teile 1-amino-4- (4'-benzoylamino)- plienyiaminoanthrachinon-2-sulfonsaures Na trium werden in 1200 Teilen 96 % iger Schwe felsäure gelöst und mit 24 Teilen Brom ver setzt. Man rührt 48 Stunden lang bei Raum temperatur und arbeitet den Farbstoff auf. Er ist ein rötlicllblaues Pulver, das sich in Wasser mit rotstichig blauer Farbe löst.
Seine Lösungsfarbe in konzentrierter Schwefelsäure ist rotstichig blau; beim Zusatz von Paraform- aldehyd erfolgt ein Umschlag nach Grün.
Der neue Farbstoff färbt urolle und andere tierische Fasern sowie Nylon in klaren, rot- stiehig blauen Tönen von hervorragender 'Valkeehtheit und guter Liehtechtheit und be sitzt ferner ein ausgezeichnetes Neutra.lzieh- vermögen.
<B> Additional patent </B> to main patent no. 287563. Process for the production of an acidic fulled dyestuff of the anthraquinone series. The subject of the present patent is a process for the preparation of an acidic wall dye of the anthraquinone series, wel Ches consists in that 1-amino-4 (4'-benzoylamino) -phenylaminoanthraehinone-2-sulfonsällre by treating with a brominating agent in the dibrominated from convicted.
Example: 53.5 parts of 1-amino-4- (4'-benzoylamino) - plienyiaminoanthraquinone-2-sulfonic acid sodium are dissolved in 1200 parts of 96% sulfuric acid and 24 parts of bromine are added. The mixture is stirred for 48 hours at room temperature and the dye is worked up. It is a reddish blue powder that dissolves in water with a reddish blue color.
Its solution color in concentrated sulfuric acid is a reddish blue; when paraformaldehyde is added, the color changes to green.
The new dye dyes urolla and other animal fibers as well as nylon in clear, reddish-blue shades of excellent valkyfastness and good lightfastness, and also has excellent neutral properties.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH287563T | 1950-09-27 | ||
| CH292303T | 1950-09-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH292303A true CH292303A (en) | 1953-07-31 |
Family
ID=25732734
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH292303D CH292303A (en) | 1950-09-27 | 1950-09-27 | Process for the production of an acid milled dye of the anthraquinone series. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH292303A (en) |
-
1950
- 1950-09-27 CH CH292303D patent/CH292303A/en unknown
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