CH292302A - 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
- CH292302A CH292302A CH292302DA CH292302A CH 292302 A CH292302 A CH 292302A CH 292302D A CH292302D A CH 292302DA CH 292302 A CH292302 A CH 292302A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- acid
- anthraquinone series
- brominating agent
- amino
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 7
- 239000002253 acid Substances 0.000 title claims description 4
- 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 claims description 3
- 239000000975 dye Substances 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 239000004677 Nylon Substances 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 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
- 210000004243 sweat Anatomy 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 230000031709 bromination Effects 0.000 claims 1
- 238000005893 bromination reaction Methods 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 description 2
- 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
- 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)
- 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. CTegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines sauren Talldarbstoffes der Anthrachinonreihe, wel ches darin besteht, dass man 1-Amino-4-(5',6', 7'. #S' - teti-ahydr onaplithyl -1' );
-a.minoanthraehi- noti '-'-stilfonsäure durch Behandeln mit einem 1)i-oniierenden Mittel in den dibromierten Ab- könumling überführt.
<I>Beispiel:</I> 47,0 Teile 1-amiiio-l-(5',6',7',8-'tetrahydro- napht hyl-1') -aminoanthrachinon - 2 - sulfonsau- res Natrium werden in 1500 Teilen 90 % iger Seliwefelsäure gelöst.
Man versetzt die Lösung finit 26 Teilen Brom und rührt die Masse 6 Stunden lang bei Raumtemperatur und her nach noch 0' Stunden lang bei 60 .
Naeh dem Aufarbeiten erhält man einen Farbstoff, der sich in Wasser mit rotstichig blauer Farbe löst. In konzentrierter Schwefel säure ist seine Lösungsfarbe klar blau; sie schlägt beim Zusatz von Paraformaldehyd nach grünblau um.
Der neue Farbstoff färbt Wolle und an dere tierische Fasern sowie Nylon in klaren, rotstieliig blauen Tönen von hervorragender Schweiss- und Walkechtheit und besitzt ferner ein ausgezeichnetes Neutralziehvermögen.
<B> Additional patent </B> to main patent no. 287563. Process for the production of an acidic fulled dyestuff of the anthraquinone series. The subject matter of the present patent is a process for the preparation of an acidic tall dari of the anthraquinone series, which consists in that 1-amino-4- (5 ', 6', 7 '. ;
-a.minoanthraehi- noti '-'- stilfonic acid by treatment with a 1) i-oniating agent in the dibrominated Ab- transferred.
<I> Example: </I> 47.0 parts of 1-amiiio-1- (5 ', 6', 7 ', 8-' tetrahydronaphthyl-1 ') -aminoanthraquinone - 2 - sulphonic acid sodium dissolved in 1500 parts of 90% strength seliulfuric acid.
26 parts of bromine are added to the solution, and the mass is stirred for 6 hours at room temperature and after a further 0 'hours at 60.
After working up, a dye is obtained which dissolves in water with a reddish blue color. In concentrated sulfuric acid, its solution color is clear blue; it changes to green-blue when paraformaldehyde is added.
The new dye dyes wool and other animal fibers as well as nylon in clear, red-stemmed blue shades of excellent sweat and milled fastness and also has excellent neutral drawability.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH287563T | 1950-09-27 | ||
| CH292302T | 1950-09-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH292302A true CH292302A (en) | 1953-07-31 |
Family
ID=25732733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH292302D CH292302A (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) | CH292302A (en) |
-
1950
- 1950-09-27 CH CH292302D patent/CH292302A/en unknown
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