CH194345A - Process for the preparation of a polyazo dye. - Google Patents
Process for the preparation of a polyazo dye.Info
- Publication number
- CH194345A CH194345A CH194345DA CH194345A CH 194345 A CH194345 A CH 194345A CH 194345D A CH194345D A CH 194345DA CH 194345 A CH194345 A CH 194345A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- diazotized
- green
- water
- polyazo
- Prior art date
Links
- -1 polyazo Polymers 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 3
- 239000000975 dye Substances 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 7
- 229920000742 Cotton Polymers 0.000 claims description 4
- 239000000243 solution Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
- 240000007817 Olea europaea Species 0.000 claims description 2
- 235000005811 Viola adunca Nutrition 0.000 claims description 2
- 235000013487 Viola odorata Nutrition 0.000 claims description 2
- 235000002254 Viola papilionacea Nutrition 0.000 claims description 2
- 244000172533 Viola sororia Species 0.000 claims description 2
- 239000012670 alkaline solution Substances 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical class [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 claims 1
- 244000154870 Viola adunca Species 0.000 claims 1
- 150000004699 copper complex Chemical class 0.000 claims 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 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
- 240000009038 Viola odorata Species 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010288 sodium nitrite 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/36—Trisazo dyes of the type
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Perfabren zur Herstellung eines Polyazofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Polya.zo- farbstoffes, dadurch gekennzeichnet, dass man diazotierte 4-Aminostilben-4'-azo-anisol- 2.2'-,disulfonsä@ure mit Aminohydroehinon- dimethyläther kuppelt,
den so erhaltenen Aminodisazofarbstoff diazotiert und in alka lischer Lösung mit 2-Naphthol-3. 6-disulfon- säure kuppelt.
Der so erhaltene Polyazofarbstoff löst sich in Wasser grün, in konzentrierter Schwefelsäure violett und färbt Baumwolle bei gutem Ziehvermögen blaustichig .grün. Die aus diesem Farbstoff hergestellte Kupfer- komplexverbindung gibt auf Baumwolle 0livfärbungen mit wesentlich verbesserter Lichtechtheit.
Ihre Lösungsfarbe in Wasser ist gelbstichig grün, in konzentrierter Bchwe- felsäure blauviolett: <I>Beispiel:</I> <B>51,1</B> Teile 4-Aminostilben-4'-azo-anisol- 2.2'-,disulfonsäure werden in der üblichen Weise diazotiert und in sodaalkalischer Lö- sung mit 15,2 Teilen A.minobydrochinon- dimethyläther gekuppelt und ,
gegebenenfalls der Farbstoff dureh Umlösen von überschüs siger Kupplungskomponente befreit. Dann wird mit 6,9 Teilen Natriumnitrit und -30 Teilen Salzsäure vom spezifischen Gewicht 1,18 diazotiert und in pyridinhaltiger Lösung mit 26 Teilen 2-naplhthol-3. 6-disulfonsaurem Natrium zusammengebracht. Nach Beendi gung der Kupplung wird der Farbstoff durch Aussalzen abgeschieden.
Perfabren for the production of a polyazo dye. The present patent relates to a process for the production of a polya.zo dye, characterized in that diazotized 4-aminostilbene-4'-azo-anisole-2.2 '-, disulfonic acid is coupled with aminohydroehinone dimethyl ether,
the aminodisazo dye thus obtained is diazotized and in alkali solution with 2-naphthol-3. 6-disulfonic acid couples.
The polyazo dye obtained in this way dissolves green in water and violet in concentrated sulfuric acid and dyes cotton with a bluish tinge of green with good drawability. The copper complex compound produced from this dye gives olive dyeings to cotton with significantly improved lightfastness.
Their solution color in water is yellowish green, in concentrated bulfuric acid blue-violet: <I> Example: </I> <B> 51.1 </B> parts 4-aminostilbene-4'-azo-anisole-2.2'- Disulfonic acid is diazotized in the usual way and coupled with 15.2 parts of A.minobydroquinone dimethyl ether in a soda-alkaline solution and,
if necessary, the dye is freed from excess coupling component by dissolving. It is then diazotized with 6.9 parts of sodium nitrite and -30 parts of hydrochloric acid with a specific weight of 1.18 and in a pyridine-containing solution with 26 parts of 2-naplhthol-3. 6-disulfonic acid sodium brought together. After the coupling has ended, the dye is deposited by salting out.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH188026T | 1935-12-04 | ||
| CH194345T | 1935-12-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH194345A true CH194345A (en) | 1937-11-30 |
Family
ID=25721604
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH194345D CH194345A (en) | 1935-12-04 | 1935-12-04 | Process for the preparation of a polyazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH194345A (en) |
-
1935
- 1935-12-04 CH CH194345D patent/CH194345A/en unknown
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