AT47155B - Process for the preparation of disazo dyes for wool. - Google Patents
Process for the preparation of disazo dyes for wool.Info
- Publication number
- AT47155B AT47155B AT47155DA AT47155B AT 47155 B AT47155 B AT 47155B AT 47155D A AT47155D A AT 47155DA AT 47155 B AT47155 B AT 47155B
- Authority
- AT
- Austria
- Prior art keywords
- wool
- preparation
- disazo dyes
- dyes
- yellow
- Prior art date
Links
- 210000002268 wool Anatomy 0.000 title claims description 5
- 238000000034 method Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title claims description 3
- 239000000975 dye Substances 0.000 title description 9
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- CWJQQASJVVAXKL-UHFFFAOYSA-N 4-(3-Methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonic acid Chemical compound O=C1CC(C)=NN1C1=CC=C(S(O)(=O)=O)C=C1 CWJQQASJVVAXKL-UHFFFAOYSA-N 0.000 description 1
- QYIMZXITLDTULQ-UHFFFAOYSA-N 4-(4-amino-2-methylphenyl)-3-methylaniline Chemical compound CC1=CC(N)=CC=C1C1=CC=C(N)C=C1C QYIMZXITLDTULQ-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Coloring (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung von Disazofarbstoffen für Wolle.
In der Stammpatentschrift Nr. 46876 sind Disazofarbstoffe beschrieben, welche durch Kombination der Tetrazo\'orbindl1ng des m-Tolidins der Konstitution
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anfärben und auch ohne Nachbehandlung mit Chromsalzen gegen weisse Wolle und Baum- wolle walkecht sind.
Es wurde nun gefunden, dass man in diesen Farbstoffen ein Motekül Pyrazolonderivat durch ein Molekül einer ortho-Oxykarbonsäure der Benzolreihe ersetzen kann und so gleichfalls zu gelben walkechten Wolifarbstoffen gelangt.
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10#6 Teile m-toluidin werden tetrazotiert und unter Eiskühlung mit einer sodaalkatischen Losung von 7#2 Teilen Salicylsüure kombiniert. Nach Bildung des Zwischenproduktes gibt man eine mit Soda neutralisierte Lösung von 13 Teilen 1-p-Sulfophenyl-3-methyl-5-pyrazolon hinzu und rührt bis zur Vollendung der Farbstoffbildung. Dann wird auf 70 erwärmt und der Farbstoff mit Salz gefüllt. Kr färbt Wolle gelb.
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**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for the preparation of disazo dyes for wool.
In the parent patent specification No. 46876 disazo dyes are described, which by combining the tetrazo \ 'orbindlng of the m-tolidine of the constitution
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dye and are millfast even without after-treatment with chromium salts against white wool and cotton.
It has now been found that a Motekül pyrazolone derivative in these dyes can be replaced by a molecule of an ortho-oxycarboxylic acid of the benzene series and thus yellow milled Woli dyes are also obtained.
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10 # 6 parts of m-toluidine are tetrazotized and combined with a soda-alkaline solution of 7 # 2 parts of salicylic acid while cooling with ice. After formation of the intermediate product, a solution of 13 parts of 1-p-sulfophenyl-3-methyl-5-pyrazolone neutralized with soda is added and the mixture is stirred until the dye has formed. Then it is heated to 70 and the dye is filled with salt. Kr dyes wool yellow.
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** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE46876X | 1909-05-15 | ||
| DE47155X | 1909-05-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT47155B true AT47155B (en) | 1911-03-27 |
Family
ID=25749041
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT47155D AT47155B (en) | 1909-05-15 | 1910-04-23 | Process for the preparation of disazo dyes for wool. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT47155B (en) |
-
1910
- 1910-04-23 AT AT47155D patent/AT47155B/en active
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