|  | |
| Names | |
|---|---|
| Preferred IUPAC name 2,3-Dimethylaniline | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.001.596 | 
| EC Number | 
 | 
| PubChem CID | |
| RTECS number | 
 | 
| UNII | |
| UN number | 1711 | 
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C8H11N | |
| Molar mass | 121.183 g·mol−1 | 
| Appearance | colorless liquid | 
| Melting point | 3.5 °C (38.3 °F; 276.6 K) | 
| Boiling point | 222 °C (432 °F; 495 K) | 
| Hazards | |
| GHS labelling: | |
|    | |
| Warning | |
| H301, H311, H331, H373, H411 | |
| P260, P261, P264, P270, P271, P273, P280, P301+P310, P302+P352, P304+P340, P311, P312, P314, P321, P322, P330, P361, P363, P391, P403+P233, P405, P501 | |
| Flash point | 97 °C (207 °F; 370 K) | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
2,3-Xylidine is the organic compound with the formula C6H3(CH3)2NH2. it is one of several isomeric xylidines. It is a colorless viscous liquid. The compound is used in the production of the drug mefenamic acid and the herbicide xylachlor.[1]
References
- ↑ M. Meyer (2012). "Xylidines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a28_455. ISBN 978-3527306732.
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