|  | |
| Names | |
|---|---|
| Preferred IUPAC name 2-(Butan-2-yl)-4,6-dinitrophenyl 3-methylbut-2-enoate | |
| Other names 2-[(2RS)-Butan-2-yl]-4,6-dinitrophenyl 3-methylbut-2-enoate (RS)-2-(Butan-2-yl)-4,6-dinitrophenyl 3-methylbut-2-enoate (RS)-2-sec-Butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Dapacryl Morocide Morrocid Acricid Endosan Ambox Dinoseb methacrylate | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.006.921 | 
| EC Number | 
 | 
| KEGG | |
| PubChem CID | |
| RTECS number | 
 | 
| UNII | |
| UN number | 2779 | 
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C15H18N2O6 | |
| Molar mass | 322.317 g·mol−1 | 
| Density | 1.2 g/cm3 | 
| Melting point | 66 to 67 °C (151 to 153 °F; 339 to 340 K) | 
| Insoluble | |
| Hazards | |
| GHS labelling: | |
|    | |
| Danger | |
| H302, H312, H360, H410 | |
| P201, P202, P264, P270, P273, P280, P281, P301+P312, P302+P352, P308+P313, P312, P322, P330, P363, P391, P405, P501 | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Binapacryl was used as a miticide and fungicide. Chemically, it is an ester derivative of dinoseb. Although binapacryl has low toxicity itself, it is readily metabolized to form dinoseb, which is highly toxic.[1]
International trade in binapacryl is regulated by the Rotterdam Convention; it has been withdrawn as a pesticide, since products were highly toxic to mammals, fish and aquatic invertebrates.[2]
References
- 1 2 Datasheet from International Programme on Chemical Safety
- ↑ Pesticide Properties DataBase: Binapacryl
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