Binapacryl
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]
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| Names | |
|---|---|
| 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) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.006.921 |
| EC Number |
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| KEGG | |
PubChem CID |
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| RTECS number |
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| UNII | |
| UN number | 2779 |
CompTox Dashboard (EPA) |
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| 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 pictograms |    |
| GHS Signal word | Danger |
GHS hazard statements |
H302, H312, H360, H400, H410 |
| P201, P202, P264, P270, P273, P280, P281, P301+312, P302+352, P308+313, 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). | |
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| Infobox references | |
International trade in binapacryl is regulated by the Rotterdam Convention; it has been withdrawn as a pesticide, since products were highly toxic to mammals, fish and aquatic invertebrates.[2]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
- Datasheet from International Programme on Chemical Safety
- Pesticide Properties DataBase: Binapacryl
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