Binapacryl
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Names | |
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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 | |
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3D model (JSmol) |
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ChEBI |
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ChEMBL |
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ChemSpider |
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ECHA InfoCard | 100.006.921 ![]() |
EC Number |
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PubChem CID |
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UNII |
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UN number | 2779 |
CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | 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) |
Solubility in water | Insoluble |
Hazards | |
GHS labelling: | |
Pictograms | ![]() ![]() ![]() |
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 |
Chemical compound
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International trade in binapacryl is regulated by the Rotterdam Convention; it has been withdrawn as a pesticide, since products were highly toxic to mammals, fish and aquatic invertebrates.[2]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
- ^ a b Datasheet from International Programme on Chemical Safety
- ^ Pesticide Properties DataBase: Binapacryl