Imiprothrin
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| Names | |
|---|---|
| Preferred IUPAC name
[2,5-Dioxo-3-(prop-2-yn-1-yl)imidazolidin-1-yl]methyl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropane-1-carboxylate | |
| Other names
Pralle; Multicide
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| Identifiers | |
3D model (
JSmol ) |
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| ChEBI | |
| ChemSpider | |
ECHA InfoCard
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100.106.762 |
| EC Number |
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C17H22N2O4 | |
| Molar mass | 318.373 g·mol−1 |
| Appearance | Golden yellow liquid |
| Odor | Slightly sweet |
| Density | 0.979 g/mL |
| Hazards | |
| GHS labelling: | |
 
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| Warning | |
| H302, H410 | |
| P264, P270, P273, P301+P312, P330, P391, P501 | |
| Flash point | 110 °C (230 °F; 383 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Imiprothrin is a synthetic
dermal routes, but to insects it acts as a neurotoxin causing paralysis. It is effective against cockroaches, waterbugs, ants, silverfish, crickets and spiders, among others.[2]
References
- ^ Imiprothrin at Sigma-Aldrich
- ^ U. S. Environmental Protection Agency, March 1998.