Mipafox
Mipafox is a highly toxic organophosphate insecticide that can cause delayed neurotoxicity and paralysis.[1] It is an irreversible acetylcholinesterase inhibitor that is resistant to oxime reactivators.[2]
Names | |
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IUPAC name
N,N′-Diisopropylphosphorodiamidic fluoride | |
Other names
Bis(isopropylamino)fluorophosphine oxide; Isopestox | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.006.130 |
EC Number |
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KEGG | |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C6H16FN2OP | |
Molar mass | 182.179 g·mol−1 |
Density | 1.2 |
Melting point | 65 °C (149 °F; 338 K) |
Boiling point | 125 °C (257 °F; 398 K) |
80 g/L | |
Hazards | |
Main hazards | Highly toxic |
GHS pictograms | |
GHS Signal word | Danger |
H301, H370 | |
P260, P264, P270, P301+310, P307+311, P321, P330, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Synthesis
Phosphoryl chloride is reacted with isopropylamine. The resulting product is then reacted with potassium fluoride or ammonium fluoride to form mipafox.[3]
References
- BIDSTRUP, PL; BONNELL, JA; BECKETT, AG (16 May 1953). "Paralysis following poisoning by a new organic phosphorus insecticide (mipafox); report on two cases". British Medical Journal. 1 (4819): 1068–72. doi:10.1136/bmj.1.4819.1068. PMC 2016450. PMID 13042137.
- Mangas, I; Taylor, P; Vilanova, E; Estévez, J; França, TC; Komives, E; Radić, Z (March 2016). "Resolving pathways of interaction of mipafox and a sarin analog with human acetylcholinesterase by kinetics, mass spectrometry and molecular modeling approaches". Archives of Toxicology. 90 (3): 603–16. doi:10.1007/s00204-015-1481-1. PMC 4833118. PMID 25743373.
- "Process for the preparation of bisisopropyl-amino-fluoro-phosphine oxide".
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