|Synonyms||isofluorophate, isofluorphate, DFP, DIFP, DIPF, diisopropyl phosphorofluoridate, PF-3, PF3, T-1703, TL 466|
|Chemical and physical data|
|Molar mass||184.146 g/mol|
|3D model (JSmol)|
|Melting point||−82 °C (−116 °F)|
|Boiling point||183 °C (361 °F) 1013 mbar|
Diisopropyl fluorophosphate is an oily, colorless liquid with the chemical formula C6H14FO3P. It is used in medicine and as an organophosphorus insecticide. It is stable, but undergoes hydrolysis when subjected to moisture, producing hydrofluoric acid.
Uses in medicine
Diisopropyl fluorophosphate is a parasympathomimetic drug irreversible anti-cholinesterase and has been used in ophthalmology as a miotic agent in treatment of chronic glaucoma, as a miotic in veterinary medicine, and as an experimental agent in neuroscience because of its acetylcholinesterase inhibitory properties and ability to induce delayed peripheral neuropathy.
Uses as toxin
The marked toxicity of esters of monofluorophosphoric acid was discovered in 1932, when Willy Lange and his PhD student Gerda von Krueger prepared the methyl, ethyl, n-propyl, and n-butyl esters and incidentally experienced their toxic effects. Another homologue of this series of esters, Diisopropyl fluorophosphate, was developed by British scientist Bernard Charles Saunders. On his search for compounds to be used as chemical warfare agents, Saunders was inspired by the report by Lange and Krueger and decided to prepare the new homologue which he labeled PF-3. It was much less effective as a chemical weapon than the G series agents. It was often mixed with mustard gas, forming a more effective mixture with significantly lower melting point, resulting in an agent suitable for use in cold weather.
In military research, due to its physical and chemical similarities and comparatively low toxicity, it is used as a simulant of G-agents (GA, GB, GD, and GF). Diisopropyl fluorophosphate is used in civilian laboratories to mimic lethal nerve gas exposure or organophosphate toxicities. It has also been used to develop a rodent model of Gulf War Syndrome.
Diisopropyl fluorophosphate is a very potent neurotoxin. Its LD50 in rats is 6 mg/kg (oral). It combines with the amino acid serine at the active site of the enzyme acetylcholinesterase, an enzyme that deactivates the neurotransmitter acetylcholine. Neurotransmitters are needed to continue the passage of nerve impulses from one neuron to another across the synapse. Once the impulse has been transmitted, acetylcholinesterase functions to deactivate the acetylcholine almost immediately by breaking it down. If the enzyme is inhibited, acetylcholine accumulates and nerve impulses cannot be stopped, causing prolonged muscle contraction. Paralysis occurs and death may result since the respiratory muscles are affected.
DFP also inhibits some proteases. It is a useful additive for protein or cell isolation procedure.
Isoflurophate, the diisopropyl ester of fluorophosphoric acid, is made by reacting isopropyl alcohol with phosphorus trichloride, forming diisopropylphosphite, which is chlorinated and further reacted with sodium fluoride to replace the chlorine atom with fluorine, thus giving diisopropyl fluorophosphate.
DIPF is a diagnostic test for the presence of the active site Ser in serine proteases. The toxin, along with other neurotoxins is inactivated by the enzyme paraoxonase, which is present in widely varying levels in humans.
Society and culture
It is marketed under many brand names including Difluorophate, Diflupyl, Diflurphate, Dyflos, Dyphlos, Fluropryl, Fluostigmine, Neoglaucit.
- MAFP (methoxy arachidonoylfluorophosphonate), a mechanistically related inhibitor
- Sarin (isopropyl methylphosphonofluridate), a related phosphofluridate
- "Isofluorphate definition". Drugs.com. Retrieved 6 September 2017.
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- Millard, C.B.; Kryger, G.; Ordentlich, A.; Greenblatt, H.M.; Harel, M.; Raves, M.L.; Segall, Y.; Barak, D.; Shafferman, A.; Silman, I.; Sussman, J.L (1999). "Crystal structures of phosphylated acetylcholinesterase: Nerve agent reaction products at atomic resolution". Biochemistry. 38 (22): 7032–9. doi:10.1021/bi982678l. PMID 10353814.
- US patent 2409039, E.E. Hardy & G.M. Kosoloapoff, "Halogenated compounds and process for making same", issued 1946-10-08, assigned to Monsanto Chemical Company
- Brenner, G. M. (2000). Pharmacology. Philadelphia, PA: W.B. Saunders Company. ISBN 0-7216-7757-6.
- Meiers, P. (2006). "History of the fluorophosphates".