Synthesis and Storage Stability of Diisopropylfluorophosphate

Diisopropylfluorophosphate (DFP) is a potent acetylcholinesterase inhibitor commonly used in toxicological studies as an organophosphorus nerve agent surrogate. However, LD50 values for DFP in the same species can differ widely even within the same laboratory, possibly due to the use of degraded DFP...

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Main Authors: Derik R. Heiss, Donald W. Zehnder, David A. Jett, Gennady E. Platoff, David T. Yeung, Bobby N. Brewer
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2016/3190891
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spelling doaj-61ca818a6a4d4101a868c5c77deaba452020-11-24T21:03:47ZengHindawi LimitedJournal of Chemistry2090-90632090-90712016-01-01201610.1155/2016/31908913190891Synthesis and Storage Stability of DiisopropylfluorophosphateDerik R. Heiss0Donald W. Zehnder1David A. Jett2Gennady E. Platoff3David T. Yeung4Bobby N. Brewer5Battelle Memorial Institute, 505 King Avenue, Columbus, OH 43201, USABattelle Memorial Institute, 505 King Avenue, Columbus, OH 43201, USANational Institute of Neurological Disorders and Stroke, National Institutes of Health, 6001 Executive Boulevard, Rockville, MD 20852, USANational Institute of Allergy and Infectious Diseases, National Institutes of Health, 5601 Fishers Lane, Rockville, MD 20892, USANational Institute of Neurological Disorders and Stroke, National Institutes of Health, 6001 Executive Boulevard, Rockville, MD 20852, USABattelle Memorial Institute, 505 King Avenue, Columbus, OH 43201, USADiisopropylfluorophosphate (DFP) is a potent acetylcholinesterase inhibitor commonly used in toxicological studies as an organophosphorus nerve agent surrogate. However, LD50 values for DFP in the same species can differ widely even within the same laboratory, possibly due to the use of degraded DFP. The objectives here were to identify an efficient synthesis route for high purity DFP and assess the storage stability of both the in-house synthesized and commercial source of DFP at the manufacturer-recommended storage temperature of 4°C, as well as −10°C and −80°C. After 393 days, the commercial DFP stored at 4°C experienced significant degradation, while only minor degradation was observed at −10°C and none was observed at −80°C. DFP prepared using the newly identified synthesis route was significantly more stable, exhibiting only minor degradation at 4°C and none at −10°C or −80°C. The major degradation product was the monoacid derivative diisopropylphosphate, formed via hydrolysis of DFP. It was also found that storing DFP in glass containers may accelerate the degradation process by generating water in situ as hydrolytically generated hydrofluoric acid attacks the silica in the glass. Based on the results here, it is recommended that DFP be stored at or below −10°C, preferably in air-tight, nonglass containers.http://dx.doi.org/10.1155/2016/3190891
collection DOAJ
language English
format Article
sources DOAJ
author Derik R. Heiss
Donald W. Zehnder
David A. Jett
Gennady E. Platoff
David T. Yeung
Bobby N. Brewer
spellingShingle Derik R. Heiss
Donald W. Zehnder
David A. Jett
Gennady E. Platoff
David T. Yeung
Bobby N. Brewer
Synthesis and Storage Stability of Diisopropylfluorophosphate
Journal of Chemistry
author_facet Derik R. Heiss
Donald W. Zehnder
David A. Jett
Gennady E. Platoff
David T. Yeung
Bobby N. Brewer
author_sort Derik R. Heiss
title Synthesis and Storage Stability of Diisopropylfluorophosphate
title_short Synthesis and Storage Stability of Diisopropylfluorophosphate
title_full Synthesis and Storage Stability of Diisopropylfluorophosphate
title_fullStr Synthesis and Storage Stability of Diisopropylfluorophosphate
title_full_unstemmed Synthesis and Storage Stability of Diisopropylfluorophosphate
title_sort synthesis and storage stability of diisopropylfluorophosphate
publisher Hindawi Limited
series Journal of Chemistry
issn 2090-9063
2090-9071
publishDate 2016-01-01
description Diisopropylfluorophosphate (DFP) is a potent acetylcholinesterase inhibitor commonly used in toxicological studies as an organophosphorus nerve agent surrogate. However, LD50 values for DFP in the same species can differ widely even within the same laboratory, possibly due to the use of degraded DFP. The objectives here were to identify an efficient synthesis route for high purity DFP and assess the storage stability of both the in-house synthesized and commercial source of DFP at the manufacturer-recommended storage temperature of 4°C, as well as −10°C and −80°C. After 393 days, the commercial DFP stored at 4°C experienced significant degradation, while only minor degradation was observed at −10°C and none was observed at −80°C. DFP prepared using the newly identified synthesis route was significantly more stable, exhibiting only minor degradation at 4°C and none at −10°C or −80°C. The major degradation product was the monoacid derivative diisopropylphosphate, formed via hydrolysis of DFP. It was also found that storing DFP in glass containers may accelerate the degradation process by generating water in situ as hydrolytically generated hydrofluoric acid attacks the silica in the glass. Based on the results here, it is recommended that DFP be stored at or below −10°C, preferably in air-tight, nonglass containers.
url http://dx.doi.org/10.1155/2016/3190891
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