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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, LD(50) values for DFP in the same species can differ widely even within the same laboratory, possibly due to the use of degraded D...

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Autores principales: Heiss, Derik R., Zehnder, Donald W., Jett, David A., Platoff, Gennady E., Yeung, David T., Brewer, Bobby N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573265/
https://www.ncbi.nlm.nih.gov/pubmed/28856029
http://dx.doi.org/10.1155/2016/3190891
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author Heiss, Derik R.
Zehnder, Donald W.
Jett, David A.
Platoff, Gennady E.
Yeung, David T.
Brewer, Bobby N.
author_facet Heiss, Derik R.
Zehnder, Donald W.
Jett, David A.
Platoff, Gennady E.
Yeung, David T.
Brewer, Bobby N.
author_sort Heiss, Derik R.
collection PubMed
description Diisopropylfluorophosphate (DFP) is a potent acetylcholinesterase inhibitor commonly used in toxicological studies as an organophosphorus nerve agent surrogate. However, LD(50) 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.
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spelling pubmed-55732652017-08-28 Synthesis and Storage Stability of Diisopropylfluorophosphate Heiss, Derik R. Zehnder, Donald W. Jett, David A. Platoff, Gennady E. Yeung, David T. Brewer, Bobby N. J Chem Article Diisopropylfluorophosphate (DFP) is a potent acetylcholinesterase inhibitor commonly used in toxicological studies as an organophosphorus nerve agent surrogate. However, LD(50) 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. 2016 /pmc/articles/PMC5573265/ /pubmed/28856029 http://dx.doi.org/10.1155/2016/3190891 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Heiss, Derik R.
Zehnder, Donald W.
Jett, David A.
Platoff, Gennady E.
Yeung, David T.
Brewer, Bobby N.
Synthesis and Storage Stability of Diisopropylfluorophosphate
title 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_short Synthesis and Storage Stability of Diisopropylfluorophosphate
title_sort synthesis and storage stability of diisopropylfluorophosphate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573265/
https://www.ncbi.nlm.nih.gov/pubmed/28856029
http://dx.doi.org/10.1155/2016/3190891
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