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Title: Effective methylation of phosphonic acids related to chemical warfare agents mediated by trimethyloxonium tetrafluoroborate for their qualitative detection and identification by gas chromatography-mass spectrometry

Journal Article · · Analytica Chimica Acta
ORCiD logo [1];  [1];  [1]
  1. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Nuclear and Chemical Sciences Division, Forensic Science Center

The effective methylation of phosphonic acids related to chemical warfare agents (CWAs) employing trimethyloxonium tetrafluoroborate (TMO·BF4) for their qualitative detection and identification by gas chromatography-mass spectrometry (GC-MS) is presented. The methylation occurs in rapid fashion (1 h) and can be conveniently carried out at ambient temperature, thus providing a safer alternative to the universally employed diazomethane-based methylation protocols. Optimization of the methylation parameters led us to conclude that methylene chloride was the ideal solvent to carry out the derivatization, and that even though methylated products can be observed surfacing after only 1 h, additional time was not found to be detrimental but beneficial to the process particularly when dealing with analytes at low concentrations (~10 μg mL-1). Due to its insolubility in methylene chloride, TMO·BF4 conveniently settles to the bottom during the reaction and does not produce additional interfering by-products that may further complicate the GC-MS analysis. We demonstrated the method to successfully methylate a variety of Schedule 2 phosphonic acids, including their half esters, resulting in derivatives that were readily detected and identified using the instrument's spectral library. Most importantly, the method was shown to simultaneously methylate a mixture of the organophosphorus-based nerve agent hydrolysis products: pinacolyl methylphosphonate (PMPA), cyclohexyl methylphosphonate (CyMPA) and ethyl methylphosphonate (EMPA) (at a 10 μg mL-1 concentration each) in a fatty acid ester-rich organic matrix (OPCW-PT-O3) featured in the 38th Organisation for the Prohibition of Chemical Weapons (OPCW) Proficiency Test. Additionally, the protocol was found to effectively methylate N,N-diethylamino ethanesulfonic acid and N,N-diisopropylamino ethanesulfonic acid that are products arising from the oxidative degradation of the V-series agents VR and VX respectively. This work described herein represents the first report on the use of TMO·BF4 as a viable, stable and safe agent for the methylation of phosphonic acids and their half esters and within the context of an OPCW Proficiency Test sample analysis.

Research Organization:
Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)
Sponsoring Organization:
USDOE
Grant/Contract Number:
AC52-07NA27344
OSTI ID:
1368027
Report Number(s):
LLNL-JRNL-682362
Journal Information:
Analytica Chimica Acta, Vol. 933, Issue C; ISSN 0003-2670
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 20 works
Citation information provided by
Web of Science

References (33)

Chemical warfare agents journal September 2008
History of chemical and biological warfare agents journal October 2005
Interaction of an organophosphate with a peripheral site on acetylcholinesterase journal January 1990
In vivo cholinesterase inhibitory specificity of organophosphorus nerve agents journal December 2005
The Tokyo subway sarin attack—lessons learned journal September 2005
Report on 640 Victims of the Tokyo Subway Sarin Attack journal August 1996
Syrian gas attack reinforces need for better anti-sarin drugs journal October 2013
Limitations and challenges in treatment of acute chemical warfare agent poisoning journal December 2013
Decontamination of VX, GD, and HD on a Surface Using Modified Vaporized Hydrogen Peroxide journal January 2007
Destruction and Detection of Chemical Warfare Agents journal September 2011
Decontamination of chemical warfare agents journal December 1992
Review of oximes available for treatment of nerve agent poisoning journal September 1994
The Role of Oximes in the Treatment of Nerve Agent Poisoning in Civilian Casualties journal January 2006
Recent advances in evaluation of oxime efficacy in nerve agent poisoning by in vitro analysis journal March 2007
Chromogenic and fluorogenic detection and discrimination of nerve agents Tabun and Vx journal January 2015
Chromogenic and fluorogenic detection of a nerve agent simulant with a rhodamine-deoxylactam based sensor journal January 2011
Chromogenic and fluorogenic reagents for chemical warfare nerve agents' detection journal January 2007
31 P-Edited Diffusion-Ordered 1 H NMR Spectroscopy for the Spectral Isolation and Identification of Organophosphorus Compounds Related to Chemical Weapons Agents and Their Degradation Products journal November 2012
Derivatization of pinacolyl alcohol with phenyldimethylchlorosilane for enhanced detection by gas chromatography–mass spectrometry journal January 2014
Determination of ethephon residues in water by gas chromatography with cubic mass spectrometry after ion-exchange purification and derivatisation with N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide journal March 2006
Determination of glyphosate, glyphosate metabolites, and glufosinate in human serum by gas chromatography–mass spectrometry journal November 2008
Derivatization of organophosphorus nerve agent degradation products for gas chromatography with ICPMS and TOF-MS detection journal March 2007
Development and validation of a sensitive solid-phase-extraction (SPE) method using high-performance liquid chromatography/tandem mass spectrometry (LC–MS/MS) for determination of risedronate concentrations in human plasma journal January 2012
Thermally assisted methylation and subsequent silylation of scheduled acids of chemical weapon convention for on-site analysis and its comparison with the other methods of methylation journal February 2011
On-matrix derivatization for dynamic headspace sampling of nonvolatile surface residues journal September 2012
Structural determination of nerve agent markers using gas chromatography mass spectrometry after derivatization with 3-pyridyldiazomethane: Structural determination of nerve agent markers journal June 2013
FIRM FINED FOR CHEMIST’S DEATH: SAFETY: Sepracor Canada admits lack of lab ventilation in worker fatality case journal May 2011
Esterification of carboxylic acids with trialkyloxonium salts journal March 1979
Total Synthesis with a Chirogenic Opening Move Demonstrated on Steroids with Estrane or 18a-Homoestrane Skeleton journal August 1995
Toward the Synthesis of (+)-Peloruside A via an Intramolecular Vinylogous Aldol Reaction journal December 2011
Urinary organic acid screening by solid-phase microextraction of the methyl esters journal August 1998
Development of fatty acid analysis by high-performance liquid chromatography, gas chromatography, and related techniques journal August 2002
A review of current trends and advances in modern bio-analytical methods: Chromatography and sample preparation journal December 2009

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