EA-1763
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| Names | |
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| Other names
N-[2-[methyl(propoxy)phosphoryl]sulfanylethyl]-N-propan-2-ylpropan-2-amine
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C12H28NO2PS | |
| Molar mass | 281.39 g·mol−1 |
| Boiling point | 316.5 °C (601.7 °F; 589.6 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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EA-1763,[1] O-PPVX, V1[2] or propyl S-2-diisopropylaminoethylmethylphosphonothiolate, is a military-grade neurotoxic organophosphonate nerve agent related to VX as it the propyl analogue of VX. It is part of the V-series.
Chemical characteristics[edit]
Little information about EA-1763's physicochemical properties has been reported.[1] V1 is a more viscous and less dense liquid than VX.[3] It is colorless, odorless and tasteless in its pure form. Impure, or in the crude form, it has a characteristic viscous amber color, giving it an appearance similar to motor oil. The impure form varies several shades of amber, from a viscous liquid of a transparent pale yellow color to a pasty liquid of a semi-transparent and cloudy dirty amber color. The smell varies from engine oil to an offensive brew of organosulfur compounds and organoamines.[4]
Its larger alkane chain pushes its melting point above that of VX. The estimated solubility of V1 in water is 4 times lower compared to VX (6.8 g/L of water at 25 °C). V1 has high solubility in organic solvents and other non-polar compounds. The stability of V1 is roughly the same as that of VX in either environment. Higher insolubility and lower volatility can slow down the process. A vapor pressure at least 3 times lower than VX is speculated.[5]
The longer alkane chain tends to stabilize the induction of electrons from P to O, making P less electrophilic.[5] It is expected that the persistence of V1 is slightly higher than that of VX, estimating the hydrolysis rate between ethyl and n-propyl paraoxon, is 1.6 times more persistent in neutral medium.[6]
The lower volatility and minimal persistence difference makes VX preferable to V1.[5]
Preparation[edit]
It is prepared by the same route as VX using propanol instead of ethanol.
References[edit]
- ^ a b John B. Samuel, Elwin C. Penski, John J. Callahan. PHYSICAL PROPERTIES OF STANDARD AGENTS, CANDIDATE AGENTS, AND RELATED COMPOUNDS AT SEVERAL TEMPERATURES (U). p 24 and 279.
- ^ Kirkpatrick, Melanie G.; diTargiani, Robert C.; Sweeney, Richard E.; Otto, Tamara C. (2016-11-25). "Use of V agents and V-analogue compounds to probe the active site of atypical butyrylcholinesterase from Oryzias latipes". Chemico-Biological Interactions. 259 (Pt B): 182–186. Bibcode:2016CBI...259..182K. doi:10.1016/j.cbi.2016.03.016. ISSN 1872-7786. PMID 27000540.
- ^ Coulter, P. B.; Callahan, J. J.; Link, R.S. Physical Constants of Thirteen V Agents. U. S. Army Chemical Warfare Laboratories Technical Report (Report). CWLR-2346.
- ^ Ledgard, J. A Laboratory History of Chemical Warfare Agents. p 223-225.
- ^ a b c cit-OPDC. The preparatory manual to chemical warfare. Vol 1: V1
- ^ CHEMICAL REVIEWS VOLUME6 4, NUMBER 4. JULY 24, 1964. page 318.