Jump to content

Methylphosphonyl difluoride

From Wikipedia, the free encyclopedia
(Redirected from Methylphosphonic difluoride)
Methylphosphonyl difluoride
Names
Preferred IUPAC name
Methylphosphonic difluoride
Other names
Methylphosphonyl difluoride
Methylphosphonoyl difluoride, EA-1251
Identifiers
3D model (JSmol)
4-04-00-03508
ChemSpider
MeSH difluoride Methylphosphonic difluoride
UNII
  • InChI=1S/CH3F2OP/c1-5(2,3)4/h1H3
    Key: PQIOSYKVBBWRRI-UHFFFAOYSA-N
  • CP(F)(F)=O
Properties
CH3POF2
Molar mass 100.00
Appearance Colorless liquid
Odor Pungent, acid-like[1]
Density 1.359 g/mL (77°F)[1]
Melting point −37 °C; −35 °F; 236 K
Boiling point 100 °C; 212 °F; 373 K
Decomposes[1]
Vapor pressure 36 mmHg (77°F)[1]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Corrosive, toxic
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Methylphosphonyl difluoride (DF), also known as EA-1251[2] or difluoro,[3] is a chemical weapon precursor. Its chemical formula is CH3POF2. It is a Schedule 1 substance under the Chemical Weapons Convention. It is used for production of sarin and soman as a component of binary chemical weapons; an example is the M687 artillery shell, where it is used together with a mixture of isopropyl alcohol and isopropyl amine, producing sarin.

Preparation

[edit]

Methylphosphonyl difluoride can be prepared by reacting methylphosphonyl dichloride with hydrogen fluoride (HF) or sodium fluoride (NaF).

Safety

[edit]

Methylphosphonyl difluoride is both reactive and corrosive. It is absorbed through skin and causes burns and mild nerve agent symptoms. It reacts with water, producing HF fumes and methylphosphonic acid as a result. It is also capable of corroding glass.

Significance in international relations

[edit]

In 2013–2014, the stockpile of chemicals covered by the CWC was removed from Syria and destroyed. Of the stockpile, 581 tons (over 96%) of the stockpile was DF. It was destroyed by the U.S. Army on the MV Cape Ray by hydrolysis.[4][5]

References

[edit]
  1. ^ a b c d e f Handbook of chemical and biological warfare agents (2nd ed.). CRC Press. 24 August 2007. ISBN 9780849314346.
  2. ^ "Physical properties of standard agents, candidate agents, and related compounds at several temperatures" (PDF). Archived (PDF) from the original on February 26, 2017.
  3. ^ U. S. Army (12 Dec 1990). Potential Military Chemical/Biological Agents and Compounds (PDF). Washington, D.C.: Headquarters, Dept. of the Army. Retrieved 12 May 2020.
  4. ^ Organization for the Prohibition of Chemical Weapons (OPCW). "U.S. Completes Destruction of Sarin Precursors from Syria on the Cape Ray". OPCW News. Retrieved 12 May 2020.
  5. ^ Trapp, Dr. Ralf. "Lessons Learned from the OPCW Mission in Syria" (PDF). OPCW. Retrieved 12 May 2020.