Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Methylphosphonyl difluoride

From Wikipedia, the free encyclopedia
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
MeSHdifluoride Methylphosphonic difluoride
UNII
  • InChI=1S/CH3F2OP/c1-5(2,3)4/h1H3
    Key: PQIOSYKVBBWRRI-UHFFFAOYSA-N
  • CP(F)(F)=O
Properties
CH3POF2
Molar mass100.00
AppearanceColorless liquid
OdorPungent, acid-like[1]
Density1.359 g/mL (77°F)[1]
Melting point−37 °C; −35 °F; 236 K
Boiling point100 °C; 212 °F; 373 K
Decomposes[1]
Vapor pressure36 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 theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Methylphosphonyl difluoride (DF), also known asEA-1251[2] ordifluoro,[3] is achemical weapon precursor. Its chemical formula is CH3POF2. It is aSchedule 1 substance under theChemical Weapons Convention. It is used for production ofsarin andsoman as a component ofbinary chemical weapons; an example is theM687artillery shell, where it is used together with a mixture ofisopropyl alcohol andisopropyl amine, producingsarin.

Preparation

[edit]

Methylphosphonyl difluoride can be prepared by reactingmethylphosphonyl dichloride withhydrogen fluoride (HF) orsodium 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 andmethylphosphonic 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 MVCape Ray by hydrolysis.[4][5]

References

[edit]
  1. ^abcdefHandbook 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. Retrieved12 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. Retrieved12 May 2020.
  5. ^Trapp, Dr. Ralf."Lessons Learned from the OPCW Mission in Syria"(PDF). OPCW. Retrieved12 May 2020.
Blood agents
Blister agents
Arsenicals
Sulfur mustards
Nitrogen mustards
Nettle agents
Other
Nerve agents
G-agents
V-agents
GV agents
Novichok agents
Carbamates
Other
Precursors
Neurotoxins
Pulmonary/
choking agents
Vomiting agents
Incapacitating
agents
Lachrymatory
agents
Malodorant agents
Cornea-clouding agents
Biological toxins
Tumor promoting agents
Other
Units, formations,
centers and institutes
Industrial facilities
Operations
and projects
Research
Operational
Disposal
Agents
Munitions
Protective equipment
Related topics
Retrieved from "https://en.wikipedia.org/w/index.php?title=Methylphosphonyl_difluoride&oldid=1284186731"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp