| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
[(E)-2-Chloroethen-1-yl]arsonous dichloride | |||
Other names
Chlorovinylarsine dichloride
2-Chloroethenyldichloroarsine (E)-2-Chlorovinylarsonous dichloride (E)-2-Chlorovinyldichloroarsine Dichloro((E)-2-chlorovinyl)arsine | |||
Identifiers | |||
3D model (JSmol)
|
|||
ChemSpider | |||
MeSH | lewisite | ||
PubChem CID
|
|||
UNII | |||
UN number | 2810 | ||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
C2H2AsCl3 | |||
Molar mass | 207.32 g/mol | ||
Density | 1.89 g/cm3 | ||
Melting point | −18 °C (0 °F; 255 K) | ||
Boiling point | 190 °C (374 °F; 463 K) | ||
Reacts with water | |||
Solubility | Ethers, hydrocarbons, THF | ||
Vapor pressure | 0.58 mmHg (25 °C) | ||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards
|
Flammable, highly toxic, corrosive, vesicant | ||
NFPA 704 (fire diamond) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Lewisite (L) (A-243) is an organoarsenic compound. It was once manufactured in the U.S., Japan, Germany[2] and the Soviet Union[3] for use as a chemical weapon, acting as a vesicant (blister agent) and lung irritant. Although the substance is colorless and odorless in its pure form, impure samples of lewisite are a yellow, brown, violet-black, green, or amber oily liquid with a distinctive odor that has been described as similar to geraniums.[4][5][6]
Lewisite is named after the US chemist and soldier Winford Lee Lewis (1878–1943). Apart from its use as a weapon of war, the compound is useless; a chemist from the United States Army's chemical warfare laboratories said that "no one has ever found any use for the compound".[7]
nrc
was invoked but never defined (see the help page).