| Soman | |
|---|---|
| Discovery | |
| Discovered by | Richard Kuhn |
| Discovered in | 1944 |
| Chemical characteristics | |
| Chemical name | 3-(fluoro-methyl-phosphoryl)oxy- 2,2-dimethyl-butane |
| Chemical family | Fluorinated organophosphorus compound |
| Chemical formula | C7H16FO2P |
| NFPA Rating | |
| Boiling point | 198 °C |
| Freezing/melting point | −42 °C |
| Vapor pressure | 0.40 mmHg (53 Pa) at 25 °C |
| Vapor relative density (air=1) | 6.3 |
| Solubility in water | Moderate |
| Density at 25 °C | 1.022 g/cm3 |
| Appearance and color | When pure, colorless liquid with fruity odor. With impurities, amber or dark brown, with oil of camphor odor |
Soman, also known by its NATO designation GD (O-Pinacolyl methylphosphonofluoridate) is an extremely toxic substance whose sole application is as one of the world's most dangerous military weapons. It is a nerve agent, interfering with normal functioning of the mammalian nervous system. As a chemical weapon, it is classified as a weapon of mass destruction by the United Nations according to UN Resolution 687, and its production is strictly controlled and stockpiling outlawed by the Chemical Weapons Convention of 1993. Soman was the third of the so-called G-series nerve agents to be discovered (along with GA (tabun), GB (sarin), and GF (cyclosarin)).
It is a volatile, corrosive and colourless liquid with a faint odour when pure. More commonly, it is a yellow to brown color and has a stronger odour described as camphor. The LCt50 for Soman is 70 mg·min/m3 in humans. It is both more lethal and more persistent than sarin or tabun, but less so than cyclosarin.
GD can be thickened for use as a chemical spray using an acryloid copolymer. It can also be deployed as a binary chemical weapon; its precursor chemicals are methylphosphonyl difluoride and a mixture of pinacolyl alcohol and an amine.
Anticholinesterases | Esters | Nerve agents | Organophosphates