CW Agent Factsheet - Sarin
Factsheet: Sarin
Compiled and written by Dr. Jean Pascal Zanders
| Category: | Casualty agent |
| Subcategory: | Nerve agent |
| Chemical name | Isopropyl methyl phosphonofluoridate |
| Code | GB |
Alternative codes and names |
First German code number: T-113. All nerve agents developed by the Germans were classified under Grün-3. |
| Formula | CH3P(O)(F)OCH(CH3)2 |
| Main characteristics | Colourless, non-persistent liquid, which gives off no odour when vaporizing. The vapour is colourless. Sarin evaporates 36 times as quickly as tabun. It can be made more persistent through the addition of certain oils or petroleum products. |
| Main effects | Nerve agents in general attack the nervous system of the human body. When a nerve receives a stimulus acetylcholine is released in order to carry the impulse to muscles and organs. Once the impulse has passed, the enzyme cholinesterase acts to prevent the accumulation of acetylcholine after its release in the nervous system. Nerve agents inhibit the functioning of cholinesterase, as a consequence of which the acetylcholine continues to act so that nervous impulses continue to be transmitted. The first symptoms a victim will experience following exposure to nerve agents are a runny nose, tightness in the chest and constriction of the pupils (miosis). The victim will then encounter difficulties breathing, drooling from the mouth and nausea. Because of the loss of control over bodily functions, vomiting, defecation and urination occurs. This phase is followed by twitching and jerking. Ultimately the victim will become comatose and will suffocate as a consequence of convulsive spasms. Sarin is a highly volatile liquid, so that inhalation as well as absorption through the skin pose a great threat. Even vapour concentrations will immediately penetrate the skin. Death may follow in one minute after direct ingestion of extremely low concentrations (0.01 mg per kg of body weight or higher). People who did not accumulate a lethal dose but did not receive immediate appropriate medical treatment may suffer permanent neurological damage. |
| Precursors | Key precursors: methylphosphonyl difluoride; methylphosphonyldichloride; diisopropyl methylphosphonochloridate Precursors: Dimethyl methylphosphonate; isopropyl methylphosphonate Other chemicals: Trimethylphosphite; phosphorus trichloride;triisopropyl phosphite |
| Comments | Sarin, developed in 1938, is the most toxic of the three G-agents made by Germany. Its name is derived from the names of the chemists involved in its creation: Schrader, Ambrose, Rüdigerand van der Linde. NATO adopted it as a standard chemical warfare agent in the early 1950s. Iraq used sarin in the 1980-88 war with Iran and had large stocks available in the 1990-91 Gulf War. The Japanese Aum Shinrikyo religious sect released an impure form of sarin in Matsumoto in 1994 and in the Tokyo underground in 1995. |

