Three Nerve Agents example essay topic

Chem Warfare It was not until the early 1930's that German chemists observed that organ o-phosphorus compounds could be poisonous. In 1934, Dr Gerhard Schrader, a chemist at IG Farben, was given the task of developing a pesticide. Two years later a phosphorus compound with extremely high toxicity was produced for the first time. According to contemporary regulations, discoveries with military implications had to be reported to the military authorities, which was also done with Schrader's discovery. This phosphorus compound, given the name tabu n, was the first of the substances later referred to as nerve agents. A factory for production of the new CW agent was built and a total of 12 000 tonnes of tabu n we reproduced during the years 1942-1945.

At the end of the war the Allies seized large quantities of this nerve agent. Up to the end of the war, Schrader and his co-workers synthesized about 2 000 -phosphorus compounds, including sar in (1938). The third of the 'classic' nerve agents, so man, was first produced in 1944. These three nerve agents are known as G agents in the American nomenclature. The manufacture of started properly and up to 1945 only about 0.5 tonne of this nerve agent was produced in a pilot plant.

Immediately after the war, research was mainly concentrated on studies of the mechanisms of the nerve agents in order to discover more effective forms of protection against these new CW agents. The results of these efforts led, however, not only to better forms of protection but also to new types of agents closely related to the earlier ones. By the mid-1950's a group of more stable nerve agents had been developed, known as the V-agents in the American nomenclature. They are approximately ten-fold more poisonous than sar in and are thus among the most toxic substances ever synthesized. The first publication of these substances appeared in 1955. The authors, R. Ghosh and J.F. Newman, described one of the substances, known as Amit on, as being particularly effective against mites.

At this time, intensive research was being devoted to the organ o-phosphorus insecticides both in Europe and in the United States. At least three chemical firms appear to have independently discovered the remarkable toxicity of these phosphorus compounds during the years 1952-53. Surprisingly enough, some of these substances were available on the market as pesticides. Nonetheless, they were soon withdrawn owing to their considerable toxicity also to mammals.

In the United States, the choice fell in 1958 on a substance known by its code name Vas suitable as a CW agent of persistent type. Full-scale production of VX started in April 1961 but its structure was not published until 1972. Physical and Chemical Properties The most important nerve agents included in modern CW arsenals are: ? Tabun, O-, with the American denomination GA.

This nerve agent is the easiest to manufacture. Consequently, it is more likely that developing countries start their CW arsenal with this nerve agent whereas industrialized countries consider tabu n to be out-of-date and of limited use.? Sarin, , with the Americandenomination GB, a volatile substance mainly taken up through inhalation.? Soman, , with the Americandenomination GD, a moderately volatile substance which can be taken up by inhalation or skin contact.? Cyclo hexyl, with the American denomination GF, a substance with low volatility which is taken up through skin contact and inhalation of the substance either as ages or aerosol.? O-ethyl S-, better known under the American denomination VX, a persistent substance which can remain on material, equipment and terrain for long periods.

Uptake is mainly through the skin but also through inhalation of the substance as a gas or aerosol. The formulae for some nerve agents are: ? Tabun, GA: (CH 3) 2 N-P ( = O) (-CN) (-OC 2 H 5)? Sarin, GB: CH 3-P ( = O) (-F) (-OCH (CH 33) 2)? Soman, GD: CH 3-P ( = O) (-F) (-CH (CH 3) C (CH 3) 3?

GF: CH 3-P ( = O) (-F) (-C 6 H 11)? VX: CH 3-P ( = O) (-SCH 2 CH 2 N [CH (CH 3) 2] 2) (-OC 2 H 5).