Chloropicrin, also known as PS (from Port Sunlight
Synthesis
Chloropicrin was discovered in 1848 by Scottish chemist
John Stenhouse. He prepared it by the reaction of sodium hypochlorite with
picric acid:
Because of the precursor used, Stenhouse named the compound chloropicrin, although the two compounds are structurally dissimilar.
Today, chloropicrin is manufactured by the reaction of nitromethane with sodium hypochlorite:
Reaction of chloroform and nitric acid also yields chloropicrin:
Properties
Chloropicrin's chemical formula is and its molecular weight is 164.38 grams/mole.
Pure chloropicrin is a colorless liquid, with a boiling point of 112 °C.
Chloropicrin is sparingly soluble in water with solubility of 2 g/L at 25 °C.
It is volatile, with a vapor pressure of 23.2 millimeters of mercury (mmHg) at 25 °C; the corresponding Henry's law constant is 0.00251 atmosphere-cubic meter per mole.
The octanol-water partition coefficient (
Kow) of chloropicrin is estimated to be 269.
Its soil adsorption coefficient (
Koc; normalized to soil organic matter content) is 25 cm
3/g.
Uses
Poison
Chloropicrin was manufactured for use as poison gas in World War I.
In World War I, German forces used concentrated chloropicrin against Allied forces as a tear gas. While not as lethal as other chemical weapons, it induced
vomiting and forced Allied soldiers to remove their masks to vomit, exposing them to more toxic gases used as weapons during the war.
It was also used by the Imperial Russian Army in hand grenades as 50% solution in sulfuryl chloride.
In February 2024, Ukraine General Oleksandr Tarnavskyi accused the Russian Armed Forces of using chloropicrin munitions.
Agriculture
In agriculture, chloropicrin is injected into soil prior to planting a crop to
fumigation soil. Chloropicrin affects a broad spectrum of
fungi,
microbes and
insects.
It is commonly used as a stand-alone treatment or in combination / co-formulation with
methyl bromide and 1,3-dichloropropene.
Chloropicrin is used as an indicator and repellent when fumigating residences for insects with sulfuryl fluoride which is an odorless gas. Chloropicrin's mode of action is unknown
(IRAC MoA 8B).
Chloropicrin may stimulate
weed germination, which can be useful when quickly followed by a more effective
herbicide.
Chloropicrin was first registered in 1975 in the US. After a 2008 re-approval, the EPA
Used as a preplant soil treatment measure, chloropicrin suppresses soilborne pathogenic fungi and some nematodes and insects. According to chloropicrin manufacturers, with a half-life of hours to days, it is completely digested by soil organisms before the crop is planted, making it safe and efficient. Contrary to popular belief, chloropicrin does not sterilize soil and does not Ozone depletion, as the compound is destroyed by sunlight. Additionally, chloropicrin has never been found in groundwater, due to its low solubility.
California
In
California, experience with acute effects of chloropicrin when used as a soil fumigant for
strawberries and other
crops led to the release of regulations in January 2015 creating buffer zones and other precautions to minimize exposure to farm workers, neighbors, and passersby.
Safety
At a national level, chloropicrin is regulated in the
United States by the United States Environmental Protection Agency as a restricted use
pesticide.
Because of its toxicity, distribution and use of chloropicrin is available only to licensed professionals and specially certified growers who are trained in its proper and safe use.
In the US, occupational exposure limits have been set at 0.1 ppm over an eight-hour time-weighted average.
High concentrations
Chloropicrin is harmful to humans. It can be absorbed systemically through inhalation, ingestion, and the skin. At high concentrations, it is severely irritating to the lungs, eyes, and skin.
Damage to protective gear
Chloropicrin and its derivative
phosgene oxime have been known to damage or compromise earlier generations of personal protective equipment. Some of the soldiers attacked mentioned a white smoke emerging from their gas masks.
See also
-
Trichloronitrosomethane
-
Tetrachlorodinitroethane
[, University of Hertfordshire, accessed 2021-03-10.]
