“…There are particular issues of remediation of chlorocarbons associated with the manufacture of lindane. Hexachlorocyclohexanes (HCHs) were first produced by chlorination of benzene in sunlight by Faraday in 1825. , Lindane, first isolated from HCH in 1912, typically constitutes 12% of the stereoisomer mixture, but it is the only insecticide among eight separable stereoisomers, whereas the α- and β-isomers (1 R ,2 R ,3 R ,4 R ,5 S ,6 S -hexachlorocyclohexane, CAS# 319–84–6, and 1 r ,2 r ,3 r ,4 r ,5 r ,6 r -hexachlorocyclohexane, CAS# 319–85–7, respectively) are more toxic to mammals. − As much as 700 000 tons of lindane were used worldwide as a broad spectrum pesticide between 1950 and 2000. , This was accompanied by at least 5 million tons of waste hexachlorocyclohexane isomers now scattered in mountainous dumps throughout the world . Therefore, lindane has been banned for agricultural use under the 2009 Stockholm Convention on Persistent Organic Pollutants .…”