Ethylmercury
Ethylmercury is a cation composed of an organic CH3CH2— species bound to a mercury(II) centre, making it a type of organometallic cation, and giving it a chemical formula C2H5Hg+. The main source of ethylmercury is thimerosal.
Synthesis and structure
Ethylmercury is a substituent of compounds: it occurs as a component of compounds of the formula C2H5HgX where X = chloride, thiolate, or another organic group. Most famously X = the mercaptide group of thiosalicylic acid as in thiomersal. In the body, ethylmercury is most commonly encountered as derivatives with a thiolate attached to the mercury. In these compounds, Hg has a linear or sometimes trigonal coordination geometry. Given the comparable electronegativities of mercury and carbon, the mercury-carbon bond is described as covalent.Toxicity
The toxicity of ethylmercury is well studied. Like methylmercury, ethylmercury distributes to all body tissues, crossing the blood–brain barrier and the placental barrier, and ethylmercury also moves freely throughout the body. Risk assessment for effects on the human nervous system have been made by extrapolating from dose-response relationships for methylmercury. Estimates have suggested that ethylmercury clears from blood with a half-life of 3–7 days in adult humans. In monkeys, it clears from brain tissue with a half-life of 24 days and blood in 7 days.It is a fungicide but has been banned from use in the U.S. on food grain and even on seeds only used to grow crops.