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Dimethylmercury
Organomercury chemical compound
Organomercury chemical compound
|NFPA-H = 4 |NFPA-F = 4 |NFPA-R = 3 |Diethylmercury |Diphenylmercury |Dimethylzinc |Dimethylcadmium |Dimethylmagnesium
Dimethylmercury is an extremely toxic organomercury compound with the formula (CH3)2Hg. A volatile, flammable, dense and colorless liquid, dimethylmercury is one of the strongest known neurotoxins. Less than 0.1 mL is capable of inducing severe mercury poisoning resulting in death.
Synthesis, structure, and reactions
The compound was one of the earliest organometallics reported, reflecting its considerable stability. The compound was first prepared by George Buckton in 1857 by a reaction of methylmercury iodide with potassium cyanide: : 2 CH3HgI + 2 KCN → Hg(CH3)2 + 2 KI + (CN)2 + Hg Later, Edward Frankland discovered that it could be synthesized by treating sodium amalgam with methyl halides: : Hg + 2 Na + 2 CH3I → Hg(CH3)2 + 2 NaI It can also be obtained by alkylation of mercuric chloride with methyllithium: : HgCl2 + 2 LiCH3 → Hg(CH3)2 + 2 LiCl The molecule adopts a linear structure with Hg–C bond lengths of 2.083 Å.
Reactivity and physical properties

Dimethylmercury is stable in water and reacts with mineral acids at a significant rate only at elevated temperatures, whereas the corresponding organocadmium and organozinc compounds (and most metal alkyls in general) hydrolyze rapidly. The difference reflects the high electronegativity of Hg (Pauling EN = 2.00) and the low affinity of Hg(II) for oxygen ligands. The compound undergoes a redistribution reaction with mercuric chloride to give methylmercury chloride(actually, this is a reversible equilibrium): : (CH3)2Hg + HgCl2 → 2 CH3HgCl Whereas dimethylmercury is a volatile liquid, methylmercury chloride is a crystalline solid.
Use
Dimethylmercury has few practical applications because of its danger to human life. It has been studied for reactions involving bonding methylmercury cations to target molecules, forming potent bactericides, but methylmercury's bioaccumulation and ultimate toxicity has led to it being largely abandoned in favor of the less toxic ethylmercury and diethylmercury compounds, which perform a similar function without the bioaccumulation hazard.
In toxicology, it still finds limited use as a reference toxin. It is also used to calibrate NMR instruments for detection of mercury (δ 0 ppm for 199Hg NMR), although diethylmercury and less toxic mercury salts are now preferred.
Around 1960, Phil Pomerantz, a man working at the Bureau of Naval Weapons, suggested that dimethylmercury be used as a fuel mix with red fuming nitric acid.
Safety
Dimethylmercury is extremely toxic and dangerous to handle. Absorption of doses as low as 0.1 mL can result in severe mercury poisoning. The risks are enhanced because of the compound's high vapor pressure. Since it is highly lipophilic, it absorbs through the skin and into body fat very easily and can permeate many materials, including many plastics and rubber compounds.
Permeation tests showed that several types of disposable latex or polyvinyl chloride gloves (typically, about 0.1 mm thick), commonly used in most laboratories and clinical settings, had high and maximal rates of permeation by dimethylmercury within 15 seconds. The American Occupational Safety and Health Administration (OSHA) advises handling dimethylmercury with highly resistant laminated gloves with an additional pair of abrasion-resistant gloves worn over the laminate pair, and also recommends using a face shield and working in a fume hood.
Dimethylmercury is metabolized after several days to methylmercury. Methylmercury crosses the blood–brain barrier easily, probably owing to formation of a complex with cysteine. It easily absorbs into the body and has a tendency to bioaccumulate. The symptoms of mercury poisoning may be delayed by months, resulting in cases in which a diagnosis is ultimately discovered, but only at a point in which it is too late or almost too late for an effective treatment regimen to be successful. Organomercury poisoning is also known as Minamata disease.
Incidents
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As early as 1865, two workers in the laboratory of Edward Frankland died after exhibiting progressive neurological symptoms following accidental exposure to the compound.
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Karen Wetterhahn, a professor of chemistry at Dartmouth College, died in 1997, ten months after spilling only a few drops of dimethylmercury onto her latex gloves. This incident resulted in improved awareness of the substance's extreme toxicity, and its ability to easily penetrate latex, compared to less porous materials such as nitrile. New OSHA material-handling guidelines were published, many institutions purged their supplies of the compound, and it became almost impossible to buy.
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Christoph Bulwin, a 40-year-old database administrator for IG Bergbau, Chemie, Energie, claimed to have been attacked with a syringe-tipped umbrella on 15 July 2011 in Hanover. Bulwin, who died a year later from mercury poisoning, had said he confiscated the syringe, which was later found to contain dimethylmercury. According to a 2020 article in Forensic Science, Medicine and Pathology, police investigations revealed a syringe containing a typical mercury thallium compound in Bulwin's car, and mercury and thallium in thermometers at his workplace. Inconclusive antemortem and postmortem blood, urine, and tissue analysis cast doubts on the assault account. The absence of an identified assailant or motive, as well as the presence of different mercury compounds in Bulwin's car, led police to conclude that the intoxication was likely self-administered, thereby terminating the preliminary investigation. The Forensic Science, Medicine and Pathology account is contradicted by other reports, including the August 24, 2022 episode of the German flagship true crime TV program Aktenzeichen XY... ungelöst that was co-edited by the Hannover criminal police and in which information was solicited from the public based on Bulwin's own umbrella scenario.
References
References
- (16 September 2004). "dimethylmercury – Compound Summary". National Center for Biotechnology Information.
- "OSHA Hazard Information Bulletins – Dimethylmercury".
- (1977). "The Chemistry of mercury". Macmillan.
- (2001). "Inorganic Chemistry". Academic Press.
- Crabtree, Robert H.. (2005). "The Organometallic Chemistry of the Transition Metals". John Wiley.
- (September 1973). "Chemistry of Organomercurials in Aquatic Systems". [[U.S. Govt. Print. Off.]].
- "Methylmercury chloride". [[National Center for Biotechnology Information]], United States [[National Institutes of Health]].
- (1998-03-10). "199Hg Standards". Northwestern University.
- Hoffman, R.. (2011-08-01). "(Hg) Mercury NMR". The Hebrew University.
- "Delayed Toxic Syndromes". [[Oak Ridge Associated Universities.
- Clark, John Drury. (2018-05-23). "Ignition!". Rutgers University Press Classics.
- (1998). "Delayed Cerebellar Disease and Death after Accidental Exposure to Dimethylmercury". [[New England Journal of Medicine]].
- Cotton, Simon. (October 2003). "Dimethylmercury and Mercury Poisoning: The Karen Wetterhahn story". [[Bristol University]] School of Chemistry.
- (October 2003). "DimethylMercury and Mercury poisoning".
- Cavanaugh, Ray. (2019-02-19). "The dangers of dimethylmercury". [[Royal Society of Chemistry]].
- (2020-09-01). "Another umbrella murder? – A rare case of Minamata disease". Forensic Science, Medicine and Pathology.
- (11 May 2012). "Umbrella stab victim dies of mercury poisoning".
- (11 May 2012). "Quecksilbervergiftung".
- (2020-09-01). "Another umbrella murder? – A rare case of Minamata disease". Forensic Science, Medicine and Pathology.
- (2022-08-30). "Heimtückischer Mord - Familienvater stirbt nach Spritzenattacke - ZDFmediathek".
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