593-74-8

colourless liquid

As inorganic reagent.

Dimethyl mercury has been used as seed disinfectants and for fungicides. It has also been used in organic synthesis.

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit
Antidotes and Special Procedures for medical personnel: The drug NAP has been used to treat mercury poisoning, with mixed success.

UN2025 Mercury compounds, solid, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. May be sensitive to light.

The first indication of the extreme toxicity of dimethylmercury (DMM) was documented in 1863 when two laboratory assistants died of DMM poisoning while synthesizing DMM in the laboratory of Frankland and Duppa. There are numerous reports of people dying from alkyl mercury compounds including a chemist who was preparing several thousand grams ofDMMin his laboratory in 1974. The extreme toxicity was revisited in 1997, when Karen Wetterhahn, an internationally renowned researcher of the carcinogenic effects of heavy metals on DNA repair proteins, died within a few months after a single exposure of less than a milliliter of DMM on her latex-covered hand. DMM is extremely toxic and lethal at a dose of approximately 400 mg of mercury (equivalent to a few drops) or about 5mgkg-1 of body weight or as little as 0.1 ml

ChEBI: Dimethylmercury is a methylmercury compound.

All alkylmercury compounds are highly toxicby all routes of exposure. There are manyserious cases of human poisoning frommethylmercury (Lu 2003). Outbreaks ofmass poisoning from consumption of contaminatedfish occurred in Japan during the1950s, causing a severe neurological disease,so-called “Minamata disease,” whichresulted in hundreds of deaths. A similaroutbreak of food poisoning from contaminatedwheat caused several hundred deathsin Iraq in 1972. A tragic death from a singleacute transdermal exposure to dimethylmercury(estimated between 0.1 to 0.5 mL) thatpenetrated into the skin through disposablelatex gloves has occurred (Blayney et al.1997; The New York Times, June 11, 1997).The symptoms reported were episodes ofnausea and vomiting occurring three monthsafter the exposure followed by onset ofataxia, slurred speech (dysarthia), and loss ofvision and hearing 2 months after that. Thedeath occurred in about six months after theaccident.
Methylmercury can concentrate in certainfetal organs, such as the brain. Thetarget organs are the brain and the centralnervous system. It can cause death, miscarriage,and deformed fetuses. Unlike inorganicmercury compounds, it can penetrate throughthe membrane barrier of the erythrocyte,accumulating at about 10 times greater concentrationthan that in the plasma (WHO1976). Its rate of excretion on the bloodlevel is very slow. It gradually accumulatesin the blood. Such accumulation was found toreach 60% equilibrium at about 90 days, culminatedafter 270 days (Munro and Willes,1978). Skin absorption exhibits the symptomsof mercury poisoning. The toxic thresholdconcentration of mercury in the wholeblood is usually in the range 40 to 50 μg/L,while the normal range should be below10 μg/L.

It is a flammable liquid; flash point 38°C (101°F). The flammability of this compound, its ease of oxidation and the energy of decomposition is relatively lower than the alkyls of lighter metals. It is mildly endothermic. The heat of formation, △H°f is ＋75.3 kJ/mol (Bretherick 1995). Unlike most other metal alkyls formed by elements of lower atomic numbers, dimethylmercury does not pose any serious fire or explosion hazard. Although it does not ignite in air, the compound is easily inflammable. It dissolves in lower alcohols without any violent decomposition. Heating with oxidizing substances can cause explosion. Violent explosion is reported with diboron tetrachloride at －63°C (－81°F) under vacuum (Wartik et al. 1971).

DMM is a colorless liquid that is volatile at room temperature (vapor pressure 62.3 mmHg) and is slightly soluble in water (water solubility 8860 mg l^-1). There are no reports on the partition behavior of DMM but it is known to readily evaporate and is thus rarely found in sediment or soil. No reports were found on the environmental persistence of DMM. While DMM vaporizes, no studies were found on long range transport. The lipophilicity ofDMMresults in its accumulation inadipose tissue, plasma proteins, and brain. DMM has not been found in fish.

In contrast to the white crystalline solids of the pure forms of methylmercury (MMM) and phenylmercury, DMM exists as a colorless liquid at room temperature with high volatility. These physical qualities enable high concentrations of the substance to be absorbed by exposure pathways of the skin and lungs that circumvent first-pass elimination. Effectively, this prolongs the systemic circulation of DMM, and extends its residence time in the body.
The additional alkyl group flanking the mercury imparts DMM with lipophilicity that exceeds its monoalkylated counterpart, and allows DMM to be sequestered in lipid-rich depots. The metabolic delay allows the neurotoxicity of DMM to remain latent for months.
The gradual conversion into MMM results in the release of DMM from depots such as lipid-rich tissues and plasma proteins, and permits its movement through barriers such as the blood–brain and placenta. A cysteine complex of the monomethylated metabolite penetrates the endothelial cells of the blood–brain barrier by mimicking methionine and using the large neutral amino acid transporter.
Thus, the toxicity of DMM is mediated by its dealkylation. Cleavage of the carbon–mercury bond generates MMM metabolites, which can form covalent bonds with cellular ligands with amphiphilic properties. The mercury center reacts with sulfur and sulfur-containing thiol groups of enzymes and thereby inhibits them, resulting in cellular dysfunction.
The metal center of DMM acts as a soft acid, and binds tightly to polarizable donor atoms in soft bases. An additional mechanism of adverse effect is the disruption of the prooxidant– antioxidant balance, causing oxidative damage to biomolecules resulting cellular damage. Within cells, mercury may interact with a variety of proteins, particularly microsomal and mitochondrial enzymes. Recent studies demonstrated that the combined administration of the antioxidants N-acetyl cysteine, zinc, and selenium mitigated DMM acute and chronic toxicity by reducing enzymatic and cellular dysfunction.