{"Abbreviation":"","Aliases":["Plumbane, tetraethyl-","Tetraethylplumbane","Tetraethyl lead","Tetra(methylethyl)lead","Czteroetylek olowiu","Lead, tetraethyl-","Tetraethylolovo","Lead tetraethide","NCI-C54988","Piombo tetra-etile"],"Boiling Point":"392 °","CAS":"78-00-2","ChEBI":"CHEBI:30182","ChemicalClasses":[],"Chirality":"achiral","Classes":["Neurotoxin"],"Color/Form":"Colorless, oily liquid","Decomposition":"Failure to cover the residue with water after emptying a tank of the compound caused explosive decomposition after several days.","Density":"1.653 at 68 °F (EPA, 1998) - Denser than water; will sink g/cm\u003csup\u003e3\u003c/sup\u003e","Dosing Info":[],"DrugClasses":[],"EINECS":"201-075-4","European Community (EC) Number":"201-075-4","Flash Point":"200 °F (EPA, 1998)","HeavyAtomCount":9,"IUPACName":"tetraethylplumbane","InChI":"InChI=1S/4C2H5.Pb/c4*1-2;/h4*1H2,2H3;","InChIKey":"MRMOZBOQVYRSEM-UHFFFAOYSA-N","Melting Point":"-202 °F (EPA, 1998)","MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e20\u003c/sub\u003ePb","MolecularWeight":"323 g/mol","Odor":"Musty odor","Physical Description":"Tetraethyl lead, liquid appears as a colorless liquid with a characteristic odor. Flash point 163 °F. Density 14 lb / gal. Insoluble in water. Toxic by inhalation and by skin absorption.","PrevSalts":[],"PubChemId":6511,"Record Description":["Tetraethyl lead, liquid appears as a colorless liquid with a characteristic odor. Flash point 163 °F. Density 14 lb / gal. Insoluble in water. Toxic by inhalation and by skin absorption.","Tetraethyllead is an organolead compound consisting of four ethyl groups joined to a central lead atom. It derives from a hydride of a plumbane.","Tetraethyl lead is an organolead compound produced by reacting ethyl chloride with a sodium-lead alloy. It was originally used as an antiknock additive in gasoline, but is now found only in some aircraft fuels. Lead is a heavy metal and stable element with the symbol Pb and the atomic number 82, existing in metallic, organic, and inorganic forms. It is mainly found in nature as the mineral galena (PbS), cerussite (PbCO3) or anglesite (PbSO4), usually in ore with zinc, silver, or copper. (L21, L419)","A highly toxic compound used as a gasoline additive. It causes acute toxic psychosis or chronic poisoning if inhaled or absorbed through the skin.","Tetraethyllead is an organolead compound consisting of four ethyl groups joined to a central lead atom. It derives from a hydride of a plumbane."],"References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Tetraethyllead","Name":"Tetraethyllead","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q266210","Name":"Tetraethyllead","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/6511","Name":"Tetraethyllead","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:30182","Name":"Tetraethyllead","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=78-00-2","Name":"Tetraethyllead","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/13426ZWT6A","Name":"Tetraethyllead","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID7023801","Name":"Tetraethyllead","Sub":false}]}],"Reported Fatal Dose":"15 mL tetraethyl lead, ie 0.35 g/kg body weight","SMILES":"CC[Pb](CC)(CC)CC","Solubility":"less than 1 mg/mL at 70 °F (NTP, 1992)","Stability/Shelf Life":"DECOMP SLOWLY @ ROOM TEMP \u0026 MORE RAPIDLY @ ELEVATED TEMP","StoreUNII":["13426ZWT6A"],"StructureBase64":"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","Title":"Tetraethyllead","UNII":"13426ZWT6A","Wikidata":"Q266210","Wikipedia":"Tetraethyllead","XLogP":null}