| Weight | 267.34 g/mol |
|---|---|
| Formula | C4H12Pb |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Tetramethyllead (75-74-1)
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- Determination of tetramethyllead and tetraethyllead in the atmosphere by a two-step enrichment method and gas chromatographicmass spectrometric isotope dilution analysis (Analytica Chimica Acta, 1981)
- The acute effects of lead alkyls. Oral administration of tetramethyllead, tetraethyllead, trimethyllead chloride, triethyllead chloride, and diethyllead dichloride to rats. (Archives of Environmental Health, 1963)
- Accumulation and depuration of tetramethyllead by rainbow trout (Water Research, 1981)
- Molecular Structure and Phase-shift of Tetramethyllead as Studied by Gas Electron Diffraction (Bulletin of the Chemical Society of Japan, 1971)
- TETRAETHYLLEAD AND TETRAMETHYLLEAD. COMPARATIVE EXPERIMENTAL PATHOLOGY: I. LEAD ABSORPTION AND PATHOLOGY. (Archives of Environmental Health, 1964)
- Direct determination of tetraethyllead and tetramethyllead in gasoline by high-performance liquid chromatography with electrochemical detection at mercury electrodes (Analytical Chemistry, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H300: Fatal if swallowed
Danger Acute toxicity, oral - Category 1, 2 - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H360: May damage fertility or the unborn child
Danger Reproductive toxicity - Category 1A, 1B -
SMILESC[Pb](C)(C)C
-
InChIKeyXOOGZRUBTYCLHG-UHFFFAOYSA-N
- Pubchem - Tetramethyllead
- Wikipedia - tetramethyllead
Tetramethyllead, also called tetra methyllead and lead tetramethyl, is a chemical compound used as an antiknock additive for gasoline. Its use is being phased out for environmental considerations. The National Institute for Occupational Safety and Health (NIOSH) in the United States has identified tetramethyllead as a potential workplace hazard.
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