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tetraethyllead
Sign in to saveAlso known as tetraethyl lead, lead tetraethyl, TEL, tetraethylplumbane, [PbEt4], PbEt4
Tetraethyllead (commonly styled tetraethyl lead), abbreviated TEL, is an organolead compound with the formula Pb(C2H5)4. It was widely used as a fuel additive for much of the 20th century, first being mixed with gasoline beginning in the 1920s. This "leaded gasoline" had an increased octane rating that allowed engine compression to be raised substantially and in turn increased vehicle performance and fuel economy. TEL was first synthesized by German chemist Carl Jacob Löwig in 1853. American chemical engineer Thomas Midgley Jr., who was working for the U.S. corporation General Motors, was the
OverviewAI-generated
Tetraethyllead is a chemical compound with the formula C₈H₂₀Pb. It has a molecular mass of 324.133 and a density of 1.65. The substance exhibits a melting point of -202 and a decomposition point of 228. Its vapor pressure is 0.2, and it has a solubility of 0.00002. The flash point is 200, with a lower flammable limit of 1.8. The ionization energy is 11.1.
Safety data indicates an immediately dangerous to life or health level of 40. The time-weighted average exposure limit is 0.075. The compound is associated with 480 PubMed entries and is referenced by 554 other encyclopedia articles.
Synthesized by Vinony from 27 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.
Chemical data
- Formula
- C8H20Pb
- Molecular weight
- 323 g/mol
- SMILES
- C[CH2].C[CH2].C[CH2].C[CH2].[Pb]
- InChIKey
- MRMOZBOQVYRSEM-UHFFFAOYSA-N
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Research
480 papers- Online measurement of tetraethyllead in aqueous samples utilizing monolith-based magnetism-enhanced in-tube solid phase microextraction coupled with chromatographic analysis.Journal of chromatography. A · 2023
- TETRAETHYLLEAD INTOXICATION.Archives of environmental health · 1964
- Tetraethyllead and tetramethyllead - Addendum: re-evaluation of the BAT values and derivation of a BLW: Assessment Values in Biological Material - Translation of the German version from 2025.The MAK collection for occupational health and safety · 2025
- Chirality Induced in Tetraethyllead through Noncovalent Interactions with a Chiral Tag.Journal of the American Chemical Society · 2026
- Toxic myoclonus.Advances in neurology · 1986
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Part of
- leaded gasoline
- Has part
- lead
- Mass
- 324.133
Show 14 more facts
- Commons category
- Tetraethyllead
- density
- 1.65
- canonical SMILES
- CC[Pb](CC)(CC)CC
- flash point
- 200
- NIOSH Pocket Guide ID
- 0601
- immediately dangerous to life or health
- 40
- melting point
- -202
- decomposition point
- 228
- vapor pressure
- 0.2
- solubility
- 0.00002
- lower flammable limit
- 1.8
- ionization energy
- 11.1
- time-weighted average exposure limit
- 0.075
- chemical formula
- C₈H₂₀Pb
via Wikidata · CC0
~32 min read
Encyclopedic overview
31 sectionsContents
- Synthesis and properties
- Reactions
- In motor fuel
- Valve wear preventive
- Antiknock agent
- "Ethyl Fluid"
- Phaseout and ban
- Leaded-fuel bans
- Europe
- North America
- South America
- Asia
- Oceania
- Africa
- In motor racing
- Aviation gasoline
- Alternative antiknock agents
- Toxicity
- History
- In fuel
- Initial controversy
- Modern findings
- Effect on crime rates
- Lingering issues over time
- See also
- References
- Further reading
- External links
- Media articles
- Official documents
- Scientific papers and journal articles
Tetraethyllead (commonly styled tetraethyl lead), abbreviated TEL, is an organolead compound with the formula Pb(C2H5)4. It was widely used as a fuel additive for much of the 20th century, first being mixed with gasoline beginning in the 1920s. This "leaded gasoline" had an increased octane rating that allowed engine compression to be raised substantially and in turn increased vehicle performance and fuel economy. TEL was first synthesized by German chemist Carl Jacob Löwig in 1853. American chemical engineer Thomas Midgley Jr., who was working for the U.S. corporation General Motors, was the first to discover its effectiveness as a knock inhibitor on December 9, 1921, after spending six years attempting to find an additive that was both highly effective and inexpensive.
Of the some 33,000 substances in total screened, lead was found to be the most effective antiknock agent, in that it necessitated the smallest concentrations necessary; a treatment of 1 part TEL to 1300 parts gasoline by weight is sufficient to suppress detonation. The four ethyl groups in the compound served to dissolve the active lead atom within the fuel. When injected into the combustion chamber, tetraethyllead decomposed upon heating into ethyl radicals, lead, and lead oxide. The lead oxide scavenges radicals and therefore inhibits a flame from developing until full compression has been achieved, allowing the optimal timing of ignition, as well as the lowering of fuel consumption. Throughout the sixty year period from 1926 to 1985, an estimated 20 trillion liters of leaded gasoline at an average lead concentration of 0.4 g/L were produced and sold in the United States alone, or an equivalent of 8 million tons of inorganic lead, three quarters of which would have been emitted in the form of lead chloride and lead bromide. Estimating a similar amount of lead to have come from other countries' emissions, a total of more than 15 million tonnes of lead may have been released into the atmosphere.
Excerpted from Wikipedia’s “tetraethyllead” article, available under the CC BY-SA 4.0 licence.