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Tetraethylplumbane
[CAS# 78-00-2]

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Identification
ClassificationOrganic raw materials >> Organometallic compound >> Organic scandium, tantalum, thallium, tungsten, antimony, lanthanum, lead, vanadium, molybdenum, chromium, ytterbium, etc.
NameTetraethylplumbane
SynonymsNSC 22314; TEL; Tetraethyllead
Molecular StructureCAS # 78-00-2, Tetraethylplumbane
Molecular FormulaC8H20Pb
Molecular Weight323.44
CAS Registry Number78-00-2
EC Number201-075-4
SMILESCC[Pb](CC)(CC)CC
Properties
SolubilityInsoluble (1.5E-5 g/L) (25 °C), Calc.*
Density1.7 g/cm3**
Melting point400 °C (decomp)***
Boiling point220 °C****
Refractive index1.5318 (20 °C)*****
Flash point82.7±22.6 °C, Calc.*
*Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2015 ACD/Labs)
**"International Chemical Safety Cards" data were obtained from the National Institute for Occupational Safety and Health (US)
***Tanaka, Yoshio
****Meinert, Richard N.
*****Jones, W. J.
Safety Data
Hazard Symbolssymbol symbol symbol   GHS06;GHS08;GHS09 Danger  Details
Risk StatementsH300+H310+H330-H300-H310-H330-H360-H373-H400-H410  Details
Safety StatementsP203-P260-P262-P264-P270-P271-P273-P280-P284-P301+P316-P302+P352-P304+P340-P316-P318-P319-P320-P321-P330-P361+P364-P391-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute hazardous to the aquatic environmentAquatic Acute1H400
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Specific target organ toxicity - repeated exposureSTOT RE2H373
Acute toxicityAcute Tox.1H310
Reproductive toxicityRepr.1AH360
Acute toxicityAcute Tox.2H300
Acute toxicityAcute Tox.2H330
Acute toxicityAcute Tox.1H330
Acute toxicityAcute Tox.1H300
SDSAvailable
up Discovery and Applications
Tetraethylplumbane, with the chemical formula Pb(C₂H₅)₄, is an organometallic compound of lead. It was first synthesized in the early 20th century, around the 1850s, by chemists who were investigating various organolead compounds for their potential applications. The synthesis typically involves the reaction of ethyl iodide with lead(II) acetate in the presence of sodium. Tetraethylplumbane was among the first organolead compounds studied and marked a significant step in the development of organometallic chemistry.

One of the primary historical applications of tetraethylplumbane was as an additive in gasoline. In the 1920s, tetraethyl lead (TEL), which is derived from tetraethylplumbane, was introduced as an anti-knock agent in internal combustion engines. It significantly improved the octane rating of fuels, allowing for more efficient engine performance and reducing engine knock. This led to widespread use in automotive fuels throughout the mid-20th century, making tetraethyl lead a crucial component in the development of high-performance vehicles.

However, the environmental and health impacts of tetraethyl lead became apparent over time. Lead is a toxic heavy metal that can cause serious health issues, including neurological damage, especially in children. As a result, concerns over lead exposure led to the gradual phasing out of leaded gasoline in many countries during the 1970s and 1980s. The introduction of unleaded gasoline alternatives diminished the demand for tetraethyl lead, leading to a decline in its use.

Despite its controversial past, tetraethylplumbane remains of interest in certain industrial applications. It can be utilized in organic synthesis as a reagent for various chemical transformations, including the introduction of ethyl groups into organic molecules. Additionally, it serves as a precursor for other organolead compounds, which continue to be studied for their potential applications in chemistry.

Moreover, research into the environmental fate of organolead compounds, including tetraethylplumbane, has led to a better understanding of lead's behavior in the environment and its impact on ecosystems. This research is critical for developing strategies to remediate contaminated sites and manage lead exposure risks.

In summary, tetraethylplumbane is an organometallic compound that played a pivotal role in the history of fuel additives, particularly in improving the performance of gasoline. While its use has declined due to health and environmental concerns, it still holds significance in organic synthesis and ongoing research regarding lead contamination and remediation.

References

Dmitri A. Katskov, Yuri M. Sadagov and Maria Banda. Fast heated ballast furnace atomizer for atomic absorption spectrometry, J. Anal. Atom. Spectrosc., 2005, 20, 227.
Market Analysis Reports
List of Reports Available for Tetraethylplumbane
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