Online Database of Chemicals from Around the World

Tetraethylplumbane
[CAS# 78-00-2]

List of Suppliers
Tianjin Zhongxin Chem-tech Co., Ltd. China Inquire  
+86 (22) 6688-0623
sales@tjzxchem.com
Chemical manufacturer since 2007
chemBlink standard supplier since 2009
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
Gelest, Inc. USA Inquire  
+1 (215) 547-1015
info@gelest.com
Chemical manufacturer
Complete supplier list of Tetraethylplumbane
Identification
Classification Organic raw materials >> Organometallic compound >> Organic scandium, tantalum, thallium, tungsten, antimony, lanthanum, lead, vanadium, molybdenum, chromium, ytterbium, etc.
Name Tetraethylplumbane
Synonyms NSC 22314; TEL; Tetraethyllead
Molecular Structure CAS # 78-00-2, Tetraethylplumbane, NSC 22314, TEL, Tetraethyllead
Molecular Formula C8H20Pb
Molecular Weight 323.44
CAS Registry Number 78-00-2
EC Number 201-075-4
SMILES CC[Pb](CC)(CC)CC
Properties
Solubility Insoluble (1.5E-5 g/L) (25 ºC), Calc.*
Density 1.7 g/cm3**
Melting point 400 ºC (decomp)***
Boiling point 220 ºC****
Refractive index 1.5318 (20 ºC)*****
Flash point 82.7±22.6 ºC, 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; Rept. Dept. Aeronautical Research Inst. Tokyo Imp. Univ. 1927, V2, P409-20.
**** Meinert, Richard N.; Journal of the American Chemical Society 1933, V55, P979-89.
***** Jones, W. J.; Journal of the Chemical Society 1935, P39-47.
Safety Data
Hazard Symbols symbol symbol symbol   GHS06;GHS08;GHS09 Danger    Details
Hazard Statements H300+H310+H330-H300-H310-H330-H360-H373-H400-H410    Details
Precautionary Statements P203-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
SDS Available
up Discovory and Applicatios
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
Related Products
4,5,6,7-Tetrafluoro-2,3-dihydro-1H-isoindole  1,1,2,2-Tetrafluoro-1,4-diiodobutane  Tetraethyl orthosilicate  Tetraethyl Orthosilicate  Tetraethyl 2,2'-(1,4-phenylenedimethylidyne)bismalonate  Tetraethylphosphinous amide  Tetraethylphosphonium fluoborate  Tetraethylphosphonium iodide  Tetraethylphosphorodiamidic chloride  2,2,6,6-Tetraethyl-4-piperidinol  Tetraethyl pyrophosphate  Tetraethyl ranelate  Tetraethylsilane  Tetraethyltin  Tetraethylurea  2,2,2,3'-Tetrafluoroacetophenone  2,2,2,2'-Tetrafluoroacetophenone  2,3,5,6-Tetrafluoroaniline  2,3,4,5-Tetrafluoroaniline  2,3,4,6-Tetrafluoroaniline