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Triethyl(methyl)lead

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Identification
Molecular formula
C7H16Pb
CAS number
607-74-5
IUPAC name
triethyl(methyl)plumbane
State
State

Triethyl(methyl)lead is a liquid at room temperature.

Melting point (Celsius)
-91.00
Melting point (Kelvin)
182.15
Boiling point (Celsius)
199.30
Boiling point (Kelvin)
472.45
General information
Molecular weight
291.41g/mol
Molar mass
291.4060g/mol
Density
1.4570g/cm3
Appearence

Triethyl(methyl)lead is a colorless liquid.

Comment on solubility

Solubility of Triethyl(methyl)plumbane

Triethyl(methyl)plumbane, with the chemical formula C5H13Pb, presents interesting characteristics regarding its solubility. As an organolead compound, it exhibits both hydrophobic and lipophilic properties. This means:

  • It is insoluble in water, which is typical for many organic lead compounds.
  • It has a relatively high solubility in organic solvents such as hexane and chloroform.

The lack of solubility in water is attributed to:

  • The high molecular weight of lead, which significantly influences the compound's interactions with water.
  • The nonpolar character of the triethyl groups that dominate its structure, rendering it incompatible with polar solvents like water.

To summarize, Triethyl(methyl)plumbane is not soluble in water but finds good compatibility with organic solvents. This solubility behavior is essential for its applications in organic synthesis and as a reagent in various chemical reactions.

Interesting facts

Interesting Facts about Triethyl(methyl)plumbane

Triethyl(methyl)plumbane is a fascinating organometallic compound that showcases the intriguing chemistry of lead in organic synthesis. Here are some key points to consider:

  • Structure and Composition: This compound features a central lead atom bonded to three ethyl groups and one methyl group, illustrating the unique bonding capabilities of lead.
  • Reactivity: As an organolead compound, triethyl(methyl)plumbane can undergo various chemical reactions, making it of interest for synthetic applications, particularly in the formation of complex organic molecules.
  • Historical Context: The study of organometallic compounds like triethyl(methyl)plumbane has been instrumental in the advancement of coordination chemistry and has contributed to a greater understanding of metal-carbon bonds.
  • Toxicity Considerations: Like other lead-containing compounds, caution is advised when handling triethyl(methyl)plumbane due to the toxic effects of lead, which can pose serious health risks.
  • Applications: While primarily of academic interest, compounds like triethyl(methyl)plumbane are studied for potential applications in catalysis and material science.

In conclusion, triethyl(methyl)plumbane represents a captivating intersection of organic and inorganic chemistry, illustrating the versatility and complexity of lead-containing compounds in chemical synthesis.

As stated by renowned chemist Paul G. Gassman, “The study of organometallic chemistry opens a window to new realms of reactivity and synthesis.” Embracing this perspective can lead to innovative applications and discoveries within the field.

Synonyms
Triethylmethyllead
Triethylmethylplumbane
METHYLTRIETHYLLEAD
Plumbane, triethylmethyl-
HSDB 5854
Methyltriethyl lead
UNII-I381XEH64W
EINECS 217-171-4
DTXSID9051799
METHYLTRIETHYLLEAD [HSDB]
Lead, triethylmethyl
Plumbane, triethylmethyl
DTXCID2030354
kgfrughbhnuhos-uhfffaoysa-n
Triethyl(methyl)plumbane
Methyltriethylplumbane
1762-28-3
Lead, triethylmethyl-
I381XEH64W
Triethyl(methyl)plumbane #
NS00081575
Q27280307