Tetraethyltin

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Tetraethyltin
Tetraethyltin.svg
Names
IUPAC name
Tetraethyltin
Other names
Tetraethyl tin
Identifiers
597-64-8 N
Abbreviations TET
ChemSpider 11212 YesY
EC Number 209-906-2
Jmol 3D model Interactive image
MeSH Tetraethyltin
PubChem 11704
UN number 3384
  • InChI=1S/4C2H5.Sn/c4*1-2;/h4*1H2,2H3; YesY
    Key: RWWNQEOPUOCKGR-UHFFFAOYSA-N YesY
  • CC[Sn](CC)(CC)CC
Properties
C8H20Sn
Molar mass 234.96 g·mol−1
Appearance Colourless liquid
Density 1.187 g cm−3
Melting point −112 °C (−170 °F; 161 K)
Boiling point 181 °C (358 °F; 454 K)
Vapor pressure {{{value}}}
Related compounds
Related Tetraalkylstannanes
Tetrabutyltin

Tetramethyltin

Related compounds
Tetraethylgermanium

Tetraethyllead

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Tetraethyltin or tetraethyl tin is a chemical compound with the formula C
8
H
20
Sn
and molecular structure (CH3CH2)4Sn, that is, a tin atom attached to four ethyl groups. It is an important example of an organotin compound, often abbreviated as TET.

Tetraethyltin is a colourless flammable liquid, soluble in diethyl ether and insoluble in water, that freezes at -112 °C and boils at 181 °C.[1][2] It is used in the electronics industry.

Tetraethyltin can be obtained by reacting ethylmagnesium bromide with tin(IV) chloride:[1]

SnCl4 + 4 (C2H5)MgBr → (CH3CH2)4Sn + 4 MgBrCl

The same reaction can be used to obtain tetra-n-propyltin and tetra-n-butyltin.[1]

Tetraethyltin is converted in the body to the more toxic triethyltin.[3]

See also

References

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  1. 1.0 1.1 1.2 G. J. M. Van Der Kerk and J. G. A. Luijten (1956), "Tetraethyltin". Organic Syntheses, volume 36, page 86; Coll. Vol. 4, p.881 (1963)
  2. SAFC corp, tetraethyltin catalog page. Accessed on 2011-01-18.
  3. Lua error in package.lua at line 80: module 'strict' not found.