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| Names | |||
|---|---|---|---|
| IUPAC name
Tetraethyltin | |||
| Other names
Tetraethyl tin Tetraethylstannane | |||
| Identifiers | |||
3D model (JSmol) |
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| Abbreviations | TET | ||
| ChemSpider | |||
| ECHA InfoCard | 100.009.007 | ||
| EC Number |
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| MeSH | Tetraethyltin | ||
PubChem CID |
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| UNII | |||
| UN number | 3384 2788 | ||
CompTox Dashboard (EPA) |
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| Properties | |||
| (CH3CH2)4Sn | |||
| Molar mass | 234.958 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) | ||
| Hazards | |||
| GHS labelling: | |||
   | |||
| Danger | |||
| H226, H300, H310, H330, H410 | |||
| P210, P233, P240, P241, P242, P243, P260, P262, P264, P270, P271, P273, P280, P284, P301+P310, P302+P350, P303+P361+P353, P304+P340, P310, P320, P321, P322, P330, P361, P363, P370+P378, P391, P403+P233, P403+P235, P405, P501 | |||
| NFPA 704 (fire diamond) | |||
| Flash point | 53 °C (127 °F; 326 K) | ||
| Related compounds | |||
Related Tetraalkylstannanes |
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Related compounds |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Tetraethyltin or tetraethyl tin is a chemical compound with the formula (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 CH3CH2MgBr → (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
- Tetraethylmethane
- Tetraethylsilane
- Tetraethylgermane
- Tetraethylplumbane
References
- 1 2 3 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)
- ↑ SAFC corp, tetraethyltin catalog page. Accessed on 2011-01-18.
- ↑ Schmid, D. O.; Cwik, S. (1975). "R receptors on lymphocytes of sheep". Animal Blood Groups and Biochemical Genetics. 6 (1): 61–62. doi:10.1111/j.1365-2052.1975.tb01351.x. PMID 1200418.
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