Chemistry:Tributyltin chloride
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Names | |
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Preferred IUPAC name
Chlorotri(butyl)stannane | |
Other names
Tributylchlorotin
TBTC | |
Identifiers | |
3D model (JSmol)
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KEGG | |
PubChem CID
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Properties | |
C12H27ClSn | |
Molar mass | 325.51 g·mol−1 |
Appearance | colorless viscous liquid |
Density | 1.20 g·cm−3 (20 °C |
Melting point | −9 °C (16 °F; 264 K) |
Boiling point | 171 °C (340 °F; 444 K) |
Refractive index (nD)
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1.4903 |
Hazards | |
Safety data sheet | External MSDS |
GHS pictograms | ![]() ![]() ![]() |
GHS Signal word | Danger |
H301, H312, H315, H317, H319, H360FD, H372, H410 | |
P201, P273, P280, P301+310+330Script error: No such module "Preview warning".Category:GHS errors, P302+352+312Script error: No such module "Preview warning".Category:GHS errors, P305+351+338 | |
Flash point | 108 °C (226 °F; 381 K) (closed cup) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Tributyltin chloride is an organotin compound with the formula (C4H9)3SnCl. It is a colorless liquid that is soluble in organic solvents.
Preparation and reactions
The compound is prepared by a redistribution reaction by combining stannic chloride and tetrabutyltin:
- 3 (C4H9)4Sn + SnCl4 → 4 (C4H9)3SnCl
Tributyltin chloride hydrolyzes to the oxide [(C4H9)3Sn]2O
Tributyltin chloride is used as a precursor to other organotin compounds[1] and reagents, such as tributyltin hydride.
Literature
- ↑ A. F. Renaldo; J. W. Labadie; J. K. Stille (1989). "Palladium-catalyzed Coupling Of Acid Chlorides With Organotin Reagents: Ethyl (E)-4-(4-nitrophenyl)-4-oxo-2-butenoate". Org. Synth. 67: 86. doi:10.15227/orgsyn.067.0086.
![]() | Original source: https://en.wikipedia.org/wiki/Tributyltin chloride.
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