Triphenyltin chloride

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Triphenyltin chloride
Ph3SnCl.png
Triphenyltin-chloride-3D-spacefill.png
Names
IUPAC name
chlorotriphenylstannane
Identifiers
639-58-7 YesY
ChEMBL ChEMBL515580 YesY
ChemSpider 12023 YesY
Jmol-3D images Image
PubChem 12540
Properties
C18H15ClSn
Molar mass 385.4747 g/mol
Appearance colourless solid
Melting point 108 °C (226 °F; 381 K)
Boiling point 240 °C (464 °F; 513 K)
organic solvents
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Triphenyltin chloride is an organotin compound with formula Sn(C6H5)3Cl. It is a colourless solid that dissolves in organic solvents. It slowly reacts with water. The main use for this compound is as a fungicide and antifoulant.[1]

Hazards[edit]

Triphenyltin chloride has been found to cause an increase in post-implantation embryonic loss as well as implantation failure in rats.[2] It also caused detrimental effects on body weight, testicular size and structure, and decreased fertility in Holtzmann rats.[3]

References[edit]

  1. ^ Davies, A. G. (2004). Organotin Chemistry. Weinheim, Germany: Wiley-VCH. ISBN 3-527-31023-1. 
  2. ^ Ema, M. (2000). "Reproductive and developmental toxicity of triphenyltin chloride in rats". Congenital Anomalities (Osaka, Japan: National Institute of Health Sciences) 40 (1): 8–13. doi:10.1111/j.1741-4520.2000.tb00903.x. ISSN 0914-3505. 
  3. ^ Golub, M. S. (2006). Metals, Fertility, and Reproductive Toxicity. CRC Press. pp. 28–31. ISBN 0-415-70040-X.