Triphenyltin chloride
Names
IUPAC name
chlorotriphenylstannane
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.010.327
UNII
  • InChI=1S/3C6H5.ClH.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H;/q;;;;+1/p-1 checkY
    Key: NJVOZLGKTAPUTQ-UHFFFAOYSA-M checkY
  • InChI=1/3C6H5.ClH.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H;/q;;;;+1/p-1/rC18H15ClSn/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
    Key: NJVOZLGKTAPUTQ-LLLCWGJXAQ
  • Cl[Sn](c1ccccc1)(c2ccccc2)c3ccccc3
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] Triphenyl tin chloride is used as a chemosterilant. Triphenyl tins used as an antifeedants against potato cutworm.

Hazards

Triphenyltin chloride is as toxic as hydrogen cyanide.[2] It also caused detrimental effects on body weight, testicular size and structure, and decreased fertility in Holtzmann rats.[3]

References

  1. ↑ Davies, A. G. (2004). Organotin Chemistry. Weinheim, Germany: Wiley-VCH. ISBN 3-527-31023-1.
  2. ↑ G. G. Graf (2005). "Tin, Tin Alloys, and Tin Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a27_049. ISBN 3527306730.
  3. ↑ Golub, M. S. (2006). Metals, Fertility, and Reproductive Toxicity. CRC Press. pp. 28–31. ISBN 0-415-70040-X.


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