Triphenyltin chloride

Triphenyltin chloride
Names


IUPAC name chlorotriphenylstannane
Identifiers
CAS Registry Number	639-58-7^Y
ChEMBL	ChEMBL515580^Y
ChemSpider	12023^Y
InChI InChI=1S/3C6H5.ClH.Sn/c31-2-4-6-5-3-1;;/h31-5H;1H;/q;;;;+1/p-1^Y Key: NJVOZLGKTAPUTQ-UHFFFAOYSA-M^Y InChI=1/3C6H5.ClH.Sn/c31-2-4-6-5-3-1;;/h31-5H;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
Jmol-3D images	Image
PubChem	12540
SMILES Cl[Sn](c1ccccc1)(c2ccccc2)c3ccccc3
Properties
Chemical formula	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)
Solubility in water	organic solvents
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Y verify (what is: Y/N?)
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

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

↑ Davies, A. G. (2004). Organotin Chemistry. Weinheim, Germany: Wiley-VCH. ISBN 3-527-31023-1.
↑ 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.
↑ Golub, M. S. (2006). Metals, Fertility, and Reproductive Toxicity. CRC Press. pp. 28–31. ISBN 0-415-70040-X.