Triphenyltin chloride

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Triphenyltin chloride
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Names
IUPAC name
chlorotriphenylstannane
Identifiers
639-58-7 YesY
ChEMBL ChEMBL515580 YesY
ChemSpider 12023 YesY
Jmol 3D model Interactive image
PubChem 12540
  • InChI=1S/3C6H5.ClH.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H;/q;;;;+1/p-1 YesY
    Key: NJVOZLGKTAPUTQ-UHFFFAOYSA-M YesY
  • 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
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
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

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