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Tributyltin chloride

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Tributyltin chloride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.014.508 Edit this at Wikidata
EC Number
  • 215-958-7
KEGG
UNII
  • InChI=1S/3C4H9.ClH.Sn/c3*1-3-4-2;;/h3*1,3-4H2,2H3;1H;/q;;;;+1/p-1
    Key: GCTFWCDSFPMHHS-UHFFFAOYSA-M
  • CCCC[Sn](CCCC)(CCCC)Cl
Properties
C12H27ClSn
Molar mass 325.51 g·mol−1
Appearance colorless viscous liquid
Density 1.20 g·cm−3 (20 °C
1.4903
Hazards
GHS labelling:
GHS06: ToxicGHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard
Danger
H301, H312, H315, H317, H319, H372, H410
P260, P261, P264, P270, P272, P273, P280, P301+P310, P302+P352, P305+P351+P338, P312, P314, P321, P322, P330, P332+P313, P333+P313, P337+P313, P362, P363, P391, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tributyltin chloride is an organotin compound with the formula (C4H9)3SnCl. It is a colorless liquid that is soluble in organic solvents. The molecule has tetrahedral geometry.

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.

Safety

The compound is almost as poisonous as hydrogen cyanide.[citation needed]

Literature

  1. ^ "Palladium-catalyzed Coupling Of Acid Chlorides With Organotin Reagents: Ethyl (E)-4-(4-nitrophenyl)-4-oxo-2-butenoate". Org. Synth. 67: 86. 1989. doi:10.15227/orgsyn.067.0086. {{cite journal}}: Cite uses deprecated parameter |authors= (help)