Triphenyltin hydroxide

Triphenyltin hydroxide
Names
	Preferred IUPAC name Triphenylstannanol
Identifiers
CAS Number	76-87-9 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	4139186
ChEBI	CHEBI:30473 ;
ChEMBL	ChEMBL506538 ;
ChemSpider	21106510 ;
ECHA InfoCard	100.000.901
EC Number	200-990-6;
Gmelin Reference	7194
KEGG	C18729;
PubChem CID	9907219;
RTECS number	WH8575000;
UNII	KKL46V5313 ;
UN number	2786 2588
CompTox Dashboard (EPA)	DTXSID1021409 DTXSID50215768, DTXSID1021409 ;
	InChI InChI=1S/3C6H5.H2O.Sn/c31-2-4-6-5-3-1;;/h31-5H;1H2;/q;;;;+1/p-1 Key: BFWMWWXRWVJXSE-UHFFFAOYSA-M ; InChI=1/3C6H5.H2O.Sn/c31-2-4-6-5-3-1;;/h31-5H;1H2;/q;;;;+1/p-1/rC18H16OSn/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,19H Key: BFWMWWXRWVJXSE-OLMCWIPIAE;
	SMILES O[Sn](c1ccccc1)(c2ccccc2)c3ccccc3;
Properties
Chemical formula	C18H16OSn
Molar mass	367.035 g·mol−1
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H301, H311, H315, H318, H330, H335, H351, H361, H372, H410
Precautionary statements	P201, P202, P260, P261, P264, P270, P271, P273, P280, P281, P284, P301+P310, P302+P352, P304+P340, P305+P351+P338, P308+P313, P310, P312, P314, P320, P321, P322, P330, P332+P313, P361, P362, P363, P391, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Triphenyltin hydroxide is an organotin compound with formula Sn(C₆H₅)₃OH. Triphenyltin hydroxide is used as a fungicide for potatoes, sugar beets, and pecans. It was first registered for use as a pesticide in the United States in 1971.^[1]

Structure

While triphenyltin hydroxide is often depicted as a monomer, it crystallizes as a polymer with a bridging hydroxide groups.^[2] The Sn-O distances are 2.18 and 2.250 Å. Many organotin compounds engage in similar aggregation equilibria.

References

^ "R.E.D. Facts: Triphenyltin Hydroxide" (PDF). U.S. EPA.
^ Christopher Glidewell; John N. Low; João A. S. Bomfim; Carlos A. L. Filgueiras; James L. Wardell (2002). "catena-Poly[[triphenyltin(IV)]-μ-hydroxo-κ²O:O] at 120 K". Acta Crystallographica Section C: Crystal Structure Communications. 58 (Pt 4): M199-201. doi:10.1107/S0108270102001798. PMID 11932514.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[1] "R.E.D. Facts: Triphenyltin Hydroxide" (PDF). U.S. EPA.

[2] Christopher Glidewell; John N. Low; João A. S. Bomfim; Carlos A. L. Filgueiras; James L. Wardell (2002). "catena-Poly[[triphenyltin(IV)]-μ-hydroxo-κ²O:O] at 120 K". Acta Crystallographica Section C: Crystal Structure Communications. 58 (Pt 4): M199-201. doi:10.1107/S0108270102001798. PMID 11932514.

[1]

[2]