Triphenyltin hydroxide
{{Chembox
| Verifiedfields = changed
| verifiedrevid = 470617074
| ImageFile = Ph3SnOH.png
| ImageSize = 170
| ImageAlt = Skeletal formula of triphenyltin hydroxide
| ImageFile1 = Triphenyltin-hydroxide-3D-spacefill.png
| ImageSize1 = 190px
| ImageAlt1 = Space-filling model of the triphenyltin hydroxide molecule
| PIN = Triphenylstannanol
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 76-87-9
| Beilstein = 4139186
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID=21106510
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 30473
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 506538
| EINECS = 200-990-6
| Gmelin = 7194
| KEGG = C18729
| PubChem = 9907219
| PubChem_Comment =
| RTECS = WH8575000
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = KKL46V5313
| UNNumber = 2786 2588
| InChI = 1/3C6H5.H2O.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;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
| InChIKey = BFWMWWXRWVJXSE-OLMCWIPIAE
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/3C6H5.H2O.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H2;/q;;;;+1/p-1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = BFWMWWXRWVJXSE-UHFFFAOYSA-M
| SMILES = O[Sn](c1ccccc1)(c2ccccc2)c3ccccc3
}}
|Section2={{Chembox Properties
| Formula = {{chem2|Sn(C6H5)3OH}}
| C=18 | H=16 | O=1 | Sn=1
| Appearance =
| Density =
| MeltingPt =
| BoilingPt =
| Solubility = }}
|Section3={{Chembox Hazards
| GHSPictograms = {{GHS05}}{{GHS06}}{{GHS07}}{{GHS08}}{{GHS09}}
| GHSSignalWord = Danger
| HPhrases = {{H-phrases|301|311|315|318|330|335|351|361|372|410}}
| PPhrases = {{P-phrases|201|202|260|261|264|270|271|273|280|281|284|301+310|302+352|304+340|305+351+338|308+313|310|312|314|320|321|322|330|332+313|361|362|363|391|403+233|405|501}}
| MainHazards =
| FlashPt =
| AutoignitionPt = }}
}}
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.{{cite web | publisher = U.S. EPA | title = R.E.D. Facts: Triphenyltin Hydroxide | url = http://www.epa.gov/oppsrrd1/REDs/factsheets/0099fact.pdf}}
Structure
While triphenyltin hydroxide is often depicted as a monomer, it crystallizes as a polymer with a bridging hydroxide groups.{{cite journal|doi=10.1107/S0108270102001798|title=catena-Poly