| Revision as of 14:25, 10 January 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 449004294 of page Triphenyltin_hydroxide for the Chem/Drugbox validation project (updated: 'ChEMBL'). |
Latest revision as of 16:53, 30 September 2023 edit Trappist the monk (talk | contribs)Administrators479,773 editsm →Structure: cite repair;Tag: AWB |
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}} |
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{{Chembox |
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{{Chembox |
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| Verifiedfields = changed |
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| verifiedrevid = 444237473 |
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| verifiedrevid = 470617074 |
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| ImageFile = Ph3SnOH.png |
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| ImageFile = Ph3SnOH.png |
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| ImageSize = |
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| ImageSize = 170 |
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| ImageAlt = |
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| ImageAlt = Skeletal formula of triphenyltin hydroxide |
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| ImageFile1 = Triphenyltin-hydroxide-3D-spacefill.png |
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| IUPACName = hydroxytriphenylstannane |
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| ImageSize1 = 190px |
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| PIN = |
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| ImageAlt1 = Space-filling model of the triphenyltin hydroxide molecule |
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| PIN = Triphenylstannanol |
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| OtherNames = |
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| OtherNames = |
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| Section1 = {{Chembox Identifiers |
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|Section1={{Chembox Identifiers |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| 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 |
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| CASNo = 76-87-9 |
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| Beilstein = 4139186 |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID=21106510 |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 30473 |
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| ChEMBL_Ref = {{ebicite|correct|EBI}} |
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| ChEMBL = 506538 |
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| EINECS = 200-990-6 |
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| Gmelin = 7194 |
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| KEGG = C18729 |
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| PubChem = 9907219 |
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| PubChem_Comment = |
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| RTECS = WH8575000 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = KKL46V5313 |
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| UNNumber = 2786 2588 |
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| 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 |
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| InChIKey = BFWMWWXRWVJXSE-OLMCWIPIAE |
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| InChIKey = BFWMWWXRWVJXSE-OLMCWIPIAE |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = BFWMWWXRWVJXSE-UHFFFAOYSA-M |
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| StdInChIKey = BFWMWWXRWVJXSE-UHFFFAOYSA-M |
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| CASNo = |
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| ChEMBL = 506538 |
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| PubChem = |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID=21106510 |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 30473 |
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| SMILES = O(c1ccccc1)(c2ccccc2)c3ccccc3 |
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| SMILES = O(c1ccccc1)(c2ccccc2)c3ccccc3 |
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}} |
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| Section2 = {{Chembox Properties |
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|Section2={{Chembox Properties |
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| C = 18 | H = 16 | O = 1 | Sn = 1 |
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| C=18 | H=16 | O=1 | Sn=1 |
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| Appearance = |
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| Appearance = |
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| Density = |
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| Density = |
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| MeltingPt = |
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| BoilingPt = |
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| BoilingPt = |
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| Solubility = }} |
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| Solubility = }} |
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| Section3 = {{Chembox Hazards |
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|Section3={{Chembox Hazards |
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| GHSPictograms = {{GHS05}}{{GHS06}}{{GHS07}}{{GHS08}}{{GHS09}} |
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| MainHazards = |
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| GHSSignalWord = Danger |
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| FlashPt = |
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| HPhrases = {{H-phrases|301|311|315|318|330|335|351|361|372|410}} |
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| Autoignition = }} |
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| 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}} |
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| MainHazards = |
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| FlashPt = |
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| AutoignitionPt = }} |
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}} |
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}} |
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'''Triphenyltin hydroxide''' is an ] with formula Sn(C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>OH. Triphenyltin hydroxide is used as a ] for potatoes, sugar beets, and pecans. It was first registered for use as a ] in the United States in 1971.<ref>{{cite web | publisher = ] | title = R.E.D. Facts: Triphenyltin Hydroxide | url = http://www.epa.gov/oppsrrd1/REDs/factsheets/0099fact.pdf}}</ref> |
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==Structure== |
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] |
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While triphenyltin hydroxide is often depicted as a monomer, it crystallizes as a ] with a ] groups.<ref>{{cite journal|doi=10.1107/S0108270102001798|title=''catena''-Poly<nowiki></nowiki>-μ-hydroxo-κ<sup>2</sup>O:O<nowiki>]</nowiki> at 120 K|author=Christopher Glidewell |author2=John N. Low |author3=João A. S. Bomfim |author4=Carlos A. L. Filgueiras |author5=James L. Wardell |volume=58|year= 2002|journal=Acta Crystallographica Section C: Crystal Structure Communications|issue=Pt 4 |pages=M199-201 |pmid=11932514 }}</ref> The Sn-O distances are 2.18 and 2.250 Å. Many organotin compounds engage in similar aggregation equilibria. |
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==References== |
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<references/> |
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] |
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] |
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{{organic-compound-stub}} |