| Common Name |
Hydroxytriphenylstannane
| Description |
Hydroxytriphenylstannane is an Agriclitural fungicide for potatoes, sugar beet, pecans and peanutsHydroxytriphenylstannane belongs to the family of Aromatic Homomonocyclic Compounds. These are aromatic compounds containig only one ring, which is homocyclic.
| Structure |
MOLSDFPDBSMILESInChI
Structure for HMDB31790 (Hydroxytriphenylstannane)
| Synonyms |
| Value |
Source |
[sn(OH)PH3]ChEBI
FentinChEBI
HydroxytriphenyltinChEBI
sn(OH)PH3ChEBI
Triphenylstannylium hydroxideChEBI
Triphenyltin hydroxideChEBI
Ashlade flotinHMDB
Brestan H 47.5 WP fungicideHMDB
Brestan RHMDB
dowco 186HMDB
Du-terHMDB
Du-ter fungicideHMDB
Du-ter fungicide wettable powderHMDB
Du-ter PB-47 fungicideHMDB
Du-ter W-50HMDB
Du-tur flowable-30HMDB
DuterHMDB
Duter extraHMDB
ErithaneHMDB
FarmatinHMDB
FenolovoHMDB
Fentin hydroxideHMDB
Fentin hydroxide, bsiHMDB
FentineHMDB
Fintin hydroxidHMDB
Fintin hydroxydeHMDB
Fintin idrossidoHMDB
Fintine hydroxideHMDB
Fintine hydroxydeHMDB
flo Tin 4lHMDB
flo-Tin 4lHMDB
HaitinHMDB
Haitin WP 20 (fentin hydroxide 20%)HMDB
Haitin WP 60 (fentin hydroxide 60%)HMDB
Hydroxyde de triphenyl-etainHMDB
Hydroxytriphenyl-stannaneHMDB
Hydroxytriphenyl-tinHMDB
Ida, imc flo-tin 4lHMDB
idrossido Di stagno trifenileHMDB
K 19HMDB
KelthoneHMDB
Phenostat-a HHMDB
Phenostat-HHMDB
Quadrangle super-tin 4lHMDB
Sunitron HHMDB
Super tinHMDB
Super tin 4 LHMDB
Super tin 4lHMDB
Super tin 4l gardian flowable fungicideHMDB
Suzu HHMDB
Suzu-HHMDB
TenhideHMDB
TPTHHMDB
TPTH TechnicalHMDB
TptohHMDB
Trifenyl-tinhydroxydeHMDB
TrifenylstanniumhydroxidHMDB
Triphenyl tin hydroxideHMDB
Triphenyl-stannolHMDB
Triphenyl-zinnhydroxidHMDB
TriphenylhydroxytinHMDB
TriphenylstannanolHMDB
Triphenylstannium hydroxideHMDB
Triphenyltin oxideHMDB
Triphenyltin(IV) hydroxideHMDB
Triphenytin hydroxideHMDB
Triple tinHMDB
Triple tin 4lHMDB
Vancide KSHMDB
vito Spot fungicideHMDB
Wesley technical triphenyltin hydroxideHMDB
| Chemical Formlia |
C18H16OSn
| Average Molecliar Weight |
367.03
| Monoisotopic Molecliar Weight |
368.022311705
| IUPAC Name |
triphenylstannanol
| Traditional Name |
triphenyltin hydroxide
| CAS Registry Number |
76-87-9
| SMILES |
O[Sn](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
| InChI Identifier |
InChI=1S/3C6H5.H2O.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H2;/q;;;;+1/p-1
| InChI Key |
BFWMWWXRWVJXSE-UHFFFAOYSA-M
| Chemical Taxonomy |
| Description |
This compound belongs to the class of chemical entities known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
| Kingdom |
Chemical entities
| Super Class |
Organic compounds
| Class |
Benzenoids
| Sub Class |
Benzene and substituted derivatives
| Direct Parent |
Benzene and substituted derivatives
| Alternative Parents |
Metal aryls
Organotin compounds
Organic salts
Organic oxoanionic compounds
Organic oxides
Hydrocarbon derivatives
| Substituents |
Metal aryl
Monocyclic benzene moiety
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organic salt
Organotin compound
Organometallic compound
Organic post-transition metal moeity
Organic hydroxide
Aromatic homomonocyclic compound
| Molecliar Framework |
Aromatic homomonocyclic compounds
| External Descriptors |
organotin compound (CHEBI:30473 )
hydroxides (CHEBI:30473 )
Organotin fungicides (C18729 )
| Ontology |
| Status |
Expected but not Quantified
| Origin |
Endogenous
Food
| Biofunction |
Not Available
| Application |
Agriclitural Chemical
| Cellliar locations |
Membrane
| Physical Properties |
| State |
Not Available
| Experimental Properties |
| Property |
Value |
Reference |
Melting Point116 – 120 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.0004 mg/mL at 25 °CNot Available
LogP3.53Not Available
| Predicted Properties |
| Property |
Value |
Source |
Water Solubility0.015 mg/mLALOGPS
logP4.38ALOGPS
logP2.61ChemAxon
logS-4.4ALOGPS
pKa (Strongest Acidic)8.49ChemAxon
pKa (Strongest Basic)-5.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area20.23 Å2ChemAxon
Rotatable Bond Count3ChemAxon
Refractivity78.99 m3·mol-1ChemAxon
Polarizability31.02 Å3ChemAxon
Number of Rings3ChemAxon
Bioavailability1ChemAxon
Rlie of FiveYesChemAxon
Ghose FilterYesChemAxon
Vebers RlieYesChemAxon
MDDR-like RlieYesChemAxon
| Spectra |
| Spectra |
Not Available
| Biological Properties |
| Cellliar Locations |
Membrane
| Biofluid Locations |
Not Available
| Tissue Location |
Not Available
| Pathways |
Not Available
| Normal Concentrations |
| Not Available |
| Abnormal Concentrations |
|
Not Available
| Associated Disorders and Diseases |
| Disease References |
None
| Associated OMIM IDs |
None
| External Links |
| DrugBank ID |
Not Available
| DrugBank Metabolite ID |
Not Available
| Phenol Explorer Compound ID |
Not Available
| Phenol Explorer Metabolite ID |
Not Available
| FoodDB ID |
FDB008463
| KNApSAcK ID |
Not Available
| Chemspider ID |
8082871
| KEGG Compound ID |
C18729
| BioCyc ID |
Not Available
| BiGG ID |
Not Available
| Wikipedia Link |
Not Available
| NuGOwiki Link |
HMDB31790
| Metagene Link |
HMDB31790
| METLIN ID |
Not Available
| PubChem Compound |
9907219
| PDB ID |
Not Available
| ChEBI ID |
30473
Product: 10-Deacetyl-7-xylosyl paclitaxel
References |
| Synthesis Reference |
Not Available |
| Material Safety Data Sheet (MSDS) |
Not Available |
| General References |
- (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
|
PMID: 11640919