Triphenylphosphine Oxide

Product Name Triphenylphosphine Oxide
CAT No. CS-T-62517
CAS No. 791-28-6
Category Impurities
Stock IN-Stock
Mol. Wt. 278.3 g/mol
Mol. For. C18H15OP
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Purity 95%
Smileys C1=CC=C(C=C1)P(=O)(C2=CC=CC=C2)C3=CC=CC=C3
Canonical Smiles C1=CC=C(C=C1)P(=O)(C2=CC=CC=C2)C3=CC=CC=C3
InchIKey FIQMHBFVRAXMOP-UHFFFAOYSA-N
Inchl InChI=1S/C18H15OP/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
IUPAC diphenylphosphorylbenzene
Controlled No
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Triphenylphosphine oxide (TPPO) is a white crystalline solid that is commonly used as a reagent in organic chemistry. It is a derivative of triphenylphosphine, which is a commonly used reducing agent. TPPO is often used as a mild oxidizing agent, as it can be easily reduced to triphenylphosphine under reducing conditions. TPPO is often used in the synthesis of organic molecules, particularly in the formation of carbon-carbon bonds. It can be used in reactions such as the Wittig reaction, which is used to form carbon-carbon double bonds. TPPO is also used in the Horner-Wadsworth-Emmons reaction, which is used to form carbon-carbon bonds between carbonyl compounds and phosphonates. Chemically, TPPO is an organophosphorus compound that contains three phenyl groups attached to a phosphorus atom. It has a molecular formula of C18H15OP and a molecular weight of 278.29 g/mol. TPPO is a polar compound, with a melting point of 156-158°C and a boiling point of 360°C. TPPO is considered to be a relatively safe reagent to use in organic chemistry, as it is not particularly reactive or toxic. However, it can be irritating to the skin and eyes, and should be handled with care. Overall, TPPO is an important reagent in organic chemistry that is widely used in the synthesis of organic molecules.

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