Thermo Scientific Chemicals

Triphenylphosphine, flake, 99%, Thermo Scientific Chemicals

Catalog number: A14089.0B
1000 g, Each
Thermo Scientific Chemicals

Triphenylphosphine, flake, 99%, Thermo Scientific Chemicals

Catalog number: A14089.0B
1000 g, Each
Quantity
Catalog number: A14089.0B
also known as A14089-0B
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Chemical Identifiers

CAS
603-35-0
IUPAC Name
triphenylphosphane
Molecular Formula
C18H15P
InChI Key
RIOQSEWOXXDEQQ-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)P(C1=CC=CC=C1)C1=CC=CC=C1
Identification (FTIR)
Conforms
Melting Point (clear melt)
78.0-85.0?C
Appearance (Color)
White
Form
Flakes
Assay (GC)
≥98.5%

Description

In the synthesis of organic compounds, phosphonium salts and other phosphorus compounds, and as a polymerization initiatorTriphenylphosphine is used in the synthesis of organic compounds due to its nucleophilicity and its reducing character. It is involved in the synthesis of biaryl compounds, phosphonium salts and other phosphorus compounds. As a reducing agent, it is used to prepare aromatic amines from the corresponding aromatic N-oxides. The anionic phosphine is usually isolated as the trisodium salt, which reacts with rhodium to form a complex that finds use in industrial hydroformylation reactions. It is also used to prepare Wilkinson's catalyst, RhCl(PPh3)3 useful to catalyze the hydrogenation of alkenes and tetrakis(triphenylphosphine)palladium(0) that is widely used to catalyse C-C coupling reactions in organic synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
In the synthesis of organic compounds, phosphonium salts and other phosphorus compounds, and as a polymerization initiatorTriphenylphosphine is used in the synthesis of organic compounds due to its nucleophilicity and its reducing character. It is involved in the synthesis of biaryl compounds, phosphonium salts and other phosphorus compounds. As a reducing agent, it is used to prepare aromatic amines from the corresponding aromatic N-oxides. The anionic phosphine is usually isolated as the trisodium salt, which reacts with rhodium to form a complex that finds use in industrial hydroformylation reactions. It is also used to prepare Wilkinson′s catalyst, RhCl(PPh3)3 useful to catalyze the hydrogenation of alkenes and tetrakis(triphenylphosphine)palladium(0) that is widely used to catalyse C-C coupling reactions in organic synthesis.

Notes
Incompatible with oxidizing agents and acids.
RUO – Research Use Only

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