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Triphenylphosphine, flake, 99%, Thermo Scientific Chemicals

Product Code. 11448036
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250 g
1000 g
5000 g

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.
TRUSTED_SUSTAINABILITY

Chemical Identifiers

CAS 603-35-0
Molecular Formula C18H15P
Molecular Weight (g/mol) 262.29
MDL Number MFCD00003043 MFCD20489348
InChI Key RIOQSEWOXXDEQQ-UHFFFAOYSA-N
Synonym triphenylphosphine, triphenyl phosphine, phosphine, triphenyl, triphenylphosphorus, triphenyl-phosphane, triphenylphosphide, phosphorustriphenyl, trifenylfosfin, trifenylfosfin czech, triphenylphosphine resin
PubChem CID 11776
IUPAC Name triphenylphosphane
SMILES C1=CC=C(C=C1)P(C1=CC=CC=C1)C1=CC=CC=C1

Specifications

Melting Point 79°C to 81°C
Density 1.2
Boiling Point 360°C
Flash Point 181°C (358°F)
Assay Percent Range 99%
Odor Mild
Quantity 5000 g
Beilstein 610776
Merck Index 14,9743
Solubility Information Insoluble in water; Soluble in benzene,acetone,carbon tetrachloride,ether,and glacial acetic acidSoluble in ether,benzene,carbon tetrachloride,glacial acetic acid,acetone,chloroform and alcohol; Insoluble in water.
Formula Weight 262.29
Percent Purity 99%
Physical Form Flakes
Chemical Name or Material Triphenylphosphine
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Product Identifier
  • Triphenylphosphine
Signal Word
  • Warning
Hazard Category
  • Acute toxicity Category 4
  • Skin sensitiser Category 1
  • Specific target organ toxicity after repeated exposure Category 2
Hazard Statement
  • H302-Harmful if swallowed.
  • H317-May cause an allergic skin reaction.
  • H373-May cause damage to organs.
Precautionary Statement
  • P280-Wear protective gloves/protective clothing/eye protection/face protection.
  • P301+P312-IF SWALLOWED: Call a POISON CENTER or doctor/physician/ if you feel unwell.
Supplemental information
  • MIXTURE LIST-Contains : Triphenylphosphine

RUO – Research Use Only

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