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Triphenylphosphine, powder, 99%, Thermo Scientific Chemicals

Catalog Number 11387725
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Quantità:
50 g
250 g
1000 g
Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso
603-35-0
C18H15P
262.29
MFCD00003043 MFCD20489348
RIOQSEWOXXDEQQ-UHFFFAOYSA-N
triphenylphosphine, triphenyl phosphine, phosphine, triphenyl, triphenylphosphorus, triphenyl-phosphane, triphenylphosphide, phosphorustriphenyl, trifenylfosfin, trifenylfosfin czech, triphenylphosphine resin
11776
triphenylphosphane
C1=CC=C(C=C1)P(C1=CC=CC=C1)C1=CC=CC=C1
Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso
603-35-0
C18H15P
262.29
MFCD00003043 MFCD20489348
RIOQSEWOXXDEQQ-UHFFFAOYSA-N
triphenylphosphine, triphenyl phosphine, phosphine, triphenyl, triphenylphosphorus, triphenyl-phosphane, triphenylphosphide, phosphorustriphenyl, trifenylfosfin, trifenylfosfin czech, triphenylphosphine resin
11776
triphenylphosphane
C1=CC=C(C=C1)P(C1=CC=CC=C1)C1=CC=CC=C1

Triphenylphosphine 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
Triphenylphosphine 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.

Solubility
Soluble in ether, benzene, carbon tetrachloride, glacial acetic acid, acetone, chloroform and alcohol. Insoluble in water.

Notes
Incompatible with oxidizing agents and acids.
TRUSTED_SUSTAINABILITY
Materiale o nome chimico Triphenylphosphine
Punto di fusione 79°C to 81°C
Densità 1.2
Punti di ebollizione 360°C
Punto d'infiammabilità 181°C (358°F)
Odore Mild
Quantità 250 g
Beilstein 610776
Indice di Merck 14,9743
Informazioni di solubilità Soluble in ether,benzene,carbon tetrachloride,glacial acetic acid,acetone,chloroform and alcohol. Insoluble in water.
Peso formulazione 262.29
Percent Purity 99%
Forma fisica Powder
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