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Triphenylphosphine

SIAL/93092 - ≥95.0% (GC)

Synonym: Phosphorustriphenyl

CAS Number: 603-35-0
Empirical Formula (Hill Notation): C18H15P
Molecular Weight: 262.29
EC Number: 210-036-0
MDL Number: MFCD00003043
Linear Formula: (C6H5)3P
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-93092-250G 250 g
$107.00
1/EA
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45-93092-1KG 1 kg
$202.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 93092-250G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 93092-1KG

 

assay ≥95.0% (GC)
bp 377 °C (lit.)
form crystals
functional group phosphine
impurities ~3% triphenylphosphine oxide
InChI 1S/C18H15P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI key RIOQSEWOXXDEQQ-UHFFFAOYSA-N
mp 77-84 °C
  79-81 °C (lit.)
Quality Level 200 
reaction suitability reaction type: Buchwald-Hartwig Cross Coupling Reaction
  reaction type: Heck Reaction
  reaction type: Hiyama Coupling
  reaction type: Negishi Coupling
  reaction type: Sonogashira Coupling
  reaction type: Stille Coupling
  reaction type: Suzuki-Miyaura Coupling
  reagent type: ligand
SMILES string c1ccc(cc1)P(c2ccccc2)c3ccccc3
solubility water: soluble 0.00017 g/L at 22 °C
vapor density 9 (vs air)
vapor pressure 5 mmHg ( 20 °C)
Application:

  • The palladium-based complexes bearing 1, 3-dibenzylbenzimidazolium with morpholine, triphenylphosphine, and pyridine derivate ligands: This study discusses the synthesis and characterization of new palladium-based complexes incorporating triphenylphosphine, providing insights into their potential catalytic activities (Aktaş et al., 2022 ).

  • Polymer-supported triphenylphosphine: This review highlights the diverse applications of polymer-supported triphenylphosphine in organic synthesis and its significant role in promoting more sustainable and efficient chemical processes (Moussa et al., 2019 ).

  • Application prospects of triphenylphosphine-based mitochondria-targeted cancer therapy: The review focuses on the utilization of triphenylphosphine for developing mitochondria-targeted drugs, emphasizing its potential in cancer therapy (Cheng et al., 2023 ).
General description: Triphenylphosphine, also referred to as PPH3, is an organophosphorous compound. It readily forms complexes with platinum-metal group salts.
Packaging: 1 kg in poly bottle
Packaging: 250 g in poly bottle
Purity ≥95.0% (GC)
bp 377 °C (lit.)
mp 77-84 °C; 79-81 °C (lit.)
UNSPSC 12352100

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