Methyltriphenylphosphonium chloride, 97%, Thermo Scientific Chemicals
Methyltriphenylphosphonium chloride, 97%, Thermo Scientific Chemicals
Methyltriphenylphosphonium chloride, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Methyltriphenylphosphonium chloride, 97%, Thermo Scientific Chemicals

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Catalog NumberQuantity
H56851.06
also known as H56851-06
5 g
Catalog number H56851.06
also known as H56851-06
Price (TWD)
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Quantity:
5 g
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Chemical Identifiers
CAS1031-15-8
IUPAC Namemethyltriphenylphosphanium chloride
Molecular FormulaC19H18ClP
InChI KeyQRPRIOOKPZSVFN-UHFFFAOYSA-M
SMILES[Cl-].C[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (unspecified)>96.0%
Methyltriphenylphosphonium chloride is used as a phase transfer catalyst in synthetic chemistry. It acts as a catalyst for regio-controlled ring-opening polymerization of substituted epoxides. It is utilized for controlling the corrosion iron. It acts as a reactant for intramolecular nitrone cycloaddition. In addition to this, it is used for neoplasm inhibition through antimitochondrial effect.

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
Methyltriphenylphosphonium chloride is used as a phase transfer catalyst in synthetic chemistry. It acts as a catalyst for regio-controlled ring-opening polymerization of substituted epoxides. It is utilized for controlling the corrosion iron. It acts as a reactant for intramolecular nitrone cycloaddition. In addition to this, it is used for neoplasm inhibition through antimitochondrial effect.

Solubility
Soluble in methanol.

Notes
Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Boudewijns, T.; Piccinini, M.; Degraeve, P.; Liebens, A.; De Vos, D. Pathway to Vinyl Chloride Production via Dehydrochlorination of 1,2-Dichloroethane in Ionic Liquid Media. ACS Catal. 2015, 5 (7), 4043-4047.
  2. Diaf, I.; Joffrin, A.; Lemière, G.; Duñach, E. Synthesis and odor evaluation of allenic derivatives. Flavour Fragance J. 2015, 30 (6), 478-484.