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Benzyltriphenylphosphonium chloride

ALDRICH/B32807 - 99%

Synonym: BTPPC; NSC 116712; Triphenyl(phenylmethyl)phosphonium chloride

CAS Number: 1100-88-5
Empirical Formula (Hill Notation): C25H22ClP
Molecular Weight: 388.87
EC Number: 214-154-3
MDL Number: MFCD00011913
Linear Formula: C6H5CH2P(Cl)(C6H5)3
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-B32807-25G 25 g
 $55.90
1/EA		 Add To Favorites
45-B32807-100G 100 g
 $98.30
1/EA		 Add To Favorites
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This image depicts SKU: B32807-100G

 

assay 99%
form powder
InChI 1S/C25H22P.ClH/c1-5-13-22(14-6-1)21-26(23-15-7-2-8-16-23,24-17-9-3-10-18-24)25-19-11-4-12-20-25;/h1-20H,21H2;1H/q+1;/p-1
InChI key USFRYJRPHFMVBZ-UHFFFAOYSA-M
mp ≥300 °C (lit.)
Quality Level 200 
reaction suitability reaction type: C-C Bond Formation
SMILES string [Cl-].C(c1ccccc1)[P+](c2ccccc2)(c3ccccc3)c4ccccc4
Application: Benzyltriphenylphosphonium chloride can be used as a reactant for the synthesis of:
• Platinum chloro-tetrazole complexes via azidation.
• Trans-stilbenes and cinnamates via Wittig olefination.
• Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment.
• Pentiptycenes for use as light-driven molecular brakes.
• Archipelago structures for formation of petroleum asphaltenes.


It is also used as a crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites.
Application: Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites

Reactant for synthesis of:
• Platinum chloro tetrazole complexes via azidation
• Trans-stilbenes and cinnamates via Wittig olefination
• Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment
• Pentiptycenes for use as light-driven molecular brakes

Reactant for formation of archipelago structures for formation of petroleum asphaltenes
Packaging: 25, 100 g in poly bottle
Purity 99%
mp ≥300 °C (lit.)
UNSPSC 12352107

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