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Tribenzylphosphine

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Tribenzylphosphine manufacturers

  • Tribenzylphosphine
  • Tribenzylphosphine pictures
  • $1.00
  • 2026-08-07
  • CAS:7650-89-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20 tons
  • TRIBENZYLPHOSPHINE
  • TRIBENZYLPHOSPHINE pictures
  • $1.00
  • 2019-07-06
  • CAS:7650-89-7
  • Min. Order: 1KG
  • Purity: 95%
  • Supply Ability: 200KG
Tribenzylphosphine Basic information
Product Name:Tribenzylphosphine
Synonyms:Tris(phenylmethyl)phosphine;Trisbenzylphosphine;Tribenzylphoshine;Einecs 231-608-6;Phosphine, tris(phenylmethyl)-;Tribenzylphosphine 98%;TRIBENZYLPHOSPHINE (TBZP);TRIBENZYLPHOSPHINE,98%
CAS:7650-89-7
MF:C21H21P
MW:304.37
EINECS:231-608-6
Product Categories:Achiral Phosphine;Aryl Phosphine;Catalysis and Inorganic Chemistry;Phosphine Ligands;Phosphorus Compounds
Mol File:7650-89-7.mol
Tribenzylphosphine Structure
Tribenzylphosphine Chemical Properties
Melting point 96-101 °C (lit.)
Boiling point 183-185°C/0.2mm
Fp 183-185°C/0.2mm
form Crystalline
color White
Water Solubility Insoluble in water.
Sensitive Air & Moisture Sensitive
BRN 650179
InChI1S/C21H21P/c1-4-10-19(11-5-1)16-22(17-20-12-6-2-7-13-20)18-21-14-8-3-9-15-21/h1-15H,16-18H2
InChIKeyIFXORIIYQORRMJ-UHFFFAOYSA-N
SMILESC(P(Cc1ccccc1)Cc2ccccc2)c3ccccc3
CAS DataBase Reference7650-89-7(CAS DataBase Reference)
EPA Substance Registry SystemPhosphine, tris(phenylmethyl)- (7650-89-7)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
RTECS SZ3865000
F 10-23
TSCA TSCA listed
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
Tribenzylphosphine Usage And Synthesis
UsesTribenzylphosphine is used as a co catalyst in preparation of coumarin derivatives via nickel-catalyzed cycloaddition, copolymerization reactions, Rh-catalyzed hydroformylation reactions, preparation of substituted allylamines by three-component coupling of alkynes, imines and organoboranes.
UsesCocatalyst in:
  • Preparation of coumarin derivatives via nickel-catalyzed cycloaddition
  • Copolymerization reactions
  • Rh-catalyzed hydroformylation reactions
  • Platinum-catalyzed oxidative hydroxylation reactions
  • Preparation of substituted allylamines by three-component coupling of alkynes, imines and organoboranes
  • Ruthenium catalyzed metathesis reactions (Degenerate ligand exchange)
reaction suitabilityreaction 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
Tribenzylphosphine Preparation Products And Raw materials
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