110231-30-6

Diphenyl-1-pyrenylphosphine Chemical Structure
110231-30-6

Chemical Structure

Diphenyl-1-pyrenylphosphine

Synonym(s): DPPP

  • CAS No.: 110231-30-6
  • Formula:C28H19P
  • Molecular Weight:386.42

IUPAC Name: diphenyl(pyren-1-yl)phosphane

InChIKey: DSYGKYCYNVHCNQ-UHFFFAOYSA-N

SMILES: P(C1=CC=CC=C1)(C2=CC=CC=C2)C3=C(C4=C56)C=CC6=CC=CC5=CC=C4C=C3

Biological Activity: Diphenyl-1-pyrenylphosphine (DPPP) is a functional organic molecule with both fluorescent properties and metal coordination ability, which is commonly used in materials and coordination chemistry research. Upon exposure to ultraviolet light, Diphenyl-1-pyrenylphosphine undergoes photoinduced phosphorus atom oxidation to form O-DPPP, triggering a transition from aggregation-induced emission (AIE) to aggregation-caused quenching (ACQ). Diphenyl-1-pyrenylphosphine reacts stoichiometrically with lipid hydroperoxides to produce fluorescent diphenyl-1-pyrenylphosphine oxide. Diphenyl-1-pyrenylphosphine can insert into cell membranes to monitor lipid peroxidation processes in living cells[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-118159
Diphenyl-1-pyrenylphosphine 98.56% Diphenyl-1-pyrenylphosphine (DPPP) is a functional organic molecule with both fluorescent properties and metal coordination ability, which is commonly used in materials and coordination chemistry research. Upon exposure to ultraviolet light, Diphenyl-1-pyrenylphosphine undergoes photoinduced phosphorus atom oxidation to form O-DPPP, triggering a transition from aggregation-induced emission (AIE) to aggregation-caused quenching (ACQ). Diphenyl-1-pyrenylphosphine reacts stoichiometrically with lipid hydroperoxides to produce fluorescent diphenyl-1-pyrenylphosphine oxide. Diphenyl-1-pyrenylphosphine can insert into cell membranes to monitor lipid peroxidation processes in living cells.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References