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Chemical Structure
Chemical Structure
Chemical Structure

N,N-Dimethyl-6-propionyl-2-naphthylamine [70504-01-7]

Research Use Only
CDX-D0077
Chemodex
CAS Number70504-01-7
Product group Chemicals
Estimated Purity>98%
Molecular Weight227.3
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    N,N-Dimethyl-6-propionyl-2-naphthylamine [70504-01-7]
  • Delivery Days Customer
    10
  • CAS Number
    70504-01-7
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Non-hazardous
  • Molecular Formula
    C15H17NO
  • Molecular Weight
    227.3
  • Scientific Description
    Chemical. CAS: 70504-01-7. Formula: C15H17NO. MW: 227.3. Synthetic. N,N-dimethyl-6-propionyl-2-naphthylamine (prodan) has both an electron-donor and an electron-acceptor substituent, resulting in a large excited-state dipole moment and extensive solvent polarity-dependent fluorescence shifts. When prodan is incorporated into membranes, their fluorescence spectra are sensitive to the physical state of the surrounding phospholipids. In membranes, prodan appears to localize at the surface, although Fourier transform infrared measurements indicate some degree of penetration into the lipid interior. Excited-state relaxation of prodan is sensitive to the nature of the linkage between phospholipid hydrocarbon tails and the glycerol backbone. Tubulin and its hydrophobic surfaces have been probed with the enviroment-sensitive probes prodan. Prodan is also used for the generation of peroxy-oxalate chemiluminescence with H2O2. - N,N-dimethyl-6-propionyl-2-naphthylamine (prodan) has both an electron-donor and an electron-acceptor substituent, resulting in a large excited-state dipole moment and extensive solvent polarity-dependent fluorescence shifts. When prodan is incorporated into membranes, their fluorescence spectra are sensitive to the physical state of the surrounding phospholipids. In membranes, prodan appears to localize at the surface, although Fourier transform infrared measurements indicate some degree of penetration into the lipid interior. Excited-state relaxation of prodan is sensitive to the nature of the linkage between phospholipid hydrocarbon tails and the glycerol backbone. Tubulin and its hydrophobic surfaces have been probed with the enviroment-sensitive probes prodan. Prodan is also used for the generation of peroxy-oxalate chemiluminescence with H2O2.
  • SMILES
    CCC(=O)C1=CC2=CC=C(C=C2C=C1)N(C)C
  • Storage Instruction
    2°C to 8°C,-20°C
  • UNSPSC
    12352200