N,N-Dimethyl-6-propionyl-2-naphthylamine

CHF 111.00
In stock
CDX-D0077-M02525 mgCHF 111.00
CDX-D0077-M05050 mgCHF 172.00
CDX-D0077-M500500 mgCHF 1'252.00
More Information
Product Details
Synonyms Prodan
Product Type Chemical
Properties
Formula C15H17NO
MW 227.3
CAS 70504-01-7
Source/Host Chemicals Synthetic.
Purity Chemicals ≥98% (HPLC)
Appearance Light yellow powder.
Solubility Soluble in methanol, DMF, acetonitrile or acetone.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key MPPQGYCZBNURDG-UHFFFAOYSA-N
Smiles CCC(=O)C1=CC2=CC=C(C=C2C=C1)N(C)C
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF

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.

Product References

(1) B.A. Rowe et al.; J. Phys. Chem. B 110(30), 15021 (2006) | (2) E. Omanovic et al.; Int. J. Environm. Anal. Chem. 85(12-13), 853 (2005) | (3) M. Lin et al.; C. Huie; Anal. Chim. Acta 339(1-2), 131 (1997) | (4) A. Chakrabarti et al.; Biochem. Biophys. Res. Commun. 226, 495 (1996) | (5) P.L.G. Chong et al.; Biochemistry 28, 8358 (1989) | (6) P.L.G. Chong et al.; Biochemistry 27, 399 (1988)

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