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

Product Code:
 
CDX-D0077
Product Group:
 
Dyes, Stains, and Probes
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
-20 °C
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Chemical Structure
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Chemical Structure

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CDX-D0077-M02525 mg£117.00
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CDX-D0077-M05050 mg£175.00
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CDX-D0077-M500500 mg£1,208.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
Prodan
Appearance:
Light yellow powder.
CAS:
70504-01-7
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Protect from light and moisture.
InChi:
InChI=1S/C15H17NO/c1-4-15(17)13-6-5-12-10-14(16(2)3)8-7-11(12)9-13/h5-10H,4H2,1-3H3
InChiKey:
MPPQGYCZBNURDG-UHFFFAOYSA-N
Long 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.
MDL:
MFCD00056615
Molecular Formula:
C15H17NO
Molecular Weight:
227.3
Package Type:
Vial
Product Description:
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.
Purity:
>98% (HPLC)
SMILES:
CCC(=O)C1=CC2=CC=C(C=C2C=C1)N(C)C
Solubility Chemicals:
Soluble in methanol, DMF, acetonitrile or acetone.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

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)