CAS 96886-70-3
:cholesteryl (pyren-1-yl)hexanoate
Description:
Cholesteryl (pyren-1-yl)hexanoate is an organic compound characterized by its ester functional group, formed from the reaction of cholesterol and pyren-1-yl hexanoic acid. This compound features a cholesteryl moiety, which contributes to its amphiphilic nature, allowing it to interact with both hydrophilic and hydrophobic environments. The presence of the pyrenyl group, a polycyclic aromatic hydrocarbon, imparts unique optical properties, making it useful in fluorescence applications. The hexanoate chain adds to its hydrophobic characteristics, influencing its solubility and interaction with biological membranes. Cholesteryl (pyren-1-yl)hexanoate is often studied in the context of lipid bilayers, drug delivery systems, and as a potential component in nanotechnology due to its ability to form organized structures. Its molecular structure and properties make it a subject of interest in various fields, including biochemistry and materials science, particularly for applications involving lipid-based formulations and fluorescent probes.
Formula:C49H64O2
InChI:InChI=1/C49H64O2/c1-32(2)11-9-12-33(3)42-25-26-43-41-24-22-38-31-39(27-29-48(38,4)44(41)28-30-49(42,43)5)51-45(50)16-8-6-7-13-34-17-18-37-20-19-35-14-10-15-36-21-23-40(34)47(37)46(35)36/h10,14-15,17-23,32-33,39,41-44H,6-9,11-13,16,24-31H2,1-5H3/t33-,39+,41+,42?,43+,44+,48+,49-/m1/s1
Synonyms:- Cholesteryl-6-pyrenylhexanoate
- ChPH
- P6Chol
- Cholest-5-en-3-ol (3beta)-, 3-pyrenehexanoate
- (3Beta,17Xi)-Cholest-5-En-3-Yl 6-(Pyren-1-Yl)Hexanoate
- Cholesteryl(pyren-1-yl)hexanoate
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