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Cholesteryl hexanoate (CAS 1062-96-0)

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Alternate Names:
Cholesteryl caproate
CAS Number:
1062-96-0
Purity:
≥98%
Molecular Weight:
484.80
Molecular Formula:
C33H56O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cholesteryl hexanoate, a chemical compound of scientific interest, has been extensively studied for its mechanisms of action and various research applications. One significant area of investigation is its utilization as a lipid-based material in the development of functional biomaterials. Cholesteryl hexanoate has been employed as a precursor or building block for the synthesis of lipids with tailored properties. Researchers have introduced cholesteryl hexanoate into lipid structures to modulate their physical and chemical characteristics through chemical modifications. This compound has been incorporated into liposomes, lipid nanoparticles, or lipid bilayers to enhance stability, control drug release, or improve encapsulationefficiency. The unique properties of cholesteryl hexanoate make it an ideal candidate for applications in drug delivery systems. It has been used to develop lipid-based nanocarriers capable of encapsulating and delivering agents to specific targets. The self-assembly properties of cholesteryl hexanoate have also been investigated for the fabrication of lipid-based nanostructures, such as micelles and vesicles, which can serve as vehicles for targeted delivery or as platforms for molecular imaging. Additionally, cholesteryl hexanoate has been explored in the field of surface modification and functionalization. Its compatibility with different substrates enables the creation of lipid-coated surfaces with desired properties, such as improved biocompatibility or controlled release capabilities. The ongoing scientific research on cholesteryl hexanoate continues to advance our understanding of its mechanisms of action and its potential applications in biomaterials, nanotechnology, and surface science. These research applications contribute to the development of innovative solutions for a wide range of scientific disciplines.


Cholesteryl hexanoate (CAS 1062-96-0) References

  1. Conformation of the oleate chains in crystals of cholesteryl oleate at 123 K.  |  Gao, Q. and Craven, BM. 1986. J Lipid Res. 27: 1214-21. PMID: 3559387
  2. Crystal nucleation studies in supercooled mesomorphic phases of cholesteryl derivatives.  |  Pochan, JM. and Gibson, HW. 1972. J Am Chem Soc. 94: 5573-7. PMID: 5053860
  3. Further studies on the fatty acid specificity of rat liver sterol-ester hydrolase.  |  Goller, HJ. and Sgoutas, DS. 1970. Biochemistry. 9: 4801-6. PMID: 5482274
  4. Effect of cholesteryl alkanoate structure on liquid crystal transition thermodynamics. Pure and in binary mixtures  |  Gibson, Harry W., and John M. Pochan. 1973. The Journal of Physical Chemistry. 77: 837-845.
  5. Synthesis and polymerization of cholesteryl 11‐methacryloyloxyundecanoate  |  Minezaki, Shigehiro, Tadao Nakaya, and Minoru Imoto. 1974. Die Makromolekulare Chemie: Macromolecular Chemistry and Physics. 175: 3017-3021.
  6. Cylindrically Symmetric Textures in Mesophases of Cholesteryl Esters.  |  Price, Fraser P., and Chan S. Bak. 1974. Liquid Crystals and Ordered Fluids. 2: 411-419.
  7. Refractive indices, densities, polarizabilities and molecular order in cholesteric liquid crystals  |  Shivaprakash, N. C., et al. 1982. Molecular Crystals and Liquid Crystals. 80: 179-193.
  8. Composition of organic matter in subducted and unsubducted sediments off the Nicoya peninsula, Costa Rica (ODP Leg 170, Sites 1039 and 1040)  |  Lutz, Rüdiger, et al. 2000. Organic geochemistry. 31: 1597-1610.
  9. A study of various cholesteryl alkanoates by a semi-empirical quantum calculation  |  Benmelouka, M., S. Bresson, and B. Khelifa. 2001. Computational materials science. 22: 185-192.
  10. Liquid-crystalline behaviours of novel chitosan derivates containing singular and cholesteryl groups  |  Cong, Yue-Hua, et al. 2009. Liquid Crystals. 36: 455-460.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cholesteryl hexanoate, 100 mg

sc-214698
100 mg
$218.00

Cholesteryl hexanoate, 1 g

sc-214698A
1 g
$437.00