Date published: 2026-5-18

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Cholesteryl linolelaidate (CAS 70190-89-5)

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Alternate Names:
3β-Hydroxy-5-cholestene 3-linolelaidate, 5-Cholesten-3β-ol 3-linolelaidate, Cholesteryl 9,12-octadecadienoate
CAS Number:
70190-89-5
Molecular Weight:
649.08
Molecular Formula:
C45H76O2
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 linolelaidate, a chemical compound of scientific interest, has been the subject of extensive research aimed at elucidating its mechanisms of action and exploring its applications in scientific investigations. One area of research focuses on its utilization as a lipid-based material in the development of functional biomaterials. Cholesteryl linolelaidate acts as a building block for the synthesis of lipids with customized properties. Researchers have investigated its incorporation into lipid structures to modulate their physical and chemical characteristics. This compound has displayed potential in the formulation of liposomes, lipid nanoparticles, and lipid bilayers, contributing to improved stability, controlled release of encapsulated substances, and enhanced encapsulation efficiency. Moreover, cholesteryl linolelaidate has been explored for its self-assembly properties, particularly in the creation of lipid-based nanostructures. These nanostructures have been investigated for various applications, including their role as drug delivery systems, gene carriers, and imaging agents. Additionally, cholesteryl linolelaidate has garnered interest in the development of functional interfaces and coatings. Its compatibility with diverse substrates enables the generation of surfaces with desired properties, such as enhanced biocompatibility and controlled release capabilities. The ongoing scientific research on cholesteryl linolelaidate continues to advance our understanding of its mechanisms of action and its potential applications in biomaterials, nanotechnology, and surface science research. These research applications contribute to the development of innovative materials and technologies across various scientific disciplines.


Cholesteryl linolelaidate (CAS 70190-89-5) References

  1. Picosecond spectral coherent anti-Stokes Raman scattering imaging with principal component analysis of meibomian glands.  |  Lin, CY., et al. 2011. J Biomed Opt. 16: 021104. PMID: 21361667
  2. Crystal structure of form II of cholesteryl palmitelaidate at 295 K.  |  Srivastava, RC. and Craven, BM. 1989. J Lipid Res. 30: 893-8. PMID: 2794779
  3. 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
  4. The 'quasi-thermal' mechanism for electron beam damage of n-paraffins.  |  Dorset, DL., et al. 1984. Ultramicroscopy. 13: 305-10. PMID: 6485130
  5. Conformational changes of cholesteryl palmitoleate in the crystal structure at low temperature.  |  Craven, BM. and Sawzik, P. 1984. J Lipid Res. 25: 857-64. PMID: 6491530
  6. Conformation and packing of unsaturated chains in crystals of cholesteryl nervonate at 123 K.  |  Sawzik, P. and Craven, BM. 1984. J Lipid Res. 25: 851-6. PMID: 6548506
  7. Structural determination and packing analysis of a cholesteryl caprate/cholesteryl laurate solid solution.  |  McCourt, MP., et al. 1994. J Lipid Res. 35: 584-91. PMID: 8006513
  8. Structural analyses of polymorphic transitions of sn-1, 3-distearoyl-2-oleoylglycerol (SOS) and sn-1, 3-dioleoyl-2-stearoylglycerol (OSO): assessment on steric hindrance of unsaturated and saturated acyl chain interactions.  |  Yano, J., et al. 1999. J Lipid Res. 40: 140-51. PMID: 9869660

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cholesteryl linolelaidate, 100 mg

sc-214700
100 mg
$71.00

Cholesteryl linolelaidate, 1 g

sc-214700A
1 g
$150.00