Date published: 2025-12-11

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1,3-Dioleoyl-2-palmitoylglycerol (CAS 1716-07-0)

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Alternate Names:
1,3-Di(cis-9-octadecenoyl)-2-hexadecanoylglycerol
Application:
1,3-Dioleoyl-2-palmitoylglycerol is A triglyceride used in making human milk replacements
CAS Number:
1716-07-0
Molecular Weight:
859.39
Molecular Formula:
C55H102O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1,3-Dioleoyl-2-palmitoylglycerol, listed under CAS number 1716-07-0, is a triacylglycerol molecule characterized by the presence of two oleic acid chains at the 1 and 3 positions and a palmitic acid chain at the 2 position on a glycerol backbone. This specific arrangement of fatty acids — two monounsaturated oleic acids and one saturated palmitic acid — provides a unique platform for studying lipid behavior and properties in various scientific disciplines. In research, this compound has been extensively used to explore the physical chemistry of fats and oils, particularly how fatty acid composition affects melting behavior, crystallization processes, and the structural organization within lipid systems. The molecule′s asymmetry, with different types of fatty acids in specific positions, makes it particularly useful in studies focusing on the phase behavior of mixed lipid systems, including the formation of liquid crystalline phases and the impact of fatty acid saturation on membrane fluidity. Additionally, 1,3-Dioleoyl-2-palmitoylglycerol has been a subject of interest in food science for understanding how triglyceride composition can influence the nutritional properties and processing characteristics of edible fats. Its unique structural features also facilitate the examination of interactions between triglycerides and other components in complex matrices, crucial for the development of food products with optimized texture and stability.


1,3-Dioleoyl-2-palmitoylglycerol (CAS 1716-07-0) References

  1. Preparation and characterization of 1,3-dioleoyl-2-palmitoylglycerol.  |  Qin, XL., et al. 2011. J Agric Food Chem. 59: 5714-9. PMID: 21510711
  2. Chemoenzymatic synthesis of 1,3-dioleoyl-2-palmitoylglycerol.  |  Wang, X., et al. 2015. Biotechnol Lett. 37: 691-6. PMID: 25367802
  3. Ultrasonic pretreatment in lipase-catalyzed synthesis of structured lipids with high 1,3-dioleoyl-2-palmitoylglycerol content.  |  Liu, SL., et al. 2015. Ultrason Sonochem. 23: 100-8. PMID: 25453210
  4. Immobilization, Regiospecificity Characterization and Application of Aspergillus oryzae Lipase in the Enzymatic Synthesis of the Structured Lipid 1,3-Dioleoyl-2-Palmitoylglycerol.  |  Cai, H., et al. 2015. PLoS One. 10: e0133857. PMID: 26218640
  5. In situ crystallization and transformation kinetics of polymorphic forms of saturated-unsaturated-unsaturated triacylglycerols: 1-palmitoyl-2,3-dioleoyl glycerol, 1-stearoyl-2,3-dioleoyl glycerol, and 1-palmitoyl-2-oleoyl-3-linoleoyl glycerol.  |  Bayés-García, L., et al. 2016. Food Res Int. 85: 244-258. PMID: 29544841
  6. Effects of the Major Structured Triacylglycerols in Human Milk on Lipid Metabolism of Hepatocyte Cells in Vitro.  |  Wu, Y., et al. 2021. J Agric Food Chem. 69: 9147-9156. PMID: 33369388
  7. Effects of Proteins and Mineral Ions on the Physicochemical Properties of 1,3-Dioleoyl-2-Palmitoylglycerol Emulsion to Mimic a Liquid Infant Formula.  |  Wang, Q., et al. 2022. Front Nutr. 9: 808351. PMID: 35769380
  8. Lipase in-situ immobilized in covalent organic framework: Enzymatic properties and application in the preparation of 1, 3-dioleoyl-2-palmitoylglycerol.  |  Feng, T., et al. 2024. Colloids Surf B Biointerfaces. 238: 113873. PMID: 38552410

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,3-Dioleoyl-2-palmitoylglycerol, 25 mg

sc-206241
25 mg
$176.00