Date published: 2025-10-18

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Lactal Hexaacetate (CAS 51450-24-9)

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CAS Number:
51450-24-9
Molecular Weight:
558.48
Molecular Formula:
C24H30O15
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Lactal hexaacetate, a derivative of lactal, has garnered attention in scientific research, particularly in the fields of organic chemistry and materials science. Its unique chemical structure, characterized by the acetylation of multiple hydroxyl groups on the lactal molecule, imparts distinct properties and reactivity compared to its parent compound. One notable research application of lactal hexaacetate lies in its use as a versatile building block for the synthesis of functionalized organic molecules and advanced materials. Chemists exploit its reactivity in various synthetic methodologies to access complex molecular architectures and novel chemical entities with potential applications in diverse fields. Additionally, lactal hexaacetate serves as a valuable precursor for the preparation of acetylated lactal derivatives, enabling the exploration of their physicochemical properties and potential applications. In materials science, lactal hexaacetate has been investigated for its potential use in the fabrication of functional materials, including polymers, nanoparticles, and thin films, due to its ability to impart desirable properties such as solubility, stability, and tunable functionality. Furthermore, researchers are exploring its utility in supramolecular chemistry and self-assembly processes for the construction of molecular assemblies and nanostructures with tailored properties and applications in nanotechnology, catalysis, and drug delivery systems. Overall, lactal hexaacetate holds promise as a versatile chemical building block for advancing research in synthetic chemistry, materials science, and nanotechnology.


Lactal Hexaacetate (CAS 51450-24-9) References

  1. Synthesis of 2-[(perfluoroalkyl) phenyl] propionic acids  |  Stahly, G. P., & Jackson, A. 1991. The Journal of Organic Chemistry. 56(18): 5472-5475.
  2. Solid-surface activated recombinant Rhizopous oryzae lipase expressed in Pichia pastoris and chemically modified variants as efficient catalysts in the synthesis of hydroxy monodeprotected glycals  |  Filice, M., Molina, M., Benaiges, M. D., Abian, O., Valero, F., & Palomo, J. M. 2017. Catalysis Science & Technology. 7(8): 1766-1775.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Lactal Hexaacetate, 1 g

sc-221823
1 g
$300.00