Date published: 2025-12-5

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Lactose Octaacetate (CAS 6291-42-5)

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Alternate Names:
β-Octaacetyllactose
CAS Number:
6291-42-5
Purity:
≥97%
Molecular Weight:
678.59
Molecular Formula:
C28H38O19
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Lactose Octaacetate is a chemically modified form of lactose, where all hydroxyl groups are acetylated, enhancing its physicochemical properties and making it a useful reagent in various areas of chemical research. This derivative is particularly important in studies of carbohydrate interactions and the physical chemistry of sugars due to its increased stability and altered solubility compared to its parent compound, lactose. In research applications, Lactose Octaacetate is utilized to investigate the impact of structural modifications on the biochemical functionality of carbohydrates. Its non-reducing sugar nature due to the acetylation of the hydroxyl groups prevents it from participating in reducing sugar reactions, such as Maillard reactions, which is beneficial for controlled experimental conditions. This compound also serves as a model compound in enzymatic studies, helping to explain the specificity and mechanism of carbohydrate-metabolizing enzymes such as esterases and acetyltransferases. Additionally, Lactose Octaacetate is used in materials science for the preparation of carbohydrate-based polymers and coatings. These materials are studied for their potential applications in encapsulating agents and controlled release matrices, where the modified sugar structures can influence the mechanical properties and degradation rates of the polymers. Through these diverse applications, Lactose Octaacetate contributes significantly to the broader understanding of carbohydrate chemistry and its implications for industrial and biochemical technologies.


Lactose Octaacetate (CAS 6291-42-5) References

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  5. Nanovesicles displaying functional linear and branched oligomannose self-assembled from sequence-defined Janus glycodendrimers.  |  Xiao, Q., et al. 2020. Proc Natl Acad Sci U S A. 117: 11931-11939. PMID: 32424105
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  7. The Rearrangement of Sugar Acetates by Aluminum Chloride. Further Studies on Neolactose and d-Altrose1  |  Richtmyer, N. K., & Hudson, C. S. 1935. Journal of the American Chemical Society. 57(9): 1716-1721.
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  10. Construction of Glycosylated Surfaces for Poly(propylene) Beads with a Photoinduced Grafting/Chemical Reaction Sequence  |  Hu, M. X., Wan, L. S., Fu, Z. S., Fan, Z. Q., & Xu, Z. K. 2007. Macromolecular rapid communications. 28(24): 2325-2331.
  11. Supramolecular hydrogels based on glycoamphiphiles: Effect of the disaccharide polar head  |  Clemente, M. J., Romero, P., Serrano, J. L., Fitremann, J., & Oriol, L. 2012. Chemistry of Materials. 24(20): 3847-3858.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Lactose Octaacetate, 25 g

sc-221829
25 g
$228.00