Date published: 2026-1-31

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D-Galactose Pentaacetate (CAS 25878-60-8)

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Application:
D-Galactose Pentaacetate is used to produce sugar nucleotides via enzymatic fucosylation synthesis
CAS Number:
25878-60-8
Molecular Weight:
390.34
Molecular Formula:
C16H22O11
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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D-Galactose Pentaacetate, a derivative of the monosaccharide D-galactose, has garnered attention in scientific research due to its structural properties and potential applications in various fields. This compound is commonly employed as a building block in the synthesis of complex carbohydrates and glycoconjugates, contributing to the study of carbohydrate chemistry, glycobiology, and glycoscience. Its five acetyl groups confer enhanced stability and solubility, facilitating its manipulation and utilization in diverse experimental settings. Researchers utilize D-Galactose Pentaacetate as a precursor molecule for the synthesis of oligosaccharides, glycopeptides, and glycomimetics with tailored structures and functionalities. By incorporating D-Galactose Pentaacetate into synthetic pathways, scientists can probe glycan-mediated interactions, such as host-pathogen recognition, cell adhesion, and immune modulation, providing insights into the roles of carbohydrates in biological processes. Furthermore, D-Galactose Pentaacetate serves as a valuable tool for the development of carbohydrate-based materials, including biomaterials, sensors, and drug delivery systems. Its chemical versatility and compatibility with various synthetic strategies make it a versatile component in the construction of carbohydrate-based scaffolds and probes for applications like biomolecular recognition studies. Overall, D-Galactose Pentaacetate offers researchers a powerful platform for exploring the complex roles of carbohydrates in biology and advancing the development of carbohydrate-based materials for scientific and technological advancements.


D-Galactose Pentaacetate (CAS 25878-60-8) References

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  2. ELAM-1 mediates cell adhesion by recognition of a carbohydrate ligand, sialyl-Lex.  |  Phillips, ML., et al. 1990. Science. 250: 1130-2. PMID: 1701274
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  4. Preparation of nucleosides derived from 2-nitroimidazole and D-arabinose, D-ribose, and D-galactose by the Vorbrüggen method and their conversion to potential precursors for tracers to image hypoxia.  |  Schweifer, A. and Hammerschmidt, F. 2011. J Org Chem. 76: 8159-67. PMID: 21905640
  5. Purification and properties of N-acetylglucosaminide alpha 1----3-fucosyltransferase from embryonal carcinoma cells.  |  Muramatsu, H., et al. 1986. Eur J Biochem. 157: 71-5. PMID: 2423330
  6. A rapid synthesis of low-nanomolar divalent LecA inhibitors in four linear steps from d-galactose pentaacetate.  |  Zahorska, E., et al. 2020. Chem Commun (Camb). 56: 8822-8825. PMID: 32628229
  7. Bitter taste of monosaccharide pentaacetate esters.  |  Malaisse, WJ. and Malaisse-Lagae, F. 1997. Biochem Mol Biol Int. 43: 1367-71. PMID: 9442931
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  9. The formation of N-acylglycosylamines of some monosaccharides. D-mannose and L-rhamnose derivatives  |  Zanlungo, A. B., Deferrari, J. O., & Cadenas, R. A. 1970. Carbohydrate Research. 14(2): 245-254.
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

D-Galactose Pentaacetate, 5 g

sc-221479
5 g
$330.00