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L-Iduronic acid sodium salt (CAS 61199-83-5)

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Alternate Names:
Sodium L-Iduronate; L-Iduronic Acid Monosodium Salt
Application:
L-Iduronic acid sodium salt is a constituent of certain mucopolysaccharides
CAS Number:
61199-83-5
Molecular Weight:
216.12
Molecular Formula:
C6H9O7•Na
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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L-Iduronic acid sodium salt is a crucial compound in glycobiology research, highly valued for its role as a fundamental component of glycosaminoglycans (GAGs) in the extracellular matrix and on cell surfaces. Its unique structure, featuring a carboxylate group and a sulfate moiety on the C2 and C3 positions, respectively, distinguishes it from its epimer, D-glucuronic acid. L-Iduronic acid plays a pivotal role in the structure and function of various GAGs, including heparan sulfate and dermatan sulfate, by imparting specific structural and biochemical properties. Researchers utilize L-Iduronic acid sodium salt as a substrate for studying the biosynthesis and modification of GAGs, including the enzymatic mechanisms involved in their polymerization and sulfation. Moreover, this compound serves as a valuable tool in investigating the interactions between GAGs and their binding partners, such as growth factors, cytokines, and extracellular matrix proteins, contributing to our understanding of cell signaling, tissue development, and pathophysiological processes. Additionally, L-Iduronic acid sodium salt finds applications in the development of biomaterials, drug delivery systems, and tissue engineering scaffolds, exploiting its unique chemical properties and biological functions. Overall, this compound plays a crucial role in advancing our understanding of glycosaminoglycan biology and its implications in various research fields, ranging from molecular biology to biomedical engineering.


L-Iduronic acid sodium salt (CAS 61199-83-5) References

  1. The acid mucopolysaccharides of connective tissue.  |  DAVIDSON, E., et al. 1956. Biochim Biophys Acta. 21: 506-18. PMID: 13363957
  2. Chemistry of beta-heparin (chondroitinsulfuric acid-B).  |  CIFONELLI, JA., et al. 1958. J Biol Chem. 233: 541-5. PMID: 13575409
  3. Uronic Acid of Chondroitin Sulfate B.  |  Hoffman, P., et al. 1956. Science. 124: 1252. PMID: 17750586
  4. Development of a Post-Column Liquid Chromatographic Chiral Addition Method for the Separation and Resolution of Common Mammalian Monosaccharides.  |  Wooke, Z., et al. 2019. J Am Soc Mass Spectrom. 30: 419-425. PMID: 30430437
  5. Composition and structure of cell wall ulvans recovered from Ulva spp. along the Swedish west coast.  |  Wahlström, N., et al. 2020. Carbohydr Polym. 233: 115852. PMID: 32059903
  6. Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporter.  |  Havelaar, AC., et al. 1998. J Biol Chem. 273: 34568-74. PMID: 9852127

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

L-Iduronic acid sodium salt, 10 mg

sc-221809
10 mg
$600.00