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2,3,4-Tri-O-pivaloyl-β-D-glucopyranuronic acid methyl ester

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Cat Number : A14-1020

2,3,4-Tri-O-pivaloyl-β-D-glucopyranuronic acid methyl ester is a chemically protected glucuronic acid derivative widely used in carbohydrate synthesis. Below is a comprehensive breakdown of its properties and applications:

Chemical Identity

  • CAS Number: 86448-98-8
  • Molecular Formula: C₂₁H₃₂O₁₀
  • Molecular Weight: 460.52 g/mol

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2,3,4-Tri-O-pivaloyl-β-D-glucopyranuronic Acid Methyl Ester (CAS No. 86448-98-8)

2,3,4-Tri-O-pivaloyl-β-D-glucopyranuronic acid methyl ester is a chemically protected glucuronic acid derivative widely used in carbohydrate synthesis. Below is a comprehensive breakdown of its properties and applications:

Chemical Identity

  • CAS Number: 86448-98-8
  • Product Code: A1251263
  • IUPAC Name: Methyl (2S,3S,4S,5R,6R)-3,4,5-tris(pivaloyloxy)-6-hydroxyoxane-2-carboxylate
  • Molecular Formula: C₂₁H₃₂O₁₀
  • Molecular Weight: 460.52 g/mol

Physical Properties

  • Appearance: White crystalline solid
  • Purity: ≥97% (typically confirmed via ¹H-NMR)
  • Melting Point: 130–134°C
  • Solubility: Soluble in DMSO, methanol, dichloromethane, and DMF.

Structural Features

  • Based on the β-D-glucopyranuronic acid backbone with pivaloyl (trimethylacetyl) groups at the 2, 3, and 4 positions.
  • A methyl ester at the carboxyl group (C6) stabilizes the uronic acid moiety.
  • The β-anomeric configuration is retained, critical for stereospecific glycosylation reactions.

Applications

  • Glycosylation Reactions: Serves as a key intermediate for synthesizing glycosides, glycoconjugates, or glycomimetics due to its stability and reactivity.
  • Pharmaceutical Research: Used to develop prodrugs or enzyme substrates, leveraging its protected functional groups for targeted modifications.
  • Biochemical Probes: Employed in studies involving carbohydrate-protein interactions.

Safety and Handling

  • Hazard Statements: Not explicitly listed, but general precautions for organic esters apply:
    • Avoid inhalation, skin contact, and ingestion.
  • Storage: Store at −20°C in a tightly sealed container to prevent moisture absorption.

Regulatory Information

  • TSCA Status: Likely listed (similar glucuronic acid derivatives are TSCA-compliant).

This compound is commercially available in gram-scale quantities for research purposes, with applications in medicinal chemistry and glycobiology.

Citations:

  1. https://pubchem.ncbi.nlm.nih.gov/compound/10782914
  2. https://www.sigmaaldrich.com/IN/en/product/sigma/a8292
  3. https://www.lookchem.com/CASDataBase_21085-72-3.htm
  4. https://synthose.com/products/TG935
  5. https://pubchem.ncbi.nlm.nih.gov/compound/171370124
  6. https://synthose.com/products/TG137
  7. https://www.amadischem.com/product-A1251262
  8. https://www.ambeed.com/products/21085-72-3.html

 

  1. COA

2. MSDS

3. Tech Data Sheets/Manuals

Size

1 MG, 10 MG, 5 MG

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