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Catalog Number:
28150
CAS Number:
13992-26-2
1-Azido-1-deoxy-β-D-galactopyranoside tetraacetate
Purity:
≥ 99.5% (HPLC)
Documents
$106.96 /250MG
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Product Information

1-Azido-1-deoxy-b-D-galactopyranoside tetraacetate is a versatile compound that plays a significant role in the field of glycoscience and bioconjugation. This azido sugar derivative is particularly valuable for researchers looking to explore glycan interactions and develop glycosylation reactions. Its unique azido functional group allows for click chemistry applications, facilitating the attachment of various biomolecules, which is essential in the development of targeted drug delivery systems and novel therapeutics.

In addition to its applications in medicinal chemistry, this compound is also utilized in the synthesis of glycoproteins and glycolipids, making it a crucial building block in the study of cell signaling and recognition processes. Its tetraacetate form enhances stability and solubility, making it easier to handle in laboratory settings. The compound's ability to participate in selective reactions further distinguishes it from similar compounds, providing researchers with a powerful tool for advancing their studies in carbohydrate chemistry and related fields.

CAS Number
13992-26-2
Purity
≥ 99.5% (HPLC)
Molecular Formula
C14H19N3O9
Molecular Weight
373.32
MDL Number
MFCD00181721
PubChem ID
4114495
Appearance
White to off-white powder
Optical Rotation
[a]20D = -14.5 to -17.5 ° (C=1 in CHCl3)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
13992-26-2
Purity
≥ 99.5% (HPLC)
Molecular Formula
C14H19N3O9
Molecular Weight
373.32
MDL Number
MFCD00181721
PubChem ID
4114495
Appearance
White to off-white powder
Optical Rotation
[a]20D = -14.5 to -17.5 ° (C=1 in CHCl3)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-Azido-1-deoxy-b-D-galactopyranoside tetraacetate is widely utilized in research focused on:

  • Glycobiology: This compound serves as a valuable tool for studying carbohydrate interactions and functions, helping researchers understand complex biological processes.
  • Drug Development: Its azido group allows for click chemistry applications, facilitating the synthesis of new drug candidates and improving drug delivery systems.
  • Bioconjugation: The compound is used in the conjugation of biomolecules, enabling the development of targeted therapies and diagnostic agents in the pharmaceutical industry.
  • Material Science: It can be incorporated into polymer matrices to create functional materials with specific properties, such as enhanced biocompatibility for medical devices.
  • Diagnostics: The compound's unique structure makes it suitable for use in assays and imaging techniques, aiding in the detection of specific biomolecules in clinical settings.

Citations