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Catalog Number:
29211
CAS Number:
47339-09-3
2,3,4,6-Tetra-O-acetyl-D-galactopyranose
Purity:
≥ 98% (HPLC)
Documents
$65.40 /100MG
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Product Information

2,3,4,6-Tetra-O-acetyl-D-galactopyranose is a versatile acetylated sugar derivative that plays a significant role in various fields, including pharmaceuticals and biochemistry. This compound is recognized for its ability to serve as a protective group in carbohydrate chemistry, facilitating the synthesis of more complex glycosides and oligosaccharides. Its unique structure enhances solubility and stability, making it an ideal candidate for applications in drug formulation and development. Researchers often utilize this compound in the synthesis of glycosyl donors, which are essential for the construction of glycosidic bonds in carbohydrate-based drugs.

In addition to its synthetic utility, 2,3,4,6-Tetra-O-acetyl-D-galactopyranose is also valuable in the study of carbohydrate interactions and biological processes. Its acetyl groups can be selectively removed, allowing for the generation of functionalized sugars that can mimic natural glycosides. This property is particularly beneficial in the development of glycomimetics, which have potential applications in targeting specific biological pathways. With its broad range of applications and ease of use, this compound is an essential tool for researchers and industry professionals working in the fields of glycoscience and medicinal chemistry.

CAS Number
47339-09-3
Purity
≥ 98% (HPLC)
Molecular Formula
C14H20O10
Molecular Weight
348.3
MDL Number
MFCD09817577
PubChem ID
315762
Appearance
White crystalline powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
47339-09-3
Purity
≥ 98% (HPLC)
Molecular Formula
C14H20O10
Molecular Weight
348.3
MDL Number
MFCD09817577
PubChem ID
315762
Appearance
White crystalline powder
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

2,3,4,6-Tetra-O-acetyl-D-galactopyranose is widely utilized in research focused on:

  • Carbohydrate Chemistry: This compound serves as a versatile building block in the synthesis of complex carbohydrates, aiding researchers in developing new glycosylation reactions.
  • Pharmaceutical Applications: It is used in the formulation of drug delivery systems, enhancing the solubility and stability of pharmaceutical compounds, which is crucial for effective treatment.
  • Food Industry: The compound acts as a sweetening agent and flavor enhancer, providing a natural alternative to synthetic sweeteners in various food products.
  • Biotechnology: It plays a role in the development of glycoproteins and other biomolecules, which are essential for vaccine production and therapeutic applications.
  • Research and Development: This chemical is instrumental in the study of carbohydrate interactions in biological systems, helping scientists understand cell signaling and immune responses.

Citations