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Catalog Number:
06764
CAS Number:
4098-06-0
3,4,6-Tri-O-acetyl-D-galactal
Purity:
≥ 99% (GC)
Synonym(s):
Tri-O-acetyl-D-galactal, 1,5-Anhydro-2-deoxy-D-lyxo-hex-1-enitol 3,4,6-tri-O-acetyl ether
Documents
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Product Information

3,4,6-Tri-O-acetyl-D-galactal is a versatile chemical compound known for its significant role in carbohydrate chemistry and glycosylation reactions. This compound, a derivative of D-galactose, features three acetyl groups that enhance its stability and reactivity, making it an ideal candidate for various applications in the pharmaceutical and biochemical industries. Researchers often utilize 3,4,6-Tri-O-acetyl-D-galactal in the synthesis of glycosides and oligosaccharides, which are crucial for developing new drugs and understanding biological processes. Its unique structure allows for selective reactions, providing an advantage over similar compounds in terms of yield and specificity.

In addition to its synthetic applications, 3,4,6-Tri-O-acetyl-D-galactal serves as an important intermediate in the production of glycoproteins and glycolipids, which are essential components in cell signaling and immune response. The compound's ability to facilitate the formation of complex carbohydrates makes it invaluable for researchers exploring cellular interactions and therapeutic targets. With its proven efficacy and broad applicability, 3,4,6-Tri-O-acetyl-D-galactal stands out as a key reagent for advancing research in glycoscience and drug development.

Synonyms
Tri-O-acetyl-D-galactal, 1,5-Anhydro-2-deoxy-D-lyxo-hex-1-enitol 3,4,6-tri-O-acetyl ether
CAS Number
4098-06-0
Purity
≥ 99% (GC)
Molecular Formula
C12H16O7
Molecular Weight
272.25
MDL Number
MFCD00064092
PubChem ID
102891
Appearance
Light yellow solidifying oil
Optical Rotation
[a]20/D= -16 to -21° (C=1 in CHCl3
Conditions
Store at 2-8 °C
General Information
Synonyms
Tri-O-acetyl-D-galactal, 1,5-Anhydro-2-deoxy-D-lyxo-hex-1-enitol 3,4,6-tri-O-acetyl ether
CAS Number
4098-06-0
Purity
≥ 99% (GC)
Molecular Formula
C12H16O7
Molecular Weight
272.25
MDL Number
MFCD00064092
PubChem ID
102891
Appearance
Light yellow solidifying oil
Optical Rotation
[a]20/D= -16 to -21° (C=1 in CHCl3
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3,4,6-Tri-O-acetyl-D-galactal is widely utilized in research focused on:

  • Carbohydrate Synthesis: This compound serves as a key intermediate in the synthesis of various oligosaccharides, which are essential for studying glycoproteins and glycolipids.
  • Drug Development: Its derivatives are explored in pharmaceutical research for developing new drugs, particularly those targeting specific carbohydrate-binding proteins.
  • Biotechnology: Used in the production of glycosylated proteins, enhancing their stability and efficacy, which is crucial for biopharmaceutical applications.
  • Food Industry: Acts as a flavoring agent or sweetener in food formulations, providing a natural alternative to synthetic sweeteners.
  • Research in Glycobiology: Facilitates the study of carbohydrate interactions in biological systems, aiding in the understanding of cellular processes and disease mechanisms.

Citations