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Catalog Number:
32426
CAS Number:
165331-08-8
2-Azidoethyl β-glucopyranoside
Purity:
≥ 98%
Synonym(s):
β-D-Glc-Et-N3, 2-Azidoethyl β-D-glucopyranoside
Documents
$127.79 /25MG
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Product Information

2-Azidoethyl b-glucopyranoside is a versatile compound with significant applications in the fields of biochemistry and medicinal chemistry. This azido sugar derivative is recognized for its ability to participate in click chemistry reactions, making it an invaluable tool for researchers looking to develop new glycosylation strategies or to create complex carbohydrate structures. Its unique azido functional group allows for selective labeling and modification, facilitating the study of glycan interactions in biological systems.

In addition to its synthetic utility, 2-Azidoethyl b-glucopyranoside can be employed in the development of glyco-conjugates and drug delivery systems, enhancing the efficacy of therapeutic agents. Researchers have utilized this compound in the synthesis of glycoproteins and glycolipids, which are crucial for understanding cellular processes and disease mechanisms. Its stability and reactivity make it a preferred choice for those aiming to explore the intricate roles of carbohydrates in biology.

Synonyms
β-D-Glc-Et-N3, 2-Azidoethyl β-D-glucopyranoside
CAS Number
165331-08-8
Purity
≥ 98%
Molecular Formula
C8H15N3O6
Molecular Weight
249.22
MDL Number
MFCD15072142
PubChem ID
18619938
Appearance
Oily syrup
Optical Rotation
[a]25D = -15.5 ± 2 ° (C=0.5 in H2O)
Conditions
Store at ≤ -10 °C
General Information
Synonyms
β-D-Glc-Et-N3, 2-Azidoethyl β-D-glucopyranoside
CAS Number
165331-08-8
Purity
≥ 98%
Molecular Formula
C8H15N3O6
Molecular Weight
249.22
MDL Number
MFCD15072142
PubChem ID
18619938
Appearance
Oily syrup
Optical Rotation
[a]25D = -15.5 ± 2 ° (C=0.5 in H2O)
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Azidoethyl b-glucopyranoside is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach various biomolecules, such as proteins or antibodies, to surfaces or other molecules for enhanced functionality.
  • Drug Development: In pharmaceutical research, it is used in the synthesis of glycosylated drugs, which can improve the pharmacokinetics and bioavailability of therapeutic agents.
  • Glycobiology: It plays a significant role in studying carbohydrate-protein interactions, helping scientists understand cell signaling and recognition processes critical in immunology and cancer research.
  • Material Science: This compound can be incorporated into polymer matrices to create smart materials with specific properties, such as responsiveness to environmental stimuli, which is valuable in developing advanced coatings and sensors.
  • Diagnostics: It is used in the development of diagnostic tools, where its azide functionality allows for click chemistry applications, facilitating the labeling and detection of biomolecules in various assays.

Citations