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

Conservar con desecante. Conservar bajo gas inerte. Conservar alejado de agentes oxidantes y fuentes de ignición.

Synonyms
β-D-Glc-Et-N3, 2-azidoetil β-D-glucopiranósido
CAS Number
165331-08-8
Purity
≥ 98%
Molecular Formula
C8H15N3O6
Molecular Weight
249.22
MDL Number
MFCD15072142
PubChem ID
18619938
Appearance
Jarabe aceitoso
Optical Rotation
[a] 25 D = -15,5 ± 2 ° (C=0,5 en H 2 O)
Conditions
Conservar a ≤ -10 °C
General Information
Synonyms
β-D-Glc-Et-N3, 2-azidoetil β-D-glucopiranósido
CAS Number
165331-08-8
Purity
≥ 98%
Molecular Formula
C8H15N3O6
Molecular Weight
249.22
MDL Number
MFCD15072142
PubChem ID
18619938
Appearance
Jarabe aceitoso
Optical Rotation
[a] 25 D = -15,5 ± 2 ° (C=0,5 en H 2 O)
Conditions
Conservar a ≤ -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.

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