2-[(Azidoacety)amino]-2-deoxy-D-mannose

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Reagent Code: #139580
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CAS Number 361154-23-6

science Other reagents with same CAS 361154-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.22 g/mol
Formula C₈H₁₄N₄O₆
badge Registry Numbers
MDL Number MFCD26961125
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in bioorthogonal chemistry for labeling and imaging biomolecules in living systems. The azide group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), allowing selective conjugation with alkyne-bearing probes such as fluorophores or biotin. Serves as a metabolic label for glycoconjugates due to its sugar backbone, facilitating the study of glycosylation processes in cells. Applied in glycobiology research to track and visualize newly synthesized glycoproteins and glycolipids without disrupting natural biological functions.

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inventory 10mg
10-20 days ฿5,100.00

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2-[(Azidoacety)amino]-2-deoxy-D-mannose
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Used in bioorthogonal chemistry for labeling and imaging biomolecules in living systems. The azide group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), allowing selective conjugation with alkyne-bearing probes such as fluorophores or biotin. Serves as a metabolic label for glycoconjugates due to its sugar backbone, facilitating the study of glycosylation processes in cells. Applied in glycobiology research to track and visualize newly synthesized glycopr
Used in bioorthogonal chemistry for labeling and imaging biomolecules in living systems. The azide group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), allowing selective conjugation with alkyne-bearing probes such as fluorophores or biotin. Serves as a metabolic label for glycoconjugates due to its sugar backbone, facilitating the study of glycosylation processes in cells. Applied in glycobiology research to track and visualize newly synthesized glycoproteins and glycolipids without disrupting natural biological functions.
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