2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl azide

Catalog No.: A91519
Biochemical Assay Reagent
2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl azide is a click chemistry reagent featuring an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) with alkyne-containing compounds, such as DBCO and BCN. This compound serves as a valuable biochemical assay reagent in various life science research applications, particularly in glycosylation studies and bioconjugation. Its stable acetylated form enhances solubility and reactivity, making it an effective tool for the synthesis of complex biomolecules and labeled substrates.
Grouped product items
Size Price Stock Qty
1g
$220.00
In stock
Bulk Size
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Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
Description2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl azide is a click chemistry reagent featuring an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) with alkyne-containing compounds, such as DBCO and BCN. This compound serves as a valuable biochemical assay reagent in various life science research applications, particularly in glycosylation studies and bioconjugation. Its stable acetylated form enhances solubility and reactivity, making it an effective tool for the synthesis of complex biomolecules and labeled substrates.
Product Information
Catalog NumA91519
FormulaC14H19N3O9
Molecular Weight373.32
CAS Number13992-25-1
SMILESCC(O[C@H]1[C@@H]([C@H](O[C@H]([C@@H]1OC(C)=O)N=[N+]=[N-])COC(C)=O)OC(C)=O)=O
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