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Click Chemistry & Bioconjugation Reagents

Ac4GlcNAz

[(2R,3S,4R,5R)-3,4,6-triacetyloxy-5-[(2-azidoacetyl)amino]oxan-2-yl]methyl acetate

N° produitCH70475N° CAS98924-81-3Pureté>=98%
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Résumé du produit

Aperçu rapide

Famille de produits
Click Chemistry & Bioconjugation Reagents
Nom chimique
[(2R,3S,4R,5R)-3,4,6-triacetyloxy-5-[(2-azidoacetyl)amino]oxan-2-yl]methyl acetate
FM
C16H22N4O10
PM
430.37
Pureté
>=98%

Ac4GlcNAz is a tetra-O-acetylated N-azidoacetylglucosamine derivative used as an azido sugar metabolic chemical reporter in glycan and O-GlcNAc labeling research. PubChem records it as CID 11495687, CAS 98924-81-3, molecular formula C16H22N4O10, molecular weight 430.37, and InChIKey HGMISDAXLUIXKM-ALTVCHKUSA-N.

The acetylated GlcNAz scaffold is used in cell-based metabolic reporter workflows, while the azide handle supports downstream alkyne-probe tagging in bioorthogonal chemistry. Published studies also report S-glyco/off-target considerations for fully protected sugar reporters, so Ac4GlcNAz should be handled as a research chemical reporter rather than as a universal selectivity claim.

Synonymes

Ac4GlcNAz; GlcNAz tetraacetate; 1,3,4,6-tetra-O-acetyl-N-azidoacetylglucosamine; 2-[(azidoacetyl)amino]-2-deoxy-D-glucopyranose 1,3,4,6-tetraacetate; N-azidoacetylglucosamine tetraacylated

Identité et spécifications

Catalog No.CH70475
Product NameAc4GlcNAz
CAS No.98924-81-3
Molecular FormulaC16H22N4O10
Molecular Weight430.37
Exact Mass430.13359291
PubChem CID11495687
InChIKeyHGMISDAXLUIXKM-ALTVCHKUSA-N
SynonymsGlcNAz tetraacetate; 1,3,4,6-tetra-O-acetyl-N-azidoacetylglucosamine
Purity>=98%

Conditions de stockage

-20 C in dark and desiccated

Caractéristiques techniques

Sugar scaffold
N-acetylglucosamine analog
Sugar protection
Tetra-O-acetyl
Chemical-reporter handle
N-azidoacetyl group
Labeling role
Metabolic glycan reporter precursor
Packaging
5 mg; 25 mg; 100 mg; Custom packaging on request
Physical form
White solid
Stability
24 months after receipt

Contexte d’application

  • Metabolic glycan labeling research: Ac4GlcNAz is used as an azido sugar reporter in studies of glycan and O-GlcNAc labeling workflows.
  • Bioorthogonal tagging workflows: the azide handle enables downstream ligation with alkyne-containing probes for detection, enrichment, or imaging workflows in research settings.
  • Reporter-comparison studies: Ac4GlcNAz appears in literature comparing metabolic sugar reporters and discussing S-glyco/off-target labeling behavior.

Informations complémentaires sur le matériau

Utilisations

Use in research workflows that require an azido GlcNAc reporter for metabolic glycan or O-GlcNAc labeling studies. Interpret labeling results with appropriate controls because published studies describe off-target and S-glyco considerations for fully protected sugar reporters.

Caractéristiques

Ac4GlcNAz combines a protected GlcNAz sugar scaffold with an azidoacetyl reporter handle. The acetylated form is used in metabolic-labeling workflows, and the azide enables downstream bioorthogonal tagging with suitable alkyne probes.

Ressources techniques associées

Sources publiques

Questions fréquentes

What is Ac4GlcNAz?

Ac4GlcNAz is a tetra-O-acetylated N-azidoacetylglucosamine derivative, also described as GlcNAz tetraacetate. PubChem records it as CID 11495687 with CAS 98924-81-3.

How is Ac4GlcNAz used in research workflows?

It is used as an azido sugar metabolic chemical reporter in glycan and O-GlcNAc labeling workflows. The azide handle can be paired with alkyne-containing probes for downstream bioorthogonal tagging.

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