N-azidoacetylmannosamine-tetraacylated (Ac4ManNAz)
Catalog#
Unit Size
Price (USD)
Availability
Qty
1084-5
5 mg
$139.00
In stock
1084-25
25 mg
$255.00
In stock
1084-100
100 mg
$645.00
In stock
The unnatural azido-containing monosaccharide building block. The azide moiety can be used for modification though chemoselective ligation chemistries including CuAAC, Cu-free click reaction or Staudinger ligation. The acetyl groups increase solubility in many solvents and make handling of this reagent easier.
Molecular weight
430.37
Chemical composition
C16H22N4O10
CAS
361154-30-5
Solubility
DMSO, DMF, DCM, THF, Chloroform
Purity
>90%
Appearance
Slightly grey amorphous solid
Storage conditions
-20°C.
Shipping conditions
Ambient temperature
- Ranzinger, R., et al. (2020). Mass Spectrometric Method for the Unambiguous Profiling of Cellular Dynamic Glycosylation. ACS Chem. Biol., 15, 10, 2692-2701. [ACSPublications]
- Loebel, C., et al. (2020). Metabolic Labeling to Probe the Spatiotemporal Accumulation of Matrix at the Chondrocyte–Hydrogel Interface. Adv. Funct. Mater. [PubMed]
- Song, S., et al. (2020). In Situ One-Step Fluorescence Labeling Strategy of Exosomes via Bioorthogonal Click Chemistry for Real-Time Exosome Tracking In Vitro and In Vivo. Bioconjugate Chem., 31(5), 1562-74. [PubMed]
- Kim, S. H., et al. (2014). Cell labeling and tracking method without distorted signals by phagocytosis of macrophages . Theranostics, 4 (4), 420-31. [PubMed]
Related Products
AZDye 488 DBCO
Excitation maximum: 494 nm
Emission maximum: 517 nm
AZDye 647 Alkyne
Excitation maximum: 648 nm
Emission maximum: 671 nm
6-Azide-Trehalose (6-TreAz)
Azide modified, non-mammalian disaccharide trehalose precursor for essential cell wall glycolipids and other metabolites.