Mannosamines [Glycoscience] — covers acetylated and azidated mannose and glucosamine amino sugar derivatives, including N-acetyl-D-mannosamine and azido analogs that serve as building blocks for modified carbohydrate chemistry. This structure enables selective modification of the amino group and specific positions in the pyranose ring.
Mannosamines and their azido derivatives are widely used in glycoscience for metabolic glycan engineering, bioorthogonal labeling based on azide-alkyne click chemistry, and the synthesis of oligosaccharides and glycoconjugates in cell biology and glycobiology research. Researchers use the azido group as a chemical marker that is inert toward biological systems yet selectively reactive under controlled conditions.
Example products in this collection: TCI T1733 68733-20-0 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-alpha-D-mannopyranose, TCI B6321 2,6-Bis(acetamido)-2,6-dideoxy-D-mannose, TCI A3648 361154-30-5 1,3,4,6-Tetra-O-acetyl-2-azidoacetamido-2-deoxy-D-mannopyranose, TCI G0463 258824-38-3 N-Glycolyl-D-mannosamine Pentaacetate, TCI A3590 2-Acetamido-1,3,4-tri-O-acetyl-6-azido-2,6-dideoxy-D-mannopyranose, TCI M3237 5505-63-5 D-Mannosamine Hydrochloride, TCI A3466 219814-62-7 2-Acetamido-6-azido-2,6-dideoxy-D-glucopyranose, TCI A2160 3615-17-6 N-Acetyl-D-mannosamine Monohydrate.
Pay attention to the azido or acetyl substitution position on the pyranose ring, the alpha/beta anomeric configuration, and the protection level of hydroxyl groups, as these determine the success of subsequent reactions. All products are genuine Tokyo Chemical Industry (TCI) Japan products, with purity, packaging, and storage conditions listed on each item's page.
Other parallel categories under Glycoscience, often used together in one laboratory workflow:
Back to Glycoscience. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — official TCI Japan distributor in Indonesia — to check availability and lead time directly from Japan.
