Description
2-Acetamido-2-deoxy-β-D-glucopyranosylamine is an N-acetylglucosamine-derived glycosylamine with CAS number 4229-38-3 and empirical formula C₈H₁₆N₂O₅. It has a molar mass of 220,22 g/mol. The molecule combines a 2-acetamido-2-deoxy glucopyranosyl core with a glycosylamine functionality, making it relevant to studies of GlcNAc chemistry, N-glycoside formation, and amino-sugar reactivity. Researchers employ such intermediates when exploring protecting-group strategies, coupling reactions, and model systems related to chitin and glycoprotein fragments. This material is available from manufacturer Carl ROTH for groups working in carbohydrate chemistry, glycobiology, and related organic synthesis. Clear identification by CAS number and formula aids traceability in purchasing and quality documentation. Typical use cases include academic teaching labs, method development, and specialised research programmes that need a defined 2-acetamido glycosylamine rather than generic amino sugars.
This article is part of Click chemistry, bioconjugation & synthesis reagents, in Biochemicals & reagents.
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Questions about 2-Acetamido-2-deoxy-b-D-glucopyranosyl a, mine, 500 mg
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2-Acetamido-2-deoxy-b-D-glucopyranosyl a, mine, 500 mg is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Click chemistry, bioconjugation & synthesis reagents, inside Biochemicals & reagents, in Microbiology lab supplies.
Click and bioconjugation reagents join two molecules under mild conditions, often an azide to an alkyne, or an NHS ester to an amine. The linker length and the reactive group are the specification. They are small bottles of a reactive compound, and moisture often ruins them.
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