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About This Item
Empirical Formula (Hill Notation):
C8H15NO6
CAS Number:
Molecular Weight:
221.21
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
231-368-2
Beilstein/REAXYS Number:
1727589
MDL number:
biological source
crab (red)
Quality Level
assay
≥99% (HPLC)
form
powder
technique(s)
HPLC: suitable
color
white to off-white
mp
211 °C (dec.) (lit.)
solubility
H2O: 50 mg/mL, clear to very slightly hazy (colorless to faint yellow solution)
application(s)
advanced drug delivery
storage temp.
−20°C
SMILES string
CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
InChI
1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6-,7-,8?/m1/s1
InChI key
OVRNDRQMDRJTHS-RTRLPJTCSA-N
General description
N-acetylglucosamine (GlcNAc) is the acetylated derivative of glucosamine (GlcN). It is an important component of proteoglycans, glycoproteins, glycosaminoglycans (GAGs), and other building units found in connective tissue.
Application
N-Acetyl-D-glucosamine has been used:
- as sugar for competitive inhibition in lectin histochemistry
- as a component in Barbour-Stonner-Kelly (BSK) medium for cultivating Borrelia burgdorferi spirochetes strains
- as a component of binding buffer to suspend Streptococcus pneumoniae strains for inhibition assay to examine the specificity of M-ficolin binding to S. pneumoniae strains
Biochem/physiol Actions
N-acetylglucosamine (GlcNAc) is mainly used in the food, cosmetics, and pharmaceutical industries.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| A8625-25G | 04061833400401 |
| A8625-10MG | 04061833400395 |
| A8625-5G | 04061833400418 |