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About This Item
Empirical Formula (Hill Notation):
C7H14O6
CAS Number:
Molecular Weight:
194.18
Beilstein:
81566
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
Quality Level
Assay
≥99.0% (HPLC)
form
powder
optical activity
[α]20/D 77.0 to 82.0°, c = 1-10% (w/v) in water
technique(s)
HPLC: suitable
color
white to off-white
mp
193-196 °C (lit.)
solubility
water: 100 mg/mL, clear, colorless
storage temp.
15-25°C
SMILES string
CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
InChI
1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
InChI key
HOVAGTYPODGVJG-VEIUFWFVSA-N
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General description
Methyl α-D-mannopyranoside is a competitor inhibitor of the binding of mannose by Escherichia coli.
Application
Methyl α-D-mannopyranoside has been used to synthesize a series of tri- and tetrahydroxylated seven-membered iminosugars in a study that worked towards a stable noeuromycin analog with a D-manno configuration. It has also been used in a study to investigate the primary mannose binding site of pradimicin A.
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
404.1 °F
Flash Point(C)
206.74 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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