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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:
41106212
PubChem Substance ID:
NACRES:
NA.85
Quality Level
Assay
≥99.0% (sum of enantiomers, HPLC)
≥99.0%
form
powder
optical activity
[α]20/D 77.0 to 82.0°, c = 10% in H2O
mol wt
194.18 g/mol
mp
187-195 °C
193-196 °C (lit.)
solubility
H2O: 0.1 g/mL, clear, colorless
application(s)
microbiology
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 compound that belongs to the class of organic compounds known as o-glycosyl compounds. It is used for the differentiation of Listeria species, Listeria monocytogenes, Listeria innocua, and Listeria welshimeri can ferment the sugar, producing acid which can be identified using an appropriate pH indicator. It has been used to synthesize a series of tri- and tetrahydroxylated seven-membered imino sugars in a study that worked towards a stable Noeuromycin (glycosyl cation mimic that strongly inhibits glycosidases) analog with a D-manno configuration. It has also been used in a study to investigate the primary mannose-binding site of Pradimicin A. (antifungal agent)
Application
Methyl α-D-mannopyranoside can be used to identify different species of Listeria based on their ability to ferment the sugar.
Other Notes
Unwanted binding of avidin to endogenous lectins
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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