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M1134

Sigma-Aldrich

L-(−)-Mannose

≥99% (GC)

Synonym(s):

L-Mannopyranose

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About This Item

Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
10030-80-5
Molecular Weight:
180.16
Beilstein:
1724628
EC Number:
233-080-2
MDL number:
MFCD00063884
UNSPSC Code:
12352201
PubChem Substance ID:
24896618
NACRES:
NA.25

Quality Level

100

Assay

≥99% (GC)

form

powder

technique(s)

gas chromatography (GC): suitable

color

beige

mp

129-131 °C (lit.)

solubility

water: 100 mg/mL, clear, colorless to very faintly yellow

SMILES string

OC[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6?/m0/s1

InChI key

WQZGKKKJIJFFOK-JFNONXLTSA-N

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General description

Mannose is a monosaccharide.

Application

L-Mannose has been used in a study to assess substrate specificity of galactokinase from Streptococcus pneumoniae. It has also been used in a study to investigate a versatile route to L-hexoses.

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)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC4905
BCCB1764
BCBV0460
BCBR5551V
BCBR5551

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Pin Guo et al.
Journal of experimental & clinical cancer research : CR, 39(1), 202-202 (2020-10-01)
Globally, colorectal cancer (CRC) affects more than 1 million people each year. In addition to non-modifiable and other environmental risk factors, Fusobacterium nucleatum infection has been linked to CRC recently. In this study, we explored mechanisms underlying the role of
Optimized
Emily Wu et al.
In vitro cellular & developmental biology. Plant : journal of the Tissue Culture Association, 50(1), 9-18 (2014-01-01)
Yang Zou et al.
Bioorganic & medicinal chemistry letters, 22(10), 3540-3543 (2012-04-20)
Galactokinases (GalKs) have attracted significant research attention for their potential applications in the enzymatic synthesis of unique sugar phosphates. The galactokinase (GalKSpe4) cloned from Streptococcus pneumoniae TIGR4 presents a remarkably broad substrate range including 14 diverse natural and unnatural sugars.
Annalisa Guaragna et al.
Organic letters, 8(21), 4863-4866 (2006-10-06)
[reaction: see text] An efficient route for the synthesis of orthogonally protected l-sugars has been opened up, starting from the heterocyclic homologating agent 1 and 2,3-O-isopropylidene-l-glyceraldehyde (2). Our synthetic path enables the synthesis of a 2,3-unsaturated-l-pyranoside, which can be suitably
Lars Andresen et al.
Journal of immunology (Baltimore, Md. : 1950), 188(4), 1847-1855 (2012-01-10)
NKG2D ligand surface expression is important for immune recognition of stressed and neotransformed cells. In this study, we show that surface expression of MICA/B and other NKG2D ligands is dependent on N-linked glycosylation. The inhibitor of glycolysis and N-linked glycosylation
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