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M1134

Sigma-Aldrich

L-(−)-Mannose

≥99% (GC)

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Synonym(s):
L-Mannopyranose
Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
Molecular Weight:
180.16
Beilstein/REAXYS Number:
1724628
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

Quality Level

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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This Item
M2069M8574M3655
L-(−)-Mannose ≥99% (GC)

M1134

L-(−)-Mannose

D-(+)-Mannose ≥99% (GC), wood

M2069

D-(+)-Mannose

D-(+)-Mannose synthetic, ≥99% (GC)

M8574

D-(+)-Mannose

D-Mannose 6-phosphate sodium salt ≥98% (HPLC)

M3655

D-Mannose 6-phosphate sodium salt

technique(s)

gas chromatography (GC): suitable

technique(s)

gas chromatography (GC): suitable

technique(s)

gas chromatography (GC): suitable

technique(s)

HPLC: suitable

solubility

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

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

solubility

water: soluble 10 g/L at 20 °C

solubility

water: 50 mg/mL, clear to cloudy, colorless

form

powder

form

powder

form

powder

form

powder

mp

129-131 °C (lit.)

mp

133-140 °C (lit.)

mp

133-140 °C (lit.)

mp

-

color

beige

color

white to off-white

color

white to off-white

color

white

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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
Optimized
Emily Wu et al.
In vitro cellular & developmental biology. Plant : journal of the Tissue Culture Association, 50(1), 9-18 (2014-01-01)
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
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
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.

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