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M2069

Sigma-Aldrich

D-(+)-Mannose

wood, ≥99%

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Synonym(s):
D-Mannopyranose
Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
Molecular Weight:
180.16
Beilstein:
1564373
EC Number:
MDL number:
PubChem Substance ID:

biological source

wood

Quality Level

Assay

≥99%

form

powder

technique(s)

gas chromatography (GC): suitable

color

white to off-white

mp

133-140 °C (lit.)

solubility

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

storage temp.

room temp

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?/m1/s1

InChI key

WQZGKKKJIJFFOK-QTVWNMPRSA-N

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This Item
63580M602063579
D-(+)-Mannose wood, ≥99%

Sigma-Aldrich

M2069

D-(+)-Mannose

-
D-(+)-Mannose ≥99%, suitable for microbiology

Millipore

63580

D-(+)-Mannose

-
D-(+)-Mannose powder, BioReagent, suitable for cell culture

Sigma-Aldrich

M6020

D-(+)-Mannose

-
D-(+)-Mannose BioUltra, ≥99.5% (sum of enantiomers, HPLC)

Sigma-Aldrich

63579

D-(+)-Mannose

Premium Grade
assay

≥99%

assay

≥99%, ≥99.0% (sum of enantiomers, HPLC)

assay

≥99%

assay

≥99.5% (sum of enantiomers, HPLC)

form

powder

form

powder

form

powder

form

solid

technique(s)

gas chromatography (GC): suitable

technique(s)

-

technique(s)

cell culture | mammalian: suitable

technique(s)

-

color

white to off-white

color

-

color

-

color

white

mp

133-140 °C (lit.)

mp

133-140 °C (lit.)

mp

133-140 °C (lit.)

mp

133-140 °C (lit.)

General description

Mannose is a monosaccharide.

Application

D-(+)-Mannose, a C-2 epimer of D-glucose, is used in the formation of glycan structure and glycosylation.
D-Mannose has been used in a study to assess the synthesis of a family of amphiphilic glycopolymers. It has also been used in a study to investigate the early detection of bronchiolitis obliterans after lung transplantation.

Biochem/physiol Actions

Mannose, a six-carbon carbohydrate, is the C-2 epimer of glucose and a critical sugar for protein glycosylation. Mannose can also be utilized by the brain as an alternative energy source.

Other Notes

From spruce, birch, or beech wood
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Quality

Predominantly α-isomer

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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25G
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Bithi Chatterjee et al.
Blood, 120(10), 2011-2020 (2012-07-14)
Dendritic cells (DCs) can capture extracellular antigens and load resultant peptides on to MHC class I molecules, a process termed cross presentation. The mechanisms of cross presentation remain incompletely understood, particularly in primary human DCs. One unknown is the extent
Fabian Suriano et al.
Biomaterials, 31(9), 2637-2645 (2010-01-16)
Polymers bearing pendant carbohydrates have a variety of biomedical applications especially in the area of targeted drug delivery. Here we report the synthesis of a family of amphiphilic block glycopolymers containing d glucose, d galactose and d mannose via metal-free
Steven J Budd et al.
Respiratory research, 13, 56-56 (2012-07-06)
Long-term lung allograft survival is limited by bronchiolitis obliterans syndrome (BOS). Mannose binding lectin (MBL) belongs to the innate immune system, participates in complement activation, and may predispose to graft rejection. We investigated mannose binding (MBL) during cold ischemia and
Conghui Liu et al.
Frontiers in immunology, 11, 1379-1379 (2020-08-15)
Cluster of differentiation 63 (CD63), a four-transmembrane glycoprotein in the subfamily of tetraspanin, has been widely recognized as a gateway from the infection of foreign invaders to the immune defense of hosts. Its role in Pacific oyster Crassostrea gigas is
E A Biessen et al.
The Journal of biological chemistry, 271(45), 28024-28030 (1996-11-08)
In search of synthetic high affinity ligands for the mannose receptor, we synthesized a series of lysine-based oligomannosides containing two (M2L) to six (M6L5) terminal alpha-D-mannose groups that are connected with the backbone by flexible elongated spacers (16 A). The

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