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M1134

Sigma-Aldrich

L-(−)-Mannose

≥99% (GC)

Sinónimos:

L-Mannopyranose

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About This Item

Fórmula empírica (notación de Hill):
C6H12O6
Número de CAS:
10030-80-5
Peso molecular:
180.16
Beilstein/REAXYS Number:
1724628
EC Number:
233-080-2
MDL number:
MFCD00063884
UNSPSC Code:
12352201
PubChem Substance ID:
24896618
NACRES:
NA.25

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Optimized
Emily Wu et al.
In vitro cellular & developmental biology. Plant : journal of the Tissue Culture Association, 50(1), 9-18 (2014-01-01)
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
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
Adriana Navarrete-Solis et al.
Journal of food science and technology, 57(2), 663-672 (2020-03-03)
Spray drying represents a viable alternative for the stabilization of juice and extract of a great diversity of plant in tropical zones, such as jackfruit from Nayarit, Mexico. The jackfruit powder allows physicochemical and microbiological stability for storage, transportation, and
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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