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Merck
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Documentos clave

M1050

Sigma-Aldrich

2α-Mannobiose

≥93% (HPLC)

Sinónimos:

α-D-Man-[1→2]-D-Man, 2-O-α-D-Mannopyranosyl-D-mannopyranose

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About This Item

Fórmula empírica (notación de Hill):
C12H22O11
Número de CAS:
15548-39-7
Peso molecular:
342.30
Número MDL:
MFCD01310887
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
24896585
NACRES:
NA.25

origen biológico

synthetic

Nivel de calidad

200

Ensayo

≥93% (HPLC)

Formulario

powder

color

white to light yellow

temp. de almacenamiento

−20°C

cadena SMILES

OC[C@H]1OC(O)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H]1O

InChI

1S/C12H22O11/c13-1-3-6(16)8(18)10(11(20)21-3)23-12-9(19)7(17)5(15)4(2-14)22-12/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8+,9+,10+,11?,12-/m1/s1

Clave InChI

HIWPGCMGAMJNRG-VXSGSMIHSA-N

Descripción general

2α-Mannobiose is a disaccharide.

Aplicación

2α-Mannobiose has been used in a study to assess affinity chromatography with monolithic capillary columns. It has also been used in a study to investigate the influence of disaccharide structure on prebiotic selectivity in vitro.

Otras notas

To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000331472
0000304433
0000260399
SLCK5854
SLCJ1267

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Hui Zhang et al.
Rapid communications in mass spectrometry : RCM, 22(10), 1579-1586 (2008-04-25)
The discrimination of isomeric disaccharides with different linkage types and different monosaccharide residues--glucose (Glc), galactose (Gal), and mannose (Man) at the non-reducing end--was investigated with tandem mass spectrometry (MS/MS) and linear discriminant analysis (LDA). Conventional matrix-assisted laser desorption/ionization (MALDI)-MS has
Mohamed Bedair et al.
Journal of chromatography. A, 1044(1-2), 177-186 (2004-09-10)
Monolithic capillary columns with surface-immobilized mannan have been introduced for affinity-based micro-column separations by nano-liquid chromatography (nano-LC) and capillary electrochromatography (CEC). Two kinds of polymethacrylate monoliths were prepared, namely poly(glycidyl methacrylate-co-ethylene dimethacrylate) and poly(glycidyl methacrylate-co-ethylene dimethacrylate-co-[2-(methacryloyloxy)ethyl]trimethyl ammonium chloride) to yield
María Luz Sanz et al.
Journal of agricultural and food chemistry, 53(13), 5192-5199 (2005-06-23)
To obtain structure-function information of a range of carbohydrates, which are available only in very small quantities, an in vitro fermentation method using 7 mg of carbohydrate, 0.7 mL of basal medium, and 1% (w/v) of fecal bacteria was validated
Christine Henry et al.
mBio, 10(1) (2019-02-14)
Fungal cell wall mannans are complex carbohydrate polysaccharides with different structures in yeasts and molds. In contrast to yeasts, their biosynthetic pathway has been poorly investigated in filamentous fungi. In Aspergillus fumigatus, the major mannan structure is a galactomannan that

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