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Merck
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M9376

Sigma-Aldrich

Methyl α-D-glucopyranoside

≥99% (GC)

Sinónimos:

Methyl α-D-glucoside

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About This Item

Fórmula empírica (notación de Hill):
C7H14O6
Número de CAS:
97-30-3
Peso molecular:
194.18
Beilstein:
81568
Número CE:
202-571-3
Número MDL:
MFCD00064086
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
24897328
NACRES:
NA.25

origen biológico

synthetic (organic)

Análisis

≥99% (GC)

formulario

powder

actividad óptica

[α]20/D 156 to 160 °, c = 10% (w/v) in water

técnicas

gas chromatography (GC): suitable

color

white

solubilidad

water: 50 mg/mL, clear, colorless

temp. de almacenamiento

room temp

cadena SMILES

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

InChI

1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6-,7+/m1/s1

Clave InChI

HOVAGTYPODGVJG-ZFYZTMLRSA-N

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Aplicación

Different concentrations of methyl α-D-glucopyranoside were used to vary echo decay times in a study that assessed the effects of cryoprotection on the structure and activity of p21ras. Methyl α-D-glucopyranoside has also been used in a study to investigate saccharide-mediated protection of chaotropic-induced deactivation of concanavalin A.

Otras notas

To gain a comprehensive understanding of our extensive range of Monosaccharides 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 1

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

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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D N Figlas et al.
Archives of biochemistry and biophysics, 340(1), 154-158 (1997-04-01)
This work provides evidence of a physical instance in which some proteins that are usually inactivated under strong chaotropic conditions may become fully resistant through the occupancy of their binding sites with suitable ligands. In this regard, we found that
C J Halkides et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 134(1), 142-153 (1998-09-19)
Electron spin-echo envelope modulation (ESEEM) spectroscopy is widely used to investigate the active sites of biological molecules in frozen solutions. Various cryoprotection techniques, particularly the addition of co-solvents, are commonly employed in the preparation of such samples. In conjunction with
Mikkel G Jørgensen et al.
Journal of bacteriology, 191(4), 1191-1199 (2008-12-09)
Toxin-antitoxin (TA) loci are common in free-living bacteria and archaea. TA loci encode a stable toxin that is neutralized by a metabolically unstable antitoxin. The antitoxin can be either a protein or an antisense RNA. So far, six different TA
Amy B Blodgett et al.
Diabetes technology & therapeutics, 13(7), 743-751 (2011-04-23)
Diabetes may alter renal glucose reabsorption by sodium (Na(+))-dependent glucose transporters (SGLTs). Radiolabeled substrates are commonly used for in vitro measurements of SGLT activity in kidney cells. We optimized a method to measure glucose uptake using a fluorescent substrate, 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-2-deoxyglucose
Sirpa Vuorinen et al.
AAPS PharmSciTech, 10(2), 566-573 (2009-05-12)
Sugar end-capped poly-D,L-lactide (SPDLA) polymers were investigated as a potential release controlling excipient in oral sustained release matrix tablets. The SPDLA polymers were obtained by a catalytic ring-opening polymerization technique using methyl alpha-D-gluco-pyranoside as a multifunctional initiator in the polymerization.
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