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M9376

Sigma-Aldrich

Methyl α-D-glucopyranoside

≥99% (GC)

Sinonimo/i:

Methyl α-D-glucoside

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About This Item

Formula empirica (notazione di Hill):
C7H14O6
Numero CAS:
97-30-3
Peso molecolare:
194.18
Beilstein:
81568
Numero CE:
202-571-3
Numero MDL:
MFCD00064086
Codice UNSPSC:
12352201
ID PubChem:
24897328
NACRES:
NA.25

Origine biologica

synthetic (organic)

Livello qualitativo

200

Saggio

≥99% (GC)

Forma fisica

solid

Attività ottica

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

tecniche

gas chromatography (GC): suitable

Colore

white

Solubilità

water: 50 mg/mL, clear, colorless

Temperatura di conservazione

room temp

Stringa SMILE

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
HOVAGTYPODGVJG-ZFYZTMLRSA-N

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Categorie correlate

Applicazioni

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.

Altre note

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Methyl α-D-mannopyranoside ≥99.0%, suitable for microbiology, enables differentiation between species of Listeria

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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
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
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
Maxime G Blanchard et al.
American journal of physiology. Cell physiology, 295(5), C1464-C1472 (2008-10-03)
The ion-trap technique is an experimental approach allowing measurement of changes in ionic concentrations within a restricted space (the trap) comprised of a large-diameter ion-selective electrode apposed to a voltage-clamped Xenopus laevis oocyte. The technique is demonstrated with oocytes expressing
Emily B Golden et al.
Biochimica et biophysica acta, 1794(11), 1643-1647 (2009-08-05)
Sweet almond beta-glucosidase is a retaining, family 1, glycohydrolase, catalyzing the highly efficient hydrolysis of a variety of glycosides. For example, the enzyme-catalyzed hydrolysis of methyl beta-D-glucopyranoside is approximately 4 x 10(15)-times faster than the spontaneous hydrolysis at 25 degrees
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