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Merck
CN

M9376

Methyl α-D-glucopyranoside

≥99% (GC)

Synonym(s):

Methyl α-D-glucoside

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About This Item

Empirical Formula (Hill Notation):
C7H14O6
CAS Number:
97-30-3
Molecular Weight:
194.18
Beilstein:
81568
EC Number:
202-571-3
MDL number:
MFCD00064086
UNSPSC Code:
12352201
PubChem Substance ID:
24897328
NACRES:
NA.25

Key Documents

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biological source

synthetic (organic)

Quality Level

200

Assay

≥99% (GC)

form

solid

optical activity

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

technique(s)

gas chromatography (GC): suitable

color

white

solubility

water: 50 mg/mL, clear, colorless

storage temp.

room temp

SMILES string

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

InChI key

HOVAGTYPODGVJG-ZFYZTMLRSA-N

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Application

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.

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 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

Regulatory Information

涉药品监管产品
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Certificates of Analysis (COA)

Lot/Batch Number
WXBF4900V
WXBF4191V
WXBF3959V
WXBF3555V
WXBF3010V

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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
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
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
Miyuki Kimura et al.
Journal of bioscience and bioengineering, 112(2), 194-201 (2011-05-21)
We studied the effects of d-glucose on transgene expression in mammalian cells by a reporter gene assay using CV-1 cells and a CMV promoter-controlled EGFP gene. Treatment of CV-1 cells with 5% D-glucose unchanged the number of fluorescent cells in
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
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