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4-Methylumbelliferyl-α-D-Glucopyranoside
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4-Methylumbelliferyl-α-D-Glucopyranoside

CAS: 17833-43-1

Ref. TM-T85134

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Estimated delivery in United States, on Tuesday 16 Jul 2024

Product Information

Name:
4-Methylumbelliferyl-α-D-Glucopyranoside
Synonyms:
  • 4-Methylumbelliferyl-α-D-Glucoside, 4-Methylumbelliferyl-α-D-Glucose, 4-MU-α-D-Glucopyranoside
  • 2H-1-Benzopyran-2-one, 7-(α-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4-methyl-
  • 4-Methylumbelliferyl A-D-Glucopyranoside
  • 4-Methylumbelliferyl α-<span class="text-smallcaps">D</span>-glucopyranoside
  • 4-Methylumbelliferyl α-<span class="text-smallcaps">D</span>-glucose
  • 4-Methylumbelliferyl α-<span class="text-smallcaps">D</span>-glucoside
  • 4-Methylumbelliferyl-A-D-Glucoside
  • 4-Methylumbelliferyl-Alpha-D-Glucopyranoside
  • 4-Methylumbelliferyl-Alpha-D-Glucoside
  • 4-Mu-Alpha-D-Glc
  • See more synonyms
  • 4-methyl-2-oxo-2H-chromen-7-yl alpha-D-glucopyranoside
  • 4-methyl-2-oxo-2H-chromen-7-yl alpha-L-galactopyranoside
  • 7-(alpha.-D-glucopyranosyloxy)-4-methyl-2H-1-Benzopyran-2-one
  • 7-(α-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-4-methyl-2H-1-benzopyran-2-one
  • 7-Hydroxy-4-Methylcumarin-Alpha-D-Glucopyranosid
  • Coumarin, 7-(α-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4-methyl-
Description:

4-Methylumbelliferyl-α-D-glucopyranoside serves as a fluorogenic substrate for α-glucosidase, used in enzymatic assays. This compound undergoes cleavage by α-glucosidase, releasing 4-methylumbelliferyl (4-MU), a compound whose fluorescence intensity varies with pH. Specifically, 4-MU exhibits excitation peaks at 320 nm and 360 nm in acidic (pH 1.97-6.72) and alkaline environments (pH 7.12-10.3), respectively, and its emission peak ranges between 445 nm and 455 nm, with brightness increasing as the pH drops. Utilizing these properties, 4-Methylumbelliferyl-α-D-glucopyranoside has been effectively applied in the measurement of α-glucosidase activity within infant blood spot samples, acting as a diagnostic marker for Fabry and Pompe diseases. These illnesses are types of lysosomal storage disorders caused by α-glucosidase enzyme deficiency.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Targetmol
Long term storage:
Notes:

Chemical properties

Molecular weight:
338.312
Formula:
C16H18O8
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Hazard Info

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