Chemodex

4-Methylumbelliferyl α-D-glucopyranoside

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Product Details
Synonyms 4-MU-α-D-Glc; 4-Methylumbelliferyl α-D-glucoside; 4-Methylumbelliferyl-α-D-Glucose; 4-MU-α-D-Glucopyranoside; 7-(α-D-glucopyranosyloxy)-4-methylcoumarin
Product Type Chemical
Properties
Formula C16H18O8
MW 338.31
CAS 17833-43-1
Source/Host Chemicals Synthetic
Purity Chemicals ≥99% (TLC)
Appearance White to off-white powder.
Solubility Soluble in DMF (5mg/ml) or DMSO (30 mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key YUDPTGPSBJVHCN-JZYAIQKZSA-N
Smiles CC=1C=2C(=CC(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=CC2)OC(=O)C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage -20°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
4-Methylumbelliferyl-α-D-glucopyranoside is a non-fluorescent but sensitive fluorogenic substrate for α-glucosidase yielding a blue fluorescent solution. 4-Methylumbelliferyl-α-D-glucopyranoside is cleaved by α-glucosidase to release the fluorescent moiety 4-methylumbelliferyl (4-MU). 4-MU fluorescence is pH-dependent with excitation maxima of 320 and 360 nm at low (1.97-6.72) and high pH (7.12-10.3), respectively, and an emission maximum ranging from 445 to 455 nm, increasing as pH decreases. 4-Methylumbelliferyl-α-D-glucopyranoside has been used to quantify α-glucosidase activity in infant blood spot samples as a biomarker of Fabry and Pompe diseases, lysosomal storage disorders characterized by a deficiency in the enzyme and and fundamental research into carbohydrate-metabolizing enzyme function. Spectral Data: λEx/λEm= 360/450 nm (cleaved product, pH-dependent).
Product References
(1) J. Butterworth & D.M. Droadhead; Clin. Chim. Acta 78, 335 (1977) | (2) D.M. Broadhead & J. Butterworth; Clin. Genet. 13, 504 (1978) | (3) C. Castilla, et al.; Int. J. Biochem. 13, 381 (1981) | (4) W.H. Porter, et al.; Clin. Chem. 32, 652 (1986) | (5) M.M. Hermans, et al.; J. Biol. Chem. 266, 13507 (1991) | (6) T. Matsui, et al.; Anal. Sci. 25, 559 (2009) | (7) P. Olivova, et al.; Clin. Chim. Acta 403, 159 (2009)
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