4-Methylumbelliferyl alpha-D-glucopyranoside CAS: 17833-43-1
MF: C16H18O8
MW: 338.31
A fluorogenic β-glucosidase substrate.

4-Methylumbelliferyl α-D-glucopyranoside (CAS 17833-43-1)

4-Methylumbelliferyl α-D-glucopyranoside | CAS 17833-43-1 is rated 5.0 out of 5 by 1.
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Alternate Names: 4-Methylumbelliferyl-α-D-glucoside
Application: 4-Methylumbelliferyl α-D-glucopyranoside is a fluorogenic β-glucosidase substrate
CAS Number: 17833-43-1
Molecular Weight: 338.31
Molecular Formula: C16H18O8
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data (including water content).
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4-Methylumbelliferyl α-D-glucopyranoside is a fluorogenic substrate useful in the assay of α-D-glucosidase activity. 4-Methylumbelliferyl α-D-glucopyranoside is described to interact with both neutral and acid α-D-glucosidase activity in studies investigating Pompe's disease.


References

1. Broadhead, D.M. and Butterworth, J. 1977. Clin. Chim. Acta. 75: 155-161. PMID: 14796
2. Butterworth, J. and Droadhead, D.M. 1977. Clin. Chim. Acta. 78: 335-342. PMID: 18303

Physical State :
Solid
Solubility :
Soluble in water, DMSO (50 mg/ml), methanol, pyridine, and acetic acid.
Storage :
Store at 4° C
Melting Point :
210-212°C (lit.)
Boiling Point :
571.9-681.9° C at 760 mmHg (Predicted)
Density :
1.5 g/cm3 (Predicted)
Refractive Index :
n20D 1.64 (Predicted)
Fluoresence :
λex 316 nm, λem 375 nm (Reaction product); λex 317 nm, λem 374 nm in pH9.0; λex 360 nm, λem 449 nm; λex 365 nm, λem 445 nm in 0.1 M Tris pH 8.0
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
WGK Germany :
3
PubChem CID :
MDL Number :
MFCD00067661
EC Number :
241-794-0
Beilstein Registry :
1690776
SMILES :

Download SDS (MSDS)

Certificate of Analysis

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Rated 5 out of 5 by from Various publications cite the use of 4 Various publications cite the use of 4-Methylumbelliferyl -D-glucopyranoside, fluorogenic substrate, in the assay of -D-glucosidase activity. -SCBT Publication Review
Date published: 2015-03-05
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