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Chemical Structure
Chemical Structure
Chemical Structure

2-(4-Methylumbelliferyl)-alpha-D-N-acetylneuraminic acid sodium salt hydrate [76204-02-9]

Research Use Only
CDX-M0096
Chemodex
CAS Number76204-02-9
Product group Chemicals
Estimated Purity>95%
Molecular Weight489.41 (anhydrous basis)
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Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    2-(4-Methylumbelliferyl)-alpha-D-N-acetylneuraminic acid sodium salt hydrate [76204-02-9]
  • Delivery Days Customer
    10
  • CAS Number
    76204-02-9
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Molecular Formula
    C21H24NNaO11 . xH2O
  • Molecular Weight
    489.41 (anhydrous basis)
  • Scientific Description
    Chemical. CAS: 76204-02-9 (anhydrous). Formula: C21H24NNaO11 . xH2O. MW: 489.41 (anhydrous basis). Synthetic Fluorogenic substrate used to measure sensitively enzymatic neuraminidase activity in fluorometric assays in mammalian and viral sources. Neuraminidase is catalyzed by the hydrolysation to form N-acetylneuraminic acid and the blue fluorescent soluble compound 4-Methylumbelliferone, which can be detected fluorometrically. Spectral data: lambdaex 315 nm - lambdaem 374 nm (pH.7.0) or lambdaex 365 nm - lambdaem 445 nm (after cleavage by neuraminidase). Used for fluorescent staining of sialidases in PAGE. - Fluorogenic substrate used to measure sensitively enzymatic neuraminidase activity in fluorometric assays in mammalian and viral sources. Neuraminidase is catalyzed by the hydrolysation to form N-acetylneuraminic acid and the blue fluorescent soluble compound 4-Methylumbelliferone, which can be detected fluorometrically. Spectral data: lambdaex 315 nm - lambdaem 374 nm (pH.7.0) or lambdaex 365 nm - lambdaem 445 nm (after cleavage by neuraminidase). Used for fluorescent staining of sialidases in PAGE.
  • SMILES
    O.CC(=O)N[C@@H]1[C@H](O)C[C@@](OC2=CC3=C(C=C2)C(C)=CC(=O)O3)(OC1[C@H](O)[C@H](O)CO)C(=O)O[Na]
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116134