CAS 15220-11-8
:Sulfate de 4-méthylumbelliférone de potassium
- Potassium 4-methylumbelliferone sulfate
- 2H-1-Benzopyran-2-one, 4-methyl-7-(sulfooxy)-, potassium salt (1:1)
- Potassium 4-methylumbelliferyl sulfate
- Coumarin, 7-hydroxy-4-methyl-, hydrogen sulfate potassium salt
- 2H-1-Benzopyran-2-one, 4-methyl-7-(sulfooxy)-, potassium salt
4-Methylumbelliferyl sulfate potassium salt, 98%
CAS :Substrate for sulfataseFormule :C10H7KO6SDegré de pureté :98%Couleur et forme :White, PowderMasse moléculaire :294.322H-1-BENZOPYRAN-2-ONE,4-METHYL-7-(SULFOOXY)-, POTASSIUM SALT
CAS :Formule :C10H7KO6SDegré de pureté :97%Couleur et forme :SolidMasse moléculaire :294.32234-Methylumbelliferyl sulfate potassium salt
CAS :Formule :C10H7KO6SDegré de pureté :(HPLC) ≥ 98%Couleur et forme :White powder or solidMasse moléculaire :294.304-Methylumbelliferyl sulphate potassium salt
CAS :4-Methylumbelliferyl sulphate potassium salt
Degré de pureté :By hplc: >99% (Typical Value in Batch COA)Couleur et forme : white solidMasse moléculaire :294.32g/mol4-Methylumbelliferyl Sulfate Potassium Salt
CAS :Applications Met-enkephalin analog found in opioid extracts of brain and adrenal chromaffin cells that is an artifact generated by trichloroacetic acid extraction. MUS is used as a fluorimetric substrate for arylsulphatase enzyme. Subsitution of the hydroxyl group of 4-methylumbelliferone (4-methyl-7-hydroxy-coumarin) causes the excitation wavelength of the umbelliferone to shift to shorter values and also brings about a decrease in fluorescence.Fluorescence: max. Abs = 334 mm; max. Em. = 370 mm
References Harinath, B., et al.: J. Neurochem., 18, 245 (1971), Marniemi, J., et al.: Int. J. Biochem., 4, 95 (1973), Bojarova, P., et al.: ChemBioChem., 9, 613 (2008),Formule :C10H7O6S·KCouleur et forme :NeatMasse moléculaire :294.324-Methylumbelliferyl sulfate, potassium salt
CAS :4-Methylumbelliferyl sulfate, potassium salt is a metabolite of 4-methylumbelliferone and has been used as a human serum marker. This molecule is conjugated with glucuronide and p-hydroxybenzoic acid to form the sulfate, glucuronide conjugate. The reaction mechanism of this compound is not known, but it is thought that the metabolism may involve oxidation at the methyl group. The analytical method for this compound can be performed using liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). This method can also be used in vitro to test antimicrobial activity against bacteria such as Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa.Formule :C10H7KO6SDegré de pureté :Min. 99.0 Area-%Masse moléculaire :294.33 g/mol4-Methylumbelliferyl sulfate potassium salt
CAS :M04140 - 4-Methylumbelliferyl sulfate potassium salt
Formule :C10H7KO6SDegré de pureté :97%Couleur et forme :SolidMasse moléculaire :294.324-Methylumbelliferyl Sulfate Potassium Salt extrapure, 99%
CAS :Formule :C10H7KO6SDegré de pureté :min. 99%Couleur et forme :White, PowderMasse moléculaire :294.304-Methylumbelliferyl sulfate potassium salt
CAS :4-Methylumbelliferyl sulfate potassium salt serves as a superior fluorogenic substrate in enzyme detection assays. Upon enzymatic hydrolysis, it releases a highly fluorescent 4-methylumbelliferone moiety, enabling real-time analysis and quantification of enzyme activities. This product is ideal for a variety of biological assay applications, including in vitro diagnostics, drug discovery, and research purposes. Its excellent sensitivity, specificity, and performance ensure accurate and consistent results every time.Formule :C10H7KO6SDegré de pureté :Min. 98 Area-%Couleur et forme :White PowderMasse moléculaire :294.32 g/mol







