M8883
4-Methylumbelliferyl phosphate
phosphatase substrate, fluorogenic, ≥98% (HPLC), powder
Synonym(s):
4-Methylumbelliferyl-phosphoric acid
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About This Item
Empirical Formula (Hill Notation):
C10H9O6P
CAS Number:
Molecular Weight:
256.15
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
222-137-7
MDL number:
Beilstein/REAXYS Number:
1687229
Product Name
4-Methylumbelliferyl phosphate,
InChI key
BCHIXGBGRHLSBE-UHFFFAOYSA-N
InChI
1S/C10H9O6P/c1-6-4-10(11)15-9-5-7(2-3-8(6)9)16-17(12,13)14/h2-5H,1H3,(H2,12,13,14)
SMILES string
CC1=CC(=O)Oc2cc(OP(O)(O)=O)ccc12
Quality Level
assay
≥98% (HPLC)
form
powder
solubility
water: 25 mg/mL, clear to very slightly hazy, colorless
fluorescence
λex 319 nm; λem 384 nm (pH 9.1), λex 360 nm; λem 449 nm (Reaction product)
storage temp.
−20°C
Related Categories
General description
Fluorogenic substrate for phosphatases.
Application
4-Methylumbelliferyl phosphate has been used as a substrate for alkaline phosphatase in the peptide-binding assay. It has also been used as a fluorogenic substrate in enzyme-linked immunosorbent assay (ELISA).
Biochem/physiol Actions
4-Methylumbelliferyl phosphate serves as a fluorogenic substrate for calmodulin-dependent protein phosphatase and in kinetic studies of alkaline phosphatase. It is a substrate for alkaline phosphatase in enzyme-linked immunosorbent assay (ELISA) procedures. 4-Methylumbelliferyl phosphate is seven times more sensitive than phenolphthalein monophosphate and 8-13 times more sensitive than with p-nitrophenyl phosphate when used in enzyme immunoassays for the detection of antibodies to human immunodeficiency viruses.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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N Bouaícha et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 40(11), 1677-1683 (2002-08-15)
Protein phosphatase inhibition assays currently used for the detection of cyanobacterial peptide hepatotoxins in drinking water require an enrichment step using C18 cartridges to achieve lower the detection limit. This paper describes a colorimetric and fluorometric protein phosphatase inhibition method
S A Rankin et al.
Journal of dairy science, 93(12), 5538-5551 (2010-11-26)
Standard practices for indirectly assessing the pasteurization status of milk products are primarily based on the thermal inactivation kinetics of the endogenous milk enzyme, alkaline phosphatase (ALP). This assessment provides an invaluable, if not required, tool for both regulatory and
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