Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
O2NC6H4OP(O)(ONa)2 · 6H2O
CAS Number:
Molecular Weight:
371.14
UNSPSC Code:
12352204
NACRES:
NA.75
PubChem Substance ID:
EC Number:
224-246-5
Beilstein/REAXYS Number:
5324661
MDL number:
InChI key
KAKKHKRHCKCAGH-UHFFFAOYSA-L
InChI
1S/C6H6NO6P.2Na.6H2O/c8-7(9)5-1-3-6(4-2-5)13-14(10,11)12;;;;;;;;/h1-4H,(H2,10,11,12);;;6*1H2/q;2*+1;;;;;;/p-2
SMILES string
O.O.O.O.O.O.[Na+].[Na+].[O-][N+](=O)c1ccc(OP([O-])([O-])=O)cc1
biological source
synthetic (organic)
product line
BioReagent
assay
≥97%
form
powder
technique(s)
cell culture | mammalian: suitable
solubility
H2O: 100 mg/mL
storage temp.
−20°C
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
4-Nitrophenyl phosphate disodium salt hexahydrate has been used:
- as a component in diethanolamine buffer to detect alkaline phosphatase-conjugated antibodies in enzyme linked immunosorbent assay (ELISA)
- to treat adherent cells in adhesion assay
- as a phosphatase substrate in in vitro phosphatase assay in substrate buffer for ELISA
Biochem/physiol Actions
p-Nitrophenyl phosphate (pNPP) is the substrate of choice for use with alkaline phosphatase in enzyme linked immunosorbent assay (ELISA) procedures. It is the substrate of choice in alkaline phosphatase systems due to its high sensitivity. This substrate produces a soluble end product that is yellow in color and can be read spectrophotometrically at 405 nm. This product is tested for use in cell culture applications. 4-nitrophenyl phosphate (pNPP), a small-molecule substrate can be used to study on alkaline phosphatases, acid phosphatases etc.
General description
Chromogenic substrate for the determination of acid and alkaline phosphatases. The reaction produces a soluble end product that is yellow in color. The reaction may be stopped with 3 N NaOH and read at 405 nm.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Serodiagnosis of Salmonella enterica serovar Typhi and S. enterica serovars Paratyphi A, B and C human infections
Chart H, et al.
Journal of Medical Microbiology, 56(9), 1161-1166 (2007)
Serodiagnosis of Echinococcus spp. infection: explorative selection of diagnostic antigens by peptide microarray
List C, et al.
PLoS Neglected Tropical Diseases, 4(8), e771-e771 (2010)
Cucurbitacin I inhibits STAT3, but enhances STAT1 signaling in human cancer cells in vitro through disrupting actin filaments
Guo H, et al.
Acta Pharmacologica Sinica, 39(3), 425-425 (2018)
Flexible, actin-based ridges colocalise with the beta1 integrin on the surface of melanoma cells
Poole K and Muller D
British Journal of Cancer, 92(8), 1499-1499 (2005)
Assays for protein-tyrosine phosphatases.
McCain DF and Zhang ZY
Methods in Enzymology, 345, 507-518 (2002)
Related Content
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service