产品名称
双(对硝基苯基)磷酸盐 钠盐, ≥99% (TLC)
InChI key
NXXNKMXTNUUECE-UHFFFAOYSA-N
InChI
1S/C12H9N2O8P.Na.H/c15-13(16)9-1-5-11(6-2-9)21-23(19,20)22-12-7-3-10(4-8-12)14(17)18;;/h1-8H,(H,19,20);;
SMILES string
[Na].OP(=O)(Oc1ccc(cc1)N(=O)=O)Oc2ccc(cc2)N(=O)=O
assay
≥99% (TLC)
form
powder
impurities
≤0.05% free p-nitrophenol
solubility
water: 20 mg/mL, clear to very slightly hazy
storage temp.
−20°C
Quality Level
Application
双( p -硝基苯基)磷酸钠盐已被用作磷酸二酯酶 (PDE) 活性估计的底物。 在 PDE 抑制试验中也用作底物。
General description
磷酸二酯酶底物
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
6-Nitrobenzimidazole derivatives: Potential phosphodiesterase inhibitors: Synthesis and structure-activity relationship
Khan KM, et al.
Bioorganic & Medicinal Chemistry, 20(4), 1521-1526 (2012)
Elution of tightly bound solutes from concanavalin A Sepharose: Factors affecting the desorption of cottonmouth venom glycoproteins
Soper AS and Aird SD
Journal of Chromatography A, 1154(1-2), 308-318 (2007)
Peter C Griffiths et al.
Advances in colloid and interface science, 144(1-2), 13-23 (2008-09-25)
Incorporation of d- or f-block metals into ligand systems that renders a metal complex surface-active or drives its partitioning into surfactant phases enables the localisation of chemical functionality at interfaces. This article discusses a number of fundamental aspects of these
Altan Ercan et al.
Journal of inorganic biochemistry, 104(1), 19-29 (2009-11-03)
The dinuclear aminopeptidase from Streptomyces griseus (SgAP) and its metal derivatives catalyze the hydrolysis of the phosphoester bis(p-nitrophenyl) phosphate (BNPP) and the phosphonate ester p-nitrophenyl phenylphosphonate with extraordinary rate enhancements at pH 7.0 and 25 degrees C [A. Ercan, H.
Meng Zhao et al.
Dalton transactions (Cambridge, England : 2003), 41(15), 4469-4476 (2012-02-23)
Two N-donor ligands (L(1) and L(2)) derived from a β-cyclodextrin (βCD) monomer and dimer were employed to mediate the hydrolytic activity and stability of the Ce(IV) ion in aqueous solution. Complexes Ce(IV)-L(1) and Ce(IV)-L(2) were prepared in situ and characterized
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