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N3129

Sigma-Aldrich

4-Nitrophenyl phosphate bis(cyclohexylammonium) salt

phosphatase substrate, chromogenic, ≥97% anhydrous basis, powder

Synonym(s):

p-Nitrophenyl phosphate bis(cyclohexylammonium) salt, PNPP

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About This Item

Linear Formula:
O2NC6H4OP(O)(O-)2 · 2C6H11NH3+
CAS Number:
52483-84-8
Molecular Weight:
417.44
Beilstein/REAXYS Number:
6553276
EC Number:
257-949-0
MDL number:
MFCD00013173
UNSPSC Code:
12352204
PubChem Substance ID:
24897623
NACRES:
NA.83

product name

4-Nitrophenyl phosphate bis(cyclohexylammonium) salt, phosphatase substrate

Quality Level

300

assay

≥97% anhydrous basis

form

powder

solubility

water: 10 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

NC1CCCCC1.NC2CCCCC2.OP(O)(=O)Oc3ccc(cc3)[N+]([O-])=O

InChI

1S/C6H6NO6P.2C6H13N/c8-7(9)5-1-3-6(4-2-5)13-14(10,11)12;2*7-6-4-2-1-3-5-6/h1-4H,(H2,10,11,12);2*6H,1-5,7H2

InChI key

KXNNUYCXODNFBD-UHFFFAOYSA-N

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Application

4-Nitrophenyl phosphate bis(cyclohexylammonium) salt has been used as a component in the colorimetric reagent for abscisic acid (ABA) assay.

Biochem/physiol Actions

p-Nitrophenyl phosphate (pNPP) is the preferred substrate for use with alkaline phosphatase in enzyme-linked immunosorbent assay (ELISA) procedures. Due to its high sensitivity, pNPP is the considered substrate in alkaline phosphatase systems. ELISA applications based on pNPP can be read in timed assays or delayed readings by stopping with alkaline solutions. This substrate yields a yellow-colored soluble end product that can be measured spectrophotometrically at 405 nm.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Brittany R Jenkins et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 35(6), e21551-e21551 (2021-05-28)
Intestinal epithelial cells (IEC) are crucial for maintaining proper digestion and overall homeostasis of the gut mucosa. IEC proliferation and differentiation are tightly regulated by well described pathways, however, relatively little is known about how cytokines shape these processes. Given
Ziad Dahabreh et al.
World journal of stem cells, 6(4), 497-504 (2014-09-27)
To compare seven commercially available bone graft substitutes (BGS) in terms of these properties and without using any additional biological growth factors. Porcine osteoprogenitor cells were loaded on seven commercially available BGS and allowed to proliferate for one week followed
Abscisic acid synthesis in Acer rubrum L. leaves?a vapor-pressure-deficit-mediated response
Bauerle WL, et al.
J. Am. Soc. Hort. Sci., 129(2), 182-187 (2004)
Leaf abscisic acid accumulation in response to substrate water content: Linking leaf gas exchange regulation with leaf abscisic acid concentration
Bauerle WL, et al.
J. Am. Soc. Hort. Sci., 131(2), 295-301 (2006)
Bjarni Ásgeirsson et al.
Biochemistry and biophysics reports, 24, 100830-100830 (2020-10-27)
Para-nitrophenyl phosphate, the common substrate for alkaline phosphatase (AP), is available as a cyclohexylamine salt. Here, we report that cyclohexylamine is a non-competitive inhibitor of APs. Cyclohexylamine inhibited four different APs. Co-crystallization with the cold-active Vibrio AP (VAP) was performed

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