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123943

Bis(4-nitrophenyl) phosphate

Name: Bis(4-nitrophenyl) phosphate
Brand: ALDRICH

99%

Synonym(s):

Di-4-nitrophenyl hydrogenphosphate

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About This Item

Linear Formula:

(O₂NC₆H₄O)₂P(O)OH

CAS Number:

645-15-8

Molecular Weight:

340.18

NACRES:

NA.22

PubChem Substance ID:

24847590

UNSPSC Code:

12352100

EC Number:

211-434-7

MDL number:

MFCD00007318

Assay:

99%

Form:

solid

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Properties

Quality Level

200

assay

99%

form

solid

mp

172-175 °C (lit.)

functional group

nitro, phosphate

SMILES string

OP(=O)(Oc1ccc(cc1)[N+]([O-])=O)Oc2ccc(cc2)[N+]([O-])=O

InChI

1S/C12H9N2O8P/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)

InChI key

MHSVUSZEHNVFKW-UHFFFAOYSA-N

Description

Application

Bis(4-nitrophenyl) phosphate(BNPP) has been used as substrate to determine the enzyme activity of root phosphodiesterases of wetland plants. BNPP has been used to study the mechanism of cleavage of BNPP using oxamido-bridged dinuclear copper(II) complexes as catalysts.

pictograms

GHS06

signalword

Danger

hcodes

H300

pcodes

P301 + P310 + P330

Hazard Classifications

Acute Tox. 2 Oral

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Studies on the reaction kinetics and the mechanism of hydrolysis of bis (4-nitrophenyl) phosphate (BNPP) catalyzed by oxamido-bridged dinuclear copper (II) complexes in micellar solution.

Xie J, et al.

Transition Met. Chem. (London), 28(7), 782-787 (2003)

Cannabidiol causes activated hepatic stellate cell death through a mechanism of endoplasmic reticulum stress-induced apoptosis.

M P Lim et al.

Cell death & disease, 2, e170-e170 (2011-06-10)

The major cellular event in the development and progression of liver fibrosis is the activation of hepatic stellate cells (HSCs). Activated HSCs proliferate and produce excess collagen, leading to accumulation of scar matrix and fibrotic liver. As such, the induction

Patterns of activities of root phosphomonoesterase and phosphodiesterase in wetland plants as a function of macrophyte species and ambient phosphorus regime.

Eliska Rejmánková et al.

The New phytologist, 190(4), 968-976 (2011-06-30)

Phosphorus (P)-limited plants produce higher amounts of root phosphatases, but research has mostly focused on phosphomonoesterases (PMEs). Because phosphate diesters can form a significant proportion of organic P in wetlands, we aimed to determine whether wetland plants produce both root

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Global Trade Item Number

SKU	GTIN
123943-10G	04061833313008
123943-1G	04061838722652
123943-5G	04061838722669