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Merck
CN

N8130

4-Nitrophenyl acetate

esterase substrate, chromogenic, ≥98% (TLC), powder or crystals

Synonym(s):

Acetic acid 4-nitrophenyl ester

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About This Item

Linear Formula:
CH3CO2C6H4NO2
CAS Number:
830-03-5
Molecular Weight:
181.15
NACRES:
NA.32
PubChem Substance ID:
24897853
UNSPSC Code:
12352204
EC Number:
212-593-5
MDL number:
MFCD00007326
Beilstein/REAXYS Number:
515874

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Product Name

4-Nitrophenyl acetate, esterase substrate

InChI key

QAUUDNIGJSLPSX-UHFFFAOYSA-N

InChI

1S/C8H7NO4/c1-6(10)13-8-4-2-7(3-5-8)9(11)12/h2-5H,1H3

SMILES string

CC(=O)Oc1ccc(cc1)[N+]([O-])=O

assay

≥98% (TLC)

form

powder or crystals

Quality Level

200

Gene Information

human ... PON1(5444)

storage temp.

−20°C

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General description

Chromogenic esterase substrate.

Application

4-Nitrophenyl acetate has been used:
  • to evaluate esterase activity in human embryonic kidney cell line
  • in carbonic anhydrase inhibition assay
  • to study its conversion to p-nitrophenol (p-NP) by the esterase activity of bovine serum albumin
  • as a substrate to determine carboxylesterase (CES) activity in mouse liver cells
  • to study the advantages of bioconjugation of cross-linked enzyme aggregates (CLEAs) and magnetic iron oxide nanoparticles (MIONPs) in magnetic CLEAs matrix

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Ox. Sol. 3 - Skin Sens. 1

Storage Class

5.1B - Oxidizing hazardous materials

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL9010
BCCF7796
BCBW1104
BCBP8051V
BCBK4587V

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Immunomodulatory, antiglycation and anti-ulcerative properties of Ruellia squarrosa Fenzl Acanthaceae
Afzal K, et al.
Tropical Journal of Pharmaceutical Research, 16(8), 1751-1755 (2017)
Beyond esterase-like activity of serum albumin. Histidine-(nitro) phenol radical formation in conversion cascade of p-nitrophenyl acetate and the role of infrared light
Kowacz M and Warszynski P
arXiv (2018)
Akın Akıncıoğlu et al.
Bioorganic & medicinal chemistry, 21(6), 1379-1385 (2013-02-12)
Sulfamides represent an important class of biologically active compounds. A series of novel sulfamides were synthesized from 1-aminoindanes, 1-aminotetralin, 2-aminoindanes and 2-aminotetralin via the reactions of free amines, benzyl alcohol and chlorosulfonyl isocyanate (CSI) followed by hydrogenolysis of the obtained
Ramón Alberto Batista-García et al.
PloS one, 9(8), e105893-e105893 (2014-08-28)
A moderate halophile and thermotolerant fungal strain was isolated from a sugarcane bagasse fermentation in the presence of 2 M NaCl that was set in the laboratory. This strain was identified by polyphasic criteria as Aspergillus caesiellus. The fungus showed
Hanna Gustafsson et al.
Colloids and surfaces. B, Biointerfaces, 100, 22-30 (2012-07-04)
Immobilization of enzymes usually improves the recyclability and stability and can sometimes also improve the activity compared to enzymes free in solution. Mesoporous silica is a widely studied material as host for immobilized enzymes because of its large internal surface
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Product Information Sheet - N8130

Product Information Sheet

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