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N4377

4-Nitrophenyl valerate

chromogenic, ≥98% (TLC), liquid

Synonym(s):

Pentanoic acid 4-nitrophenyl ester

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About This Item

Empirical Formula (Hill Notation):
C11H13NO4
CAS Number:
1956-07-6
Molecular Weight:
223.23
UNSPSC Code:
12352204
PubChem Substance ID:
24897702
NACRES:
NA.83
MDL number:
MFCD00057614

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Product Name

4-Nitrophenyl valerate, liquid

SMILES string

CCCCC(=O)Oc1ccc(cc1)N(=O)=O

InChI

1S/C11H13NO4/c1-2-3-4-11(13)16-10-7-5-9(6-8-10)12(14)15/h5-8H,2-4H2,1H3

InChI key

RJQXEHRFVKJLJO-UHFFFAOYSA-N

assay

≥98% (TLC)

form

liquid

color

faintly yellow to dark yellow

storage temp.

−20°C

Quality Level

200

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This Item
N813021742N3627
4-Nitrophenyl valerate liquid

Sigma-Aldrich

N4377

4-Nitrophenyl valerate

4-Nitrophenyl acetate esterase substrate

Sigma-Aldrich

N8130

4-Nitrophenyl acetate

4-Nitrophenyl octanoate ≥90.0% (GC)

Sigma-Aldrich

21742

4-Nitrophenyl octanoate

4-Nitrophenyl stearate lipase substrate

Sigma-Aldrich

N3627

4-Nitrophenyl stearate

assay

≥98% (TLC)

assay

≥98% (TLC)

assay

≥90.0% (GC)

assay

≥90% (TLC)

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

200

form

liquid

form

powder or crystals

form

liquid

form

powder

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

color

faintly yellow to dark yellow

color

-

color

-

color

-

Application

4-Nitrophenyl valerate has been used as a substrate solution to measure the rate of p-nitrophenol formation using p-nitrophenyl valerate as substrate.[1] It has also been used as a substrate to measure general esterase activity in hepatopancreas extracts.[2]

Biochem/physiol Actions

4-Nitrophenyl valerate acts as a model substrate for carboxylesterase and butyrylcholinesterase.[3]

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000511459
0000511458
0000511460
0000511458
0000511459

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Sonja Kübelbeck et al.
Macromolecular bioscience, 18(7), e1800095-e1800095 (2018-06-06)
Herein, the synthesis of enzyme-polymer conjugates is reported. Four different activated polymers (mPEG-aldehyde, mPEG-NHS, maltodextrin-aldehyde, carboxymethyl cellulose aldehyde) are conjugated to the surface of protease, α-amylase, and lipase using two different strategies (reductive amination and alkylation with NHS-activated acid). Although
Lincoln A MacKenzie et al.
Toxicon : official journal of the International Society on Toxinology, 60(3), 406-419 (2012-05-23)
An enzyme capable of hydrolysing pectenotoxins (PTXs) and okadaic acid (OA) esters within the hepatopancreas of the Greenshell™ mussel Perna canaliculus was isolated and characterized. The enzyme was purified by sequential polyethylene glycol fractionation, anion exchange, hydrophobic interaction, gel filtration
Xia Wen et al.
Toxicology, 416, 15-22 (2019-01-28)
Hepatic carboxylesterases (Ces) catalyze the metabolism of drugs, environmental toxicants, and endogenous lipids and are known to be regulated by multiple nuclear receptors. Perfluorooctanoic acid (PFOA) is a synthetic fluorochemical that has been associated with dyslipidemia in exposed populations. In
Andrés M Attademo et al.
Ecotoxicology (London, England), 20(1), 274-282 (2010-11-30)
Activity of B-esterases (BChE: butyrylcholinesterase and CbE: carboxylesterase using two model substrates: α-naphthyl acetate and 4-nitrophenyl valerate) in a native frog, Leptodactylus chaquensis from rice fields (RF1: methamidophos and RF2: cypermethrin and endosulfan sprayed by aircraft) and non-contaminated area (pristine
Mikael Skaanning Jørgensen et al.
Microbial cell factories, 13(1), 33-33 (2014-03-08)
The industrially applied filamentous fungus Trichoderma reesei has received substantial interest due to its highly efficient synthesis apparatus of cellulytic enzymes. However, the production of heterologous enzymes in T. reesei still remains low mainly due to lack of tools for
View All Related Papers

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