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N4377

Sigma-Aldrich

4-Nitrophenyl valerate

chromogenic, ≥98% (TLC), liquid

Sinónimos:

Pentanoic acid 4-nitrophenyl ester

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About This Item

Fórmula empírica (notación de Hill):
C11H13NO4
Número de CAS:
1956-07-6
Peso molecular:
223.23
MDL number:
MFCD00057614
UNSPSC Code:
12352204
PubChem Substance ID:
24897702
NACRES:
NA.83

product name

4-Nitrophenyl valerate, liquid

assay

≥98% (TLC)

form

liquid

color

faintly yellow to dark yellow

storage temp.

−20°C

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

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. It has also been used as a substrate to measure general esterase activity in hepatopancreas extracts.

Biochem/physiol Actions

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

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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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
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
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
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
Brittany N Szafran et al.
Molecules (Basel, Switzerland), 23(12) (2018-12-06)
Endocannabinoid-metabolizing enzymes are downregulated in response to lipopolysaccharide (LPS)-induced inflammation in mice, which may serve as a negative feedback mechanism to increase endocannabinoid levels and reduce inflammation. Increased plasma levels of the pro-inflammatory cytokine interleukin-6 (IL-6) and decreased fatty acid
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