Chemodex

4-Nitrophenyl acetate

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Specifications / Handling

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Product Details
Synonyms 4-NPA: 4-Nitrophenyl ester acetic acid; p-Acetoxynitrobenzene; p-Nitrophenyl acetate; p-NPA; NSC2633
Product Type Chemical
Properties
Formula C8H7NO4
MW 181.15
CAS 830-03-5
RTECS AJ1150000
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (TLC)
Appearance Powder or crystals.
Solubility Soluble in chloroform, ethanol or methanol.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key QAUUDNIGJSLPSX-UHFFFAOYSA-N
Smiles O=C(OC1=CC=C(C=C1)N(=O)=O)C
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
Product Specification Sheet
Datasheet Download PDF Download PDF

Scientific Background Information

Product Description
4-Nitrophenyl acetate is a chromogenic substrate widely used in enzymology, analytical chemistry and biochemical research. Upon hydrolysis by esterases, lipases and other hydrolase enzymes, it releases the chromophore 4-nitrophenol, which can be readily monitored spectrophotometrically at 405 nm due to its strong absorbance in alkaline solution. The enzymes initially release 4-nitrophenol. The assay is then performed or stopped under alkaline conditions, converting it to the p-nitrophenoxide ion, which has a strong absorbance at 405 nm. This is why enzyme activity is almost always monitored at 405 nm. This property makes 4-nitrophenyl acetate an ideal substrate for enzyme activity assays, kinetic studies, inhibitor screening and method development. It is also used as an intermediate in organic synthesis and chemical research.
Product-specific References
(1) W.N. Aldridge; Biochem. J. 53, 110 (1953) | (2) K.M. Loomes & T.M. Kitson; Biochem. J. 238, 617 (1986) | (3) P. Ascenzi, et al.; BBRC 424, 451 (2012) | (4) A. Hammid, et al.; Drug Metab. Dispos. 50, 1483 (2022) | (5) Q. Song, et al.; Polym. Chem. 14, 4712 (2023) | (6) P. Jankovic & D. Kalafatovic; Methods Enzymol. 697, 423 (2024)
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