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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914258Generated: October 26, 2026

Tromethamine hydrochloride → 4-Nitrophenol

https://huagongshe.com/reaction/1914258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTromethamine hydrochlorideHCID 93573—
Reactant4-NitrophenolateHCID 644235—
Reactant(4-Nitrophenyl)acetateHCID 6931101—
Reactantp-NitrophenylferulateHCID 178490568—
SolventDimethyl SulfoxideHCID 679—
SolventSodium AcetateHCID 517045—
Product4-NitrophenolHCID 980—

Reaction Steps

A p-nitrophenylferulate stock solution is made by dissolving p-nitrophenylacetate in dimethylsulfoxide (DMSO) to constitute a 0.1 M solution. Before assay, a sample of the stock solution is diluted 100-fold in 50 mM sodium acetate pH 5.0 to make a 1 mM solution. A 100 μl volume of 1 mM p-nitrophenylferulate is mixed with each dilution of the enzyme and then incubated at 25° C. for 10 minutes. Substrate alone, enzyme alone, and buffer alone are run as controls. p-Nitrophenol standard solutions of 0.25, 0.2, 0.1, 0.05, and 0.02 mM are prepared by diluting a 10 mM stock solution in 50 mM sodium acetate pH 5.0. At 10 minutes, 50 μl of 1.0 M Tris-HCl pH 8.0 buffer is added to each well (including samples, substrate control, enzyme control, reagent control, and standards), mixed, and the absorbance at 405 nm immediately measured on a SPECTRAMAX™ 340 PC plate reader (Molecular Devices, Sunnyvale, Calif., USA). One unit of feruloyl esterase activity is defined as the amount of enzyme capable of releasing 1 μmole of p-nitrophenolate anion per minute at pH 5, 25° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609933B2
Source datasetuspto-grants-2013_12
ORD IDord-5b67f0f84b55475da90280ec74c02115
Source noteuspto-grants-2013_12