3-Nitrobenzoic acid forms molecular adducts with commercially important herbicides and pesticides such as amitrole[1].
Application
3-Nitrobenzoic acid was used to investgate the role of ozone as additional decomposition or finishing reagent in the degradation of o-, m- and p-nitobenzoic acids[2].
Legal Information
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In an attempt to produce complete oxidation of a biological matrix, bovine liver, ozone was investigated as an additional, potentially non-contaminating, oxidizing reagent after nitric acid digestion. Experiments were carried out to determine the decomposition efficiency of residual carbon species
Biodegradation rates of benzoate and related aromatic compounds, 3-nitrobenzoate, 4-chlorobenzoate, 4-chlorophenol, and 2,4-dichlorophenol by unexposed (unacclimated) and long-term exposed (acclimated) biomass were quantified using a modified fed-batch technique. The acclimated biomass was taken after approximately 1-year of operation from three
Reproductive toxicology. m-Nitrobenzoic acid.
Environmental health perspectives, 105 Suppl 1, 325-326 (1997-02-01)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 82(1), 235-246 (2011-08-25)
The influence of beryllium, magnesium, calcium, strontium and barium cations on the electronic system of 3-nitrobenzoic acid was studied in comparison with studied earlier alkali metal ions. The vibrational FT-IR (in KBr and ATR techniques) and (1)H and (13)C NMR
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