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Benzoic acid and its salts are used as food preservatives, represented by the E numbers E210, E211, E212, and E213. Benzoic acid inhibits the growth of mold, yeast [23] and some bacteria. It is either added directly or created from reactions with its sodium, potassium, or calcium salt. The mechanism starts with the absorption of benzoic acid ...
Another silver ion causes the neighboring group substitution of the benzoate ester to give the oxonium salt (5). A second S N 2 substitution by the benzoate anion gives the desired diester (6). The mechanism of the Prévost reaction. In the final step hydrolysis of the ester groups gives the anti-diol.
The archetypal reaction is the alkaline hydrolysis of ethyl benzoate (R=R'=H) in a water/ethanol mixture at 30 °C. Measurement of the reaction rate k 0 combined with that of many substituted ethyl benzoates ultimately result in a reaction constant of +2.498. [3] [needs update] [non-primary source needed] Scheme 2. Hydrolysis of benzoic acid esters
Across a sample of 23 nicotine salts available for public purchase, the three most common acids used in the formation of nicotine salts were lactic acid, benzoic acid and levulinic acid. [8] Benzoic acid is the most used acid to create a nicotine salt. [9] Nicotine pyruvate is another form of nicotine salt. [10] A chemical reaction with a ...
Although the maximum rate of biotransformation of benzoic acid to hippuric acid varied between 17.2 and 28.8 mg.kg-1.h-1 among the six individuals, the mean value (23.0 mg.kg-1.h-1) was fairly close to that provided by daily maximum dose (0.5 g.kg-1.day-1) recommended in the treatment of hyperammonaemia in patients with inborn errors of ureagenesis
Ammonium benzoate, a white powder-like substance, is the ammonium salt of benzoic acid. [1] This compound is prepared by the reaction of benzoic acid and ammonia . Reactions
Benzoic acid was shown to be genotoxic in vitro. [22] Benzoic acid therefore might have a role in benzotrichloride carcinogenicity, but benzotrichloride has more carcinogenic potential than benzoic acid, suggesting that an intermediate in hydrolysis is responsible for at least part of the carcinogenicity. [1]
It reacts with water to produce hydrochloric acid and benzoic acid: C 6 H 5 COCl + H 2 O → C 6 H 5 COOH + HCl. Benzoyl chloride is a typical acyl chloride. It reacts with alcohols to give the corresponding esters. Similarly, it reacts with amines to give the amide. [5] [6]