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The major cause of benzene in soft drinks is the decarboxylation of benzoic acid in the presence of ascorbic acid (vitamin C, E300) or erythorbic acid (a diastereomer of ascorbic acid, E315). Benzoic acid is often added to drinks as a preservative in the form of its salts sodium benzoate (E211), potassium benzoate (E 212), or calcium benzoate ...
Benzoic acid is cheap and readily available, so the laboratory synthesis of benzoic acid is mainly practiced for its pedagogical value. It is a common undergraduate preparation. Benzoic acid can be purified by recrystallization from water because of its high solubility in hot water and poor solubility in cold water. The avoidance of organic ...
Benzoic acid is generally not used directly due to its poor water solubility. Concentration as a food preservative is limited by the FDA in the U.S. to 0.1% by weight. [ 8 ] Sodium benzoate is also allowed as an animal food additive at up to 0.1%, per the Association of American Feed Control Officials. [ 9 ]
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Benzotrichloride is a poorly water-soluble, clear to yellowish liquid with a penetrating odor. It hydrolyzes rapidly to benzoic acid and hydrochloric acid with a half life of about 2.4 minutes, thus making the compound unstable in the presence of water. [2]
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 ...
Benzoyl chloride is produced from benzotrichloride using either water or benzoic acid: [2] C 6 H 5 CCl 3 + H 2 O → C 6 H 5 COCl + 2 HCl C 6 H 5 CCl 3 + C 6 H 5 CO 2 H → 2 C 6 H 5 COCl + HCl. As with other acyl chlorides, it can be generated from the parent acid and standard chlorinating agents such as phosphorus pentachloride, thionyl ...
Benzyl alcohol is subsequently metabolized to benzoic acid. The conjugates of benzoic acid ( hippuric acid and the glucuronide of benzoic acid) are rapidly eliminated in urine. [ 1 ] When given in large doses to laboratory animals, benzyl benzoate can cause hyperexcitation, loss of coordination, ataxia , convulsions , and respiratory paralysis .