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While there are alternatives to using sodium benzoate as a preservative, the casual consumption of such a drink is unlikely to pose a significant health hazard to a particular individual (see, for example, the EPA IRIS document on benzene [8]). The UK Food Standards Agency has stated that people would need to drink at least 20 litres (5.5 gal ...
Sodium benzoate also known as benzoate of soda is the sodium salt of benzoic acid, widely used as a food preservative (with an E number of E211) and a pickling agent. It appears as a white crystalline chemical with the formula C 6 H 5 COONa.
The efficacy of benzoic acid and benzoate is thus dependent on the pH of the food. [24] Benzoic acid, benzoates and their derivatives are used as preservatives for acidic foods and beverages such as citrus fruit juices (citric acid), sparkling drinks (carbon dioxide), soft drinks (phosphoric acid), pickles and other acidified foods.
The ingredients in Diet Coke include carbonated water, caramel color, aspartame, phosphoric acid, potassium benzoate, natural flavors, citric acid and caffeine.
Polychlorinated biphenyls (containing 60 or more percent chlorine by molecular weight) – Polychlorinated dibenzo-p-dioxins – Polychlorinated dibenzofurans – Polygeenan: 53973-98-1 Ponceau MX: 3761-53-3 Ponceau 3R: 3564-09-8 Potassium bromate: 7758-01-2 Potassium dimethyldithiocarbamate: 128-03-0 Pravastatin sodium: 81131-70-6 Prednisolone ...
The ingredient Sodium Benzoate ("Benzoate of Soda" under "...Nutrition Info" [3]) is a common preservative. Scientists have shown that when mixed with ascorbic acid (vitamin C), it turns into benzene, a known carcinogen. [4] Sodium benzoate in beverages that also contain vitamin C may, therefore, be problematic. [5]
Beauty products like dry shampoo keep getting recalled for containing benzene, a human carcinogen linked to cancer. Experts reveal why benzene is even in dry shampoo, plus ways you can reduce your ...
Benzyl benzoate is produced industrially by the reaction of sodium benzoate with benzyl chloride in the presence of a base, or by transesterification of methyl benzoate and benzyl alcohol. [8] It is a byproduct of benzoic acid synthesis by toluene oxidation. [ 11 ]