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  2. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    For humans, the World Health Organization's International Programme on Chemical Safety (IPCS) suggests a provisional tolerable intake would be 5 mg/kg body weight per day. [32] Cats have a significantly lower tolerance against benzoic acid and its salts than rats and mice. Lethal dose for cats can be as low as 300 mg/kg body weight. [41]

  3. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen. The benzoyl group has a mass of 105 amu. The term "benzoyl" should not be confused with benzyl, which has the formula − ...

  4. Propiophenone - Wikipedia

    en.wikipedia.org/wiki/Propiophenone

    It is also prepared commercially by ketonization of benzoic acid and propionic acid over calcium acetate and alumina at 450–550 °C: [1] C 6 H 5 CO 2 H + CH 3 CH 2 CO 2 H → C 6 H 5 C(O)CH 2 CH 3 + CO 2 + H 2 O. Ludwig Claisen discovered that α-methoxystyrene forms this compound when heated for an hour at 300 °C (65% yield). [2] [3]

  5. Molar mass - Wikipedia

    en.wikipedia.org/wiki/Molar_mass

    The molar mass of atoms of an element is given by the relative atomic mass of the element multiplied by the molar mass constant, M u ≈ 1.000 000 × 10 −3 kg/mol ≈ 1 g/mol. For normal samples from Earth with typical isotope composition, the atomic weight can be approximated by the standard atomic weight [ 2 ] or the conventional atomic weight.

  6. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    The esters of propionic acid have fruit-like odors and are sometimes used as solvents or artificial flavorings. [15] In biogas plants, propionic acid is a common intermediate product, which is formed by fermentation with propionic acid bacteria. Its degradation in anaerobic environments (e.g. biogas plants) requires the activity of complex ...

  7. The best benzoyl peroxide products, according to ... - AOL

    www.aol.com/news/best-benzoyl-peroxide-products...

    This includes hyaluronic acid, glycerin, ceramides and niacinamide, according to our experts. Concentration: The strength of your over-the-counter benzoyl peroxide will range from 2.5% to 10%. The ...

  8. Benzoyl-CoA - Wikipedia

    en.wikipedia.org/wiki/Benzoyl-CoA

    Benzoyl-CoA is the thioester derived from benzoic acid and coenzyme A.The term benzoyl-CoA also include diverse conjugates of coenzyme A and aromatic carboxylic acids. Benzoate, vanillin, anthranilic acid, 4-ethylphenol, p-cresol, phenol, aniline, terephthalic acid, [3-hydroxybenzoic acid, and phenylalanine are all metabolized to benzoy

  9. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol has low acute toxicity with an LD 50 of 1.2 g/kg in rats. [5] It oxidizes rapidly in healthy individuals to benzoic acid, conjugated with glycine in the liver, and excreted as hippuric acid. Very high concentrations can result in toxic effects including respiratory failure, vasodilation, hypotension, convulsions, and paralysis.