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  2. Benzophenone - Wikipedia

    en.wikipedia.org/wiki/Benzophenone

    Benzophenone is a naturally occurring organic compound with the formula (C 6 H 5) 2 CO, generally abbreviated Ph 2 CO. Benzophenone has been found in some fungi, fruits and plants, including grapes. [4] It is a white solid with a low melting point and rose-like odor [5] that is soluble in organic solvents. Benzophenone is the simplest ...

  3. Oxybenzone - Wikipedia

    en.wikipedia.org/wiki/Oxybenzone

    Oxybenzone or benzophenone-3 or BP-3 (trade names Milestab 9, Eusolex 4360, Escalol 567, KAHSCREEN BZ-3) is an organic compound belonging to the class of aromatic ketones known as benzophenones. It takes the form of pale-yellow crystals that are readily soluble in most organic solvents.

  4. Benzene in soft drinks - Wikipedia

    en.wikipedia.org/wiki/Benzene_in_soft_drinks

    Benzene in soft drinks has to be seen in the context of other environmental exposure. Taking the worst example found to date of a soft drink containing 87.9 ppb benzene, [5] someone drinking a 350 ml (12 oz) can would ingest 31 μg (micrograms) of benzene, almost equivalent to the benzene inhaled by a motorist refilling a fuel tank for three ...

  5. What happens to your body when you drink, and why it's never ...

    www.aol.com/happens-body-drink-why-never...

    In a typical day, about 100 people die in a car accident in the U.S.; but the National Safety Council estimates there will be more than 400 during the two-day period of Dec. 31 and Jan. 1. Dr ...

  6. Sodium benzoate - Wikipedia

    en.wikipedia.org/wiki/Sodium_benzoate

    The human body rapidly clears sodium benzoate by combining it with glycine to form hippuric acid which is then excreted. [26] The metabolic pathway for this begins with the conversion of benzoate by butyrate-CoA ligase into an intermediate product, benzoyl-CoA , [ 28 ] which is then metabolized by glycine N -acyltransferase into hippuric acid.

  7. Benzophenone imine - Wikipedia

    en.wikipedia.org/wiki/Benzophenone_imine

    Benzophenone imine can be prepared by the thermal decomposition of benzophenone oxime: [2]. 2 (C 6 H 5) 2 C=NOH → (C 6 H 5) 2 C=NH + (C 6 H 5) 2 C=O. Benzophenone imine can also be synthesized by addition of phenylmagnesium bromide to benzonitrile followed by careful hydrolysis (lest the imine be hydrolyzed): [3]

  8. Benzone - Wikipedia

    en.wikipedia.org/wiki/Benzone

    Benzophenone-n, a class of compounds derived from benzophenone, including Oxybenzone; Dioxybenzone; and mostly used in sunscreens This page was last edited on 15 ...

  9. How Much Alcohol Is Safe to Drink Without Putting Your Health ...

    www.aol.com/lifestyle/much-alcohol-safe-drink...

    A new federal report shows that one drink per day could raise the risk of liver damage and several cancers. The report follows a recommendation by the U.S. Surgeon General on safe alcohol ...