Phenylacetic acid explained

Phenylacetic acid (conjugate base phenylacetate), also known by various synonyms, is an organic compound containing a phenyl functional group and a carboxylic acid functional group. It is a white solid with a strong honey-like odor. Endogenously, it is a catabolite of phenylalanine. As a commercial chemical, because it can be used in the illicit production of phenylacetone (used in the manufacture of substituted amphetamines), it is subject to controls in countries including the United States and China.[1]

Occurrence

Phenylacetic acid has been found to be an active auxin (a type of plant hormone),[2] found predominantly in fruits. However, its effect is much weaker than the effect of the basic auxin molecule indole-3-acetic acid. In addition the molecule is naturally produced by the metapleural gland of most ant species and used as an antimicrobial. It is also the oxidation product of phenethylamine in humans following metabolism by monoamine oxidase and subsequent metabolism of the intermediate product, phenylacetaldehyde, by the aldehyde dehydrogenase enzyme; these enzymes are also found in many other organisms.

Preparation

This compound may be prepared by the hydrolysis of benzyl cyanide:

Reactions

Phenylacetic acid undergoes ketonic decarboxylation to form ketones.[3] It can be condensed with itself to form dibenzyl ketone, or with a large excess of another carboxylic acid (in the form of an acid anhydride), such as with acetic anhydride to form phenylacetone.

Applications

Phenylacetic acid is used in some perfumes, as it possesses a honey-like odor even in low concentrations. It is also used in penicillin G production and diclofenac production. It is also employed to treat type II hyperammonemia to help reduce the amounts of ammonia in a patient's bloodstream by forming phenylacetyl-CoA, which then reacts with nitrogen-rich glutamine to form phenylacetylglutamine. This compound is then excreted from the patient's body. It's also used in the illicit production of phenylacetone, which is used in the manufacture of methamphetamine.

The sodium salt of phenylacetic acid, sodium phenylacetate, is used as a pharmaceutical drug for the treatment of urea cycle disorders, including as the combination drug sodium phenylacetate/sodium benzoate (Ammonul).[4]

Phenylacetic acid is used in the preparation of and derived from several pharmaceutical drugs, including camylofin, bendazol, triafungin, phenacemide, lorcainide, phenindione, phenelzine and cyclopentolate.

In popular culture

In the crime drama Breaking Bad, phenylacetic acid is featured twice as a precursor to methamphetamine, first in the episode titled "A No-Rough-Stuff-Type Deal", then in "Salud".[5]

See also

Notes and References

  1. Web site: List of Regulated Drug Precursor Chemicals in China. 27 April 2015. dead. https://web.archive.org/web/20150817022812/http://www.chemsafetypro.com/Topics/China/Drug_Precursor_Chemicals_List.html. 17 August 2015.
  2. Wightman, F. . Lighty, D. L. . Identification of phenylacetic acid as a natural auxin in the shoots of higher plants . Physiologia Plantarum . 1982 . 55 . 1 . 17–24 . 10.1111/j.1399-3054.1982.tb00278.x .
  3. Book: 10.1002/14356007.a15_077 . Ketones . Ullmann's Encyclopedia of Industrial Chemistry . 2000 . Siegel . Hardo . Eggersdorfer . Manfred . 9783527306732 .
  4. Web site: Sodium Phenylacetate and Sodium Benzoate Monograph for Professionals . Drugs.com . 16 November 2019 . en.
  5. Web site: Chemistry Views . . The Chemistry of Breaking Bad . Harnisch . Falk . Salthammer . Tunga . https://web.archive.org/web/20240208125657/https://www.chemistryviews.org/details/ezine/5416791/The_Chemistry_of_Breaking_Bad/ . 8 February 2024 .