Hippuric acid

Hippuric acid
Structural formula of hippuric acid
Ball-and-stick model of the hippuric acid molecule
Names
IUPAC name
Benzoylaminoethanoic acid
Other names
  • Hippuric acid
  • N-Benzoylglycine
  • Benzoyl glycocoll
  • Benzoyl amidoacetic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.098
KEGG
UNII
Properties
C9H9NO3
Molar mass 179.18 g·mol−1
Density 1.371 g/cm3
Melting point 187 to 188 °C (369 to 370 °F; 460 to 461 K)
Boiling point 240 °C (464 °F; 513 K) (decomposes)
Hazards
Safety data sheet Material Safety Data Sheet
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Hippuric acid (Gr. hippos, horse, ouron, urine) is a carboxylic acid and organic compound. It is found in urine and is formed from the combination of benzoic acid and glycine. Levels of hippuric acid rise with the consumption of phenolic compounds (such as fruit juice, tea and wine). The phenols are first converted to benzoic acid, and then to hippuric acid and excreted in urine.[1]

Hippuric acid crystallizes in rhombic prisms which are readily soluble in hot water, melt at 187 °C, and decompose at about 240 °C. High concentrations of hippuric acid may also indicate a toluene intoxication; however, scientists have called this correlation into question because there are other variables that affect levels of hippuric acid.[2] When many aromatic compounds such as benzoic acid and toluene are taken internally, they are converted to hippuric acid by reaction with the amino acid, glycine.

Synthesis

A modern synthesis of hippuric acid involves the acylation of glycine with benzoyl chloride:[3]

Reactions

Hippuric acid is readily hydrolysed by hot caustic alkalis to benzoic acid and glycine. Nitrous acid converts it into benzoyl glycolic acid, C6H5C(=O)OCH2CO2H. Its ethyl ester reacts with hydrazine to form hippuryl hydrazine, C6H5CONHCH2CONHNH2, which was used by Theodor Curtius for the preparation of hydrazoic acid.

History

Justus von Liebig showed in 1829 that hippuric acid differed from benzoic acid,[4] and in 1834 determined its constitution,[5] while in 1853 French chemist Victor Dessaignes (1800–1885) synthesized it by the action of benzoyl chloride on the zinc salt of glycine.[6] It was also formed by heating benzoic anhydride with glycine,[7] and by heating benzamide with monochloroacetic acid.

See also

References

  1. ↑ "Human Metabolome Database: Showing metabocard for Hippuric acid (HMDB0000714)". www.hmdb.ca. Retrieved 2018-09-21.
  2. ↑ Pero, RW (2010). "Health consequences of catabolic synthesis of hippuric acid in humans". Current clinical pharmacology. 5 (1): 67–73. doi:10.2174/157488410790410588. PMID 19891605.
  3. ↑ A. W. Ingersoll and S. H. Babcock. "Hippuric acid". Organic Syntheses. ; Collective Volume, 2, p. 0328
  4. ↑ Liebig, Justus (1829) "Ueber die Säure, welche in dem Harn der grasfressenden vierfüssigen Thiere enthalten ist" (On the acid which is contained in the urine of grass-eating, four-footed animals), Annalen der Physik und Chemie, 17 : 389–399.
  5. ↑ Liebig, Justus (1834) "Ueber die Zusammensetzung der Hippursäure" (On the composition of hippuric acid), Annalen der Physik und Chemie, 32 : 573–574.
  6. ↑ Dessaignes V. (1853). "Ueber die Regeneration der Hippursäure" [On the regeneration of hippuric acid]. Annalen der Chemie und Pharmacie. 87 (3): 325–327. doi:10.1002/jlac.18530870311. See also: Dessaignes (1853) "Note sur la régénération de l'acide hipparique," Comptes rendus, 37 : 251–252.
  7. ↑ Curtius T. (1884). "Synthese von Hippursäure und Hippursäureäthern" [Synthesis of hippuric acid and hippuric acid esters]. Berichte der deutschen chemischen Gesellschaft. 17 (2): 1662–1663. doi:10.1002/cber.18840170225.
  •  This article incorporates text from a publication now in the public domain: Chisholm, Hugh, ed. (1911). "Hippuric Acid". Encyclopædia Britannica (11th ed.). Cambridge University Press.
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