Salicyluric acid

Salicyluric acid is the glycine conjugate of salicylic acid and is the primary form in which salicylates are excreted from the body,[1] via the kidneys. The pathway is very similar to the pathway of benzoic acid excretion as hippuric acid.

Salicyluric acid
Identifiers
CAS Number
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.006.965
Chemical and physical data
FormulaC9H9NO4
Molar mass195.174 g·mol−1
3D model (JSmol)
Melting point164–165 °C (327–329 °F)
SMILES
  • c1ccc(c(c1)C(=O)NCC(=O)O)O
InChI
  • InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
  • Key:ONJSZLXSECQROL-UHFFFAOYSA-N

References
  1. Schrör K (2016). "Biotransformations of Salicylic Acid". Acetylsalicylic acid (Second ed.). Weinheim. p. 70. ISBN 978-3-527-68502-8.


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