Date published: 2025-10-13

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m-Tolylacetic acid (CAS 621-36-3)

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Alternate Names:
3-Methylphenylacetic acid
CAS Number:
621-36-3
Molecular Weight:
150.17
Molecular Formula:
C9H10O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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m-Tolylacetic acid functions as a precursor in the synthesis of agrochemicals. It acts as a building block in the production of various organic compounds, contributing to the development of new chemical entities. At the molecular level, m-Tolylacetic acid undergoes specific chemical reactions to form key intermediates, enabling the creation of diverse chemical structures. Its mechanism of action involves participating in organic synthesis processes, facilitating the formation of complex molecules with potential applications in various research and development endeavors. Through its involvement in synthesis pathways, m-Tolylacetic acid plays a role in the advancement of chemical innovation and the exploration of new molecular entities.


m-Tolylacetic acid (CAS 621-36-3) References

  1. The pharmacological properties of a novel MCH1 receptor antagonist isolated from combinatorial libraries.  |  Nagasaki, H., et al. 2009. Eur J Pharmacol. 602: 194-202. PMID: 19041642
  2. Identification of two novel, potent, low-liability antinociceptive compounds from the direct in vivo screening of a large mixture-based combinatorial library.  |  Reilley, KJ., et al. 2010. AAPS J. 12: 318-29. PMID: 20422341
  3. Biotransformation of the Fluorinated Nonsteroidal Anti-Inflammatory Pharmaceutical Flurbiprofen in Activated Sludge Results in Accumulation of a Recalcitrant Fluorinated Aromatic Metabolite.  |  Yanaç, K. and Murdoch, RW. 2019. Glob Chall. 3: 1800093. PMID: 31565381
  4. Biodegradation of Microtoxic Phenylpropanoids (Phenylpropanoic Acid and Ibuprofen) by Bacteria and the Relevance for Their Removal from Wastewater Treatment Plants.  |  Wittich, RM., et al. 2023. Genes (Basel). 14: PMID: 36833369
  5. Mixture-based heterocyclic combinatorial positional scanning libraries: discovery of bicyclic guanidines having potent antifungal activities against Candida albicans and Cryptococcus neoformans.  |  Blondelle, SE., et al. 1999. Antimicrob Agents Chemother. 43: 106-14. PMID: 9869574

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

m-Tolylacetic acid, 5 g

sc-235541
5 g
$27.00