Date published: 2026-2-11

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(−)-Menthyloxyacetic acid (CAS 40248-63-3)

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Alternate Names:
(−)-Menthyl carboxymethyl ether
CAS Number:
40248-63-3
Molecular Weight:
214.30
Molecular Formula:
C12H22O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(−)-Menthyloxyacetic acid is a derivative of (−)-menthol, which is a well-known compound with a characteristic minty odor. In biochemistry, (−)-menthyloxyacetic acid is of interest due to its potential role as a precursor in the biosynthesis of certain products. (−)-Menthyloxyacetic acid undergo enzymatic transformations in certain organisms, leading to the formation of biologically active molecules. The structural features of (−)-menthyloxyacetic acid make it a suitable substrate for specific enzymes, allowing for the production of diverse chemical entities. The reactivity of (−)-Menthyloxyacetic acid under biological conditions provides insight into the mechanisms of enzymatic catalysis and metabolic pathways. The study of (−)-menthyloxyacetic acid in biochemistry contributes to our understanding of product biosynthesis and enzymatic reactions in living organisms.


(−)-Menthyloxyacetic acid (CAS 40248-63-3) References

  1. Tailored cellulose esters: synthesis and structure determination.  |  Liebert, TF. and Heinze, T. 2005. Biomacromolecules. 6: 333-40. PMID: 15638537
  2. Enantiomeric resolution, thermodynamic parameters, and modeling of clausenamidone and neoclausenamidone on polysaccharide-based chiral stationary phases.  |  Luo, X., et al. 2019. Chirality. 31: 423-433. PMID: 31017738
  3. Ketones from Nickel-Catalyzed Decarboxylative, Non-Symmetric Cross-Electrophile Coupling of Carboxylic Acid Esters.  |  Wang, J., et al. 2019. Angew Chem Int Ed Engl. 58: 12081-12085. PMID: 31287943
  4. An enantiomeric interaction in the metabolism and tumorigenicity of (+)- and (-)-benzo[a]pyrene 7,8-oxide.  |  W. Levin, M.K. Buening, A.W. Wood, R.L. Chang, B. Kedzierski, D.R. Thakker, D.R. Boyd, G.S. Gadaginamath, R.N. Armstrong, H. Yagi, J.M. Karle, T.J. Slaga, D.M. Jerina, A.H. Conney. 1980. Journal of Biological. 255: 9067-9074.
  5. Novel, racemic or nearly-racemic antibacterial bromo- and chloroquinols and γ-lactams of the verongiaquinol and the cavernicolin type from the marine sponge Aplysina (= Verongia) cavernicola†  |  Michele D'Ambrosio, Antonio Guerriero, Francesco Pietra. 1984. Helvetica Chimica Acta. 67: 1484-1492.
  6. Effects of a 6-fluoro substituent on the solvolytic properties of the diastereomeric 7,8-diol 9,10-epoxides of the carcinogen benzo[a]pyrene  |  H. Yagi, J. M. Sayer, D. R. Thakker, W. Levin, and D. M. Jerina, et al. 1987. J. Am. Chem. Soc. 109: 838–846.
  7. Synthesis of (R,R) and (S,S) bicyclo[3.3.0]octane-2,6-dione interactions between non-conjugated chromophores  |  Joëlle Pérard-Viret, André Rassat ∗. 1994. Tetrahedron: Asymmetry. 5: 1-4.
  8. Attempted Resolution and Racemization of Beckmann-Derived CTV-Lactam and the Use of Chirabite-AR® to Determine the Optical Purity of the Supramolecular Scaffold  |  Marlon R. Lutz Jr., Elizabeth Ernst, Matthias Zeller, Jacob Dudzinski, Peter Thoresen, Daniel P. Becker. 2018. European Journal of Organic Chemistry. 2018: 4639-4645.
  9. Novel optically active 2D materials based on λ-zirconium phosphate and chiral monocarboxylic acids: Synthesis and characterization  |  Hussein Alhendawi, Ernesto Brunet, Elena Rodríguez Payán & Huda Alkahlout. 2021. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 99: 217–226.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(−)-Menthyloxyacetic acid, 1 g

sc-252995
1 g
$47.00