L-Menthol
L-Menthol (CAS No.: 2216-51-5) is a naturally occurring monoterpene predominantly isolated from peppermint and other mint oils or produced via synthetic routes, typically appearing as a clear to white crystalline solid at ambient conditions. As the principal bioactive stereoisomer of menthol, it is widely studied in biomedical research for its modulatory effects on sensory ion channels, most notably as an agonist of the transient receptor potential melastatin 8 (TRPM8) channel, leading to increased intracellular calcium levels and the elicitation of cooling sensations. In addition to its well-characterized role in sensory neurobiology and analgesia, L-menthol exhibits inhibitory activity against enzymes such as acetylcholinesterase at low millimolar concentrations and has demonstrated the ability to modulate gene expression related to DNA topology and cell proliferation, including topoisomerases, in cancer cell models, where it reduces cell viability at micromolar to millimolar levels. Preclinical studies further indicate antinociceptive effects in animal models, supporting its utility in pain and inflammation research. These diverse pharmacological properties make L-menthol a valuable tool compound for investigating ion channel signaling, neurophysiology, and potential anticancer mechanisms, with experimental concentrations and dosing regimens varying depending on specific in vitro or in vivo study designs.
| Physical Appearance | A crystalline solid |
| Storage | -20°C |
| M.Wt | 156.27 |
| Cas No. | 2216-51-5 |
| Formula | C10H20O |
| Synonyms | L-Menthol; (1R,2S,5R)-(?)-Menthol; NSC 62788 |
| Solubility | ≥2.05 mg/mL in H2O; ≥27.5 mg/mL in EtOH; ≥35.7 mg/mL in DMSO |
| Chemical Name | (1R,2S,5R)-2-isopropyl-5-methylcyclohexan-1-ol |
| Canonical SMILES | C[C@H]1C[C@@H](O)[C@H](C(C)C)CC1 |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |







