α-Linolenic Acid
α-Linolenic Acid (CAS No.: 463-40-1) is a plant-derived essential omega-3 polyunsaturated fatty acid widely distributed in vegetable oils and recognized as a critical component of human nutrition and lipid metabolism. As a precursor to longer-chain omega-3 fatty acids, including eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid, it plays a central role in maintaining cellular membrane composition and modulating bioactive lipid mediator synthesis. In biomedical research, α-linolenic acid is studied for its involvement in cardiovascular physiology, inflammation, and metabolic regulation, with evidence indicating that it can influence thrombotic processes through modulation of PI3K/Akt signaling pathways and exhibit anti-arrhythmic properties. It is further implicated in pathways related to oxidative metabolism, as it can undergo β-oxidation for energy production or be incorporated into lipid storage pools. Experimental studies commonly employ α-linolenic acid in cell-based and in vivo models to investigate lipid signaling, cardiometabolic disease mechanisms, and cancer biology, with observed biological activities typically occurring in the nanomolar to micromolar concentration range depending on the assay system. Its broad utility in drug discovery and nutritional research stems from its role as both a metabolic substrate and a modulator of signaling networks relevant to chronic disease pathogenesis.
| Physical Appearance | Liquid |
| Storage | -20°C |
| M.Wt | 278.43 |
| Cas No. | 463-40-1 |
| Formula | C18H30O2 |
| Synonyms | ALA; C18:3 n-3; C18:3 (9Z,12Z,15Z); FA 18:3 |
| Solubility | insoluble in H2O; ≥48 mg/mL in DMSO; ≥51.9 mg/mL in EtOH |
| Chemical Name | (9Z,12Z,15Z)-octadeca-9,12,15-trienoic acid |
| Canonical SMILES | CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O |
| 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. |







