Ferulic acid sodium

• CAT Number: I002810
• CAS Number: 24276-84-4
• Molecular Formula: C10H9NaO4
• Molecular Weight: 216.17
• Purity: ≥95%
• Target: Immunology/Inflammation
• Solubility: DMSO:15mg/mL
• Storage: Store at -20C
• IUPAC Name: sodium;(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
• InChI: 1S/C10H10O4.Na/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13;/h2-6,11H,1H3,(H,12,13);/q;+1/p-1/b5-3+
• InChIKey: NCTHNHPAQAVBEB-WGCWOXMQSA-M
• SMILES: COC1=C(C=CC(=C1)/C=C/C(=O)[O-])O.[Na+]

Ferulic acid sodium (Cat No.: I002810) is a water-soluble derivative of ferulic acid, a natural phenolic compound with strong antioxidant, anti-inflammatory, and neuroprotective properties. It scavenges free radicals, protects against oxidative stress, and enhances cellular defense mechanisms. Used in skincare, pharmaceuticals, and food supplements, it helps prevent aging, cardiovascular diseases, and neurodegenerative disorders. Ferulic acid sodium also stabilizes other antioxidants like vitamin C and E, making it a valuable ingredient in cosmetic and therapeutic formulations for improved stability and efficacy.

Reference

[1]. Lampiasi N, et al. The molecular events behind ferulic acid mediated modulation of IL-6 expression in LPS-activated Raw 264.7 cells. Immunobiology. 2015 Nov 10.
[2]. Yu CL, et al. Ferulic Acid Protects Against Lead Acetate-Induced Inhibition of Neurite Outgrowth by Upregulating HO-1 in PC12 Cells: Involvement of ERK1/2-Nrf2 Pathway. Mol Neurobiol. 2015 Nov 26.
[3]. Ana Lúcia B. Zeni, et al. Ferulic acid exerts antidepressant-like effect in the tail suspension test in mice: Evidence for the involvement of the serotonergic system. European Journal of Pharmacology 679 (2012) 68–74