Ferulic acid

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Ferulic acid is a powerful antioxidant naturally found in the cell walls of plants such as rice bran, oats, apples, and coffee. It is widely used in skincare for its ability to neutralize free radicals, protect against environmental damage, and enhance the effectiveness of other antioxidants.

One of ferulic acid’s key benefits is its ability to stabilize and boost the potency of vitamins C and E, making it a common ingredient in antioxidant serums. By preventing oxidative stress caused by UV exposure and pollution, it helps reduce signs of aging, including fine lines, wrinkles, and hyperpigmentation. Ferulic acid also has anti-inflammatory properties, which can soothe the skin and reduce redness.

Due to its photoprotective qualities, ferulic acid is often included in daytime skincare formulations to provide an added layer of defense against sun damage. It is commonly found in serums, creams, and anti-aging treatments, particularly those focused on brightening and skin repair.

Gentle yet highly effective, ferulic acid is suitable for most skin types and works well in combination with other antioxidants to promote a healthier, more radiant complexion. With consistent use, it helps improve skin tone, texture, and overall resilience against environmental stressors.

Ferulic acid (Wikipedia)

Ferulic acid is a hydroxycinnamic acid derivative and a phenolic compound. It is an organic compound with the formula (CH3O)HOC6H3CH=CHCO2H. The name is derived from the genus Ferula, referring to the giant fennel (Ferula communis). Classified as a phenolic phytochemical, ferulic acid is an amber colored solid. Esters of ferulic acid are found in plant cell walls, covalently bonded to hemicellulose such as arabinoxylans. Salts and esters derived from ferulic acid are called ferulates.

Ferulic acid
Names
Preferred IUPAC name
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid
Other names
2-propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-
ferulic acid
3-(4-hydroxy-3-methoxyphenyl)-2-propenoic acid
3-(4-hydroxy-3-methoxyphenyl)acrylic acid
3-methoxy-4-hydroxycinnamic acid
4-hydroxy-3-methoxycinnamic acid
(2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoic acid
Coniferic acid
trans-ferulic acid
(E)-ferulic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.007.892 Edit this at Wikidata
UNII
  • InChI=1S/C10H10O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)/b5-3+ checkY
    Key: KSEBMYQBYZTDHS-HWKANZROSA-N checkY
  • InChI=1/C10H10O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)/b5-3+
    Key: KSEBMYQBYZTDHS-HWKANZROBE
  • COc1cc(ccc1O)/C=C/C(=O)O
Properties
C10H10O4
Molar mass 194.186 g·mol−1
Appearance Crystalline powder
Melting point 168 to 172 °C (334 to 342 °F; 441 to 445 K)
0.78 g/L
Acidity (pKa) 4.61
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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