Malic acid is an alpha hydroxy acid (AHA) naturally found in apples, pears, and other fruits, known for its gentle exfoliating, hydrating, and brightening properties. Unlike stronger AHAs such as glycolic or lactic acid, malic acid has a larger molecular structure, which means it penetrates the skin more slowly, reducing the risk of irritation while still delivering effective exfoliation. This makes it a great option for those with sensitive or reactive skin who want to experience the benefits of chemical exfoliation without excessive dryness or redness.
One of malic acid’s key benefits is its ability to promote cell turnover, helping to smooth rough skin, fade discoloration, and improve overall radiance. It works by breaking down the bonds between dead skin cells, allowing them to shed more easily and reveal fresher, healthier skin underneath. Because it has both humectant and keratolytic properties, malic acid not only exfoliates but also attracts moisture to the skin, making it a hydrating AHA that helps maintain the skin’s natural moisture barrier.
Malic acid is often used in combination with other exfoliating acids, such as glycolic or lactic acid, in peels, cleansers, and serums to create a balanced exfoliation process. It is particularly effective for addressing concerns like dullness, fine lines, hyperpigmentation, and uneven skin tone, while also helping to refine the appearance of pores. Additionally, its antioxidant properties help protect the skin from oxidative stress and environmental damage.
While malic acid is considered one of the gentler AHAs, it can still increase sun sensitivity, so daily sunscreen use is essential when incorporating it into a skincare routine. It works well alongside hydrating ingredients like hyaluronic acid, ceramides, and soothing agents like aloe vera, making it a well-rounded ingredient for improving skin texture and radiance without excessive irritation.
Malic acid is an organic compound with the molecular formula HO2CCH(OH)CH2CO2H. It is a dicarboxylic acid that is made by all living organisms, contributes to the sour taste of fruits, and is used as a food additive. Malic acid has two stereoisomeric forms (L- and D-enantiomers), though only the L-isomer exists naturally. The salts and esters of malic acid are known as malates. The malate anion is a metabolic intermediate in the citric acid cycle.
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![]() DL-Malic acid
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Names | |
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Preferred IUPAC name
2-Hydroxybutanedioic acid | |
Other names
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Identifiers | |
3D model (JSmol)
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ChEBI |
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.027.293 |
EC Number |
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E number | E296 (preservatives) |
KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C4H6O5 | |
Molar mass | 134.09 g/mol |
Appearance | Colorless |
Density | 1.609 g⋅cm−3 |
Melting point | 130 °C (266 °F; 403 K) |
558 g/L (at 20 °C) | |
Acidity (pKa) | pKa1 = 3.40 pKa2 = 5.20 pKa3 = 14.5 |
Hazards | |
GHS labelling: | |
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Flash point | 203 °C |
Related compounds | |
Other anions
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Malate |
Related carboxylic acids
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Succinic acid Tartaric acid Fumaric acid |
Related compounds
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Butanol Butyraldehyde Crotonaldehyde Sodium malate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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