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Common Name(s): 3,5-dimethoxy-4-hydroxycinnamic acid,sinapinic acid
CAS Number: 530-59-6
DESCRIPTION
What It Does: Provides antioxidant activity with natural uv absorption for combined photoprotection and antioxidant defense.
Why It's Used: Natural uv-absorbing antioxidant from cruciferous sources providing both direct free radical scavenging and uv energy absorption.
How It Works: Two methoxy groups enhance electron-donating capacity for radical scavenging. cinnamate chromophore absorbs uv (290-330nm) via pi-pi transitions. anti-inflammatory via cox-2 inhibition. potential for natural uv filter activity.
Typically Found In: Natural sunscreen boosters,antioxidant serums,photoprotection products
TECHNICAL DETAILS
Primary Category: Active ingredient – phenylpropanoid antioxidant
Secondary Functions: Uv absorption,photoprotection,anti-inflammatory
Application Areas:
Facial Skincare
Body Care
Hair Care
Beard Care
Color Cosmetics (Makeup)
Dietary/Oral Supplements
Typical Concentration Range: 0.1%–1%
SOURCING & ETHICS
Vegan Status: Yes – from cruciferous plants
Halal Status: Yes
Source Notes: Plant-derived extract or synthetic.
SKIN COMPATIBILITY
Irritancy Rating: 1/5 – very low
Comedogenicity Rating: 0/5 – non-comedogenic
Sensitivity Concerns: Non-irritating; well-tolerated.
Safe for Sensitive Skin: Yes
SAFETY & COMPATIBILITY
Safety Profile: Excellent safety profile. ewg score: 1.
Works Well With: Vitamin c,vitamin e,ferulic acid,spf,other antioxidants
Avoid Combining With: No significant incompatibilities
SCIENTIFIC NOTE
Sinapic acid's uv absorption maximum (320nm, log ε~4.3) falls in the uvb/uva-ii range, comparable to synthetic uvb filters. unlike synthetic filters, sinapic acid simultaneously provides direct antioxidant protection while absorbing uv, making it a dual-action photoprotective ingredient.
Last Verified: 2026-03-12
Primary Sources: Cosing database,nair et al. sinapic acid uv absorption study