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Compounds · Aldehydes · Phenylpropanoid pathway

Cinnamaldehyde

Also known as Cinnamal · 3-Phenyl-2-propenal — an analysis may use any of these names

Cinnamon bark, hot sweetness, almost a taste. A single molecule responsible for the whole cinnamon tree in everyone’s memory.

CAS
104-55-2
Formula
C9H8O
Molar mass
132.16
Odour threshold
—
Boiling point
≈ 248 °C at atmospheric pressure
Volatility
150 °C290 °C

Must be declared on the label

This compound is on the list of allergens that must be declared individually on cosmetic labels in the European Union, as one of the 24 substances listed before Regulation 2023/1545. Name to use on the label: CINNAMAL.

The declaration threshold is 0.001% in leave-on products and 0.01% in rinse-off products. This is an EU requirement — see the regulations page for why it matters beyond the EU. This is not legal advice.

Where it comes from

Biosynthetic pathway: Phenylpropanoid pathway — plants build them around a six-carbon aromatic ring.

Why it sits where it does

An aromatic aldehyde with a conjugated double bond linked to the benzene ring. A flat, stable structure, boiling at around 248 degrees.

Where else you meet it

Cinnamon bark is almost its only source. The synthetic version is widely used in confectionery.

Dictionary entries that mention this compound