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Benzyl cinnamate

Phenylmethyl 3-phenylprop-2-enoate

Cinnamic acid benzyl ester · Cinnamein (trans)

Phenylpropenoid benzenoid ester · C₁₆H₁₄O₂

Chemical structure of Benzyl cinnamate
2D structure PubChem / NCI CIR

Chemical info

CAS number CAS
103-41-3
Molecular formula
C₁₆H₁₄O₂
Molecular weight
238.28 g/mol
Aroma
Warm balsamic, sweet, with a soft cinnamon edge.

Safety

Low concern · EU listed allergen

Benzyl cinnamate appears chiefly in Peru balsam and styrax. Practical data indicate very low irritation and sensitization risk; some authors consider its inclusion among the 26 EU fragrance allergens overcautious.

Skin. An 8 percent patch test on 25 volunteers caused neither irritation nor sensitization. An HRIPT at 4 percent on 101 volunteers gave no reactions. Among 1,072 dermatitis patients, under 1 percent reacted at 1–2 percent.

Peru balsam sensitive patients may cross-react: 3 of 102 reacted to 2 percent benzyl cinnamate.

Oral. Acute oral LD50 is 3.76 g/kg in guinea pigs and 3.28 g/kg in rats. Rabbit dermal LD50 exceeds 3 g/kg.

Subchronic. Rats fed 10,000 ppm for 19 weeks showed no macroscopic effects. NOAEL is 500 mg/kg/day.

Mutagenicity. Non-mutagenic in the Bacillus subtilis rec assay.


Usage guidelines

EU mandatory declaration
Above 100 ppm wash-off or 10 ppm leave-on
IFRA limit (leave-on)
2.1 percent
Rat subchronic NOAEL
500 mg/kg/day
Concern level
Low

Found in essential oils

Principal sources
Peru balsam0.4 – 30.1 %
Styrax1.7 %

Notes

The source oils for benzyl cinnamate are Peru balsam and styrax, which themselves carry dermal limits. Adding a constituent-specific limit may be redundant.