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Benzyl salicylate

Phenylmethyl 2-hydroxybenzoate

Salicylic acid benzyl ester · o-Hydroxybenzoic acid benzyl ester

Phenolic ester · C₁₄H₁₂O₃

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

Chemical info

CAS number CAS
118-58-1
Molecular formula
C₁₄H₁₂O₃
Molecular weight
228.24 g/mol
Aroma
Soft floral-balsamic, faintly sweet-spicy, used as a fixative.

Safety

Low concern · EU listed allergen

Benzyl salicylate is a mildly substituted phenol, a weak acid that can be corrosive to tissues at high concentrations. Listed among the 26 EU fragrance allergens, practical data show very low risk in non-Japanese populations.

Skin. A 30 percent patch test on 25 volunteers caused no sensitization. In 10,503 patch tests of consumer products containing under 2 percent benzyl salicylate, no reactions were attributable to the compound. In 100 consecutive dermatitis patients, no irritant or allergic reactions to 1 percent.

Clear population differences exist. In Japan, 3.4 percent of 5,087 dermatitis patients reacted to 2 percent. In Europe and North America, the rate is 0.76 percent in 2,640 patients.

Oral. Acute oral LD50 in rats is 2.23 g/kg; rabbit dermal LD50 is 14.15 g/kg, indicating very low toxicity.

Reproductive. Salicylates generally inhibit growth and cause congenital abnormalities in animals. Benzyl salicylate has weak in vitro estrogenic activity at 10⁻⁵ M, with an opposite effect at 10⁻⁴ M. It is unlikely to reach toxic doses through practical essential oil exposure.

Mutagenicity. Non-mutagenic in the Ames test.


Usage guidelines

EU mandatory declaration
Above 100 ppm wash-off or 10 ppm leave-on
IFRA limit (leave-on)
8.0 percent
Concern level
Low (higher in Japanese populations)

Found in essential oils

Principal sources
Ylang-ylang0.3 – 3.9 %
Carnation3.9 %
Tuberose2.6 %

Notes

Benzyl salicylate absorbs UV light. The compound was historically used as a mild sunscreen ingredient. Today its main role is as a fixative for floral notes in fine perfumery.