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Benzyl acetate

Phenylmethyl ethanoate

Acetic acid benzyl ester · Acetic acid phenylmethyl ester

Benzenoid ester · C₉H₁₀O₂

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

Chemical info

CAS number CAS
140-11-4
Molecular formula
C₉H₁₀O₂
Molecular weight
150.17 g/mol
Aroma
Pronounced jasmine, sweet, with a soft fruity facet.

Safety

Low concern · Safe at standard use

Benzyl acetate is a major constituent of many floral absolutes, notably jasmine. The compound is safe at practical use levels, although its vapor can irritate mucous membranes.

Skin. An 8 percent patch test on 25 volunteers caused no sensitization. On 100 dermatitis patients, 5 percent benzyl acetate produced no irritant or allergic reactions. The compound is non-phototoxic in vitro.

Mucous membranes and respiratory tract. Vapor can irritate mucous membranes, eyes and respiratory passages.

Oral. Acute oral LD50 is 2.49–3.69 g/kg in rats, 2.64 g/kg in rabbits. May cause vomiting and diarrhea if ingested.

Subchronic. Rats fed 860–2,150 mg/kg/day for 28 days lost weight, with increased mortality and neuronal necrosis in cerebellum, hippocampus and pyriform cortex. Glycine attenuated toxicity, suggesting glycine depletion as a mechanism.

Reproductive. Developmental NOAEL in rats is 500 mg/kg/day on gestation days 6–15. The high dose of 1,000 mg/kg/day increased skeletal malformations without maternal toxicity.

Mutagenicity. Non-mutagenic in the Ames test, but active in some mouse lymphoma assays.


Usage guidelines

JECFA group ADI
0–5 mg/kg (benzoic acid and salts)
Rat developmental NOAEL
500 mg/kg/day
Concern level
Low

Found in essential oils

Principal sources
Jasmine15.0 – 24.5 %
Ylang-ylang0.4 – 12.4 %
Narcissus9.5 – 9.6 %
Hyacinth8.1 %
Jasmine sambac4.3 %
Champaca (orange)0.1 – 4.0 %
Jonquil1.0 %

Pharmacokinetics

Benzyl acetate is rapidly and almost completely metabolized through benzyl alcohol to benzoic acid in humans, excreted as hippuric acid. After dermal application in rats, virtually all the absorbed dose is excreted within 24 hours.

Gavage produces benzoic acid plasma concentrations many times higher than equivalent feed administration, as gavage saturates the benzoic acid elimination pathway.


Notes

Benzyl acetate is the key carrier of the jasmine note in commercial perfumery and cosmetics. Synthetically it is produced from benzyl alcohol and acetic acid.