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EUGENYL PHENYLACETATE

CAS
—
EC
—
Material type
synthetic aroma chemical
Canonical source
arctander
Formulation

Usage guidance

Suggested min
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Suggested max
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Cost
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Stock
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Compatibility tags
carnationorientalamberfloraltobaccospicy
How it behaves

Olfactory profile

Family
sweet
Note tendency
Base
Descriptors
honey

A warm, sweet-spicy ester with a rich clove-eugenol facet softened by a honeyed, faintly floral phenylacetate character. Less pungent and sharper than eugenol itself, with a rounded balsamic depth that lingers as a smooth spicy-sweet drydown.AI · claude-opus-4-7

Intensity
5 / 10
Tenacity
7 / 10
Volatility
3 / 10
Members

The rest of this material

Composition, IFRA restriction figures, allergen concentrations and where this material is bought are part of Perfume Foundry’s curated library and need an account. Create one or sign in.

chemicals · No. 1375

Arctander monograph

Perfume and Flavor Chemicals, page 563.

tenacity · excellent
sweetspicy
MW
—
BP
320°C
MP
—
Sp.Gr.
1.15
Refractive n
—
Rotation
—
Appearance

Pale straw-colored, viscous liquid.

Solubility

Insoluble in water, soluble in alcohol and oils.

Odor

Mild, but warm and sweet, slightly spicy odor of excellent tenacity.

Uses in perfumery

This material is occasionally used in perfume compositions as a modifier in Carnation bases, where a particularly delicate and discrete Spice-note is desirable, and iso-Eugenol does not cover the full olfactory picture. However, the iso-Eugenyl ester is generally preferred over this material. It finds some use in Lilac bases where it may introduce the warm and rich undertones, often difficult to obtain.

Production

Produced from Phenylacetyl chloride and Sodium eugenol

Identity
Aliases · 2
Eugenol phenylacetateiso-Eugenol phenylacetate
Compliance note. Restriction data is sourced directly from IFRA publications and preserved with its document excerpt. Perfume Foundry is a compliance-support tool — not a substitute for a qualified safety assessor (CPSR / PIF).