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ETHYL-3-PHENYLPROPIONATE

CAS
—
EC
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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
white-floralfruityhoney-accordchypregourmandoriental
How it behaves

Olfactory profile

Family
sweet
Note tendency
Middle
Descriptors
fruitysweet

A soft, sweet fruity-floral note with a rounded balsamic-cinnamic character reminiscent of honey and ripe stone fruit. Has a gentle, slightly powdery warmth that bridges floral and gourmand facets, adding body and a natural nuance to blossom accords.AI · claude-opus-4-7

Intensity
5 / 10
Tenacity
5 / 10
Volatility
5 / 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. 1340

Arctander monograph

Perfume and Flavor Chemicals, page 546.

MIDDLEtenacity · moderatepower · strongG.R.A.S.FEMA 2455
sweetfruityhoneylikefloral
MW
178.23
BP
240°C
MP
—
Sp.Gr.
1.02
Refractive n
—
Rotation
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Appearance

Colorless, somewhat oily liquid.

Solubility

Almost insoluble in water, soluble in alcohol and oils, slightly soluble in propylene glycol.

Odor

Sweet, very light, fruity-honeylike odor. Milder, more rosy-honeylike and more hyacinth-like than the methylester.

Flavor

Sweet, fresh-fruity-floral taste with a honey-like note.

Uses in perfumery

This ester finds use in many types of floral fragrance, e.g. lilac, rose, appleblossom, sweet pea, etc. and in oriental bases with patchouli oil and phenylacetates. Its fruity notes tend to appear strawberry-like if the concentration is too high in a perfume base, but the ester can be advantageously utilized with the skilled combination of chemicals with a similar rate of evaporation.

Uses in flavor

In flavor compositions it can be used for various types of fruit and honey complexes. It is also used in combination with cinnamon and other spices for certain types of candy.

Production

1) from hydrocinnamic acid and ethanol by normal esterification. 2) by hydrogenation of ethyl cinnamate.

Identity
Aliases · 2
Ethyl hydrocinnamateEthyldihydrocinnamate
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).