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HEPTYL-ISO-EUGENOL

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
carnationorientalfloral-spicyamberfougere
How it behaves

Olfactory profile

Family
sweet
Note tendency
Base
Descriptors
fruitysweet

A warm, sweet-spicy clove-eugenol character extended by a long alkyl chain, giving it a softer, more diffusive and less pungent profile than eugenol itself. Rounded, slightly powdery and balsamic with a subtle carnation-floral facet that persists quietly on the 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. 1539

Arctander monograph

Perfume and Flavor Chemicals, page 637.

tenacity · high
sweetfruity
MW
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BP
276°C
MP
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Sp.Gr.
0.97
Refractive n
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Rotation
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Appearance

Pale yellowish or straw-colored viscous liquid.

Solubility

Insoluble in water, soluble in alcohol and oils. Insoluble in propylene glycol.

Odor

Mild and very sweet, also fruity and very tenacious odor, remotely reminiscent of overripe fruit (apples). Contrary to the Heptyl eugenol this ether is not tarry, not leather-like.

Uses in perfumery

Suggested for use in perfume compositions.

Production

Produced by isomerization of Heptyl eugenol, or from iso-Eugenol in alcoholic alkali solution with Heptyl bromide.

Identity
Aliases · 2
3-Methoxy-4-heptoxy propenyl benzeneiso-Eugenol heptylether
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).