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HELIOTROPINE

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
orientalgourmandwhite-floralpowderyfougereamber
How it behaves

Olfactory profile

Family
sweet
Note tendency
Base
Descriptors
floralspicysweetwarm

Sweet, powdery, almond-like floral with a distinct cherry-vanilla nuance. Recalls heliotrope flowers and marzipan, with a soft creamy warmth that lingers into the drydown.AI · claude-opus-4-7

Intensity
6 / 10
Tenacity
7 / 10
Volatility
4 / 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. 1484

Arctander monograph

Perfume and Flavor Chemicals, page 614.

MIDDLEtenacity · highpower · strongG.R.A.S.FEMA 2911
sweetfloralspicytenacious
MW
150.14
BP
263°C
MP
37°C
Sp.Gr.
0.2
Refractive n
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Rotation
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Appearance

White or colorless crystals.

Solubility

Soluble in cold water, somewhat better in hot water. Soluble in alcohol and oils, somewhat soluble in propylene glycol. Insoluble in glycerin. Volatile with steam.

Odor

Very sweet floral, warm slightly spicy and tenacious odor, sometimes described as 'Cherry-like' (American type Cherry).

Flavor

Sweet, spicy-floral taste of considerable power.

Uses in perfumery

Heliotropine is very extensively used in perfume compositions - from the very expensive types all the way down to household fragrances and industrial perfumes. Concentrations may vary from less than one percent to more than ten percent, but floral effects are usually obtained with a few percent.

Uses in flavor

Heliotropine finds extensive use in flavor compositions, although the power of Heliotropine as a flavoring agent is often underestimated, and the concentration should be kept at a minimum in order to achieve truly pleasant and 'non-perfumey' effects.

Production

1) by oxidation of iso-Safrole, which is obtained by isomerization of Safrole, a distillation isolate from Brazilian Ocotea pretiosa oil or Chinese Camphor oil. 2) from Catechol (Pyrocatechol).

Identity
Aliases · 5
3,4-Methylene dioxybenzaldehydeDioxymethylene protocatechuic aldehydePiperonalPiperonyl aldehydeProtocatechualdehyde methylene ether
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).