Heliotropin (Piperonal) (CAS 120-57-0) — Sweet Base Note Fragrance Ingredient




Heliotropin (Piperonal)

CAS 120-57-0

Origin
Note
IFRA
Generally safe
Data as of: Mar 2026

What Is Heliotropin (Piperonal)?

Heliotropin, also known as Piperonal, is a sweet, vanilla-like aromatic compound used in perfumes and flavorings. You’ll encounter it in gourmand fragrances, bakery products, and some floral compositions. This ingredient matters because it bridges floral and edible scent worlds, creating comforting yet sophisticated accords. Its stability makes it a perfumer’s favorite for long-lasting sweet notes.

Safety Profile

GENERALLY SAFE

Generally safeUse with awarenessProfessional use
Approved for food and fragrance use
Potential skin sensitizer at high concentrations
CAS
120-57-0
Formula
Mixture
MW
Variable
Odor Family
Layer 1 · Enthusiast

What Does Heliotropin (Piperonal) Smell Like?

Piperonal greets you with an intense, powdery sweetness reminiscent of fresh-baked almond cookies, then unfolds into a creamy vanilla-heliotrope heart. Like a pastry shop at dawn, it balances gourmand warmth with floral delicacy. The dry-down reveals subtle cherry-almond nuances that linger close to skin, creating an intimate sillage. Unlike pure vanilla, it carries a crisp, almost minty edge that prevents cloying sweetness.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

L’Heure Bleue(Guerlain, 1912)

Piperonal provides the iconic powdery-anisic backbone of this melancholic masterpiece, blending with iris and carnation to create its twilight haze.

Shalimar(Guerlain, 1925)

Used sparingly to soften the citrus-vanilla contrast, adding a delicate cherry blossom nuance to the legendary oriental structure.

Layer 2

2D Molecular Structure

Piperonal

SMILES: O=CC1=CC=C2OCOC2=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Piperonal is a benzodioxole derivative synthesized from safrole or catechol. The methylenedioxy bridge contributes to its stability and distinctive odor profile. Modern production often uses peroxidation of isosafrole, yielding this crystalline solid that sublimes readily. Its planar structure allows excellent diffusion, while the aldehyde group provides reactivity for Schiff base formation in perfumery.

Physical & Chemical Properties

Boiling Point 263 °C
Melting Point 37 °C
Flash Point 129 °C
Density 1.337 g/cm³

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-6 hours)
Blending
Excellent
Application Typical % Range Notes
Fine Fragrance 1-3% 0.5-5% Adds powdery sweetness
Soaps 0.5-1% 0.2-2% Stable in alkaline media
Candles 2-4% 1-6% Good heat resistance

Classic Accords

+ Vanilla + Tonka = Gourmand
+ Mimosa + Iris = Powdery floral
+ Citrus + Musk = Soft oriental

Tip: Use with ionones to create velvety floral effects or with ethyl maltol for candy-like accents.

Alternatives & Comparisons

1
Vanillin CAS 121-33-5

When a simpler, more straightforward vanilla character is needed without the floral-powdery complexity.

2
Ethyl Vanillin CAS 121-32-4

For three times the potency and more caramelized sweetness when projecting power is required.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. IFRA, REACH, EU Cosmetics Regulation standards update periodically. Consult current IFRA Standards Library before formulating. Not legal or regulatory advice.

IFRA Status

No restrictions under IFRA 49th Amendment. Listed as safe for use in current categories.

EU Allergen Declaration

Not listed in EU allergen regulation (EC) No 1223/2009.

RIFM Assessment

RIFM-reviewed with no significant safety concerns at reported use levels.

Sustainability

Most piperonal is synthesized from petrochemical precursors, though some is still derived from sustainable sassafras oil in regions where cultivation is permitted. New catalytic processes have reduced environmental impact compared to traditional synthesis routes.

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Industry & Science Data

Odor Detection Threshold
1 ppb
in air (orthonasal)
Ref: van Gemert, Odour Thresholds (2011)
Commercial Price
$20–$40/kg
synthetic grade, bulk market
Indicative 2024 pricing. Varies by purity & volume.
Global Usage Rank
#32 most used
by global fragrance volume
Source: IFRA Usage Survey 2015
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References

  1. Bickers et al. (2005). Safety assessment of piperonal. Food and Chemical Toxicology. PMID 15979073

Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Mar 2026.

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Physicochemical Properties

DTXSID: DTXSID7025924

Physical Properties

Molecular Weight 150.133 g/mol🔬 EPA CompTox
Density 1.42 g/cm^3🔬 EPA CTX
Boiling Point 263.356 °C🔬 EPA CTX
Melting Point 36.769 °C🔬 EPA CTX
Flash Point 103.7 °C🔬 EPA CTX
Refractive Index 1.615 Dimensionless📊 OPERA
Molar Volume 112.277 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.05 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 1.23 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.23 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.23 Log10 unitless📊 OPERA
Water Solubility 0.023 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 0.01 mmHg🔬 EPA CTX
Viscosity 3.175 cP📊 OPERA
Surface Tension 51.1 dyn/cm📊 OPERA
Thermal Conductivity 134.063 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 35.53 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 1 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 39.167 cm^3/mol📊 OPERA
Polarizability 15.527 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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