o-Methoxybenzaldehyde (CAS 0135-02-04) — Sweet Heart Note Fragrance Ingredient

Sweet · Floral

o-Methoxybenzaldehyde

CAS 0135-02-04

Origin
synthetic
Note
Heart
IFRA
Generally safe
Data as of: Apr 2026

What Is o-Methoxybenzaldehyde?

o-Methoxybenzaldehyde is a synthetic aromatic compound used in perfumery to create sweet, almond-like scents with a hint of floral character. You might encounter it in gourmand fragrances, body care products, or as a flavoring agent. This ingredient matters because it provides a cost-effective alternative to natural heliotropin, allowing perfumers to craft warm, comforting fragrances without relying on botanical extracts.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions in consumer products
Potential mild skin sensitivity at high concentrations
CAS
0135-02-04
Formula
Mixture
MW
Variable
Odor Family
Sweet · Floral
Layer 1 · Enthusiast

What Does o-Methoxybenzaldehyde Smell Like?

o-Methoxybenzaldehyde opens with a bright, cherry-like sweetness reminiscent of marzipan, quickly revealing a deeper almond core dusted with vanilla powder. As it develops, subtle floral facets emerge – imagine heliotrope petals dipped in honey. The dry-down is surprisingly tenacious for an aromatic aldehyde, leaving a soft, powdery trail that blends beautifully with vanilla and tonka bases. When overdosed, it can exhibit a sharp, almost medicinal edge that requires careful balancing with woody notes.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

L'Heure Bleue(Guerlain, 1912)

Used as a heliotrope substitute in the powdery heart, contributing to the fragrance’s nostalgic, almond-tinged floralcy that defines its twilight melancholy.

Chergui(Serge Lutens, 2001)

Amplifies the honeyed tobacco accord, adding a gourmand dimension that bridges between hay-like coumarin and sweet amber notes.

Bois Farine(L’Artisan Parfumeur, 2003)

Provides the signature ‘flour sack’ accord, blending with iris and sandalwood to create a uniquely edible woody fragrance.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

o-Methoxybenzaldehyde is an aromatic aldehyde with a methoxy group ortho to the formyl group. Industrially produced through the oxidation of o-methoxytoluene or via the Reimer-Tiemann reaction on guaiacol. The ortho substitution creates steric hindrance that affects its reactivity compared to unsubstituted benzaldehydes. Unlike its para isomer (anisaldehyde), it exhibits greater stability against oxidation while maintaining good solubility in both polar and non-polar solvents.

Physical & Chemical Properties

Boiling Point238-240 °C
Density1.119 g/cm³
Refractive Index1.555-1.558
Flash Point>100 °C

Perfumer Guide

Note Position
Heart
Volatility
Medium (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Used as heliotropin modifier
Soap0.5-1%Up to 2%Provides lasting sweet notes
Candles0.2-0.5%Up to 1%Heat-stable gourmand character

Classic Accords

+ Vanilla + Coumarin = Gourmand Base + Rose + Violet = Powdery Floral + Tonka + Amber = Sweet Oriental

Tip: Stabilize in ethanol before adding to oil bases to prevent crystallization in cold formulas.

Alternatives & Comparisons

1
Heliotropin CAS 120-57-0

The natural benchmark for powdery almond notes, but more expensive and prone to discoloration in formulations.

2
Anisaldehyde CAS 123-11-5

Offers similar sweet characteristics but with stronger floral-hawthorn aspects and less powderiness.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

No IFRA restrictions under Amendment 51. Usage compliant up to 100% in all categories.

RIFM Assessment

RIFM evaluation concluded safe use at current industry levels with no sensitization concerns.

Sustainability

As a purely synthetic material, o-Methoxybenzaldehyde avoids agricultural supply chain issues. Production typically uses petrochemical feedstocks, though some manufacturers are exploring bio-based routes from lignin derivatives. The compound’s stability reduces formulation waste compared to more labile natural alternatives.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH. ISBN 978-3-527-30364-6

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

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