Cinnamic aldehyde dimethyl acetal (CAS 4364-06-01) — Spicy Heart Note Fragrance Ingredient

Spicy · Sweet

Cinnamic aldehyde dimethyl acetal

CAS 4364-06-01

Origin
synthetic
Note
Heart
IFRA
Use with awareness
Data as of: Apr 2026

What Is Cinnamic aldehyde dimethyl acetal?

Cinnamic aldehyde dimethyl acetal is a synthetic fragrance ingredient that adds warm, spicy-cinnamon notes to perfumes and scented products. You’ll find it in holiday candles, potpourri, and festive fragrances. This molecule matters because it provides a longer-lasting cinnamon aroma than natural cinnamon oil, without the skin sensitivity risks of raw cinnamaldehyde.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Stabilized form reduces skin reactivity
Derived from known allergen precursors
CAS
4364-06-01
Formula
Mixture
MW
Variable
Odor Family
Spicy · Sweet
Layer 1 · Enthusiast

What Does Cinnamic aldehyde dimethyl acetal Smell Like?

A warm embrace of baked goods and mulled wine, with the powdered sugar sweetness of cinnamon toast. Opens with a crisp, almost metallic top note that quickly melts into honeyed cinnamon hearts. The dry-down reveals woody vanillic undertones, like the lingering scent on wool sweaters after a Christmas market visit. Unlike raw cinnamon, this acetal lacks harsh edges, presenting as rounded and gourmand.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Spicebomb(Viktor&Rolf, 2012)

Provides the smooth cinnamon backbone without overwhelming spice, complementing the leather and tobacco accords.

Angel(Mugler, 1992)

Used sparingly to soften the patchouli-chocolate accord with a powdered cinnamon effect.

Cinnabar(Estée Lauder, 1978)

Creates the illusion of aged spice cabinets through its mellowed cinnamon character.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Cinnamic aldehyde dimethyl acetal is an acetal derivative of cinnamaldehyde, where the aldehyde group has been protected with methanol. This modification increases stability against oxidation while reducing skin sensitization potential. Industrially produced via acid-catalyzed acetalization of cinnamaldehyde with methanol, the reaction typically uses p-toluenesulfonic acid as catalyst. The acetal functional group makes the molecule more resistant to nucleophilic attack compared to its parent aldehyde.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointEstimated 250-260 °C
Density~1.05 g/cm³ (estimated)

Perfumer Guide

Note Position
Heart
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Spice modifier in oriental bases
Home Fragrance1-3%Up to 8%Holiday candle formulations

Classic Accords

Tip: Use with citrus top notes to prevent the fragrance from becoming too heavy.

Alternatives & Comparisons

1
Cinnamyl acetate CAS 103-54-8

When a fruitier, less spicy cinnamon effect is desired.

2
Methyl dihydrojasmonate CAS 24851-98-7

For similar warmth without the gourmand associations.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. Considered less sensitizing than cinnamaldehyde.

EU Allergen Declaration

Not listed as EU allergen when pure, but may contain traces of cinnamaldehyde.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

RIFM evaluation pending as of 2023; considered lower risk than parent aldehyde.

Sustainability

Synthetic production avoids cinnamon bark harvesting pressures. The acetalization process reduces waste compared to traditional isolation methods. Energy-intensive methanol use presents opportunities for green chemistry improvements.

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References

  1. Bickers et al. (2005). Cinnamaldehyde review. Contact Dermatitis. PMID 16128757

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

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