p-Tolylacetaldehyde (CAS 0104-09-06) — Floral Top to Middle Note Fragrance Ingredient

Floral · Green

p-Tolylacetaldehyde

CAS 0104-09-06

Origin
synthetic
Note
Top to Middle
IFRA
Generally safe
Data as of: Apr 2026

What Is p-Tolylacetaldehyde?

p-Tolylacetaldehyde is a synthetic aromatic compound used in perfumery to add floral and green nuances. It’s found in many modern fragrances, particularly those aiming for a fresh, slightly powdery character. This aldehyde matters because it bridges natural and synthetic accords, offering perfumers a versatile tool for creating complex scent profiles with excellent stability.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated concentrations
Potential mild irritant at high concentrations
CAS
0104-09-06
Formula
Mixture
MW
Variable
Odor Family
Floral · Green
Layer 1 · Enthusiast

What Does p-Tolylacetaldehyde Smell Like?

p-Tolylacetaldehyde opens with a crisp, green freshness reminiscent of crushed stems, evolving into a delicate floralcy akin to hyacinth petals dusted with powdered sugar. As it dries, it reveals a subtle almond-like nuance wrapped in clean muskiness, behaving like a shy dancer who gradually gains confidence on stage. The dry-down leaves a lingering impression of starched linens dried in a spring garden.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chanel No. 19(Chanel, 1971)

Used to amplify the green galbanum note while softening the floral heart with its powdery-aldehyde character.

Vent Vert(Balmain, 1947)

Provides structural support to the hyper-green accord, preventing it from becoming too sharp or linear.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

p-Tolylacetaldehyde belongs to the aromatic aldehyde class, featuring a para-methyl substituted benzene ring. Industrially synthesized via Friedel-Crafts alkylation followed by oxidation, this compound demonstrates typical aldehyde reactivity while offering superior stability compared to aliphatic aldehydes. The electron-donating methyl group influences both its olfactory character and chemical behavior.

Physical & Chemical Properties

Boiling Point220-222 °C
Density1.015 g/cm³

Perfumer Guide

Note Position
Top to Middle
Volatility
Medium (2-4 hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Adds diffusive floral-green facets
Functional Fragrance0.5-1%Up to 2%Provides fresh linen character

Classic Accords

+ Galbanum + Rose = Classic green floral + Ionones + Musks = Powdered violet

Tip: Use with ionones to create sophisticated powder notes without excessive sweetness.

Alternatives & Comparisons

1
Phenylacetaldehyde CAS 122-78-1

More honeyed and intense, useful when a stronger floral impact is desired.

2
Helional CAS 1205-17-0

Offers similar green freshness but with better water solubility for functional applications.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions currently apply to p-Tolylacetaldehyde.

EU Allergen Declaration

Not listed in EU allergen regulations.

RIFM Assessment

RIFM evaluation confirms safe use at current industry concentrations.

Sustainability

As a synthetic material, p-Tolylacetaldehyde production avoids agricultural impacts but requires petrochemical feedstocks. Modern manufacturing processes have significantly reduced energy consumption and waste generation compared to early synthesis methods.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.
  2. Arctander, S. (1969). Perfume and Flavor Chemicals. Allured.

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

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