2-Phenylpropionaldehyde (CAS 93-53-8) — Floral Middle Note Fragrance Ingredient

Floral · Sweet

2-Phenylpropionaldehyde

CAS 93-53-8

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

What Is 2-Phenylpropionaldehyde?

2-Phenylpropionaldehyde is a synthetic fragrance ingredient used in perfumes and flavored products. It adds a sweet, floral-hyacinth character with honey-like undertones. You’ll encounter it in floral perfumes, soaps, and some food flavorings. This aldehyde is valued for its ability to create rich, complex floral effects at low concentrations. It helps perfumers mimic natural flower scents while providing better stability than some botanical extracts.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
IFRA-approved within limits
Potential sensitizer at high concentrations
CAS
93-53-8
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does 2-Phenylpropionaldehyde Smell Like?

2-Phenylpropionaldehyde opens with a burst of intense floralcy reminiscent of hyacinth and lilac, layered over a surprising honeyed sweetness. As it evolves, the scent reveals a subtle green stem-like quality that prevents it from becoming cloying. The dry-down carries a faint almond-like nuance that adds sophistication. This molecule behaves like a chameleon – in small doses it enhances floral bouquets, while higher concentrations showcase its distinctive honey-floral character with an almost waxy texture.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chanel No. 5(Chanel, 1921)

Used sparingly to enhance the aldehydic floralcy, contributing to the perfume’s legendary complexity without overpowering the delicate balance.

L'Air du Temps(Nina Ricci, 1948)

Helps create the perfume’s signature carnation-hyacinth accord, adding a sweet floral depth to the spicy carnation notes.

Layer 2

2D Molecular Structure

Hydratropaldehyde

SMILES: CC(C=O)C1=CC=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Phenylpropionaldehyde is an aromatic aldehyde with the phenyl group attached to an aliphatic aldehyde chain. It’s synthesized through the hydroformylation of styrene or oxidation of 2-phenylpropanol. The molecule lacks chirality but exhibits interesting conformational flexibility that influences its odor profile. Its chemical stability makes it valuable in formulations requiring long shelf life.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Floral modifier
Soap0.1-0.5%Up to 1%Provides floral depth

Classic Accords

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

Alternatives & Comparisons

1
Lilial CAS 80-54-6

When a cleaner, more diffusive floralcy is needed without the honeyed aspects of phenylpropionaldehyde.

2
Phenylacetaldehyde CAS 122-78-1

For a greener, more hyacinth-like floral character without the sweetness.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA standards.

RIFM Assessment

RIFM has evaluated this material and found it safe for use at current levels.

Sustainability

As a synthetic material, 2-phenylpropionaldehyde production avoids agricultural impacts but requires petrochemical feedstocks. Modern production methods aim to minimize waste and energy use.

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References

  1. Bickers et al. (2003). Safety assessment of aryl alkyl aldehydes. Food and Chemical Toxicology. PubChem

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

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Ingredient Data Sheet

CAS 93-53-8

Physical Properties

Molecular Weight134.17 g/mol🔬 PubChem
LogP (Octanol-Water)1.9🔬 PubChem
Boiling Point92 °C🔬 EPA CompTox
Vapor Pressure0.1575 mmHg @ 25°C📊 OPERA
Flash Point79 °C🔬 EPA CompTox
Involatility Index0.0147💻 Calculated
log Kp (skin permeability)-2.169💻 Calculated
SMILESCC(C=O)C1=CC=CC=C1🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated
Volatility ClassSlow💻 Calculated
Persistence Score1.1 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsfloralgreenhoney• leffingwell
Functional Groupsaldehydearomatic💻 RDKit
2-Phenylpropionaldehyde has an intense, green, floral odor reminiscent of hyacinth.📖 Fenaroli

Regulatory Status

IFRA ListedYes — see IFRA Standards for category limits⚖️ IFRA 51
EU Annex IIIListed (restricted)⚖️ IFRA 51
IOFI ClassificationArtificial📖 Fenaroli
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID0052629

Physical Properties

Molecular Weight 134.178 g/mol🔬 EPA CompTox
Density 1.005 g/cm^3🔬 EPA CTX
Boiling Point 207.071 °C🔬 EPA CTX
Melting Point 9.837 °C📊 OPERA
Flash Point 75.75 °C🔬 EPA CTX
Refractive Index 1.506 Dimensionless📊 OPERA
Molar Volume 136.824 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.96 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 1.993 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.993 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.45 Log10 unitless📊 OPERA
Water Solubility 0.02 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.243 mmHg🔬 EPA CTX
Viscosity 2.283 cP📊 OPERA
Surface Tension 33.738 dyn/cm📊 OPERA
Thermal Conductivity 138.734 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 17.07 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 2 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 40.625 cm^3/mol📊 OPERA
Polarizability 16.105 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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