2-Cyclohexylpropanal (CAS 2109-22-0) — Green Top to Mid Note Fragrance Ingredient

Green · Floral

2-Cyclohexylpropanal

CAS 2109-22-0

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

What Is 2-Cyclohexylpropanal?

2-Cyclohexylpropanal is a synthetic fragrance ingredient used to add fresh, green, and slightly floral nuances to perfumes. You’ll encounter it in modern floral and citrus fragrances, often lending a crisp, clean character. This aldehyde is prized for its ability to bridge top and heart notes, providing longevity while maintaining brightness. Its subtle complexity makes it valuable for creating sophisticated scent profiles that evolve beautifully on skin.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions under IFRA
Low skin sensitization potential
CAS
2109-22-0
Formula
Mixture
MW
Variable
Odor Family
Green · Floral
Layer 1 · Enthusiast

What Does 2-Cyclohexylpropanal Smell Like?

2-Cyclohexylpropanal opens with a burst of crisp green freshness, like crushed stems after rain, quickly revealing a delicate floralcy reminiscent of lily petals floating in a citrus-infused spring stream. The heart develops a subtle waxy character akin to freshly peeled cucumber skin, while the dry-down leaves a whisper of clean muskiness—like sun-warmed linen drying in an alpine meadow. Its moderate persistence allows it to serve as both a top note enhancer and heart note anchor, bridging citrus and floral elements with remarkable versatility.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau de Cartier(Cartier, 2001)

Used here to amplify the violet leaf accord, adding a dewy green freshness that contrasts beautifully with the woody base. Its aliphatic character helps unify citrus and floral elements.

Pleasures(Estée Lauder, 1995)

Provides a crisp green counterpoint to the white flowers, creating the illusion of stems freshly cut from the bouquet. Its subtle floralcy enhances the naturalistic effect.

Layer 2

2D Molecular Structure

Cyclohexaneacetaldehyde, .alpha.-methyl-

SMILES: CC(C=O)C1CCCCC1

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Cyclohexylpropanal belongs to the aliphatic aldehydes class, characterized by its cyclohexyl group attached to a propanal chain. Synthesized through hydroformylation of cyclohexylpropene or oxidation of the corresponding alcohol, this molecule lacks chirality but displays conformational flexibility that contributes to its odor profile. The aldehyde functional group makes it reactive in perfumery applications, often forming Schiff bases with amines to create novel odorants. Its moderate chain length gives it balanced volatility between traditional C8-C12 aldehydes.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointEstimated 210-220°C
DensityApprox. 0.89 g/cm³

Perfumer Guide

Note Position
Top to Mid
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Adds green-floral freshness
Functional Products0.1-0.5%Up to 1%For clean, fresh effects

Classic Accords

+ Violet Leaf + Bergamot = Modern Green + Lilial + Hedione = Floral Freshness

Tip: Stabilize in ethanol before adding to water-based formulations to prevent aldehyde degradation.

Alternatives & Comparisons

1
Adoxal CAS 141-13-9

For stronger green marine effects with similar floralcy but greater diffusion.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted under IFRA standards. Listed on IFRA Transparency List Amendment 49.

RIFM Assessment

RIFM evaluation ongoing; preliminary data suggests low sensitization potential at typical use levels.

Sustainability

As a synthetic material, 2-Cyclohexylpropanal avoids agricultural resource use. Modern production methods employ green chemistry principles with high atom economy. Being petroleum-derived, its carbon footprint depends on production facility energy sources, but typical synthesis routes have lower environmental impact than many natural ingredient extractions.

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References

  1. IFRA Transparency List Amendment 49 IFRA Official

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

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Ingredient Data Sheet

CAS 2109-22-0

Physical Properties

Molecular Weight140.22 g/mol🔬 PubChem
LogP (Octanol-Water)3🔬 PubChem
Boiling Point191 °C🔬 EPA CompTox
Vapor Pressure0.4169 mmHg @ 25°C📊 OPERA
Flash Point71.4 °C🔬 EPA CompTox
Involatility Index0.0379💻 Calculated
log Kp (skin permeability)-1.425💻 Calculated
SMILESCC(C=O)C1CCCCC1🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated
Volatility ClassSlow💻 Calculated
Persistence Score0.6 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsfloralgreen• leffingwell
Functional Groupsaldehyde💻 RDKit
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: DTXSID10862833

Physical Properties

Molecular Weight 140.226 g/mol🔬 EPA CompTox
Density 0.897 g/cm^3📊 OPERA
Boiling Point 193.773 °C📊 OPERA
Melting Point 9.842 °C📊 OPERA
Flash Point 69.25 °C📊 OPERA
Refractive Index 1.448 Dimensionless📊 OPERA
Molar Volume 155.882 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.052 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.052 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.052 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.44 Log10 unitless📊 OPERA
Water Solubility 0.006 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.341 mmHg📊 OPERA
Viscosity 3.021 cP📊 OPERA
Surface Tension 30.299 dyn/cm📊 OPERA
Thermal Conductivity 130.94 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 0 count💻 Computed
Molar Refractivity 41.722 cm^3/mol📊 OPERA
Polarizability 16.54 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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