2,4,6-Trimethylcyclohex-3-enecarbaldehyde (CAS 1423-46-7) — Green Top to middle Note Fragrance Ingredient

Green · Woody

2,4,6-Trimethylcyclohex-3-enecarbaldehyde

CAS 1423-46-7

Origin
synthetic
Note
Top to middle
IFRA
Use with awareness
Data as of: Apr 2026

What Is 2,4,6-Trimethylcyclohex-3-enecarbaldehyde?

2,4,6-Trimethylcyclohex-3-enecarbaldehyde is a synthetic fragrance ingredient used in modern perfumery to create fresh, green, and slightly woody aromas. It’s often found in fine fragrances, body care products, and household cleaners. This aldehyde is valued for its ability to add a crisp, natural character to floral and citrus compositions, enhancing their vibrancy and longevity.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Safe in regulated products
May cause skin irritation in high concentrations
CAS
1423-46-7
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does 2,4,6-Trimethylcyclohex-3-enecarbaldehyde Smell Like?

2,4,6-Trimethylcyclohex-3-enecarbaldehyde opens with a sharp, green freshness reminiscent of crushed leaves and freshly cut grass. As it evolves, it reveals a slightly woody undertone with a hint of citrusy brightness, like a sunlit forest after rain. The dry-down is clean and slightly herbaceous, leaving a subtle, natural impression that blends well with floral and woody notes.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Green Tea(Elizabeth Arden, 1999)

Used to enhance the fresh, green tea character, adding a crisp, natural edge to the citrus and floral notes.

Un Jardin Sur Le Nil(Hermès, 2005)

Contributes to the vibrant, green accord that mimics the lush vegetation along the Nile.

Eau de Cartier(Cartier, 2001)

Adds a fresh, green facet to the citrus top notes, enhancing the overall brightness.

L'Eau d'Issey(Issey Miyake, 1992)

Used to amplify the aquatic freshness, providing a green, natural undertone.

Chanel No. 19(Chanel, 1971)

Enhances the green, galbanum note, adding depth and complexity to the floral heart.

Layer 2

2D Molecular Structure

2,4,6-Trimethylcyclohex-3-enecarbaldehyde

SMILES: CC1CC(C)=CC(C)C1C=O

Chemistry, Properties & Perfumer Guide

The Chemistry

2,4,6-Trimethylcyclohex-3-enecarbaldehyde is a synthetic aldehyde with a cyclohexene ring structure. It is typically synthesized through the Diels-Alder reaction or by oxidation of corresponding alcohols. Its molecular structure features a conjugated system that contributes to its green, fresh odor profile. The compound is chiral, and its enantiomers may exhibit slightly different olfactory characteristics.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available
Vapor PressureNot available
SolubilityNot available

Perfumer Guide

Note Position
Top to middle
Volatility
Moderate (1-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Adds freshness and green character
Body Care0.5-2%Up to 5%Enhances clean, natural scents
Household Cleaners0.1-1%Up to 3%Provides a fresh, green note

Classic Accords

Tip: Use in small amounts to avoid overpowering other notes; works well with citrus and floral ingredients.

Alternatives & Comparisons

1
Hexyl Cinnamal CAS 101-86-0

Offers a similar green character but with a sweeter, floral undertone.

2
Cyclamen Aldehyde CAS 103-95-7

Provides a fresh, floral-green note with better stability in formulations.

3
Triplal CAS 68039-49-6

A stronger green note with a more pronounced leafy character.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific restrictions under IFRA standards.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

RIFM has assessed this ingredient as safe for use in current practices.

Sustainability

As a synthetic ingredient, 2,4,6-Trimethylcyclohex-3-enecarbaldehyde is produced in controlled laboratory settings, reducing the environmental impact associated with natural extraction. Its synthesis can be optimized for minimal waste and energy use, making it a sustainable choice for modern perfumery.

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References

  1. PubChem. 2,4,6-Trimethylcyclohex-3-enecarbaldehyde. PubChem
  2. IFRA Standards Library. IFRA
  3. RIFM Safety Assessment. RIFM

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

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Ingredient Data Sheet

CAS 1423-46-7

Physical Properties

Molecular Weight152.23 g/mol🔬 PubChem
LogP (Octanol-Water)1.9🔬 PubChem
Boiling Point214 °C🔬 EPA CompTox
Vapor Pressure0.39 mmHg @ 25°C📊 OPERA
Flash Point66 °C🔬 EPA CompTox
Involatility Index0.0341💻 Calculated
log Kp (skin permeability)-2.28💻 Calculated
SMILESCC1CC(=CC(C1C=O)C)C🔬 PubChem

Volatility & Performance

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

Odor & Flavor

Primary Descriptorsgreenwoody• leffingwell
Functional Groupsaldehydealkene💻 RDKit

Regulatory Status

IFRA ListedYes — see IFRA Standards for category limits⚖️ IFRA 51
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: DTXSID5052678

Physical Properties

Molecular Weight 152.237 g/mol🔬 EPA CompTox
Density 0.92 g/cm^3🔬 EPA CTX
Boiling Point 203 °C🔬 EPA CTX
Melting Point -0.36 °C📊 OPERA
Flash Point 66 °C🔬 EPA CTX
Refractive Index 1.496 Dimensionless📊 OPERA
Molar Volume 164.291 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.964 Log10 unitless📊 OPERA
LogD (pH 5.5) 2.964 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.964 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.83 Log10 unitless📊 OPERA
Water Solubility 0.014 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.506 mmHg🔬 EPA CTX
Viscosity 2.758 cP📊 OPERA
Surface Tension 30.985 dyn/cm📊 OPERA
Thermal Conductivity 122.261 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 1 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 48.003 cm^3/mol📊 OPERA
Polarizability 19.03 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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