2,6-Nonadienal diethyl acetal (CAS 67674-36-6) — Green Top Note Fragrance Ingredient

Green · Sweet

2,6-Nonadienal diethyl acetal

CAS 67674-36-6

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

What Is 2,6-Nonadienal diethyl acetal?

2,6-Nonadienal diethyl acetal is a synthetic fragrance ingredient used to impart fresh, green, cucumber-like notes in perfumes and scented products. It’s commonly found in fine fragrances, body care products, and air fresheners. This ingredient matters because it provides a crisp, watery freshness that mimics natural cucumber and melon aromas, enhancing modern aquatic and green fragrance compositions.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated products
Use in moderation due to potency
CAS
67674-36-6
Formula
Mixture
MW
Variable
Odor Family
Green · Sweet
Layer 1 · Enthusiast

What Does 2,6-Nonadienal diethyl acetal Smell Like?

2,6-Nonadienal diethyl acetal bursts with an intense, watery-green freshness reminiscent of freshly cut cucumbers and honeydew melon rind. The top note is sharply vegetal with a dewy, almost metallic edge that evolves into a softer, rounded heart of green tea leaves and young bamboo shoots. Dry-down reveals a whisper of clean linen and aquatic nuances, leaving a transparent trail that’s refreshing without being overpowering.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau de Campagne(Sisley, 1974)

Used to amplify the tomato leaf accord, creating a hyper-realistic garden effect that’s both earthy and refreshing.

Provides the wet, dewy melon facet that mimics the freshness after tropical rainfall.

Layer 2

2D Molecular Structure

(2E,6Z)-1,1-diethoxynona-2,6-diene

SMILES: CCOC(OCC)\C=C\CC\C=C/CC

Chemistry, Properties & Perfumer Guide

The Chemistry

2,6-Nonadienal diethyl acetal belongs to the acetal class of fragrance compounds, formed by the reaction of 2,6-nonadienal with ethanol. This protection of the aldehyde group enhances stability while maintaining the characteristic green odor. The molecule features a nine-carbon chain with two double bonds (2,6 positions) that are crucial for its fresh green character. Industrial synthesis typically involves acetalization of trans-2,cis-6-nonadienal under acidic conditions.

Physical & Chemical Properties

Boiling PointNot publicly available
DensityNot publicly available

Perfumer Guide

Note Position
Top
Volatility
Medium (1-2 hours)
Blending
Good with citrus and green notes
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Provides fresh top notes
Functional Fragrances0.01-0.1%Up to 0.3%For soap and detergent applications

Classic Accords

Tip: Use sparingly in citrus colognes to add a dewy, rain-kissed dimension.

Alternatives & Comparisons

1
Melonal CAS 106-72-9

When a sweeter, more candied melon effect is desired without the cucumber freshness.

2
Verdox CAS 88-41-5

For a more woody-green character with better stability in alkaline formulations.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. No specific usage limits established.

RIFM Assessment

RIFM has evaluated related nonadienal compounds but no specific assessment found for this acetal derivative.

Sustainability

As a synthetic material, 2,6-Nonadienal diethyl acetal doesn’t rely on agricultural production. However, its synthesis requires petrochemical feedstocks. The acetal group improves stability, potentially reducing waste from degradation compared to the parent aldehyde. Future green chemistry approaches may optimize the synthesis route.

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References

  1. Bauer, K. 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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Physicochemical Properties

DTXSID: DTXSID0047034

Physical Properties

Molecular Weight 212.333 g/mol🔬 EPA CompTox
Density 0.868 g/cm^3📊 OPERA
Boiling Point 263.637 °C📊 OPERA
Melting Point -48.282 °C📊 OPERA
Flash Point 87.714 °C📊 OPERA
Refractive Index 1.453 Dimensionless📊 OPERA
Molar Volume 243.454 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.201 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.201 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.201 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.56 Log10 unitless📊 OPERA
Water Solubility 0.001 mol/L📊 OPERA
Henry's Law Constant 0.001 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.042 mmHg📊 OPERA
Viscosity 1.985 cP📊 OPERA
Surface Tension 26.339 dyn/cm📊 OPERA
Thermal Conductivity 137.764 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 18.46 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 9 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 65.841 cm^3/mol📊 OPERA
Polarizability 26.101 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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