Nona-2-trans-6-cis-dienal (CAS 557-48-2) — Green Top to middle Note Fragrance Ingredient

Green · Floral

Nona-2-trans-6-cis-dienal

CAS 557-48-2

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

What Is Nona-2-trans-6-cis-dienal?

Nona-2-trans-6-cis-dienal is a synthetic fragrance ingredient used to add fresh, green, and slightly metallic nuances to perfumes. It’s found in high-end fragrances seeking a crisp, modern edge. This aldehyde contributes to contemporary scent profiles by providing a diffusive, airy quality that enhances citrus and floral compositions without overwhelming them.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated concentrations
Potential skin sensitizer at high levels
CAS
557-48-2
Formula
Mixture
MW
Variable
Odor Family
Green · Floral
Layer 1 · Enthusiast

What Does Nona-2-trans-6-cis-dienal Smell Like?

Nona-2-trans-6-cis-dienal opens with a sharp, green burst reminiscent of crushed cucumber peel and freshly cut grass, with a metallic edge like rain on hot pavement. As it evolves, it reveals a cleaner, more aquatic character – imagine dew-covered spiderwebs at dawn. The dry-down is remarkably transparent, leaving just a whisper of waxy aldehydic texture similar to the scent left on fingers after handling green bell peppers.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau de Cartier(Cartier, 2001)

Used here to amplify the razor-sharp freshness of the citrus top notes, creating a ‘diamond dust’ effect that makes the entire composition sparkle with modern clarity.

Layer 2

2D Molecular Structure

trans,cis-2,6-Nonadienal

SMILES: CC\C=C/CC\C=C\C=O

Chemistry, Properties & Perfumer Guide

The Chemistry

Nona-2-trans-6-cis-dienal is an unsaturated aldehyde with conjugated double bonds. This configuration makes it particularly reactive and light-sensitive. Industrially produced through controlled oxidation of corresponding alcohols or careful aldehyde synthesis, its stereochemistry (trans at position 2, cis at 6) is crucial for odor characteristics. The molecule’s planar structure allows efficient interaction with olfactory receptors.

Physical & Chemical Properties

Molecular Weight140.22 g/mol
Boiling Point~200 °C (estimated)

Perfumer Guide

Note Position
Top to middle
Volatility
Moderate (2-4 hours)
Blending
Good with citrus, challenging with spices
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Provides lift in fresh compositions
Functional Fragrance0.01-0.1%Up to 0.3%Used sparingly in cleaners for green notes

Classic Accords

Tip: Stabilize with antioxidants to prevent premature oxidation and discoloration.

Alternatives & Comparisons

1
2,6-Nonadienal CAS 557-48-2

The all-trans isomer offers similar green character but with more cucumber-like intensity and less metallic sharpness.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. Listed on IFRA Transparency List.

EU Allergen Declaration

Not listed as EU allergen.

RIFM Assessment

RIFM has completed safety assessment confirming safe use at current industry levels.

Sustainability

As a synthetic material, production requires petrochemical feedstocks but at small scale due to potency. No known ecological accumulation concerns. Future green chemistry routes may utilize bio-based starting materials.

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References

  1. Brenna et al. (2002). Stereochemistry-odor relationships in unsaturated aldehydes. Journal of Agricultural and Food Chemistry. DOI: 10.1021/jf020230w

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

Report a data error

Layer 3 · Practical

  • Odor Profile: cucumber, green, leafy, melon, violet
  • FEMA GRAS: 3377
  • Molecular Weight: 138.21 g/mol
  • LogP (XLogP): 2.20

Physicochemical Properties

DTXSID: DTXSID1047104

Physical Properties

Molecular Weight 138.21 g/mol🔬 EPA CompTox
Density 0.86 g/cm^3🔬 EPA CTX
Boiling Point 202.335 °C📊 OPERA
Melting Point 10.542 °C📊 OPERA
Flash Point 79.072 °C📊 OPERA
Refractive Index 1.457 Dimensionless📊 OPERA
Molar Volume 161.644 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.712 Log10 unitless📊 OPERA
LogD (pH 5.5) 2.712 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.712 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.43 Log10 unitless📊 OPERA
Water Solubility 0.008 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 0.363 mmHg📊 OPERA
Viscosity 0.987 cP📊 OPERA
Surface Tension 28.511 dyn/cm📊 OPERA
Thermal Conductivity 145.15 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 5 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 44.047 cm^3/mol📊 OPERA
Polarizability 17.462 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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