6-Nonenal, (6E)- (CAS 2277-20-5) — Green Top Note Fragrance Ingredient

Green · Citrus

6-_Nonenal, (6E)_-

CAS 2277-20-5

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

What Is 6-_Nonenal, (6E)_-?

6-Nonenal is a synthetic compound used in perfumery to create green, cucumber-like, and fatty notes. It’s often found in fragrances aiming for aquatic or fresh vegetable effects. This aldehyde is powerful at low concentrations, contributing to modern, ozonic scent profiles. Its unique aroma makes it valuable for creating cutting-edge perfumes that break from traditional floral or woody themes.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Safe in regulated concentrations
Can cause skin irritation at high levels
CAS
2277-20-5
Formula
Mixture
MW
Variable
Odor Family
Green · Citrus
Layer 1 · Enthusiast

What Does 6-_Nonenal, (6E)_- Smell Like?

6-Nonenal delivers a sharp, green burst reminiscent of freshly cut cucumbers and watermelon rind, with an underlying fatty, slightly metallic edge. As it evolves, the fatty character becomes more pronounced, akin to the oiliness of crushed leaves, while retaining a watery freshness. The dry-down reveals a subtle, lingering greenness that blends seamlessly with woody and musky bases.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

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

Used to enhance the aquatic, fresh cucumber facet that defines this iconic fragrance, contributing to its modern, watery transparency.

Un Jardin sur le Nil(Hermès, 2005)

Adds a crisp, green vegetal note that complements the mango and grapefruit, creating a vivid garden effect.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

6-Nonenal is an unsaturated aldehyde with the formula C9H16O. It belongs to the class of nonenals, which are known for their potent green and fatty odors. The compound is typically synthesized through the oxidation of corresponding alcohols or via hydroformylation of unsaturated hydrocarbons. Its (E)-isomer is particularly significant in perfumery due to its intense aroma.

Physical & Chemical Properties

Boiling Point198 °C
Density0.865 g/cm³

Perfumer Guide

Note Position
Top
Volatility
Medium (1-2 hours)
Blending
Good with citrus and woody notes
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Used for fresh, green top notes
Functional Fragrances0.05-0.2%Up to 0.5%Adds freshness to detergents and cleaners

Classic Accords

Tip: Use sparingly to avoid overpowering other notes; blends well with citrus and ozonic molecules.

Alternatives & Comparisons

1
Nonanal CAS 124-19-6

Less green and more fatty, suitable for softer, less vegetal effects.

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

More intense cucumber note, used when a stronger green character is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions currently apply to 6-Nonenal.

EU Allergen Declaration

Not listed as an EU allergen.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

RIFM has assessed 6-Nonenal as safe for use in current fragrance applications at typical levels.

Sustainability

6-Nonenal is synthesized from petrochemical sources, with no known natural occurrence. Its production is energy-intensive but requires minimal quantities due to its potency. Future green chemistry approaches may offer more sustainable synthesis routes.

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References

  1. PubChem Compound Summary for 6-Nonenal PubChem
  2. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press.

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

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