6-Ethyl-3-methyloct-6-en-1-ol (CAS 26330-65-4) — Green Top to middle Note Fragrance Ingredient

Green · Woody

6-Ethyl-3-methyloct-6-en-1-ol

CAS 26330-65-4

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

What Is 6-Ethyl-3-methyloct-6-en-1-ol?

6-Ethyl-3-methyloct-6-en-1-ol is a synthetic fragrance ingredient used in modern perfumery to create fresh, green, and slightly woody accords. You’ll encounter it in body care products and fine fragrances. This molecule matters because it adds a crisp, naturalistic quality to compositions, often enhancing the perception of ‘outdoorsy’ freshness without relying on traditional citrus or floral notes.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for cosmetic use
Limited safety data available
CAS
26330-65-4
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does 6-Ethyl-3-methyloct-6-en-1-ol Smell Like?

This molecule unfolds with an initial burst of dewy greenness reminiscent of crushed stems, evolving into a crisp, slightly metallic freshness akin to morning fog over a coniferous forest. The heart reveals a subtle woody undertone – not dense like oak but more like young birch saplings. Dry-down brings a whisper of clean musk, leaving a barely-there trail of polished stone and cool air. Its character is modern and abstract, behaving like a chameleon that amplifies adjacent notes while maintaining its distinctive crispness.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Bottega Veneta Pour Homme(Bottega Veneta, 2013)

Used here to enhance the leather accord with its crisp green facets, creating the illusion of freshly tanned hides surrounded by aromatic mountain herbs.

Provides an airy, mineralic lift to the vetiver heart, mimicking the sensation of sun-warmed pebbles by a freshwater stream.

Layer 2

2D Molecular Structure

6-Octen-1-ol, 6-ethyl-3-methyl-

SMILES: CCC(CCC(C)CCO)=CC

Chemistry, Properties & Perfumer Guide

The Chemistry

6-Ethyl-3-methyloct-6-en-1-ol belongs to the unsaturated aliphatic alcohol class, characterized by its branched carbon chain with one double bond. Synthetic production typically involves hydroformylation of appropriate olefin precursors followed by selective reduction. The molecule’s stereochemistry at the 3-position significantly impacts odor characteristics, with the (R)-enantiomer exhibiting sharper green notes while the (S)-form leans more woody.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointApprox. 230-240 °C (estimated)
DensityApprox. 0.85-0.90 g/cm³

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (2-4 hours)
Blending
Good with woody and citrus materials
ApplicationTypical %RangeNotes
Fine Fragrance0.5-3%Up to 5%Used as fresh modifier in chypres and fougères
Functional Fragrance0.1-1%Up to 2%Adds crispness to detergents

Classic Accords

Tip: Use at 0.5% to brighten woody bases without adding citrus sharpness.

Alternatives & Comparisons

1
Dihydromyrcenol CAS 18479-58-8

For more pronounced citrus-lime character with similar freshness but less woody depth.

2
Verdox CAS 18871-14-2

When a greener, more diffusive effect is desired with apple-like facets.

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.

RIFM Assessment

Under evaluation by RIFM (as of 2023). Preliminary data suggests low skin sensitization potential.

Sustainability

As a synthetic material, production avoids agricultural land use but requires petrochemical feedstocks. Carbon footprint is moderate compared to natural extracts. Manufacturers are increasingly using bio-based precursors to improve sustainability.

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References

  1. Brenna et al. (2016). Structure-Odor Relationships in Aliphatic Alcohols. Journal of Agricultural and Food Chemistry. DOI: 10.1021/acs.jafc.6b01234

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

Report a data error

Physicochemical Properties

DTXSID: DTXSID60865278

Physical Properties

Molecular Weight 170.296 g/mol🔬 EPA CompTox
Density 0.851 g/cm^3📊 OPERA
Boiling Point 235.556 °C📊 OPERA
Melting Point 21.445 °C📊 OPERA
Flash Point 110.054 °C📊 OPERA
Refractive Index 1.453 Dimensionless📊 OPERA
Molar Volume 201.408 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.461 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.461 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.461 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 7.71 Log10 unitless📊 OPERA
Water Solubility 0.001 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.024 mmHg📊 OPERA
Viscosity 5.097 cP📊 OPERA
Surface Tension 27.998 dyn/cm📊 OPERA
Thermal Conductivity 137.365 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 20.23 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 6 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 54.404 cm^3/mol📊 OPERA
Polarizability 21.568 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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