2-Methyl-2-hepten-6-ol (CAS 1569-60-4) — Green Top to middle Note Fragrance Ingredient

Green · Floral

2-Methyl-2-hepten-6-ol

CAS 1569-60-4

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

What Is 2-Methyl-2-hepten-6-ol?

2-Methyl-2-hepten-6-ol is a synthetic fragrance ingredient used to add fresh, green nuances to perfumes and scented products. You’ll encounter it in modern floral and citrus compositions. This molecule matters because it provides a crisp, natural-smelling green character that helps bridge top notes to heart notes in fragrances, creating a sense of movement and evolution in the scent.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Limited safety data available
CAS
1569-60-4
Formula
Mixture
MW
Variable
Odor Family
Green · Floral
Layer 1 · Enthusiast

What Does 2-Methyl-2-hepten-6-ol Smell Like?

2-Methyl-2-hepten-6-ol delivers a vibrant green freshness reminiscent of crushed leaves and unripe fruits. The opening is sharp and slightly metallic, like freshly cut stems, evolving into a cleaner, more floral-green character. In drydown, it retains a subtle vegetal quality that blends well with citrus and floral materials. The overall effect is like walking through a dew-covered garden at dawn – moist, alive, and slightly pungent.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Vent Vert(Balmain, 1947)

Used to enhance the radical green freshness that made this fragrance revolutionary. Provides the ‘snapped stem’ effect that defines the composition.

Eau Dynamisante(Clarins, 1987)

Contributes to the invigorating green-herbal character that defines this energizing fragrance, pairing with citrus and woody notes.

Layer 2

2D Molecular Structure

6-Methylhept-5-en-2-ol

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

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Methyl-2-hepten-6-ol is an unsaturated aliphatic alcohol with molecular formula C8H16O. As a synthetic material, it’s typically produced through aldol condensation reactions followed by selective hydrogenation. The molecule features both a double bond and hydroxyl group, making it moderately reactive. The specific stereochemistry influences its odor profile, with different isomers exhibiting varying intensity and character.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor ThresholdLow ppm range

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Green modifier
Functional Fragrance0.1-0.5%Up to 1%Freshness booster

Classic Accords

+ Galbanum + Violet Leaf = Ultra-green + Citronellol + PEA = Green floral

Tip: Use to add naturalistic green effects without excessive harshness.

Alternatives & Comparisons

1
Leaf Alcohol CAS 928-96-1

For a more intense green character with grassy aspects.

2
Styrallyl Acetate CAS 151-05-3

When a fruitier green note 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.

RIFM Assessment

Not currently evaluated by RIFM.

Sustainability

As a synthetic material, 2-Methyl-2-hepten-6-ol has minimal environmental impact in production. Being petroleum-derived, its sustainability depends on the manufacturer’s energy sources and waste management practices. It offers an alternative to natural green materials that may have agricultural impacts.

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References

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

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    Physicochemical Properties

    DTXSID: DTXSID8051754

    Physical Properties

    Molecular Weight 128.215 g/mol🔬 EPA CompTox
    Density 0.849 g/cm^3📊 OPERA
    Boiling Point 175 °C🔬 EPA CTX
    Melting Point -41.494 °C📊 OPERA
    Flash Point 67.875 °C🔬 EPA CTX
    Refractive Index 1.446 Dimensionless📊 OPERA
    Molar Volume 151.888 cm^3/mol📊 OPERA

    Partition & Solubility

    LogP (Octanol-Water) 2.569 Log10 unitless📊 OPERA
    LogD (pH 5.5) 2.569 Log10 unitless📊 OPERA
    LogD (pH 7.4) 2.569 Log10 unitless📊 OPERA
    LogKoa (Octanol-Air) 5.68 Log10 unitless📊 OPERA
    Water Solubility 0.023 mol/L📊 OPERA
    Henry's Law Constant 0 atm-m3/mole📊 OPERA

    Transport Properties

    Vapor Pressure 0.36 mmHg📊 OPERA
    Viscosity 3.044 cP📊 OPERA
    Surface Tension 26.527 dyn/cm📊 OPERA
    Thermal Conductivity 142.121 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 3 count💻 Computed
    Aromatic Rings 0 count💻 Computed
    Molar Refractivity 40.506 cm^3/mol📊 OPERA
    Polarizability 16.058 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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