3,7-Dimethyl-2,6-octadien-1-ol (CAS 624-15-7) — Floral Top to middle Note Fragrance Ingredient

Floral · Green

3,7-Dimethyl-2,6-octadien-1-ol

CAS 624-15-7

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

What Is 3,7-Dimethyl-2,6-octadien-1-ol?

3,7-Dimethyl-2,6-octadien-1-ol is a synthetic fragrance molecule that mimics aspects of natural floral scents. You’ll encounter it in perfumes, soaps, and household products where a fresh, floral-green character is desired. This ingredient matters because it provides perfumers with a stable, cost-effective alternative to natural extracts, allowing consistent scent profiles across batches while reducing reliance on botanical sources.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions in current use
Potential mild skin sensitivity at high concentrations
CAS
624-15-7
Formula
Mixture
MW
Variable
Odor Family
Floral · Green
Layer 1 · Enthusiast

What Does 3,7-Dimethyl-2,6-octadien-1-ol Smell Like?

This molecule delivers a crisp, green-floral character reminiscent of lily-of-the-valley with subtle citrus undertones. The initial impression is sharply green, like crushed stems, evolving into a cleaner floral heart with dew-covered petals. As it dries down, it reveals a soft woody-musky base that prevents the floralcy from becoming cloying. The overall effect is fresh and transparent, with excellent diffusion that makes it valuable in modern floral compositions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Diorissimo(Christian Dior, 1956)

Used as a synthetic lily-of-the-valley note to create the fragrance’s signature floralcy without relying on natural extracts, providing stability and consistency.

Pleasures(Estée Lauder, 1995)

Contributes to the fresh green floral accord that defines this modern classic, blending seamlessly with rose and peony notes.

Layer 2

2D Molecular Structure

3,7-Dimethyl-2,6-octadienol

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

Chemistry, Properties & Perfumer Guide

The Chemistry

3,7-Dimethyl-2,6-octadien-1-ol belongs to the terpenoid alcohol class. While it occurs naturally in some plants, commercial production typically involves synthetic routes starting from citral or myrcene. The molecule exists in several stereoisomeric forms, with the trans-isomer being most common in fragrance applications. Industrial synthesis often involves selective hydrogenation of citral derivatives followed by careful purification to achieve the desired olfactory profile.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Floral-green modifier
Functional Products0.1-1%Up to 3%Freshness booster

Classic Accords

Tip: Use with citrus top notes to enhance freshness or with white florals to add green dimensionality.

Alternatives & Comparisons

1
Hydroxycitronellal CAS 107-75-5

Offers similar floralcy but with less green character and more sweetness, useful when a softer floral effect is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No current IFRA restrictions.

RIFM Assessment

Currently under review by RIFM with preliminary data suggesting low risk at typical usage levels.

Sustainability

As a synthetic material, this ingredient reduces pressure on natural resources while offering consistent quality. Production typically uses petroleum-derived precursors, though some manufacturers are exploring bio-based routes using renewable feedstocks. The molecule’s efficiency means relatively small quantities are needed in formulations.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

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

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Ingredient Data Sheet

CAS 624-15-7

Physical Properties

Molecular Weight154.25 g/mol🔬 PubChem
LogP (Octanol-Water)2.9🔬 PubChem
Boiling Point230 °C🔬 EPA CompTox
Vapor Pressure0.03 mmHg @ 25°C📊 OPERA
Flash Point42.2 °C🔬 EPA CompTox
Involatility Index0.0026💻 Calculated
log Kp (skin permeability)-1.582💻 Calculated
SMILESCC(=CCCC(=CCO)C)C🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score2.6 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsgeraniumrose• leffingwell
Functional Groupsalcoholalkene💻 RDKit
“Mild and sweet, floral Rose-type odor. Warm and yet slightly dry undertones, but there are great variations according to the quality and origin of the Geraniol.”📖 Arctander

Flavor Notes (Arctander)

“Its taste is somewhat disappointing, somewhat bitter unless used at very low concentration. Nerol is generally preferred for better sweetness. However, Geraniol finds its way into multitude of flavor types, such as Apple, Apricot, Strawberry, Raspberry, Plum, Peach, Honey, Cherry, Lemon, Cassia, Cin”📖 Arctander

Regulatory Status

FEMA NumberFEMA 2507⚖️ FEMA GRAS
GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID7041380

Physical Properties

Molecular Weight 154.253 g/mol🔬 EPA CompTox
Density 0.874 g/cm^3📊 OPERA
Boiling Point 228.59 °C📊 OPERA
Melting Point 8.903 °C📊 OPERA
Flash Point 86.275 °C📊 OPERA
Refractive Index 1.471 Dimensionless📊 OPERA
Molar Volume 177.941 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.47 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 3.491 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.491 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 7.65 Log10 unitless📊 OPERA
Water Solubility 0.003 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.024 mmHg📊 OPERA
Viscosity 3.178 cP📊 OPERA
Surface Tension 27.866 dyn/cm📊 OPERA
Thermal Conductivity 141.229 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 4 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 49.714 cm^3/mol📊 OPERA
Polarizability 19.708 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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