4-Methyl-3-decen-5-ol (CAS 81782-77-6) — Green Top to Middle Note Fragrance Ingredient

Green · Citrus

4-Methyl-3-decen-5-ol

CAS 81782-77-6

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

What Is 4-Methyl-3-decen-5-ol?

4-Methyl-3-decen-5-ol is a synthetic fragrance ingredient often found in modern perfumes and body care products. It contributes a fresh, slightly metallic green character with aquatic nuances. This molecule matters because it helps create crisp, contemporary scent profiles that mimic natural freshness without relying on traditional citrus or herbal notes.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions in cosmetic use
Not classified as a known allergen
CAS
81782-77-6
Formula
Mixture
MW
Variable
Odor Family
Green · Citrus
Layer 1 · Enthusiast

What Does 4-Methyl-3-decen-5-ol Smell Like?

4-Methyl-3-decen-5-ol opens with a startling freshness – like crushed cucumber skin meeting cold stainless steel. As it develops, the initial sharpness softens into a watery green heart reminiscent of aloe vera gel or young bamboo shoots. The dry-down reveals subtle woody-musky undertones that anchor the freshness, leaving a clean impression comparable to rain-washed leaves. Throughout its evolution, it maintains a futuristic, almost ozonic quality that distinguishes it from traditional green notes.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Cool Water(Davidoff, 1988)

Used to enhance the modern aquatic character, contributing to the fragrance’s signature crispness alongside calone and lavender.

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

Provides subtle green freshness that complements the lotus and melon notes, creating a dewy, contemporary effect.

Layer 2

2D Molecular Structure

4-Methyl-3-decen-5-ol

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

Chemistry, Properties & Perfumer Guide

The Chemistry

4-Methyl-3-decen-5-ol belongs to the family of unsaturated aliphatic alcohols, characterized by its branched decenol structure. The molecule features a double bond at the 3-position and a methyl group at the 4-position, which contribute to its stereochemical complexity. Industrial synthesis typically involves hydroformylation of appropriate alkene precursors followed by reduction. The specific isomerism of this compound significantly impacts its olfactory properties, with different stereoisomers exhibiting varying intensity and character.

Physical & Chemical Properties

Boiling Point~220 °C (estimated)
Density~0.85 g/cm³ (estimated)

Perfumer Guide

Note Position
Top to Middle
Volatility
Medium (1-3 hours)
Blending
Good with modern accords
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%For fresh top notes
Functional Fragrance0.1-0.5%Up to 1%In detergents and soaps

Classic Accords

+ Calone + Melon = Modern Aquatic + Galaxolide + Bergamot = Fresh Laundry + Violet Leaf + Apple = Crisp Green

Tip: Use with citrus or ozonic notes to enhance freshness without traditional lemon/citronella character.

Alternatives & Comparisons

1
Floralozone CAS 67634-15-5

Provides similar modern freshness with more pronounced floral aspects when a softer effect is desired.

2
Dihydroterpinyl acetate CAS 58985-18-5

Offers comparable green freshness but with more herbal character for traditional applications.

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, preliminary data suggests low sensitization potential.

Sustainability

As a synthetic material, 4-Methyl-3-decen-5-ol has consistent quality and reduced environmental impact compared to some natural alternatives. Production can be optimized for atom economy, and it doesn’t require agricultural land or seasonal harvesting. Modern synthesis routes aim to minimize hazardous byproducts.

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References

  1. Brenna et al. (2012). Synthetic routes to aliphatic alcohols for fragrance applications. Journal of Agricultural and Food Chemistry. ACS Publication

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

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Physicochemical Properties

DTXSID: DTXSID8052560

Physical Properties

Molecular Weight 170.296 g/mol🔬 EPA CompTox
Density 0.846 g/cm^3📊 OPERA
Boiling Point 234.731 °C📊 OPERA
Melting Point -4.174 °C📊 OPERA
Flash Point 94.421 °C📊 OPERA
Refractive Index 1.453 Dimensionless📊 OPERA
Molar Volume 201.408 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.917 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.917 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.917 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 0.02 mmHg📊 OPERA
Viscosity 8.832 cP📊 OPERA
Surface Tension 27.742 dyn/cm📊 OPERA
Thermal Conductivity 145.145 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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