Ethyl linoleate (CAS 544-35-4) — Woody Base Note Fragrance Ingredient

Woody · Balsamic

Ethyl linoleate

CAS 544-35-4

Origin
synthetic
Note
Base
IFRA
Generally safe
Data as of: Apr 2026

What Is Ethyl linoleate?

Ethyl linoleate is a synthetic fragrance ingredient often used as a fixative in perfumes and personal care products. It’s found in body lotions, soaps, and some fine fragrances. This ingredient helps extend the longevity of scents on skin, making it valuable for creating perfumes that last throughout the day without needing reapplication.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated products
Check for skin sensitivity
CAS
544-35-4
Formula
Mixture
MW
Variable
Odor Family
Woody · Balsamic
Layer 1 · Enthusiast

What Does Ethyl linoleate Smell Like?

Ethyl linoleate has a mild, fatty odor with faint herbal undertones. It serves primarily as a fixative rather than a distinctive scent note, subtly enhancing and prolonging other fragrance components. In formulations, it provides a smooth, slightly waxy background that helps blend sharper top notes into the heart accord. Its dry-down is virtually odorless but crucial for maintaining structural integrity in complex compositions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Synthetic Jungle(Frederic Malle, 2021)

Used as an invisible backbone to amplify the longevity of green floral notes without adding detectable odor.

Chance Eau Tendre(Chanel, 2010)

Employed as a skin-smoothing fixative to extend the delicate jasmine and white musk accord.

Layer 2

2D Molecular Structure

9,12-Octadecadienoic acid (9Z,12Z)-, ethyl ester

SMILES: CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC

Chemistry, Properties & Perfumer Guide

The Chemistry

Ethyl linoleate is an ethyl ester of linoleic acid, belonging to the fatty acid ester class. It’s typically synthesized through esterification of linoleic acid with ethanol. As a synthetic compound, it doesn’t occur naturally in significant quantities. The molecule’s long carbon chain and ester group contribute to its fixative properties by slowing the evaporation of more volatile fragrance components.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointApprox. 200-220°C (estimated)

Perfumer Guide

Note Position
Base
Volatility
Very low (hours-days)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Fixative base note
Body Care0.5-2%Up to 3%Skin-smoothing agent

Classic Accords

+ Citrus oils = Long-lasting freshness + Woody notes = Enhanced diffusion

Tip: Use in trace amounts to extend citrus top notes without altering their character.

Alternatives & Comparisons

1
Ethyl oleate CAS 111-62-6

Similar fixative properties with slightly more pronounced fatty odor profile.

2
Isoamyl laurate CAS 6309-51-9

Offers comparable fixative effects with a fruitier background note.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted by IFRA. No usage limitations reported.

RIFM Assessment

Recognized as safe for current usage levels in fragrance applications by RIFM.

Sustainability

As a synthetic material, ethyl linoleate production avoids agricultural impacts but requires petrochemical feedstocks. Modern manufacturing processes focus on energy efficiency and reduced solvent use. Being used in small quantities, its environmental footprint per finished product is minimal.

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References

  1. Bickers et al. (2003). Safety assessment of fatty acid derivatives. Food and Chemical Toxicology. PMID 14505838

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

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Physicochemical Properties

DTXSID: DTXSID1060269

Physical Properties

Molecular Weight 308.506 g/mol🔬 EPA CompTox
Density 0.87 g/cm^3📊 OPERA
Boiling Point 370.67 °C📊 OPERA
Melting Point -22.403 °C📊 OPERA
Flash Point 122.833 °C📊 OPERA
Refractive Index 1.465 Dimensionless📊 OPERA
Molar Volume 349.382 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 7.354 Log10 unitless📊 OPERA
LogD (pH 5.5) 7.354 Log10 unitless📊 OPERA
LogD (pH 7.4) 7.354 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 9.37 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg📊 OPERA
Viscosity 5.693 cP📊 OPERA
Surface Tension 29.567 dyn/cm📊 OPERA
Thermal Conductivity 151.311 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 26.3 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 15 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 96.597 cm^3/mol📊 OPERA
Polarizability 38.294 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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