Ethyl nonanoate (CAS 123-29-5) — Sweet Top Note Fragrance Ingredient

Sweet · Citrus

Ethyl nonanoate

CAS 123-29-5

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

What Is Ethyl nonanoate?

Ethyl nonanoate is a synthetic ester commonly used in perfumery for its fruity, waxy aroma. It’s found in artificial flavorings and some personal care products. This ingredient matters because it provides cost-effective fruity notes that mimic natural sources, allowing for consistent fragrance performance across different product formulations.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated products
Check for individual sensitivity
CAS
123-29-5
Formula
Mixture
MW
Variable
Odor Family
Sweet · Citrus
Layer 1 · Enthusiast

What Does Ethyl nonanoate Smell Like?

Ethyl nonanoate bursts with a crisp, fruity character reminiscent of green apples and unripe bananas, with a subtle waxy undertone like candle wax. The top note is bright and slightly tart, evolving into a smoother, creamier heart that suggests coconut flesh. Dry-down reveals a faintly musky, clean laundry quality that lingers close to the skin.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Paco Rabanne Invictus(Paco Rabanne, 2013)

Used for its crisp fruity accent that complements the marine accord, adding a sporty freshness to the grapefruit top notes.

Dior Sauvage(Christian Dior, 2015)

Provides subtle fruity undertones that bridge the citrus top and ambroxan base, enhancing the fragrance’s versatility.

Layer 2

2D Molecular Structure

Ethyl nonanoate

SMILES: CCCCCCCCC(=O)OCC

Chemistry, Properties & Perfumer Guide

The Chemistry

Ethyl nonanoate is a straight-chain fatty acid ester formed from ethanol and nonanoic acid. Industrially produced via esterification, it’s part of the ethyl ester family known for fruity odors. The molecule lacks chirality, making synthesis straightforward. Its relatively simple structure contributes to good stability in various pH conditions.

Physical & Chemical Properties

Boiling Point198 °C
Density0.865 g/cm³

Perfumer Guide

Note Position
Top
Volatility
Medium (1-2 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Fruity accent note
Functional Fragrances0.1-0.5%Up to 1%Clean fruity effects

Classic Accords

+ Galbanum + Bergamot = Green Fruity + Vanillin + Ethyl Maltol = Candy

Tip: Use to brighten citrus compositions or add realism to tropical fruit accords.

Alternatives & Comparisons

1
Ethyl octanoate CAS 106-32-1

More intense fruity character with stronger pear-like notes, useful when more projection is desired.

2
Ethyl decanoate CAS 110-38-3

Longer-lasting waxy-fruity note for fragrances requiring extended fruity dry-down.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions. Approved for all applications.

RIFM Assessment

RIFM assessment confirms safe use at current industry levels.

Sustainability

Synthesized from petrochemical feedstocks, ethyl nonanoate offers consistent quality without agricultural variability. Production is energy-efficient compared to some natural alternatives. Being synthetic, it doesn’t contribute to overharvesting of natural resources.

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References

  1. PubChem Compound Summary for Ethyl nonanoate CID 31277

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

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Ingredient Data Sheet

CAS 123-29-5

Physical Properties

Molecular Weight186.29 g/mol🔬 PubChem
LogP (Octanol-Water)4🔬 PubChem
Boiling Point119 °C🔬 EPA CompTox
Flash Point94.4 °C🔬 EPA CompTox
log Kp (skin permeability)-0.996💻 Calculated
SMILESCCCCCCCCC(=O)OCC🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated

Odor & Flavor

Primary Descriptorsfattygrapenuttywaxy• leffingwell
Functional Groupsesterether💻 RDKit
“Slightly fatty-oily, fruity and nut-like odor with a winy undertone. Fatty-nutty and delicately fruity, Apricot-type taste with a trace of a rosy note.”📖 Arctander
Ethyl nonanoate has a slightly fatty, oily, nutty, fruity, odor reminiscent of cognac with a rosy-fruity note.📖 Fenaroli

Flavor Notes (Arctander)

“Slightly fatty-oily, fruity and nut-like odor with a winy undertone. Fatty-nutty and delicately fruity, Apricot-type taste with a trace of a rosy note. It is widely used in flavor compositions for imitation Apple, Apricot, Quince, Cognac, Coffee, Grape, Pear, Quince, Wine, as well as in numerous ber”📖 Arctander

Sensory Thresholds

Odor Detection Threshold0.147 ppm (n=7)📖 van Gemert

Regulatory Status

FEMA NumberFEMA 2447⚖️ FEMA GRAS
GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
IOFI ClassificationNature Identical📖 Fenaroli
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: DTXSID1047651

Physical Properties

Molecular Weight 186.295 g/mol🔬 EPA CompTox
Density 0.863 g/cm^3🔬 EPA CTX
Boiling Point 227.5 °C🔬 EPA CTX
Melting Point -33.067 °C🔬 EPA CTX
Flash Point 94.275 °C🔬 EPA CTX
Refractive Index 1.427 Dimensionless📊 OPERA
Molar Volume 213.592 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.257 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.257 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.257 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.82 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0.001 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 0.09 mmHg📊 OPERA
Viscosity 1.83 cP📊 OPERA
Surface Tension 27.959 dyn/cm📊 OPERA
Thermal Conductivity 139.816 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 8 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 54.785 cm^3/mol📊 OPERA
Polarizability 21.719 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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