Ethyl 10-undecenoate (CAS 692-86-4) — Sweet Top-Middle Note Fragrance Ingredient

Sweet · Citrus

Ethyl 10-undecenoate

CAS 692-86-4

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

What Is Ethyl 10-undecenoate?

Ethyl 10-undecenoate is a synthetic ester used in perfumery for its fruity, waxy character. It’s found in artificial fruit flavors and some floral fragrances. This ingredient matters because it provides cost-effective fruity notes that persist longer than natural extracts, making modern fragrances more accessible.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Approved for fragrance use
Avoid undiluted skin contact
CAS
692-86-4
Formula
Mixture
MW
Variable
Odor Family
Sweet · Citrus
Layer 1 · Enthusiast

What Does Ethyl 10-undecenoate Smell Like?

Ethyl 10-undecenoate opens with a burst of ripe pear skin and banana esters, slightly waxy like a candle shop. The heart reveals cleaner fruity tones reminiscent of laundry detergent fruitiness. Dry-down leaves a faint, pleasant vinyl-like impression that blends well with woody bases.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Synthetic Jungle(Editions de Parfums Frederic Malle, 2021)

Used to amplify the hyper-realistic green apple and pear notes in this futuristic floral composition.

Aventus(Creed, 2010)

Provides subtle fruity lift to the pineapple top note in this modern masculine classic.

Layer 2

2D Molecular Structure

Ethyl undec-10-enoate

SMILES: CCOC(=O)CCCCCCCCC=C

Chemistry, Properties & Perfumer Guide

The Chemistry

Ethyl 10-undecenoate belongs to the ester class, specifically undecenoic acid esters. It’s produced via esterification of 10-undecenoic acid with ethanol. The double bond at position 10 makes it more reactive than saturated esters. Industrial synthesis typically uses acid catalysts under reflux conditions.

Physical & Chemical Properties

Boiling Point258-260 °C
Density0.879 g/cm³
Refractive Index1.438-1.442

Perfumer Guide

Note Position
Top-Middle
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Fruity modifier
Functional Fragrance0.5-2%Up to 3%Laundry fruitiness

Classic Accords

+ Galbanum + Hedione = Futuristic Green + Iso E Super = Modern Woody-Fruity

Tip: Use with citrus top notes to prevent waxy buildup in dry-down.

Alternatives & Comparisons

1
Ethyl decadienoate CAS 3025-30-7

More pear-like character with less waxiness, but higher cost.

2
Allyl amyl glycolate CAS 67634-00-8

Stronger tropical fruit effect with better diffusion.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No restrictions under IFRA 49th Amendment.

RIFM Assessment

RIFM assessed – no significant safety concerns at current usage levels.

Sustainability

Synthetic production from petrochemical feedstocks raises some environmental concerns, but small usage quantities minimize impact. No known natural sources exist for this specific ester.

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References

  1. PubChem: Ethyl 10-undecenoate CID XXXXX
  2. IFRA Standards Library IFRA 49th

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

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Physicochemical Properties

DTXSID: DTXSID4044828

Physical Properties

Molecular Weight 212.333 g/mol🔬 EPA CompTox
Density 0.878 g/cm^3🔬 EPA CTX
Boiling Point 262.5 °C🔬 EPA CTX
Melting Point -38 °C🔬 EPA CTX
Flash Point 144.2 °C🔬 EPA CTX
Refractive Index 1.441 Dimensionless📊 OPERA
Molar Volume 241.699 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.719 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.719 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.719 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.69 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.007 mmHg📊 OPERA
Viscosity 2.498 cP📊 OPERA
Surface Tension 29.06 dyn/cm📊 OPERA
Thermal Conductivity 142.909 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 10 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 63.776 cm^3/mol📊 OPERA
Polarizability 25.283 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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