Ethyl sorbate (CAS 2396-84-1) — Green Top Note Fragrance Ingredient

Green · Sweet

Ethyl sorbate

CAS 2396-84-1

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

What Is Ethyl sorbate?

Ethyl sorbate is a synthetic fragrance ingredient primarily used in perfumery and flavoring. It’s found in fruity scents and some cosmetic products. This ester contributes fresh, green apple-like notes that enhance modern fragrance compositions.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Use standard ester precautions
CAS
2396-84-1
Formula
Mixture
MW
Variable
Odor Family
Green · Sweet
Layer 1 · Enthusiast

What Does Ethyl sorbate Smell Like?

Ethyl sorbate bursts with crisp, green apple peel freshness that evolves into a juicy pear-like heart. The top note has a slightly tart, unripe fruit character reminiscent of gooseberries. As it dries down, it reveals a softer, almost floral undertone with a clean, slightly waxy finish. The overall effect is bright and uplifting, making it excellent for creating modern fruity-floral accords.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Green Apple Fantasy(FruityScents, 2018)

Used as the primary top note to create a hyper-realistic green apple effect, combined with cis-3-hexenol for leafiness.

Summer Orchard(Nature’s Bliss, 2020)

Provides the crisp apple-pear transition note that bridges citrus top notes to floral heart.

Layer 2

2D Molecular Structure

2,4-Hexadienoic acid, ethyl ester, (2E,4E)-

SMILES: CCOC(=O)\C=C\C=C\C

Chemistry, Properties & Perfumer Guide

The Chemistry

Ethyl sorbate is an ester formed from sorbic acid and ethanol. As a synthetic material, it’s typically produced through acid-catalyzed esterification. The molecule features a conjugated diene system that contributes to its fresh, fruity odor character. Its relatively small molecular weight gives it good volatility for top note applications.

Physical & Chemical Properties

Boiling PointApprox. 195-200°C
AppearanceColorless to pale yellow liquid

Perfumer Guide

Note Position
Top
Volatility
Medium (1-2 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-3%Up to 5%Fruity top note accent
Functional Fragrance0.1-1%Up to 2%Freshness booster

Classic Accords

+ Hexenyl acetate = Apple orchard + Galbanum = Green fantasy

Tip: Combine with cis-3-hexenol for enhanced green apple realism.

Alternatives & Comparisons

1
Ethyl-2-methylbutyrate CAS 7452-79-1

More intense apple character but less fresh green quality.

2
Hexyl acetate CAS 142-92-7

Softer, riper apple note with less tartness.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions apply.

RIFM Assessment

Considered safe for current use levels in fragrance applications.

Sustainability

As a synthetic material, ethyl sorbate has minimal environmental impact in production. Its efficient synthesis from readily available precursors makes it a sustainable choice for fruity notes compared to some natural extracts.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press.

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

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Physicochemical Properties

DTXSID: DTXSID80883712

Physical Properties

Molecular Weight 140.182 g/mol🔬 EPA CompTox
Density 0.933 g/cm^3🔬 EPA CTX
Boiling Point 196 °C🔬 EPA CTX
Melting Point 0.628 °C📊 OPERA
Flash Point 69.275 °C🔬 EPA CTX
Refractive Index 1.454 Dimensionless📊 OPERA
Molar Volume 151.301 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.417 Log10 unitless📊 OPERA
LogD (pH 5.5) 2.417 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.417 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.14 Log10 unitless📊 OPERA
Water Solubility 0.048 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.95 mmHg📊 OPERA
Surface Tension 27.387 dyn/cm📊 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 3 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 41.002 cm^3/mol📊 OPERA
Polarizability 16.255 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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