5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone (CAS 0698-10-2) — Sweet Heart to base Note Fragrance Ingredient

Sweet · Balsamic

5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone

CAS 0698-10-2

Origin
synthetic
Note
Heart to base
IFRA
Use with awareness
Data as of: Apr 2026

What Is 5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone?

5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone is a synthetic aroma chemical used to add caramel-like sweetness to fragrances and flavors. You might encounter it in gourmand perfumes or food products. This ingredient matters because it creates rich, dessert-like accords that evoke warmth and comfort, making fragrances more inviting and delicious.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Safe in regulated concentrations
Potential skin sensitizer at high levels
CAS
0698-10-2
Formula
Mixture
MW
Variable
Odor Family
Sweet · Balsamic
Layer 1 · Enthusiast

What Does 5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone Smell Like?

This furanone derivative delivers an intense, warm caramel sweetness with a slightly burnt sugar nuance. The top note is a burst of rich toffee that evolves into a heart of maple syrup and brown sugar. The dry-down reveals a subtle roasted coffee undertone, adding depth to its gourmand character. It behaves like liquid dessert, lingering on the skin with a comforting, edible quality.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Angel(Mugler, 1992)

Used as a supporting note to enhance the gourmand chocolate-patchouli accord, adding caramelized depth to the fragrance’s edible personality.

La Vie Est Belle(Lancôme, 2012)

Contributes to the praline-iris accord, providing a warm, sugary sweetness that balances the floral powdery notes.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone belongs to the furanone class of compounds, known for their potent sweet and caramel-like aromas. While structurally similar to some naturally occurring furanones in roasted foods, this specific molecule is produced synthetically. Its synthesis typically involves cyclization of appropriate hydroxy-keto acid precursors. The molecule’s stereochemistry significantly impacts its odor profile, with different enantiomers exhibiting varying intensity of sweet characteristics.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointEstimated 250-300°C
DensityApprox. 1.05 g/cm³

Perfumer Guide

Note Position
Heart to base
Volatility
Medium (2-6 hours)
Blending
Good with vanillin, maltol
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Used for gourmand accents
Functional Fragrance0.1-0.5%Up to 1%Adds warmth to detergents

Classic Accords

Tip: Use with vanillic materials to create complex gourmand effects without overpowering.

Alternatives & Comparisons

1
Furaneol CAS 3658-77-3

More strawberry-like character, used when a fruitier sweet note is desired while maintaining similar caramel undertones.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific IFRA restrictions. General furanone guidelines apply.

RIFM Assessment

RIFM has evaluated structurally similar furanones; this specific compound requires further study.

Sustainability

As a synthetic material, this furanone is produced through controlled chemical processes with minimal environmental impact compared to natural extraction. Its high potency means small quantities are effective, reducing overall material usage in formulations.

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References

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

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    Ingredient Data Sheet

    CAS 0698-10-2

    Physical Properties

    Molecular Weight142.15 g/mol🔬 PubChem
    LogP (Octanol-Water)0.9🔬 PubChem
    log Kp (skin permeability)-2.928💻 Calculated

    Sensory Thresholds

    Odor Detection Threshold0.0024 ppm (n=11)📖 van Gemert
    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.

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