Homofuraneol

Aroma chemical · Gourmand / Fruity

caramel, sweet, fruity, butterscotch — heart note.

Aroma illustration for Homofuraneol: caramel cubes and a caramel drizzle and bright abstract fruit-coloured spheres, for its caramel and fruity notes. It illustrates smell associations, not the material or its source.Skeletal formula of Homofuraneol (2-Ethyl-4-hydroxy-5-methyl-3(2H)-furanone), C7H10O3, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Homofuraneol smells like (caramel, fruity), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 33931). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Homofuraneol is the ethyl homologue of furaneol, a caramel-sweet furanone found in soy sauce and fruit. It exists as a mixture of two tautomers.

What Homofuraneol smells like

Suppliers describe homofuraneol as sweet, fruity, caramel and butterscotch; one gives sweet, caramel, fruity and bread-like for the tautomer mixture, and Flavornet lists caramel. It is reported in soy sauce, cheese, melon, coffee, strawberry and pineapple, and PubChem links it to natural-product databases.

Leading note
Caramel
Clear facets
Butterscotch
Supporting facets
Fruity
Faint facets
Bready
Character
Sweet, warm
  • caramel
  • sweet
  • fruity
  • butterscotch

What makes Homofuraneol distinctive

A caramel furanone with more butterscotch and bread than strawberry.

How Homofuraneol is used

Used for caramel, cooked-sugar and fruity-sweet effects in gourmand accords.

Typical role: modifier (used in small amounts to change the character of a blend).

How Homofuraneol differs from similar materials

Furaneol
Furaneol is caramel with cooked strawberry and pineapple; homofuraneol, its ethyl homologue, leans more to butterscotch and bread.

Each difference compares the published descriptions of the two materials. Smell varies with grade, supplier and dilution; compare them side by side on blotters before substituting one for another.

Formulation considerations

A tautomeric mixture; often used diluted (one formula gives it at 20%).

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Gourmand / Fruity
Note position
Heart note
Physical form at room temperature
Liquid
Also known as
2-Ethyl-4-hydroxy-5-methyl-3(2H)-furanone, Ethyl furaneol
CAS number
27538-10-9
Molecular formula
C7H10O3
Molecular weight
142.15 g/mol
IUPAC name
2-ethyl-4-hydroxy-5-methylfuran-3-one

The CAS number, formula and molecular weight are taken from PubChem compound 33931, whose own record lists this CAS number; checked 24 October 2026.

Safety and compliance

The IFRA Standards Library lists a Standard covering Homofuraneol:

  • "Ethyl and Methyl furaneol" — Restriction, 51st Amendment, published 2023-06

Limits differ by product category and are set out in the Standard itself; this page does not reproduce them. The list above reflects the library as read on 19 October 2026.

Hazard classification of the neat substance, as PubChem summarises it, read 26 October 2026. Companies notifying the ECHA C&L Inventory classify it (550 reports): H302 harmful if swallowed (85.5% of reports); H315 causes skin irritation (71.5% of reports); H319 causes serious eye irritation (71.5% of reports). 80 of the reports find it does not meet the hazard criteria. Unless it is harmonised, this is the notifiers' own classification, not a binding one.

This page is general information, not a safety assessment or a specification. Confirm identity, composition, IFRA status and allergen content from your supplier's documents for the lot you hold.

Materials it works with

Used in formulas and accords

Used in 7 published formulas

Homofuraneol is an ingredient in 4 perfume formulas and 3 accords in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Homofuraneol

Is Homofuraneol natural or synthetic?

The molecule occurs in nature. Commercial Homofuraneol may be made by synthesis or obtained from natural sources, so check the supplier's specification if the distinction matters to you.

What is the CAS number of Homofuraneol?

27538-10-9. It was checked against PubChem on 24 October 2026.

Which published formulas use Homofuraneol?

Homofuraneol is used in 7 published formulas in the RUŌOD Lab Formula & Accord Library, including Banana Bread, Cherry Lacquer and Fig Jam Brioche. Each is listed with a link under "Used in formulas and accords" on this page.

Is Homofuraneol covered by an IFRA Standard?

Yes. The IFRA Standards Library lists a Standard covering it: "Ethyl and Methyl furaneol" — Restriction, 51st Amendment. The limits depend on the product category; read the Standard itself before formulating.

Sources

Your own records, next to the reference

Keep your own record of Homofuraneol — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.