Ethyl Cyclopentenolone

Aroma chemical · Gourmand / Woody

maple, caramel, brown sugar, roasted, sweet — heart note.

Aroma illustration for Ethyl Cyclopentenolone: a maple leaf and a drop of syrup and caramel cubes and a caramel drizzle, for its maple and caramel notes. It illustrates smell associations, not the material or its source.Skeletal formula of Ethyl Cyclopentenolone (3-Ethyl-2-hydroxy-2-cyclopenten-1-one), C7H10O2, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Ethyl Cyclopentenolone smells like (maple, caramel), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 62752). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Ethyl cyclopentenolone is the ethyl homologue of cyclotene, a very powerful maple and caramel material. It is often supplied at 50% in propylene glycol.

What Ethyl Cyclopentenolone smells like

ChemicalBook describes ethyl cyclopentenolone at 1% as sweet, caramel, maple and fenugreek; a Parchem specification lists sweet, brown, caramellic, maple, brown sugar, rum, whiskey and furanone. An aroma supplier calls it a very powerful maple-caramellic, coffee-roast material with nutty, burnt-sugar facets. PubChem links it to natural-product databases.

Leading note
Maple
Clear facets
Caramel
Supporting facets
Brown sugar
Faint facets
Roasted coffee, rum
Character
Powerful, warm
  • maple
  • caramel
  • brown sugar
  • roasted
  • sweet

What makes Ethyl Cyclopentenolone distinctive

Darker and more layered than cyclotene, with roast and rum beside the maple.

How Ethyl Cyclopentenolone is used

Used in traces for maple, caramel and roasted effects in gourmand accords.

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

How Ethyl Cyclopentenolone differs from similar materials

Cyclotene
Cyclotene gives a clean maple-syrup sweetness; its ethyl homologue is darker and more layered, with roast and rum facets, according to a supplier.

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

Very powerful; one supplier gives about 0.005% in fine fragrance.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Gourmand / Woody
Note position
Heart note
Physical form at room temperature
Solid
Also known as
3-Ethyl-2-hydroxy-2-cyclopenten-1-one
CAS number
21835-01-8
Molecular formula
C7H10O2
Molecular weight
126.15 g/mol
IUPAC name
3-ethyl-2-hydroxycyclopent-2-en-1-one

The CAS number, formula and molecular weight are taken from PubChem compound 62752, whose own record lists this CAS number; checked 24 October 2026.

Safety and compliance

Hazard classification of the neat substance, as PubChem summarises it, read 26 October 2026. Companies notifying the ECHA C&L Inventory report it as not meeting the GHS hazard criteria (1,407 of 1,448 reports). 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 5 published formulas

Ethyl Cyclopentenolone is an ingredient in 3 perfume formulas and 2 accords in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Ethyl Cyclopentenolone

Is Ethyl Cyclopentenolone natural or synthetic?

The molecule occurs in nature. Commercial Ethyl Cyclopentenolone 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 Ethyl Cyclopentenolone?

21835-01-8. It was checked against PubChem on 24 October 2026.

Which published formulas use Ethyl Cyclopentenolone?

Ethyl Cyclopentenolone is used in 5 published formulas in the RUŌOD Lab Formula & Accord Library, including Burnt Sugar Smoke Accord, Ginger Biscuit Tin and Hazelnut Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

  • PubChem — compound 62752, checked 24 October 2026.
  • PubChem — GHS classification (the ECHA C&L Inventory notifications and any harmonised EU entry), read 26 October 2026.
  • ChemicalBook — 21835-01-8 — odour database.
  • Parchem — ethyl cyclopentenolone — distributor's description.
  • Olfactory profile: the RUŌOD Lab team's synthesis of the published descriptions above, reviewed 24 October 2026. Evidence: more than one published description. Classification and the short description: revision 1. Descriptions of odour are judgement, not measurement.

Your own records, next to the reference

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