Ethyl Acetoacetate

Aroma chemical · Fruity

fruity, ethereal, sweet, green apple — top note.

Aroma illustration for Ethyl Acetoacetate: green apples, for its green apple note. It illustrates smell associations, not the material or its source.Skeletal formula of Ethyl Acetoacetate (Ethyl 3-oxobutanoate), C6H10O3, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Ethyl Acetoacetate smells like (green apple), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 8868). Stereochemistry is not shown; the coloured background is decoration.
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By the RUŌOD Lab TeamRevision 1Updated

In short

Ethyl acetoacetate is a keto ester with a sweet, ethereal fruity odour. It is used for fresh, slightly green fruit effects in top notes.

What Ethyl Acetoacetate smells like

Ethyl acetoacetate is a fruity, ethereal, sweet ester reminiscent of green apples, with a rum-like facet. Prodasynth gives fruity, sweet, rum-like; Pell Wall ethereal, fruity-apple, sweet, rum-like. Arctander, as quoted by Pell Wall, notes its occasional use to support ethereal, winey, brandy-like and fresh-citrus top notes, and to give alcohol an 'aged' note. It can slowly react with aldehydes and lose impact.

Leading note
Ethereal green apple
Supporting facets
Rum-like, winey, brandy
Faint facets
Tutti-frutti
Character
Light, ethereal, sweet
  • fruity
  • ethereal
  • sweet
  • green apple

What makes Ethyl Acetoacetate distinctive

A light, boozy apple — ethereal and rum-like, suited to giving a brandy-like age to a top note.

How Ethyl Acetoacetate is used

Used occasionally in light, winey and brandy-like top notes; it is also the starting material for Fructone.

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

How Ethyl Acetoacetate differs from similar materials

Fructone
Fructone, made from it, is sweeter, rounder and more tenacious; ethyl acetoacetate is a lighter, ethereal apple with a rum note.

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.

Identity and classification

Type
Aroma chemical
Origin
Synthetic
Odour family
Fruity
Note position
Top note
Physical form at room temperature
Liquid
Also known as
Ethyl 3-oxobutanoate
CAS number
141-97-9
Molecular formula
C6H10O3
Molecular weight
130.14 g/mol
IUPAC name
ethyl 3-oxobutanoate

The CAS number, formula and molecular weight are taken from PubChem compound 8868, whose own record lists this CAS number; checked 19 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 classify it (2,392 reports): H319 causes serious eye irritation (17.4% of reports). 1,836 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

Ethyl Acetoacetate is also suggested as a partner on the pages for Fraistone.

Used in formulas and accords

Used in 4 published formulas

Ethyl Acetoacetate is an ingredient in 1 perfume formula and 3 accords in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Ethyl Acetoacetate

Is Ethyl Acetoacetate natural or synthetic?

Ethyl Acetoacetate is synthetic — it is made by chemical synthesis.

What is the CAS number of Ethyl Acetoacetate?

141-97-9. It was checked against PubChem on 19 October 2026.

Which published formulas use Ethyl Acetoacetate?

Ethyl Acetoacetate is used in 4 published formulas in the RUŌOD Lab Formula & Accord Library, including Açaí Accord, Apple Cellar and Gardenia Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

Your own records, next to the reference

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