Styrallyl Acetate

Aroma chemical · Green / Fruity

green, gardenia, fruity, rhubarb — top to heart note.

Aroma illustration for Styrallyl Acetate: large waxy white flowers, bright abstract fruit-coloured spheres and rhubarb stalks, for its gardenia, fruity and rhubarb notes. It illustrates smell associations, not the material or its source.Skeletal formula of Styrallyl Acetate (1-Phenylethyl acetate), C10H12O2, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Styrallyl Acetate smells like (gardenia, fruity, rhubarb), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 62341). Stereochemistry is not shown; the coloured background is decoration.
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By the RUŌOD Lab TeamRevision 1Updated

In short

Styrallyl acetate is the key note of gardenia. It has a green, fruity and fresh floral character.

What Styrallyl Acetate smells like

Styrallyl acetate is a sharp, green, fruity-floral material with a distinctive rhubarb tartness. Supplier descriptions speak of the greenness of crushed leaves and the tart bitterness of rhubarb stalk; Moellhausen gives fresh, green, rhubarb, and Symrise describes it as strong, radiant, herbal-green-fruity and floral similar to gardenia, though not tenacious. Its two mirror-image forms differ, one leaning jasmine-gardenia and fruity, the other green and strawberry-like; perfumery uses the mixture.

Leading note
Green rhubarb
Supporting facets
Gardenia-like floral, fruity
Faint facets
Herbal
Character
Sharp, tart, green, radiant
  • green
  • gardenia
  • fruity
  • rhubarb

What makes Styrallyl Acetate distinctive

Rhubarb. Few materials have its tart, green-stalk sourness, and it is the traditional green top note of gardenia accords — although a distributor points out that this is a perfumer's convention rather than a resemblance to the flower itself.

Where the descriptions disagree: Its gardenia character is the least consistent element across sources.

How Styrallyl Acetate is used

Used for a sharp green-fruity lift in floral and fresh compositions, and traditionally in gardenia accords. It is a top note and does not last long.

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

How Styrallyl Acetate differs from similar materials

Benzyl Acetate
Benzyl acetate is the diffusive fruity-floral jasmine ester; styrallyl acetate is greener and tarter, with rhubarb, and gardenia-like.

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

Strong and diffusive.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Green / Fruity
Note position
Top to heart note
Physical form at room temperature
Liquid
Also known as
1-Phenylethyl acetate
CAS number
93-92-5
Molecular formula
C10H12O2
Molecular weight
164.2 g/mol
IUPAC name
1-phenylethyl acetate

The CAS number, formula and molecular weight are taken from PubChem compound 62341, 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 report it as not meeting the GHS hazard criteria (1,775 of 1,775 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

Styrallyl Acetate is also suggested as a partner on the pages for Styrallyl Alcohol.

Used in formulas and accords

Used in 13 published formulas

Styrallyl Acetate is an ingredient in 4 perfume formulas, 8 accords and 1 base in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Styrallyl Acetate

Is Styrallyl Acetate natural or synthetic?

The molecule occurs in nature. Commercial Styrallyl Acetate 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 Styrallyl Acetate?

93-92-5. It was checked against PubChem on 19 October 2026.

Which published formulas use Styrallyl Acetate?

Styrallyl Acetate is used in 13 published formulas in the RUŌOD Lab Formula & Accord Library, including Aperol Spritz Accord, Champagne Accord and Dried Fruits 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 Styrallyl Acetate — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.