Allyl Phenoxyacetate

Aroma chemical · Fruity / Green

pineapple, honey, green, fruity — heart note.

Aroma illustration for Allyl Phenoxyacetate: a pineapple, honeycomb and a drop of honey and green leaves, for its pineapple, honey and green notes. It illustrates smell associations, not the material or its source.Skeletal formula of Allyl Phenoxyacetate (Allyl 2-phenoxyacetate), C11H12O3, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Allyl Phenoxyacetate smells like (pineapple, honey, green), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 24117). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Allyl phenoxyacetate is an allyl ester with a fruity pineapple-honey odour and a green, galbanum-like facet. It is used to add juicy fruitiness to green accords.

What Allyl Phenoxyacetate smells like

Allyl phenoxyacetate is a strong, sweet material in which pineapple is joined by honey. Symrise describes it as green, sweet and herbal-fruity, reminiscent of chamomile, with nuances of honey, galbanum and pineapple; Pell Wall Perfumes lists sweet, fresh, honey, pineapple and chamomile, with a hint of cocoa. The descriptions agree on three threads — a honeyed sweetness, a green herbal chamomile tone and a pineapple fruitiness — and none of them clearly leads.

Leading note
No single note leads in the published descriptions
Clear facets
Honey, chamomile, pineapple
Supporting facets
Green, galbanum-like
Faint facets
Cocoa
Character
Sweet, green, herbal
  • pineapple
  • honey
  • green
  • fruity

What makes Allyl Phenoxyacetate distinctive

Honey. Several allyl esters smell of pineapple and some of chamomile, but allyl phenoxyacetate is the one whose descriptions consistently add a honeyed sweetness, which is why it is mentioned for honey and chocolate accords rather than only for fruit.

Where the descriptions disagree: On how widely it is used: one reference compilation says it is rarely used in perfumery outside honey bases, while suppliers present it as a working fruity-honey material.

How Allyl Phenoxyacetate is used

Used in traces for honey, pineapple and fruity-green effects; Pell Wall Perfumes notes that it is also useful in chocolate accords. It is a flavour material as well, for candy and beverages.

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

How Allyl Phenoxyacetate differs from similar materials

Allyl Amyl Glycolate
Allyl amyl glycolate is the sharper, more metallic galbanum-pineapple; allyl phenoxyacetate softens a similar green-fruity pairing with honey and chamomile.
Allyl Cyclohexylpropionate
Allyl cyclohexylpropionate is the cleaner, smoother pineapple; allyl phenoxyacetate is honeyed and more herbal.

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

Allyl esters must meet IFRA's specification on free allyl alcohol, and this material has its own IFRA Standard. Check both.

Identity and classification

Type
Aroma chemical
Origin
Synthetic
Odour family
Fruity / Green
Note position
Heart note
Physical form at room temperature
Liquid
Also known as
Allyl 2-phenoxyacetate
CAS number
7493-74-5
Molecular formula
C11H12O3
Molecular weight
192.21 g/mol
IUPAC name
prop-2-enyl 2-phenoxyacetate

The CAS number, formula and molecular weight are taken from PubChem compound 24117, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

The IFRA Standards Library lists Standards covering Allyl Phenoxyacetate:

  • "Allyl phenoxyacetate" — type not stated in the library listing, 49th Amendment, published 2020-01
  • "Allyl esters" — Specification, 44th Amendment, published 2009-01

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 (1,578 reports): H302 harmful if swallowed (100% of reports); H312 harmful in contact with skin (96.4% of reports); H317 may cause an allergic skin reaction (95.2% of reports); H315 causes skin irritation (93.6% of reports). A skin sensitiser classification concerns handling the neat material and the dose in a finished product; the IFRA Standards, where they apply, set the limits. 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

Allyl Phenoxyacetate is also suggested as a partner on the pages for Cyclogalbanate.

Used in formulas and accords

Not currently used in any published formula.

The Formula & Accord Library lists Allyl Phenoxyacetate here as soon as a published formula, accord or base uses it.

Further reading

Questions about Allyl Phenoxyacetate

Is Allyl Phenoxyacetate natural or synthetic?

Allyl Phenoxyacetate is synthetic — it is made by chemical synthesis.

What is the CAS number of Allyl Phenoxyacetate?

7493-74-5. It was checked against PubChem on 19 October 2026.

Is Allyl Phenoxyacetate covered by an IFRA Standard?

Yes. The IFRA Standards Library lists Standards covering it: "Allyl phenoxyacetate" — type not stated in the library listing, 49th Amendment; "Allyl esters" — Specification, 44th 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 Allyl Phenoxyacetate — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.