Phenylacetic Acid

Aroma chemical · Animalic / Gourmand

honey, animalic, sweet, waxy — base note.

Aroma illustration for Phenylacetic Acid: honeycomb and a drop of honey, an abstract swirl of warm fur-like strokes and a wax candle, for its honey, animalic and waxy notes. It illustrates smell associations, not the material or its source.Skeletal formula of Phenylacetic Acid, C8H8O2, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Phenylacetic Acid smells like (honey, animalic, waxy), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 999). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Phenylacetic acid gives the animalic, honeyed depth of honey and beeswax notes. In dilution it is sweet; neat it is sharp and urinous.

What Phenylacetic Acid smells like

Phenylacetic acid has a sweet, animal, honey-like odour in dilute solution that becomes persistent and disagreeable when concentrated, in ChemicalBook's description. Perfumery glossaries describe it as warm and golden at proper dilution, with a faintly urinous, barnyard edge at higher levels, and as a more naturalistic honey than synthetic 'honey' molecules. It is a volatile component of honey and also occurs in rose and narcissus. A 1980s patent notes its animal note can be too pronounced to harmonise.

Leading note
Animalic honey
Clear facets
Sweet
Supporting facets
Urinous, barnyard
Faint facets
Waxy
Character
Warm, heavy, animalic, persistent
  • honey
  • animalic
  • sweet
  • waxy

What makes Phenylacetic Acid distinctive

Honey as it really smells: golden and sweet, with the faintly urinous, animal undertone that makes natural honey more than sugar.

Concentration and dilution

Warm, golden honey at proper dilution; urinous and disagreeable at concentration.

How Phenylacetic Acid is used

Used in small amounts as a honey modifier and in animalic bases, and in rose, narcissus and tobacco compositions.

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

How Phenylacetic Acid differs from similar materials

Methyl Phenylacetate
The methyl ester is a lighter, brighter honey with jasmine; the acid is heavier, waxier and more animalic.
p-Cresyl Phenylacetate
p-Cresyl phenylacetate pairs honey with narcissus and leather; the acid is honey with a urinous edge, without the floral narcotic note.
Ethyl Phenylacetate
Ethyl phenylacetate is a sweet floral honey with rose and fruit; the acid is heavier and animalic.
Linden Blossom Absolute
Linden is a green, citrus-tea honey with a soft hay drydown; phenylacetic acid is heavy, animalic honey.

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 solid acid; dissolve before use and dose from dilution. It can react with alcohols over time to form esters.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Animalic / Gourmand
Note position
Base note
Physical form at room temperature
Solid
CAS number
103-82-2
Molecular formula
C8H8O2
Molecular weight
136.15 g/mol
IUPAC name
2-phenylacetic acid

The CAS number, formula and molecular weight are taken from PubChem compound 999, 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 (1,864 reports): H319 causes serious eye irritation (85.5% of reports); H318 causes serious eye damage (14.4% of reports). 1 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

Phenylacetic Acid is also suggested as a partner on the pages for Allyl Phenoxyacetate, Isobutyl Phenylacetate, Methyl Phenylacetate, p-Cresyl Phenylacetate and Phenylethyl Acetate.

Used in formulas and accords

Used in 9 published formulas

Phenylacetic Acid is an ingredient in 5 perfume formulas and 4 accords in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Phenylacetic Acid

Is Phenylacetic Acid natural or synthetic?

The molecule occurs in nature. Commercial Phenylacetic Acid 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 Phenylacetic Acid?

103-82-2. It was checked against PubChem on 19 October 2026.

Which published formulas use Phenylacetic Acid?

Phenylacetic Acid is used in 9 published formulas in the RUŌOD Lab Formula & Accord Library, including Beeswax Throne, Cured Leaf 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 Phenylacetic Acid — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.