Phenylacetaldehyde

Aroma chemical · Green / Floral

green, honeyed, hyacinth, floral — top to heart note.

Aroma illustration for Phenylacetaldehyde: green leaves, honeycomb and a drop of honey and spikes of blue hyacinth flowers, for its green, honeyed and hyacinth notes. It illustrates smell associations, not the material or its source.Skeletal formula of Phenylacetaldehyde, C8H8O, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Phenylacetaldehyde smells like (green, honeyed, hyacinth), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 998). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Phenylacetaldehyde is an aldehyde with a powerful green, honeyed hyacinth note. It is used in hyacinth, rose and honey accords.

What Phenylacetaldehyde smells like

Phenylacetaldehyde is a very strong, green-floral aldehyde with a honeyed sweetness and a hyacinth character. Symrise describes it as very strong, green, floral, sweet and hyacinth-type; other data sheets give green, sweet, floral-honey, with harsh hyacinth notes on dilution. Neat it is harsh and green, and it oxidises and polymerises readily, so it is usually supplied stabilised or diluted. Sigma-Aldrich's broader flavour profile adds honey, chocolate, cherry and wine-like notes.

Leading note
Green hyacinth
Clear facets
Honey
Supporting facets
Sweet floral
Faint facets
Rose, bitter almond
Character
Green, sharp, sweet, powerful
  • green
  • honeyed
  • hyacinth
  • floral

What makes Phenylacetaldehyde distinctive

Hyacinth with honey. Several materials give a green hyacinth; phenylacetaldehyde adds a distinct honeyed sweetness, and it is the harshest and most powerful of the family's aldehydes.

Concentration and dilution

Harsh and green neat; its hyacinth character is described as appearing on dilution.

How Phenylacetaldehyde is used

Used in small amounts to brighten and sharpen floral accords — rose, hyacinth and lilac — and to add a soft honey effect. It needs restraint, and its instability means stabilised or diluted grades are the norm.

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

How Phenylacetaldehyde differs from similar materials

Phenylacetaldehyde Dimethyl Acetal
The dimethyl acetal is described as less pungent, without the aldehyde's bitter-almond note, and more stable; it adds an earthy, mushroom-like nuance. (compared directly by a cited source)
Hydratropic Aldehyde
Hydratropic aldehyde is fresh, leafy and tart, a lilac-hyacinth green; phenylacetaldehyde is sweeter and honeyed.
Trifernal
Trifernal is a bitter, crushed-foliage green with grass and tomato-leaf notes; phenylacetaldehyde is a sweet, honeyed hyacinth.
p-Tolylacetaldehyde
p-Tolylacetaldehyde (lilac acetaldehyde) is described as green-fruity, forest-like and sweeter.

An asterisk marks a difference that a cited source states directly. The others compare the published descriptions of each material. Smell varies with grade, supplier and dilution; compare them side by side on blotters before substituting one for another.

Formulation considerations

Unstable and prone to polymerisation; often supplied diluted. Covered by an IFRA Standard.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Green / Floral
Note position
Top to heart note
Physical form at room temperature
Liquid
CAS number
122-78-1
Molecular formula
C8H8O
Molecular weight
120.15 g/mol
IUPAC name
2-phenylacetaldehyde

The CAS number, formula and molecular weight are taken from PubChem compound 998, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

The IFRA Standards Library lists a Standard covering Phenylacetaldehyde:

  • "Phenylacetaldehyde" — Restriction, 49th Amendment, published 2020-01

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 (1,836 reports): H302 harmful if swallowed (99.8% of reports); H317 may cause an allergic skin reaction (96.8% of reports); H314 causes severe skin burns and eye damage (80% of reports); H318 causes serious eye damage (78.6% 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

Phenylacetaldehyde is also suggested as a partner on the pages for alpha-Terpineol, Anther, Hydratropic Aldehyde, p-Tolylacetaldehyde, Styrallyl Alcohol and Trifernal.

Used in formulas and accords

Used in 8 published formulas

Phenylacetaldehyde is an ingredient in 1 perfume formula and 7 accords in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Phenylacetaldehyde

Is Phenylacetaldehyde natural or synthetic?

The molecule occurs in nature. Commercial Phenylacetaldehyde 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 Phenylacetaldehyde?

122-78-1. It was checked against PubChem on 19 October 2026.

Which published formulas use Phenylacetaldehyde?

Phenylacetaldehyde is used in 8 published formulas in the RUŌOD Lab Formula & Accord Library, including Galbanum Courtyard, Gardenia Accord and Mimosa Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Is Phenylacetaldehyde covered by an IFRA Standard?

Yes. The IFRA Standards Library lists a Standard covering it: "Phenylacetaldehyde" — Restriction, 49th 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 Phenylacetaldehyde — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.