Pinoacetaldehyde

Aroma chemical · Aquatic / Woody

marine, pine, ozonic, watery, balsamic — top to heart note.

Aroma illustration for Pinoacetaldehyde: blue sea waves, a pine branch and cone and swirls of fresh air, for its marine, pine and ozonic notes. It illustrates smell associations, not the material or its source.Skeletal formula of Pinoacetaldehyde (6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-propanal), C12H18O, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Pinoacetaldehyde smells like (marine, pine, ozonic), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 118111). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Pinoacetaldehyde is IFF's marine-pine aldehyde, a fresh, watery and ozonic note over a clean pine heart with balsamic undertones.

What Pinoacetaldehyde smells like

Fraterworks describes Pinoacetaldehyde as a bracing burst of oceanic freshness wrapped around a clean pine heart — watery and ozonic, evocative of windswept shores, anchored by soft balsamic undertones — with six hours of substantivity and strong top-note impact. The Fragrance Foundry likens it to a beta-pinene fortified with ozonic facets.

Leading note
Marine pine
Clear facets
Ozonic
Supporting facets
Watery
Faint facets
Balsamic
Character
Fresh, transparent
  • marine
  • pine
  • ozonic
  • watery
  • balsamic

What makes Pinoacetaldehyde distinctive

Pine needles and sea air carried by one aldehyde.

How Pinoacetaldehyde is used

Used in aquatic and fougère accords, marine compositions and pine notes.

Typical role: lift (adds diffusion and radiance, especially at the top); modifier (used in small amounts to change the character of a blend).

How Pinoacetaldehyde differs from similar materials

Ozofleur
Ozofleur is metallic ozone with no conifer; pinoacetaldehyde adds pine needles and a balsamic side to its marine air.

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
Aquatic / Woody
Note position
Top to heart note
Physical form at room temperature
Liquid
Also known as
6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-propanal
CAS number
33885-51-7
Molecular formula
C12H18O
Molecular weight
178.27 g/mol
IUPAC name
3-(6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl)propanal

The CAS number, formula and molecular weight are taken from PubChem compound 118111, whose own record lists this CAS number; checked 24 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 (1,585 reports): H302 harmful if swallowed (85.4% of reports); H315 causes skin irritation (85.4% of reports); H317 may cause an allergic skin reaction (85.4% of reports); H319 causes serious eye irritation (85.4% of reports); H400 very toxic to aquatic life (84% of reports); H410 very toxic to aquatic life with long lasting effects (84% of reports). 232 of the reports find it does not meet the hazard criteria. 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

Pinoacetaldehyde is also suggested as a partner on the pages for Red Seaweed CO2 Extract.

Used in formulas and accords

Used in 2 published formulas

Pinoacetaldehyde is an ingredient in 1 perfume formula and 1 accord in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Pinoacetaldehyde

Is Pinoacetaldehyde natural or synthetic?

Pinoacetaldehyde is synthetic — it is made by chemical synthesis.

What is the CAS number of Pinoacetaldehyde?

33885-51-7. It was checked against PubChem on 24 October 2026.

Which published formulas use Pinoacetaldehyde?

Pinoacetaldehyde is used in 2 published formulas in the RUŌOD Lab Formula & Accord Library: Cookies & Cream Accord and Harbour Rope. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

  • PubChem — compound 118111, checked 24 October 2026.
  • PubChem — GHS classification (the ECHA C&L Inventory notifications and any harmonised EU entry), read 26 October 2026.
  • Fraterworks — Pinoacetaldehyde — distributor's description.
  • The Fragrance Foundry — Pino Acetaldehyde — distributor's description.
  • Olfactory profile: the RUŌOD Lab team's synthesis of the published descriptions above, reviewed 26 October 2026. Evidence: more than one published description. Classification and the short description: revision 1. Descriptions of odour are judgement, not measurement.

Your own records, next to the reference

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