Triplal

Aroma chemical · Green / Citrus

green, leafy, sharp, fresh — top note.

Aroma illustration for Triplal: green leaves, for its green and leafy notes. It illustrates smell associations, not the material or its source.Skeletal formula of Triplal (Ligustral), C9H14O, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Triplal smells like (green, leafy), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 93375). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Triplal (also known as Ligustral) is a synthetic aldehyde with a powerful green, leafy note.

What Triplal smells like

Triplal (IFF; also known as ligustral) is a powerful green aldehyde with the smell of freshly cut grass and hedge clippings, and a tart citrus-peel side. IFF's description is a powerful, green, grassy odour that connotes the concentrated, refreshing tartness of lemon and bergamot peels. A perfumery glossary adds a crisp, tart quality with a metallic backbone, and notes that at high concentration it is almost caustic.

Leading note
Sharp cut-grass green
Clear facets
Tart citrus peel
Supporting facets
Metallic, hedge leaves
Character
Sharp, tart, crisp, powerful
  • green
  • leafy
  • sharp
  • fresh

What makes Triplal distinctive

Its citrus tartness. Plenty of materials smell of cut green leaves; Triplal pairs that with the zest of lemon and bergamot peel and a metallic crispness, which is why it suits fresh citrus and green colognes so well.

Concentration and dilution

Almost caustic at high concentration; its fresh, grassy-citrus character shows in dilution.

How Triplal is used

Used in traces for a natural, sharp green top note in fresh, citrus, floral and functional fragrances.

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

How Triplal differs from similar materials

Isocyclocitral
Isocyclocitral is leafier, earthier and more humid, with weedy and stem notes; Triplal is tarter and more citrus-peel-like, with a metallic edge.
Stemone
Stemone is a fig-leaf and ivy green with a hint of anise; Triplal is cut grass and hedge with citrus-peel tartness.
Vertoliff
Vertoliff, a close cyclohexene-carbaldehyde relative, is described with more lime and unripe-peel freshness.

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

Very strong; covered by an IFRA Standard.

Identity and classification

Type
Aroma chemical
Origin
Synthetic
Odour family
Green / Citrus
Note position
Top note
Physical form at room temperature
Liquid
Also known as
Ligustral, 2,4-Dimethyl-3-cyclohexenecarboxaldehyde
CAS number
68039-49-6
Molecular formula
C9H14O
Molecular weight
138.21 g/mol
IUPAC name
2,4-dimethylcyclohex-3-ene-1-carbaldehyde

The CAS number, formula and molecular weight are taken from PubChem compound 93375, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

The IFRA Standards Library lists a Standard covering Triplal:

  • "Dimethylcyclohex-3-ene-1-carbaldehyde (mixed isomers)" — 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. It has a harmonised EU classification (Regulation (EC) No 1272/2008, Annex VI): H317 may cause an allergic skin reaction. Companies notifying the ECHA C&L Inventory classify it (2,481 reports): H315 causes skin irritation (99.8% of reports); H317 may cause an allergic skin reaction (99.7% of reports); H411 toxic to aquatic life with long lasting effects (62.7% of reports); H319 causes serious eye irritation (43.3% of reports); H412 harmful to aquatic life with long lasting effects (37% of reports). 4 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

Triplal is also suggested as a partner on the pages for 2-Isobutyl-3-methoxypyrazine, Cyclogalbanate, Isocyclocitral and Vertoliff.

Used in formulas and accords

Used in 6 published formulas

Triplal is an ingredient in 4 accords and 2 bases in the Formula & Accord Library.

Further reading

Questions about Triplal

Is Triplal natural or synthetic?

Triplal is synthetic — it is made by chemical synthesis.

What is the CAS number of Triplal?

68039-49-6. It was checked against PubChem on 19 October 2026.

Which published formulas use Triplal?

Triplal is used in 6 published formulas in the RUŌOD Lab Formula & Accord Library, including Cranberry Base, Fig Accord and Green Apple Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Is Triplal covered by an IFRA Standard?

Yes. The IFRA Standards Library lists a Standard covering it: "Dimethylcyclohex-3-ene-1-carbaldehyde (mixed isomers)" — 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 Triplal — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.