Estragole

Aroma chemical · Aromatic / Green

anise, tarragon, herbal, sweet — top to heart note.

Aroma View image for Estragole, illustrating its anise, tarragon and herbal notes. It shows smell associations, not the material or its source.Skeletal formula of Estragole (Methyl chavicol), C10H12O, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an approved image of what Estragole smells like — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 8815). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Estragole, also called methyl chavicol, is a phenylpropene and the main constituent of tarragon and many basil oils. It has a sweet anise-tarragon odour.

What Estragole smells like

Estragole (methyl chavicol), an isomer of anethole, has an odour reminiscent of anise but different in character: fresh, green and spicy, greener and more pungent than anethole and more herbal, with a faintly medicinal or camphoraceous edge at high concentration. A fragrance review describes it, against anethole, as more bitter, fresh-herbaceous and phenolic. It is the main constituent of tarragon oil and is abundant in basil. IFRA limits it because of genotoxicity concerns.

Leading note
Green herbal anise
Clear facets
Tarragon
Supporting facets
Basil
Faint facets
Phenolic, bitter
Character
Fresh, green, pungent, herbal
  • anise
  • tarragon
  • herbal
  • sweet

What makes Estragole distinctive

Anise made green: the tarragon-basil version of the anise note, less sweet and more pungent than anethole.

Concentration and dilution

At high concentration a faintly medicinal, camphoraceous edge can appear.

How Estragole is used

Used in herbal and anisic accords and in tarragon and basil reconstructions; IFRA restricts it.

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

How Estragole differs from similar materials

Anethole
Anethole is the sweeter, purer anise; estragole is greener, more pungent, herbal and bitter. (compared directly by a cited source)
Basil Oil
Exotic basil is estragole-led, adding herbaceous, green and spicy notes to its anise. (compared directly by a cited source)
Tarragon Oil
Tarragon oil is mostly estragole, with a green, herbaceous, celery-like edge. (compared directly by a cited source)

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

Covered by an IFRA Standard, which also counts estragole contributed by natural oils. Check the limit for your product category.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Aromatic / Green
Note position
Top to heart note
Physical form at room temperature
Liquid
Also known as
Methyl chavicol, 4-Allylanisole
CAS number
140-67-0
Molecular formula
C10H12O
Molecular weight
148.2 g/mol
IUPAC name
1-methoxy-4-prop-2-enylbenzene

The CAS number, formula and molecular weight are taken from PubChem compound 8815, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

The IFRA Standards Library lists a Standard covering Estragole:

  • "Estragole" — Restriction, 51st Amendment, published 2023-06

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 (1,959 reports): H302 harmful if swallowed (99.8% of reports); H317 may cause an allergic skin reaction (99.3% of reports); H341 suspected of causing genetic defects (98.4% of reports); H351 suspected of causing cancer (98.4% of reports); H315 causes skin irritation (11% of reports); H412 harmful to aquatic life with long lasting effects (10.6% of reports). 1 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

Estragole is also suggested as a partner on the pages for Dihydroanethole.

Used in formulas and accords

Not currently used in any published formula.

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

Further reading

Questions about Estragole

Is Estragole natural or synthetic?

The molecule occurs in nature. Commercial Estragole 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 Estragole?

140-67-0. It was checked against PubChem on 19 October 2026.

Is Estragole covered by an IFRA Standard?

Yes. The IFRA Standards Library lists a Standard covering it: "Estragole" — Restriction, 51st 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 Estragole — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.