Isoeugenol

Aroma chemical · Spicy / Floral

carnation, spicy, floral, sweet — heart to base note.

Aroma illustration for Isoeugenol: a ruffled pink carnation and a heap of warm spices, for its carnation and spicy notes. It illustrates smell associations, not the material or its source.Skeletal formula of Isoeugenol, C10H12O2, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Isoeugenol smells like (carnation, spicy), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 853433). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Isoeugenol is a phenol related to eugenol with a sweeter, floral-spicy carnation note.

What Isoeugenol smells like

Isoeugenol is warm, sweet and spicy-floral, with a clove-and-carnation profile and soft woody undertones. A glossary finds it softer and rounder than eugenol, faintly sweet and phenolic with a smoky, balsamic undertow, and gives an odour threshold of a few parts per billion. It is a strong skin sensitiser, and IFRA restricts it tightly.

Leading note
Carnation
Clear facets
Clove
Supporting facets
Smoky, balsamic
Faint facets
Woody
Character
Warm, sweet, rounded, potent
  • carnation
  • spicy
  • floral
  • sweet

What makes Isoeugenol distinctive

The carnation molecule: softer and rounder than eugenol, more flower than spice.

How Isoeugenol is used

Used in carnation, spicy floral and oriental compositions at low levels, within IFRA limits.

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

How Isoeugenol differs from similar materials

Eugenol
Eugenol is the sharper, more medicinal clove; isoeugenol is softer and rounder, more carnation. (compared directly by a cited source)
Isoeugenyl Acetate
A glossary finds the acetate softer and slower; it is more balsamic and fruity. (compared directly by a cited source)
Methyl Isoeugenol
Methyl isoeugenol is milder, a sweet clove-carnation that Arctander counts among the most carnation-like eugenol derivatives.
Methyl Diantilis
Givaudan places Methyl Diantilis in the same spicy register as isoeugenol, with an added powdery, carnation-like, vanilla aspect and no discolouration. (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

A strong skin sensitiser; a declarable allergen covered by an IFRA Standard with low limits. Use sparingly.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Spicy / Floral
Note position
Heart to base note
Physical form at room temperature
Liquid
CAS number
97-54-1
Molecular formula
C10H12O2
Molecular weight
164.2 g/mol
IUPAC name
2-methoxy-4-[(E)-prop-1-enyl]phenol

The CAS number, formula and molecular weight are taken from PubChem compound 853433, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

The IFRA Standards Library lists a Standard covering Isoeugenol:

  • "Isoeugenol" — 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.

Isoeugenol is one of the 26 fragrance allergens listed individually in Annex III of the EU Cosmetics Regulation (label name: Isoeugenol), which must be named on cosmetic labels above 0.001% in leave-on and 0.01% in rinse-off products. Regulation (EU) 2023/1545 extended the list; see the fragrance allergens list.

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 (1,995 reports): H317 may cause an allergic skin reaction (99.7% of reports); H302 harmful if swallowed (99.5% of reports); H315 causes skin irritation (99.5% of reports); H319 causes serious eye irritation (98.9% of reports); H312 harmful in contact with skin (96.4% of reports); H335 may cause respiratory irritation (10.9% 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

Isoeugenol is also suggested as a partner on the pages for Benzyl Isoeugenol, Carnation Absolute, Methyl Diantilis, Methyl Eugenol and Methyl Isoeugenol.

Used in formulas and accords

Used in 5 published formulas

Isoeugenol is an ingredient in 5 accords in the Formula & Accord Library.

Further reading

Questions about Isoeugenol

Is Isoeugenol natural or synthetic?

The molecule occurs in nature. Commercial Isoeugenol 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 Isoeugenol?

97-54-1. It was checked against PubChem on 19 October 2026.

Which published formulas use Isoeugenol?

Isoeugenol is used in 5 published formulas in the RUŌOD Lab Formula & Accord Library, including Gardenia Accord, Mango Accord and Mimosa Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Is Isoeugenol covered by an IFRA Standard?

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