Methyl Salicylate

Aroma chemical · Aromatic / Floral

wintergreen, minty, sweet, medicinal — top to heart note.

Aroma illustration for Methyl Salicylate: wintergreen leaves and berries and mint leaves, for its wintergreen and minty notes. It illustrates smell associations, not the material or its source.Skeletal formula of Methyl Salicylate (Oil of wintergreen (synthetic)), C8H8O3, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Methyl Salicylate smells like (wintergreen, minty), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 4133). Stereochemistry is not shown; the coloured background is decoration.
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By the RUŌOD Lab TeamRevision 1Updated

In short

Methyl salicylate is the ester that makes up nearly all of wintergreen and sweet birch oils. It has a strong, sweet minty-medicinal odour and is also a trace constituent of tuberose and ylang ylang.

What Methyl Salicylate smells like

Methyl salicylate is the smell of wintergreen: sweet, minty and medicinal, instantly recognisable from liniments and root beer. Perfumer & Flavorist notes that, though both methyl and ethyl salicylate read as wintergreen, the methyl ester has a slightly harsh, phenolic undertone; perfumery listings describe a penetrating medicinal core, camphoraceous and slightly phenolic. It is warmer and sweeter than menthol and lacks its cold blast. It makes up nearly all of wintergreen oil, and occurs in tuberose and other white flowers.

Leading note
Wintergreen
Clear facets
Medicinal
Supporting facets
Phenolic, sweet
Character
Sharp, sweet, penetrating, warm
  • wintergreen
  • minty
  • sweet
  • medicinal

What makes Methyl Salicylate distinctive

Its harshness. Of the wintergreen salicylates it is the sharp, penetrating, medicinal one — the 'dental clinic' smell in excess, a cool green lift in traces.

Concentration and dilution

So strong that it is used in traces; in excess it reads as clinical.

How Methyl Salicylate is used

Used in traces in fougère, green and forest compositions and in tuberose and other white-floral accords; IFRA restricts it.

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

How Methyl Salicylate differs from similar materials

Ethyl Salicylate
Perfumer & Flavorist notes that the methyl ester has a slightly harsh, phenolic undertone; ethyl salicylate is softer, sweeter and more floral-fruity. (compared directly by a cited source)
Wintergreen Oil
Wintergreen oil is around 96–99% methyl salicylate; the natural oil adds a sweet, fruity top and a smooth, faintly woody dryout. (compared directly by a cited source)
Methyl Benzoate
Methyl benzoate is a sweeter floral with a cresol-wintergreen phenolic side; methyl salicylate is wintergreen itself.

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

Recognisable and easily overdone; at high levels the blend reads as a liniment. It is toxic if swallowed in quantity, so label and store with care.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Aromatic / Floral
Note position
Top to heart note
Physical form at room temperature
Liquid
Also known as
Oil of wintergreen (synthetic)
CAS number
119-36-8
Molecular formula
C8H8O3
Molecular weight
152.15 g/mol
IUPAC name
methyl 2-hydroxybenzoate

The CAS number, formula and molecular weight are taken from PubChem compound 4133, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

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): H302 harmful if swallowed; H317 may cause an allergic skin reaction; H361d suspected of damaging the unborn child; H412 harmful to aquatic life with long lasting effects. Companies notifying the ECHA C&L Inventory classify it (2,210 reports): H302 harmful if swallowed (96.9% of reports). 6 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

Methyl Salicylate is also suggested as a partner on the pages for Ethyl Salicylate and Wintergreen Oil.

Used in formulas and accords

Used in 7 published formulas

Methyl Salicylate is an ingredient in 1 perfume formula and 6 accords in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Methyl Salicylate

Is Methyl Salicylate natural or synthetic?

The molecule occurs in nature. Commercial Methyl Salicylate 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 Methyl Salicylate?

119-36-8. It was checked against PubChem on 19 October 2026.

Which published formulas use Methyl Salicylate?

Methyl Salicylate is used in 7 published formulas in the RUŌOD Lab Formula & Accord Library, including Marshmallow Accord, Narcotic Floral Accord and Oolong/Jasmine Tea Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

Your own records, next to the reference

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