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Wintergreen

GREENS, HERBS AND FOUGERES  /  green · fresh · sweet
Wintergreen
Wintergreen perfume ingredient
CategoryGREENS, HERBS AND FOUGERES
Subcategorygreen · fresh · sweet
Origin
VolatilityTop Note
BotanicalGaultheria procumbens
Appearancepale yellow to reddish brown clear oily liquid
Odor StrengthMedium
Producing CountriesNorth America
PyramidTop

Sharp, cool, medicinal mint that is not mint. Wintergreen is methyl salicylate: the burning-clean smell of muscle rubs, old-fashioned candy, and birch bark.

  1. Scent
  2. The Full Story
  3. Fun Fact
  4. Extraction & Chemistry
  5. In Perfumery

Scent

Sharp, cooling, medicinal. Not menthol but often confused with it. The specific clean sharpness of methyl salicylate. Sweeter than eucalyptus, less herbal than peppermint, more medicinal than either.

Evolution over time

Immediately

Immediately

Sharp medicinal-cool burst, penetrating
After a few hours

After a few hours

Cooling subsides, sweet-clean remains
After a few days

After a few days

Faint medicinal trace, mostly dissipated within hours

The Full Story

Wintergreen (Gaultheria procumbens) leaves contain up to 98% methyl salicylate (CAS 119-36-8). This single molecule dominates so completely that wintergreen oil and synthetic methyl salicylate are indistinguishable.

Methyl salicylate has a sharp, clean, cooling character often described as minty, though chemically unrelated to menthol. It activates cold-sensitive receptors (TRPM8). The compound is also the primary aromatic in sweet birch bark (Betula lenta).

In perfumery, methyl salicylate functions as a top-note modifier. Used sparingly in fougere, green, and forest compositions. Overdose reads as athletic liniment.

Explore all seven extraits in the Discovery Set.

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Related: Alpha Pinene · Angelica · Angelica Root · Angelica Root Oil · Artemisia · Barrenwort · Beachheather · Behini Tree

Did You Know?

Did you know?
Methyl salicylate is toxic in concentrated form. As little as 5 ml of wintergreen oil can be lethal to a child. Despite its candy-like smell, it is the most common cause of fatal salicylate poisoning in young children.

Extraction & Chemistry

Extraction method: Steam distillation of Gaultheria procumbens leaves. Oil is 96-99% methyl salicylate. Most commercial supply is now synthetic.

Molecular FormulaC8H8O3
CAS Number68917-75-9
Botanical NameGaultheria procumbens
IFRA StatusNo known restrictions
SynonymsTEABERRY · CHECKERBERRY
Physical Properties
Odor StrengthMedium
Lasting Power8 hours at 100.00%
Appearancepale yellow to reddish brown clear oily liquid
Flash Point185.00 °F. TCC ( 85.00 °C. )
Specific Gravity1.17618 to 1.18200 @ 25.00 °C.
Refractive Index1.52900 to 1.54100 @ 20.00 °C.

In Perfumery

Top-note modifier providing medicinal sharpness and cooling. CAS 119-36-8. Used sparingly to cut sweetness. Functions in fougere, green, and forest compositions. Also found in birch tar accords.

From the raw to the worn

This is what it becomes.