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PARA-METHYL METHYLSALICYLATE

CAS
—
EC
—
Material type
synthetic aroma chemical
Canonical source
arctander
Formulation

Usage guidance

Suggested min
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Suggested max
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Cost
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Stock
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Compatibility tags
cassiefloralleatherrosespicy
How it behaves

Olfactory profile

Family
sweet
Note tendency
Middle
Descriptors
floralspicyherbaceoussweet

A wintergreen-like methyl salicylate character with an added methyl group giving a slightly heavier, sweeter, and more tenacious profile. Sharp minty-medicinal opening softens into a warm balsamic sweetness reminiscent of root beer and birch. Less piercing than methyl salicylate itself, with a rounder herbal-anisic facet.AI · claude-opus-4-7

Intensity
6 / 10
Tenacity
5 / 10
Volatility
6 / 10
Members

The rest of this material

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chemicals · No. 2119

Arctander monograph

Perfume and Flavor Chemicals, page 909.

tenacity · moderate
sweetherbaceousspicyfloral
MW
—
BP
235°C
MP
—
Sp.Gr.
1.16
Refractive n
—
Rotation
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Appearance

Colorless liquid.

Solubility

Almost insoluble in water, soluble in alcohol and oils.

Odor

Sweet, mild, herbaceous-spicy odor, weaker than Methylsalicylate, more floral.

Flavor

Spicy-wintergreen-like taste, more floral-woody than Methylsalicylate.

Uses in perfumery

This phenolester finds a little use in perfume compositions, partly in mild or sweet leather-like notes, or in spicy floral fragrances of Tuberose-Cassie type.

Production

Produced by condensation of Acetoacetaldehyde with Ethylacetoacetate, followed by Methyl-esterification.

Identity
Aliases · 3
Methyl-2-hydroxy-para-toluateMethyl-meta-cresotinateMethyl-para-methylsalicylate
Compliance note. Restriction data is sourced directly from IFRA publications and preserved with its document excerpt. Perfume Foundry is a compliance-support tool — not a substitute for a qualified safety assessor (CPSR / PIF).