Methyl Salicylate (CAS 119-36-8) — Sweet Top Note Fragrance Ingredient




Methyl Salicylate

CAS 119-36-8

Origin
Note
IFRA
Use with awareness
Data as of: Mar 2026

What Is Methyl Salicylate?

Methyl salicylate is the compound responsible for the wintergreen scent found in candies, chewing gums, and topical pain relievers like Bengay. It’s nature’s version of wintergreen, originally extracted from plants but now commonly synthesized. This ingredient matters because it bridges medicinal and gourmand worlds—its cooling, minty aroma signals relief in balms while adding a nostalgic candy-shop sweetness to fragrances.

Safety Profile

USE WITH AWARENESS

Generally safeUse with awarenessProfessional use
GRAS (Generally Recognized As Safe) for food use
Skin sensitizer at high concentrations
CAS
119-36-8
Formula
Mixture
MW
Variable
Odor Family
Layer 1 · Enthusiast

What Does Methyl Salicylate Smell Like?

Methyl salicylate bursts with an intense, almost metallic sweetness reminiscent of crushed wintergreen leaves—a hyperrealistic blend of peppermint oil and root beer. The opening has a cooling, medicinal sharpness that quickly mellows into a warm, candy-like sweetness. Unlike true mint oils, it lacks herbaceousness, instead developing a smooth, vanillic undertone during dry-down. In high concentrations, it can smell like a pharmacy counter; properly diluted, it evokes nostalgic memories of holiday candies and vintage soda fountains.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Joop! Homme(Joop!, 1989)

Used as a bold top note to amplify the fragrance’s signature sweet-oriental character, methyl salicylate provides an unexpected wintergreen twist that cuts through the dense honey and tobacco base.

Angel Muse(Mugler, 2016)

Here it adds a playful, candy-like dimension to the hazelnut-vanilla accord, creating a gourmand effect that’s both comforting and slightly medicinal—like a sophisticated cough drop.

Layer 2

2D Molecular Structure

Methyl salicylate

SMILES: COC(=O)C1=C(O)C=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Methyl salicylate is an ester formed from salicylic acid and methanol. Naturally occurring in wintergreen (Gaultheria procumbens) and sweet birch (Betula lenta), it’s now primarily synthesized via esterification of salicylic acid. The molecule’s simple structure—a benzene ring with ester and hydroxyl groups—gives it both volatility for top notes and tenacity from the aromatic ring. Its chirality (the natural form is R-(-)-methyl salicylate) influences odor perception, with synthetic racemic mixtures often smelling harsher than the naturally derived material.

Physical & Chemical Properties

Boiling Point 222 °C
Density 1.174 g/cm³
Refractive Index 1.535-1.538
Flash Point 96 °C
Solubility 1.4 g/L in water

Perfumer Guide

Note Position
Top to Middle
Volatility
Moderate (1-3 hours)
Blending
Good with vanillic and balsamic notes
Application Typical % Range Notes
Fine Fragrance 0.1-0.5% Up to 1% Adds sweet-minty lift
Functional Products 0.5-2% Up to 5% For analgesic/masking effects
Flavorings 0.01-0.1% Up to 0.2% Wintergreen flavor enhancer

Classic Accords

+ Vanilla + Tonka = Gourmand
+ Peppermint + Eucalyptus = Medicinal
+ Tobacco + Honey = Oriental

Tip: Use traces to brighten vanilla-heavy bases without overpowering; pairs exceptionally well with coumarin derivatives.

Alternatives & Comparisons

1
Ethyl Salicylate CAS 118-61-6

A softer, fruitier alternative with less medicinal sharpness; lasts longer in the dry-down but lacks the iconic wintergreen punch.

2
Isopropyl Salicylate CAS 6144-94-7

Even more diffusive with a clean, almost laundry-like character; useful when a less gourmand effect is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. IFRA, REACH, EU Cosmetics Regulation standards update periodically. Consult current IFRA Standards Library before formulating. Not legal or regulatory advice.

IFRA Status

Not restricted under IFRA standards, though recommended maximum use level is 0.6% in leave-on products due to sensitization potential (IFRA 49th Amendment).

EU Allergen Declaration

Not listed as an EU-regulated allergen.

GHS Classification

H302 Harmful if swallowed
H315 Causes skin irritation
H319 Causes serious eye irritation

RIFM Assessment

RIFM evaluation confirms safe use at current industry levels, with a recommended dermal limit of 0.2 mg/cm² based on sensitization data.

Sustainability

While naturally derived methyl salicylate exists (primarily from wintergreen oil), over 95% of global supply is synthesized from petrochemical-derived salicylic acid. Sustainable routes using fermentation-derived salicylic acid are emerging. The synthetic process has moderate environmental impact due to methanol usage, but the molecule’s potency means minimal quantities are needed in formulations.

Explore Methyl Salicylate

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

Industry & Science Data

Global Usage Rank
#25 most used
by global fragrance volume
Source: IFRA Usage Survey 2015
Are you a producer or supplier of Methyl Salicylate? Contact us to be featured.

References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press. ISBN 9781420090869
  2. PubChem Compound Summary for Methyl Salicylate CID 4133

Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Mar 2026.

Report a data error

Physicochemical Properties

DTXSID: DTXSID5025659

Physical Properties

Molecular Weight 152.149 g/mol🔬 EPA CompTox
Density 1.18 g/cm^3🔬 EPA CTX
Boiling Point 222.891 °C🔬 EPA CTX
Melting Point -8.321 °C🔬 EPA CTX
Flash Point 95.014 °C🔬 EPA CTX
Refractive Index 1.547 Dimensionless📊 OPERA
Molar Volume 125.756 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.55 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 2.492 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.486 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.55 Log10 unitless📊 OPERA
Water Solubility 0.016 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 0.076 mmHg🔬 EPA CTX
Viscosity 6.706 cP📊 OPERA
Surface Tension 42.445 dyn/cm📊 OPERA
Thermal Conductivity 149.393 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 46.53 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 1 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 39.908 cm^3/mol📊 OPERA
Polarizability 15.821 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

Similar Posts