Methyl mercaptan (CAS 74-93-1) — Musky Top Note Fragrance Ingredient

Musky · Spicy

Methyl mercaptan

CAS 74-93-1

Origin
synthetic
Note
Top
IFRA
Professional use
Data as of: Apr 2026

What Is Methyl mercaptan?

Methyl mercaptan is a sulfur-containing compound that people rarely encounter directly but may notice in trace amounts in natural gas (as an odorant) or certain fermented foods. Despite its extremely low concentration in consumer products, it plays a crucial role in creating complex fragrance profiles. This potent molecule is used by perfumers in minute quantities to add animalic depth or tropical fruit nuances to compositions, demonstrating how even unpleasant-smelling ingredients can be transformative when skillfully blended.

Safety Profile

PROFESSIONAL USE
Generally safeUse with awarenessProfessional use
Highly toxic at high concentrations
Requires specialized handling
CAS
74-93-1
Formula
Mixture
MW
Variable
Odor Family
Musky · Spicy
Layer 1 · Enthusiast

What Does Methyl mercaptan Smell Like?

Methyl mercaptan assaults the nose with an intensely pungent, garlicky sulfurous character reminiscent of rotten cabbage or skunk spray. At ultra-dilute concentrations (parts per billion), it transforms into a complex tropical nuance – think durian fruit’s controversial allure or the sulfury top notes of passionfruit. In perfumery, it’s used in homeopathic doses to add animalic verve to chypres or create the illusion of fresh-cut tropical fruits. The molecule’s volatility means it disappears quickly, but its olfactory impact lingers, modifying how we perceive subsequent notes in the fragrance pyramid.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Jungle L'Éléphant(Kenzo, 1996)

Methyl mercaptan contributes to the controversial tropical fruit accord, blending with cardamom and clove to create an unexpectedly addictive fragrance that walks the line between repulsive and irresistible.

Secretions Magnifiques(État Libre d’Orange, 2006)

Used here in a bold artistic statement, methyl mercaptan amplifies the blood-and-milk accord with its metallic sulfurous edge, creating one of perfumery’s most challenging compositions.

Layer 2

2D Molecular Structure

Methanethiol

SMILES: CS

Chemistry, Properties & Perfumer Guide

The Chemistry

Methyl mercaptan (CH₃SH) is the simplest thiol, consisting of a methane group bonded to a sulfhydryl group. Industrially produced by reacting methanol with hydrogen sulfide over catalysts, this volatile compound is notorious for its extremely low odor threshold (0.002 ppm). The sulfur-hydrogen bond is responsible for both its penetrating odor and high reactivity. While naturally occurring in some foods and bodily processes, synthetic production allows precise control over purity for fragrance applications. The molecule’s small size and polarity contribute to its high volatility and water solubility.

Physical & Chemical Properties

Boiling Point5.95 °C
Vapor Pressure1.5 atm at 20°C
Density0.8665 g/cm³ (liquid)

Perfumer Guide

Note Position
Top
Volatility
Extremely high (<15 min)
Blending
Specialist use only
ApplicationTypical %RangeNotes
Fine Fragrance0.0001-0.001%Up to 0.005%Used in parts-per-million for effect
Functional Fragrance0.00001%Up to 0.0001%Masking agent in industrial applications

Classic Accords

+ Grapefruit + Blackcurrant = Tropical Fantasy + Civet + Oakmoss = Animalic Chypre

Tip: Always pre-dilute to 0.1% or lower before incorporating into blends to avoid olfactory fatigue and overshooting.

Alternatives & Comparisons

1
Ethyl Mercaptan CAS 75-08-1

Slightly less pungent with a more pronounced onion character, useful when a softer sulfur note is desired while maintaining tropical fruit effects.

2
Furfuryl Mercaptan CAS 98-02-2

Offers coffee-roasted sulfur nuances at higher concentrations but can mimic passionfruit at ultra-dilute levels with greater stability.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

Not specifically restricted by IFRA but falls under general thiol limitations. Use requires expert justification.

GHS Classification

H220 Extremely flammable gas H280 Contains gas under pressure H331 Toxic if inhaled H410 Very toxic to aquatic life

RIFM Assessment

RIFM assessment recommends extreme caution due to toxicity profile, with usage only by qualified professionals in ventilated environments.

Sustainability

As an industrial chemical produced in controlled settings, methyl mercaptan’s environmental impact comes primarily from accidental releases rather than fragrance use. The minuscule quantities used in perfumery (typically micrograms per bottle) make its carbon footprint negligible compared to its functional role in gas leak detection systems that prevent methane emissions.

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References

  1. Nagata Y. (2003). Measurement of odor threshold by triangle odor bag method. Japan Ministry of Environment.
  2. Arctander S. (1969). Perfume and Flavor Chemicals. Allured Publishing.

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

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Ingredient Data Sheet

CAS 74-93-1

Physical Properties

Molecular Weight48.11 g/mol🔬 PubChem
LogP (Octanol-Water)0.5🔬 PubChem
Boiling Point5.9 °C🔬 EPA CompTox
Vapor Pressure0.0075 mmHg @ 25°C📊 OPERA
Flash Point-17.8 °C🔬 EPA CompTox
Involatility Index0.0012💻 Calculated
log Kp (skin permeability)-2.638💻 Calculated
SMILESCS🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score1.8 / 5💻 Calculated

Odor & Flavor

Primary Descriptorscabbage• leffingwell
Functional Groupsthiol💻 RDKit
“In spite of the extremely repulsive odor of this material, the human tolerance towards Methyl mercaptan is very high. Isolated cases of sickness from inhaling the gas are generally ascribed to psychological objection to the odor. The material is NOT classified as toxic.”📖 Arctander
Methyl mercaptan has an objectionable odor of decomposing cabbage or garlic.📖 Fenaroli

Flavor Notes (Arctander)

“It finds some use in flavor compositions, but more in the "reconstitution" of Coffee flavor. Particularly in products made from”📖 Arctander

Sensory Thresholds

Odor Detection Threshold0.0014 ppm (n=31)📖 van Gemert

Regulatory Status

FEMA NumberFEMA 2716⚖️ FEMA GRAS
GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
IOFI ClassificationNature Identical📖 Fenaroli
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID5026382

Physical Properties

Molecular Weight 48.1 g/mol🔬 EPA CompTox
Density 0.939 g/cm^3🔬 EPA CTX
Boiling Point 5.952 °C🔬 EPA CTX
Melting Point -122.444 °C🔬 EPA CTX
Flash Point -22.667 °C🔬 EPA CTX
Refractive Index 1.408 Dimensionless📊 OPERA
Molar Volume 59.09 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 0.979 Log10 unitless📊 OPERA
LogD (pH 5.5) 0.979 Log10 unitless📊 OPERA
LogD (pH 7.4) 0.974 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 1.35 Log10 unitless📊 OPERA
Water Solubility 0.407 mol/L🔬 EPA CTX
Henry's Law Constant 0.003 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 1350.356 mmHg🔬 EPA CTX
Viscosity 0.285 cP📊 OPERA
Surface Tension 21.076 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 0 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 14.578 cm^3/mol📊 OPERA
Polarizability 5.779 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.

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