2-Methyl-3-furanthiol (CAS 28588-74-1) — Spicy Heart to base Note Fragrance Ingredient

Spicy · Balsamic

2-Methyl-3-furanthiol

CAS 28588-74-1

Origin
synthetic
Note
Heart to base
IFRA
Use with awareness
Data as of: Apr 2026

What Is 2-Methyl-3-furanthiol?

2-Methyl-3-furanthiol is a powerful synthetic aroma compound that creates meaty, savory notes. You’ll encounter it in savory flavorings and some niche fragrances. This molecule matters because it’s one of the most potent meat-like aroma chemicals known, detectable at extremely low concentrations.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
GRAS for flavor use
Extremely potent – handle carefully
CAS
28588-74-1
Formula
Mixture
MW
Variable
Odor Family
Spicy · Balsamic
Layer 1 · Enthusiast

What Does 2-Methyl-3-furanthiol Smell Like?

At first sniff, 2-methyl-3-furanthiol delivers an explosive punch of roasted meat juices – think sizzling bacon fat and beef broth reduction. The top note has a slightly sulfurous edge that quickly mellows into a rich, umami heart reminiscent of pan-seared foie gras. As it dries down, it reveals subtle toasted bread crust nuances with lingering savory depth. In dilution, it can suggest roasted coffee or chocolate.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Ombre Nomade(Louis Vuitton, 2018)

Used in trace amounts to add animalic depth to the oud accord, creating a leathery, carnivorous effect that contrasts with the rose.

Bacon Classic(Demeter, 2004)

The key meaty component in this novelty fragrance, providing authentic fried bacon realism when combined with smoky pyrazines.

Layer 2

2D Molecular Structure

2-Methyl-3-furanthiol

SMILES: CC1=C(S)C=CO1

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Methyl-3-furanthiol belongs to the furan-thiol class of heterocyclic compounds. While found naturally in cooked meats through Maillard reactions, commercial production typically involves organic synthesis routes starting from furfural derivatives. The molecule’s extreme potency stems from its sulfur-containing functional group combined with the furan ring structure, creating strong receptor binding affinity.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor Threshold0.0004 ppb

Perfumer Guide

Note Position
Heart to base
Volatility
Medium (2-4 hours)
Blending
Challenging
ApplicationTypical %RangeNotes
Fine Fragrance0.001-0.01%Up to 0.1%Animalic accent
Functional Fragrance0.0001-0.001%Up to 0.01%Savory notes

Classic Accords

+ Castoreum + Vanilla = Animalic leather + Guaiacol + Maltol = Barbecue smoke

Tip: Always pre-dilute to 0.1% or below before incorporating into blends due to extreme potency.

Alternatives & Comparisons

1
2-Furanmethanethiol CAS 98-02-2

Less meaty but more coffee-like, useful when a roasted rather than animalic effect is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific restrictions. Classified as a sulfur compound requiring careful handling.

GHS Classification

H315 Skin irritation H319 Eye irritation H335 Respiratory irritation

RIFM Assessment

RIFM has evaluated this material and established a safe exposure level for fragrance use.

Sustainability

As a synthetic material, production avoids agricultural impacts. However, sulfur-containing compounds require careful waste management. Most manufacturers recover solvents and byproducts.

Explore 2-Methyl-3-furanthiol

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References

  1. Blank et al. (2002). Identification of the Key Aroma Compounds in Cooked Beef. Journal of Agricultural and Food Chemistry. DOI: 10.1021/jf025599+

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

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Ingredient Data Sheet

CAS 28588-74-1

Physical Properties

Molecular Weight114.17 g/mol🔬 PubChem
LogP (Octanol-Water)1.5🔬 PubChem
Boiling Point57 °C🔬 EPA CompTox
log Kp (skin permeability)-2.331💻 Calculated
SMILESCC1=C(C=CO1)S🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated

Odor & Flavor

Primary Descriptorsfishyroastedsweet• leffingwell
Functional Groupsthiolaromatic💻 RDKit
2-Methyl-3-furanthiol has an odor and taste of roasted meat. -📖 Fenaroli

Sensory Thresholds

Odor Detection Threshold0.0004 ppm (n=16)📖 van Gemert
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: DTXSID5047118

Physical Properties

Molecular Weight 114.16 g/mol🔬 EPA CompTox
Density 1.146 g/cm^3🔬 EPA CTX
Boiling Point 174.34 °C📊 OPERA
Melting Point 29.322 °C📊 OPERA
Flash Point 56.549 °C📊 OPERA
Refractive Index 1.536 Dimensionless📊 OPERA
Molar Volume 101.114 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.943 Log10 unitless📊 OPERA
LogD (pH 5.5) 1.912 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.338 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 3.68 Log10 unitless📊 OPERA
Water Solubility 0.018 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 2.846 mmHg📊 OPERA
Viscosity 1.763 cP📊 OPERA
Surface Tension 35.838 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 13.14 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 31.553 cm^3/mol📊 OPERA
Polarizability 12.509 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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