2-Ethyl-4-methylthiazole (CAS 15679-12-6) — Spicy Middle Note Fragrance Ingredient

Spicy · Woody

2-Ethyl-4-methylthiazole

CAS 15679-12-6

Origin
synthetic
Note
Middle
IFRA
Use with awareness
Data as of: Apr 2026

What Is 2-Ethyl-4-methylthiazole?

2-Ethyl-4-methylthiazole is a synthetic aroma chemical used to create savory, roasted notes in fragrances and flavors. You’ll encounter it in gourmand perfumes and some food flavorings. This molecule matters because it adds realistic meaty or nutty nuances that are hard to achieve naturally, making it valuable for creating complex savory accords in modern perfumery.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for fragrance use
Strong odor – use sparingly
CAS
15679-12-6
Formula
Mixture
MW
Variable
Odor Family
Spicy · Woody
Layer 1 · Enthusiast

What Does 2-Ethyl-4-methylthiazole Smell Like?

2-Ethyl-4-methylthiazole bursts with an intensely savory, roasted character reminiscent of seared meat and toasted nuts. The initial impression is powerfully umami, like the crust on a perfectly grilled steak. As it evolves, it reveals earthy, slightly sulfurous undertones that recall roasted coffee beans or fried onions. In drydown, it leaves a lingering, warm, almost brothy quality that blends beautifully with woody and spicy notes. Its tenacity is moderate, making it useful for creating savory heart notes that persist without overwhelming.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Ombre Leather(Tom Ford, 2018)

Used sparingly to enhance the leather’s natural animalic character, adding depth to the suede accord.

Black Saffron(Byredo, 2012)

Provides subtle savory contrast to the bright citrus opening and warm woody base.

Layer 2

2D Molecular Structure

Thiazole, 2-ethyl-4-methyl-

SMILES: CCC1=NC(C)=CS1

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Ethyl-4-methylthiazole belongs to the thiazole class of heterocyclic compounds, characterized by a five-membered ring containing both sulfur and nitrogen atoms. While thiazoles occur naturally in some roasted foods, this specific compound is synthesized for perfumery use. Common synthetic routes involve the reaction of α-haloketones with thioamides. The ethyl and methyl substitutions at positions 2 and 4 respectively create its distinctive odor profile.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor ThresholdExtremely low (ppb range)

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Good with woody and spicy notes
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Used sparingly for savory effects
Functional Fragrance0.01-0.1%Up to 0.5%Masking agent in some products

Classic Accords

Tip: Use in trace amounts (0.1% or less) to avoid overwhelming compositions with meaty notes.

Alternatives & Comparisons

1
2-Isobutylthiazole CAS 18640-74-9

More green, tomato leaf character compared to the roasted quality of 2-ethyl-4-methylthiazole.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. No specific usage limits established.

RIFM Assessment

No comprehensive RIFM evaluation published as of 2023.

Sustainability

As a synthetic material, 2-ethyl-4-methylthiazole has minimal environmental impact in production compared to natural extracts requiring agricultural land use. Its potency means very small quantities are needed, reducing overall material consumption in formulations.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press.

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

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Physicochemical Properties

DTXSID: DTXSID6065923

Physical Properties

Molecular Weight 127.21 g/mol🔬 EPA CompTox
Density 1.054 g/cm^3📊 OPERA
Boiling Point 161.5 °C🔬 EPA CTX
Melting Point -14.288 °C📊 OPERA
Flash Point 54.21 °C📊 OPERA
Refractive Index 1.524 Dimensionless📊 OPERA
Molar Volume 121.229 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.751 Log10 unitless📊 OPERA
LogD (pH 5.5) 1.733 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.751 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.56 Log10 unitless📊 OPERA
Water Solubility 0.532 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 4.636 mmHg📊 OPERA
Viscosity 2.582 cP📊 OPERA
Surface Tension 33.993 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 12.89 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 1 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 37.103 cm^3/mol📊 OPERA
Polarizability 14.709 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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