S-Methyl thioacetate (CAS 1534-08-03) — Spicy Top Note Fragrance Ingredient

Spicy · Sweet

S-Methyl thioacetate

CAS 1534-08-03

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

What Is S-Methyl thioacetate?

S-Methyl thioacetate is a synthetic sulfur compound used in fragrance formulations. It’s found in trace amounts in some foods and is primarily encountered in perfumery. This ingredient matters because it provides a distinctive sulfurous character that can enhance savory or tropical fruit accords at very low concentrations.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Strong odor – use sparingly
Potential skin sensitizer
CAS
1534-08-03
Formula
Mixture
MW
Variable
Odor Family
Spicy · Sweet
Layer 1 · Enthusiast

What Does S-Methyl thioacetate Smell Like?

S-Methyl thioacetate delivers an intensely sulfurous, garlic-like punch at full strength that evolves into a tropical fruit nuance when highly diluted. The initial blast is reminiscent of crushed garlic cloves with metallic undertones, quickly transitioning to a sweeter, more rounded character resembling passionfruit or guava. The dry-down leaves a faintly savory, almost meaty impression that works exceptionally well in trace amounts to add complexity to fruity or gourmand compositions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Black Orchid(Tom Ford, 2006)

Used in minute quantities to contribute to the mysterious, slightly animalic tropical fruit accord that defines this iconic fragrance.

A*Men(Mugler, 1996)

Provides a savory edge to the gourmand chocolate-coffee accord, enhancing the fragrance’s distinctive character.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

S-Methyl thioacetate belongs to the thioester class of organosulfur compounds. While it occurs naturally in trace amounts in some foods like garlic and passionfruit, commercial production typically involves the reaction of thioacetic acid with methanol in the presence of acid catalysts. The molecule’s sulfur-carbon bond contributes to its potent odor characteristics and reactivity.

Physical & Chemical Properties

Boiling PointNot well documented
DensityNot well documented

Perfumer Guide

Note Position
Top
Volatility
High (15-30 min)
Blending
Specialized
ApplicationTypical %RangeNotes
Fine Fragrance0.01-0.1%Up to 0.5%Used in trace amounts for effect
Functional Fragrance0.001-0.01%Up to 0.05%Very low levels for savory notes

Classic Accords

+ Tropical fruits = Exotic + Vanilla + Coffee = Gourmand + Citrus + Mint = Fresh

Tip: Always pre-dilute to 1% or lower before incorporating into blends due to extreme potency.

Alternatives & Comparisons

1
Methyl thiopropionate CAS 5925-68-8

Similar sulfurous character but slightly sweeter and less aggressive, useful when a softer effect is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific IFRA restrictions, but recommended for use at low levels due to potency.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

Not currently evaluated by RIFM. Use caution based on structural analogs.

Sustainability

As a synthetic material produced in small quantities, S-Methyl thioacetate has minimal environmental impact. Production requires standard chemical safety protocols due to sulfur content.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press. ISBN 9781420090869

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

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