Pyrazine, 2-ethyl-3-methoxy- (CAS 25680-58-4) — Green Top to heart Note Fragrance Ingredient

Green · Woody

Pyrazine, 2-ethyl-3-methoxy-

CAS 25680-58-4

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

What Is Pyrazine, 2-ethyl-3-methoxy-?

2-Ethyl-3-methoxypyrazine is a synthetic aroma chemical that creates earthy, green, and bell pepper-like scents. It’s found in perfumes and some food flavorings. This molecule matters because it’s incredibly potent – just tiny amounts can transform a fragrance, adding realistic vegetable garden or forest floor nuances.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
IFRA approved with restrictions
Extremely potent – requires careful dosing
CAS
25680-58-4
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does Pyrazine, 2-ethyl-3-methoxy- Smell Like?

A powerhouse of vegetal realism, 2-ethyl-3-methoxypyrazine bursts with crushed green bell pepper, fresh pea pods, and damp earth. The initial sharpness evolves into a sophisticated earthy heart reminiscent of truffles and forest undergrowth. At ultra-dilute concentrations, it contributes a mysterious green nuance that lingers subtly in the dry-down. This molecule is famously responsible for the characteristic ‘green’ smell of bell peppers at just parts-per-billion concentrations.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Encre Noire(Lalique, 2006)

Used minimally to enhance the ink-like earthiness, contributing to the fragrance’s stark, damp forest character without overpowering the vetiver.

Green Irish Tweed(Creed, 1985)

Provides subtle vegetal undertones that complement the violet leaf, creating a dewy morning garden effect.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Ethyl-3-methoxypyrazine belongs to the alkylmethoxypyrazine class, known for their extremely low odor thresholds. While found naturally in bell peppers and certain wines (as ‘ladybug taint’), commercial versions are synthesized. Key production methods include condensation reactions of dihydrazines with diketones followed by methylation. The methoxy group at position 3 and ethyl group at position 2 create its distinctive odor profile. Chirality isn’t significant for this particular pyrazine derivative.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Top to heart
Volatility
Moderate (1-3 hours)
Blending
Challenging
ApplicationTypical %RangeNotes
Fine Fragrance0.001-0.01%Up to 0.05%Extremely potent – use in ppm ranges
Functional Fragrance0.0001-0.001%Up to 0.005%For green fabric softeners

Classic Accords

Tip: Always pre-dilute to 0.1% or lower before incorporating into blends.

Alternatives & Comparisons

1
3-Isobutyl-2-methoxypyrazine CAS 24683-00-9

More intense bell pepper character, used when stronger green notes are desired. Also found naturally in Sauvignon Blanc grapes.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific restrictions under current IFRA standards (as of Amendment 49).

RIFM Assessment

RIFM has evaluated similar pyrazines but no specific assessment found for this compound.

Sustainability

As a synthetic material, production avoids agricultural land use but requires petrochemical feedstocks. The extreme potency means minimal quantities are needed per formulation, reducing overall environmental impact compared to less potent naturals.

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References

  1. Maga, J. A. (1982). Pyrazines in Foods. CRC Critical Reviews in Food Science and Nutrition. DOI:10.1080/10408398209527346

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

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