3-Methylbutanal diethyl acetal (CAS 3842-03-03) — Green Top Note Fragrance Ingredient

Green · Woody

3-Methylbutanal diethyl acetal

CAS 3842-03-03

Origin
synthetic
Note
Top
IFRA
Generally safe
Data as of: Apr 2026

What Is 3-Methylbutanal diethyl acetal?

3-Methylbutanal diethyl acetal is a synthetic fragrance ingredient used to add fruity, green, and slightly woody notes to perfumes and scented products. It’s commonly found in fine fragrances, body care items, and household cleaners. This molecule matters because it provides a fresh, natural-like aroma without relying on natural extracts, making formulations more consistent and sustainable.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated products
Check for individual sensitivities
CAS
3842-03-03
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does 3-Methylbutanal diethyl acetal Smell Like?

3-Methylbutanal diethyl acetal opens with a burst of green apple peel and unripe banana, evolving into a heart of fresh-cut grass with a subtle almond undertone. The dry-down reveals a whisper of clean linen and wet stones, making it surprisingly versatile for both fresh and warm compositions. Its behavior is linear yet complex, like sunlight filtering through a leafy canopy.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Green Irish Tweed(Creed, 1985)

Used here to amplify the naturalistic green accord, enhancing the illusion of dew-covered clover leaves without overpowering the violet leaf.

Eau Sauvage(Dior, 1966)

Provides a crisp, modern edge to the classic citrus-aromatic structure, complementing the rosemary and basil notes.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

3-Methylbutanal diethyl acetal belongs to the acetal class of compounds, formed by the reaction of 3-methylbutanal with ethanol. Its synthesis typically involves acid-catalyzed acetalization under controlled conditions. The molecule’s stability comes from its protected aldehyde group, which prevents oxidation while allowing controlled release of the fruity aldehyde character during fragrance evaporation.

Physical & Chemical Properties

Boiling PointNot publicly available
DensityNot publicly available

Perfumer Guide

Note Position
Top
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Adds fresh top notes
Body Care0.1-1%Up to 3%Provides clean scent profile

Classic Accords

Tip: Use with citrus oils to enhance freshness or with woody notes to create naturalistic green effects.

Alternatives & Comparisons

1
Hexenal diethyl acetal CAS 67723-63-5

When a greener, leafier character is desired without the fruity aspects.

2
3-Methylbutanal CAS 590-86-3

For a more direct aldehyde impact when acetal protection isn’t needed.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under current IFRA standards.

EU Allergen Declaration

Not listed as an EU allergen.

RIFM Assessment

No significant safety concerns identified by RIFM.

Sustainability

As a synthetic material, 3-Methylbutanal diethyl acetal reduces pressure on natural resources. Its production can be optimized for energy efficiency, and it doesn’t contribute to deforestation or habitat loss associated with some natural materials.

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References

  1. PubChem Compound Summary for 3-Methylbutanal diethyl acetal PubChem
  2. Bauer, K. et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

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

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