4-Methyl-1-oxaspiro[5.5]undecene (CAS 68228-06-08) — Woody Base Note Fragrance Ingredient

Woody · Balsamic

4-Methyl-1-oxaspiro[5.5]undecene

CAS 68228-06-08

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

What Is 4-Methyl-1-oxaspiro[5.5]undecene?

4-Methyl-1-oxaspiro[5.5]undecene is a synthetic fragrance ingredient used to add woody, ambery nuances to perfumes. You’ll find it in modern amber and woody fragrances where it contributes depth and warmth. This molecule matters because it helps create sophisticated, long-lasting fragrance bases without relying solely on natural materials, making scents more consistent and sustainable.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions in current IFRA guidelines
Limited toxicity data – use standard precautions
CAS
68228-06-08
Formula
Mixture
MW
Variable
Odor Family
Woody · Balsamic
Layer 1 · Enthusiast

What Does 4-Methyl-1-oxaspiro[5.5]undecene Smell Like?

A complex woody-amber note with intriguing duality. Opens with a crisp, almost ozonic top that quickly unfolds into a warm, slightly nutty heart reminiscent of toasted cedar. The dry-down reveals a sophisticated ambery base with whisper-like hints of vanilla and leather. Unlike traditional amber materials, it carries an airy, modern quality – like sunlight filtering through aged wooden beams in a minimalist loft.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Ambre Sultan(Serge Lutens, 2000)

Used as a modern amber enhancer, adding lift to the traditional amber accord while maintaining depth.

Terre d'Hermès(Hermès, 2006)

Provides a contemporary woody facet to the flinty mineral accord, bridging citrus top to vetiver base.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

A synthetic oxaspiro compound belonging to the cyclic ether class. The spiro structure (two rings sharing one carbon atom) creates unique conformational rigidity that influences its odor properties. Typically synthesized through acid-catalyzed cyclization of appropriate diol precursors. The methyl group at position 4 introduces subtle steric effects that modify its volatility and scent profile compared to unsubstituted analogs.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor Threshold0.003 ppm in air (estimated)

Perfumer Guide

Note Position
Base
Volatility
Low (8+ hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Base note modifier
Home Fragrance0.5-2%Up to 3%Amber accord component

Classic Accords

Tip: Use with ionones to create a seamless transition between floral heart and woody base notes.

Alternatives & Comparisons

1
Ambroxan CAS 6790-58-5

More marine/dry ambery character, better for fresh applications but lacks the woody depth.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted under IFRA standards.

RIFM Assessment

Under evaluation by RIFM as of 2023.

Sustainability

As a synthetic material, production can be optimized for minimal environmental impact through green chemistry principles. Doesn’t rely on natural resource extraction, though energy inputs for synthesis should be considered. Biodegradability studies pending.

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References

  1. Frater et al. (1998). Synthesis and Olfactory Properties of Spirocyclic Ethers. Helvetica Chimica Acta.

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

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