Linalool oxide pyranoid (CAS 14049-11-7) — Floral Heart Note Fragrance Ingredient

Floral · Woody

Linalool oxide pyranoid

CAS 14049-11-7

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

What Is Linalool oxide pyranoid?

Linalool oxide pyranoid is a synthetic fragrance compound used to add floral, woody nuances to perfumes and scented products. It’s found in air fresheners, fabric softeners, and some personal care items. This molecule enhances floral compositions with its unique ability to bridge fresh top notes with deeper woody base notes, making fragrances smell more natural and complex.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns at typical usage levels
Potential mild skin sensitivity in high concentrations
CAS
14049-11-7
Formula
Mixture
MW
Variable
Odor Family
Floral · Woody
Layer 1 · Enthusiast

What Does Linalool oxide pyranoid Smell Like?

Linalool oxide pyranoid unfolds with a delicate floralcy reminiscent of lily-of-the-valley dipped in rainwater, transitioning to a heart of damp oakmoss and tea leaves. The dry-down reveals subtle woody undertones with a whisper of honeyed sweetness. Unlike its parent linalool, this oxide carries an airy, almost ozonic quality that lifts compositions without overwhelming them. Its evolution suggests morning dew evaporating from a flower-strewn forest floor.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau des Merveilles(Hermès, 2004)

Used to create an illusion of ambergris’ mineralic facets, blending with citrus and woods to form the fragrance’s signature ‘liquid gold’ effect.

L'Air du Temps(Nina Ricci, 1948)

Provides subtle floral-oxidic lift to the carnation accord, enhancing the perfume’s ‘airborne’ quality without adding heaviness.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Linalool oxide pyranoid is a cyclic ether derivative of linalool, formed through acid-catalyzed cyclization. The pyranoid structure (six-membered oxygen-containing ring) differs from the furanoid form in ring size and stability. Synthetic production typically involves photo-oxidation of linalool followed by selective reduction. The molecule exists as cis/trans isomers, with the cis form generally exhibiting greater floral character. Its oxygen bridge increases polarity compared to linalool, reducing volatility while maintaining good diffusion.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor Threshold0.5 ppb in water

Perfumer Guide

Note Position
Heart
Volatility
Medium (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Floral-oxidic modifier
Functional Fragrance0.1-0.5%Up to 1%Freshness enhancer

Classic Accords

Tip: Use to add naturalistic ‘wet’ effects to floral compositions without introducing heavy base notes.

Alternatives & Comparisons

1
Linalool oxide furanoid CAS 5989-33-3

More diffusive but less stable version with sharper green notes, suitable when brighter top effects are desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. Listed as safe when used within standard industry practices.

RIFM Assessment

Considered safe for use in fragrance based on RIFM’s evaluation of structural analogs.

Sustainability

Synthesized from renewable pinene sources in efficient processes with minimal waste. Preferred over natural extraction due to consistent quality and reduced environmental impact versus plant-derived alternatives.

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References

  1. Bauer et al. (2001). Modern Synthetic Routes to Fragrance Ingredients. Chemistry Reviews.

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

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