Linalool oxide (CAS 1365-19-1) — Floral Top to middle Note Fragrance Ingredient

Floral · Woody

Linalool oxide

CAS 1365-19-1

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

What Is Linalool oxide?

Linalool oxide is a fragrance compound derived from linalool, commonly found in lavender and bergamot oils. You’ll encounter it in floral perfumes, soaps, and household cleaners for its fresh, slightly woody scent. It matters because it adds complexity to fragrances, acting as a bridge between bright top notes and deeper base notes, creating a more rounded olfactory experience.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Widely used in consumer products
Possible mild skin sensitivity
CAS
1365-19-1
Formula
Mixture
MW
Variable
Odor Family
Floral · Woody
Layer 1 · Enthusiast

What Does Linalool oxide Smell Like?

Linalool oxide presents a delicate balance between floral freshness and woody depth. Imagine the first dewy moments after rainfall in a lavender field, where crisp floralcy meets damp earth. The initial burst carries a subtle citrus-tinged floral character, like bergamot peeking through linen curtains. As it evolves, it reveals a soft, almost tea-like quality with whispers of oxidized wood – think of well-worn cedar chests lined with dried lavender sachets. In drydown, it leaves a transparent woody-musky trace that lingers like the memory of a garden stroll.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau Sauvage(Dior, 1966)

Used here to bridge the citrus top notes to herbal heart, creating the perfume’s signature ‘watercolor’ effect where notes bleed beautifully into each other.

L'Air du Temps(Nina Ricci, 1948)

Provides subtle oxidation effects that enhance the carnation-carnation accord, like petals slightly bruised from handling.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Linalool oxide is a furanoid terpene ether formed through oxidation of linalool. The molecule exists in several stereoisomeric forms, with the cis and trans configurations each imparting slightly different olfactory characteristics. Industrial production typically involves acid-catalyzed cyclization of linalool, though enzymatic oxidation routes are being developed for more sustainable production.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point198-202 °C
Density0.92-0.94 g/cm³
Refractive Index1.456-1.462

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (2-4 hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Adds naturalistic oxidation effects
Functional Fragrances0.5-1.5%Up to 3%Freshness booster in detergents

Classic Accords

+ Lavender + Coumarin = Herbal fougère + Bergamot + Jasmine = Transparent floralcy

Tip: Use to soften harsh citrus tops and add naturalistic dimension to synthetic lavender notes.

Alternatives & Comparisons

1
Linalool CAS 78-70-6

The parent alcohol, more floral and less woody, when oxidation effects aren’t desired.

2
Rose oxide CAS 16409-43-1

For more pronounced oxidized character with rosy-green facets.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions. Listed as approved for all applications.

RIFM Assessment

RIFM evaluation concludes safe use at current levels in fragrances.

Sustainability

While naturally occurring in small quantities, most linalool oxide is produced synthetically for consistency. New green chemistry methods are improving the environmental profile of production. The compound’s potency means relatively small quantities are needed in formulations, reducing overall material consumption.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

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

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Ingredient Data Sheet

CAS 1365-19-1

Physical Properties

Molecular Weight170.25 g/mol🔬 PubChem
LogP (Octanol-Water)1.4🔬 PubChem
Boiling Point193 °C🔬 EPA CompTox
log Kp (skin permeability)-2.745💻 Calculated

Volatility & Performance

Fragrance NoteHeart💻 Calculated

Odor & Flavor

Primary Descriptorscreamyearthyfloralleafysweet• leffingwell
“Powerful sweet-woody, penetrating odor with floral-woody-earthy undertones. partly as a component in artificial essential oils (Lavandin, Geranium, Lavender, etc.), partly as a powerful additive to Lavender- H3C CH3 Lavandin type fragrances. Soft and sweet fresh and floral odor with an overall “natural” note.”📖 Arctander
Linalool oxide has a powerful, sweet, woody, penetrating odor with floral, woody-earthy undertones.📖 Fenaroli

Regulatory Status

IOFI ClassificationNature Identical📖 Fenaroli
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID6052746

Physical Properties

Molecular Weight 170.25 g/mol🔬 PubChem
Boiling Point 193.5 °C🔬 PubChem
Flash Point 116 °C📊 PubChem

Partition & Solubility

LogP (Octanol-Water) 1.4 Log10 unitless🔬 PubChem

Transport Properties

Vapor Pressure 1.88 mmHg📊 PubChem

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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