Geranyl ethyl ether (CAS 40267-72-9) — Floral Top to middle Note Fragrance Ingredient

Floral · Sweet

Geranyl ethyl ether

CAS 40267-72-9

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

What Is Geranyl ethyl ether?

Geranyl ethyl ether is a synthetic fragrance compound that mimics the fresh, floral aspects of geranium and rose. It’s found in body care products, air fresheners, and some fine fragrances. This ingredient matters because it provides a cost-effective way to achieve natural-smelling floral notes without relying on plant extracts, making products more sustainable and consistent in scent.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns in current use
Limited toxicology data available
CAS
40267-72-9
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does Geranyl ethyl ether Smell Like?

Geranyl ethyl ether opens with a bright, citrusy-rose character reminiscent of crushed geranium leaves. The heart reveals a softer floralcy, like rose petals dipped in lemon zest, with a subtle green undertone. As it dries down, it leaves a clean, slightly sweet herbal impression that lingers close to the skin. The overall effect is like walking through a sunlit herb garden where rosemary and geraniums grow side by side.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau de Rochas(Rochas, 1970)

Used here to enhance the citrus-floral bouquet, adding a crisp, dewy quality to the classic cologne structure without overpowering the delicate citrus notes.

White Linen(Estée Lauder, 1978)

Provides a clean, soapy floral accent that complements the aldehydes, creating the impression of freshly laundered linens drying in a flower garden.

Layer 2

2D Molecular Structure

2,6-Octadiene, 1-ethoxy-3,7-dimethyl-

SMILES: CCOCC=C(C)CCC=C(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

Geranyl ethyl ether is an aromatic ether derived from geraniol. As a synthetic molecule, it’s typically produced through Williamson ether synthesis by reacting geraniol with ethyl bromide under basic conditions. The ether linkage makes it more stable than its alcohol counterpart, with reduced volatility and increased resistance to oxidation. Its molecular structure features a monoterpene skeleton with a terminal double bond that contributes to its fresh character.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointApprox. 220-230°C (estimated)
SolubilitySoluble in alcohol, oils; insoluble in water

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (1-3 hours)
Blending
Good with citrus, other florals
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Adds fresh floral lift
Soap & Detergent0.5-1.5%Up to 2%Stable in alkaline systems

Classic Accords

+ Citronellol + Linalool = Rose reconstruction + Bergamot + Galbanum = Spring floral

Tip: Use to extend rose notes in citrus colognes where geraniol might be too sweet.

Alternatives & Comparisons

1
Geranyl acetate CAS 105-87-3

More fruity and less green, with similar floral character but higher volatility.

2
Rose oxide CAS 16409-43-1

For a more metallic, dewy rose effect when realism is 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 on IFRA Transparency List.

RIFM Assessment

Not currently evaluated by RIFM. Considered low priority due to limited use volume.

Sustainability

As a synthetic material, geranyl ethyl ether reduces pressure on natural geranium crops. Production typically uses petrochemical feedstocks, though bio-based routes from pinene are theoretically possible. The ether structure makes it more stable than geraniol, potentially reducing fragrance loss and extending product lifespan.

Explore Geranyl ethyl ether

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

References

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

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

Report a data error

Ingredient Data Sheet

CAS 40267-72-9

Physical Properties

Molecular Weight182.3 g/mol🔬 PubChem
LogP (Octanol-Water)3.8🔬 PubChem
Boiling Point220 °C🔬 EPA CompTox
Vapor Pressure1 mmHg @ 25°C📊 OPERA
Flash Point85.7 °C🔬 EPA CompTox
Involatility Index0.0798💻 Calculated
log Kp (skin permeability)-1.114💻 Calculated

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassSlow💻 Calculated
Persistence Score0.5 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsfloralsweet• leffingwell
“The odor is fattier and less woody than that Mainly: 2-wans-3,7-Dimethyl-2,6-nonadien-l- of Geraniol, but since the commercial prod- 01. uct is far from pure, it is not possible to give more than an approximate odor description.”📖 Arctander
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: DTXSID1068223

Physical Properties

Molecular Weight 182.307 g/mol🔬 EPA CompTox
Density 0.841 g/cm^3📊 OPERA
Boiling Point 227.887 °C📊 OPERA
Melting Point -34.587 °C📊 OPERA
Flash Point 81.943 °C📊 OPERA
Refractive Index 1.451 Dimensionless📊 OPERA
Molar Volume 219.811 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.926 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.926 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.926 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.74 Log10 unitless📊 OPERA
Water Solubility 0.003 mol/L📊 OPERA
Henry's Law Constant 0.001 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.375 mmHg📊 OPERA
Viscosity 1.674 cP📊 OPERA
Surface Tension 25.536 dyn/cm📊 OPERA
Thermal Conductivity 131.021 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 9.23 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 6 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 59.19 cm^3/mol📊 OPERA
Polarizability 23.465 Å^3📊 OPERA

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.

Similar Posts