(-)-.alpha.-Gurjunene (CAS 489-40-7) — Woody Middle Note Fragrance Ingredient

Woody · Balsamic

(-)-.alpha.-Gurjunene

CAS 489-40-7

Origin
synthetic
Note
Middle
IFRA
Use with awareness
Data as of: Apr 2026

What Is (-)-.alpha.-Gurjunene?

(-)-α-Gurjunene is a specialized fragrance ingredient primarily used in high-end perfumery. While not commonly encountered in everyday products, it appears in niche fragrances seeking woody, balsamic complexity. This molecule matters because it adds depth and naturalistic warmth to compositions, particularly those aiming for forest-like or resinous profiles.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
No major restrictions at typical usage levels
Limited safety data – professional formulation advised
CAS
489-40-7
Formula
Mixture
MW
Variable
Odor Family
Woody · Balsamic
Layer 1 · Enthusiast

What Does (-)-.alpha.-Gurjunene Smell Like?

(-)-α-Gurjunene offers a rich, woody-balsamic profile with facets of aged cedar and warm resins. It evolves from initial peppery-woody top notes to a heart of dry, slightly smoky amber. The dry-down reveals subtle leathery undertones with exceptional tenacity. The odor profile is distinctly three-dimensional, making it valuable for creating forest floor and incense accords.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Bois d'Encens(Armani Privé, 2004)

Used as a supporting note to enhance the incense theme, adding dry woody complexity to the frankincense heart.

Oud Wood(Tom Ford, 2007)

Contributes to the faux-oud effect with its woody-balsamic character, blending with cardamom and sandalwood.

Layer 2

2D Molecular Structure

alpha-Gurjunene

SMILES: [H][C@@]12CC[C@@H](C)[C@@]3([H])CCC(C)=C3[C@]1([H])C2(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

(-)-α-Gurjunene is a sesquiterpene hydrocarbon with a bicyclic molecular structure. As the (-)-enantiomer of α-gurjunene, it exhibits distinct olfactory properties from its (+) counterpart. Synthetically produced through catalytic isomerization of other sesquiterpenes, its chirality is carefully controlled during synthesis. The molecule’s rigidity contributes to its excellent stability in fragrance bases.

Physical & Chemical Properties

Boiling Point254-256 °C (estimated)
Density0.905-0.915 g/cm³ (estimated)

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Woody accent note
Home Fragrance1-3%Up to 8%Base note for woody diffusions

Classic Accords

Tip: Use in trace amounts with citrus top notes to prevent flattening of the fragrance pyramid.

Alternatives & Comparisons

1
β-Caryophyllene CAS 87-44-5

Offers similar woody-spicy character but with more pronounced clove notes and better solubility in ethanol bases.

2
Cedrene CAS 11028-42-5

Provides comparable dry woodiness but with less balsamic depth, useful when a cleaner wood note 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 as safe at all usage levels per IFRA 51st Amendment.

RIFM Assessment

Under evaluation by RIFM. Preliminary data suggests low sensitization potential at typical fragrance concentrations.

Sustainability

Synthetic production avoids depletion of natural sources. Current manufacturing methods use bio-based precursors from terpene streams, reducing petrochemical dependence. The molecule’s stability contributes to longer-lasting fragrances, potentially reducing reapplication frequency.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH. DOI:10.1002/3527600093
  2. IFRA Standards Library. 51st Amendment. IFRA Standards

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

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Ingredient Data Sheet

CAS 489-40-7

Physical Properties

Molecular Weight204.35 g/mol🔬 PubChem
LogP (Octanol-Water)4.1🔬 PubChem
Boiling Point261 °C🔬 EPA CompTox
Vapor Pressure0.01 mmHg @ 25°C📊 OPERA
Flash Point101.3 °C🔬 EPA CompTox
Involatility Index0.0008💻 Calculated
log Kp (skin permeability)-1.036💻 Calculated
SMILESCC1CCC2C(C2(C)C)C3=C(CCC13)C🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score4.3 / 5💻 Calculated

Odor & Flavor

Functional Groupsalkene💻 RDKit
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: DTXSID0052126

Physical Properties

Molecular Weight 204.357 g/mol🔬 EPA CompTox
Density 0.933 g/cm^3📊 OPERA
Boiling Point 265.301 °C📊 OPERA
Melting Point 31.67 °C📊 OPERA
Flash Point 85.223 °C📊 OPERA
Refractive Index 1.512 Dimensionless📊 OPERA
Molar Volume 215.593 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 5.416 Log10 unitless📊 OPERA
LogD (pH 5.5) 5.416 Log10 unitless📊 OPERA
LogD (pH 7.4) 5.416 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.9 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0.01 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.009 mmHg📊 OPERA
Surface Tension 31.466 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 0 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 0 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 64.74 cm^3/mol📊 OPERA
Polarizability 25.665 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.

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