Guaiazulene (CAS 489-84-9) — Woody Heart Note Fragrance Ingredient




Guaiazulene

CAS 489-84-9

Origin
Note
IFRA
Generally safe
Data as of: Mar 2026

What Is Guaiazulene?

Guaiazulene is a deep blue aromatic compound originally derived from guaiac wood oil, now mostly synthesized. It appears in niche perfumes and skincare for its striking color and subtle woody-earthy scent. This rare ingredient matters because it provides both visual drama and a smooth, slightly medicinal aroma profile that perfumers use to add depth to modern compositions.

Safety Profile

GENERALLY SAFE

Generally safeUse with awarenessProfessional use
Used in cosmetics and pharmaceuticals
May stain fabrics due to intense color
CAS
489-84-9
Formula
Mixture
MW
Variable
Odor Family
Layer 1 · Enthusiast

What Does Guaiazulene Smell Like?

Guaiazulene greets the nose with a cool, faintly camphoraceous whisper reminiscent of antique apothecary cabinets. As it unfolds, the scent reveals dry cedar shavings and distant wood smoke, with a peculiar mineral edge like wet slate. The dry-down lingers as a soft, earthy hum—imagine the scent left on your hands after handling well-aged hardwood. Though subtle in projection, it adds remarkable tenacity and chromatic intrigue to fragrances.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Bois d’Encens(Armani Privé, 2004)

Used here for its visual impact and dry woody facets that enhance the incense accord, creating a meditative blue-hued smokiness.

Blue Sapphire(Boadicea the Victorious, 2010)

The azure color provides visual theater while the molecule’s mild antiseptic quality tempers sweet amber notes.

Layer 2

2D Molecular Structure

Guaiazulene

SMILES: CC(C)C1=CC2=C(C)C=CC2=C(C)C=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Guaiazulene is a sesquiterpene with a unique azulene skeleton, isomeric with naphthalene. First isolated from guaiac wood oil, modern production involves synthesis from vetivazulene or dehydrogenation of sesquiterpenes. The conjugated 7-membered ring system creates its signature blue color and stability against oxidation. Unlike most aromatic compounds, it’s non-benzoid with distinctive electron distribution that influences both its hue and mild polarity.

Physical & Chemical Properties

Appearance Deep blue crystalline solid
Melting Point 31-33 °C
Boiling Point 153 °C (0.05 mmHg)

Perfumer Guide

Note Position
Base
Volatility
Low (hours-days)
Blending
Good
Application Typical % Range Notes
Colorant 0.01-0.1% Up to 0.5% Primarily for visual effect
Fragrance 0.5-2% Up to 3% Adds dry woody facets

Classic Accords

+ Vetiver + Patchouli = Dark Earth
+ Ambergris + Sea Notes = Oceanic Mineral

Tip: Dissolve in ethanol before adding to oil phases to prevent speckling.

Alternatives & Comparisons

1
Chamazulene CAS 529-05-5

Similar blue colorant from chamomile with gentler, herbal aroma for sensitive applications.

2
Vetivazulene CAS 529-05-5

More greenish hue and pronounced rooty-earthy scent for darker compositions.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. IFRA, REACH, EU Cosmetics Regulation standards update periodically. Consult current IFRA Standards Library before formulating. Not legal or regulatory advice.

IFRA Status

Not restricted by IFRA. Listed as colorant CI 75130.

RIFM Assessment

RIFM assessment confirms safe use at current levels in fragrance applications.

Sustainability

Historically extracted from endangered guaiacum trees, modern synthesis from renewable terpene sources reduces ecological impact. The manufacturing process requires careful solvent management, but the molecule’s stability and potency result in low environmental load per use.

Explore Guaiazulene

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Industry & Science Data

Odor Detection Threshold
50 ppb
in air (orthonasal)
Ref: van Gemert, Odour Thresholds (2011)
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References

  1. Surburg & Panten (2006). Common Fragrance and Flavor Materials.
  2. PubChem Guaiazulene CID 3515

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

Report a data error

Physicochemical Properties

DTXSID: DTXSID7045996

Physical Properties

Molecular Weight 198.309 g/mol🔬 EPA CompTox
Density 0.97 g/cm^3🔬 EPA CTX
Boiling Point 296.151 °C📊 OPERA
Melting Point 31.722 °C🔬 EPA CTX
Flash Point 113.05 °C🔬 EPA CTX
Refractive Index 1.573 Dimensionless📊 OPERA
Molar Volume 206.172 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 5.19 Log10 unitless📊 OPERA
LogD (pH 5.5) 5.19 Log10 unitless📊 OPERA
LogD (pH 7.4) 5.19 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 7.43 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0.001 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.002 mmHg📊 OPERA
Viscosity 10.281 cP📊 OPERA
Surface Tension 34.848 dyn/cm📊 OPERA
Thermal Conductivity 115.84 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 0 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 0 count💻 Computed
Rotatable Bonds 1 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 67.93 cm^3/mol📊 OPERA
Polarizability 26.93 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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