Borneol (CAS 507-70-0) — Woody Top Note Fragrance Ingredient

Borneol

CAS 507-70-0

Origin
Note
IFRA
Generally safe
Data as of: Mar 2026

What Is Borneol?

Borneol is a naturally occurring organic compound found in various plants like rosemary and camphor. It’s commonly used in fragrances for its woody, camphoraceous scent. This ingredient matters because it adds a refreshing, medicinal quality to perfumes and is valued in aromatherapy for its potential calming effects.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated products
Avoid excessive use in sensitive products
CAS
507-70-0
Formula
Mixture
MW
Variable
Odor Family
Layer 1 · Enthusiast

What Does Borneol Smell Like?

Borneol offers a crisp, woody aroma with strong camphoraceous undertones. It starts with a sharp, almost medicinal top note that gradually mellows into a warm, earthy heart. The dry-down reveals a subtle sweetness, reminiscent of dried herbs left in the sun. Its scent profile is clean and invigorating, like a walk through a pine forest after rain.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau Sauvage(Dior, 1966)

Borneol adds a fresh, woody-camphoraceous edge to this classic citrus chypre, enhancing its aromatic masculinity.

Pour Un Homme(Caron, 1934)

Used here to complement lavender, giving a crisp medicinal quality to this barbershop staple.

Layer 2

2D Molecular Structure

endo-Borneol

SMILES: CC1(C)[C@@H]2CC[C@@]1(C)[C@@H](O)C2

Chemistry, Properties & Perfumer Guide

The Chemistry

Borneol is a bicyclic organic compound belonging to the terpenoid class. It exists as two enantiomers: (+)-borneol and (-)-borneol, which differ in their optical rotation. Naturally occurring in essential oils like rosemary and camphor, it can also be synthesized from pinene. Its structure features a hydroxyl group attached to a camphor-like skeleton, contributing to its distinctive scent and properties.

Physical & Chemical Properties

Boiling Point210 °C
Melting Point208 °C
Density0.91 g/cm³

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Adds woody-camphoraceous character
Aromatherapy0.5-2%Up to 5%Used for its refreshing properties

Classic Accords

+ Lavender + Oakmoss = Fougère + Citrus + Herbs = Cologne

Tip: Use borneol to add a crisp, medicinal quality to woody or herbal compositions.

Alternatives & Comparisons

1
Camphor CAS 76-22-2

More intense camphoraceous note, use when stronger medicinal character is desired.

2
Isoborneol CAS 124-76-5

Similar scent profile but with slightly sweeter, less sharp characteristics.

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

No IFRA restrictions apply to borneol.

RIFM Assessment

RIFM has assessed borneol as safe for use in current practices.

Sustainability

Borneol can be sourced sustainably from plant-derived essential oils or produced synthetically. Synthetic production reduces pressure on natural sources and ensures consistent quality. Both methods have low environmental impact when properly managed.

Explore Borneol

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References

  1. PubChem Compound Summary for Borneol PubChem CID 6552009

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

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Ingredient Data Sheet

CAS 507-70-0

Physical Properties

Molecular Weight154.25 g/mol🔬 PubChem
LogP (Octanol-Water)2.7🔬 PubChem
Boiling Point212 °C🔬 EPA CompTox
Vapor Pressure0.03 mmHg @ 25°C📊 OPERA
Flash Point65.6 °C🔬 EPA CompTox
Involatility Index0.0026💻 Calculated
log Kp (skin permeability)-1.724💻 Calculated
SMILESCC1(C2CCC1(C(C2)O)C)C🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score2.5 / 5💻 Calculated

Odor & Flavor

Primary Descriptorscamphoraceousmintysharpwoody• leffingwell
Functional Groupsalcohol💻 RDKit
“Dry-camphoraceous, woody-peppery odor. The dryness is characteristic and constitutes the main difference from the odor of iso- Bornedol. The odor of Bornedol is often com- pared to that of a good grade Rosemary oil (in which Bornedol is present).”📖 Arctander
Borneol has a pungent, camphor-like odor and burning taste somewhat reminiscent of mint.📖 Fenaroli

Flavor Notes (Arctander)

“slightly burning taste. Bornedol is used in Nut and Spice flavor interest to the creative perfumer or flavorist.”📖 Arctander

Sensory Thresholds

Odor Detection Threshold3.2495 ppm (n=26)📖 van Gemert

Regulatory Status

FEMA NumberFEMA 2157⚖️ FEMA GRAS
GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
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: DTXSID3052143

Physical Properties

Molecular Weight 154.253 g/mol🔬 EPA CompTox
Density 1.038 g/cm^3🔬 EPA CTX
Boiling Point 205.667 °C🔬 EPA CTX
Melting Point 205.345 °C🔬 EPA CTX
Flash Point 60 °C🔬 EPA CTX
Refractive Index 1.502 Dimensionless📊 OPERA
Molar Volume 155.364 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.905 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 2.848 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.848 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.57 Log10 unitless📊 OPERA
Water Solubility 0.004 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 8.583 mmHg🔬 EPA CTX
Viscosity 7.835 cP📊 OPERA
Surface Tension 34.232 dyn/cm📊 OPERA
Thermal Conductivity 125.116 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 20.23 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 45.855 cm^3/mol📊 OPERA
Polarizability 18.178 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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