Javanol (CAS 198404-98-7) — Woody Base Note Fragrance Ingredient




Javanol

CAS 198404-98-7

Origin
Note
IFRA
Generally safe
Data as of: Mar 2026

What Is Javanol?

Javanol is a synthetic sandalwood fragrance ingredient developed by Givaudan. It’s found in premium perfumes, body care products, and fabric softeners. This luxurious molecule mimics natural sandalwood but with enhanced performance. Its importance stems from sustainability – providing sandalwood’s iconic creamy-woody scent without depleting endangered natural resources.

Safety Profile

GENERALLY SAFE

Generally safeUse with awarenessProfessional use
IFRA approved without restrictions
Non-allergenic per RIFM
CAS
198404-98-7
Formula
Mixture
MW
Variable
Odor Family
Layer 1 · Enthusiast

What Does Javanol Smell Like?

Javanol unfolds like liquid velvet – a radiant burst of creamy sandalwood with lactonic undertones that evoke warm milk swirling in polished teak. The initial sharpness mellows into a plush woody embrace, with lingering coconut-like sweetness that persists on skin for days. Unlike natural sandalwood oils, it maintains remarkable clarity without resinous thickness.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Santal 33(Le Labo, 2011)

Javanol’s durability amplifies the fragrance’s signature cedar-sandalwood accord, creating the cult ‘pickle juice’ effect that lasts through showers.

Baccarat Rouge 540(Maison Francis Kurkdjian, 2015)

Used sparingly to ground the ethereal amber-saffron notes with a velvety woody foundation.

Layer 2

2D Molecular Structure

{1-Methyl-2-[(1,2,2-trimethylbicyclo[3.1.0]hex-3-yl)methyl]cyclopropyl}methanol

SMILES: CC1(CO)CC1CC1CC2CC2(C)C1(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

Javanol is a captive synthetic molecule (2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)butan-1-ol) developed through terpene chemistry. Its structure mimics key odorants in Santalum album while eliminating variability. The synthesis involves cyclization of terpene precursors followed by selective hydrogenation. The molecule’s ten-carbon skeleton and hydroxyl group create optimal volatility and substantivity.

Physical & Chemical Properties

Appearance Colorless to pale yellow liquid
Boiling Point ~300°C (estimated)
Flash Point >100°C

Perfumer Guide

Note Position
Base
Volatility
Very low (days)
Blending
Excellent
Application Typical % Range Notes
Fine Fragrance 1-3% 0.5-5% Provides long-lasting woody signature
Fabric Care 0.1-0.5% Up to 1% Survives washing cycles

Classic Accords

+ Ambroxan = Modern woody-amber
+ Vanillin = Creamy gourmand

Tip: Use below 5% to avoid overwhelming compositions with its tenacious woody character.

Alternatives & Comparisons

1
Ebanol CAS 68039-49-6

More affordable sandalwood substitute with sharper initial profile but less creaminess.

2
Sandalore CAS 65113-99-7

Softer, more powdery alternative when subtle woodiness is desired.

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 under any IFRA standard (2023).

RIFM Assessment

RIFM assessment confirms safe use up to 5.4% in fine fragrances.

Sustainability

As a synthetic, Javanol reduces pressure on endangered Indian sandalwood (Santalum album). Its production requires no agricultural land and generates consistent quality. Givaudan’s manufacturing process has been optimized for reduced solvent use and energy consumption.

Explore Javanol

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Industry & Science Data

Odor Detection Threshold
0.050 ppb
in air (orthonasal)
Ref: Kraft et al., Chemistry & Biodiversity (2000)
Commercial Price
$200–$400/kg
synthetic grade, bulk market
Indicative 2024 pricing. Varies by purity & volume.
Major Producers & Suppliers
Givaudan (Switzerland)
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References

  1. Givaudan Patent WO2001070695 Original synthesis
  2. Bickers et al. (2005) Food Chem Toxicol Safety assessment

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

Report a data error

Physicochemical Properties

DTXSID: DTXSID8051837

Physical Properties

Molecular Weight 222.372 g/mol🔬 EPA CompTox
Density 0.949 g/cm^3🔬 EPA CTX
Boiling Point 265.425 °C🔬 EPA CTX
Melting Point 109.679 °C📊 OPERA
Flash Point 136 °C🔬 EPA CTX
Refractive Index 1.509 Dimensionless📊 OPERA
Molar Volume 224.494 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.8 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 4.186 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.186 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 9.23 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.011 mmHg🔬 EPA CTX
Surface Tension 37.437 dyn/cm📊 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 3 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 67.022 cm^3/mol📊 OPERA
Polarizability 26.569 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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