Dihydromyrcenol (CAS 18479-58-8) — Citrus Top Note Fragrance Ingredient




Dihydromyrcenol

CAS 18479-58-8

Origin
Note
IFRA
Generally safe
Data as of: Mar 2026

What Is Dihydromyrcenol?

Dihydromyrcenol is a fresh, citrusy aroma chemical commonly used in modern fragrances. You’ll encounter it in fresh fougères, aquatic colognes, and laundry-type scents. This ingredient matters because it creates the crisp ‘just-showered’ effect in many contemporary masculine fragrances, blending citrus brightness with woody undertones.

Safety Profile

GENERALLY SAFE

Generally safeUse with awarenessProfessional use
IFRA unrestricted
No known allergen concerns
CAS
18479-58-8
Formula
Mixture
MW
Variable
Odor Family
Layer 1 · Enthusiast

What Does Dihydromyrcenol Smell Like?

Dihydromyrcenol bursts with an intense citrus-lime freshness reminiscent of freshly peeled grapefruit, quickly revealing a clean woody character like freshly sanded pine. The top notes have a bracing, almost metallic clarity that evolves into a transparent woody-herbal heart. Dry-down reveals subtle floral nuances hiding beneath its primary crispness, leaving a long-lasting impression of alpine air and sun-bleached driftwood. Its odor profile is remarkably stable, maintaining linear freshness without the harshness of some citrus synthetics.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Cool Water(Davidoff, 1988)

Provides the signature aquatic freshness that defines this genre, blending with lavender and mint to create the illusion of ocean breezes.

Polo Sport(Ralph Lauren, 1994)

Forms the crisp backbone of this sporty fragrance, enhancing mint and ozone notes while preventing sweetness from dominating.

L’Eau d’Issey Pour Homme(Issey Miyake, 1994)

Contributes to the watery transparency, working with calone to create its distinctive ‘rain on hot stones’ effect.

Layer 2

2D Molecular Structure

1,1,5-Trimethyl-6-heptenol

SMILES: CC(CCCC(C)(C)O)C=C

Chemistry, Properties & Perfumer Guide

The Chemistry

Dihydromyrcenol is a monoterpenoid alcohol derived from myrcene. Industrially produced via selective hydrogenation of myrcene followed by hydration, it exists as a mixture of isomers. The molecule’s stability comes from its saturated structure, making it resistant to oxidation while maintaining excellent volatility. Its relatively simple structure belies complex odor properties due to precise stereochemical arrangements.

Physical & Chemical Properties

Boiling Point 198-200 °C
Density 0.85 g/cm³
Flash Point 75 °C
Solubility Insoluble in water, soluble in alcohol

Perfumer Guide

Note Position
Top to middle
Volatility
Medium-high (1-3 hours)
Blending
Excellent
Application Typical % Range Notes
Fine Fragrance 5-15% Up to 25% Core fresh modifier
Functional Fragrance 1-5% Up to 10% Laundry freshness booster

Classic Accords

+ Calone + Hedione = Aquatic
+ Lavandin + Coumarin = Modern Fougère
+ Galaxolide + Bergamot = Shower Fresh

Tip: Use to brighten woody bases without adding citrus volatility.

Alternatives & Comparisons

1
Myrcenol CAS 543-39-5

More floral and less woody, used when needing softer citrus character.

2
Linalool CAS 78-70-6

For more floral-citrus effects with less woody dryness.

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 (48th Amendment).

RIFM Assessment

RIFM assessment confirms safe use at current industry levels.

Sustainability

Synthesized from turpentine derivatives, making it renewable when sourced from managed pine forests. Production requires careful solvent management but generates minimal waste compared to some aroma chemicals.

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Industry & Science Data

Global Usage Rank
#19 most used
by global fragrance volume
Source: IFRA Usage Survey 2015
Are you a producer or supplier of Dihydromyrcenol? Contact us to be featured.

References

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

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

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Physicochemical Properties

DTXSID: DTXSID8029317

Physical Properties

Molecular Weight 156.269 g/mol🔬 EPA CompTox
Density 0.832 g/cm^3🔬 EPA CTX
Boiling Point 193 °C🔬 EPA CTX
Melting Point -18.22 °C📊 OPERA
Flash Point 76 °C🔬 EPA CTX
Refractive Index 1.444 Dimensionless📊 OPERA
Molar Volume 186.627 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.074 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.074 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.074 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.24 Log10 unitless📊 OPERA
Water Solubility 0.006 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.15 mmHg🔬 EPA CTX
Viscosity 4.834 cP📊 OPERA
Surface Tension 26.96 dyn/cm📊 OPERA
Thermal Conductivity 137.202 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 5 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 49.562 cm^3/mol📊 OPERA
Polarizability 19.648 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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