Dihydroisojasmone (CAS 95-41-0) — Floral Heart Note Fragrance Ingredient

Floral · Sweet

Dihydroisojasmone

CAS 95-41-0

Origin
synthetic
Note
Heart
IFRA
Generally safe
Data as of: Apr 2026

What Is Dihydroisojasmone?

Dihydroisojasmone is a synthetic fragrance ingredient used to add floral, fruity nuances to perfumes and scented products. You’ll encounter it in fine fragrances, body care items, and household cleaners. This versatile molecule mimics natural floral scents while offering superior stability, making it a perfumer’s secret weapon for creating long-lasting, sophisticated accords.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
IFRA compliant
Check local regulations
CAS
95-41-0
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does Dihydroisojasmone Smell Like?

Dihydroisojasmone opens with a dewy floralcy reminiscent of jasmine petals dipped in honey, quickly revealing a plush fruity core like overripe apricots in sunlight. As it dries, the scent develops woody-amber undertones that add depth without heaviness, leaving a skin-hugging sillage that’s intimate yet persistent. The overall effect is like a silk scarf fluttering in an orchard breeze – weightless but unforgettable.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

J'adore(Dior, 1999)

Used here to amplify the floral bouquet with its honeyed fruitiness, creating the signature ‘golden water’ effect that makes this fragrance shimmer.

Chance Eau Tendre(Chanel, 2010)

Provides the soft jasmine-tea nuance that balances the citrus top notes, giving this fresh floral its distinctive ‘petal-soft’ character.

Layer 2

2D Molecular Structure

2-Hexylcyclopent-2-enone

SMILES: CCCCCCC1=CCCC1=O

Chemistry, Properties & Perfumer Guide

The Chemistry

Dihydroisojasmone belongs to the cyclic ketone class, specifically a hydrogenated derivative of isojasmone. While jasmone occurs naturally in jasmine absolute, this synthetic version offers greater stability and purity. Industrially produced via hydrogenation of isojasmone or through condensation reactions of appropriate precursors, its structure allows for excellent tenacity in fragrance formulations. The molecule’s conformational flexibility contributes to its ability to bridge floral and fruity olfactive spaces.

Physical & Chemical Properties

Boiling Point250 °C (estimated)
Density0.91 g/cm³ (estimated)

Perfumer Guide

Note Position
Heart
Volatility
Medium (2-4 hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Floral enhancer
Body Care0.5-1%Up to 2%Adds sophistication

Classic Accords

+ Hedione = Modern floral + Galaxolide = Clean musk

Tip: Use with ionones to create seamless floralcy or with ethyl maltol for fruity gourmand effects.

Alternatives & Comparisons

1
Isojasmone CAS 11050-62-7

The natural counterpart with greener, more volatile characteristics, preferred when authenticity to jasmine absolute is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

No restrictions under IFRA 49th Amendment.

RIFM Assessment

RIFM assessment confirms safe use at current industry levels.

Sustainability

As a synthetic material, dihydroisojasmone reduces pressure on natural jasmine crops while offering consistent quality. Production typically follows green chemistry principles with high atom economy. Future developments may explore bio-synthetic routes using engineered microorganisms.

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References

  1. Bauer, K. et al. (2001). Common Fragrance and Flavor Materials. ISBN 9783527612482

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

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Physicochemical Properties

DTXSID: DTXSID3052640

Physical Properties

Molecular Weight 166.264 g/mol🔬 EPA CompTox
Density 0.914 g/cm^3🔬 EPA CTX
Boiling Point 249 °C🔬 EPA CTX
Melting Point 23.877 °C📊 OPERA
Flash Point 114 °C🔬 EPA CTX
Refractive Index 1.474 Dimensionless📊 OPERA
Molar Volume 180.098 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.3 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 3.366 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.366 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.76 Log10 unitless📊 OPERA
Water Solubility 0.002 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg🔬 EPA CTX
Surface Tension 33.061 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 17.07 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 5 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 50.647 cm^3/mol📊 OPERA
Polarizability 20.078 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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