Citronellyl propionate (CAS 141-14-0) — Floral Middle Note Fragrance Ingredient

Floral · Citrus

Citronellyl propionate

CAS 141-14-0

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

What Is Citronellyl propionate?

Citronellyl propionate is a synthetic fragrance ingredient commonly found in perfumes, soaps, and household products. It contributes a fresh, floral-citrus scent with fruity undertones. This ester is valued for its ability to enhance floral compositions while adding a natural, dewy freshness that mimics certain botanical extracts.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No significant restrictions
Potential mild skin sensitivity
CAS
141-14-0
Formula
Mixture
MW
Variable
Odor Family
Floral · Citrus
Layer 1 · Enthusiast

What Does Citronellyl propionate Smell Like?

Citronellyl propionate opens with a bright burst of citrusy rose, like peeling a ripe tangerine near a bouquet of garden roses. The heart reveals a juicy peach nectar quality, softening into a clean, green-herbal drydown reminiscent of crushed geranium leaves. Unlike simpler citronellol derivatives, it carries exceptional diffusion – a single drop can fill a room with its dewy, morning-garden character that lingers for hours without becoming cloying.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau Dynamisante(Clarins, 1987)

Used here to amplify the citrus-rose accord while adding a sporty freshness. The propionate ester’s fruity facets bridge between bergamot top notes and floral heart.

L'Eau d'Issey(Issey Miyake, 1992)

Provides the watery floralcy that defines this aquatic. Its moderate volatility helps sustain the lotus note without overwhelming delicate cyclamen.

Layer 2

2D Molecular Structure

Citronellyl propionate

SMILES: CCC(=O)OCCC(C)CCC=C(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

Citronellyl propionate is an ester formed from citronellol and propionic acid. Industrially produced via acid-catalyzed esterification, it’s a staple of synthetic floral bases. The propionate group enhances fruity characteristics compared to the acetate analog. While chiral centers exist in citronellol, commercial material is typically racemic. Its balanced hydrophobicity (XLogP ~3.2) contributes to good tenacity in both alcohol and oil-based formulations.

Physical & Chemical Properties

Boiling Point242 °C (estimated)
Density0.89 g/cm³ (estimated)

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Very Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Floral modifier
Functional Fragrance0.5-2%Up to 5%Soap/detergent stability

Classic Accords

+ Galbanum + Jasmine = Spring Floral + Lemon + Rosemary = Mediterranean

Tip: Use to add diffusion to rose bases – 0.5% can replace 2% citronellol while reducing waxiness.

Alternatives & Comparisons

1
Citronellyl acetate CAS 150-84-5

More citrusy, less fruity. Preferred when brighter top notes are needed. Higher volatility.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under current IFRA standards (Amendment 49).

RIFM Assessment

RIFM assessment confirms safe use at current industry levels.

Sustainability

As a purely synthetic material, production avoids agricultural land use. Typical synthesis from petrochemical precursors carries standard hydrocarbon processing impacts. Biocatalytic production routes are being explored to reduce energy inputs.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH. ISBN 9783527600090

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

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Physicochemical Properties

DTXSID: DTXSID8047187

Physical Properties

Molecular Weight 212.333 g/mol🔬 EPA CompTox
Density 0.882 g/cm^3🔬 EPA CTX
Boiling Point 262.524 °C📊 OPERA
Melting Point -41.652 °C📊 OPERA
Flash Point 91.791 °C📊 OPERA
Refractive Index 1.444 Dimensionless📊 OPERA
Molar Volume 240.398 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.543 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.543 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.543 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.33 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.021 mmHg📊 OPERA
Viscosity 2.402 cP📊 OPERA
Surface Tension 27.395 dyn/cm📊 OPERA
Thermal Conductivity 135.461 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 26.3 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 7 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 63.91 cm^3/mol📊 OPERA
Polarizability 25.336 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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