Geranyl propionate (CAS 105-90-8) — Floral Top to Mid Note Fragrance Ingredient

Floral · Sweet

Geranyl propionate

CAS 105-90-8

Origin
synthetic
Note
Top to Mid
IFRA
Generally safe
Data as of: Apr 2026

What Is Geranyl propionate?

Geranyl propionate is a floral-fruity synthetic fragrance ingredient often used in perfumes and body care products. It provides a fresh, rosy character with hints of pear and citrus. This ester is prized for its ability to add naturalistic fruitiness to floral compositions, making scents feel more approachable and vibrant.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Not restricted by IFRA
No known allergen status
CAS
105-90-8
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does Geranyl propionate Smell Like?

Geranyl propionate bursts with a luminous, wet freshness reminiscent of dewy rose petals and just-peeled citrus zest. The opening has a sparkling pear-like juiciness that gradually softens into a rounded floral heart. As it dries, a subtle green stemminess emerges, keeping the sweetness in check. The dry-down reveals a whisper of clean musk, leaving a lingering impression of sun-warmed fruit on a wooden cutting board.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chance Eau Tendre(Chanel, 2010)

Used here to amplify the fruity facets of the grapefruit-quince opening, creating a dewy, luminous effect that enhances the white floral heart.

Adds a juicy, fresh-picked quality to the peony and rose accord, making the floral bouquet feel alive and dewy rather than powdery.

Layer 2

2D Molecular Structure

Geranyl propionate

SMILES: CCC(=O)OC\C=C(/C)CCC=C(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

Geranyl propionate is an ester formed from geraniol and propionic acid. Industrially produced via acid-catalyzed esterification, this molecule features the characteristic ten-carbon skeleton of monoterpenoids. The propionate esterification increases volatility compared to geraniol while maintaining good stability. Its chiral center at C-2 means it exists as (R)- and (S)-enantiomers, though commercial material is typically racemic.

Physical & Chemical Properties

Boiling Point253 °C
Density0.906 g/cm³
Refractive Index1.456
Flash Point>100 °C

Perfumer Guide

Note Position
Top to Mid
Volatility
Medium (2-4 hours)
Blending
Very Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Floral-fruity modifier
Body Care0.5-3%Up to 5%Adds freshness without harshness

Classic Accords

+ Rose Alcohol + Citronellol = Rosy Fruity + Hexyl Acetate + Linalool = Pear Blossom

Tip: Use to bridge citrus top notes with floral hearts, especially in modern fruity-floral compositions.

Alternatives & Comparisons

1
Geranyl acetate CAS 105-87-3

For a more citrusy, slightly sharper fruity effect with similar floral character but less pear-like roundness.

2
Phenethyl propionate CAS 122-70-3

When a rosier, honeyed fruitiness is desired with less green character and better persistence.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions apply to geranyl propionate under current standards (as of 50th Amendment).

RIFM Assessment

RIFM assessment confirms safe use at current industry levels with no significant toxicological concerns.

Sustainability

As a synthetic ingredient, geranyl propionate has consistent quality without natural variation. Production uses established esterification chemistry with good atom economy. The geraniol precursor can be derived from renewable pinene sources rather than petrochemicals in many modern production routes.

Explore Geranyl propionate

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH. ISBN 9783527600214

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

Report a data error

Physicochemical Properties

DTXSID: DTXSID8051540

Physical Properties

Molecular Weight 210.317 g/mol🔬 EPA CompTox
Density 0.935 g/cm^3🔬 EPA CTX
Boiling Point 265.283 °C🔬 EPA CTX
Melting Point -35.19 °C📊 OPERA
Flash Point 106.275 °C🔬 EPA CTX
Refractive Index 1.459 Dimensionless📊 OPERA
Molar Volume 233.437 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.286 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.286 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.286 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.63 Log10 unitless📊 OPERA
Water Solubility 0.001 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.022 mmHg📊 OPERA
Viscosity 2.674 cP📊 OPERA
Surface Tension 27.659 dyn/cm📊 OPERA
Thermal Conductivity 136.483 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 6 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 63.852 cm^3/mol📊 OPERA
Polarizability 25.313 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.

Similar Posts