Geranyl hexanoate (CAS 10032-02-07) — Sweet Middle Note Fragrance Ingredient

Sweet · Floral

Geranyl hexanoate

CAS 10032-02-07

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

What Is Geranyl hexanoate?

Geranyl hexanoate is a synthetic fragrance ingredient used to add fruity, floral nuances to perfumes and scented products. You’ll encounter it in body lotions, soaps, and fine fragrances where a fresh, slightly sweet character is desired. This ester matters because it provides stability and longevity to fruity-floral accords, helping maintain scent profiles in products that undergo heat or storage stress.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Patch test for sensitive skin
CAS
10032-02-07
Formula
Mixture
MW
Variable
Odor Family
Sweet · Floral
Layer 1 · Enthusiast

What Does Geranyl hexanoate Smell Like?

Geranyl hexanoate bursts with a crisp, fruity top note reminiscent of underripe bananas and pear skins, layered over a dewy rose petal heart. As it evolves, the scent reveals a candied citrus quality like bergamot marmalade, settling into a soft, musky base with whispers of green tea leaves. The dry-down maintains remarkable tenacity for a fruity ester, leaving a clean trail of sun-warmed apricots on skin.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau de Sud(Annick Goutal, 1996)

Used here to amplify the citrus-herbal accord, providing a juicy counterpoint to bitter orange and basil with its rounded fruity character.

Un Jardin sur le Nil(Hermès, 2005)

Contributes to the luminous mango facet, blending with grapefruit and carrot seed to create the illusion of sun-ripened tropical fruits.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Geranyl hexanoate belongs to the ester class, formed via Fischer esterification between geraniol and hexanoic acid. This synthetic process yields higher purity than natural extraction. The molecule features a monoterpene backbone (geranyl) esterified with a medium-chain fatty acid (hexanoate), giving it balanced volatility. Its chiral center at the geraniol moiety influences odor perception, with the (R)-enantiomer exhibiting brighter fruity characteristics compared to the more floral (S)-form.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point~250 °C (estimated)
Density~0.89 g/cm³ (estimated)

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Fruity modifier in floral bouquets
Body Care0.5-1.5%Up to 2%Adds freshness to shower gels

Classic Accords

+ Citronellol + Ethyl maltol = Tropical fruit + Hedione + Galaxolide = Shampoo floral

Tip: Use with ionones to create dimensional stone fruit effects without excessive sweetness.

Alternatives & Comparisons

1
Geranyl acetate CAS 105-87-3

For brighter, more citrus-forward fruity notes with faster evaporation. Preferred in top note constructions.

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

Considered safe for current fragrance use levels based on RIFM’s 2015 assessment.

Sustainability

As a synthetic material, geranyl hexanoate avoids agricultural land use but depends on petrochemical feedstocks. Green chemistry approaches using bio-based geraniol are being developed. Its production generates minimal waste when using modern catalytic processes.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press. ISBN 9781420090869

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

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