Geranial (CAS 141-27-5) — Citrus Top Note Fragrance Ingredient

Citrus · Sweet

Geranial

CAS 141-27-5

Origin
synthetic
Note
Top
IFRA
Use with awareness
Data as of: Apr 2026

What Is Geranial?

Geranial is a citrusy, lemon-like aroma molecule found in many essential oils like lemongrass and lemon verbena. You encounter it in citrus-scented cleaning products and zesty perfumes. This aldehyde gives bright, fresh top notes that make fragrances feel instantly uplifting and energetic. It’s prized for its ability to cut through heavier scents with a sparkling clarity.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Common food flavoring agent
Potential skin sensitizer at high concentrations
CAS
141-27-5
Formula
Mixture
MW
Variable
Odor Family
Citrus · Sweet
Layer 1 · Enthusiast

What Does Geranial Smell Like?

Geranial bursts with an intense, piercing lemon character—like the zest of a Meyer lemon amplified tenfold. It has a metallic sharpness in its opening that quickly mellows into a warmer, rosier citrus tone reminiscent of lemon drops. The dry-down reveals subtle herbal undertones, as if lemon leaves were crushed between fingers. Unlike simpler citrus notes, it maintains presence for hours, evolving from electric brightness to a sophisticated citrus-tea nuance.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau Sauvage(Dior, 1966)

Geranial provides the razor-sharp citrus sparkle that defines this classic cologne, cutting through the herbal heart with laser precision.

Light Blue(Dolce & Gabbana, 2001)

Used alongside limonene to create the photorealistic Sicilian lemon top note that made this fragrance iconic.

Layer 2

2D Molecular Structure

(2E)-3,7-dimethylocta-2,6-dienal

SMILES: CC(C)=CCC\C(C)=C\C=O

Chemistry, Properties & Perfumer Guide

The Chemistry

Geranial (C10H16O) is an α,β-unsaturated aldehyde and one of the two isomers of citral (along with neral). It’s synthesized via oxidation of geraniol or through the condensation of acetone with citronellal. The trans-configuration of its double bonds gives it a more intense citrus character than its cis counterpart neral. Industrially, it’s often produced via the dehydration of linalool followed by isomerization.

Physical & Chemical Properties

Boiling Point229 °C
Density0.893 g/cm³
Refractive Index1.489-1.491

Perfumer Guide

Note Position
Top
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Adds piercing citrus brightness
Functional Fragrances1-3%Up to 10%Boosts cleaning product freshness

Classic Accords

Tip: Stabilize in ethanol before blending to prevent polymerization.

Alternatives & Comparisons

1
Neral CAS 106-26-3

The sweeter, less aggressive citral isomer for softer citrus effects.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No restrictions under IFRA 51st Amendment.

EU Allergen Declaration

Must be declared when present >0.001% in leave-on products (EU Regulation No 1223/2009).

GHS Classification

H315 H317

RIFM Assessment

RIFM evaluation confirms safe use at current industry levels with sensitization risk below threshold.

Sustainability

Most geranial today is synthesized from turpentine-derived pinene or petrochemical precursors. Emerging bioengineering routes use modified yeast strains to produce citral from sugar, offering more sustainable options. Natural extraction from lemongrass remains niche due to low yields.

Explore Geranial

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References

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

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

Report a data error

Perfumer’s Notes

Odor: mint;lemon

MW: 152.23

LogP: 3

Odor Threshold: 0.12

Physicochemical Properties

DTXSID: DTXSID20881217

Physical Properties

Molecular Weight 152.237 g/mol🔬 EPA CompTox
Density 0.889 g/cm^3🔬 EPA CTX
Boiling Point 228.083 °C🔬 EPA CTX
Melting Point 10.717 °C📊 OPERA
Flash Point 99.1 °C🔬 EPA CTX
Refractive Index 1.457 Dimensionless📊 OPERA
Molar Volume 177.753 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.139 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 3.058 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.058 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.01 Log10 unitless📊 OPERA
Water Solubility 0.005 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.044 mmHg🔬 EPA CTX
Viscosity 1.373 cP📊 OPERA
Surface Tension 25.346 dyn/cm📊 OPERA
Thermal Conductivity 133.582 mW/(m*K)📊 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 4 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 48.365 cm^3/mol📊 OPERA
Polarizability 19.174 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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