2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- (CAS 24634-61-5) — Citrus Non-olfactive Note Fragrance Ingredient

Citrus · Floral

2,_4-_Hexadienoic acid, potassium salt (1:1)_, (2E,_4E)_-

CAS 24634-61-5

Origin
synthetic
Note
Non-olfactive
IFRA
Use with awareness
Data as of: Apr 2026

What Is 2,_4-_Hexadienoic acid, potassium salt (1:1)_, (2E,_4E)_-?

2,4-Hexadienoic acid potassium salt is a synthetic compound primarily used as a preservative in food and cosmetics. Consumers may encounter it in processed foods, personal care products, and some household items. This ingredient helps prevent microbial growth, extending product shelf life while maintaining safety standards.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for use in regulated products
Potential irritant in high concentrations
CAS
24634-61-5
Formula
Mixture
MW
Variable
Odor Family
Citrus · Floral
Layer 1 · Enthusiast

What Does 2,_4-_Hexadienoic acid, potassium salt (1:1)_, (2E,_4E)_- Smell Like?

This compound is primarily functional rather than aromatic, with minimal odor impact in formulations. In pure form, it may present faint metallic or chemical notes that dissipate quickly. As a preservative, it’s used at concentrations well below olfactory detection thresholds, making its sensory contribution negligible in finished products.

Layer 2

2D Molecular Structure

Potassium (E,E)-hexa-2,4-dienoate

SMILES: [K+].C\C=C\C=C\C([O-])=O

Chemistry, Properties & Perfumer Guide

The Chemistry

2,4-Hexadienoic acid potassium salt is the potassium salt of sorbic acid, a polyunsaturated fatty acid. It’s produced synthetically through ketene chemistry, reacting crotonaldehyde with ketene to form the acid, followed by neutralization with potassium hydroxide. The (2E,4E)-configuration is most common in commercial preparations. This white, water-soluble powder dissociates in solution to exert antimicrobial activity through disruption of microbial cell membranes.

Physical & Chemical Properties

AppearanceWhite crystalline powder
SolubilityFreely soluble in water

Perfumer Guide

Note Position
Non-olfactive
Volatility
N/A
Blending
N/A
ApplicationTypical %RangeNotes
Cosmetics0.1-0.3%Up to 0.6%Preservative system component
Food0.05-0.2%Up to 0.3%Anti-mold agent

Classic Accords

Tip: Use in water-based systems where microbial protection is needed without affecting fragrance profile.

Alternatives & Comparisons

1
Potassium sorbate CAS 24634-61-5

More common food-grade form with identical antimicrobial properties.

2
Sodium benzoate CAS 532-32-1

Alternative preservative effective in acidic formulations.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted by IFRA – primarily used as preservative rather than fragrance ingredient.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

Evaluated as food additive; extensive safety data available through JECFA and EFSA.

Sustainability

Synthesized from petrochemical feedstocks with established industrial processes. While not renewable, it’s used at very low concentrations. Proper wastewater treatment is recommended due to potential aquatic toxicity at high concentrations.

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References

  1. EFSA Panel on Food Additives (2015). Re-evaluation of sorbic acid and its salts. EFSA Journal. EFSA Journal 13(6):4144

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

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Physicochemical Properties

DTXSID: DTXSID7027835

Physical Properties

Molecular Weight 150.218 g/mol🔬 EPA CompTox
Density 0.681 g/cm^3🔬 EPA CTX
Boiling Point 209 °C📊 OPERA
Melting Point 201.5 °C🔬 EPA CTX

Partition & Solubility

LogP (Octanol-Water) -1.79 Log10 unitless📊 OPERA
LogD (pH 5.5) -2.72 Log10 unitless📊 OPERA
LogD (pH 7.4) -4.57 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.81 Log10 unitless📊 OPERA
Water Solubility 0.02 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.331 mmHg📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 40.13 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 2 count💻 Computed
Aromatic Rings 0 count💻 Computed

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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