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Ferric 2-ethylhexanoate
[CAS# 7321-53-1]

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Identification
ClassificationOrganic raw materials >> Organometallic salt
NameFerric 2-ethylhexanoate
Synonyms2-ethylhexanoate;iron(3+)
Molecular StructureCAS # 7321-53-1, Ferric 2-ethylhexanoate
Molecular FormulaFe(C8H15O2)3
Molecular Weight485.46
CAS Registry Number7321-53-1
EC Number230-794-6
SMILESCCCCC(CC)C(=O)[O-].CCCCC(CC)C(=O)[O-].CCCCC(CC)C(=O)[O-].[Fe+3]
Safety Data
Hazard Symbolssymbol symbol   GHS02;GHS08 Danger  Details
Risk StatementsH226-H304-H360D-H361  Details
Safety StatementsP203-P210-P233-P240-P241-P242-P243-P280-P301+P316-P303+P361+P353-P318-P331-P370+P378-P403+P235-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Reproductive toxicityRepr.1BH360D
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
SDSAvailable
up Discovery and Applications
Ferric 2-ethylhexanoate is an important coordination compound of iron that has garnered attention in various industrial applications, particularly in the fields of catalysis and materials science. This compound features ferric iron (Fe³⁺) coordinated with 2-ethylhexanoate, a fatty acid that imparts unique properties to the metal complex. The discovery of ferric 2-ethylhexanoate can be traced back to the exploration of metal fatty acid complexes, which are known for their utility in enhancing the performance of various chemical processes.

The synthesis of ferric 2-ethylhexanoate typically involves the reaction of ferric chloride with 2-ethylhexanoic acid. This reaction leads to the formation of the ferric complex, characterized by its solubility in organic solvents, which differentiates it from other iron compounds that are more insoluble in non-polar media. The ability of ferric 2-ethylhexanoate to solubilize in organic solvents makes it particularly valuable in applications where metal ions need to be incorporated into organic matrices or used as catalysts in organic reactions.

One of the primary applications of ferric 2-ethylhexanoate lies in the field of catalysis. This compound acts as a catalyst in various polymerization processes, including the production of polyurethanes and polyesters. The presence of ferric ions can facilitate the polymerization reaction by promoting the formation of free radicals or by participating directly in the reaction mechanism. As a result, ferric 2-ethylhexanoate enhances the efficiency of polymer production while also improving the properties of the resulting materials, such as their thermal stability and mechanical strength.

In addition to its catalytic applications, ferric 2-ethylhexanoate is also utilized in the formulation of coatings and paints. The compound serves as a drying agent, where it accelerates the curing process of alkyd resins and other binders used in surface coatings. The incorporation of ferric 2-ethylhexanoate in coating formulations results in faster drying times and improved film formation, making it an essential ingredient in the production of high-performance coatings for various substrates.

Moreover, the biocompatibility and non-toxicity of ferric 2-ethylhexanoate have led to its investigation in the biomedical field. Studies have explored its potential use as a contrast agent in magnetic resonance imaging (MRI) due to the paramagnetic properties of ferric ions. The compound’s ability to enhance imaging contrast may facilitate better visualization of tissues and blood flow in medical diagnostics.

Furthermore, ferric 2-ethylhexanoate is examined for its role in agriculture, where it may serve as a micronutrient source for plants. Iron is an essential element for plant growth, and the availability of ferric iron in a soluble form can improve iron uptake in crops, thereby enhancing their growth and yield.

In summary, ferric 2-ethylhexanoate is a versatile compound with significant applications across various industries, including catalysis, coatings, biomedicine, and agriculture. Its discovery and subsequent utilization stem from the unique properties imparted by the coordination of ferric ions with 2-ethylhexanoate, which enhance its solubility and reactivity. Ongoing research continues to explore new applications and formulations that leverage the beneficial characteristics of this compound.

References

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