36309-62-3

Usage

Uses

Used in Polymer Industry:
2,4-Imidazolidinedione, 5-butyl-5-phenylis used as a cross-linking agent for improving the physical and chemical properties of polymers, such as their strength, durability, and heat resistance. This enhancement is crucial for the development of high-performance materials in various applications.
Used in Resin and Coating Production:
In the resin and coating industry, 2,4-Imidazolidinedione, 5-butyl-5-phenylis utilized as a raw material, contributing to the creation of resins and coatings with superior properties. Its inclusion in these products results in improved performance and durability.
Used as a Curing Agent in Thermosetting Resins:
2,4-Imidazolidinedione, 5-butyl-5-phenylis employed as a curing agent in the production of thermosetting resins, which are essential for various industrial applications due to their heat resistance and rigidity.
Used as a Flame Retardant in Plastics:
This chemical is also used as a flame retardant in plastics, providing an essential safety feature in products that require resistance to ignition and fire spread.
Used in Adhesives and Sealants:
2,4-Imidazolidinedione, 5-butyl-5-phenylis utilized in the formulation of adhesives and sealants, where its properties contribute to the creation of strong, durable, and heat-resistant bonding agents.
Used in Automotive Coatings:
In the automotive industry, 2,4-Imidazolidinedione, 5-butyl-5-phenyl- is used in coatings to enhance the durability and heat resistance of vehicle finishes, ensuring long-lasting protection and appearance.
It is important to handle 2,4-Imidazolidinedione, 5-butyl-5-phenylwith care due to its potential to cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be implemented when working with this chemical to ensure the well-being of individuals and the environment.

Upstream product

• 343596-01-0 2-Phenyl-2-trimethylsilanyloxy-hexanenitrile 
• 1009-14-9 phenyl butyl ketone 
• 506-87-6 ammonium carbonate 
• 693-04-9 butyl magnesium bromide 
• 100-47-0 benzonitrile 
• 109-72-8 n-butyllithium 
• 111068-23-6 2-Hydroxy-2-phenyl-hexanenitrile 

Relevant academic research and scientific papers

Synthesis, structure, and solvatochromic properties of pharmacologically active 5-substituted 5-phenylhydantoins

A series of 5-substituted 5-phenylhydantoins was synthesized and their UV absorption spectra were recorded in the region 200-400 nm in selected solvents of different polarity. The effects of solvent dipolarity/polarizability and solvent-solute hydrogen-bonding interactions were analyzed by means of the linear solvation energy relationship concept proposed by Kamlet and Taft. The lipophilicities of the investigated hydantoins were estimated by calculation of their log P values. The quantitative relationship between the ratio of the contributions of specific solvent interactions and the corresponding lipophilicity parameter is discussed. The correlation equations were combined with the corresponding ED50 values and different physicochemical parameters to generate new equations that demonstrate the reasonable relationships between solute-solvent interactions and the structure-activity parameters. In order to determine a spectroscopic assignment of the absorption bands in different solvents, quantum chemical calculations were done. Springer-Verlag 2011.

Modified Bucherer-Bergs reaction for the one-pot synthesis of 5,5′-disubstituted hydantoins from nitriles and organometallic reagents

Diverse sets of 5,5′-disubstituted hydantoins can conveniently be made in moderate to good yields (40-92%) by a one-pot process involving treatment of aromatic, heteroaromatic or aliphatic nitriles with an organometallic reagent (RLi or RMgX) followed by

Effects of log P and phenyl ring conformation on the binding of 5- phenylhydantoins to the voltage-dependent sodium channel

Binding to the neuronal voltage-dependent sodium channel (NVSC) was evaluated for 12 5-phenylhydanteins which systematically varied either log P and/or 5-phenyl ring orientation. The linear correlation of log P with in vitro sodium channel binding activit