Compound Profile

1,4-Diiodobenzene 

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1,4-Diiodobenzene is a chemical compound that is commonly used in various industrial applications, including in the production of pharmaceuticals, dyes, and advanced materials. This compound plays a crucial role in everyday life as it is a key building block for the manufacture of a wide range of products that are essential for modern living. Its significance lies in its versatility and utility in various industries, making it a valuable component in the production of items that we rely on daily.

Table of Contents:

💡  Commercial Applications

1,4-Diiodobenzene, also known as p-Diiodobenzene, plays a crucial role in various commercial and industrial applications. This compound is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and dyes. Additionally, it is utilized in the manufacturing of organic electronic materials and as a precursor in the preparation of liquid crystals.

In the realm of drug and medication applications, 1,4-Diiodobenzene serves as a starting material for the production of radiopharmaceuticals used in positron emission tomography (PET) imaging. Due to its ability to easily undergo various chemical reactions, this compound is employed in the creation of novel molecules with potential medical benefits. Furthermore, p-Diiodobenzene is utilized in the synthesis of contrast agents for magnetic resonance imaging (MRI) procedures.

⚗️  Chemical & Physical Properties

1,4-Diiodobenzene is a white crystalline solid with a faint odor similar to that of iodine. The compound is sparingly soluble in water but soluble in organic solvents, giving it a relatively low volatility.

With a molar mass of approximately 314.9 g/mol and a density of around 2.65 g/cm³, 1,4-Diiodobenzene is heavier than common food items such as sugar and salt. This compound possesses a higher molar mass and density compared to many organic molecules found in food.

1,4-Diiodobenzene has a melting point of about 96°C and a boiling point of approximately 283°C. These values are significantly higher than the melting and boiling points of most common food items, such as water and oils. This compound exhibits high thermal stability compared to food substances.

The compound is insoluble in water but soluble in organic solvents, exhibiting a low viscosity in solution. This property contrasts with many common food items, which tend to be more water-soluble and less viscous. The solubility in water and viscosity of 1,4-Diiodobenzene are distinct from those of typical food compounds.

🏭  Production & Procurement

1,4-Diiodobenzene is typically produced through the iodination of benzene using iodine and a suitable oxidizing agent, such as nitric acid. This reaction results in the substitution of two iodine atoms at the 1 and 4 positions on the benzene ring, yielding 1,4-Diiodobenzene as the final product.

The procurement of 1,4-Diiodobenzene usually involves purchasing the chemical from specialized chemical suppliers that produce and distribute a variety of organic compounds. The compound is typically available in liquid form, packaged in sealed containers to prevent leakage or contamination during transportation.

Once procured, 1,4-Diiodobenzene can be safely transported using standard chemical transportation methods, such as shipping containers or drums equipped with appropriate labeling and safety precautions. It is important to follow proper handling procedures to ensure the integrity of the compound and prevent any accidental exposure or spillage during transit.

⚠️  Safety Considerations

Safety considerations for 1,4-Diiodobenzene include its potentially harmful effects if inhaled, ingested, or if it comes into contact with the skin or eyes. It is important to handle this chemical with caution, using appropriate personal protective equipment such as gloves, goggles, and a lab coat. Additionally, 1,4-Diiodobenzene should be stored in a well-ventilated area, away from heat sources and incompatible materials.

Hazard statements for 1,4-Diiodobenzene include being harmful if swallowed, causing skin irritation, and being toxic to aquatic life with long-lasting effects. This chemical should be kept away from food, drink, and animal feed. In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical advice if necessary. Proper disposal methods should be followed to prevent environmental contamination.

Precautionary statements for 1,4-Diiodobenzene include wearing protective gloves and eye protection when handling this chemical. It should only be used in a well-ventilated area to avoid inhalation of fumes. In case of accidental exposure, seek medical advice immediately. Proper labeling of containers and thorough cleaning of equipment after use are also important safety measures to prevent accidents and exposure to this hazardous chemical.

🔬  Potential Research Directions

Potential research directions for 1,4-Diiodobenzene include exploring its utility as a building block in organic synthesis reactions due to its unique reactivity.

Additionally, studies could investigate the potential applications of 1,4-Diiodobenzene in the development of new materials with desirable properties.

Furthermore, research may focus on the environmental impact of 1,4-Diiodobenzene and strategies for its efficient synthesis to minimize waste.

1,4-Dibromobenzene is a compound similar in structure to 1,4-Diiodobenzene, with bromine atoms occupying the para positions on the benzene ring. This compound is commonly used in organic synthesis reactions and as a starting material for the preparation of various organic compounds. Due to the similar size and properties of iodine and bromine, 1,4-Dibromobenzene exhibits similar chemical reactivity to 1,4-Diiodobenzene.

1,4-Dichlorobenzene is another compound with a molecular structure analogous to that of 1,4-Diiodobenzene, except with chlorine atoms substituted at the para positions on the benzene ring. Like its iodine and bromine counterparts, 1,4-Dichlorobenzene is utilized in organic synthesis reactions and as a precursor for the production of various organic compounds. The presence of chlorine atoms results in unique chemical reactivity compared to 1,4-Diiodobenzene.

1,4-Difluorobenzene is a compound that shares structural similarities with 1,4-Diiodobenzene, except with fluorine atoms positioned at the para positions on the benzene ring. This compound is widely employed in organic chemistry for various synthetic processes and as a building block for the synthesis of diverse organic molecules. The presence of fluorine atoms imparts distinct chemical properties to 1,4-Difluorobenzene when compared to 1,4-Diiodobenzene.

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