Compound Profile

4-Iodotoluene 

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4-Iodotoluene is a chemical compound that is used in various industries, including pharmaceuticals, agrochemicals, and materials science. It is commonly employed as a building block in the synthesis of various organic compounds due to its versatile reactivity. Despite its seemingly niche application, 4-Iodotoluene plays a significant role in everyday life as it is a crucial component in the production of numerous consumer products. Its importance lies in its ability to serve as a foundational element in the creation of a wide range of chemical substances that ultimately impact various aspects of our daily routines, from medications to pesticides to plastics.

Table of Contents:

💡  Commercial Applications

4-Iodotoluene, a chemical compound consisting of a toluene molecule with an iodine atom substitution, has a variety of commercial and industrial applications. It is commonly utilized as an intermediate in the manufacturing of dyes, pharmaceuticals, and other specialty chemicals. Additionally, it is employed in the synthesis of various organic compounds due to its reactivity and ability to undergo substitution reactions.

In the realm of drug and medication applications, 4-Iodotoluene plays a vital role in the production of certain pharmaceuticals. It is utilized as a key building block in the synthesis of different drugs, including antiseptics, antibiotics, and other medicinal compounds. Its ability to undergo functional group transformations makes it a valuable component in drug development processes, contributing to the advancement of pharmaceutical research and innovation.

⚗️  Chemical & Physical Properties

4-Iodotoluene is a colorless liquid with a strong aromatic odor. It is commonly used as an intermediate in the synthesis of various organic compounds due to its reactivity.

The molar mass of 4-Iodotoluene is approximately 218.05 g/mol, and its density is around 1.72 g/cm³. In comparison, common food items such as sugar and salt have molar masses that range from approximately 58.08 g/mol to 58.44 g/mol and densities that range from approximately 1.59 g/cm³ to 2.14 g/cm³.

The melting point of 4-Iodotoluene is around -39°C, and its boiling point is approximately 202°C. These values differ significantly from common food items such as butter and chocolate, which have melting points and boiling points closer to room temperature.

4-Iodotoluene is sparingly soluble in water and has a low viscosity. In contrast, common food items like sugar and salt are highly soluble in water and have a wide range of viscosities depending on their concentration.

🏭  Production & Procurement

4-Iodotoluene is primarily produced through the iodination of toluene, a process that involves the substitution of a hydrogen atom on the benzene ring with an iodine atom. This reaction typically takes place in the presence of a catalyst, such as iodine or an iron salt, under specific temperature and pressure conditions.

In order to procure 4-Iodotoluene, one must generally look to specialty chemical suppliers or manufacturers that have the capability to produce this compound on a commercial scale. The compound may be purchased in varying quantities, typically ranging from small laboratory sizes to bulk quantities for industrial applications.

Transportation of 4-Iodotoluene is typically done in sealed containers, such as drums or bottles, to prevent exposure to air and moisture which could lead to degradation. The compound is usually shipped in compliance with regulations for hazardous materials, with proper labeling and documentation to ensure safe handling during transit.

Overall, the production and procurement of 4-Iodotoluene involves specialized chemical processes and handling procedures to ensure the quality and safety of the compound for its various applications in research, pharmaceuticals, and other industries.

⚠️  Safety Considerations

Safety considerations for 4-Iodotoluene should be taken seriously due to its potential hazards. This chemical is flammable and can release harmful vapors when exposed to heat or flames. Additionally, 4-Iodotoluene may cause skin and eye irritation upon contact. It is important to handle this substance with care in a well-ventilated area and wear appropriate personal protective equipment, such as gloves and safety goggles, to minimize the risk of exposure.

Hazard statements for 4-Iodotoluene include: “Highly flammable liquid and vapor”, “Causes skin irritation”, and “Causes serious eye irritation.” These statements indicate the potential dangers associated with this chemical and the importance of taking precautions when working with it. It is crucial to follow safety guidelines and proper handling procedures to protect against these hazards and minimize the risk of harm.

Precautionary statements for 4-Iodotoluene include: “Keep away from heat, sparks, open flames, and hot surfaces”, “Avoid breathing vapor or mist”, and “Wear protective gloves and eye protection.” These statements provide guidance on how to safely handle this chemical and reduce the likelihood of accidents or injuries. By following these precautions, individuals can mitigate the risks associated with 4-Iodotoluene exposure and ensure a safe working environment.

🔬  Potential Research Directions

Research on 4-Iodotoluene, a halogenated aromatic compound, is still in its nascent stage. One potential direction for investigation could involve exploring its uses as a precursor in organic synthesis. Additionally, researchers may be interested in studying its reactivity towards different functional groups to uncover potential applications in medicinal chemistry or materials science.

Another avenue of research could focus on the environmental impact of 4-Iodotoluene. This could involve studying its stability, degradation pathway, and potential toxicity to assess its risk to ecosystems and human health. Understanding these factors is crucial for developing strategies for environmental remediation and regulatory policies.

Furthermore, research could be directed towards enhancing the synthesis methods of 4-Iodotoluene to improve efficiency, yield, and selectivity. This could involve exploring new catalytic systems, reaction conditions, or alternative precursors to streamline the production process. Developing more sustainable and cost-effective synthetic routes could enable greater utilization of 4-Iodotoluene and its derivatives in various industrial applications.

Lastly, investigations into the biological activity of 4-Iodotoluene and its derivatives could open up new possibilities for drug discovery and development. Understanding their interactions with biological targets, mechanisms of action, and potential therapeutic benefits could lead to the identification of novel drug candidates with improved efficacy and reduced side effects. This area of research holds promise for the discovery of new treatments for various diseases.

One similar compound to 4-Iodotoluene is 3-Iodotoluene, which differs from the former by the position of the iodine atom on the toluene ring. This compound is also an iodine-substituted derivative of toluene, possessing similar chemical properties and reactivity as 4-Iodotoluene due to the shared benzene ring structure. 3-Iodotoluene can be used in organic synthesis as a starting material for various chemical reactions.

Another analogous compound to 4-Iodotoluene is 4-Bromotoluene, where the iodine atom is replaced with a bromine atom on the toluene ring. Despite the substitution of halogens, 4-Bromotoluene exhibits comparable physical and chemical properties to 4-Iodotoluene due to the similar electronegativities and sizes of iodine and bromine. This compound is used in various organic reactions, serving as a building block for the synthesis of more complex molecules.

Additionally, 4-Fluorotoluene is a related compound to 4-Iodotoluene, with a fluorine atom substituting the iodine atom on the toluene ring. Although fluorine is smaller and more electronegative than iodine, 4-Fluorotoluene shares some chemical properties with 4-Iodotoluene, making it a valuable compound in organic chemistry research. 4-Fluorotoluene can participate in a variety of reactions, offering opportunities for the synthesis of diverse organic compounds.

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