2-Chlorotoluene 

2-Chlorotoluene is a chemical compound that is primarily used in the production of various industrial products such as dyes, pesticides, and pharmaceuticals. While not directly relevant to everyday life for most individuals, 2-Chlorotoluene plays a crucial role in the manufacturing processes of numerous consumer goods that we use on a daily basis. Its versatility and importance in various industries make it an essential component in the global economy.

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💡  Commercial Applications

2-Chlorotoluene is primarily used in commercial and industrial applications such as in the production of pesticides, dyes, and other chemicals. It is also used as a solvent, in the manufacturing of pharmaceuticals, and as an intermediate in the synthesis of various compounds.

In terms of drug and medication applications, 2-Chlorotoluene is not commonly used. Its potential for toxicity and harmful effects on human health make it unsuitable for use in pharmaceuticals. Its main uses lie in industrial processes rather than in the medical field.

⚗️  Chemical & Physical Properties

2-Chlorotoluene is a colorless liquid with a strong odor reminiscent of paint thinner. It is commonly used in the production of dyes, pharmaceuticals, and other chemicals.

With a molar mass of 126.59 g/mol and a density of 1.09 g/mL, 2-Chlorotoluene is heavier than common food items such as water and most fruits. Its density is similar to that of milk.

2-Chlorotoluene has a melting point of -50°C and a boiling point of 159°C. These values are significantly higher than those of common food items like butter and sugar, which have lower melting and boiling points.

While 2-Chlorotoluene is only slightly soluble in water, it has a higher viscosity compared to most common food items like juice or soda. Its solubility in water is much lower than that of sugar, salt, or vinegar, and its viscosity is more similar to oils and fats.

🏭  Production & Procurement

2-Chlorotoluene, a chemical compound commonly used in the production of dyes, pesticides, and pharmaceuticals, is typically produced through the chlorination of toluene. This process involves the reaction of toluene with chlorine gas in the presence of a catalyst, resulting in the formation of 2-Chlorotoluene as the primary product.

Once produced, 2-Chlorotoluene can be procured through various chemical suppliers or manufacturers. It is commonly transported and stored in sealed containers to prevent any leakage or spillage during transit. The compound is generally shipped in bulk quantities to industrial customers for further processing or utilization in various applications.

Chemical distributors and manufacturers play a key role in the procurement and supply chain of 2-Chlorotoluene, ensuring that the compound reaches its intended end users safely and efficiently. Proper handling and storage procedures are followed to maintain the integrity and quality of the product throughout the transportation process. Customers seeking to procure 2-Chlorotoluene should work with reputable suppliers to ensure compliance with safety regulations and quality standards.

⚠️  Safety Considerations

Safety considerations for 2-Chlorotoluene include the potential for skin and eye irritation upon contact. It is also important to note that 2-Chlorotoluene may be harmful if swallowed, inhaled, or absorbed through the skin. Proper handling procedures should be followed to minimize risk of exposure, such as wearing appropriate personal protective equipment, working in a well-ventilated area, and avoiding skin contact.

Hazard statements for 2-Chlorotoluene include “Causes skin irritation,” “Causes serious eye irritation,” and “Harmful if swallowed, inhaled, or absorbed through skin.” These statements highlight the potential risks associated with exposure to this chemical, emphasizing the need for caution when handling or working with 2-Chlorotoluene. It is important to be aware of these hazards and take appropriate measures to protect oneself and others from potential harm.

Precautionary statements for 2-Chlorotoluene include “Wear protective gloves/eye protection/face protection,” “IF ON SKIN: Wash with plenty of soap and water,” and “IF INHALED: Remove person to fresh air and keep comfortable for breathing.” These statements outline recommended safety measures to follow when working with 2-Chlorotoluene in order to minimize the risk of adverse health effects. By adhering to these precautions, individuals can help ensure their safety and well-being when handling this chemical.

🔬  Potential Research Directions

Potential research directions for 2-Chlorotoluene include investigating its environmental impact, particularly in terms of its persistence and bioaccumulation in various ecosystems.

Furthermore, studies could explore its potential health effects on humans and other organisms, including its toxicity, carcinogenicity, and potential for mutagenicity.

Additionally, research could focus on the development of environmentally friendly methods for the synthesis of 2-Chlorotoluene, as well as exploring its potential use as a starting material for the synthesis of other important chemical compounds.

One similar compound to 2-Chlorotoluene is 2-Bromotoluene, which has a similar molecular structure with a bromine atom instead of a chlorine atom attached to the toluene ring. This substitution results in a slightly different reactivity and physical properties when compared to 2-Chlorotoluene. Despite this difference, both compounds share similar chemical functionalities due to their common toluene backbone.

Another compound closely related to 2-Chlorotoluene is 2-Iodotoluene, where an iodine atom is substituted for the chlorine atom. This change in the halogen group can influence the compound’s reactivity and stability but still maintains the fundamental aromatic structure of the toluene molecule. Despite their differences, both 2-Chlorotoluene and 2-Iodotoluene exhibit similar chemical behaviors due to their shared structural similarities.

Lastly, 2-Fluorotoluene is a compound analogous to 2-Chlorotoluene but with a fluorine atom in place of the chlorine atom on the toluene ring. This substitution alters the compound’s physical and chemical properties, but still preserves the underlying aromatic structure of the molecule. Like 2-Chlorotoluene, 2-Fluorotoluene exhibits some similar chemical reactivity due to their common toluene framework.

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