Compound Profile

3-Fluorophenol 

0

3-Fluorophenol, a derivative of phenol in which a hydrogen atom on the aromatic ring is replaced by a fluorine atom, is a compound of growing importance in various industries due to its unique chemical properties. Despite its niche applications, 3-Fluorophenol plays a significant role in everyday life.

One notable application of 3-Fluorophenol is in the pharmaceutical industry. It is utilized as a building block in the synthesis of various drugs and pharmaceutical compounds. Its fluorine atom imparts desirable properties to these molecules, such as increased metabolic stability and improved bioavailability, making it a valuable tool in drug discovery and development.

Additionally, 3-Fluorophenol is employed in the production of agrochemicals, such as herbicides and insecticides, due to its ability to enhance the biological activity of these compounds. This utilization contributes to the efficacy of agricultural products, ultimately benefiting food production and supply chain management.

Moreover, 3-Fluorophenol is also utilized in the manufacture of advanced materials, such as specialty polymers and coatings. These materials find applications in various consumer products, including electronics, textiles, and packaging, enhancing their performance and durability.

In conclusion, while 3-Fluorophenol may not be a household name, its impact on everyday life is undeniable. From pharmaceuticals to agriculture to consumer goods, this compound plays a crucial role in advancing various industries and improving the quality of products we interact with on a daily basis.

Table of Contents:

💡  Commercial Applications

3-Fluorophenol, a chemical compound with the molecular formula C6H5FO, has several commercial and industrial applications. It is commonly used as a precursor in the manufacture of various pharmaceuticals, agrochemicals, and dyes. Additionally, 3-Fluorophenol is utilized as an intermediate in the production of organic compounds and in the synthesis of fine chemicals.

In terms of drug and medication applications, 3-Fluorophenol is frequently employed as a building block in the pharmaceutical industry. It serves as a key starting material in the synthesis of numerous active pharmaceutical ingredients (APIs) and drug molecules. Furthermore, 3-Fluorophenol plays a crucial role in the development of medications for various therapeutic purposes, including antivirals, antibiotics, and anti-inflammatory drugs.

Due to its versatile properties and broad utility, 3-Fluorophenol has become a valuable asset in the field of chemical research and development. Its significance in both commercial and industrial settings underscores its importance as a foundational compound in the synthesis of a wide range of products. As researchers continue to explore new applications for 3-Fluorophenol, its potential for further advancements in various sectors remains promising.

⚗️  Chemical & Physical Properties

3-Fluorophenol is a colorless crystalline solid with a characteristic sweet odor. The compound is commonly used in organic synthesis and as a building block for pharmaceuticals due to its unique chemical properties.

With a molar mass of approximately 126.11 g/mol and a density of about 1.37 g/cm³, 3-Fluorophenol is heavier than common food items like water (molar mass of 18.02 g/mol, density of 1 g/cm³) and sugar (molar mass of 342.3 g/mol, density of 1.59 g/cm³).

3-Fluorophenol has a melting point of 30-33°C and a boiling point of 174-176°C. In comparison to common food items like butter (melting point of 32-35°C, boiling point above 100°C) and chocolate (melting point of 34-38°C, boiling point above 100°C), 3-Fluorophenol exhibits relatively lower melting and boiling points.

The compound is sparingly soluble in water and exhibits low viscosity. This contrasts with common food items like salt (highly soluble in water) and honey (high viscosity), indicating that 3-Fluorophenol has different solubility and viscosity properties in comparison.

🏭  Production & Procurement

Production of 3-Fluorophenol typically involves the reaction of phenol with a fluorinating agent, such as bromine trifluoride or hydrofluoric acid. This results in the substitution of a hydrogen atom on the phenol ring with a fluorine atom, yielding 3-Fluorophenol as the final product.

Procurement of 3-Fluorophenol can be achieved through various chemical suppliers or manufacturers who specialize in the production of fluorinated organic compounds. It is commonly available in both bulk quantities for industrial use and smaller quantities for research purposes. Transportation of 3-Fluorophenol is typically done in sealed containers, following regulations for the safe handling and transportation of hazardous chemicals.

Upon arrival, 3-Fluorophenol should be stored in a cool, dry place away from sources of heat or ignition. Proper labeling and documentation of the chemical should be maintained to ensure safe handling and traceability. It is important to follow proper disposal procedures for any unused or waste material containing 3-Fluorophenol to prevent environmental contamination.

⚠️  Safety Considerations

Safety Considerations for 3-Fluorophenol:

When handling 3-Fluorophenol, it is important to take precautions to avoid exposure to this hazardous substance. 3-Fluorophenol is corrosive and can cause skin and eye irritation upon contact. It is also flammable and may release toxic fumes when heated or exposed to fire. Therefore, it is essential to wear appropriate personal protective equipment, such as gloves, goggles, and a lab coat, when working with this compound.

Due to its hazardous nature, 3-Fluorophenol should be stored in a well-ventilated area away from sources of heat or ignition. It is also important to handle this chemical in a fume hood to minimize the risk of inhalation of toxic vapors. In case of accidental exposure, it is recommended to flush the affected area with plenty of water and seek medical attention if necessary. Additionally, proper waste disposal procedures should be followed to prevent environmental contamination.

Hazard Statements for 3-Fluorophenol:

3-Fluorophenol is classified as a hazardous substance that can cause severe skin and eye irritation. It is also flammable and may release toxic fumes when exposed to heat or fire. Therefore, it is important to handle this compound with caution and follow proper safety protocols to minimize the risk of harm.

Precautionary Statements for 3-Fluorophenol:

When working with 3-Fluorophenol, it is important to wear appropriate personal protective equipment, such as gloves, goggles, and a lab coat, to minimize the risk of exposure. It is also essential to work in a well-ventilated area, such as a fume hood, to prevent inhalation of toxic vapors. In case of accidental exposure, it is recommended to flush the affected area with plenty of water and seek medical attention if necessary. Additionally, proper waste disposal procedures should be followed to prevent environmental contamination.

🔬  Potential Research Directions

One potential research direction for 3-Fluorophenol is its use as a building block in the synthesis of complex organic molecules. The fluorine atom can introduce unique physical and chemical properties to the resulting compounds, making them valuable for various applications in pharmaceuticals, materials science, and agrochemicals.

Another area of interest could be exploring the reactivity of 3-Fluorophenol towards different reagents and conditions to discover new reaction pathways and transformation methods. Understanding the mechanisms of these reactions can provide insights into the fundamental behavior of fluoroaromatic compounds and expand the synthetic toolbox available to organic chemists.

Additionally, investigations into the environmental fate and toxicity of 3-Fluorophenol may be warranted to assess its potential impact on human health and the ecosystem. Studies could focus on its biodegradability, bioaccumulation potential, and interactions with other pollutants to inform regulatory decisions and pollution control strategies.

One similar compound to 3-Fluorophenol is 4-Fluorophenol, which has a molecular structure identical to that of 3-Fluorophenol except for the position of the fluorine atom on the phenol ring. This subtle difference in positioning can lead to variations in chemical reactivity and biological activity.

Another related compound is 2-Fluorophenol, which also shares a similar molecular structure to 3-Fluorophenol but with the fluorine atom located at a different position on the phenol ring. Despite this difference, 2-Fluorophenol exhibits comparable physical and chemical properties to 3-Fluorophenol due to their shared core structure.

A further compound akin to 3-Fluorophenol is 2,4-Difluorophenol, which contains two fluorine atoms attached to the phenol ring. This compound presents increased molecular complexity compared to 3-Fluorophenol, potentially resulting in altered chemical and biological behaviors. The presence of multiple fluorine atoms can lead to enhanced interactions with other molecules, influencing its overall reactivity.

Related Articles

How Metalloids Power Innovation Across the Modern Economy

Wedged between metals and nonmetals on the periodic table, the metalloids are...

Lanthanides at the Core of Modern Technology

Tucked away at the bottom of the periodic table, the lanthanides—or rare...

Mesitylene

As we navigate the complex landscape of modern chemistry, certain compounds stand...

5alpha-Androstane-3beta,17beta-diol

5alpha-Androstane-3beta,17beta-diol, also known as 5-androstenediol, is a hormone produced naturally in the...

You cannot copy content of this page