2,3-Dibromopropanol 

2,3-Dibromopropanol is a chemical compound that has various practical applications in everyday life. It is commonly used in the manufacturing of pharmaceuticals as well as in the production of flame retardants and pesticides. Additionally, it is utilized in the synthesis of other organic compounds that are essential in a wide range of industries, including healthcare, agriculture, and manufacturing. Overall, 2,3-Dibromopropanol plays a significant role in the development and production of numerous consumer products that impact our daily lives.

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💡  Commercial Applications

2,3-Dibromopropanol, also known as 1-bromo-2,3-propanediol, finds commercial applications in the manufacturing of flame retardants and surfactants. It is commonly used as a flame retardant in plastics and textiles due to its ability to inhibit combustion and reduce fire hazards.

In the industrial sector, 2,3-Dibromopropanol serves as a key intermediate in the synthesis of various organic compounds. It is utilized in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactivity and versatile nature make it a valuable building block in the chemical industry.

While mostly known for its commercial and industrial uses, 2,3-Dibromopropanol also has significance in the pharmaceutical field. It can be employed as an intermediate in the synthesis of certain drugs and medications. Its chemical properties make it suitable for incorporation into pharmaceutical formulations for various therapeutic purposes.

⚗️  Chemical & Physical Properties

2,3-Dibromopropanol is a colorless liquid with a sweet, pungent odor. It is a highly flammable substance that should be handled with care due to its potential hazards.

With a molar mass of 213.90 g/mol and a density of 2.019 g/cm3, 2,3-Dibromopropanol is relatively heavier compared to common food items like sugar (molar mass of 342.30 g/mol) and water (density of 1 g/cm3).

2,3-Dibromopropanol has a melting point of -50°C and a boiling point of 125°C. These values are considerably lower than many common food items like butter (melting point around 30-35°C) and water (boiling point of 100°C).

This compound is sparingly soluble in water and exhibits a high viscosity. In comparison, common food items like sugar dissolve readily in water and have a lower viscosity, making them easier to mix and handle.

🏭  Production & Procurement

2,3-Dibromopropanol is typically produced through the bromination of 1,3-diol compounds. This reaction involves the addition of elemental bromine to the C2 and C3 positions of the diol, resulting in the formation of 2,3-Dibromopropanol as the primary product. The process is usually carried out in the presence of a suitable solvent and catalyst under controlled conditions to ensure high selectivity and yield.

The procurement of 2,3-Dibromopropanol can be achieved through various chemical suppliers or specialty manufacturers. The compound is commonly available in liquid form and is often stored and transported in sealed containers to prevent degradation or contamination. Due to its sensitive nature, proper handling, storage, and shipping practices are essential to maintain the integrity of the product and ensure its safe delivery to end-users or industrial customers.

Transportation of 2,3-Dibromopropanol is typically carried out in accordance with established regulations for the handling and shipment of hazardous chemicals. The compound may be classified as a hazardous material due to its potential toxicity and reactivity, requiring special precautions during transportation. Proper labeling, packaging, and documentation are necessary to comply with legal requirements and ensure the safety of personnel involved in the transportation process.

⚠️  Safety Considerations

Safety considerations for 2,3-Dibromopropanol include its potential to cause skin and eye irritation upon contact. It is also flammable and may release harmful fumes when exposed to heat or fire. Proper ventilation and personal protective equipment should be used when handling this compound to minimize the risk of exposure and adverse health effects.

In terms of hazard statements, 2,3-Dibromopropanol is classified as harmful if swallowed, causing irritation to the respiratory system and skin. It may also cause damage to organs through prolonged or repeated exposure. Additionally, it is toxic to aquatic life and should be handled with caution to prevent environmental harm.

Precautionary statements for 2,3-Dibromopropanol include recommendations to wear protective gloves, clothing, and eye protection when handling the compound. It should be kept away from heat, sparks, and open flames due to its flammable nature. Proper storage and disposal methods should be followed to minimize the risk of adverse effects on human health and the environment.

🔬  Potential Research Directions

One potential research direction for 2,3-Dibromopropanol is its role as a building block in the synthesis of various organic compounds. Investigating its reactivity with different functional groups could lead to the development of novel chemical reactions.

Another promising avenue of research is the study of the biological activity of 2,3-Dibromopropanol. Understanding its potential as a pharmaceutical agent or its toxicity profile could provide valuable insights for drug discovery and development.

Furthermore, exploring the environmental fate and impact of 2,3-Dibromopropanol is a critical research area. Investigating its degradation pathways, persistence in the environment, and potential health risks can contribute to the development of sustainable practices for its use and disposal.

One similar compound to 2,3-Dibromopropanol is 1,2-Dibromopropanol, which has a molecular structure consisting of a propyl chain with two bromine atoms attached at the first and second carbon positions. This compound is also a colorless liquid that is soluble in water and commonly used in various chemical reactions and organic synthesis processes.

Another similar compound is 1,3-Dibromopropanol, which shares the same propyl backbone but has bromine atoms attached at the first and third carbon positions. Like 2,3-Dibromopropanol, this compound is also used in organic synthesis and chemical reactions due to its reactivity and utility in creating various chemical compounds.

2,2-Dibromopropanol is another similar compound, with a molecular structure featuring two bromine atoms attached to the second carbon position of a propyl chain. This compound exhibits similar physical and chemical properties to 2,3-Dibromopropanol and is often used in the same applications due to its comparable reactivity and usefulness in organic synthesis processes.

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