Compound Profile

3-Bromopropionic acid 

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3-Bromopropionic acid is a chemical compound that may seem esoteric to the layperson, but it plays a crucial role in various industries and applications that impact everyday life. This compound is commonly used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also employed in research laboratories for its ability to serve as a precursor in the synthesis of more complex molecules. In addition, 3-Bromopropionic acid is utilized in the manufacturing of polymers and materials, contributing to the development of everyday products such as plastics, coatings, and adhesives. Overall, the significance of this compound lies in its widespread application across diverse sectors that ultimately influence the quality and functionality of numerous consumer goods and services.

Table of Contents:

💡  Commercial Applications

3-Bromopropionic acid, also known as β-bromopropionic acid, finds various commercial and industrial applications due to its versatile chemical properties. It is commonly used in the synthesis of pharmaceuticals, agrochemicals, and dyes. Additionally, it is utilized as a reagent in organic synthesis to introduce the bromo group into various organic compounds.

In the realm of drug and medication applications, 3-Bromopropionic acid plays a crucial role as an intermediate in the synthesis of pharmaceutical compounds. It is used in the production of certain drugs that target specific biological pathways or receptors in the human body. Furthermore, it is employed in the development of new medications with potential therapeutic benefits for various medical conditions.

The utilization of 3-Bromopropionic acid extends to the pharmaceutical industry where it is an essential component in the synthesis of active pharmaceutical ingredients (APIs). This compound serves as a building block for the creation of drugs that exhibit specific biological activities or pharmacological effects. Its incorporation into drug molecules enables the development of novel therapies for treating diverse health conditions.

⚗️  Chemical & Physical Properties

3-Bromopropionic acid is a colorless to pale yellow liquid with a pungent odor. It is known to have a sharp, vinegar-like smell that can be detected even at low concentrations.

With a molar mass of approximately 138.99 g/mol and a density of 1.68 g/cm³, 3-Bromopropionic acid is heavier than common food items like water (molar mass: 18.02 g/mol, density: 1.00 g/cm³) and sugar (molar mass: 342.30 g/mol, density: 1.59 g/cm³).

The melting point of 3-Bromopropionic acid is around -18°C, while its boiling point is approximately 196-197°C. These values differ significantly from common food items such as butter (melting point: 32-35°C, boiling point: 150-180°C) and salt (melting point: 801°C, boiling point: 1,413°C).

3-Bromopropionic acid is moderately soluble in water and has a relatively high viscosity compared to common food items. It forms a clear, colorless solution when added to water, but its viscosity is noticeably higher than that of substances like vinegar or lemon juice.

🏭  Production & Procurement

3-Bromopropionic acid, also known as beta-bromopropionic acid, is primarily produced through the reaction between propionic acid and bromine. This chemical reaction typically takes place under controlled conditions in the presence of a catalyst, yielding the desired product as the end result. The purification process involves various techniques to ensure the purity of the final 3-Bromopropionic acid product.

Procurement of 3-Bromopropionic acid can be achieved through chemical suppliers who specialize in the production and distribution of fine chemicals. The compound is typically available in varying quantities, ranging from small laboratory quantities to bulk quantities for industrial applications. Transportation of 3-Bromopropionic acid is carried out following strict regulations regarding the handling and shipping of hazardous chemicals, ensuring safety throughout the transportation process.

When procuring 3-Bromopropionic acid, it is crucial to adhere to safety guidelines provided by regulatory authorities to prevent any potential hazards during storage and handling. Proper storage conditions, such as storing in a dry and well-ventilated area away from incompatible substances, are necessary to maintain the integrity of the compound. Additionally, the labeling and documentation of 3-Bromopropionic acid shipments are essential to facilitate traceability and regulatory compliance throughout the procurement and transportation process.

⚠️  Safety Considerations

Safety considerations for 3-Bromopropionic acid include its corrosive nature, which can cause severe skin and eye irritation upon contact. It is also harmful if swallowed or inhaled, leading to respiratory distress and gastrointestinal issues. Special precautions should be taken when handling this chemical, such as wearing appropriate personal protective equipment, working in a well-ventilated area, and avoiding direct skin contact.

Hazard statements for 3-Bromopropionic acid include “Causes severe skin burns and eye damage” and “Toxic if swallowed or inhaled.” These statements highlight the potential dangers associated with this chemical, emphasizing the importance of handling it with care and following proper safety protocols. It is crucial to be aware of these hazards when working with 3-Bromopropionic acid to prevent accidents and minimize risks to health.

Precautionary statements for 3-Bromopropionic acid recommend wearing protective gloves, clothing, eye protection, and face protection to avoid skin and eye contact. It is advised to work in a well-ventilated area or use a fume hood to prevent inhalation of the chemical. In case of contact, thorough washing with water and seeking medical attention is necessary. Proper storage and disposal methods should also be followed to prevent accidental exposure and environmental contamination. Overall, strict adherence to these precautionary measures is crucial to ensure safe handling of 3-Bromopropionic acid and minimize potential risks to health and safety.

🔬  Potential Research Directions

One potential research direction for 3-Bromopropionic acid includes its use in organic synthesis as a starting material for the preparation of various compounds. The reactivity of the bromine atom in 3-Bromopropionic acid allows for the introduction of new functional groups, making it a versatile building block for the creation of complex molecules.

Another area of interest in the study of 3-Bromopropionic acid is its potential as a pharmaceutical intermediate. Researchers are exploring its role in the synthesis of biologically active molecules that could have applications in the development of new drugs. By modifying the structure of 3-Bromopropionic acid, new compounds with enhanced pharmacological properties may be discovered.

Additionally, the investigation of the toxicological properties of 3-Bromopropionic acid is a pressing research direction. Understanding its potential effects on human health and the environment is crucial for assessing its safety in various applications. This research may involve studies on its metabolism, bioaccumulation, and potential risks associated with exposure.

One similar compound to 3-Bromopropionic acid is 4-Bromobutyric acid. This compound has a molecular structure similar to 3-Bromopropionic acid, with an additional carbon atom in the alkyl chain. This structural similarity results in similar chemical properties and reactivity between the two compounds.

Another similar compound is 2-Bromopropionic acid. With a molecular structure identical to 3-Bromopropionic acid but differing in the position of the bromine atom, 2-Bromopropionic acid exhibits similar chemical properties and reactions. The only difference lies in the positional isomerism of the bromine atom in the alkyl chain.

Additionally, 3-Iodopropionic acid is a compound closely related to 3-Bromopropionic acid. This compound substitutes the bromine atom with an iodine atom, resulting in a similar molecular structure with different halogen substitution. The similarities in structure lead to comparable chemical behavior and reactivity between the two compounds.

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