3-Hydroxypropionic acid

3-Hydroxypropionic acid, a naturally occurring compound found in various living organisms, holds significance in everyday life due to its potential applications in the production of biodegradable plastics, biofuels, and other sustainable chemicals. With the increasing global focus on environmental sustainability and transitioning away from traditional petrochemical-based products, the development and utilization of 3-Hydroxypropionic acid as a renewable resource has the potential to have a meaningful impact on various industries and the environment at large.

Table of Contents:

💡  Commercial Applications

3-Hydroxypropionic acid, also known as malic acid, plays a crucial role in various commercial and industrial applications. It is commonly used in the production of biodegradable polymer poly(3-hydroxypropionate) which has potential applications in the manufacturing of biodegradable plastics. Additionally, 3-Hydroxypropionic acid is utilized in the synthesis of various pharmaceuticals, herbicides, and insecticides, making it a valuable compound in the chemical industry. Its properties as a precursor for the synthesis of valuable products have sparked interest in the development of sustainable processes for its production.

In the realm of drug and medication applications, 3-Hydroxypropionic acid shows promise as a potential therapeutic agent for various medical conditions. Studies have suggested its anti-inflammatory properties that could be beneficial in the treatment of inflammatory diseases such as rheumatoid arthritis. Furthermore, its role as a precursor for the synthesis of various pharmaceutical compounds opens up avenues for the development of novel drugs targeting specific biological pathways. The potential medicinal applications of 3-Hydroxypropionic acid highlight its versatility and importance in the pharmaceutical industry.

In conclusion, 3-Hydroxypropionic acid holds significant commercial and industrial value due to its diverse applications in the production of biodegradable polymers, pharmaceuticals, and other chemical products. Its potential as a therapeutic agent in the field of medicine further underscores its importance in advancing healthcare technologies. As research continues to uncover new applications for this compound, 3-Hydroxypropionic acid is poised to play a significant role in shaping various industries in the years to come.

⚗️  Chemical & Physical Properties

3-Hydroxypropionic acid, also known as beta-hydroxypropionic acid, is a colorless to light yellow liquid with a mild sour smell. It is commonly found in nature as a metabolic product of various microorganisms.

With a molar mass of 90.08 g/mol and a density of 1.22 g/cm^3, 3-Hydroxypropionic acid is similar in molar mass to acetic acid but has a slightly higher density. In comparison to common food items, it has a lower molar mass than table sugar but a higher density than milk.

3-Hydroxypropionic acid has a melting point of 9 to 11 °C and a boiling point of 206 °C. These properties make it a relatively low-melting and high boiling compound compared to common food items like butter and sugar, which have significantly higher melting points and lower boiling points.

This compound is highly soluble in water, forming a clear solution, and has a low viscosity. In comparison to common food items like salt and sugar, 3-Hydroxypropionic acid exhibits higher solubility in water but lower viscosity, making it easier to dissolve and mix with other substances.

🏭  Production & Procurement

3-Hydroxypropionic acid is primarily produced through microbial fermentation processes utilizing various microorganisms such as genetically engineered bacteria or yeast. These microorganisms are capable of converting renewable feedstocks, such as sugars, into 3-Hydroxypropionic acid through metabolic pathways.

The procurement of 3-Hydroxypropionic acid involves various methods, including extraction from fermentation broth or chemical synthesis. Extraction from fermentation broth typically involves separation and purification processes to obtain the desired product in high purity. Alternatively, chemical synthesis routes involve the use of precursor chemicals to produce 3-Hydroxypropionic acid.

Once produced or procured, 3-Hydroxypropionic acid can be transported in liquid form using appropriate containers or tanks. It is essential to ensure proper handling and storage conditions during transportation to maintain the integrity and quality of the product. Additionally, transportation routes must comply with safety regulations to prevent any risks or hazards associated with the handling of 3-Hydroxypropionic acid.

⚠️  Safety Considerations

Safety Considerations for 3-Hydroxypropionic acid:

When handling 3-Hydroxypropionic acid, it is important to wear appropriate personal protective equipment such as gloves, goggles, and a lab coat to prevent skin and eye irritation. It is also crucial to work in a well-ventilated area to avoid inhaling fumes and to minimize the risk of exposure through inhalation. Additionally, proper storage of 3-Hydroxypropionic acid in a cool, dry place away from incompatible substances is essential to prevent potential chemical reactions or spills that could lead to hazardous situations.

Hazard Statements for 3-Hydroxypropionic acid:

3-Hydroxypropionic acid may cause skin irritation and serious eye damage. It is harmful if swallowed, inhaled, or absorbed through the skin. This chemical can cause respiratory irritation and may be toxic to aquatic life with long-lasting effects. It is important to handle 3-Hydroxypropionic acid with caution and follow proper safety protocols to prevent adverse health effects and environmental harm.

Precautionary Statements for 3-Hydroxypropionic acid:

When working with 3-Hydroxypropionic acid, always wear protective gloves, eye protection, and a face mask to minimize exposure and prevent skin and respiratory irritation. Avoid inhaling fumes or vapors, and ensure proper ventilation in the working area. In case of skin contact, wash affected areas with soap and water. In case of eye contact, rinse eyes with water for several minutes while removing contact lenses if present. If swallowed, seek medical advice immediately and do not induce vomiting. Store 3-Hydroxypropionic acid in a tightly sealed container away from heat, sparks, and open flames.

🔬  Potential Research Directions

One potential research direction for 3-Hydroxypropionic acid is its application as a precursor for the production of various chemicals and materials. This includes polymers, solvents, and pharmaceutical compounds, highlighting its versatility as a building block in organic synthesis.

Another avenue of research could focus on optimizing the microbial production of 3-Hydroxypropionic acid through metabolic engineering techniques. This involves manipulating the metabolic pathways of microorganisms to enhance the efficiency and yield of 3-Hydroxypropionic acid production, which is essential for economic viability.

Furthermore, research on the potential industrial scale-up of 3-Hydroxypropionic acid production could be explored. This includes investigating fermentation conditions, downstream processing methods, and cost-effective strategies to make 3-Hydroxypropionic acid production more feasible for commercial applications.

One similar compound to 3-Hydroxypropionic acid is Lactic acid, also known as 2-Hydroxypropanoic acid. Both compounds have a hydroxy group attached to a carbon chain, with Lactic acid having the hydroxy group on the second carbon instead of the third. Lactic acid is found in sour milk and is produced in the muscles during intense exercise.

Another compound similar to 3-Hydroxypropionic acid is Hydroxybutyric acid, also known as 3-Hydroxybutanoic acid. This compound has an additional carbon in the carbon chain compared to 3-Hydroxypropionic acid, with the hydroxy group attached to the third carbon. Hydroxybutyric acid is a ketone body produced in the liver during fasting or prolonged exercise.

A third similar compound is Mandelic acid, also known as α-Hydroxyphenylacetic acid. This compound has a hydroxy group attached to a benzene ring, with a carboxylic acid group attached to the carbon chain. Mandelic acid is used in skincare products as an exfoliant and antibacterial agent due to its ability to penetrate the skin and unclog pores.

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