3-Methyladipic acid plays a significant role in everyday life as it is utilized in the production of polymers, specifically in the manufacturing of nylon. Nylon is a widely used synthetic polymer found in various consumer goods such as clothing, carpets, ropes, and bristles for brushes. Therefore, 3-Methyladipic acid is essential in enhancing the durability and flexibility of these everyday products, ultimately impacting the quality and functionality experienced by individuals in their daily lives.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
3-Methyladipic acid has several commercial and industrial applications. It is commonly used in the production of polymers, specifically as a monomer for the synthesis of various copolymers. Additionally, it can be utilized in the manufacturing of specialty chemicals and additives for a wide range of industries.
In the realm of drug and medication applications, 3-Methyladipic acid has been studied for its potential use in the treatment of metabolic disorders. Research has shown promising results in improving metabolic function and insulin sensitivity in animal studies. However, further clinical trials are required to determine its efficacy and safety in human subjects.
In conclusion, 3-Methyladipic acid offers diverse applications in both commercial and industrial settings, as well as potential therapeutic benefits in the field of medicine. Its unique properties and versatile nature make it a valuable compound for various industries and research purposes.
⚗️ Chemical & Physical Properties
3-Methyladipic acid is a white crystalline solid with no distinct odor. It is typically found in a powdered form and is non-volatile at room temperature. The compound is stable under normal conditions and does not easily decompose.
The molar mass of 3-Methyladipic acid is approximately 146.14 g/mol, with a density of around 1.4 g/cm³. In comparison to common food items, such as sugar and salt, 3-Methyladipic acid has a slightly higher molar mass and density. However, it is still considered a relatively light compound.
3-Methyladipic acid has a melting point of approximately 139-141°C and a boiling point of around 358-360°C. In comparison to common food items like butter and chocolate, 3-Methyladipic acid has a higher melting point and boiling point. This makes it more stable and less likely to undergo physical changes at higher temperatures.
3-Methyladipic acid is sparingly soluble in water, with a lower viscosity compared to common food items like honey and syrup. Its solubility in water is limited due to the non-polar nature of the compound, making it less likely to dissolve in aqueous solutions. The viscosity of 3-Methyladipic acid is relatively low, giving it a more fluid consistency than thicker food items.
🏭 Production & Procurement
3-Methyladipic acid is typically produced through the oxidation of m-xylene, a derivative of benzene. The process involves the reaction of m-xylene with nitric acid, resulting in the formation of 3-Methyladipic acid as a primary product.
3-Methyladipic acid can be procured through various chemical suppliers and manufacturers who specialize in producing organic acids. It is typically available in both solid and liquid forms, depending on the specific requirements of the end user. The acid can be transported in sealed containers or drums to ensure its safe delivery to the desired destination.
The transportation of 3-Methyladipic acid is typically conducted via road tanker trucks or rail tank cars, depending on the volume and distance of the shipment. It is important to follow proper handling and storage guidelines to prevent any potential hazards during transportation. Additionally, proper documentation and labeling are required to comply with regulatory standards.
⚠️ Safety Considerations
Safety Considerations for 3-Methyladipic acid:
3-Methyladipic acid is a chemical compound that must be handled with care due to its potential hazards. When working with this substance, it is important to wear appropriate personal protective equipment, such as gloves, goggles, and a lab coat, to prevent skin contact and inhalation. Proper ventilation should be maintained in the area where 3-Methyladipic acid is being used to minimize the risk of exposure.
In the event of accidental exposure to 3-Methyladipic acid, immediate action should be taken to prevent further harm. If skin contact occurs, the affected area should be washed thoroughly with soap and water. In case of eye contact, the eyes should be rinsed with water for at least 15 minutes while seeking medical attention. If 3-Methyladipic acid is inhaled, the individual should be moved to fresh air and monitored closely for any signs of distress.
Hazard Statements for 3-Methyladipic acid:
3-Methyladipic acid poses certain hazards that individuals should be aware of when working with this compound. Hazard statements for 3-Methyladipic acid include “Causes skin irritation,” “Causes serious eye irritation,” and “May cause respiratory irritation.” These statements indicate the potential risks associated with exposure to 3-Methyladipic acid and underscore the importance of following safety precautions.
Precautionary Statements for 3-Methyladipic acid:
To minimize the risks associated with 3-Methyladipic acid, it is important to take certain precautionary measures when handling this substance. Precautionary statements for 3-Methyladipic acid include “Wear protective gloves/eye protection/face protection,” “IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing,” and “IF INHALED: Remove person to fresh air and keep comfortable for breathing.” By adhering to these precautionary statements, individuals can reduce the likelihood of harm when working with 3-Methyladipic acid.
🔬 Potential Research Directions
One potential research direction for 3-Methyladipic acid could involve investigating its potential as a building block for the synthesis of novel polymers with unique properties. These polymers could be explored for applications in various fields such as materials science, biotechnology, and pharmaceuticals.
Another research avenue could focus on studying the environmental fate and degradation pathways of 3-Methyladipic acid. Understanding how this compound behaves in different environmental conditions can provide valuable insights into its potential impact on ecosystems and human health. This research could also inform efforts to develop more sustainable processes for the production and use of 3-Methyladipic acid.
Furthermore, exploring the reactivity of 3-Methyladipic acid with other compounds could lead to the discovery of new chemical reactions and applications. Investigating its interactions with various reagents, catalysts, or biomolecules could uncover novel synthetic pathways or potential therapeutic targets. This line of research has the potential to expand our knowledge of organic chemistry and contribute to the development of innovative technologies.
🧪 Related Compounds
One similar compound to 3-Methyladipic acid is 2-Methyladipic acid. This compound is structurally related to 3-Methyladipic acid, but differs in the location of the methyl group on the carbon chain. In 2-Methyladipic acid, the methyl group is attached to the second carbon atom of the adipic acid chain.
Another compound similar to 3-Methyladipic acid is 4-Methyladipic acid. This compound also shares the same basic structure as 3-Methyladipic acid, but the methyl group is attached to the fourth carbon atom of the adipic acid chain. This slight structural difference can lead to variations in the chemical properties and behavior of the compound.
A further compound exhibiting similarity to 3-Methyladipic acid is Dimethyladipic acid. This compound contains two methyl groups attached to the adipic acid chain, rather than just one as in 3-Methyladipic acid. This difference in structure can result in altered chemical reactivity and physical properties compared to the single methyl group-containing compound.
