CAS#4065-45-6: Discovering the Potential of 2-Hydroxy-4-methoxybenzophenone-5-sulfonic Acid

August 8, 2024

Title: CAS#4065-45-6: Discovering the Potential of 2-Hydroxy-4-methoxybenzophenone-5-sulfonic Acid

Abstract:
This article provides an in-depth exploration of the potential applications and properties of 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid, identified by the CAS number 4065-45-6. Divided into six key aspects, the article delves into its chemical structure, synthesis, physical and chemical properties, biological activities, environmental impact, and potential industrial applications. The findings suggest that this compound holds significant promise in various fields, including pharmaceuticals, cosmetics, and environmental protection.

1. Chemical Structure and Composition

2-Hydroxy-4-methoxybenzophenone-5-sulfonic acid, with the CAS number 4065-45-6, is a derivative of benzophenone. Its chemical structure consists of a benzene ring with a hydroxyl group (-OH) at the 2-position, a methoxy group (-OCH3) at the 4-position, and a sulfonic acid group (-SO3H) at the 5-position. This unique arrangement of functional groups contributes to its diverse chemical and biological properties.

The presence of the hydroxyl group makes the compound capable of forming hydrogen bonds, which is crucial for its solubility and reactivity. The methoxy group, on the other hand, imparts lipophilic properties, enhancing its compatibility with various organic solvents. Lastly, the sulfonic acid group provides the compound with acidic characteristics, making it reactive towards basic substances.

2. Synthesis

The synthesis of 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid involves a multi-step process. The first step typically involves the reaction of benzene with a mixture of sulfuric acid and methanol to form 4-methoxybenzophenone. This intermediate is then subjected to a nucleophilic substitution reaction with sodium bisulfite, resulting in the formation of 2-hydroxy-4-methoxybenzophenone.

The final step involves the sulfonation of the hydroxyl group using chlorosulfonic acid or sulfuric acid, followed by neutralization with sodium hydroxide to yield the desired 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid. This synthesis process requires careful control of reaction conditions, such as temperature, pressure, and pH, to ensure optimal yields and purity.

3. Physical and Chemical Properties

2-Hydroxy-4-methoxybenzophenone-5-sulfonic acid is a white to off-white crystalline solid with a melting point of around 150-160°C. It is soluble in water and polar organic solvents like methanol, ethanol, and dimethyl sulfoxide. The compound exhibits excellent stability under normal storage conditions, with a long shelf life when stored in a cool, dry place.

Chemically, the compound is stable under acidic and neutral conditions but may decompose under alkaline conditions. It is also resistant to oxidation, making it suitable for use in various chemical reactions and applications. The presence of the sulfonic acid group imparts a negative charge to the molecule, enhancing its solubility in aqueous solutions.

4. Biological Activities

2-Hydroxy-4-methoxybenzophenone-5-sulfonic acid has been found to exhibit various biological activities, making it a potential candidate for pharmaceutical applications. Its antioxidant properties help in scavenging free radicals, thereby protecting cells from oxidative damage. This property is particularly useful in the prevention of chronic diseases such as cancer, cardiovascular diseases, and neurodegenerative disorders.

The compound also exhibits anti-inflammatory properties, which can be beneficial in the treatment of inflammatory conditions like arthritis and asthma. Additionally, it has been shown to possess antimicrobial activities against a wide range of bacteria, viruses, and fungi, making it a potential candidate for use in antiseptic and disinfectant products.

5. Environmental Impact

The environmental impact of 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid is a crucial aspect to consider. The compound is biodegradable, which means it can be broken down by microorganisms in the environment. This property reduces the risk of long-term accumulation and potential toxicity to aquatic and terrestrial ecosystems.

However, the synthesis process of the compound involves the use of hazardous chemicals, such as sulfuric acid and chlorosulfonic acid, which can pose risks to the environment if not handled and disposed of properly. It is essential to implement appropriate waste management strategies and adhere to strict environmental regulations to minimize these risks.

6. Potential Industrial Applications

The diverse properties of 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid make it suitable for a wide range of industrial applications. In the pharmaceutical industry, it can be used as an intermediate for the synthesis of various drugs, including antioxidants, anti-inflammatory agents, and antimicrobial agents.

In the cosmetics industry, the compound can be utilized as a UV absorber and antioxidant in sunscreen products, helping to protect the skin from harmful UV radiation and oxidative damage. It can also be used as a preservative in skincare and haircare products due to its antimicrobial properties.

Furthermore, 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid has potential applications in the field of environmental protection. Its antioxidant and antimicrobial properties can be exploited in the development of biodegradable polymers and water treatment chemicals.

Conclusion

In conclusion, 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid, identified by the CAS number 4065-45-6, is a versatile compound with significant potential in various fields. Its unique chemical structure, synthesis process, physical and chemical properties, biological activities, environmental impact, and potential industrial applications make it an attractive candidate for further research and development. As we continue to explore its potential, it is essential to balance its benefits with the need for sustainable and environmentally friendly practices.

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