Unlock the Secrets of CAS 112-15-2: The Ultimate Guide to 2-(2-ethoxyethoxy)ethyl Acetate

Abstract

This article provides an in-depth exploration of CAS 112-15-2, also known as 2-(2-ethoxyethoxy)ethyl acetate. It serves as an ultimate guide, covering various aspects of this compound, including its chemical structure, synthesis methods, properties, applications, safety considerations, and environmental impact. By delving into these areas, the article aims to unlock the secrets of this chemical, offering valuable insights for researchers, chemists, and anyone interested in the field of organic chemistry.

Introduction to CAS 112-15-2

CAS 112-15-2, or 2-(2-ethoxyethoxy)ethyl acetate, is an organic compound belonging to the ester family. It is a colorless liquid with a sweet, fruity odor. This compound is widely used in various industries, including pharmaceuticals, agriculture, and perfumery. Understanding the properties, synthesis, and applications of CAS 112-15-2 is crucial for researchers and professionals in these fields.

Chemical Structure and Properties

The chemical structure of CAS 112-15-2 consists of an ethyl acetate group attached to a 2-(2-ethoxyethoxy)ethyl chain. This structure contributes to its unique properties, such as solubility in organic solvents and volatility. The presence of the ethoxy groups enhances its solubility and stability, making it suitable for various applications. Additionally, the sweet, fruity odor of CAS 112-15-2 is attributed to the ethyl acetate group.

Synthesis Methods

The synthesis of CAS 112-15-2 can be achieved through various methods, including the esterification reaction between ethyl acetate and 2-(2-ethoxyethoxy)ethanol. This reaction is typically carried out in the presence of a catalyst, such as sulfuric acid or hydrochloric acid. Another method involves the reaction of ethyl chloroacetate with 2-(2-ethoxyethoxy)ethanol in the presence of a base, such as sodium hydroxide or potassium hydroxide. These methods provide a reliable and efficient way to produce CAS 112-15-2 in the laboratory.

Applications

CAS 112-15-2 finds extensive applications in various industries. In the pharmaceutical industry, it is used as a solvent for certain drugs and as a flavoring agent in oral medications. In agriculture, it serves as a herbicide and insecticide. Additionally, CAS 112-15-2 is utilized in the production of perfumes and fragrances, where it contributes to the sweet, fruity notes in many scents.

Safety Considerations

While CAS 112-15-2 is widely used, it is important to consider its safety profile. This compound is classified as a hazardous material due to its potential for causing irritation to the eyes, skin, and respiratory system. Proper handling, storage, and disposal procedures are essential to minimize the risks associated with its use. It is also important to be aware of the potential health effects of long-term exposure to CAS 112-15-2.

Environmental Impact

The environmental impact of CAS 112-15-2 is a significant concern. This compound is known to be persistent in the environment, meaning it can accumulate in soil and water over time. Its potential to bioaccumulate in organisms also raises concerns about its impact on wildlife and ecosystems. Proper waste management and the development of alternative, less harmful compounds are crucial for minimizing the environmental impact of CAS 112-15-2.

Conclusion

Unlocking the secrets of CAS 112-15-2: The Ultimate Guide to 2-(2-ethoxyethoxy)ethyl Acetate provides a comprehensive overview of this organic compound. From its chemical structure and properties to its synthesis methods, applications, safety considerations, and environmental impact, this guide offers valuable insights for anyone interested in the field of organic chemistry. By understanding the intricacies of CAS 112-15-2, researchers and professionals can make informed decisions regarding its use and development of safer alternatives.

Keywords: CAS 112-15-2, 2-(2-ethoxyethoxy)ethyl acetate, chemical structure, synthesis, properties, applications, safety, environmental impact

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