Exploring the Chemical Properties and Applications of CAS Number 203794 83 0

Understanding CAS 3794-83-0 A Closer Look at 2-Amino-4-Methylphenol

In the realm of chemistry, the Chemical Abstracts Service (CAS) Registry Number provides a unique identifier for chemical substances. One such compound, denoted by the CAS number 3794-83-0, is 2-amino-4-methylphenol. This article will delve into the significance of this compound, its properties, applications, safety considerations, and environmental impact.

What is 2-Amino-4-Methylphenol?

2-Amino-4-methylphenol is an organic compound characterized by an amino group (-NH2) and a methyl group (-CH3) attached to a benzene ring. The IUPAC name for this compound is 4-methyl-2-aminophenol, which indicates the positions of the functional groups on the benzene ring. It is a white to yellowish powder that is soluble in water and various organic solvents.

Chemically, 2-amino-4-methylphenol belongs to the family of phenolic compounds, which are known for their wide range of applications in various industries. The presence of the amino group enhances its ability to participate in chemical reactions, making it a versatile component in synthesis.

Properties of 2-Amino-4-Methylphenol

The compound exhibits various physical and chemical properties that are noteworthy. Here are some of its key characteristics

- Molecular Formula C7H9N1O1 - Molecular Weight 139.15 g/mol - Melting Point Approximately 90-93°C - Boiling Point 250°C - Solubility Soluble in water, ethanol, and most organic solvents.

These properties indicate that 2-amino-4-methylphenol can easily interact with other chemicals, which is crucial for its application in industrial processes.

2-Amino-4-methylphenol finds its utility in several fields

1. Dyes and Pigments This compound is used as an intermediate in the production of various azo dyes. Azo dyes are widely utilized in the textile industry for coloring fabrics due to their vivid colors and stability.

2. Pharmaceuticals The properties of 2-amino-4-methylphenol make it a desirable candidate in the pharmaceutical industry for the synthesis of various active pharmaceutical ingredients (APIs). Its ability to form stable bonds with other molecules allows it to be part of complex organic structures.

3. Chemical Synthesis As a chemical intermediate, it serves as a building block for the synthesis of numerous organic compounds. Its reactivity makes it valuable for researchers and manufacturers in developing new materials.

4. Laboratory Reagents In research settings, 2-amino-4-methylphenol can be utilized in assays and experiments that require specific organic compounds.

Safety and Handling

While 2-amino-4-methylphenol is beneficial in various applications, it’s essential to consider its safety and handling requirements. The compound may pose several hazards if not managed properly

- Toxicity It is recommended to handle this compound using appropriate safety measures. Prolonged exposure can lead to skin irritation and respiratory issues.

- Environmental Impact Like many organic chemicals, improper disposal could lead to environmental contamination. Appropriate waste management practices must be adhered to, ensuring that it does not enter water bodies or soil systems.

To ensure safety, personal protective equipment (PPE) such as gloves, goggles, and lab coats should be utilized when handling this compound.

Conclusion

2-Amino-4-methylphenol, with its CAS number 3794-83-0, plays a vital role in multiple industries due to its unique properties and applications. From dyes to pharmaceuticals, its versatility cannot be understated. However, as with any chemical, it is imperative to handle it with care, considering both safety and environmental factors. As research continues to advance, the potential applications of 2-amino-4-methylphenol could expand, leading to further innovations in chemical synthesis and product development. Whether in a laboratory setting or industrial use, understanding this compound is essential for harnessing its full potential while ensuring a safe and sustainable approach to chemistry.