This article provides a comprehensive overview of Tetraacetylethylenediamine, also known as CAS 10543-57-4, exploring its alternative names, chemical properties, uses, safety considerations, and environmental impact. The article aims to offer a detailed and accessible insight into this compound, highlighting its significance in various industries and research fields.
Tetraacetylethylenediamine, with the CAS number 10543-57-4, is a chemical compound that has gained attention for its diverse applications. It is commonly referred to by several alternative names, which reflect its chemical structure and properties. This article delves into the details of Tetraacetylethylenediamine, examining its various aspects to provide a comprehensive understanding of this compound.
Tetraacetylethylenediamine is a derivative of ethylenediamine, which is a diamine compound. It contains four acetyl groups attached to the ethylenediamine backbone. This structure contributes to its unique chemical properties, including high solubility in organic solvents and its ability to form coordination complexes with metal ions. The presence of the acetyl groups also makes it less reactive compared to ethylenediamine, which is a key factor in its applications.
The molecular formula of Tetraacetylethylenediamine is C8H12N2O4, and its molecular weight is 196.20 g/mol. It is a white crystalline solid that is stable under normal conditions. The compound has a melting point of approximately 150°C and a boiling point of around 300°C. These physical properties make it suitable for various applications, including synthesis and as a ligand in coordination chemistry.
In addition to its CAS number, Tetraacetylethylenediamine is known by several alternative names. These include diacetylhydrazine, N,N'-diacetyl-1,2-ethanediamine, and ethylenediamine tetraacetate. These names reflect the chemical structure and properties of the compound, providing different perspectives on its composition and usage.
The name "diacetylhydrazine" emphasizes the presence of two acetyl groups, while "N,N'-diacetyl-1,2-ethanediamine" highlights the acetyl groups attached to the ethylenediamine backbone. The name "ethylenediamine tetraacetate" is particularly useful in the context of coordination chemistry, as it indicates the compound's ability to form coordination complexes with metal ions.
Tetraacetylethylenediamine finds applications in various industries, including pharmaceuticals, agriculture, and coordination chemistry. In the pharmaceutical industry, it is used as a ligand in the synthesis of coordination complexes, which have potential applications in drug development. In agriculture, it is used as a fertilizer component to enhance plant growth.
In coordination chemistry, Tetraacetylethylenediamine is particularly valuable due to its ability to form stable coordination complexes with metal ions. These complexes are used in catalysis, sensors, and materials science. The compound's versatility in forming coordination bonds with different metals makes it a valuable tool in research and development.
As with any chemical compound, Tetraacetylethylenediamine requires careful handling and storage to ensure safety. The compound is considered hazardous and poses certain risks, including skin and eye irritation, respiratory irritation, and potential toxicity if ingested or inhaled. It is important to follow proper safety protocols, including the use of personal protective equipment (PPE) and proper ventilation, when working with this compound.
The Material Safety Data Sheet (MSDS) provides detailed information on the safe handling, storage, and disposal of Tetraacetylethylenediamine. It is crucial to review and adhere to the guidelines provided in the MSDS to minimize potential risks associated with the compound.
The environmental impact of Tetraacetylethylenediamine is a concern due to its potential to contaminate soil and water sources. The compound is not biodegradable and can persist in the environment for extended periods. Therefore, proper waste management and disposal practices are essential to minimize its impact on ecosystems.
Research is ongoing to develop more environmentally friendly alternatives to Tetraacetylethylenediamine. This includes exploring biodegradable ligands and developing sustainable synthesis methods that reduce the environmental footprint of chemical production.
Tetraacetylethylenediamine, also known as CAS 10543-57-4, is a versatile compound with diverse applications across various industries. Its unique chemical properties, including high solubility and coordination ability, make it a valuable tool in research and development. However, its potential hazards and environmental impact necessitate careful handling and responsible use. This article has provided a comprehensive overview of Tetraacetylethylenediamine, covering its chemical properties, alternative names, applications, safety considerations, and environmental impact.
Keywords: Tetraacetylethylenediamine, CAS 10543-57-4, ethylenediamine, acetyl groups, coordination complexes, safety, environmental impact.
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