This article provides a comprehensive overview of N,N'-Diphenyl-p-Phenylenediamine (D₁₄, 98%) - Certified Pure, 95% Purity, a highly pure form of the chemical compound. The article delves into the chemical properties, applications, synthesis methods, safety considerations, and market trends of this compound. It aims to serve as a reference for researchers, chemists, and industry professionals interested in understanding the significance and uses of this compound in various fields.
N,N'-Diphenyl-p-Phenylenediamine, also known as D₁₄, is a chemical compound with the molecular formula C₁₆H₁₄N₂. It is a derivative of p-phenylenediamine, characterized by two phenyl groups attached to the para position of the benzene ring. This compound is widely recognized for its purity, with a certified purity of 98% and an additional 95% purity guarantee. The high purity of D₁₄ makes it a valuable compound in various applications, including pharmaceuticals, dyes, and organic synthesis.
N,N'-Diphenyl-p-Phenylenediamine is a crystalline solid with a melting point of approximately 150°C. It is sparingly soluble in water but more soluble in organic solvents such as ethanol, acetone, and chloroform. The compound is a strong base and can react with acids to form salts. Its chemical structure allows for various substitution reactions, making it a versatile starting material in organic synthesis.
The high purity of N,N'-Diphenyl-p-Phenylenediamine (D₁₄, 98%) - Certified Pure, 95% Purity makes it suitable for a wide range of applications. In the pharmaceutical industry, it is used as a precursor for the synthesis of dyes, antioxidants, and pharmaceutical intermediates. In the dye industry, it serves as a key component in the production of azo dyes, which are widely used in textiles, plastics, and paints. Additionally, D₁₄ finds applications in the field of organic synthesis, where it is utilized as a building block for the creation of complex molecules.
The synthesis of N,N'-Diphenyl-p-Phenylenediamine involves several methods, each with its own advantages and limitations. One common synthesis method is the Sandmeyer reaction, which involves the reaction of a diazonium salt with a phenylhydrazine derivative. Another method is the reduction of o-phenylenediamine with sodium cyanide, followed by hydrolysis. These methods require careful control of reaction conditions to ensure the desired purity of the final product.
Handling N,N'-Diphenyl-p-Phenylenediamine (D₁₄, 98%) - Certified Pure, 95% Purity requires adherence to safety protocols. The compound is toxic if ingested, inhaled, or absorbed through the skin. It is essential to wear appropriate personal protective equipment, such as gloves, goggles, and lab coats, when working with this compound. Proper ventilation and waste disposal procedures should also be followed to minimize the risk of exposure.
The market for N,N'-Diphenyl-p-Phenylenediamine (D₁₄, 98%) - Certified Pure, 95% Purity has been growing steadily, driven by the increasing demand in the pharmaceutical and dye industries. The compound's high purity and versatility make it a sought-after material. As the global market for organic synthesis continues to expand, the demand for high-purity chemicals like D₁₄ is expected to rise further.
N,N'-Diphenyl-p-Phenylenediamine (D₁₄, 98%) - Certified Pure, 95% Purity is a highly pure form of the chemical compound that finds extensive applications in various industries. Its chemical properties, synthesis methods, safety considerations, and market trends highlight its significance in the field of organic chemistry. As research and development continue to advance, the demand for high-purity chemicals like D₁₄ is likely to increase, making it an essential compound for future innovations.
Keywords: N,N'-Diphenyl-p-Phenylenediamine, D₁₄, Certified Pure, 95% Purity, chemical properties, applications, synthesis methods, safety considerations, market trends
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