The Chemical Profile of 2-Amino-4-nitrophenol (CAS 99-57-0): Synthesis and Safety Considerations
2-Amino-4-nitrophenol, a compound identified by CAS number 99-57-0, is a key organic chemical with substantial importance, particularly as a pharmaceutical intermediate. Its detailed chemical profile, encompassing its synthesis, properties, and safety aspects, provides essential knowledge for its effective utilization in various industrial and research settings.
The synthesis of 2-Amino-4-nitrophenol is a critical process for ensuring a consistent and high-purity supply for downstream applications. While specific proprietary synthesis routes may vary, general chemical principles involve the introduction of amino and nitro groups onto a phenol ring. Manufacturers often focus on optimizing these 2-amino-4-nitrophenol synthesis pathways to maximize yield and minimize impurities, thereby ensuring the quality required for pharmaceutical intermediate manufacturing. The continuous refinement of these processes is vital for meeting industry demands.
Understanding the physical and chemical properties of 2-Amino-4-nitrophenol is fundamental. It presents as a dark yellow to brown solid, a characteristic that aids in its identification. Its melting point, typically ranging from 140-143°C, is a key parameter for quality control. The compound's molecular formula (C6H6N2O3) and molecular weight (154.12) define its basic chemical identity. Its solubility profile, being slightly soluble in water but more soluble in common organic solvents, dictates the choice of reaction media and purification techniques. These 2-amino-4-nitrophenol properties are critical for its successful application in diverse chemical processes.
The applications of 2-Amino-4-nitrophenol are broad, ranging from its primary use as a pharmaceutical intermediate to its roles in dye synthesis and biochemical research. As a pharmaceutical intermediate, it serves as a precursor for numerous drug molecules, contributing to the development of new therapies. Its utility as a fluorescent probe also highlights its value in advanced analytical techniques. The versatility of these 2-amino-4-nitrophenol applications underscores its significance in the chemical industry.
Crucially, comprehensive 2-amino-4-nitrophenol safety considerations must always be observed. Handling this compound requires adherence to strict safety protocols, including the use of appropriate personal protective equipment (PPE) such as gloves, eye protection, and laboratory coats. Work should be conducted in well-ventilated areas or under fume hoods to minimize inhalation exposure. Proper storage, away from incompatible materials and protected from light and moisture, is also essential for maintaining product quality and preventing hazardous reactions. Safety Data Sheets (SDS) provide detailed information to guide safe handling and emergency procedures.
In essence, 2-Amino-4-nitrophenol (CAS 99-57-0) is a vital chemical compound with a well-defined profile. Its synthesis, chemical characteristics, broad applications, and the critical importance of safety measures collectively define its role in modern industry. Continued research into its properties and applications promises further advancements in fields ranging from pharmaceuticals to chemical engineering.
Perspectives & Insights
Molecule Vision 7
“While specific proprietary synthesis routes may vary, general chemical principles involve the introduction of amino and nitro groups onto a phenol ring.”
Alpha Origin 24
“Manufacturers often focus on optimizing these 2-amino-4-nitrophenol synthesis pathways to maximize yield and minimize impurities, thereby ensuring the quality required for pharmaceutical intermediate manufacturing.”
Future Analyst X
“The continuous refinement of these processes is vital for meeting industry demands.”