Overview
Dinaphthol, chemically known as 2,2'-dihydroxy-1,1'-binaphthyl (BINOL), is a chiral organic compound with significant applications in asymmetric synthesis. It is widely recognized for its role as a ligand in catalytic reactions, particularly in the pharmaceutical and agrochemical industries. The compound's unique structure allows it to facilitate enantioselective transformations, making it invaluable in the production of optically active molecules. Dinaphthol is typically synthesized through the oxidative coupling of 2-naphthol or via other specialized methods. Its purity and enantiomeric excess are critical for its effectiveness in industrial applications. The compound is available in various grades, with high-purity versions being essential for sensitive chemical processes.
Physical and Chemical Properties
Dinaphthol appears as a white to off-white crystalline powder with a melting point range of 210-215°C. It is soluble in organic solvents such as ethanol, acetone, and dichloromethane but exhibits negligible solubility in water. The compound's chiral nature is due to the restricted rotation around the central bond, which gives rise to its atropisomeric properties. The molecular weight of dinaphthol is 286.33 g/mol, and its stability under normal conditions makes it suitable for long-term storage when kept away from moisture and light. Its solubility profile and thermal stability are key factors in its widespread use in organic synthesis and industrial applications.
Main Applications
Dinaphthol is primarily used as a chiral ligand in asymmetric catalysis, enabling the synthesis of enantiomerically pure compounds. This is particularly important in the pharmaceutical industry, where the production of single-enantiomer drugs is often required for efficacy and safety. The compound is also employed in the synthesis of agrochemicals, fragrances, and advanced materials. In addition to its role in catalysis, dinaphthol serves as a building block for the preparation of other chiral compounds and polymers. Its versatility and effectiveness in promoting stereoselective reactions have made it a staple in research laboratories and industrial settings alike.
Safety and Storage
Dinaphthol should be handled with care to avoid inhalation or skin contact, as it may cause irritation. Proper personal protective equipment, including gloves and goggles, should be worn when working with the compound. It is advisable to use the material in a well-ventilated area or under a fume hood to minimize exposure. Storage conditions for dinaphthol include keeping the compound in a cool, dry place, away from direct sunlight and moisture. The container should be tightly sealed to prevent contamination and degradation. Long-term stability can be ensured by storing the material in an inert atmosphere if necessary.
B2B Procurement Guide
When procuring dinaphthol, B2B buyers should prioritize suppliers with a proven track record of delivering high-purity products. Certificates of analysis (CoA) should be requested to verify the compound's purity and enantiomeric excess. Bulk purchasing can often lead to cost savings, but it is essential to ensure that storage facilities meet the required conditions. Price ranges for dinaphthol vary based on purity and quantity, with typical costs ranging from $50 to $200 per kilogram. Buyers should also consider the supplier's reliability, lead times, and compliance with regulatory standards. Establishing long-term relationships with reputable suppliers can streamline procurement processes and ensure consistent quality.
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