The Chemical Properties and Versatility of 3-Hydroxypyridine
Understanding the fundamental chemical properties of an intermediate is crucial for any formulator or researcher looking to utilize it effectively. 3-Hydroxypyridine, bearing the CAS number 109-00-2, is an organic compound distinguished by its pyridine ring structure with a hydroxyl group at the third position. This seemingly simple arrangement imbues the molecule with a fascinating reactivity and versatility that is highly valued across multiple industries, from pharmaceuticals to agrochemicals and beyond.
Chemically, 3-Hydroxypyridine exhibits dual functionality due to the presence of both the nitrogen atom in the pyridine ring and the phenolic hydroxyl group. The nitrogen atom contributes to the compound's basicity and its ability to coordinate with metal ions, making it a potential ligand in coordination chemistry. The hydroxyl group, on the other hand, confers weak acidic properties and allows for participation in hydrogen bonding, crucial for solubility in polar solvents like water and many organic solvents. This amphoteric nature, combined with the aromatic character of the pyridine ring, allows 3-Hydroxypyridine to undergo a wide range of chemical transformations, including electrophilic aromatic substitution, nucleophilic attack, and various derivatization reactions at the hydroxyl group. Its molecular weight is approximately 95.10 g/mol, and it typically presents as a colorless to pale yellow liquid or solid, with its physical state often dependent on purity and ambient temperature. Its solubility profile is a significant advantage, facilitating its use in diverse reaction media.
The versatility of 3-Hydroxypyridine stems directly from these chemical properties. In organic synthesis, it serves as an excellent building block for constructing more complex molecules. For instance, the hydroxyl group can be readily functionalized through etherification or esterification, while the pyridine ring can be modified through various substitution reactions. These reactions are fundamental to creating the active ingredients found in many pharmaceuticals, such as those used to treat neuromuscular disorders, or in agrochemicals like herbicides that require specific structural features for biological activity. The reactivity of 3-Hydroxypyridine is a key reason why manufacturers prioritize its high purity, often specifying an assay of 98% or greater. Such purity ensures predictable reaction outcomes and minimizes unwanted byproducts in downstream syntheses.
For industrial buyers, understanding these chemical characteristics helps in selecting the right grade and supplier of 3-Hydroxypyridine. Whether you are looking to buy 3-Hydroxypyridine for pharmaceutical intermediates, agrochemical synthesis, or cosmetic ingredient development, partnering with a reputable manufacturer, such as those found in China, who can guarantee consistent quality and purity is essential. The ability to source this compound reliably allows researchers and manufacturers to unlock its full potential, driving innovation and product development across multiple sectors.
Perspectives & Insights
Molecule Vision 7
“10 g/mol, and it typically presents as a colorless to pale yellow liquid or solid, with its physical state often dependent on purity and ambient temperature.”
Alpha Origin 24
“Its solubility profile is a significant advantage, facilitating its use in diverse reaction media.”
Future Analyst X
“The versatility of 3-Hydroxypyridine stems directly from these chemical properties.”