5-Hydroxytiabendazole

Introducing 5-Hydroxytiabendazole, a versatile and highly specialized chemical compound that holds immense potential in various scientific and industrial applications. With its unique molecular structure and exceptional purity, this compound has captured the attention of researchers and professionals across diverse fields, from pharmaceutical development to material science innovations.

At the heart of 5-Hydroxytiabendazole lies a captivating chemical identity. Boasting the CAS number 948-71-0 and the reference number 86-MM0602.02, this compound is a derivative of the well-known Tiabendazole, a widely used fungicide. However, the strategic placement of a hydroxyl group at the 5-position of the benzimidazole ring sets 5-Hydroxytiabendazole apart, endowing it with distinct properties and expanded potential.

The molecular formula of C10H7N3OS, combined with a molecular weight of 217.25 g/mol, gives 5-Hydroxytiabendazole its characteristic light yellow color and a melting point range of 284-287°C. Its IUPAC name, 2-(1,3-thiazol-4-yl)-1H-benzimidazol-5-ol, further highlights the compound's structural complexity and the intricate interplay of its functional groups.

Pharmaceutical Research and Development

In the realm of pharmaceutical research and development, 5-Hydroxytiabendazole shines as a valuable asset. Its structural similarity to Tiabendazole, a well-established anthelmintic and fungicidal agent, suggests the potential for exploring novel therapeutic applications. Researchers may leverage the unique properties of 5-Hydroxytiabendazole to develop innovative drug candidates targeting a range of health conditions, from parasitic infections to fungal diseases.

The strategic placement of the hydroxyl group on the benzimidazole core can lead to enhanced pharmacological profiles, improved bioavailability, or targeted mechanisms of action. By delving into the nuances of 5-Hydroxytiabendazole's chemical structure and reactivity, scientists can unlock new avenues for therapeutic breakthroughs, ultimately benefiting patients and advancing the field of modern medicine.

Material Science and Chemical Synthesis

Beyond the pharmaceutical realm, 5-Hydroxytiabendazole also finds applications in the realm of material science and chemical synthesis. Its unique molecular architecture, characterized by the presence of a thiazole ring, a benzimidazole moiety, and a strategically positioned hydroxyl group, makes it a versatile building block for the creation of novel materials and compounds.

In the field of material science, researchers may explore the integration of 5-Hydroxytiabendazole into polymeric structures or coatings, leveraging its chemical properties to enhance the performance characteristics of the resulting materials. This could lead to the development of advanced materials with improved thermal stability, mechanical strength, or optical properties, opening up new possibilities in various industries.

Furthermore, the compound's reactivity and selectivity make it a valuable reagent in organic synthesis, enabling chemists to construct complex molecules with tailored functionalities. By harnessing the potential of 5-Hydroxytiabendazole, researchers can push the boundaries of chemical innovation, unlocking new avenues for scientific discovery and technological advancements.

Handling and Storage

As with any specialized chemical compound, proper handling and storage of 5-Hydroxytiabendazole are of utmost importance. This compound is classified as a hazardous material, with a hazard class of 9 and a UN number of 3077. It is considered very toxic to aquatic life, with the potential for long-lasting effects.

When handling 5-Hydroxytiabendazole, it is crucial to adhere to strict safety protocols, including the use of personal protective equipment (PPE) such as gloves, goggles, and a face mask. Avoid release to the environment, and in the event of a spill, collect the spillage and dispose of it in accordance with local, regional, and national regulations.

For optimal storage