CAS 5488-16-4: A Versatile Intermediate for Organic Synthesis
In the realm of organic chemistry, the availability of versatile intermediates is fundamental for the creation of complex molecules and novel materials. 2,5-Dihydroxy-1,4-Benzenediacetic Acid, identified by its CAS Number 5488-16-4, is one such compound that offers significant utility to researchers and chemical manufacturers. This molecule, characterized by a benzene ring substituted with two hydroxyl groups and two acetic acid moieties, serves as a valuable building block in a variety of synthetic pathways.
The inherent structure of 2,5-Dihydroxy-1,4-Benzenediacetic Acid makes it particularly well-suited for reactions involving its functional groups. The carboxylic acid groups can readily undergo esterification, amidation, or salt formation, while the phenolic hydroxyl groups can be involved in etherification, esterification, or oxidation reactions. This reactivity profile opens doors to a wide range of chemical transformations, enabling the synthesis of more complex organic structures.
A significant application area for CAS 5488-16-4 is in the field of coordination chemistry and the synthesis of Metal-Organic Frameworks (MOFs). As a di-carboxylic acid linker, it can coordinate with various metal ions to form porous crystalline structures. These MOFs are gaining increasing attention for their potential in gas adsorption, catalysis, and separation technologies. Researchers often seek out such specific linker molecules to tailor the properties of their MOFs, and 2,5-Dihydroxy-1,4-Benzenediacetic Acid provides a unique structural motif due to its hydroxyl substituents.
For chemists engaged in the development of new pharmaceuticals, agrochemicals, or advanced materials, sourcing a reliable supply of high-quality intermediates like 2,5-Dihydroxy-1,4-Benzenediacetic Acid is crucial. We understand the demands of the chemical industry and are proud to be a leading manufacturer and supplier in China, providing this essential intermediate. Our commitment ensures that when you buy 2,5-Dihydroxy-1,4-Benzenediacetic Acid from us, you are obtaining a product with a minimum purity of 97%, backed by stringent quality control measures.
The versatility of this compound extends beyond MOFs. It can also be used in the synthesis of polymers, dyes, and other fine chemicals. Its aromatic nature, combined with the presence of reactive functional groups, allows for its incorporation into polymer backbones or its use as a precursor for functional monomers. The ability to modify and build upon this structure makes it an indispensable tool in an organic chemist's arsenal. When evaluating where to purchase CAS 5488-16-4, consider the importance of purity and consistent supply chain management.
Our aim is to support innovation by providing essential chemical building blocks. We offer competitive 2,5-Dihydroxy-1,4-Benzenediacetic Acid prices, particularly for bulk orders, making advanced synthesis more accessible. Whether you are performing small-scale research or large-scale manufacturing, our team is ready to assist with your procurement needs. We encourage you to reach out for a quote or sample to experience the quality and service we provide.
In conclusion, 2,5-Dihydroxy-1,4-Benzenediacetic Acid (CAS 5488-16-4) is a testament to the importance of well-defined intermediates in driving progress in organic chemistry and material science. As a dedicated 2,5-Dihydroxy-1,4-Benzenediacetic Acid supplier, we are committed to facilitating your research and production efforts with a consistently high-quality product.
Perspectives & Insights
Data Seeker X
“The inherent structure of 2,5-Dihydroxy-1,4-Benzenediacetic Acid makes it particularly well-suited for reactions involving its functional groups.”
Chem Reader AI
“The carboxylic acid groups can readily undergo esterification, amidation, or salt formation, while the phenolic hydroxyl groups can be involved in etherification, esterification, or oxidation reactions.”
Agile Vision 2025
“This reactivity profile opens doors to a wide range of chemical transformations, enabling the synthesis of more complex organic structures.”