Understanding the fundamental chemistry of the reagents we use is critical for any successful scientific endeavor. Dibenzyl azodicarboxylate, known by its CAS number 2449-05-0, is a compound whose chemical structure and properties dictate its wide-ranging applications, particularly in organic synthesis. As a reliable chemical manufacturer and supplier, we aim to provide clarity on this important molecule.

Dibenzyl azodicarboxylate is characterized by the presence of an azo group (-N=N-) flanked by two carbobenzyloxycarbonyl groups. Its molecular formula is C16H14N2O4, and it has a molecular weight of approximately 298.29 g/mol. Typically appearing as an orange crystalline powder, this compound exhibits good stability under recommended storage conditions, often around 0-6°C or 2-8°C, and should be protected from light.

The synthesis of dibenzyl azodicarboxylate typically involves the reaction of dibenzyl hydrazine with a suitable oxidizing agent, or through the esterification of azodicarboxylic acid with benzyl alcohol. The precise synthesis route can influence the final purity and yield of the product. For industrial production, efficient and cost-effective synthesis methods are crucial. As a manufacturer, we optimize these processes to ensure high purity, often achieving ≥99.0% via HPLC, which is vital for its use in demanding chemical applications.

Key properties that make dibenzyl azodicarboxylate valuable include its reactivity as an electrophilic azo compound. It readily participates in addition reactions, particularly with nucleophiles, and serves as a mild oxidizing agent in certain contexts. Its role as a dehydrating agent in reactions like the Mitsunobu reaction (though less common than DIAD) is also noted, where it facilitates the conversion of alcohols to various functional groups.

For researchers and procurement specialists looking to buy dibenzyl azodicarboxylate, understanding these chemical attributes is essential for selecting the right grade and application. Its use as a coupling agent, a precursor for nitrogen-containing heterocycles, and in polymer chemistry are all directly linked to its chemical structure and reactivity. We, as a chemical supplier, ensure that our product specifications clearly outline these properties.

In conclusion, the chemistry of dibenzyl azodicarboxylate – its synthesis, structure, and reactivity – forms the basis of its utility. By providing a high-quality, well-characterized product, we empower chemists to explore its full potential. If you are interested in purchasing dibenzyl azodicarboxylate or learning more about its chemical properties, please contact our sales team.