Date published: 2025-9-5

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Anhydrides

Santa Cruz Biotechnology now offers a broad range of anhydrides for use in various applications. Anhydrides are a class of organic compounds that are formed by the removal of water from two molecules of carboxylic acids, resulting in a compound with two acyl groups bonded to the same oxygen atom. These highly reactive compounds are crucial in synthetic organic chemistry for their ability to act as acylating agents, facilitating the formation of esters, amides, and other derivatives through nucleophilic acyl substitution reactions. Anhydrides are pivotal in polymer chemistry, where they are used to produce polyesters and polyamides, materials that have significant industrial applications due to their strength, durability, and versatility. In biochemistry, anhydrides play a role in the synthesis of biomolecules and the study of enzymatic mechanisms, particularly those involving acyl transfer reactions. Environmental scientists study anhydrides to understand their reactivity and potential impact on ecosystems, as well as to develop methods for their safe handling and disposal. Additionally, anhydrides are employed in materials science to modify surface properties, enhance adhesion, and create advanced materials with specific structural and functional characteristics. They are also vital in analytical chemistry as reagents for derivatization, improving the detection and analysis of various compounds using techniques such as gas chromatography and mass spectrometry. By offering a diverse selection of anhydrides, Santa Cruz Biotechnology supports a wide range of scientific endeavors, enabling researchers to select the appropriate anhydride for their specific experimental needs. This extensive range of anhydrides facilitates innovation and discovery across multiple scientific disciplines, including chemistry, biology, environmental science, and materials science. View detailed information on our available anhydrides by clicking on the product name.

Items 61 to 62 of 62 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Methylcyclohexene-1,2-dicarboxylic anhydride

11070-44-3sc-279439
5 g
$97.00
(0)

Methylcyclohexene-1,2-dicarboxylic anhydride is characterized by its unique cyclic anhydride structure, which imparts significant electrophilic properties. The presence of two anhydride groups allows for versatile reactivity, enabling it to participate in Diels-Alder reactions and other cycloaddition processes. Its steric configuration influences reaction kinetics, promoting selective pathways in synthetic applications. Additionally, the compound's ability to form stable adducts with amines and alcohols highlights its role in creating complex molecular architectures.

3-Bromophthalic anhydride

82-73-5sc-266531
sc-266531A
1 g
5 g
$143.00
$420.00
(0)

3-Bromophthalic anhydride is an anhydride distinguished by its brominated aromatic structure, which enhances its electrophilic reactivity. The presence of the bromine atom increases the electron-withdrawing effect, facilitating nucleophilic attack on the carbonyl groups. This compound exhibits unique reaction kinetics, often leading to regioselective outcomes in cycloaddition reactions. Its planar geometry allows for effective π-stacking interactions, influencing solubility and reactivity in various organic transformations.