Date published: 2025-9-13

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Lactones

Santa Cruz Biotechnology now offers a broad range of lactones for use in various applications. Lactones, a group of cyclic esters, are integral to scientific research due to their diverse chemical properties and versatile applications. These compounds, formed through the intramolecular esterification of hydroxy acids, serve as essential intermediates in organic synthesis, facilitating the creation of complex molecules through various ring-opening and polymerization reactions. In the field of materials science, lactones are utilized in the production of biodegradable polymers and resins, which are critical for developing sustainable materials with reduced environmental impact. Researchers in environmental science leverage lactones to study natural processes and to design eco-friendly chemical solutions. In biochemistry, lactones play a crucial role in the study of enzyme mechanisms and metabolic pathways, offering insights into fundamental biological processes. They are also important in flavor and fragrance chemistry, where their unique aromatic properties are harnessed to create a wide range of scents and flavors. Analytical chemists use lactones as standards and reagents to facilitate the identification and quantification of compounds in complex mixtures. The ability of lactones to participate in various chemical transformations makes them valuable tools in synthetic chemistry, enabling the development of novel compounds and materials. Their broad applicability across multiple scientific disciplines underscores their importance in driving innovation and expanding our understanding of chemical and biological systems. View detailed information on our available lactones by clicking on the product name.

Items 451 to 452 of 452 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Desertomycin A

121820-50-6sc-362018
1 mg
$192.00
1
(0)

Desertomycin A is a notable lactone distinguished by its unique cyclic structure, which imparts significant strain and reactivity. This strain facilitates rapid intramolecular reactions, leading to the formation of various derivatives. The compound exhibits intriguing solubility characteristics, allowing for selective interactions with nucleophiles. Its distinct electronic properties, influenced by the lactone ring, enhance its potential for diverse synthetic pathways, making it a fascinating target for chemical research.

(6S)-6-[2-(1,3-Benzodioxol-5-yl)ethyl]-5,6-dihydro-4-methoxy-2H-pyran-2-one

19902-91-1sc-503365
2.5 mg
$230.00
(0)

(6S)-6-[2-(1,3-Benzodioxol-5-yl)ethyl]-5,6-dihydro-4-methoxy-2H-pyran-2-one, as a lactone, showcases unique cyclic ester characteristics that contribute to its stability and reactivity. The presence of the methoxy group enhances electron density, promoting nucleophilic attack at the carbonyl carbon. Its rigid structure allows for specific conformational orientations, influencing reaction pathways and selectivity in cyclization reactions. Additionally, the lactone's ability to undergo ring-opening reactions under certain conditions expands its utility in synthetic chemistry.