Date published: 2025-9-18

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Esters

Santa Cruz Biotechnology now offers a broad range of esters for use in various applications. Esters, characterized by their functional group -COO-, are versatile and widely utilized compounds in scientific research due to their unique chemical properties and reactivity. These organic compounds are formed by the reaction of an acid (usually a carboxylic acid) and an alcohol, resulting in a wide variety of structures and functionalities. In organic synthesis, esters serve as key intermediates in the production of polymers, plasticizers, and synthetic flavors and fragrances, making them essential for industrial and materials chemistry. Analytical chemists frequently use esters in methods such as gas chromatography to analyze complex mixtures, owing to their volatility and distinctive fragmentation patterns. Esters are also crucial in environmental science, where they are studied to understand their role in natural processes like the formation of natural products and biodegradation pathways. In biochemical research, esters are employed to study enzyme specificity and mechanisms, particularly esterases and lipases, which play significant roles in metabolic pathways and lipid metabolism. The versatility of esters extends to their use in the development of novel materials, including biodegradable plastics and advanced composites. By offering a diverse selection of esters, Santa Cruz Biotechnology supports a wide range of scientific endeavors, enabling researchers to select the appropriate ester for their specific experimental needs. This extensive range of esters facilitates innovation and discovery across multiple scientific disciplines, including organic chemistry, materials science, environmental science, and analytical chemistry. View detailed information on our available esters by clicking on the product name.

Items 231 to 234 of 234 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Lauric Acid ethyl ester

106-33-2sc-204790
sc-204790A
100 mg
500 mg
$15.00
$17.00
(0)

Lauric acid ethyl ester, an ester, showcases distinctive solubility characteristics owing to its long hydrophobic carbon chain and ethyl group. This structure allows for effective interactions with both polar and non-polar solvents, enhancing its emulsifying properties. The compound's reactivity is influenced by its ester functional group, which can undergo transesterification and hydrolysis, making it versatile in various chemical pathways. Its unique molecular interactions contribute to its behavior in diverse applications.

Isobutyl acrylate

106-63-8sc-357365
sc-357365A
100 ml
500 ml
$37.00
$130.00
(0)

Isobutyl acrylate, an ester, exhibits unique reactivity due to its acrylate functional group, which facilitates rapid polymerization through free radical mechanisms. This compound's branched isobutyl structure enhances its compatibility with various monomers, promoting diverse copolymer formations. Its low viscosity and high volatility contribute to efficient processing in coatings and adhesives, while its ability to form hydrogen bonds influences its interactions with other polar substances, enhancing its performance in various formulations.

2-Ethoxyethyl acrylate

106-74-1sc-358739
sc-358739A
25 g
100 g
$400.00
$800.00
(0)

2-Ethoxyethyl acrylate is an ester characterized by its unique ability to participate in Michael addition reactions, enhancing its versatility in polymer synthesis. The ethoxyethyl group imparts a degree of flexibility, allowing for improved chain mobility and reduced glass transition temperature in polymers. Its moderate polarity facilitates solubility in a range of solvents, while the acrylate moiety promotes rapid crosslinking under UV light, making it suitable for applications requiring quick curing times.

Triethylene glycol dimethacrylate

109-16-0sc-251327
sc-251327A
250 ml
1 L
$82.00
$209.00
(0)

Triethylene glycol dimethacrylate is an ester notable for its multifunctional nature, enabling it to act as a crosslinking agent in polymer networks. Its structure allows for strong hydrogen bonding interactions, enhancing the mechanical properties of the resulting materials. The presence of methacrylate groups facilitates efficient radical polymerization, leading to rapid network formation. Additionally, its low viscosity aids in processing, ensuring uniform distribution in formulations.