|Reaxis C125 – Stannous Neodecanoate||Stannous Neodecanoate||Request A Sample|
|Reaxis C129 – Stannous Octoate||Stannous Octoate||Request A Sample|
|Reaxis C154 – Stannous Chloride Dihydrate||Stannous Chloride, Dihydrate||Request A Sample|
|Reaxis C160 – Stannous Oxalate||Stannous Oxalate||Request A Sample|
|Reaxis C162||Stannous Chloride, Anhydrous||Request A Sample|
|Reaxis C188||Stannous Oxide||Request A Sample|
|Reaxis C216||Dioctyltin Dilaurate||Request A Sample|
|Reaxis C220||Monobutyltin Tris-(2-ethylhexanoate)||Request A Sample|
|Reaxis C233||Dibutyltin Diacetate||Request A Sample|
|Reaxis C233T||Dibutyltin Diacetate||Request A Sample|
|Reaxis C248||Dibutyltin Oxide||Request A Sample|
|Reaxis C248LC||Dibutyltin Oxide||Request A Sample|
The Role of Esterification in Industrial Manufacturing
Esterification is a pivotal process in industrial manufacturing, contributing to the production of a plethora of specialty chemicals with applications in the production of bulk and commodity chemicals. This chemical reaction combines an acid and an alcohol to form an ester, a component critical in various industrial applications from pharmaceuticals to adhesives and coatings.
The importance of esterification stems from the versatility of esters themselves. Depending on the specific acid and alcohol used, esters can have wide-ranging physical and chemical properties, making them adaptable to many different applications, including coatings, adhesives and sealants, composites, elastomers, personal care and lubricants. They can be found in pharmaceuticals where they are used as pro-drugs, in adhesives and coatings due to their bonding capabilities and resistance properties, and in plastics for their flexibility and durability.
In addition to their versatility, the esterification process is commonly used due to its relative simplicity and cost-effectiveness. Under the right conditions, acids and alcohols readily react to form esters, making it an accessible reaction for many industrial processes. The ability to create complex molecules through a straightforward process underscores the esterification reaction’s importance in the chemical industry and manufacturing.
Inorganic Tin and Organotin Compounds: Essential Ingredients for Esterification
Tin catalysts are commonly used in the synthesis of a wide range of mono- and polyesters and alkyds. In regard to polyesters, tin catalysts are used primarily in the production of saturated polyesters used in various coatings applications. Saturated Polyester polyols are one of the key raw materials used in producing polyurethanes. Tin catalysts are also used in the synthesis of unsaturated polyesters, such as those used in the production of various plastic composites. Inorganic tin and organotin catalysts such as REAXIS®C125, Stannous Neodecanoate, REAXIS®C129, Stannous Octoate, Stannous Chloride (both in dihydrate as REAXIS®C154 and anhydrous as REAXIS®C162), REAXIS®C160, Stannous Oxalate, REAXIS®C188, Stannous Oxide, REAXIS®C216, Dioctyltin Dilaurate, REAXIS®C220, Monobutyltin Tris-(2-Ethylhexanoate), REAXIS®C233, Dibutlytin Diacetate, and REAXIS®C248, Dibutyltin Oxide are commonly employed.
Reaxis: Supplying Key Esterification Catalysts for Industrial Manufacturing
At Reaxis, we understand the critical role esterification plays in industrial manufacturing, and we are committed to supplying high-quality, performance-enhancing inorganic tin and organotin catalysts for these processes. The aforementioned catalysts are integral to our offering, each possessing unique properties that contribute to the overall efficiency and quality of industrial manufacturers’ end products. By leveraging our extensive knowledge of these catalysts and the esterification process, along with a long history of commercial production experience, we support our customers in delivering innovative and reliable chemical solutions.
- Manufacturing Chemist, “Revolutionizing industrial applications of ester hydrogenation,” https://www.manufacturingchemist.com/news/article_page/Revolutionising_industrial_applications_of_ester_hydrogenation/139571
- Pon Pure Chemicals Group, “Esters: Its Chemical Nature, Properties and Uses”
- American Chemical Society, “Hydrogenation of Carboxylic Acids, Esters, and Related Compounds over Heterogeneous Catalysts: A Step toward Sustainable and Carbon-Neutral Processes,” https://pubs.acs.org/doi/10.1021/acs.chemrev.2c00550