Basuri, Pallab et al. published their research in ACS Sustainable Chemistry & Engineering in 2022 | CAS: 31566-31-1

Glyceryl monostearate (cas: 31566-31-1) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Application In Synthesis of Glyceryl monostearate

Accelerated Non-Enzymatic Fatty Acid Esterification during Microdroplet Collision: A Method for Enhanced Sustainability was written by Basuri, Pallab;Kumar, Jenifer Shantha;Das, Subhashree;Pradeep, Thalappil. And the article was included in ACS Sustainable Chemistry & Engineering in 2022.Application In Synthesis of Glyceryl monostearate The following contents are mentioned in the article:

Accelerated non-enzymic and metal-free “reaction and extraction” of sugar esters at the interface of two immiscible liquid microdroplets is demonstrated. The bimol. reaction occurs by collision of microdroplets originating from two home-built electrospray sonic ion sources, carrying sugar mols. in water and long-chain fatty acids in toluene, resp. Our method shows that the rate of reaction is enhanced ~107 times in comparison to the bulk, initiated by ultrasonic activation. Such a high rate of reaction in the microdroplets can be attributed to factors such as surface activity, concentration enhancement, partial solvation, and temperature-assisted dehydration of the species occurring in microdroplets. We provide evidence for an interfacial nucleophilic addition-elimination reaction mechanism. This method of synthesis is extended to 18 similar reactions. Microdroplet synthesis offers a sustainable method for biphasic reactions, eliminating the need for phase transfer reagents and activating agents such as acids/bases, metals, or enzymes. This study involved multiple reactions and reactants, such as Glyceryl monostearate (cas: 31566-31-1Application In Synthesis of Glyceryl monostearate).

Glyceryl monostearate (cas: 31566-31-1) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Application In Synthesis of Glyceryl monostearate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics