Born, Max team published research on Propellants, Explosives, Pyrotechnics in 2022 | 7748-36-9

7748-36-9, Oxetan-3-ol is a useful research compound. Its molecular formula is C3H6O2 and its molecular weight is 74.08 g/mol. The purity is usually 95%.
Oxetan-3-ol is a synthetic hydroxy compound with the chemical formula C6H12O3. It is an organic solvent that can be used in reactions involving vinyl alcohol and oxetane, such as ring-opening polymerization and cationic polymerization. Oxetan-3-ol has also been shown to react with ethyl bromoacetate to form the corresponding oxetane, which can be used as a bioisostere for chloropropane, a potential replacement for chlorofluorocarbons., Application of C3H6O2

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 7748-36-9, formula is C3H6O2, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , Application of C3H6O2

Born, Max;Plank, Jakob;Klapotke, Thomas M. research published 《 Energetic Polymers: A Chance for Lightweight Reactive Structure Materials?》, the research content is summarized as follows. Today′s ammunition still consists of about 70 wt% structure-providing materials such as metals providing no energetic contribution. Therefore, reactive structure materials (RSMs) offer tremendous room for improvement. While current research focuses on rather heavy, metal-based materials (e. g., alloys, thermites), energetic polymers appear as an under-recognized opportunity for very lightweight RSMs. Unfortunately, suitable polymers are unavailable as energetic polymer research has almost exclusively focused on elastic binders with the least possible glass transition temperature An application as RSM, however, requires rigid polymers with a glass transition above operational temperatures Accordingly, monomers with fundamentally different structures are required. The first step in this particular direction is 3-(2,4,6-trinitrophenoxy)oxetane (TNPO). Herein, we report the synthesis of its homopolymer and investigate its polymerization behavior by copolymerization with prior art energetic oxetanes. All polymers were intensively studied by vibrational and multinuclear (1H, 13C, 14N) NMR spectroscopy, elemental anal., gel permeation chromatog., and differential scanning calorimetry (DSC). Hereby, DSC revealed the high effect of the TNPO repeating unit on the glass transition temperature The performance of all polymers was calculated using the EXPLO5 code to evaluate the potential performance range of polymeric RSMs. Further, their shock and friction sensitivity was determined by BAM standard procedures.

7748-36-9, Oxetan-3-ol is a useful research compound. Its molecular formula is C3H6O2 and its molecular weight is 74.08 g/mol. The purity is usually 95%.
Oxetan-3-ol is a synthetic hydroxy compound with the chemical formula C6H12O3. It is an organic solvent that can be used in reactions involving vinyl alcohol and oxetane, such as ring-opening polymerization and cationic polymerization. Oxetan-3-ol has also been shown to react with ethyl bromoacetate to form the corresponding oxetane, which can be used as a bioisostere for chloropropane, a potential replacement for chlorofluorocarbons., Application of C3H6O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts