Lisovskaya, Alexandra; Shadyro, Oleg; Schiemann, Olav; Carmichael, Ian published an article in 2021. The article was titled 《OH radical reactions with the hydrophilic component of sphingolipids》, and you may find the article in Physical Chemistry Chemical Physics.Safety of 2-Aminopropane-1,3-diol The information in the text is summarized as follows:
In this work, using the example of model compounds, we studied the reactions resulting from the interaction of OH radicals with the hydrophilic part of sphingolipids. We compared the stopped-flow EPR spectroscopy and pulse radiolysis with optical detection methods to characterize radical intermediates formed in the reaction of OH radicals with glycerol, serinol and N-boc-serinol. Quantum chem. calculations were also performed to help interpret the observed exptl. data. It was shown that H-abstraction from the terminal carbon atom is the main process that is realized for all the studied compounds The presence of the unsubstituted amino group (-NH2) is seen to completely change the reaction properties of serinol in comparison with those observed in glycerol and N-boc serinol. The results came from multiple reactions, including the reaction of 2-Aminopropane-1,3-diol(cas: 534-03-2Safety of 2-Aminopropane-1,3-diol)
2-Aminopropane-1,3-diol(cas: 534-03-2) belongs to anime. Amines have a free lone pair with which they can coordinate to metal centers. Amine–metal bonds are weaker because amines are incapable of backbonding, but they are still important for sensing applications.While stronger than hydrogen bonds, amine–metal bonds are still weaker than both covalent and ionic bonds.Safety of 2-Aminopropane-1,3-diol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts