Formation of neutral complexes of boric acid with 1,3-diols in organic solvents and in aqueous solution was written by Bachelier, Nicolas;Verchere, Jean-Francois. And the article was included in Polyhedron in 1995.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:
From solubility measurements in organic media and extraction experiments, the values of the stability constants of neutral 1:1 complexes (HBL) formed between boric acid (HB) and 1,3-diols (L) were obtained in aqueous solution (Kcw) and in organic solvents (Kcs). The values of the partition coefficients of the diols (PL) and (PHBL) between H2O and the organic solvents also were calculated Generally, the addition of a diol to an aqueous solution of borax is accompanied by a decrease of pH due to the prevailing formation of borate species but, in the case of 2-methyl-2,4-pentanediol, the pH increased, in agreement with the formation of a single neutral complex. A modification of a previous potentiometric procedure yields simultaneously the values of the stability constants of the neutral and anionic complexes in aqueous solution This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4HPLC of Formula: 115-84-4).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.HPLC of Formula: 115-84-4
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts