Kwon, TaeOk et al. published their research in Solvent Extraction Research and Development, Japan in 2004 | CAS: 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. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.HPLC of Formula: 115-84-4

Equilibrium of boron extraction with 2-butyl-2ethyl-1,3-propanediol in 2-ethylhexanol was written by Kwon, TaeOk;Kawano, Yuka;Toorisaka, Eiichi;Takanashi, Hirokazu;Yamagishi, Toshio;Hirata, Makoto;Hano, Tadashi. And the article was included in Solvent Extraction Research and Development, Japan in 2004.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

Boron extraction equilibrium was investigated by using 2-butyl-2-ethyl-1,3-propane-diol (BEPD) dissolved in 2-ethylhexanol (EH) as the organic solvent at various boric acid concentrations, extractant concentrations and pH values. The distribution ratio of boron increased with the initial concentration of BEPD in the organic phase for all boron concentrations examined in this study. At each BEPD concentrations, the distribution ratio of boron was constant with minimal effect of boron concentration The effect of pH on boron extraction with BEPD in EH was also examined, and the results verified the fact that boron extraction with BEPD in 2-ethylhexanol was effective in acidic and weakly alk. media (pH < 9), but at pH values above 8 boron was stripped from the organic phase. 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. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.HPLC of Formula: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts