Extraction of boric acid with aliphatic 1,3-diols and other chelating agents was written by Egneus, Birgitta;Uppstrom, Leif. And the article was included in Analytica Chimica Acta in 1973.Application of 115-84-4 The following contents are mentioned in the article:
Some 40 compounds were investigated with reference to their boric acid extraction properties. Preliminary tests showed that aliphatic 1,3-diols with at least 6 C atoms possess superior extraction qualities compared to diketones, hydroxyketones, hydroxyamines, and other species investigated. The 1,3-diols were further studied with attention to size and steric configuration. The extraction equilibrium involved were investigated for 2,2-diphenylpropanediol-1,3. The constants derived showed that this diol, in spite of its large hydrophobic groups, has a smaller reaction constant than the previously investigated 2,2-diethylpropanediol-1,3 and 2-ethylhexanediol-1,3. The extraction capacity has a maximum for 1,3-diols with 8-9 C atoms. The largest B distribution was obtained with 2,2,4-trimethylpentanediol-1,3, which seems to form a very stable ester with boric acid in CHCl3 at room temperature The ester formation is supported by NMR and ir spectra. The effect of geminal substituents in the 2-position is discussed. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application of 115-84-4).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Application of 115-84-4
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts