Synthetic ester lubricants was written by Barnes, R. S.;Fainman, M. Z.. And the article was included in Lubrication Engineering in 1957.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:
Phys. properties and coefficients of friction were determined for esters of neopentyl glycol, tri(hydroxymethyl)ethane, tri(hydroxymethyl)propane, pentaerythritol, 2-butyl-2-ethyl-1,3-propanediol, and 2,2,4-trimethyl-1,3-pentanediol with n-C9, n-C10, n-C14 and n-C18 acids from natural sources, highly branched acids obtained by the Oxo process, and mixed normal and branched acids obtained by caustic extraction of the liquid product from CO hydrogenation. Study of the thermal decomposition at 260° of selected esters indicated that its rate is generally greatly increased by H in the β position. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Safety of 2-Butyl-2-ethylpropane-1,3-diol).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Safety of 2-Butyl-2-ethylpropane-1,3-diol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts