Talk:2,3-Dimethylpentane

Data for the enantiomers
Most experimental data seems to use the racemic mixture. Is there literature on the enantiomers? There may be a paper in Chimiké Listy volume 51 (1957) by Lukes and Langthaler, whose title translates into "degradation of branched optically active tertiary bases", but I don't have access to it. The racemic mixture seems to be very hard to crystallize (glass transition at 123 K). Perhaps the pure enantiomers can be crystallized? --Jorge Stolfi (talk) 04:06, 6 November 2018 (UTC)