The author of 《Chiral discrimination of secondary alcohols by both 1H-NMR and HPLC after labeling with a chiral derivatization reagent, 2-(2,3-anthracenedicarboximide)cyclohexane carboxylic acid》 were Ohtaki, Takashi; Akasaka, Kazuaki; Kabuto, Chizuko; Ohrui, Hiroshi. And the article was published in Chirality in 2005. Recommanded Product: 591-70-8 The author mentioned the following in the article:
Enantiomeric discrimination of chiral secondary alcs. was performed by both reversed-phase HPLC and 1H-NMR after labeling with a chiral fluorescent derivatization reagent, 2-(2,3-anthracenedicarboximide)cyclohexanecarboxylic acid. It was possible to discriminate by HPLC the chirality of alcs. up to C30 having a chiral hydroxyl group at the middle of the straight alkyl chain, and by 1H-NMR, alcs. up to C16. For alcs. having one straight alkyl and one isoalkyl group with the same carbon numbers at both sides of a hydroxyl group, it was possible to discriminate the chiralities of alcs. up to C19 by both 1H-NMR and HPLC. The 1H-NMR methods also made it possible to determine absolute configurations empirically. In the experimental materials used by the author, we found Octadecan-9-ol(cas: 591-70-8Recommanded Product: 591-70-8)
Octadecan-9-ol(cas: 591-70-8) belongs to hydroxy-containing compounds. Hydroxy groups participate in the dehydration reactions that link simple biological molecules into long chains.Recommanded Product: 591-70-8 The joining of a fatty acid to glycerol to form a triacylglycerol removes the −OH from the carboxy end of the fatty acid.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts