Safety of Octadecan-9-olOn March 31, 2002, Ohrui, Hiroshi; Terashima, Hanae; Imaizumi, Keiichiro; Akasaka, Kazuaki published an article in Proceedings of the Japan Academy, Series B: Physical and Biological Sciences. The article was 《A solution of the “”intrinsic problem”” of diastereomer method in chiral discrimination: Development of a method for highly efficient and sensitive discrimination of chiral alcohols》. The article mentions the following:
Very potent fluorescent chiral labeling reagents for alcs., (R,R)- and (S,S)-2-(anthracene-2,3-dicarboximido)cyclohexanecarboxylic acids, were developed. By labeling with them, the enantiomeric discriminations of primary alcs. having a Me branching at the carbon from 2 to 9 by 1H-NMR and from 2 to 16 by HPLC were achieved. Further, HPLC separations of all four optical isomers of Me branched secondary alcs. and enantiomers of 9-nonadecanol were also achieved. The experimental process involved the reaction of Octadecan-9-ol(cas: 591-70-8Safety of Octadecan-9-ol)
Octadecan-9-ol(cas: 591-70-8) belongs to hydroxy-containing compounds. Hydroxy-containing compounds engage in intermolecular hydrogen bonding increasing the electrostatic attraction between molecules and thus to higher boiling and melting points than found for compounds that lack this functional group. Organic compounds, which are often poorly soluble in water, become water-soluble when they contain two or more hydroxy groups, as illustrated by sugars and amino acid.Safety of Octadecan-9-ol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts