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Cyclic fatty acids: Separation from straight‐chain fatty acids by urea adducting
Author(s) -
Eisenhauer R. A.,
Beal R. E.
Publication year - 1968
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/bf02668964
Subject(s) - chemistry , urea , stearic acid , organic chemistry , fatty acid , adduct , fraction (chemistry) , oleic acid , crystallization , palmitic acid , chromatography , biochemistry
A mixture containing 37% cyclic and 63% straight‐chain fatty acids, made by high‐temperature treatment of linseed oil fatty acids with alkali, was separated by the urea adduct method to give unsaturated cyclic fatty acids (nonadduct) in 95% purity and 90–95% yeild. Previous reports from this Laboratory describe a process for separating cyclic fatty acids from stearic acid by hydrogenation followed by crystallization at −40C. The urea adduct method avoids hydrogenation and low‐temperature crystallization, and furthermore, unsaturated cyclic and unsaturated straight‐chain products can be recovered as individual fractions. Then, by readducting the unsaturated straight‐chain fatty acid fraction, the small amounts of palmitic and stearic acids are removed leaving an unsaturated fraction containing oleic, nonconjugated and conjugated linoleic and some unsaturated cyclic fatty acids.