The thermal decomposition reactions of cholic acid (1), methyl cholate
(2), 3 alpha-acetoxy-7 alpha,12 alpha-dihydroxy-5 beta-methylcholanat
e (3), 3 alpha,7 alpha-diacetoxy-12 alpha-hydroxy-5 beta-methylcholana
te (4), 3 alpha,7 alpha-diacetoxy-12 alpha-oxo-5 beta-methylcholanate
(5) and 3 alpha,7 alpha,12 alpha-triacetoxy-5 beta-methylcholanate (6)
were studied by DTA and TGA. The thermal decomposition of cholic acid
proceeds as a one stage process in the range 200-420 degrees C. The e
sterification of the carboxylic group of cholic acid results in consid
erable increase of the thermal stability of compound (2). The endother
mic peaks at about 100 degrees C occurring only in compounds (1) and (
2) can be attributed to desolvation and release of hygroscopically bou
nd water. The thermal decomposition reactions of the dried compound (2
) and compounds (3), (4) and (5) are found to proceed in two stages. D
uring the first stage, the thermal degradation of (5) leads to the for
mation of a completely deacetylated compound and two monodeacetylated
compounds with the predominant product resulting from the elimination
of the acetate group at C-3. Degradation of the carbon skeleton takes
place during the second stage.