“…[34,37,75,76] The alleged identification of 'a second atranol isomer' requires confirmation. [37] As the free haematommic acids are very labile, or because they are mainly present as ethyl esters, which are formed during the processing of the resinoids with ethanol, attention was rather focused on ethyl haematommate 28 and ethyl chlorohaematommate 36. [22,34] Actually, very little is known about the sensitizing potential of the acids, either isolated or present at low levels, in oakmoss extracts.…”