A series of unsaturated branched esters were purified by preparative g
as chromatography and their odor thresholds were determined using sens
ory panel methods. In general, unsaturated branched esters had higher
odor thresholds than their saturated counterparts. Double bond positio
n and configuration had marked influences on the odor threshold. In mo
st cases the addition of a double bond in the C-2 position of the acid
resulted in significantly higher odor thresholds while the addition o
f a double bond in positions further away from the acid carbonyl had a
smaller effect on the odor threshold. Ethyl 2-methyl-4-pentenoate had
the lowest odor threshold (0.01 mu L/10(3) L) of the esters tested wh
ile methyl (E)-2-methyl-2-butenoate (methyl tiglate; 130 mu L/10(3) L)
had the highest odor threshold.