It's a weird little bugger; both of the optical isomers are active, but unlike all the other psychedelic amphetamines, the two isomers produce different subjective effects. The L isomer has actions at the 5HT2a receptor in the same way that other psychedelic amphetamines do (but has a much lower affinity than the normally encountered psych. amphetamines - hence the higher dose), but the D isomer has the entactogenic activity that's shown by MDMA.
As I'm yet to hear of a clandestine sythesis that was resolved into the optical isomers, what you get with a dose of MDA is essentially two related, but distinctly different pharmacological activities; that's what makes MDA different to any other psychedelic you're likely to come across.
It would be interesting to see if IAP had that same quirk of optical isomers with different pharmacological profiles