Hi guys,
So a while back some spice was extracted from Mimosa and after three pulls and a freeze precipitation 0.405mg of yellow-white crystals were left on a weighing scale.

These had some slight contamination: bits of pipette rubber were present, as well as some of the lye soup. So the plan then became to do a wash.
It was decided to not do Sodium Bicarbonate as it was gathered that shop bought Bicarbonate of Soda (Dr. Oetker) would do the trick. Bicarbonate of Soda was mixed in the room temp water until it became a saturated solution. The solution was then added to DMT dissolved in heated naphtha. Separation occurred and the dirty parts clearly stayed in the bicarb solution on the bottom. The naphtha was siphoned off from a measuring cylinder and into a dish for freeze precip. However, after this freeze precip there were now only 0.215mg of white spice left.

My question is why was almost half lost? Was the first pull just really dirty (it doesn't look it)? Is shop bought bicarb bad? Bubbles were noticed on the jar in which agitation occurred, were they crystals getting stuck?
I was just wondering how much everyone normally loses in a clean. This was the first process done after extraction there was no re-x or anything like that. Any ideas would be much appreciated.
Nature is not mute; it is man who is deaf. - Big T