Note: This is addition to the question above.
Since Dimethyltryptamine is an indole alkaloid (aromatic) does that mean that an aromatic non polar solvent like Dichloromethane/Toluene/Xylene can dissolve it to some extent even in its protonated form? For example during aqueous biphasic systems (the defatt)?
(I ask specifically for DCM, since its the most polar of the above mentioned solvents, i have ongoing project involving small scale experimentation with Acacias and Grasses and i dont want to skip the defatt, DCM will be used as extraction solvent, however im not convinced about its use during the defatt).
While aliphatic solvents like Heptane for example (as non polar as it gets) presumably could be more effective than aromatics when it comes to the defatting procedure because: they wont dissolve any amounts of salts; low polarity.
After all, likes dissolves likes. Right?
I'm not chemist nor do i qualify myself as one, help me!