So swim found some pure Iso and read up on it
at wiki it said :-
Unlike ethanol or methanol, isopropanol can be separated from aqueous solutions by adding a salt such as sodium chloride, sodium sulfate, or any of several other inorganic salts, since the alcohol is much less soluble in saline solutions than in salt-free water [5] The process is colloquially called salting out, and causes concentrated isopropanol to separate into a distinct layer.
So swim thought this :- if say cannabis or salvia was left in iso for a period of time - then filtered then mixed with water.
Salt added to separate the water from solvent,
surely the salvianorin or thc would stay disolved in the iso on separation and the contaminants would stay in the water - at least partially.
This idea could lead to a clener di-terpenoid extraction and beats my last salvia extraction idea - or so it would seem.
Comments or suggestions on what else iso can be used for(anything to do with the kinda chemistry discussed here) would be greatly appreciated.
at wiki it said :-
Unlike ethanol or methanol, isopropanol can be separated from aqueous solutions by adding a salt such as sodium chloride, sodium sulfate, or any of several other inorganic salts, since the alcohol is much less soluble in saline solutions than in salt-free water [5] The process is colloquially called salting out, and causes concentrated isopropanol to separate into a distinct layer.
So swim thought this :- if say cannabis or salvia was left in iso for a period of time - then filtered then mixed with water.
Salt added to separate the water from solvent,
surely the salvianorin or thc would stay disolved in the iso on separation and the contaminants would stay in the water - at least partially.
This idea could lead to a clener di-terpenoid extraction and beats my last salvia extraction idea - or so it would seem.
Comments or suggestions on what else iso can be used for(anything to do with the kinda chemistry discussed here) would be greatly appreciated.