Dear all,
after reading several discussions on this forum it became apparent to me that it seems to be a common practice for many people to use DCM as solvent for the extraction of DMT.
While being a versatile solvent for many ways of application, for DMT it is actually not recommendable to use DCM due to a specific reaction with DMT, resulting in the formation of a quaternary ammonium salt byproduct, i.e. N-chloromethyl-N,N-dimethyltryptamine chloride.
If it is desired to use alkyl halides as solvent, then it is better to use chloroform (CHCl3) instead of DCM, or otherwise any other non polar solvent.
A detailed description of these findings can be found in the original article:
Dunlop & Olson, 2018 - "Reaction of N,N-Dimethyltryptamine with Dichloromethane Under Common Experimental Conditions." ACS Omega 3(5): 4968–4973.
Just FYI
Best regards
noo
after reading several discussions on this forum it became apparent to me that it seems to be a common practice for many people to use DCM as solvent for the extraction of DMT.
While being a versatile solvent for many ways of application, for DMT it is actually not recommendable to use DCM due to a specific reaction with DMT, resulting in the formation of a quaternary ammonium salt byproduct, i.e. N-chloromethyl-N,N-dimethyltryptamine chloride.
If it is desired to use alkyl halides as solvent, then it is better to use chloroform (CHCl3) instead of DCM, or otherwise any other non polar solvent.
A detailed description of these findings can be found in the original article:
Dunlop & Olson, 2018 - "Reaction of N,N-Dimethyltryptamine with Dichloromethane Under Common Experimental Conditions." ACS Omega 3(5): 4968–4973.
Just FYI
Best regards
noo