69ron
Rising Star
Diethyl ether, DCM, xylene, and chloroform should all extract this so called "Jungle Spice" or "Dark Spice" according to posts I've read from other SWIMs.
Diethyl ether, like DCM and chloroform, will extract a lot of DMT N-Oxide. When impure, it looks like brown goo and will prevent your DMT from crystallizing if there is enough present. When pure it looks like yellow goo. It doesn't crystallize no matter how pure it is. It is active however, but SWIMs tests found it is slightly less potent than DMT and is more gentle, so it's probably not the "Jungle Spice" people are talking about.
Naphtha and heptane cannot extract any N-Oxides. N-Oxides are too polar to be extracted by those solvents. I don't know if xylene can extract N-Oxides or not.
N-Oxides of DMT can be generated in a few minutes in certain cases. For example, heating DMT with a fan blowing over it seems to make DMT N-Oxide rather quickly.
When using a solvent like diethyl ether, you’re going to extract a larger array of alkaloids. For example, if you extracted from Anadenanthera colubrina using naphtha or heptane, only a tiny bit of alkaloids would get extracted. Most would not get extracted. You would extract DMT and 5-MeO-DMT almost exclusively. Alkaloids that would be excluded include DMT N-Oxide, 5-MeO-DMT N-Oxide, bufotenine, bufotenine N-Oxide, serotonin, and a few others. But if you extracted with diethyl ether, nearly all the alkaloids would get extracted.
Diethyl ether, DCM and chloroform are very similar solvents and they usually extract a wider range of alkaloids compared with the more non-polar solvents like naphtha and heptane.
The only solvents that are better are the alcohols usually, but they are water soluble and can’t usually be used in an A/B extraction. However, isopropyl alcohol can be used as a sort of non-polar solvent in an A/B extraction if the water is saturated with salt (sodium chloride). Isopropyl alcohol is insoluble in water saturated with salt and forms a separate layer. This is useful sometimes when you’re trying to extract an alkaloid that is very water soluble and won’t easily get extracted by the true non-polar solvents.
Diethyl ether, like DCM and chloroform, will extract a lot of DMT N-Oxide. When impure, it looks like brown goo and will prevent your DMT from crystallizing if there is enough present. When pure it looks like yellow goo. It doesn't crystallize no matter how pure it is. It is active however, but SWIMs tests found it is slightly less potent than DMT and is more gentle, so it's probably not the "Jungle Spice" people are talking about.
Naphtha and heptane cannot extract any N-Oxides. N-Oxides are too polar to be extracted by those solvents. I don't know if xylene can extract N-Oxides or not.
N-Oxides of DMT can be generated in a few minutes in certain cases. For example, heating DMT with a fan blowing over it seems to make DMT N-Oxide rather quickly.
When using a solvent like diethyl ether, you’re going to extract a larger array of alkaloids. For example, if you extracted from Anadenanthera colubrina using naphtha or heptane, only a tiny bit of alkaloids would get extracted. Most would not get extracted. You would extract DMT and 5-MeO-DMT almost exclusively. Alkaloids that would be excluded include DMT N-Oxide, 5-MeO-DMT N-Oxide, bufotenine, bufotenine N-Oxide, serotonin, and a few others. But if you extracted with diethyl ether, nearly all the alkaloids would get extracted.
Diethyl ether, DCM and chloroform are very similar solvents and they usually extract a wider range of alkaloids compared with the more non-polar solvents like naphtha and heptane.
The only solvents that are better are the alcohols usually, but they are water soluble and can’t usually be used in an A/B extraction. However, isopropyl alcohol can be used as a sort of non-polar solvent in an A/B extraction if the water is saturated with salt (sodium chloride). Isopropyl alcohol is insoluble in water saturated with salt and forms a separate layer. This is useful sometimes when you’re trying to extract an alkaloid that is very water soluble and won’t easily get extracted by the true non-polar solvents.