the pen is blue
Australian psychedelic shred machine.
Hey folks!
First time poster long time observer,
I've recently delved into the beautiful world of dmt extraction and making some beautiful progress.
My most recent setup went like this:
100 grams of acacia acuminata bark.
3 cups of water
2 cups of vinegar
100 grams of sodium hydroxide
I started my process by freezing and defrosting the 100 grams of aca x2 in a large plastic container which was immersed with 250ml of water to moisten the aca.
After x2 freeze I then placed this within a stainless steel pot, and added an additional 2 cups of water and 2 cups of vinegar.
I then brought this mixture to a light simmer and periodically stirred this mixture with a potato masher (including mashing this mixture) every 5 minutes (lid on)
After approximately 60 minutes of boiling, I then allowed the mixture to become Luke warm before then transferring the contents in a fine sieve and filtering out the heavy particulates. I then placed the aca bark into a muslin cloth and squeezed until a majority of the acidic solution was out. This transfer was all into a glass bowl.
I then transferred this solution back into the stainless steel pot (which was cleaned before I retransferred)
I then added sodium hydroxide at around 20 gram increments until the entire 100 grams was added to the now basic solution, ( I also stirred the entire time that I was adding the sodium hydroxide).
Whilst this solution was cooling down I placed the lid back on to contain evaporants.
After the basic solution had cooled down to 40 degrees Celsius. I then poured my solution into 2 jars around the 3/4 full mark (around 750ml capacity glass jar). I then poured 75ml of naptha into the solution and agitated until the naptha was not visibly present. I then allowed the solution to settle bringing the naptha back to the surface and repeated this process x5.
I then left this for 24 hours, and pulled my naptha out being cautious not to remove any of the basic solution. I placed this into a graduated flask and placed a fan in front of this to aid in evaporation.
Once 1/2 of the napthalene had evaporated I then placed into to glass bowls and placed cling film over the tops of each making sure that the film is tight. And then placed into a freezer at -18 degrees Celsius.
After 24 hours I pulled my bowls out of the freezer and poured the remaining naptha back into the basic solutions. I then allowed these to dry over the course of 8 hours in front of a fan (upright) with the room temperature not being higher than 20 degrees centigrade.
My yield from this first pull was .46 grams
First time poster long time observer,
I've recently delved into the beautiful world of dmt extraction and making some beautiful progress.
My most recent setup went like this:
100 grams of acacia acuminata bark.
3 cups of water
2 cups of vinegar
100 grams of sodium hydroxide
I started my process by freezing and defrosting the 100 grams of aca x2 in a large plastic container which was immersed with 250ml of water to moisten the aca.
After x2 freeze I then placed this within a stainless steel pot, and added an additional 2 cups of water and 2 cups of vinegar.
I then brought this mixture to a light simmer and periodically stirred this mixture with a potato masher (including mashing this mixture) every 5 minutes (lid on)
After approximately 60 minutes of boiling, I then allowed the mixture to become Luke warm before then transferring the contents in a fine sieve and filtering out the heavy particulates. I then placed the aca bark into a muslin cloth and squeezed until a majority of the acidic solution was out. This transfer was all into a glass bowl.
I then transferred this solution back into the stainless steel pot (which was cleaned before I retransferred)
I then added sodium hydroxide at around 20 gram increments until the entire 100 grams was added to the now basic solution, ( I also stirred the entire time that I was adding the sodium hydroxide).
Whilst this solution was cooling down I placed the lid back on to contain evaporants.
After the basic solution had cooled down to 40 degrees Celsius. I then poured my solution into 2 jars around the 3/4 full mark (around 750ml capacity glass jar). I then poured 75ml of naptha into the solution and agitated until the naptha was not visibly present. I then allowed the solution to settle bringing the naptha back to the surface and repeated this process x5.
I then left this for 24 hours, and pulled my naptha out being cautious not to remove any of the basic solution. I placed this into a graduated flask and placed a fan in front of this to aid in evaporation.
Once 1/2 of the napthalene had evaporated I then placed into to glass bowls and placed cling film over the tops of each making sure that the film is tight. And then placed into a freezer at -18 degrees Celsius.
After 24 hours I pulled my bowls out of the freezer and poured the remaining naptha back into the basic solutions. I then allowed these to dry over the course of 8 hours in front of a fan (upright) with the room temperature not being higher than 20 degrees centigrade.
My yield from this first pull was .46 grams
