as a rule of thumb the extraction of marihuana with carbon dioxide of density 0.9 g/ml at 40 degrees C for 34 min and of hashish for 18 min can be suggested. The application of the proposed extraction times ensured at least a 95% recovery for the main neutral cannabinoids.
In PCT/GB02/00620 the applicant discloses a method of preparing a herbal drug extract (botanical drug substance) from medicinal cannabis. The process comprises: 1. a heating step to decarboxylate the acid form of the cannabinoids to theirneutral form; 2. a first extraction with a specified volume of liquid carbon dioxide for 6 8 hours; and 3. a step to reduce the proportion of non-target materials, referred to as winterisation, which step precipitates out waxes.
More specifically, PCT/GB02/00620 describes a process wherein: step 1 comprises heating chopped cannabis (2 3 mm) at 100 150° C. for sufficient time to allow decarboxylation; step 2 comprises CO2 extraction using: a) a coarse powder(the particles are passed through a 3 mm mesh); b) a packing density of 0.3; and c) supercritical conditions of 600 bar at 35° C. for 4 hours, although other combinations of temp and pressure ranging from 10 35° C. and 60 600 bar (bothsuper critical and sub critical conditions) could, it is acknowledged, be used; and step 3 comprises conducting an ethanolic precipitation at -20° C. for 24 hours and removing the waxy material by filtration.
The supercritical method disclosed in PCT/GB02/00620 produced: a) a high THC extract containing: 60% THC (Δ9-tetrahydrocannabinol) 1 2% CBD (cannabidiol) 4 5% other minor cannabinoids including CBN (cannabinol) (Quantative yields were9% wt/wt based on dry weight of medicinal cannabis); and b) a high CBD extract containing: 60% CBD 4% THC 2% other cannabinoids (Quantative yields were 9% wt/wt based on dry weight of medicinal cannabis).
Clearly as the resulting BDS is to be used in a pharmaceutical product it is essential that the process is safe, scalable to GMP and gives high degrees of product consistency and, preferably also good yields.
The principles of supercritical fluid extraction (SFE) have been known since the work of Baron Cagniard de le Tour in 1822 when it was noted that the gas-liquid boundary disappeared when the temperature of certain materials was increased byheating them in a closed glass container. From this early work the critical point of a substance was first discovered. The critical point is the temperature above which a substance can co-exist in gas, liquid and solid phases. It was later found thatby taking substances to or above their critical temperature and pressure they could be used as sophisticated solvents for extraction and fractionation of complex mixtures.
People have been talking about supercritical fluid extraction of essential oils of cannabis online since OG's dawn and before I imagine. I can only personally attest to the talk at OG but perhaps others remember when butane extraction was referred to as supercritical fluid extraction. The Lycaeum and its ilk may have been responsible; I believe supercritical fluid extraction was the name given to the first successful butane extraction of DMT performed at the DMT Vaults in the fall of 1998.
What I have yet to see is anyone posting the results of a true supercritical extraction. To claim that there's no reason to pursue this as the above poster does is willful ignorance. There's no point in informing someone as to why CO2 and organic solvents might be slightly different to inhale at high temperatures should complete evaporation of solvent prove impractical if the person clearly thinks that CO2 and all organic solvents on that list are equally kosher to put in your resin.
Alright look at the last section of the last link posted at the top here. Because it is extremely awesome and will blow everyone's mind I will post a portion here below.
Looks like Eden Labs is violating INDRA's patent huh.
More than that, I'm grateful you've taken the time to inform me of the error of my ways and to remind me to be grateful that my feeble mind can understand current methods. Now I can stop trying to improve my product and can rest assured that things are as good as they're going to get.
It's a good thing you don't want to start a flame war over anything silly. You're a fucking bitch, I bet your oil gets about as hard as your dick.
Oil of catnip was extracted via the supercritical fluid carbon dioxide in an
SFT1000 Supercritical Fluid Processing Unit (SFPU). The dried catnip (consisting of
Page 4 leaves, stems, and buds) was crushed and 17.533g were packed into a 50mL stainless steel vessel. After securing the vessel into place, the SFPU was set to the appropriate conditions. The conditions were checked using the “system status” function, and conditions were altered using the “rest parameter editor” function. The initial
temperature for the SFE/SFR was set to 40°C while the initial pressure setpoint was
2000 psi. During this time, the vessel filled with liquid carbon dioxide. The pressure was
raised in increments of 2000 psi by use of a pneumatic pump until the desired pressure
of 6000 psi was obtained. The SFPU operated in the static mode for 30 minutes
allowing the carbon dioxide time to soak through the catnip. After this time, the unit was
set to dynamic mode for 7 minutes, and the restrictor valve was opened manually 13 full
turns (completely opened is 17 turns) in the counter clockwise direction. It was
important to monitor the restrictor valve temperature at this time using the “system
status” function. If the temperature, set to approximately 60°C, fell below 5°C, the
restrictor valve had to be turned in the clockwise direction to maintain the temperature
above the freezing point. During this time, supercritical carbon dioxide extracted the oil
from the sample and carried it to the collection jar. After the completion of the 7
minutes, the pressure setpoint was reset to zero using the “rest parameter editor.” (The
mode was still dynamic). The restrictor valve was turned in the counter clockwise
direction allowing a rapid fall in pressure. When the pressure fell below 1200 psi, the
“open depressurization valve” function was selected to provide the final rapid
depressurization.