"The liver converts the tri-chromes into 11 hydroxy THC which is 4 times as potent as when smoked."
Got a link?
Your recipe for cannabutter is fine, but no different than a hundred others I've seen.
#50 | Posted by nullifidian at 2009-10-04 12:46 AM
The only thing that isn't complete in that recipe is that I didn't explain how heat is the reason for the tri-chrome bonds breaking and fat is what they attach to. Delta-9-THC vaporizes quickly into 11-hydroxy-THC when smoked, but some is lost the longer and hotter the burn as O2 is added. When introduced into a suspension (butter) and digested via the liver the effects are more pronounced.
Here's a chart of smoking versus eating (minus the heat, fat) that I got form this useful forum thread.
Try it and let me know what you believe to be the case. It can also be made into an oil which can go onto salads or into other foods with as strong an effect. This is particularly useful for avoiding the stench of burning weed and the possible harm to the lungs from smoke inhalation.
Tetrahydrocannabinol
Main article: Tetrahydrocannabinol
Tetrahydrocannabinol (THC) is the primary psychoactive component of the plant. Medically, it appears to ease moderate pain (analgetic) and to be neuroprotective. THC has approximately equal affinity for the CB1 and CB2 receptors.[5] Its effects are perceived to be more cerebral.[citation needed]
delta-9-Tetrahydrocannabinol (Δ9-THC, THC) and delta-8-tetrahydrocannabinol (Δ8-THC), mimic the action of anandamide, a neurotransmitter produced naturally in the body. The THCs produce the high associated with cannabis by binding to the CB1 cannabinoid receptors in the brain.
11-Hydroxy-THC
11-Hydroxy-Δ9-
tetrahydrocannabinol (11-OH-THC) is the main active metabolite of THC which is formed in the body after cannabis is smoked[1]. 11-hydroxy-THC has been shown to be active in its own right[2], but the effects produced are not necessarily identical to those of THC[3]; it is plausible that the biphasic action of cannabis might be explained by the action of the active metabolite of THC rather than by other compounds present in the plant such as cannabidiol, so that 11-hydroxy-THC might be responsible for causing certain effects such as sleepiness and increased appetite which are characteristically delayed and occur as the initial "high" is wearing off.
11-hydroxy-THC is subsequently metabolised further to 11-carboxy-THC, which is not psychoactive but may still play a role in the analgesic and anti-inflammatory effects of cannabis.