General Description
Off-white crystals or olive to light purple waxy solid. Forms monohydrate (melting point: 102-106°F).
Reactivity Profile
OLIVETOL(500-66-3) is incompatible with acid chlorides, acid anhydrides and oxidizing agents.
Air & Water Reactions
Sensitive to air. Insoluble in water.
Fire Hazard
This chemical is probably combustible.
Chemical Properties
light purple to brown crystalline mass
Chemical Properties
OLIVETOL is an off-white crystals or olive to light purple waxy solid. Forms monohydrate (melting point: 102-106°F). Olivetol is a member of the class of resorcinols that is resorcinol in which the hydrogen at position 5 is replaced by a pentyl group. It has a role as a lichen metabolite.
Physical properties
light purple to brown crystalline mass.
Application
Olivetol is a precursor in various syntheses of tetrahydrocannabinol.
Definition
ChEBI: A member of the class of resorcinols that is resorcinol in which the hydrogen at position 5 is replaced by a pentyl group.
Preparation
olivetol can also be formed through hydrolysis of intermediate polyketide CoAs or spontaneous cyclization.
Biological Activity
Olivetol (5-Pentylresorcinol, 5-n-Amylresorcinol) is a naturally occurring organic compound being a precursor in various syntheses of tetrahydrocannabinol. It acts as a competitive inhibitor of the cannabinoid receptors CB1 and CB2.?
Safety
Olivetol is still a very new product. It has not been researched nearly enough to prove it's safe to use. So far, no one has reported any adverse side effects as far as we know. Until more information is available, carefully control your THC intake instead of relying on an untested gelcap.
storage
Store at 2-8°C, stored under nitrogen
Mode of action
When you look at olivetol's molecular structure, it'll look very familiar. It's as if someone took a THC molecule and sliced it in two. Olivetol, like THC, works by binding with the CB1 receptors that exist all over your body and brain. But, olivetol is thought to be smaller and stickier than THC, so that helps it reduce a raging high in two ways. First, it slips into any open receptors before THC can get there to block them—so you won't get any higher. Second, it bumps into THC molecules that are already lodged in a CB1 receptor to knock them loose and take their place. That's how it brings you down.
According to numerous personal accounts, olivetol works, but we don't know exactly how it does so. More research and investigation is needed, but in theory it's very similar to how Narcan acts to reverse opiate overdoses.
