Buy 3-MeO-PCP Online wholesale from the manufacturer, high quality at a low price with shipping worldwide.3-meo-pcp with the formal name of 1-[1-(3-methoxyphenyl)cyclohexyl]-piperidine is classified as a dissociative compound. Buy 3-MeO-PCP online overnight without prescription
Firstly. 3-Methoxyphencyclidine (commonly known as 3-MeO-PCP or 3-MeO) is a lesser-known novel dissociative substance of the arylcyclohexylamine class that produces dissociative, anesthetic, and hallucinogenic effects when administered. It is structurally related to arylcyclohexylamines like PCP, MXE, and 3-MeO-PCE.
Secondly, 3-MeO-PCP was first synthesized in 1979 to investigate the structure-activity relationship of phencyclidine (PCP) derivatives. Its activity in humans was not described until 1999 when a chemist using the pseudonym John Q. Beagle reported qualitative similarities to PCP along with comparable potency.
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Like other substances of its class, particularly methoxetamine (MXE), phencyclidine (PCP), and 3-MeO-PCE, it is know to primarily induce a state refer to as “dissociative anesthesia”, although the extent to which this occurs is reporte to be highly dose-dependent and variable in its effects. It is commonly taken orally and nasally, although it may also be smok and injected.
Today, 3-MeO-PCP is rarely sell on the streets and almost exclusively obtain as a gray area research chemical through the use of online vendors, where it is commonly use as a recreational substance and, more rarely and controversially, as an entheogen.
3-Methoxyphencyclidine, or 3-MeO-PCP, is a synthetic dissociative of the arylcyclohexylamine class. 3-MeO-PCP contains cyclohexane, a six-member saturated ring, bonded to two additional rings at R1. One of these rings is a piperidine ring, a nitrogenous six member ring, bonded at its nitrogen group. The other ring is an aromatic phenyl ring, substituted at R3 with a methoxy group.
3-MeO-PCP is a PCP derivative and structurally analogous to 4-MeO-PCP.
3-MeO-PCP acts as an NMDA receptor antagonist. A specific subtype of glutamate receptor, NMDA (N-Methyl-D-Aspartate). Modulates the transmission of electrical signals between neurons in the brain and spinal cord; for the signals to pass, the receptor must be open.