3-MEO-PCE Powder | Buy 3-MEO-PCE Powder


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Buy 3-MEO-PCE powder online

3-MEO-PCE Powder or 3-methoxyeticyclidine also called methoxieticyclidine is a new dissociative chemical belonging to the class of arylcyclohexylamines which causes hallucinogenic and dissociative effects when consumed. Due to its structure, it is presented as an analogue of the PCE.

3-methoxyeticyclidine powder became popular in 2010 and sold in the online chemicals market or the darkweb as a legal alternative to ketamine or PCP. We have little information on the toxicity, metabolism and pharmacological properties of this compound, and its use in humans is highly uncertain. We strongly recommend that you use harm reduction practices when using this substance.

Is 3-MEO-PCE Powder legal?

N-ethyl-1- (3-methoxyphenyl) cyclohexan-1-amine or 3-MEO-PCE crystal vendor is classified as a drug from the arylcyclohexylamine group. Ayrlcyclohexylamines have a preference for use because of their structures which include a cyclohexane ring linked in an aromatic process with an amine group. 3-MeO-PCE powder USA comes with a phenyl process with a methoxy R3 recombinant to (CH3-O-) attached to a cyclohexane ring. An aminoethyl chain -NCH2CH3 is attached to the same R 1 carbon of the cyclohexanone ring. This compound along with MXE, has an amino-ethyl chain at the expense of the amino-methyl chain found in ketamine or DCK. It is an analogue to MXE, but lacks a ketone replaced by R2. It is also similar to 3-MeO-PCP but does not have the complementary carbons to add to a piperidine ring.

3-MEO-PCE Powder
3-MEO-PCE Powder


It largely acts as an antagonist of NMDA receptors. NMDA receptors allow the spine and neurons of the brain to better accept the electrical signals circulating there; provided that the receiver is ready. Dissociatives block NMDA receptors by shutting them down. A disconnection of the neurons leads to difficulties in moving, a loss of sensation, an almost similar failure of the famous “k hole”.

3-MeO-PCE powder erowid has properties of 61 nM Ki for the NMDA receptor, 2097 nM for the histamine H2 receptor, 115 nM for the serotonin transporter, 4519 nM for the σ1 receptor, 743 nM for the transporter dopamine, 964 nM for the alpha-2A adrenergic receptor or 525 nM for the σ2 receptor.

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