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5-MeO-MiPT BUY, 5-Methoxy-N-methyl-N-isopropyltryptamine, sometimes referred to as "Moxy", is an entactogenic and hallucinogenic drug belonging to the family of substances known as tryptamines. It is the known hallucinogenic N-methyl-N-isopropyl homolog of 5-MeO-DMT. It is comparable in structure and pharmacodynamics to the drugs 5-MeO-DiPT, DiPT and MiPT.
Prior to the publication of its synthesis and pharmacology by Repke, Grotjahn and Shulgin in the Journal of Medicinal Chemistry in 1985, the use of this drug in humans was unknown. Today, it is mostly purchased as a gray-zone research chemical from online vendors and used as an entheogen and recreational drug. It is rarely sold on the street.
The process that produces this. Although there may be other mechanisms of action, such as inhibition of MAO, 5-HT2A receptor agonism is thought to be the main cause of the hallucinogenic and entactogenic effects of 5-MeO-MiPT.
I will now begin to break down and discuss the complicated and wide range of effects that the 5-MeO-MiPT experience includes, based on the preset index of potential subjective effects that you can find here.
Physical effects:
Three distinct elements make up the physical effects of 5-MeO-MIPT, and each one becomes stronger as the dosage increases. These are explained below and typically consist of:
Unplanned tactile experiences: The 5-MeO body high is characterized by a pleasant, comforting, soothing and penetrating glow. In addition, there is a cool and sharp tingling sensation that occurs at various random times throughout the course of itself. Although there may be other mechanisms of action such as inhibition of MAO, 5-HT2A receptor agonism is thought to be the main cause of the hallucinogenic and entactogenic effects of 5-MeO-MiPT.
During the journey, it can continue to be a steady presence for others, gradually increasing at the beginning of the journey and reaching its maximum when the summit is reached.
Stimulation and sedation: 5-MeO-MIPT can have both energizing and sedative effects on the physical energy level of a tripper. Physical energy levels appear to follow an unexpected wave pattern. This appears to be largely environment dependent and can be energizing and stimulating during physically strenuous activities such as dancing or jogging. On the other hand, quiet environments such as dimly lit rooms with cozy furniture can have a calm, serene and even slightly soothing effect.
Nausea: This is a common side effect that often disappears as soon as the person feels better. Occasionally, initial vomiting may also occur. Compared to other psychedelics such as psilocin, LSD and 2C-E, the effectiveness of this drug can be considered quite modest. It has been reported that this drug is significantly less physically stimulating and has a much lower tendency to cause unpleasant physical reactions than 5-MeO-DIPT.
Cognitive effects: Many people describe the 5-MeO-MIPT mind space as insightful, sometimes calming and occasionally extremely stimulating. This material generates a significant amount of
far-reaching cognitive consequences of psychedelics. Typically, the most notable of these consequences consist of:
The self-observation component only appears when the user is alone in an environment without social interaction.
Increased affection, sociability and empathy are traits that only manifest themselves regularly in social situations where you are with other people. Although these emotions are somewhat gentler and less intense than those induced by drugs such as MDMA and 2C-B, they are still strong enough to have long-lasting therapeutic benefits. These emotions include kindness, affection and empathy.
What is 5-MeO-MiPT?
5-Methoxy-N-methyl-N-isopropyltryptamine (also known as 5-MeO-MiPT and Moxy) is a psychedelic substance of the tryptamine class. It has become increasingly popular in recent years due to its tactile effects, which serve to increase libido and sexual pleasure.
5-MeO-MiPT is chemically related to tryptamines such as 5-MeO-DMT and 5-MeO-DiPT. It produces its psychoactive effects through activity at serotonin receptors in the brain.
The synthesis and pharmacology of 5-MeO-MiPT was first described by David Repke and Alexander Shulgin in 1985. Its effects on humans were documented in Shulgin's book TiHKAL ("Tryptamines I have known and loved").
Chemical properties of 5-MeO-MiPT
5-MeO-MiPT is a synthetic indole alkaloid molecule of the tryptamine class. Tryptamines share a core structure consisting of a bicylindole heterocycle linked to an amino group at R3 via an ethyl side chain. 5-MeO-MiPT is substituted at R5 of its indole heterocycle with a methoxy (MeO) functional group CH3O-; it also contains a methyl group and an isopropyl chain attached to the terminal amine RN of its tryptamine backbone (MiPT).
What are the effects of 5-MeO-MiPT?
The psychedelic effects of 5-MeO-MiPT are thought to be due to its efficacy at the 5-HT2A receptor as an [[agonist # agonists | partial agonist]] and additional mechanisms of action such as inhibition of MAO (i.e. digestive enzymes in the stomach). have also been speculated, although this has yet to be scientifically proven.
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