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Specification
Product Name: 4-HO-DMT
IUPAC Name: 3-[2-(Dimethylamino)ethyl]-1H-indol-4-ol
Other Names: Psilocin, Psilocine, Psilocyn, Psilotsin, 4-HO-DMT, 4-OH-DMT
Molecular Formula: None
Molar Mass: 237.26 g·mol−1
Effect: stimulant, psychedelic
Purity of the substance: 99.9%
Physical properties: Crystals, Powder
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  • 4-HO-DMT for sale online from USA vendor

Table of Contents

  1. History and Culture
  2. Chemistry
  3. Pharmacology
  4. Physical Effects
  5. Visual Effects
  6. Hallucinatory States
  7. Cognitive Effects
  8. Multi-Sensory and Transpersonal Effects
  9. Combination Effects
  10. Research Findings
    • Antidepressant Effects
    • Toxicity and Harm Potential
    • Tolerance and Addiction Potential
  11. Legal Status

Introduction to Psilocin

4-Hydroxy-N,N-dimethyltryptamine, commonly known as 4-HO-DMT or psilocin, belongs to the tryptamine class of naturally-occurring psychedelic substances. It serves as the primary psychoactive component in certain species of mushrooms. Structurally akin to the potent visionary entheogen DMT (N,N-dimethyltryptamine), psilocin presents intriguing properties for researchers and enthusiasts alike.

Discovery and Characteristics

Albert Hofmann, in 1958, isolated and christened psilocin. Its psychoactive effects are believed to stem from its chemical affinity to serotonin, a crucial neurotransmitter governing various sensory and cognitive functions within the brain. Psilocin's ability to interact with serotonin receptor sites underpins its psychedelic nature, leading to altered states of consciousness.

Natural Occurrence and Synthetic Form

Psilocin commonly coexists with psilocybin in considerable amounts within psilocybin-containing mushrooms. However, its synthetic manifestation is exceptionally rare. Anecdotal testimonies often describe pure psilocin as a more lucid and intense version of psilocybin mushrooms, reflecting its unique psychoactive properties.

Safety and Considerations

Unlike many heavily regulated substances, psilocin isn't deemed addictive or physiologically toxic. Nonetheless, users should exercise caution due to potential adverse psychological reactions such as severe anxiety, paranoia, or psychosis, particularly among individuals predisposed to mental health disorders. Embracing harm reduction practices is strongly encouraged for those engaging with psilocin.

In conclusion, understanding psilocin's intricacies offers insights into its therapeutic potential and risks, contributing to informed discourse surrounding psychedelic substances.

Unveiling Psilocin: History and Culture

Discovery and Naming

Psilocin and its phosphorylated inactive precursor, psilocybin, were initially identified and named in 1958 by Swiss chemist Albert Hofmann. Hofmann extracted these compounds from laboratory-cultivated specimens of the entheogenic mushroom Psilocybe mexicana before exploring their synthetic pathways.

The Chemistry of Psilocin

Psilocin, also recognized as 4-HO-DMT, represents an organic indole alkaloid molecule belonging to the tryptamine class of chemicals. Tryptamines, including psilocin, share a fundamental structure characterized by a bicyclic indole heterocycle linked at R3 to an amino group via an ethyl side chain. At R4 of its indole heterocycle, psilocin features a hydroxyl (-OH) functional group, along with two methyl groups (CH3-) bound to the terminal amine RN of the ethyl side chain. This configuration renders psilocin the 4-hydroxy structural analog of DMT and the dephosphorylated analog of psilocybin.

Psilocin can be derived from the dephosphorylation of natural psilocybin under strongly acidic or alkaline conditions through hydrolysis, a process mirroring its metabolic activation within the human body.

Concerning its physical attributes, 4-HO-DMT exhibits relative instability in solution due to its phenolic hydroxy (-OH) group. In the presence of oxygen, it readily forms bluish and dark black degradation products. Hence, it is advisable to store psilocin under optimal chemical storage conditions—cool, dry, and away from light—to mitigate excessive degradation.

Understanding the chemical intricacies of psilocin elucidates its behavior and potential applications within scientific and cultural contexts.

Navigating Psilocin Dosage

Understanding Thresholds

  • Threshold: 5 mg

Levels of Experience

  • Light: 10 - 15 mg
  • Common: 15 - 25 mg
  • Strong: 25 - 40 mg
  • Heavy: 40 mg and above

Psilocin dosage ranges provide a framework for understanding the spectrum of experiences associated with its consumption. Adhering to recommended thresholds and levels ensures safer and more controlled psychedelic encounters.

Unraveling the Pharmacology of Psilocin

Psilocin: The Active Agent

Psilocin emerges as the pharmacologically active compound within the body subsequent to the ingestion of psilocybin or certain species of psychedelic mushrooms.

Mechanisms of Action

Psilocybin undergoes rapid dephosphorylation within the body, converting into psilocin. Psilocin acts as an agonist or partial agonist at serotonin receptors, particularly 5-HT2A, 5-HT2C, and 5-HT1A. Notably, psilocin exhibits functional selectivity by activating phospholipase A2 rather than phospholipase C, the usual pathway of serotonin. Structurally akin to serotonin, psilocin differs by the hydroxyl group being on the 4-position rather than the 5 and the dimethyl groups on the nitrogen. Its primary effects are attributed to its partial agonist activity at 5-HT2A serotonin receptors in the prefrontal cortex.

Neurotransmitter Interaction

Psilocin does not significantly affect dopamine receptors, unlike LSD. It only influences the noradrenergic system at very high dosages.

Psychedelic Effects and Subjective Experiences

Psilocin's psychedelic effects are believed to stem from its interactions at the 5-HT2A receptor as a partial agonist. However, understanding how these interactions culminate in the psychedelic experience remains a subject of ongoing scientific investigation.

Anecdotal reports depict the effects of psilocin as powerful and visionary, characterized by a profound, all-encompassing headspace and immersive visuals featuring intricate geometry. The onset of effects is rapid and challenging, often reported to be more lucid and anxiety-provoking than when orally ingesting psilocybin mushrooms. This intensity may overwhelm individuals inexperienced with psychedelics.

Disclaimer: The effects outlined herein draw from the Subjective Effect Index (SEI), a compilation of anecdotal user reports and personal analyses by contributors to PsychonautWiki. Consequently, they should be approached with a degree of skepticism. Additionally, these effects may not manifest predictably or reliably, with higher doses heightening the likelihood of experiencing the full spectrum of effects. Moreover, adverse effects, including addiction, severe injury, or death, become more probable with higher doses.

Exploring Physical Effects of Psilocin

Psilocin induces a myriad of physical effects that contribute to the overall psychedelic experience. Understanding these phenomena enhances awareness and facilitates informed engagement with the substance.

Sedation and Relaxation

  • Psilocin's effects often include a sense of relaxation, accompanied by mild sedation.
  • Compulsive yawning is a common occurrence during psilocin experiences.

Perception of Bodily Heaviness

  • Users may perceive a feeling of bodily heaviness, especially during the initial phases of the trip.
  • Certain species of mushrooms, such as Psilocybe azurescens, may accentuate this sensation.

Spontaneous Physical Sensations

  • Referred to as the "body high," psilocin induces a pleasurable tingling sensation or glow.
  • This sensation intensifies throughout the onset and peaks of the experience, offering euphoria or tranquility, depending on the dosage.

Physical Euphoria

  • Psilocin's ability to induce physical euphoria varies among individuals and may not be as reliably induced as with other substances.
  • Physical discomfort can also manifest unexpectedly.

Changes in Felt Bodily Form

  • Users may experience a sense of warmth or unity, feeling physically connected to objects or surroundings.
  • This sensation is typically comforting and peaceful.

Tactile Enhancement

  • While less pronounced than with other psychedelics, psilocin may heighten tactile sensations, such as slight itchiness or ticklishness on the skin.

Other Physical Effects

  • Changes in felt gravity, nausea, excessive yawning, brain zaps, watery eyes, muscle contractions, olfactory hallucinations, frequent urination, pupil dilation, runny nose, increased salivation, and, rarely, seizures may occur.

Visual Effects

Psilocin induces a range of visual effects, including enhancements, distortions, and hallucinations, characterized by intricate patterns, distortions of perception, and intensified colors.

Hallucinatory States

  • Users may experience hallucinations, including machinescapes, transformations, internal and external hallucinations, shadow people, and more, often influenced by set and setting.

Cognitive Effects

Psilocin induces profound cognitive effects, such as relaxation, enhanced emotionality, empathy, affection, sociability, language suppression, cognitive euphoria, analysis enhancement, creativity enhancement, feelings of impending doom, catharsis, rejuvenation, memory suppression, ego death, addiction suppression, and various thought patterns.

Multi-Sensory and Transpersonal Effects

  • Synesthesia, spirituality enhancement, existential self-realization, unity, and interconnectedness may manifest, akin to other entheogenic substances.

Combination Effects

  • Psilocin's effects may be intensified or altered when combined with substances like cannabis, dissociatives, MDMA, alcohol, or benzodiazepines.

Understanding the physical effects of psilocin enriches the psychedelic experience, fostering responsible and informed use of the substance.

Research Findings

Antidepressant Effects

  • Preliminary studies suggest potential antidepressant effects of psilocin, with observations of decreased depression scores in terminal cancer patients and individuals with unipolar treatment-resistant depression post-treatment.

  • Psilocin's mechanism of action in treating depression remains under investigation, with hypotheses centered around its impact on the medial prefrontal cortex and serotonin receptor agonism.

Toxicity and Harm Potential

  • Psilocin exhibits low toxicity relative to dose, with few physical side effects associated with acute exposure.

  • Lethal dosage studies in rats indicate a high LD50, although extrapolation to human lethal dosage remains uncertain.

  • Despite its low physical toxicity, responsible use of psilocin is strongly advised to mitigate potential risks.

Tolerance and Addiction Potential

  • Psilocin is non-addictive and may lead to decreased desire for continued use over time.

  • Tolerance develops rapidly after ingestion, with effects diminishing within days and cross-tolerance observed with other psychedelics.

Legal Status

  • Psilocin is classified as a Schedule I drug under the Convention on Psychotropic Substances in many countries, including the United States, Canada, and several European nations.

  • Possession, sale, and production of psilocin and psilocybin-containing mushrooms are generally prohibited, although exceptions exist for religious or medical use in some jurisdictions.

Understanding the current research and legal landscape surrounding psilocin informs safe and responsible use practices, promoting informed decisions and harm reduction strategies.

Frequently Asked Questions (FAQ)

Q: What is psilocin?

A: Psilocin is a naturally occurring psychedelic compound found in certain species of mushrooms. It is the primary psychoactive constituent responsible for the hallucinogenic effects experienced after ingestion.

Q: How does psilocin work in the body?

A: Psilocin acts as an agonist or partial agonist at serotonin receptors in the brain, particularly the 5-HT2A, 5-HT2C, and 5-HT1A receptors. Its effects are thought to result from its interactions with these receptors, although the precise mechanisms are still under investigation.

Q: What are the physical effects of psilocin?

A: Psilocin induces a range of physical effects, including sedation, perception of bodily heaviness, spontaneous physical sensations, physical euphoria, changes in felt bodily form, tactile enhancement, and various other sensations such as nausea, excessive yawning, and muscle contractions.

Q: What are the visual effects of psilocin?

A: Psilocin induces a variety of visual effects, including enhancements in color and visual acuity, distortions in perception such as drifting and tracers, and complex geometric patterns.

Q: Is psilocin addictive?

A: Psilocin is not considered to be addictive, and the desire to use it may decrease with repeated use. It is most often self-regulating, and tolerance develops rapidly after ingestion.

Q: What is the legal status of psilocin?

A: Psilocin is classified as a Schedule I drug in many countries, meaning its possession, sale, and production are generally prohibited. However, some jurisdictions may allow exceptions for religious or medical use.

Q: Are there any research findings on psilocin?

A: Preliminary research suggests potential antidepressant effects of psilocin, as well as low toxicity relative to dose. Studies are ongoing to explore its therapeutic potential and safety profile further.

These FAQs provide basic information about psilocin and address common inquiries regarding its effects, mechanisms of action, legal status, and research findings.

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