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'''Psilacetin''' (also known as '''O-Acetylpsilocin''', '''4-Acetoxy-DMT''', or '''4-AcO-DMT''') is a synthetically produced psychoactive drug and has been suggested by David Nichols to be a potentially useful alternative to [[Psilocin#Psilocybin|psilocybin]] for pharmacological studies, as they are both believed to be prodrugs of [[psilocin]].<ref>Improvements to the Synthesis of Psilocybin and a Facile Method for  
'''Psilacetin''' (also known as '''O-Acetylpsilocin''', '''4-Acetoxy-DMT''', or '''4-AcO-DMT''') is a synthetically produced psychoactive drug and has been suggested by David Nichols to be a potentially useful alternative to [[Psilocin#Psilocybin|psilocybin]] for pharmacological studies, as they are both believed to be prodrugs of [[psilocin]].<ref>Improvements to the Synthesis of Psilocybin and a Facile Method for  
Preparing the O-Acetyl Prodrug of Psilocin | http://www.erowid.org/archive/rhodium/pdf/nichols/nichols-psilocin.pdf<ref> However, many report that psilacetin's effects differ greatly from that of psilocybin and psilocin suggesting that it may be active intself before metabolism.  
Preparing the O-Acetyl Prodrug of Psilocin | http://www.erowid.org/archive/rhodium/pdf/nichols/nichols-psilocin.pdf</ref> However, many report that psilacetin's effects differ greatly from that of psilocybin and psilocin suggesting that it may be active intself before metabolism.  


=Chemistry=
=Chemistry=
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*[[Tryptamines]]
*[[Tryptamines]]
*[[Psilocin]]
*[[Psilocin]]
=References=
<references/>

Revision as of 09:05, 28 February 2014

Psilacetin (4-AcO-DMT)

The skeletal formula of Psilacetin (4-AcO-DMT).
Dosage
Threshold 5 - 10mg
Light 10 - 20mg
Common 20 - 30mg
Strong 30 - 40mg
Heavy 40mg +
Duration
Total Duration 6 - 8 hours
Onset 20 - 60 minutes
Initial effects 15 - 30 minutes
Peak 3 - 6 hours
Coming down 3 - 5 hours
After effects 2 - 5 hours

Psilacetin (also known as O-Acetylpsilocin, 4-Acetoxy-DMT, or 4-AcO-DMT) is a synthetically produced psychoactive drug and has been suggested by David Nichols to be a potentially useful alternative to psilocybin for pharmacological studies, as they are both believed to be prodrugs of psilocin.[1] However, many report that psilacetin's effects differ greatly from that of psilocybin and psilocin suggesting that it may be active intself before metabolism.

Chemistry

General formula of a tryptamine molecule.
Skeletal formula of Psilacetin molecule.

Psilacetin is made up of a tryptamine backbone with an acetoxy group attached to carbon R4 of the indole ring, and two methyl groups substituted onto the nitrogen RN1 and RN2.

Pharmacology

Psilacetin acts as a 5-HT2A, 5-HT2C and 5-HT1A partial agonist; the psychedelic effects are believed to come from Psilacetin's efficacy at the 5-HT2A receptors. At high doses, there is some efficacy to noradrenaline receptors.

Subjective effects

The physical effects of psilacetin can be broken down into two components all of which progressively intensify proportional to dosage. These are described below and generally include:

  • Spontaneous tactile sensations - the body high of psilacetin can be described as a pleasurable, warm, soft and all encompassing tingling sensation. This maintains a consistent presence that steadily rises with the onset and hits its limit once the peak has been reached.
  • Sedation - in terms of its effects on the physical energy levels of the tripper psilacetin is considered by most to be relaxing, stoning and mildly sedating. This sense of sedation is accompanied by compulsive yawning, a runny nose and watering eyes.

The head space of psilacetin is described by many as extremely relaxing, profound and stoning in its style when compared to other commonly used psychedelics such as LSD or 2C-B which tend to be energetic and stimulating. It contains a large number of psychedelic typical and unique cognitive effects.

The most prominent of these typical effects generally include:

psilacetin presents a full and complete array of possible visual enhancements which generally includes:

As for visual distortions and alterations, effects experienced are detailed below:

The visual geometry that is present throughout this trip can be described as more similar in appearance to that of psilocin, ayahuasca and 2C-E than LSD. They can be comprehensively described as structured in their organization, organic in geometric style, intricate in complexity, large in size, fast and smooth in motion, colourful in scheme, glossy in colour, blurred in their edges and rounded in their corners. They have a very "natural" feel to them and at higher dosages are significantly more likely to result in states of Level 7B visual geometry over Level 7A.

psilacetin and its various other forms produce a full range of high level hallucinatory states in a fashion that is more consistent and reproducible than that of many other commonly used psychedelics. These effects generally include:

  • External hallucinations
  • Internal hallucinations - this particular effect commonly contains hallucinations with scenarios, landscapes, settings, concepts and autonomous entity contact. They are more common within dark environments and can be described as internal in their manifestation, lucid in believability, interactive in style and almost exclusively of religious, spiritual, mystical or a transcendental nature in their overall theme.

The auditory effects of psilacetin are common in their occurrence and exhibit a full range of effects which commonly includes:

Toxicity and Harm Potential

Lethal Dosage

The LD50 of Psilacetin has been extrapolated from animal results to 800mg for an average human.

Tolerance and Addiction Potential

Psilacetin tolerance lasts for approximately a week, meaning that it is very difficult to form an addiction to this substance. It also has a high cross-tolerance, affecting the potency of other tryptamines.

Legal Issues

Possession and sale of Psilacetin is unscheduled in most countries.

  • UK: Could be considered illegal under the 1971 Misuse of Drugs Act as it metabolises into psilocin.
  • USA: Could be considered illegal under the Federal Analog Act as an analogue of psilocin.

See Also

References

  1. Improvements to the Synthesis of Psilocybin and a Facile Method for Preparing the O-Acetyl Prodrug of Psilocin | http://www.erowid.org/archive/rhodium/pdf/nichols/nichols-psilocin.pdf