Library

MK-801

Potency is in the microgram range; calibrated 0.1 mg precision scale or volumetric dosing is mandatory. Subjective duration (20-48 h) far exceeds the 2 h rat plasma half-life because of high receptor affinity and slow dissociation. Animal studies show rapid formation of Olney's lesions in the retrosplenial cortex at equivalent doses to 1 mg/kg; human relevance unknown but caution advised. Users commonly report pronounced macropsia/micropsia, spatial warping and auditory hallucinations rather than classic dissociative euphoria. Severe amnesia, insomnia and thought-disorder are typical above 100 ug.

Also known as: Dizocilpine

Classification

  • Psychoactive: Dissociative
  • Tag: Arylcyclohexyl-related NMDA antagonist
  • Tag: Diarycycloheptene
  • Tag: Habit-Forming
  • Tag: Hallucinogen
  • Tag: Research-Chemical
  • Tag: Tentative

Effects

  • Nystagmus
  • Incoordination
  • Impaired Balance
  • Insomnia
  • Profound Dissociation
  • Time Dilation
  • Ego Fragmentation
  • Motor Control Loss
  • Cognitive Impairment
  • Memory Suppression
  • Auditory Hallucination
  • Visual Distortion
  • Open Eye Visuals
  • Voices
  • Warping
  • Size Distortion

Routes of Administration

Oral / Sublingual

Dosage

  • Threshold: 25 ug
  • Light: 25-50 ug
  • Common: 50-100 ug
  • Strong: 100-300 ug
  • Heavy: 300 ug

Duration

  • Onset: 0.25-1 h
  • Comeup: 1-2 h
  • Peak: 4-10 h
  • Offset: 8-24 h
  • After Effects: 24-72 h

Insufflated

Dosage

  • Threshold: 25 ug
  • Light: 25-50 ug
  • Common: 50-80 ug
  • Strong: 80-250 ug
  • Heavy: 250 ug

Duration

  • Onset: 0.166-0.5 h
  • Comeup: 1-2 h
  • Peak: 3.5-9 h
  • Offset: 10-24 h
  • After Effects: 24-72 h
  • Total Duration: 24-48 h

Intramuscular

Dosage

  • Threshold: 15 ug
  • Light: 15-30 ug
  • Common: 30-100 ug
  • Strong: 100-250 ug
  • Heavy: 250 ug

Duration

  • Onset: 0.083-0.25 h
  • Comeup: 0.5-1.5 h
  • Peak: 4-10 h
  • Offset: 10-24 h
  • After Effects: 24-72 h
  • Total Duration: 24-48 h

Rectal

Dosage

  • Threshold: 25 ug
  • Light: 25-50 ug
  • Common: 50-100 ug
  • Strong: 100-300 ug
  • Heavy: 300 ug

Duration

  • Onset: 0.25-0.75 h
  • Comeup: 1-2 h
  • Peak: 4-10 h
  • Offset: 8-24 h
  • After Effects: 24-72 h

Oral

Dosage

  • Heavy: 2.0 mg+
  • Light: 0.05 mg - 0.30 mg
  • Common: 0.30 mg - 1.0 mg
  • Strong: 1.0 mg - 2.0 mg
  • Threshold: 0.05 mg

Duration

  • Onset: 0.25-1 h
  • Peak: 4-10 h
  • Offset: 12-24 h
  • After Effects: 24-72 h
  • Total Duration: 24-48 h

Sublingual

Dosage

  • Heavy: 2.0 mg+
  • Light: 0.05 mg - 0.30 mg
  • Common: 0.30 mg - 1.0 mg
  • Strong: 1.0 mg - 2.0 mg
  • Threshold: 0.05 mg

Duration

No data available for this section yet.

Harm Reduction

Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.

Sources

Substance data is aggregated from the following public harm-reduction and reference sources.

Links

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MK-801 - DrugsPRO vodič o supstancama

MK-801: Potency is in the microgram range; calibrated 0.1 mg precision scale or volumetric dosing is mandatory. Subjective duration (20-48 h) far exceeds the 2 h rat plasma half-life because of high receptor affinity and slow dissociation. Animal studies show rapid formation of Olney's lesions in th

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