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Isoproscaline

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Interactions
Tolerance
Harm Potential
Legality
Isoproscaline molecule structureIsoproscaline molecule structure
Chemical Class

Isoproscaline is a psychedelic phenethylamine and an analogue of mescaline, closely related to proscaline. It replaces mescaline's 4-propoxy group with a branched isopropoxy group while retaining the 3,4,5-substitution pattern on the benzene ring. It was first synthesized by David E. Nichols and colleagues, and appears in PiHKAL. Related compounds include escaline, allylescaline, and methallylescaline.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold30 mg
Light40-50 mg
Moderate50-60 mg
Strong60-80 mg
Heavy80+ mg

Wikipedia reports that in PiHKAL, Alexander Shulgin lists a psychedelic dose as being 40-80 mg, with effects lasting 10-16 hours; the route is not specified there. An 80 mg experience report describes a slight descent at 6-7 hours and a slow, pleasant descent until about the 12th hour, with mild irritability the following day.

Duration

Onset1-3 hours
After Effects1-12 hours
Total10-20 hours

Subjective Effects

Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.

Isoproscaline produces a psychedelic state described as warm, social, and emotionally genuine, with a long duration and a notably gentle trajectory. Reports describe a lengthy period before the body settles, followed by a sustained plateau of talkative, contented engagement with other people, music, and food. The decline is slow and smooth rather than abrupt, with mild irritability sometimes noted the following day.

Physical

Both mental and physical stimulation are typical, accompanied by restlessness, muscle tension, sweating or chills, decreased appetite, pupil dilation, and difficulty sleeping.

Muscle tension

Autonomic

Pupil dilation

Cognitive

The headspace is characterized by euphoria, empathy, and insight, with emotions felt vividly and without dulling; a softening of ego boundaries and, in some cases, confusion are also reported.

Confusion

Emotional

Euphoria

Visual

Visual activity spans brightened color and both closed- and open-eye imagery.

Hallucinatory States

Tactile

Pharmacology

Pharmacodynamics

The hallucinogenic and entheogenic effects of isoproscaline are most likely produced through agonism at the 5-HT2A serotonin receptor in the brain, the mechanism thought to be shared by hallucinogenic tryptamines and phenethylamines. No direct binding or functional data for isoproscaline itself is available.

Pharmacokinetics

Absorption & half-lifenot documented yetMetabolitesnone documented yet

Interactions

Interactions not written up yet

An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.

Check TripSit

Tolerance

Tolerance not written up yet

Harm Potential

Harm Potential not written up yet

History & Culture

Isoproscaline, or 4-isopropoxy-3,5-dimethoxyphenethylamine, is an analogue of mescaline closely related to proscaline. It was first synthesized by David E. Nichols and colleagues.

Legality

Legality not written up yet

Article Status

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    Step 1 · Automated synthesis

    An autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.

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Recent changes7 human edits · latest

Times are UTCNewest first

24 January 2026

  1. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  2. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  3. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  4. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  5. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  6. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  7. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

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