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Pentylone

Pentylone molecule structurePentylone molecule structure

Pentylone is a stimulant of the substituted cathinone class1, first synthesized in the 1960s. Reports of euphoria vary, with some describing little or none and others reporting entactogenic effects at certain doses. Pentylone was identified alongside three other cathinones in an NRG-1 product sample.2 It has been included in products with variable compositions.2 Reported adverse effects include paranoia, agitation, and insomnia, and effects can persist for several days at high doses.

Dosage & Duration

Log in Piru

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~10 mg
Light10-20 mg
Moderate20-40 mg
Strong40+ mg

Duration

After Effects1-6 hours
Total3-4 hours

Subjective Effects

Subjective Effects not written up yet

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Marquis(MQ)
white → yellow2 → yellow3
Mecke(ME)
white → yellow2 → brown1
Mandelin(MD)
yellow2 → brown3 → brown2
Liebermann(LB)
white → brown3
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Pharmacology

Pharmacodynamics

Pentylone inhibits the reuptake of dopamine, norepinephrine, and serotonin, with lower measured inhibitory concentrations at the norepinephrine and dopamine transporters than at the serotonin transporter.3 It also promotes serotonin release,3 which was observed at a test concentration of 100 µM, although the relevance of this action is unclear. In rat drug-discrimination testing, pentylone fully substituted for methamphetamine and cocaine.4

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 timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Full Tolerance
The case report described NRG-3 as a mixture of pentylone and MDPV.5 Tolerance was reported with repeated intranasal use of this mixture, with the usual dose increasing from 100 mg to 200 mg. The time needed for tolerance to develop and pentylone's individual contribution were not established.

Harm Potential

Addiction & Dependence

Psychological

Moderate

Pentylone is considered habit-forming.

Toxicity

cardiovascular

Pentylone has sometimes caused pronounced cardiovascular effects, including notable tachycardia and chest pain.

psychiatric and central nervous system

Reports describe paranoia, agitation, insomnia, and delirium with persecutory and grandiose themes after several days of behavioral changes.

Psychosis Risk

Case reports describe paranoia and delirium marked by persecutory and grandiose themes, especially with large doses or individual vulnerability.

Seizure Risk

Animal data report clonic convulsions in 3 of 7 mice eight hours after 100 mg/kg intraperitoneal administration.

History & Culture

Pentylone was developed in the 1960s and described in a UK patent in 1969. Reports of its use emerged around 2010, when it appeared on the research chemical market.…

Legality

By Country

Illegal5
United States flagUnited StatesIllegal
Canada flagCanadaIllegal (analog/blanket ban)
Germany flagGermanyIllegal
Sweden flagSwedenIllegal
United Kingdom flagUnited KingdomIllegal

References

Citations

  1. Pentylone in orange 'Nike tick' pills. Victoria Department of Health (2023). https://www.health.vic.gov.au/drug-alerts/pentylone-in-orange-nike-tick-pills1
  2. Analysis of NRG 'legal highs' in the UK: identification and formation of novel cathinones. Drug Testing and Analysis (2011). https://doi.org/10.1002/dta.204123
  3. Monoamine transporter and receptor interaction profiles of a new series of designer cathinones. Neuropharmacology (2014). https://doi.org/10.1016/j.neuropharm.2013.11.0081234
  4. Discriminative and locomotor effects of five synthetic cathinones in rats and mice. ResearchGate, author-uploaded Psychopharmacology manuscript (2015). https://doi.org/10.1007/s00213-014-3755-31
  5. Case Report of an Acute Psychosis Episode Induced by Emerging Cathinone-Like Designer Drug Available on Internet. French Association of Medical Research Advancement (2016). https://www.afpremed.org/downloads/atlanta2016n.pdf1
  6. Health Canada Drug Analysis Service and Cannabis Laboratory — HC DAS and CL classification framework for psychoactive substances in the illicit drug market (updated 2026-07-06). health-infobase.canada.ca (n.d.). https://health-infobase.canada.ca/src/data/DAS/newLayout/20260706_ClassificationTable_Public.csv1
  7. Drug Classification — Health Canada's Drug Analysis Platform. health-infobase.canada.ca (n.d.). https://health-infobase.canada.ca/drug-analysis-service/drug-classification.html1
  8. Controlled Drugs and Substances Act — current consolidated Schedule I. laws-lois.justice.gc.ca (n.d.). https://www.laws-lois.justice.gc.ca/eng/acts/C-38.8/section-sched95314.html1
  9. Controlled Drugs and Substances Act — section 2 definitions. laws-lois.justice.gc.ca (n.d.). https://www.laws-lois.justice.gc.ca/eng/acts/C-38.8/section-2.html1
  10. Controlled Drugs and Substances Act — section 4. laws-lois.justice.gc.ca (n.d.). https://www.laws-lois.justice.gc.ca/eng/acts/C-38.8/section-4.html1

Further Reading

  1. Westphal et al. 2012 - Mass, NMR and IR spectroscopic characterization of pentedrone and pentylone and identification of their isocathinone by-products

Article Status

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