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Adrafinil

Adrafinil molecule structureAdrafinil molecule structure
Adrafinil
Olmifon, CRL 40028

Adrafinil is a eugeroic stimulant of the benzhydryl class that acts as a prodrug for modafinil.citation needed Discovered in 1974 by chemists at the French pharmaceutical company Laboratoires Lafon during screening for analgesic compounds, it was formerly marketed under the brand name Olmifon. It promotes wakefulness and alertness without amphetamine-like effects. Long-term use is not advised due to potential liver stress from elevated hepatic enzymes associated with its metabolism.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~100 mg
Light100-250 mg
Moderate250-400 mg
Strong400-600 mg
Heavy600+ mg

Duration

Onset45-120 minutes
Come Up45-60 minutes
Peak4.5-6 hours
Offset1-3 hours
After Effects1-6 hours
Total6-12 hours

Subjective Effects

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

Effects vary widely by individual, dose, and context.

Physical

The physical effects of adrafinil can be broken down into several components.

Increased heart rateDizzinessNausea

Cognitive

The cognitive effects of adrafinil can be broken down into several components.

Adapted from the Modafinil subjective effects documentation. Adrafinil is a prodrug of modafinil and is reported to produce an effectively identical experience, with a slower onset. Forked from Subjective Effect Documentation byJosie Kins August 2015.

Reagent Testing

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

Marquis(MQ)
white → yellow2 → orange2 → brown2
Mecke(ME)
white → orange2 → red2 → brown2
Mandelin(MD)
yellow2 → brown3
Liebermann(LB)
white → orange2 → brown2
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Pharmacology

Pharmacodynamics

Adrafinil is a prodrug that is primarily converted to modafinil in vivo, producing nearly identical pharmacological effects once the active metabolite has accumulated to sufficient concentrations.citation needed In animal studies, its locomotor-stimulating effects are blocked by α1-adrenergic and α2-adrenergic receptor antagonists, suggesting involvement of postsynaptic adrenergic signaling in its wakefulness-promoting activity. However, neither adrafinil nor modafinil has been found to bind the α1-adrenergic receptor directly, and the evidence for adrenergic agonism is considered weak. Modafinil has been identified as a weak, atypical inhibitor of the dopamine transporter, and this action may account for some or all of its pharmacological effects.

Pharmacokinetics

Adrafinil is metabolized hepatically and may follow one of two pathways: the primary route converts it to the active metabolite modafinil, while a secondary route produces inactive modafinilic acid directly without prior conversion to modafinil.citation needed This dual pathway may account for adrafinil's lower potency relative to modafinil. Modafinil is itself further metabolized to inactive modafinilic acid and modafinil sulfone. As a prodrug, adrafinil requires time for its active metabolite to accumulate to effective concentrations in the bloodstream.

Interactions

Caution

Use caution

These combinations are not usually physically harmful, but may produce undesirable effects, such as physical discomfort or overstimulation. Extreme use may cause physical health issues. Synergistic effects may be unpredictable. Care should be taken when choosing to use this combination.

AcebutololAceclofenacAcemetacinAcetylsalicylic acidAclidinium
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Tolerance

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

Full Tolerance
Repeated adrafinil use over time can reduce sensitivity to many effects, leading users to need larger doses for similar results.
Baseline Reset
1-2 weeks
Half Tolerance
3-7 days
Cross Tolerance

Benzhydryl eugeroics (modafinil, armodafinil)

Harm Potential

Addiction & Dependence

Psychological

Low

Adrafinil is considered not addictive with a low potential for abuse. It does not appear to be capable of causing psychological dependence among most users.

Toxicity

Hepatic

Prolonged use may cause elevated liver enzymes and slight hepatotoxicity due to the requirement for hepatic metabolism to convert adrafinil to its active metabolite modafinil; occasional use at typical doses appears to carry minimal hepatic risk.

Psychosis Risk

Mania has been reported as a side effect, particularly in individuals with a predisposition to mood disorders such as bipolar disorder. Confusion, aggression, and overstimulation may also occur but are described as transitory effects that resolve upon discontinuation.citation needed

Seizure Risk

Adrafinil is contraindicated in individuals with epilepsy.citation needed

History & Culture

Discovery and Development

Adrafinil was discovered in 1974 by two chemists working at the French pharmaceutical company Laboratoires Lafon.citation needed The compound emerged unexpectedly during a screening program aimed at identifying novel analgesic agents. Rather than demonstrating pain-relieving

Legality

International

World Anti-Doping Agency Prohibited List (2004)1

By Country

Illegal1
Norway flagNorwayIllegal
Controlled / restricted19
United States flagUnited StatesRestricted
Austria flagAustriaRestricted
Brazil flagBrazilRestricted
Colombia flagColombiaRestricted
Czech Republic flagCzech RepublicRestricted
Denmark flagDenmarkRestricted
Finland flagFinlandRestricted
France flagFranceRestricted
Germany flagGermanyRestricted
Italy flagItalyRestricted
Laos flagLaosRestricted
Mexico flagMexicoRestricted
Netherlands flagNetherlandsRestricted
Poland flagPolandRestricted
Portugal flagPortugalRestricted
Russia flagRussiaRestricted
South Korea flagSouth KoreaRestricted
Spain flagSpainRestricted
Ukraine flagUkraineRestricted
Prescription3
Australia flagAustraliaPrescription only
China flagChinaPrescription only
New Zealand flagNew ZealandPrescription only

References

Source Pages

  1. DrugBank
  2. Erowid
  3. Erowid: Adrafinil Health
  4. Isomer Design (TiHKAL/PiHKAL)
  5. PsychonautWiki
  6. TripSit Factsheets
  7. Wikipedia

Citations

  1. Ameline A, Gheddar L, Raul JS, & Kintz P. (2020). Identification of adrafinil and its main metabolite modafinil in human hair. Self-administration study and interpretation of an authentic case. 5(4), 322-326. https://doi.org/10.1080/20961790.2019.17044821
  2. Poisons Standard. tga.gov.au (n.d.). https://www.tga.gov.au/resources/publication/publications/poisons-standard-february-20261
  3. Internationales Übereinkommen gegen Doping im Sport, Anlage I (Verbotsliste 2026; BGBl. III Nr. 219/2025). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/Dokumente/BgblAuth/BGBLA_2025_III_219/BGBLA_2025_III_219.pdf1
  4. Internationales Übereinkommen gegen Doping im Sport, Anlage I (Verbotsliste 2026; BGBl. III Nr. 219/2025). ris.bka.gv.at (n.d.). https://ris.bka.gv.at/Dokumente/Bundesnormen/NOR40275236/NOR40275236.html1
  5. Internationales Übereinkommen gegen Doping im Sport, Anlage I (Verbotsliste 2026; BGBl. III Nr. 219/2025). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/NormDokument.wxe?Abfrage=Bundesnormen&Gesetzesnummer=20011421&Paragraf=1&Uebergangsrecht=1
  6. Lei nº 14.597/2023, art. 175, VIII; Lista Proibida 2026 do Código Mundial Antidopagem. planalto.gov.br (n.d.). https://www.planalto.gov.br/ccivil_03/_ato2023-2026/2023/lei/l14597.htm1
  7. Lei nº 14.597/2023, art. 175, VIII; Lista Proibida 2026 do Código Mundial Antidopagem. gov.br (n.d.). https://www.gov.br/abcd/pt-br/composicao/atletas/substancias-e-metodos-proibidos/arquivos-lista-de-substancias-proibidas/lista_proibida_2026_pt-br_v-3semlogo.pdf/%40%40download/file1
  8. Lei nº 14.597/2023, art. 175, VIII; Lista Proibida 2026 do Código Mundial Antidopagem. gov.br (n.d.). https://www.gov.br/esporte/pt-br/noticias-e-conteudos/esporte/abcd-divulga-lista-de-substancias-e-metodos-proibidos-20261
  9. 2026年兴奋剂目录公告;《反兴奋剂条例》. sport.gov.cn (n.d.). https://www.sport.gov.cn/kjs/n5084/c29328536/part/29328879.pdf1
  10. 2026年兴奋剂目录公告;《反兴奋剂条例》. samr.gov.cn (n.d.). https://www.samr.gov.cn/zw/zfxxgk/fdzdgknr/bgt/art/2023/art_ab59ecfc91ce456399fcf3357ea54622.html1

Further Reading

  1. Lowe et al. 2021 - Adrafinil Psychostimulant and Purported Nootropic

Article Status

  • Josie Kins avatar
    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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    Step 2 · First-pass review

    A first pass manual review and edit of article prose and copy has been performed by subject-matter expert Lyrea. This does not guarantee factual accuracy. An additional human review for each of this article's citations is yet to be performed.

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    No one has reviewed this article's citations yet. That second pass checks each claim against the source it cites.

Recent changes8 human edits · latest

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13 August 2026

  1. Lyrea · Updated the article

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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