Skip to main content
Lyrea avatar

Not yet reviewed — this article is pending editorial review by Lyrea.

Citation noticeOur citation system is being overhauled

References and citation markers may currently be incomplete, mismatched, or incorrect. This system is being rebuilt and reviewed before the full site launch.

Butyrfentanyl

Butyrfentanyl molecule structureButyrfentanyl molecule structure
Psychoactive Class
Chemical Class

Butyrfentanyl is a potent short-acting synthetic opioid and analog of fentanyl, possessing approximately one quarter of its parent compound's potency. It has no established clinical applications and is sold exclusively as a designer drug. One of the earliest references to this compound appears in documentation by The College on Problems of Drug Dependence. As with other fentanyl analogs, butyrfentanyl carries significant risk of respiratory depression and fatal overdose, demanding extreme caution.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~400 µg
Light400-800 µg
Moderate800-1500 µg
Strong1.5-3 mg
Heavy3+ mg

This substance exhibits significantly greater potency compared to conventional opioids, making precise dose measurement and gradual titration essential for risk reduction.

Duration

After Effects1-4 hours

Subjective Effects

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

Butyrfentanyl produces a short-acting opioid experience broadly comparable to that of fentanyl, though at roughly one quarter of its potency. The experience is dominated by analgesia, sedation, and opioid euphoria rather than any meaningful sensory alteration. Its effect profile mirrors that of other fentanyl analogs, including a pronounced risk of life-threatening respiratory depression at higher doses.

Physical

Physical effects center on pain relief and a heavy, sedated body feeling, accompanied by itching and nausea. Respiratory depression scales with dose and can become life-threatening.

Sedation

Sedation

Uncomfortable

Nausea

Cognitive

The headspace is a typical opioid state centered on euphoric contentment and relaxation, without notable perceptual or hallucinatory components.

Reagent Testing

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

Marquis(MQ)
white → orange2
Mecke(ME)
white → yellow2
Mandelin(MD)
yellow2 → orange2 → red2 → brown2 → yellow2
Simons(SI)
No reaction
No reaction
Powered by PROtestkit.eu

Pharmacology

Pharmacodynamics

Butyrfentanyl acts as an agonist at μ-opioid receptors. In radioligand displacement assays using [3H]fentanyl, it exhibits a Ki of 32 ± 4.1 nM, indicating substantially lower binding affinity than fentanyl itself (Ki 1.06 ± 0.15 nM) and roughly one quarter of its potency as an opioid agonist.

Pharmacokinetics

Butyrfentanyl is rapidly cleared from the body. In studies of urinary excretion following injection, nearly all of the administered dose was excreted or metabolized within the first 3 hours, with only very low concentrations detectable thereafter.

Metabolitesnone 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.

Cross Tolerance

Opioids (fentanyl, morphine, heroin, oxycodone, and other μ-opioid receptor agonists)

Harm Potential

Addiction & Dependence

Psychological

High

Classified as habit-forming. As a potent synthetic opioid and fentanyl analog, it carries significant abuse potential.

Toxicity

Respiratory

Can cause serious respiratory depression that may be life-threatening in overdose.

History & Culture

Butyrfentanyl first appears in scientific literature through documentation by the College on Problems of Drug Dependence, where it was referenced as an N-butyramide fentanyl analog. Pharmacological characterization of the compound—including analgesic efficacy studies, opioid receptor binding

Legality

International

UN Single Convention on Narcotic Drugs 1961 (Schedule I, added March 2017)

By Country

Illegal4
United States flagUnited StatesIllegal
China flagChinaIllegal
Switzerland flagSwitzerlandIllegal
United Kingdom flagUnited KingdomIllegal (analog/blanket ban)

References

Citations

  1. 我国管制毒品目录(2026年7月更新,540种+三大类). ga.sz.gov.cn (n.d.). https://ga.sz.gov.cn/SZJDZX/SZBMFW/content/post_12898420.html1
  2. 非药用类麻醉药品和精神药品列管办法. gaj.panjin.gov.cn (n.d.). https://gaj.panjin.gov.cn/2015_10/08_00/content-235605.html1
  3. 麻醉药品和精神药品管理条例 (Regulations on the Administration of Narcotic Drugs and Psychotropic Substances), third revision. xzfg.moj.gov.cn (n.d.). https://xzfg.moj.gov.cn/front/law/detail?LawID=17441
  4. 三部门联合发布最新版《非药用类麻醉药品和精神药品目录》. btgaj.xjbt.gov.cn (n.d.). https://btgaj.xjbt.gov.cn/c/2025-07-28/8428464.shtml1
  5. 国家禁毒委召开新闻发布会宣布整类列管芬太尼类物质. gat.xinjiang.gov.cn (n.d.). https://gat.xinjiang.gov.cn/gat/jwyw/201904/351d88c2400d4f51961d48c44fd48492.shtml1
  6. Commission on Narcotic Drugs: Extract from the Report of the 38th WHO Expert Committee on Drug Dependence. unodc.org (n.d.). https://www.unodc.org/documents/commissions/CND/CND_Sessions/CND_59Reconvened/ECN72016_CRP13_V1610192.pdf12
  7. Betäubungsmittelverzeichnisverordnung (BetmVV-EDI), SR 812.121.11, consolidated text as at 13 March 2026. fedlex.data.admin.ch (n.d.). https://fedlex.data.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/2011/363/20260313/de/html/fedlex-data-admin-ch-eli-cc-2011-363-20260313-de-html-3.html1
  8. BetmVV-EDI amendment of 18 August 2017 (AS 2017 5003). fedlex.data.admin.ch (n.d.). https://fedlex.data.admin.ch/filestore/fedlex.data.admin.ch/eli/oc/2017/539/de/pdf-a/fedlex-data-admin-ch-eli-oc-2017-539-de-pdf-a.pdf1
  9. Betäubungsmittelverzeichnisverordnung (BetmVV-EDI), SR 812.121.11, consolidated text as at 1 December 2015. fedlex.data.admin.ch (n.d.). https://fedlex.data.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/2011/363/20151201/de/pdf-a/fedlex-data-admin-ch-eli-cc-2011-363-20151201-de-pdf-a.pdf1
  10. Betäubungsmittelkontrollverordnung (BetmKV), SR 812.121.1, consolidated text as at 23 January 2023. fedlex.admin.ch (n.d.). https://www.fedlex.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/2011/362/20230123/de/html/fedlex-data-admin-ch-eli-cc-2011-362-20230123-de-html-3.html1

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.

  • Step 2 · First-pass reviewPending

    Not yet reviewed — this article is pending editorial review by Lyrea.

  • Step 3 · Citation reviewPending

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

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

All changes to this article · Site-wide recent changes

Suggest an edit

Spotted a mistake, an outdated claim, or something missing from the Butyrfentanyl article? Send the editors a private note. Feedback lands in a moderation queue and is never shown on the site.

Wish to give generalised feedback? You can do so here.