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Flualprazolam

Flualprazolam molecule structureFlualprazolam molecule structure
8-Chloro-6-(2-fluorophenyl)-1-methyl-4H-benzo[f][1,2,4]triazolo[4,3-a][1,4]diazepine
Flualp, F-Alp, 2'-Fluoro-Alprazolam

Flualprazolam is a synthetic depressant of the triazolobenzodiazepine class and a fluorinated analog of alprazolam (Xanax)citation needed. It first appeared on the research chemical market in 2017, though its developmental origins remain unclear. Flualprazolam is notably more potent than alprazolam, producing effects at lower doses with a relatively rapid onset. It has reportedly been deceptively sold as alprazolam despite differing in substantive ways, posing significant harm reduction concerns.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~0.05 mg
Light0.05-0.25 mg
Moderate0.25-0.5 mg
Strong0.5-1 mg
Heavy1+ mg

Reported to be more potent by weight than alprazolam, with user estimates ranging from roughly 1.5 to 5 times stronger; onset of effects is relatively rapid.

Duration

Onset10-30 minutes
Peak1-2 hours
Offset2-6 hours
After Effects6-24 hours
Total5-8 hours

Subjective Effects

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

The experience is dominated by heavy sedation, anxiety relief, and muscle relaxation, with a relatively rapid onset and greater potency than alprazolam. Central nervous system depression dampens feelings and perceptions rather than altering them, producing a calm, blunted state that can progress into sleep at higher doses. Memory of the period after ingestion frequently becomes unreliable, and compulsive redosing during these gaps is a recognized hazard.

Physical

Pronounced muscle relaxation and a heavy, sedated body feeling are the primary physical effects, often accompanied by dizziness, impaired coordination and reaction time, and slowed breathing at higher doses. Prolonged fatigue and hangover-like lethargy can persist after the main effects subside.

Sedation

Muscle relaxation

Uncomfortable

Cognitive

The headspace is calm, quieted, and disinhibited, with reduced anxiety and dampened emotional response. Thought slows noticeably, and confusion and anterograde amnesia become prominent at moderate to high doses; paradoxical aggression, irritability, and outbursts of anger have also been reported.

Suppressions

Cognitive effects are dominated by suppression, consistent with reduced information flow between neurons and general dampening of feelings and perceptions.

Thought decelerationConfusion

Reagent Testing

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

Zimm(ZI)
white → pink1 → purple2
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Pharmacology

Pharmacodynamics

Flualprazolam acts as a positive allosteric modulator at the GABA-A receptor via the benzodiazepine binding site, enhancing the activity of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA).citation needed This mechanism is consistent with its classification as a triazolobenzodiazepine. It appears to be more potent by weight than its parent compound alprazolam, from which it is derived as the 2'-fluoro substituted analog.

Pharmacokinetics

Limited pharmacokinetic data is available for flualprazolam.1 It is reported to have a significantly longer elimination half-life than alprazolam, though specific values have not been well characterized.citation needed Seven flualprazolam metabolites were tentatively identified. Several cytochrome P450 and UDP-glucuronosyltransferase isozymes, under which CYP3A4 and UGT1A4, were shown to be involved in flualprazolam metabolism using in vitro incubations with pooled human liver S9 fraction or HepaRG cells.2

Interactions

Dangerous

Highest risk

These combinations are considered extremely harmful and should always be avoided. Reactions to these drugs taken in combination are highly unpredictable and have a potential to cause death.

AlcoholGHB/GBLOpioidsTramadol

Unsafe

Avoid

There is considerable risk of physical harm when taking these combinations, they should be avoided where possible.

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.

DXMKetamineMXE
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Tolerance

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

Full Tolerance
Tolerance to sedative-hypnotic effects can emerge quickly, often after only several days of uninterrupted use. Reports suggest flualprazolam can sharply accelerate cross-tolerance with benzodiazepines, so limiting use to short periods is strongly advised.
Cross Tolerance

Benzodiazepines, Other GABAergic depressants

Baseline Reset
Tolerance generally returns to baseline within 7-14 days after cessation. However, following prolonged or intensive use, this recovery period may extend significantly longer in proportion to the duration and intensity of prior consumption.

Harm Potential

Addiction & Dependence

Psychological

High

Considered highly addictive with a high potential for abuse.citation needed The short-lasting euphoric effects (1-2 hours) encourage compulsive redosing while still intoxicated. Rapidly increases benzodiazepine cross-tolerance, making short-term use strongly advised.

Physical

Extremely High

Regular use leads to physical dependence with potentially life-threatening withdrawal. Discontinuation after prolonged use can cause dizziness, physical weakness, tremors, sleep disturbances, sweating, nausea, hallucinations, depression, and seizures. Gradual dose tapering under medical supervision is necessary; abrupt cessation is dangerous.

Psychosis Risk

Paradoxical reactions including aggression, violent behavior, and suicidal behavior occur rarely in the general population (below 1% incidence). These effects occur with greater frequency in recreational abusers, individuals with mental disorders, children, and those on high-dosage regimens. Hallucinations may occur as a withdrawal symptom.

Seizure Risk

Has anticonvulsant properties during use (seizure suppression). However, there is an increased risk of seizures following discontinuation, particularly after heavy or long-term use. Paradoxically, some benzodiazepines can cause seizures in epileptics. Substances that lower seizure threshold should be avoided during withdrawal.

History & Culture

Flualprazolam was first synthesized in 1976 as part of broader benzodiazepine research,citation needed representing the triazolo analog of fludiazepam and structurally related to alprazolam as its 2'-fluoro derivative. Despite its early synthesis, the compound was never developed for

Legality

International

Flualprazolam is not listed under the 1961 Single Convention on Narcotic Drugs. It is listed in Schedule II of the 1971 Convention on Psychotropic Substances. It is not listed under the 1988 Convention against Illicit Traffic in Narcotic Drugs and Psychotropic Substances.

By Country

Illegal14
United States flagUnited StatesSchedule I
Australia flagAustraliaIllegal
Chile flagChileIllegal
Czech Republic flagCzech RepublicIllegal
Finland flagFinlandIllegal
Germany flagGermanyIllegal
Indonesia flagIndonesiaIllegal
Netherlands flagNetherlandsIllegal
Poland flagPolandIllegal
South Korea flagSouth KoreaIllegal
Sweden flagSwedenIllegal
Thailand flagThailandIllegal
Turkey flagTurkeyIllegal
United Kingdom flagUnited KingdomIllegal
Controlled / restricted2
Japan flagJapanRestricted
Norway flagNorwayRestricted
Prescription2
Argentina flagArgentinaPrescription only
Austria flagAustriaPrescription only

References

Source Pages

  1. Bluelight: Flualprazolam Discussion Thread
  2. Erowid Experience Vaults: Flualprazolam
  3. Isomer Design (TiHKAL/PiHKAL)
  4. PsychonautWiki
  5. TripSit Factsheets
  6. Wikipedia

Citations

  1. Designer benzodiazepine rat pharmacokinetics: A comparison of alprazolam, flualprazolam and flubromazolam. (n.d.). https://doi.org/10.1016/j.taap.2023.1164591
  2. Toxicokinetics and Analytical Toxicology of Flualprazolam: Metabolic Fate, Isozyme Mapping, Human Plasma Concentration and Main Urinary Excretion Products. Journal of Analytical Toxicology, 44(6), 549–558 (July 2020). https://doi.org/10.1093/jat/bkaa0191
  3. Ley 21.704 (Convenio sobre Sustancias Sicotrópicas de 1971), modificada por la Decisión 63/12 de la Comisión de Estupefacientes. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/nacional/ley-21704-232689/texto1
  4. CND Decision 63/12: Inclusion of flualprazolam in Schedule IV of the Convention on Psychotropic Substances of 1971 (March 4, 2020). (n.d.). https://www.unodc.org/documents/commissions/CND/Drug_Resolutions/2020-2029/2020/Decision_63_12.pdf1
  5. UNODC Laboratory and Scientific Service — Substance Details: Flualprazolam. (n.d.). https://www.unodc.org/LSS/Substance/Details/0915776e-f185-450f-9e4b-a40a676aa1fc1
  6. Customs (Prohibited Imports) Regulations 1956. legislation.gov.au (n.d.). https://www.legislation.gov.au/F1996B03651/2025-03-01/2025-03-01/text/original/pdf1
  7. Psychotropenverordnung (PV), Anlage 1, Punkt 2. ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/Dokumente/BgblAuth/BGBLA_2021_II_8/BGBLA_2021_II_8.html1
  8. Psychotropenverordnung (PV), Anlage 1, Punkt 2. ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/Dokumente/Bundesnormen/NOR40267457/NOR40267457.html1
  9. Psychotropenverordnung (PV), Anlage 1, Punkt 2. ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/NormDokument.wxe?Abfrage=Bundesnormen&Gesetzesnummer=10011040&Paragraf=51
  10. Psychotropenverordnung (PV), Anlage 1, Punkt 2. ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/NormDokument.wxe?Abfrage=Bundesnormen&Gesetzesnummer=10011040&Paragraf=301

Further Reading

  1. Forensic Toxicology - Fatal Flualprazolam Intoxication Case Report
  2. Forensic Toxicology - Flualprazolam Review Article
  3. Journal of Forensic Sciences - Flualprazolam Distribution Study
  4. Reddit: r/researchchemicals Flualprazolam Review

Article Status

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

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    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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Recent changes8 human edits · latest

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20 August 2026

  1. Lyrea · Added a citation in PharmacologyPharmacokinetics

  2. Lyrea · Added a source: using in vitro incubations with pooled human liver S9 fraction or HepaRG cells

  3. Lyrea · Reworded 14 words in PharmacologyPharmacokinetics

  4. Lyrea · Reworded 25 words in PharmacologyPharmacokinetics

  5. Lyrea · Updated the article

19 August 2026

  1. Lyrea · Changed a word in Dosage & DurationRoutes 1 › Dose ranges › Light

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

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