Flualprazolam
Flualprazolam is a synthetic depressant of the triazolobenzodiazepine class and a fluorinated analog of alprazolam (Xanax)1. It first appeared on the research chemical market in 20171, though its developmental origins remain unclear. Flualprazolam is notably more potent than alprazolam2, producing effects at lower doses with a relatively rapid onset. It has reportedly been deceptively sold as alprazolam despite differing in substantive ways21, posing significant harm reduction concerns.
Dosage & Duration
Dosage
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
Subjective Effects
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
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.
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).34 This mechanism is consistent with its classification as a triazolobenzodiazepine.3 It appears to be more potent by weight than its parent compound alprazolam, from which it is derived as the 2'-fluoro substituted analog.35
Pharmacokinetics
Limited pharmacokinetic data is available for flualprazolam.5 It is reported to have a significantly longer elimination half-life than alprazolam, though specific values have not been well characterized.5
Dangerous
Highest riskThese 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.
Unsafe
AvoidThere is considerable risk of physical harm when taking these combinations, they should be avoided where possible.
Caution
Use cautionThese 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.
Tolerance
Benzodiazepines, Other GABAergic depressants
Harm Potential
Addiction & Dependence
Psychological
HighConsidered highly addictive with a high potential for abuse.6 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 HighRegular 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,6 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…
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
References
Source Pages
Citations
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- Driving Under the Influence of Flualprazolam: 10 Case Reports. (n.d.). https://doi.org/10.1093/jat/bkab10512
- FLUALPRAZOLAM (Street Name: Flualp). (n.d.). https://www.deadiversion.usdoj.gov/drug_chem_info/flualp.pdf123
- A case of fatal multidrug intoxication involving flualprazolam: distribution in body fluids and solid tissues. (n.d.). https://pmc.ncbi.nlm.nih.gov/articles/PMC9715448/12
- Designer benzodiazepine rat pharmacokinetics: A comparison of alprazolam, flualprazolam and flubromazolam. (n.d.). https://doi.org/10.1016/j.taap.2023.116459123
- Critical Review Report: FLUALPRAZOLAM — Expert Committee on Drug Dependence, Forty-second Meeting, Geneva, 21-25 October 2019. (n.d.). https://ecddrepository.org/sites/default/files/2023-04/final_flualprazolam.pdf12345
- News: December 2019 – WHO: World Health Organization recommends 12 NPS for scheduling. www.unodc.org (n.d.). https://www.unodc.org/LSS/Announcement/Details/021820a0-8746-42a4-9ee3-47ce50b30ca31
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- 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
- UNODC Laboratory and Scientific Service — Substance Details: Flualprazolam. (n.d.). https://www.unodc.org/LSS/Substance/Details/0915776e-f185-450f-9e4b-a40a676aa1fc1
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Further Reading
Automated synthesisInformation aggregated and synthesized using an autonomous workflow built by Josie Kins.
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