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Flunitrazolam

Flunitrazolam molecule structureFlunitrazolam molecule structure
Flunitrazolam
FNTZ, Flunazolam

Flunitrazolam is a novel synthetic depressant of the triazolobenzodiazepine class that first emerged on the research chemical market in 2016.citation needed It has no known precedent in the scientific literature prior to its appearance for sale online. Flunitrazolam is notable for its extreme potency, being active in the low microgram range—a characteristic shared with compounds like flubromazolam and clonazolam. As with all benzodiazepines, it carries significant risk of dependence, and its ultra-potent nature makes accurate dosing particularly critical.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~30 µg
Light30-80 µg
Moderate80-150 µg
Strong150-300 µg
Heavy300+ µg

Duration

Onset20-40 minutes
Peak1-2 hours
Offset2-4 hours
After Effects1-12 hours
Total4-8 hours

Subjective Effects

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

The experience is dominated by powerful sedation, hypnosis, and anxiety relief, consistent with a highly potent triazolobenzodiazepine active at doses as low as 0.1 mg. Its effect profile is broadly comparable to related compounds such as flunitrazepam, clonazolam, and flubromazolam, with a pronounced hypnotic character that readily progresses into sleep at higher doses. Memory of the period following ingestion is frequently impaired or lost entirely, and blackouts are a recognized risk even at seemingly modest amounts given the compound's microgram-level potency.

Physical

Heavy sedation and pronounced muscle relaxation define the body experience, accompanied by a loss of motor coordination that makes movement clumsy and unsteady.

Sedation

Cognitive

The headspace is one of diminished anxiety and mental quieting rather than stimulation or alteration of perception. Anterograde amnesia is a defining feature, with recall of events after dosing often fragmentary or absent, culminating in full blackouts at higher doses.

Suppressions

Reagent Testing

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

Morr(MO)
pink2 → green1
Simons(SI)
No reaction
No reaction
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Pharmacology

Pharmacodynamics

Flunitrazolam acts as a positive allosteric modulator at the GABA-A receptor benzodiazepine binding site, enhancing the inhibitory effects of gamma-aminobutyric acid (GABA). As a triazolobenzodiazepine, it incorporates a fused triazole ring into the benzodiazepine scaffold, which substantially increases potency compared to its parent compound flunitrazepam, rendering it active in the microgram range. The anticonvulsant properties of benzodiazepines may also involve binding to voltage-dependent sodium channels. Very little direct pharmacological research has been conducted on flunitrazolam specifically, and much of its presumed mechanism is inferred from its structural similarity to other benzodiazepines.

Pharmacokinetics

In a self-administration study of Flunitrazolam, the urine was analysed of the volunteer. 7-Amino-Flunitrazolam was detectable for up to 37 hours, Desnitro-Flunitrazolam and 7-Acetamido-Flunitrazolam were also identified. The area response of Desnitro-Flunitrazolam was always lower than compared to the 2 other metabolites and re-analysis showed chemical instability. Hydroxylated forms of Flunitrazolam were not identified in HLMs or urine samples.citation needed

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 a few days of uninterrupted use.
Cross Tolerance

Benzodiazepines (all)

Baseline Reset
Following cessation of use, tolerance generally returns to baseline within 7-14 days. However, individuals with prolonged or intensive use patterns may require significantly longer periods for complete tolerance reset, proportional to the duration and intensity of their usage history.

Harm Potential

Addiction & Dependence

Psychological

High

High abuse potential similar to other potent benzodiazepines.citation needed Compulsive redosing is commonly reported, and rebound anxiety following use can contribute to cycles of dependence and addiction.

Physical

Extremely High

Extremely physically addictive with potentially life-threatening withdrawal. Abrupt discontinuation after regular use can result in hypertension, seizures, or death.citation needed Gradual tapering over weeks is essential; abrupt cessation is dangerous.

Seizure Risk

Unusually for a benzodiazepine, high to very high doses have reportedly caused seizures without additional triggers such as withdrawal. This proconvulsant effect at high doses is atypical for the drug class. Seizures are also a significant risk during withdrawal from chronic use.citation needed

History & Culture

Flunitrazolam is a novel designer benzodiazepine with no documented history prior to its emergence on the online research chemical market. Unlike many benzodiazepines which were first developed by pharmaceutical companies and later diverted to recreational use, flunitrazolam appears to have been

Legality

International

The fetched UNODC ICE record identifies Flunitrazolam as a benzodiazepine NPS and shows no international-control schedule entry. A direct text search of the fetched schedules in the official INCB editions of the 1961, 1971 and 1988 conventions found no occurrence of flunitrazolam. This international result does not determine national analogue or generic-law coverage.

By Country

Illegal15
Argentina flagArgentinaIllegal
Belgium flagBelgiumIllegal
Czech Republic flagCzech RepublicIllegal
Denmark flagDenmarkIllegal
Finland flagFinlandIllegal
Germany flagGermanyIllegal (analog/blanket ban)
Indonesia flagIndonesiaIllegal
Italy flagItalyIllegal
Poland flagPolandIllegal
Singapore flagSingaporeIllegal (analog/blanket ban)
South Africa flagSouth AfricaIllegal (analog/blanket ban)
South Korea flagSouth KoreaIllegal
Sweden flagSwedenIllegal
Switzerland flagSwitzerlandIllegal
United Kingdom flagUnited KingdomIllegal
Controlled / restricted4
Brazil flagBrazilRestricted
Canada flagCanadaRestricted
France flagFranceRestricted
Russia flagRussiaRestricted
Prescription1
Australia flagAustraliaPrescription only

References

Source Pages

  1. Bluelight: Flunitrazolam Experiences and Dosage Discussion
  2. Erowid Experience Report: Flunitrazolam
  3. Isomer Design (TiHKAL/PiHKAL)
  4. PsychonautWiki
  5. TripSit Factsheet: Flunitrazolam
  6. TripSit Factsheet: Flunitrazolam
  7. TripSit Factsheets
  8. Wikipedia

Citations

  1. Decreto 122/2026, Anexo I. boletinoficial.gob.ar (n.d.). https://www.boletinoficial.gob.ar/detalleAviso/primera/338915/20260302?anexos=11
  2. Decreto 122/2026, Anexo I. mpf.gob.ar (n.d.). https://www.mpf.gob.ar/procunar/files/2019/09/Anexo-decreto-122-2026.pdf1
  3. Decreto 122/2026, Anexo I. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/nacional/ley-23737-138/actualizacion1
  4. Therapeutic Goods (Poisons Standard—June 2026) Instrument 2026, Schedule 4 and Appendix D clause 5. legislation.gov.au (n.d.). https://www.legislation.gov.au/F2026L00633/asmade/2026-05-28/text/original/epub/OEBPS/document_1/document_1.html1
  5. Therapeutic Goods (Poisons Standard—June 2026) Instrument 2026, Schedule 4 and Appendix D clause 5. pubchem.ncbi.nlm.nih.gov (n.d.). https://pubchem.ncbi.nlm.nih.gov/compound/Flunitrazolam1
  6. Royal Decree of 6 September 2017 regulating narcotic, psychotropic and soporific substances, Annex IVB (as amended). ejustice.just.fgov.be (n.d.). https://www.ejustice.just.fgov.be/eli/arrete/2017/09/06/2017031231/justel1
  7. Royal Decree of 6 September 2017 regulating narcotic, psychotropic and soporific substances, Annex IVB (as amended). afmps.be (n.d.). https://www.afmps.be/fr/humain/produits_particuliers/subst_specialement_reglementees/stupefiants_et_psychotropes/substances1
  8. Royal Decree of 6 September 2017 regulating narcotic, psychotropic and soporific substances, Annex IVB (as amended). afmps.be (n.d.). https://www.afmps.be/sites/default/files/content/INSP/NARC/annex%20IV_non%20official%20consolidated%20version.pdf1
  9. Royal Decree of 6 September 2017 regulating narcotic, psychotropic and soporific substances, Annex IVB (as amended). afmps.be (n.d.). https://www.afmps.be/sites/default/files/content/INSP/NARC/kb-ar-20170906.pdf1
  10. Portaria SVS/MS No. 344/1998, Annex I, List B1, as updated by ANVISA RDC No. 835 of 13 December 2023. gov.br (n.d.). https://www.gov.br/anvisa/pt-br/assuntos/medicamentos/controlados/lista-substancias1

Further Reading

  1. Tripsitter: Flunitrazolam Fact Sheet
  2. van Vrancken et al. 2021 - Designer Benzodiazepine Toxicity in Netherlands

Article Status

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Recent changes8 human edits · latest

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20 August 2026

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