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    GBL molecular structure

    GBL Stats & Data

    Gamma-bl Blue nitro Revivarant Renewtrient 1,4-lactone
    PubChem
    MW86.09
    FormulaC4H6O2
    LogP-0.6
    IUPACoxolan-2-one
    InChIKeyYEJRWHAVMIAJKC-UHFFFAOYSA-N
    Chemical Class Butyrolactone
    Psychoactive Class Depressant

    Interaction Warnings

    ⚠ dissociatives

    This combination can result in an increased risk of vomiting during unconsciousness and death from the resulting suffocation. If this occurs, users should attempt to fall asleep in the recovery position or have a friend move them into it.

    ⚠ stimulants

    It is dangerous to combine GBL, a depressant, with stimulants due to the risk of excessive intoxication. Stimulants decrease the sedative effect of GBL, which is the main factor most people consider when determining their level of intoxication. Once the stimulant wears off, the effects of GHB will be significantly increased, leading to intensified disinhibition as well as other effects. If combined, one should strictly limit themselves to only dosing a certain amount of GHB per hour.

    Pharmacology

    DrugBank
    State Solid

    Description

    One of the furans with a carbonyl thereby forming a cyclic lactone. It is an endogenous compound made from gamma-aminobutyrate and is the precursor of gamma-hydroxybutyrate. It is also used as a pharmacological agent and solvent.

    Mechanism of Action

    GBL is a rapidly- and short-acting prodrug to GHB with an uneven conversion rate into the same. (1g GHB = 1.6 ml GBL)

    Pharmacodynamics

    GBL can be converted to GHB prior to ingestion with a strong base, or after ingestion via blood lactonases.

    Receptor Profile

    Receptor Actions

    Agonists
    Gamma-hydroxybutyrate (GHB) receptor agonist
    GABA-B receptor agonist (via conversion to GHB)

    History & Culture

    GBL has a long history as an industrial chemical, primarily valued as a solvent and intermediate in the synthesis of other compounds. Its commercial applications have included use as a flavoring agent, stain remover, wheel cleaner, paint stripper, superglue remover, and as a solvent in certain wet aluminum electrolytic capacitors. The recreational history of GBL is closely intertwined with the scheduling of GHB. Following restrictions placed on GHB, GBL was marketed as a nutritional supplement under brand names such as Revivarant and Renewtrient, capitalizing on its property as a GHB prodrug that enhances sleep-related growth hormone secretion. These products were eventually prohibited by the FDA. In response to tightening regulations on both substances, home synthesis kits emerged that enabled users to convert GBL and 1,4-butanediol into GHB, effectively circumventing restrictions on the scheduled substance. The relative accessibility of GBL's precursors has contributed to its popularity in certain recreational contexts, particularly among young people in French nightclub scenes where it can be produced with readily available materials. Both GBL and GHB are colloquially referred to as "K.-o.-Tropfen" (knockout drops) in German-speaking countries. While concerns have been raised regarding the potential use of GBL as a drug-facilitated sexual assault agent—particularly as an alternative to scheduled GHB—the available evidence suggests such use is not widespread, especially when compared to alcohol, partly due to GBL's distinctively strong taste.

    Subjective Effects

    Physical

    The physical effects of GBL can be broken down into several components which progressively intensify proportional to dosage.

    • Stimulation and Sedation: At lower dosages GBL is physically stimulating, encouraging movement and wakefulness. At higher dosages, however, it becomes physically sedating, encouraging sleep and lethargy.
    • Respiratory depression: In cases of GBL overdoses, many reportedly experience an abnormal pattern of breathing characterized by progressively deeper and sometimes faster breathing, followed by a gradual decrease that results in a temporary stop in breathing called an apnea.
    • Euphoria
    • Nausea
    • Motor control loss
    • Dizziness
    • Dehydration
    Cognitive

    The cognitive effects of GBL can be broken down into several components which progressively intensify proportional to dosage.

    • Empathy, love and sociability enhancement: Unlike alcohol which merely increases sociability through disinhibition, GBL presents strong entactogenic effects which although weaker than that of MDMA are still prominent and well defined.
    • Disinhibition
    • Information processing suppression
    • Thought deceleration
    • Amnesia
    • Euphoria
    • Anxiety suppression

    Forked from Subjective Effect Documentation by Josie Kins, September 2015. Via dose.wiki (CC0).

    Toxicity

    PsychonautWiki PubChem DrugBank

    GBL is not active in its own right; its mechanism of action stems from its identity as a prodrug of GHB, meaning that it is rapidly converted into GHB in the body. GBL is not considered to be as safe as GHB used responsibly or medicinally, since it is theorized to display additional toxic effects on the body in difference to GHB. The LD50 is above the active dosage, and there is no danger of acute toxicity. However, it can become dangerous when used as a recreational drug, abused, or in combination with other drugs. There have been many negative reports from recreational users who have overdosed, combined GBL with alcohol or other drugs, or accidentally dosed themselves unexpectedly or way above the common dosage range.

    LD50

    • LD50: 17.2 mL/kg (Oral, Rat) (581)

    Carcinogenicity

    Group 3: Not classifiable as to its carcinogenicity to humans

    Organ-specific toxicity

    GBL itself may also produce neurotoxic effects, in addition to the effects of GHB, to which it is converted to by the body. In multiple studies, GHB has been found to impair spatial memory, working memory, learning and memory in rats with chronic administration. These effects are associated with decreased NMDA receptor expression in the cerebral cortex and possibly other areas as well.

    Community Effects

    TripSit
    Positive
    relaxation

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    GBL is converted to GHB very rapidly (on the order of minutes); GHB elimination half‑life is commonly cited around 30–60 minutes, but clinical effects can outlast plasma levels due to receptor dynamics and stacking.
    Addiction Potential
    High with frequent use: tolerance can build in days; physical dependence and medically dangerous withdrawal have been repeatedly documented, especially with around‑the‑clock redosing patterns.

    No tolerance chart. Our decay curves for these drugs were estimates, and a curve can make tolerance look longer-lasting than it is, which is the dangerous direction.

    How fast tolerance to these drugs fades after a break has not been measured well enough to draw, so don't count on a dose you used to take still being safe: after time off, start with a much smaller amount and don't use alone. Mixing sedatives with each other, with alcohol or with opioids sharply raises the risk of a fatal overdose. If you've been using regularly, don't stop suddenly: withdrawal from benzodiazepines, alcohol or GHB/GBL can cause seizures or delirium, so get medical help to cut down gradually. With GHB and GBL, tolerance drops after you stop, so the amount you used to take can cause an overdose, and the gap between the dose you want and an overdose is small and hard to judge.

    Sources: FRANK: benzodiazepines · Alcohol and Drug Foundation: GHB · FDA 2020: benzodiazepine boxed warning · FDA 2019: gabapentinoids and breathing · NHS: alcohol use disorder · FRANK: GHB

    Cross-Tolerances

    GHB
    1,4-Butanediol

    Experience Report Analysis

    Erowid
    80 Reports
    42 Single-substance
    1997–2022 Date Range
    24 With Age Data
    20 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 42 experience reports (42 single-substance Erowid)

    42 Reports
    20 Effects Detected
    9 Positive
    7 Adverse
    4 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Each bar is the share of reports mentioning the effect; its whisker, and the band on the rows below, is the 95% interval: where the share could plausibly be with other reports of the same kind.

    Positive Effects 9

    Euphoria 38.1% (95% interval 25 to 53 percent) 70%
    Stimulation 38.1% (95% interval 25 to 53 percent) 70%
    Empathy 23.8% (95% interval 14 to 38 percent) 70%
    Tactile Enhancement 23.8% (95% interval 14 to 38 percent) 70%
    Sedation 21.4% (95% interval 12 to 36 percent) 70%
    Music Enhancement 14.3% (95% interval 7 to 28 percent) 70%
    Color Enhancement 9.5% (95% interval 4 to 22 percent) 70%
    Focus Enhancement 9.5% (95% interval 4 to 22 percent) 70%
    Introspection 7.1% (95% interval 2 to 19 percent) 70%

    Adverse Effects 7

    Anxiety 47.6% (95% interval 33 to 62 percent) 70%
    Nausea 23.8% (95% interval 14 to 38 percent) 70%
    Confusion 23.8% (95% interval 14 to 38 percent) 70%
    Sweating 9.5% (95% interval 4 to 22 percent) 70%
    ⚠ Psychosis 9.5% (95% interval 4 to 22 percent) 70%
    Increased Heart Rate 9.5% (95% interval 4 to 22 percent) 70%
    ⚠ Seizure 7.1% (95% interval 2 to 19 percent) 70%
    Show 4 neutral or unclassified mentions
    Hospital 26.2% (95% interval 15 to 41 percent)
    Auditory Effects 16.7% (95% interval 8 to 31 percent)
    Open-Eye Visuals 11.9% (95% interval 5 to 25 percent)
    Visual Distortions 9.5% (95% interval 4 to 22 percent)

    Also reported in combinations. In the 38 GBL reports where another drug was taken too, 10 (26.3%) mention hospital, emergency services or an overdose, 3 (7.9%) a seizure and 2 (5.3%) psychosis. In the 42 single-substance reports: 26.2%, 7.1% and 9.5%. These are not in the figures above: they cannot be put down to GBL alone, and a mention is not always something that happened to the writer.

    Dosage Distribution

    Dose distribution from experience reports, one dose per report (the first listed). Doses above Q3 + 3×IQR, far above what people typically take, are left out of the median and range and listed under each route: most are real heavy doses or overdoses, not mistakes.

    Median: 2.2 ml IQR: 1.5–5.0 ml n=22

    1 report gave a dose above the typical range (20 ml), so it is not in the figures above. Listing a dose here does not mean it is safe.

    Show the report

    Real-World Dose Distribution

    Erowid

    From 9 of 71 recorded dose entries: those that state a weight (mg, g or µg), in routes with at least five of them. Values above Q3 + 3×IQR, far above what people typically take, are left out; they can include real heavy doses and overdoses, not only mistakes.

    Oral (n=8)

    Median: 2000.0mg 25th: 1225.0mg 75th: 2000.0mg 90th: 2180.0mg

    Common Combinations

    Most co-occurring substances, as a share of all 80 reports filed under GBL; whiskers are 95% intervals

    Form / Preparation

    Most common forms and preparations, as a share of the 52 reports that give one; whiskers are 95% intervals

    Redose Patterns

    Redosing behavior across 65 reports

    10.8% (95% interval 5 to 21 percent) Redosed
    1.2 Avg Doses
    27m Median Interval

    Legal Status

    Country Status Notes
    Australia Border Controlled Substance Illegal to import without a permit. Importation of a commercial quantity (over 1 kg) is punishable by up to life imprisonment and/or an AUD $825,000 fine.
    Austria Illegal (NPSG) Since January 1, 2012, possession, production, and sale are prohibited under the Neue-Psychoaktive-Substanzen-Gesetz (New Psychoactive Substances Act).
    Canada Schedule VI (CDSA) Controlled under Schedule VI of the Controlled Drugs and Substances Act. Vendors must collect purchase information. Import and export are prohibited, punishable as an indictable offence (up to 10 years) or summary conviction (up to 18 months). Personal possession is not illegal.
    Germany Controlled Distribution Not listed in the Betäubungsmittelgesetz (Narcotics Act), but distribution is controlled. Possession is not illegal unless intended for human consumption or GHB synthesis, in which case the Arzneimittelgesetz (Medicines Act) may apply.
    Hong Kong Schedule 1 (Dangerous Drugs Ordinance) Controlled as a dangerous drug under Schedule 1 of the Dangerous Drugs Ordinance, Cap.134, with exemption clause at Paragraph 16D. Unauthorized possession punishable by a fine of HK$1,000,000 and imprisonment for 7 years upon indictment.
    Israel Proscribed Substance Classified as a proscribed substance since 2007. Possession, production, and distribution are prohibited under national drug control legislation.
    Netherlands Legal (Industrial Use) Freely available as a cleaning agent. Retailers do not require a license to sell the substance for legitimate industrial purposes.
    Poland Controlled Drug Classified as a drug under national pharmaceutical legislation. Handling requires a pharmaceutical license; unauthorized possession and distribution are prohibited.
    Sweden Health-Endangering Substance Not classified as a narcotic drug but designated a health-endangering substance. Legislation enacted in April 2011 enabled GBL to be treated as a controlled substance when not used for legitimate industrial purposes.
    Switzerland Illegal (GHB Analog) Considered an ester analog of GHB, making it controlled under Buchstabe B of Swiss narcotics legislation. Industrial use remains permitted with appropriate authorization.
    Turkey Illegal Classified as a controlled drug. Possession, production, supply, and importation are prohibited under national drug legislation.
    United Kingdom Conditionally Controlled Under Regulation 4B of the Misuse of Drugs Regulations 2001, it is lawful to import, export, produce, supply, or possess GBL for legitimate purposes. The substance becomes controlled when a person handles it knowing or believing it will be used for human ingestion.
    United States List I Controlled Chemical Regulated as a List I controlled chemical under federal law. As a GHB analog, it is treated as a Schedule I controlled substance under the Controlled Substances Act when intended for human consumption.

    Harm Reduction

    drugs.wiki

    GBL is a prodrug rapidly converted to GHB in vivo; relative to GHB it is more potent by volume and has a faster, sharper onset, which increases overdose risk from small mismeasurements. GBL is a skin/mucosal irritant solvent; always dilute in a non‑alcoholic drink before swallowing, avoid contact with eyes/skin, and never inject or insufflate. The dose‑response curve is steep: recreational doses lie close to doses causing unrousable sleep and, at higher levels or when mixed with other depressants, life‑threatening respiratory depression. Redosing too soon causes stacking: wait at least 2 hours between doses and reduce any redose; dopamine‑rebound wakefulness 3–5 hours later can create a strong compulsion to redose but increases risk of dependence. Food reduces/slow s absorption; many HR groups suggest dosing at least 2 hours after eating and avoiding further redose until effects fully plateau. Never combine with alcohol, benzodiazepines, opioids, barbiturates, Z‑drugs, or other depressants; ketamine with G markedly increases loss of consciousness and breathing problems. If someone becomes unrousable, place them in the recovery position, keep airway clear, monitor breathing, and seek emergency help; do not ‘wake’ them with stimulants or give more substances. Tolerance can develop in days with frequent use; withdrawal may begin within 1–6 hours after the last dose and can escalate to agitation, delirium, tachycardia, and life‑threatening complications — medical supervision is essential for dependent users. Concentration varies by source and bottles; unknown dilution is common — start low (0.3–0.5 mL), measure precisely to 0.1 mL, and label doses/times to avoid mistakes. GHB/GBL may reduce efficacy of some HIV medications; avoid co‑use and consult a clinician if on antiretrovirals. As a solvent, GBL can degrade some plastics; prefer glass (or chemically resistant equipment) for storage/measurement, clearly label, add a food‑safe dye to avoid accidental ingestion, and keep locked away from children/pets. Do not drive or operate machinery; some HR groups advise waiting at least 24 hours after last dose before driving due to residual impairment and stacking.

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