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    Phenibut molecular structure

    Phenibut Stats & Data

    Phgaba Noofen Bifren Fenibut Anvifen
    NPS DataHub
    MW179.22
    FormulaC10H13NO2
    CAS1078-21-3
    SMILESNCC(CC(=O)[O-])c1ccccc1.[H+]
    InChIKeyDAFOCGYVTAOKAJ-UHFFFAOYSA-N
    Phenethylamines; Others; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Psychoactive Class Depressant

    Receptor Profile

    Receptor Actions

    Agonists
    GABA-B receptor agonist (full)
    GABA-A receptor agonist (at higher doses)
    Other
    Voltage-gated calcium channel alpha-2-delta subunit ligand

    History & Culture

    1960s–1974

    Phenibut was synthesized during the 1960s at the Department of Organic Chemistry at the Al Gertsen Leningrad Pedagogical Institute under the supervision of Professor V. V. Perekalin. Following its development, the compound was researched for potential applications in treating various conditions including anxiety, depression, post-traumatic stress disorder, insomnia, and general weakness or asthenia. Early research indicated that while phenibut shared certain properties with traditional sedatives, it produced less impairment and fewer "narcotic-like" effects in animal studies. The compound was initially introduced under the brand name Citrocard during the late 1960s to early 1970s. On December 18, 1974, phenibut was officially added to the State Drug Register under Order No. 1126 by the USSR's Ministry of Public Health, establishing it as an approved neuropsychotropic medication.

    1975–present

    Phenibut gained notable recognition for its inclusion in Soviet space program protocols. According to Neumyvakin (1978), the substance was available to Russian cosmonauts during the Soyuz-19 mission in 1975. The compound has since been cited as a mandated component of cosmonaut medical kits, though the precise extent of its utilization throughout the broader Soviet and Russian space programs remains unclear.

    2000s–present

    While phenibut has maintained continuous pharmaceutical availability in Russia since its initial release, the substance has seen minimal expansion into medical settings beyond Russian borders and remains unapproved for clinical use in most other countries. However, beginning in the 2000s and accelerating through the 2010s, phenibut became widely accessible internationally through the nutritional supplement industry, marketed and sold without prescription in many regions where it lacks pharmaceutical approval.

    Subjective Effect Notes

    In comparison to other commonly used GABAgenic depressants such as alcohol or benzodiazepines, this compound is significantly longer lasting, more euphoric and more recreational.

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    1.5-3 hours
    1.5-3 hours
    3-4 hours
    4-6 hours
    6-24 hours
    Total: 4-10 hours
    Rectal
    30-60 minutes hours
    1-3 hours
    1-24 hours
    Total: 4-10 hours

    Community Effects

    TripSit
    Negative
    anxiety insomnia psychosis

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

    Full tolerance 1h Half tolerance 10d Baseline ~14d

    Cross-Tolerances

    Alcohol
    30% ●○○
    GHB
    30% ●○○
    GBL
    30% ●○○
    Gabapentin
    80% ●○○
    Pregabalin
    80% ●○○

    Experience Report Analysis

    Erowid BlueLight
    120 Reports
    2004–2025 Date Range
    104 With Age Data
    34 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 145 experience reports (120 Erowid + 25 Bluelight)

    145 Reports
    104 Effects Detected
    33 Positive
    53 Adverse
    18 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 33

    Anxiety Suppression 56.5% 92%
    Stimulation 46.2% 84%
    Euphoria 40.0% 87%
    Sedation 39.3% 84%
    Sociability Enhancement 32.0% 81%
    Music Enhancement 30.3% 90%
    Focus Enhancement 26.9% 82%
    Contentment 24.0% 85%
    Hypersomnia 24.0% 81%
    Peace 24.0% 85%
    Empathy 23.4% 80%
    Joy 20.0% 81%
    Tactile Enhancement 18.3% 70%
    Color Enhancement 15.8% 85%
    Thought Acceleration 12.0% 87%
    Body High 10.4% 75%
    Relaxation 8.0% 90%
    Geometric Imagery 8.0% 90%
    Libido Enhancement 8.0% 75%
    Bliss 8.0% 88%

    Adverse Effects 53

    Nausea 26.9% 86%
    Dizziness 24.0% 85%
    Confusion 19.3% 88%
    Headache 18.6% 88%
    Body Load 16.0% 84%
    Focus Suppression 16.0% 79%
    Insomnia 16.0% 81%
    Motor Impairment 13.1% 80%
    Thought Disorganization 12.0% 75%
    Vomiting 12.0% 92%
    Memory Suppression 11.1% 78%
    Sweating 8.3% 85%
    Heaviness 8.0% 80%
    Disinhibition 8.0% 80%
    Panic 8.0% 95%
    Ataxia 8.0% 85%
    Metallic Taste 8.0% 95%
    Increased Heart Rate 7.5% 70%
    Muscle Tension 6.7% 70%
    Pain Enhancement 4.0% 75%

    Dosage Distribution

    Dose distribution from experience reports

    Median: 2000.0 mg IQR: 1000.0–3000.0 mg n=49

    Real-World Dose Distribution

    62K Doses

    From 188 individual dose entries

    Oral (n=155)

    Median: 1250.0mg 25th: 775.0mg 75th: 2000.0mg 90th: 3000.0mg
    mg/kg median: 17.082 mg/kg 75th: 31.538

    Insufflated (n=6)

    Median: 75.0mg 25th: 50.0mg 75th: 100.0mg 90th: 125.0mg
    mg/kg median: 1.115 mg/kg 75th: 1.47

    Common Combinations

    Most co-occurring substances in experience reports

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 24.51 mg/kg IQR: 11.765–32.68 mg/kg n=48

    Redose Patterns

    Redosing behavior across 74 reports

    27.0% Redosed
    1.4 Avg Doses
    60m Median Interval

    Legal Status

    Country Status Notes
    Australia Schedule 9 Classified as a prohibited substance as of February 1st, 2018. Possession, importation, supply, and manufacture are illegal.
    Canada Uncontrolled Not a controlled substance under Canadian law. Legal to possess without license or prescription.
    Germany Potentially NpSG May be controlled under the Neue-psychoaktive-Stoffe-Gesetz (New Psychoactive Substances Act) as of July 18, 2019. Whether this legislation applies to phenibut remains legally unclear.
    Italy Schedule 1 Classified as a Schedule 1 controlled substance. Possession, production, and distribution are prohibited.
    Latvia Prescription medication Available as an unscheduled prescription drug marketed under the brand name 'Noofen.' Also sold as 'Cognifen' in combination with ipidacrine for cognitive impairment associated with vascular disorders.
    Russia Approved pharmaceutical Added to the State Drug Register in 1974 under Order No. 1126 by the USSR Ministry of Public Health. Remains available as a neuropsychotropic medication for conditions including anxiety, depression, PTSD, insomnia, and vestibular disorders.
    Switzerland Not controlled Not listed under Buchstabe A, B, C, or D of controlled substances legislation. Generally considered legal to possess.
    United Kingdom Not specifically controlled Not a controlled substance under the Misuse of Drugs Act 1971. However, production, supply, or importation may potentially be prohibited under the Psychoactive Substances Act 2016, which applies blanket restrictions on psychoactive substances with exemptions for alcohol, nicotine, and medicinal products.
    United States Federally uncontrolled Not a federally scheduled substance. Legal to possess without license or prescription. Sales, distribution, and labeling are regulated by FDA rules when sold for human consumption. Note that Alabama classified phenibut as a Schedule II controlled substance at the state level as of November 21st, 2021.
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