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    5-APB molecular structure

    5-APB Stats & Data

    Nrg-3 6-apb Benzofury Head candy 5apb 6apb
    NPS DataHub
    MW175.23
    FormulaC11H13NO
    CAS286834-85-3
    IUPAC1-(1-benzofuran-6-yl)propan-2-amine
    SMILESCC(N)Cc1ccc2ccoc2c1
    InChIKeyFQDAMYLMQQKPRX-UHFFFAOYSA-N
    Phenethylamines; Arylalkylamines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Amphetamine
    Psychoactive Class Psychedelic / Stimulant
    Half-Life Unknown in humans; long duration of action suggests a multi-hour elimination phase. Estimates in user communities span roughly 4–8 h but are not from controlled PK studies.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (partial)
    5-HT2B receptor agonist (potent)
    5-HT2C receptor agonist
    TAAR1 agonist
    Inhibitors
    Serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI)
    Other
    Serotonin-norepinephrine-dopamine releasing agent (SNDRA)

    History & Culture

    1993–2000

    The development of 5-APB emerged from research into benzofuran-based entactogens during the 1990s. Medicinal chemist David E. Nichols and colleagues at Purdue University conducted foundational work on benzofuran analogues, examining the role of the MDA dioxole ring structure in interacting with serotonergic neurons. This research was motivated in part by efforts to identify a potentially non-neurotoxic alternative to MDMA, which was being investigated as a possible adjunct to psychotherapy but was also raising concerns about neurotoxic effects. 5-APB and its positional isomer 6-APB were formally described in a patent by Karin Briner and colleagues at Eli Lilly and Company in 2000. These compounds were studied as serotonin 5-HT2C receptor agonists for potential therapeutic applications, though they were not developed further for medical use.

    2010–present

    Recreational use of 5-APB was not documented until 2010, when it emerged for sale on the global research chemical market. The compound became particularly prominent in the United Kingdom's "legal highs" market, where 5-APB and related benzofuran entactogens were sold under the brand name "Benzofury" and gained a following in the rave scene. This period of legal availability was relatively short-lived. Following recommendations from the Advisory Council on the Misuse of Drugs, 5-APB and related analogues were classified as controlled substances in the UK in 2014, effectively ending the legal sale of benzofuran entactogens in that country. Similar regulatory actions followed in other jurisdictions.

    Effect Profile

    Curated + 95 Reports
    Psychedelic 7.6

    Strong visuals, auditory effects, and body load with moderate headspace

    Visual Intensity×3
    10106.0
    Headspace Depth×3
    75.13.3
    Auditory Effects×1
    1010
    Body Load / Somatic Effects×1
    10106.7
    Catalog Erowid BlueLight
    Empathogen 10.0

    Strong empathy, euphoria, stimulation, and sensory enhancement

    Empathy / Social Openness×3
    10104.0
    Euphoria / Mood Elevation×2
    101010
    Stimulation×1
    10106.7
    Sensory Enhancement×1
    101010
    Catalog Erowid BlueLight
    Stimulant 8.8

    Strong stimulation, euphoria, focus, and anxiety/jitters

    Stimulation / Energy×3
    1010
    Euphoria / Mood Lift×2
    1010
    Focus / Productivity×2
    104.7
    Anxiety / Jitters×1
    1010
    Catalog Erowid

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    19 minutes - 1.0 hours
    45 minutes - 1.5 hours
    2-4 hours
    1.5-3 hours
    6-48 hours
    Total: 7-8 hours
    Insufflated
    4-15 minutes
    19-40 minutes
    2-4 hours
    1.5-3 hours
    4-24 hours
    Total: 7-8 hours
    Rectal
    10-30 minutes
    45 minutes - 1.5 hours
    2.5-4 hours
    2-3 hours
    6-24 hours
    Total: 7-8 hours

    Empirical Duration

    Erowid Reports
    Onset Come Up Peak Offset
    Oral (22 reports)

    Community Effects

    TripSit
    Positive
    euphoria visual enhancement empathy music enhancement sociability warmth
    Negative
    nausea vomiting jaw clenching hyperthermia

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; long duration of action suggests a multi-hour elimination phase. Estimates in user communities span roughly 4–8 h but are not from controlled PK studies.
    Addiction Potential
    Moderate. Psychological reinforcement and binge-redose patterns are reported; physical dependence is uncommon but repeated frequent dosing can increase compulsive use risk.

    Tolerance Decay

    Full tolerance 1d Half tolerance 7d Baseline ~14d

    Pattern inferred from user reports across benzofurans and MDMA-like agents. Acute tolerance develops within a session; effects are notably blunted by redosing late. Subjective tolerance partially subsides over 1–2 weeks, with baseline often reported after 3–5 weeks. Data quality: anecdotal/community-derived.

    Cross-Tolerances

    MDMA
    60% ●○○
    MDA
    60% ●○○
    6-APB
    70% ●○○
    5-MAPB
    70% ●○○

    Experience Report Analysis

    Erowid BlueLight
    89 Reports
    2010–2025 Date Range
    85 With Age Data
    33 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 95 experience reports (89 Erowid + 6 Bluelight)

    95 Reports
    56 Effects Detected
    17 Positive
    19 Adverse
    20 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 17

    Euphoria 73.7% 91%
    Stimulation 65.2% 78%
    Music Enhancement 63.1% 89%
    Empathy 54.7% 85%
    Tactile Enhancement 45.3% 90%
    Color Enhancement 35.8% 80%
    Contentment 33.3% 80%
    Sociability Enhancement 33.3% 75%
    Body High 29.5% 89%
    Focus Enhancement 24.2% 75%
    Numbness 16.7% 80%
    Taste Distortion 16.7% 85%
    Love 16.7% 80%
    Empathogenic Connection 16.7% 85%
    Tingling 16.7% 80%
    Introspection 9.5% 75%
    Creativity Enhancement 9.0% 70%

    Adverse Effects 19

    Jaw Clenching 36.8% 75%
    Anxiety 33.7% 70%
    Body Load 33.3% 82%
    Nausea 30.5% 82%
    Confusion 28.1% 70%
    Pupil Dilation 26.3% 80%
    Sweating 20.0% 90%
    Headache 18.0% 70%
    Diarrhea 16.7% 70%
    Emotional Blunting 16.7% 75%
    Sociability Suppression 16.7% 80%
    Irritability 16.7% 65%
    Increased Heart Rate 13.5% 70%
    Muscle Tension 11.5% 80%
    Motor Impairment 9.0% 70%
    Memory Suppression 5.6% 70%
    Seizure 4.5% 70%
    Appetite Suppression 3.4% 70%
    Psychosis 3.4% 70%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    View data table
    Effect Heavy (n=38)
    Euphoria 84.2%
    Visual Distortions 68.4%
    Music Enhancement 68.4%
    Stimulation 68.4%
    Empathy 65.8%
    Color Enhancement 47.4%
    Jaw Clenching 47.4%
    Tactile Enhancement 42.1%
    Sweating 36.8%
    Nausea 34.2%
    Sedation 34.2%
    Anxiety 34.2%
    Confusion 31.6%
    Pupil Dilation 26.3%
    Auditory Effects 26.3%

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 89 experience reports.

    Limited tier coverage — most reports fall within the Heavy range. Effects at other dose levels may not be represented.

    Oral dose range: 90.0–150.0 mg (median 100.0 mg)
    Effect Heavy (n=38)
    euphoria
    84%
    visual distortions
    68%
    music enhancement
    68%
    stimulation
    68%
    empathy
    66%
    color enhancement
    47%
    jaw clenching
    47%
    tactile enhancement
    42%
    sweating
    37%
    nausea
    34%
    sedation
    34%
    anxiety
    34%
    confusion
    32%
    pupil dilation
    26%
    auditory effects
    26%
    body high
    24%
    focus enhancement
    21%
    open-eye visuals
    18%
    headache
    18%
    creativity enhancement
    16%

    Showing top 20 of 30 effects

    Dosage Distribution

    Dose distribution from experience reports

    Median: 100.0 mg IQR: 90.0–150.0 mg n=53

    Real-World Dose Distribution

    62K Doses

    From 133 individual dose entries

    Oral (n=98)

    Median: 100.0mg 25th: 70.0mg 75th: 133.75mg 90th: 166.0mg
    mg/kg median: 1.25 mg/kg 75th: 1.911

    Insufflated (n=17)

    Median: 57.0mg 25th: 25.0mg 75th: 78.0mg 90th: 116.8mg
    mg/kg median: 0.779 mg/kg 75th: 1.236

    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: 1.373 mg/kg IQR: 1.136–2.028 mg/kg n=50

    Redose Patterns

    Redosing behavior across 71 reports

    40.8% Redosed
    1.6 Avg Doses
    130m Median Interval

    Legal Status

    Country Status Notes
    Brazil Illegal Listed on Portaria SVS/MS nº 344. Possession, production, and sale are prohibited under Brazilian drug control legislation.
    France Narcotic Classified as a narcotic substance since May 9, 2018, alongside other benzofuran-derived compounds.
    Germany Anlage II BtMG Controlled under Anlage II of the Betäubungsmittelgesetz (Narcotics Act, Schedule II) since July 17, 2013. Manufacturing, possession, import, export, purchase, sale, procurement, or dispensing without a license is illegal.
    Japan Controlled substance Designated as a controlled substance effective September 16, 2015.
    Netherlands Legal (under review) Currently unscheduled, though it belongs to a substance group that may be prohibited under recently passed New Psychoactive Substances (NPS) legislation.
    Switzerland Controlled (Verzeichnis E) Specifically named as a controlled substance under Verzeichnis E of Swiss drug control legislation.
    United Kingdom Class B Initially classified as a Temporary Class Drug on June 10, 2013. Made a permanent Class B, Schedule 1 substance on June 10, 2014 alongside all other benzofuran entactogens and structurally related compounds.
    United States Unscheduled (Analogue Act applies) Not specifically scheduled at the federal level. However, due to structural similarity to MDA, it may be prosecuted under the Federal Analogue Act if sold or possessed with intent for human consumption.

    Harm Reduction

    drugs.wiki

    Product mislabeling and salt-form variability are common in the benzofuran market; material sold as “Benzo Fury” may contain 5‑APB, 6‑APB, mixtures, or unrelated actives—use multi-reagent testing and consider sending a small sample to a drug-checking service before dosing. The come-up can be slow (often 60–120 min) with a wave-like rise; premature redosing in the first 2–3 hours markedly increases risk of over-intoxication, nausea, and cardiovascular strain. 5‑APB is commonly encountered as the HCl or succinate salt; by weight, HCl contains more active base than succinate—doses should be reduced if the material is HCl or unusually pure. Reagent behavior can resemble MDMA on some tests (e.g., Marquis/Mecke dark reactions), so use a panel (e.g., Froehde, Simon’s) rather than a single reagent and avoid assuming MDMA results confirm MDMA. As a serotonergic entactogen with stimulant properties, 5‑APB should not be combined with MAOIs, DXM, tramadol, triptans, or serotonergic supplements (5‑HTP) due to serotonin toxicity risk; combining with other stimulants amplifies hypertension, hyperthermia, and arrhythmia risk. Benzofurans show concerning 5‑HT2B activity in vitro discussions; although clinical data are limited, frequent use may pose a theoretical valvulopathy risk—pace use (e.g., several weeks between sessions) and avoid if you have heart disease. Manage environment and temperature: take breaks from heat, sip water regularly, and include electrolytes on long sessions; avoid heavy alcohol (dehydration, masking warning signs). Common adverse effects include jaw clenching, nausea/vomiting on come-up, headaches during/after, insomnia, and transient anxiety—dose control, cool ambient temperature, and avoiding redose can mitigate these. Insufflation is irritating and may increase intensity but reduce duration; oral administration is generally preferred for smoother effects. Cross-tolerance with MDMA/MDA and similar entactogens is reported; spacing uses reduces “muted” effects and post-acute low mood. Because benzo fury-era products were often adulterated, be cautious with pressed pellets or unusually colored powders, and titrate with an accurate milligram scale after reagent testing.

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