Home
    Disclaimer
    6-APB molecular structure

    6-APB Stats & Data

    6apb Benzofury Nrg-3
    PubChem
    MW175.23
    FormulaC11H13NO
    LogP2.1
    IUPAC1-(1-benzofuran-6-yl)propan-2-amine
    InChIKeyFQDAMYLMQQKPRX-UHFFFAOYSA-N
    Chemical Class Amphetamine
    Psychoactive Class Psychedelic / Stimulant
    Half-Life Unknown in humans (no controlled PK). Long subjective duration (7–10 h oral) and residual stimulation suggest slow redistribution and/or active metabolites.

    Pharmacology

    Metabolites

    3-Carboxymethyl-4-hydroxyamphetamine
    4-Carboxymethyl-3-hydroxyamphetamine

    History & Culture

    1993–2000

    The benzofuran entactogens emerged from academic research into the structure-activity relationships of MDMA and related compounds. In 1993, medicinal chemist David E. Nichols and colleagues at Purdue University investigated 5-APDB and 6-APDB as serotonin releasing agents and entactogens, examining the role of the MDA dioxole ring structure in serotonergic neuron interactions.[cite:doi-10-1021-jm00075a027] This research was partly motivated by efforts to identify potential non-neurotoxic alternatives to MDMA, which was gaining recognition as a potentially useful adjunct in psychotherapy while simultaneously being linked to neurotoxic effects. Following this foundational work, 6-APB and its structural relative 5-APB were first described in the scientific literature in 2000 by Karin Briner and colleagues at Eli Lilly and Company in a patent application.[cite:url-patents-google-com-us7045545b1] At this time, the compounds were specifically studied as serotonin 5-HT2C receptor agonists for potential medical applications rather than as recreational substances.[cite:url-patents-google-com-us7045545b1]

    2010–2014

    Despite being characterized in the scientific literature a decade earlier, human recreational use of 6-APB was not documented until 2010, when the compound emerged for sale on the global research chemical market.[cite:doi-10-1007-s00213-020-05648-z] It became particularly prominent in the United Kingdom's "legal highs" market, where it was sold under the brand name "Benzofury" in distinctive bright orange packaging that became instantly recognizable.[cite:uk-ho-circular-008-2013] The compound's conspicuous branding attracted significant media attention during this period. 6-APB became one of the most frequently cited research chemicals in media coverage critical of legal highs, contributing to calls for regulatory action. This ultimately led to classification as a Temporary Class Drug in June 2013,[cite:uk-si-2013-1294] followed by permanent scheduling as a Class B substance alongside all other benzofuran entactogens in June 2014,[cite:url-legislation-gov-uk-made] effectively ending its presence in the legal market.

    Effect Profile

    Curated + 137 Reports
    Psychedelic 7.6

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

    Visual Intensity×3
    10102.1
    Headspace Depth×3
    75.41.7
    Auditory Effects×1
    10100.8
    Body Load / Somatic Effects×1
    10103.1
    Catalog Erowid BlueLight
    Empathogen 10.0

    Strong empathy, euphoria, stimulation, and sensory enhancement

    Empathy / Social Openness×3
    10103.5
    Euphoria / Mood Elevation×2
    10106.4
    Stimulation×1
    10105.6
    Sensory Enhancement×1
    10105.0
    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
    104.8
    Anxiety / Jitters×1
    1010
    Catalog Erowid

    Empirical Duration

    Erowid Reports
    Onset Come Up Peak Offset
    Oral (20 reports)

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans (no controlled PK). Long subjective duration (7–10 h oral) and residual stimulation suggest slow redistribution and/or active metabolites.
    Addiction Potential
    Moderate: empathogenic reinforcement and long duration can encourage session extension and redosing; clear pharmacodynamic tolerance develops within a session, which limits multi‑day use but can prompt higher single‑session dosing.

    Tolerance Decay

    Full tolerance 1d Half tolerance 4d Baseline ~14d

    Within‑session tolerance is common and encourages redosing; spacing sessions by several weeks reduces cumulative serotonergic and potential 5‑HT2B‑mediated risks.

    Cross-Tolerances

    MDMA
    60% ●○○
    MDA
    60% ●○○
    5‑APB / 5‑MAPB
    70% ●○○

    Experience Report Analysis

    Erowid BlueLight
    80 Reports
    2010–2025 Date Range
    76 With Age Data
    32 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 130 experience reports (80 Erowid + 57 Bluelight)

    130 Reports
    128 Effects Detected
    48 Positive
    52 Adverse
    28 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 48

    Euphoria 71.5% 91%
    Stimulation 65.4% 85%
    Music Enhancement 53.9% 86%
    Empathy 45.4% 86%
    Sociability Enhancement 38.0% 85%
    Tactile Enhancement 33.1% 84%
    Color Enhancement 31.5% 75%
    Body High 29.2% 85%
    Tingling 28.0% 82%
    Contentment 26.0% 80%
    Libido Enhancement 20.0% 84%
    Focus Enhancement 17.0% 78%
    Visual Trails 16.0% 84%
    Joy 14.0% 89%
    Drowsiness 14.0% 79%
    Introspection 13.1% 79%
    Patterning 12.0% 80%
    Thought Acceleration 12.0% 80%
    Creativity Enhancement 10.0% 70%
    Morphing 10.0% 85%

    Adverse Effects 52

    Jaw Clenching 41.6% 85%
    Nausea 29.3% 86%
    Pupil Dilation 26.9% 89%
    Anxiety 26.2% 79%
    Dry Mouth 22.0% 83%
    Headache 21.5% 80%
    Sweating 20.0% 85%
    Insomnia 20.0% 83%
    Thought Loops 18.0% 76%
    Confusion 17.7% 90%
    Teeth Grinding 16.0% 88%
    Thought Disorganization 16.0% 79%
    Focus Suppression 14.0% 74%
    Increased Heart Rate 12.5% 70%
    Body Temperature Change 12.0% 81%
    Restlessness 12.0% 78%
    Motor Impairment 9.2% 75%
    Paranoia 8.0% 80%
    Vomiting 8.0% 90%
    Stomach Cramps 8.0% 72%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    View data table
    Effect Strong (n=17) Heavy (n=21)
    Euphoria 76.5% 85.7%
    Music Enhancement 76.5% 61.9%
    Visual Distortions 52.9% 76.2%
    Empathy 64.7% 71.4%
    Stimulation 52.9% 71.4%
    Jaw Clenching 58.8% 42.9%
    Color Enhancement 52.9% 42.9%
    Tactile Enhancement 47.1% 38.1%
    Sedation 41.2% 28.6%
    Sweating 41.2% 28.6%
    Nausea 35.3% 33.3%
    Headache 35.3% 0%
    Anxiety 29.4% 33.3%
    Confusion 29.4% 33.3%
    Auditory Effects 29.4% 23.8%

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 80 experience reports.

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

    Oral dose range: 100.0–150.0 mg (median 115.0 mg)
    Effect Strong (n=17) Heavy (n=21)
    euphoria
    76%
    86%
    music enhancement
    76%
    62%
    visual distortions
    53%
    76%
    empathy
    65%
    71%
    stimulation
    53%
    71%
    jaw clenching
    59%
    43%
    color enhancement
    53%
    43%
    tactile enhancement
    47%
    38%
    sedation
    41%
    29%
    sweating
    41%
    29%
    nausea
    35%
    33%
    headache
    35%
    anxiety
    29%
    33%
    confusion
    29%
    33%
    auditory effects
    29%
    24%
    focus enhancement
    29%
    19%
    pupil dilation
    18%
    29%
    body high
    24%
    24%
    muscle tension
    24%
    motor impairment
    24%

    Showing top 20 of 30 effects

    Risk Escalation

    Sentiment Analysis

    Average frequency of positive vs adverse effects across dose tiers

    Strong n=17
    10 positive 44.7% 10 adverse 30.6%
    Heavy n=21
    10 positive 44.8% 8 adverse 28.0%
    View effect breakdown

    Adverse Effects

    Effect Strong (n=17) Heavy (n=21) Change
    Jaw Clenching
    59%
    43%
    -27%
    Sweating
    41%
    29%
    -30%
    Nausea
    35%
    33%
    -5%
    Headache
    35%
    0%
    Anxiety
    29%
    33%
    +13%
    Confusion
    29%
    33%
    +13%
    Pupil Dilation
    18%
    29%
    +62%
    Muscle Tension
    24%
    0%
    Motor Impairment
    24%
    0%
    Memory Suppression
    14%
    0%
    Increased Heart Rate
    12%
    0%
    Seizure
    10%
    0%

    Positive Effects

    Effect Strong (n=17) Heavy (n=21) Change
    Euphoria
    76%
    86%
    +12%
    Music Enhancement
    76%
    62%
    -19%
    Empathy
    65%
    71%
    10%
    Stimulation
    53%
    71%
    +34%
    Color Enhancement
    53%
    43%
    -18%
    Tactile Enhancement
    47%
    38%
    -19%
    Focus Enhancement
    29%
    19%
    -35%
    Body High
    24%
    24%
    1%
    Creativity Enhancement
    12%
    19%
    +61%
    Introspection
    12%
    14%
    +21%

    Dosage Distribution

    Dose distribution from experience reports

    Median: 115.0 mg IQR: 100.0–150.0 mg n=47

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 1.378 mg/kg IQR: 1.152–2.101 mg/kg n=44

    Redose Patterns

    Redosing behavior across 65 reports

    43.1% Redosed
    1.7 Avg Doses
    130m Median Interval

    Harm Reduction

    drugs.wiki

    - Onset is slow (often 60–120 min oral). Premature redosing is a leading cause of unexpectedly high total intake; wait at least 2 hours before considering any booster.

    - Intranasal use is discouraged due to strong nasal irritation and variable absorption; oral is the safer, more predictable ROA.

    - Salt form matters. By weight, pure 6‑APB succinate delivers about 72% of the active base compared with HCl; many commercial succinate batches contain substantial excess succinic acid, further lowering potency. Calibrate doses conservatively and test new batches.

    - Product variability and mislabeling are common; recent Swiss and Dutch drug‑checking alerts continue to find 6‑APB in place of MDMA in pills and, in rare cases, mixtures or adulterants. Use reagent testing and, where available, lab‑based drug checking before consumption.

    - Duration is longer than MDMA; plan dosing early in the day if sleep is needed the same night, and expect residual stimulation into the following day.

    - Hydration and temperature: during dancing/heat, sip isotonic fluids (~300 mL/hour), take cool‑down breaks, and avoid overhydration; isotonic drinks reduce hyponatremia risk compared with plain water.

    - Serotonin‑toxicity risk increases with MAOIs, SSRIs/SNRIs, tramadol/DXM, or other serotonergic releasers; avoid such combinations and seek urgent care if confusion, hyperthermia, rigidity, or clonus occur.

    - 5‑HT2B receptor agonists (e.g., fenfluramine metabolite norfenfluramine) are linked to valvular heart disease with chronic exposure. Because benzofurans can activate 5‑HT2B in vitro, frequent or high‑dose 6‑APB use may plausibly elevate long‑term valvulopathy risk; spacing use and avoiding chronic patterns is prudent.

    - Polydrug stimulant combinations (e.g., with amphetamine) amplify cardiovascular strain and should be avoided; if undertaken, significantly reduce doses and do not redose during the peak.

    - Recent market reviews indicate 6‑APB continues to circulate as an NPS in parts of Europe; quality and composition vary year‑to‑year—further reason to test batches and titrate cautiously.

    ← Back to 6-APB