Home
    Disclaimer
    2C-B molecular structure

    2C-B Stats & Data

    Bees Erox Nexus Venus Bdmpea 2cb 2-cb
    NPS DataHub
    MW296.59
    FormulaC10H15BrClNO2
    CAS56281-37-9
    IUPAC4-Bromo-2,5-dimethoxyphenethylamine.hydrochloride
    SMILES[Cl-].NCCc1cc(OC)c(Br)cc1OC.[H+]
    InChIKeyUJTWHDAMHSIRDK-UHFFFAOYSA-N
    Phenethylamines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Phenethylamine
    Psychoactive Class Psychedelic / Stimulant
    Half-Life Unknown in humans; effective duration typically 4–6 h orally (see duration).

    Pharmacology

    DrugBank
    State Solid

    Description

    2C-B (4-bromo-2,5-dimethoxyphenethylamine) is a synthetic psychedelic substance derived from mescaline. It was invented in 1974 by a man named Alexander Shulgin — the godfather of MDMA and creator of the entire 2C- family of substances. Shulgin invented well over 200 psychoactive compounds in his research lab dubbed “The Farm.” Shulgin considered 2C-B to be one of his greatest creations. In one of his books — PiHKAL (phenethylamines I Have Known And Loved) — he listed 2C-B among his “magic half dozen”. The other five include mescaline, DOM, 2C-E, 2C-I, 2C-T2, and 2C-T7. The effects of 2C-B have been described as a combination between LSD and MDMA — but this is a simplification. In reality, the 2C-B experience is entirely unique. The qualities of 2C-B made it popular as a sex-enhancement drug in the 80s. The German pharmaceutical company Drittewelle started producing the drug under the name “Nexus.” It was sold in sex shops as a way to boost libido, sexual connection and increase stamina and energy. 2C-B is still considered by many to be the best psychedelic to use during sex of all time. In Shulgin’s own words, 2C-B “... is, in my opinion, one of the most graceful, erotic, sensual, introspective compounds I have ever invented.” 2C-B reached mainstream popularity sometime after 1985 when MDMA was officially banned. It was used as a legal alternative to MDMA. 2C-B and the rest of the 2C- family were later banned in 1995.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (partial)
    5-HT2C receptor agonist (partial)

    History & Culture

    1974–1975

    2C-B was first synthesized in 1974 by American chemist Alexander Shulgin while investigating novel psychedelic compounds based on the chemical structure of mescaline, specifically exploring homologues of DOB. Its psychoactive properties were discovered on June 25, 1975, when Shulgin tested the compound on himself and described it as "beautifully active." He subsequently published his findings on 2C-B alongside those for 2C-D in the scientific literature that same year, proposing both compounds for potential use in psychedelic-assisted psychotherapy. Shulgin's comprehensive documentation of 2C-B was later included in his 1991 book PiHKAL (Phenethylamines I Have Known And Loved), where he listed it among the "magical half-dozen" psychedelic phenethylamines he considered most important. This distinguished group also included mescaline, DOM, 2C-E, 2C-T-2, and 2C-T-7. In subsequent interviews, Shulgin repeatedly identified 2C-B as his personal favorite psychedelic compound.

    1970s–present

    Following its discovery, 2C-B found its first applications among a small circle of American psychotherapists during the 1970s. These practitioners considered it one of the most suitable substances for therapeutic contexts due to its relatively short duration, mild side effect profile, and gentle overall character compared to other psychedelics. Therapists who employed 2C-B in clinical settings reported that it facilitated a warm, empathetic connection between practitioner and patient. They found that the substance helped break down ego defenses and inner resistances, allowing patients to access suppressed emotions and repressed memories. However, some accounts suggest that therapeutic use was eventually discontinued due to gastrointestinal side effects and the compound's lack of strong entactogenic properties compared to other options.

    1985–1995

    After MDMA was classified as a Schedule I substance in the United States in 1985, 2C-B emerged as a popular alternative in the recreational drug scene. It was first encountered as a novel designer drug in the United States that same year and gained traction in raves and club settings, where users appreciated its minimal comedown and clear, euphoric headspace. During the late 1980s and early 1990s, several companies legally manufactured and marketed 2C-B as an over-the-counter sexual enhancer. The German pharmaceutical company Drittewelle produced it under the brand name "Erox" for sale in adult stores and some nightclubs across European countries including Germany. In the Netherlands, it was sold in smart shops under the name "Nexus" as a legal ecstasy alternative. In Japan, it was marketed as "Performax" until the country scheduled the substance in the summer of 1998. The U.S. Drug Enforcement Administration reported its distribution in Miami in the form of yellow pills marketed as an aphrodisiac. The increasing popularity of 2C-B as both a recreational substance and commercial product led to regulatory action. It was placed in Schedule I in the United States in 1994, with permanent scheduling following in 1995. Most other countries enacted similar controls throughout the mid-1990s, and by 1999 it was illegal in most of the world. The compound was added to Schedule II of the UN Convention on Psychotropic Substances in March 2001. Despite these restrictions, interest in 2C-B resurged in the 2000s with the emergence of the research chemicals scene and the development of darknet markets.

    1993–1996

    2C-B was legally sold in Southern Africa from 1993 until early 1996, during which time it was adopted as an entheogen by traditional healers among the Sangoma, Nyanga, and Amagqirha peoples. The substance was marketed specifically as medicine for Sangomas under the name "Ubulawu Nomathotholo," which roughly translates to "Medicine of the Singing Ancestors." These practitioners reportedly used 2C-B in place of their traditional plant medicines during this period.

    Subjective Effect Notes

    physical: The physical effects of 2C-B can be broken down into five components all of which progressively intensify proportional to dosage.

    cognitive: The head space of 2C-B is described by many as one which is both insightful and relatively normal in its thought processes even at moderate to high dosages.

    Effect Profile

    Curated + 536 Reports
    Psychedelic 5.9

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

    Visual Intensity×3
    8103.2 12/24
    Headspace Depth×3
    49.32.8 5/24
    Auditory Effects×1
    6100.6 8/24
    Body Load / Somatic Effects×1
    59.22.5 10/24
    Catalog Erowid BlueLight

    User Experiences

    Visuals "During meditation, visual distortions manifested themselves as visual drifting (breathing) of the walls, color shifting, and the symmetrical texture repetition of abstract imagery (eyes and shrooms..." Effect Index
    Auditory Effects "2cb is really one of a kind with its cartoony visuals and signature body high and music enhancement yet sociability." Bluelight
    Body Load "I am stricken with nasty nausea and discomfort, along with intense sweating." Effect Index
    Empathogen 4.4

    Strong sensory enhancement with mild euphoria and stimulation, low empathy

    Empathy / Social Openness×3
    39.15.2 10/24
    Euphoria / Mood Elevation×2
    58.16.3 15/24
    Stimulation×1
    46.82.5 7/24
    Sensory Enhancement×1
    8103.1 5/24
    Catalog Erowid BlueLight

    User Experiences

    Sensory Enhancement "The purpose of this trip was to reduce my current Post-Traumatic Stress Disorder symptoms from a sexual assault that occurred a year ago." Effect Index
    Euphoria "They had a large property with a beautiful pool and garden, and it was in a textbook idyllic suburb on an incredible sunny summer day." Effect Index
    Stimulation "In that situation it should best be taken with someone with experience, and someone whose energy is there to guide you through the experience, someone whose energy seeks to guide your mood to a..." Bluelight

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    19-45 minutes
    45 minutes - 1.5 hours
    2-4 hours
    1-2 hours
    2-4 hours
    Total: 4-8 hours
    Insufflated
    1-10 minutes
    10-19 minutes
    2-3 hours
    1-2 hours
    2-4 hours
    Rectal
    4-19 minutes
    19-40 minutes
    2-4 hours
    1-2 hours
    2-4 hours
    Intravenous
    0 minutes
    12-30 minutes
    1.5-2 hours
    2-4 hours

    Empirical Duration

    Erowid Reports
    Onset Come Up Peak Offset
    Oral (36 reports)

    Community Effects

    TripSit
    Positive
    dissociation

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; effective duration typically 4–6 h orally (see duration).
    Addiction Potential
    Low: classical-psychedelic–like pharmacology with rapid tolerance; compulsive use uncommon though situational/sexual reinforcement can occur.

    Tolerance Decay

    Full tolerance 0h Half tolerance 3d Baseline ~7d

    Psychedelic tolerance is marked after one session and tends to return close to baseline within 1–2 weeks; spacing experiences by at least 2 weeks is common HR advice.

    Cross-Tolerances

    LSD
    50% ●○○
    psilocybin
    50% ●○○
    mescaline
    60% ●○○

    Experience Report Analysis

    Erowid BlueLight
    394 Reports
    1994–2025 Date Range
    211 With Age Data
    34 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 444 experience reports (394 Erowid + 142 Bluelight)

    444 Reports
    148 Effects Detected
    69 Positive
    48 Adverse
    31 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 69

    Color Enhancement 59.9% 86%
    Music Enhancement 50.0% 84%
    Euphoria 47.3% 90%
    Empathy 43.7% 84%
    Stimulation 42.3% 80%
    Surface Breathing 40.0% 84%
    Joy 38.0% 87%
    Sociability Enhancement 38.0% 84%
    Tactile Enhancement 36.2% 84%
    Contentment 30.0% 80%
    Patterning 28.0% 86%
    Awe 28.0% 82%
    Focus Enhancement 27.7% 80%
    Introspection 26.6% 80%
    Insight 22.0% 82%
    Morphing 22.0% 86%
    Love 22.0% 85%
    Visual Trails 22.0% 84%
    Body High 21.2% 84%
    Emotional Openness 20.0% 82%

    Adverse Effects 48

    Anxiety 45.8% 78%
    Confusion 32.6% 79%
    Nausea 28.6% 86%
    Body Load 16.0% 80%
    Muscle Tension 14.2% 80%
    Fear 14.0% 83%
    Paranoia 12.0% 76%
    Entity Imagery 10.0% 77%
    Depersonalization 10.0% 80%
    Stomach Cramps 10.0% 84%
    Headache 9.0% 80%
    Motor Impairment 9.0% 75%
    Memory Suppression 8.6% 77%
    Dry Mouth 8.0% 70%
    Vomiting 8.0% 92%
    Body Temperature Change 8.0% 81%
    Tremor 8.0% 78%
    Sweating 7.7% 87%
    Pupil Dilation 7.7% 85%
    Thought Loops 7.7% 82%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    Insufflated

    View data table
    Effect Strong (n=14) Heavy (n=19)
    Visual Distortions 100.0% 73.7%
    Color Enhancement 92.9% 73.7%
    Anxiety 71.4% 57.9%
    Euphoria 64.3% 36.8%
    Confusion 35.7% 63.2%
    Music Enhancement 50.0% 57.9%
    Stimulation 57.1% 26.3%
    Auditory Effects 42.9% 52.6%
    Tactile Enhancement 42.9% 42.1%
    Nausea 35.7% 36.8%
    Empathy 35.7% 36.8%
    Focus Enhancement 35.7% 26.3%
    Motor Impairment 28.6% 0%
    Closed-Eye Visuals 28.6% 10.5%
    Sedation 28.6% 0%

    Oral

    View data table
    Effect Light (n=12) Common (n=64) Strong (n=49) Heavy (n=17)
    Visual Distortions 83.3% 89.1% 89.8% 100.0%
    Color Enhancement 41.7% 57.8% 73.5% 64.7%
    Music Enhancement 58.3% 50.0% 61.2% 70.6%
    Stimulation 58.3% 65.6% 55.1% 41.2%
    Euphoria 50.0% 54.7% 51.0% 52.9%
    Tactile Enhancement 25.0% 54.7% 40.8% 29.4%
    Confusion 33.3% 46.9% 28.6% 52.9%
    Empathy 33.3% 51.6% 49.0% 52.9%
    Anxiety 16.7% 46.9% 46.9% 41.2%
    Focus Enhancement 25.0% 26.6% 30.6% 41.2%
    Closed-Eye Visuals 25.0% 34.4% 34.7% 41.2%
    Sedation 16.7% 35.9% 28.6% 17.6%
    Introspection 0% 35.9% 28.6% 23.5%
    Nausea 25.0% 29.7% 30.6% 35.3%
    Auditory Effects 0% 25.0% 26.5% 35.3%

    Subjective Effect Ontology

    Experience Reports

    Structured effect tags extracted from 536 Erowid & Bluelight experience reports using a controlled vocabulary of 220+ canonical effects across 15 domains.

    Auditory

    music enhancement 222 46.2% auditory effects 110 21.2%

    Cognitive

    confusion 145 28.7% focus enhancement 123 25.0% introspection 118 29.2%

    Emotional

    euphoria 210 49.1% anxiety 203 44.1% empathy 194 41.3%

    Gastrointestinal

    nausea 127 27.4%

    Motor

    stimulation 188 38.8%

    Tactile

    tactile enhancement 161 31.4%

    Visual

    visual distortions 332 63.3% color enhancement 266 58.5% closed eye visuals 112 25.0%

    14 unique effects extracted · Derived from Erowid & Bluelight reports

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 394 experience reports.

    Insufflated dose range: 11.0–25.0 mg (median 20.0 mg)
    Effect Strong (n=14) Heavy (n=19)
    visual distortions
    100%
    74%
    color enhancement
    93%
    74%
    anxiety
    71%
    58%
    euphoria
    64%
    37%
    confusion
    36%
    63%
    music enhancement
    50%
    58%
    stimulation
    57%
    26%
    auditory effects
    43%
    53%
    tactile enhancement
    43%
    42%
    nausea
    36%
    37%
    empathy
    36%
    37%
    focus enhancement
    36%
    26%
    motor impairment
    29%
    closed-eye visuals
    29%
    10%
    sedation
    29%
    sweating
    29%
    10%
    hospital
    21%
    26%
    introspection
    21%
    open-eye visuals
    21%
    10%
    body high
    14%
    21%

    Showing top 20 of 25 effects

    Oral dose range: 19.0–25.0 mg (median 20.0 mg)
    Effect Light (n=12) Common (n=64) Strong (n=49) Heavy (n=17)
    visual distortions
    83%
    89%
    90%
    100%
    color enhancement
    42%
    58%
    74%
    65%
    music enhancement
    58%
    50%
    61%
    71%
    stimulation
    58%
    66%
    55%
    41%
    euphoria
    50%
    55%
    51%
    53%
    tactile enhancement
    25%
    55%
    41%
    29%
    confusion
    33%
    47%
    29%
    53%
    empathy
    33%
    52%
    49%
    53%
    anxiety
    17%
    47%
    47%
    41%
    focus enhancement
    25%
    27%
    31%
    41%
    closed-eye visuals
    25%
    34%
    35%
    41%
    sedation
    17%
    36%
    29%
    18%
    introspection
    36%
    29%
    24%
    nausea
    25%
    30%
    31%
    35%
    auditory effects
    25%
    26%
    35%
    dissociation
    17%
    22%
    16%
    29%
    pupil dilation
    9%
    14%
    29%
    thought loops
    25%
    9%
    10%
    18%
    body high
    25%
    19%
    24%
    muscle tension
    25%
    14%
    20%
    18%

    Showing top 20 of 34 effects

    Risk Escalation

    Sentiment Analysis

    Average frequency of positive vs adverse effects across dose tiers (Insufflated)

    Strong n=14
    9 positive 46.0% 8 adverse 30.4%
    Heavy n=19
    8 positive 40.1% 5 adverse 35.8%
    View effect breakdown

    Adverse Effects

    Effect Strong (n=14) Heavy (n=19) Change
    Anxiety
    71%
    58%
    -18%
    Confusion
    36%
    63%
    +77%
    Nausea
    36%
    37%
    3%
    Motor Impairment
    29%
    0%
    Sweating
    29%
    10%
    -63%
    Seizure
    14%
    0%
    Psychosis
    14%
    0%
    Pupil Dilation
    14%
    0%
    Memory Suppression
    10%
    0%

    Positive Effects

    Effect Strong (n=14) Heavy (n=19) Change
    Color Enhancement
    93%
    74%
    -20%
    Euphoria
    64%
    37%
    -42%
    Music Enhancement
    50%
    58%
    +15%
    Stimulation
    57%
    26%
    -53%
    Tactile Enhancement
    43%
    42%
    -1%
    Empathy
    36%
    37%
    3%
    Focus Enhancement
    36%
    26%
    -26%
    Introspection
    21%
    0%
    Body High
    14%
    21%
    +47%

    Risk Escalation

    Sentiment Analysis

    Average frequency of positive vs adverse effects across dose tiers (Oral)

    Light n=12
    8 positive 39.6% 6 adverse 23.6%
    Common n=64
    11 positive 39.1% 13 adverse 16.2%
    Strong n=49
    10 positive 42.5% 13 adverse 16.0%
    Heavy n=17
    8 positive 47.0% 10 adverse 24.1%
    View effect breakdown

    Adverse Effects

    Effect Light (n=12) Common (n=64) Strong (n=49) Heavy (n=17) Change
    Confusion
    33%
    47%
    29%
    53%
    +58%
    Anxiety
    17%
    47%
    47%
    41%
    +146%
    Nausea
    25%
    30%
    31%
    35%
    +41%
    Pupil Dilation
    9%
    14%
    29%
    +212%
    Thought Loops
    25%
    9%
    10%
    18%
    -29%
    Muscle Tension
    25%
    14%
    20%
    18%
    -29%
    Jaw Clenching
    17%
    11%
    6%
    12%
    -29%
    Headache
    12%
    8%
    12%
    -5%
    Memory Suppression
    9%
    8%
    12%
    +25%
    Increased Heart Rate
    5%
    10%
    12%
    +151%
    Motor Impairment
    6%
    10%
    +64%
    Sweating
    6%
    8%
    +32%
    Seizure
    6%
    0%
    Psychosis
    5%
    0%

    Positive Effects

    Effect Light (n=12) Common (n=64) Strong (n=49) Heavy (n=17) Change
    Color Enhancement
    42%
    58%
    74%
    65%
    +55%
    Music Enhancement
    58%
    50%
    61%
    71%
    +21%
    Stimulation
    58%
    66%
    55%
    41%
    -29%
    Euphoria
    50%
    55%
    51%
    53%
    5%
    Tactile Enhancement
    25%
    55%
    41%
    29%
    +17%
    Empathy
    33%
    52%
    49%
    53%
    +58%
    Focus Enhancement
    25%
    27%
    31%
    41%
    +64%
    Introspection
    36%
    29%
    24%
    -34%
    Body High
    25%
    19%
    24%
    -2%
    Creativity Enhancement
    11%
    10%
    -6%
    Pain Relief
    3%
    0%

    Dosage Distribution

    Dose distribution from experience reports

    Insufflated

    Median: 20.0 mg IQR: 11.0–25.0 mg n=46

    Oral

    Median: 20.0 mg IQR: 19.0–25.0 mg n=144

    Real-World Dose Distribution

    62K Doses

    From 519 individual dose entries

    Oral (n=308)

    Median: 20.0mg 25th: 15.0mg 75th: 25.0mg 90th: 33.6mg
    mg/kg median: 0.305 mg/kg 75th: 0.384

    Insufflated (n=94)

    Median: 15.0mg 25th: 10.0mg 75th: 25.0mg 90th: 30.0mg
    mg/kg median: 0.214 mg/kg 75th: 0.373

    Rectal (n=11)

    Median: 16.0mg 25th: 12.5mg 75th: 20.0mg 90th: 25.0mg
    mg/kg median: 0.267 mg/kg 75th: 0.312

    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

    Insufflated

    Median: 0.301 mg/kg IQR: 0.176–0.441 mg/kg n=45

    Unknown

    Median: 0.278 mg/kg IQR: 0.259–0.294 mg/kg n=5

    Oral

    Median: 0.315 mg/kg IQR: 0.242–0.424 mg/kg n=128

    Rectal

    Median: 0.286 mg/kg IQR: 0.243–0.301 mg/kg n=8

    Redose Patterns

    Redosing behavior across 263 reports

    19.8% Redosed
    1.3 Avg Doses
    61m Median Interval

    Legal Status

    UN Convention on Psychotropic Substances Schedule II (added March 2001)
    Country Status Notes
    Argentina Schedule I Classified as a Schedule I controlled substance alongside similar phenethylamines such as 2C-I and 2C-T-2.
    Australia Schedule 9 Considered a prohibited substance under the Poisons Standard. First placed on Schedule One of the Drugs Misuse and Trafficking Act in 1994 and included on the list of substances subject to import and export controls. Also falls under the Australian analogue act provisions.
    Austria Illegal (SMG Schedule V) Prohibited under the Suchtmittelgesetz (SMG). Specifically listed in Schedule V of the Suchtgiftverordnung, making possession, production, and sale illegal.
    Belgium Illegal Added to the list of illegal psychotropic substances on April 30, 2002. Production, distribution, and possession are prohibited.
    Brazil Controlled Listed on Portaria SVS/MS nº 344, making production, distribution, and possession illegal.
    Canada Schedule III (CDSA) Classified under the Controlled Drugs and Substances Act as '4-bromo-2,5-dimethoxybenzeneethanamine and any salt, isomer or salt of isomer thereof.' Originally scheduled in April 1997, then rescheduled in an amendment effective October 31, 2016 to include other 2C-x analogues.
    Chile Controlled Added to Ley 20.000 (known as Ley de drogas) in August 2007 along with many other psychoactive substances.
    Croatia Illegal Prohibited as a result of being classified as a 2,5-dimethoxyphenylethanamine derivative.
    Czech Republic Schedule II Possession of more than 200 mg is punishable by up to two years imprisonment. Smaller amounts may result in a fine. The 200 mg threshold serves as a guideline which courts may adjust based on circumstances.
    Denmark List B Classified as a Category B controlled substance under Danish drug legislation.
    Estonia Schedule I Classified as a Schedule I controlled substance, prohibiting possession, production, and distribution.
    Finland Controlled (hard-drug category) Listed in the government decree on substances, preparations, and plants considered to be narcotic drugs, classified in the hard-drug category.
    Germany Anlage I BtMG Controlled under Anlage I of the Betäubungsmittelgesetz (Narcotics Act) since January 31, 1993, listed as 'Bromdimethoxyphenethylamin' (BDMPEA). Manufacturing, possession, import, export, purchase, sale, procurement, and dispensing without a license are prohibited.
    Italy Tabella I Listed in Tabella I of 'Tabelle delle sostanze stupefacenti e psicotrope,' making possession, purchase, and sale illegal.
    Japan Scheduled Controlled since Summer 1998. Prior to scheduling, it was marketed as a sexual enhancement product under the name 'Performax.'
    Latvia Schedule I Classified as a Schedule I controlled substance, prohibiting possession, production, and distribution.
    Luxembourg Prohibited Classified as a prohibited substance since 2001.
    Netherlands List I (Opiumwet) Scheduled as a hard drug under the Opium Law on July 9, 1997. The Netherlands became the first country to ban 2C-B and related phenethylamines (2C-I, 2C-T-2, 2C-T-7) following the emergence of these substances as alternatives.
    Norway Schedule II Classified as Schedule II since March 22, 2004, listed under the name 4-bromo-2,5-dimethoxyphenethylamine.
    Poland Schedule I (I-P group) Listed in the I-P group under 'Wykaz środków odurzających i substancji psychotropowych.' Possession has been illegal since 2015.
    Russia Controlled (narcotic) Banned as a narcotic drug since October 2011. Possession of 10 mg or more carries criminal penalties.
    Serbia Controlled Classified as a controlled substance under national drug legislation.
    Spain Category 2 Added to Category 2 prohibited substances in 2002.
    Sweden Schedule I Currently classified as Schedule I. First regulated on April 1, 1999 as a 'health hazard' under the Act on the Prohibition of Certain Goods Dangerous to Health (SFS 1999:58), then promoted to Schedule I effective June 1, 2002.
    Switzerland Controlled (Verzeichnis D) Listed in Anhang D (Verzeichnis D) of the Verordnung des EDI über die Verzeichnisse der Betäubungsmittel (DetMV). Possession is illegal.
    Turkey Illegal Classified as a controlled drug. Possession, production, supply, and import are prohibited.
    United Kingdom Class A Controlled as a Class A substance under the Misuse of Drugs Act due to the phenethylamine catch-all clause, applying to all drugs in the 2C family. Production, supply, and possession are illegal. Possession carries a maximum sentence of seven years imprisonment; supply is punishable by life imprisonment and an unlimited fine.
    United States Schedule I Classified as a Schedule I controlled substance. Initially scheduled on January 6, 1994, with permanent scheduling effective June 2, 1995 following a DEA proposal in December 1994. Manufacturing, purchasing, possession, and distribution without a DEA license are prohibited.

    Harm Reduction

    drugs.wiki

    Harm-reduction justifications and key points:

    - Steep dose–response: multiple harm-reduction services and Erowid emphasize that 1–2 mg can markedly change intensity; start low and titrate with an accurate 0.001 g scale or volumetric dosing to mitigate accidental overdosing.

    - Intranasal route is far more potent per mg, has rapid onset, and is notably painful; prefer tiny, well-measured amounts or a volumetric nasal spray; expect a shorter, sharper experience.

    - Typical oral active window is ~4–6 h with an additional 2–4 h of residual stimulation; plan set/setting, nutrition, and sleep accordingly.

    - Tablets/pills labeled as 2C-B vary widely and are sometimes confused with MDMA presses; Swiss drug checking shows many different 2C-B presses around ~13–16 mg and occasional mislabeling or admixture; always reagent-test and, where possible, use professional drug checking.

    - Reagent expectations for 2C‑B: Marquis usually yellow→green within ~10–60 s (may darken later), Mecke/Froehde yellowish; Simon’s negative. Read within the first minute and avoid expired reagents to reduce false interpretations.

    - Avoid MAOIs: historical guides and community data warn of significant potentiation and risk when MAOIs are combined with 2C‑x phenethylamines.

    - Combining with strong stimulants or high alcohol loads increases cardiovascular strain and disinhibition; several harm-reduction guides list tachycardia/hypertension among common physical effects of 2C‑x; avoid driving for the rest of the day.

    - MDMA+2C‑B ("nexus flip"): commonly reported but increases total serotonergic/stimulant load; if attempted, reduce each dose and stagger timing (e.g., 2C‑B after MDMA peak) to lower risk of overheating, anxiety, and confusion.

    - SSRIs/SNRIs frequently blunt 2C‑x psychedelic effects; cross-tolerance with other serotonergic psychedelics is expected for 1–2 weeks—plan adequate spacing.

    - Safer sniffing: if using intranasally, employ fine powder or isotonic solution, avoid caustic adulterants, and rinse with sterile saline after ~20–30 min to reduce mucosal injury.

    - Set/setting and anxiety: even at ‘party’ doses, acute panic can occur; have a trusted sober sitter and benzodiazepines reserved for emergencies only, at minimal doses due to respiratory/coordination risks.

    - Do not rely on blotters labeled 2C‑B: 2C‑B is typically sold as powder/capsules or pressed pills; blotters often indicate NBOMe/NBOH/DOx which have microgram potency and higher risk profiles.

    - Driving/next-day: performance impairment can persist beyond the subjective offset; harm-reduction leaflets advise waiting until the following day (≥24 h) before driving.

    - Hydration/temperature: mild stimulant properties and environment (e.g., clubs) can raise body temperature—sip water regularly, take cool-down breaks, and avoid overhydration.

    - Testing for identity vs. strength: reagent tests confirm likely class but not dose; only a lab or LC–MS quantitation can confirm mg content—assume variability and calibrate dose with your own product.

    ← Back to 2C-B