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2C-B

2C-B molecule structure2C-B molecule structure
4-Bromo-2,5-dimethoxyphenethylamine
Nexus, Bees, Venus, Bromo Mescaline, BDMPEA
Chemical Class

2C-B is a synthetic psychedelic of the phenethylamine class and perhaps the most well-known member of the 2C-x family, which are structurally related to mescaline.citation needed First synthesized by Alexander Shulgin in 19741, he saw the possibility as an aid in psychiatric therapy.2 2C-B is characterized by warm, colorful visuals, mild entactogenic qualities, and a prominent body component.citation needed It is generally considered more manageable than classical psychedelics like LSD or psilocybin, though it is notably dose-sensitive.

Dosage & Duration

Dosage3

Doses are population estimates that vary widely between individuals.

Threshold~2 mg
Light2-15 mg
Moderate15-25 mg
Strong25-40 mg
Heavy40+ mg
Bioavailability
Low

2C-B exhibits a notably steep dose-response relationship, particularly within the 12–24 mg range, where differences of just 2 mg can substantially alter both the intensity and qualitative nature of the experience. Careful, incremental dosing is recommended when establishing individual sensitivity.

Duration3

Onset20-75 minutes
Come Up15-30 minutes
Peak2-4 hours
Offset1-2 hours
After Effects2-4 hours
Total4-8 hours
Half-life
1.2-2.5 hours

Subjective Effects

Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.

Effects vary widely by individual, dose, and context.

Physical

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

Increased bodily controlEnhancement of touch

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.

Visual

Enhancements

2C-B presents a full and complete array of possible visual enhancements.

Geometry

The visual geometry that is present throughout this trip can be described as more similar in appearance to that of LSD than that of 2C-E, psilocin, or ayahuasca. They can be comprehensively described as unstructured in their organization, algorithmic in geometric style, intricate in complexity, large in size, fast and smooth in motion, colourful in scheme, glossy in colour, sharp in their edges and angular in their corners. They seem high in algorithmic visuals such as fractals and at higher dosages are significantly more likely to result in states of Level 7A visual geometry over Level 7B.

Hallucinatory States

Like LSD, while 2C-B is capable of producing a full range of low and high level hallucinatory states, this is extremely rare and inconsistent at higher levels but common at lower levels.

External hallucinations

Auditory

The auditory effects of 2C-B are more common than some psychedelics in their occurrence and are capable of producing a full range of effects.

Forked from Subjective Effect Documentation byJosie Kins September 2013.

See also: Psychedelic Intensity Scale, Effects of psychedelics (visual, cognitive, miscellaneous)

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Marquis(MQ)
white → yellow2 → green2
Mecke(ME)
white → yellow2 → orange1 → green2 → brown2
Mandelin(MD)
yellow2 → green2 → brown3
Robadope(RB)
orange1 → pink1 → pink1 → pink2 → purple2
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Pharmacology

Pharmacodynamics

2C-B functions primarily as a partial agonist at the serotonin 5-HT2 receptor family, with potent binding at 5-HT2A, 5-HT2C, and to a lesser degree 5-HT2B.citation needed Some studies have reported low efficacy or antagonism at 5-HT2A and 5-HT2C, while others have consistently measured near-full efficacy at these sites. Beyond the 5-HT2 receptors, 2C-B shows modest affinity for 5-HT1A and 5-HT1B receptors and has been characterized as a non-competitive serotonin transporter inhibitor of very low potency. Research in rat models has also demonstrated that 2C-B increases dopamine levels, which may contribute to its psychoactive profile.4

Pharmacokinetics

2C-B appears to have relatively low oral bioavailability as a result of substantial first-pass metabolism in the liver. It is metabolized by hepatocytes through oxidative deamination and demethylation, with deamination catalyzed by both MAO-A and MAO-B.citation needed Species differences exist in the metabolic products; human, monkey, and rabbit hepatocytes produce the demethylated metabolite B-2-HMPE, while dog, rat, and mouse hepatocytes do not.5 The primary metabolite BDMPAA reaches plasma concentrations approximately 280-fold higher than 2C-B itself after oral dosing. The elimination half-life in humans ranges from 1.2 to 2.5 hours.citation needed

Interactions

Dangerous

Highest risk

These combinations are considered extremely harmful and should always be avoided. Reactions to these drugs taken in combination are highly unpredictable and have a potential to cause death.

Unsafe

Avoid

There is considerable risk of physical harm when taking these combinations, they should be avoided where possible.

Caution

Use caution

These combinations are not usually physically harmful, but may produce undesirable effects, such as physical discomfort or overstimulation. Extreme use may cause physical health issues. Synergistic effects may be unpredictable. Care should be taken when choosing to use this combination.

2C-T-x compounds5-MeO-xxT tryptaminesAmphetaminesCannabisCocaineDOx compoundsMAOIsMescalineNBOMe compounds
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Tolerance

Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Full Tolerance
Unlike most serotonergic psychedelics, 2C-B exhibits an unusual tolerance profile. Tolerance develops slowly even with repeated consecutive use, and the substance can often be redosed multiple times with minimal reduction in effect intensity. Some users report sustained multi-day use with only gradual tolerance accumulation.
Cross Tolerance

Partial cross-tolerance with serotonergic psychedelics (asymmetric; other psychedelics may reduce 2C-B effects, but 2C-B typically does not diminish effects of subsequent psychedelic use)

Baseline Reset
Tolerance appears to diminish relatively quickly, with effects returning to near-baseline levels after 5-7 days of abstinence.

Harm Potential

Reported adverse effects of 2C-B include visual focusing difficulty, trembling, sweating, nausea, abdominal pain, tachycardia, jaw clenching, dizziness, confusion, and memory impairment.citation needed At oral doses over 20 to 30 mg, 2C-B may cause frightening hallucinations, tachycardia, hypertension, and hyperthermia.

Addiction & Dependence

Psychological

Extremely Low

2C-B is considered non-addictive with a low potential for abuse. Like other serotonergic psychedelics, it possesses a self-regulating quality that discourages compulsive use patterns.

Physical

Extremely Low

2C-B does not produce physical dependence. Withdrawal effects following discontinuation have not been reported.

Toxicity

Cardiovascular

Acute cardiovascular effects including elevated blood pressure, increased heart rate, and hyperthermia occur during intoxication, particularly at higher doses; theoretical risk of cardiac valvulopathy exists with frequent long-term use due to 5-HT2B agonism, though this has not been documented in 2C-B users specifically.citation needed

Central Nervous System

At typical recreational doses, 2C-B is unlikely to be neurotoxic; severe neurological impairment has been reported in isolated case reports involving unknown doses or possible adulterants.citation needed

Psychosis Risk

Adverse psychological reactions including anxiety, paranoia, delusions, and psychosis are possible, particularly in those predisposed to mental disorders. One case report documents persistent psychosis following a single dose.8 Individuals with a family history of schizophrenia or early onset mental illness should exercise extreme caution.

Seizure Risk

Seizures are rare but have been documented in at least one case report involving an unknown dose that also produced serotonin syndrome.citation needed Risk may increase in susceptible individuals or when combined with seizure threshold-lowering substances.

History & Culture

Discovery and Early Research

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

Trip Reports

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Legality

International

UN Convention on Psychotropic Substances Schedule II (added March 2001)9

By Country

Illegal34
United States flagUnited StatesIllegal
Argentina flagArgentinaIllegal
Australia flagAustraliaIllegal
Austria flagAustriaIllegal
Belgium flagBelgiumIllegal
Brazil flagBrazilIllegal
Canada flagCanadaIllegal
Chile flagChileIllegal
China flagChinaIllegal
Croatia flagCroatiaIllegal
Czech Republic flagCzech RepublicIllegal
Denmark flagDenmarkIllegal
Estonia flagEstoniaIllegal
Finland flagFinlandIllegal
Germany flagGermanyIllegal
India flagIndiaIllegal
Indonesia flagIndonesiaIllegal
Ireland flagIrelandIllegal (analog/blanket ban)
Italy flagItalyIllegal
Japan flagJapanIllegal
Latvia flagLatviaIllegal
Luxembourg flagLuxembourgIllegal
Netherlands flagNetherlandsIllegal
Norway flagNorwayIllegal
Philippines flagPhilippinesIllegal
Poland flagPolandIllegal
Russia flagRussiaIllegal
Singapore flagSingaporeIllegal
South Africa flagSouth AfricaIllegal
Sweden flagSwedenIllegal
Switzerland flagSwitzerlandIllegal
Thailand flagThailandIllegal
Turkey flagTurkeyIllegal
United Kingdom flagUnited KingdomIllegal
Controlled / restricted7
Iceland flagIcelandRestricted
Mexico flagMexicoRestricted
Serbia flagSerbiaRestricted
South Korea flagSouth KoreaRestricted
Spain flagSpainRestricted
Ukraine flagUkraineRestricted
United Arab Emirates flagUnited Arab EmiratesRestricted
Legal / decriminalized1
Portugal flagPortugalDecriminalized

References

Source Pages

  1. Bluelight thread: ‘2C-B as a party drug?’
  2. Disregard Everything I Say
  3. Drug Users Bible by Dominic Milton Trott
  4. Erowid
  5. Erowid: 2C-B FAQ
  6. Isomer Design (TiHKAL/PiHKAL)
  7. PiHKAL: 2C-B Entry #20
  8. PsychonautWiki
  9. The Drug Classroom
  10. TripSit Factsheets
  11. TripSit Wiki
  12. Wikipedia

Citations

  1. C. B. Poulie, A. A. Jensen, A. L. Halberstadt, & J. L. Kristensen. (2020). DARK Classics in Chemical Neuroscience: NBOMes. ACS Chemical Neuroscience. https://doi.org/10.1021/acschemneuro.9b005281
  2. Alexander T. Shulgin, & M. F. Carter. (1975). Centrally active phenethylamines. Psychopharmacology Communications. https://isomerdesign.com/bitnest/external/Psychopharmacol.Commun/1.1.931
  3. Alexander Shulgin, & Ann Shulgin. (1991). PiHKAL: A Chemical Love Story. https://www.erowid.org/library/books_online/pihkal/pihkal020.shtml12
  4. T. Páleníček, M. Fujáková, M. Brunovský, J. Horáček, I. Gorman, M. Balíková, L. Rambousek, K. Syslová, P. Kačer, P. Zach, V. Bubeníková-Valešová, & F. Tylš. (2013). Behavioral, neurochemical and pharmaco-EEG profiles of the psychedelic drug 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in rats. Psychopharmacology, 225, 75–93. https://doi.org/10.1007/s00213-012-2797-71
  5. H. Carmo, F. Remião, A. Carvalho, A. Fernandes, M. de Boer, J. A. Boess, P. de Wolff, M. L. Bastos, & F. Carvalho. (2004). Metabolic pathways of 4-bromo-2,5-dimethoxyphenethylamine (2C-B): analysis of phase I metabolism with hepatocytes of six species including human. Toxicology. https://doi.org/10.1016/j.tox.2004.10.0031
  6. D. S. Theobald, & H. H. Maurer. (2007). Identification of monoamine oxidase and cytochrome P450 isoenzymes involved in the deamination of phenethylamine-derived designer drugs (2C-series). Biochemical Pharmacology. https://doi.org/10.1016/j.bcp.2006.09.0221
  7. B. V. Dean, S. J. Stellpflug, A. M. Burnett, & K. M. Engebretsen. (2013). 2C or not 2C: phenethylamine designer drug review. Journal of Medical Toxicology. https://doi.org/10.1007/s13181-013-0295-x12
  8. Persistent psychosis after ingestion of a single tablet of '2C-B'. Progress in Neuro-Psychopharmacology & Biological Psychiatry, 35(1), 293–294 (January 2011). https://doi.org/10.1016/j.pnpbp.2010.10.0181
  9. World Health Organization / UNODC. (2001). 4-Bromo-2,5-dimethoxyphenethylamine (2C-B) — WHO Expert Committee on Drug Dependence Information Repository. https://ecddrepository.org/en/4-bromo-25-dimethoxyphenethylamine1
  10. Disposición ANMAT No. 3634/2002, Article 2 (Lista II, Ley No. 19.303). argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/nacional/disposici%C3%B3n-3634-2002-76920/actualizacion1

Further Reading

  1. Acute Pharmacological Effects of 2C-B in Humans
  2. Alcohol and Drug Foundation: 2C-B Facts
  3. KnowDrugs: 2C-B Substance Profile
  4. Recovery Village – 2C-B Addiction Profile
  5. Release UK: 2C-B Harm Reduction Guide
  6. Substance UVic Drug-Checking One-Sheet
  7. Talk to Frank: 2C family overview

Article Status

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    Step 1 · Automated synthesis

    An autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.

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    A first pass manual review and edit of article prose and copy has been performed by subject-matter expert Lyrea. This does not guarantee factual accuracy. An additional human review for each of this article's citations is yet to be performed.

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    No one has reviewed this article's citations yet. That second pass checks each claim against the source it cites.

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1 September 2026

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  4. Lyrea · Added a source: A qualitative descriptive analysis of effects of psychedelic phenethylamines and tryptamines

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