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    25E-NBOH molecular structure

    25E-NBOH Stats & Data

    2c-e-nboh Nboh-2c-e
    NPS DataHub
    MW315.41
    FormulaC19H25NO3
    CAS1391489-79-4
    IUPAC2-({[2-(4-ethyl-2,5-dimethoxyphenyl)ethyl]amino}methyl)phenol
    SMILESCCc1cc(OC)c(CCNCc2ccccc2O)cc1OC
    InChIKeySYBINTRPEZWFLZ-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

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (potent)
    5-HT2C receptor agonist
    5-HT2B receptor agonist (cardiotoxic risk)

    History & Culture

    25E-NBOH was first synthesized in 2010 by Martin Hansen at the University of Copenhagen, where it was developed as a brain imaging agent for research purposes. The compound was part of a broader effort to create selective serotonin receptor ligands suitable for neuroimaging applications. The substance subsequently appeared on the recreational drug market, with the first confirmed identification occurring in Brazil in 2018 when it was detected on seized blotter paper. It has since been identified in several European countries, including Slovenia and France. The broader NBOH series, encompassing related compounds such as 25B-NBOH, 25C-NBOH, and 25I-NBOH, gained recognition from European drug monitoring authorities around 2016. Within recreational contexts, 25E-NBOH has been marketed as a cost-effective alternative to LSD and has reportedly been misrepresented and sold as LSD in some instances, following a pattern common to many novel psychoactive substances distributed on blotter paper.

    Effect Profile

    Curated + 10 Reports
    Psychedelic 8.2

    Strong visuals, auditory effects, headspace, and body load

    Visual Intensity×3
    10
    Headspace Depth×3
    8
    Auditory Effects×1
    10
    Body Load / Somatic Effects×1
    8
    Stimulant 4.2

    Mild stimulation, anxiety/jitters, and focus with low euphoria

    Stimulation / Energy×3
    5
    Euphoria / Mood Lift×2
    3
    Focus / Productivity×2
    4
    Anxiety / Jitters×1
    5

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

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

    Experience Report Analysis

    Erowid
    10 Reports
    2019–2022 Date Range
    10 With Age Data
    16 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 10 experience reports (10 Erowid)

    10 Reports
    16 Effects Detected
    6 Positive
    5 Adverse
    5 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 6

    Music Enhancement 80.0% 70%
    Stimulation 70.0% 70%
    Euphoria 60.0% 70%
    Color Enhancement 50.0% 70%
    Focus Enhancement 40.0% 70%
    Tactile Enhancement 30.0% 70%

    Adverse Effects 5

    Nausea 40.0% 70%
    Anxiety 40.0% 70%
    Muscle Tension 40.0% 70%
    Pupil Dilation 30.0% 70%
    Confusion 30.0% 70%

    Real-World Dose Distribution

    62K Doses

    From 14 individual dose entries

    Sublingual (n=5)

    Median: 1.8mg 25th: 1.5mg 75th: 1.8mg 90th: 1.92mg

    Form / Preparation

    Most common forms and preparations reported

    Legal Status

    Country Status Notes
    United Kingdom Class A Controlled under the Misuse of Drugs Act 1971 through the N-benzylphenethylamine catch-all clause, which covers structurally related compounds regardless of specific scheduling. Class A classification carries the most severe penalties under UK drug law, including up to seven years imprisonment for possession and life imprisonment for supply offenses.
    United States Unscheduled (Analogue Act applies) Not explicitly listed under the Controlled Substances Act of 1970. However, due to structural similarity to NBOMe-class compounds, it may be prosecuted under the Federal Analogue Act of 1986 when sold or possessed for human consumption, effectively treating it as a Schedule I substance. Manufacturing, purchasing, possessing, or distributing without DEA authorization could result in federal prosecution.
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