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    ETH-LAD molecular structure

    ETH-LAD Stats & Data

    N-ethyl-nor-lsd ethlad
    NPS DataHub
    MW337.46
    FormulaC21H27N3O
    CAS65527-62-0
    IUPAC(6~{a}~{R},9~{R})-~{N},~{N},7-triethyl-6,6~{a},8,9-tetrahydro-4~{H}-indolo[4,3-fg]quinoline-9-carboxamide
    SMILESCCN(CC)C(=O)C1CN(CC)C2Cc3cnc4cccc(C2=C1)c34
    InChIKeyMYNOUXJLOHVSMQ-DNVCBOLYSA-N
    2020/5.2 Δ9 10-Ergolene; 2021/5.2 Δ9 10-Ergolene; 2022/5.2 Δ9 10-Ergolene
    Chemical Class Lysergamide
    Psychoactive Class Psychedelic

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (partial)
    5-HT2C receptor agonist
    5-HT1A receptor agonist (high affinity)
    Other
    dopamine D1, D2, D3, D4, D5 receptor binding (lower affinity)

    History & Culture

    ETH-LAD was first described in the scientific literature by Japanese researcher Tetsukichi Niwaguchi and colleagues in 1976. Nearly a decade later, American researchers Andrew J. Hoffman and David E. Nichols conducted preclinical pharmacological studies of the compound in 1985, examining its properties as part of broader investigations into lysergamide structure-activity relationships. The effects of ETH-LAD in humans were subsequently investigated by Alexander Shulgin, with initial observations communicated via personal correspondence with Nichols in 1986. Shulgin later published his findings in a 1994 literature review and provided comprehensive documentation in his 1997 book TiHKAL (Tryptamines I Have Known and Loved), where he characterized the compound as producing distinctive visual effects compared to LSD. Shulgin also noted concerns about the compound's apparent instability in solution, observing a significant drop in potency after several months of storage even under favorable conditions. ETH-LAD remained relatively obscure outside of research contexts until it emerged as a novel designer drug in Europe around 2016. It has since been marketed alongside other lysergamides such as 1P-LSD and AL-LAD as a grey-market research chemical, commercially distributed through online vendors catering to the psychedelic research community. A prodrug variant, 1P-ETH-LAD, has also been developed and appeared on the designer drug market.

    Effect Profile

    Curated + 32 Reports
    Psychedelic 8.8

    Strong visuals, headspace, auditory effects, and body load

    Visual Intensity×3
    10104.9
    Headspace Depth×3
    10102.7
    Auditory Effects×1
    10102.2
    Body Load / Somatic Effects×1
    10105.4
    Catalog Erowid BlueLight

    Community Effects

    TripSit
    Positive
    visual enhancement euphoria color enhancement
    Negative
    nausea body load vasoconstriction

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

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

    Cross-Tolerances

    LSD
    90% ●○○
    Psilocybin
    80% ●○○
    Psilocin
    80% ●○○
    Mescaline
    60% ●○○
    DMT
    80% ●○○
    5-MeO-DMT
    80% ●○○
    2C-B
    60% ●○○
    2C-E
    60% ●○○

    Experience Report Analysis

    Erowid BlueLight
    23 Reports
    2014–2024 Date Range
    20 With Age Data
    24 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 32 experience reports (23 Erowid + 9 Bluelight)

    32 Reports
    78 Effects Detected
    38 Positive
    18 Adverse
    22 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 38

    Color Enhancement 59.4% 95%
    Music Enhancement 46.9% 90%
    Empathy 43.5% 70%
    Stimulation 40.6% 75%
    Euphoria 37.5% 82%
    Focus Enhancement 34.8% 70%
    Warping 33.3% 85%
    Patterning 33.3% 83%
    Morphing 33.3% 85%
    Introspection 25.0% 75%
    Entity Imagery 22.2% 80%
    Visual Vibration 22.2% 85%
    Texture Rippling 22.2% 80%
    Contentment 22.2% 82%
    Sociability Enhancement 22.2% 82%
    Appetite Increase 22.2% 85%
    Creativity Enhancement 22.2% 82%
    Tactile Enhancement 21.9% 70%
    Body High 18.8% 85%
    Brightness Enhancement 11.1% 90%

    Adverse Effects 18

    Nausea 46.9% 92%
    Body Load 44.4% 89%
    Confusion 43.7% 83%
    Muscle Tension 39.1% 70%
    Anxiety 37.5% 88%
    Increased Heart Rate 30.4% 70%
    Motor Suppression 22.2% 82%
    Panic 22.2% 85%
    Memory Suppression 13.0% 70%
    Thought Loops 12.5% 85%
    Stomach Cramps 11.1% 80%
    Tremor 11.1% 75%
    Vomiting 11.1% 95%
    Temporal Disorientation 11.1% 90%
    Auditory-Visual Synesthesia 11.1% 80%
    Fear 11.1% 80%
    Focus Suppression 11.1% 75%
    Fatigue 11.1% 70%

    Real-World Dose Distribution

    62K Doses

    From 20 individual dose entries

    Oral (n=10)

    Median: 0.17mg 25th: 0.15mg 75th: 0.29mg 90th: 0.4mg
    mg/kg median: 0.003 mg/kg 75th: 0.004

    Sublingual (n=8)

    Median: 0.18mg 25th: 0.1mg 75th: 0.2mg 90th: 0.2mg
    mg/kg median: 0.003 mg/kg 75th: 0.003

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 0.003 mg/kg IQR: 0.002–0.004 mg/kg n=7

    Redose Patterns

    Redosing behavior across 16 reports

    6.2% Redosed
    1.1 Avg Doses

    Legal Status

    Country Status Notes
    Austria Gray area (NPSG may apply) Not explicitly scheduled by name. However, it may fall under the Neue-Psychoaktive-Substanzen-Gesetz (New Psychoactive Substances Act) as a structural analogue of LSD.
    Germany NpSG controlled Controlled under the Neue-psychoaktive-Stoffe-Gesetz (New Psychoactive Substances Act) since July 18, 2019. Production and import with intent to market, administration to others, and trading are criminally punishable. Possession is prohibited but not subject to criminal penalty.
    Latvia Illegal (LSD analogue) While not officially scheduled by name, it is controlled as a structural analogue of LSD under an amendment to drug legislation enacted on June 1, 2015.
    Poland NPS class (illegal) Classified as a New Psychoactive Substance under Polish drug law. Both possession and distribution are prohibited.
    Switzerland Controlled (Verzeichnis E) Specifically named as a controlled substance under Verzeichnis E of Swiss narcotics legislation since December 1, 2015.
    Turkey Illegal Classified as a controlled drug under Turkish legislation. Possession, production, supply, and importation are all prohibited.
    United Kingdom Class A Specifically named in the Misuse of Drugs Act 1971 as a Class A controlled substance since January 7, 2015. Class A carries the most severe penalties, including up to 7 years imprisonment for possession.
    United States Unscheduled (analogue liability) Not specifically scheduled under the Controlled Substances Act. However, as a structural analogue of LSD (Schedule I), sale for human consumption or use for illicit non-medical purposes may be prosecuted under the Federal Analogue Act.
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