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    DET molecular structure

    DET Stats & Data

    T-9 Diethyltryptamine
    NPS DataHub
    MW252.79
    FormulaC14H21ClN2
    CAS7558-72-7
    IUPACN,N-diethyl-1H-indole-3-ethanamine, hydrochloride
    SMILES[Cl-].CCN(CC)CCc1cnc2ccccc12.[H+]
    InChIKeyGHDJWZZXXNZUST-UHFFFAOYSA-N
    Tryptamines; 2020/5.1 Indol-3-alkylamine; 2021/5.1 Indol-3-alkylamine; 2022/5.1 Indol-3-alkylamine
    Chemical Class Tryptamine
    Psychoactive Class Psychedelic

    Pharmacology

    DrugBank
    State Solid

    Description

    Diethyltryptamine (DET) is an orally active hallucinogenic agent and a substituted form of tryptamine.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (partial)
    5-HT2B receptor agonist
    5-HT2C receptor agonist

    History & Culture

    DET was first synthesized in 1956 by Hungarian chemist Stephen Szára, with his findings published the following year. More systematic studies were subsequently conducted by Szára and colleagues, as well as independently by Böszörményi and colleagues. Despite being a close structural analog of DMT, DET has remained extremely uncommon with little history of human use outside of clinical research settings. The substance emerged during a period when researchers were investigating the transmethylation hypothesis—the theory that endogenous production of psychoactive agents might explain hallucinatory symptoms in certain psychiatric conditions. This was the era of "psychotomimesis," when scientists sought drugs that could reliably produce states resembling psychosis, hoping such models might inform treatment approaches for mental illness. It was during this period, in 1956, that Humphry Osmond proposed at a New York Academy of Sciences meeting the term "psychedelic" as a less pejorative alternative to existing terminology such as "psychotomimetic." Clinical studies with DET were conducted in the late 1950s and early 1960s under research conditions now recognized as ethically problematic. One study involved unemployed men from a depressed mining area who received intramuscular injections in a partially soundproofed clinic equipped with one-way mirrors and microphones for observation. Other early research was conducted at the Lexington, Kentucky Public Health Service Hospital—a facility that functioned primarily as a federal prison for drug offenders—using hospitalized patients, individuals with schizophrenia, people with alcohol dependence, and prisoners as research subjects.

    Effect Profile

    Curated + 13 Reports
    Psychedelic 7.6

    Strong visuals and headspace with moderate body load

    Visual Intensity×3
    10
    Headspace Depth×3
    9
    Auditory Effects×1
    0
    Body Load / Somatic Effects×1
    6

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    30 minutes - 1.5 hours
    30 minutes - 1.0 hours
    2-4 hours
    1-2 hours
    2-8 hours
    Total: 2-4 hours
    Smoked
    1-4 minutes
    2.0-4.0 hours
    1.0-6.0 hours
    Total: 2-4 hours
    Intramuscular
    4-15 minutes
    15-30 minutes
    1-2 hours
    1-2 hours
    1-4 hours
    Total: 2-4 hours

    Community Effects

    TripSit
    Positive
    visual enhancement euphoria introspection
    Negative
    nausea body load

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

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

    Cross-Tolerances

    LSD
    30% ●○○
    Psilocybin
    30% ●○○
    Psilocin
    30% ●○○
    Mescaline
    30% ●○○
    DMT
    30% ●○○
    5-MeO-DMT
    30% ●○○
    2C-B
    30% ●○○
    2C-E
    30% ●○○

    Experience Report Analysis

    Erowid
    13 Reports
    1995–2022 Date Range
    7 With Age Data
    11 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 13 experience reports (13 Erowid)

    13 Reports
    11 Effects Detected
    6 Positive
    2 Adverse
    3 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 6

    Euphoria 61.5% 70%
    Music Enhancement 61.5% 70%
    Empathy 46.2% 70%
    Stimulation 46.2% 70%
    Color Enhancement 38.5% 70%
    Tactile Enhancement 38.5% 70%

    Adverse Effects 2

    Anxiety 46.2% 70%
    Nausea 38.5% 70%

    Real-World Dose Distribution

    62K Doses

    From 20 individual dose entries

    Smoked (n=6)

    Median: 27.5mg 25th: 21.25mg 75th: 52.5mg 90th: 67.5mg
    mg/kg median: 0.644 mg/kg 75th: 0.84

    Oral (n=8)

    Median: 56.0mg 25th: 32.0mg 75th: 103.25mg 90th: 190.1mg
    mg/kg median: 1.222 mg/kg 75th: 2.122

    Form / Preparation

    Most common forms and preparations reported

    Redose Patterns

    Redosing behavior across 13 reports

    15.4% Redosed
    1.5 Avg Doses
    90m Median Interval

    Legal Status

    UN Convention on Psychotropic Substances 1971 (Schedule I)
    Country Status Notes
    Australia Schedule 9 Controlled under the Poisons Standard. Classified as a substance subject to abuse or misuse; manufacture, possession, sale, or use is prohibited except for approved medical or scientific research, analytical, teaching, or training purposes with Commonwealth and/or State or Territory Health Authority approval.
    Canada Schedule III (CDSA) Controlled under the Controlled Drugs and Substances Act. Canadian scheduling differs significantly from the United States system in terms of penalties and associated restrictions.
    Germany Anlage I BtMG Listed in Anlage I of the Betäubungsmittelgesetz (Narcotics Act) since January 24, 1974. Manufacturing, possession, import, export, purchase, sale, procurement, or dispensing without a license is prohibited.
    Italy Tabella I Listed in Tabella I of the Tabelle delle sostanze stupefacenti e psicotrope (Tables of Narcotic and Psychotropic Substances). Possession, purchase, and sale are illegal.
    New Zealand Class A Controlled as a Class A substance, the most restrictive category under New Zealand drug legislation, carrying the most severe penalties.
    South Africa Undesirable Dependence Producing Substance Classified under the Drug and Drug Trafficking Act No. 140 of 1992 as an undesirable dependence-producing substance, subjecting it to criminal penalties for unauthorized possession or distribution.
    Switzerland Verzeichnis D Specifically named as a controlled substance under Verzeichnis D of Swiss narcotics legislation.
    United Kingdom Class A / Schedule 1 Controlled as a Class A, Schedule 1 substance under the Misuse of Drugs Act 1971. Purchasing or possessing without a Home Office license is illegal.
    United States Schedule I Controlled under the Controlled Substances Act as a Schedule I hallucinogen, indicating high abuse potential and no accepted medical use. Manufacturing, buying, possessing, or distributing without a DEA license is a federal offense.
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