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Ethylisopropyltryptamine
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    Ethylisopropyltryptamine

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    Ethylisopropyltryptamine
    Ethylisopropyltryptamine.svg
    Clinical data
    ATC code
    • none
    Legal status
    Legal status
    • DE: NpSG (Industrial and scientific use only)
    • UK: Class A
    Identifiers
    • N-ethyl-N-[2-(1H-indol-3-yl)ethyl]propan-2-amine
    CAS Number
    ChemSpider
    UNII
    Chemical and physical data
    Formula C15H22N2
    Molar mass 230.355 g·mol−1
    3D model (JSmol)
    Melting point 71 to 73 °C (160 to 163 °F)
    • CCN(C(C)C)CCc1c[nH]c2ccccc12
    • InChI=1S/C15H22N2/c1-4-17(12(2)3)10-9-13-11-16-15-8-6-5-7-14(13)15/h5-8,11-12,16H,4,9-10H2,1-3H3 checkY
    • Key:HQZLBYMOYCJZRF-UHFFFAOYSA-N checkY
      (verify)

    Ethylisopropyltryptamine (EiPT) is a chemical of the tryptamine family that and produces psychedelic and hallucinogenic effects. It was probably first synthesized by American psychopharmacologist, Alexander Shulgin.

    Chemistry

    EiPT is short for N-ethyl-N-isopropyl-tryptamine. The full chemical name of this structure is N-ethyl-N-[2-(1H-indol-3-yl)ethyl]propan-2-amine. EiPT is a tryptamine, which all belong to a larger family of compounds known as indolethylamines. EiPT is closely related to the compounds diethyltryptamine (DET) and DIPT.

    Dosage

    In his book TiHKAL, Alexander Shulgin lists a dosage for EiPT as being 24-40 mg taken orally.

    Effects

    Very little is known about the psychopharmacological properties of EiPT, but reports suggest it produces psychedelic effects that can last 4–6 hours. According to Shulgin, this compound tends to produce nausea, dysphoria, and other unpleasant side-effects. It also lacks the hallucinatory and visual properties usually associated with psychedelic drugs.

    Dangers

    There have been no reported deaths or hospitalizations from EiPT, but its safety profile is unknown.

    Legality

    EiPT is unscheduled and uncontrolled in the United States, but possession and sales of EiPT could be prosecuted under the Federal Analog Act because of its structural similarities to DET.

    See also

    External links


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