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CAS 1137-04-8

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5-Methoxy-α-methyltryptamine

Description:
5-Methoxy-α-methyltryptamine (5-MeO-α-MT) is a synthetic tryptamine derivative known for its psychoactive properties. It is structurally related to serotonin and other tryptamines, featuring a methoxy group at the 5-position and an α-methyl group on the ethylamine side chain. This compound is often studied for its potential effects on serotonin receptors, particularly the 5-HT2A receptor, which is implicated in mood regulation and perception. 5-MeO-α-MT is typically encountered as a white crystalline powder and is soluble in organic solvents. Its psychoactive effects can include alterations in mood, perception, and consciousness, similar to other hallucinogenic substances. However, the specific pharmacological profile and safety profile of 5-MeO-α-MT are not as well-documented as those of more widely known psychedelics. As with many psychoactive substances, its use may carry risks, including psychological distress or adverse reactions, particularly in unregulated settings. Research into its effects and potential therapeutic applications is ongoing, contributing to the broader understanding of tryptamine compounds in neuroscience and psychopharmacology.
Formula:C12H16N2O
InChI:InChI=1S/C12H16N2O/c1-8(13)5-9-7-14-12-4-3-10(15-2)6-11(9)12/h3-4,6-8,14H,5,13H2,1-2H3
InChI key:InChIKey=OGNJZVNNKBZFRM-UHFFFAOYSA-N
SMILES:C(C(C)N)C=1C=2C(NC1)=CC=C(OC)C2
Synonyms:
  • 1-(5-methoxy-1H-indol-3-yl)propan-2-amine
  • 1H-Indole-3-Ethanamine
  • 1H-Indole-3-ethanamine, 5-methoxy-α-methyl-
  • 2-(1H-Indol-3-Yl)-Ethylamine
  • 2-(1H-Indol-3-Yl)Ethanamine
  • 3-(2-Aminoethyl)-1H-Indole
  • 3-(Beta-Aminoethyl) Indole
  • 5-Meo Amt
  • 5-Methoxy-1H-Indole-3-Propane-2-Amine
  • 5-Methoxy-A-Methyltryptamine
  • See more synonyms
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Found 1 products.
  • a,O-Dimethyl serotonin
    Biosynth
    + Info

    a,O-Dimethyl serotonin

    Controlled Product
    CAS:
    <p>a,O-Dimethyl serotonin is a monoamine compound that is synthesized by the enzymatic decarboxylation of 5-hydroxytryptophan. It has been shown to increase dopamine levels and inhibit the enzyme activity of serotonin in mice. This drug also binds to 5-ht2 receptors and induces the release of serotonin from nerve cells. A linear calibration curve was obtained using bufotenin as a standard. This drug has been used in analytical toxicology for determining the uptake of serotonin into human lung tissue and its effect on 5-ht1a receptors. In addition, a study was conducted with perennial ryegrass to determine whether this drug inhibits plant toxin synthesis. The results showed that it did not have an inhibitory effect on plant toxins and may even promote their synthesis.</p>
    Formula:C12H16N2O
    Purity:Min. 95%
    Molecular weight:204.27 g/mol

    Ref: 3D-FD22257

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