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Atomfair 5-Methoxy-alpha-methyltryptamine 5-MeO-AMT C12H16N2O

Description 5-Methoxy-alpha-methyltryptamine (5-MeO-AMT) is a research chemical belonging to the tryptamine class, with the molecular formula C12H16N2O and CAS number 30379-58-9 . Its IUPAC name is 1-(5-methoxy-1H-indol-3-yl)propan-2-amine . This compound is structurally related to serotonin and other tryptamine derivatives, featuring a methoxy group at the 5-position and an alpha-methyl substitution on the side chain. It is supplied as a high-purity analytical reference standard, ideal for spectroscopic analysis, pharmacological studies, and forensic applications. Proper handling and storage under controlled conditions are recommended to ensure stability and integrity.

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Description

Description

5-Methoxy-alpha-methyltryptamine (5-MeO-AMT) is a research chemical belonging to the tryptamine class, with the molecular formula C12H16N2O and CAS number 30379-58-9. Its IUPAC name is 1-(5-methoxy-1H-indol-3-yl)propan-2-amine. This compound is structurally related to serotonin and other tryptamine derivatives, featuring a methoxy group at the 5-position and an alpha-methyl substitution on the side chain. It is supplied as a high-purity analytical reference standard, ideal for spectroscopic analysis, pharmacological studies, and forensic applications. Proper handling and storage under controlled conditions are recommended to ensure stability and integrity.

  • CAS No: 30379-58-9
  • Molecular Formula: C12H16N2O
  • Molecular Weight: 204.27
  • Exact Mass: 204.126263138
  • Monoisotopic Mass: 204.126263138
  • IUPAC Name: 1-(5-methoxy-1H-indol-3-yl)propan-2-amine
  • SMILES: CC(CC1=CNC2=C1C=C(C=C2)OC)N
  • Synonyms: 5-Methoxy-alpha-methyltryptamine, 1137-04-8, 5-meo-amt, 1-(5-methoxy-1H-indol-3-yl)propan-2-amine, Alpha-O

Application

5-Methoxy-alpha-methyltryptamine is primarily used in neuropharmacological research due to its structural similarity to endogenous neurotransmitters. It serves as a reference standard in mass spectrometry and chromatographic analysis for forensic and clinical toxicology. Researchers also investigate its potential interactions with serotonin receptors in central nervous system studies.

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