MET fumarate

$127.00$660.00

Buy MET Fumarate (N-Methyl-N-ethyltryptamine Fumarate)


MET Fumarate is a high-purity tryptamine analog used for serotonin receptor research. Stable fumarate salt form ideal for advanced analytical studies.

Product Information Table

Property Value
Product Name MET Fumarate
IUPAC Name N-ethyl-N-methyl-1H-indole-3-ethanamine fumarate
Molecular Formula C13H18N2 · C4H4O4
Molecular Weight ~318.35 g/mol (fumarate salt)
Form Crystalline powder
Purity ≥98%
Appearance Off-white to beige
Applications 5-HT receptor research, tryptamine analog studies
Storage Store sealed, in cool, dark conditions

Buy MET Fumarate – High-Purity N-Methyl-N-ethyltryptamine for Tryptamine Research

MET Fumarate (N-Methyl-N-ethyltryptamine Fumarate) is a tryptamine-class research chemical related structurally to DMT and DET. Known for its fast-acting properties in some in vitro models, MET is studied for its interaction with serotonin receptors, especially 5-HT2A, and for its role in CNS neurotransmission modeling.

The fumarate salt form offers enhanced stability and solubility, making it ideal for receptor binding assays, structure-activity relationship (SAR) comparisons, and chemical neuroscience studies. It is provided in ≥98% pure crystalline form, intended for research use only.


🧪 Key Product Details

  • Chemical Name: N-Methyl-N-ethyltryptamine fumarate

  • Common Name: MET Fumarate

  • IUPAC Name: N-ethyl-N-methyl-1H-indole-3-ethanamine fumarate

  • Molecular Formula (Freebase): C13H18N2

  • Molecular Formula (Fumarate): C13H18N2 · C4H4O4

  • Molecular Weight: ~318.35 g/mol (salt form)

  • CAS Number: [Unlisted / research only]

  • Form: Crystalline fumarate salt

  • Purity: ≥98%

  • Appearance: Off-white to beige crystalline powder

  • Application: Receptor binding research, SAR studies

  • Storage: Airtight, cool, and dry environment

  • Legal Status: Not for human or veterinary use


  How It Works

MET (N-Methyl-N-ethyltryptamine) is a substituted tryptamine believed to act as an agonist at serotonin 5-HT receptors, particularly 5-HT2A and 5-HT1A. Structurally, it is similar to DMT, but the added ethyl group modifies its binding affinity and metabolic profile.

In laboratory settings, researchers use MET to study:

  • Serotonin receptor activity and selectivity

  • Central nervous system (CNS) simulation models

  • SAR comparison with DMT, MET, and other analogs

  • In vitro metabolic breakdown and binding kinetics

The fumarate form is more chemically stable than the freebase, enabling longer shelf life and greater solubility for aqueous-based studies.


⚠️ Safety and Warning Guidelines

  • Research Use Only: MET Fumarate is not approved for human ingestion or therapeutic use.

  • Protective Measures: Always use PPE – gloves, goggles, lab coat.

  • Handling Protocols: Conduct experiments under fume hoods with spill containment in place.

  • Storage Conditions: Store in a sealed container in a cool, dry, and dark environment.

  • Disposal Requirements: Follow your local and institutional hazardous waste guidelines.

  • Legal Compliance: This compound may be restricted in some regions. Verify legality before ordering or handling.

Must only be handled by trained personnel in certified research facilities.


  Research Applications of MET Fumarate

  • In vitro serotonergic receptor studies

  • Tryptamine analog comparisons for SAR mapping

  • Neuropharmacology simulations of indole-based compounds

  • Neurotransmitter interaction and transporter mapping models


⚠️ Usage Disclaimer

This product is sold strictly for research and analytical purposes. Not for human or animal consumption under any condition.


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