MiPT fumarate

$84.00$336.00

MiPT Fumarate is a high-purity N-isopropyl tryptamine compound for serotonin receptor research. Stable fumarate form ideal for SAR studies and CNS assays.

Product Information Table

Property Value
Product Name MiPT Fumarate
IUPAC Name N-[2-(1H-indol-3-yl)ethyl]-N-methylpropan-2-amine fumarate
Molecular Formula C14H20N2 · C4H4O4
Molecular Weight ~312.36 g/mol
Form Crystalline powder (fumarate salt)
Purity ≥98%
Appearance White to off-white powder
Applications Tryptamine analog research, serotonin agonist studies
Storage Store sealed in cool, dry environment

Buy MiPT Fumarate – High-Purity N-Methyl-N-isopropyltryptamine for Tryptamine Research

MiPT Fumarate is a lab-grade compound belonging to the tryptamine class of research chemicals, structurally similar to DMT and MET. Known for its unique N-isopropyl substitution, MiPT has become a key molecule in serotonergic receptor binding studies, particularly those involving 5-HT2A and 5-HT1A receptors.

Provided in its fumarate salt form, MiPT ensures greater stability and solubility for in vitro studies. With ≥98% purity, this compound is ideal for advanced research into indole-based receptor agonists, neurochemical mapping, and SAR (Structure-Activity Relationship) evaluations. It is not intended for human or veterinary consumption.


  Key Product Details

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

  • Common Name: MiPT Fumarate

  • IUPAC Name: N-[2-(1H-indol-3-yl)ethyl]-N-methylpropan-2-amine fumarate

  • Molecular Formula (Salt): C14H20N2 · C4H4O4

  • Molecular Weight: ~312.36 g/mol (fumarate salt)

  • Form: Crystalline powder (fumarate)

  • Purity: ≥98%

  • Appearance: White to off-white powder

  • Application: Serotonin receptor research, tryptamine analog studies

  • Storage: Store in sealed container, cool and dry environment

  • Legal Status: For research use only; not approved for human consumption


 How It Works

MiPT acts as a serotonin receptor agonist, with its primary activity at 5-HT2A, the same receptor associated with other tryptamines like DMT. The addition of an isopropyl group instead of ethyl or methyl significantly alters the molecule’s binding affinity and selectivity.

In lab research, MiPT is studied for:

  • Receptor subtype binding efficiency

  • Tryptamine SAR comparisons

  • Neurochemical transporter interaction

  • Comparative modeling alongside DMT, MET, and DIPT

Its fumarate form enhances chemical stability and water solubility, ensuring consistency across long-term research trials.


 Safety and Warning Guidelines

  • Intended for Lab Use Only: MiPT is not approved for medical or recreational use.

  • Protective Measures: Researchers must wear gloves, eye protection, and lab coats.

  • Handling Procedures: Use only in certified labs, preferably under a fume hood.

  • Storage Instructions: Keep in a cool, dry area. Protect from direct light and humidity.

  • Disposal: Follow institutional and local hazardous waste protocols.

  • Legal Status: May be restricted under analogue laws. Researchers must verify regional legality before ordering.

  • Exposure Warning: In case of skin or eye contact, rinse with water and seek medical advice if irritation persists.

Only trained professionals should handle MiPT in controlled lab environments.


  Research Applications of MiPT

  • Serotonin receptor agonist mapping

  • CNS activity modeling in vitro

  • Tryptamine analog SAR studies

  • Glutamate and dopamine pathway interaction assessments


 Usage Disclaimer

This product is intended strictly for scientific, forensic, or analytical research purposes. It is not for human or animal consumption.


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