Buy 5‑MeO‑MiPT Powder Online - (5‑methoxy‑N‑methyl‑N‑isopropyltryptamine) — Forensic / Research Reference
Buy 5‑MeO‑MiPT powder is a synthetic tryptamine derivative related to the indole‑ethylamines naturally occurring in plants and mammals.
It appears as a white to off‑white crystalline powder in forensic samples since the early 2000s.
All handling is restricted to licensed research or toxicology laboratories.
Organic / Inorganic Chemistry
| Property | Description |
|---|---|
| IUPAC name | N‑[2‑(5‑methoxy‑1H‑indol‑3‑yl)ethyl]‑N‑methylpropan‑2‑amine |
| Empirical formula | C₁₅H₂₂N₂O |
| Molar mass | 246.35 g · mol⁻¹ |
| Functional groups | Indole ring, secondary amine (N‑methyl‑N‑isopropyl), methoxy ether. |
| Physical form | Crystalline or amorphous solid (pale beige to tan). |
| Solubility | Freely soluble in polar organic solvents; low in water. |
| Reactivity | Base forms salts with acids (e.g., HCl); sensitive to oxidation and UV light. |
Chemical Biology
- Mechanistic interest: Selective serotonin (5‑HT₂A/2C/1A) receptor agonist in in‑vitro studies.
- Biotransformation: O‑demethylation (→ 5‑HO‑MiPT), N‑dealkylation, oxidative deamination.
- Toxicology: Data limited; acute stimulation, hyperthermia, confusion reported clinically for related tryptamines.
- No approved medical use.
Computational Chemistry
| Descriptor | Result (typical B3LYP/6‑31G*) |
|---|---|
| Geometry | Planar indole with side‑chain dihedral ≈ 65°. |
| HOMO–LUMO gap | 4.6 eV → moderately stable molecule. |
| Dipole moment | 2.5 D. |
| Pred. log P | 2.9 → lipophilic organic amine. |
| Polar surface area | 42 Ų. |
| Use | Structure–activity relationship (SAR) studies within tryptamine series. |
Environmental Chemistry
- Volatility: Low; present as solid residue.
- Persistence: Slowly oxidized and photo‑degraded in soil/water.
- Transformation products: indole‑2‑ones, N‑oxide derivatives, methoxyphenols.
- Waste disposal: Complete destruction by high‑temperature incineration (≥ 1000 °C).
Laboratory Equipment (for licensed analysis)
| Instrument | Purpose |
|---|---|
| GC‑MS (EI) | Primary screening; base peak m/z = 58 (N‑isopropyl fragment). |
| LC‑MS/MS | Quantitative toxicology assay; [M+H]⁺ = 247.1802. |
| FTIR | 3320 cm⁻¹ (N–H), 1610 cm⁻¹ (C=C), 1250 cm⁻¹ (C–O–CH₃). |
| NMR (¹H / ¹³C) | Indole aromatics 6.9–7.5 ppm; methyl groups ~1.2 ppm. |
| UV‑Vis | λₘₐₓ ≈ 278 nm (aromatic π→π*). |
Facilities require: controlled‑substance storage, fume hood, 0.1 mg balances, calibration standards.
Consumables
- LC‑grade acetonitrile / methanol + 0.1 % formic acid.
- Amber autosampler vials with PTFE septa.
- Nitrile gloves, protective eyewear, lab coat.
- PTFE filters (0.22 µm).
- Reference standards under valid DEA/MHRA licence.
Regulation & Safety
| Category | Description |
|---|---|
| Controlled status | Schedule I (US CSA, 21 CFR 1308.11); Class A (UK); EU Annex I NPS –– no approved use. |
| Hazard statements | H301 (Toxic if swallowed), H331 (Toxic if inhaled), H370 (Causes organ damage). |
| PPE requirements | Lab coat, gloves, safety goggles, respirator if dust risk. |
| Storage | Locked controlled‑drug cabinet, ≤ –20 °C, away from light and oxidants. |
| Handling precautions | Work in ventilated hood; avoid aerosol formation. |
| Disposal | Licensed hazardous‑waste incineration. |
Chemical Informatics
| Identifier | Value |
|---|---|
| SMILES | CC(C)N(C)CCC1=CNC2=CC=C(OC)C=C12 |
| InChIKey | CHZVERDGACCTDJ‑UHFFFAOYSA‑N |
| Molecular weight | 246.35 g mol⁻¹ |
| TPSA | 42 Ų |
| Rotatable bonds | 5 |
| log P (pred) | 2.9 |
| Applications | Reference for forensic mass spectral libraries and QSAR datasets of tryptamine analogues. |
Ethical and Legal Notice
⚠️ Controlled‑Substance Warning
5‑MeO‑MiPT is classified internationally as a Schedule I psychedelic tryptamine.
Synthesis, possession, or distribution without appropriate licence is illegal.
This dossier is intended solely for forensic, regulatory, and scientific reference to support public‑health oversight.




Reviews
There are no reviews yet.