5-MeO-MiPT 15mg Pellets

Name: 5-MeO-MiPT 15mg Pellets
SKU: 235
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€9

Price is per pellet

Category: Research Chemicals

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5‑MeO‑MiPT 15mg Pellets – (5‑Methoxy‑N‑methyl‑N‑isopropyltryptamine) — Analytical & Regulatory Overview

5‑MeO‑MiPT 15mg Pellets is a synthetic indole‑alkylamine belonging to the tryptamine class.
It has been identified in “research chemical” samples formatted as tablets or pellets (e.g., nominal 15 mg each), intended for unregulated use before scheduling.
All such materials are now prohibited substances, controlled under Schedule I (US) and Class A (UK) law.

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 solid (white–beige).
Solubility	Freely soluble in methanol, ethanol, or chloroform.
Salt form used	Commonly hydrochloride or fumarate for analytical reference.

Chemical Biology

Mechanism: Agonist activity at 5‑HT₁A and 5‑HT₂A/2C receptors.
Metabolism: O‑demethylation → 5‑HO‑MiPT; oxidative de‑amination via MAO.
Pharmacology: Produces psychoactive mind‑altering effects; no approved medical indication.
Toxicology: Limited data; potential CNS over‑stimulation and hyperthermia.

Computational Chemistry

Descriptor	Typical Value
HOMO‑LUMO gap	≈ 4.6 eV
Dipole moment	2.5 D
Pred. log P	2.9
Polar surface area	42 Å²
Rotatable bonds	5
Cytochrome P450 binding (virtual)	Predicted CYP2D6 substrate likelihood > 0.7
QSAR applications	Used for indole family structure‑activity studies.

Environmental Chemistry

- Degradation: Photolysis and oxidation to indole‑2‑ones and methoxyphenols.
- Bioaccumulation factor: Low (moderate lipophilicity and rapid oxidation).
- Persistence: Decomposes slowly in neutral soil at ambient temperatures.
- Disposal: High‑temperature combustion (≥ 1000 °C) in licensed facility.

Laboratory Equipment (for licensed analysis)

Instrument	Purpose
GC‑MS (EI)	Screening and identification — base ion m/z  58.
LC‑QTOF‑MS	High‑resolution confirmation [M+H]⁺ = 247.1802.
¹H‑NMR	Methyl resonances ~1.2 ppm; aromatic protons 6.8–7.5 ppm.
FTIR	N–H stretch  ≈ 3330 cm⁻¹; C–O  ≈ 1250 cm⁻¹.
UV–Vis	λₘₐₓ ~ 278 nm (aromatic π→π*).

Facility requirements: DEA/Home Office research licence, Class II fume hood, trace‑quantity balances.

Consumables

- LC‑grade acetonitrile / water + 0.1 % formic acid.
- Amber autosampler vials (PTFE liners).
- 0.22 µm PTFE syringe filters.
- Reference standard solutions (≤ 1 mg · mL⁻¹ under licence).
- Nitrile gloves, safety glasses, lab coats.

Regulation & Safety

Category	Details
Controlled status	Schedule I (US Controlled Substances Act); Class A (Psychoactive Substances Act UK).
Permitted use	Forensic and scientific research in approved facilities only.
GHS classification	H301 (Toxic if swallowed) · H331 (Toxic if inhaled) · H370 (Target‑organ toxicant).
Handling precautions	Avoid dust; use local exhaust ventilation and PPE.
Storage	≤ –20 °C, protected from light, in locked controlled‑substance safe.
Waste	Incineration with acid gas scrubbing; document chain of custody.

Chemical Informatics

Descriptor	Representative Value
SMILES	`CC(C)N(C)CCC1=CNC2=CC=C(OC)C=C12`
InChIKey	`CHZVERDGACCTDJ‑UHFFFAOYSA‑N`
Molecular weight	246.35 g mol⁻¹
log P	2.9
TPSA	42 Å²
Rotatable bonds	5
Applications	Forensic mass‑spectral libraries; QSAR training sets for serotonergic ligands.

Ethical and Legal Notice

⚠️ Controlled‑Substance Advisory
5‑MeO‑MiPT is an internationally scheduled psychedelic compound.
Its manufacture, distribution, or possession is illegal without explicit research authorization.
This document serves only as a scientific and regulatory reference for chemical and forensic professionals.