5-MeO-MiPT Powder

€45

Price is per 0.5g

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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 Å².
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 Å²
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.