Buy 6-APB Pellets 120mg Online – (6‑(2‑Aminopropyl)benzofuran) — Forensic & Regulatory Technical Summary
Buy 6-APB Pellets 120mg is an aromatic heterocyclic amine structurally related to MDMA, combining a benzofuran ring and an aminopropyl side chain.
Any “pellet” or “tablet” form (e.g., 120 mg) encountered in casework is treated as illicit formulation and analyzed only by accredited forensic laboratories.
Organic / Inorganic Chemistry
| Property | Description |
|---|---|
| IUPAC name | 1‑(benzofuran‑6‑yl)propan‑2‑amine |
| Formula | C₁₁H₁₃NO |
| Molar mass | 175.23 g ⋅ mol⁻¹ |
| Functional groups | Secondary amine (–NH–), aromatic C=C, ether oxygen (furan ring) |
| Melting point | ≈ 115–118 °C (HCl salt) |
| Solubility | Polar solvents (e.g., methanol, water as HCl salt); low in non‑polar media. |
| Reactivity | Basic; forms salts with strong acids; oxidizable to quinone/furanone derivatives. |
Chemical Biology
- Mechanistic interest: Functions as a monoamine‑releasing amphetamine analogue in theoretical pharmacodynamic models.
- No approved medical or research use outside controlled substance licences.
- Biotransformation: Phase I oxidation → O‑desmethyl‑6‑APB; Phase II conjugation (sulfate / glucuronide).
- Toxicological profile: Serotonergic overstimulation, hyperthermia, cardiovascular stress, neurotoxicity at high dose.
- Forensic use: Analytical reference compound for LC‑MS toxicology detection panels.
Computational Chemistry
| Parameter | Example Result (DFT B3LYP/6‑31G*) |
|---|---|
| Optimized geometry | Planar benzofuran; amine side‑chain dihedral ≈ 62°. |
| HOMO–LUMO gap | ≈ 4.3 eV → moderate kinetic stability. |
| Dipole moment | 2.0 D. |
| Log P (predicted) | 2.5 → intermediate lipophilicity. |
| Polar surface area | 32 Ų. |
| Computational utility | Benchmark structure in QSAR and machine‑learning sets for amine–aromatic systems. |
Environmental Chemistry
- Chemical stability: Aromatic benzofuran ring yields slow biodegradation.
- Degradation pathways: Photo‑oxidation and hydroxyl radical attack produce carboxybenzofuran acids.
- Aquatic impact: Potential acute toxicity to microorganisms; data limited.
- Disposal: High‑temperature incineration ≥ 1000 °C with acid‑gas filtration.
Laboratory Equipment (for Authorized Analysis)
| Instrument | Application |
|---|---|
| LC‑MS/MS (QqQ) | Quantitative assay (m/z 176 → 159 → 131). |
| GC‑MS (EI) | Mass spectral confirmation ions: 44, 77, 105. |
| FTIR / Raman | Diagnostic bands at 3400 cm⁻¹ (N–H), 1600 cm⁻¹ (C=C), 1260 cm⁻¹ (C–O). |
| ¹H‑NMR / ¹³C‑NMR | Confirms benzofuran substitution pattern and amine chain. |
| UV‑Vis | λₘₐₓ ≈ 275 nm (π → π*). |
Facility requirements:
Class II fume hoods, analytic balances (0.1 mg precision), dry & secure controlled‑substance storage.
Consumables
- Amber vials with PTFE septa.
- HPLC‑grade acetonitrile / methanol / formic acid (0.1 %).
- PTFE 0.22 µm syringe filters.
- Calibrated micropipettes, weighing boats, nitrile gloves, safety glasses.
- Biohazard bags for waste under controlled destruction protocol.
Regulation & Safety
| Classification | Detail |
|---|---|
| Controlled status | Schedule I (US DEA); Class A (UK Misuse of Drugs Act); EU Annex I NPS listing. |
| Permitted use | Investigative, toxicological, and regulatory testing only. |
| GHS Hazards | H301 (Toxic if swallowed), H331 (Toxic if inhaled), H370 (Causes organ damage). |
| PPE | Lab coat, nitrile gloves, safety goggles, respirator (P3 filter). |
| Storage | ≤ –20 °C in locked controlled‑substance cabinet, away from oxidants. |
| Handling | Weigh using enclosed balance chamber; dispose via licensed hazardous‑waste facility. |
Chemical Informatics
| Identifier | Value |
|---|---|
| SMILES | CC(N)CC1=CC2=C(O1)C=CC=C2 |
| InChIKey | QWUWCCQZLGKZHM‑UHFFFAOYSA‑N |
| Molecular weight | 175.23 g mol⁻¹ |
| PSA | 32.3 Ų |
| Rotatable bonds | 2 |
| Informatics use | Reference structure in forensic spectral libraries and QSAR toxicology datasets. |
Ethical and Legal Notice
⚠️ Compliance Reminder:
Any press‑formed “pellet” or measured “dose” of 6‑APB is deemed illicit manufacture under global drug‑control frameworks.
The compound may be handled only by licensed laboratories for analytical and regulatory purposes.
This document supports science, public‑health, and regulatory awareness — not production or distribution.
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