Buy 2‑MMC Capsules 220mg Online — Forensic Analytical Reference Material
Buy 2‑MMC Capsules 220mg (2‑methylmethcathinone) is a synthetic β‑keto phenethylamine, derived from the cathinone scaffold found in Catha edulis.
It is used exclusively as a calibration standard for forensic screening and mass‑spectrometric confirmation of designer cathinones.
The 220 mg capsule format facilitates sealed, pre‑measured aliquots for reference preparation in quality‑controlled analytical workflows.
Organic / Inorganic Chemistry
| Parameter | Value |
|---|---|
| IUPAC Name | 2‑(methylamino)‑1‑(2‑methylphenyl)‑1‑propanone |
| Molecular Formula | C₁₁H₁₅NO |
| Molecular Mass | 177.24 g mol⁻¹ |
| Functional Groups | Aromatic ring, β‑keto carbonyl, secondary amine |
| Chemical Family | Substituted cathinones |
| Physical Form | Crystalline powder encapsulated (220 mg) |
| Melting Point (base) | ≈ 195 °C |
| Boiling Point (base) | ≈ 245 °C (thermal decomp.) |
| pKa (amine) | 8.8 |
| Solubility | Methanol, ethanol, acetone (soluble); water (limited) |
| Storage | ≤ –20 °C under desiccation and light exclusion |
| Purity (Analytical) | ≥ 99 % (by HPLC) |
Chemical Biology
- Mechanism: Stimulant via monoamine transporter interaction (DAT > SERT).
- Usage in Lab: Benchmark compound for forensic spectral libraries and metabolite identification.
- In vitro studies: Supports research into dopaminergic and serotonergic uptake assays.
- Metabolic Pathways: N‑demethylation → alcohol reduction → oxidation to acidic metabolites.
- Toxicological Profile: CNS stimulant; strictly controlled; not for biological administration.
Computational Chemistry
| Descriptor | Predicted Value (B3LYP/6‑31G*) |
|---|---|
| Dipole Moment | 2.91 D |
| HOMO–LUMO Gap | 5.73 eV |
| Hydrogen‑Bond Acceptors | 2 |
| Hydrogen‑Bond Donors | 1 |
| Rotatable Bonds | 4 |
| log P (pred.) | 2.3 |
| Polar Surface Area (TPSA) | 38 Ų |
| Binding Energy (DAT model)** | –9.4 kcal mol⁻¹ |
| Binding Energy (SERT model)** | –8.7 kcal mol⁻¹ |
Environmental Chemistry
- Persistence: Stable under neutral pH; moderately photosensitive (β‑keto degradation under UV).
- Photolysis Half‑Life: ≈ 5 h at 365 nm.
- Hydrolysis: Negligible between pH 5–9.
- log Kow: 2.3 → moderate bioaccumulation potential.
- Primary Degradation Products: Benzoic acid derivatives and methcathinone metabolites.
- Waste Treatment: Advanced oxidation (ozone, UV/H₂O₂) or thermal destruction (≥ 1100 °C).
Laboratory Equipment
| Instrument | Application |
|---|---|
| GC–MS (EI) | Molecular ion 177 m/z · Fragments 58, 105, 131 m/z |
| LC–MS/MS (ESI⁺) | [M + H]⁺ = 178 m/z → product ions 160, 132 m/z |
| FTIR (ATR) | C=O 1694 cm⁻¹ · NH 3310 cm⁻¹ · Ar–CH 3030 cm⁻¹ |
| ¹H NMR (CDCl₃) | δ 7.0–7.3 (aromatic), δ 3.0 (β‑CH₂), δ 1.1 (CH₃) |
| HPLC Conditions | C18 column; Acetonitrile:H₂O (60:40 + 0.1 % formic acid); Rt ≈ 3.6 min |
Laboratory Consumables
- LC–MS‑grade acetonitrile and methanol.
- Amber vials (1.5 mL) with PTFE‑lined caps.
- 0.22 µm PTFE filters.
- Precision balance (± 0.01 mg).
- Certified pipettes and tips (Class A).
- PPE: gloves, lab coat, safety glasses, P3 respirator mask.
Regulation & Safety
| Aspect | Information |
|---|---|
| Legal Status | Listed under Schedule I / Class B controlled substances. |
| Permitted Use | Authorized forensic and analytical reference use only. |
| GHS Signal Word | Danger |
| Hazard Statements | H301, H311, H331 — Toxic if swallowed, inhaled, or through skin. |
| Precautionary | P280, P260 — Use PPE · Avoid inhalation/dust exposure. |
| Spill Response | Absorb on vermiculite/activated carbon; seal for licensed disposal. |
| Waste Disposal | High‑temperature incineration at licensed facility (≥ 1100 °C). |
Chemical Informatics
| Field | Entry |
|---|---|
| SMILES | CC(C(=O)C1=CC=CC=C1C)NC |
| InChIKey | RWBQCCOWZKUPCH-UHFFFAOYSA-N |
| Molecular Weight | 177.24 g mol⁻¹ |
| TPSA | 38 Ų |
| log P | 2.3 |
| Rotatable Bonds | 4 |
| QSAR Usage | Data point for β‑keto phenethylamine SAR modelling and neuroactive compound predictors. |
| Database Links | PubChem CID 12788532 · NIST Forensic ChemDB · ChemIDplus Ref. |
Compliance Notice
⚠️ Controlled‑Substance Advisory
2‑MMC and derivatives are prohibited under the UN Convention (1971) and national drug laws (Schedule I/Class B/Annex I).
Handling and storage require institutional licensing, secure inventory control, and periodic auditing.
This document is for scientific and regulatory reference only — not for promotion or sale.
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