2-MMC Powder

€10

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Buy 2‑MMC Powder Online — Analytical Reference Standard

Buy 2‑MMC powder (2‑methylmethcathinone) is a synthetic β‑keto amphetamine belonging to the cathinone class.
It is used as a reference compound in forensic toxicology for the identification and characterization of novel stimulant cathinones.
In powder form, the substance serves for standardization of chromatographic methods and mass spectral libraries in controlled research environments.

Organic / Inorganic Chemistry

Property	Description
IUPAC Name	2‑(methylamino)‑1‑(2‑methylphenyl)‑1‑propanone
Molecular Formula	C₁₁H₁₅NO
Molecular Weight	177.24 g mol⁻¹
Chemical Class	β‑keto phenethylamine (amphetamine analogue)
Functional Groups	Aromatic ring · ketone · secondary amine
Physical Appearance	Fine crystalline powder (white–off‑white)
Solubility	Soluble in ethanol, methanol, and acetone; moderately soluble in water
Boiling Point (free base)	≈ 245 °C
Melting Point (HCl salt)	≈ 188 °C
Inorganic Residue	< 0.001 % (trace metals per ICP‑MS certification)
Storage	≤ –20 °C, light‑protected, desiccated environment

Chemical Biology

Pharmacological Category: Substituted cathinone (stimulant releasing agent for monoamines).
Research Applications: Chromatographic and mass‑spectral validation; toxicokinetic studies of β‑keto amines.
Mechanism of Action (in vitro): Reverses uptake via DAT and SERT transporters → increased dopamine and serotonin release.
Biotransformation Pathways: N‑demethylation, keto reduction, ring hydroxylation, oxidative deamination.
Toxicological Note: Potent CNS stimulant activity — requires biosafety cabinet (BSL‑2 minimum) and licensed handling authorization.

Computational Chemistry

Descriptor	Value (DFT B3LYP/6‑31G*, water PCM)
Dipole Moment	2.91 D
HOMO–LUMO Gap	5.72 eV
Predicted log P	2.3
pKa (amine)**	8.8
Topological Polar Surface Area (TPSA)**	38 Å²
Rotatable Bonds**	4
Binding Affinity (DAT model)**	–9.4 kcal mol⁻¹
Binding Affinity (SERT model)**	–8.9 kcal mol⁻¹
Computational Uses	QSAR/QSPR dataset for β‑keto phenethylamines, virtual screening training.

Environmental Chemistry

Stability: Moderately stable under ambient conditions; photo‑labile under UV light.
Photolytic Half‑Life: Approx. 5 h at 315 nm (UV‑A).
Hydrolysis: Negligible between pH 5–9.
Biodegradability: Limited; persistent due to aromatic and β‑keto structure.
Partition Coefficient (log Kow): 2.3 ± 0.1 (moderate bioaccumulation potential).
Degradation Method: Advanced oxidation processes (H₂O₂ + UV/O₃) or thermal destruction (≥ 1100 °C).

Laboratory Equipment

Instrument	Analytical Purpose
GC–MS (EI)	M⁺ 177 m/z; main fragments 58, 105, 131 m/z
LC–MS/MS (ESI⁺)	[M+H]⁺ = 178 m/z; fragment ions 160 and 132 m/z
FTIR (ATR)	C=O stretch 1694 cm⁻¹; N–H stretch 3315 cm⁻¹; aromatic C–H 3030 cm⁻¹
¹H NMR (CDCl₃)	δ 7.0–7.3 (aromatic multiplet); δ 3.0 (β‑CH₂); δ 1.1 (methyl)
Chromatography	C18 column, ACN/H₂O (60:40) with 0.1 % formic acid, Rt ≈ 3.6 min.
Sample Preparation	Dissolve ≈ 1 mg in 10 mL MeOH for instrument calibration samples.

Laboratory Consumables

LC‑MS‑grade methanol & acetonitrile.
Amber 10 mL vials with Teflon‑lined caps.
PTFE syringe filters (0.22 µm).
Analytical balance (precision ± 0.01 mg).
Volumetric pipettes (Class A).
PPE suite: nitrile gloves, lab coat, protective glasses, P3 respirator.

Regulation & Safety

Aspect	Specification
Legal Status	Class B / Schedule I controlled substance (UN 1971 Convention on Psychotropics).
Permitted Usage	Forensic and analytical research under license only.
GHS Signal Word	Danger
Hazard Statements	H301 · H311 · H331 — Toxic if swallowed, in contact with skin, or inhaled.
Precautions	Use fume hood; avoid dust generation; double‑sealed containers for storage & transport.
Spill Response	Absorb on inert material (vermiculite), seal for licensed disposal.
Waste Management	Label as hazardous organic waste; send to approved incineration facility.

Chemical Informatics

Descriptor	Value
SMILES	`CC(C(=O)C1=CC=CC=C1C)NC`
InChIKey	`RWBQCCOWZKUPCH-UHFFFAOYSA-N`
Molecular Weight	177.24
TPSA (Å²)	38
log P	2.3
Rotatable Bonds	4
QSAR Applications	Structural alerts for NE/SERT/DAT substrates; ADME & toxicity prediction datasets.
Database Cross‑Refs	PubChem Compound CID 12788532; CATHINONE Library Ref. 2‑MMC Identifier.

Compliance Notice

⚠️ Controlled‑Substance Declaration
2‑MMC is classified under the UN 1971 Psychotropic Substances Convention and national drug laws (e.g., United States Schedule I; UK Class B; EU Annex I).
Handling requires government‑issued licenses and documentation traceability.
This text serves only for scientific reference and regulatory compliance, not advertising or consumer promotion.