Description
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Order High-Purity 4-MMC for Laboratory Research
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Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: (RS)-2-(methylamino)-1-(4-methylphenyl)propan-1-one
- Standard CAS Registry Number: 1189805-46-6 (Base) | 1189726-22-4 (Hydrochloride Salt Form)
- Molecular Formula: C₁₁H₁₅NO · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 177.24 g/mol (Base) | 213.71 g/mol (Refined HCl Salt variant)
- Physical Presentation: Translucent to off-white large crystal structures or compressed crystalline powder blocks
- Structural Classification: Substituted synthetic cathinone derivative featuring a methyl group bound explicitly at the para (4th) position of the phenyl ring core.
Theoretical Pharmacology & Documented Adverse Effects
Legal Status & European Regulations
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- European Union (EU-Wide Prohibition): Following comprehensive assessments by European health authorities, 4-MMC (Mephedrone) is formally scheduled and classified as an illegal drug across all EU Member States. Furthermore, under Delegated Regulation (EU) 2026/314, rigid Category I restrictions apply to the precursor building blocks required for synthesis, completely halting domestic manufacturing within European territory. National frameworks—such as Germany’s NpSG and equivalent narcotic acts in France and the Netherlands—restrict distribution solely to state-authorized installations holding specialized government permits.
- United Kingdom: Controlled rigidly as a Class B substance under the Misuse of Drugs Act 1971 and universally restricted under the Psychoactive Substances Act 2016, criminalizing all forms of unauthorized supply, domestic transfer, or importation into British territory.
Authorized Research Use & Safety Warning
Frequently Asked Questions (FAQ)
As a highly potent phenethylamine and substituted cathinone derivative, exposure to 4-MMC carries substantial cardiovascular and neurological risks. Documented adverse reactions include severe hypertensive strain, rapid heart rate (tachycardia), dangerous spikes in core body temperature (hyperthermia), peripheral vasoconstriction, and profound psychomotor agitation. Prolonged exposure or high doses may lead to permanent organ damage or structural cardiovascular complications.
The molecular structure of 4-MMC differs from 3-MMC solely by the positioning of the methyl group on the aromatic ring. While 3-MMC features a methyl group attached at the 3rd (meta) position, 4-MMC incorporates the methyl group substitution at the 4th (para) position. This positional variation significantly alters the compound’s target receptor affinity, notably changing its overall serotonin-to-dopamine release ratio.
No. This compound is synthesized and handled strictly as an analytical reference standard. It is not approved for human or veterinary consumption, and any such application is completely illegal and carries life-threatening health and legal consequences.
