Description
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Order High-Purity 3-MMC Crystals for Laboratory Research
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Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: 2-(methylamino)-1-(3-methylphenyl)propan-1-one
- Standard CAS Registry Number: 1246816-62-5 (Base Form) | 1246998-31-3 (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: Highly stable, translucent to off-white large crystalline structures or compressed crystal blocks
- Structural Classification: Substituted synthetic cathinone derivative featuring a methyl group bound at the meta (3rd) 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, 3-MMC 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 under the Class B framework of the Misuse of Drugs Act 1971, 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 3-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), vasoconstriction, and profound psychomotor agitation. Prolonged exposure or high doses may lead to permanent organ damage or structural cardiovascular complications.
The molecular structure of 3-MMC differs from mephedrone (4-MMC) solely by the positioning of the methyl group on the phenyl ring. While mephedrone features a methyl group attached at the 4th (para) position, 3-MMC incorporates the methyl group substitution at the 3rd (meta) position. This slight structural variation noticeably shifts its lipophilicity, clearance kinetics, and target receptor affinity.
No. In the majority of jurisdictions, including the European Union and the United Kingdom, 3-MMC is a heavily controlled substance. Unauthorized possession, supply, or importation is a criminal offense. Legal access is strictly limited to authorized scientific research institutions and requires specialized permits for forensic or legitimate laboratory research purposes.
