Description
Buy 3-CMC Small Crystals Online | Secured Tracked Logistics EU
Order High-Purity 3-CMC Small Crystals for Laboratory Research
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Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: 1-(3-chlorophenyl)-2-(methylamino)propan-1-one
- Standard CAS Registry Number: 1049677-59-9 (Base) | 1607439-32-6 (Hydrochloride Salt Form)
- Molecular Formula: C₁₀H₁₂ClNO · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 197.66 g/mol (Base) | 234.12 g/mol (Refined HCl Salt variant)
- Physical Presentation: Highly defined, translucent to off-white small crystal aggregates or fine crystalline structures
- Structural Classification: Substituted synthetic cathinone derivative featuring a chlorinated halogen atom substitution at the meta (3rd) position of the phenyl ring .
Theoretical Pharmacology & Documented Adverse Effects
Legal Status & European Regulations
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- European Union (EU-Wide Prohibition): Following a delegated risk assessment by European health authorities, 3-CMC is formally classified and scheduled 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 permits .
- United Kingdom: Strictly prohibited under the Psychoactive Substances Act 2016 (and scheduled directly as a Class B substance under the Misuse of Drugs Act 1971), criminalizing unauthorized production, supply, or importation into British territory .
Authorized Research Use & Safety Warning
Frequently Asked Questions (FAQ)
As a potent phenethylamine and substituted cathinone derivative, exposure to 3-CMC 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 fatality.
The molecular structure of 3-CMC differs from 4-CMC based entirely on the positioning of the chlorine atom on the aromatic ring . In 3-CMC, the chlorine substitution occurs at the 3rd (meta) position, whereas in 4-CMC, it is situated at the 4th (para) position . This structural variation significantly alters the compound’s chemical properties, lipophilicity, and its interaction with biological transporters.
No. In the majority of jurisdictions, including the European Union and the United Kingdom, 3-CMC is a heavily controlled substance . Unauthorized possession, supply, or importation is a criminal offense . Legal access is typically restricted to authorized scientific institutions and requires specific permits for forensic or legitimate research purposes .
