3-CMC (3-Chloromethcathinone) | 220mg Analytical Research Profile
Are you seeking validated analytical data on Buy 3-CMC capsules – 220mg for neuropharmacological or forensic investigations? 3-Chloromethcathinone (3-CMC) is a synthetic substituted cathinone featuring a chlorine atom at the meta (3-) position of the phenyl ring. Within the scientific community, it is a primary subject for researchers investigating monoamine transporter kinetics, synaptic reuptake inhibition, and the structure-activity relationships of halogenated phenethylamines.
For laboratories looking to buy research chemicals online, utilizing standardized 220mg capsules ensures precise volumetric control and eliminates the weighing variability common with bulk powders in behavioral modeling.
Chemical Structure & Pharmacodynamics
The pharmacological profile of 3-CMC is heavily influenced by the electronegativity of the chlorine substituent. Its structural relationship to 3-MMC and 4-CMC (Clephedrone) provides a unique window into synaptic signaling:
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Receptor Interaction: 3-CMC acts primarily as a triple reuptake inhibitor, modulating the levels of dopamine, serotonin, and norepinephrine. Researchers study how the meta-position substitution affects the binding affinity compared to para-substituted isomers.
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Neurochemical Stability: In a standardized 220mg capsule format, the compound is protected from atmospheric moisture and oxidation, ensuring that the chemical integrity remains intact for the duration of the experimental protocol.
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Halogenation Effects: The presence of the chlorine atom is a key variable in investigating the metabolic pathways and potential neurotoxicological thresholds of the cathinone class.
Primary Research Applications
Buy 3-CMC capsules – 220mg analytical standards are essential for several advanced scientific domains:
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Neuropharmacological Mapping: Exploring the compound’s effect on the mesolimbic reward system and its implications for studying mood disorders and cognitive focus.
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Forensic Toxicology: Establishing precise retention times and fragmentation patterns using LC-MS/MS to differentiate 3-CMC from other emerging stimulants in biological matrices.
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Behavioral Modeling: Assessing the dose-response relationship of 220mg increments on locomotor activity, executive function, and psychological reinforcement.
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Enzymatic Kinetic Studies: Identifying the specific CYP450 enzymes involved in the degradation of 3-CMC to predict drug-drug interactions.
Technical Specifications
| Feature | Details |
| IUPAC Name | 1-(3-chlorophenyl)-2-(methylamino)propan-1-one |
| CAS Number | 1049677-59-9 |
| Molecular Formula | $C_{10}H_{12}ClNO$ |
| Formulation | 220mg Standardized Capsules |
| Purity Grade | High-Purity Analytical Grade ($\ge$98%) |
Safety, Regulatory Status, and Procurement
3-CMC is intended strictly for laboratory research and forensic applications. It is not for human or veterinary consumption.
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Regulatory Compliance: Researchers must verify the legal status of 3-CMC within their jurisdiction. Many countries have placed halogenated cathinones under restrictive schedules or general analog bans.
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Handling Protocols: Due to its potential potency, 3-CMC should be handled in a controlled laboratory environment using appropriate Personal Protective Equipment (PPE).
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Documentation: Every shipment includes a detailed Safety Data Sheet (SDS) covering solubility, toxicological data, and secure disposal procedures.
Why Source Buy 3-CMC capsules – 220mg Through Verified Channels?
Reliable scientific data depends on the consistency of the research material. Sourcing through a legitimate research chemical supplier ensures that each 220mg capsule contains a standardized assay free from unreacted synthesis precursors or heavy metal residues.



