3-FMA Pellets – 50mg

3-FMA

PRODUCT DETAILS TABLE

 

Specification Details
Brand Biosynlab
Product Name 3-FMA (3-Fluoromethamphetamine)
IUPAC Name 1-(3-fluorophenyl)-N-methylpropan-2-amine
CAS Number 351-03-1
Molecular Formula C₁₀H₁₄FN
Molecular Weight 167.23 g/mol
Chemical Class Fluorinated substituted amphetamine / Phenethylamine derivative
Purity ≥99.2% (HPLC Verified)
Appearance White to off-white crystalline powder
Melting Point 215-218°C (hydrochloride salt)
Solubility Soluble in ethanol, methanol, DMSO; sparingly soluble in water
Storage -20°C, desiccated, away from light
Packaging Amber glass vial with PTFE seal
Quantities 250mg, 500mg, 1g, 5g, 10g, 25g, bulk
Analysis COA, NMR, MS, FTIR included
Shipping Express courier, tracked
Regions USA, UK, Germany, Netherlands, EU, Australia, Canada

Introduction

 

3-FMA (3-Fluoromethamphetamine) represents a cutting-edge fluorinated amphetamine derivative increasingly utilized in neuropharmacological research and analytical chemistry applications. As a structural analog of methamphetamine featuring a fluorine substituent at the 3-position of the phenyl ring, 3-FMA offers unique pharmacokinetic properties that make it valuable for receptor binding studies and structure-activity relationship (SAR) investigations. Biosynlab delivers pharmaceutical-grade 3-FMA with certified ≥99.2% purity, supporting research institutions across the USA, United Kingdom, European Union, and beyond.

The strategic fluorination of the phenyl ring in 3-FMA alters lipophilicity, metabolic stability, and binding affinity compared to non-fluorinated parent compounds. This structural modification creates distinct pharmacological properties that researchers are actively characterizing through in vitro assays and receptor profiling studies. Biosynlab’s synthesis and analytical protocols ensure batch-to-batch consistency critical for reproducible scientific outcomes.

Chemical Properties & Structural Analysis

3-Fluoromethamphetamine belongs to the phenethylamine chemical class, specifically the substituted amphetamine subclass. The addition of the electronegative fluorine atom at the meta position creates electron-withdrawing effects that influence the compound’s interaction with monoamine transporters and receptors.

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