3-FA Pellets 50mg

3-FA analytical chemistry: Analytical Overview, Structure, and Research Significance

Introduction

Within the field of analytical and forensic chemistry, 3-FA (3-Fluoroamphetamine) has gained growing attention due to its distinctive structure and valuable role in comparative chemical analysis. As a fluorinated amphetamine analog, 3-FA offers researchers the opportunity to study the effects of fluorine substitution on molecular behavior, reactivity, and detection profiles.

The 50 mg pellet format provides a consistent, controlled reference amount suitable for laboratory-based evaluation. Scientists use 3-FA to investigate molecular interactions, chromatographic behavior, and structure–activity relationships (SAR) among substituted amphetamines and related compounds.

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Chemical Structure and Classification of 3-FA fluorinated amphetamines

3-FA (3-Fluoroamphetamine) belongs to the phenethylamine and amphetamine classes, sharing a core backbone with well-known analogs such as amphetamine, 2-FA, and 4-FA. The defining structural feature of 3-FA is the fluorine atom substitution on the third position of the benzene ring.

• Molecular Formula: C9H12FN

• Molecular Weight: 153.20 g/mol

• Chemical Class: Substituted Amphetamine

• Functional Groups: Aromatic Ring, Primary Amine, Fluorine Substituent

The introduction of fluorine significantly influences 3-FA’s electronegativity and chemical stability, giving it distinct spectroscopic and chromatographic signatures when analyzed in laboratory conditions.

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Spectroscopic and Analytical Identification of lab tested 3-FA for sale

To accurately characterize and differentiate 3-FA from other fluorinated analogs, researchers employ several analytical methods. Each method provides a unique data set that contributes to a complete molecular profile.

1. Gas Chromatography–Mass Spectrometry (GC-MS)

GC-MS remains a cornerstone in compound identification. For 3-FA, its fragmentation pattern is distinct due to the fluoro-substitution, yielding a reliable mass spectral signature. Analysts can confirm the identity and purity of 3-FA through its consistent retention time and mass ion peaks.

2. Fourier Transform Infrared Spectroscopy (FT-IR)

In FT-IR spectroscopy, 3-FA exhibits prominent C–F bond stretching vibrations between 1000–1300 cm⁻¹, making it easily distinguishable from non-fluorinated amphetamines. The IR spectrum also shows characteristic amine absorption bands and aromatic C–H stretching signals.

3. Nuclear Magnetic Resonance (NMR) Spectroscopy

¹H and ¹³C NMR techniques provide detailed information on 3-FA’s structure, confirming the substitution position of the fluorine atom and the integrity of the aromatic ring. The fluorine atom also introduces coupling effects visible in both spectra, reinforcing structural verification.

Collectively, these analytical methods enable laboratories to build complete spectral reference data for 3-FA, ensuring reproducibility and traceability in scientific research.

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Analytical and Research Applications of high purity 3-Fluoroamphetamine

3-FA’s significance in research lies primarily in its structural distinctiveness and analytical clarity. Scientists utilize it to study:

• Structure–Activity Relationships (SAR): Understanding how fluorine substitution modifies electronic distribution.

• Chromatographic Retention Behavior: Comparing polarity and volatility with related compounds such as 2-FA and 4-FA.

• Spectral Fingerprinting: Enhancing identification accuracy in forensic chemical libraries.

• Thermal Stability and Reactivity: Observing the compound’s response to controlled temperature variations.

Because of its predictable and stable analytical behavior, 3-FA serves as a valuable model compound in the study of fluorinated amphetamines and other substituted aromatic systems.

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Physicochemical Properties and 3-FA analytical chemistry

The fluorine atom’s inclusion enhances molecular stability and impacts both chromatographic separation and mass spectral fragmentation, providing consistent analytical outcomes.

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Comparative Analytical Behavior: 2-FA, 3-FA, and 4-FA

Researchers frequently compare fluorinated amphetamine isomers to understand how the fluorine’s position on the benzene ring affects the compound’s physical and analytical behavior.

3-FA’s meta-substitution gives it intermediate properties, making it ideal for comparative chromatography and spectral analysis research.

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Research Significance in Forensic Chemistry of high purity 3-Fluoroamphetamine

In forensic and toxicological studies, compounds like 3-FA serve as reference materials for method validation, spectral matching, and chemical classification. Its consistent analytical pattern supports:

• Calibration of detection instruments (GC-MS, LC-MS)

• Expansion of forensic spectral databases

• Improvement of compound differentiation algorithms

Through its reproducible chemical signature, 3-FA enhances method reliability and standardization in forensic science.

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Storage and Laboratory Handling To buy 3-FA pellets online

Proper storage conditions are essential for maintaining the integrity and reproducibility of analytical results.
3-FA Pellets (50 mg) should be:

• Stored in a cool, dry environment, protected from direct sunlight.

• Kept in airtight containers to prevent moisture absorption.

• Labeled and logged under controlled inventory conditions.

All research and analytical handling must adhere to local laboratory safety regulations, ensuring sample traceability and compliance with standard research protocols.

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Spectroscopic Reference Data Compilation of lab tested 3-FA for sale

Advanced laboratories often compile multi-spectral databases that include 3-FA’s:

• GC-MS retention times and ion fragmentation patterns

• FT-IR absorbance spectra for C–F and amine groups

• ¹H/¹³C NMR chemical shifts and coupling constants

• UV-Vis absorbance data for aromatic resonance analysis

These datasets form the backbone of compound recognition systems, improving automated identification accuracy across analytical networks.

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Future Research Directions of 3-FA fluorinated amphetamines

Current trends in fluorinated amphetamine research are evolving with the integration of digital and AI-driven analytical tools. 3-FA remains a compound of focus for future developments in:

• Machine-learning based spectral identification systems

• High-resolution mass spectrometry calibration

• Isomer differentiation algorithms

• Comparative electronic property modeling

As computational chemistry advances, compounds like 3-FA will continue to support the development of predictive analytical models and automated detection frameworks.

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Conclusion of 3-FA analytical chemistry

3-FA (3-Fluoroamphetamine) represents a cornerstone in the analytical exploration of fluorinated amphetamines. Its molecular structure, spectral clarity, and consistent performance under laboratory conditions make it invaluable for analytical, forensic, and educational research.

By studying 3-FA through GC-MS, FT-IR, NMR, and UV-Vis techniques, scientists can expand their understanding of fluorine substitution effects, improve detection methods, and build stronger analytical frameworks for future compound identification.

As research continues to evolve, 3-FA’s role as a benchmark in fluorinated amphetamine analysis ensures its lasting relevance in the fields of 3-FA analytical chemistry and molecular characterization.