2C-B-FLY Pellets 10mg

buy 2C-B-FLY pellets online: Analytical Chemistry Overview, Structure, and Research Applications

Introduction

Among modern analytical reference materials, 2C-B-FLY has captured significant scientific interest for its unique benzodifuran ring system and complex molecular behavior. Classified within the 2C family of substituted phenethylamines, 2C-B-FLY (chemically known as 8-bromo-2,3,6,7-benzodifuranethylamine) represents a rare fusion of phenethylamine and benzodifuran frameworks.

In the laboratory, 2C-B-FLY Pellets (10 mg) serve as a consistent form for controlled analysis and molecular characterization. Through its intricate structure, researchers can investigate structure–activity relationships (SARs), spectral identification, and chromatographic properties that distinguish it from other 2C analogs.

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Chemical Identity and Molecular Formula of high purity benzodifuran compound

The defining feature of 2C-B-FLY is its bicyclic benzodifuran ring, fused to the traditional phenethylamine backbone and substituted with a bromine atom at the 8-position.

• IUPAC Name: 8-Bromo-2,3,6,7-benzodifuranethylamine

• Molecular Formula: C12H10BrNO2

• Molecular Weight: 296.12 g/mol

• Chemical Class: Substituted Phenethylamine (Benzodifuran derivative)

• Functional Groups: Aromatic ring, primary amine, ether linkages

This complex configuration influences its spectroscopic and chromatographic behavior, allowing for precise differentiation in analytical environments with 2C-B-FLY pellets for sale

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Analytical Characterization and Methods of Identification

Due to its sophisticated structure, 2C-B-FLY is studied using several complementary analytical techniques. Each provides a layer of verification and insight into the molecule’s properties and stability.

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

In GC-MS analysis, 2C-B-FLY demonstrates a unique fragmentation pattern influenced by its fused ring system and bromine substitution. The molecular ion peak is readily identifiable, and its retention time differs significantly from related 2C compounds such as 2C-B or 2C-E.
This distinct spectral signature makes GC-MS one of the most effective tools for compound verification and purity assessment.

2. Fourier Transform Infrared Spectroscopy (FT-IR)

FT-IR spectroscopy reveals multiple characteristic absorption bands linked to the C–O–C ether bridges of the benzodifuran structure. Key absorbance peaks are typically observed around 1100–1300 cm⁻¹ (C–O stretching) and 1500–1600 cm⁻¹ (aromatic C=C vibrations).
These spectral markers serve as definitive identifiers when differentiating 2C-B-FLY from other lab tested benzodifuran derivatives.

3. Nuclear Magnetic Resonance (NMR) Spectroscopy

In ¹H and ¹³C NMR, the benzodifuran moiety produces complex splitting patterns. The presence of bromine causes chemical shift deshielding effects, confirming its substitution site.
NMR provides detailed atomic connectivity data, essential for confirming molecular structure, purity, and isomeric integrity.

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Physical and Chemical Properties of 2C-B-FLY analytical chemistry

These physical properties contribute to 2C-B-FLY’s predictable analytical performance, allowing reproducible results across laboratories.

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Analytical Significance and Research Applications of lab tested benzodifuran derivatives

The scientific relevance of 2C-B-FLY extends well beyond its structure — it serves as a benchmark compound for understanding how ring fusion and halogenation affect electronic and molecular behavior.

Researchers employ 2C-B-FLY in various analytical studies to:

• Examine fluorination and bromination effects on electron density distribution.

• Compare chromatographic mobility among the 2C analog family.

• Develop mass spectral databases for halogenated phenethylamines.

• Explore structure–property correlations within benzodifuran derivatives.

Because of its well-defined molecular architecture, 2C-B-FLY is ideal for method validation, spectral calibration, and compound identification training in forensic laboratories.

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Spectral Analysis Insights of 2C-B-FLY pellets for sale

GC-MS Findings

The GC-MS fragmentation spectrum of 2C-B-FLY exhibits predictable ionization pathways. The bromine isotope peaks (m/z 79 and 81) appear distinctly, confirming halogen substitution. The difuran ring contributes to a stable base ion peak, distinguishing it from other 2C derivatives.

FT-IR Observations

Infrared analysis identifies C–O–C asymmetric stretches, aromatic ring modes, and amine N–H vibrations, offering multiple verification points for compound identity.

NMR Observations

The NMR spectrum provides an in-depth structural confirmation. Proton signals on the aromatic ring are shifted due to bromine’s inductive effects, while ¹³C NMR reveals deshielding in the benzodifuran carbons, consistent with the fused ring system.

These results together form a robust analytical fingerprint for 2C-B-FLY.

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Comparative Analysis: 2C-B-FLY vs. 2C-B

While 2C-B and 2C-B-FLY share the same bromine substitution, their core structures differ dramatically. The benzodifuran fusion in 2C-B-FLY significantly enhances its molecular rigidity and electron delocalization, altering its spectral characteristics.

This comparison highlights why 2C-B-FLY remains an essential compound for advanced analytical chemistry and forensic reference studies.

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Laboratory Handling and Storage Methods To buy 2C-B-FLY pellets online

For consistency in analytical outcomes, 2C-B-FLY Pellets (10 mg) should be stored in airtight containers, protected from light and moisture. The compound maintains stability under room temperature if stored in a dry, cool environment.
All handling must comply with standard laboratory safety protocols, including the use of gloves, goggles, and fume hoods when preparing samples for spectroscopic or chromatographic analysis.

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Applications in Forensic and Analytical Research

2C-B-FLY’s precise structure and unique spectral identity make it a valuable reference material for multiple fields of research:

• Forensic chemistry: Development of GC-MS and LC-MS detection libraries.

• Academic research: Comparative structural and electronic studies.

• Analytical method development: Validation of new chromatographic separation techniques.

• Spectroscopic calibration: Benchmarking spectral instruments for halogenated compounds.

Its stability and reproducibility make it suitable for long-term analytical reference, ensuring consistency in data collection across laboratories worldwide.

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Future Research Directions of 2C-B-FLY analytical chemistry

Ongoing research into benzodifuran-based compounds like 2C-B-FLY continues to enhance our understanding of heterocyclic aromatic systems and halogen substitution effects.
Emerging analytical techniques, such as high-resolution time-of-flight mass spectrometry (TOF-MS) and AI-based spectral recognition, are improving the accuracy of compound identification and comparison.

Future studies aim to expand digital spectral libraries, enabling automated compound classification and machine learning–assisted forensic identification — areas where to buy 2C-B-FLY pellets online plays a crucial foundational role.

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Conclusion To 2C-B-FLY analytical chemistry

2C-B-FLY (8-Bromo-2,3,6,7-benzodifuranethylamine) stands as one of the most structurally intricate and analytically significant members of the 2C family. Its fused benzodifuran ring system, halogen substitution, and distinctive spectral profile make it invaluable to modern forensic, analytical, and academic research.

Through analytical techniques such as GC-MS, FT-IR, and NMR, scientists continue to uncover the intricate behaviors of 2C-B-FLY, contributing to a deeper understanding of structure–activity relationships, molecular reactivity, and spectral differentiation in substituted phenethylamines.

The high purity benzodifuran compound stability, reproducibility, and unique analytical fingerprint ensure its continuing relevance in chemical identification and reference material development across global research networks.