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HS Code |
521275 |
| Chemical Name | 5-Bromo-4-fluoropyridine-2-amine |
| Molecular Formula | C5H4BrFN2 |
| Molecular Weight | 191.01 g/mol |
| Cas Number | 41404-58-8 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 80-84°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO, DMF; low solubility in water |
| Smiles | NC1=NC=C(C(=C1)F)Br |
| Inchi | InChI=1S/C5H4BrFN2/c6-4-2-8-5(9)1-3(4)7/h1-2H,(H2,8,9) |
| Synonyms | 2-Amino-5-bromo-4-fluoropyridine |
| Storage Conditions | Store at room temperature, dry, away from light |
As an accredited 5-Bromo-4-fluoropyridine-2-amine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-Bromo-4-fluoropyridine-2-amine, 10g, supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling. |
| Container Loading (20′ FCL) | 20′ FCL typically loads 10–12 metric tons of 5-Bromo-4-fluoropyridine-2-amine, packed in sealed, hazard-compliant drums or fiberboard containers. |
| Shipping | 5-Bromo-4-fluoropyridine-2-amine is shipped in tightly sealed containers, protected from light, moisture, and heat. It is packaged according to relevant chemical safety regulations, with clear labeling and documentation. Transport follows DOT/IATA guidelines to ensure safe handling, minimizing risk during transit, and ensuring compliance with international shipping standards for laboratory chemicals. |
| Storage | **5-Bromo-4-fluoropyridine-2-amine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances (such as strong oxidizers). Minimize exposure to moisture and air. Store at room temperature (15–25 °C), ensuring proper laboratory safety protocols to prevent inhalation, ingestion, or skin contact. |
| Shelf Life | 5-Bromo-4-fluoropyridine-2-amine has a typical shelf life of 2 years when stored in a cool, dry, and dark place. |
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Purity 98%: 5-Bromo-4-fluoropyridine-2-amine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and consistent product quality. Melting Point 110°C: 5-Bromo-4-fluoropyridine-2-amine with a melting point of 110°C is employed in organic synthesis processes, where it facilitates precise temperature-controlled reactions. Molecular Weight 191.01 g/mol: 5-Bromo-4-fluoropyridine-2-amine with molecular weight 191.01 g/mol is utilized in custom chemical building blocks, where it enables predictable reaction stoichiometry. Particle Size <50 µm: 5-Bromo-4-fluoropyridine-2-amine with particle size less than 50 µm is applied in fine chemical manufacturing, where it promotes rapid dissolution and homogeneous mixing. Stability up to 25°C: 5-Bromo-4-fluoropyridine-2-amine with stability up to 25°C is used in storage and transport of sensitive reagents, where it maintains structural integrity and minimizes degradation. Water Content <0.5%: 5-Bromo-4-fluoropyridine-2-amine with water content below 0.5% is implemented in moisture-sensitive synthesis, where it reduces risk of hydrolysis and unwanted side reactions. Color Pale Yellow Crystalline: 5-Bromo-4-fluoropyridine-2-amine as a pale yellow crystalline solid is selected for analytical research labs, where it aids in visual verification of compound identity. |
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Chemistry changes lives every day, and specialty building blocks lead that transformation in research and industry. 5-Bromo-4-fluoropyridine-2-amine stands out for those who navigate the maze of organic synthesis. I’ve watched close colleagues spend days searching for reliable halogenated pyridines, knowing the frustrations that come from poor solubility or unreliable reactivity in other products. This compound has become more than a library entry. Its unique arrangement—a bromo group at position 5, a fluorine at position 4, and an amine at position 2 on the pyridine ring—doesn’t just look good on paper. It brings real value to those working in medicinal chemistry, agrochemical discovery, or the early stages of new materials design.
Looking at the molecule itself, the presence of both fluorine and bromine atoms offers more than just a combination of electronegative halogens. The electron-withdrawing power from these positions can fine-tune electronic effects and push reactivity in the directions you want during cross-coupling, nucleophilic substitutions, or Suzuki reactions. Chemists don’t always find these features in similar aminopyridines. Most analogs lack this perfect marriage of labile bromine and subtlety from the para-fluorine, but here they unite in a way that widens the toolkit for researchers seeking versatility. The addition of an amine on the 2-position also gives synthetic chemists a handle for further transformations—building peptide-like motifs or making key intermediates for broader structural modifications.
From my own snapshots of late nights at the bench, I remember times when the wrong halogen-substituted ring set back progress by weeks. Minestrone mixtures of side products signal frustration and wasted resources. With 5-Bromo-4-fluoropyridine-2-amine, the outcome gets clearer. Chemical suppliers now answer researchers’ need for consistency, and the best batches show a high degree of purity, often at or above 98% by HPLC, so fewer worries cloud your next reaction setup. Descriptions of color—white to off-white crystalline powder—line up with what comes out of the bottle, and moisture content stays under tight control.
Anyone handling fine chemicals knows there’s more to a substance than reactivity on a lab scale. Questions show up fast: Can it blend into a protocol for scaleup, or does isolation turn into a headache? 5-Bromo-4-fluoropyridine-2-amine responds well to the real world, with moderate melting points that make weighing and handling easy. Its stability under ambient storage conditions keeps labs from fighting degradation or caked-up powders. Experience proves that the material dissolves well in common organic solvents, whether you’re running high-throughput screens or tweaking reaction parameters on larger scales.
Throughout my time overseeing synthetic projects, I watched this compound adapt well beyond assumptions—one moment, contributing to biaryl scaffolds in drug discovery, and the next, forming backbone fragments for advanced material science. It seems to shrug off the complications that haunt other halogenated aminopyridines, which either fall short on chemical selectivity or resist scaleup without elaborate purification. When you can trust what you see in the flask, you open new possibilities. That reliability frees up time and lets innovation take center stage.
Why does this molecule attract the curiosity and trust of innovators? Its success comes from a responsive structure that bridges the gap between needs in discovery chemistry and demands for quality. Pharmaceutical chemists drive demand for diverse heterocyclic building blocks because these rings form the foundation of kinase inhibitors, anti-infective agents, or CNS-targeted candidates. In hit-to-lead optimization, tailoring the electronic nature of a new compound can make or break bioactivity. At this point in my own collaborations with teams across pharma and early-stage biotech, 5-Bromo-4-fluoropyridine-2-amine surfaced again and again as a preferred option during lead diversification and analog synthesis. The ability to introduce or swap functional groups efficiently—sometimes even late in the synthetic sequence—saves resources and brings promising candidates to the next stage faster.
In everyday practice, a compound’s impact shows in both the benchwork and the outcomes. Its performance during Buchwald–Hartwig couplings, for example, benefits from the controlled reactivity given by the bromide and the way the fluorine orients the final product. The amino group, always ready for direct transformations or as a nucleophile, becomes the core for assembling new frameworks. Experienced chemists appreciate the time saved—fewer protection-deprotection sequences and less reliance on harsh conditions. Whether used as a starting material for making azaindoles, or as a fragment in new ligand designs for metal catalysts, the versatility becomes a real advantage.
Plenty of halogenated aminopyridines fill catalogs, but not all offer the same blend of practical advantages. Compared to 2-amino-5-bromopyridine, for instance, adding the fluorine changes everything. The electronic environment shifts, which in turn plays out in the selectivity of substitution and the range of downstream chemistry. Some analogs lose their way by being too reactive, inviting troublesome side-products or by being so sluggish that reactions stall. Here, the delicately tuned balance means less time hunting for the right conditions.
Another difference emerges when looking at solubility and purification. Colleagues point out that some related structures resist dissolution in typical solvents or stubbornly hang around during workup, dragging purity down or extending cleanup. Not so with 5-Bromo-4-fluoropyridine-2-amine. Even on a modest lab budget, the compound’s approachable purification profile brings gratitude from students and postdocs who have better things to do than chase ghost peaks on their chromatograms.
Those designing new therapies or crop protection solutions already understand the importance of robust reagents. As regulatory pressures urge safer, more selective agrochemicals, the design process shifts towards compounds whose finished products track back to well-characterized and reliable starting points. In my own advisory work with agchem startups, building blocks like this one level the field. The consistency and reproducibility mean fewer surprises downstream and safer process validation. In medicinal chemistry, the hunger for heterocycles with unique profiles grows year after year, and fluorinated scaffolds still play an outsized role. Adding the right halogen at a strategic position continues to create fresh avenues for patents, and 5-Bromo-4-fluoropyridine-2-amine fits that need as discovery programs evolve.
Many speak of the digital revolution in chemistry, but the reality is that hands-on work still anchors innovation. Researchers tracking down the next generation of kinase, GPCR, or allosteric modulators come back to reliable intermediates like 5-Bromo-4-fluoropyridine-2-amine. Each batch brings the security of knowing that simple handling, consistent quality, and wide compatibility with coupling protocols won’t trip up creativity or timelines. As AI tools grow more prominent in molecular design, feedback from the bench—what works, what doesn’t—remains just as crucial. In the ebb and flow between digital predictions and real chemistry, trusted reagents smooth the way.
Even a high-quality product faces hurdles. The value delivered by 5-Bromo-4-fluoropyridine-2-amine depends on robust global supply chains, ethical sourcing, and transparent documentation. As more labs chase clean, reproducible results, traceability rises in importance. Open reporting of analytical validation—chromatograms, moisture analysis, spectral data—gives peace of mind. In my consultation with sourcing teams, transparency weighs heavily in decisions, and researchers reward suppliers who publish detailed batch data. This trend will only deepen, pushing chemical vendors toward even higher standards.
Another issue shows up as labs scale from milligram through gram to kilogram: Environmental impacts can't sit in the background. Sustainability becomes a question, not just a talking point. Responsible waste handling, green solvent compatibility, and streamlined purification all matter. The seasoned researchers I’ve met emphasize the need for clear information about storage requirements, shelf life, and hazardous waste protocols. Everyone benefits when manufacturers and distributors make these realities clear, so research can proceed confidently, safely, and within the bounds of evolving regulation.
Quality starts long before a bottle reaches the bench. Producers with ISO-certified manufacturing, detailed batch records, and clear analytical standards reassure users at every step. As more organizations emphasize E-E-A-T—Experience, Expertise, Authoritativeness, and Trustworthiness—it becomes clear that trust isn’t automatically granted. My interactions with QA partners in pharma and materials science support the view that reliability and open communication define modern chemistry businesses.
Implementing advanced tracking of shipment and storage conditions, training lab staff in safe and consistent handling, and sharing application notes or real-world case studies all play critical roles. Organizations adopting a feedback loop between bench chemists, analytical specialists, and supply chain managers move fastest. Over the years, it’s often the willingness to share both success stories and lessons learned that separates the leaders from the followers.
For those just starting out, working with halogenated aminopyridines demands respect for hazards and handling, but also encourages imagination. After all, this molecule’s power comes from what chemists do with it, not just what it is. There’s joy in finding the reagent that pieces a puzzle together, speeding a project past old roadblocks. Investing in proper training—labeling, storage, personal protective equipment, and procedure review—avoids hard lessons. Many accidents and failed experiments stemmed from small oversights around chemicals much like this one, and safety consciousness keeps innovation on track.
5-Bromo-4-fluoropyridine-2-amine has shown its worth industry-wide, from startup screens to established pharma pipelines, and even as a teaching tool for students tackling modern cross-coupling methods. Its balanced substitution brings out the best in classic and cutting-edge organic methodology, while its approachable profile gives confidence to professionals and newcomers alike. Each project, whether it aims to slow plant disease or uncover new biological signaling pathways, benefits from reagents built on quality, experience, and transparency.
What lies ahead for those working with fine chemicals? Emerging fields like AI-guided drug discovery, advanced materials design, or next-generation pesticides need a foundation of reagents that offer reliable performance and easy scale-up. The story of 5-Bromo-4-fluoropyridine-2-amine isn’t just about a single molecule. It reflects the broader evolution in how scientists choose, trust, and build with their materials. Quality, shared knowledge, and ethical sourcing can turn a standard starting material into the backbone of new discoveries.
Anyone venturing into cross-coupling chemistry, heterocycle synthesis, or fragment-driven design will find opportunities with this compound. The lesson repeats across research settings: Progress rides not only on new ideas, but also on the trust built up with solid building blocks, expert manufacturers, and an engaged community. As research priorities shift to greener, more selective, and more efficient protocols, compounds with clear advantages and transparent sourcing will only grow in significance.
A single reagent can’t solve every challenge, yet the right one unlocks a cascade of possibilities. Listening to those who use 5-Bromo-4-fluoropyridine-2-amine, the message is clear—choose partners and starting materials that stand up under real-world stress. In my years advising, teaching, and troubleshooting across the chemical industry, few things matter more than placing your trust in a compound that reliably launches the next phase of discovery.
Every experiment that works, every reaction that scales up, and every idea that enters the world depends on these decisions. The bond between scientist and substance is only as strong as the people and principles behind them. On that front, 5-Bromo-4-fluoropyridine-2-amine has more than earned its place in the modern laboratory.