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HS Code |
519418 |
| Productname | 5-Bromo-3-fluoropyridine |
| Casnumber | 407-13-2 |
| Molecularformula | C5H3BrFN |
| Molecularweight | 175.99 |
| Appearance | Colorless to light yellow liquid |
| Boilingpoint | 188-190 °C |
| Density | 1.71 g/cm3 |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=CN=C1Br)F |
| Inchi | InChI=1S/C5H3BrFN/c6-4-1-5(7)3-8-2-4/h1-3H |
| Solubility | Soluble in organic solvents |
| Refractiveindex | 1.565 |
| Storage | Store in a cool, dry place |
As an accredited 5-Bromo-3-fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-Bromo-3-fluoropyridine is supplied in a sealed amber glass bottle, 25 grams, labeled with chemical name, purity, and safety information. |
| Container Loading (20′ FCL) | Container loading for 5-Bromo-3-fluoropyridine (20′ FCL): 8–10 metric tons, securely packed in drums, compliant with chemical safety regulations. |
| Shipping | 5-Bromo-3-fluoropyridine is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material and should be handled and transported according to local, national, and international regulations. Ensure proper labeling, use of secondary containment, and compatibility with packaging to prevent leaks and exposure during transit. |
| Storage | 5-Bromo-3-fluoropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container away from sources of ignition and moisture. Ensure storage conditions minimize exposure to air and humidity to maintain chemical stability and prevent decomposition. |
| Shelf Life | 5-Bromo-3-fluoropyridine is stable under recommended storage conditions; shelf life is typically 2-3 years when stored sealed, dry, and cool. |
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Purity 98%: 5-Bromo-3-fluoropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity levels. Molecular weight 176.98 g/mol: 5-Bromo-3-fluoropyridine with molecular weight 176.98 g/mol is used in agrochemical discovery, where its defined mass contributes to precise formulation development. Melting point 30–32°C: 5-Bromo-3-fluoropyridine with a melting point of 30–32°C is used in research-scale reactions, where easy solid-to-liquid transition facilitates efficient handling and dosing. Stability temperature up to 40°C: 5-Bromo-3-fluoropyridine with stability temperature up to 40°C is used in ambient storage applications, where it provides extended shelf-life and maintains chemical integrity. Particle size <100 µm: 5-Bromo-3-fluoropyridine with particle size less than 100 µm is used in automated pharmaceutical processing, where uniform dispersion and reaction rates are achieved. Water content <0.5%: 5-Bromo-3-fluoropyridine with water content below 0.5% is used in anhydrous synthesis reactions, where it prevents hydrolysis and preserves product quality. Assay ≥99%: 5-Bromo-3-fluoropyridine with assay of at least 99% is used in advanced material synthesis, where it assures reproducibility and minimizes side reactions. |
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5-Bromo-3-fluoropyridine entered my radar about a decade ago, fresh out of university when organic synthesis started to look less like a wall of confusing SMILES notations and more like a world of opportunity. This compound has since grown more common in labs designing new pharmaceuticals, crop protection agents, and advanced materials. 5-Bromo-3-fluoropyridine pushes new frontiers in synthetic chemistry, helping researchers bridge the gap between discovery and invention with more confidence and control.
The name says a lot about what’s going on at a molecular level. You get a six-membered pyridine ring—a familiar skeleton in chemical libraries—spruced up with bromine at position 5 and fluorine at position 3. Both halogen groups offer targetable handles that make this molecule stand out from plain pyridines or even other substituted versions. Chemistry has taught me that positions and substitutions matter; a single atom in the right spot will dictate not just how something reacts, but how it solves real research headaches.
In the field, I’ve seen the 5-bromo and 3-fluoro arrangement help craft new building blocks. Bromine acts as an excellent leaving group in cross-coupling reactions, transforming sluggish bonds into effective links. Fluorine delivers unique electronic characteristics and metabolic stability. This setup lets you push work past the limitations of standard halopyridines, sidestepping issues like rapid degradation or unmanageable reaction pathways.
There’s no cutting corners with chemical purity, and this fact hit home for me after spending days chasing down sources of contamination in a batch run. Any reputable source will offer 5-Bromo-3-fluoropyridine with a reliable purity benchmark, most typically at or above 98%. This isn’t just a number for a spec sheet—subtle impurities mess with yields, waste expensive catalysts, and skew biological testing results. The model CAS number, 407-10-7, helps researchers identify the molecule in global databases, ensuring clear and reproducible science.
Standard specifications usually describe the compound as a white to off-white crystalline solid, easily handled and stored in normal laboratory conditions. Unlike some finicky pyridines prone to discoloration or decomposition, batches of 5-Bromo-3-fluoropyridine from established suppliers resist the urge to turn yellow or degrade, letting project timelines glide rather than stall.
My first hands-on experience with 5-Bromo-3-fluoropyridine happened during an attempt to synthesize a lead compound for a kinase inhibitor series. Years later, that lesson sticks: reliable intermediates save time and effort across drug discovery, agrochemical research, and functional material projects. Modern medicinal chemists use this molecule to introduce the pyridine motif into candidate drugs, taking advantage of its precise reactivity profile. This approach gives medicinal projects a better chance to survive metabolic testing and patent scrutiny.
For those who work with Suzuki, Buchwald-Hartwig, or Sonogashira couplings, the bromine atom proves its worth every time. It reacts smoothly under normal or even slightly stubborn conditions, attaching aryl, alkynyl, or amine groups with impressive yields. The fluorine keeps metabolic breakdown under control, meaning researchers worry less about bioactivity vanishing after just one round of testing. Every synthetic chemist chasing a new scaffold or analog in lead optimization knows how valuable these properties become once timelines tighten.
It’s easy to lump halopyridines into one broad category of interchangeable reagents, but that idea quickly falls apart. 4-bromopyridine, for example, runs into more problems when used in complex cross-coupling pathways due to its electronic setup. 2-fluoropyridine won’t deliver the same activation site for robust coupling. 5-Bromo-3-fluoropyridine carves out its niche by balancing reactivity and control, letting researchers push ambitious programs without spending weeks tweaking reaction conditions.
Comparisons with other multifunctional intermediates show small changes make a big difference. Adding a fluoro atom at position 3 (compared to unsubstituted 5-bromopyridine) shifts the electron density, drawing down side-reactions and often boosting selectivity for targeted couplings. Older generation precursors without fluorine additions won’t compare for projects seeking improved metabolic stability or bioactive library diversity.
5-Bromo-3-fluoropyridine has made itself useful in every lab I’ve seen that values speed, reliability, and versatility. Classic cross-coupling chemistry gives it a home—the kind of workflow that appears in academic theses and industrial strategies alike. Medicinal teams in pharma push it as an intermediate in kinase and GPCR inhibitor development, taking advantage of the molecule’s unique profile to design potent, selective candidates. Crop protection researchers expand pyridine chemistries to improve selectivity and minimize off-target environmental effects, sometimes shaving months off optimization cycles.
Material science groups start with 5-Bromo-3-fluoropyridine as the root of new polymers or functionalized resins. Every time I talk to an engineer balancing performance and durability, they mention how a tailored pyridine backbone offers more control over key polymer characteristics like thermal stability, electronic conductivity, or adhesion strength. You get more than a simple chemical—work accelerates, and data comes back stronger and more actionable.
No molecule, even one as well-behaved as this, comes without its cautions. 5-Bromo-3-fluoropyridine earns its place in a well-ventilated chemical hood and gets the respect of standard PPE: gloves, goggles, dedicated containers. Years of vigilance taught me not to get lax, especially when handling halogenated aromatics. The compound handles long-term storage well under cool, dry conditions away from light, letting it sit on the shelf without drama or hazard.
Researchers who take safety seriously see fewer surprises—no unexpected decompositions, no storage-related surprises. Any spills clean up easily using conventional absorbents, no exotic protocols or panic-inducing hazards. Consistent labeling matters. Early on, careless labeling once cost me a week’s work; these days, containers stay clearly marked with CAS numbers, names, and date of receipt, keeping mixes safe and easy to trace.
Real research lives and dies on dependable building blocks. In my own experience, a temperamental intermediate will sabotage weeks of work, while a reliable one powers up creativity and risk-taking. 5-Bromo-3-fluoropyridine stands out because it fills an awkward gap—offering the high cross-coupling reactivity of a bromopyridine, tempered with the fine control and metabolic tweaks that fluoro groups provide. Researchers working on next-generation active ingredients in pharma or ag don’t just want off-the-shelf reagents; they lean on fine-tuned intermediates that open up unexplored structure-activity relationships.
The blend of synthetic utility and downstream stability means new projects can get to the proof-of-concept stage faster, testing more ideas with less wasted effort. Project managers and lab heads should recognize how the right intermediate nips inefficiency in the bud, translating directly to time and cost savings that show up on the balance sheet.
Medicinal chemistry has always demanded a deeper playbook. As resistance develops against classic treatments and patent space gets congested, new molecules must stand out. Fluorinated intermediates like 5-Bromo-3-fluoropyridine answer both calls—broadening the scope for analog synthesis and extending metabolic half-life, which raises the odds of success for every compound that enters the clinic. Not every group needs this specific reagent, but teams wanting to move from basic skeletons to more sophisticated frameworks will see big gains.
My peers in agrochemical research talk about growing pressure to deliver targeted protection without introducing legacy pollution to crops or soil. The fine-tuned reactivity of this compound lets them introduce new features into candidate pesticides, narrowing spectrums and reducing unintended effects. In this space, progress isn’t just faster—it’s smarter, supporting a leaner, greener R&D pipeline.
Any chemist who’s pulled a late-night TLC and found nothing but starting material understands how valuable reliable reactants become. Batch-to-batch consistency forms the backbone of any scale-up program. I’ve worked with various 5-Bromo-3-fluoropyridine samples across research and pilot programs; only those from recognized suppliers with transparent quality control deliver reproducible outcomes, saving both money and morale.
Researchers run better routes, avoid side-reactions, and gather cleaner data. Analytical teams rarely run into headaches during characterizations—NMR and LC-MS spectra reveal clean, predictable results. This isn’t just a backroom concern. Regulatory approval and IP protection both get easier when intermediates are robust and paperwork clean.
The chemical supply chain has felt more turbulence in recent years than ever before. Import restrictions, shifting regulatory landscapes, and quality scandals cast a long shadow over specialty reagent sourcing. Choosing 5-Bromo-3-fluoropyridine from a trusted network of production partners means fewer interruptions. The pandemic reinforced for every research team I know the importance of reliable channels and documented quality at every step.
Sourcing responsibly continues to be a crucial piece of success. Researchers and procurement teams examine supplier certifications, following programs that document ethical production and environmental stewardship. I remember navigating a shortage of high-purity halopyridines a few years back; relationships with reputable vendors, well-audited production, and full traceability proved invaluable.
Innovation doesn’t stop at a single building block. As more projects demand creative combinations and precisely tailored scaffolds, 5-Bromo-3-fluoropyridine takes on new life in the hands of inspired chemists. The ability to plug this molecule into fast, modular syntheses or slow, stepwise functionalizations lets scientists work on their terms. As regulatory bodies and customers alike push for safer, longer-lasting, and more efficient molecules in medicine and agriculture, intermediates like this will only grow in importance.
The landscape won’t stand still. Advancements in catalysis and discovery screening keep stretching the boundaries of what pyridine chemistries can achieve. In my collaborations with biotech startups and large research consortia, the push never stops for greener processes, faster optimization, and smarter material design. By leaning on the precision and adaptability of 5-Bromo-3-fluoropyridine, labs everywhere get a real edge.
Not every lab has immediate access to the compound, especially in regions with tight regulations or limited supplier footprints. Partnerships between research-focused suppliers and international distributors could help manage these bottlenecks. Digital supply chain tracking, with clear documentation for every lot and movement, reduces risk and bolsters trust—especially when shifting economic policies create volatility overnight.
Another hurdle appears at the intersection of pricing, purity, and sustainability. As global attention focuses on green chemistry, both researchers and suppliers explore more efficient routes to synthesize and purify 5-Bromo-3-fluoropyridine. Catalytic and continuous-flow techniques cut down on waste, boost atom economy, and improve energy usage. Groups like the ACS Green Chemistry Institute push for public-private partnerships, pilot programs, and knowledge sharing to keep raising the bar.
Educating young chemists and new lab members about the practical and strategic importance of reliable intermediates deserves more focus. Workshops, online seminars, and open-access research help spread best practices, closing gaps between academic and industrial settings.
Years ago, synthesizing a handful of analogs took weeks for even small libraries. Today, with the dependable building blocks provided by compounds such as 5-Bromo-3-fluoropyridine, progress moves a lot faster—collaborators pool resources, computational chemists model new scaffolds, and teams pivot quickly in response to new data. Reliable intermediates act as bridges, carrying projects from hope to reality.
Whether your work focuses on unearthing drug leads, advancing eco-friendly crop solutions, or designing next-gen composite materials, the real-world impact of choosing dependable intermediates deserves respect. Each time a new paper or patent emerges, there’s often an unsung chemical hero in the mix—one that let the research move forward without a hitch.
Science always asks for a blend of daring and discipline. Having worked alongside researchers who thrive on creative risk, I’ve seen the difference reliable chemistry makes. 5-Bromo-3-fluoropyridine represents a kind of quiet backbone—the tool that lets visionaries move confidently toward breakthroughs. As the research landscape keeps evolving, and demand for new active ingredients or functional materials spikes, having the right molecular springboard makes all the difference.
The compound doesn’t do the heavy lifting by itself; it hands control back to the people crafting each reaction and strategy. Better chemical building blocks let smarter solutions rise to the top. With a future full of more connected science, tighter timelines, and global collaboration, 5-Bromo-3-fluoropyridine will help teams respond to new problems and seize new opportunities.