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HS Code |
116467 |
| Product Name | 2-Bromo-5-Chloro-3-Hydroxypyridine |
| Cas Number | 159613-46-8 |
| Molecular Formula | C5H3BrClNO |
| Molecular Weight | 208.44 |
| Appearance | White to off-white solid |
| Melting Point | 98-102°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Conditions | Store at 2-8°C, in a tightly sealed container |
| Smiles | C1=C(C=NC(=C1Cl)O)Br |
| Inchi | InChI=1S/C5H3BrClNO/c6-4-2-8-3(7)1-5(4)9/h1-2,9H |
| Synonyms | 3-Hydroxy-2-bromo-5-chloropyridine |
As an accredited 2-Bromo-5-Chloro-3-Hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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If you spend any time in the world of fine chemicals, names like 2-Bromo-5-Chloro-3-Hydroxypyridine are more than just tongue-twisters—they’re useful, practical tools that keep labs and production lines moving. This compound, often recognized by its CAS number 78491-02-8, may not catch headlines, but its value runs deep for professionals chasing precision and efficiency in pharmaceutical and agrochemical research.
You notice the difference with this pyridine derivative not only in its structure, but in the consistency high-purity batches bring to scientific work. Its molecular formula—C5H3BrClNO—gives it a specific edge, letting chemists tap into both halogen and hydroxyl chemistry within a single scaffold. In my years running reactions for contract research projects, I learned that having both bromine and chlorine on the same ring provides a flexibility that saves more than time; it shores up confidence in downstream steps. That small change, just shifting a chlorine here or adding a bromine there, reshapes synthetic pathways dramatically.
Getting reliable outcomes depends on purity and traceability, something I’ve prioritized throughout my career. Analytical tools like NMR, HPLC, and GC-MS all trace the product’s integrity, helping us avoid unpleasant surprises. Most sources today deliver 2-Bromo-5-Chloro-3-Hydroxypyridine above 98% purity, and some go as high as 99%. Scrutiny of lot-to-lot reproducibility clears the path for both research and large-scale manufacturing. That kind of accountability builds trust, especially in regulated environments where a single impurity can lead to hours of troubleshooting.
Colleagues often ask me why certain compounds find broad application in R&D. This compound’s halogen pattern, with bromo at the 2-position and chloro at the 5-position, opens up unique cross-coupling possibilities. Suzuki and Buchwald-Hartwig couplings respond differently depending on placement and reactivity of these atoms. Whenever faced with a challenging target structure, I’ve seen this molecule serve as a launch pad, enabling cross-couplings that fizzle when using simpler 3-hydroxypyridines. Its dual halogen setup creates a springboard for multiple selective transformations, which cuts down the number of synthesis steps and saves valuable resources.
Not every intermediate offers the same utility. The distinct placement of both bromine and chlorine aside the reactive hydroxy group means chemists gain controlled activation points on the ring for further modification. While many pyridine derivatives end up as dead ends or require laborious protection-deprotection steps, this one invites exploration. In small-molecule discovery, that flexibility proves invaluable—I’ve seen speed bumps turn into fast lanes in more projects than I can count.
With tighter global regulations and ever-stricter benchmarks for new molecule approval, sloppy chemistry gets weeded out quickly. Consistency goes beyond just numbers on a COA; in my experience, subtle impurities can derail an entire synthetic program, and those issues often only become apparent with sensitive target compounds. The better suppliers today respond to this by using tighter control during recrystallization and drying, coupled with regular batch validation.
The real-world advantage of 2-Bromo-5-Chloro-3-Hydroxypyridine reveals itself in both batch and flow chemistry. In process development, where cost pressures and timelines drive every decision, I’ve spent more hours than I care to remember optimizing catalyst loads or troubleshooting purification issues. This compound, with its clear reactivity and predictable behavior, simplifies many complex methodological headaches. Its bromo function enables reliable palladium-catalyzed couplings, while the 5-chloro adds an orthogonal handle for further late-stage diversification or selective activation.
Plenty of pyridine-based intermediates line the shelves—2-bromo-3-hydroxypyridine, 5-chloro-3-hydroxypyridine, and countless others. Each brings certain perks, but the combined 2-bromo/5-chloro variation stands out when sites of substitution need to be managed carefully, or when selectivity is paramount. As a synthetic chemist, the greatest frustration often comes from protecting groups and additional sequences just to get a ring decorated correctly; this compound’s natural substitution pattern tackles that concern head-on. So for multi-step syntheses or programs demanding high throughput, the right pre-functionalized core saves weeks of effort.
Pharmaceutical innovators leverage this compound for its scaffolding potential. I’ve witnessed its use in assembling kinase inhibitors and anti-infectives. Small tweaks—swapping the halogen for larger or more exotic groups—can rapidly generate libraries for screening. In agrochemicals, scientists push for enhanced selectivity and safety in plant-protection products, and that exchange of substituents lets them experiment with off-target profiles and environmental breakdown rates. Innovation hinges on being able to make small, controlled changes with minimal fuss, and this molecule delivers that edge.
As demand increases, suppliers adapt production strategies and invest in robust safety data—something I appreciate after watching projects hit walls simply because supplies dried up or data transparency lagged. Reliable manufacturers today back up their quality with transparent analytics and ensure that documentation supports regulatory filings, which matters for both emerging start-ups and established multinational programs.
Working with this intermediate over years has taught me the importance of storage conditions and handling. Moisture and light can trigger unwanted hydrolysis or oxidation in sensitive heterocycles, so investing in well-sealed packaging and dry, low-light warehouses pays off down the line. By keeping stock fresh, chemists avoid unnecessary re-testing and maintain a smooth production run without those dreaded late-stage surprises.
Labs and commercial teams look for compounds that ease transitions from bench to pilot to plant. This molecule, thanks to its structural balance and availability, integrates into most automated synthesis platforms without major adaptation. Automation in chemical research grows in importance every year, and intermediates that behave consistently across varying scales and instruments smooth out the path from design to development. My own switch from manual to semi-automated synthesis ten years ago highlighted which compounds performed well—and this one earned its spot as a favorite of both the analytical and operations teams.
The rise of green chemistry and focus on sustainable processes shaped how suppliers and users treat reagents. Chlorinated and brominated intermediates require careful handling, both to guard operator safety and ensure waste is managed correctly. Training team members to respect hazards, coupled with sound use of fume hoods and good laboratory hygiene, reduces both health risks and environmental impact. Many firms now recover halide waste streams or invest in more benign halogenation alternatives, a trend I’ve seen accelerate as awareness grows and regulations tighten.
Using this compound taught me a few hard lessons about patience and foresight. Early in my career, I jumped the gun and scaled up a reaction before getting a solid read on its stability. Under mild basic conditions, the hydroxy group played tricks, sometimes competing in unexpected places. With time, I learned tricks for gentle deprotection and for purifying via column chromatography, and I respect just how subtle differences among similar intermediates can set a project up for smooth sailing or hours of troubleshooting.
Establishing strong analytical controls remains non-negotiable. I’ve made it a habit to benchmark every fresh lot by verifying proton NMR and comparing against established standards, both for spot-checking and for building a reference database. Minor discrepancies often trace back to residual solvents or oversight in final drying. Experienced suppliers take pride in full traceability—from starting material to finished bottle—and offer documentation that holds up to the scrutiny of strict regulatory agencies and IP filings.
Supply chain hiccups hurt downstream users most—no one wants to find a flagship compound can’t be resupplied, or that purity fluctuates between shipments. Over the years, I developed a short list of suppliers who consistently met not just regulatory requirements but also the unspoken expectations of seasoned chemists. Some rebuild their processes to minimize cross-batch contamination, others focus on ultra-clean glassware or advanced drying technology. Longevity in the business relies not just on price, but on delivering real, tested value with every package.
Researchers look beyond traditional applications for new possibilities. Recent years brought a surge of interest in pyridine-centered scaffolds for novel anti-cancer therapies, driven by the rising need for kinase modulation and targeted therapies. This compound’s substitution pattern offers more than a routine stepping stone—it lets medicinal chemists build complexity incrementally, designing compounds for better bioavailability or target specificity. Teams working on next-generation electronics or specialty dyes also find the ring system advantageous, since subtle electronic tweaks can lead to marked changes in device performance or pigment stability.
Keeping things running smoothly means not just buying reliable material, but also understanding how it interacts with other reagents and solvents. I’ve seen surprises—some pleasant, some not—when the compound forms unexpected complexes or resists dissolution in standard solvents. Careful adjustment of pH and controlled addition order, especially in multi-step one-pot reactions, improves yields and reproducibility, something anyone scaling up to kilogram levels truly appreciates.
More researchers tackle difficult targets with creative process chemistry, and this intermediate helps shorten tedious protection-deprotection routes. By thinking strategically about where to install each functional group, chemists transform what used to be multi-stage bottlenecks into streamlined syntheses. A few groups I know have leveraged the dual halogenation to create new macrocycles or polypyridyl ligands, stepping into areas like catalysis and advanced materials. As discovery platforms move faster, demand for such versatile intermediates won’t slow down anytime soon.
Global supply chains face shifting demands and shocks, from sudden tariffs to new environmental standards. As someone who’s monitored compliance shifts, I’ve noticed that suppliers who publish robust lifecycle data and invest in greener synthetic methods win more contracts and customer loyalty. In turn, chemists downstream trust intermediates produced responsibly—both for repeatable results and to meet regulatory approval under current frameworks.
With each wave of new drug or agrochemical development, easy access to trusted intermediates matters more than ever. Intellectual property stakes often mean selecting or even modifying intermediates for exclusivity, and reliable availability lets chemists experiment fearlessly. As teams emphasize efficiency, safety, and sustainability, the intermediates they pick must check all those boxes. Years in custom synthesis have made me value not just the chemistry, but the network that delivers it, and 2-Bromo-5-Chloro-3-Hydroxypyridine has certainly earned that trust for more than a few successful projects.
Science keeps moving forward, demanding faster, cleaner, and smarter ways to unlock new molecules. Products like 2-Bromo-5-Chloro-3-Hydroxypyridine, with their unique positional substitutions and reliable sourcing, enable breakthroughs in both early-stage discovery and scalable manufacturing. As automation, green chemistry, and precision medicine rise, flexible intermediates underpin whole industries of progress. The experiences of years spent poring over NMR spectra and optimizing reaction times shape my appreciation for such workhorses. More than just a reagent, this compound typifies the kind of reliable, value-driven chemistry that pushes boundaries, supports new discoveries, and helps teams deliver safer, more effective solutions to the world.