|
HS Code |
780890 |
| Name | 3-Chloro-5-bromopyridine |
| Chemical Formula | C5H3BrClN |
| Molecular Weight | 208.44 g/mol |
| Cas Number | 182442-43-3 |
| Appearance | Pale yellow to brown crystalline solid |
| Boiling Point | 243-245 °C |
| Melting Point | 49-52 °C |
| Density | 1.80 g/cm³ (at 25°C) |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
| Refractive Index | 1.615 (estimated) |
| Smiles | C1=CC(=CN=C1Cl)Br |
| Inchi | InChI=1S/C5H3BrClN/c6-4-1-2-8-5(7)3-4/h1-3H |
| Synonyms | 5-Bromo-3-chloropyridine |
As an accredited 3-Chloro-5-bromopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "3-Chloro-5-bromopyridine, 25g", with hazard symbols, tightly sealed, and tamper-evident cap. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 3-Chloro-5-bromopyridine: securely packed in 200 kg drums, totaling approximately 80 drums per container. |
| Shipping | 3-Chloro-5-bromopyridine is typically shipped in tightly sealed containers to protect against moisture and contamination. It is classified as a hazardous material and must be transported in accordance with local, national, and international chemical shipping regulations, including adequate labeling. The chemical should be kept away from incompatible substances during transit. |
| Storage | 3-Chloro-5-bromopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container protected from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent leaks or spills. Handle with appropriate personal protective equipment. |
| Shelf Life | 3-Chloro-5-bromopyridine has a shelf life of at least 2 years when stored in a cool, dry, airtight container. |
|
Purity 99%: 3-Chloro-5-bromopyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures enhanced reaction specificity and yield. Melting Point 64–67°C: 3-Chloro-5-bromopyridine with a melting point of 64–67°C is used in fine chemical manufacturing, where controlled melting behavior supports efficient solid-state processing. Molecular Weight 192.45 g/mol: 3-Chloro-5-bromopyridine with molecular weight 192.45 g/mol is used in agrochemical development, where precise dosing and formulation are facilitated. Stability Temperature up to 120°C: 3-Chloro-5-bromopyridine with stability temperature up to 120°C is used in catalyst research, where thermal stability preserves compound integrity during high-temperature reactions. Particle Size <20 µm: 3-Chloro-5-bromopyridine with particle size less than 20 µm is used in advanced material applications, where fine dispersion promotes uniform blending and surface reactivity. Moisture Content <0.5%: 3-Chloro-5-bromopyridine with moisture content below 0.5% is used in electronics material synthesis, where low moisture prevents hydrolysis and enhances product reliability. Assay ≥98.5%: 3-Chloro-5-bromopyridine with assay not less than 98.5% is used in pigment precursor production, where consistent assay ensures reproducible color strength and quality. |
Competitive 3-Chloro-5-bromopyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Chemicals like 3-Chloro-5-bromopyridine do their work mostly in the background, yet they touch daily life more than most of us realize. People who spend time in research labs quickly learn that every new drug, pigment, or advanced material usually depends on these unsung heroes. Take a step away from the glossy headlines about new medicines and think about the scaffold upon which such discoveries rest; often, it’s intermediates such as 3-Chloro-5-bromopyridine providing that foundation.
I started out in the lab thinking everything important had to glitter with promise. Over time, I learned key differences are often found not just at the top of the value chain but down where meticulous synthetic work happens. The clean geometry of a pyridine ring, halogenated at strategic points, offers more than a straightforward substrate. 3-Chloro-5-bromopyridine has won respect among chemists as a reliable intermediate in making pharmaceuticals, crop protection agents, and specialty materials. Its presence in synthetic routes supports the assembly of larger, more complex molecules. Without it, many transformations just don’t work as efficiently or cleanly. The combination of the chloro and bromo substituents means the compound sits perfectly for selective reactivity; chemists get balance and flexibility without compromising on yield, a feature colleagues in process chemistry talk about all the time.
3-Chloro-5-bromopyridine carries a blueprint for reliability in advanced synthesis. I've seen time and again that one of the halogens—either bromine or chlorine—serves as an excellent leaving group in cross-coupling reactions. Imagine palladium-catalyzed Suzuki or Buchwald–Hartwig couplings; the bromine leaves, new functional groups slide into place, and the work proceeds. In the same molecule, the other substituent hangs on, providing chemists with a handle for the next critical step. This strategic difference is not a trivial upgrade—it's the sort of detail that marks the difference between an easy, scalable synthesis and one bogged down by low yields or too many byproducts.
Compare 3-Chloro-5-bromopyridine to analogs like 3-bromopyridine or 3-chloropyridine and the advantages become practical, not abstract. With just one halogen, selectivity can get tricky—sometimes, you burn a lot of time protecting and deprotecting parts of your molecule, juggling reactivity, and managing side reactions. The dual-substituted scaffold saves this trouble and opens easier multi-step routes, especially in pharmaceutical manufacturing, where every wasted hour or impure run costs money and, more importantly, time in delivering solutions to those who need them. As a result, this compound fits into an expanding class of halogenated heterocycles designed for targeted reactivity—a simple adjustment in bench synthesis but a huge leap in process efficiency.
Scientists, both in academic and industrial circles, debate purity and consistency just as heatedly as end-results. People who source 3-Chloro-5-bromopyridine care about knowing that every batch delivers the same performance. Days in the lab have convinced me that variability in starting materials always catches up later. Specifications often hold the spotlight: chemical purity should not dip below 98%, moisture and residual solvents must remain tightly controlled, and no one wants traces of metal or other byproducts lingering in their flask. These are not arbitrary values; they translate directly into cleaner reactions, smoother workups, and lower costs in downstream purification.
Reliable suppliers now provide 3-Chloro-5-bromopyridine with these strict markers in mind. The industry moved past the days of “good enough.” Smart sourcing managers ask for supporting analytical data—NMR, HPLC, GC-MS reports—since even small shifts in impurity profiles can damage a synthetic pathway or upset biological systems later down the chain. Whenever I've joined discussion panels, one recurring pain point is precisely this: a mismatch between what’s on the label and what’s in the bottle. Investing time up front to check the integrity of intermediates like this one prevents headaches and extra costs once the project really gets rolling.
At a research level, the attention on 3-Chloro-5-bromopyridine has increased as more teams focus on making smaller, more precise libraries of compounds. Pharmaceutical chemists prefer intermediates that fit into modular synthesis, so they can swap out side groups and tune bioactivity while preserving the molecular core. This approach, structure-activity relationship (SAR) studies, speeds up the identification of promising leads and, ultimately, the path toward testing new drugs.
Agrichemical research benefits in similar ways. Modern crop protection relies on selective agents—compounds effective at targeting pests without spilling over into unwanted environmental harm. Many of the best new candidates are built on halogenated pyridines, because their structure gives predictable biological function and robust stability in the field. Speaking to colleagues, I keep hearing how halogenation patterns tip activity toward efficacy or target selectivity. For a laboratory or manufacturing line, this means fewer steps spent tailoring the base molecule, and more focus on innovation and final formulation.
In electronics, advanced materials, and dyes, fine-tuning optical properties or charge transport demands unique building blocks. 3-Chloro-5-bromopyridine makes the short list because the substituents can be exchanged cleanly for aryl, alkyl, or other functional groups. Over the years, I’ve seen that reliable coupling reactions give chemists the power to explore properties like fluorescence, conductivity, or photostability in new ways. Rather than labor over custom synthesis from scratch, labs can jump into creative territory more quickly.
Chemicals with both chlorine and bromine atoms automatically confront scrutiny—especially as global regulations on halogenated substances get stricter. Responsible handling starts at the bench and goes all the way to shipment and disposal. While the toxicity profile of pyridines is well-known, deliberate protocols keep risks at bay: personal protective equipment, good ventilation, strict attention to spill management, and careful storage away from heat or open flame are essentials. In industry, automated systems reduce direct exposure and closed-loop processes control emissions and waste.
Environmental impact matters even before the material reaches the consumer. Many manufacturers now shift closer to green chemistry approaches: higher atom economy, reduced use of hazardous solvents, and more energy-efficient purification steps. A few years back, I started seeing sustainability as not just a marketing buzzword but an operational necessity. Finding suppliers who document environmentally friendly practices builds confidence on both sides of the transaction—something scientists, procurement officers, and regulatory inspectors all appreciate.
Waste management presents its own challenges. Both brominated and chlorinated byproducts call for controlled incineration or chemical neutralization facilities, rather than casual dumping or sewer disposal. Professionals want to see a clear path for cradle-to-grave management. Speaking from experience, a supplier who stands behind solid environmental records rises to the top of every shortlist. Certificates of analysis matter just as much as proof of safe, conscientious disposal practices.
A closer look at published literature and patent filings drives home the growing use of 3-Chloro-5-bromopyridine across multiple sectors. Chemists cite it in synthetic work exploring kinase inhibitors, anti-cancer candidates, and enzyme blockers. Market data places halogenated pyridines in the growth phase for specialty intermediates, with incremental jump year after year as more applications come online for pharmaceuticals and agrochemicals. That trend reflects a feedback loop—better quality and more consistent supply encourages broader experimental use, which then builds into more robust demand.
Peer-reviewed studies reinforce how the differences in positional halogenation affect coupling yields, biological properties, and downstream modifications. For example, a switch in halogen position often stands between a low-potency and a high-potency candidate drug. The confidence in this intermediate also comes from wide compatibility with standard cross-coupling technologies; most chemistry students learn on Suzuki, Stille, or Negishi reactions, so using a well-behaved substrate eases the learning curve and powers new discoveries.
If productivity on the bench depends on fewer purification steps and higher yields, 3-Chloro-5-bromopyridine wins out over less functionalized pyridines. In practice, these advances translate into cost saving, more rapid lead optimization, and even a smaller environmental footprint—the fewer steps you run, the less waste, solvent, and energy you consume.
The difference between success in a small flask and success at manufacturing scale comes down to how forgiving a chemical is. I’ve learned that some starting materials tolerate a rare impurity at milligram scale, but those blips magnify unpredictably once the process moves to kilogram or ton production. Here, 3-Chloro-5-bromopyridine’s consistency supports both bench-scale discovery and full-scale process chemistry. Most companies working in pharma or specialty materials invest significant time upfront making sure their intermediates perform identically batch after batch.
Process chemists praise intermediates they can trust—batch-to-batch variation is more than an inconvenience, it’s a drag on productivity. With global supply chains under pressure, a reliable intermediate brings peace of mind. Every experienced chemist can recall costly setbacks from switching suppliers and discovering subtle differences in reactivity, solubility, or contaminant profile. By anchoring process development in standardized intermediates, teams avoid surprises and deliver projects on time.
I heard one operations manager say, “The right intermediate short-circuits troubleshooting down the line.” That goes for tech transfer, regulatory filings, and safety reviews. With 3-Chloro-5-bromopyridine, supply is supported by analytical reports, transparent sourcing, and documented handling procedures. As manufacturers tie quality to real-world performance, repeatable success brings new confidence in pushing synthetic boundaries.
Research on heterocyclic compounds shows no signs of slowing. Pharmaceutical pipelines fill with new candidates built on flexible, functionalized pyridine scaffolds. In this landscape, the advantage shifts toward intermediates like 3-Chloro-5-bromopyridine, which can handle both the operational needs of discovery chemistry and the tight margins of scale-up. Teams prize options that allow for quick adjustment—changing a bromo group for a thiol, replacing chlorine with an amine, attaching a bulky functional group, or switching to a fluorinated analog—all without rebuilding the entire synthetic route.
Sustainability raises the bar. Legislation and consumer awareness both drive chemists and sourcing managers toward greener processes, lower carbon footprints, and safer end-products. Suppliers who develop and document cleaner, safer production practices win wider market share. I talk with people inside and outside industry, and pressure mounts to cut down hazardous waste and streamline purification, which again speaks to the value of well-behaved, versatile intermediates.
Digital tools also play a growing role. Automated synthesis planning, machine-learning-driven route selection, and real-time supply chain tracking all favor starting materials with solid track records. A digitally documented COA, linked batch testing data, and automated regulatory-compliance logs now factor into big purchasing decisions—gone are the days when a handwritten assay sheet sufficed. Professionals trust data-backed sources, and those who offer transparent, up-to-date documentation attract more long-term partners.
The mark of a standout chemical comes not just from the certificate of analysis, but from the hours saved and problems avoided downstream. 3-Chloro-5-bromopyridine outpaces many alternatives precisely because users get to work quickly and reliably, not stuck managing legacy issues from inconsistent material. Flexible substitution lets researchers construct more varied libraries with less rework. In comparative terms, less functionalized versions introduce roadblocks, while more complex analogs push up costs and risk. Research progress slows down every time a new batch arrives that doesn’t deliver on expectations. Frequent communication with suppliers and solid reporting keep these troubles at bay.
Material handling sheds light as well. The compound’s manageable volatility and solubility mean typical good laboratory practices offer adequate safety. Compared to less stable analogs, 3-Chloro-5-bromopyridine stores and ships easily, cutting down on special handling costs. This makes a difference for small institutes and startups, who work with tight budgets and staff who carry out multiple roles. Scalability also matters; as a compound moves from small-lot synthesis to larger campaigns, its performance in simple, repeatable steps removes uncertainty and preserves limited resources.
With the landscape changing, professionals want more than just reliable supply. One persistent call is for wider access to granular analytical data, including impurity profiles traced to original lots. In my experience, this data should always ship alongside material, not as an extra or afterthought, since it saves time in project troubleshooting and regulatory filings. Supplier transparency becomes a form of risk management: everyone wants to avoid unexpected delays once high-profile projects reach clinical trial or pilot production.
Another challenge rests on the balance between availability and sustainable practices. The industry’s leaders focus on greener solvents, minimized byproduct streams, lower energy input, and closed-cycle solvent recovery. If I had a wish-list for future production of 3-Chloro-5-bromopyridine, it would include not only technical refinements but a broader shift to renewables and low-impact logistics.
Looking ahead, the real value to users will come from the combination of reliable, repeatable quality and open, proactive communication about changes at the source. As digital tools become easier to use, rapid, batch-level traceability should move from luxury to standard practice. Product sheets, batch COA, and shipping records can now move electronically. This means more time saved, fewer disputes settled after the fact, and airtight audit trails, which global regulatory trends demand.
At every step—from the research bench to mass production—those with hands-on experience in synthetic chemistry appreciate products that allow progress without repeated workarounds. 3-Chloro-5-bromopyridine, with its dual functionality, offers that edge. It’s a quiet workhorse that lets both seasoned professionals and newcomers deliver better results, faster.