|
HS Code |
488526 |
| Product Name | 5-Bromo-2-Iodopyridine |
| Chemical Formula | C5H3BrIN |
| Molecular Weight | 283.90 g/mol |
| Cas Number | 183437-25-8 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | 78-81°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Conditions | Store at room temperature, in a dry and well-ventilated place |
| Synonyms | 2-Iodo-5-bromopyridine |
| Smiles | C1=CC(=NC=C1I)Br |
| Inchi | InChI=1S/C5H3BrIN/c6-4-1-2-5(7)8-3-4/h1-3H |
As an accredited 5-Bromo-2-Iodopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of 5-Bromo-2-Iodopyridine, labeled with chemical name, purity, hazard warnings, and CAS number. |
| Shipping | 5-Bromo-2-Iodopyridine is shipped in tightly sealed containers, protected from light and moisture. It should be transported as a hazardous material according to local and international regulations, including UN identification and appropriate labeling. The chemical is typically shipped at ambient temperature, with documentation for safety and handling procedures included. |
| Storage | 5-Bromo-2-Iodopyridine should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Store at room temperature and handle using appropriate personal protective equipment (PPE), including gloves and eye protection, to minimize exposure and ensure laboratory safety. |
| Purity 98%: 5-Bromo-2-Iodopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized impurity formation. Melting Point 70°C: 5-Bromo-2-Iodopyridine at a melting point of 70°C is used in organometallic coupling reactions, where it provides efficient process temperature control. Molecular Weight 282.89 g/mol: 5-Bromo-2-Iodopyridine with molecular weight 282.89 g/mol is used in agrochemical development, where accurate compound dosing is critical for reproducibility. Particle Size ≤40 µm: 5-Bromo-2-Iodopyridine with particle size ≤40 µm is used in fine chemical manufacturing, where it promotes superior dispersion and reaction kinetics. Stability Temperature ≤25°C: 5-Bromo-2-Iodopyridine with stability temperature ≤25°C is used in storage of chemical libraries, where long-term compound integrity is maintained. |
Competitive 5-Bromo-2-Iodopyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Any chemist stepping into a synthesis lab today will recognize the unique fingerprint of halogenated pyridines in modern research and manufacturing. Over decades, our plant has worked hands-on with dozens of compounds. Out of this crowd, 5-Bromo-2-Iodopyridine stands out—not just in terms of its dual halogen substitutions, but because of how it pushes boundaries in both medicinal and electronic chemistry.
Our experience with 5-Bromo-2-Iodopyridine dates back to the surge in demand for versatile heterocyclic building blocks. As the industry began exploring deeper heteroaromatic substitutions, requests for this particular molecule increased. Every batch we’ve produced reflects not only precision, but a deep acknowledgment of what this molecule brings to synthesis.
At its core, 5-Bromo-2-Iodopyridine is a six-membered aromatic ring with a bromine at the fifth position and an iodine at the second. This precise arrangement does more than decorate the molecule with two heavy atoms. It offers selective reactivity not available in monosubstituted or non-halogenated pyridines. The iodine atom brings a more labile leaving group—critical for cross-coupling pathways. Meanwhile, the bromine stands ready for further tailored functionalization, often during late-stage modifications.
Those making active pharmaceutical ingredients need control at every step, especially when multi-step synthetic routes cross over. With 5-Bromo-2-Iodopyridine, the iodine’s reactivity speeds up Suzuki, Sonogashira, and Buchwald-Hartwig reactions. Chemists use this faster route whenever they want more yield per step or shorter cycle times. The bromine stays largely untouched until needed—a feature that simplifies purification and subsequent transformations.
We don’t cut corners during halogenation. Modern chemical manufacturing is all about reliable handling, efficient use of raw materials, and minimizing byproducts. Asking our team, they’ll describe how controlling temperature profiles during iodination goes hand-in-hand with precise addition of the bromine source. Each run draws on years of batch data, giving us confidence that every kilogram shipped matches promised purity and crystal structure.
5-Bromo-2-Iodopyridine isn’t a compound that will tolerate sloppy technique. Impurities at even low ppm levels can lead to catalyst poisoning during further transformations. So throughout our facility, we monitor every stage with a combination of in-line analysis and classic bench tests. Routine checks with NMR and HPLC ensure the substitution pattern hasn’t drifted, especially given the close reactivity of neighboring positions on the pyridine ring.
One of our largest clients specializes in kinase research. Their medicinal chemistry team shifted toward custom kinase inhibitors featuring pyridine cores, but found that monosubstituted pyridines limited their SAR studies. By feeding 5-Bromo-2-Iodopyridine into their workflow, they expanded their toolkit overnight—attaching diverse aryl groups at the iodine position in one step, then using the bromine handle for sumoylation-ready adjuncts. This kind of double substitution expands molecular diversity without requiring multiple protection-deprotection steps, which saves them time and resources.
On the electronics front, another customer sought a new ligand design. With our compound, they reported that the dihalogenated pyridine core allowed more predictable coordination to palladium and platinum metals. Direct evidence from their lab indicated improved catalytic lifetimes in OLED production—something that neither bromopyridine nor iodopyridine alone could deliver.
Most catalogs list melting point, purity, and molecular weight, but those are just factsheets. Our feedback from customers points to something deeper—batch-to-batch consistency. Twenty grams may sound trivial, but when the next series of vials comes from a different production day, yield consistency and impurity profiles remain the deciding factor for international buyers. In-house, we chase this challenge—no two upstream halogen sources behave the same, nor do trace metal residues always fall in line. Yet with disciplined process control and a refusal to let marginal material out the door, our shipments have given medicinal, agrochemical, and material science labs a new baseline of reliability.
In terms of solubility and shelf stability, the dual halogens actually ease storage for most users. Some strictly chlorinated pyridine derivatives degrade via ambient hydrolysis; our records show that 5-Bromo-2-Iodopyridine ships worldwide without incident, as long as the containers are kept dry and away from direct sunlight. Regular audits in our inventory show that even after six months, batches retain both color and melting point—a strong signal that our purification protocols work.
Experienced manufacturers know that not every dihalogenated pyridine behaves the same. We fielded multiple requests to substitute fluorine or chlorine for either halogen, yet each change in element brings a new set of physical properties and reaction challenges. In the lab, bromine and iodine together prove most forgiving for both handling and sequential metal-catalyzed reactions. Iodopyridines alone often react too quickly for controlled transformations, leaving little room for selectivity. Adding bromine to the mix, especially in our unique arrangement, hands users more subtlety—selective coupling with the iodine first, holding the bromine for the next desired step.
5-Bromo-2-Iodopyridine outperforms in cross-coupling applications not just because of its reactivity gradient but because its electronic effects on the ring steer product distribution. We’ve run dozens of side-by-side comparisons with similar dihalogenated pyridines. Bromine at other positions often introduces steric hindrance, dropping the yield of subsequent steps. Placing it at the fifth position on the ring leaves both ortho and para sites open, making for easier manipulation by skilled hands.
Not a year goes by without a customer spotting something new about this compound in their process. All those years in manufacturing taught us never to underestimate these insights. Mid-sized pharma companies reported that switching from 2-bromopyridine to its bromo-iodo cousin lowered their catalyst loading by up to 25%, primarily due to the enhanced leaving group ability of iodine. In one memorable case, a customer telephoned us to explain how their GC traces cleaned up almost overnight: better starting material led to tidier downstream workups and fewer side impurities.
Our synthesis team learned to filter out the tiniest traces of polyhalogenated byproducts, which hide among desired crystals. Achieving high isomeric purity starts with using crisp, temperature-stable reagents, followed by a stepwise crystallization that doesn't rush cooling. One shift in pressure during solvent removal can skew the halogen balance, so we keep careful logs for every batch. No automation beats hands-on checking for subtle changes in odor or color as a signal to halt or progress the process.
Scaling 5-Bromo-2-Iodopyridine from gram to multi-kilogram demand brings familiar headaches and new surprises. Halogen reagents are not always consistent between suppliers; sometimes a lot of iodine flakes carries trace metal ions, throwing off color and reactivity. Our purchase team established close partnerships with primary producers, choosing sources with predictable impurity profiles and long histories of safe, ethical production.
The demands of regulatory compliance grew sharper over time. Many jurisdictions raised the bar for maximum allowed residual solvents and heavy metals. Our R&D staff worked directly with process chemists to tune purification parameters, sometimes rerunning entire lots if limits approached warning levels. Full transparency matters—each customer gets a copy of the analytical run, and even nonconformances show up in our internal investigation logs. In a business where every contaminant or trace unknown could spell the difference in a patent filing or toxicological review, running those extra checks earned client trust.
Supplier reliability never looked more important than during global transport disruptions. More than once, air-freighted shipments of raw iodo intermediates never left their overseas docks. We responded by keeping buffer stock at separate facilities, linked by domestic road and rail routes. Emergency production runs taught us the value of keeping blends stable—overdried powders sometimes clump or lose flow, so maintaining optimal storage humidity made recovery faster during forced shutdowns.
Large-scale buyers in Asia began requesting biodegradable solvent alternatives for reprocessing spent mother liquors. In response, our not-so-huge but hungry technical group set up pilot runs with green solvents, swapping out classic chlorinated hydrocarbons for less persistent alternatives. The first batches weren’t pretty—low yields and puzzling side products. But with time, stepwise adjustments closed the gap. Now, we’re confident sending out orders processed through both traditional and eco-friendlier lines, with analytical paperwork to back each claim.
Chemists in small or medium labs sometimes call for direct pointers before placing new orders. A common uncertainty: at what stage should the iodine or bromine be replaced in a multi-step synthesis? Decades of feedback shaped our advice—start with the iodine. The increased reactivity means easy coupling with a minimal risk of competitive halogen exchange. Once the newly introduced substituent locks in place, the fifth-position bromine can be replaced under milder or more targeted conditions. This two-stage approach leads to fewer byproducts and builds confidence during scale-up.
New users often want data on thermal stability and decomposition products. From our own thermal analysis, 5-Bromo-2-Iodopyridine boasts better temperature resistance on storage compared to many fluorinated counterparts. Still, exposure to strong bases or transition metal complexes at high temperatures sometimes liberates free iodine—a known pathway for color change or reactivity loss. So keeping reaction conditions within validated windows staves off these headaches.
Running a chemical manufacturing plant is a contact sport, not an exercise in theory. Operators spot issues days before paperwork shows trouble. A faint lingering odor, slight yellow tint, or sluggish filtration—each one prompts checks and sometimes preemptive tweaks. For 5-Bromo-2-Iodopyridine, our approach centers around never ignoring small anomalies. Even if analytical tests pass, real-world processability tells the truth: if the product behaves differently at scale than at bench, customers lose time and money. We share these observations as part of our documentation, giving end-users more insight into possible operational quirks.
Continuous investment in equipment pays back over the years. Upgrading crystallizers and drying ovens cut moisture retention and improved batchwise reproducibility. Years back, we learned the hard way that inefficient oven airflow caused “hot spots” in big trays, so some users received crumbly, off-spec powder. Now, tighter controls and direct feedback loops between production and QA teams ensure a more uniform product, from pilot scale to full commercial runs.
It pays to keep track of where the wider market is heading. More medicinal chemists push for late-stage halogen exchange and increasingly complex library synthesis. In agricultural R&D, new pesticide candidates rely on dual functionalization to meet regulatory hurdles for safety and efficacy. A generation ago, supplying a few grams of 5-Bromo-2-Iodopyridine sufficed. Now, kilo quantities leave our dock every month, integrated into longer and more varied supply chains.
Circle back to the unique advantages of 5-Bromo-2-Iodopyridine, and the biggest keeps coming up: flexibility. Not every reaction pathway will suit the next user, but having both bromine and iodine at your fingertips means fewer synthetic detours. It reduces waste, slashes reaction time, and, in many cases, means fewer resources eaten up during purification. That matters not just for the environment but for the hard math in chemical process economics.
Sustainability is no longer a buzzword. Our clients—especially those with global brands—demand deeper scrutiny not just into product purity, but the impact of every step in the process. Each batch of 5-Bromo-2-Iodopyridine reflects this shift. We switched to energy monitoring on production lines, invested in solvent recovery, and prioritized waste minimization without sacrificing reliability. Whether tracking the carbon footprint of a single kilogram or replacing legacy reagents with cleaner alternatives, the soul of modern manufacturing is adaptability.
Direct conversations with our end-users help us detect shifts in demand early. They want confidence that what they buy will work from the first gram to the hundredth kilo. Having direct lines of communication—without a forest of intermediaries—means we can adapt at the speed industry requires. Post-delivery support remains a mainstay of our ethos, answering questions on everything from optimal storage conditions to troubleshooting unexpected color changes.
It’s clear from years on the front line: technicians and process chemists want more than a spec sheet. They appreciate knowledge gained from thousands of hours on the shop floor, catching small details before they become big headaches. Our experience with 5-Bromo-2-Iodopyridine adds up to more than just analytical numbers—it’s confidence, problem-solving built on lived reality, and determination to improve with every run.
Many products claim to be pure or versatile, but in practice, performance in the user’s hands is the real test. Whether it’s handling tons for a new crop protection candidate or just small bottles for medicinal chemistry trials, our commitment to reliability and openness defines every lot produced. We look forward to new challenges and new ideas that push both us and our molecular toolkit in new directions.