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HS Code |
144272 |
| Chemical Name | 2-Bromo-5-nitropyridine |
| Cas Number | 4487-59-6 |
| Molecular Formula | C5H3BrN2O2 |
| Molecular Weight | 203.99 g/mol |
| Appearance | Yellow to brown solid |
| Melting Point | 53-57 °C |
| Density | 1.81 g/cm³ |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥ 97% |
| Smiles | C1=CC(=NC=C1Br)[N+](=O)[O-] |
| Inchi | InChI=1S/C5H3BrN2O2/c6-4-1-2-5(8(9)10)7-3-4/h1-3H |
| Synonyms | 5-Nitro-2-bromopyridine |
| Storage Condition | Store in a cool, dry place |
As an accredited 2-Bromo-5-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Bromo-5-nitropyridine, labeled with product name, hazard symbols, and batch information. |
| Container Loading (20′ FCL) | 20′ FCL: Standard 20-foot full container load for bulk shipment of 2-Bromo-5-nitropyridine, securely packed in sealed drums. |
| Shipping | 2-Bromo-5-nitropyridine is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material due to its toxic and irritant properties. Appropriate labeling and documentation are required, and transportation follows international and local regulations for chemicals to ensure safety during transit. |
| Storage | 2-Bromo-5-nitropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and reducing agents. Protect from light and moisture. Avoid sources of ignition. Store at ambient temperature and ensure proper labeling. Handle in accordance with good industrial hygiene and safety practices. |
| Shelf Life | 2-Bromo-5-nitropyridine is stable for at least 2 years when stored in a cool, dry place, protected from light. |
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Purity 98%: 2-Bromo-5-nitropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high product yield and minimal impurities are ensured. Molecular Weight 189.98 g/mol: 2-Bromo-5-nitropyridine at a molecular weight of 189.98 g/mol is used in agrochemical development, where precise stoichiometric calculations improve formulation efficiency. Melting Point 61–64°C: 2-Bromo-5-nitropyridine with a melting point of 61–64°C is used in solid-state organic synthesis, where controlled thermal processing optimizes reaction kinetics. Stability Temperature up to 120°C: 2-Bromo-5-nitropyridine stable up to 120°C is used in chemical R&D labs, where elevated temperature reactions proceed without decomposition. Particle Size <50 microns: 2-Bromo-5-nitropyridine with particle size under 50 microns is used in advanced electronic material production, where uniform dispersion enhances film homogeneity. |
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Every laboratory and production site values consistency. In my own experience, chasing after reliable sources for specialty chemicals often turns into a long search. 2-Bromo-5-nitropyridine stands out on this front. Its molecular layout, with a bromine atom on the second position and a nitro group on the fifth, lets chemists approach synthesis with control. This kind of compound finds its place where precision counts, whether that’s for pharmaceuticals or crop protection. The C5H3BrN2O2 molecule brings not only structure — it opens doors to a range of downstream transformations.
The need for safe, efficient chemical building blocks only grows. I’ve watched research teams rely on intermediates like 2-Bromo-5-nitropyridine because it can speed up a project or unlock new routes for development. Its structure means it reacts smartly — not just to any reagent but to those carefully picked for a certain synthesis. That makes a difference if you’re looking to attach a new group, fine-tune a ring, or build complex molecules found in drugs and advanced materials.
Chemistry, especially at scale, rewards attention to detail. For 2-Bromo-5-nitropyridine, purity impacts not just research outcomes but safety. Most reputable vendors offer it at a purity of 98% or above, often as a yellow crystalline powder with a molecular weight of just over 216 g/mol. Years ago, I learned the hard way how an off-spec shipment could throw off months of careful planning. Small differences in melting point or appearance sometimes hint at process hiccups, so a documented batch analysis often means the difference between progress and setback.
It’s easy to think about intermediates as just another tool for the bench. But 2-Bromo-5-nitropyridine reaches far outside the fume hood. In development work, it helps jumpstart complex reactions. For instance, I know teams that use it as a starting point for making pyridine-based pharmaceuticals, thanks to its ability to undergo substitution or coupling reactions cleanly. These capabilities also place it in the development chain for agrochemical actives — critical for protecting food supply. The nitro group flags it to synthetic chemists for further reduction or transformation, while the bromo group provides an anchor for Suzuki or Buchwald-Hartwig reactions.
I’ve worked with plenty of pyridine derivatives, yet few offer the kind of versatility 2-Bromo-5-nitropyridine brings. It distinguishes itself from close relatives like 2-Chloro-5-nitropyridine or 3-Bromo-5-nitropyridine by the position and strength of its leaving group. The reactivity differences change the way each derivative handles nucleophilic substitutions. This often means fewer by-products and cleaner isolations for the chemist — something no one complains about when product purity counts. Experiences in the lab prove that even slight changes in structure can shift boiling and melting points, reactivity, and appearance. Over the years, more synthetic developers have gravitated towards 2-Bromo-5-nitropyridine when selectivity or reaction yield tips the balance.
Handling compounds with nitro and bromo groups always calls for respect and diligence. There’s always a temptation to focus on yield or reactivity, but I’ve seen the consequences of neglecting safety training. 2-Bromo-5-nitropyridine’s handling requires well-ventilated workspaces, gloves, and eye protection — a basic ritual in synthetic work. Waste management cannot stay an afterthought, either. Compounds with nitro groups, especially when handled in scale-up, demand tailored disposal strategies. Facilities adopting sustainable practices lock in better results over the long term. In advanced labs, I’ve seen chemists push for better containment, using sealed systems and scrubbing setups that cut exposure and keep releases out of the air and water.
Innovation comes from partnerships between researchers, suppliers, and end-users. In the past decade, the move toward greener and more efficient syntheses pushed many companies to examine the impact of their intermediates. 2-Bromo-5-nitropyridine’s adaptability makes it a favorite for method developers. It allows for cross-coupling reactions that once needed more costly or less stable partners. For example, the increased functional group tolerance in modern catalysis means more chemists can swap the bromo group for custom additions with lower temperatures and less hazardous reagents.
Sourcing high-quality specialty chemicals often turns into a test of trust. I’ve seen the effects of supply interruptions, especially when global events shake trade networks. Reliable access remains top of mind at every stage — from small research lots to multi-kilogram production. Quality documentation, including lot-specific certificates and trackable specifications, guides purchasing decisions. Transparency around origin and testing processes reassures both auditors and end-users. I’ve noticed more chemical vendors investing in digital quality tracking to trace everything from synthesis batch to delivery truck, reflecting a real shift in priorities over the last five years.
Pyridine derivatives won’t be leaving the scene anytime soon. Their value comes from their broad reach — spanning medicines, crop sciences, dyes, and advanced materials. 2-Bromo-5-nitropyridine often tracks with these trends. Today’s pharmaceutical development cycles run lean, so demand for intermediates that accelerate timelines isn’t going down. One thing stands out: the push for new bio-active molecules lifts all the specialty intermediates with it. As more startups and research collaborations pop up, requests for quality-controlled, reliable chemical intermediates only grow.
Ask any synthetic chemist about bottlenecks, and intermediates land right near the top of the list. Years ago, I’d spend evenings troubleshooting why a custom pyridine coupling didn’t work out, only to realize later a cheap batch of intermediate was the culprit. This builds an appreciation for compounds like 2-Bromo-5-nitropyridine, whose reproducibility and expected structure replace uncertainty with confidence. The bromine at position 2 gives excellent reactivity for carbon–carbon and carbon–nitrogen closures, while the nitro group serves as a functional handle for stepwise building. These features often mean fewer steps and tools required for downstream modifications.
Not all pyridines behave the same. While 2-Bromo-5-nitropyridine holds a distinct position, competitors like 3-Bromo-5-nitropyridine or other halogenated analogs carry different profiles. The reason behind selecting the bromo substituent often ties to reactivity. Many chemists look for optimal leaving groups when planning nucleophilic substitutions or cross-coupling reactions. I’ve noticed in project retrospectives that switching from chloro to bromo opens new reaction channels, often leading to better yields and selectivity. These subtle changes in molecular design turn minor building blocks into strategic levers for success.
Anyone involved in drug or agrochemical R&D quickly learns the importance of flexible intermediates. 2-Bromo-5-nitropyridine plays a silent but essential role in the background, helping research teams attach functional groups or form rings found in active ingredients. Its reliability keeps costs lower and predictability higher, a balance many industry leaders prefer. Just as with active pharmaceutical ingredients, lot-traceability and analytical proof often drive purchasing decisions as much as the molecule itself.
The pressure to improve green metrics in chemical production sees compounds like 2-Bromo-5-nitropyridine in a new light. Researchers look for intermediates that can be processed under milder conditions, with less waste. The rise of catalytic methods, minimizing heavy metals and harsh solvents, means more reactions go through this intermediate now than in years past. It also serves as a template; developers work on redesigning its synthesis from more sustainable feedstocks, sometimes dialing down the energy required or recycling process streams. Real progress often begins when industry veterans and new innovators ask, “How do we make this step safer and cleaner?”
At the bench scale, students and postdocs value ease of handling and predictable reactivity. 2-Bromo-5-nitropyridine demands dry, dark storage because light and moisture can kick off unwanted side reactions. At higher volumes, process chemists adjust techniques to minimize waste and maximize throughput. Modern pilot plants swap batch reactors for flow systems, controlling addition rates and heat more effectively. I’ve watched as facilities evolve — replacing open vessels with closed, instrumented ports — all to keep yields high and operators safe.
No chemical reaches its potential without careful storage and supervision. The bromine and nitro groups make this compound sensitive to certain triggers. In my own work, careful container choices — amber glass, moisture-tight seals — often make the difference between stocks staying potent or breaking down. Inventory tracking systems help labs keep tabs, flagging old bottles before degradation becomes a risk. Ongoing education, especially for new researchers, prevents careless handling or overuse.
Great chemistry always circles back to the people using it. Training, safety culture, and a sense of purpose matter as much as the reactants and tools in use. Teams who shape their routines around responsible handling, transparent communication, and regular audits rarely find themselves wrestling with surprise incidents. Many of the positive examples I’ve seen start with open information-sharing and owning up to near-misses, paving the way for safer, more productive labs.
The way forward for specialty intermediates like 2-Bromo-5-nitropyridine centers on blending innovation with responsibility. The next round of improvement rests not just with chemical engineers but across procurement, logistics, and compliance officers. Streamlined logistics reduce delays and wasted motion, while meaningful safety reviews drive incremental improvements in waste management and energy use. Many companies focus on supplier partnerships — not just as a cost exercise, but to ensure the integrity of their supply chain and the reliability of their products.
Anyone serious about building a life in the lab knows that impact grows over time. The right intermediate allows more than just reaction completion; it leads to complex natural products, advanced polymers, and life-saving therapies. In this way, 2-Bromo-5-nitropyridine delivers where it counts. Years from now, I expect demand only to increase as researchers push boundaries in bioactive design. The momentum comes from trust — in science, in each other, and in quality products that don’t cut corners.
Wider distribution of information around specialty chemicals pays dividends. Whether through peer-reviewed articles, supplier workshops, or just lunchtime talks in the lab, security comes from informed workers and up-to-date practices. I’ve watched junior researchers grow from careful instruction, gaining confidence as they move from sample prep to scaled synthesis. The knowledge that accompanies a bottle of 2-Bromo-5-nitropyridine can shape not only project success but also laboratory culture and reputation.
No single group carries the burden of safe, effective synthesis. Collaboration between academia, industry, and regulatory bodies ensures that strong practices outlast any single project. Routine surveys, open data sharing, and regular supplier evaluations build a foundation for stronger, more transparent markets. In my own work, partnerships with trusted suppliers speed troubleshooting and reinforce standards, making the difference when deadlines loom or quality needs verification.
This compound might look unremarkable on paper to the untrained eye, but my experience tells a different story. Every breakthrough, whether in a university lab or a global manufacturing site, depends on fundamentals like trustworthy intermediates. 2-Bromo-5-nitropyridine delivers exactly what creative chemists and production specialists need — reliability, flexibility, and performance. As the field grows more complicated, the value of well-characterized, dependable materials only becomes clearer. The quiet workhorse in cancer research or crop protection tomorrow may just start with this single bottle on the shelf today.