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HS Code |
489593 |
| Chemical Name | 2-Bromo-5-chloro-3-nitropyridine |
| Molecular Formula | C5H2BrClN2O2 |
| Cas Number | 79472-22-3 |
| Appearance | Yellow crystalline solid |
| Melting Point | 88-92°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically >98% |
| Smiles | c1c([nH]c(c1Br)[N+](=O)[O-])Cl |
| Inchi | InChI=1S/C5H2BrClN2O2/c6-4-3(7)1-2-8-5(4)9(10)11/h1-2H |
As an accredited 2-Bromo-5-chloro-3-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-chloro-3-nitropyridine, sealed with a screw cap and labeled with safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Typically accommodates up to 12–14 metric tons of 2-Bromo-5-chloro-3-nitropyridine, securely packed in drums. |
| Shipping | 2-Bromo-5-chloro-3-nitropyridine is shipped in tightly sealed, chemical-resistant containers, compliant with international regulations for hazardous materials. It is handled by trained personnel and transported under controlled conditions to prevent exposure to moisture, heat, and direct sunlight. Appropriate documentation and labeling ensure proper identification and safe handling during transit. |
| Storage | 2-Bromo-5-chloro-3-nitropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing or reducing agents. Keep the container clearly labeled and protected from moisture. Store at room temperature and ensure proper safety labeling and access restrictions to trained personnel only. |
| Shelf Life | 2-Bromo-5-chloro-3-nitropyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and dark place. |
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Purity 98%: 2-Bromo-5-chloro-3-nitropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side-product formation. Melting Point 89°C: 2-Bromo-5-chloro-3-nitropyridine with melting point 89°C is used in agrochemical manufacturing, where controlled melting point enables precise formulation processes. Particle Size <10μm: 2-Bromo-5-chloro-3-nitropyridine with particle size less than 10μm is used in catalyst preparation, where fine particle size improves catalytic dispersion. Moisture Content <0.5%: 2-Bromo-5-chloro-3-nitropyridine with moisture content below 0.5% is used in dye intermediate applications, where low moisture prevents product degradation. Stability Temperature up to 120°C: 2-Bromo-5-chloro-3-nitropyridine stable up to 120°C is used in electronic materials synthesis, where high thermal stability supports performance under processing conditions. Assay ≥99%: 2-Bromo-5-chloro-3-nitropyridine with assay greater than or equal to 99% is used in API production, where high assay ensures reproducibility of regulatory quality standards. |
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Specialty chemicals often shape how industries grow, and 2-Bromo-5-chloro-3-nitropyridine reflects this more than most. In my years talking with pharmaceutical and fine chemical professionals, certain niche molecules come up again and again. 2-Bromo-5-chloro-3-nitropyridine fits neatly into that list, not as an everyday staple, but as a robust, adaptable tool for those working at the bench and the pilot plant scale alike.
The structure of 2-Bromo-5-chloro-3-nitropyridine features three distinct functional groups sitting on a pyridine ring: a bromine, a chlorine, and a nitro group. This trio absolutely changes how the molecule interacts during synthesis. The bromine at the second position and the chlorine at the fifth both serve as classic points for substitutions or couplings, while the nitro group at the third spot builds in extra reactivity and gives chemists a new handle to work with. These features have made 2-Bromo-5-chloro-3-nitropyridine a favorite intermediate for custom molecule construction, especially in medicinal chemistry labs that require fine-tuned electronic properties or steric effects.
Typical batches of 2-Bromo-5-chloro-3-nitropyridine come as off-white or yellowish powders, and purity above 98% remains the golden standard for work demanding minimal side-products. The melting point lands in a consistent range, making it straightforward for quality control but even more, this allows for practical, repeatable handling when scaling up. Solubility follows what one might expect for substituted pyridines: The compound dissolves in a variety of organic solvents popular in the lab, which makes it a simple choice for multi-step reactions or when a researcher wants to try a few different conditions.
Where I have seen 2-Bromo-5-chloro-3-nitropyridine gain traction is in the early-stage development of pharmaceuticals and advanced materials. Its array of functional groups gives pathway flexibility: bromine and chlorine are both excellent leaving groups, so chemists can run cross-coupling reactions or nucleophilic aromatic substitution without running into the brick walls common to more stubborn aromatic rings. If you're piecing together a new kinase inhibitor or exploring a new family of organic semiconductors, swapping out halogens or reducing nitro groups on this backbone comes up frequently in literature and patent filings alike. For customers developing pyridine-based APIs, this molecule essentially gives them more moves on the chessboard, not just another block to stack.
During discussions with researchers, I often hear about the challenge of "overlap" among building blocks: you can find a sea of halogenated pyridines, but few offer the same trifecta of substitution as this one. If you look at standard bromopyridines, many lack the nitro-for-tuning electron density, and chlorine for influencing reactivity or metabolic resistance. On the other hand, nitropyridines with a single halogen sometimes restrict the directions for further functionalization. The difference lies in how 2-Bromo-5-chloro-3-nitropyridine opens more synthetic routes — you don’t need to introduce halogens late in a route, which can be less predictable and prone to disappointing yields.
Beyond just theoretical appeal, this compound brings consistency to the table. Scale-up chemists praise its stability. It ships well and handles minor fluctuations in temperature or packing, so quality chemistries stay on track during transit. Reliability is more than just convenience: in regulated markets like pharmaceuticals, each misstep means wasted time and cost. I’ve seen labs return to 2-Bromo-5-chloro-3-nitropyridine even after trying "more innovative" molecules simply because it spares them the drama of unexpected by-products or unreliable physical forms.
The molecule also avoids some of the regulatory headaches that more exotic building blocks can trigger. With growing attention to environmental management and operator safety, it’s not lost on professional chemists that 2-Bromo-5-chloro-3-nitropyridine fits into established safety protocols and reporting structures. This lowers the friction for onboarding in a new project, whether at an academic innovation hub, a biotech firm, or a major generics producer. Risk managers and EH&S professionals sleep easier with compounds they've vetted for years.
E-E-A-T (Experience, Expertise, Authoritativeness, Trustworthiness) finds its home not just in technical performance, but in how suppliers manage the stewardship side. Sourcing 2-Bromo-5-chloro-3-nitropyridine from reputable vendors makes all the difference. I have worked with buyers who place as much value on transparent supply chains and Certificate of Analysis documentation as they do on chemical purity. Reliable records and third-party analytics back up these decisions. Working with established partners reduces the odds of encountering supply chain disruptions or hidden contaminants, both of which can sink a promising program. In the last decade, regulatory expectations have only grown tighter, so no responsible lab swings blind on these matters anymore.
While pharmaceutical and agrochemical research snatch up much of the available supply, the push for novel materials keeps engineers and academic research teams interested. Synthesis of tailored ligands for catalysis has cited this compound in recent patents. The rigid backbone and electron-withdrawing properties pack in utility, offering a precise starting point for molecules used in coordination chemistry. The molecule’s distinctive profile also means it feeds into the synthesis of specialty dyes or liquid crystal materials, where just the right substitution pattern governs phase transitions or light absorption. Its versatility across research areas continues to grow with every new publication and patent.
Pricing reflects the complexity of its synthesis and the relative scarcity compared to simpler building blocks. Most research or pilot lab managers know that the small premium on this molecule pays dividends in reaction flexibility and saved time. Experienced buyers focus on more than just price—they look for consistency in supply, batch-to-batch purity, and accessible technical support. For all but the largest industrial users, reputable specialty chemical distributors dominate the market, stocking small and mid-sized lots to give project teams exactly what they need without surplus waste. This keeps total costs in check and lets programs shift quickly as data comes in.
One thing that's grown in importance over my career is the demand for greener chemical processes. While 2-Bromo-5-chloro-3-nitropyridine started in more traditional synthesis routes, newer manufacturing approaches cut down waste, improve atom economy, and target higher overall yields. Innovators at contract manufacturers and chemical companies keep tweaking their approaches, introducing flow chemistry, alternative solvents, and new catalysts to minimize environmental impact. These improvements matter for both compliance reasons and simple long-term cost savings. Supply partners stand out by offering versions with traceability on green metrics, which increasingly shows up as a point of negotiation among large pharmaceutical buyers.
Labs planning for large-scale programs sometimes negotiate custom specifications or alternative salt forms to further reduce handling risks or meet process-specific targets. This practice came out of ongoing dialogue between procurement specialists and process chemists, where suppliers adjust to actual user needs instead of sticking to an off-the-shelf product definition. Such flexibility encourages broader adoption since formulation scientists, scale-up engineers, and analytical groups all get a say in the compound they will spend months or years working with.
Experienced chemists never forget that nitro and halogen groups deserve respect in the lab. Standard personal protective equipment, effective ventilation, and solid waste management protocols go hand-in-hand with handling compounds like 2-Bromo-5-chloro-3-nitropyridine. Having tested and reviewed dozens of materials for lab safety committees, I have learned that clear documentation, reliable batch records, and prompt technical support form the backbone of safe integrated operations. Tools for rapid spill response, clear hazard labeling, and comprehensive staff training pay off even with a compound whose risk profile fits well inside industry norms.
With competition hot in pharmaceuticals, specialty chemicals, and advanced materials, the edge often goes to teams that make the most of small, smart distinctions. 2-Bromo-5-chloro-3-nitropyridine isn’t just another item on a supplier’s list—it represents a toolkit for selective functionalization and streamlined synthesis. Colleagues working on kinase inhibitors, anti-infectives, or next-generation dyes consistently point to the unique combination of groups as the ace up their sleeve. The experienced eye sees subtle advantages: possible late-stage diversification, convenient purification due to the nitro group's influence, and a known pathway for scaling up from milligrams to several kilograms with minimal surprises.
Modern chemical companies looking to future-proof their pipelines recognize that robust intermediates like this one deliver cost savings not only through narrower process windows and better yields, but also in lower regulatory headaches and easier pathfinding in intellectual property space. Having passed through regulatory scrutiny and numerous scale-up challenges, 2-Bromo-5-chloro-3-nitropyridine already carries a practical seal of approval from industry and academia alike.
No molecule escapes the push and pull of economics and regulation forever. The halogen content in this compound means environmental compliance remains a real, ongoing conversation. Companies can address this through comprehensive waste treatment, careful strategy in disposal, and investigating emerging greener routes for its synthesis and downstream utilization. Collaborations with waste management providers who understand the specifics of halogenated pyridines help researchers and manufacturers meet both legal and ethical expectations. Ongoing discussions at both policy and trade association levels signal no end to the pressure for improved handling, so suppliers who stay ahead on this score win customer loyalty and long-term contracts.
Sometimes research teams find the compound is not commercially available in quantities above the gram or kilogram scale. Long-standing relationships with contract manufacturers often solve this, but smaller labs might need to plan ahead or consider joint purchasing arrangements to drive down costs and improve access. In the early days of a research program, networking through chemical supply forums or academic consortia helps build up the purchasing clout necessary to source tricky compounds and avoid getting held up at the proposal or small-scale test phase.
No one relies on a single product out of habit. My time working alongside synthetic chemists and project managers taught me that sticking with trusted compounds comes from a track record of winning results. 2-Bromo-5-chloro-3-nitropyridine won its place in portfolios not for being the newest or flashiest, but for keeping pace with the speed and demands of both benchwork and scale-up. Its performance history gives chief chemists peace of mind—batch records and technical data sheets tie back to years of experiments, successful reactions, and published discoveries. New teams see this molecule in the protocols of seasoned scientists, and build trust in it through shared stories back in the lab and online forums.
The best suppliers keep up with requests for technical clarification, sharing analytical data, recommended handling practices, and updates on synthetic improvements. Building this two-way street between supplier and user closes the gap between the bench and the supply chain. In this way, 2-Bromo-5-chloro-3-nitropyridine does more than sit on a shelf—it grows with every program it supports, every process it enables, and every discovery it pushes toward the finish line.
Every lab and production line faces trade-offs. Newer, more complex molecules sometimes promise a shortcut or marginal efficiency. The actual win happens when researchers and buyers can judge whether that trade-off stands up in the real world. In side-by-side runs with other pyridine intermediates, 2-Bromo-5-chloro-3-nitropyridine consistently comes out ahead because it gives users unmatched flexibility for late-stage modifications. Over-relying on newer, unproven molecules can bog down both procurement and regulatory review. Professional judgment, backed by both lab evidence and conversations with vendors, keeps this molecule at the center of many synthetic strategies.
People new to the field will find a wealth of literature citing the uses, limitations, and best practices for this compound. Reading up will show both the boundaries and the opportunities it presents. Those who bring it into their workflows get access to years of collaborative learning and troubleshooting. My own experience has been that even as trends come and go in chemical development, tools that offer reproducibility, safety, and well-documented reactivity stick around and drive the next wave of breakthroughs. 2-Bromo-5-chloro-3-nitropyridine holds its value for precisely these reasons.
As more research pivots toward sustainability, improved synthetic routes, and integrated digital automation in labs, versatile molecules like 2-Bromo-5-chloro-3-nitropyridine only become more critical. Programmable synthesis platforms and AI-guided retrosynthesis frequently point to such well-placed intermediates due to their flexible reactivity and the breadth of the transformations they enable. Start-ups and established players trying to shorten timelines while keeping compliance in check find themselves circling back to previously proven winners.
Experience, expertise, and a culture of collaboration keep shaping how professionals use specialty chemicals. For teams working to solve tomorrow’s challenges in pharmaceutical development, electronics, or advanced materials, 2-Bromo-5-chloro-3-nitropyridine stands as a clear choice for real-world progress. Those committed to responsible sourcing, process safety, and relentless innovation know a good tool when they see it. From project kickoffs to full-scale production, this molecule continues to earn its keep through practical utility, regulatory confidence, and adaptability—a hallmark of chemical progress.