|
HS Code |
864229 |
| Product Name | 3-Bromo-4-Nitropyridine N-Oxide |
| Cas Number | 945212-72-6 |
| Molecular Formula | C5H3BrN2O3 |
| Molecular Weight | 218.99 g/mol |
| Appearance | Yellow solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO and DMF |
| Synonyms | 3-Bromo-4-nitro-1-oxidopyridin-1-ium |
| Smiles | c1c([n+](=O)[O-])cc(Br)nc1[N+](=O)[O-] |
| Inchikey | QSRQOYALHDWTII-UHFFFAOYSA-N |
| Storage Conditions | Store in a cool, dry place, away from light |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 3-Bromo-4-Nitropyridine N-Oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 3-Bromo-4-Nitropyridine N-Oxide, labeled with hazard symbols, product code, and safety information. |
| Shipping | 3-Bromo-4-Nitropyridine N-Oxide is securely packaged in compliance with hazardous material regulations. It is shipped in sealed, chemical-resistant containers and clearly labeled for laboratory use. Temperature and handling instructions may apply. Delivery utilizes certified carriers to ensure safe and prompt arrival, accompanied by a Material Safety Data Sheet (MSDS). |
| Storage | Store **3-Bromo-4-Nitropyridine N-Oxide** in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong reducing agents. Protect from direct sunlight and moisture. Clearly label the container and keep it away from foodstuffs and acids. Use appropriate chemical storage cabinets for hazardous materials. |
Applications of 3-Bromo-4-Nitropyridine N-Oxide in Industrial ManufacturingAs a core manufacturer specializing in advanced pyridine derivatives, we supply 3-Bromo-4-Nitropyridine N-Oxide to facilitate critical reactions in specialized sectors. Its application spans high-value pharmaceutical intermediates and niche agrochemical actives, where its unique reactivity supports precise syntheses under tightly regulated conditions. Below, we outline key downstream scenarios with a focus on compliance, industrial composition, process flows, and finished products relevant to our clients' end uses. 1. Advanced Pharmaceutical Intermediate SynthesisLeading API producers employ this compound as a building block in the targeted preparation of heterocycle-based pharmacophores, especially in the synthesis of kinase inhibitors, antineoplastic agents, and pyridine-based anti-infectives. The material’s electron-withdrawing properties enable controlled bromination and nitration reactions, allowing chemists to achieve specific substitution patterns essential for bioactivity and regulatory approvals. Strict validation ensures that all process byproducts meet health authority standards, with focus on impurity profiling and traceability. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Crop Protection Active Ingredient ManufacturingSpecialty agrochemical producers utilize this raw material during the multi-step synthesis of selective herbicide and fungicide actives. Its electron-rich pyridine core, combined with halogen positions, provides an essential scaffold for subsequent alkylation or ring closure, forming complex molecules with high field efficacy. These operations require tight controls over purity and isomer ratios to comply with international maximum residue limits and pre-registration data packages for crop safety and environmental fate. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemical Synthesis for Liquid Crystal PrecursorsManufacturers of specialty electronic chemicals use this nitropyridine oxide as a precursor in the highly selective synthesis of liquid crystal monomers and related compounds for advanced display technologies. Its precise halogenation enables downstream Suzuki or Stille coupling reactions, yielding biphenyl and pyridine derivatives with stringent stereochemistry and high purity. Electronic grade synthesis imposes additional controls on metal ion and halide residues given the sensitivity of end-use displays to trace contaminants. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Research Reagent and Analytical Reference Materials ProductionProducers of certified reference materials and specialty reagents supply this compound to research labs and pharmaceutical quality control units. The precise structure, with controllable halogen and nitro positions, fits demand for high-purity analytical standards used in method validation or impurity profiling. Manufacturing for this sector demands the strictest batch consistency and extended documentation, with comprehensive impurity elucidation to meet accreditation criteria for analytical standard suppliers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Specialty Dye and Pigment Intermediate ManufacturingChemical manufacturers in the dye and pigment sector utilize this compound in the controlled synthesis of azo and heterocyclic dye precursors. Its nitro and bromo functionalities act as key activation points for diazotization or cross-coupling, enhancing chromophore development and improving solubility in processable pigment lines. Maintaining low metal and halogen contamination is critical, given the requirements for stable color, fastness properties, and environmental discharge restrictions for final pigment preparations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Bromo-4-Nitropyridine N-Oxide 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!
Our team has been working hands-on with pyridine derivatives for more than a decade. The chemical complexity and practical challenges of 3-Bromo-4-Nitropyridine N-Oxide have taught us plenty. In our facility, every kilogram starts with high-purity base pyridine and carefully sourced brominating and nitrating agents. Quality keeps our process honest—nobody wants a run ruined by impurities or improperly oxidized intermediates.
We produce 3-Bromo-4-Nitropyridine N-Oxide for advanced chemical synthesis. Researchers and process engineers rely on its reactivity and unique electronic properties—specifically, the precise placement of bromine and nitro functions alongside the N-oxide—because those functional groups open doors. Medicinal chemists come to us looking to build small molecule libraries where this compound serves as a crucial intermediate. Scale-up projects in pharmaceutical and agrochemical development depend on consistency. We know because we've supplied production from gram to multi-kilogram scale—each time, keeping the process tight and reproducible.
In practice, we typically deliver 3-Bromo-4-Nitropyridine N-Oxide as an off-white to pale yellow crystalline solid. Our final product hits a purity above 98% by HPLC—our QC lab cross-verifies every lot, making sure water and residual solvents stay well below accepted process limits. We avoid the easy route of relaxed moisture conditions, which means a product that won’t surprise you with sticky clumping or side-product contamination. Melting point remains within a tight range with every batch, and we include spectral and chromatographic data for full transparency. Many buyers ask about particle size or solubility during method development. We’ve found it dissolves smoothly in most polar organic solvents, and our technical staff stands by to share real-world results from our own processing steps.
No two synthesis routes are identical. We keep flexibility in mind when choosing parameters for each production campaign. Temperature control sits front and center during both nitration and bromination to keep isomer content low. By recycling reagent streams, we keep both environmental impact and input costs in check. Our batch records aren’t just regulatory paperwork—they’re also our reference for troubleshooting. When a customer encountered product variability due to shipping conditions, we re-examined our packaging and included desiccant packets in every container. These details only surface after years of actual work with the material.
Some labs ask us for small amounts of 3-Bromo-4-Nitropyridine N-Oxide for early-stage research. Others come with inquiries that demand drum quantities for pilot-plant work. Handling larger lots calls for a different mindset. Scaling up this particular compound brings its own set of headaches: sensitivity to moisture, dusting during transfer, and the need for trained personnel familiar with nitrogen oxides and brominated aromatics. In the early days, we underestimated dust suppression—leading to operator complaints and minor equipment malfunctions. We quickly realized the dust loves to travel, even through seemingly tight seals. These days, we use sealed charging and transfer equipment, minimizing both environmental exposure and waste.
Shipping regulations for N-oxide compounds can turn simple logistical plans into puzzles. Regulatory requirements vary from destination to destination. Early on, a container held at customs due to incomplete paperwork triggered a full review of our documentation protocols. We now include product identification with each shipment and double-check that every regulatory box is ticked for international orders. No manufacturer is perfect, but those bruises taught us the cost of mixing chemical skill with incomplete paperwork. Ensuring the chain of custody and complete batch traceability became a core part of our process after that lesson.
From experience, chemists often ask how 3-Bromo-4-Nitropyridine N-Oxide lines up against other pyridine-based products. Many of those inquiries home in on reactivity and selectivity. Compared to its non-oxidized cousin, 3-Bromo-4-Nitropyridine, the N-oxide brings an electron-donating twist that makes it behave very differently in coupling and substitution reactions. That means in palladium- or copper-catalyzed transformations, the N-oxide can steer selectivity and yield. Some researchers see improved rates or new pathways in reactions that would otherwise stall or give unwanted side products. We’ve had clients report that the N-oxide survived conditions where other brominated pyridines would decompose, giving them higher overall yield and easier purification.
The nitro group at the fourth position not only serves as a useful synthetic handle but also gives the molecule electron-withdrawing punch. In synthetic schemes, this can change the way the pyridine ring participates in further modification. It can open up possibilities for nucleophilic aromatic substitution or reduction schemes that are tough to achieve with hydrogen or halide in the same spot. By comparison, materials like 3-Bromo-2-Chloropyridine may offer reactivity at a different position, but the N-oxide variant supports a different profile in terms of downstream transformations and ease of deprotection. Some of our industrial partners report that for select bioconjugation and material science applications, the N-oxide form ends up more tolerant under their reaction conditions. These distinctions aren’t just details—they help determine whether a project moves forward or gets stuck troubleshooting poor conversions week after week.
Bringing a compound like 3-Bromo-4-Nitropyridine N-Oxide out of the literature and into the warehouse means more than reading a published procedure. Each new order, each scale-up request, comes with the need for quality assurance and flexibility. Mistakes surface as off-spec color or unwanted byproducts, often traced to one corner of the production line—a slightly colder reactor wall, a brief power fluctuation, or residual water in a supposedly dry tank.
It took several unsuccessful batches before hitting reliable yields above 80%. Controlling temperature ramp rates during both bromination and oxidation proved critical. Nitrogen inerting and closed-loop temperature control gave us the reliability needed for consistent output. For us, every failed batch represents both a cost and a lesson. After one equipment upgrade, we noticed trace iron contamination in the finished product. Diagnostics traced it back to a gasket on a recently installed glass-lined reactor. Swapping the gasket and checking the rest of the line restored our high purity levels. Success in this business doesn’t come from chasing shortcuts or ignoring borderline analytical results.
Part of our process investment focuses on in-line analytical techniques. Near-infrared spectroscopy flags off-target species before the product leaves the reactor. Time spent developing and validating new analytical methods directly translates into reduced rework and higher confidence for every customer—especially those in regulated industries.
We welcome feedback from partners who use 3-Bromo-4-Nitropyridine N-Oxide in their own work. A biotech group utilizing our compound in the late-stage functionalization of drug candidates reported a two-fold increase in coupling efficiency due to the clean, moisture-free batches we supplied. Another client in the specialty electronics sector praised the N-oxide version for fine-tuning the electrical properties of their custom pyridine-based materials, particularly where its higher electron density made a difference in performance metrics.
Researchers in academic labs also share both hiccups and success stories. A graduate student once flagged an aberrant melting point in a sample set, which led us to retest a batch and spot a slight deviation. This alert let us tighten the reaction protocol even further. Such exchanges keep us sharp and remind us why technical support matters as much as output.
Chemical manufacturing always brings environmental responsibilities. At our facility, we manage waste streams from pyridine derivatives through a combination of internal recycling and outside treatment partnerships. Spent acids from the nitration process pass through dedicated neutralization units, while recovered solvents go through rigorous purification before reuse. After complaints from nearby businesses over odor years ago, we invested in new scrubber technology and real-time air quality monitoring. By keeping local impact in check, we build trust with both the public and the regulatory agencies.
Continuous process innovation remains part of our ethos. In early campaigns, product variability and waste rates ran too high for comfort. We overhauled our oxidation protocol with catalytic regimes that improved selectivity and reduced byproduct formation. These changes dropped effluent load and increased overall output. Partnerships with raw material suppliers help ensure a consistent feedstock and prevent surprises mid-campaign. No manufacturer operates in isolation—a robust supply web supports both quality and continuity.
Manufacturers aren't just vendors; we’re the foundation for downstream innovation. Our own team leans on a steady stream of feedback from both scientists and engineers who use 3-Bromo-4-Nitropyridine N-Oxide in real-world applications. No datasheet or certificate of analysis can replace the experience of seeing how a material functions in the hands of a creative research chemist.
Over the years, we’ve supported clients during challenging troubleshooting periods. When an agrochemical project ran into oxidative degradation issues, we adjusted our packaging and introduced argon blanketing for shipping. In early-stage drug development work, we’ve helped optimize protocols by providing technical notes on reactivity, solubility, and storage—drawn directly from our own experiments rather than secondary literature.
Educational collaborations with university labs give us an early read on which challenges and needs will likely shape tomorrow’s chemical landscape. By discussing results openly and sharing both failures and successes, we help move the field forward. If a customer encounters unexpected analytical results, we pull batch data, review our process, and exchange ideas openly. That approach leads to real improvement, not just incremental updates.
Making and supplying 3-Bromo-4-Nitropyridine N-Oxide goes beyond filling orders. Our commitment runs through each drum, bag, and bottle we produce. Customers new and old know they can call with questions that dig deep into synthetic challenges rather than sticking to order numbers. We know most breakthroughs and optimizations don’t show up in newsletters or glossy presentations. Actual discoveries come from the informal back-and-forth between manufacturer and chemist.
In our shop, we rely on substance over sales talk. By sharing practical knowledge—what worked, what didn’t, and what might save time or resources for the next project—we support genuine progress. The compound itself plays only part of the story. Its reliability, consistency, and performance come from the steady hands of our production staff and the open dialogue with every user.
We invite every scientist, scale-up manager, and R&D team using 3-Bromo-4-Nitropyridine N-Oxide to keep the conversation open. If your project runs into unexpected reactivity, variable yields, or analytical confusion, we want to hear about it. Those insights keep our own operation sharp and teach us more than any textbook ever could.
Staying close to both the raw chemistry and the ever-evolving needs of research partners means we improve every year. Every batch we’ve produced stands as a testament to that commitment. By investing in people and processes, we aim to deliver a product that doesn’t just fill a specification—but gives real value on every bench and production floor it reaches.
Because each gram carries the work of many hands, and every order contributes to the next breakthrough, we’re ready to support your synthesis challenges with experience, transparency, and ongoing improvement.