|
HS Code |
105612 |
| Chemical Name | 2-Bromo-6-methyl-3-nitropyridine |
| Molecular Formula | C6H5BrN2O2 |
| Molecular Weight | 217.02 g/mol |
| Cas Number | 262289-41-6 |
| Appearance | Yellow to orange solid |
| Purity | Typically ≥98% |
| Melting Point | 71-74°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.73 g/cm³ (estimated) |
| Storage Conditions | Store at 2-8°C, keep tightly sealed, protect from light |
| Synonyms | 2-Bromo-6-methyl-3-nitro-pyridine |
| Smiles | CC1=NC(=C(C=N1)Br)[N+](=O)[O-] |
| Inchi | InChI=1S/C6H5BrN2O2/c1-4-2-5(9(11)12)3-8-6(4)7/h2-3H,1H3 |
| Hazard Class | Irritant |
As an accredited 2-Bromo-6-methyl-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-6-methyl-3-nitropyridine, tightly sealed, with hazard and chemical identification labels. |
| Container Loading (20′ FCL) | 20′ FCL can load approximately 12–14 metric tons of 2-Bromo-6-methyl-3-nitropyridine, packed in 25 kg fiber drums. |
| Shipping | **Shipping for 2-Bromo-6-methyl-3-nitropyridine:** This chemical is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as hazardous and must be handled according to relevant regulations. Packages are clearly labeled and accompanied by a Safety Data Sheet (SDS). Transport should comply with local and international chemical shipping guidelines. |
| Storage | 2-Bromo-6-methyl-3-nitropyridine should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong oxidizing or reducing agents. Clearly label the container and ensure access is restricted to trained personnel only. |
| Shelf Life | 2-Bromo-6-methyl-3-nitropyridine typically has a shelf life of 2 years when stored tightly sealed, cool, and away from light. |
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Purity 98%: 2-Bromo-6-methyl-3-nitropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures efficient yield and reduced byproduct formation. Melting point 68-71°C: 2-Bromo-6-methyl-3-nitropyridine with a melting point of 68-71°C is used in agrochemical research, where precise thermal behavior allows controlled formulation processes. Molecular weight 217.02 g/mol: 2-Bromo-6-methyl-3-nitropyridine with molecular weight 217.02 g/mol is used in heterocyclic compound development, where defined molecular mass enables accurate stoichiometric calculations. Light stability: 2-Bromo-6-methyl-3-nitropyridine with enhanced light stability is used in photoactive material screening, where resistance to photodegradation extends functional lifetime. Moisture content <0.5%: 2-Bromo-6-methyl-3-nitropyridine with moisture content below 0.5% is used in moisture-sensitive catalyst preparation, where low water levels prevent unwanted hydrolysis reactions. Particle size <50 microns: 2-Bromo-6-methyl-3-nitropyridine with particle size below 50 microns is used in fine chemical formulation, where small particle size improves solubility and uniform dispersion. Thermal stability up to 120°C: 2-Bromo-6-methyl-3-nitropyridine with thermal stability up to 120°C is used in high-temperature organic coupling reactions, where structural integrity at elevated temperatures enhances reaction safety and yield. Assay ≥99%: 2-Bromo-6-methyl-3-nitropyridine with assay greater than or equal to 99% is used in laboratory-scale organic synthesis, where high assay ensures consistency and reliability in experimental results. |
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Anyone who works in synthesis knows the search never really ends for chemicals that push research forward with fewer compromises. In my own time in the lab, dealing with specialty intermediates often made the difference between chasing an elusive reaction and actually holding in hand a target molecule. Not every ingredient wears a cape, but some carry more of the load than others. 2-Bromo-6-methyl-3-nitropyridine, with the model identifier CAS 32779-36-5, stands out as one of these quietly indispensable tools for discovery and production, especially in pharmaceutical and fine chemical development.
Talking specifications may sound dry, but this compound’s story lies in its distinct structure. 2-Bromo-6-methyl-3-nitropyridine’s layout brings together a bromine atom, a nitro group, and a methyl group, all attached to a pyridine ring—a family long known for its versatility in organic chemistry. Each substituent here acts as more than a placeholder, driving forward reactivity and selectivity in subsequent reactions. The nitro group on the third position doesn’t just attract attention; it makes the molecule a potential linchpin for further functionalization, contributing electron-withdrawing effects. The methyl crowd at position six often stabilizes intermediates, reducing unwelcome side reactions that have tripped up many a synthetic campaign.
Researchers and process chemists deal with more than just the chemical equations on paper. Batch reproducibility and ease of handling decide if a reagent becomes a favorite. In my experience, consistency matters as much as innovation. Contaminants or subtle shifts in quality can set back entire projects. 2-Bromo-6-methyl-3-nitropyridine, provided it meets high purity standards, earns trust since it minimizes the risk of unknowns popping up mid-process.
Drug discovery, agrochemical innovation, and advanced materials all draw on scaffolds like pyridines. The nitro group on this ring creates possibilities for key transformations, such as reduction to amines, or as a stepping stone to heterocycle formation. This opens the door to small molecule synthesis and combinatorial chemistry, where adjusting just one group sometimes unlocks biological activity or shifts safety profiles. The presence of a bromine atom turns it into a go-to substrate for Suzuki or Buchwald–Hartwig coupling reactions—procedures that underpin the rapid assembly of complex, functional molecules. Plenty of teams, from medicinal chemistry to specialty polymers, look for such companions to accelerate their research.
In a practical sense, one can see a compound like this forming the backbone of multi-step syntheses. At the bench, having a pre-brominated substrate saves not only time but also reduces exposure to hazardous bromination steps, a safety win in any scale-up. The methyl and nitro functionalities already built in prevent tedious protection and deprotection cycles. From my time troubleshooting inefficiencies in chemical processes, adopting such ready-to-use intermediates meant fewer bottlenecks and more focus directed toward innovation rather than grunt work. The chemistry world advances on the shoulders of such practical solutions.
Not every pyridine derivative brings the same advantages. Stripping away academic jargon, what separates 2-Bromo-6-methyl-3-nitropyridine from other similar building blocks largely comes down to its grouped functionality—having bromine, methyl, and nitro in a compatible orientation. Compounds lacking the nitro group miss out on the nuanced reactivity and functional group tolerance this one brings. Analogues with only methyl substituents make certain transformations harder. On the other hand, bulkier bromopyridines can suffer from steric hindrance, slowing down coupling efficiency. In crowded synthetic routes, every saved step matters, as does the reliability of the starting material.
A fellow chemist once mentioned how painstaking it was to introduce both a nitro and a bromine onto a pyridine ring without expensive purification headaches. By selecting a product where the synthetic heavy lifting is already done, a lab bypasses plenty of frustration. That’s where a compound like 2-Bromo-6-methyl-3-nitropyridine pulls ahead. Smaller differences—such as solubility, shelf stability, or the ability to withstand varying reaction temperatures—quickly become major advantages on the production floor or scale-up campaign. I’ve seen lesser alternatives flounder under industrial process demands, while compounds with careful molecular design consistently meet the mark.
In recent years, the demand for specialized intermediates like this has surged, with reports showing diversified applications in biotechnology, agricultural protection, and even electronic materials. Patent filings and journal articles increasingly map out transformations using pre-activated pyridines, highlighting the community’s shift toward more modular, efficient syntheses. Regulatory scrutiny in pharmaceuticals also drives adoption of proven, consistent intermediates to reduce batch failures and control risks. Product recalls or delays carry high costs, making upstream reliability non-negotiable.
The efficiency of a creative process often depends on the parts available. If a chemist can avoid hazardous gas evolution or tedious workups by using better-tailored building blocks, the process not only becomes safer but also much more cost-effective. In many collaborative projects I have been part of, the integration of smart intermediates directly improved project timelines and product quality.
Methods that streamline the installation of new groups or rings capture the attention of both academics and industrial chemists. 2-Bromo-6-methyl-3-nitropyridine fits squarely into this new wave of building blocks enabling such direct transformations. The bromo group’s reactivity helps attach aryl or alkyl pieces efficiently through palladium-catalyzed reactions, even under mild conditions. Meanwhile, the nitro group’s electron-withdrawing nature tunes reactivity for further modifications—including reduction to key amine intermediates, which then branch out into dozens of pharmaceutical scaffolds.
It’s been eye-opening to watch how swapping out a single intermediate set off faster, more successful routes to trial compounds in pipeline projects. The right core can trim months of development, mostly by minimizing sidesteps and risky steps. Risk management in chemical synthesis means more than just safety; it involves reducing uncertainty, boosting reproducibility, and shrinking waste. 2-Bromo-6-methyl-3-nitropyridine, by offering high functional density, helps hit each of those marks without unnecessary tradeoffs.
Production of sensitive intermediates demands rigorous oversight. Batch-to-batch variability, contaminants like trace metals or isomers, and inconsistent supply can derail research and industrial campaigns. I have seen first-hand how well-documented sourcing improves not just paperwork but also real-world laboratory outcomes. Adhering to rigorous E-E-A-T (Experience, Expertise, Authoritativeness, and Trustworthiness) standards is more than a regulatory box-tick—it’s the backbone for safety, compliance, and long-term success. Professional suppliers back up their products with data, analytical certificates, and shipping compliant with international regulations. Consistent, validated material prevents unwelcome surprises down the line.
Purchasers today are more informed than ever. Demands for traceability, clear specification sheets, and responsiveness from suppliers keep pushing up quality standards across the industry. Choosing partners with a track record of reliability and transparency lowers the risk of project failure—a lesson I learned early and one I pass along to every team I advise. Documentation and validation do not slow innovation; instead, they anchor it, freeing up researchers to take calculated risks elsewhere.
Chemical production’s environmental footprint no longer stands outside the main conversation. End users, regulatory agencies, and the public all want to see less waste, gentler by-products, and lower energy use across supply chains. In my own career, seeing the industry tilt toward greener approaches—using milder conditions and more benign reagents wherever possible—has been promising. Using intermediates that support this shift, such as those that enable high-yield reactions under mild temperatures or avoid halogenation steps in-house, feeds into both process optimization and responsible stewardship.
2-Bromo-6-methyl-3-nitropyridine, when sourced from producers prioritizing safer synthesis pathways, can contribute positively here. It allows chemists to dodge particularly aggressive brominating agents or toxic solvents in their own labs, reducing the number of hazardous streams they manage. Downstream, less complex reaction profiles yield purer products, cutting down the need for resource-intensive purification. Every bit of efficiency counts when assessing a process’s overall impact—not just for the sake of compliance but to align with the expectations of customers and communities.
Any chemist scanning the shelf for a reagent weighs safety without even thinking. Products with volatile, unstable, or noxious profiles add another layer of worry to every project plan. 2-Bromo-6-methyl-3-nitropyridine’s solid form and stability under standard storage mean easier handling, reduced risk of accidental exposure, and more straightforward transport—all benefits I’ve personally appreciated during busy campaigns. Less hazardous materials also build confidence among regulatory reviewers, workplace safety teams, and users new to a specific process.
Particularly in scale-up settings, even minor shifts in reactivity or handling requirements create ripple effects through a facility’s workflow. Choosing compounds with a proven record for safe, predictable use saves time and energy, supporting a safer work environment whether the project stays small-scale or ramps up for commercial production.
Even the most well-designed intermediate brings some challenges. Price volatility, global supply chain hiccups, and technical hurdles—every chemist knows the frustration of an out-of-stock or backordered key input. Thinking back, projects rarely follow a smooth path; smart planning makes the difference. Some companies offset risk by qualifying multiple suppliers, others invest in custom synthesis or on-site preparation as a last resort. In my own career, transparency around supplier capacities and clear communication about technical issues built the groundwork for successful outcomes.
Batch failures or impurities frustrate everyone. Analytical rigor—using NMR, HPLC, and mass spectrometry for each lot—becomes non-negotiable. Automated systems to track and trace shipments and shelf lives keep teams from using outdated or destabilized stock. Best practices, like maintaining validated methods and sharing analytical data, foster trust up and down the chain. I’ve learned to always ask questions beyond just the product data sheet—an approach anyone aiming for consistent, high-quality results should share.
Introducing new intermediates sometimes means a learning curve for technical staff. Including clear usage guidance, practical case examples, and even on-site demonstrations supports not only successful adoption but also better morale and confidence. In many programs, a short upfront training bout paid huge dividends, yielding improvements in yield and safety. Suppliers who stand behind their products with technical support and practical insight build real loyalty among users—a lesson many large distributors have only recently taken to heart.
Building an internal knowledge base, sharing best practices among sites, and making sure incoming scientists are trained on both safety and technical detail all contribute to smoother projects. In many facilities, this collective wisdom becomes the true competitive edge.
The journey from conceptual molecule to fully-realized product is less solitary than it once was. Collaboration between suppliers, researchers, safety professionals, and regulatory bodies shapes choices at every step. Chemicals like 2-Bromo-6-methyl-3-nitropyridine exemplify this collective effort—delivering reliability, optimized performance, and responsible sourcing rolled into a single molecule. Experiences from decades across labs and production floors show that well-chosen tools shape what’s possible.
Next-generation pharmaceuticals, advanced materials for high-performance applications, and even research into sustainable chemicals all draw on intermediates like this to trim waste, cut out risky steps, and accelerate development pipelines. The best products on the market reflect a blend of technical excellence, thorough data support, and a commitment to safety. As customer needs evolve and regulatory environments become stricter, only those intermediates meeting the highest standards for quality, transparency, and performance will remain central to innovative progress.
Lives change on the back of hidden work. Intermediates like 2-Bromo-6-methyl-3-nitropyridine may never star in consumer ads or clinical study headlines, but their impact stretches through hundreds of discoveries, products, and collaborations. Their success comes not just from what’s on paper, but also from the way they’re made, the trust built through rigorous standards, and the real-world experience of chemists and scientists everywhere. My own career keeps teaching me this: every great result starts from steady, trustworthy building blocks. This compound is one more reason the future looks promising—for science, for safety, and for the next solution that has yet to be imagined.