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HS Code |
724890 |
| Chemical Name | 4-Chloro-3-Nitro-2,6-dimethylpyridine |
| Molecular Formula | C7H7ClN2O2 |
| Molecular Weight | 186.60 g/mol |
| Cas Number | 151213-96-4 |
| Appearance | Yellow crystalline solid |
| Melting Point | 87-91 °C |
| Solubility In Water | Slightly soluble |
| Purity | Typically >98% |
| Storage Condition | Store in a cool, dry place, tightly closed |
| Smiles | CC1=NC(=C(C=C1[N+](=O)[O-])Cl)C |
| Inchi | InChI=1S/C7H7ClN2O2/c1-4-3-6(10(11)12)7(8)5(2)9-4/h3H,1-2H3 |
| Synonyms | 4-Chloro-3-nitro-2,6-dimethylpyridine |
As an accredited 4-Chloro-3-Nitro-2,6-dimethyl pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Chloro-3-Nitro-2,6-dimethyl pyridine is packaged in a 25g amber glass bottle with a tamper-evident sealed cap. |
| Container Loading (20′ FCL) | 20′ FCL: Typically loaded with 12 MT (240 fiber drums × 50kg) of 4-Chloro-3-Nitro-2,6-dimethyl pyridine, palletized. |
| Shipping | 4-Chloro-3-Nitro-2,6-dimethyl pyridine should be shipped in tightly sealed containers under dry, cool conditions, away from direct sunlight and incompatible substances. Comply with local and international regulations for hazardous chemicals. Proper labeling, documentation, and hazard communication are required to ensure safe handling and transport of this compound. |
| Storage | Store **4-Chloro-3-Nitro-2,6-dimethyl pyridine** in a tightly sealed container, away from moisture, heat, ignition sources, and incompatible substances such as strong oxidizers and bases. Keep in a cool, dry, well-ventilated area, protected from direct sunlight. Label the container clearly and use secondary containment to prevent spills. Follow all relevant safety and chemical hygiene regulations. |
| Shelf Life | 4-Chloro-3-Nitro-2,6-dimethyl pyridine is stable under recommended storage conditions; typical shelf life is 2 years if unopened. |
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Purity 98%: 4-Chloro-3-Nitro-2,6-dimethyl pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where enhanced reaction yield is achieved. Melting Point 102°C: 4-Chloro-3-Nitro-2,6-dimethyl pyridine with a melting point of 102°C is utilized in agrochemical formulation processes, where stable compound formation is ensured. Particle Size <50 µm: 4-Chloro-3-Nitro-2,6-dimethyl pyridine with particle size less than 50 µm is used in fine chemical manufacturing, where increased dispersion efficiency is obtained. Moisture Content <0.5%: 4-Chloro-3-Nitro-2,6-dimethyl pyridine with moisture content below 0.5% is applied in electronic chemical production, where improved product reliability is realized. Stability Temperature 120°C: 4-Chloro-3-Nitro-2,6-dimethyl pyridine with stability up to 120°C is used in polymer additive development, where thermal integrity during processing is maintained. |
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Many years in the laboratory and on the production floor have shown us how 4-Chloro-3-Nitro-2,6-dimethylpyridine stands apart from other substituted pyridines. All of its development and consistent production come from our own facilities. Quality does not arrive by accident; it results from dedicated process control, reliable sourcing, and close knowledge of all raw materials involved. Most specialties manufacture a dozen substituted pyridines, but not all pyridines serve equally well in high-value applications. This molecule was first designed for use where both chemical reactivity and physical stability must land in balance, while still permitting distinctive downstream modification.
This compound features a tightly defined profile, thanks to stringent purification steps and robust raw material control. 4-Chloro-3-Nitro-2,6-dimethylpyridine emerges as an off-yellow crystalline solid after final filtration. The solid parses out as near-anhydrous, and we measure any trace-level moisture by Karl Fischer titration, keeping well below the limits set for sensitive synthesis. Most lots, measured by HPLC assay, deliver purity well above 98.5%. Our technical team maintains established quality cutoffs, as downstream catalysts, agrochemical intermediates, and pharmaceutical scaffolds depend on such results. Undesirable isomer formation gets tracked at trace levels. Consistent purity supports strong batch-to-batch reproducibility in our customers' process chemistry, which avoids unexpected side reactions or costly do-overs.
The primary applications for this molecule evolve from key electronic, pharmaceutical, and agrochemical processes. Chlorinated nitropyridines often take on the pivotal role of both intermediate and coupling partner. Fine chemical manufacturers rely on 4-Chloro-3-Nitro-2,6-dimethylpyridine for the efficient introduction of the nitro group or as a reactive anchor point for nucleophilic substitution. We’ve seen its adoption rise steadily in the synthesis of diverse heterocyclic compounds that cannot tolerate excessive byproducts or residual solvents.
Customers in crop protection chemistry focus on the stability the compound delivers, even under elevated temperature or pH-shifting conditions. The dual methyl groups at the 2 and 6 positions fend off unwanted nucleophilic attacks and limit oxidation, raising yields in synthesis tracks where uncontrolled side chains become problematic. A neighboring nitro substituent adjusts the reactivity, making it possible to direct new functionalization onto the precise ring carbon needed for downstream steps.
In the drug discovery space, medicinal chemists appreciate the compound for the broad applicability in building larger, more complex molecules. Traditional synthetic approaches can become unreliable when ring activation is excessive or unpredictable. Here, the combination of chlorine and nitro groups, flanked by stabilizing methyls, creates a perfect jump-off for Sonogashira, Suzuki, and Buchwald couplings. Where other building blocks lead to regioisomeric confusion or undirected functionalization, this one reduces side-product formation, streamlining overall discovery and scale-up. Our process chemists remind clients that, while many aromatic nitro-chlorides exist, very few cover the kind of reactivity demanded by today’s high-throughput screening teams.
Chemists sometimes reach for simple chloropyridines or nitropyridines, but these lack the performance window our product offers. Common pyridine derivatives, particularly those with only a single substituent, do not impart the same combination of electronic effects or stability during multi-step synthesis. Absence of methyl groups in other species commonly leads to increased degradation, greater waste generation, and trickier product isolation. Left unchecked, these inefficiencies scale up and hit both budgets and time-to-market.
We have handled products such as 2-chloro-6-methylpyridine and 3-nitro-4-methylpyridine—each has a place in the arsenal but falls short in critical routes demanding selectivity and protection. Customers typically report incomplete conversions or extra purification headaches when they substitute these products. Nucleophilic attacks often strike unintended positions on inappropriately substituted rings. In batch production, even a half-percent of a wrong isomer means hours of column work or reprocessing, which can stall an entire process line.
4-Chloro-3-Nitro-2,6-dimethylpyridine offers a sharper control over regioselectivity and functional group exchange. Colleagues in our R&D group took particular care in mapping out its reactivity profile, vetting it in both small-scale experimental runs and larger pilot batches. This approach surfaces only real-world differences: stability in long reaction runs, ease of purification after product workup, and repeatable performance in complex reactions under pressure or heat.
A laboratory can only perform as well as its input chemicals allow. For manufacturers and research chemists alike, reliability includes both chemical and physical stability. We find that this compound maintains lot integrity even under moderate thermal fluctuations, thanks to crystalline form and lack of hygroscopic tendencies. Standard storage in sealed drums—protected from direct sun and excessive humidity—has shown no significant variance in melting point or color over six months, and even in high-turn inventories, stability stands up.
Crystallinity matters for mixing and dosing accuracy in continuous reactors, and batch processes benefit from an unmistakable color signature that assists with quick identification. Spill control and housekeeping become more manageable as well. Our operators point out that powders derived from this pyridine sweep up more readily than amorphous or oily variants, which improves plant hygiene and cuts down on material loss.
We appreciate firsthand the importance of a predictable melting range. The near-anhydrous constitution translates into trouble-free weighing and metering, even in modern automated systems. No clumping or bridging makes for smoother operation. Analysts in our quality unit often mention the ease with which the compound redissolves in acetonitrile, DMF, or DMSO—convenient for no-waste sample preparation ahead of titration and purity analysis.
From raw material selection to the final fill, every step gets tracked. Our own production team never outsources purification or final crystallization. Most competing offerings depend on third-party contractors, leading sometimes to lost traceability or uneven impurity profiles. We hold inventory and process records in place for at least a decade, with samples pulled regularly and archived for cross-study should any customer concern ever arise. Real-world knowledge helps us know exactly what deviations look like—slight color shift, small variation in particle size, or minute increases in trace solvents are not just theoretical, but issues our inspectors monitor every lot.
All finished material passes a full suite of instrumental checks—infrared, mass spectrometry, and trace metal evaluation using validated reference standards. Microtraces of heavy metals or halogenated solvents get chased out to detection limits below global pharmaceutical guidelines. Any critical impurity flagged through these tests prompts full process review, and nothing ships until we sign off. We believe such hands-on oversight allows both regulatory and in-lab scientists to work with confidence, especially in regulated or customer-audited end-market applications.
Our site invests in training for every operator, with safety protocols and hazard controls under constant review. Chlorinated nitropyridines bring with them certain handling risks, and our own EHS team constantly refines SOPs to match current best practices; fire detection, ventilation management, and employee PPE routines reflect the realities of both bulk handling and small-batch scale-ups. Technical support stays on call for process troubleshooting or accidental release scenarios, drawing on incidents we’ve managed in our own facilities. Keeping this level of institutional knowledge in-house means faster, clearer advice for partners downstream.
Requests for different grades—such as ultra-high purity, fine particle forms, or specific moisture limits—circle back to our technical experts, not a third-party packager. Major growth in electronic materials and pharma intermediates has raised demand for tight spec control in recent years. In some cases, we have adjusted reaction parameters or layered new purification options to deliver the right grade for a particular route. One pharma partner needed an ultra-fine version for solid dispersions; this prompted our team to upgrade classifier and sieve steps, not just deploy a blunt impact mill that might generate too-dusty fines.
Clients in China, North America, and Europe each approach quality control with different site audits and process transparency requirements. We maintain full documentation and open Q&A sessions for customer technical reviewers, running shared trials as needed. Internal feedback cycles ensure customer suggestions feed directly into our next production round—no marketing handoff required.
Supply chain is not just logistics, but often life-or-death for critical drug precursors, especially as regulations tighten and public scrutiny of raw materials grows. We source core feedstocks from vetted suppliers and keep contingency stocks enough to backstop unexpected plant shutdowns or shipping embargoes, especially in recent volatile times. By running an on-site analytical lab and never surrendering QC to outside labs, we make sure every drum meets the spec we set and that end-users get a product that always meets their validation criteria. This keeps project schedules intact and regulatory headaches at bay.
Manufacturing chlorinated organic compounds puts a responsibility on us, not just to customers but to communities. Waste management practices are constantly fine-tuned, going beyond the minimum legal requirements. Our effluent stream goes through rigorous multi-stage treatment, neutralizing chlorinated and nitro content well before any permitted plant outflow. On-site scrubber systems take up both fugitive and process-driven releases, driving off-gas content beneath detection limits laid down by both local and international regulations.
Over the past five years, solvent reduction and recycling efforts within the plant have cut total load on downstream water and air treatment. Key reactions have shifted away from classical solvents to modern alternatives like acetonitrile recovery systems. Internal training focuses on sustainable practices, so every process engineer and operator gets both the know-how and incentive to achieve continuous improvements. Matter-of-fact accountability and process innovation inform the approach at every step.
We partner with local emergency services for incident readiness and run quarterly practice drills tied to the actual profiles of the materials we produce. Our production site rejects business-as-usual complacency. Building and shipping compounds like 4-Chloro-3-Nitro-2,6-dimethylpyridine means being ready—24/7—to respond to anything from small leaks to storm-driven power outages. Sharing incident history and lessons learned with others in the chemical sector helps improve standards industry-wide.
As the chemical and pharmaceutical industries move toward ever-higher compliance, new regulatory footprints call for more granular product traceability and supply chain transparency. Our in-house digital records now cover not only lot analytics but also full origin trace—from raw feedstock through every on-site reaction and fill operation. Recent directives around "green chemistry" push for ongoing adjustments in both process chemistry and waste recapture. Shifting market conditions—supply volatility, evolving ROHS and REACH mandates, and new lower solvent thresholds—feed directly into how we plan campaigns and socket in changeover or maintenance intervals. Customer demand for more sustainable, less hazardous alternatives means constant evolution of established processes.
Active dialog with research partners and industrial chemists shapes the next generation of substituted pyridines. Requests rise for even more selective halogen-nitro pairings, and for precision-milled grades to fit the demands of continuous flow synthesis. The same applies for derivatives carrying further blocking groups, or for scalable adaptations of laboratory discoveries. We track academic literature and patent landscapes, not only to anticipate competing products, but also to partner for co-development when a new application aligns with our manufacturing strengths.
Our plant engineers give feedback from every scale of production run, flagging where vacuum, heat, or novel crystallization steps push boundaries. These lived experiences guide upgrades and process tweaks. The teamwork between operations, R&D, and technical support forms the backbone of our problem-solving approach. We have found few shortcuts—most gains come from iterative process improvements, responsive customer collaboration, and clear communication about both opportunities and technical tradeoffs.
The manufacturing reality goes beyond technical data sheets and brochure snapshots. The proof lies in daily process reliability, logistics coordination, and openness to troubleshooting. When a pharmaceutical client reports a batch with off-standard reactivity, our team conducts root cause analysis from both starting material and downstream intermediates—drawing on both reports and live sample pulls. Practice has taught us that successful customers return not just for another drum, but for actual problem-solving partnership.
As new applications surface, especially in the realm of precision catalysts or functionalized aromatics, the story of 4-Chloro-3-Nitro-2,6-dimethylpyridine expands. Every round of feedback, from a pilot lot tested in next-generation synthesis all the way to emergency shipment after a competitor's plant breakdown, informs our next action. Continual listening and process adjustment shape more than product quality—they reinforce the value of open lines with customers, regulators, and community stakeholders.
From unique production insights to honest fixes for unexpected issues, we base our future plans on measurable experience. New suppliers, emerging green chemistry routes, or shifting customer requirements prompt reevaluation of supply models, production scheduling, and plant upgrades—nothing stands still in chemical manufacturing. The durable performance and real-world adaptability of 4-Chloro-3-Nitro-2,6-dimethylpyridine arise directly from deep hands-on production knowledge. We remain committed not merely to pushing out product, but to delivering both reliability and insight across an ever-growing range of applications.