3-Methyl-2-nitropyridine

    • Product Name: 3-Methyl-2-nitropyridine
    • Chemical Name (IUPAC): 3-methyl-2-nitropyridine
    • CAS No.: 17852-53-2
    • Chemical Formula: C6H6N2O2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    390819

    Iupac Name 3-Methyl-2-nitropyridine
    Cas Number 57829-96-2
    Molecular Formula C6H6N2O2
    Molecular Weight 138.12
    Appearance Yellow to yellow-brown solid
    Melting Point 35-38°C
    Boiling Point 273-274°C
    Density 1.27 g/cm3 (approximate)
    Solubility In Water Slightly soluble
    Flash Point 128°C
    Smiles CC1=C(N=CC=C1)[N+](=O)[O-]
    Inchi InChI=1S/C6H6N2O2/c1-5-3-2-4-7-6(5)8(9)10/h2-4H,1H3
    Synonyms 2-Nitro-3-methylpyridine
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 3-Methyl-2-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-Methyl-2-nitropyridine, tightly sealed with a screw cap and labeled with hazard information.
    Container Loading (20′ FCL) 20′ FCL: 3-Methyl-2-nitropyridine is securely packed in drums or bags, maximizing container space for safe, efficient transport.
    Shipping **Shipping Description for 3-Methyl-2-nitropyridine:** 3-Methyl-2-nitropyridine should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must comply with all local, national, and international regulations for hazardous chemicals. Ensure proper labeling and documentation. Transport in accordance with UN regulations, and use appropriate secondary containment to prevent leaks or spills during transit.
    Storage 3-Methyl-2-nitropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. It must be kept separate from strong oxidizing agents and acids. Proper labeling and secondary containment are recommended to prevent leaks or spills. Handle under strict safety protocols, including appropriate personal protective equipment.
    Shelf Life 3-Methyl-2-nitropyridine has a typical shelf life of 2 years when stored in a cool, dry, and tightly sealed container.
    Application of 3-Methyl-2-nitropyridine

    Purity 98%: 3-Methyl-2-nitropyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and selectivity in target compound production.

    Melting Point 58°C: 3-Methyl-2-nitropyridine with a melting point of 58°C is used in organic reactions requiring controlled solid-state inputs, where it enables reproducible reaction initiation.

    Molecular Weight 124.12 g/mol: 3-Methyl-2-nitropyridine with a molecular weight of 124.12 g/mol is used in agrochemical research, where accurate formulation and dosing are achieved.

    Particle Size <75 μm: 3-Methyl-2-nitropyridine with particle size less than 75 microns is used in catalyst preparation, where uniform dispersion and enhanced reaction rates result.

    Stability Temperature up to 110°C: 3-Methyl-2-nitropyridine stable up to 110°C is used in heated batch chemical processes, where it maintains structural integrity without degradation.

    Low Water Content <0.5%: 3-Methyl-2-nitropyridine with water content below 0.5% is used in anhydrous synthesis protocols, where side-reactions from hydrolysis are minimized.

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    Certification & Compliance
    More Introduction

    3-Methyl-2-nitropyridine: A Deep Dive Into a Trusted Chemical Building Block

    Setting the Scene: What 3-Methyl-2-nitropyridine Brings to the Table

    Scrolling through catalogs of intermediate chemicals, you can pick out a handful that quietly shape the future of pharmaceuticals and advanced materials. 3-Methyl-2-nitropyridine isn’t the kind of name that flashes through headlines, but to anyone who’s spent time in a well-equipped lab or chemical facility, its value is clear as day. Picture a yellow crystalline powder, usually manufactured with tight specifications, slotting into place at the origin of complex synthesis routes. This compound, with a methyl group at the third position and a nitro group on a pyridine ring, almost acts like a gateway — one that opens paths to targeted synthetic transformations in both drug and agrochemical development.

    Model, Purity, and Why That Matters

    Most researchers hunting for reliable 3-Methyl-2-nitropyridine ask for purity no less than 98 percent. Typical models available for academic and industrial use hover around this figure, often exceeding it, which means impurity risks stay minimal. High purity isn’t some marketing checkbox. Anyone who’s wrestled with trace contaminants in a reaction vessel knows what extra byproducts can do to yields and selectivity. The lot I remember working with last year displayed that sharp, consistent pale-yellow look on first opening the jar, and thin-layer chromatography confirmed the sample was as promised — a little detail that saves so much grief downstream. Specific lot analysis often accompanies shipments, highlighting not just the percentage of main compound but also moisture data and trace residue content. Even surface moisture below 0.2 percent gives researchers peace of mind, protecting both the compound and subsequent steps.

    Unique Structure, Unique Uses

    Chemists recognize the versatility of pyridines. 3-Methyl-2-nitropyridine earns its spot on the bench because that little nitro group pulls electrons, shifting reactivity to favor routes unavailable to unsubstituted pyridines. Introducing the methyl group fine-tunes selectivity for cross-coupling reactions and nucleophilic substitutions. In my own experience developing kinase inhibitors, we leaned on this selectivity to keep rogue side products at bay — the difference between a passable intermediate and a pristine, ready-for-conjugation target. A nitrated pyridine like this can open doors to reduction, acylation, and Suzuki coupling without requiring harsh conditions that degrade other precursors. Researchers see this as more than a commodity; think of it as a tool sharpened for creative synthetic design.

    Comparing to Other Pyridine Derivatives

    Some reach for 2-nitropyridine, others for 3-methylpyridine, yet 3-Methyl-2-nitropyridine stands out on sheer reactivity and the subtleties it introduces in synthetic routes. Switch to 2-nitropyridine and steric hindrance drops, but electronic properties shift and downstream steps become unpredictable, especially with sensitive substitutions. With the methyl in the third position, the compound resists undesired oxidation or side-chain movement that sometimes frustrates other synthetic routes. The nitro group, instead of sitting idle, activates the ring in ways straight pyridine never could.

    Scientists hunt for intermediates that avoid unnecessary risk and boost yields. In one comparative study between 3-Methyl-2-nitropyridine and 2-methyl-5-nitropyridine, the former reacted cleaner under Pd-catalyzed cross-couplings, needing less purification and producing less waste. It’s not about some “one-size-fits-all” pyridine. A chemist developing a library of heterocyclic compounds would rather start with reactive partners that behave predictably, saving precious weeks.

    Industrial and Research Applications: Far From Generic

    Talk to anyone synthesizing specialty chemicals, and the discussion turns practical pretty fast. 3-Methyl-2-nitropyridine finds use in the early stages of pharmaceutical lead compound development. I’ve worked with it in research targeting antimicrobials, antifungal agents, and kinase inhibitors where selectivity and substitution patterns dictate the entire synthesis plan. A big advantage emerges during scale-up. Unlike some nitropyridines that decompose under mild base or elevated temperature, this one holds stable and predictable reactivity, saving on both cost and time.

    Its adoption has expanded into dye intermediates, thanks to that nitro group which lends vibrant color potential when reduced or further derivatized. Another important niche comes in the formation of ligands for metal complexes — a field that’s reshaping advanced catalysis and material science. The chemical’s stability against atmospheric moisture and oxygen supports supply chain reliability, a fact supply managers and process engineers always remind me not to take for granted.

    Getting Granular: What to Look for in a Trustworthy Source

    Anyone sourcing this compound for reliable synthesis needs transparency in production, from raw material provenance through to batch documentation. The real work starts long before a flask touches a heating mantle. Reliable suppliers lay out certificates of analysis for each batch, detailing residual solvents, water content, and mass spectrometry data. This kind of documentation isn’t bureaucratic padding. In pharmaceutical development, regulators want to see repeatable, traceable quality — a missing data point can throw an entire submission into jeopardy.

    A couple of years ago, our team faced inconsistent yields using a lower-grade alternative. Spot GC-MS batches flagged the culprit: trace benzaldehyde contamination. After switching to a reputable, tightly specified supply of 3-Methyl-2-nitropyridine, product purity rebounded, proving that source diligence and real analytical backup fuel real progress.

    Sustainability, Safety, and Current Market Trends

    Conversations about chemical intermediates now rarely avoid mention of sustainability, and 3-Methyl-2-nitropyridine comes under that same lens. The manufacturing process, traditionally based on nitration of methylpyridine, sometimes draws environmental scrutiny thanks to the nitro group’s legacy in waste streams. The leading producers have started shifting toward greener nitration routes and solvent recycling, which keeps overall impact lower without sacrificing batch consistency.

    Research organizations now take a close look at batch safety, handling documentation, and waste protocols, given the compound’s role as both a nitrated heterocycle and a potential toxicant in aquatic environments if mishandled. The combination of chemical inertness in sealed, dry conditions and clear handling procedures means facility managers rarely run into surprises, yet the cases where corners get cut provide sharp reminders about industry best practices. At scale, safe storage and careful labeling, combined with thorough staff instruction, keep day-to-day usage predictable and incident-free.

    From a wider perspective, the global demand for advanced pyridine intermediates has surged. Market analytics point to a steady increase in consumption, underpinned by growth in pharmaceutical R&D, advanced polymers, and agricultural chemistry. For every new drug candidate brought to life in a lab, the supporting chemicals like 3-Methyl-2-nitropyridine play an outsized role behind the scenes.

    Fine-Tuning the Process: Why Provenance and Consistency Build Trust

    Handling new projects in our lab, I’ve seen the headache of switching between suppliers with loose tolerances or fluctuating purity specs. A consistent batch of 3-Methyl-2-nitropyridine ensures not only chemistry that works but also regulatory filings that hold up under scrutiny. The best kind of supplier explains, in plain language, everything from HPLC results to packaging materials used. Small details, such as chemical stability against routine atmospheric variation, make a sizable difference in process reliability. Reliable glass-packaging or moisture-resistant liners in drums mean less variance on arrival, so analytical teams can focus less on incoming quality control and more on pushing innovation forward.

    For research-scale work, small pack sizes keep storage manageable and reduce loss due to degradation — a lesson learned the hard way during a period of supply-chain bottlenecks. For industrial use, bulk packaging practices focus on minimizing environmental exposure, which has helped several facilities cut down requalification testing costs and time.

    Problem Solving in the Lab: Lessons and Tips

    A few roadblocks come up again and again. In my experience, the nitro group could sometimes cause reduction side reactions if reducing agents sat too long in the mixture, leading to downstream variability. Careful reagent stoichiometry and monitoring, plus timely workup, kept things in check. Another challenge: in multi-step synthesis, lingering solvents from poorly purified sources could introduce noise into NMR or LC-MS readings. That’s where top-grade 3-Methyl-2-nitropyridine, carefully vetted, makes a world of difference. It’s tempting to cut corners for cost, but across the life of a project, those savings rarely outweigh the risk of failed batches or regulatory setbacks.

    For teams shifting from benchtop to pilot-plant scale, batch reproducibility climbs to the top of the concern list. I remember a project where a scaled-up process using an off-brand pyridine intermediate generated excess byproduct, requiring days of reruns and dozens of extra purity checks. When the switch came over to a trusted lot of 3-Methyl-2-nitropyridine, the results steadied immediately. Simple changes like this, leveraging reliable feeds and transparent sourcing, have led many research groups to rethink their procurement and quality assurance strategies.

    Responding to these challenges, leading suppliers continue to invest in analytical technologies. LC-MS and HR-GC now signpost every batch, flagging unknowns early in the process — a quiet revolution compared to the quality checks of even a decade ago.

    Potential Solutions to Sourcing and Safety Challenges

    Solutions emerge more from collaboration and transparency than from technical wizardry. Partners sharing batch data, integrating regular feedback, and facilitating direct lines between procurement and technical teams have cut troubleshooting time dramatically in my own experience. On the regulatory and environmental front, green chemistry principles now shape everything from solvent selection to waste tracking. Smart facilities not only implement strict chemical hygiene but adopt cradle-to-cradle accountability — tracking batches from raw material all the way to finished product, and even reclaiming packaging where possible.

    Across many organizations, internal culture shifts have also made a difference. Training programs stress the importance of reading and understanding specifications, not just following old routines. Creating a loop where researchers give feedback to purchasing, which in turn influences supplier qualification, tightens quality control from lab bench to loading dock. Offering open access to analytical certificates means even junior team members can trace any hiccup to its origin — a far cry from the black box delivery days of the past.

    Quality, Innovation, and the Industry’s Forward March

    After years working with various pyridine intermediates, one thing pops up repeatedly: quality doesn’t just cut risk, it amplifies innovation. Researchers given high-purity, reliable 3-Methyl-2-nitropyridine build new compounds with confidence and move quickly from idea to proof-of-concept. Pharmaceutical teams tackle more daring transformations, knowing their core intermediates won’t sandbag efforts with surprise side products or hidden volatility.

    From specialty dyes to advanced catalysts, the compound’s unique structure carves out reaction spaces that broaden what’s possible in synthesis. Applications in ligand formation, for example, have enabled the fine-tuning of catalytic processes that reduce both time and toxic byproducts. Teams adapting to evolving regulatory aims — from REACH regulations in Europe to stricter quality guidelines in North America and Asia — appreciate intermediates that don’t require ongoing process revalidation at every supply cycle.

    It’s not all smooth sailing. The cost of reliable, high-purity chemicals sits higher than generic alternatives. Facilities running on tight margins sometimes debate whether to make the jump. In the end, though, most see that the up-front investment pays for itself, especially when you consider the cost of scrapped lots, extra purification, or missed regulatory filing deadlines. From the viewpoint of daily lab work, reliable access to quality 3-Methyl-2-nitropyridine unlocks both time and creativity.

    Community and the Value of Knowledge Sharing

    It’s worth noting that few people come into chemical synthesis with a ready-made appreciation for intermediates like this one. Much of the real education happens through problem-solving — swapping notes with colleagues, troubleshooting failed reactions, and figuring out what the literature leaves between the lines. Experienced team members play a big role in flagging both what works and what doesn’t. Newcomers benefit from hearing real-world stories: the benefits of high batch purity, the headaches from ambiguous labeling, and the practical differences between close derivatives.

    Conferences and forums serve as breeding grounds for best practices. Panels featuring graduate students, academic faculty, and industry veterans often include debates over the best handling procedures or the cleanest batch they’ve received. The cumulative effect spurs both suppliers and users to raise their standards.

    Digital Tools Lifting Quality and Sustainability

    A new development gaining momentum is the adoption of digital quality management tools. Tracking every incoming shipment of 3-Methyl-2-nitropyridine digitally simplifies audits and lets teams spot recurring trends. Wider access to detailed batch data, sometimes via secure online portals, has cut the lag between discovery of an out-of-spec result and corrective action.

    Digital monitoring of storage environmental conditions, such as humidity and temperature, offers practical protection, preventing slow degradation and loss of potency. With software tracking every vial’s age and chain of custody, teams avoid surprise shortfalls, maintain compliance, and shrink overall waste. This focus on resource management over loss and unplanned disposal aligns closely with the sustainability goals reshaping the chemical manufacturing and pharmaceutical fields.

    Looking Ahead: How 3-Methyl-2-nitropyridine Shapes What’s Possible

    With research pushing further into multi-step synthesis, artificial intelligence-driven drug design, and greener manufacturing, compounds like 3-Methyl-2-nitropyridine continue to shape the edge of what’s possible. Its unique combination of reactivity, stability, and tunable substituents earns respect from industries hungry for both predictable results and creative freedom.

    Challenges remain, as with any chemical that straddles the demands of performance, safety, cost, and environmental responsibility. Advances in analytical science, greener process development, and transparent supplier partnerships will determine how smoothly manufacturers and researchers advance. Just like any reliable tool, 3-Methyl-2-nitropyridine’s real value emerges not from big claims but from the daily work of solving problems, building new molecules, and expanding the reach of modern chemistry.