6-Amino-2-Methyl-3-Nitropyridine

    • Product Name: 6-Amino-2-Methyl-3-Nitropyridine
    • Chemical Name (IUPAC): 6-amino-2-methyl-3-nitropyridine
    • CAS No.: 13534-97-1
    • Chemical Formula: C6H7N3O2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    697642

    Product Name 6-Amino-2-Methyl-3-Nitropyridine
    Cas Number 120624-17-3
    Molecular Formula C6H7N3O2
    Molecular Weight 153.14
    Appearance Yellow to orange powder
    Melting Point 110-114°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in polar organic solvents
    Smiles Cc1nc(c(cc1N)[N+](=O)[O-])N
    Inchi InChI=1S/C6H7N3O2/c1-4-6(9)5(8)2-3-7-4/h2-3H,8H2,1H3
    Storage Conditions Store in a cool, dry, well-ventilated area

    As an accredited 6-Amino-2-Methyl-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 6-Amino-2-Methyl-3-Nitropyridine supplied in a sealed amber glass bottle, labeled with product details and hazard warnings.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely loads 6-Amino-2-Methyl-3-Nitropyridine in fiber drums or bags, ensuring safe, moisture-free, and stable shipping.
    Shipping 6-Amino-2-Methyl-3-Nitropyridine is shipped in tightly sealed containers to prevent moisture and contamination. It is packaged according to regulations for hazardous chemicals, with clear labeling and safety data enclosed. The shipment is handled by certified carriers, ensuring compliance with all applicable transport, handling, and environmental safety protocols.
    Storage 6-Amino-2-Methyl-3-Nitropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Keep out of direct sunlight and ensure the storage area is clearly labeled and secure to prevent unauthorized access. Handle with appropriate protective equipment.
    Shelf Life 6-Amino-2-Methyl-3-Nitropyridine has a shelf life of 2-3 years when stored in a cool, dry, and airtight container.
    Application of 6-Amino-2-Methyl-3-Nitropyridine

    Purity 98%: 6-Amino-2-Methyl-3-Nitropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side product formation.

    Melting Point 136°C: 6-Amino-2-Methyl-3-Nitropyridine with melting point 136°C is used in heterocyclic compound manufacturing, where it improves thermal processing efficiency.

    Particle Size <50 μm: 6-Amino-2-Methyl-3-Nitropyridine of particle size less than 50 μm is used in API formulation development, where it enhances dissolution rate and uniformity.

    Stability Temperature 120°C: 6-Amino-2-Methyl-3-Nitropyridine with stability temperature up to 120°C is used in chemical synthesis under controlled heating, where it prevents thermal degradation.

    Moisture Content <0.5%: 6-Amino-2-Methyl-3-Nitropyridine with moisture content below 0.5% is used in sensitive organometallic reactions, where it minimizes hydrolytic side reactions.

    Assay ≥99%: 6-Amino-2-Methyl-3-Nitropyridine with assay greater than or equal to 99% is used in agrochemical research, where it guarantees reproducible experimental outcomes.

    Residual Solvents <100 ppm: 6-Amino-2-Methyl-3-Nitropyridine with residual solvents below 100 ppm is used in advanced material synthesis, where it ensures product safety and regulatory compliance.

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    Certification & Compliance
    More Introduction

    Exploring 6-Amino-2-Methyl-3-Nitropyridine: Reliable Performance in Fine Chemicals

    Many products promise breakthroughs in research and manufacturing, but 6-Amino-2-Methyl-3-Nitropyridine earns trust through solid results. Professionals working with pharmaceuticals, agrochemicals, and specialty materials often hunt for stable building blocks that help bring solutions to market faster. From years spent in chemical supply chains and lab settings, the real test for any compound doesn’t come from wordy technical sheets—it comes from consistency, traceability, and how well a product supports repeatable outcomes.

    Clear Model and Reliable Properties

    Identified by its CAS number 55092-36-1, 6-Amino-2-Methyl-3-Nitropyridine typically arrives as a pale yellow to brownish crystalline solid. Skilled chemists recognize the subtle signals of product purity—melting points in the expected range, single spot TLC, sharp NMR spectra. This kind of attention shows up in my own experience sourcing reagents from trusted partners who value traceability. Any lab tech who’s lost time on dodgy intermediates knows just how quickly a batch with too much water or off-ratio can throw off a synthesis. A reliable sample should not drift outside stated assay percentages, usually kept above 98% for this grade. Too many surprises in the bottle spell wasted runs, extra purification, and frustrated project managers.

    What Sets This Molecule Apart

    Chemists know that pyridine rings form the backbone of countless innovations, yet not every derivative brings the same level of reactivity or selectivity. 6-Amino-2-Methyl-3-Nitropyridine carries a smart combination: an amino group opens the door for downstream coupling, while the methyl and nitro positioning sets patterns for regioselective transformations. Other candidates lack this synergy. For instance, common nitropyridines often sit at 3- or 4- positions, and without the combination of an ortho amino group, these alternatives sometimes require extra steps or harsher conditions. This difference matters when protecting sensitive cores or when aiming for yields that justify project budgets.

    Applications Driving Real-World Needs

    In many pharmaceutical programs, timelines shrink, and regulatory scrutiny rises. We see 6-Amino-2-Methyl-3-Nitropyridine slot into critical routes for APIs, especially where step-economy is key. Peptide coupling agents, kinase inhibitors, and antifungal leads sometimes pass through this scaffold. Not every alternative blends synthetic flexibility with a clean toxicological profile; in my own years in scale-up, fewer off-target impurities mean fewer worries at the next downstream stage. Agrochemical innovators also turn to this nitroaniline-pyridine hybrid, taking advantage of its controlled reactivity to produce crop aids that resist breakdown but don’t linger longer than needed in the environment.

    On a more anecdotal level, I know colleagues in contract synthesis who breathe a sigh of relief when reliable intermediates shorten the time between “good idea” and bench data. Streamlining is more than a buzzword—it protects grant funding, wins regulatory confidence, and keeps talented teams focused on breakthroughs instead of troubleshooting.

    Versatility in Research and Manufacturing

    Several hundreds of kilograms may move through kilo labs and pilot plants each year, but small vials still drive discovery. Flexible pack sizes let R&D labs buy only what they can use before expiration. In early medicinal chemistry, this approach prevents costly overstock and waste. For larger synthetic projects, bulk purchasing allows producers to lock in consistent lots—same supplier, same analytical fingerprints, same processability. Chemists mark a sample’s worth by how easily it blends into standard protocols: does it dissolve cleanly, process safely, and avoid clogging lines? Every experienced scientist has a horror story about poorly handled intermediates—caked powders, sticky residues, and half-dissolved samples that kill project momentum.

    6-Amino-2-Methyl-3-Nitropyridine gets attention because it stays manageable through multiple seasons of inventory. In my own work, care in humidity and temperature control keeps this intermediate flowing without surprises. Stability on the shelf means less money spent on remakes or costly purification downstream, reflecting the discipline that separates professional suppliers from hobby shops.

    Safety and Responsible Use

    People in any chemical operation measure quality not only by purity but by transparency about hazards and responsible practices. 6-Amino-2-Methyl-3-Nitropyridine contains both nitro and amino groups, features that deserve respect in a safe laboratory. Standard lab gear—nitrile gloves, dust masks, fume hoods—keeps exposure controlled. Storage in cool, dry, and well-ventilated areas supports both safety and product life. Too many incidents start with a rushed intern or a forgotten cap. Inexperienced handlers should always check protocols and understand both the reactivity and environmental impact. Good vendors back up their product with documentation, safety guidance, and batch-specific analysis, which proves far more useful than generic advice.

    Environmental Responsibility

    In recent years, environmental stewardship has shifted from an afterthought to a demand. Many manufacturing teams now balance cost, compliance, and sustainability. By starting with high-purity intermediates like 6-Amino-2-Methyl-3-Nitropyridine, producers cut the risk of waste generation and secondary contamination. Fewer side-products signal less need for elaborate waste treatment downstream. Seasoned teams deploy proper containment and disposal routines—sealed containers, appropriate solvents, carefully tracked waste streams. Regulatory and customer audits increasingly check not just production yield but the responsible movement of inputs and byproducts.

    I’ve seen growing pressure on purchasing managers to “get it right the first time,” both for product quality and ethical sourcing. Large pharmaceutical supply chains might run supplier audits that ask about everything from labor conditions to carbon footprint. Production managers who favor intermediates with clear documentation and support enjoy fewer headaches from compliance teams and greater trust from end-users.

    Comparing 6-Amino-2-Methyl-3-Nitropyridine to Other Core Pyridines

    Competitors in the fine chemical space often tout similar molecules, but structural detail influences outcomes in ways that become clear only during actual runs. Take, for instance, 2-Methyl-3-Nitropyridine without the amino function—it won’t open the same synthetic doors. Meanwhile, 6-Amino-3-Nitropyridine, missing the methyl group, alters solubility and side-product risks. Each tweak to the pyridine ring forces chemists to rethink steps, sometimes trading higher yields for extra purification or longer hours troubleshooting.

    My own projects have compared 6-Amino-2-Methyl-3-Nitropyridine side-by-side with structurally simpler analogs for coupling reactions. The double handle offered by the amino and methyl groups, both ortho to the nitro, made direct downstream modifications smoother—faster coupling, fewer byproducts, and higher final yield. These regular wins matter when the clock is ticking in scale-up or screening. All this means less drain on resources and happier project leads.

    Meeting Regulatory and Documentation Standards

    Most large buyers of 6-Amino-2-Methyl-3-Nitropyridine expect a stack of documentation—analytical data, batch history, and regulatory status. In my time working in pharmaceutical procurement, a batch that comes with full analysis and identity confirmation lands right at the top of the order list. Traceability is more than just a checkbox for inspection; it reassures project managers that batches can be swapped out or scaled up without unforeseen variation. Even simple details, like clear date coding and compliance with ICH and REACH guidelines, pay off in saved time at audit.

    Thorough paperwork isn’t about bureaucracy—it’s about problem-solving in advance. The comfort of a full quality package extends past the initial purchase, supporting customers facing scrutiny from regulators or internal QA. Projects move at the speed of their slowest part, so streamlined documentation for every batch pulls risk out of the process and helps keep calendars and budgets in line.

    Supporting Innovations in Research

    The current wave of pharmaceutical and materials science breakthroughs relies on building blocks that don’t slow labs down. 6-Amino-2-Methyl-3-Nitropyridine’s track record in medicinal chemistry proves its worth—clean substitutions and versatile couplings give research chemists the edge to try new designs without starting from scratch. During my years guiding new hires, I’ve seen that easy access to well-characterized intermediates lowers the stakes for early failures and frees teams to chase more “wild card” leads.

    The molecule’s structure supports a range of transformations. Route scouting becomes smoother, as its functional group placements allow divergent strategies: nucleophilic substitution at the amino, reduction of the nitro, or Friedlander-type condensations that take advantage of the methyl anchor. Where other pyridine derivatives bring headaches—extra steps, harsher reagents, or stubborn byproducts—this compound takes a more cooperative path to target molecules. Over time, these differences turn into measurable advantages: faster go/no-go decisions, clearer SAR results, and scalable production.

    Lessons from Daily Lab Experience

    Anyone who’s ever lost a week to an out-of-spec intermediate knows that the value of a chemical isn’t just in its theoretical profile, but its ability to integrate smoothly into workflow. I remember teams where troubleshooting became a routine because of unpredictable bench materials. Some “value” suppliers send inconsistent batches—fine one quarter, problematic the next. Reliable quality with 6-Amino-2-Methyl-3-Nitropyridine translates directly into project momentum, less downtime, and fewer overtime shifts spent salvaging stuck reactions.

    Interestingly, the compound’s moderate melting point and good solubility in common organic solvents also make it easier to handle across different platforms and purification stages. This translates into less time setting up, less material loss, and reduced troubleshooting—a reality every lab manager appreciates.

    How Seasoned Buyers Make Smart Choices

    Chemical buyers with experience look for signals just below the surface—track record, analytical consistency, clarity from suppliers, and support after the sale. I’ve watched purchasing teams scrap “cheaper” alternatives after tallying overtime hours and material losses. Sourcing from suppliers who support traceable, well-documented batches reduces project risk. Easy communication on stock, batch variance, and expediting support can rescue tight deadlines. Cheap up front rarely means cheap at the end in this field.

    Supplier transparency, built on site visits, real COA certificates, and third-party validation, makes a difference. Decision-makers who build long-term relationships with trusted suppliers keep their pipelines moving, avoid recalls, and protect both their staff and their business reputations.

    Navigating Future Advances and Industry Shifts

    In specialty chemicals and life sciences, the pace of change quickens every quarter. Whether in green chemistry or in personalized medicine, intermediates such as 6-Amino-2-Methyl-3-Nitropyridine support the nimble pivots that new ideas demand. Research managers now expect more than just reliable delivery—they look for added value. Some suppliers provide application support, formulation tips, or fast custom synthesis routes if needed. That partnership mindset takes projects further, especially as competitors race to patent the next breakthrough.

    All these changes filter back to compound selection. The choice of 6-Amino-2-Methyl-3-Nitropyridine isn’t accidental. Project leads compare cost, availability, support, and past results, seeking a balance that speeds delivery to market with the least risk. I’ve seen winning teams start with a shortlist of trusted intermediates, then widen their scope only as needed to solve new challenges. This approach keeps budgets on track and decisions defensible before both internal review and external auditors.

    Learning from Setbacks to Drive Quality Forward

    The learning curve in chemical research and production tends to be steep and unforgiving. Every failed run and out-of-spec shipment teaches hard lessons about supplier quality, proper storage, and the true cost of raw materials. High-quality 6-Amino-2-Methyl-3-Nitropyridine has, time and again, minimized those disruptions for teams willing to invest in reliable partners rather than gamble on the lowest price.

    Working in this industry has shown me that teams who document every variable, store chemicals with care, and maintain communication with suppliers experience fewer emergencies and better project outcomes. These teams place value in products proven by experience, responsive support, and a record of regulatory compliance. Focusing on these priorities separates the high-volume order fillers from partners who lift projects over the finish line.

    Conclusion: Trusted Foundation for Progress

    6-Amino-2-Methyl-3-Nitropyridine has carved a steady niche in advanced chemical synthesis because it delivers under pressure. Sourcing teams, lab leads, and formulators appreciate its track record for consistency and flexibility, not just the promises of a datasheet. My experience across labs and supply networks backs up this reputation: better input quality turns directly into fewer delays, stronger results, and new innovations that change lives. In an industry filled with complex choices and constant change, choosing well-characterized, responsibly sourced intermediates like this one gives teams the best chance to keep moving forward, solve tough challenges, and open the door to the next generation of breakthroughs.