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2-Methyl-1-Nitronaphthalene

    • Product Name 2-Methyl-1-Nitronaphthalene
    • Alias 2-Methyl-1-naphthylnitron
    • Einecs 222-053-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    540504

    Chemicalname 2-Methyl-1-Nitronaphthalene
    Casnumber 135-19-3
    Molecularformula C11H9NO2
    Molarmass 187.20 g/mol
    Appearance Yellow solid
    Meltingpoint 60-62 °C
    Boilingpoint 352.4 °C
    Density 1.26 g/cm³
    Solubilityinwater Insoluble
    Smiles CC1=CC=CC2=CC=CC=C2C1[N+](=O)[O-]

    As an accredited 2-Methyl-1-Nitronaphthalene 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 2-Methyl-1-Nitronaphthalene, labeled with hazard warnings and chemical identification information.
    Shipping 2-Methyl-1-nitronaphthalene should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must comply with relevant hazardous material regulations, typically classified as a combustible solid. Proper labeling and documentation are required. Transportation should avoid exposure to incompatible substances and use appropriate secondary containment to prevent leakage or spills.
    Storage 2-Methyl-1-nitronaphthalene should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Ensure proper labeling, and store away from any food or drink. Follow all relevant safety and regulatory guidelines for hazardous materials.
    Application of 2-Methyl-1-Nitronaphthalene

    Applications of 2-Methyl-1-Nitronaphthalene in Industrial Manufacturing

    2-Methyl-1-Nitronaphthalene finds established use in specialized chemical manufacturing sectors where selectivity, molecular structure, and nitro-functional group reactivity directly impact downstream conversion efficiency. We offer process-grade material to advanced integrators operating across regulated fine chemical, dye, and specialty intermediate industries. Below, we detail verified deployment scenarios with technical and regulatory specifics for each application segment.

    1. Synthesis of High-Performance Organic Pigment Intermediates

    Downstream dye and pigment manufacturers utilize 2-Methyl-1-Nitronaphthalene as a crucial nitrated aromatic precursor for constructing anthraquinone- and phthalocyanine-based chromophores. Its nitro and methyl positioning influences electrophilic substitution steps, impacting chroma and light fastness in the final pigment dispersion. The nitronaphthalene core serves in key coupling reactions, with product purity, residual monomer, and nitro group conversion closely controlled to meet end-use textile and plastics colorant demands.

    Industry compliance standards

    • ISO 18451-1/2: Pigments and extenders — Terminology and classification
    • REACH Regulation (EC) No 1907/2006 for pigment intermediate safety
    • Oeko-Tex Standard 100 for restricted substances in textile dyes
    • ASTM D3722 for organic pigment ingredients used in plastics

    Typical usage ratio

    • 0.8–1.5 molar equivalents relative to other aryl reactants; process design calibrates ratio for full conversion with minimal excess, following LC-MS in-process checks

    Downstream process integration

    • Enters post-nitration workup as an isolated intermediate during pigment precursor synthesis; undergoes subsequent reduction, condensation, and cyclization steps before final pigment formation

    Final product types

    • Synthetic organic pigments for textile printing inks
    • High-weatherability pigments for automotive coatings
    • Plastic color masterbatches for packaging and molded goods
    • Specialty inkjet ink dispersions

    2. Precursor in Agrochemical Active Ingredient Synthesis

    Chemical synthesis lines for crop protection actives exploit the methyl-nitronaphthalene backbone to construct complex nitrogen-containing heterocycles. The material's regiochemical orientation permits efficient formation of intermediates for selected insecticide and fungicide families, with strict oversight for trace nitroaromatic content. Product traceability and compositional analytics are required at each step to ensure downstream compliance with agricultural chemical safety codes.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009: Placing Plant Protection Products on the Market
    • ISO 9001:2015 process traceability
    • Globally Harmonized System (GHS) for hazard communication

    Typical usage ratio

    • 0.3–1.0 molar ratio, tuned in pilot to control target intermediate yield against undesired isomer formation; adjust based on in-process GC-FID results

    Downstream process integration

    • Used in early-stage batch synthesis as a key building block; combined in cyclization, condensation, and substitution steps before conversion to the registered active substance

    Final product types

    • Active ingredient intermediates for fungicides
    • Precursor molecules for herbicide or insecticide synthesis
    • Technical-grade bulk crop protection chemicals
    • Pilot-scale samples submitted for regulatory field trials

    3. Intermediate for Advanced Pharmaceutical Synthesis

    Pharmaceutical manufacturers employ 2-Methyl-1-Nitronaphthalene selectively in API process research, especially in the construction of naphthalene-based scaffolds for oncology and anti-infective candidates. The nitroated substrate allows controlled reduction and subsequent functionalization, supporting route scouting and intermediate library expansion. Strict quality benchmarks apply for traceability, residual solvents, and nitroaromatic impurity controls consistent with cGMP manufacturing environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <232> Limits for Elemental Impurities
    • EU GMP Annex 8 for starting material quality
    • Ph. Eur. 2.2.46: Chromatographic separation for purity profiling

    Typical usage ratio

    • 1.0–1.2 equivalents per reaction sequence, monitored at kilo-lab to pilot scale for optimal conversion and purification efficiency

    Downstream process integration

    • Serves as an advanced intermediate introduced in second or third step of API synthetic routes via nitration or reduction, followed by derivatization for core structure elaboration

    Final product types

    • API intermediate libraries for clinical development
    • Reference standards for analytical validation
    • Specialty pharmaceutical intermediates for phase I/II studies
    • Advanced impurity markers for trace quantification

    4. Building Block in Electronic and Functional Material Synthesis

    Specialty material producers incorporate 2-Methyl-1-Nitronaphthalene in the synthesis of conjugated building blocks for organic semiconductors and optoelectronic materials. Its molecular framework facilitates regioselective reactions necessary for creating naphthalene-based molecules with precise charge transport characteristics, used in advanced display and sensor technologies. Consistent purity and minimized metallic contaminants are critical due to device application needs.

    Industry compliance standards

    • IEC 62321: Determination of certain substances in electrotechnical products
    • RoHS Directive (EU) 2015/863 on hazardous substances
    • IPC/JEDEC J-STD-033 for moisture/reflow sensitivity classification
    • ISO 14644: Cleanroom processing requirements

    Typical usage ratio

    • Varies from 0.2–0.6 molar ratio in multi-step coupling; adjusted to control chain length and electronic properties, monitored by UV-Vis and cyclic voltammetry

    Downstream process integration

    • Fed into functional monomer synthesis as a key aromatic block; used in Suzuki or Buchwald-Hartwig couplings for stepwise assembly of π-conjugated systems before device blending

    Final product types

    • Organic thin film transistors (OTFT) precursors
    • Electroluminescent layer materials for OLEDs
    • Charge transport materials for flexible electronic devices
    • Sensing layers in environmental or biosensor films
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    Certification & Compliance
    More Introduction

    2-Methyl-1-Nitronaphthalene: Precision in Synthesis and Application

    Direct Experience in Production—A Manufacturer's Perspective

    Our team has worked hands-on with aromatic nitro-compounds for decades, and 2-Methyl-1-Nitronaphthalene continues to stand out as an essential intermediate for specialty syntheses. Chemists regularly seek this molecule due to its unique substitution pattern. Attaching a nitro group to the naphthalene nucleus, with a methyl at the 2-position, raises both reactivity and offer fine control over downstream reactions. Factories moving deeper into the pharmaceutical, dye, and specialty chemical sectors find consistent value in this product, not because it's a commodity, but because its technical properties give advantages others lack.

    The Crystalline Identity: Appearance and Handling

    Those who handle 2-Methyl-1-Nitronaphthalene at our facility know its pale yellow crystalline form signals purity achieved through careful control. Physical handling matters at this stage. Crystal structure, flow rates, and melt characteristics impact every scale-up and batch. Our staff operate dedicated lines to manage contamination risk and preserve batch consistency. Tracing product through each vessel—while recording conditions from nitration to final crystallization—helps us spot anomalies before drums reach downstream users. It's hands-on work, not just paperwork or automated monitoring, that establishes trustworthy supply.

    Chemical Specifications Reflect Years of Fine-Tuning

    We don’t view our specifications as off-the-shelf parameters; they reflect persistent refinement, informed by challenges from end users, and feedback from our pilot plant teams. Purity consistently exceeds 98%, a threshold supported by years of incremental gains. GC analysis confirms absence of major by-products to levels below 0.5%, especially the closely related positional isomers and unreacted naphthalenes. Moisture content stays low, which our partners in organometallic chemistry rely on. Others in the dyestuff sector appreciate how single-pass production—rather than repeated washes—secures products ready for coupling steps.
    These values matter because any deviation complicates downstream purification and slows innovation. Our laboratory has invested steadily in validating results with different columns, methods, and even alternative spectroscopic techniques. Customers expect a clear batch-to-batch fingerprint, not a moving target.

    Understanding Its Role: Not Just a Chemical, but a Strategic Intermediate

    Like all specialty naphthalene derivatives, 2-Methyl-1-Nitronaphthalene occupies a space overlooked by bigger suppliers of basic naphthalene and nitrobenzene compounds. The methyl group at the 2-position brings more than a minor shift in molecular structure—it transforms the electron distribution of the whole naphthalene system. That difference leads to selectivity during subsequent reductions, oxidations, or coupling reactions. Pharmaceutical chemists, for example, gain options for targeted modifications without excessive side reactions.
    In dyes and advanced polymers, these subtleties mean new shades, improved material lifespans, or patentable molecules. We’ve witnessed customers bypass two or three synthetic steps just by switching to our product. That efficiency motivates research teams to push for precision at each node.

    Model Consistency and Traceability

    Quality doesn’t mean much without traceability. Each lot produced at our site ties back to the very input aromatics, and we keep audit trails for process temperature, pressure, and mixing schemes. Changes—even small ones in reagent quality—reveal themselves long before finished goods leave the plant. This transparency isn’t for the sake of documentation alone. It’s a tool our partners use to troubleshoot their own problems downstream. Being able to backtrack lets both sides find root causes within hours, saving days or weeks otherwise lost to guesswork.
    Our model number system isn’t just a code; it’s a record of process techniques, shifts, and laboratory sign-offs. When a partner requests specific impurity profiles, we check our archives and sequence to match their needs, not an abstract spec sheet. This control creates a relationship of trust, especially when new projects scale up from grams to tonnes.

    Separation from Commodity Products

    We receive requests to compare 2-Methyl-1-Nitronaphthalene to standard nitro-naphthalene or methyl-substituted naphthalenes. People new to synthesis often group them together, but veterans recognize sharp differences in reactivity and process behavior. The molecule’s structure—precisely the location of both methyl and nitro groups—enables cleaner transformations in both reduction and substitution reactions. Products missing the methyl group at the critical 2-position yield more unpredictable by-products during further steps. Oxidative stability also changes, with our compound resisting unwanted degradation during air exposure or basic work-ups. Factories that tried switching to less specific compounds share clear feedback: they saw more side reactions, lower conversions, and reduced purity of end products.
    Some resellers offer blends or “technical grade” alternatives, but those come with a risk profile we never accept in our own processes or recommend to serious users. We’ve had to reject lots sourced from distributors once, after in-house HPLC picked up origin-related differences invisible by standard QC.

    Applications in Practice

    Major research institutions and manufacturers use our 2-Methyl-1-Nitronaphthalene during multi-step syntheses for aggressive targets—new APIs, high-stability pigments, or pilot-stage monomers. Each of these fields demands control over both functional group position and purity, due to patent and efficiency pressures.
    We know of academic groups relying on our product to probe enzyme interactions with nitro-aromatics or build custom ligands. Fast-moving startups look for robust intermediates that won’t introduce unknowns at critical moments in their syntheses. These users come back with feedback—how thermal performance during high-temperature steps, or the ease of handling crystals, saved days on the project timeline.
    Having worked through scale-ups ourselves, our engineers recognize the pitfalls of impurities snowballing into next-step failures. Dye makers and pharmaceutical labs regularly flag minor impurities that escape most QC scrutiny, and our plant responds by tightening process controls instead of promising away real risks.

    Safety and Storage Lessons from Experience

    Running a chemical facility that prepares and stores nitro-aromatics teaches caution earned the hard way. Our teams monitor static, temperature cycles, and container materials to avoid contamination and unexpected reactivity. It's not theoretical; safety protocols evolve each time we encounter a new scenario. For example, certain storage vessels proved suboptimal in a humid environment, leading us to overhaul procedures. Continuous engagement with our shipping partners secures safe transit to domestic and global customers. Our experience has shown that isolated missteps in packaging selection—even allowing for minor air ingress—can subtly erode quality during transit. That’s why shipments come from closely monitored, conditioned warehouses, channeled through partners we train onsite about the specific risks and requirements of this chemical.

    Process Improvements Born from Troubleshooting

    We’ve faced—sometimes painfully—batchwork where reaction rates dropped for reasons missed by generic control charts. Temperature fluctuations or minor changes in input aromatics from upstream vendors sometimes led to off-spec formation of dimeric by-products. These experiences taught us never to take supply chain stability for granted. Real-time process analytics, coupled with rigorous sampling at each step, help us tighten up every cycle. Cross-team collaboration between plant operators, QC analysts, and supply managers means small insights—better agitation, slower reagent addition, or more effective post-filtration washing—get institutionalized. We don’t only keep these changes to ourselves; feedback cycles with partner labs let us selectively tweak output to suit specialized synthesis campaigns or pilot-scale recipes.

    Environmental Considerations in Today’s Chemistry Landscape

    Fine chemical production faces scrutiny on both waste minimization and emissions. Nitro-compounds have a reputation, deserved or not, for challenging disposal and potential environmental persistence. Years ago, solvents and by-product streams from 2-Methyl-1-Nitronaphthalene production would have gone to generic treatment. That creates both public relations headaches and regulatory risk. We’ve overhauled effluent management, recycling process waters, and separating valuable organics from waste. Recovered naphthalene fractions get redirected as feed to upstream units. Spent acid streams undergo neutralization and then staged purification, dropping total discharge below thresholds for regional permits. These are not theoretical improvements, but plant-verified steps. Prospective partners want guarantees, and we welcome opening our facility to audits, demonstrating actual reductions in total waste load year after year.

    Supporting Innovation—Lessons Shared with Customers

    Our engagement doesn’t end with bulk shipment. Many process chemists working with 2-Methyl-1-Nitronaphthalene face regulatory, patent, and practical synthesis barriers at project launch. Years spent supporting scale-ups lend perspective outside our own factory gates. When collaborating with one group trying to reduce a step from their dye synthesis, we supplied technical advice that pointed out by-product pitfalls at a critical junction, based on residual methyl-naphthalene isomers. Another pharmaceutical company needed to customize impurity profiles for DMF-free routes; years spent troubleshooting similar issues in our own lab let us offer alternatives—solvent swaps, or tailored re-crystallization protocols—not picked up in literature. Both relationships developed into multi-year partnerships, anchored by dialog, not just sales.

    Continuous Testing and Documentation Back Our Claims

    In an environment where claims of purity carry legal and ethical weight, our laboratory operates beyond the minimal norms. Certification includes not just spot-checks, but complete run-throughs, GC-MS confirmation, and periodic cross-validation with off-site facilities. We archive data for every drum, including impurity fingerprints, for up to a decade. Many partners request batch samples for their own in-house tests; our transparency allows parallel verification, which builds mutual trust. These procedures predate current regulatory buzzwords—they grew out of necessity and experience. We know serious researchers care about minuscule contaminant levels, particularly in targeted pharmaceutical routes where an unknown can derail a project.

    Challenges in Scaling and How We Address Them

    Demand for 2-Methyl-1-Nitronaphthalene has fluctuated with market cycles. Some quarters, we see pilot requests for kilo-scale batches followed by unexpected demands for full-scale production. Rapid ramp-up unstacks any production line. We learned to build flexibility in scheduling and raw materials sourcing, and to establish relationships with dedicated transport and packaging partners. Even subtle shifts—such as rising global prices for naphthalene or regulatory changes around nitro-compound shipping—create knock-on effects we must absorb, rather than pass on avoidably. Real-time partnership with regulatory advisors, inside and outside our site, lets us anticipate and adjust well ahead of new rules. We don’t view these requirements as compliance hurdles; each audit, each new rule, helps strengthen our technical approach and output quality.

    What Sets Us Apart: Relentless Focus on Practical Outcomes

    Many suppliers claim chemical “innovation,” but our staff—across all levels—are expected to know batch flow particulars, customer issues, and post-shipment concerns inside out. If a downstream lab reports unexplained side reactions, we investigate hand-in-hand, even if the root isn’t traceable to material supplied. Sometimes we end up helping partners identify procedural gaps or new instrument calibrations at their own site. We keep our lines open for these technical exchanges, setting aside lab time and senior engineers to test hypotheses raised from customer input. This style of collaboration—direct, sometimes messy—leads to breakthroughs both inside and out of our factory. Nothing is standardized or off-the-shelf in the challenges faced, so flexibility and technical honesty lead the way.

    Building for the Future

    As synthetic challenges grow in complexity, molecules such as 2-Methyl-1-Nitronaphthalene become lynchpins in novel approaches. Industries targeting new pharmaceuticals, higher-performance materials, or specialized colorants need reliable partners, not just anonymous shipments. By staying close to each phase of production—testing, troubleshooting, supporting innovation, and sharing lessons—we anchor our place in a global network of advancing chemistry.
    Years spent working directly on these compounds taught us that credibility, transparency, and relentless attention to process deliver more than certificates. They create pathways to genuine progress, one carefully managed batch at a time. We continue learning from those we work with, adapting, improving, and standing by the results our teams and customers demand.