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3-Methyl-2-Nitroanisole

    • Product Name 3-Methyl-2-Nitroanisole
    • Alias 3-methoxy-2-nitrotoluene
    • Einecs 629-099-6
    • 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

    678797

    Cas Number 5437-37-6
    Molecular Formula C8H9NO3
    Molecular Weight 167.16 g/mol
    Iupac Name 1-methoxy-3-methyl-2-nitrobenzene
    Appearance Yellow to brown liquid
    Boiling Point 272-273°C
    Density 1.209 g/cm³
    Solubility In Water Insoluble
    Flash Point 118°C
    Refractive Index 1.552
    Purity Typically ≥ 98%
    Synonyms 2-Nitro-3-methylanisole
    Smiles COC1=C(C=CC=C1C)[N+](=O)[O-]

    As an accredited 3-Methyl-2-Nitroanisole 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 100 grams of 3-Methyl-2-Nitroanisole, tightly sealed; labelled with hazard symbols and product details.
    Shipping 3-Methyl-2-Nitroanisole is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Transport must comply with all local and international chemical safety regulations. Appropriate hazard labeling and documentation are required. Protective packaging is used to prevent leaks or spills during transit, ensuring safe and secure delivery to the destination.
    Storage 3-Methyl-2-Nitroanisole should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Protect from light and moisture. Use appropriate chemical storage cabinets and ensure proper grounding and ventilation to prevent accumulation of vapors.
    Application of 3-Methyl-2-Nitroanisole

    Applications of 3-Methyl-2-Nitroanisole in Industrial Manufacturing

    As the direct manufacturer of 3-Methyl-2-Nitroanisole, we carefully support global downstream industries that depend on high-purity intermediates for specialized synthesis. This product finds real-world application in several focused sectors where its properties and reactivity are essential to high-value chemical transformations. Below, explore practical manufacturing scenarios utilizing this raw material with precise compliance, formulation, and process integration details.

    1. Advanced Agrochemical Synthesis

    Chemical manufacturers use this material as a building block in the construction of select herbicide and fungicide molecules, leveraging its methyl and nitro substituents for later-stage coupling and cyclization steps. The compound typically undergoes nitration or reduction reactions that position it for formation of heterocyclic and aromatic crop protection actives. Consistent quality and traceability are crucial throughout the formulation process to meet regulatory expectations and production stability.

    Industry compliance standards

    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH, EC 1907/2006)
    • U.S. EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)
    • ISO 9001:2015 (Quality Management System for chemical synthesis and handling)
    • Good Laboratory Practice (GLP) for analytical purity and impurity profiling

    Typical usage ratio

    • 5–25% of the active ingredient intermediate batch; the percentage depends on target molecular architecture, selected downstream coupling partners, and yield optimization parameters

    Downstream process integration

    • Charged into the multi-step organic synthesis reactor during the aromatic coupling or ring closure phase after initial substrate activation

    Final product types

    • Phenoxyalkanoic acid herbicides
    • Systemic triazole fungicides
    • Broad-acre agricultural chemical actives (formulated into EC and SC product grades)
    • Granular and liquid crop protection agents

    2. Pharmaceutical Intermediate Manufacturing

    In regulated pharmaceutical supply chains, this compound acts as a custom intermediate during the synthesis of certain active pharmaceutical ingredients (APIs) where ortho-substituted aromatic frameworks are required. Typical processes utilize its electron-withdrawing group to direct substitution and reduction steps, which are essential in producing molecules for targeted therapeutic classes such as CNS agents and anti-infectives. Manufacturers prioritize documentation and traceable GMP compliance through all process steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Pharmacopoeia monographs (e.g., USP, Ph. Eur.) for related starting materials and impurities
    • U.S. FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Quality management per ISO 13485 for pharmaceutical intermediates

    Typical usage ratio

    • 8–18% in multi-step synthesis, tailored by batch scale and yield in target molecule assembly; ratio fine-tuned based on stoichiometric conversion rates

    Downstream process integration

    • Fed into API synthesis lines after initial halogenation or methylation, typically followed by reduction and protection/deprotection cycles under GMP-controlled conditions

    Final product types

    • Nitroaromatic precursor APIs for neuroactive drugs
    • Anti-microbial and broad-spectrum antibiotic intermediates
    • Niche CNS pharmaceutical compounds with ortho-methyl group requirements
    • R&D pilot lots for clinical and scale-up trials

    3. Fine Chemical Dye Intermediate Production

    The compound's unique substitution pattern makes it valuable in the manufacturing of high-performance azo and anthraquinone dyes. During pigment synthesis, downstream operators capitalize on its controlled reactivity to introduce select nitro and methoxy moieties for improved chromatic properties, stability, and light fastness. These dye intermediates must meet both regulatory dye purity thresholds and strict end-use specifications in specialty textile and plastics sectors.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for restricted dye substances and contaminants)
    • REACH Annex XVII (restrictions on use of hazardous aromatic amines in dyes)
    • ISO 14001 (Environmental Management for effluent-heavy dye processes)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)

    Typical usage ratio

    • 3–12% of dye intermediate reaction mixture; exact proportion depends on chromophore structure and pigment shade requirements

    Downstream process integration

    • Introduced during the diazotization and coupling steps when assembling complex aromatic dye molecules, typically following sulfonation or prior to reduction

    Final product types

    • Reactive azo dyes for cotton and cellulosic textiles
    • Anthraquinone pigment intermediates for polymer coloration
    • Solvent dyes for plastics and coatings
    • Specialty high-stability colorants for digital and industrial inks

    4. Specialty Aroma and Fragrance Chemical Synthesis

    The molecule is used within select aroma chemical production schemes, functioning as a key intermediate in the synthesis of complex methoxy-substituted aromatic compounds. Industrial fragrance houses value its high purity for constructing raw materials that contribute specific top, middle, or base notes in finished aromas. Careful process control is essential to avoid contamination, while compliance with international fragrance regulations is paramount throughout material handling and conversion.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • Regulation (EC) No 1223/2009 (Cosmetics Regulation, applicable to ingredients used in fine fragrances)
    • IFRA Code of Practice for handling aromatic nitro compounds
    • Internal ISO 9001:2015 QA/QC standard for batch traceability and purity

    Typical usage ratio

    • 2–7% in aroma chemical synthesis formulations; varying usage reflects the required olfactory intensity and target molecule conversion efficacy

    Downstream process integration

    • Added during the core construction step prior to etherification, methylation, or further substitution phases in the aroma molecule synthesis train

    Final product types

    • Base notes for fine fragrance blends
    • Methoxy-aromatic intermediates for use in flavor and fragrance dispersions
    • Olfactory chemicals for cosmetic applications
    • Perfumery accords for personal and home care products

    5. Polymeric Material Additive Manufacturing

    This compound serves as a specialty intermediate for the functionalization of polymer additives—especially antioxidants and UV stabilizers—within advanced plastics manufacturing lines. Its nitro and methoxy groups improve the grafting efficiency during reactions on polymer backbones, allowing downstream processors to achieve precise material performance targets for weathering, thermal stability, and color retention. Consistency and impurity control are critical to ensure additive compatibility and downstream polymer safety.

    Industry compliance standards

    • FDA 21 CFR 177.1520 (Olefin Polymers for Articles Intended for Repeated Use)
    • EU Regulation (EU) No 10/2011 (Plastic Materials and Articles Intended to Come Into Contact with Food)
    • ISO 10993-5 for biocompatibility (for medical grade polymers, if applicable)
    • ISO 9001:2015 for additive supply chain management

    Typical usage ratio

    • 0.5–4% by mass (weight% of total additive formulation); selected according to polymer type, target stabilization performance, and processing temperature

    Downstream process integration

    • Combined with monomers or polymer matrix pre-mix during compounding or masterbatch production phase, followed by melt-blending and extrusion

    Final product types

    • Antioxidant and UV-blocking masterbatches for polyethylene, polypropylene, and PET
    • Stabilizer additives for high-performance engineering plastics
    • Polymer blends for automotive and outdoor applications
    • Plastic packaging material with extended shelf-life properties
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    Certification & Compliance
    More Introduction

    3-Methyl-2-Nitroanisole: Designed by Chemists for Real-World Applications

    Proudly Manufactured With Purpose

    Every kilogram of 3-Methyl-2-Nitroanisole that leaves our reactors has a story written by our chemists—one told through precise measurements, tight controls, and practical knowledge from years in the trade. We’ve synthesized this molecule for clients who expect more than just high purity; they trust us to keep standards high, batch after batch, because downstream processes rely on consistency.

    Formulated under supervision in our facility, the product typifies our approach to specialty intermediates for the fine chemical and pharmaceutical sectors. Our team constantly assesses product by GC and NMR to assure typical purity levels not less than 99%. Careful monitoring of moisture and residual solvents sets our output apart. Color stays light yellow, and our crystallization and filtration techniques keep ash and solids at a low—tangible signs of attention to process detail.

    Going Beyond Raw Material: Who Actually Needs This Compound?

    We work daily with customers developing advanced intermediates for active pharmaceutical ingredients and crop protection molecules. R&D teams tell us that a troublesome impurity load or too wide melting range can throw their project off course. That’s why our internal guidelines control the allowed content of side-products like methyl- or nitro-isomers. Chemists buying 3-Methyl-2-Nitroanisole for a nitroaromatic coupling or as a masked methoxy group know better than anyone that even minor quality shifts can cascade downstream, impacting both yield and ease of product isolation.

    Our product supports oxidative or reductive transformations, delivering reliable results in multistep synthesis. Its electron-rich aromatic ring, moderated by the nitro and methyl substituents, opens up multiple practical applications.

    What Sets 3-Methyl-2-Nitroanisole Apart in the Market?

    Several methyl-nitro anisole isomers exist, but not all display the balance of reactivity and selectivity found here. Our molecule, with the nitro at position 2 and methyl at position 3, shows unique behavior in nucleophilic aromatic substitution and directed ortho-metalation. Chemists choose this isomer because positional effects influence both product outcome and safety. A simple swap to another regioisomer can increase side reactions or demand new purification steps—not cost effective in scaleup or process chemistry.

    In contrast to nitroanisole compounds that carry the methyl group at the 4 position, ours favors certain regioselective substitutions, which matters in complex molecule synthesis. Customers working with m-substituted aromatic frameworks know that this placement impacts downstream reactivity, particularly in building advanced building blocks for pharmaceuticals or electronics.

    Controlled Synthesis and Quality Backed by Experience

    Our synthesis starts from pharmaceutical-grade methylanisole. Nitration proceeds under cold, rigorously monitored conditions. Purification steps include repeated distillation and crystallization, not just to hit a spec, but to minimize unwanted isomers and byproducts. Every shift in process—temperature, acid ratio, stirring rate—receives documentation and real-time adjustment. Years doing this at scale means our operators recognize the batch where the color has deepened or the odor changes; subtle hints a less seasoned manufacturer might overlook.

    Final analysis covers more than main compound content. We examine acid-insoluble matter, check for color change during storage, monitor for environmental and process contaminants. A lot with less than 0.1% non-volatile residue looks and handles differently than an average technical grade. In the hands of chemists translating bench chemistry to production, this matters—yield climbs and filtration steps compress, saving costly hours.

    Practical Handling and Integration Into Complex Flows

    We’ve designed our packaging and shipment to safeguard the delicate balance of purity, solubility, and odor. Sturdy sealed drums, inert blanketing, and carefully matched inner liners cut down on contamination risk, even in humid or high-temperature logistics legs. Attention to detail in physical product form—crystalline solid, not cake or paste—reduces handling losses.

    Some end-users process the product directly into Grignard, lithiation, or reduction reactions. Here, physical homogeneity cuts down on undissolved residues and shortens post-processing time. By focusing on low water content and minimal cross-isomer mixing, our material dissolves fast—welcome efficiency gains in kilo-lab or plant reactors. Workers don’t lose valuable time clearing clogged feed lines or filtering off unexpected particulates.

    Supporting Sustainable Development and Safe Processing

    From experience, we know sustainability matters to both procurement teams and plant chemists. Our process engineers continually revise our nitration stages to cut roadblock waste, close material loops, and capture recycle streams. Years back, traditional acid-use ratios resulted in regular off-gassing and spent acid drums. We’ve since modernized to internal acid recovery units and closed-loop cooling systems—these investments aren’t just regulatory compliance, they support a stable supply and match the Green Chemistry goals of our most forward-looking partners.

    We monitor for exposure risks throughout synthesis and packaging. Engineering controls—full-scale local exhaust, specialty coated reaction vessels, real-time NOx detection—don’t just exist on paper. Workers expect more than slogans about zero incidents; our training protocols embed continuous monitoring and fast isolation measures, ensuring that even in process upsets, hazards remain contained.

    Clients have pushed us to clarify supply chain traceability. We identify raw materials from origin, log batch-wise quality deviations, and provide transparent documentation. In a world focused on responsible sourcing, we do more than check boxes. Our QC and compliance team reviews each order, checking against internal audit records. Buyers get direct access to certificates and can even trace testing logs—a real benefit for audits and regulatory documentation in highly scrutinized sectors.

    Direct Collaboration With End Users

    Our customers develop active compounds in pharmaceuticals, intermediates in agricultural chemicals, and specialty chemicals in precision electronics. We’ve spent many long days on their plant floors, solving scale-up kinks, ensuring the transition from lab-bench bottles to ton-level flow goes smooth. Sometimes, an apparently small tweak—improved drying protocol or better filtration—unlocks major cost savings and reliability at application point.

    The conversations rarely sound like textbook chemistry. Instead, end-users bring us up to speed with their process needs: batch times too slow, filtration clogging, color stability issues in product intermediates. Rather than just shipping out drums, we study the application environment. For crop protection chemical manufacturers, for example, low nitrophenol content not only meets environmental standards but saves time spent on downstream washing and neutralization. In electronics spheres, even trace ionic contamination disrupts semi-conductor performance—our samples undergo independent testing before bulk deliveries.

    We never treat process deviations lightly. If an application turns up issues—crystallization not matching past behavior, unexpected side-products, or solvent partitioning—our technical team visits the client site, shoring up troubleshooting and sharing solutions tested in our own reactors. Many problems reveal their root much faster over a process walk-through than through distant email chains.

    Tackling Risk: Chemical Reliability Starts at the Source

    Quality, to us, means more than passing a certificate. It’s a daily challenge of managing risk in the plant, anticipating the variables that can slip through routine analytics. Our chemists, having spent years coaxing color purity and eliminating background contaminants, understand these details serve real customer demands—not just a distant specification.

    Many projects demand 3-Methyl-2-Nitroanisole above all for its reliability. Customers in the pharmaceutical industry report that reducing batch-to-batch impurities translated directly into regulatory confidence and speedier scale-up approvals. With ever-strict requirements, regulators look at more than just “pass/fail”—trace elements and unidentified impurities can hold up projects. By investing time refining and validating each part of process, we reduce unknowns that can stymie complex molecule launches.

    In crop chemistry, impurities not only challenge product efficacy but can push residue profiles across borders. Our regular screenings dig into nitro and methoxy ring byproducts far beyond traditional analysis, ensuring our partners don’t get regulatory headaches or field rejections.

    Transparent Support for Changing Industry Needs

    Clients push the boundaries of what’s possible with this molecule. We develop new grades—ultra-low moisture, specialty micronized forms—after months of collaboration and feedback. Analytical techniques have kept pace; our internal labs run qNMR, multi-stage GC-MS, and moisture titrations, not just the basics. Rather than limiting ourselves to “fit-for-use” assessments, we check parameters relevant for the actual application environment.

    Customers scaling up often ask for data on shelf stability and handling. Over the years, we’ve lengthened the stability window, cut down caking, and engineered packaging that isn’t just tough, but simple to handle from drum to reactor. Upgrades in transportation materials and labeling grew out of requests from hazardous material teams, ensuring our shipments meet evolving rules and real-life handling challenges.

    Sometimes clients need tailored blends or fine-particle lots for special catalysts or formulation steps. Requests lead to direct pilot trials—we sample, run the practical tests on our own equipment, and only then release new production lines. In this way, actual process performance always trumps theoretical advantage.

    Comparing To Other Products: What Our Experience Has Taught Us

    For chemists choosing between 3-Methyl-2-Nitroanisole and its close cousins, the decision rarely concerns cost alone. We’ve seen frequent misuse of similar isomers—2-Nitro-4-methylanisole, 4-Nitro-2-methylanisole, and others—in early R&D, only for downstream kinetics or isomer separations to expose critical differences. Our isomer’s substitution pattern stabilizes reactive intermediates and directs subsequent chemistry toward cleaner, more selective results.

    Clients used to settling for technical-grade, high-impurity material find the gains in throughput and reproducible results offset higher up-front investment. In electronics manufacturing, trace metallic or halogen residues spell disaster for device yield rates—our extra cleaning and testing measures directly support their bottom line.

    This knowledge comes only from years of close collaboration. Each pilot run, each troubleshooting session, adds to our practical playbook. We never approach a client’s process challenge as solved until their own numbers, yields, and final project results confirm the value of our product.

    Scaling Up Responsibly: The Manufacturer’s Perspective

    We see firsthand the mounting pressure to deliver material at scale, on tight timelines, and with ever-closer regulatory scrutiny. Planners and engineers work side by side with quality control teams, weighing every possible efficiency gain against safety and environmental obligations. Rather than viewing ourselves as mere suppliers, we see this as craft—each stage designed for safety, sustainability, and supply chain resilience.

    Our continuous investments—process automation, in-line analytics, guided training—reflect a long-term view. Toxicity, explosion potential, and nitro compound handling aren’t just theoretical—they demand lived safety culture. When a vessel alarm sounds, the operator recognizes it immediately; response is automatic, no time lost checking manuals. Auditors visit our site not just for forms, but for open-door process tours. We invite client partners to witness the full path, from raw material receipt to the packed outgoing drums.

    Looking to the future, we expect to see demands shift again—tighter impurity restrictions, new applications, smarter logistics. We rely on lessons learned, decades of on-site troubleshooting, and honest feedback from customers to refine both our chemistry and our service.

    Connecting Experience to Product Performance

    Every kilo of 3-Methyl-2-Nitroanisole we ship draws upon real manufacturing experience. We understand how a seemingly minor process change—slower cooling, altered charge order, tighter filtration protocols—can make product tougher to handle or shortcut a client’s overall project. Feedback from users translates directly into process tweaks, stronger packing standards, and fresh operator training sessions.

    Our facility upholds a standard earned over years of practice and collaboration. Analytical scientists, process engineers, and shift leaders share responsibility for every batch—quality, safety, and delivery that keep production lines running without downstream headaches.

    For those building next-generation pharmaceuticals, crop protectants, or sophisticated electronics, the right choice of intermediate can make or break project success. By drawing upon hard-won manufacturing experience and constantly improving at every stage, we aim to support your team and your products far beyond the basic material supply.