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4-Methyl-2-Nitroanisole

    • Product Name 4-Methyl-2-Nitroanisole
    • Alias 4-methyl-2-nitro-1-methoxybenzene
    • Einecs 624-725-5
    • 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

    391542

    Cas Number 4567-24-6
    Molecular Formula C8H9NO3
    Molecular Weight 167.16 g/mol
    Iupac Name 1-methoxy-4-methyl-2-nitrobenzene
    Appearance Pale yellow to yellow liquid
    Boiling Point 275-276°C
    Melting Point N/A (liquid at room temperature)
    Density 1.16 g/cm³
    Solubility In Water Practically insoluble
    Flash Point 121°C
    Refractive Index 1.548
    Smiles CC1=CC(=C(C=C1)OC)[N+](=O)[O-]

    As an accredited 4-Methyl-2-Nitroanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Methyl-2-Nitroanisole is supplied in a sealed, amber glass bottle containing 25 grams, labeled with hazard and safety information.
    Shipping 4-Methyl-2-Nitroanisole should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Use appropriate secondary containment and ensure labeling complies with hazardous material regulations. Transport under ambient conditions unless otherwise specified, and follow local, national, and international guidelines for hazardous chemicals during shipping.
    Storage 4-Methyl-2-Nitroanisole should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from direct sunlight. Use appropriate chemical-resistant containers and label them clearly. Ensure access is restricted to trained personnel and comply with all relevant safety guidelines and regulations.
    Application of 4-Methyl-2-Nitroanisole

    Applications of 4-Methyl-2-Nitroanisole in Industrial Manufacturing

    4-Methyl-2-Nitroanisole serves as a specialized intermediate in chemical synthesis, supporting targeted industrial sectors with stringent requirements on traceability and product consistency. All applications shown reflect established, real-world downstream pathways and end products relied upon by high-volume manufacturers for further synthesis or formulation.

    1. Synthesis of Pharmaceutical Building Blocks

    Pharmaceutical manufacturers utilize 4-Methyl-2-Nitroanisole as a key precursor in producing aromatic amines and heterocyclic scaffolds for advanced drug intermediates. During active pharmaceutical ingredient development, its electron-withdrawing nitro group offers reliable selectivity for reduction and condensation steps, enabling efficient assembly of small-molecule APIs such as antihypertensives and antimicrobials. Plant-level process controls monitor residual nitro content and trace metal contamination in all reaction batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) general chapters on residual solvents
    • EU GMP EudraLex, Volume 4, Part II—Basic Requirements for Active Substances
    • 21 CFR 210/211 (cGMP for Finished Pharmaceuticals, USA)

    Typical usage ratio

    • Employed at 0.85%–2.3% molar ratio relative to main synthesis substrate; exact ratio depends on the targeted pharmaceutical intermediate, downstream step, and process scale.

    Downstream process integration

    • Charged as a starting material for catalytic reduction and nucleophilic aromatic substitution; introduced during the initial batch synthesis stage in pressure reactors; monitored for conversion to downstream amine or heterocycle intermediates via HPLC.

    Final product types

    • Aryl amine drug intermediates
    • Heterocyclic core building blocks for API synthesis
    • Pharmaceutical fine chemicals for multi-step API assembly

    2. Agrochemical Intermediate Production

    Major agrochemical formulators adopt this nitroanisole derivative to construct substituted anilines—essential components in the synthesis of selective herbicides and fungicide active ingredients. Its methyl and methoxy groups impart defined physicochemical properties, improving downstream reactivity in coupling and cyclization reactions. Process engineers ensure fully documented raw material traceability in compliance with crop protection regulatory audits and residue analysis guidelines.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU)
    • OECD Guideline on Good Laboratory Practice (GLP)

    Typical usage ratio

    • Used at 1.5%–3.2% by weight of total batch charge for intermediate synthesis, with actual ratio determined by coupling efficiency and target agrochemical structure.

    Downstream process integration

    • Added to main reaction vessel prior to catalytic hydrogenation or condensation stage; inclusion point calibrated by pilot batch trials to minimize unreacted nitroates in final technical concentrate.

    Final product types

    • Selective herbicide intermediates
    • Active ingredient scaffolds for fungicides
    • Precursor compounds for insecticide formulation

    3. Specialty Dye Intermediate Manufacturing

    Dye and pigment companies incorporate 4-Methyl-2-Nitroanisole to build azo and anthraquinone dye precursors, especially for colorants needing precise electron-donating and -withdrawing substituent positioning. The nitro group’s controlled reactivity allows fine-tuning of colorfastness and light stability for high-performance industrial and textile dye systems. Quality assurance teams focus on achieving strict impurity profiles to meet application-specific and environmental guidelines.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for dyes in textiles)
    • EN 71-3:2019 (safety of toy dyes)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, manufacturing restricted substances list for dyes)
    • ISO 9001 for batch dye production traceability

    Typical usage ratio

    • Dosage lies between 0.6%–1.2% by mass, adjusted according to chromatic yield and desired shade intensity; validated through pilot runs on each dye variant.

    Downstream process integration

    • Fed directly into diazotization and coupling chambers to generate dye intermediates; subsequent sulfonation or reduction adapts the precursor for the required chromophore.

    Final product types

    • Azo dye intermediates for textile printing
    • Anthraquinone dye components
    • Industrial pigment precursors

    4. Fine Chemical Synthesis and Research-Scale Applications

    Institutes and fine chemical producers use this compound as a controlled-input substrate in bench- to pilot-scale synthesis protocols for high-purity aromatic derivatives and custom intermediates. Its distinct substitution pattern enables stepwise derivatization, forming advanced intermediates that serve as reference materials, flavors, or trace marker compounds. Researchers document each batch under laboratory best practices to meet analytical and synthetic standard requirements.

    Industry compliance standards

    • ISO/IEC 17025 General Requirements for the Competence of Testing and Calibration Laboratories
    • ACS reagent-grade specifications
    • GLP (Good Laboratory Practice) for synthetic chemistry

    Typical usage ratio

    • Applied at 0.5–5 mmol/L in reaction protocols, set according to scale, yield optimization, and downstream derivatization chain.

    Downstream process integration

    • Employed in stepwise synthetic routes for methylated or aminated aromatic intermediates, following multi-stage purification and isolation for specificity and purity validation.

    Final product types

    • High-purity analytical standards
    • Custom reference intermediates
    • Research-scale aromatic derivatives for process development
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    Certification & Compliance
    More Introduction

    4-Methyl-2-Nitroanisole: A Manufacturer’s Perspective

    Getting to Know 4-Methyl-2-Nitroanisole

    As a long-term manufacturer working with nitroanisol derivatives, we have seen the demand for 4-Methyl-2-Nitroanisole steadily rise over the years. This compound, also known as 1-methoxy-4-methyl-2-nitrobenzene, finds use in a niche segment of specialty chemicals, particularly where selectivity and purity make a marked difference. Our facility has produced several metric tons of this substance, refining our process with each production run to meet the ever-tightening quality targets from end users.

    Our Approach to Manufacturing

    Few intermediates pose such a distinctive challenge in both synthesis and purification as 4-Methyl-2-Nitroanisole. We rely on a selective nitration process that prevents over-nitration and preserves the integrity of the aromatic ring. The starting material, p-cresyl methyl ether, undergoes nitration in controlled conditions to produce the desired mononitro derivative with the methyl and methoxy groups in the required positions. The yield and purity depend not just on raw material quality, but on careful control of temperature, reaction kinetics, and separation techniques.

    Through years of refining our techniques, we have settled on a multi-step distillation process that removes contaminants and ensures colorless to pale yellow crystals, surpassing 99% purity. From a synthetic chemist’s perspective, the oxidative stability is notable. Trace isomers and colored byproducts can affect performance for downstream applications, so our team consistently invests in better separation columns and purification resins. By doing so, we meet the demands of both domestic users and overseas partners who depend on credible, repeatable quality.

    Technical Specifications: Precision in Practice

    Our typical batches of 4-Methyl-2-Nitroanisole conform to strict parameters. Purity by gas chromatography usually exceeds 99%. Water content is kept below 0.1%, as any residual moisture can impact subsequent reactions—this matters most to pharmaceutical and agrochemical developers relying on the compound as a key intermediate. The melting point consistently falls within the 49–52°C range, and the product remains stable in its sealed containers during transport and warehousing.

    Each lot undergoes full analytical screening—including nuclear magnetic resonance and mass spectrometry—to verify proper substitution. We have learned, time after time, that customers’ confidence hinges on batch-to-batch consistency. Even minor deviations in melting point or spectral profile hint at impurities that could cause headaches further along the supply chain. Every order leaves our site with a complete analytical report from our in-house laboratory. This trust, built over many years, forms the backbone of our business relationships.

    Applications: Where We See Real Value

    We see the most interest in 4-Methyl-2-Nitroanisole coming from the pharma and pesticide sectors. The compound acts as a central intermediate in the synthesis of more complex chemical structures—most notably, for manufacturers aiming to build nitrogen-containing heterocycles or other aromatic systems. Its chemical stability and predictable reactivity make it ideal for forming robust C-N bonds, nitrated aromatics, or as a stepping stone to valuable specialty molecules.

    Some of our partners use it to synthesize methylated aromatic amines via reduction, or to prepare advanced dyestuffs. Others have us tailor-make specific grades for pilot projects where the downstream yield hinges on minute differences in starting material quality. We have witnessed faster development cycles for those clients who care about the precise substitution pattern and low impurity profile of their 4-Methyl-2-Nitroanisole supply, as it reduces the need for additional purification steps later on.

    Our feedback channel with end-users reveals that in pharma intermediates, even slight deviations in isomeric purity can affect biological activity down the line. As regulations tighten in Europe, the United States, and Southeast Asia, our customers face greater scrutiny on their own synthetic processes. Reliable intermediates save their chemists headaches. By partnering directly with manufacturers—we produce, analyze, and ship—clients eliminate the uncertainty introduced by complicated supply chains and untraceable sourcing.

    Differences from Other Nitroanisoles and Analogues

    Over years of producing nitroaryl ethers, we have compared 4-Methyl-2-Nitroanisole to its close structural relatives—such as 2-Methyl-4-Nitroanisole, 4-Nitroanisole, and 4-Methyl-3-Nitroanisole. The location of both the methyl and nitro groups on the aromatic ring leads to clear performance differences. For example, 4-Methyl-2-Nitroanisole’s ortho relationship between nitro and methoxy groups impacts physicochemical properties like electron density, melting point, solubility, and reactivity with nucleophiles. These factors go on to shape its effectiveness in specific reactions.

    Clients sometimes ask for alternative isomers, but few meet the same standards when they transition to regulated, large-scale synthesis. We have tested alternate routes with mixed nitroanisoles in real reactions and found differences in regioselectivity and the efficiency of subsequent transformations. The methyl group positioned at the para site (relative to the methoxy) in 4-Methyl-2-Nitroanisole gives intermediates greater stability in some hydrogenation reactions, a property less pronounced in meta- or ortho-substituted analogues.

    In dye and pigment applications, the shade and consistency of the end product relate closely to precursor choice. Slight shifts in substitution patterns—not obvious at first glance—can cause shifts in color or crystallinity. Experienced users notice the difference almost immediately, which is why we maintain several grades and isomer-specific production lines for our long-term partners. Some aromatic nitro derivatives, if handled incorrectly, also produce higher levels of environmental residues or problematic byproducts; we have streamlined our manufacturing technologies to address these issues, storing and recycling mother liquors and recovering solvents for repeated use. This way, we respond to both product quality demands and environmental requirements.

    Impact on the End-User: Lessons from the Field

    Working directly with research labs and production chemists has taught us a lot about what matters at the bench and on the plant floor. Researchers need clear documentation, not just for specification sheets but also for the entire manufacturing pathway. Wherever possible, we open our books to customers, walking them through our synthetic route, quality control routines, and strategies for impurity removal.

    Small mistakes in upstream chemistry translate into major delays for our customers’ own milestones. On several occasions, we’ve been called to troubleshoot unexplained yield drops in a partner’s process, only to discover subtle differences in raw material composition from other sources. These are hard lessons, and they drive our investment in process transparency.

    In downstream synthesis, particularly those going toward active pharmaceutical ingredients, trace impurities sourced from the aromatic precursor stage can sometimes survive all the way to the final step. Our close relationship with end-users has led us to develop enhanced purification and tracking systems, allowing both parties to spot issues early. The shared risk, and the shared solutions, have allowed us to help partners scale up from kilogram trials to multi-ton campaigns without the usual stumbling blocks.

    Environmental, Health, and Safety Realities

    Handling, storing, and transporting 4-Methyl-2-Nitroanisole involves a set of responsibilities for any manufacturer. Years of compliance audits and regulatory updates have shaped our facility layout and work culture. The nitro group adds a degree of hazard—raising concerns over combustibility, acute toxicity, and safe disposal of waste streams. Our teams receive ongoing training to recognize and manage these risks, both for personal safety and environmental protection.

    On our site, we use closed-system reactors and continuous monitoring to minimize operator exposure. All effluents undergo rigorous neutralization, and every drum shipped receives full documentation tracing its origin and chain of custody. This isn’t just a regulatory requirement; it keeps our communities and our team safe. Over time, we have adopted greener chemistry principles, aiming for higher atom efficiency and lower solvent waste. By investing in solvent recycling, catalytic transformation, and energy-efficient equipment, we reduce our environmental footprint—an ongoing priority as the landscape of chemical regulation evolves.

    For end-users, the safety data sheets and disposal guidance we supply help downstream users avoid occupational hazards and environmental fines. By supplying a high-purity material, we lower the risk of unexpected side reactions or dangerous byproducts during further processing. People often overlook this link—how robust manufacturing upstream prevents safety or environmental headaches downstream.

    Supply Chain Considerations and Traceability

    Chemical supply chains face more scrutiny every year. Our experience as an origin manufacturer shows that transparency and traceability pay off. Clients ask detailed questions, not just about the product itself but about the handling and logistics as it moves between continents. We have developed a lot tracking system that links every batch of 4-Methyl-2-Nitroanisole we produce, from raw material intake to delivery. This makes auditable chain-of-custody records available to any end-customer or regulator who asks.

    Espionage and cross-contamination worry both us and our partners. We use physical and electronic safeguards. Packaging follows international guidelines for hazardous materials, and shipment documentation includes not only chemical and safety data but also a transparent trail of custody. For shipments passing through multiple countries, we prepare additional certifications to guarantee clearance and prevent product delays.

    During the pandemic, global movements slowed and we heard more concern about unreliable sourcing. Our ability to synthesize consistently from local and import-sourced feedstocks meant we maintained uninterrupted supply lines—even as shipping costs soared and certain raw materials temporarily dried up. By integrating upstream synthesis and downstream analytics in-house, we buffered clients against uncertainty no distributor can match.

    Continuous Improvement: Facing Tomorrow’s Challenges

    Our technical group meets every quarter to survey new research, regulatory trends, and customer feedback. Over the years, we found that improving 4-Methyl-2-Nitroanisole quality is less about adding bells and whistles, and more about eliminating uncertainty. Projects now underway target even tighter process controls and more sustainable inputs. Where possible, we share data with users evaluating our compounds for future synthesis campaigns, using real analytics and stress-testing to anticipate hurdles.

    Adopting process analytical technology reduced production downtime, lowered energy consumption, and helped us spot deviations within minutes, not hours. Continuous feedback loops from our customers showed that smarter, in-line monitoring gives us a head start on problems that could result in waste or delayed delivery. Investment in staff and lab upgrades matters too; in our experience, operator skill and hands-on attention make a greater difference than technology alone.

    We pay attention to guidance from regulatory bodies, research published by academic collaborators, and trends across industries. Stricter quality, health, and environmental standards show no sign of slowing. By anticipating stricter purity and traceability requirements, we cut future migration snags and offer buyers a reliable partner for the long haul.

    Building Partnerships, Not Deliveries

    Selling 4-Methyl-2-Nitroanisole isn’t just about quotas or quarterly numbers. It’s about forming relationships with researchers, formulators, and industrial chemists who trust us to deliver not only chemicals, but stability and knowledge. Every customer presents a different context: pilot production runs, full-scale process launches, or exploratory R&D. We have walked beside start-ups, established pharmaceuticals, dye makers, and agrichemical giants. Each conversation shapes our support structure, and every technical hurdle, whether in downstream synthesis or environmental compliance, adds to our playbook.

    We have watched customers grow from first contact to commercial launches with our 4-Methyl-2-Nitroanisole at the heart of novel process technology. Having direct access to our technical and quality assurance teams breaks through red tape and simplifies troubleshooting. For us, every successful project validates both the product and the philosophy behind its production. Our role goes beyond supply—we empower users with every piece of experience and scientific know-how gathered on our shop floor.

    Closing Thoughts: What Years of Experience Have Shown Us

    Making and supplying 4-Methyl-2-Nitroanisole is a cumulative process—balancing technology, transparency, and close listening. Regulations, specifications, and end-user expectations shift, but the essentials remain the same: quality, safety, reliable logistics, and technical partnership. As we look ahead, we continue refining every batch, sharing hard-won knowledge, and building the kind of trust only direct manufacturers can offer. For chemists and businesses needing more than just a drum of chemicals, our approach to 4-Methyl-2-Nitroanisole means confidence—and results—every step of the way.