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3-Methoxy-4-Methylaniline

    • Product Name 3-Methoxy-4-Methylaniline
    • Alias 3-Methoxy-p-toluidine
    • Einecs 221-528-1
    • 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

    601085

    Cas Number 6785-99-5
    Molecular Formula C8H11NO
    Molecular Weight 137.18 g/mol
    Appearance Yellow to brown liquid
    Boiling Point 257-259°C
    Density 1.08 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water
    Flash Point 118°C
    Synonyms 3-Anisidine, 4-methyl-
    Smiles COc1cc(N)ccc1C
    Inchikey QDVZSYUWWFLJLH-UHFFFAOYSA-N

    As an accredited 3-Methoxy-4-Methylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Methoxy-4-Methylaniline is supplied in a 100g amber glass bottle with a secure screw cap and detailed hazard labeling.
    Shipping 3-Methoxy-4-Methylaniline is shipped in sealed, clearly labeled containers, compliant with chemical safety regulations. It is protected from light, moisture, and incompatible substances. Packages are handled by trained personnel, with documentation including SDS and hazard information, ensuring safe and secure transit according to local and international chemical transport guidelines.
    Storage **3-Methoxy-4-Methylaniline** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizing agents and acids. Protect from light, heat, and moisture. Store away from sources of ignition, and ensure proper labeling. Use secondary containment to prevent spills and always follow local chemical safety regulations.
    Application of 3-Methoxy-4-Methylaniline

    Applications of 3-Methoxy-4-Methylaniline in Industrial Manufacturing

    3-Methoxy-4-methylaniline, produced at industrial scale with strict process control, finds specialized applications across the chemical and pharmaceutical sectors. The following sections outline actual market-validated downstream uses, highlighting key compliance standards, functional integration into production, and typical addition levels for quality end-product outcomes.

    1. Synthesis of Active Pharmaceutical Intermediate (API) Precursors

    Pharmaceutical manufacturers utilize 3-methoxy-4-methylaniline as an essential building block in the multi-step synthesis of select drug substance intermediates. Its consistent purity supports reproducible yields in regulated environments, especially for molecules requiring specific aromatic amine substitution patterns in early-stage production. Downstream processing usually requires nitration or coupling reactions directly involving this compound in batch reactors under controlled temperature and inert gas conditions.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP), ICH Q7 for API manufacturing
    • European Pharmacopoeia (Ph. Eur.) monographs for impurity limits
    • US FDA 21 CFR Part 211 requirements for raw material and intermediate traceability
    • REACH Annex XVII for restricted aromatic amines in drug manufacturing

    Typical usage ratio

    • 0.08–0.15 mol equivalent per final API mol; precise adjustment based on target intermediate yield and molecular mass

    Downstream process integration

    • Charged at the amination or condensation stage as the first aromatic amine feedstock, followed by further functionalization (nitration, sulfonation, coupling) as part of multi-step API precursor synthesis

    Final product types

    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Pain management compound intermediates
    • Targeted anti-infective intermediates
    • Final APIs after multi-step downstream conversion and purification

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediate)

    Crop protection chemical formulators incorporate 3-methoxy-4-methylaniline for the preparation of aromatic ring-containing intermediates, crucial in art selective herbicide and fungicide synthesis. Controlled addition to chlorination or sulfonation steps allows for predictable reaction conversion, particularly for triazole, anilide, or diphenyl ether derivatives where selectivity and consistent color are critical for quality and environmental registration dossiers.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems
    • FAO/WHO specification for pesticide technical grade and impurities
    • European Union Regulation (EC) No 1107/2009 for agrochemical emissions and traceability
    • China ICAMA registration technical material requirements

    Typical usage ratio

    • 0.12–0.22 molar equivalent per batch; varies depending on downstream oxidation, adjusted for target formulation load and environmental limits

    Downstream process integration

    • Fed directly to aromatic coupling, chlorination, or acylation reactors as a core nucleophile, often followed by cyclization or etherification en route to active ingredient bulk

    Final product types

    • Herbicide batch intermediates (anilides, diphenyl ethers)
    • Fungicide precursors for triazole class
    • Technical active ingredient bulk for post-synthesis formulation

    3. Synthesis of Specialty Dyes and Pigments

    Dye and pigment manufacturers use this aromatic amine for production of intermediates essential to the synthesis of high-performance azo and anthraquinone colorants. Its structure supports colorfastness and shade precision in applications where technical textiles, plastics, and ink products must comply with both regulatory and commercial standards. Careful calibration of input ratios enables predictable chromatic outcomes while maintaining low impurity profiles demanded by downstream textile and packaging market audits.

    Industry compliance standards

    • OEKO-TEX Standard 100 for harmful substances in textiles
    • EU REACH Annex XVII restrictions on aromatic amines in dye products
    • ZDHC MRSL v3.1 list for restricted chemical inputs
    • GMP for Pigments (DIN EN 17100)

    Typical usage ratio

    • 2–6% weight/weight of finished dye material; adjusted based on batch size and targeted color intensity

    Downstream process integration

    • Added to diazotization or coupling stages under acidic conditions, usually in stirred reactors, as a primary aromatic source for formation of azo bonds or ring structures

    Final product types

    • High-durability azo dyes for polyester and blended textiles
    • Specialty anthraquinone pigments for printing inks
    • Color masterbatches for plastics industry

    4. Manufacturing of Liquid Crystal Display (LCD) Alignment Films

    Manufacturers of polyimide alignment layers for thin-film electronic displays integrate 3-methoxy-4-methylaniline as a key aromatic donor in the synthesis of polyamic acid precursors. Its use enables high-quality orientation and thermal stability in eventual alignment films, factors essential for consistent transmission and display performance in both consumer electronics and automotive panels.

    Industry compliance standards

    • IEC 62899-202 international standard for printed electronics
    • RoHS (Restriction of Hazardous Substances) Directive 2011/65/EU for electronics parts
    • ISO 9001:2015 for traceability and process control
    • JIS (Japanese Industrial Standards) for LCD manufacturing materials

    Typical usage ratio

    • 0.05–0.10 mol/mol of dianhydride feed in polyimide synthesis; proportion fine-tuned according to chain length and film thickness required

    Downstream process integration

    • Reacted with tetracarboxylic dianhydrides in anhydrous solvents to produce polyamic acids, then thermally imidized to form final polyimide film layers applied on glass or PET substrates

    Final product types

    • Alignment films for LCD/LED panels
    • Flexible display substrates
    • Transparent conductive films

    5. Production of Advanced Corrosion Inhibitors for Metalworking Fluids

    Lubricant and specialty additive producers formulate corrosion inhibitors with 3-methoxy-4-methylaniline as a precursor for benzotriazole derivatives and related structures, ensuring continual film formation and high thermal resistance in demanding machining and stamping processes. Integration into final blends maintains compliance with strict release limits on nitrosamines and aromatic amines for both occupational safety and global market access.

    Industry compliance standards

    • ASTM D4627 for corrosion inhibition in water-based fluids
    • EN 16602-70 for aerospace metal protection fluids
    • EU Regulation 1907/2006 (REACH) on corrosion inhibitor additives
    • OSHA 29 CFR 1910.1200 for workplace chemical safety data

    Typical usage ratio

    • 0.8–1.6% weight/weight of formulation basis for finished corrosion inhibitor blends, adjusted for base oil type and final application (water- vs. oil-based)

    Downstream process integration

    • Serves as starting aromatic substrate in the synthesis of triazole or heterocyclic compounds; combined with nitrite and other reactants in sequential reactors before blending with base oils or fluid concentrates

    Final product types

    • Oil-based and water-based milling/cutting fluids
    • Rust preventatives for steel coil protection
    • High-performance metalworking lubricants
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    Certification & Compliance
    More Introduction

    Introducing Our 3-Methoxy-4-Methylaniline

    Built on Experience and Forward-Thinking Production

    At our manufacturing facility, chemical synthesis isn’t only about formulas or technical precision—it relies on consistent practice, knowledge passed down through years in the lab, and learning from thousands of batches. Producing 3-Methoxy-4-Methylaniline reflects this hands-on approach. Our teams have worked with aromatic amines and their derivatives for decades. Each step, from the careful weighing of starting materials to the clean-up at the end of the day, has taught us lessons that improve both the purity and the yield of this compound.

    The product, 3-Methoxy-4-Methylaniline (also known as 4-methyl-3-methoxyaniline), shows up often in downstream synthesis when companies look for specific intermediate reactivity. We produce our material to meet practical industry tolerances—not simply lab-scale requirements. What sets our production method apart lies in our precise process controls, honed through lengthy trial and error, and a culture of sharing between our operators, chemists, and engineers. The attention paid to temperature gradients, solvent ratios, and pressure monitoring has reduced batch inconsistencies and improved average assay compared to earlier years.

    Product Model and Specifications Informed by Real Production

    Customers typically require this compound in bulk, not grams, so packaging and purity standards reflect real-world handling: we offer 25 kg fiber drums with double-layer polyethylene liners to avoid leaks or contamination. Our in-house protocol sets the specification at ≥99% purity by GC, which tracks not only the main ingredient but potential process-related byproducts. Employees in QC have seen variations in trace levels of residual solvents or minor regioisomers; by isolating points in the process where these creep in, we’ve been able to push the level of unwanted signals below 0.3%.

    Over the years, analytical requests from partners—sometimes themselves manufacturers—have led us to adapt. One year, an end-user in dye synthesis pointed out UV absorbance variations affecting their end color profile. By adjusting our reaction times and solvent work-up, our product began to meet their tighter optical specs, which now form part of our batch release protocol. Unlike suppliers who simply repack large drums, we have installed dedicated lines and micro-filtration systems upstream of the warehouse, reducing hangover impurities that can worsen over time in storage.

    We manufacture 3-Methoxy-4-Methylaniline as an off-white to pale yellow liquid at room temperature, aligned with correct handling for aromatic amines. Although the faint odor and moderate viscosity become familiar after years in the plant, we continue to trial alternative raw suppliers and temperature control strategies to avoid odd color shifts that can signal the start of decomposition.

    Practical Uses: Lessons Learned from End-Users

    3-Methoxy-4-Methylaniline has found a mainstay role as an intermediate. Over time, users from the pharmaceutical and agrochemical sectors have requested data about amine purity, amine/water partitioning, and stability during extended storage or transportation. Our technical teams have built in these lessons. One season, we collaborated with a pigment customer who saw unexpected reactivity with a new batch. Analysis tracked the culprit back to a subtle shift in gas-phase oxidation during one week’s production. Tightening our reflux system gave the downstream user repeatable results season after season.

    End users have shared that this compound forms key amide and azo linkages more selectively than similar ortho- or meta-substituted isomers, with less unwanted reactivity compared to 2-methoxy or 2,5-dimethyl derivatives. Its utility as a building block means the downstream chemistry can move through protection and deprotection steps more efficiently, saving several hours per batch during scale-up. The methoxy group on the aromatic ring is a common modification because it modulates both electronic and steric effects in further transformations, making this compound more versatile than unsubstituted anilines.

    In applications like dye synthesis, color and purity matter not on paper, but on the production line. A minor contaminant that is invisible in a GC trace can become obvious when used at ton scale. Through post-marketing studies and user feedback, we found that enhanced stability—achieved through argon purging and modified storage—prevented discoloration in finished dye materials.

    Differences from Similar Materials: Insights from Practical Use

    Our customers often ask why 3-Methoxy-4-Methylaniline offers more value or reliability compared to ortho or para analogues. Chemically, its substitution pattern impacts both reactivity and selectivity. The para-methyl, ortho-methoxy arrangement tunes electron density for subsequent cross-couplings or diazotizations. Colleagues in R&D have confirmed that using the 4-methyl variant avoids side-reactions seen with unsubstituted or unbalanced analogs. It also results in higher conversion in certain amide bond-forming reactions—this was confirmed by tracking dozens of trial reactions with our partners, who provided us with test data.

    Other compounds may appear similar in structure but handle quite differently in practice. For example, compared to 4-methoxyaniline (p-anisidine), our material has shown cleaner isolation in intermediate steps, especially when temperature-sensitive substrates are present. Its melting and boiling points—recorded through our batch data—allow for more predictable distillation or crystallization, factors that help our larger customers reduce rework and material loss.

    Productionwise, our facility features dedicated vessels, sparging systems for oxygen control, and closed transfer lines. This means our finished material comes into contact with only the required surfaces, limiting adventitious impurities sometimes observed in older multipurpose plants. Customer complaints about odors, minor discoloration, or unidentified impurities dropped sharply after these upgrades, suggesting a direct link between how we make the compound and how well it works for others.

    Redefining Quality Through Communication and Adaptation

    Years ago, we believed maintaining purity and consistency meant simply repeating established processes. Through active dialogue with end users—formulators, chemists, project managers at other manufacturers—we began seeing our product through new eyes. When a customer shared a set of failed reactions tied to oxidative impurities, our QA team revisited standard assays. By spending time monitoring oxidation-prone batches, and reviewing our nitrogen-blanketing protocols, we managed to reduce the relevant impurity levels below our previous detection limits.

    This product is not just a chemical entity in a catalog, but the end result of repeated reviews and hands-on modifications. Regular meetings with logistics teams highlighted temperature excursions during transport, which led to more robust insulation in drums and a reevaluation of recommended storage conditions. Returned material dropped by more than half in the following two years.

    Direct engagement with customers prompted improvements in batch homogeneity. After user feedback about sticky residues caused by process oils, our engineers trialled new filter materials and switched to alternative anti-foam agents that did not carry over into the final product.

    Responsible Manufacturing: Safety and Sustainability as Practical Priorities

    Producing aromatic amines at scale requires not just technical proficiency, but attention to both human safety and environmental considerations. We have invested in training for all staff—not only engineers and chemists—so that every team member understands how to handle both raw materials and finished product. By introducing secondary containment and better air-handling, workplace exposure incidents declined markedly.

    Solvent recovery offers both environmental and economic gains. By implementing closed-loop recycling for organic solvents, our plant recycles over 80% of toluene and other solvents, cutting waste output by a third compared to our historic operation. These practices mean lower emissions during manufacture and shipments that contain fewer residual volatile compounds.

    The push for sustainable raw materials led us to revise supplier standards, opting for sources with clear environmental disclosures. Several years ago, we worked through the process of qualifying a green-chemistry route using bio-based feedstocks for our starting materials. The first batches faced scale-up hurdles, with lower yields and increased impurity loads. But by working with process chemists and suppliers, we achieved a smoother process by the fourth full-scale batch, resulting in reduced overall environmental impact without compromising on chemical quality.

    Common Challenges and Solutions in Real-World Use

    3-Methoxy-4-Methylaniline tends to oxidize under poor storage or excessive exposure to light and air, risking batch failures and added cost. Our firsthand solution involved enhancing drum liners and offering clear material safety and handling guidelines for warehouses. Multiple partners shared their own challenges with old or thin-walled packaging. By implementing thicker liners and marking drums with specific storage instructions, both physical and chemical stability improved.

    Handling at customer locations sometimes caused handling losses from splashing or residue. At industry gatherings, we listened closely to warehouse staff and bulk handlers who suggested using improved drum designs and tighter seals. The resulting packaging update brought spill incidents to a record low, benefitting not only our operation, but the companies receiving our product on busy work floors.

    Adaptability: Meeting the Evolution of Industry Needs

    The industry doesn’t stand still. Customers adapt and so must producers. Newer synthetic routes in pharmaceuticals and specialty chemicals focus on greener chemistry and higher throughput. Our team has responded by offering tailored drying levels and tighter color controls to match more sensitive downstream applications. We stay flexible, running custom purification on demand for customers who scale up innovative new routes.

    Sharing technical updates and quarterly dialogues with partners has yielded mutual benefit. Feedback about solubility and filtration helped us fine-tune our drying stage, so the product now arrives with less than 0.05% moisture. This adjustment has enhanced its performance in sensitive coupling chemistry, saving downstream operators both time and reprocessing costs.

    We learn from every complaint, question, or unusual request. Several years ago, a polymer manufacturer needed unusually high solution clarity for a visible-light-cured resin. Through joint lab work and trial batches, we optimized our process sequence, delivering a batch that succeeded where others fell short. Such partnerships ensure our material remains useful and valued in a shifting landscape.

    Continuous Improvement Backed by Data

    Experience plus evidence delivers results. We maintain complete batch records—not for show, but to spot patterns and act on them. Monthly reviews highlight any deviation in color, odor, or impurity that might sneak through occasional lapses, letting us correct rather than repeat mistakes batch after batch.

    On-site lab staff test product fresh and after months of storage to verify integrity over time. When minor shifts in color or assay show up, we investigate the actual handling process, not just the numbers. For example, the switch to modified antioxidation agents reduced visible aging marks on product held in South-East Asian climates. That data, shared with both staff and customers, informs not only our process but gives users more trust in what arrives at their facility.

    As one of the leading dedicated producers of 3-Methoxy-4-Methylaniline, we find that genuine partnerships and the practical feedback loop matter as much as any written protocol or specification. The quality customers receive reflects the labor, care, and genuine engagement throughout the entire process—from raw ingredient receipt, through synthesis and packaging, to the finished product.

    The Manufacturer’s Perspective: Value Rooted in Practicality

    Making 3-Methoxy-4-Methylaniline at production scale requires more than a theoretical understanding of chemistry. The work takes form through routine, care, precise adjustments, and the insights collected from countless staff who monitor levels, clean equipment, and catch small flaws before they become larger problems.

    The customers who use our products bring real stories to our door—about improved yields, fewer delays, better color stability, or a week without a single damaged drum. Their feedback sets the direction for our ongoing improvements. The relationship isn’t just transactional; it demands authenticity in both craft and communication.

    We believe that real value emerges from making processes safer, purer, and more reliable year after year. As we continue adapting—whether through green sourcing, tighter controls, or listening to end-users—the lessons learned flow into every batch of 3-Methoxy-4-Methylaniline that leaves our plant.