Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3,5-Dimethoxyaniline

    • Product Name 3,5-Dimethoxyaniline
    • Alias m-Xylidine
    • Einecs 210-158-6
    • 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

    402431

    Cas Number 102-64-9
    Iupac Name 3,5-Dimethoxyaniline
    Molecular Formula C8H11NO2
    Molecular Weight 153.18 g/mol
    Appearance Light yellow to brown solid
    Melting Point 62-66 °C
    Boiling Point 285-287 °C
    Density 1.13 g/cm³
    Solubility In Water Slightly soluble
    Refractive Index 1.574
    Smiles COC1=CC(N)=CC(OC)=C1
    Pubchem Cid 77443

    As an accredited 3,5-Dimethoxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle, screw-capped, labeled "3,5-Dimethoxyaniline," chemical formula, CAS number, and hazard warnings displayed.
    Shipping 3,5-Dimethoxyaniline is shipped in tightly sealed containers, stored in a cool, dry, and well-ventilated area. Containers are clearly labeled and handled according to local and international regulations for chemical transport. Personnel must use appropriate protective gear during handling to prevent exposure and ensure safety during storage and transit.
    Storage 3,5-Dimethoxyaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Proper labeling and secondary containment are recommended to prevent accidental spills and ensure safe handling and storage conditions.
    Application of 3,5-Dimethoxyaniline

    Applications of 3,5-Dimethoxyaniline in Industrial Manufacturing

    3,5-Dimethoxyaniline serves as a key intermediate in a range of high-value downstream sectors, delivering reliable performance in advanced chemical synthesis and specialized manufacturing environments. The following application scenarios demonstrate industrial integration of this raw material within established production chains where documented regulatory oversight and proven compatibility support its sustained global adoption.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers incorporate 3,5-dimethoxyaniline as a building block in the synthesis of active pharmaceutical ingredients (APIs), particularly for the preparation of substituted anilines required in anti-inflammatory and antipyretic drug classes. The aromatic amine moiety delivers selectivity in electrophilic aromatic substitution, with carefully monitored addition rates to ensure purity and minimize side reactions during multistep transformations under GMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs regulating raw materials
    • US FDA 21 CFR Part 210 & 211 for finished pharmaceuticals
    • Chinese Pharmacopoeia (ChP) API raw material guidance

    Typical usage ratio

    • Applied between 0.8 – 2.0 molar equivalents, with precise ratio determined by API synthesis route and consecutive functional group conversions

    Downstream process integration

    • Charged during the initial condensation or coupling reaction, frequently under nitrogen atmosphere to prevent oxidative degradation; incorporation monitored via HPLC during scale-up

    Final product types

    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Paracetamol and related phenacetin derivatives
    • Custom pharmaceutical intermediates for small-molecule pipelines

    2. Agrochemical Synthesis

    Chemical crop protection companies employ this raw material for the targeted synthesis of particular aniline-derived herbicides and fungicides. Its electron-donating methoxy substituents allow precise control during aromatic nitration, halogenation, and diazotization steps critical for downstream agrochemical activity, with process design based on field efficacy data and regulatory residue limits.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • OECD Principles of Good Laboratory Practice (GLP)
    • European Union Regulation (EC) No 1107/2009 for plant protection products
    • US EPA 40 CFR Part 180 Tolerances and Exemptions for pesticide chemical residues

    Typical usage ratio

    • Utilized in 10–20% weight of total intermediates during coupling, adjusted for target molecule structure and batch yields

    Downstream process integration

    • Introduced during the stage of aromatic amine derivatization, typically prior to diazotization or carbonylation, in closed system reactors with LC-MS batch monitoring to ensure trace impurity removal

    Final product types

    • Triazine-based herbicides
    • Aniline-derivative fungicide precursors
    • Nitroaniline intermediate compounds for selective pesticides

    3. Dye and Pigment Intermediate Production

    Producers of specialty dyes and pigments rely on this material to introduce specific methoxy patterns in aromatic rings for improved chromophore stability. It directly participates in azo dye coupling and oxidative cyclization, where exact dosing impacts shade consistency, solubility, and UV resistance of the final pigment dispersions. Quality management enforces batch reproducibility and chromatographic purity throughout multi-ton scale manufacturing.

    Industry compliance standards

    • REACH (EC 1907/2006) substance registration for dye/pigment production
    • ISO 9001:2015 certified quality management for colorant synthesis
    • ZDHC MRSL for restricted substances in textile applications
    • EN 71-3 toy safety requirements for heavy metal content in pigments

    Typical usage ratio

    • Ranges from 5–15% by mass in coupling with diazonium salts, matched to target pigment intensity and solubility profile

    Downstream process integration

    • Charged at the initial amination or coupling stage under alkaline aqueous conditions, with pH and temperature control; followed by purification steps such as extraction and recrystallization

    Final product types

    • Azo dyes for textiles and inkjet inks
    • Methoxy-substituted pigment lakes
    • Colorants for plastics and synthetic fibers

    4. Fine Chemical Synthesis for Electronic Materials

    Manufacturers in the electronic chemicals sector leverage this amine for tailoring functional moieties within high-purity organic semiconductors and dye-sensitized solar cell (DSSC) components. The compound’s dual methoxy groups modulate electron density, supporting reliable performance in functional small molecules and specialty polyanilines applied in emerging optoelectronic devices, with attention to contamination control at sub-ppm levels.

    Industry compliance standards

    • IEC 60749 reliability test methods for semiconductor devices
    • JEITA ET-7304 polymeric material purity guidelines
    • RoHS (Directive 2011/65/EU) hazardous substance restrictions for electronic applications
    • IATF 16949:2016 for automotive electronic chemical ingredients

    Typical usage ratio

    • Applied at 1–4 mol% relative to polymerizable monomer units, with fine-tuned levels based on required conductivity or dye layer absorption

    Downstream process integration

    • Added to the reaction mix during polymer backbone functionalization or dye precursor formation, under inert gas environment to suppress oxidative byproducts; monitored by GC-MS for trace metal residues

    Final product types

    • Conductive polymers for OLED and OPV layers
    • Dye-sensitized solar cell sensitizers
    • Organic thin-film transistor active layers

    5. Organic Synthesis for Perfume Ingredient Intermediates

    Companies focused on fragrance raw material synthesis incorporate 3,5-dimethoxyaniline into intermediates for musk and anisic compounds. The compound supports regioselective substitution and esterification enabling downstream olfactory-active molecules, with controlled addition crucial for purity and olfactory profile targeting in large-scale aroma chemical production lines governed by IFRA standards and European safety regulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9001:2015 for process and quality management systems
    • REACH (EC 1907/2006) raw material registration

    Typical usage ratio

    • Incorporated at 3–8% by weight during precursor synthesis, dependent on fragrance molecule complexity and synthetic yield optimization

    Downstream process integration

    • Reacted via Friedel–Crafts acylation or esterification following controlled substitution, with in-process GC analysis for isomer distribution monitoring

    Final product types

    • Anisic aldehyde and ester intermediates
    • Musk ketone and related aroma chemicals
    • Scent ingredient intermediates for cosmetics and detergents
    Free Quote

    Competitive 3,5-Dimethoxyaniline prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    3,5-Dimethoxyaniline: A Closer Look at Practical Applications and Manufacturing Insights

    Practical Value in Modern Industry

    At our facility, we have watched 3,5-Dimethoxyaniline become one of the go-to intermediates in synthesis across several sectors. Our daily production emphasizes the demands of pharmaceuticals and agricultural compounds but also notices its growing footprint in dyes, specialty polymers, and chemical research. This aniline derivative, known by CAS number 104-92-7, comes up in both new research discussions and established multi-ton batch orders. Its two methoxy groups at the 3- and 5-positions on the aniline ring unlocks pathways that plain aniline or mono-methoxylated anilines can’t fulfill.

    Each molecule can participate in fine-tuned reactions. In our reactors, purity and positional selectivity matter—down to the last decimal—and that drives discussions about quality with both established partners and new clients. Its white to off-white crystalline appearance may seem unremarkable, but chemists recognize the stability and reactivity made possible by those methoxy groups. Over years of working with this compound, we have refined our processes to squeeze out any minor isomeric impurities or colored byproducts. Feedback often touches on reliable melting range, low residual moisture, and tight GC area purity.

    Distinctive Features in Manufacturing

    One thing we encounter in our work is the comparison between 3,5-Dimethoxyaniline and its regioisomers, or even with simpler anilines. The dual methoxy pattern in the meta-positions sometimes draws confusion from those only familiar with mono-substituted types, like 4-methoxyaniline. Mono-methoxy anilines usually push the electron-donating effect at a single site and open up a different profile in coupling reactions. By contrast, the 3,5-pattern yields milder reactivity, but introduces more pronounced selectivity in certain syntheses. We have seen custom dyestuff chemistries count on this difference. A handful of organic electronics teams now seek out the symmetrical substitution for thin-film processing.

    Operationally, producing this compound involves careful temperature controls and timing during methylation and amination stages. Overheating or overexpression of reagents can tip the balance toward unwanted regioisomers. Every batch is carefully monitored for signs of these byproducts, which can alter not just color, but the solubility profile vital for downstream applications. Tight process controls let us deliver a final product with predictable solubility in organic solvents—something both formulation teams and pilot plant engineers appreciate.

    Usage Insights From a Manufacturer’s Perspective

    In recent years, we have worked with a growing roster of medicinal chemistry labs that use 3,5-Dimethoxyaniline as a starting block for anti-infective and anti-tumor agents. The methoxy groups offer protection against premature oxidation or unwanted deamination, and their influence on electronic structure sometimes opens up new binding motifs in lead discovery campaigns. Downstream, we periodically receive requests for kilogram-scale supply with custom particle sizing or purification levels, especially as regulatory requirements shift.

    On the pigments and dyes side, our partners rely on the reproducibility of our batches, especially when scaling from grams to pallet-sized quantities. Poorly controlled manufacturing of similar compounds—like 2,4-dimethoxyaniline or 3,4,5-trimethoxyaniline—can lead to visible shade shifts or reduced batch stability in colorant formulations. This underlines the value in working with manufacturers who monitor every stage, from initial raw material selection to final packaging.

    The Role in Large-Scale Organic Synthesis

    Production of 3,5-Dimethoxyaniline on a multi-ton scale brings unique challenges compared to more commoditized aromatic amines. Our tanks see repeated stress testing during the amination process; inconsistent heat transfer or reagent feed can compromise yield. Process optimization efforts over the past decade have given us insights not only for this specific product but for broader aniline derivative manufacture.

    This is a compound that rarely sees direct end-use without transformation. Instead, it acts as a vital building block. In our experience, clients often modify it through acylation, diazotization, or coupling—each operation placing fresh demands on the raw material’s purity. A dye manufacturer, for example, addressed us with issues caused by trace levels of 3,4-dimethoxyaniline in a competitor’s material, which complicated azo coupling yields. By tightening our fractionation protocols, we helped them stabilize their finished color consistency.

    Comparison With Other Aniline Derivatives

    Many in the marketplace treat all methoxyanilines as interchangeable. Our technical support teams field recurring questions about the difference between, say, 3-methoxyaniline, 4-methoxyaniline, or 3,5-dimethoxyaniline. In day-to-day plant operations, these differences are significant. Electron density shifts alter their participation in electrophilic substitution, which in turn affects everything from reactivity to heat stability of downstream products. The symmetrical substitution on the 3,5-variant can mean less interference in multi-step synthesis—something process chemists engaged in scale-up often cite as a key reason for selecting this material.

    Older grades produced with less strict controls frequently caused trouble in pharmaceutical synthesis. In contrast, our modern approach delivers reproducible batches with tightly managed side products and minimal colorants formation. Over the years, more medicinal chemistry projects have chosen 3,5-dimethoxyaniline over former favorites due to its improved reliability and influence on pharmacophoric development.

    Real-World Challenges for Producers

    Working with aryl amines always requires due diligence around worker safety and environmental release. In our factory, we incorporate enclosed handling and high-efficiency scrubbing to minimize emission risks. Historical practices in some regions cut corners with vented systems, spreading odors and possible health effects. By investing in recovery and containment, we meet new regulatory developments in most export markets and have helped clients facing chemical safety audits to explain sourcing and compliance with ease.

    Logistics matter. As the raw aniline derivatives see global demand spikes, we’ve noticed transport regulation changes tied to environmental performance and hazardous material categories. We lean into our relationships with vetted forwarders and maintain up-to-date compliance protocols to avoid shipment delays at customs. Companies sourcing from casual traders or unchecked exporters often find themselves at odds with customs and port officials—delays that have never helped a production schedule.

    Feedback and Collaboration Across Industries

    Through years of supplying 3,5-Dimethoxyaniline, we have developed a responsive model to customer feedback. Dye houses may ask for tighter control of moisture, while pilot pharma plants flag the need for reduced heavy metals or ultralow residual solvents. Each feedback point feeds directly into process improvements and batch test regimes. In the early days, most communication focused on spec sheets and Certificates of Analysis. Lately, dialogue has shifted toward robust documentation for REACH, TSCA, and other international chemical registration regimes.

    In R&D collaborations, we’ve witnessed how incremental purity improvements let advanced syntheses push yield envelopes even further. Some partners use our aniline derivative as a stepping stone in complex heterocycle development; others explore its application in agrochemical formulation where adjuvant stability is essential. Where we see repeat orders and expanded joint development, it reflects how our practical, factory-level optimization enables their innovation.

    Production and Handling Details

    Day-to-day production involves more than quality checkpoints and analytics. In our facility, operators are trained to handle this compound through contained systems, limiting potential exposure. Waste streams from methylation or amination sometimes contain minor side-products that require dedicated treatment. Overhead mitigation costs, including solvent recovery or distillation, factor into our pricing—but ensure less environmental risk for us and downstream users.

    Compared with older decades, automated packaging has reduced both contamination risk and exposure incidents. Today’s packed drums or bags keep out atmospheric moisture and cross-contamination with other aromatic amines. Those who’ve worked in chemical warehouses know the frustration that comes from poorly sealed packaging—moisture pick-up, color changes, and even clumping can ruin a downstream process and complicate scale-up.

    Meeting Evolving Technical Demands

    We’ve learned that customer requirements rarely stand still. A few years ago, typical orders sought purity above 98 percent and modest control on water content. Since then, advance in API development and high-performance dyes sparked requests for even tighter specifications—upward of 99 percent and water well below 0.1 percent. Mass spec and NMR checks are more common, demanded not just by regulatory agencies, but also by the internal QC teams of our advanced customers.

    There’s clear competitive pressure to continually refine both analytical tools and isolation techniques. In our plant, that means new GC setups and the use of deeper vacuum for final drying. Older purification frameworks sufficed for industrial colorants but not for pharmaceutical or high-tech polymer intermediates. We test for aldehydic and nitro impurities, as even minor traces can catalyze downstream decomposition.

    Looking at Sustainability and Supply Security

    Chemical manufacturing faces new scrutiny from global buyers, from scrutiny over solvent use to local regulatory registration. Our ongoing investment in solvent reuse cuts both emissions and costs, responding to questions from end users about carbon footprint. Every ton of 3,5-Dimethoxyaniline set aside for re-blend means less waste and avoids the inefficiency of single-use solvents that dominated industry practices of the past.

    Some customers now list supply chain robustness as a top concern, especially after witnessing recent logistics bottlenecks. Our response is local warehousing in multiple regions and buffer stocks at key depots. This lets us ride out delays in upstream feedstocks or restrictions in port traffic. Shipments of uncontrolled or grey-market materials often risk flagging at customs, so traceable batches with full quality documentation have become a differentiator.

    Who Typically Uses 3,5-Dimethoxyaniline?

    We see orders rolling in from pharmaceuticals, dyestuffs, intermediate manufacturers, agrochemical producers, and research institutions. Common stories from users include improved batch-to-batch consistency and fewer downstream issues compared with generic grades sourced from less controlled producers. Pharma groups highlight the ability to scale up from small-lab to pilot plant without facing impurities that block downstream chemistry. Dyestuff companies appreciate the reliable chromophore formation, with clean transitions in hue and minimal unexpected color shifts.

    Custom synthesis teams value not having to revisit raw material qualification with every shipment. In our experience, the more meticulous the downstream process, the more crucial fully characterized, well-handled starting materials. Any lapse at our end magnifies as expensive cGMP or regulatory-quality syntheses down the line.

    Potential Solutions to Industry Issues

    We have addressed challenges by building both technical and human capacity. Training staff to monitor every stage—the methylation control, amination timing, post-reaction clean-ups—has cut incidents of off-spec batches. Auditing supply chains has weeded out unreliable or unsafe raw reagent vendors, boosting both consistency and confidence for stakeholders further down the line.

    Some partners want ever-improving documentation—mass spectrometry scans, heavy metals assessments, full spectral data, detailed impurity profiles. We have opened up data sharing portals and standardized reporting interfaces, because delays and hiccups often come from mismatched paperwork, not just missed specs.

    Supply disruptions have led us to lean towards vertical integration for certain critical inputs. Bringing feedstock processing in-house means less vulnerability to market swings triggered by upstream shortages or regulation in distant regions. These sorts of precautions keep the flow of 3,5-Dimethoxyaniline steady in a world of shifting geopolitical risk.

    Conclusion: Why Commitment to Quality Matters

    No two compounds serve all markets equally well. Feedback from long-term partners makes clear: reliable production and transparency in manufacturing ensure success, not just on paper but across thousands of kilograms in real-world processes. 3,5-Dimethoxyaniline may be a single line item in a complex synthesis, but small differences upstream can mean major differences in yield, cost, and quality outcomes downstream. The experience of hands-on manufacturing brings home these principles time and again.