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

3,4,5-Trimethoxyaniline

    • Product Name 3,4,5-Trimethoxyaniline
    • Alias m-Anisidine
    • Einecs 216-481-3
    • 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

    219519

    Cas Number 13727-37-8
    Molecular Formula C9H13NO3
    Molecular Weight 183.21 g/mol
    Iupac Name 3,4,5-Trimethoxyaniline
    Appearance Light yellow to brown solid
    Melting Point 74-77°C
    Boiling Point 322.2°C at 760 mmHg
    Density 1.188 g/cm3
    Solubility Slightly soluble in water
    Flash Point 148.3°C
    Smiles COC1=CC(=CC(=C1OC)N)OC
    Pubchem Cid 69701
    Refractive Index 1.577

    As an accredited 3,4,5-Trimethoxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a screw cap, labeled "3,4,5-Trimethoxyaniline," includes hazard symbols and handling instructions.
    Shipping 3,4,5-Trimethoxyaniline is generally shipped as a solid chemical in tightly sealed containers to prevent moisture ingress and contamination. The packaging must comply with local and international transport regulations, including labeling for laboratory chemicals. It should be kept away from strong oxidizers and stored in a cool, dry place during shipping.
    Storage 3,4,5-Trimethoxyaniline should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Protect from light and moisture. Label the container clearly, and ensure storage complies with local chemical safety regulations. Use secondary containment to prevent accidental spills or leaks.
    Application of 3,4,5-Trimethoxyaniline

    Applications of 3,4,5-Trimethoxyaniline in Industrial Manufacturing

    3,4,5-Trimethoxyaniline serves as a specialized intermediate in various industrial manufacturing sectors, supporting stringent process requirements and compliance frameworks for downstream high-value products. Below, we detail its application scenarios with precise information on standards, formulation, process entry points, and end product types.

    1. Pharmaceutical Synthesis – Active Pharmaceutical Ingredient (API) Intermediates

    Pharmaceutical manufacturers incorporate this intermediate for the synthesis of certain APIs, particularly those in the antihypertensive, antiviral, and anticancer agent classes where methoxy-aniline derivatives are present in molecular scaffolds. The chemical enters multi-step organic synthesis routes, participating in selective amination and heterocycle formation steps under validated process controls, directly impacting the bioactivity of the resultant compound.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) as outlined in ICH Q7
    • USP and European Pharmacopoeia (Ph. Eur.) monographs for synthesis quality
    • FDA and EMA guidelines for starting material traceability and impurity profiles
    • International Conference on Harmonisation (ICH Q3A/B) impurity limits

    Typical usage ratio

    • Batch formulas range from 0.3% to 1.5% w/w relative to total organic intermediates, determined by stoichiometry in multi-step API synthesis and adjusted to target specific impurity thresholds

    Downstream process integration

    • Charged during intermediate condensation or ring closure steps before final API salt formation; reaction monitored for conversion coefficient and controlled under in-process analytical QC

    Final product types

    • Antiviral and antihypertensive drugs (e.g., methoxyphenyl-substituted imidazoles, pyridines)
    • Active pharmaceutical ingredients containing aromatic amines

    2. High-Performance Dye and Pigment Manufacturing

    Dye and pigment producers utilize this material as a methoxy-functionalized aromatic amine for synthesizing complex azo, anthraquinone, and triarylmethane dye structures, where it confers bathochromic shift and enhanced thermal stability. Its introduction occurs during diazotization and coupling reactions for specialty colorants under controlled pH and temperature conditions.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textile dyes
    • REACH Annex XVII and SVHC regulations specific to aromatic amines
    • ISO 9001:2015 quality management system for pigment producers
    • DIN EN 71-3 for toy and consumer product colorants

    Typical usage ratio

    • Between 2.0% and 6.0% by total dye mass, set based on targeted chromophore structure and shade intensity requirements

    Downstream process integration

    • Enters the process post-diazotization as the primary amino precursor for azo bond formation or as a substitution reagent in aryl amination stages

    Final product types

    • Reactive and disperse dyes for polyester and cellulose fibers
    • Organic pigments for printing inks and plastic color masterbatches
    • Specialty colorants for electronics and packaging materials

    3. Advanced Agrochemical Intermediate Manufacturing

    Agrochemical formulators employ 3,4,5-trimethoxyaniline for producing aromatic amine-substituted herbicide and fungicide building blocks, where its electron-donating methoxy groups adjust bioactivity and environmental persistence. This raw material enters amidation and coupling reactions within multi-step synthetic routes for pre-emergence weed control and disease management agents.

    Industry compliance standards

    • FAO and WHO Specifications for Plant Protection Products (FAO/WHO-JMPS)
    • ISO 17025 certification for lab analysis and purity control
    • Regulation (EC) No 1107/2009 on market authorization of active substances in EU
    • US EPA Pesticide Registration standards for chemical intermediates

    Typical usage ratio

    • Generally used at 1.5–4.0% of intermediate synthesis mass, adjusted by crop application spectrum and target compound potency

    Downstream process integration

    • Introduced during early-stage aromatic amine alkylation or condensation step, enabling precise molecular substitution before formulation into technical concentrates

    Final product types

    • Herbicide and fungicide active ingredients with substituted aniline cores
    • Finished crop protection technical concentrates and suspension concentrates (SC)

    4. Liquid Crystal Monomer and Display Material Synthesis

    Producers of advanced display materials use this intermediate in bespoke liquid crystal formulations and organic electronic monomer synthesis. Its three methoxy groups influence molecular orientation and electric dipole moments, essential for customizing reactivity during aryl diamine polymerization, allowing fine-tuning of nematic and smectic phase transitions.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances) Directive for display components
    • ISO 14001 for environmental management in electronics manufacturing
    • Sony Green Partner Environmental Quality Approval Program
    • IPC-4101 specification for base materials used in printed circuit boards

    Typical usage ratio

    • Loading levels typically between 0.8% and 2.0% of reactive monomer batch, tailored to electro-optical requirements and phase behavior mapping

    Downstream process integration

    • Feeds into Suzuki coupling, Buchwald–Hartwig amination, or polycondensation steps during advanced monomer synthesis prior to LC mixture compounding

    Final product types

    • Nematic liquid crystal monomers for LC displays
    • Specialty organic semiconductors for OLED and OTFT applications

    5. Fine Chemical and Analytical Reagent Production

    Producers of fine chemicals and analytical reagents utilize this intermediate for creating calibration standards, derivatization agents, and specialty assay substrates. Its defined substitution pattern ensures reproducibility in analytical protocols. The material enters diazonium salt formation and subsequent coupling or functionalization stages under high-precision batch control.

    Industry compliance standards

    • ISO 17034 General requirements for the competence of reference material producers
    • ACS Reagent Grade specifications and purity criteria
    • EN ISO/IEC 17025 requirements for chemical analysis traceability
    • GMP as required for pharmaceutical analytical reagents

    Typical usage ratio

    • Formulated at 0.5–3.0% in analytical or calibration mixtures, based on assay sensitivity and linearity calibration curve requirements

    Downstream process integration

    • Charged into diazotization or arylation stages for the generation of primary or secondary calibration standards and functionalization reagents

    Final product types

    • Certified analytical reference materials (CRMs) for spectrophotometry and chromatography
    • Custom high-purity derivatization reagents for analytical labs
    Free Quote

    Competitive 3,4,5-Trimethoxyaniline 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

    Introducing 3,4,5-Trimethoxyaniline: A Core Ingredient for Advanced Chemical Synthesis

    A Manufacturer’s Insight into 3,4,5-Trimethoxyaniline

    Chemical manufacturing relies on building blocks that meet high expectations for quality, purity, and consistent performance in complex transformations. 3,4,5-Trimethoxyaniline, known by the molecular formula C9H13NO3 and the CAS number 3173-80-0, stands out as a valuable intermediate in both research and industrial use. In our years of producing specialty organics, this compound has served as a reliable material for clients working in pharmaceutical development, agrochemicals, and high-value materials research.

    What Sets 3,4,5-Trimethoxyaniline Apart

    The aryl amine backbone of 3,4,5-Trimethoxyaniline, with methoxy groups at three contiguous positions on the benzene ring, gives it distinctive properties. The three methoxy substituents direct the course of substitution reactions, broadening the scope of downstream chemistry compared to simpler anilines. Many clients point to its reactivity and versatility as the foundation for constructing novel heterocyclic systems or devising unique analogues in drug discovery pipelines.

    Speaking from production experience, its pale yellow crystalline form sharply distinguishes it from less-substituted anilines both visually and chemically. Methoxy groups raise its electron density, making this material more nucleophilic and reactive in electrophilic aromatic substitution compared to lower methoxylated anilines. This aspect proves helpful during azo coupling or Friedel–Crafts alkylations, where regioselectivity means less troubleshooting and higher efficiency in synthesis design.

    Many commonly used anilines—like p-anisidine or 4-methoxyaniline—show limited flexibility because of single-site substitution. Broadening the substitution to three locations on the aromatic ring opens new synthetic possibilities. Over time, work with academic research groups and process development labs has shown that 3,4,5-Trimethoxyaniline handles more demanding reaction conditions, with superior stability and less tendency toward oxidation or degradation during storage and application.

    Specifications Backed by Process Rigor

    Customers expect consistent purity and particle characteristics, especially when scaling up beyond gram-scale synthesis. Our facility produces 3,4,5-Trimethoxyaniline to strict analytic parameters, generally meeting purity levels above 99% as measured by HPLC. Moisture content remains below 0.5%, and trace metal analysis confirms contamination remains far beneath international standards for pharmaceuticals and electronics. Rigorous lot tracking and full transparency in process documentation ensure every kilogram matches published certificate-of-analysis values. We have engaged in third-party testing for critical trace contaminants—such as residual solvents and related nitroso compounds—despite strict controls on process solvents, because end users in fine chemistry require these assurances.

    This attention to detail supports demanding use cases: medicinal chemists rely on fine-resolution NMR and MS spectra to confirm structure, while those in dye or pigment manufacturing seek batch-to-batch color consistency. Direct communication between our production team and end users has driven optimizations in drying methods, minimizing the risk of caking or particle growth during long-term storage. By listening to customer feedback, we often adjust crystal size distributions to better fit automated solid-dosing equipment, which streamlines workflows in industrial settings.

    From Synthesis to Application: Real-World Use

    The relevance of 3,4,5-Trimethoxyaniline extends throughout the value chain of specialty chemistry. It routinely fills gaps left by simpler anilines in diverse applications:

    Pharmaceutical clients often highlight regulatory compliance needs. By sourcing 3,4,5-Trimethoxyaniline from a manufacturer committed to traceability and documentation, they bypass regulatory delays and costly repeats of analytical characterization. Our production lines offer the flexibility for custom grades, matching appearance, impurity profile, and bulk density to unique process requirements. By maintaining a direct connection with users, we nimbly address shifts in market demand, for instance supplying research-grade or high-volume commercial lots with the same consistency.

    Manufacturing Challenges and Direct Solutions

    Over the years, scaling up production of 3,4,5-Trimethoxyaniline motivated improvements across synthesis, purification, and logistics. At bench scale, reaction parameters may seem dialed in, but scaling to hundreds of kilograms exposes every process variable. The starting material availability, rigorous control of substitution patterns, and optimized purification methods all play crucial roles. Thermal profile management keeps yields high while preventing unwanted by-products; downstream, careful work-up avoids introducing residual reagents or solvents.

    Process engineers at our plant designed filtration and crystallization protocols to maintain the narrowest possible particle size distribution. High shear mixers prevent agglomeration, and post-reaction washing removes trapped mother liquor. These details matter less at gram scale but can destroy lot integrity during multi-ton runs. Transparent communication with raw material suppliers secures stable input quality, while real-time monitoring foresees and corrects process drift before it impacts any shipment.

    Long-term partners in pharmaceutical and agrochemical companies have stressed the problem of nitrosamine contamination—a major concern across the industry. Our quality team implemented in-process monitoring specifically targeting these impurities, not relying solely on end-point testing. We have installed in-line drying technology to guarantee the lowest achievable residual moisture content, which helps preserve product stability and avoids degradation during global transit. Changes in packaging—using specialized liners—preclude environmental contamination, a common pitfall for lesser-quality imports that suffer during shipping and storage.

    Key Differences from Alternative Aromatic Amines

    In side-by-side comparisons, 3,4,5-Trimethoxyaniline differs from more common or less substituted anilines. Products like aniline, o-toluidine, or mono-methoxyanilines support only basic electrophilic aromatic substitution and offer less structural variety in final products. The density and positioning of methoxy groups in 3,4,5-Trimethoxyaniline lead to different reactivity, allowing selective manipulation at other positions or stabilization of intermediates that do not persist with other substrates. By offering this unique substitution pattern, we furnish a starting material that delivers distinct chemical outcomes unavailable from common anilines.

    Bulk aniline and lower methoxylated analogues, while cost-effective, often show limitations in downstream application—lower yields, more side-products, instability, or difficulty in achieving regulatory compliance. Feedback from our customers has shown that investing in a precisely substituted intermediate gives gains in operational efficiency, finished product quality, and intellectual property differentiation. The balance among reactivity, purity, and physical stability defines the competitive edge of our product.

    Trial batches supplied to major research hubs have shown less batch-to-batch variability in chromatographic behavior versus off-the-shelf mono- and di-methoxyanilines. Researchers who formerly struggled with color changes, residue on crystallization, or ambient sensitivity comment on the straightforward handling and reproducibility of our 3,4,5-Trimethoxyaniline lots. These real-world results led us to further tighten process controls and advise clients on best storage practices to extend usable shelf life.

    Regulatory Alignment and Documentation

    A responsible manufacturer recognizes the importance of regulatory transparency. For pharmaceutical, agricultural, and specialty applications, our documentation details every step from raw material assessment through final packaging. Traceability governs our management practices—each batch receives a unique identifier linked to full synthesis, purification, and distribution records.

    Customer audits have driven our team to adopt international best practices for handling, waste disposal, and cross-contamination prevention. Regular updates to standard operating procedures reflect lessons from past inspections and evolving global standards. Regulatory environments now demand certification of source, proof of absence of banned substances, and quantified analysis of impurities. By meeting and exceeding these requirements, we help streamline customer compliance processes and support uninterrupted global trade.

    Local and international clients frequently request electronic access to analytical data and process audit trails as part of supplier qualification. Our digital records management grants immediate access, eliminating delays on new project initiation or troubleshooting. Each certificate of analysis comes with detailed breakdowns—NMR, HPLC, MS, and elemental analysis—removing guesswork and speeding up onboarding or regulatory submissions downstream.

    Sustainability Initiatives in our Process

    As environmental considerations move to the forefront, our team looks for process improvements that conserve resources and reduce waste during the production of 3,4,5-Trimethoxyaniline. Solvent recovery units reclaim and recycle large portions of process fluids, both reducing environmental load and cutting customer costs through operational efficiency. Byproduct streams—once a waste liability—now enter secondary reactions, either for sale in lower-value applications or as harmless discharge with proper treatment.

    Wherever possible, we select greener reagents and look for lower-energy steps, reducing the factory’s carbon footprint. In discussions with end users, we answer concerns about lifecycle impact by providing third-party sustainability reports. These provide credible data on energy input, water use, and emissions per kilogram produced. We believe direct accountability links cleaner chemistry to downstream market value, especially where ethical sourcing factors into customer purchasing decisions. Environmental agencies increasingly look for documented improvements; our internal culture encourages continual process revision to stay ahead of regulatory and social trends.

    Challenges in Handling and Logistics

    Consistent quality only matters if the product reaches formulators, chemists, and engineers in optimal condition. 3,4,5-Trimethoxyaniline, though more stable than some aromatic amines, still reacts to improper packaging, temperature, and humidity swings. We invested in packaging upgrades—such as anti-static liners and vapor barrier sacks—to safeguard every shipment. Regional partners receive detailed guidelines on storage: away from direct sunlight, sealed in cool, dry rooms. Unlike low-quality alternatives, our product resists clumping, remains free-flowing, and avoids color drift over time.

    For customers with just-in-time production models, shipping and customs demands careful management. We routinely coordinate with freight forwarders and customs brokers to ensure regulatory paperwork accompanies each consignment, minimizing border delays. Emergency inventory programs offer backup for clients with unpredictable consumption rates; small-lot availability reduces financial risk for startups while fulfilling large blanket orders keeps global supply chains running without interruption.

    Our logistics team continuously refines routes, calendar timing, and hazard declarations on material safety data sheets. Recent adjustments in national chemical registration laws prompted us to pre-qualify overseas distribution partners, so customers never experience avoidable downtime. Responsiveness to changing regulations, combined with technical support from chemists, ensures 3,4,5-Trimethoxyaniline maintains its relevance and reliability as markets and rules shift.

    Supporting Innovation into the Future

    From process optimization to end-user application, 3,4,5-Trimethoxyaniline stands as a central intermediate shaped by real-world feedback and technical progress. Customers return for consistent quality, not only because the finished product is robust, but because our team stands behind every shipment with deep experience and openness to collaboration. The evolution of new materials, pharmaceuticals, and crop science tools relies on materials that respond predictably to sophisticated chemical transformations.

    Chemical manufacturing faces continual demand for compounds that stretch beyond commodity standards. The three methoxy groups on 3,4,5-Trimethoxyaniline symbolize not only diverse chemistry, but the manufacturer’s commitment to delivering specialty materials with minimal surprises. In practice, we grow alongside our customers as needs change—responding with faster turnaround, clarified documentation, and flexible lot sizes to fit evolving project requirements.

    Open lines of communication with partners and users define our way of working. Whether improving step-yields, troubleshooting impurities, or designing more sustainable packaging, knowledge gained in one area flows straight to product and service improvement. As new challenges emerge—whether stricter regulatory codes, specialized reaction conditions, or sudden market realignments—we stand ready to adapt, ensuring 3,4,5-Trimethoxyaniline continues powering innovation across advanced sectors.