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2,4-Dimethoxyaniline

    • Product Name 2,4-Dimethoxyaniline
    • Alias 2,4-Dimethoxybenzenamine
    • Einecs 208-677-4
    • 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

    711268

    Cas Number 120-84-5
    Molecular Formula C8H11NO2
    Molecular Weight 153.18 g/mol
    Iupac Name 2,4-dimethoxyaniline
    Appearance Light yellow to brown crystalline solid
    Melting Point 61-63 °C
    Boiling Point 274 °C
    Density 1.13 g/cm³
    Solubility In Water Slightly soluble
    Flash Point 140 °C
    Pubchem Cid 88231
    Smiles COC1=CC(=C(C=C1)N)OC

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2,4-Dimethoxyaniline, labeled with hazard warnings, product details, and supplier information.
    Shipping 2,4-Dimethoxyaniline should be shipped in secure, tightly sealed containers, compliant with all relevant chemical handling regulations. It must be labeled as a hazardous chemical, stored away from incompatible substances, and protected from moisture and extreme temperatures. Ensure proper documentation and packaging according to international and local shipping standards for hazardous materials.
    Storage 2,4-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 the chemical from light and moisture. Ensure containers are clearly labeled, and access is restricted to trained personnel. Use secondary containment to prevent spills or leaks.
    Application of 2,4-Dimethoxyaniline

    Applications of 2,4-Dimethoxyaniline in Industrial Manufacturing

    As a direct manufacturer of 2,4-Dimethoxyaniline, we support a range of mature downstream sectors where this aromatic amine plays a critical role in formulating performance-driven chemical intermediates. The following application scenarios demonstrate specific integration points and compliance measures for each industry, focusing on established, high-purity requirements and practicable manufacturing data.

    1. Dye and Pigment Intermediate Synthesis

    Downstream colorant producers utilize 2,4-Dimethoxyaniline as a building block for azo dyes, particularly in the production of bright red and orange pigments with high tinting strength and light fastness. The material participates in the diazotization and subsequent coupling reactions, contributing essential electron-donating effects that influence chromatic properties. Process engineers adjust input ratios according to shade and purity specifications, responding to end-market quality controls in textiles, plastics, and inks.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for pigment raw materials
    • OEKO-TEX Standard 100 for dyes used in textiles
    • ISO 105 series for color fastness requirements
    • China GB/T 17650 for industrial dye manufacture

    Typical usage ratio

    • 3–8% by weight in diazo component for azo dye formulation; adjusted based on molecular weight of the coupling partner and desired pigment intensity

    Downstream process integration

    • Introduced during the primary diazotization step under controlled acidic conditions, followed by coupling with various aromatic compounds to yield target pigments

    Final product types

    • Disperse red and orange dyes for synthetic fibers
    • Specialty pigments for plastic coloring
    • Organic printing inks for textiles and packaging
    • Technical coatings for automotive and industrial equipment

    2. Pharmaceutical Intermediate Manufacturing

    2,4-Dimethoxyaniline acts as a key precursor in active pharmaceutical ingredient (API) synthesis, especially for certain analgesic and antipyretic agents. Its chemical structure facilitates selective acylation, alkylation, or condensation routes, enabling medicinal chemists to construct complex heterocyclic rings that undergo further functionalization. Pharmaceutical sites operate GMP-compliant lines and enforce rigorous raw material traceability, necessitating batch purity assurance and documentation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP–NF Monographs (where applicable)
    • European Pharmacopoeia (Ph. Eur.) for APIs containing aromatic amine segments
    • 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to core API scaffold in multi-step synthesis; calculated per target yield and impurity profile

    Downstream process integration

    • Charged into the initial condensation or protection/deprotection stage; may participate in selective demethylation or amide bond formation depending on the API structure

    Final product types

    • Paracetamol (Acetaminophen) derivatives
    • Antihistamine intermediates
    • Custom research compounds for small molecule libraries
    • Potential intermediate for non-steroidal anti-inflammatory drugs (NSAIDs)

    3. Agrochemical Synthesis (Herbicide Precursors)

    Specialty agrochemical manufacturers employ 2,4-Dimethoxyaniline as a primary intermediate in the development of selective herbicide molecules. The compound undergoes targeted coupling with chlorinated and sulfonated partners to produce active molecules with high plant selectivity. Formulation chemists tune the additive amount based on target crop safety profiles and residual environmental parameters demanded by end-use markets for post-emergent applications.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) – Technical Material Standards
    • US EPA 40 CFR Part 180 for pesticide tolerances
    • China GB 1886.174 for pesticide intermediates
    • ISO 9001:2015 Quality Management System for agrochemical manufacturing

    Typical usage ratio

    • Ranges from 2–6% by weight in relation to the total synthetic batch, depending on the target molecule’s substitution pattern and reactivity

    Downstream process integration

    • Fed into nucleophilic substitution or aromatic coupling sequences during active ingredient construction; often followed by purification and crystallization

    Final product types

    • Selective herbicide actives for broadleaf weed control
    • Intermediates for sulfonylurea compounds
    • Functionalized aromatic base stocks for crop protection R&D

    4. Polymer Additives for High-Performance Materials

    Industrial polymerization facilities leverage 2,4-Dimethoxyaniline as a chain stopper or reactive modifier in specialty polyimide and polyamide production. Its integration as a comonomer or end-capping agent imparts tailored physical properties such as increased thermal resistance and controlled molecular weight distribution. Engineers select input ratios to balance cost, mechanical requirements, and downstream compounding processes, especially for high-spec electronics and aerospace-grade films.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive) for electronic components
    • UL 94 for flammability of polymeric materials
    • ISO 9001:2015 for quality management in polymer synthesis
    • ASTM D5208 for UV stability in polymer films

    Typical usage ratio

    • Commonly 0.5–2.5% by weight as a reactive additive or end group modifier, selected based on molecular weight targets for the final polymer

    Downstream process integration

    • Added during the prepolymer stage, either as a terminating agent for molecular weight control or as a functional monomer impacting chain structure and cross-link density

    Final product types

    • Heat-resistant polyimide films
    • Specialty polyamide fibers for high-strength textiles
    • Electrical insulation materials for microelectronics
    • Engineered plastics for aerospace interiors

    5. Fine Chemicals for Photographic Chemicals

    The production of high-purity developers and stabilizers in photographic processing relies on 2,4-Dimethoxyaniline for its role in synthesizing aromatic developer agents with refined reactivity profiles. Chemical control teams use the amine for condensation reactions to tailor redox properties, optimizing for rapid image development and minimal fogging. Batch process adjustments depend on the silver ion concentration and targeted grain structure in final photographic emulsions.

    Industry compliance standards

    • ISO 18911:2010 Processed Silver-Gelatin Photographic Films—Storage Practices
    • ANSI IT9.17 for photographic system safety
    • GMP for specialty fine chemicals
    • REACH registration for fine chemical usage in EU

    Typical usage ratio

    • Typically 1–4% by weight in developer component formulations, modifiable based on emulsion formulation details

    Downstream process integration

    • Used in the synthesis of aromatic reducer agents, often reacting under mild conditions followed by fine purification for photo-grade standards

    Final product types

    • Color and black & white photographic developers
    • Photographic fixer solutions
    • Stabilizer blends for silver halide emulsions
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    Certification & Compliance
    More Introduction

    2,4-Dimethoxyaniline: Meeting New Demands in Chemical Synthesis

    At our facility, we prioritize building our product line around real-world feedback, from lab-scale research to commercial manufacturing. 2,4-Dimethoxyaniline often comes up during conversations with chemists who need reliability and ease of handling in an aromatic amines portfolio. Through years of production experience, we recognize that the balance between reactivity and selectivity gives 2,4-Dimethoxyaniline strong appeal across multiple sectors. Its chemical structure—featuring methoxy groups in ortho and para positions—translates into consistent performance, especially when downstream processes require targeted substitutions on the aromatic ring.

    Bridging the Gaps in Traditional Amines

    Many aromatic amines can present operators with two main obstacles: purity concerns and batch consistency. Crude batches are prone to variable impurity profiles, and variable impurity brings unpredictable yields. After years in manufacturing, we have learned to synthesize 2,4-Dimethoxyaniline to rigorous standards, delivering batches with controlled assay values and trace-level impurity profiles. Across pigments, pharmaceuticals, and specialty chemical synthesis, impurities can sap color quality, hinder drug intermediates, or affect downstream formulation processes. With our manufacturing approach, every supply lot undergoes tailored purification and analytical checks, accounting for the realities of commercial production instead of lab-scale idealism.

    What Sets 2,4-Dimethoxyaniline Apart

    It’s easy to reach for unsubstituted aniline or for its mono-methoxy analogues. In practice, product developers find that 2,4-Dimethoxyaniline delivers increased versatility. The dual methoxy substitution alters electron distribution on the aromatic ring, enabling different coupling and acylation reactions. This distinction becomes significant for anyone who’s spent time optimizing reaction conditions for azo dye precursors, active pharmaceutical ingredients, or advanced materials. Over the years, we’ve seen how these extra methoxy groups broaden opportunities for creative molecular design, while at the same time providing a level of chemical stability that’s not always available with single-substitution options.

    Our product achieves a high assay (typically >99.0% by GC), but numbers alone only tell part of the story. From our vantage point, reproducibility matters more in the long run than a single certificate of analysis. We’ve worked through supply chain disruptions and seen firsthand how subtle production shifts can change impurity fingerprints—sometimes enough to impact critical downstream assays. By controlling raw material sources and finetuning reactor parameters, we help chemists working on high-value projects sidestep unwanted surprises. Anyone who’s worked on scaling up a pigment or a drug intermediate knows what it’s like to trace a color shift or a bioactivity loss right back to invisible process changes.

    Specifications and Handling Insights from Decades in Manufacture

    2,4-Dimethoxyaniline comes as an off-white to pale yellow crystalline solid. Its melting point sits in a comfortable range for easy storage and handling, which simplifies logistics both here at the plant and throughout the customer supply chain. Volatiles remain minimal during transit, which reduces loss and waste compared with more volatile analogues. Consistent melting point values (typically ~62–64°C in our production runs) tell us quite a bit about product integrity, especially after seasonal temperature swings in the warehouse. This physical stability is relevant not just for our quality control team, but also for downstream formulators seeking to avoid rework due to sticky or amorphous materials.

    Solubility profiles make a difference for practical workflows. 2,4-Dimethoxyaniline dissolves readily in common organic solvents such as ethanol, ether, and chloroform, with limited water solubility. This allows for flexibility in both extraction and reaction set-ups—a benefit that customers in dye and pharmaceutical labs cite as a recurring strength.

    Usage Experience across Industries

    The synthesis of complex dyes repeatedly calls for this compound as a reliable precursor in coupling reactions. Anyone fabricating azo pigments for plastics, inks, or coatings has likely struggled with byproduct color variability—especially at scale, where minor changes in intermediate quality show up loud and clear in end-use performance. From our production line, customers receive batches engineered to eliminate these pitfalls; a steady impurity fingerprint keeps color development in the target shade, batch after batch, year after year.

    Pharmaceutical development teams have taken advantage of 2,4-Dimethoxyaniline as an intermediate for fine chemicals and active molecules. The dual methoxy groups lend themselves to selective synthetic transformations, enabling the construction of medicinal scaffolds while minimizing risks posed by oxidative or reductive side-reactions. Medicinal chemists working on new molecular entities often face the challenge of developing synthetic routes that permit structural diversity; our experience tells us that this molecule frequently provides just the right combination of reactivity and selectivity for multi-step flow systems.

    Materials scientists value its use in monomer synthesis for advanced polymers or specialty surface coatings. The electron-donating methoxy groups alter both reactivity and the resulting polymer’s properties, leading to differences in crosslinking and thermal characteristics that can be harnessed for specific industrial needs. Over years of supply partnerships, customers have credited material performance gains to consistent upstream intermediate quality—a fact that reinforces our ongoing process investment.

    Why Not Just Use Mono-Methoxyanilines?

    There's often a temptation to swap in more readily available mono-methoxy or unsubstituted analogues—on the surface, this can look appealing from a procurement angle. Our long-term project partners have shared countless cases showing reduced functional group compatibility or yield drop-offs when less substituted amines are used. Chemistry teams looking to push the limits of their process windows—higher throughputs, better yields, lower waste—turn to 2,4-Dimethoxyaniline for more reliable results. Its chemical fingerprint intersects favorably with common starting materials, supporting broader substrate scopes during optimization. Where one methoxy group may not fully block unwanted side-reactions, the two present here tighten selectivity windows, giving researchers an edge when playing for both speed and precision in product development.

    Balancing Cost and Reliability

    Every process manager faces the cost–performance tradeoff. Our plant has weathered raw material price cycles long enough to know that thoughtful sourcing coupled with efficient reaction design pays dividends in batch-to-batch repeatability. Reliable end results matter more over the life of a product cycle than momentary spot pricing. Through optimized plant economics, we keep costs in line while holding to the purity and physical property standards that professional users demand. Contract partners who have switched from lower-cost suppliers tell us the time saved from fewer failed batches and cleaner reactions outweighs minor upcharges on input materials.

    Safety, Scale, and the Path to Reliable Supply

    Manufacturing aromatic amines, especially those with multiple substitutions, often means adapting reactor conditions and work-up to larger batch sizes. Over the years, our process engineers have refined protocols to limit dust emissions and manage solvent recovery, supporting both operator safety and sustainability goals. Due to its relatively low volatility, 2,4-Dimethoxyaniline presents fewer inhalation and containment concerns versus some more volatile aromatic amines—a practical consideration that customers mention as a reason for selecting this molecule for pilot or commercial-scale operations.

    For scaling customers, consistent supply reassurance ranks high. We manage risk by maintaining multiple input streams and validating every supplier before any upstream switch hits our line. As producers, we feel a responsibility to communicate early about any raw material issues, helping downstream partners plan with a transparency that avoids last-minute disruptions. Decades in the chemical sector taught us that trust builds not on slogans but on tangible delivery and long-term supply security.

    How Customers Shape Our Specifications

    Our team reviews every customer requirement specification in detail, adapting analytical protocols beyond generic methods to count for real-life variables: moisture, aromatics profile, and even color indices. Chemists working under tight regulatory conditions—whether for pigment migration in food-contact plastics or for pharmaceutical ingredient dossiers—often bring unique approval criteria. Since we experience these audits alongside our customers, we align our output with the most demanding settings, not just baseline technical data.

    Process Evolution and Future Trends

    The industry’s needs rarely sit still. Lately, we’ve seen increased demand for sustainably manufactured aromatic amines, with customers seeking new green chemistry initiatives. Our plant team deploys selective catalytic methods and solvent recycling for cleaner process footprints. Fractional crystallization and high-vacuum techniques help us boost yield while cutting solvent demand. The challenge: make these improvements without shifting impurity signatures or end-use performance.

    End users keep us grounded. Application chemists send back feedback that steers our equipment upgrades or packaging decisions. Small adjustments to bulk packaging or drum lining reduce cross-contamination risk, especially for pharmaceutical intermediates. Logistics teams, both at our site and at the customer’s, have stressed the value in well-sealed containment for aromatic amines—less odor, less product loss, and fewer headaches during regulatory inspections. Collective knowledge from across our supply and client networks sharpens our future process enhancements, feeding innovation in plant infrastructure and shipping container options.

    Comparing with Other Products—What Matters Most

    Our customers constantly compare 2,4-Dimethoxyaniline with both classic anilines and niche analogues. Experience tells us that it stands apart on several fronts: first, the twin methoxy functionality supports chemical versatility. Second, commercial users see immediate differences in manageable melting point and solvent compatibility. Third, the long view shows that product consistency, more than a single analyte number, serves as the foundation of complex syntheses and marketable product outcomes. Whether in the development of innovative polymers, formulation of advanced coatings, or scale-up of pharmaceutical intermediates, gaps in input stability immediately echo into efficiency and product quality changes. This has made 2,4-Dimethoxyaniline more than just a niche intermediate—it’s a mainstay where process predictability and high performance are needed.

    As a manufacturer, we take our stewardship role seriously. Chemists need more than a commodity—they look for a collaborative partner in the supply chain, one who has weathered process ups and downs and can be trusted to deliver no matter the market climate. 2,4-Dimethoxyaniline occupies a unique position in our lineup, bringing both history and adaptability to industries pushing the frontier of chemical innovation. We see its relevance deepening wherever customization and precision matter most, and we remain committed to pushing our own production standards to match the evolving demands of the life sciences, pigment, and materials industries.

    Through many production campaigns, technology changes, and cycles of customer feedback, our focus stays rooted in application-driven quality and process transparency. Each batch results from concrete dialogue with end users—a continuous effort to balance innovation, reliability, and responsible production. Working alongside the industry as it evolves, we recognize how 2,4-Dimethoxyaniline has grown from a specialty chemical to a practical solution for modern manufacturing, equal parts chemistry and partnership.