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2-Methoxyaniline

    • Product Name 2-Methoxyaniline
    • Alias o-Anisidine
    • Einecs 202-963-8
    • 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

    633080

    Cas Number 90-04-0
    Molecular Formula C7H9NO
    Molecular Weight 123.15 g/mol
    Iupac Name 2-Methoxyaniline
    Other Names o-Anisidine
    Appearance Brownish liquid
    Melting Point −1.5 °C
    Boiling Point 225 °C
    Density 1.094 g/cm³
    Solubility In Water Slightly soluble
    Odor Aromatic amine-like
    Refractive Index 1.577

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

    Packing & Storage
    Packing 2-Methoxyaniline, 500g, is supplied in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 2-Methoxyaniline is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled as a hazardous material, following relevant regulations for flammable, toxic chemicals. Appropriate labeling, documentation, and safety precautions, such as secondary containment and ventilation, are required during transport to ensure safe and compliant shipping.
    Storage 2-Methoxyaniline should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents and acids. Protect from light and moisture. Store on secondary containment to prevent spills and adhere to all applicable safety and chemical storage guidelines. Use appropriate labeling to identify the chemical clearly.
    Application of 2-Methoxyaniline

    Applications of 2-Methoxyaniline in Industrial Manufacturing

    2-Methoxyaniline acts as a vital intermediate in several specialized chemical sectors. As the original manufacturer, we ensure high-purity production for demanding downstream integrations across dyes, pharmaceuticals, pesticides, high-end pigment synthesis, and advanced polymer manufacturing. Below, we detail key industrial applications—including formulation specifics, regulatory frameworks, and the end uses realized by our customers.

    1. Dye Intermediates for Azo Dye Production

    In dye manufacturing, 2-Methoxyaniline serves as a critical amine component in the synthesis of azo dye intermediates. Manufacturers introduce it during the diazotization and coupling stages, resulting in vibrant, high-fastness dyes for textiles and paper. Customer formulations frequently adjust the input to control tone strength and compatibility with different fiber types. Strict batch-to-batch homogeneity is maintained to satisfy the repeatability demands of continuous production lines.

    Industry compliance standards

    • REACH Regulation (EU)
    • OEKO-TEX® Standard 100 (for dyes in textiles)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 15–25% of total amine feed in diazotization baths; the exact percentage depends on target dye molecular weight and chromatic requirements.

    Downstream process integration

    • Introduced after acidification and temperature adjustment in the amine dissolution tank.
    • Undergoes diazotization to form diazonium salt before coupling with aromatic compounds.
    • Strict in-process monitoring prevents over- or under-coupling, which affects final color strength.

    Final product types

    • Reactive dyes for cellulose fibers
    • Acid dyes for wool, silk, and polyamide
    • Direct dyes for paper and cotton
    • Intermediates for specialty pigments

    2. Pharmaceutical Intermediates in Analgesic Synthesis

    Major API manufacturers employ 2-Methoxyaniline as a building block during multi-step syntheses of certain analgesic drugs. It participates in amide or ether coupling reactions, forming heterocyclic systems. The material’s purity profile must minimize residual solvents and secondary amines to meet strict ICH guidelines. Careful input metering allows process development teams to optimize yields while controlling side chain isomerism.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF and EP Monographs for impurities
    • 21 CFR Part 211 (FDA cGMP)
    • Ph. Eur. 2.4.24 (Residue on ignition test)

    Typical usage ratio

    • 0.8–1.1 molar equivalents relative to the core acid or halide reactant, tuned per specific API route and impurity control requirements.

    Downstream process integration

    • Added during the amidation or etherification step in protected or open systems.
    • Purification by crystallization or preparative chromatography follows, ensuring residual raw material falls below pharmacopeial thresholds.
    • In-process analytics confirm complete conversion before isolation of intermediates.

    Final product types

    • Precursors for paracetamol derivatives
    • Key intermediates in central-acting analgesics
    • Starting material for specialty antipyretic compounds
    • Small-molecule research chemicals

    3. Agrochemical Synthesis for Herbicides

    Producers of selective herbicides utilize 2-Methoxyaniline as a core nucleophile for the synthesis of complex aromatic rings found in modern crop protection agents. The compound enters condensation or alkylation processes, forming functional groups that determine selectivity and environmental stability. Tight material quality controls ensure process reproducibility essential for agrochemical regulatory submissions.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17034:2016 (Reference materials for agrochemicals)
    • EPA 40 CFR Part 180 (US pesticide residue tolerances)
    • EU Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • 10–22% of batch weight in synthetic cropside active ingredient reactors; adjusted for molecular backbone structure.

    Downstream process integration

    • Introduced into closed-system reactors during nucleophilic aromatic substitution or Mannich-type condensation stages.
    • Reaction monitored for complete conversion by HPLC or GC.
    • Final stage filtration and drying ensure removal of unreacted amine, supported by robust QC documentation.

    Final product types

    • Active materials for selective cereal herbicides
    • Intermediates for growth regulator formulations
    • Building blocks for systemic weed control products
    • Precursors for phenoxy acid derivatives

    4. Pigment Intermediate for Specialty Organic Pigments

    Specialty pigment manufacturers select 2-Methoxyaniline for its capacity to introduce methoxy-functionalized aromatic rings into high-performance pigment structures. The material participates in oxidative coupling or acylation chemistries, conferring enhanced color depth and stability. Operations incorporate inline monitoring and traceability protocols, critical for coloring agents used in automotive coatings, plastics, and electronics.

    Industry compliance standards

    • EN 71-3 (Toy safety for colorants)
    • ASTM D476: Standard Classification for Dry Pigmentary Titanium Dioxide Products
    • ISO 1248: Pigments — Methods of test
    • Automotive OEM individual substance restriction lists

    Typical usage ratio

    • 5–12% as a co-reactant in pigment synthesis; outcome depends on desired chromatic shift and lightfastness requirements.

    Downstream process integration

    • Supplied to condensation step for arylamine-pigment core formation.
    • Post-coupling oxidative treatments yield required color stability and hue intensity.
    • Final pigment paste undergoes rigorous particle size and dispersibility testing before being shipped to downstream users.

    Final product types

    • Automotive-grade pigment dispersions
    • High-performance engineering plastics colorants
    • Special effect pigments for coatings
    • Color concentrates for electronic device components

    5. Polymer Stabilizer Synthesis

    Chemical companies engaged in polymer and plastics modification rely on 2-Methoxyaniline as a precursor for certain antioxidant and stabilizer intermediates. The compound reacts in Mannich or phenolic stabilization chemistries, strengthening light and thermal resistance in polymers. Precise dosing strategies and raw material quality control assure end customers of consistent additive performance batch after batch.

    Industry compliance standards

    • EU Plastics Regulation (EU) No 10/2011
    • FDA 21 CFR §177 (Indirect food additives: polymers)
    • ISO 14001: Environmental management
    • ISO 9001:2015 (Quality system for industrial additives)

    Typical usage ratio

    • 2–6% as an intermediate for stabilizer synthesis per polymer batch; levels vary with polymer resin type and regulatory allowance.

    Downstream process integration

    • Fed into block reactors during pre-polymer additive production stage.
    • Intermediate stabilizer isolated and blended with polymer granules.
    • Final extrusion or molding operations integrate the stabilized blend for enhanced end-use durability.

    Final product types

    • Antioxidant masterbatches
    • UV-resistance additives for polyolefins
    • Thermo-resistant polycarbonate and ABS compounds
    • Stabilized engineering thermoplastics for outdoor use
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    Certification & Compliance
    More Introduction

    Introducing 2-Methoxyaniline: Benefits in Modern Chemical Manufacturing

    What Sets 2-Methoxyaniline Apart?

    In the world of specialty chemicals, 2-Methoxyaniline, also known as o-Anisidine, delivers a blend of stability and performance that experienced manufacturers appreciate in day-to-day operations. This aromatic amine has long held a key role as an intermediate, bridging the gap between basic building blocks and sophisticated end-products. As a chemical manufacturer, the detail that jumps out is the way 2-Methoxyaniline’s molecular structure—specifically the methoxy group at the ortho position—serves as a unique contributor in countless synthesis routes. The presence of the methoxy group not only alters electron density but brings subtle advantages during downstream reactions.

    We have worked with a broad range of aromatic amines, and experience tells us that 2-Methoxyaniline occupies a distinct spot due to its reactivity profile and manageable physical handling properties. Its melting point and solubility make it less cumbersome than some of the more volatile or toxic alternatives. For operators who have lined up production campaigns of dyes, pigments, and pharmaceuticals, safe and consistent handling means fewer interruptions and improved throughput. Unlike its closely related cousins—aniline and its alternative methoxy- or methyl-substituted analogues—o-Anisidine offers a specific pattern for nucleophilic substitution or diazotization, allowing for targeted synthesis of specialized azo compounds and heterocycles.

    Applications Backed by Decades of Reliability

    Production lines for azo dyes have long relied on dependable access to 2-Methoxyaniline. The demand isn’t only about volume; it’s about tight batch-to-batch consistency that keeps color match and purity up to demanding standards. Having run reactors that use both 2-Methoxyaniline and similar intermediates, differences in processing are easy to spot. For example, the shelf-life and liquid stability of 2-Methoxyaniline, compared with more oxidation-prone counterparts like para-anisidine, save a lot of headaches. Less downtime for cleaning, fewer blown gaskets from off-gassing, and easy transfer between containers lead to more confident scheduling and fewer late shipments.

    Manufacturers in pharmaceutical synthesis see another side: the molecular behavior of 2-Methoxyaniline during coupling and catalytic steps. Certain analgesics, anti-tubercular compounds, and agricultural actives trace their roots back to o-Anisidine intermediates. Purity levels of 99.5% or higher are not just technical bragging points, but a necessity to keep unwanted byproducts or regulatory red flags from entering the picture. These things matter most when you’re scaling up from gram-scale feasibility to months-long production runs. Each kilogram that matches the spec reduces risk all along the chain.

    Specifications Shaped by Real-World Experience

    In the plant, clear, pale yellow to brownish liquids signal well-made 2-Methoxyaniline, free from visible particulate or tar-like residues. Its molecular formula, C7H9NO, may seem straightforward, but we pay close attention to byproducts that can crop up from impurities upstream such as nitroanisole or over-reduced anilines. Over the years, refining washing and crystallization techniques has paid off, leading to final products with lower water content and a sharper melting range.

    Shipping stability matters for end-users who may stockpile this intermediate for extended periods. The material holds up well in standard iron drums or HDPE containers under shaded storage, with no special refrigeration needed for short-term logistics. Plant engineers frequently comment on the unexpectedly mild odor and the manageable volatility below 50°C, which eases air handling requirements compared to other aromatic amines.

    No Substitute for Consistency

    Many newcomers to fine chemical synthesis ask whether switching among isomeric anilines is feasible, but downstream performance shows why 2-Methoxyaniline can’t simply be replaced in certain colorant or pharmaceutical routes. Take azo coupling—using para-anisidine in the same step shifts absorbance, alters shade, and can introduce regulatory ambiguity in textile applications that are closely scrutinized in the EU and North America. In the pharma sector, only the ortho-methoxy group provides the electronic steering to drive selectivity in ring-closure reactions or the correct bioactivity in many APIs.

    By direct comparison in our own pilot labs, reactions employing 2-Methoxyaniline tend to proceed with fewer side-products and less tar formation, especially when run under batch conditions with consistent heating profiles. This translates to less lost material in post-reaction workup and higher isolation yields. Production planners notice the intangible benefit in reduced energy costs and diminished need for downstream purification, especially with large, month-long campaigns.

    Addressing Challenges and Solutions

    Nothing replaces hands-on troubleshooting when dealing with aryl amines and their derivatives. Sensitivity to atmospheric oxidation represents a concern, particularly when handling bulk quantities in open tanks or poorly sealed reactors. Cylindrical storage vessels and nitrogen blanketing, established from years of handling similar chemicals, keep product within specification. Preservation of color and reduction in quinonoid byproduct formation demands strict monitoring, a process our plant teams have honed with real-time colorimetry and titration checks—small process changes like these prevent subtle quality drift.

    Operators working with 2-Methoxyaniline quickly learn the importance of personal protective equipment and effective fume extraction. Despite relatively mild volatility, the long-term health profile means exposure limits must be respected. By upgrading to enclosed transfer systems and local exhaust hoods, production runs progress with fewer incidents and stronger compliance records. We worked closely with engineering teams to select chemical-resistant sealants that avoid leaching or cross-contamination, based on firsthand experiences with system fouling.

    Why Purity and Traceability Matter

    End-users in ink and dye manufacturing often request documentation not only on key physical properties but also on trace residuals—particularly metals, solvents, and secondary amines. We introduced batch-level chromatography checks to monitor for off-spec intermediates like meta-anisidine or nitroresidues. Customers count on this because their own downstream processes react sensitively even to minute compositional differences.

    Over the years, regulatory bodies have grown increasingly strict about trace contaminants. We have learned this lesson firsthand, occasionally needing to adapt production parameters or alter solvent choice to remain within global thresholds such as those set by REACH and TSCA. Full batch records and chain-of-custody tracking safeguard both our customers and ourselves. The price premium for this level of traceability is often justified by fewer rejected shipments and strengthened relationships with valued partners.

    Distinct Properties and Market Advantages

    Chemists appreciate 2-Methoxyaniline’s distinctive melting point and boiling point, giving it a handling advantage against similar C7H9NO isomers. These thermal properties influence reaction temperatures, crystallization points, and operational safety margins. In our own facilities, we’ve found that yield losses tied to uncontrolled distillation events fall when operators handle feedstock with a clearly defined phase transition range.

    Unlike simple aniline—prone to rapid oxidation and darkening upon exposure to air—2-Methoxyaniline holds color and resist decomposition under similar conditions. This matters to anyone formulating high-value colorants and coatings who needs reproducible results. By adjusting pH and storage temperature, formulating shelf-stable intermediates becomes far easier than with more reactive or hydrophilic analogues. Benchmarking our product against national and international standards has become second nature; third-party analysis nearly always confirms the extra tightness in quality and impurity control our customers expect.

    Environmental Responsibility and Future Outlook

    As a long-term manufacturer of specialty aromatics, we recognize the sharpened focus on health and safety, both for production workers and downstream consumers. The drive toward cleaner synthesis means reevaluating waste streams and solvent recovery at every stage. Implementing closed-loop washing and distillation—not just for compliance but to drive down the cost per kilogram—has become part of daily operations. The byproduct load from 2-Methoxyaniline synthesis is both manageable and well understood, which contrasts sharply with more problematic aromatic compounds, some of which require offsite incineration.

    In a time where public scrutiny tracks the fate of even minor intermediates, transparent stewardship stands out. Customers often want to know about emissions controls, effluent treatment, and accident discipline—not just specs and price points. This honest dialogue leads to process improvements that wouldn’t emerge in a less collaborative environment.

    Real-World Insights from the Factory Floor

    Years of production rounds have taught us the value of small process tweaks. Switching to finer mesh filtration during the final crystallization means fewer downstream interruptions from solids. Upgrading heat exchangers and ensuring steady temperature control reduce the formation of side products and unwanted tars. Operators recognize the familiar sweet-phenolic odor of 2-Methoxyaniline even in low concentrations, a practical reminder to check for leaks or fugitive emissions before they spiral into costly downtime.

    Direct feedback from production teams reveals strengths and limitations that statistics in a brochure can never capture. Fewer tank cleanouts, less corrosion on storage lines, and easier pumping routines—real advantages that only come out after handling drums and tankfuls day in and day out. Experience tells us that a reliable 2-Methoxyaniline supply remains one of the most requested asks from long-term customers.

    Comparative Perspective: Working with 2-Methoxyaniline and Other Anilines

    Each aromatic amine presents a learning curve. 2-Methoxyaniline stands out for its intermediate volatility and solid-liquid handling, making transfer, weighing, and metering tasks less prone to spillage and loss. Operations involving meta- or para-isomers frequently call for stricter light and temperature controls, while hydrophilic anilines draw in water, causing caking or clumping in bulk bins. Over time, the pattern becomes clear: less wastage and lower maintenance when working with o-Anisidine.

    Process engineers striving for predictable kinetics in batch or continuous operations find that reaction times, heat input, and filtration steps proceed with fewer hitches using 2-Methoxyaniline. The balance between reactivity and stability allows researchers to optimize reactions for yield rather than fighting unplanned degradation or side reactions. The difference shows not only in quality-control results but in actual bottom-line costs by the end of the month.

    Listening to Customers: Insights that Drive Change

    Customers point to specific requirements in shade, particle size, or chemical purity. We respond with tangible changes—improved trace analysis, more rigorous pre-shipment inspections, flexible lot sizes, and clear documentation to meet exacting pharma, pigment, or agrochemical standards. These tweaks evolve from open channels: technical queries that come from users on the line, not just in R&D. It’s often these real-world conversations, not sales brochures, that shape the improvements we choose to roll out.

    Production managers tell us clear documentation and rapid, reliable delivery reduce project delays and keep finished products moving to market on time. By addressing lingering pain points and adapting packaging, we maintain trust and ensure repeat business.

    Ongoing Commitment to Quality and Support

    Sustained, real-world performance—batch after batch—reflects strict in-process controls used in every kilogram produced. In-plant monitoring, layered hygiene, and refined logistics networks ensure each shipment meets or exceeds industry benchmarks. These operational realities make a difference for chemists, QC teams, and downstream manufacturers. Decades of observing subtle differences in isomer behavior, impurity profiles, and batch-to-batch reliability give us the confidence to continue investing in smarter, greener, and safer processes for the future.

    Reliable supply of 2-Methoxyaniline supports stronger innovation in color chemistry, pharmaceuticals, and advanced materials. By building trust through practical action, not just claims, the pathway to future specialty chemicals—smarter, safer, and more sustainable—remains wide open.