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2-Fluoro-3-Methylaniline

    • Product Name 2-Fluoro-3-Methylaniline
    • Alias 2-Fluoro-m-toluidine
    • Einecs 610-044-7
    • 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

    139585

    Iupac Name 2-fluoro-3-methylaniline
    Molecular Formula C7H8FN
    Molecular Weight 125.15 g/mol
    Cas Number 57872-41-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 203-205 °C
    Density 1.114 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Flash Point 96 °C
    Synonyms 2-Fluoro-m-toluidine, 3-Methyl-2-fluoroaniline
    Refractive Index 1.553

    As an accredited 2-Fluoro-3-Methylaniline 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 25 grams of 2-Fluoro-3-Methylaniline, securely sealed with a screw cap and labeled with safety information.
    Shipping 2-Fluoro-3-Methylaniline is shipped in tightly sealed containers, compliant with relevant chemical safety regulations. It should be transported at ambient temperature, away from heat and incompatible substances. Proper labeling and documentation are required, and only trained personnel should handle transportation. Shipping must adhere to local, national, and international hazardous material guidelines.
    Storage 2-Fluoro-3-methylaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. The storage area should be clearly labeled, protected from direct sunlight, and equipped to contain spills. Store at room temperature and avoid exposure to moisture to ensure chemical stability and safety.
    Application of 2-Fluoro-3-Methylaniline

    Applications of 2-Fluoro-3-Methylaniline in Industrial Manufacturing

    2-Fluoro-3-Methylaniline supports precision synthesis in advanced industrial environments, serving as a critical intermediate for several established downstream sectors. As an experienced manufacturer, we address specific industry needs with consistently monitored quality and batch traceability, enabling downstream partners to maintain compliance, streamline integration, and achieve product performance goals in demanding regulatory landscapes.

    1. Agrochemical Active Ingredient Synthesis

    This intermediate plays a critical role in the construction of selective herbicide and fungicide molecules for the crop protection sector. Production teams exploit its unique substitution pattern to build modern active substances with targeted biological properties. Integration typically occurs in early-stage coupling or acylation reactions during the synthesis of phenylurea or anilide actives. Adaptive usage maintains reactant balance, supporting reliable yields and downstream formulation accuracy.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001 Quality Management Systems
    • European Regulation (EC) No 1107/2009 (Plant Protection Products)
    • US EPA Pesticide Registration (FIFRA)

    Typical usage ratio

    • 5–18% of total batch mass, adjusted based on the parent pesticide molecule’s target substitution and total desired activity. Chemists optimize input in relation to downstream moiety construction and process scale.

    Downstream process integration

    • Enters as a starting material in N- or C-coupling with carbonyl or isocyanate intermediates, followed by purification, crystallization, and formulation blending for solid or liquid technical actives.

    Final product types

    • Technical herbicides (e.g., substituted phenylureas)
    • Systemic fungicides (custom-developed anilide derivatives)

    2. Pharmaceutical Intermediate for Small Molecule API Synthesis

    Process teams in pharmaceutical manufacturing employ this compound to build fluorinated aromatic scaffolds within various drug candidate synthesis routes. Its structure enables regioselective amide or imine formation, which helps access targeted intermediates for antihypertensives, CNS agents, and oncology candidates. Usage ratios reflect strict process validation, with full traceability maintained for regulatory review and batch QA.

    Industry compliance standards

    • ICH Q7 GMP (Active Pharmaceutical Ingredients)
    • USP/NF (United States Pharmacopeia/ National Formulary)
    • EU EudraLex Volume 4
    • China Pharmacopoeia (when supplied to Chinese manufacturers)

    Typical usage ratio

    • 0.5–6% of the synthetic batch, with adjustment per target molecule complexity and desired fluorine content. Ratios determined via process development and route optimization data.

    Downstream process integration

    • Introduced during key reductive amination, Buchwald–Hartwig amination, or ring closure steps. Also used for fragment coupling or as an intermediate for further fluorination and diversification.

    Final product types

    • Fluorinated antihypertensive APIs (e.g., selective receptor antagonists)
    • Intermediates for CNS drug candidates
    • Oncology molecule scaffolds

    3. Dye and Pigment Intermediate Production

    This aniline derivative serves in the creation of specialty azo, anthraquinone, and triarylmethane dyestuffs where the substituted aromatic ring provides fastness and altered shade properties. Technical teams apply it in the preparation of diazo components via controlled diazotization and coupling, resulting in dyes that meet high-performance and regulatory requirements for textiles, inks, and plastics.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile Safety)
    • REACH Regulation (EC) No 1907/2006 (Chemical Registration)
    • ISO 105 (Textile Color Fastness Testing)
    • GMP for Colors (21 CFR part 74/82, US FDA where applicable)

    Typical usage ratio

    • 10–20% in diazotization batches for azo dyes, and 1–8% in multi-component pigment syntheses. Formulators adjust for target color strength, solubility, and lightfastness performance.

    Downstream process integration

    • Charged into the reactor for stepwise diazotization/coupling, followed by oxidation or condensation for pigment precursors; further purification precedes final blending and milling for end-use applications.

    Final product types

    • Acid and disperse dyes for polyester or nylon textiles
    • Special effect pigments for plastics and coatings
    • Organic colorants for inkjet printing inks

    4. Specialty Chemical Intermediate for Electronic Materials

    R&D and process teams in the electronics sector leverage this compound when constructing high-purity functionalized aromatic cores for use in electronic-grade polymers and advanced resins. Its fluorinated, methylated profile imparts specific properties—thermal stability, electron transport optimization, and improved film formation—essential for next-generation OLED and liquid crystal device fabrication.

    Industry compliance standards

    • IEC 61249-2-21 (Halogen-Free Materials for Electronics)
    • UL 94 (Flammability of Plastic Materials)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001 (Quality Management for Electronics Manufacturing)

    Typical usage ratio

    • 1–4% as a functional monomer or crosslinker modifier in prepolymer or resin blend systems. Tuning is based on dielectric, mechanical, and processing requirements for each target device platform.

    Downstream process integration

    • Introduced during monomer synthesis for step-growth polymerizations, or used in condensation/functionalization steps for polyimide and epoxy resin manufacturing; followed by purification, film casting, or compounding for final device use.

    Final product types

    • OLED functional layer polymers
    • High-purity liquid crystal alignment materials
    • Halogen-modified epoxy laminates for PCBs
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    Certification & Compliance
    More Introduction

    2-Fluoro-3-Methylaniline: Reliability from Direct Chemical Manufacturing

    Purpose-Driven Production and Real-World Insights

    Years of experience have taught us that handling aromatic amines demands focus and consistency at every step, especially for compounds like 2-Fluoro-3-Methylaniline. This material, characterized by its substituted aniline backbone with unique fluorine and methyl groups, requires careful attention during synthesis and purification. We refine production protocols so each batch reflects not only laboratory controls but the realities of scale-up and industrial use.

    Model variants in this class depend on how precisely the methyl and fluoro groups attach to the ring. We produce 2-Fluoro-3-Methylaniline in liquid form, often shipped as a clear to pale yellow fluid, with purity benchmarks established through gas chromatography. Typical purity levels exceed 99%; the trace levels of related anilines and isomers are tightly monitored to safeguard consistency in downstream reactions. Most of the demand we see stems from the pharmaceutical and agrochemical fields, but this compound finds use across a spectrum that values its reactivity.

    Why Substitution Patterns Matter

    Subtle shifts in atomic arrangement give 2-Fluoro-3-Methylaniline its set of properties. Our clients depend on this molecule for its balance of reactivity, safety, and stability. The ortho-fluorine increases the stability of certain reaction intermediates compared to the non-fluorinated methyl-anilines, especially under oxidative or acidic conditions. We’ve seen process chemists point out better yields and fewer by-products when using this version as a building block, particularly in C-N coupling and heterocycle assembly.

    Every batch is designed with downstream chemistry in mind. Changing the fluoro group’s position, or skipping it altogether, alters both the electronic properties and the way derivatives behave under hydrogenation, halogenation, and amide formation. Some aniline derivatives oxidize too easily or don’t provide the desired selectivity. Our experience with 2-Fluoro-3-Methylaniline suggests that this molecule holds its own in challenging coupling reactions, minimizing over-reduction and helping to avoid tedious rework.

    Handling and Consistency: More Than Meets the Eye

    Years in the factory have shown which handling protocols matter most. Every drum and container undergoes checks for residual moisture because this aniline, like many of its kind, can pick up water and degrade in storage. We support each delivery with analysis certificates – but also with decades of hands-on knowledge. Our logistics team understands shipping laws for amines; we guide customers through safe unloading, especially during humid months, to prevent hydrolysis and discoloration.

    We have worked alongside formulation teams who require more than certificates. They bring us questions about reactivity under continuous flow, shelf-life under various temperatures, or the appearance of trace fluoride impurities in their end product. Our chemists respond by tracing every possible by-product through the full process, often fine-tuning reaction conditions upstream to prevent headaches downstream. For example, we have improved isolation steps to address color concerns without impacting the product’s utility.

    Insight into Industrial Applications

    Process chemists often integrate 2-Fluoro-3-Methylaniline into multi-step syntheses where a stable yet reactive aromatic amine is needed. In-house testing has shown that the compound’s electron profile allows for efficient N-arylation and C-H functionalization without excessive side reactions. We work with teams scaling up from grams to tons, so every insight gained at the pilot stage translates into more predictable results later. The pharmaceutical sector seeks this molecule for creating kinase inhibitors and other advanced intermediates. Meanwhile, agrochemical developers value the selective transformations enabled by subtle substitutions like the ortho-fluorine.

    We further support those making dyes and pigments, where amine purity shapes both color fastness and yield. Still, the unique aspect of 2-Fluoro-3-Methylaniline lies in the fluoro/methyl substitution, which offers both enhanced stability and improved performance over classic anilines. We frequently collaborate with customers exploring new catalyst systems, or examining how this compound influences the regioselectivity of transformations compared to more basic methyl-aniline or fluoro-aniline alternatives.

    Process Learnings from Manufacturing

    Batch-to-batch reproducibility drives client decisions. We’ve adjusted reactor pressure, chosen better solvents, or tailored the order of reactant addition – all to ensure minimal impurities and low colored by-products. The bottom line always shows in real-world outcomes: does the 2-Fluoro-3-Methylaniline perform reliably for lengthy syntheses, and are handling losses low enough to matter on a production scale? Giving honest answers to these questions enables clients to plan confidently.

    Throughout production, we study how minor fluctuations in reaction temperature or raw material quality influence final product performance. Our in-house analytics, from NMR to HPLC, are not only about ticking regulatory boxes but about identifying trends early, so we can tweak steps before problems arise. Old habits die hard – we still pull archive samples and run headspace analysis, even after the product leaves the door, to spot potential changes over shelf life.

    Safety in Practice and Experience

    Handling substituted anilines brings known risks: contact sensitivity, vapor pressure under heat, and the ever-present risk of trace impurities. We have spent time improving local exhaust systems in production halls and working closely with occupational safety inspectors to minimize fume exposure. This isn’t only about passing audits; it’s about keeping a safe environment for those blending and packaging these chemicals day in, day out.

    Clients sometimes call for advice on accidental exposure or unusual odor profiles, often during summer transport. Our on-call team responds promptly because we know timing matters. Over the years, we have simplified decontamination steps and storage protocols for warehouse staff as well as end users who may never have handled a substituted aniline before. Our training modules reflect both regulatory best practices and the lessons learned the hard way on an actual factory floor.

    Comparing 2-Fluoro-3-Methylaniline with Related Amines

    Not all anilines respond equally in the lab or plant. Where a simple methyl-aniline might break down during hydrogenation, the fluoro-methyl derivative stands up to a broader range of catalyst systems and elevated temperatures. Direct feedback from formulation chemists shows their preference for this molecule over unsubstituted analogs during amide coupling and electrophilic aromatic substitution.

    We have supplied side-by-side samples to customers for pilot trials. Results commonly back our experience: the 2-Fluoro-3-Methylaniline version provides improved selectivity during functionalization, and often leads to fewer purification steps when generating downstream heterocyclic compounds. Technical staff appreciate a product less prone to unwanted oxidation, with a higher boiling point than the non-fluorinated equivalents, making it easier to handle during scale-up. One recurring finding: projects that switched from standard methyl-aniline to our fluorinated grade saw a 10-15% boost in isolated yield over multiple runs—enough to justify the investment in specialty substitution.

    Supporting Research and Custom Solutions

    We regularly work with clients on custom scale-ups, especially as new patent-protected intermediates arise. Our R&D team partners with project leaders to translate milligram validation into kilogram scale, troubleshooting every step. Bench chemists want more than theoretical guidance; they prefer real feedback rooted in production realities. This transparency strengthens trust and leads to better repeat orders.

    Sometimes a customer asks about possible polymorphs or solvation effects during purification. These are not abstract queries; they directly impact downstream synthesis and batch reproducibility. Experience has shown that controlling the cooling rate post-reaction can minimize undesirable crystal habits or oiling out—a lesson learned through practical batches, not just simulations.

    Understanding Market Evolution

    Over the past decade, the shift towards more selective fluorinated intermediates has become clear. Skeptics once doubted the extra production steps could justify the additional utility, but outcomes speak for themselves. We have watched regulatory shifts push for cleaner profiles and phase out uncontrolled aniline derivatives. Older plants struggled to adapt, but with facility upgrades and granular process tracking, specialty derivatives like 2-Fluoro-3-Methylaniline became not just viable, but favored for their reliability in both classic and novel synthetic routes.

    The growing emphasis on traceability has encouraged us to track every ingredient, solvent residue, and by-product signature. Our internal systems catalog this data and provide it during audits. External labs have confirmed that our grades consistently meet international benchmarks for both pharmaceutical and agrochemical starting materials, reflecting both the stringency of our controls and years of accumulated production experience.

    Partnering for Innovation

    Chemistry evolves; so do expectations from those who rely on advanced intermediates. We have learned not only to react to customer needs, but to anticipate possible headaches in large-scale work. By maintaining long-term relationships and keeping open channels with both purchasing leads and hands-on process chemists, we spot opportunities for improvement that generic sellers rarely consider.

    Recent projects have involved working with partners to shorten their synthetic routes by taking advantage of 2-Fluoro-3-Methylaniline’s versatile profile. In one case, a process redesign allowed bypassing a tedious protecting group step, saving both time and cost. These solutions grow out of experience and flexibility during production, rather than static catalogs or fixed recipes.

    Troubleshooting and Proactive Adjustments

    No production process runs without occasional issues. Sometimes the raw fluorobenzene needs tighter QC, or a change in catalyst supplier shakes up the reduction’s selectivity. We don’t wait for complaints to arrive; continuous process monitoring allows us to intervene early and keep customers informed if a batch requires special handling. Our willingness to take calls late at night, and to ship small test batches mid-campaign, stems from the direct accountability that comes with manufacturing at scale.

    Our lab staff work closely with both seasoned colleagues and newer recruits, ensuring that knowledge built up over decades survives staff changes or equipment upgrades. Internal training days incorporate both theory and practical troubleshooting, focusing on not just what should happen, but how to respond when an instrument throws an unexpected result. This culture makes a difference in the way we support customers and adapt to changing industry needs.

    Future Trends and Sustainable Chemistry

    The push towards greener syntheses shapes our thinking each year. For every batch of 2-Fluoro-3-Methylaniline, we evaluate possible waste streams and their treatment – not out of obligation, but because the chemical industry cannot afford complacency. We have piloted alternative solvents and explored catalytic changes that limit hazardous by-product formation. Many times the drive for new approaches comes straight from the field, as our clients explore biosynthetic integrations or enzyme-based catalysis.

    We also keep in step with stricter environmental impact monitoring, confirming our waste management aligns with new local and international guidelines. For clients looking to lower their carbon footprint, we offer transparent reporting about material and energy inputs per ton of product delivered. Our aim: continuous improvement guided by both industry standards and hands-on factory experience.

    Direct Connections and Accountability

    As direct manufacturers, we see every step, from raw material sourcing to final drum filling. This gives us practical insight into both routine and challenge batches and lets us answer technical questions with confidence. Clients don’t have to unravel a supply chain or wonder about storage conditions back at the warehouse. This accountability means troubleshooting happens faster, and knowledge flows both ways. If a customer encounters an issue in pilot or full-scale production, our technical team steps in with context that only comes from real-time, direct experience—whether that’s advice on shelf-life extension, safe mixing, or optimum temperatures for high-yield crystallizations.

    Wrapping Up Real-World Value

    2-Fluoro-3-Methylaniline isn’t only a molecular structure in a database. It’s a result of accumulated know-how, repeated refinement, and years of close collaboration with those who put it to work. Its strengths—reliable batch performance, flexible reactivity, and tolerance of varied production conditions—have all grown out of hands-on practice in the plant and ongoing dialogue with formulation and process experts. We remain committed to improving both process and product, always open to new challenges from partners wanting to push chemistry farther.