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3-Fluoro-2-Methylaniline

    • Product Name 3-Fluoro-2-Methylaniline
    • Alias 3-Fluoro-o-toluidine
    • Einecs 631-296-6
    • 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
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    Specifications

    HS Code

    135473

    Chemical Name 3-Fluoro-2-Methylaniline
    Molecular Formula C7H8FN
    Molecular Weight 125.15 g/mol
    Cas Number 58760-13-3
    Appearance Colorless to pale yellow liquid
    Boiling Point 210-212°C
    Density 1.13 g/mL at 25°C
    Purity Typically ≥98%
    Refractive Index 1.565-1.570
    Flash Point 94°C
    Solubility Soluble in organic solvents, slightly soluble in water

    As an accredited 3-Fluoro-2-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 100 grams of 3-Fluoro-2-Methylaniline, sealed with a red cap and labeled with hazard warnings.
    Shipping 3-Fluoro-2-Methylaniline is shipped in tightly sealed, chemical-resistant containers, protected from light, moisture, and incompatible substances. Transport complies with relevant hazardous material regulations, ensuring labeling and documentation are accurate. Handle with care to prevent leaks or spills, and store in cool, dry conditions during transit to maintain stability and safety.
    Storage 3-Fluoro-2-methylaniline should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. The storage area should be equipped with appropriate spill containment and clearly labeled. Handle with care, using protective equipment to prevent inhalation, ingestion, or contact with skin and eyes.
    Application of 3-Fluoro-2-Methylaniline

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

    As a committed chemical raw material manufacturer specializing in high-purity substituted anilines, we supply 3-Fluoro-2-Methylaniline to advanced manufacturing sectors. This intermediate plays a crucial role in diverse downstream transformations within the fields of pharmaceutical synthesis, agrochemical actives, dye manufacture, and specialty material monomers. Each application scenario leverages the compound’s unique reactivity profile, supporting formulated outputs that demand reliable performance and traceable compliance.

    1. Pharmaceutical API Synthesis – Non-Steroidal Antiinflammatory Intermediates

    Leading pharmaceutical producers incorporate 3-Fluoro-2-Methylaniline as a key aromatic amine intermediate during the assembly of select NSAID and central nervous system drug APIs. Its ortho-fluoro functionality allows for specific acetylation and ring-construction strategies, supporting stringent impurity control during multi-step synthesis. In typical workflows, manufacturers regulate input levels according to targeted yield curves, with the feed point just prior to heterocycle formation or direct coupling stages.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) monographs for intermediate purity
    • European Pharmacopoeia (Ph. Eur.) compliance for starting materials
    • FDA 21 CFR Part 211 (cGMP for finished pharmaceuticals)

    Typical usage ratio

    • Employed at 0.7–1.2 molar equivalents relative to core ketone or acid intermediates, adjusted based on stoichiometric efficiency and target batch size

    Downstream process integration

    • Added at the nucleophilic substitution or amide coupling stage, preceding final ring closure or functional group modifications in multi-step API assembly

    Final product types

    • Anti-inflammatory actives (e.g., related to fenamic acid derivatives)
    • CNS pharmaceutical intermediates with fluoroaromatic motifs
    • Bulk drug substances requiring ortho-fluoro compatibility

    2. Agrochemical Synthesis – Herbicide and Fungicide Precursors

    Major agrochemical firms utilize 3-Fluoro-2-Methylaniline as a fluorinated aromatic building block during the construction of selective herbicide and fungicide molecules, capitalizing on its resistance to metabolic degradation. Process engineers introduce this compound into Suzuki or Buchwald coupling lines, where its methyl and fluoro pattern ensures targeted bioactivity. Formula optimization depends on the target molecule, with batch documentation following regulatory dossiers.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP)
    • EU REACH Annex VII–X for intermediate registration
    • China National Pesticide Standards (GB/T 1604, GB 2763)

    Typical usage ratio

    • Ranged from 5%–15% by weight of total formulated intermediates; precise proportion confirmed via route scouting and final active concentration

    Downstream process integration

    • Feeding into palladium-catalyzed aryl-amine bond formation, followed by core scaffold closure or side chain extension prior to formulation

    Final product types

    • Fluorinated triazole and anilide herbicides
    • Fungicidal actives for broad-acre crop protection
    • Custom pesticide intermediates for contract manufacturing

    3. Dyes & Pigments – Synthetic Dye Intermediate

    Colorants manufacturers source high-purity 3-Fluoro-2-Methylaniline to create tailored azo and anthraquinone dye scaffolds, meeting requirements for textile and specialty ink systems where lightfastness and chemical resistance are critical. The fluoro-substituted aromatic amine enters diazotization and coupling processes, influencing shade strength and wash durability in finished pigment dispersions and liquid dye concentrates.

    Industry compliance standards

    • OEKO-TEX Standard 100 (input material restrictions)
    • ZDHC MRSL Conformance Guidance
    • EU REACH (Annex XVII) for dye intermediates
    • ISO 105 industrial colorfastness standards

    Typical usage ratio

    • Used at 1–3% by weight of total dye precursor batch; proportional usage refined by color strength and target fastness properties

    Downstream process integration

    • First step diazotization followed by aromatic coupling for monoazo/anthraquinone dye core assembly; post-functionalization for pigment stabilization

    Final product types

    • Reactive and disperse dyes for synthetic textile fibers
    • High-performance industrial inkjet pigments
    • Custom colorant dispersions for coating or plastics

    4. Electronic Specialty Chemicals – Advanced Monomer Synthesis

    Producers of functional polymers and electronic materials rely on 3-Fluoro-2-Methylaniline to supply tailored monomer units necessary for synthesizing high-glass-transition copolymers or specialty polyamides. Its substitution pattern enables unique thermal and dielectric properties in the resulting backbone. The monomer enters polymerization streams at the controlled copolymer feed-in stage, with precise dosing reflecting the required final performance envelope.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for restricted substances
    • IEC 61249-2-21 for base materials in printed wiring boards
    • UL 94 for polymer flammability rating
    • ISO 9001 for electronic material quality systems

    Typical usage ratio

    • Incorporated at 2–10 mol% in targeted copolymer formulations; precisely adjusted for dielectric property optimization in insulating layers

    Downstream process integration

    • Fed into controlled batch or continuous monomer feed tanks for step-growth or chain-polymerization; sequencing verified via in-process QA

    Final product types

    • High-temperature-resistant epoxy and polyamide resins
    • PCB substrate materials with custom dielectric constants
    • Functional polyimide coatings for semiconductors and flexible circuits

    5. Fine Chemical Custom Synthesis – Contracted Intermediate Manufacture

    Custom chemical manufacturers select 3-Fluoro-2-Methylaniline as a starter molecule for small-molecule libraries, advanced screening compounds, and specialty fine intermediates. The input concentration and process route reflect end-use client requirements, such as SAR variant synthesis, with process documentation aligned to global audit expectations. Integration occurs at the first or second transformation step, depending on the lab-scale or pilot-scale batch design.

    Industry compliance standards

    • ISO 13485 for intermediates in pharma/diagnostic devices
    • GMP and GLP (as required for regulatory filings)
    • REACH intermediates registration (substance tracking and traceability)
    • Custom specification sheets (client-validated)

    Typical usage ratio

    • Applied at 1 to 5 mmol per 10 mmol target product in small-batch synthesis; adaptability determined by end-client structure requirements

    Downstream process integration

    • Processed via acylation, halogenation, or cyclization in initial steps; exact synthetic position based on project specification and IP protocols

    Final product types

    • Hit-to-lead discovery compounds for pharma R&D
    • Material science intermediates for OLED, OPV, or battery research
    • Reference reagents for chemical screening kits
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    Certification & Compliance
    More Introduction

    3-Fluoro-2-Methylaniline: Precision, Experience, and Advancements from the Manufacturer’s Floor

    Building a Foundation in Aromatic Amine Chemistry

    Manufacturing 3-Fluoro-2-Methylaniline begins on a foundation of deep-rooted expertise in the synthesis and purification of aromatic amines. The craft goes far beyond a simple catalog entry, as working with these materials involves handling challenges that stem from their sensitive nature and the demands placed by customers in pharmaceuticals, agrochemicals, and specialty materials. At our site, the product takes shape in reactors engineered to handle such conditions — lined, cleaned, and checked by hands that know the impact an off-ratio impurity or substandard lot will have further down the customer’s process. The actual work with 3-Fluoro-2-Methylaniline offers insights a spreadsheet can’t capture: the importance of consistent batch quality, clear communication between production and QC, and process adaptation as global regulations tighten around fluorinated building blocks.

    What Sets 3-Fluoro-2-Methylaniline Apart

    Within aromatic amine offerings, 3-Fluoro-2-Methylaniline stands out for its unique position on the benzene ring. The ortho-methyl and meta-fluoro arrangement changes reactivity compared to the more common mono-substituted anilines or other fluoro-aniline isomers. The methyl group brings more than just a minor steric effect; paired with a carefully introduced fluorine atom, it can fundamentally reshape hydrogen bonding, shift electron density, and alter solubility. This is not a small difference — downstream reactions (like acylation, sulfonation, or cross-coupling) move at a different pace or lead to products that offer better pharmacokinetics or improved field performance. Researchers and process chemists who moved from unsubstituted or para-substituted variants see sharper selectivity for certain transformations, less overreaction, and — in the case of some modern crop science applications — reduced generation of side-products that require costly cleanup.

    Manufacturing Realities: Purity, Scale, and Consistency

    Operating a chemical plant that regularly turns out 3-Fluoro-2-Methylaniline brings a distinct set of realities. First, the choice of starting materials — typically fluoro-toluenes or their nitro derivatives — can dictate end-product purity. Handling these raw materials safely and efficiently, minimizing worker exposure, and preventing emissions, all draw on experience honed batch by batch. In the plant, controlling moisture, temperature ramps, and catalyst quality becomes crucial, especially if markets demand low ppm impurities or if certain nitroso or dimeric byproducts threaten compliance. Over time, designing for robustness means less downtime, fewer off-spec drums, and client relationships that last beyond a single PO.

    The expectations for analytical support have also grown. Running a single HPLC trace at release no longer passes muster. Now, customers demand full impurity profiling (GC-MS, NMR, and occasionally chiral methods if racemization is deemed risky), reproducibility across monthly batches, and validated cleaning to minimize cross-contact with structurally similar compounds. We keep documentation updated, run annual validations, and track even micron-scale deviations. Quality doesn’t happen by accident; it comes from integrating lab findings into daily routines, recalibrating instruments ahead of schedule, and empowering operators to raise a flag when something doesn’t look or smell right.

    Why 3-Fluoro-2-Methylaniline Matters: Real-World Use Cases

    This aromatic amine’s main stage sits inside the walls of pharma labs and pesticide R&D centers. Medicinal chemists searching for better kinase inhibitors or improved CNS penetration know that a strategic methyl or fluoro can flip a switch for efficacy, bioavailability, or reduced off-target binding. Several fluoro-methyl aniline motifs appear as core intermediates in blockbuster patent filings, and only tailored suppliers can keep up with the volume and regulatory scrutiny required.

    In the agrochemical sphere, programs striving for next-generation fungicides or safer herbicides also turn toward substituted aniline cores. Here, introducing a fluorine at the 3-position and a methyl at the 2-position gives better weed selectivity or pest control in combination with specific side chains. Crop scientists report better rainfastness, persistence, and lower toxicity to beneficial insects compared to non-fluorinated analogs. Our direct work with pilot batches, feedback from formulation chemists, and reformulation for global field trials taught us long ago not to chase after purity alone. Downstream, seemingly minor processing residues, solubility issues, or odor traces quickly snowball into failed pilot runs or rejected field lots.

    Experience Informs Product Development and Scale-Up

    Scaling from grams to hundreds of kilograms means more than swapping flasks for reactors. You keep learning what water content in a raw material will do to a diazotization or hydrogenation. You see how batch-to-batch fluorine content tracks with air humidity, how a temperature spike can introduce stubborn dimeric byproducts that only sharp eyes (and a persistent odor) spot. Each plant campaign brings new facts to light: a clogged filter cloth, a slower reaction when it rains too much outside, a new solvent that helps separate trace over-reduced residues.

    Product improvement comes directly from listening to the plant floor, engaging with QC techs on thorny outlier results, and keeping ongoing dialog with customer R&D teams. Many of our most robust purification tweaks started from feedback — a finished 3-Fluoro-2-Methylaniline lot that worked in a pilot-scale amide coupling but left sticky residues during large-scale API trials. By taking this feedback into production meetings, adjusting cycle times, or switching to smaller lot sizes for sensitive programs, the product now fits better not just at release but years down the line, when customer regimens migrate from lab to commercial scale.

    Handling, Safety, and Regulatory Knowledge

    Plant teams regularly go beyond SDS compliance to make sure every container of 3-Fluoro-2-Methylaniline travels safely. Drumming, venting, and labeling follow evolving ADR, IMDG, and country-specific guidelines. Workers receive training for accidental exposure and containment. Teams run fire drills and use updated monitoring. Documentation also covers new global requirements where needed: RoHS for electronics use, REACH preregistration as substances get flagged, and attention to upcoming PFAS regulations. Regular visits from inspectors and client audits shape how recordkeeping, monitoring, and training adapt. These efforts mean customers and third parties can trust traceability, residue control, and multi-year compliance records.

    Differences from Other Aromatic Amines

    Comparing 3-Fluoro-2-Methylaniline to classic anilines or other fluoroaniline isomers reveals clear performance gaps. For instance, while 4-fluoroaniline or 2-methylaniline deliver value for legacy syntheses, they often fall short for modern programs that demand lower toxicity, greater metabolic stability, or sharper regioselectivity in follow-on steps. Dual substitution with both methyl and fluoro groups gives more tunable electronic effects, reshaping the reactivity profile in cross-couplings and nucleophilic aromatic substitutions. This difference isn’t only theoretical; long practice has shown that many patented agro and pharma intermediates now depend on this motif for key building steps and side-chain elaborations. Less common side reactions, improved product yields, and easier separation from starting material residues give the product a performance edge that translates into less project risk and more efficient manufacturing for our partners.

    Specification: What Customers Are Asking For

    Most of the clients we supply ask for material above 98% purity by HPLC, with well-defined GC and NMR impurity profiles. Moisture and volatile residuals stay below specified thresholds to avoid issues in moisture-sensitive coupling reactions. The hue of the final product, its odor signature, and any trace contamination often matter just as much: a faint residue in a catalyst line or a stubborn aftertaste in polysiloxane formulations would stand out straight away. Every batch ships with a certificate that summarizes PCR, micro traces, and — where customers request it — targeted screening for nitroaniline impurities, chloride levels, and trace solvents. No two customers have the exact same downstream demands, and the margin for error narrows as projects approach launch.

    Solutions to Industry-Wide Challenges

    The challenges tied to 3-Fluoro-2-Methylaniline go beyond technical hurdles. Access to high-quality precursors can tighten unexpectedly when supply chains tangle. Responding to this requires strong supplier relationships, sometimes custom synthesis of upstream blocks, and more rigorous inventory management. Capacity allocation during busy seasons — especially as downstream clients face their own surprises — brings pressure to deliver without compromising documentation or safety.

    Cost pressures follow changing regulatory and customer landscapes, as global procurement teams now factor in not just chemical price but HSE profiles, multi-year audit histories, and the transparency of process changes. Where solvent bans or emission caps shape operations, adapting reactor venting, solvent recovery, and waste handling protocols becomes daily work, not a box to check off. The best solutions have come from cross-functional workshops, investing in safer process routes, and directly addressing feedback from both major and emerging customers. Rather than racing to the lowest cost, our team prioritizes steady supply, unwavering compliance, and a readiness to troubleshoot in real time.

    Fact-Driven Product Development and Customer Partnerships

    Product stewardship requires ongoing attention to market trends and laboratory data. New methods for fluorination, greener routes to anilines, and high-throughput screening in the client’s own hands change expectations almost every quarter. Regular engagement, technical exchanges, and site visits do more than keep us competitive; they remind all stakeholders of the long tail that an excipient or core intermediate like 3-Fluoro-2-Methylaniline casts through the value chain. Manufacturers that treat this chemical as a one-size-fits-all commodity ignore real history: even a one-week deviation in impurity profile, or a late shipment due to regulatory delay, can derail a project milestone for months.

    We track and communicate stability data, freeze/thaw sensitivities, and multiple year shelf lives to support our partners’ regulatory filings. This open data exchange underpins joint NDAs, rapid troubleshooting, and better transparency in times of unexpected change. The feedback loop running from customer pilot plants back to our own reactors keeps improving the product over time. As more teams push the frontiers — in targeted therapies, greener pest management, or smart coatings — 3-Fluoro-2-Methylaniline’s unique mix of reactivity, processability, and regulatory acceptance keeps it in focus as a preferred intermediate or building block.

    Conclusion: Real Chemistry, Real Experience

    3-Fluoro-2-Methylaniline remains a workhorse for innovation-driven industries. Meeting its strict specifications, adapting to evolving customer and regulatory demands, and supplying it reliably all rely on long-standing manufacturing experience, lab discipline, and clear lines of communication. Years of scaling up this molecule, refining each step from raw material sourcing through to handling and documentation, make a measurable difference to customers who need more than a simple catalog solution. As new challenges arise, the accumulated learning and commitment from plant, lab, and commercial teams ultimately drive the product’s reputation and utility across fields as diverse as agrochemicals, pharmaceuticals, and specialty materials.