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HS Code |
201952 |
| Cas Number | 445-23-4 |
| Molecular Formula | C7H8FNO |
| Molecular Weight | 141.14 g/mol |
| Iupac Name | 3-fluoro-4-methoxyaniline |
| Appearance | Light yellow to beige solid |
| Melting Point | 63-66°C |
| Boiling Point | 256-258°C |
| Density | 1.184 g/cm³ |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | COC1=CC(=CC(=C1)F)N |
| Inchi | InChI=1S/C7H8FNO/c1-10-7-3-5(9)2-6(8)4-7/h2-4H,9H2,1H3 |
| Refractive Index | 1.574 |
As an accredited 3-Fluoro-4-Methoxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-Fluoro-4-Methoxyaniline is supplied in a sealed 25g amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 3-Fluoro-4-Methoxyaniline is shipped in sealed containers, protected from moisture, light, and incompatible substances. Proper chemical labeling and documentation accompany the package. It is transported according to applicable chemical and hazardous goods regulations, ensuring safety, stability, and compliance throughout transit. Personal protective equipment is recommended during handling and unpacking. |
| Storage | Store 3-Fluoro-4-Methoxyaniline in a tightly sealed container, away from direct sunlight and sources of ignition, at room temperature in a cool, dry, well-ventilated area. Keep separate from strong oxidizing agents and acids. Use secondary containment to avoid spillage and ensure proper chemical labeling. Follow standard laboratory procedures for handling hazardous chemicals, including use of personal protective equipment. |
Applications of 3-Fluoro-4-Methoxyaniline in Industrial ManufacturingAs a dedicated manufacturer of 3-Fluoro-4-Methoxyaniline, we deliver high-purity raw material to key industries where advanced aromatic amine intermediates are essential for enabling downstream innovation. The following sections present proven, large-scale application scenarios where this compound plays a critical role, each grounded in specific industry standards, precise formulation know-how, and established production workflow—from regulated pharmaceutical synthesis to fine chemicals and specialty agrochemicals. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisOur 3-Fluoro-4-Methoxyaniline is widely integrated within pharmaceutical plants as a building block for the synthesis of targeted APIs, especially within non-steroidal anti-inflammatory drugs (NSAIDs) and next-generation oncology candidates. Formulators value its electronic and steric profile for regioselective amination and substitution steps in multi-stage API production, meeting stringent control on impurities and residual solvents as dictated by international pharmacopoeias. Industry compliance standards
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2. Advanced Agrochemical Synthesis: Herbicide and Acaricide PrecursorsLeading agrochemical manufacturers deploy this compound as a reactive aromatic amine in the synthesis of fluoro-methoxyphenyl urea and triazine derivatives, which form critical components of modern herbicide and acaricide actives. The high fluorine content offers improved metabolic stability in target actives, while the methoxy group provides compatibility with select crop chemistries in global regulatory markets. Industry compliance standards
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3. Specialty Dye and Pigment Intermediate for Electronic and Performance TextilesWithin advanced pigment and electronic dye industries, our material serves as a tailored intermediate, enabling synthesis of fluorinated azo and anthraquinone dyes with high resistance to UV degradation and solvent attack. Producers targeting OLED display materials and technical textile dyeing implement customized downstream modifications for superior performance and colorfastness. Industry compliance standards
Typical usage ratio
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4. Fine Chemical Intermediate for Custom Synthesis: Heterocycle and API Scaffold DevelopmentResearch-based fine chemical companies use our compound to construct complex heterocyclic scaffolds and as a customization point in the development of advanced functional molecules. Its defined reactivity and substitution pattern allow controlled introduction of functional groups vital for building premium structure-activity relationship libraries, and also scaling up pilot production under ISO and GMP-compliant settings. Industry compliance standards
Typical usage ratio
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In a chemical manufacturer’s workshop, the subtleties between two aromatic amines can reflect months of careful research and process development. 3-Fluoro-4-Methoxyaniline stands out in that regard. Over the years, those of us working directly with aromatic fluoro anilines have come to appreciate how its unique substitution pattern creates value across pharmaceutical synthesis, agrochemical building blocks, and advanced material intermediates. Unlike standard aniline derivatives, this compound rewards the craftsman willing to respect its nuances.
Direct from experienced reactors and carefully monitored purification columns, our product comes as a pale solid, showing consistent melting behavior batch after batch. With the model identified as C7H8FNO (CAS 82419-36-1), 3-Fluoro-4-Methoxyaniline packs both electron-donating and electron-withdrawing groups onto the aromatic ring, altering its reactivity profile in a way hard to replicate with alternatives. To meet demanding downstream chemistry, we control for purity through chromatography, routinely exceeding 98% by HPLC. Attention is paid to residual solvents, metal traces, and moisture, since small changes here can trigger unexpected side reactions in later steps. Our extensive in-house analytics were designed after years of learning what matters most to synthetic chemists who cannot tolerate surprises.
Packing also plays a practical role. We ship in sealed, double-lined bags, minimizing atmospheric moisture exposure. Each lot receives its own unique analytical certificate—chemists want to know exactly what enters their flask. For those pushing grams or scaling up to multikilo, consistency is critical. No batch varies beyond our preset QC thresholds, and every deviation is logged with rationale and corrective action. Over time, our processes have eliminated the trial-and-error phase many chemists endure when changing suppliers.
Aromatic halogenated anilines have become mainstays as starting points for complex molecules, but every substitution alters how a molecule behaves amid typical reagents. 3-Fluoro-4-Methoxyaniline finds usage in early drug discovery as a privileged motif for library construction, yet also holds power in scale-up campaigns where reproducibility and low impurity levels reduce headaches at the isolation stage. We saw this early in a custom synthesis contract for a pharmaceutical partner: alternative isomers led to pigment-forming byproducts or sluggish coupling reactions, whereas this specific combination sped up the reaction while minimizing side reactivity.
These traits have broader reach than just pharma. In fine chemicals, the combination of fluorine and methoxy substituents enables regioselective functionalization, opening the door to highly tailored intermediates in herbicides and active agro molecules. We have observed, through our own implementation, that the electron-rich nature combined with resistance to traditional electrophilic attack lets chemists introduce further complexity at alternative positions. It’s more than just a ‘basic building block’—it’s a platform for creative molecular construction. Our ongoing collaborations with research institutes push its application envelope further into advanced material science, including certain sensor molecules and organic electronics. Each trial returns new feedback, which we build into our next lot improvement cycles.
Anyone who has run a failed Buchwald coupling or suffered an unexpected color change after adding a fresh lot knows the importance of starting material consistency. 3-Fluoro-4-Methoxyaniline, coming directly from our reactors under rigidly defined safety parameters, saves time spent on laborious in-house purification. We keep a sharp focus on analytical control at every step because leftover reactants can easily poison catalysts or lead to costly purification later down the line.
Not all aniline derivatives behave the same during downstream chemistry. Fluorinated analogs often create tough soluble impurities during oxidation or metalation if not thoroughly free of halide scavengers and acidic traces. We cut through these risks by implementing continuous feedback loops on our drying and filtration equipment. As the manufacturer, we control every lever from raw material selection to reactor maintenance, which means the most current process tweaks get folded back into the next production run.
Our own chemists have tested para-methoxyaniline and meta-fluoroaniline as alternatives in bond-forming reactions, only to find significant differences in yield and process reliability. While similar at a quick glance—or, to those who just scan CAS numbers—the subtle interplay of substituent effects becomes evident on scale. The ortho effect from the fluorine group alters electron density enough to change regioselectivity, giving a different product distribution during acylation or nitration.
Process engineers face plenty of pain when switching from traditional anilines to something more esoteric. Impurities, volatility, and unwelcome tars haunt scale-ups if the starting material profile shifts. In supplying 3-Fluoro-4-Methoxyaniline, we keep phone lines open for feedback. That customer feedback loop exposed the way trace moisture, so minor you’d miss it without Karl Fischer titration, can spark changes in shelf life and transformation efficiency. We don’t treat impurity control as a formality—each process review dives into specifics with our QA group pulling historical trendlines for key specifications. Years spent climbing the learning curve benefit each next batch.
Compared with other fluoroaniline products, ours emphasizes not only structural purity, but reproducibility across multi-kilo lots. The real-world differences surface in palladium-catalyzed aminations, where the reaction rate can drop by half if the halide content or amine to metal ratio drifts off target. We consistently observe better catalyst life and lower side product formation with our own 3-Fluoro-4-Methoxyaniline as opposed to commodity grades. Chemists aiming for intermediate purification, not just functional group introduction, appreciate the effort invested upstream.
There’s little glamour in vessel cleaning, but cross-contamination remains a real source of trouble, as those with scale-up scars can confirm. We track vessel histories and validate our cleaning cycles, with special attention for anything running before a new 3-Fluoro-4-Methoxyaniline campaign. During early years, our teams would learn of faint coloration or tacky texture from subtle cross-traffic of reagents. These findings helped shape our current batch scheduling and cleaning validation, translating directly to reliability in the final packages customers receive.
Strict solvent segregation also carries strong justification. Some solvents can drive isomerization or hydrolysis when traces are present, leading to lower than expected yields or brown-toned byproducts forming lingerie at the interface. By controlling solvents from drum to disposal we’ve cut the odds of these minor losses, and our product survives even the most critical NMR or GC-MS scrutiny. Customer audits occasionally bring hidden process flaws into daylight, but we welcome outside review—it’s another set of eyes, another chance to catch a process inefficiency before it costs anyone time or money. The fact that we run our own facility means that tweaks and upgrades go into effect immediately, for the benefit of everyone downstream.
Years of synthesis and troubleshooting inform each process update. Subtle changes like column temperature or raw material supplier have taught us to document every detail. Our technical team consists of chemists who have moved from bench to plant—every failed TLC or stubborn emulsion has its lesson, and these lessons shape our day-to-day operations. Direct communication between our process chemists and operators keeps knowledge fresh, reducing reliance on distant third-party analyses.
Routine engagement with our customer’s technical teams lets us learn how their reaction conditions interact with our product. By providing grams-for-trial or custom packaging, we invest in their process success, not just our output. These exchanges bring issues like trace leaching from liners or minute corrosion effects into play, which we can address on our side. Over time, that close technical relationship has led to late-stage process improvements, sometimes as small as switching to a more inert liner type after discovering tiny yields losses in a downstream coupling.
With supply chains under scrutiny for both sustainability and transparency, our operation anchors on traceable sourcing and responsible waste minimization. Working with European and North American raw materials gives confidence in regulatory compliance without sacrificing performance. Our waste tracking extends from toluene distillation residue to fluorine neutralization streams, audited for environmental impact.
Investment in on-site treatment and energy-efficient equipment started years back, encouraged by both local regulations and rising customer expectations. As a direct manufacturer, we guide every barrel from formula to drum—a visible chain of custody that traders often cannot provide. Many customers ask for this transparency before awarding long-term contracts. We deliver not only product but also detailed batch histories, if required for reimbursement or regulatory filings. In-house, we keep our packaging to recyclable formats wherever possible, without trading away chemical stability. These efforts pay off both in customer trust and risk minimization—no stalled deliveries caused by missing paperwork or incomplete traceability records.
Sourcing hiccups have plagued many of our peers. We’ve sidestepped bottlenecks by building supplier redundancy, qualifying at least two routes for key precursors and maintaining reserve batches of 3-Fluoro-4-Methoxyaniline for urgent requests. Our planners track global shipping disruptions and recalibrate buffer stock to anticipate delays. In past quarters, a single transportation hold-up would trigger a scramble for suitable material substitutes; today, our planning environment means no gaps in supply, no last-minute switching to inferior alternatives.
On the user end, headaches surface most often in reaction selectivity, yield drift, and downstream impurity profiles. Because we work so closely with our customers, we often know about off-spec products and botched reactions before a formal complaint lands. Early intervention, sometimes sending a sample for NMR troubleshooting or ramping up analytical support, helps keep projects on schedule. As the primary source, our team directly oversees reevaluation of suspect lots and can initiate a fresh batch if quality falls short. Unlike intermediaries, we don’t deflect responsibility or push blame down the chain—each outcome reflects our underlying processes, and we adjust accordingly.
Feedback from our research collaborations hints at future directions for 3-Fluoro-4-Methoxyaniline: greater integration into high-purity applications such as OLED synthesis, and tighter impurity control for radiolabeling or very sensitive pharmacology programs. Each year brings stricter impurity requirements—sometimes down to the sub-ppm level—and a growing call for custom packaging or documentation. Because we design and build our own processes, these requests are built into our update cycles rather than tacked on as afterthoughts.
Competition in specialty aromatics keeps everyone sharp. We continually compare new analytical techniques, reviewing our data integrity and keeping abreast of regulatory changes in both export controls and end-use declarations. This diligence shields our customers from unpleasant surprises months after purchase. Our technical teams regularly join conferences and supplier meetings to track shifting requirements and local implementation hurdles.
Industry talk often circles back to a single word—confidence. Our approach with 3-Fluoro-4-Methoxyaniline has always flowed from hands-on manufacturing: every process step certified, every specification shaped by direct reaction feedback. Clients aren’t simply picking from a catalog but entering a working partnership, shaped by our open feedback lines and willingness to talk through real chemical problems.
Our focus doesn’t stop at metrics or regulatory compliance—although both matter. It extends into collaborative troubleshooting, continual improvement, and a certain pride that can’t come from reselling or anonymous sourcing. We carry all the experience, scars, and practical ingenuity of a manufacturer who stands behind their material on the line, not just on paper.
Chemists hungry for reliability seek more than just a number on a spec sheet—they seek partners ready to answer the next question, run the next analysis, and share the lessons learned from a hundred production runs. In 3-Fluoro-4-Methoxyaniline, we deliver a product born from deep technical roots, ongoing learning, and a commitment to putting practical value in every shipment.