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HS Code |
718391 |
| Chemicalname | 3-Fluoro-2-Methoxyaniline |
| Casnumber | 55750-85-9 |
| Molecularformula | C7H8FNO |
| Molecularweight | 141.14 g/mol |
| Appearance | Pale yellow to brown liquid |
| Boilingpoint | 239 °C |
| Density | 1.19 g/cm³ |
| Purity | Typically ≥98% |
| Refractiveindex | 1.566 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | COC1=C(C=CC=C1F)N |
| Inchikey | LOQULNZSFWKCHD-UHFFFAOYSA-N |
As an accredited 3-Fluoro-2-Methoxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-Fluoro-2-Methoxyaniline, sealed with a screw cap and labeled with safety information. |
| Shipping | 3-Fluoro-2-Methoxyaniline is shipped in securely sealed containers to prevent leakage and contamination. It is classified as a hazardous material, and must be transported according to local and international chemical safety regulations. Proper labeling and documentation are required, and the package should be handled by trained personnel wearing appropriate protective equipment. |
| Storage | **Storage for 3-Fluoro-2-Methoxyaniline:** Store 3-Fluoro-2-Methoxyaniline in a tightly sealed container, away from light, moisture, ignition sources, and incompatible substances such as strong oxidizers and acids. Keep in a cool, dry, and well-ventilated area. Clearly label the storage container, and handle only with appropriate personal protective equipment in place to prevent skin or eye contact. |
Applications of 3-Fluoro-2-Methoxyaniline in Industrial Manufacturing3-Fluoro-2-Methoxyaniline serves as a key intermediate for multiple downstream industries. As the actual manufacturer, we supply customers who integrate this molecule in the synthesis of active pharmaceutical ingredients, crop protection compounds, high-performance materials, pigments, and specialty fine chemicals. Below, we detail industrial application scenarios with focus on formulation, compliance, production integration, and end-use product categories. 1. Pharmaceutical API Intermediate SynthesisMany pharmaceutical companies use this compound during the assembly of fluorinated aniline building blocks for non-steroidal anti-inflammatory drugs and other APIs. Our product supports nucleophilic aromatic substitution reactions, facilitating the creation of heterocyclic scaffolds essential for patented molecules. Downstream processors focus on strict impurity profiles and validated scale-up procedures. Our QC approach enables batch traceability, ensuring minimal residual solvents suitable for regulated environments. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisMajor crop protection players employ our raw material for selective synthesis of fluorinated amine intermediates, critical for next-generation herbicides, fungicides, and insecticides. The methoxy and fluorine substituents introduce specific physicochemical profiles, supporting soil stability and bioactivity. Downstream partners favor our material due to controlled moisture content and consistent batch purity that allow for continuous production regimes without intermediate purification. Industry compliance standards
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3. Specialty Dye and Pigment ManufacturingTextile, ink, and plastics manufacturers integrate 3-Fluoro-2-Methoxyaniline into advanced azo and anthraquinone dye synthesis. The unique substitution pattern modifies chromophore absorption, enabling production of stable, high-shade purity dyes resistant to UV degradation. Customers require strict control of amino and methoxy substituents, which directly affect color yield and fastness properties in mass coloration and high-value specialty printing applications. Industry compliance standards
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4. Fine Chemical and Electronic Material ProductionManufacturers of organic electronic intermediates and high-purity fine chemicals incorporate 3-Fluoro-2-Methoxyaniline for selective functional group introduction on core scaffold. Its structural features support the controlled synthesis of OLED emitter precursors, photoactive resins, and electronic grade monomers. We supply our material under low-metal, high-purity specifications necessary for electronics, ensuring minimal contamination risk across high-value, small-batch operations. Industry compliance standards
Typical usage ratio
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The manufacturing of 3-Fluoro-2-Methoxyaniline—known among chemists by its CAS number 86604-78-6—reflects countless hours spent refining our approach to small-batch aromatic amines. Over the course of a decade producing fluorinated anilines, subtle details in crystalline appearance, moisture content, and even the odor become signals of consistency. This molecule, bearing a fluorine at the meta position and a methoxy at the ortho, sets itself apart both structurally and functionally from relatives in the aniline family. Such a layout influences reactivity: we see the fluorine not simply as a passive substituent, but as an active director in downstream reactions, supporting key steps in pharmaceutical and agrochemical intermediate synthesis.
Crafting each batch relies on carefully sourced fluorinated intermediates and strict preservation of lab atmosphere. Trace water, depending on the lot, can impact yield and purity. Unlike plainer anilines, storage and transport require vigilance since even slight hydrolysis or oxidation can create off-spec byproducts detectable by GC-MS or HPLC. Through experience, we’ve established protocols that minimize air and light exposure from synthesis to bottling, recognizing how a few hours’ delay in sealing can diminish value for the most precise applications.
Often the specs come as a list: purity not less than 98.0%; colorless to pale yellow crystals; melting point typically close to 40°C. In practice, these numbers mean nothing if the product doesn’t behave reliably for our research partners and production engineers. Slight differences in residual solvents, mainly from outdated drying steps or uneven distillation, change the course of scaling up reactions. This is a recurring lesson in producing 3-Fluoro-2-Methoxyaniline for larger installations—what works in a 500 g flask does not behave the same in a 100 L reactor. Regular feedback from customer labs helps us adjust batch protocols, preventing surprises like off-odors or outlier melting points that slow timelines and cost tens of thousands in rework and delays.
Years of close collaboration with pharmaceutical and agricultural R&D teams taught us how small contaminants influence enzyme inhibition or receptor binding studies. In one project, a 0.3% unknown detected by HPLC ended up interfering with a late-stage N-alkylation. We traced the issue to a subtle difference in solvent dryness and calibrated our purification train to exclude co-distilling byproducts, delivering future batches with improved consistency. This level of scrutiny proves essential when adoption for regulatory filing or clinical research is on the table.
Comparisons between 3-Fluoro-2-Methoxyaniline and 4-fluoro-, 2-fluoro-, or even non-fluorinated methoxyanilines expose chemical realities only seen by steady-handed manufacturers. The position of fluorine severely alters both electronic character and downstream handling: for example, para-fluoro variants exhibit greater resistance to nucleophilic substitution under many conditions, while ortho arrangements create challenges with steric hindrance and solubility.
We’ve noticed customers running into bottlenecks when they sub in a more commonly available 4-fluoro-2-methoxyaniline just to save on marginal costs. Their conversions drop, catalytic loads spike, or isolation demands balloon beyond original budget estimates. Over time, our records show that proper matching of positional isomer to intended chemical task, especially during palladium-catalyzed couplings, clears hurdles both logistical and economic. The 3-fluoro pattern often improves selectivity in heterocycle construction and biaryl bridge formation, reduces side products, and allows shorter workups.
In our line, understanding these subtleties means sharing lessons. Even packaging matters—this material prefers amber glass, low headspace, and argon flush, keeping oxidative degradation at bay for months longer than standard bottling. Chemists who rely on predictable response during scale-up gravitate to these extra measures, saving time during bench work and kilo-lab translation. Consistency from drum to drum has opened doors to collaborations that would have slipped away had off-spec material arrived.
Through every kilo batch, we see the value in in-depth analytical work. Gas chromatography with flame ionization detection, tandem with UV-Vis and NMR, has become our gold standard. Early in the process, we leaned too heavily on TLC and melting point alone. These crude markers let minor impurities slip through—each of which can catalyze unwanted side-reactions or, in rare cases, trigger regulatory flags during import and export inspection.
Adaptation came as clients in drug discovery began examining every trace for risk assessment due to strict ICH Q3A/B regulations on genotoxic impurities. Response meant investing in higher-grade columns, better reference standards, and cross-lab syntheses for product comparison. Through this, repeatability improved. Batch-to-batch consistency gave research departments confidence to order larger lots and prompted fewer retest requests.
Waste stream analysis forms another foundation. Even after product isolation, solvent recovery, and purification, we route aqueous and organic phases through proprietary testing before neutralization and safe discharge. Environmental controls often add hours of effort, but reports from each batch reassure buyers and regulators alike that process risk is low. Our own anecdotal study over 24 months showed that strict waste controls have reduced downstream cross-contamination cases, which proved a costly headache for several peer producers in fluorinated aromatic lines.
Scaling up doesn’t always go to plan. Early pilot batches of 3-Fluoro-2-Methoxyaniline taught difficult lessons about agitation speed and temperature control during diazotization and nucleophilic aromatic substitution. Excess exotherm produced a brown tinge in two drum lots—color alone indicated over-oxidation. Remediation required five days of repurification, rerunning column chromatography at twice the planned cost, and reinstructing the team that five degrees off protocol was the difference between commercial and waste.
We’ve learned to identify heat and light sensitivity early on, incorporating soft LED lighting in storage rooms and slower cooling ramps in crystallization. Our QA lab frequently splits production lots, running stability studies at different humidity and temperature settings. Patterns emerge: humidity above 60% raises water content in product drums, reducing shelf life and increasing risk of reaction failure for customers. So, routines changed across our warehousing, from the choice of spill-absorbent to twice-weekly ambient checks. Deliberate practice on these basics beats out racing to hit every order fast.
Chemists in pharmaceutical lead optimization and crop protection both value molecules like 3-Fluoro-2-Methoxyaniline for reasons shaped by everyday project goals. It acts as an intermediate in synthesis of heterocycles, where electron-rich aromatic partners must combine with precision. One pharmaceutical client, after switching to our material for an N-arylation, noted a consistent five percent yield bump attributed to lower unknown impurities. Their process engineer confirmed, after extensive internal batch runs, that the lower propensity for hydrolysis allowed them to skip a pre-reaction drying step, saving both time and solvent.
Another customer specializing in fungicide development employs this molecule as a core building block for several triazole derivatives. They pointed out that our fluorinated aniline’s improved purity reduced downstream purification headaches. Since the molecule’s fingerprint—both in NMR and mass spec—falls in a relatively unique window, traceability of end products for regulatory registration grows simpler. Compliance departments embrace less ambiguity when each synthetic link in a pesticide’s route stems from a well-documented, well-characterized intermediate.
We see the same motivation in custom projects requiring 3-Fluoro-2-Methoxyaniline as a scaffold for probe development or PET tracer synthesis. Each time, feedback links clean conversions to the care we put into process control and documentation. Our files are filled with similar tales: customers who approached after failed trial runs with products sourced elsewhere, then reversed course with reproducible outputs once supplied with our consistently managed batches.
Throughout the last decade, demand for 3-Fluoro-2-Methoxyaniline tracks closely with the boom in targeted organic syntheses. Researchers worldwide explore the subtle action of fluorine in pharmaceutical scaffolding. In-house, we started with annual runs of sub-50 kilos; today those numbers approach several tonnes based on steady demand from crop science innovators, small-molecule drug developers, and custom synthesis houses. The climb required shifting from semi-manual to largely automated lines.
Logistics remain a perennial challenge, as cool chain reliability and hazardous material regulations evolve. Each country applies unique labels and restrictions to aromatic amines, pressing us to collaborate with trusted freight partners. We supplement each shipment with detailed certificates of analysis and transit stability records—practice born from experience rather than regulatory obligation. Unplanned customs spot checks have been survived mostly through these records and clear chain of custody, saving weeks against tight project deadlines for international partners.
Bottlenecking sometimes follows market shocks—shortages of halogenated raw materials, or spikes in demand from generic drug launches or sudden regulatory approvals generate temporary shortages industry-wide. Our advantage lies in long-term supplier contracts and buffer inventory in three continents, allowing production continuity even as peers pause to secure precursors. Such decisions aren’t easily visible to end users, but behind every delivered drum stands months of advance planning and relationship management.
It’s easy to claim high purity on a data sheet; it’s harder to respond effectively when a client’s pilot run stumbles. Open lines of communication with customers allowed our technical staff to adapt crystallization and filtration methods over time. In several cases, project feedback revealed recurring solubility issues in aryl halide couplings—finding that a brief heat treatment during solidification improved dissolution in common polar aprotic solvents. Other clients experienced minor fouling in metered pumps caused by crystallite size variations; this prompted tweaks in cooling and batch timing, mitigating flow problems without excessive filter changes or wasted labor.
A continuing theme emerges: feedback loops drive our most useful improvements. Six years ago, we fielded repeated queries over faint byproduct peaks in LC-MS traces. Instead of generic responses, we committed to side-by-side testing with our largest customers, running parallel syntheses and purification, then directly sharing chromatograms. That collaborative approach seeded protocol refinements and invited external audits that now serve as selling points to new business partners.
Being solely a manufacturer, not a reseller, means advice comes seasoned by real process data, not theoretical best practices. We keep client confidentiality sacrosanct, but encourage those trialing our material to share details about downstream chemistry and equipment. In one story, a customer’s switch from batch to flow chemistry flagged a previously unnoticed foaming in their quencher—a side effect of residual solvent vapor pressure, which we resolved with an extra vacuum stripping step before bottling. Details matter, and so does open dialogue.
Environmental stewardship for us means investing in plant upgrades and training, not just ticking regulatory boxes. Many steps in aromatic amine production generate acid and solvent-laden effluent. Early iterations of our process relied on standard wastewater neutralization and activated carbon. Over time, marginal improvements—tightening condensation containment, solvent recovery, and waste sorting—paid off in both reduced emissions and community trust.
Our plant workers receive yearly refreshers on spill control and emergency procedures tailored to fluorinated intermediate production. This practical education far surpasses what generic safety posters convey and lowers risk to both staff and the surrounding neighborhood. In several audits, local environmental agencies praised our adoption of continuous air quality monitoring and flue gas scrubbing rather than the intermittent or threshold-based models adopted elsewhere.
We extend the same care to vendors, specifying low-residual solvent requirements and firm delivery protocols. Accountability isn’t just regulatory; it’s a shared industry reality where one careless entrance of contaminated solvent tankers can disrupt entire months of output. Experience shows that these invisible ripple effects—from upstream suppliers to downstream chemical users—get minimized only by thorough documentation and transparency across all links in the supply chain.
For users of 3-Fluoro-2-Methoxyaniline, sourcing direct means a shorter chain between questions and answers. Project leads want relevant insights—how to store unopened drums, what to watch for as shelf life approaches, which solvent systems optimize downstream purification. These details rarely come from intermediaries with less skin in the game. Over the years, we’ve shortened both feedback cycles and turnaround times by working directly with the chemists and engineers driving their own research.
Paperwork—COAs, analytical support, reprocessing records—are prepared by the same people responsible for day-to-day process control. We don’t rely on detached sales offices to relay technical updates; instead, technical management stays engaged from inquiry through post-delivery troubleshooting. Repeat orders from the same handful of pharmaceutical and agrochemical giants validate that this hands-on approach wins out over the polished, but often less knowledgeable, channels.
We see these results not as exceptional, but as the product of hundreds of lessons learned in climbing from hand-prepped flasks to full-scale reactors. Direct feedback, shared troubleshooting, and access to both failures and successes produced a resilience in both product and process. Whether the client’s concern centers on process safety, minimizing regulatory headaches, or shaving hours from production timelines, we work from the conviction that the best answers come from those who do the daily work of manufacturing itself.
Chemical production never stands still. The demand profile for 3-Fluoro-2-Methoxyaniline will continue to shift as medicinal chemistry chases new scaffolds and crop science pursues next-generation actives. As the original manufacturer, we commit ongoing investment to analytical infrastructure, routine process assessments, and incremental improvements in both environmental and safety domains. These upgrades come not from outside pressure, but internal drive fueled by years of watching small slip-ups spiral into costly setbacks when left unaddressed.
Underlying all these efforts is an understanding that every bottle we produce becomes part of someone else’s pivotal research program, pilot batch, or production run. That responsibility shapes each improvement, troubleshooting call, and project partnership we build. Only through hands-on experience and open lines of technical exchange can a manufacturer truly deliver more than just a specification—they deliver reliability, accountability, and opportunity for those pushing chemical synthesis forward.