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HS Code |
761776 |
| Product Name | 2-Fluoronicotinic Acid Methyl Ester |
| Cas Number | 241155-13-7 |
| Molecular Formula | C7H6FNO2 |
| Molecular Weight | 155.13 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 215-217 °C |
| Density | 1.244 g/cm3 |
| Purity | Typically ≥97% |
| Solubility | Soluble in organic solvents (e.g., ethanol, dichloromethane) |
As an accredited 2-Fluoronicotinic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Fluoronicotinic Acid Methyl Ester (5 grams) is a sealed amber glass bottle with a printed chemical label. |
| Shipping | 2-Fluoronicotinic Acid Methyl Ester is shipped in secure, chemical-resistant containers, typically under ambient conditions. It is packaged to prevent leaks and contamination, accompanied by appropriate hazard labeling and documentation per regulatory guidelines. Shipping complies with local and international regulations for chemical transport, ensuring safety during transit and handling. |
| Storage | 2-Fluoronicotinic Acid Methyl Ester should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, well-ventilated area. Keep it separate from incompatible substances such as strong oxidizers. Store at recommended temperatures, typically at or below room temperature (20-25°C), and ensure proper labeling to avoid accidental misuse or exposure. |
Applications of 2-Fluoronicotinic Acid Methyl Ester in Industrial ManufacturingAs a direct manufacturer of 2-Fluoronicotinic Acid Methyl Ester, we supply this high-purity intermediate to specialty sectors where its integrity, synthesis reliability, and traceability are critical for downstream performance. Our production is optimized for scalable supply to regulated industries with stringent compliance and precise compositional controls. Below, we detail its established applications across leading chemical manufacturing fields, focusing on scenario-specific integration, sector standards, typical formulation ratios, and commercial end products. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisThis raw material functions as a critical pyridine-based building block within the multistep synthesis of several advanced pharmaceutical intermediates, particularly in fluoroquinolone antibiotics and CNS-targeted small molecules. Its methyl ester group enables selective transformations under mild conditions, which helps maintain purity and minimization of side impurities. Contract manufacturing organizations and pharmaceutical groups use it in process development pathways requiring validated traceability and full regulatory compliance, integrated under controlled synthetic stages to ensure batch release aligns with global pharmacopeial standards. Industry compliance standards
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2. Crop Protection Intermediate ManufacturingLeading agrochemical formulators utilize this material to build molecular frameworks found in modern pesticide actives, including selective herbicides and insecticides. Its fluorinated structure imparts valuable metabolic stability, which is critical for extending the environmental half-life of actives in the field. Large-scale batch manufacturing applies it as a defined intermediate in multi-step processes that must comply with regional agchem regulation, particularly regarding impurity thresholds and formulary documentation for eventual product registration. Industry compliance standards
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3. Specialty Dye Intermediate ProductionThe fine chemical sector employs this raw material as a fluorinated precursor in the synthesis of certain advanced azo, anthraquinone, and pyridine-based dyes, particularly those required for technical textiles and optoelectronic applications. Its controlled reactivity profile allows for safe integration in multi-stage chromophore construction, where government and industry standards demand reproducible color indices and traceability in the textile supply chain. Quality control laboratories use dedicated HPLC and NMR methods to monitor the conversion, minimizing off-hue by-products in the final formulation. Industry compliance standards
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4. Electronic Chemical Intermediate FabricationHigh-purity electronics chemical producers integrate this material as a precursor for synthesizing certain N-heterocyclic molecules and ligands used in photoresist components and organic semiconductors. Its electronic structure and selective transformation capability support the formation of high-stability compounds needed in semiconductor patterning and OLED device manufacturing. Production utilizes enclosed synthesis lines, monitored for metal and halide contamination, and documentation aligns with major global electronics production quality standards. Industry compliance standards
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Chemistry always rewards attention to detail. Over decades of running full-scale lines and bench-scale reactors, the value of specialized intermediates becomes crystal clear—each one brings new pathways into reach. 2-Fluoronicotinic Acid Methyl Ester stands out in our catalog for precisely that reason. We work with a variety of heterocyclic building blocks, but this ester offers a unique blend of reactivity and selectivity that helps both research and industry craft new molecules with intention. Whether navigating medicinal, electronic, or agricultural sectors, the appeal of fluorinated pyridines lies in their performance and adaptability.
Our manufacturing process produces 2-Fluoronicotinic Acid Methyl Ester under carefully controlled moisture and temperature gradients. We maintain high GC purity, run tight controls on residual solvents, and always validate lot-to-lot consistency with NMR and mass spectrometry. Over years of daily operation, we have observed that slight variations in precursor quality or drying time lead to noticeable shifts in color and shelf stability. The ester typically arrives as a colorless to pale yellow liquid, settling into storage bottles with a crisp, faint aroma reminiscent of other methylated pyridines.
Staff in our packaging hall often remark that it pours with a smooth, almost syrupy viscosity—distinct from more volatile methyl esters. The liquid remains stable under ambient warehouse conditions, but we always recommend keeping the containers tightly closed, particularly since exposure to humidity can trigger hydrolysis back to the free acid.
Even small operators appreciate direct shipment from our facility, forgoing intermediaries and benefiting from our stock rotation discipline. We believe consistent, fresh batches set the foundation for reliable downstream chemistry.
Workflows in our customer labs often center around catalyst development, medicinal chemistry, or complex ligand synthesis for crop protection agents. For project chemists in these spaces, 2-Fluoronicotinic Acid Methyl Ester opens valuable doors. It serves as an activated, regioselective handle for nucleophilic aromatic substitution (SNAr), direct amination, or Suzuki cross-coupling. Teams exploring new kinase inhibitors or pyridine-based ligands quickly see how the fluorine atom on the 2-position tweaks both electronics and steric crowding.
Brands in agrochemicals leverage this compound to introduce tailored fluorine motifs, which can improve metabolic durability or bioactivity. In pharmaceutical synthesis, the methyl ester acts as a protected, easily unmasked variant of 2-fluoronicotinic acid, making late-stage diversification more straightforward. Electronics manufacturers, searching for the elusive blend of UV resistance and electronic fine-tuning, likewise recognize its value.
We follow published data showing the methyl ester’s behavior under various coupling conditions. It offers clean transformations to amides, acids, and even arylated derivatives, often sidestepping troublesome byproducts common with halogenated pyridines. Our partnerships with R&D labs have confirmed its predictable transformation profiles, saving both time and materials on scale-up runs.
Manufacturers always ask if there’s a clear reason to choose this product over the acid or its other derivatives. Our experience consistently points to the ester’s well-balanced mix of processability and versatility. The acid itself often crystallizes out prematurely or reacts sluggishly in multi-step routes. The ethyl ester, though similar, brings a higher boiling point, which complicates cleanup and downstream modification—especially when pursuing rapid hydrolysis.
We watch project teams compare fluoro-substituted pyridines at different positions (2, 3, or 4). The 2-position fluorine brings sharper electron-withdrawing properties, impacting reactivity patterns in a way that benefits select cross-coupling and heterocyclic ring construction. In contrast, the 4-fluoro analogs may not deliver the same substitution precision in subsequent steps. These nuances aren’t always obvious in catalog listings, but after years of scale-up syntheses, they stand out as real time- and yield-savers.
We find that some clients look at straight methyl nicotinate as a cheaper alternative, often overlooking the value induced by the fluorine substituent. Clients focused on SAR (structure-activity relationship) surveys report significant differences in in vivo results once substitutions move from hydrogen to fluorine, or as functional group location shifts. Such stories reinforce our commitment to purity and batch reliability—the performance edge in your final product starts with the starting materials.
Product reliability matters most at large scale. Our reactors run multi-hundred-kilo quantities per month during peak demand cycles, filling both steady schedule orders and one-off research campaigns. We routinely customize batch size for specialized requests, providing both drum and bottle options. Our in-process controls allow tweaks to drying, solvent content, or packaging based on customer feedback.
Experiences from the first drum line we launched show that small variations in esterification catalyst quality ripple through the downstream supply chain. By investing in better QA routines and real-time monitoring, we have lifted customer yields and shaved days off of lead times. Clients launching critical path syntheses often stop by our plant to see the operation firsthand. These visits lead to tighter collaboration on specification targets or custom processing needs—distance disappears when chemists speak directly to operators.
Delivering globally means we secure materials and logistics routes that withstand regulatory audits and customs checks. Each order flows from our production batch history, so clients can trace the entire lifecycle of the ester. For multinational pharma and agrochem companies, this transparency delivers peace of mind and cuts distractions at regulatory review stages.
Handling 2-Fluoronicotinic Acid Methyl Ester calls for respect, just like any moderately reactive pyridine intermediate. Experienced hands know not to treat the methyl ester as fully benign: it will hydrolyze or transesterify in strong acid or base, and careless open handling leads to losses from volatilization. Personal protective equipment—gloves, eyewear, proper ventilation—remain everyday realities, enforced on our floor as mandatory routine.
Over the years, we have learned that proper ventilation and careful drum selection are not theoretical matters. Early in our manufacturing experience, a batch shift left too long in a poorly sealed drum led to partial hydrolysis and an off-odor that made downstream processing both wasteful and frustrating.
After investing in better drum linings and upgraded damp rooms, such mishaps dropped sharply. Now, containers sport desiccant packs and robust seals, holding up to months of warehouse storage without visible product degradation. More importantly, full material safety training forms part of every new hire’s onboarding, reinforcing respect for both personal and environmental well-being.
Our regular waste audits provide real-world feedback about the impact of our processes. By switching to more targeted extraction solvents and recovering more of the methyl ester from mother liquors, we have steadily reduced production waste and solvent loading. These incremental improvements translate directly into greener operations and improved working environments for our employees.
Customers expect performance. Each reactor load of 2-Fluoronicotinic Acid Methyl Ester gets signed off by our senior chemists. They check for purity spikes, byproduct anomalies, and color changes that signal a process deviation. We have stood in the lab at 6:45 am, dialing into conference calls with customers in different time zones, swapping chromatograms and notes about impurity profiles. Scrutiny does not fade with routine—if anything, it deepens with familiarity.
The learning curve never truly plateaus. As automation, new analytical instruments, and control systems become more common, so do expectations on traceability and documentation. All raw materials feed into monitored supply chains, and finished esters land in containers with QR-coded batch histories. This foundation, built on hands-on experience, lets our customers document each stage of their own syntheses with confidence.
It makes no sense for a manufacturer to operate in a vacuum. Our teams spend as much time responding to unique user challenges as they do managing internal efficiency targets. Pharmas working on fast-tracked clinical candidates want insight into trace impurity origins. Agrochemical innovators need flexibility in both sample size and shipment method to accommodate shifting regulatory landscapes and new trial regions.
From our factory floor, we see every special synthesis as an opportunity to refine process steps, dial in final purity, or try greener solvents. In the last year alone, direct feedback from contract research labs led to the introduction of single-lot, zero-residual-methanol grades, skipping filtration steps and minimizing post-reaction purification. Once, a customer facing a stalled coupling agreed to send us a bench sample. Within a day, our technical staff replicated their problem, modified the ester feed rate, and brought both the conversion and selectivity in line with their targets.
We have even seen joint troubleshooting sessions—customer QA leads calling in from three different continents—resolve material handling hiccups simply by swapping transport packaging or pre-cooled drums. These stories, repeated across the seasons, continue to confirm the wisdom of direct channels between producer and user.
Being a manufacturer means taking the long view. As global demand shifts, synthetic methods move from traditional batch routes to continuous flow, and stricter environmental rules tighten, the way 2-Fluoronicotinic Acid Methyl Ester enters the supply chain continues to evolve. Our process development team tracks improvements in esterification catalysts, cleaner methylating reagents, and improved energy management—all of which trickle down to safer, more robust products.
Not every lesson comes easily. Early in our move to automated extraction, we discovered that aggressive solvent flushing increased the risk of minor impurity formation. Tweaks to residence time and temperature brought both product purity and solvent waste under better control.
We keep one eye on the regulatory future, aligning production documentation and process changes to the next wave of compliance needs—whether they relate to global hazard labeling, improved transport safety, or end-of-life management. Such moves, though strategic, mean investment in both infrastructure and staff education. The goal: make the ester available with increased safety and minimal environmental impact while supporting growing user demand.
Over decades of production, countless user stories, and a steady rhythm of process upgrades, one thing rings true—chemical manufacturing delivers real value when practicality, reliability, and responsiveness come together. The story of 2-Fluoronicotinic Acid Methyl Ester isn’t just a tale of a chemical bottle on a shelf. It’s the result of a daily commitment to process care, honest documentation, and a respect for the needs of chemists at every level.
Our teams—operators, analysts, product managers—bring their own ideas from the floor and listen to feedback from labs around the world. We’ve learned to respond quickly to changing project timelines, regulatory requests, and custom formulation needs, because real users and evolving projects keep the business honest and vital.
For every reaction that starts with our 2-Fluoronicotinic Acid Methyl Ester, there is a daily reality behind the scenes. Clean reactors, tightly monitored storage, careful hands at the filling station—all contribute to the quiet success of ongoing innovation in pharmaceuticals, agrochems, and materials. It’s a job that changes every day, but the foundation remains the same: careful production, responsible management, and open lines of communication make the difference between another catalog commodity and a partnership built on trust.