|
HS Code |
439417 |
| Chemical Name | Methyl 2-fluoropyridine-4-carboxylate |
| Molecular Formula | C7H6FNO2 |
| Molecular Weight | 155.13 g/mol |
| Cas Number | 126187-90-0 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 243-246°C |
| Density | 1.28 g/cm3 |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | COC(=O)C1=CC=NC(=C1)F |
As an accredited methyl 2-fluoropyridine-4-carboxylate 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 methyl 2-fluoropyridine-4-carboxylate, sealed with a screw cap, labeled with hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 14 metric tons on pallets (drums or fiber drums), securely packed to prevent leakage or contamination during transit. |
| Shipping | **Shipping Description:** Methyl 2-fluoropyridine-4-carboxylate should be shipped in tightly sealed, chemical-resistant containers under ambient conditions. Ensure proper labeling according to relevant chemical regulations. Avoid contact with incompatible materials and protect from moisture and physical damage during transit. Transport using licensed carriers in compliance with local, national, and international chemical shipping regulations. |
| Storage | Store methyl 2-fluoropyridine-4-carboxylate in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, and well-ventilated area, ideally at room temperature. Ensure proper labeling and avoid strong oxidizers and acids. Handle with suitable personal protective equipment and follow local regulations for chemical storage and disposal. |
| Shelf Life | Methyl 2-fluoropyridine-4-carboxylate has a typical shelf life of 2-3 years when stored in a cool, dry place. |
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Purity 98%: Methyl 2-fluoropyridine-4-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced byproduct formation. Molecular weight 157.12 g/mol: Methyl 2-fluoropyridine-4-carboxylate with molecular weight 157.12 g/mol is used in agrochemical research, where it provides accurate stoichiometric calculations for formulation development. Melting point 61°C: Methyl 2-fluoropyridine-4-carboxylate with melting point 61°C is used in solid-phase peptide synthesis, where it affords reliable processing at moderate temperatures. Low moisture content (<0.5%): Methyl 2-fluoropyridine-4-carboxylate with low moisture content is used in heterocyclic compound manufacturing, where it prevents hydrolytic degradation during reactions. Stability temperature up to 120°C: Methyl 2-fluoropyridine-4-carboxylate with stability temperature up to 120°C is used in heated reaction protocols, where it maintains compound integrity for consistent results. Particle size <50 microns: Methyl 2-fluoropyridine-4-carboxylate with particle size below 50 microns is used in fine chemical blending, where it promotes uniform dispersion in composite matrices. |
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Talking about chemical intermediates, it always comes down to the realities behind the lab door—what we run in our reactors, how handling affects each batch, which properties actually make life easier for process engineers, and how consistent output shapes the final product. From our day-to-day operations, methyl 2-fluoropyridine-4-carboxylate presents unique advantages in synthesis, scale, and application that are worth sharing frankly, based on hands-on familiarity rather than marketing jargon.
Our running model for this compound is based on controlled-flow nitration, followed by esterification and fluorination under strict moisture exclusion. The result: a solid batch-to-batch consistency in purity and isomer control. Typical output runs as a clear, off-white to light yellow powder or crystalline solid, depending on downstream requirements. We run analytical checks using in-house NMR, GC, and HPLC; chromosomes on purity have clocked in above 99% in our facility for most runs, with byproducts tightly suppressed by reaction control rather than post-processing. Years of working with various pyridine esters taught us that careful chemistry upfront beats heavy downstream purification every time if you aim for reliability at scale.
Organic chemists and process engineers often reach for methyl 2-fluoropyridine-4-carboxylate when they’re seeking a blend of reactivity, selectivity, and manageable safety profile. It gets regular use as an intermediate in the synthesis of heterocyclic drugs and crop protection agents. The fluorine atom at the 2-position strongly influences electronic properties and the downstream reactivity of the pyridine ring, often allowing access to unique substitution patterns across synthetic routes. What matters in the real world is not only lab yield, but scalability—this compound keeps its performance even when the batch scale grows from grams to tons, which cuts risk during tech transfer and scale-up.
In production, the methyl ester offers predictable hydrolysis, and pyridine derivatives carry inherent solvent and catalyst compatibility, so engineers rarely face surprises with solvent switches or catalyst fouling. Researchers have scaled up nucleophilic substitutions, Suzuki couplings, and even more exotic heterocycle construction on this backbone without needing to overhaul reactor design or modify process controls. These properties offer real headroom for process development and continuous-flow adaptation, which more lab-centric molecules frequently stumble over.
Think about the daily grind in a fluorinated pyridine campaign. At the bench level, certain isomers or ester types can be finicky, either from a reactivity standpoint or safety handling. Hot fluorination chemistries often mean complicated containment and waste neutralization, which can drag on cost and time. Our methyl 2-fluoropyridine-4-carboxylate sidesteps several persistent bottlenecks: clean fluorine incorporation at the 2-position reduces side-product formation typical in multi-step fluorinations for other pyridines, so waste management simplifies, and downstream purifications see fewer byproducts bleeding through columns.
Comparing methyl and ethyl esters, methyl esters tend to offer more controllable saponification and better solubility profiles in typical process solvents, easing both reaction work-up and purification. We’ve watched dogged issues like solid caking or undesired hydrolysis rates that crop up with longer chain esters or carboxylic acid forms. Handling powder or crystalline methyl esters uprights workflow, minimizing filtration headaches and waste, especially in humid climates where deliquescence or clumping can sabotage timelines.
Process stability gets overlooked in many introductory product guides, but for production teams, it is everything. On the floor, we’ve had to break up production blocks due to highly exothermic side reactions in similar pyridine derivatives. Through repeated optimization, we built our procedure around moderate temperatures and staged reagent addition for the fluorination. This heads off runaway reactions and stranded inventory, meaning we avoid costly plant downtime.
Batch reproducibility means a lot more than just matching the HPLC peak area. It means avoiding process interruptions, same-day batch correction, and keeping downstream users confident in what they’re getting every time. We don’t see the same instrument drift or product oiling with this compound as with unsubstituted or 3-fluorinated analogs. This delivers predictable pack density and volumetric handling when filling drums or bags.
Pharmaceutical process teams gravitate toward this intermediate during early lead optimization. The fluorinated site boosts metabolic stability in final drug molecules, with the carboxylate moiety offering easy derivatization points for amide, acid, or heterocyclic coupling. Over the last decade, we’ve seen heavy demand in the field of kinase inhibitors, as well as new antibiotics that require stable, electron-deficient pyridine frameworks. For regulatory filings, consistent upstream intermediate quality supports faster IND packages by smoothing over variability in impurity profiles — something we report thoroughly from each lot.
In crop protection, these fluorinated pyridine esters serve as modular building blocks, entering into urea, amide, or heterocycle scaffolds. Field chemists can rely on its hydrolysis and coupling efficiency, and regulatory agencies increasingly ask for traceable fluorinated inputs to support environmental testing. Tiered impurity review and batch traceability become part of our routine, not just a compliance tick box.
Materials chemists in the electronics sector have come to us looking for functionalized pyridines capable of supporting advanced ligand formation or as precursors to new types of conductive polymers. While this market takes only a fraction of our output, continual improvement on particle size and purity ensures researchers get consistent reactivity and minimize unknown variables in experimental setups.
Handling fluorinated intermediates never goes without respect in a production environment. Methyl 2-fluoropyridine-4-carboxylate offers a good balance between reactivity and manageable safety, especially compared to more volatile or dust-forming analogs. The melting point sits high enough to support safe storage, and its solubility limits airborne dust risk during transfer. We’ve established closed transfer systems and dust suppression where appropriate, based on real incidents during the scale-up of similar compounds.
Our own process generates manageable levels of HF and acidic byproducts, all captured through in-line scrubbing and neutralization. Through years of pilot runs, operational teams flagged specific steps where HF-offgassing could pose a challenge. We re-engineered our reactor seals and scrubber capacities around those needs. Effluent management for this material runs within standard protocols, with no need for specialty waste handlers or off-site incineration. That keeps costs rational and wins approval during regular audits.
Every drum shipped leaves our site with full analytical backup, run on the same instruments as those used for internal quality assurance. We keep archives of every sample batch, following batch genealogy back to the reactor clean-out and equipment logs. This kind of traceability gives lot-to-lot confidence, supports customer audits, and calms regulatory nerves in downstream manufacturing.
We’ve seen trends come and go: green chemistry slogans, the latest “sustainable” solvents, digital tracking fads. At the end of the day, large pharma teams and specialty manufacturers come back to us for one reason: steadfast output, real-world documentation, and candid problem-solving. Our methyl 2-fluoropyridine-4-carboxylate pipeline doesn’t rely on “magic bullet” techniques; it reflects years of careful fine tuning, hundreds of hours logged fixing operator issues, and reams of analytical data proving each adjustment’s worth.
Our team grew skeptical of chasing A.I.-driven process controls until statistical feedback from years of batch data proved incremental tweaks could lock in purity at scale. Now we apply targeted analytics at each stage, checking for both out-of-trend readings and insidious shifts in impurity profiles. There is no shortcut; quality follows from technical discipline and actual feedback, not after-the-fact corrections.
Big customers tell us supply reliability counts more than theoretical performance. A research division can’t afford to halt because a kilo lot fails analytical checks or shows unexpected color. We maintain dialogue with downstream users not because compliance demands it, but because process changes ripple outward—days of wasted filtration or remakes cost way more than chasing single-molecule performance improvements. We answer technical questions based on genuine test bench and plant experience, not scripted sales answers.
Shipping on schedule means tracking not just product readiness, but each step—cleaning, packaging, transporter protocols, suitable labeling. Years of exporting to strict regulatory regions taught us to plan for everything from customs paperwork to label legibility in winter.
Our compound often comes up for evaluation in side-by-side trials with similarly fluorinated pyridine esters. Some labs try to swap in cheaper non-fluorinated intermediates, only to learn the hard way how fluorine’s presence shifts reactivity and final compound performance. We’ve collaborated directly with process development teams to troubleshoot side reactions and adjust reactivity through solvent tweaks, or reaction order. The effort invested at this stage saves weeks of frustration and late-stage surprises for formulation or QC teams downstream.
Batch feedback cycles extend far beyond simple pass/fail metrics. Customers report on product handling, filtration behavior, safety issues, and packaging needs. Our operational team cycles this data back into both plant upgrades and documentation—updating maintenance SOPs, packaging lines, and handling advice.
Unwanted solidification or caking during humid summer shipping almost derailed several overseas shipments—nothing replaced actual stress testing with different liner films and overpackaging to arrive at an approach that kept both the product and workforce safe. Engineers don’t want theoretical advice; they want to hear what actually worked in a similar shipping lane and climate. By building feedback loops between our operations, logistics partners, and end users, we’ve tightened tolerances and reduced incident frequency.
Some synthetic campaigns generate downstream clogs or decomposition with off-grade intermediates. We run bulk stability testing under forced aging to supply real shelf-life and handling limits, not just generic “best by” conventions. Having handled both clear and borderline-lot material, our plant operators can point out subtle cues—a slight hue shift, a persistent trace odor—signaling not just purity concerns but potential batch history issues upstream.
Our aim is not to flood the market or undercut by price. The specialty applications really shaping health care, agriculture, and material science rely on secure, long-term access to reagents that don’t throw new process risk into already tight schedules. We commit engineering, capital, and critical talent to the production of each batch, with the bulk routed by long-term planning, not speculative inventory. Our advice to customers has always followed a “no-surprises” path: request a real batch sample, stress it under actual process conditions, and keep communication lines open.
Smaller lots or custom particle sizing can be arranged, but our principal production strength hinges on well-validated process streams, robust batch records, and expert troubleshooting. As new applications emerge in drug discovery, crop resilience, or advanced materials, we adjust process development, analytical checks, and reporting requirements to line up with real user feedback, regulatory expectations, and export logistics.
Long experience manufacturing methyl 2-fluoropyridine-4-carboxylate shapes how we approach each aspect of the business—from upstream sourcing, reactor tuning, and analytical QA, to packaging, client communication, and logistics. When a chemist picks up this material from our production line, it reflects the combined practical know-how of our entire operation, not just what worked in the literature or shrunk in a test tube. We value every insight fed back from customers, process engineers, regulators, and plant operators. Each lot, drum, or kilo reflects a work ethic that values progress, learning, and real partnership in the specialty chemical sector.