|
HS Code |
391605 |
| Chemical Name | 3-fluoropyridine-2-carboxylic acid |
| Molecular Formula | C6H4FNO2 |
| Molecular Weight | 141.10 |
| Cas Number | 407-01-6 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 123-126°C |
| Solubility | Soluble in polar organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CC(=NC=C1F)C(=O)O |
| Inchi | InChI=1S/C6H4FNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3H,(H,9,10) |
| Pka | Approx. 3.3 (for carboxylic acid group) |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Hazard Classification | Irritant (may cause skin and eye irritation) |
| Pubchem Cid | 98894 |
As an accredited 3-fluropyridine-2-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 3-Fluoropyridine-2-carboxylic acid is supplied in a sealed amber glass bottle with a screw cap and labeling. |
| Container Loading (20′ FCL) | 20′ FCL container can load approximately 10 metric tons of 3-fluoropyridine-2-carboxylic acid, packed in 25 kg fiber drums. |
| Shipping | 3-Fluoropyridine-2-carboxylic acid is shipped in tightly sealed containers, protected from moisture and light. Packages are clearly labeled with chemical and hazard information. Transportation complies with local and international chemical regulations, ensuring secure handling. Appropriate documentation accompanies each shipment. Suitable precautions are taken to prevent leakage, contamination, or exposure during transit. |
| Storage | Store 3-fluoropyridine-2-carboxylic acid in a tightly sealed container, away from moisture and incompatible substances such as strong bases and oxidizers. Keep in a cool, dry, and well-ventilated area, protected from direct sunlight. Ensure storage area is clearly labeled and follow all relevant safety protocols. Avoid inhalation, ingestion, or contact with skin and eyes during handling. |
| Shelf Life | 3-Fluoropyridine-2-carboxylic acid should be stored in a cool, dry place; shelf life typically exceeds two years if unopened. |
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Purity 99.5%: 3-fluropyridine-2-carboxylic acid with a purity of 99.5% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal byproduct formation. Melting point 158°C: 3-fluropyridine-2-carboxylic acid featuring a melting point of 158°C is used in solid-phase organic synthesis, where stable processing conditions are required. Particle size ≤10 μm: 3-fluropyridine-2-carboxylic acid with a particle size ≤10 μm is used in catalyst preparation, where fine particles improve mixing and reaction efficiency. Moisture content <0.2%: 3-fluropyridine-2-carboxylic acid with a moisture content below 0.2% is used in API (Active Pharmaceutical Ingredient) manufacturing, where low moisture prevents hydrolysis and degradation. Chemical stability up to 120°C: 3-fluropyridine-2-carboxylic acid with chemical stability up to 120°C is used in heat-sensitive process steps, where decomposition rates are minimized. Molecular weight 140.09 g/mol: 3-fluropyridine-2-carboxylic acid with a molecular weight of 140.09 g/mol is used in analytical method development, where accurate quantification is achieved. |
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Chemists and research professionals in pharmaceuticals, agrochemical development, and fine chemical synthesis have welcomed advances that help improve efficiency in complex molecule construction. 3-Fluoropyridine-2-carboxylic acid has shown its merit as a key intermediate in several of these demanding fields. Known for its consistent quality and tightly controlled specifications, this compound supports reliable synthesis-building decisions around the world.
3-Fluoropyridine-2-carboxylic acid’s molecular formula, C6H4FNO2, situates it within an important class of pyridine-based acids. The structure, featuring a fluorine substituent at the 3-position and a carboxylic acid group at the 2-position, makes this material uniquely reactive in a set of transformations that other pyridine derivatives cannot easily match. Many researchers describe the consistent melting point and defined reaction profile—which means fewer headaches trying to troubleshoot unexpected results.
My own early career focused on medicinal chemistry, and I quickly saw the value of highly pure intermediates. Working through multiple failed attempts at coupling reactions—often turned sour by contaminated reagents—I realized the waste of time and frustration poor quality intermediates can cause. What stands out about 3-fluoropyridine-2-carboxylic acid is how its purity above 98 percent supports robust yields and predictable conversions.
In drug development, the presence of a fluoro group changes the character of the final molecule significantly. The rate of metabolic breakdown drops, and the biological target affinity can shift, which matters deeply for discovering effective drug candidates. Fine-tuning these properties begins with reliable starting materials, and access to consistently pure 3-fluoropyridine-2-carboxylic acid takes the uncertainty out of these efforts.
On the agrochemical side, pyridine derivatives play a vital role in new crop protection materials. Fields rely on compounds that fight off pests while not compromising environmental safety. The unique substitution pattern here—fluorine at position three, carboxyl at position two—lets chemists build complex structures that would otherwise require more convoluted multi-step processes. That means less chemical waste, lower manufacturing costs, and clearer regulatory pathways.
It’s tempting to lump all pyridine carboxylic acids into the same category. This overlooks how much difference a single fluorine can make. For those who’ve struggled to direct reactivity or steer regioselectivity, 3-fluoropyridine-2-carboxylic acid offers a welcome degree of control over the synthesis outcome. Unlike the better-known 2-pyridinecarboxylic acid or its 3- and 4- position isomers, the 3-fluoro variant brings an electron-withdrawing effect that shifts reaction rates and site selectivity.
In my hands, using the fluorinated analog meant far fewer by-products in Suzuki couplings and aromatic substitutions. Downstream purification runs shorter. Solubility shifts, so controlling precipitation and crystal form gets easier. Neighbors in the lab reported similar advantages in transition metal-catalyzed cross-couplings, where electron density really rules the day.
Researchers constantly battle issues stemming from impurities and batch variation. Some compounds, especially those sourced at scale or through multiple distributors, display shifting purities, colorations, or unidentified contaminants. With this acid, purification to above 98 percent means LC-MS and NMR characterization rarely delivers surprises. Analysts who rely on clean mass spec traces and clear proton signals see more of what they expect and less noise to decode.
The physical form—usually a white or near-white powder—gives easy weighing, straightforward transfer, and rapid dissolution in a variety of laboratory solvents. That’s a relief on long days, when scraping sticky residues or fighting with inhomogeneous crystals can make even basic procedures drag. Over time, less time wasted on workups yields more time on developing useful chemistry.
Echoing conversations in labs from Boston to Basel, reproducibility means fewer late night troubleshooting sessions. My own experience chasing down batch-specific problems showed the hidden costs of drifting purity and inconsistent reactivity. With 3-fluoropyridine-2-carboxylic acid made to a clear, high specification, each reaction step delivers the yield, selectivity, and speed promised by published protocols.
Chemistry teams working on tight deadlines for patent filings or regulatory submissions rest easier when intermediates do their job the same way, each time. When scaling up, the headache of translating bench results to pilot plant work shrinks dramatically as a result of clean, pure, and consistent input materials.
The pressure to innovate in pharmaceuticals and agrochemicals grows fiercer as regulatory expectations, supply interruptions, and intellectual property constraints tighten. Erratic quality in key intermediates can derail promising projects and stall product launches.
Practical approaches to these challenges include selecting reputable suppliers who forward full analytical documentation and provide transparency about sourcing. Strong relationships and regular communication between buyers and manufacturers help root out specification drift and allow for up-front negotiation of needed certificates of analysis or trace-level impurity profiling.
Routine in-lab QC remains a wise investment. Even trusted intermediates can drift in composition if storage, transport, or re-packing gets careless. In my workflow, spot-checking incoming batches by HPLC or GC before launching a major synthetic route quickly saved wasted time downstream. The cost of a few analytical runs fades next to the hours recovered by heading off surprises early.
Working with halogenated compounds—including those bearing fluorine—carries responsibility for careful waste management and exposure controls. While 3-fluoropyridine-2-carboxylic acid does not rise to the same hazard class as the more volatile fluorinated reagents, safety protocols require glove and goggle use. Clean technique, sturdy containment, and well-ventilated workspaces help avert accidental exposures. Choosing intermediates with a well-documented safety profile reduces risk and aids compliance with both internal and regulatory guidelines.
Green chemistry efforts also turn attention towards atom economy and waste reduction. When a versatile intermediate like this one lets teams eliminate unnecessary steps, both costs and chemical footprint shrink. Sourcing from suppliers who follow responsible manufacturing standards closes the loop to more sustainable chemistry. Practicing chemists increasingly demand a traceable chain of custody and audit-ready documentation as part of regular procurement.
Beyond drug research and crop protection, 3-fluoropyridine-2-carboxylic acid finds roles in material science, specialty dye synthesis, and as a ligand precursor in some catalytic systems. Academic groups aiming to publish novel method development or mechanistic studies value intermediates with unique substitution profiles and well-characterized reactivity. Faculty principal investigators often encourage students to work with reliable compounds to support reproducible results and easier peer review.
Custom synthesis outfits appreciate the flexibility this acid gives. Its structure opens the door for late-stage functionalization, a strategy that wins time in fast-moving discovery programs. In material design, this acid’s properties enable structural motifs in polymers or specialty coatings, where fluorination can modulate properties like hydrophobicity or thermal stability.
In highly regulated fields, documentation and traceability matter deeply. Reputable producers of 3-fluoropyridine-2-carboxylic acid back every batch with thorough analytical data—NMR, HPLC, and mass spectrometry at a minimum. Access to impurity profiling, elemental analysis, and residual solvent testing rounds out the information both R&D and QA teams want on file.
Meeting the needs of developing generic drugs, new chemical entities, or proprietary crop protection products always means ticking boxes that regulators and internal reviewers set. The availability of rigorous lot-release documentation, full traceability, and a record of stability data supports safe, compliant advancement of research and eventual product approval.
Supply chain disruptions for key reagents can paralyze research timelines and jeopardize product launches. Over the past decade, several highly specialized intermediates saw availability drop as single-source manufacturers were hit by natural disasters, regulatory crackdown, or transportation bottlenecks. Diversifying approved suppliers for materials like 3-fluoropyridine-2-carboxylic acid insulates projects against such shocks.
Procurement professionals within both large corporations and research-focused startups have adopted robust vetting processes. These involve on-site audits, periodic requalification, and ongoing supplier performance tracking. A close working relationship with the chemistry team ensures that technical requirements match what partners provide. Transparent communication about delivery schedules, storage recommendations, and shelf-life management further smooths the path from lab-bench discovery to pilot and commercial scale applications.
Back in a period spent troubleshooting a scale-up of a fluorinated benzamide in a pharma project, a contaminated batch of a related intermediate—supplied by a new vendor—derailed a month’s timeline. The cost in overtime, lost material, and opportunity haunted the project review meeting for months. Instituting a workflow that featured pre-committed, high-purity intermediates, including 3-fluoropyridine-2-carboxylic acid, restored progress and took much of the firefighting out of the weekly meetings.
This kind of lesson sticks. Chemists and managers alike share stories of syntheses that either succeeded beautifully or failed spectacularly depending on the integrity of key intermediates. Many now demand up-front analytical support, a process that increasingly includes digital access to NMR and HPLC traces, impurity reporting, and even validated SOPs for storage and handling.
With growing worldwide focus on chemical regulation, transparent sourcing and clear regulatory compliance now factor into nearly every purchasing decision. Both pharmaceutical and crop science partners want intermediates sourced through responsible channels, compliant with local and international standards, and ready for audit if a question arises. 3-fluoropyridine-2-carboxylic acid, when supplied with a thorough dossier, sits neatly within these requirements.
Compliance doesn’t end on paper. Real-world storage, transport, and inventory tracking ensure this compound arrives with predictable viability and clean identity. Smart facilities invest in purpose-built storage spaces, temperature control, and periodic re-testing to confirm intermediates remain fresh and potent between procurement and use.
Across several sectors, decision-makers weigh the upfront cost of premium intermediates against the high internal costs of troubleshooting, rework, and delays. Experience shows that committing to high-purity 3-fluoropyridine-2-carboxylic acid sharpens project predictability and relieves back-end bottlenecks. Teams tasked with ultra-fast discovery, scale-up, or process validation lean heavily on reliable input materials with a strong analytical pedigree.
The gap between academic and industrial environments closes as both sides recognize the technical and business risks from batch drift, unexpected impurity profiles, and supply interruptions. The narrative has shifted: no longer just a commodity, this intermediate forms a linchpin in streamlined, modern synthetic workflows. Those leading innovation understand that strong science rides on the quality of its foundations.
Process chemists hunting for route improvements and cost savings see wins when intermediates feature predictable reactivity and clean conversion profiles. 3-fluoropyridine-2-carboxylic acid, with well-documented kinetics and solvent compatibility, fits the trend toward telescoped syntheses—where fewer isolations and purifications speed timelines and cut expenses.
Lessons learned over years of process optimization show that small investments in reliable materials pay off fast. Selective reactivity and easy downstream processing count more than the apparent sticker price of the input chemical. Looking at the entire project journey, from lab notebook to final product pallets, advantages compound at each step.
As the industry focus swings to ever more complex molecules and the hunt for next-generation pharmaceuticals or smart materials continues, the appeal of diverse, reactive intermediates strengthens. Open data exchanges and advanced analytical support drive more informed decisions about reagent selection. Firms pushing the boundaries of green chemistry and atom economy find their efforts supported by robust, well-understood intermediates like 3-fluoropyridine-2-carboxylic acid.
Collaboration between suppliers, end-users, and regulatory partners fuels greater transparency, cleaner processes, and better products. Ongoing investment in material quality pays dividends in time saved, headaches avoided, and progress accelerated.
In over a decade’s work with chemical synthesis—both early discovery and late-stage development—one clear lesson stands out: the difference between smooth progress and drawn-out troubleshooting often traces to the quality of your intermediates. 3-Fluoropyridine-2-carboxylic acid has stepped up as a trustworthy option for chemists and engineers aiming for strong, reproducible results.
A chemical’s journey from supplier to the heart of critical research and manufacturing passes through many hands. When those hands trust the reliability, purity, and documentation that ride with each shipment, projects hit their marks more often. The field continues to demand intermediates that not only promise quality but deliver it, again and again.