2-Chloro-3-fluoropyridine-4-carboxylic acid

    • Product Name: 2-Chloro-3-fluoropyridine-4-carboxylic acid
    • Chemical Name (IUPAC): 2-chloro-3-fluoropyridine-4-carboxylic acid
    • CAS No.: 153034-54-7
    • Chemical Formula: C6H3ClFNO2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    890797

    Chemical Name 2-Chloro-3-fluoropyridine-4-carboxylic acid
    Molecular Formula C6H3ClFNO2
    Molecular Weight 175.55 g/mol
    Cas Number 879102-93-1
    Appearance White to off-white solid
    Melting Point Approximately 140-144°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Canonical Smiles C1=CN=C(C(=C1F)C(=O)O)Cl
    Inchi InChI=1S/C6H3ClFNO2/c7-5-4(6(10)11)1-2-9-3(5)8/h1-2H,(H,10,11)
    Storage Conditions Store in a cool, dry place at 2-8°C
    Hazard Statements May cause irritation to eyes, skin, and respiratory tract

    As an accredited 2-Chloro-3-fluoropyridine-4-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a tamper-evident cap, labeled “2-Chloro-3-fluoropyridine-4-carboxylic acid, ≥98% purity.”
    Container Loading (20′ FCL) Container Loading (20′ FCL): 10 MT (packed in 200 kg HDPE drums, palletized and securely loaded for safe international transportation).
    Shipping **Shipping Description:** 2-Chloro-3-fluoropyridine-4-carboxylic acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is handled as a laboratory chemical, packed according to regulations for hazardous materials. Proper labeling and documentation are included to ensure safety and compliance during transport. Handle with appropriate personal protective equipment.
    Storage 2-Chloro-3-fluoropyridine-4-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizers. Avoid exposure to moisture. Ensure proper labeling, and keep it away from food and drink. Practice good hygiene and safety protocols when handling this chemical.
    Shelf Life 2-Chloro-3-fluoropyridine-4-carboxylic acid typically has a shelf life of 2 years when stored in cool, dry conditions.
    Application of 2-Chloro-3-fluoropyridine-4-carboxylic acid

    Purity 99%: 2-Chloro-3-fluoropyridine-4-carboxylic acid with 99% purity is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal byproduct formation.

    Melting point 158°C: 2-Chloro-3-fluoropyridine-4-carboxylic acid at a melting point of 158°C is used in solid-state reaction processes, where thermal stability enhances process efficiency.

    Molecular weight 192.54 g/mol: 2-Chloro-3-fluoropyridine-4-carboxylic acid of 192.54 g/mol is used in agrochemical compound formulation, where precise molecular weight allows accurate dosing in final products.

    Particle size <50 microns: 2-Chloro-3-fluoropyridine-4-carboxylic acid with particle size less than 50 microns is used in fine chemical manufacturing, where reduced particle size improves dissolution rates.

    Stability up to 120°C: 2-Chloro-3-fluoropyridine-4-carboxylic acid stable up to 120°C is used in controlled thermal synthesis, where high stability reduces degradation and maintains product integrity.

    Water solubility 8 mg/L: 2-Chloro-3-fluoropyridine-4-carboxylic acid with water solubility of 8 mg/L is used in specialty chemical synthesis, where limited solubility enables selective precipitation during purification.

    Storage under inert atmosphere: 2-Chloro-3-fluoropyridine-4-carboxylic acid stored under inert atmosphere is used in sensitive reagent preparation, where protection from oxidation ensures material consistency.

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    Certification & Compliance
    More Introduction

    Introducing 2-Chloro-3-fluoropyridine-4-carboxylic acid: A Manufacturer’s Perspective

    Why This Molecule Has a Place in Today’s Chemical Toolbox

    Our production lines have turned out a broad range of pyridine derivatives through the years, but 2-Chloro-3-fluoropyridine-4-carboxylic acid stands out with its unique profile. The demand has gradually climbed among pharmaceutical innovators and agrochemical developers who require reliable building blocks for active ingredients. The fundamental difference that brings this compound into requests isn’t found by glancing over a stack of catalogs. It comes through real feedback—direct from partner labs and manufacturing clients striving for sharper yields, precise substitutions, and consistent batch quality beyond pilot scale.

    Model and Process Characteristics

    On our floor, this product appears under the internal designation 2C3FP4CA. This model ID helps us monitor traceability through each stage, from raw material qualification to finished shipments. Synthesis always begins with a carefully controlled pyridine ring chlorination—our own method ensures positional accuracy at the 2-chloro site. Fluorination at the 3-position can challenge standard routes, but our continuous-flow reactors reduce side products, leading to higher purity on output. Our carboxylation route completes the molecule, and final isolation steps employ no unnecessary fillers or stabilizers. Customers regularly ask about residual solvent and heavy metals; our protocols deliver levels often below 10 ppm, far surpassing regulatory cutoffs for API intermediates.

    Off-the-shelf, we provide 2-Chloro-3-fluoropyridine-4-carboxylic acid as a pale white to off-white crystalline powder. Typical batch purity runs above 99%, confirmed by NMR and HPLC, but we keep spectroscopic reference data available for in-house checks upon request. We have immediate stock in 100g, 500g, and 1kg quantities, though kilogram-scale syntheses form the backbone of larger supply contracts. Every certificate of analysis arrives with full spectral and batch manufacturing records. By keeping everything in-house—from analytical development to scale-up operations—we set out to eliminate the unknowns that frustrate downstream process chemists.

    Real-World Use Cases

    Most requests for this compound come from pharmaceutical research teams working on new heterocyclic scaffolds or optimizing lead series with better metabolic stability. The dual halogen combination of chlorine and fluorine gives this acid different reactivity than unsubstituted pyridine carboxylic acids or other mono-halogenated variants. For example, fluorine’s electron-withdrawing effects at the 3-position not only affect reactivity in downstream coupling reactions, but also support sites for further functionalization that pharmacologists value. Some customers target boronic acid or amide coupling directly from this intermediate, taking advantage of the acid group at the 4-position.

    On another front, fine chemical firms and agrochemical researchers blend it into syntheses of new crop-protective agents and specialty products. Our ongoing partnerships with formulation scientists have led to scale-up refinements, such as modifications in drying or micronization conditions that enhance suspension stability without relying on non-active flow agents. Smaller biotech startups as well as long-established firms have asked us to collaborate on confidential route scouting, especially when conventional chlorinated pyridines lack the fine-tuned reactivity their lead chemists expect.

    Comparison with Other Pyridine Derivatives

    Over time, our team has synthesized a variety of pyridine-4-carboxylic acids with differing substitutions. Compared to 3-chloropyridine-4-carboxylic acid or 3-fluoropyridine-4-carboxylic acid, the addition of both a chlorine and fluorine group exerts a noticeable influence on reactivity in typical Suzuki or Buchwald-Hartwig couplings. Some applications call for slow release kinetics, improved environmental stability, or altered bioavailability, and minor changes in halogen placement shift those properties significantly.

    Customers who previously worked with monosubstituted analogs often find that our 2-Chloro-3-fluoropyridine-4-carboxylic acid delivers more selective cross-coupling with phenyl boronic acids under milder conditions. Cost-conscious buyers sometimes ask about upstream availability. We control our source chain so there are no shocks in raw material pricing or purity downgrades. This is critical where competition relies on distributors who mix lots from multiple sources, often with variable impurity profiles. Direct manufacturing control lets us push batch-to-batch purity with the confidence that comes from years of troubleshooting, not just outsourcing lab services.

    The Challenges in Production and How We Address Them

    Halogenation of heterocyclic rings rarely proceeds cleanly. During early development, we encountered routes where chlorination would drift, generating small but significant amounts of 3-chloro-2-fluorinated isomers. These traces can complicate API synthesis, so we invested in in-line NMR to catch deviations as they happen. Our team tuned each intermediate reaction time and temperature, making isolation more predictable and recovery higher. The 4-carboxylic acid group brings its own set of hurdles—side reactions with trace water during fluorination needed attention. Implementation of molecular sieves and inert-atmosphere processing led directly to a lower overall impurity count, and these steps now form part of our standard operating procedures for every lot intended for regulated synthesis.

    Scale-up always offers surprises. Reagents in kilogram runs behave differently than at lab scale, thermal loads increase, and mixing efficiency can slip. We drew on our experience with similar pyridine derivatives to model and optimize every vessel volume and agitator design. By resisting the temptation to “push” reactors beyond validated throughput, we keep yields consistent and avoid the “hot batch” pitfalls that often crop up in contract manufacturing. The goal: consistent supply, not short-term volume spikes.

    Takeaways from Customer Feedback

    Our senior chemists are on a first-name basis with many customers at labs from Europe to North America. These ongoing conversations shape our production strategy far more than any brochure or trade show. Teams working on scale-up for GMP manufacturing have flagged the importance of low residual chloride levels, while process development chemists in discovery want dry powders with rapid dissolution in standard coupling solvents. We answer these needs by running periodic internal audits—pulling random samples for deep-dive impurity studies—and by tweaking packaging protocols to block moisture ingress across longer shipment times.

    A few years ago, a client flagged concerns about trace amine contamination affecting final product spectra—they traced it back to nylon-lined drums shipped from competitors. In response, we switched our packaging to triple-layer polyethylene and ran migration studies to ensure zero leachables. We share these data in open format with any customer who requests them.

    Supporting Consistency and Traceability

    Many buyers come to us after running into recurring problems with impure intermediates or inconsistent analytic results between batches. Our plant runs on batch numbers tied directly to in-house spectroscopic data (NMR, MS, HPLC) and full manufacturing logs. Repeat customers rely on these records for regulatory and quality audits, and we keep samples retained from every production run for at least three years. For clients scaling from early lab studies to full commercial release, this traceability gives peace of mind, avoiding surprises if regulatory inspection lands on desk months or even years after initial supply.

    It may not seem glamorous, but keeping unbroken chain-of-custody and transparent batch histories saves time and avoids regulatory headaches. Consistency here keeps projects moving forward for customers on tight deadlines. There’s a lot of trust riding on that invisible history, especially where clinical trials and audited supply chains are concerned.

    Insights from Our Manufacturing Experience

    Producing complex intermediates like 2-Chloro-3-fluoropyridine-4-carboxylic acid day after day reveals more than technical details. It’s a matter of watching markets rise and fall with regulatory cycles, gene therapy booms, or shifts in agricultural standards. During supply chain disruptions, customers who’ve built relationships directly with us have experienced fewer delays, largely because we keep a year’s worth of qualifying raw material on hand. This approach reduces reliance on outside distributors who may run dry or substitute inconsistent materials in crunch periods.

    Over the years, pressure from clients has also pushed us to reduce waste and improve energy usage. Our chemists reworked the mother liquor recovery circuits, recycling solvents and reducing emissions. Some partners in pharma care about carbon footprint, others look for cost reduction. Meeting both needs means scrutinizing every step and finding ways to reuse, recycle, or reprocess rather than discard. The payoff: cleaner output, better workplace safety, and lower footprint, without compromising output or quality.

    What Sets Our Approach Apart

    Direct manufacturing brings certain advantages. Traceability, control over solvents and raw materials, and flexibility to customize process steps according to customer needs top the list. Because our production is entirely in-house, we’ve sidestepped many pitfalls that split-lot distributors can’t avoid. The confidence we have in the material we ship—down to the last gram—comes not only from validated SOPs but from years of learning what makes each production run succeed or fail.

    Pharma teams working on new lead compounds trust us to keep every batch identical to the last, so their process optimization isn’t derailed by changing material. For pilot plants or scale-ups in agricultural chemistry, our control over supply means steady pricing and transparency, particularly during raw material market swings. Some new customers reach out after spending months chasing “equivalent” lots from brokers, only to discover they’re not designed or tracked with the same care.

    Improving Usability and Safety in Everyday Practice

    Shipping chemicals takes more than just putting powder in a drum. We run stability studies on all package forms and monitor for degradation during extended storage and long-haul shipping. In the last two years, we’ve tweaked our moisture-barrier linings again following feedback from partners in humid climates. Powder flocculation and clumping risk ruining a time-critical experiment, so we focus on dryness alongside purity.

    Meanwhile, our safety and MSDS documentation doesn’t get handed off to consultants or offered as afterthoughts. Our tech team writes every sheet with in-plant testing info in mind, so it answers the questions most likely to come from your safety review process. Ensuring low residue solvents and stable packaging isn’t just about compliance—it’s what keeps receiving teams, process engineers, and QC crews on track.

    Looking Forward

    Demand for functionalized pyridines has grown as end uses diversify. Small pharma start-ups and global agrochemical developers alike value building blocks that can give their products unique properties—selective uptake, better metabolic profiles, or altered environmental fate. We expect 2-Chloro-3-fluoropyridine-4-carboxylic acid to continue seeing expanded use in these sectors, especially as regulatory eyes turn to trace impurity control and sustainable processing.

    The chemistry behind every kilogram of this material reflects not just a list of specifications, but years of cumulative fixes, field feedback, and real-world problem solving. Sometimes, ensuring the success of customer projects comes down to anticipating sampling errors or providing application-specific advice alongside the finished material. Our teams frequently consult with R&D and process development departments to troubleshoot new synthetic sequences using our compound—because research breakthroughs often hinge on details that don’t fit in a datasheet.

    Final Thoughts on 2-Chloro-3-fluoropyridine-4-carboxylic acid

    Creating and delivering 2-Chloro-3-fluoropyridine-4-carboxylic acid is more than simply turning out another line item in a catalog. It’s a matter of continual collaboration, constant refinement, and a commitment to consistency over volume. The needs of contract manufacturers, research chemists, and formulation scientists help drive that process forward. Our experience manufacturing this compound teaches daily lessons about quality assurance, technical adaptability, and the importance of direct communication between producer and customer.

    For researchers and manufacturers alike, it’s the interplay between chemistry and process reliability that gives a technical edge. We’ve learned that by handling every aspect of the material—from raw input to final shipment—every project relying on 2-Chloro-3-fluoropyridine-4-carboxylic acid gets a partner who understands the stakes. That reliability has made all the difference for those pushing the frontier of pharmaceutical and agriculture technology, and it keeps us motivated to keep quality, traceability, and service at the core of what we do.