2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid

    • Product Name: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid
    • Chemical Name (IUPAC): 2-chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid
    • CAS No.: 690632-78-5
    • Chemical Formula: C7H3ClF3NO2
    • 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

    149971

    Product Name 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid
    Cas Number 395-43-1
    Molecular Formula C7H3ClF3NO2
    Molecular Weight 225.55
    Appearance White to off-white solid
    Melting Point 109-113°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Smiles C1=CC(=C(N=C1Cl)C(=O)O)C(F)(F)F
    Inchi InChI=1S/C7H3ClF3NO2/c8-5-3-4(7(14)15)6(12-2-5)1-10(9,11)13/h2-3H,1H2,(H,14,15)
    Storage Temperature Store at room temperature

    As an accredited 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 25g amber glass bottle with a secure, tamper-evident cap and chemical-resistant labeling for safety and identification.
    Container Loading (20′ FCL) 20′ FCL loads 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid securely packed in drums or bags, maximizing container space efficiently.
    Shipping 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with hazardous material regulations, ensuring safe transport. Temperature and handling precautions are observed to prevent degradation or accidental release during transit. Shipping documentation includes proper labeling and safety data sheets for regulatory compliance.
    Storage Store 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, well-ventilated area, separated from incompatible substances like strong bases and oxidizers. Ensure the storage area is equipped with spill containment and clearly labeled. Handle using proper personal protective equipment to avoid exposure.
    Shelf Life Shelf life of 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid: Stable for 2 years when stored cool, dry, and protected from light.
    Application of 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid

    Purity 98%: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting Point 120°C: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with a melting point of 120°C is used in agrochemical formulations, where it provides thermal stability during processing.

    Particle Size <10 µm: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with a particle size below 10 µm is used in fine chemical manufacturing, where it allows for enhanced reactivity and dispersion.

    Stability Temperature up to 150°C: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with stability up to 150°C is used in catalyst development, where it maintains structural integrity under elevated reaction conditions.

    Molecular Weight 243.57 g/mol: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with a molecular weight of 243.57 g/mol is used in QSAR modeling, where precise molecular metrics improve predictive analytics.

    Assay ≥99%: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with an assay of at least 99% is used in specialty chemical synthesis, where high-purity input reduces impurity interference.

    Residual Solvent <0.1%: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with residual solvent content below 0.1% is used in electronic material applications, where minimal contamination enhances device reliability.

    Water Content ≤0.5%: 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylicacid with water content at or below 0.5% is used in moisture-sensitive reactions, where it minimizes hydrolysis risk.

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    Certification & Compliance
    More Introduction

    2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid: Practical Insights from the Manufacturing Floor

    Facing Demands in Modern Chemistry

    Working with specialty fluorinated heterocyclic compounds puts a manufacturer right at the crossroad of global research needs and technical demands. 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid, known among production teams as a resilient intermediate, reflects years of accumulated expertise in handling reactive halopyridines and introducing trifluoromethyl groups with high selectivity. In our facility, this molecule carries the identifier CTFPCA-303, though the number matters less than the reality: researchers expect consistent yields, clear documentation, and scalable batches every single production cycle.

    What sets this molecule apart from a sea of pyridine derivatives deals most with that trifluoromethyl substitution at the 5-position. The presence of both an electron-withdrawing chlorine and a carboxylic acid group influences reactions downstream, demanding careful control during synthesis and rigorous analytical oversight. These subtle electronic shifts underpin both its distinct reactivity and the value it holds for medicinal chemistry projects, as well as for crop science innovators hunting for robust new actives.

    The Day-to-Day of Reliable Synthesis

    Production teams engaging directly with 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid know that consistency is the metric clients care about most. From charge-in through distillation, workers adjust temperatures and atmospheres to coax the right balance from sensitive intermediates, especially during chlorination and trifluoromethylation steps. With these, subtle changes in the order of reagent addition and purification protocol spell the difference between a batch that satisfies quality demands and a time-consuming rework.

    Our methods skip shortcuts that compromise stability. Avoiding residual solvent, controlling trace water, and confirming the absence of byproduct isomers remain daily priorities. In the lab, we subject every lot to HPLC and NMR scrutiny. Even though some would consider this overkill, experience teaches that single-molecule contaminants or minor changes in substitution patterns can send an entire client’s trial off in the wrong direction.

    Specifications Shaped by Experience

    Years of cumulative feedback from downstream chemists have honed the way we define and test our 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid. Experienced hands avoid the temptation to advertise technical-grade material or cut corners on purity. Every batch targets at least a 98% area by HPLC, capped with water content below 0.2%. Moisture can play havoc with coupling reactions, and a few stubborn residuals tend to hide unless analytical teams calibrate their gear thoroughly. Standard lots appear as an off-white crystalline powder, blending easily in polar organic solvents. Each lot’s actual melting point, often in the 178–182°C range, serves as an added fingerprint confirming process control.

    Product form stays granular, never sticky. Finely divided powder invites caking, making storage and weighing tricky, so our post-crystallization drying cycles stretch longer than most. This keeps both bench chemists and kilo-lab preparers happy, avoiding the messy clean-ups after pipetting clumpy material.

    End Use and Application: Beyond Generalizations

    From firsthand conversations with research partners, the adoption of 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid runs the gamut from pharmaceutical R&D to agrochemical lead optimization. In pharmaceutical routes, chemists prize it for its activating effects in Suzuki and amide-coupling steps. The molecule survives harsh coupling conditions, with the chlorine offering an additional handle for further functionalization. This dual-reactivity profile shows up repeatedly in patent filings, particularly where researchers chase lead molecules with improved metabolic stability.

    Agrochemical developers lean on its trifluoromethyl group, which increases lipophilicity and bioactivity in new crop protection candidates. Over the years, production has responded to demands for larger batches—sometimes up to hundreds of kilograms—requiring process tweaks to maintain safety and batch homogeneity. Nobody gets a pass around here for delivering variable lots, especially when global regulatory requirements get stricter each year.

    Standing Apart from Other Pyridine Carboxylic Acids

    Users with firsthand product experience quickly appreciate the difference that a single position shift in trifluoromethyl or carboxyl groups can make. Compared with more commonly used isomers—such as 2-chloro-3-(trifluoromethyl)pyridine-5-carboxylic acid or 2-chloro-6-(trifluoromethyl)pyridine-3-carboxylic acid—the 5-position trifluoromethyl of this product lends different chemical attitudes in cross-coupling steps. This can mean increased selectivity or altered pharmacokinetics depending on the downstream application. In technical discussions, chemists frequently cite the reduced tendency toward byproduct formation during amidation and improved crystallinity after reaction workups.

    Production teams must remember that closely related isomers sometimes sneak into processes at outside suppliers. A proper manufacturing partner monitors for these side products, avoiding headache for their clients later on. In our process, specific purification steps weed out these cousin structures, and any lot failing to reach target purity on their own gets reprocessed. The trick comes from years spent fine-tuning synthetic steps and learning where even small temperature drifts or reagent excesses can throw off selectivity.

    Experience in Bulk Manufacturing: Lessons Learned

    Scaling up from grams in the lab to scores of kilograms brings its own set of challenges. High exotherms during chlorination require solid engineering controls and constant vigilance from process teams. Every worker who has handled the scale-up of this material knows the risk of localized over-reaction, so batch records log temperature at short intervals and keep a close eye on color and clarity changes in the reaction mixture.

    On the logistical side, granulation and drying facilities must avoid cross-contamination with structurally similar halopyridines. Tanks and lines receive thorough cleaning, all documented, before every run. For customers using the acid in regulated environments, traceability and recall readiness cannot become afterthoughts. Over time, robust data tracking and outside QA audits have become part of the daily routine. These measures keep our material compliant with the shifting landscape of chemical and safety regulations—protecting both our people and partners down the supply chain.

    Supporting Researchers with Real-World Solutions

    Real value for customers comes not just from a clean drum delivered on time, but from a living partnership with the client’s technical teams. Over the years, pharmaceutical innovators have requested custom batch sizes, unique packaging, or adjusted particle sizes. Each request generates internal discussion: drying time, drum linings, or sieving steps all affect the quality of final material. When one major client asked for sub-100 micron powder for improved solubility, an entire drying and sifting approach was validated from lab through full production to ensure performance in their downstream reactor.

    Maintaining open lines of communication lets the manufacturing side solve problems before they disrupt a critical synthesis. In practice, this means process teams remain responsive, replacing or reformulating shipments if stability or appearance shifts during transit. A recent batch destined for export changed color during ocean freight—a sure sign of air exposure. Rather than debate responsibility, we took back the entire lot for retesting and replaced it in record time with zero surcharge. Actions like that keep partners coming back, year after year.

    Documenting Quality, Not Just Selling It

    Documentation stands as more than a regulatory box to tick. Over many cycles, we have built a library of batch records, QA reports, and stability studies, providing deeper insight into lot-to-lot consistency and guideline compliance. For all lots of 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid, detailed reports accompany the shipment—containing full spectra, chromatograms, and impurity profiles. End-users benefit from this transparency, often sharing feedback for further specification tightening.

    Such data-driven approaches decrease the learning curve for customers piloting a new synthetic route. For some, the difference between a robust scale-up campaign and an early-stage failure boils down to the quality of supplied intermediates and the clarity of communication. Our documents open up our processes to scrutiny, and clients with strict regulatory submissions feel confident referencing these records in their own files.

    Handling and Storage: A Manufacturer’s Perspective

    Factories run better when raw materials behave predictably. That requires proper storage conditions—dry, sealed, and away from excessive heat. 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid handles well in this respect. Once dried post-crystallization, it resists atmospheric pickup of water, though longer-term field experience shows that extended exposure in high humidity will eventually lead to clumping. We keep drums lined and sealed with double gaskets for longer storage; most customers see no shift in handling for a year or longer if they keep the packaging closed.

    Anecdotal observations suggest the acid maintains its appearance and reactivity over field storage conditions much better than many halogenated analogues. Still, best practice dictates using a lot within twelve months of manufacture for key pharma or agrochemical applications, aiming for minimal change in appearance, flow, or reactivity that would otherwise compromise productivity on the user side.

    Looking to the Future: Trends and Potential Complications

    Recent years have seen a global tightening on permissible residues and process impurities, especially for active pharmaceutical intermediates and crop chemistry building blocks. Regulations frequently shift, with authorities in multiple countries updating lists of allowable trace elements and byproducts. This puts pressure on all manufacturers to audit not just their main synthesis, but also every raw material, solvent, and packaging item for potential liability.

    In practice, this means process safety and analytical testing sit front and center now more than ever. Research partners expect documentation on elemental impurities, solvent residues, and—if applicable—genotoxic impurities at levels far below thresholds seen a decade prior. Our manufacturing routines regularly incorporate these advanced tests, using modern equipment and participating in outside proficiency programs to validate methods and results.

    Material traceability can no longer operate as an afterthought. From the moment starting material stocks arrive on-site, tracking continues at every reaction, filtration, and drying step—ending only when the finished acid leaves our facility with a matching set of production and QA records. Manufacturers who slip here find themselves locked out of global supply chains, particularly those feeding into the most tightly regulated markets.

    Building Trust: The Human Touch

    What ultimately distinguishes a specialist manufacturer isn’t a fancy certificate or website claim—it’s the trust earned through years of reliable delivery and field-proven technical support. Many long-term clients reach out directly to discuss subtleties in their syntheses, ask detailed questions about trace impurity levels, or request updates to documentation in line with evolving regulations. These moments reflect real partnership, a level of open technical exchange that can’t be faked.

    Every batch of 2-Chloro-5-(trifluoromethyl)pyridine-3-carboxylic acid carries the weight of prior experience, close attention to technical change, and the commitment to take responsibility for performance, from drum to flask. In markets defined by speed and innovation, consistency and openness remain rare strengths. Over time, this approach shapes not just chemical supply, but the real progress chemists achieve with the raw materials we provide.