6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester

    • Product Name: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester
    • Chemical Name (IUPAC): methyl 6-(trifluoromethyl)pyridine-2-carboxylate
    • CAS No.: 352018-76-5
    • Chemical Formula: C8H6F3NO2
    • Form/Physical State: Liquid
    • 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

    173261

    Product Name 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester
    Cas Number 766557-02-6
    Molecular Formula C8H6F3NO2
    Molecular Weight 205.13 g/mol
    Appearance Colorless to light yellow liquid
    Purity Typically ≥ 98%
    Boiling Point 219-220°C
    Density 1.37 g/cm³
    Smiles COC(=O)c1cccc(n1)C(F)(F)F
    Inchi InChI=1S/C8H6F3NO2/c1-14-8(13)6-3-2-4-12-7(6)5(9,10)11/h2-4H,1H3
    Solubility Soluble in most organic solvents
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Refractive Index n20/D 1.481

    As an accredited 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in a sealed 25g amber glass bottle, labeled with product name, purity, hazard symbols, and storage instructions for laboratory use.
    Container Loading (20′ FCL) 20′ FCL loads 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester in secure drums or bags, ensuring safe, efficient bulk transport.
    Shipping **6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester** should be shipped in a tightly sealed container, protected from light and moisture. Package according to all applicable regulations for hazardous chemicals, including appropriate labeling. Transport at ambient temperature unless otherwise specified. Ensure compatibility with shipping materials and include safety documentation (SDS) with the shipment.
    Storage Store **6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester** in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep container tightly closed when not in use. Store separately from incompatible substances such as strong oxidizers and acids. Use appropriate chemical storage containers made of materials compatible with esters and fluorinated compounds.
    Shelf Life 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester is stable for at least two years when stored in a cool, dry place.
    Application of 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester

    Purity 98%: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures superior reaction yield and product consistency.

    Melting Point 56-58°C: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester with melting point 56-58°C is used in organic synthesis, where defined melting behavior aids in controlled crystallization and formulation processes.

    Molecular Weight 205.15 g/mol: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester of molecular weight 205.15 g/mol is used in agrochemical research, where exact molecular mass supports accurate formulation and dosing.

    Stability Temperature up to 80°C: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester with stability temperature up to 80°C is used in chemical process optimization, where thermal stability allows for safe handling under moderate reaction conditions.

    Particle Size < 50 µm: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester with particle size < 50 µm is used in high-precision analytical applications, where fine particle size provides improved dissolution rates and homogeneous mixture preparation.

    Water Content < 0.5%: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester with water content < 0.5% is used in moisture-sensitive reactions, where minimal water presence reduces side reactions and enhances final product quality.

    GC Assay ≥ 99%: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester with GC assay ≥ 99% is used in API development, where high assay by gas chromatography guarantees analytical traceability and regulatory compliance.

    Residual Solvents < 0.1%: 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester with residual solvents < 0.1% is used in finished product manufacturing, where low solvent content meets stringent safety and purity requirements.

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    Certification & Compliance
    More Introduction

    6-Trifluoromethyl-pyridine-2-carboxylic Acid Methyl Ester: A Manufacturer’s Perspective

    Introduction to a Distinctive Intermediate

    Producing 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester brings both technical challenge and a sense of pride to our team. Those in pharmaceutical, agrochemical, and materials science fields know how a single compound can influence the output and efficiency of a whole production chain. This ester, CAS 31574-18-4, stands out among pyridine derivatives for its trifluoromethyl group, lending increased metabolic stability and altered electronic properties—a marked difference from many non-fluorinated counterparts and even from similar pyridine esters. The chemistry of fluorination doesn’t forget nuances; it impacts reactivity and downstream applications in ways that traditional esters rarely replicate.

    Insight into the Chemistry and Production Challenges

    Manufacturing this compound goes beyond simple esterification or carboxyl group manipulation. In practice, synthesis is more than a handful of steps; it demands precise control of temperature, careful management of reagents like methylating agents, and rigorous exclusion of water. One misstep and impurities form—impurities that could reduce yields or complicate purification. The trifluoromethyl group creates synthetic hurdles, particularly in controlling regioselectivity and avoiding defluorination under strong conditions. We scale up using equipment lined for resistance to aggressive fluorinated intermediates, and each batch runs with multi-point quality checks. Over time, we’ve learned not to underestimate the impact of minor variables—solvent grade, stirring rates, even pressure variances. These practical realities influence both consistency and safety, from pilot scale to full production runs.

    Why Structural Features Matter in Application

    The appeal for many researchers and manufacturers lies in the unique balance between lipophilicity and electron-withdrawing effect that the trifluoromethyl group imparts. In drug discovery, improved metabolic stability often means longer half-lives for active compounds incorporating this ester as a building block. In crop protection formulas, the robust structure counters rapid hydrolysis, maintaining the active principle’s persistence on foliage or in soil. Those using non-fluorinated methylpyridine esters often encounter issues of rapid breakdown or lower activity, while this compound stands as a solution where durability is essential.

    We routinely work with formulation teams who specify this intermediate for their ring-opening or cross-coupling reactions, reporting cleaner reaction profiles and higher selectivity. Having the methyl ester instead of an acid or an amide often facilitates easier transformations under milder conditions, saving production time and reducing waste. These solid results in process chemistry are not just laboratory theory—years of customer feedback and our own pilot trials reinforce them.

    Pushing Standards in Purity and Process

    As chemical manufacturers, the pressure comes from knowing small variations can shift the entire reactivity or safety profile of a substance. For this trifluoromethylated methyl ester, color, odor, and melting range alone do not speak to quality—a misconception for manufacturers less experienced in fluorinated heterocycles. High-pressure liquid chromatography, NMR, and mass spec analyses are necessary, each iteration indicating where the purification route needs recalibration. Without these checks, co-eluting byproducts from incomplete trifluoromethylation or side-reactions might creep in, risking the reproducibility of downstream syntheses. Our team implements periodic validation of analytical protocols, recognizing that aging equipment or subtle changes in calibration standards could impact detection. Analogues without the same substitution pattern generally tolerate broader impurity specs; in this business, that level of laxity leads to failure in critical end-use steps.

    Although some chemical resellers and intermediates suppliers focus mostly on batch-to-batch price, our experience says long-term relationships rely on robust lot data, open communication, and quick troubleshooting. We share spectral data with customers, and on occasion, a batch with less than optimal clarity or an atypical impurity triggers an investigation—not finger pointing, but root-cause analysis. As a manufacturer, accountability is direct and personal, spanning from reactor operator to QC chemist to product manager. These relationships shape our standards for this product and have raised the bar for all our pyridine esters.

    Safety, Handling, and Environmental Responsibility

    Working at the manufacturer level, daily contact with fluorinated compounds reinforces the need for caution and oversight. Many outside the plant underestimate the volatility or reactivity of these intermediates. Spills are rare because staff work with full knowledge of exposure limits and proper PPE, not just for individual safety but for environmental containment. Waste management takes on added urgency because fluorinated residues resist breakdown and challenge typical treatment protocols. We treat spent solvents and washings separately, tracking them through the facility, and work steadily to reduce overall waste volume per unit product.

    Customers sometimes ask about “green chemistry” adaptations or alternatives, and this is where we draw on direct experience. We use closed systems for solvent transfers and run energy audits on our reactors annually, looking for potential reductions in heating and cooling demands. Routes under development prioritize minimal byproducts and, where feasible, solvent recycling. Not every fluorine or methyl operation will be fully sustainable, but steady incremental improvement toward greener standards is part of our ongoing commitment.

    Why Experienced Manufacturing Matters for Complex Pyridine Esters

    The intricacies of fluorine chemistry play out not just in a technical sense, but also economically. 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester draws higher development costs at the front end, often requiring custom synthesis capacity. Earlier in our manufacturing journey, we underestimated the maintenance cycles for gaskets and pumps exposed to aggressive intermediates, resulting in unplanned downtime and higher repair costs. Years of troubleshooting and process optimization have cut these costs over time, but we remain vigilant—experience shows where potential failure points could impact safety, output, or customer confidence.

    The process also requires tighter supplier control for raw materials. Not all methylating agents perform equally, and minor contaminations in fluorinating agents lead to batch loss or extended rework. Routine supplier audits and specification updates help secure consistent quality at scale. The complexity of this product sets it apart from simpler pyridine esters or unsubstituted methyl esters, where bulk chemicals sometimes mask underlying process weaknesses. For this compound, weaknesses become obvious quickly—either in yield, impurity profile, or stability under storage.

    Application in Synthesis and Innovation

    One of the highlights for chemists developing novel pharmaceuticals is the versatility of this methyl ester as a synthetic intermediate. The electron-withdrawing trifluoromethyl group not only shifts pKa values but alters the molecular recognition profile in ligand-based discovery. Our end-users, mainly in R&D or scale-up environments, choose this product for building blocks in kinase inhibitors, anti-infectives, or complex crop protection agents.

    Process chemists report that the methyl ester function allows rapid hydrolysis to the acid or transformation to amides, nitriles, or other esters under finely controlled conditions. The combination of reactivity, stability, and downstream compatibility often outpaces other available esters. Our own process trials mirror these experiences—shorter reaction times and fewer purification challenges compared to less specialized esters.

    Having direct control over production means we can respond early to requests for custom modifications, whether a deuterated version for metabolic tracing or a multi-kilogram scale order with tighter impurity specs. The dialogue with customer teams continually improves our understanding of how the product enables high-value transformations downstream. That feedback loops directly into the way we tune batch size, quality assurance, and even storage facilities.

    Differentiation from Other Pyridine Derivatives

    The chemical landscape is crowded with pyridine derivatives, but few offer the structural features and practical handling insights of 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester. Substituting a methyl group for a trifluoromethyl, or shifting the ester function to another position on the ring, alters reactivity and process compatibility. Classic methylpyridine esters often fall short in thermal and chemical stability during higher-temperature steps. Some manufacturers try to push generalized pyridine esters as one-size-fits-all intermediates, but field reports speak otherwise; end-products that fail regulatory criteria or lack shelf life have costly implications. Our extensive production and troubleshooting record with this trifluoromethylated ester underscores the need for careful matching of intermediates to the specific downstream chemistry.

    For those working in halogenated heterocycle synthesis, trifluoromethyl groups display increased resistance to metabolic breakdown and oxidative degradation. This property carries practical advantages in active ingredient design for both pharmaceuticals and agrochemicals. Other options may include difluorinated analogues or non-fluorinated esters, but such substitutions often result in lower biological activity or premature breakdown in use conditions.

    Commitment to Technical Support and Collaboration

    As producers, our commitment doesn’t end with an invoice or shipping notice. We work closely with clients to resolve any doubts about application methods, storage needs, or analytical procedures. Sometimes an off-specification analytical result or an unexpected solubility profile points to an edge case in formulation—these challenges are chances to improve. Clients reach out for support not just during early project phases but well after their own product launch, seeking insights or troubleshooting advice that only a manufacturer with direct synthesis and QC experience can provide.

    Internal knowledge sharing plays a strong role in how we structure support. Production chemists and quality assurance teams log unexpected findings systematically, so expertise builds up and is shared instead of being lost as personnel change. Our customers benefit from this institutional memory in questions concerning new transformations, alternative solvents, or analytical checks for trace impurities. This expertise differentiates direct manufacturers—materials suppliers trading only on inventory don’t carry the same level of practical background or resolve process quirks as rapidly.

    Managing Supply Chain and Scaling Challenges

    Running a plant that produces specialty pyridine esters means responding quickly to fluctuations in supply or demand. Global disruptions over the past years have shown how quickly raw material routes can become unavailable or delayed. For this ester, reliance on pure starting materials and qualified reagents means stockpiling beyond just-in-time models; extended lead times for fluorinating agents or methyl sources form a key point of contingency planning. Coordination between procurement, logistics, and technical staff keeps the line running and orders fulfilled even during challenging periods.

    Routine preventative maintenance on synthesis and handling equipment reduces the risk of unplanned shutdowns. Batch production scheduling, blending, and tank cleaning cycles are set up to minimize cross-contamination and maximize throughput, while separate filling and packaging rooms keep exposure risks low. These operational strategies take years to refine and are informed directly by experience with fluorinated compounds, which can clog, corrode, or otherwise compromise standard plant infrastructure.

    What Long-Term Experience Delivers to Users

    Clients ordering this intermediate receive more than just a drum or flask of chemical. They gain access to the cumulative expertise of a team attentive to purity, application, and handling concerns. Numerous process improvements over the years—optimized workup protocols, new purification steps, solvent recycling initiatives—have translated into fewer product recalls and higher end-user satisfaction. Our laboratory follows stability testing protocols tailored for this ester, tracking the integrity of each batch under differing storage and transit conditions. The resultant confidence shortens development cycles and allows clients to move smoothly from bench to kilo-lab to plant scale.

    Periodically, end-users request unique grades for specific applications, such as higher purity levels for regulated pharma production or alternative solvent systems for specialized reactions. Our ability to adapt protocols and deliver flexible batch sizes stems from the core knowledge base developed on the production line—not marketing abstractions. Where academic or generic suppliers often struggle to trace impurity sources or explain production inconsistencies, we leverage process records and analytical archives to resolve issues at their roots.

    Trends and Future Directions

    No specialty chemical market stays static—customer expectations and regulatory guidelines continue to tighten, especially for compounds used in human or environmental applications. We continually monitor the literature and reach out to R&D chemists developing next-generation processes involving new trifluoromethylation methods, green solvent approaches, or continuous processing. Expanding scale production while maintaining quality benchmarks presents an ongoing challenge—and competitive opportunity. Surging demand for fluoroaromatics in drug, materials, and technology sectors drives us to invest not just in larger reactors, but in better emission controls and process safety upgrades.

    Sustainable chemistry guidance grows more relevant with each passing year. Our experience suggests that effective progress begins with solvent reduction and energy minimization, but continues through to waste tracking and potential closed-loop recycling. Early trials with renewable solvent systems or reduced-waste workups sometimes fail, but learnings feed into future design and equipment purchase decisions. Increased transparency—batch histories, analytical data, emissions control—forms part of E-E-A-T best practices, earning trust with clients and regulators alike.

    Leveraging Direct Manufacturer Knowledge

    Producing 6-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester at commercial scale requires more than following a recipe. Years of investment yield a product line trusted not only for physical consistency, but for the cascade of real-world insight that backs each shipment. In a shifting regulatory and market landscape, choosing material right from a manufacturer means having a direct line to the people who understand the compound’s chemistry, processing requirements, and optimal use cases. This unimpeachable chain of custody and accumulated best practices grants customers reliability unavailable from intermediaries.

    From the reactor to the customer loading dock, every step in the process reflects experience, commitment, and a willingness to engage with evolving technical needs. As we continue refining production and application, it’s clear that understanding the nuances of fluorinated pyridine esters like this one benefits everyone—from the formulation chemist seeking reproducible results, to the regulatory officer assessing batch records, to the end user applying advanced active ingredients in real-world scenarios.