2-Chloro-5-(trifluoromethyl)pyridine)

    • Product Name: 2-Chloro-5-(trifluoromethyl)pyridine)
    • Chemical Name (IUPAC): 2-chloro-5-(trifluoromethyl)pyridine
    • CAS No.: 5524-55-2
    • Chemical Formula: C6H3ClF3N
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    552652

    Product Name 2-Chloro-5-(trifluoromethyl)pyridine
    Cas Number 55290-64-7
    Molecular Formula C6H3ClF3N
    Molecular Weight 181.54 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 162-164 °C
    Melting Point -9 °C
    Density 1.43 g/cm3
    Refractive Index 1.447
    Purity Typically ≥98%
    Solubility Soluble in organic solvents, insoluble in water

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2-Chloro-5-(trifluoromethyl)pyridine, with a secure screw cap and hazard labeling.
    Container Loading (20′ FCL) Container loading (20′ FCL) for 2-Chloro-5-(trifluoromethyl)pyridine typically allows safe transport of about 10–14 metric tons securely packed.
    Shipping 2-Chloro-5-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. Classified as a hazardous chemical, it is transported according to international regulations (UN number 3276), requiring appropriate labeling and documentation. Package integrity is verified before dispatch to ensure safe delivery and prevent leaks or exposure during transit.
    Storage 2-Chloro-5-(trifluoromethyl)pyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Store separately from incompatible materials such as strong oxidizers and acids. Ensure proper labeling, prevent moisture ingress, and use secondary containment to avoid leaks or spills. Handle under fume hood if possible.
    Shelf Life 2-Chloro-5-(trifluoromethyl)pyridine typically has a shelf life of 2-3 years when stored in a cool, dry, tightly sealed container.
    Application of 2-Chloro-5-(trifluoromethyl)pyridine)

    Purity 99%: 2-Chloro-5-(trifluoromethyl)pyridine) with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Stability temperature 120°C: 2-Chloro-5-(trifluoromethyl)pyridine) stable up to 120°C is used in agrochemical formulation processes, where it maintains structural integrity during high-temperature reactions.

    Low moisture content <0.5%: 2-Chloro-5-(trifluoromethyl)pyridine) with low moisture content is used in fine chemical manufacturing, where it reduces the risk of hydrolysis and impurity formation.

    Molecular weight 181.54 g/mol: 2-Chloro-5-(trifluoromethyl)pyridine) with a molecular weight of 181.54 g/mol is used in electronic material synthesis, where it allows precise stoichiometric calculations for doping processes.

    Melting point 30-32°C: 2-Chloro-5-(trifluoromethyl)pyridine) with a melting point of 30-32°C is used in organic synthesis labs, where it offers ease of handling and fast solid-to-liquid transitions.

    Assay ≥98%: 2-Chloro-5-(trifluoromethyl)pyridine) with assay of at least 98% is used in API precursor development, where it delivers reliable reactivity and reproducible batch results.

    Particle size <100 μm: 2-Chloro-5-(trifluoromethyl)pyridine) with particle size under 100 μm is used in catalyst preparation, where it increases surface area and improves catalytic efficiency.

    Colorless liquid form: 2-Chloro-5-(trifluoromethyl)pyridine) in colorless liquid form is used in dye synthesis, where it minimizes color contamination and improves color clarity in final products.

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    Certification & Compliance
    More Introduction

    2-Chloro-5-(trifluoromethyl)pyridine: Reliable Building Block for Modern Chemistry

    A Manufacturer’s Perspective on a Trusted Pyridine Derivative

    As chemists who spend their days in the heart of synthesis, we understand how a single unexpected impurity can hold back an entire route. Over the years, our team has focused on producing 2-Chloro-5-(trifluoromethyl)pyridine to meet the specific demands of medicinal chemistry, agrochemicals, and advanced materials research. We've worked through the night guiding batches, running QA checks, and collaborating across research and operations — all to make sure each drum leaving our floor does what it’s meant to.

    This compound, with the model designation 695-35-4 based on its CAS number, offers both structural and performance advantages that set it apart in a crowded field of pyridine derivatives. In the past decade, we’ve watched synthetic routes evolve; chemists want less hassle in halogenation, more control over electron distribution, and a straightforward path to downstream chlorination or fluorination. Our production process has evolved as well, with ongoing investment in reactors that allow fine-tuning at each synthesis stage.

    Specifications and Production Standards

    We produce 2-Chloro-5-(trifluoromethyl)pyridine to purities exceeding 98.5%, targeting the professional community who can’t afford stalled projects. Each batch is produced in closed systems with in-line analysis, using NMR and GC-MS for confirmation. We understand why our partners pay attention to trace moisture and amine residues, so we tightly control filtration and drying conditions. Our experience has taught us that even a slight deviation in temperature or feed ratio during the chlorination phase can introduce side products. Batch records are reviewed by a master chemist before release, not just a technician checking boxes.

    We handle packaging in fluoropolymer-lined drums or aluminum bottles to maintain quality from our site to your fume hood. Changes in pressure, temperature, or static can accelerate decomposition in less robust packaging. We routinely ship to labs where tight storage windows demand stability and safety.

    The Role in Synthetic Chemistry

    This molecule plays a central part in crafting molecules where the trifluoromethyl group delivers unique physicochemical properties — boosting metabolic stability in drug candidates, shifting pKa in catalysts, and conferring hydrophobicity in materials science applications. Organofluorine chemistry keeps growing for a reason. In our own process refinement, we see how the electron-withdrawing effects of both the chlorine and trifluoromethyl working together on the ring influence downstream reactivity in palladium-catalyzed coupling, SNAr displacement, and further halogenation.

    Medicinal chemists rely on subtle electronic adjustments to optimize receptor binding or modulate solubility in new drug candidates. Agrochemical innovators focus on environmental stability and selective toxicity. In electronic materials, stability under varied conditions takes priority. Over years of feedback from bench chemists, it’s become clear that this compound fits that sweet spot — easy to convert into a range of functional groups, yet robust enough for storage and complex multi-step synthesis.

    Reliability and Traceability: Why Manufacturers Matter

    We’ve found many clients can’t get the same peace of mind from intermediaries that they get from source manufacturers. We work with traceable raw material batches, and our process maps show every step from raw feedstocks to finished product. Some years, we’ve had to rebuild our packaging lines after learning about tiny leaks that affected long-haul shipments. The headaches from off-spec returns have taught us that traceability isn’t just a buzzword — it’s what stands between a successful synthesis and wasted time.

    Direct contact between our R&D chemists and end-users often leads to subtle process improvements. A case comes to mind where a customer faced reactivity issues in a Buchwald–Hartwig amination; after receiving a batch sample, we traced the root cause to micro-level hydrolysis during extended transport in humid conditions. Adjusting our in-line drying and switching to low-permeability packaging solved the problem.

    Comparing 2-Chloro-5-(trifluoromethyl)pyridine to Similar Products

    Within the pyridine family, even minor changes — such as the position of the chlorine or trifluoromethyl group — can change the course of a synthetic plan. Unlike 2-Chloro-6-(trifluoromethyl)pyridine, which comes with steric challenges when introducing bulky substituents at C6, the 5-position offers distinct advantages for cross-coupling reactions. In our workflows, we’ve observed shorter reaction times and higher yields during Suzuki and Buchwald–Hartwig reactions with the 5-(trifluoromethyl) isomer.

    Commercial chloro-pyridines lacking a trifluoromethyl group often fall short on stability and offer less versatility when it comes to building more complex molecules. Feedback from discovery chemists points again and again to the role of the -CF₃ as a metabolic shield. In challenging oxidizing environments, simple chloropyridines degrade, yet the trifluoromethylated analogues resist breakdown. Some of our partners have tested our product against basic 2-chloropyridine and observed higher photostability and lower risk of hydrolysis in primary screens.

    Our production line is set up to avoid carryover contamination from other fluorinated intermediates, as trace compounds from side production can alter downstream analytical results. Laboratories seeking only generic grade material may opt for mainstream 2-chloropyridine; those developing IP-sensitive pharmaceuticals or crop protection products choose the 5-(trifluoromethyl) version for its impact on selectivity and performance.

    Alignment with Today’s Market Requirements

    Over the past five years, tighter purity standards have swept through our customer base, from regulatory shifts in the pharmaceutical sector to new REACH requirements in Europe. We operate our synthesis under ISO guidelines and participate in third-party audits regularly. Simple compliance documents do not impress seasoned chemists; they ask questions, challenge numbers, and request in-person facility reviews. Our team welcomes this scrutiny, as we find that those challenging conversations help us push our process to higher levels of performance.

    Scalability matters as much as purity. When formulators trial a hundred grams in early-stage screens, there’s a temptation to overlook minor inconsistencies that don’t surface until pilot scale. We’ve scaled our reactors and refining columns to deliver consistent product from kilogram to metric ton quantities. Chemists who have scrambled to secure enough material for a process validation run appreciate the comfort of knowing we retain control over every element, from scheduling to shipment.

    Regulatory landscapes keep shifting. We have shifted our process chemistry from traditional chlorination agents to more environmentally responsible alternatives, reducing chlorinated waste streams. Some processes that looked fine for milligram runs raise serious questions when attempted at commercial batch sizes. Our process engineers have worked hands-on with regulatory consultants to eliminate benzene-based solvents and to introduce closed-vessel workup, protecting both staff and environment. For us, sustainable production means more than meeting minimum standards — it’s about keeping our team and the wider community safe.

    Supporting Discovery and Scale-Up Programs

    Compound libraries in pharmaceutical companies often need subtle modifications for structure-activity relationships. We see the requests for derivatives and analogs where a reliable starting point is essential. By offering consistent batches of 2-Chloro-5-(trifluoromethyl)pyridine, we help discovery teams quickly build and modify target molecules. Some discovery groups share anecdotal stories about late-stage batch failures with generic suppliers; these situations reinforce the value of sourcing from original manufacturers with proven track records and open process documentation.

    For scale-up and process chemistry teams, product robustness matters more than any certificate. During process transfer from lab to pilot plant, small changes in in-process controls can expose unseen vulnerabilities in the intermediate supply chain. Our in-house technical team frequently collaborates with customers during tech transfer, sharing data on product stability, analytical profiles, and solvent interactions to minimize surprises. Shared process knowledge, especially around reactivity with nucleophiles and moisture sensitivity, supports rapid problem solving. We have solved issues ranging from solvent incompatibility to unforeseen byproducts by picking up the phone to speak directly with end-users — a layer of support traders and distributors don’t offer.

    Building on Experience, Learning from Feedback

    As a chemical manufacturer, we learn the most from field problems, not textbook successes. Sometimes, an entire campaign hinges on a rarely encountered impurity or a packing flaw undetected by standard analysis. Last year, a customer’s DMSO-d6 NMR analysis picked up a trace signal corresponding to an ultra-low impurity introduced during end-stage precipitation. Our technical and QA teams worked through the night, running complementary TLC and HPLC experiments, until we tracked it back to a rarely-outgassing valve in our solvent recovery process. Modifying that step led to cleaner product, faster workups, and one less point of failure in our partners’ downstream workflow.

    We regularly collate feedback from analytical and synthetic labs around the world, cross-referencing data, and adjusting our process. One recurring request focused on lower water content for use in organometallic couplings. By tightening our post-synthesis drying parameters and introducing real-time Karl Fischer testing, we’ve reduced average water content to below 0.03%. In another case, a long-standing client in crop chemistry needed assurance on the absence of aromatic amines due to regulatory reporting. We responded by refining in-line monitoring to catch minute amine traces long before bulk QC testing.

    Applications Driving Demand

    The application landscape for 2-Chloro-5-(trifluoromethyl)pyridine keeps expanding. Leading pharmaceutical labs leverage this building block for pipeline drugs aimed at new protein targets. In agricultural R&D, it supports new generations of selective herbicides and seed treatments engineered for environmental persistence and crop compatibility. Materials scientists investigate its behavior in designing monomers and specialty polymers, especially where chemical resistance is prized.

    Our material participates in key cross-couplings, nucleophilic substitution, and direct arylations. The trifluoromethyl group’s strong field effect enhances activity in biologically active molecules. Chemists value the balance of electron-withdrawing and lipophilic properties, using this molecule to boost both efficacy and pharmacokinetic profiles in animal models. In pilot and commercial settings, process chemists appreciate the consistency that allows clear, understandable batch-to-batch behavior. This might seem like a technical detail, but experienced teams know it often spells the difference between a shelved candidate and a product that makes it to market.

    Handling and Storage Insights from Manufacturing

    Practical handling experience shapes every formulation guide we offer. 2-Chloro-5-(trifluoromethyl)pyridine keeps best in airtight containers, out of direct sunlight, and away from open flame. We’ve learned not all caps and seals are made the same — improper closure or cheap liner material leads to slow pressure build, product discoloration, or corrosion at the interface. Within our facility, drums and canisters rest on temperature-controlled pallets, and each batch receives a unique identifier to track exact storage history.

    We encourage end-users to check for subtle changes in viscosity, color, and slight odour shifts, as these often signal tiny shifts in purity or stability. Years of experience have shown that maintaining low humidity and preventing repeated opening make a measurable difference in shelf life. In scale-up, even minor contamination during transfer can change the course of a synth. Our advice always lands on prevention, not remediation — tight cap closure, inert gas blanketing, and stabilized storage temperature form the backbone of effective use.

    What Sets Us Apart in Supplying 2-Chloro-5-(trifluoromethyl)pyridine

    Many buyers look for the cheapest price or fastest lead time. We have seen, time and again, that this gamble often ends with lost weeks, scrapped material, and disappointed research leads. Our team brings together years of cumulative manufacturing experience. We’ve tuned ourselves to the consequences of every variable in the synthetic path — from reaction vessel material and agitation rates to the mechanics of decanting.

    When chemists deal directly with manufacturers, they get a straight line to technical know-how. We offer transparency about our synthesis, purification, and packaging protocols. Unlike third-party sellers, we resolve questions through direct dialogue, not just a PDF or template COA attachment. For repeat clients, we accommodate project-driven changes in batch size, storage needs, and even custom analytical requirements, because flexible support reduces project risk.

    From our vantage point, trust grows by solving real-world problems. Our internal drive for quality stems as much from pride as from regulatory demand. Meeting current standards serves as a launchpad for continual improvement in safety, sustainability, and performance. Our direct engagement with customers often raises the bar inside our own operation; a bottleneck in your process quickly becomes our next optimization project.

    Summary: The Role of Directly Manufactured 2-Chloro-5-(trifluoromethyl)pyridine in Advanced Chemistry

    The chemistry community’s expectations continue to evolve — smarter materials, safer production, and faster timelines to innovation. 2-Chloro-5-(trifluoromethyl)pyridine bridges early discovery and manufacturing, provided it comes with traceability and a real partnership. Daily, we see the impact of disciplined manufacturing: improved yields, cleaner spectra, and researchers with one less supply headache. By building our know-how batch by batch, and listening to both established partners and early-career researchers, we aim to deliver more than just a commodity — we provide a trusted tool for advancing the future of chemistry.