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HS Code |
132419 |
| Chemical Name | 5-bromo-2-chloro-4-(trifluoromethyl)pyridine |
| Cas Number | 122144-98-3 |
| Molecular Formula | C6H2BrClF3N |
| Molecular Weight | 260.44 |
| Appearance | White to off-white solid |
| Melting Point | 42-44°C |
| Density | 1.79 g/cm3 (estimated) |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents such as DMSO and DMF |
| Smiles | C1=CN=C(C(=C1Br)C(F)(F)F)Cl |
| Inchi | InChI=1S/C6H2BrClF3N/c7-4-2-12-3(8)1-5(4)6(9,10)11 |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Hazard Class | Harmful if swallowed or inhaled |
As an accredited 5-bromo-2-chloro-4-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 5-bromo-2-chloro-4-(trifluoromethyl)pyridine, sealed with a tamper-evident cap and labeled. |
| Container Loading (20′ FCL) | 20′ FCL container holds 12 MT of 5-bromo-2-chloro-4-(trifluoromethyl)pyridine, packed in 200 kg UN-approved drums. |
| Shipping | **Shipping Description:** 5-Bromo-2-chloro-4-(trifluoromethyl)pyridine should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport according to applicable regulations for hazardous chemicals. Required labeling and documentation should indicate potential irritant properties. Handle with care to avoid spills or exposure during transit. Store in a cool, well-ventilated area upon arrival. |
| Storage | Store 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep container tightly closed and properly labeled. Store away from incompatible substances such as strong oxidizers. Use appropriate chemical-resistant containers. Follow all relevant safety protocols and local regulations for hazardous chemical storage. |
| Shelf Life | 5-Bromo-2-chloro-4-(trifluoromethyl)pyridine is typically stable for 2-3 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 5-bromo-2-chloro-4-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and consistent compound quality. Melting Point 60–63°C: 5-bromo-2-chloro-4-(trifluoromethyl)pyridine with a melting point of 60–63°C is used in agrochemical research formulations, where it promotes stable dispersion and precise application. Molecular Weight 278.43 g/mol: 5-bromo-2-chloro-4-(trifluoromethyl)pyridine at a molecular weight of 278.43 g/mol is used in heterocycle coupling reactions, where it supports accurate stoichiometric calculations and efficient reaction progress. Water Content <0.5%: 5-bromo-2-chloro-4-(trifluoromethyl)pyridine with water content less than 0.5% is used in moisture-sensitive catalysis, where it minimizes side reactions and increases product purity. Stability Temperature up to 120°C: 5-bromo-2-chloro-4-(trifluoromethyl)pyridine stable at temperatures up to 120°C is used in thermal scale-up studies, where it maintains structural integrity and predictable performance. Particle Size <100 μm: 5-bromo-2-chloro-4-(trifluoromethyl)pyridine with particle size less than 100 μm is used in fine chemical blending, where it allows uniform mixing and optimized reaction kinetics. |
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Working in chemical synthesis means knowing how each compound fits into the bigger picture of a process chain—so every molecule counts. Among the specialty pyridines, 5-bromo-2-chloro-4-(trifluoromethyl)pyridine stands out for its essential role in advanced pharmaceuticals, crop protection, and high-performance material science. From experience on the production floor and in formulation labs, this compound’s structure—a pyridine ring featuring bromine, chlorine, and a trifluoromethyl group—enables precise and selective transformations that make it valuable in modern chemistry.
Our manufactured material consistently meets strict quality standards, designed for downstream reactions such as cross-coupling, nucleophilic substitution, and as a key intermediate in the synthesis of complex heterocycles. Typical material leaves our facility in the range of 98% to 99.5% purity, as per validated HPLC and NMR results. Colour and state remain consistent lot-to-lot: a white to off-white crystalline powder, powder flow characteristics tuned for automated dosing in both pilot and industrial scale syntheses. Moisture content and trace metal levels are tightly controlled, crucial for customers who run catalyst-sensitive processes.
Researchers and process chemists value this pyridine for more than its purity—it’s about how the halogen and trifluoromethyl functionality unlock reactivity. The bromine and chlorine atoms direct regioselective transformations, and the electron-withdrawing trifluoromethyl group not only improves metabolic stability for medicinal chemists but can tune properties in agrochemical molecules. Reproducibility, batch after batch, becomes a critical requirement for those scaling up: unexpected side products or fluctuating impurity profiles can ruin a week’s work. Years spent guiding new chemists through process troubleshooting taught us that a reliable supplier has to live up to the trust placed by development and manufacturing teams.
Scaling up halogenated pyridines isn’t just about following a textbook reaction. During our earliest production campaigns, phase separation issues, byproduct formation, and handling volatility of intermediates posed learning curves. Over several process improvements, we found that precise pH control and low-temperature crystallization minimized unwanted hydrodebromination. Strict monitoring of reaction exotherms, especially during halogen exchange steps, ensures quality. Our batch records reflect real adjustments driven by plant realities: a five-minute drift in holding temperature leads to color impurities; a momentary drop in agitation increases unreacted starting material. These are problems only hands-on work reveals.
Medicinal chemistry has become more focused on polar, halogenated motifs for target interactions, and this compound answers that need. The pyridine ring serves as a recognized pharmacophore, while trifluoromethyl and halogen substituents enhance target affinity and ADME properties. Contract research organizations rely on its performance during multi-step syntheses of kinase inhibitors, CNS-active agents, and more. On the agricultural side, this molecule has formed the base of several patented herbicide and fungicide actives, providing environmental stability and robust biological profiles. Over the past decade, we’ve collaborated with product development labs tuning formulation ratios and impurity benchmarks to keep up with evolving global regulations.
Many customers want to know what sets this compound apart from 2-chloropyridine or 4-trifluoromethylpyridine, both of which see heavy usage. The structural difference is no small matter. Bromo-chloro-trifluoromethyl substitution patterns unlock Suzuki, Stille, and Negishi couplings not possible with mono-substituted or unsubstituted analogs. This enables assembly of more complicated scaffolds with fewer protection/deprotection sequences and higher overall yields. Traditional mono-halopyridines often lead to regioisomer mixtures or mid-reaction stalling; we’ve seen our product outperform those standards repeatedly by delivering cleaner conversions and easier purification, especially at scale.
Handling this compound needs a deliberate safety approach, one we developed from actual plant experience. The halogen and trifluoromethyl groups confer low volatility under ambient conditions, so both operator exposure and environmental release risks remain minimal when standard containment is used. That said, even trace vapors can be irritating—proper local exhaust and personal protection works best. Waste solvent from purifications must meet halogenated organic disposal standards. We run regular waste stream characterization, not just to maintain compliance but to stay ahead of shifting regional frameworks. Easy as it can be to focus only on the target molecule, the real mark of sustainable production comes from these details.
Early efforts at manufacturing this compound sometimes produced inconsistent impurity profiles. By overhauling analytical support—adding GC-MS fingerprinting alongside routine NMR and HPLC—we reduced inter-batch variation to well below 0.5% for identified impurities. Simply running a single purity assay doesn’t catch unknowns; method validation and reference standard calibration matter for downstream users. A joint project with a European pharma partner led us to install a new moisture analyzer after a residual solvent batch failed to meet their ICH guidelines. These are the subtle but crucial infrastructure choices that lead to trust-based supply relationships.
Environmental standards tighten year after year, mandating lower volatility organic emissions and cleaner production. This motivates us to keep investing in greener solvents, recovery units, and alternative workup strategies. Several seasons back, a regional inspection highlighted solvent losses during fractional distillation—forcing us to convert the whole process to a closed-loop setup. Training operators on these changes goes hand in hand with physical upgrades. Product stewardship becomes more than paperwork—it’s something lived day to day. We take pride in watching the numbers from condenser output drop while yield stays high, a testament to combining chemistry know-how with practical engineering.
From years of direct technical support and site visits, the key lesson is clear: chemists need not only molecules, but advice rooted in practical experience. Process engineers scaling up for the first time have questions about stir rates, filtration aids, and whether a batch will clump during drying. We pass along not just theoretical knowledge, but real-world troubleshooting from our own process logs. Processing notes—like which grades of silica work best during purification, or how to completely dry out a stubbornly moist batch—make the difference between laboratory success and a full-scale hiccup. These details accumulate only over years.
No project can move forward without dependable delivery. Over time, we adapted our inventory strategy after hearing from contract manufacturers who had projects delayed by late or inconsistent shipments. Building up safety stock, qualifying second and third sources of raw materials, and investing in larger drying ovens cut lead times and let us promise—and deliver—faster shipments. Customers stay up to date on lot status, COA issuance, and site logistics, often visiting to witness production in person. Supply consistency is not about slogans—it comes from work done on the ground with attention to every factor influencing workflow.
Many users explore novel coupling or cyclization chemistry using challenging pyridines. This product’s electronic structure allows chemists to achieve transformations not otherwise accessible via cheaper or widely available building blocks. Our technical team has fielded dozens of calls regarding reaction optimization—whether it’s a tricky metal-catalyzed coupling or a multi-step alkylation. In response, we’ve assembled a set of troubleshooting guides and sample application notes based on real lab experience. Knowing how base selection, temperature profile, or order of addition influences yield can save teams enormous amounts of trial-and-error.
Feedback from customers has shaped our production and support practices more than any grand strategic plan. One key account flagged issues with particle size consistency during automated dispensing, prompting us to introduce a secondary milling and sieving step. From that update arose improved reproducibility across solid dosing instruments and less product wastage. Another customer required a certificate of analysis formatted to their ERP requirements—this led to retooling our data output and integrating digital batch records. Real market needs steer many of our updates, ensuring the product is not only high-purity but engineered for ease of use and reliable documentation.
Over the last five years, demand from the pharmaceutical and agrochemical innovation pipeline has pushed us to increase batch sizes and invest in new reactor systems. The compound’s growing use in the synthesis of new kinase inhibitors, insecticides, and advanced materials reflects how versatile, multi-functional building blocks have moved to the forefront of discovery chemistry. Innovation doesn’t only flow from university labs—process tweaks and new application methods often originate from feedback sessions with production chemists and pilot plant teams. That cross-pollination fuels product evolution.
Customers frequently turn to us for support with regulatory filings in the US, EU, or Japan when using this compound as a key starting material. Detailed impurity profiling, full traceability, complete analytical data sets, and transparent change control processes help streamline submissions. Experience with regulatory dossiers has taught us that full compliance is not just about product specs—documentation matters as much as the molecules themselves. We have worked side by side with customers on impurity qualification, impurity fate studies, and even on-site audits, giving peace of mind that every batch meets the letter and spirit of regulatory expectations.
Other substituted pyridines often suffer from limited reactivity or less predictable outcomes in functionalization steps. Through years of comparative trials, we have seen 5-bromo-2-chloro-4-(trifluoromethyl)pyridine stand out. Its dual-halide and trifluoromethyl arrangement gives synthetic chemists a greater toolkit—allowing for sequential halide exchange, site-specific metalation, and late-stage derivatization. Many commercial alternatives fail under the same conditions, with catalysts poisoned or isomerization occurring. The molecular architecture we produce holds up to rigorous screening, letting customers push forward on shorter timelines and with fewer headaches.
Our vision has always focused on building relationships, not transactions. Direct feedback from synthetic chemistry teams, production operators, and analytical specialists shapes how we prioritize investments and process tweaks. Partnering often means sending extra samples to facilitate testing, opening plant doors for audits, and sharing parts of our own process development journey. A two-way dialogue uncovers needs we would otherwise miss, from packaging preferences to documentation updates and logistics support. Over time, mutual trust proves more durable than batch-to-batch competition—the market rewards those who earn it through action.
Inevitably, production hits speed bumps: raw material shortages, sudden shifts in regulatory limits, unexpected analytical discrepancies. What matters is response speed and transparency. Our staff tracks every deviation or issue, updating customers proactively and rolling out countermeasures where possible. Once, a sudden region-wide shortage of a key halogen source jeopardized several batches; instead of delaying shipments indefinitely, we leveraged site inventory and reprioritized synthetic routes to meet existing purchase orders on time. Customers knew the situation the moment we did, with regular updates until deliveries resumed as normal. Working through these situations builds resilience and a level of trust no brochure can capture.
Having produced and supported customers’ programs based on 5-bromo-2-chloro-4-(trifluoromethyl)pyridine for many years, the value of specialty manufacturing becomes clear. Process control isn't just a technical requirement—it's at the heart of delivering reliable, user-friendly, and innovative building blocks for scientific progress. Every batch reflects our practical knowledge, continual learning, and dedication to quality, safety, and partnership. The results show up not only in assay values but in the long-term successes of the chemists, engineers, and companies who trust our material in their breakthrough projects.