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HS Code |
501255 |
| Product Name | 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine |
| Cas Number | 658118-93-5 |
| Molecular Formula | C6H3BrF3NO |
| Molecular Weight | 257.00 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CN=C(C(=C1O)Br)C(F)(F)F |
| Inchi | InChI=1S/C6H3BrF3NO/c7-4-3(6(9,10)11)1-2-12-5(4)8/h1-2,8H |
| Storage Conditions | Store at 2-8°C, dry, tightly sealed |
| Synonyms | 5-Bromo-2-hydroxy-4-trifluoromethylpyridine |
As an accredited 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25-gram amber glass bottle, sealed with a screw cap, and labeled with safety and identification information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine: Securely packed in drums, maximizing space, ensuring safe transit, compliant with chemical transport regulations. |
| Shipping | 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It should be handled as a hazardous chemical, following all relevant safety and regulatory guidelines. Shipping typically occurs via ground or air, compliant with international dangerous goods regulations (such as IATA and DOT standards). |
| Storage | Store 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, sources of ignition, and incompatible substances such as strong acids, bases, and oxidizing agents. Protect from moisture and store at room temperature. Label clearly and handle only with appropriate protective equipment in compliance with relevant safety guidelines. |
| Shelf Life | 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine is stable for at least 2 years when stored in a cool, dry place. |
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Purity 98%: 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction selectivity and product yield. Melting Point 142°C: 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine with a melting point of 142°C is used in active pharmaceutical ingredient (API) development, where it contributes to formulation stability during processing. Particle Size < 50 μm: 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine with a particle size less than 50 μm is used in fine chemical manufacturing, where it enhances dissolution rates and process uniformity. Moisture Content < 0.5%: 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine with moisture content below 0.5% is used in agrochemical formulation, where it prevents hydrolytic degradation during storage. Stability Temperature up to 80°C: 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine with stability up to 80°C is used in organic synthesis workflows, where it maintains compound integrity under elevated temperature conditions. |
Competitive 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine prices that fit your budget—flexible terms and customized quotes for every order.
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People often imagine chemical manufacturing as process charts and numbers, but real value lives beyond the batch sheet. On our shop floor, we work daily with advanced intermediates, and 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine stands out in both the reaction vessel and its applications. Over the years, we’ve worked intimately with this unique pyridine derivative — from selecting raw bromine and trifluoromethyl sources to controlling critical reaction parameters unique to its synthesis. The chemistry has never been academic for us. Each batch has revealed much about the product’s strengths and the subtle pitfalls that can accompany this particular substitution pattern.
This compound, known in our process area by its shorthand, often serves as a linchpin in creating more complex molecules within pharmaceuticals, agrochemicals, and specialty organic schemes. The halogenation and subsequent trifluoromethylation of pyridines is not trivial. Our team has experimented and optimized the route for years, always seeking cleaner reactions and minimal side products. We learned early that even slight deviations in moisture or reaction temperature shift the purity spectrum, and we've refined our controls — maintaining high standards batch after batch. These lessons came directly from running hundreds of syntheses, not from speculative papers or distributor catalog blurbs.
Working up close with 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine, it's clear the arrangement of functional groups offers a rare mix of reactivity and selectivity. The bromine at position 5 influences the activation of the aromatic ring, guiding downstream transformations reliably. That makes it valuable where targeted coupling or halide exchange matters. Unlike monosubstituted pyridines, or even some 2,5-disubstituted analogues, the extra electron-withdrawing nature provided by the trifluoromethyl group at position 4 supports dense electron-deficient intermediates, which means the product works well in cross-coupling and nucleophilic aromatic substitution — routes we’ve directly validated in our pilot plant. Colleagues in the pharma sector often reach out for insights, especially those running SAR campaigns on novel heterocyclic leads. We've seen the compound’s structure bring an advantage precisely where four- or five-membered rings would otherwise stagnate due to instability.
The hydroxy group at the ortho position changes how the pyridine interacts with both organic and inorganic reagents. Crystalizing this intermediate often gives us well-defined, easily handled material compared with more labile hydroxypyridines. Some newer chemists first expect trouble, due to past problems with related hydroxyhalopyridines, but they soon notice the unexpected robustness. That comes from the exact positions of the groups, not just the functional identities.
Scaling this compound from a 50-liter glass vessel to multi-hundred-kilogram output provides an education in itself. Bromination can run hot; we keep live monitoring on our jacketed reactors, because a run-away batch leads to discoloration or hard-to-remove byproducts. We’ve learned more from reworking a few tough batches than from all the perfect lab runs combined. Real production means tracking every parameter, from solvent drying through to argon purges and precise sampling — we test, not once or twice, but at every stage. That approach keeps our typical purity above 98%, based on HPLC and NMR we run in-house. People sometimes ask why we bother running all those intermediate checks. Experience tells us: if the purity falls on this molecule by even half a percent, downstream users hit trouble, from chromatography headaches to failed couplings.
In our workshop, we don’t settle for ‘good enough’. Before shipping, we rely on experienced eyes to catch conformity not just in numerical purity, but in physical form and color. Batches present as pale yellow to off-white, crystalline material — not dusty orange or sticky residues that hint at problems upstream. Over time, we’ve noticed these signs correlate closely to trace side-reaction products. We care about these details not because we’re perfectionists, but because we’ve seen customers lose weeks of work from minor impurities.
Many buyers compare 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine to other pyridine derivatives, like 2-hydroxy-4-trifluoromethylpyridine or even the simpler 2,5-dibromopyridine. On paper, these look similar. In practice, they behave very differently in multi-step syntheses. Take downstream Suzuki-Miyaura coupling for example; the 5-bromo position provides a sweet spot for coupling selectivity, especially when competing with possible reactions at the hydroxy group. Non-brominated analogues force a reliance on less predictable reactions, often delivering more side products and less yield.
We see requests for alternative halogens — chlorine or iodine — but each change brings a new set of handling and reactivity issues. Chlorinated versions can need higher temperatures and lead to less clean separations, while iodinated pyridines bump up material cost without always providing extra benefit in most common cross-coupling sequences. In the end, our preference comes straight from lab and pilot-plant evidence: the bromo substituent at this position fits well in Pd-catalyzed reactions, giving a balance of reactivity and cost that makes synthesis smoother for downstream users.
Our customer base includes pharmaceutical R&D, custom synthesis shops, academic labs, and agrochemical developers. Feedback and collaborative projects over many years have built a practical sense of what works — and what doesn’t — for this intermediate. In heterocycle elaboration or fluorinated motif incorporation, this compound delivers steric and electronic effects that fuel new activity profiles or boost physicochemical stability. Some prefer other derivatives when aiming for selectivity at other ring positions, but for introducing unique, highly polar groups, or building out pyridine cores for kinase inhibitors, nothing else balances the needs quite like this one.
We’ve also seen the molecule serve as a key intermediate in multi-step APIs that made it into late clinical phases, and even in specialized agrochemical actives that required tough environmental fate metrics. Certain research groups choose it as a starting material for radiolabeling. In their hands, the hydroxy substituent forms a friendly gateway toward selective O-alkylation or further aromatic substitutions. Plenty of clients have started with a handful of milligrams on the bench and come back for kilogram or greater scale after their medicinal chemistry teams confirm unique bioactivity.
Some competitors lean on generic descriptions in their listings, missing a big part of the story: in practice, trace metals, sulfonate byproducts, and even subtle process regents can persist if the process isn’t tightly optimized. Purification by repeated recrystallization and careful filtration is needed, but overdoing it can reduce yield or introduce other quality control headaches. That’s why our production floor never rests on written procedures alone; we constantly refine conditions based on close observation and years of in-house trial.
Decades of direct manufacture have shaped how we guarantee what arrives at the customer’s dock. Clients often share horror stories from material bought through brokers who can’t trace lots or audit their actual manufacturing source. We only release lots that our own chemists have monitored from raw material intake to packed drum. Transparency beats hollow guarantees. As people working with tough molecules, our teams treat quality checks as non-negotiable. Each delivery comes tied to a batch history, chromatograms, and spectra, rather than a generic certificate from a faceless trader.
Supply chain disruptions or raw material shortages can sometimes slow output. In these cases, we keep customers updated, offering not just timelines but, when possible, alternative synthetic strategies or route adjustments that keep projects alive. Real relationships have come out of these hard times. This willingness to speak openly — to say exactly where the process stands — has built the trust that gets projects through tough situations.
On the manufacturing side, handling 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine introduces both routine and unique safety concerns. Although not shock-sensitive or prone to violent exotherms, the compound’s fine particulate nature demands careful dust management and reliable personal protective equipment for all staff. We enforce bench-level and storage-level controls to mitigate inhalation and minimize any risk of skin exposure. Over the years, no rule had more impact than installing improved local exhaust and air quality monitoring. Storage requires cool, dry rooms, separate from incompatible chemicals or moisture sources, and our in-house protocols call for regular inventory review to prevent slow degradation.
Environmental stewardship matters to us beyond compliance. Each reaction step — from handling trifluoromethyl sources to final crystallization — generates chemical waste that deserves full traceability. Our waste processing partners operate under direct contract: no offloading to unclear handlers. We retain full transparency on solvent, halogen byproduct, and organofluorine disposal. Continuous improvement within these protocols arose not because regulators insisted, but because as manufacturers, we see firsthand the consequences of any lapses. That view shapes every step, every drum we pack, every sample we send.
Some users approach us armed with a concise target molecule, clear procedures, and a synthetic sequence built upon years of literature precedent. Others start barely beyond a rough concept, unsure which intermediates hold potential. Our team fields both kinds of requests. Having manufactured hundreds of intermediates, we guide users through the real-world implications of selecting 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine over seemingly similar products. We’ve collaborated on custom routes, pilot campaigns, even scale transfers. This hands-on approach is driven not by ‘service philosophy’ but by tangible practice. We’ve stood in their shoes, frustrated by unexpected product behavior. Our guidance stems straight from lessons learned beneath the fume hood and on the production floor.
Take the adjustment needed for Suzuki coupling partners: a small shift in base or solvent can bring the desired product over 15% higher yield when this compound replaces other pyridine analogues. This didn’t come from guesswork — our technical team helped optimize the run, set reagent stoichiometry, and ensure that the process made commercial sense at scale. Our pride comes from helping users avoid the missteps we've climbed out of ourselves.
Long-term success with such synthetic intermediates involves much more than the molecule itself. Colleagues in research, QC, and downstream manufacturing know that problems with one batch can set back entire projects. We support them not through canned support scripts but through direct access to the manufacturing team, who can interpret spectra, troubleshoot side reactions, and communicate the implications of process changes. This hands-on troubleshooting cannot be faked; it comes only from living the process year after year.
We’ve invested heavily in continuous process improvement, building out analytical capacity with in-house NMR, HPLC, and mass spec tied to each lot’s journey. Any anomaly — a retention time drift, minor impurity, or unexpected crystallization habit — triggers in-depth review by the same chemists who run final packaging. This practice, carried out by people who have spent years understanding the quirks of brominated and trifluoromethylated pyridines, lowers risk for end users and saves significant time down the line.
Development in pharmaceuticals, materials science, and agrochemicals pushes our demands for quality and flexibility. The future for 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine will only grow alongside applications where high-value substitutions and rugged motifs drive performance. With innovations in catalysis, process intensification, and green chemistry, we adapt our own practices, always ready to re-invest in purification, analytics, and process controls that deliver ever better outcomes. This approach comes from manufacturing not just one product, but from supporting complex chemistries through every breakthrough and challenge.
What’s next for us centers on new demand — customers looking for ever cleaner, more selective intermediates, willing to pay for true quality and support. Recent collaborative projects between our senior chemists and external researchers have opened new synthetic directions, where this compound’s unique structure enables shortcuts in multi-step routes or brings robust new properties into advanced materials design. We share these lessons openly, trusting in the mutual benefit from a deeper understanding of what manufacturing expertise adds to cutting-edge chemical development.
After years of working, troubleshooting, and refining our handling of 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine, our perspective grows from daily contact, not hollow routine. The value sits in every kilogram we release, guided by real chemists who safeguard not just the batch but the entire downstream project chain. As the science grows, so do our procedures — adapting, improving, and supporting the next generation of innovations where this compound brings something truly unique to the laboratory bench or the plant reactor. True understanding comes not from data sheets, but from lived practice.