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HS Code |
334409 |
| Chemical Name | 2-bromo-3-trifluoromethyl-5-hydroxypyridine |
| Molecular Formula | C6H3BrF3NO |
| Cas Number | 1119436-25-1 |
| Appearance | White to off-white solid |
| Solubility | Soluble in organic solvents (e.g., DMSO, DMF) |
| Smiles | C1=CC(=C(N=C1Br)C(F)(F)F)O |
| Inchi | InChI=1S/C6H3BrF3NO/c7-5-4(6(8,9)10)3(12)1-2-11-5/h1-2,12H |
| Purity | Typically >95% |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Hazard Classification | May cause irritation to skin, eyes, and respiratory tract |
As an accredited 2-bromo-3-trifluoromethyl-5-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2-bromo-3-trifluoromethyl-5-hydroxypyridine, 5 grams," with hazard symbols, lot number, and safety instructions. |
| Container Loading (20′ FCL) | 20′ FCL loaded with securely packed drums of 2-bromo-3-trifluoromethyl-5-hydroxypyridine, ensuring safe, moisture-free chemical transport. |
| Shipping | **Shipping Description for 2-bromo-3-trifluoromethyl-5-hydroxypyridine:** Ships in a tightly sealed container under ambient conditions. Protect from moisture and direct sunlight. Handled in accordance with standard chemical shipping regulations. Includes safety documentation (SDS). Suitable for air and ground transport; ensure labeling for hazardous organic compounds. Intended for laboratory use only. |
| Storage | 2-Bromo-3-trifluoromethyl-5-hydroxypyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature or as specified by the manufacturer. Use appropriate personal protective equipment when handling the chemical. |
| Shelf Life | 2-Bromo-3-trifluoromethyl-5-hydroxypyridine typically has a shelf life of 2 years when stored in a cool, dry, and dark place. |
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Purity 98%: 2-bromo-3-trifluoromethyl-5-hydroxypyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting Point 120°C: 2-bromo-3-trifluoromethyl-5-hydroxypyridine with a melting point of 120°C is applied in organic synthesis workflows, where it provides thermal stability for controlled reactions. Molecular Weight 258.01 g/mol: 2-bromo-3-trifluoromethyl-5-hydroxypyridine with a molecular weight of 258.01 g/mol is used in agrochemical research, where accurate dosing and reproducibility are required. Stability Temperature 40°C: 2-bromo-3-trifluoromethyl-5-hydroxypyridine with a stability temperature of 40°C is utilized in catalyst manufacturing, where prolonged storage without decomposition is critical. Particle Size <10 μm: 2-bromo-3-trifluoromethyl-5-hydroxypyridine with a particle size under 10 μm is used in fine chemical production, where improved solubility and reactivity are achieved. |
Competitive 2-bromo-3-trifluoromethyl-5-hydroxypyridine prices that fit your budget—flexible terms and customized quotes for every order.
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Handling halogenated pyridines on a production scale reveals a lot about where value comes from in the supply chain. Our experience with 2-bromo-3-trifluoromethyl-5-hydroxypyridine shows how careful process design and real understanding of each reaction step matter more than any generic promises. In our line, this compound, with CAS 690632-70-5 and a molecular formula of C6H3BrF3NO, plays a crucial role for customers working on next-generation pharmaceuticals and agrochemicals. We learned early that even slight changes in synthesis impact subsequent transformations. Consistency here isn't just a lab concept; it determines whether your downstream products meet their mark or end up as wasted time and reagents.
The finished product usually appears as a pale yellow to off-white powder. Experienced chemical workers know that color can tell you almost as much as chromatography—our own QC teams rely on direct visual inspection almost as much as on the HPLC or NMR data. Purity matters greatly; our batches routinely go above 98% by HPLC, but the key metric for real-world users isn’t a percentage: it’s whether anything left behind throws off the next step. Moisture control shows up at this scale too, since the trifluoromethyl group and bromine don’t play nicely with residual water—you get more side reactions, stickier crystals, and headaches in purification.
We handle demand from both small-scale R&D and pilot-scale production lines. Clients developing kinase inhibitors, crop protection agents, or advanced materials often route their syntheses through this molecule because the 5-hydroxy substitution introduces further functional group compatibility. We’ve seen teams use it for Suzuki couplings, nucleophilic aromatic substitution, and as an entry point for introducing fluorinated rings into their active ingredients. The bromine at position 2 boosts reactivity for metal-catalyzed bond construction, something you don’t get from the chlorinated or iodinated variants as cleanly.
As production scales up, operational details weigh heavily. Manual addition of starting materials gives way to semi-automatic feeding, jacketed reactors replace flasks, and each variable—order of addition, temperature ramp, solvent dryness—makes its mark. We noticed over the years that production runs exceeding 10 kilos need solvent control tighter than ±1% by volume, as variation drives formation of troublesome by-products.
Comparing this compound to other pyridines, the combination of trifluoromethyl and hydroxy substitution has a practical advantage. The trifluoromethyl makes the ring more electron-deficient and resistant to unwanted oxidation, and in our operations, we see lower formation of colored impurities—a cleaner work-up, less extensive post-reaction treatments. Other halogenated pyridines either go off-color faster during storage or force longer purification.
Regioselectivity is another honest differentiator. Crafting 2-bromo-3-trifluoromethyl-5-hydroxypyridine with high selectivity avoids contamination by its regioisomers. We don’t just talk about 'isomeric purity' as a checkbox; we actively monitor by NMR and LC-MS, since even trace amounts of mis-substituted isomers can poison follow-up reactions or confuse SAR studies in pharma. Customers have called to report failed scale-ups traced to reagent sources with unrecognized isomer content—details only visible with honest QC, not just a printed certificate.
Solubility windows also distinguish this compound. Whereas unsubstituted or methyl-substituted variants dissolve either too readily or form oiling-out sludges in common solvents, 2-bromo-3-trifluoromethyl-5-hydroxypyridine sits in the workable middle; users often blend in THF, MeCN, or DCM without the clumping, precipitation, or micro-particulate issues that turn a reaction tank into a cleanup project. On our floor, our techs optimize filtration and drying to give customers material they can pour, not dig out by the scoopful.
Our synthesis protocol grew from direct hands-on experience over two decades. Early on, we sourced raw materials from three continents, finding that even on-paper identical bromine donors or fluorinating agents acted differently due to trace metals or stabilizers. These differences manifested as changes in exotherm profiles and batch reproducibility, so we eventually partnered with select suppliers and defined pre-treatment steps.
On the plant floor, a single filter clog or extractor malfunction can burn eight hours of man-hours and drain yield by a percentage point per cycle. Our process prioritizes safety—hydrogen bromide evolution control, temperature ramp monitoring, ventilation upgrades—because nobody seems to mention the real risks outside reaction schemes. These steps aren’t just for compliance; equipment corrosion, batch-to-batch variation, and worker exposure all translate to lost time and actual accidents if not controlled with practical expertise.
Frequent testing using both in-house and outside labs ensures we discover outliers before our customers do. We often pick up trace impurities even major laboratories miss, thanks to SOPs designed by chemists who actually run and scale these reactions. This real-world knowledge shapes every batch, rather than a distant office or rote checklist.
Every kilo of 2-bromo-3-trifluoromethyl-5-hydroxypyridine we ship supports projects with demanding regulatory and performance requirements. We’ve supplied material for active pharmaceutical ingredient (API) intermediates slated for registration in the US and EU. Drug innovators lean on reliable supply since synthetic bottlenecks often hold back the entire R&D effort. Our compound’s stable storage and well-documented synthesis back up regulatory dossiers that scrutiny demands—our own experience filling out DMF and technical packages means we know what to document, not just what looks good in a brochure.
Agrochemical groups and advanced material outfits find value in this intermediate too. Need for robust C–C or C–N bond formation, where byproduct unpredictability can ruin a run, pushes buyers away from off-the-shelf catalog material. We’ve seen how consistent purity reduces downstream rework, shrinks the number of purification cycles, and trims scrap rates. These hard details drive up efficiency, make deadlines feasible, and frankly reduce headache for all involved.
We have also partnered with analytical development labs, providing reference standards and scaled-up batches to support method validation. Direct communication between our plant chemists and end users reduces errors—real people discussing actual use cases always outperform templated data sheets.
Drawing on firsthand shipping and storage challenges, 2-bromo-3-trifluoromethyl-5-hydroxypyridine’s stability in ambient conditions saves real costs compared to similar analogs that demand cold or inert atmosphere storage. The crystalline powder resists atmospheric moisture, and we package in high-density polyethylene bottles with desiccants—a lesson learned after one too many experiences with sticky clumps during rainy seasons.
Solubilizing for reactions presents no outsized trouble. For routine Suzuki or Buchwald-Hartwig couplings, you can use moderately polar organics; for less routine transformations, we’ve offered technical support to match best solvents or blending ratios, based on actual dissolution data rather than theory. End users in the Northern hemisphere have called in winter to troubleshoot solids handling—our advice, based on years running bulk shipments through freezing temperatures and humid summers, means fewer surprises and less batch re-processing.
Transport rules can trip up even savvy procurement teams. Our compliance team tracks UN ‘Dangerous Goods’ shipping codes but, more importantly, shares handling and labeling tips, since past shipments delayed at customs taught us that regulations often shift faster than databases update. We prevent delays with full shipment documentation and preventative advice rather than after-the-fact apologies.
Scaling up this molecule, from grams to tens of kilos, forced us to rework filtration steps and rethink crystallization temperatures. Some early attempts yielded fine precipitates that passed through standard filter papers, which doubled drying times and caused agglomerates. To mitigate that, we switched to graduated nucleation cooling and mixed-solvent washes, balancing yield with user preferences for easy redissolution. This level of care shows up every production run, not simply as a set of specs but as a history of improvements born out of production hiccups and responses.
We realized years ago that every customer batch runs into unique hurdles: one pharma group needed packaging compatible with restricted cleanrooms, an academic lab required anhydrous forms with residual water under 0.1%, a large custom manufacturer needed micron-sized powders for inline feeding. Flexible line design in our facility allows us to meet real needs based on actual experience, not by pushing generic options.
Technical hiccups? Regular dialogue between production, QA, and R&D solves issues faster than top-down fixes. Our approach—continuous problem-solving and both feet on the ground—translates to reliable material, less troubleshooting on your end, and stronger partnerships.
Demand for halogenated and fluorinated heterocycles continues to rise in both pharma and crop protection. In response, we upgraded reactor capacity and implemented batch-tracking that links every outgoing shipment to a specific lot traceable back through raw material origins. We invest in staff technical training, as even a minor slip in reagent quality or a missed water check can cascade into real loss of quality—or worse, production downtime.
We focus on sustainability, not as a marketing checkbox, but in how we source starting materials, contain waste, and recycle solvents. Our efforts to cut halogenated solvent volumes and minimize waste byproducts aim to hold down both costs and environmental footprint. This kind of approach meets increasing demand for greener supply chains across the board.
We also maintain an R&D program dedicated to process improvement, not simply resting on our existing protocol. Recent process tweaks brought reaction times down by 12% and cut waste by nearly a third—details that show up in cycle time, not theory. Success in chemical manufacturing rarely fits a one-size-fits-all solution; our ongoing innovation and transparency help customers develop new applications and scale their own operations.
Real-world chemistry doesn’t rely on abstract assurances; it thrives on facts, hard-earned skills, and lessons from hundreds of cycles. We believe in sharing what we learn, supporting innovation, and meeting every challenge head-on with practical expertise. 2-bromo-3-trifluoromethyl-5-hydroxypyridine remains one of those products where hands-on experience and close customer partnerships make the defining difference. Our story with this compound is grounded in daily realities—direct observation, direct communication, and commitment to delivering reliable solutions for tough applications.