|
HS Code |
197424 |
| Product Name | 2,5-Dibromo-3-fluoropyridine |
| Cas Number | 351003-85-7 |
| Molecular Formula | C5H2Br2FN |
| Molecular Weight | 270.88 |
| Appearance | white to off-white solid |
| Melting Point | 45-49°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in organic solvents |
| Smiles | C1=CN=C(C(=C1Br)F)Br |
| Inchi | InChI=1S/C5H2Br2FN/c6-3-1-4(8)5(7)9-2-3/h1-2H |
| Storage Temperature | Store at 2-8°C |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 2,5-Dibromo-3-fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram sample of 2,5-Dibromo-3-fluoropyridine is supplied in a sealed amber glass bottle with a safety cap. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** 2,5-Dibromo-3-fluoropyridine is typically packed in 25kg fiber drums; 20′ FCL accommodates about 8-10 MT. |
| Shipping | 2,5-Dibromo-3-fluoropyridine is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. Packaging adheres to international transport regulations for hazardous chemicals. The shipment includes detailed labeling and safety documentation, and is handled by authorized personnel to ensure safe delivery. Temperature and stability requirements are maintained throughout transit. |
| Storage | 2,5-Dibromo-3-fluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Avoid exposure to moisture and light. Clearly label the storage container and keep it in a designated chemical storage cabinet, preferably for hazardous or halogenated organic compounds. |
| Shelf Life | 2,5-Dibromo-3-fluoropyridine is stable under recommended storage conditions; shelf life is typically two years when stored in a cool, dry place. |
|
Purity 98%: 2,5-Dibromo-3-fluoropyridine with purity 98% is used in pharmaceutical intermediates synthesis, where high product yield and reduced by-products are achieved. Molecular weight 255.89 g/mol: 2,5-Dibromo-3-fluoropyridine of molecular weight 255.89 g/mol is used in agrochemical precursor fabrication, where precise molecular incorporation is facilitated. Melting point 60-62°C: 2,5-Dibromo-3-fluoropyridine with melting point 60-62°C is used in crystal engineering research, where controlled crystallization enables reproducible solid forms. Particle size <50 µm: 2,5-Dibromo-3-fluoropyridine of particle size less than 50 µm is used in fine chemical compounding, where uniform dispersion enhances reaction efficiency. Stability temperature up to 120°C: 2,5-Dibromo-3-fluoropyridine with stability temperature up to 120°C is used in high-temperature catalytic processes, where thermal stability ensures consistent reactivity. Water content <0.1%: 2,5-Dibromo-3-fluoropyridine with water content less than 0.1% is used in moisture-sensitive syntheses, where minimized hydrolysis boosts product integrity. |
Competitive 2,5-Dibromo-3-fluoropyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
For researchers and chemical manufacturers working on the cutting edge, certain compounds open doors to projects that just don’t move forward with more basic materials. 2,5-Dibromo-3-fluoropyridine stands out among those. It’s not just another halogenated heterocycle; the presence of both bromine and fluorine atoms on a pyridine ring makes it a genuine tool for creativity in synthesis.
In my own work with pharmaceutical intermediates, introducing small changes—like placing a fluorine atom next to bromines on pyridine—has given molecules new reactivity and stronger resistance to metabolic breakdown. This single molecule, with its unique arrangement, brings that benefit straight to a chemical development bench. The structure makes it a solid candidate for nucleophilic substitutions or coupling reactions. With bromine at the two and five positions, and fluorine at the three position of the pyridine ring, the compound resists some common pitfalls encountered with mono-substituted pyridines, like unwanted side reactions or unpredictable reactivity.
Quality matters, every single time. When sourcing 2,5-Dibromo-3-fluoropyridine, the demand usually lands around 97% purity or higher, and for some labs, even a decimal or two on that number changes the outcome of a project. Impurities in multi-step syntheses lead to problematic byproducts that show up later, and anyone who has been caught in the cycle of tracing back impurities in a finished pharmaceutical ingredient can appreciate the assurance that comes from tight specification controls.
In terms of form, most samples arrive as an off-white to pale yellow solid. Some variation appears between manufacturers based on the synthesis route and purification steps, but a visibly off-color sample almost always signals trouble. Moisture pick-up can sometimes be an issue, especially if the product sits open to air, so a tightly sealed container is almost mandatory for storage. Instead of thinking of this compound as just another checkmark on a synthetic route, I treat it as a hard-won milestone product—exposing cheaper variants to moisture or oxygen shortens their shelf life, affecting project timelines and reliability.
Medicinal chemistry doesn’t revolve around a handful of common building blocks anymore. Today's drug discovery often weaves together niche heterocyclic scaffolds and strategic halogenation to tune metabolic properties, binding affinity, and even patentability. The appeal of 2,5-Dibromo-3-fluoropyridine lies in the control it grants: fluorine’s small size and strong electronegativity can lower the basicity of the pyridine ring, subtly shifting compound behavior in bioassays. Bromines can act as leaving groups for Suzuki or Sonogashira couplings, introducing aromatic or alkynyl fragments that were previously out of reach with other pyridine options.
The reach extends beyond pharmaceuticals. In my conversations with material scientists, similar halogenated pyridines often serve as key intermediates in developing custom ligands for metal complexes, specialty polymers, or high-performance coatings. The thermal stability boosts offered by both bromine and fluorine substituents can make or break project outcomes.
I remember working with 2,5-dibromopyridine once, and we battled with poor selectivity during cross-couplings due to the absence of fluorine. Swapping out the hydrogen with a fluorine at the three position not only lowers the electron density on the ring, but also curbs side reactivity with common metal catalysts. Compared with monobrominated or mono-fluorinated pyridines, this compound gives researchers a double handle to manipulate while retaining the stability that fluorine confers.
Most halogenated pyridines only allow access to a narrow set of chemical transformations, usually limited by the positions and types of substituents present. The di-bromination pattern combined with fluorination widens the plays researchers can execute: from building fused heterocycles to constructing rigid pharmacophores for kinase inhibitors or CNS-active drugs.
Getting specialty intermediates once meant three months of paperwork and customs headaches, waiting for a product that sometimes didn’t match the catalog grade. Places with the best reputation for 2,5-Dibromo-3-fluoropyridine production set the bar with transparent impurity profiles, batch-specific data, and direct conversation with chemists behind the scenes. Price swings still happen, since the raw materials (like elemental bromine or fluorine sources) track with larger commodity markets. But the rise of established specialty suppliers has brought better consistency and fewer interruptions during scale-up.
Labs sometimes try to make this compound in-house if they’re not working at commercial scale, but the inconvenience and safety concerns with handling brominating reagents or selective fluorination agents steer most folks towards buying verified lots. Lengthy purification—column chromatography under anhydrous conditions, fraction collection, and NMR verification—demands both patience and robust infrastructure, often limiting DIY approaches to the most urgent or low-volume runs.
Handling halogenated pyridines calls for respect. Brominated and fluorinated intermediates don’t compare to benign solvents in terms of safety profile or environmental impact. Years spent in the lab have hammered home that a liter of unstable material in the wrong hands causes more pain and paperwork than a properly managed kilogram. Proper PPE, fume hood use, and careful waste management all matter here.
Efforts to design greener production processes are ongoing. Some manufacturers have moved away from harsh halogenation reagents, looking at catalytic processes or two-step synthesis schemes that minimize side waste. For anyone in synthetic chemistry, checking supplier production practices and environmental credentials provides one more layer of peace of mind. Every time we opt for a supplier with a responsible record, that choice ripples down the line: less hazardous waste, safer working conditions, fewer regulatory headaches.
In my own experience crafting fragment libraries for drug screening, introducing a fluorine atom offers more than a way to shift physical properties—it changes how a molecule interacts with targets, sometimes amplifying or dampening biological activity by an order of magnitude. Adding bromine at multiple positions gives two launching pads for cross-coupling, letting chemists rapidly iterate analogs for SAR studies. Speed matters here; the quicker we can make and test analogs, the faster breakthroughs reach the clinic.
Outside of pharma, the same backbone has value in electronics development. Organic light-emitting diodes and specialty dyes often start with halopyridines. The unique electronic character of this compound means it can act as either electron acceptor or donor, depending on the system, providing key flexibility during material design.
Batch variation still trips up unsuspecting buyers. One lot might pass an NMR and GC-MS check with flying colors, but a small contaminant below detection limits can ruin reactivity, especially in low catalyst-load couplings. Collaborating with suppliers to obtain up-to-date spectra and COA documentation has saved my group from more than one failed synthesis. If there’s one lesson to pass on to newcomers, it’s to maintain a dialogue with suppliers and request thorough verification—don’t lean solely on catalog claims.
The cost spread can seem dramatic. On one side, specialty aggregator websites list the compound at premium pricing, banking on in-stock guarantees and fast shipping for time-sensitive projects. Direct inquiries to producers or regional chemical trading houses sometimes unlock better rates, or fresh lots with full transparency around origin. For larger programs needing repeated batches, building a direct relationship and negotiating contract supply cuts recurring headaches and extra markups.
From an investment perspective, buying higher grade at a premium sometimes saves more in labor and troubleshooting than bargain material ever could. Labs running into batch-to-batch reactivity losses or purification bottlenecks lose expensive person-hours fixing shortcuts made at the buying stage.
Choosing the right specialty intermediate like 2,5-Dibromo-3-fluoropyridine speeds projects and decides whether ideas survive beyond the proposal. A collaboration on kinase inhibitor scaffolds illustrated this perfectly: switching from a common 2,3-dibromopyridine to this compound unlocked regioselective couplings, shaving a month off the campaign. In that sense, it enables scientific curiosity and risk-taking—chemists aren’t boxed in by their toolkit’s limits.
The shrinking world of specialty chemicals means more researchers can work with rare building blocks that once took months or years to source. Scientists in smaller institutions or less-resourced labs have increasingly fair access, leveling the playing field for innovation.
Continuous improvement at the supplier level makes a difference over months and years. Suppliers committed to clean processes, robust logistics, and thorough technical support win repeat business, and it’s in their interest to keep up with emerging best practices around purity, employee safety, and sustainability.
End users—researchers, process chemists, and developers—play their part through vigilance and feedback. Documenting successful runs, flagging odd reactivity patterns, and reporting back to suppliers builds a foundation for incremental improvement. The market for 2,5-Dibromo-3-fluoropyridine will keep evolving as new applications emerge, but the basics of sound sourcing and clear communication won’t ever lose their place.
With broader access comes greater responsibility. Chemical buyers and users should stick to reliable, established sources, demanding batch-specific quality data, up-to-date safety information, and full regulatory transparency. That approach protects both human health and intellectual property, keeping workflow disruptions to a minimum. The choice to work with vetted suppliers isn’t just about compliance; it’s about sustaining creative, reliable research environments.
Safety data sheets and hazard labeling remain critical—halogenated pyridines don’t belong in the hands of untrained users. From spill management to waste disposal, even a minor slip carries consequences. I’ve seen careful planning save entire projects from operational risk or regulatory scrutiny, especially in academic or contract environments where resources are tight.
Better access to technical data, application notes, and troubleshooting forums creates shared knowledge. A decade ago, figuring out a failed coupling or stability issue meant weeks of solo struggle. Now, shared experiences through scientific networks or supplier-hosted Q&As can make a difference the same day an issue arises. Markets follow demand; as requests for more sustainable production and documentation climb, so will supplier offerings.
Innovation in the world of halogenated heterocycles keeps raising expectations for reagents like 2,5-Dibromo-3-fluoropyridine. As applications grow and methods improve, the industry will keep refining both product quality and the way it interacts with the end user. As long as those in the lab pay attention to the details—never settling for unverified purity or lacking process transparency—there’s every reason to expect bigger discoveries built on the foundation this specialty building block provides.