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HS Code |
824623 |
| Iupac Name | 2,5-dibromopyridine-4-carboxylic acid |
| Molecular Formula | C6H3Br2NO2 |
| Molecular Weight | 296.90 g/mol |
| Cas Number | 7682-42-4 |
| Appearance | White to off-white powder |
| Melting Point | Above 250°C (decomposes) |
| Solubility In Water | Slightly soluble |
| Synonyms | 2,5-Dibromonicotinic acid |
| Smiles | C1=CN=C(C(=C1Br)C(=O)O)Br |
| Pubchem Cid | 27092 |
As an accredited 4-Pyridinecarboxylic acid, 2,5-dibromo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Pyridinecarboxylic acid, 2,5-dibromo- is packaged in a 25-gram amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | 20′ FCL can load approximately 12 metric tons of 4-Pyridinecarboxylic acid, 2,5-dibromo-, packed in 25 kg fiber drums. |
| Shipping | 4-Pyridinecarboxylic acid, 2,5-dibromo- is shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. Transport is in compliance with hazardous materials regulations, typically using ground or air freight. Appropriate labeling and documentation are provided to ensure safe and secure delivery to the designated laboratory or facility. |
| Storage | 4-Pyridinecarboxylic acid, 2,5-dibromo- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and keep container tightly closed when not in use. Ensure proper labeling, and follow all safety guidelines for handling chemicals. |
| Shelf Life | 4-Pyridinecarboxylic acid, 2,5-dibromo- is stable for at least 2 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 4-Pyridinecarboxylic acid, 2,5-dibromo- with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal yield and product consistency. Melting Point 240°C: 4-Pyridinecarboxylic acid, 2,5-dibromo- with a melting point of 240°C is used in fine chemical manufacturing, where thermal stability facilitates high-temperature reactions without decomposition. Molecular Weight 292.90 g/mol: 4-Pyridinecarboxylic acid, 2,5-dibromo- with molecular weight 292.90 g/mol is used in structure–activity relationship studies, where defined molar mass supports accurate reagent dosing. Stability Temperature 200°C: 4-Pyridinecarboxylic acid, 2,5-dibromo- with stability up to 200°C is used in catalyst design applications, where temperature resilience enhances catalyst lifetime and process reliability. Particle Size <50 μm: 4-Pyridinecarboxylic acid, 2,5-dibromo- with particle size less than 50 μm is used in tablet formulation processes, where fine particles improve blend uniformity and compaction properties. |
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Working on the production floor, watching the transformation of raw materials into specialized compounds, gives a real sense of respect for the complexities behind seemingly simple molecules. 4-Pyridinecarboxylic acid, 2,5-dibromo-, known in the lab by its model designation as 2,5-dibromonicotinic acid, takes a unique path through the synthesis line. Anyone involved in chemical manufacturing learns to appreciate the subtleties that set one compound apart from another, and 2,5-dibromonicotinic acid is no exception. From carefully measured reactions and purification stages, this product emerges with its characteristic structure, not just different in formula but in the way it behaves during applications and in the challenges it poses during production.
In the early days of producing halogenated pyridine derivatives, we noticed each position on the ring changed not only chemical properties but also handling requirements and market demands. As technology advanced, more industries started looking for specific brominated pyridine acids like 2,5-dibromonicotinic acid. It didn’t happen overnight; a few decades ago, requests mostly covered the mono-brominated or chlorinated variants. The two bromo groups at the 2 and 5 positions proved to have distinctive reactivity, especially for those in pharmaceutical and agrochemical research.
Anyone pressing a batch through a reactor sees how subtle shifts in temperature or choice of brominating agent can swing purity and yield. It’s not a generic bromination; the work-up, filtration, and crystallization steps take constant monitoring. Small errors in stoichiometry or timing launch headaches with side reactions or sticky byproducts. As a manufacturer who walks those halls daily, I know the significance of product consistency. End users developing advanced materials or performing functional group transformations aren’t just picking a base molecule — they’re counting on reproducibility and traceability with every batch.
For someone outside the lab, the difference between a mono- and a dibrominated pyridine acid may seem minor. Having seen both courses run for customers, the nuances matter. The 2,5-dibromo arrangement activates the molecule for subsequent cross-coupling (Suzuki, Stille, or Buchwald–Hartwig reactions), a favorite tool in modern pharmaceuticals. Mono-brominated or chlorinated analogues don’t deliver the same reactivity profile. The dibromo configuration opens wider synthetic pathways for downstream elaboration. Compared to 3,5-dibromonicotinic acid, which shifts electronic and steric environments, the 2,5 isomer proves more versatile in building certain biheteroaromatic frameworks.
The acidity from the pyridinecarboxylic group, paired with the electron-withdrawing nature of the bromine atoms, changes both solubility and reactivity. Blending that with the increasing demand among research teams for new medicinal scaffolds, we’ve seen real growth in requests for this specific isomer. Working with kilogram-scale runs has taught us to fine-tune asset utilization: solvent recovery, careful temperature ramps, and advanced filtration give near-white crystalline product with minimal mother liquor loss. Fine control over particle size and purity ensures researchers have a product that slides easily into chromatographic purification or further derivatization, without unexpected impurities ruining a run.
Every product we produce faces the reality of not only the internal requirements but also our clients’ practical needs. On the floor, the fine off-white or pale-yellow crystals of 2,5-dibromonicotinic acid signal a clean batch. Moisture sensitivity varies depending on storage and packaging, so we pay close attention to how we transfer and seal the product. Cakes pressed out from filtration show a firm texture, not a powdery mess. Each lot passes through rigorous HPLC and NMR checks, chasing down traces of mono-brominated or over-brominated impurities that sneak past less experienced manufacturers.
It’s not just about analytical numbers, either. Packing consistency matters, especially for multinational shipments. Over the years, we learned to invest in robust, airtight drums lined with polyethylene inner sacks. The product holds up well during routine handling yet moves easily for those dissolving it in DMF, DMSO, or other polar aprotic solvents. Most direct users—those in R&D for pharmaceuticals, materials, or crop-protection products—prefer a clean, flowable solid. This makes the compound easier to weigh, dispense, and store, maintaining high throughput at their own benches or pilot plants.
From conversations with QC chemists, synthetic planners, and even startups, it’s clear that no two clients see value in exactly the same features. The dibromo pattern suits some transformations much better than a chloro or mono-bromo cousin. Suzuki–Miyaura coupling is a good example: the 2,5-dibromo motif reacts selectively and efficiently, offering up both positions for possible elaboration. Structural differences between the 2,5 and, say, 3,5 or 2,6 versions aren’t just academic. These impact the orientation of substituents on the final molecular backbone, translating to material properties or biological activity.
Users in OLED or display materials seek specific electronic behaviors; a slight change in halide pattern shifts the entire device performance. Agricultural innovators want selective functionalization on a core scaffold, often building upwards from pyridine carboxylic acids. Pharmaceutical researchers experiment with ring substitutions to impart metabolic stability or tune receptor binding. Having watched multiple projects succeed or stall on availability and quality, I’ve become a strong believer in prompt communication about specification limits: residual solvent content, bromine levels, melting point range, and flow property all must match user needs, not some arbitrary catalog line.
Scaling from gram to multi-kilogram runs exposes every hidden weak point. The early lab-scale processes miss small factors—filtration times, heat transfer, and solvent recovery—that explode in importance as volumes grow. Bringing 2,5-dibromonicotinic acid to reliable scale required process specialists willing to revisit every parameter. A team approach, rooted in daily coordination between chemists, operators, and analysts, reduced downtime and upped batch yields. We invested in high-purity bromination precursors, coupled with real-time analytics, to catch any deviation before it hit downstream steps.
Quality is a lived value, not a slogan. Several clients began buying in small quantities, then increased orders after verifying that every lot matched the same NMR, HPLC, and melting point specs. A sudden spike in orders from pharma research proved our production flexes smoothly, moving from a single batch to parallel runs over multiple vessels. Each scale-up uncovers minor changes: the color of the filtrate, particle compaction in drums, storage stability during hot conditions, and other factors. Feedback from users leads to continuous small improvements.
Standing in the warehouse or lab, you learn quickly that customer decisions are shaped by far more than just price per kilo. Regulatory requirements, purity assurances, long-term accessibility, and batch traceability matter as much as raw specs. 2,5-dibromonicotinic acid resonates with those who must meet tight impurity profiles, often set by global regulatory agencies or IP teams. With major end uses in building active pharmaceutical intermediates or complex electronic materials, there’s little room for error.
Unlike some competitors, we don’t switch routes or raw materials based on short-term price swings. Sticking to established, well-characterized synthetic regimes gives us an edge in batch-to-batch consistency. New users frequently comment on lot robustness after running their own spectra, confirming that our direct, in-house production methods minimize extraneous byproducts. Even specific requests, like larger particle size ranges for custom formulation, get addressed quickly because our team knows each part of the workflow.
A successful manufacturer maintains a close relationship with both the product and its users. Supporting a specialty product like 2,5-dibromonicotinic acid means more than shipping bags or containers. Each inquiry tells us something about application trends, whether pharmaceutical, agricultural, or material science. Requests sometimes come in for custom purities or micronized product. Direct feedback from end users informs adjustments in production or handling; for instance, one client required specially dried material for anhydrous work. By talking directly with customers, we implement these changes seamlessly.
Our QC chemists track performance in user labs as well as in our own. It’s satisfying to see compounds we’ve produced become building blocks for advanced materials or drug candidates. The market moves quickly: research pivots, patent filings surge or fade, and new synthesis routes emerge. By keeping production flexible and maintaining dialogue with actual users, we ensure the material fits the evolving demands of innovative projects across the globe.
The synthesis and purification of 2,5-dibromonicotinic acid demand careful attention to operational detail at every turn. Filtering out side-products, safely containing bromine vapors, and managing exothermic bromination all become routine tasks. Decades of refining have taught us to preempt common bottlenecks—improving reaction vessel design, vacuum drying with nitrogen blanketing, and regular calibration of all analytical equipment on the line.
Logistics play a big part, too. Schedules often adjust on short notice. International regulations impact both shipping and documentation, especially with brominated organics. Real-world experience shows that robust labeling, clear documentation, and compliance with shipping authorities prevent costly delays. We don’t just hand off product at the loading dock; follow-through during transit ensures safe, compliant, and efficient delivery.
It’s easy to lump all pyridinecarboxylic acids together, but as a direct manufacturer, differences stand out during handling and processing. Monobromo and dichloro analogs tend to crystallize differently, requiring alternate handling. Solubility in common solvents, reactivity under standard conditions, and susceptibility to side-reactions all find their own quirks tied to substitution patterns on the ring. For example, the 2,5-dibromo isomer holds up better under certain C–N cross-coupling conditions due to increased reactivity at both positions, which is not always matched by isomers like 3,5-dibromonicotinic acid.
More selective end users zero in on these subtleities, choosing the brominated versions for advanced synthetic applications that need both predictability and robust yields. The added weight and electron-withdrawing properties of the two bromines affect packing, shelf life, and downstream synthesis steps. Direct conversations with those leading projects gives us updates on practical issues—such as needs for increased flow or improved thermal stability—that in turn inform our internal R&D. By producing multiple related pyridinecarboxylic acids and comparing real production datasets, we map out how these differences translate practically, guiding both our own process innovations and careful application recommendations for our clients.
Working with established pharma houses, mid-sized materials labs, and emerging biotech startups has underscored just how much is at stake with specialty chemicals. A single failed batch disrupts entire project timelines. Our repeated investment in process validation, employee training, and analytical improvements reflects this reality. Customers rely on a manufacturer not just for material but for a partnership around technical issues. By troubleshooting solvent incompatibilities or helping to interpret spectral data, our technical teams share in the ultimate outcomes of our product’s use.
Supporting customers means anticipating their next moves. Regulatory registration in different countries adds a layer of complexity; as rules change or new controls come into force, we update documentation and batch practices so users stay ahead of compliance issues. Industry trends also shape our product improvements. Whether it’s responding to requests for green chemistry routes, or adapting drying and grinding practices to regional climate needs, our production remains rooted in real-world results and direct user feedback.
Behind every drum of 4-Pyridinecarboxylic acid, 2,5-dibromo- sent to a client, there’s a team committed to transparency and safety. Safety in particular forms the backbone not just of our manufacturing process but our entire supply approach. Brominated organics demand thorough training, proper facilities, and meticulous attention to containment. Decades spent optimizing these practices directly benefit those who use our materials; our careful approach reduces the risk of off-spec product or dangerous incidents down the supply chain.
Our batch records, analytical reports, and regulatory documentation always remain open to scrutiny. Partnering with users to ensure consistent, transparent supply fosters the kind of trust needed for real progress. We’ve seen how fast research pivots—timelines tighten, new projects launch, priorities shift. The stability and reliability of a manufacturing partner who understands both the molecule and the market brings value in ways beyond the chemical itself.
The landscape for advanced building blocks keeps changing. As regulatory expectations rise and synthetic demands evolve, the need for reliable, consistent specialty chemicals stands stronger than ever. We respond by investing steadily in process refinement, analytical upgrades, and skilled staff. Customers purchasing 2,5-dibromonicotinic acid trust that product to build tomorrow’s active ingredients, crop protectants, and new electronic materials. That trust shapes every batch we produce.
Having worked on both start-up R&D benches and high-volume production lines, I understand how the smallest inconsistency in a chemical impacts both progress and morale. A direct line from manufacturer to user shortens the feedback loop and accelerates innovation. Keeping the process open, open to improvement, rooted in reliable chemistry and honest reporting, we aim to support the biggest leaps in research and application. 4-Pyridinecarboxylic acid, 2,5-dibromo- is more than a catalog listing; it is the work of real people, meeting the needs of real innovation every day.