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HS Code |
835562 |
| Productname | 2-Bromo-3-Fluoro-6-Picoline |
| Casnumber | 138806-59-8 |
| Molecularformula | C6H5BrFN |
| Molecularweight | 190.01 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Density | 1.616 g/cm³ (at 20°C, estimated) |
| Smiles | CC1=NC=C(F)C(Br)=C1 |
| Inchi | InChI=1S/C6H5BrFN/c1-4-2-5(8)6(7)3-9-4/h2-3H,1H3 |
| Solubility | Slightly soluble in water; soluble in common organic solvents |
| Refractiveindex | n20/D 1.565 (estimated) |
| Storagecondition | Store in a cool, dry, well-ventilated area |
As an accredited 2-Bromo-3-Fluoro-6-Picoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap, labeled "2-Bromo-3-Fluoro-6-Picoline, 25g," including hazard symbols and batch information. |
| Shipping | 2-Bromo-3-Fluoro-6-Picoline is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous chemical, following all regulatory requirements for transport, including labeling and documentation. Transport is typically by ground or air, compliant with IATA, DOT, and IMO regulations for chemicals. |
| Storage | **2-Bromo-3-Fluoro-6-Picoline** should be stored in a tightly sealed container, away from direct sunlight and moisture. Keep it in a cool, well-ventilated, and dry area, separated from incompatible substances such as strong oxidizers. Store at room temperature and ensure proper labeling. Access should be restricted to trained personnel, and standard laboratory safety procedures should be followed. |
Applications of 2-Bromo-3-Fluoro-6-Picoline in Industrial Manufacturing2-Bromo-3-Fluoro-6-Picoline serves as a key intermediate in advanced chemical syntheses for pharmaceutical, agrochemical, and specialty chemical industries. As a direct manufacturer, we supply this material to integrated production lines with strict adherence to global compliance frameworks and precise process controls, targeting high-value applications in mature sectors. Below are core downstream applications, each with specific regulatory, formulation, and production context. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisManufacturers use this compound as a building block in multi-step synthesis of novel pyridine-based APIs. The fluorine and bromine substitutions make it suitable for selective coupling reactions and heterocycle construction, commonly under palladium-catalyzed conditions. This intermediate enables structure-activity optimization for central nervous system or anti-infective agents, and batch records must document all raw material controls for regulatory filings. Industry compliance standards
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2. Agrochemical Intermediate in Herbicide ManufacturingMajor crop protection companies incorporate this material for synthesis of pyridine-derived herbicides, using its electron-deficient pyridine ring for substitution reactions within protected synthetic flows. Quality-controlled raw material input is essential, as final product bioactivity depends on precise incorporation of fluoro and bromo functions. The downstream process aligns with regulatory traceability for global market entry. Industry compliance standards
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3. Intermediate for Electronic Chemicals and OLED Material SynthesisElectronic materials producers use 2-Bromo-3-Fluoro-6-Picoline for heteroaromatic core formation in high-performance OLED and semiconductor chemicals. The molecule provides stability and desired electronic effects as a precursor in synthesis of hole/electron transport materials and alignment layers. Traceability and contamination control at every handling step are mandatory for this segment. Industry compliance standards
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4. Building Block for Specialty Fine Chemicals in Flavor & Fragrance DevelopmentFragrance and aroma chemical producers apply this pyridine derivative as a base for synthesis of specialty intermediates. Its substituted pyridine core enables complex aroma note development through functionalization, assisting development of unique compounds for perfumery and food flavoring. Production tracks closely to IFRA, FEMA, and local regulations for consumer safety and export documentation. Industry compliance standards
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Reliable chemicals form the backbone of modern research and industrial development. Among the nuanced building blocks, 2-Bromo-3-Fluoro-6-Picoline has stepped forward in both scale and significance. As a manufacturer with deep roots in pyridine chemistry and halogenated heterocycles, we have witnessed demand for intermediates that offer greater selectivity for downstream pharmaceutical and agrochemical synthesis. Our insights stem from years spent perfecting the controlled halogenation and methylation of picoline derivatives.
This compound, with the chemical formula C6H5BrFN, stands out for its well-defined 6-membered aromatic ring, selectively functionalized at the 2- (bromo), 3- (fluoro), and 6- (methyl) positions. The introduction of both bromine and fluorine onto the pyridine framework is not trivial. It requires careful balance: temperature controls, reagents with the right purity, a stepwise halogenation protocol. With years of practice, our team evens out the yield and manages the isomer challenge far better than when we first started.
The resulting compound—2-Bromo-3-Fluoro-6-Picoline—gains value from such precision. It achieves a purity of 98% or higher without extensive reprocessing, offering a crystalline form that resists atmospheric moisture and minimizes handling loss. We see this not as an academic purity number, but as a guarantee: a manufacturer’s proof that downstream reactions begin on sound footing.
The question that comes up regularly from formulation chemists and R&D directors is not simply about the existence of a bromo-fluoropyridine, but why such a structure matters. For scientists in the labs, this compound is more than just a catalog entry—it delivers a versatile anchor point for advanced molecular design.
The bromine atom at the 2-position supports reliable cross-coupling—Suzuki, Stille, Buchwald–Hartwig routines—central to building new C–C or C–N bonds without over-halogenation side reactions. Our path from raw picoline to a mono-brominated, mono-fluorinated pyridine, avoids the confusion of multiple regioisomers that often complicates reaction workups. With us, R&D teams see fewer surprises from batch to batch, and that steadiness drives real innovation.
The fluoro group at the 3-position shows more than just a shift on NMR spectra: it imparts subtle electronic modulation that medicinal chemists crave. Fluorine’s influence on bioactivity, binding affinity, and metabolic stability is well-documented. When biologists want to create fluorinated analogs to tune potency or reduce unwanted side effects, they find that this particular location on the pyridine ring is crucial. Through controlling the fluorination process, we avoid over-fluorinated species and guarantee the selectivity researchers expect.
The methyl group at the 6-position, often overlooked by non-specialists, stops unwanted polymerization and gives just enough steric bulk to prevent double substitutions. What seems like a small twist in the synthetic route can save weeks of troubleshooting for customers scaling up processes or working with sensitive enzymatic transformations.
Drug discovery projects and crop protection programs each have their signature challenges. New kinase inhibitors and fungicides draw on halogenated pyridines as critical intermediates. Without reliable sources for 2-Bromo-3-Fluoro-6-Picoline, screening projects grind to a crawl. Leadership in these industries means staying a step ahead of evolving regulatory demands, managing shrinking timelines, and facing patent cliffs.
We have shipped this compound to pharmaceutical innovation centers, contract research organizations, and in-house agrochemical labs alike. Many report improved yields in their palladium-catalyzed cross-coupling reactions. Several have traced superior biological activity in their lead series back to just this sort of halogen-pyridine backbone. Our own customer feedback points to reduced impurities and easier purification—the blend of attributes that lets real work move forward faster.
Some ask about alternatives: why not stick with the simpler mono-substituted bromopyridine, or the more common 3-fluoro-6-methylpyridine? Experience teaches that each choice locks in certain trade-offs. A 2-bromopyridine, for instance, tends to be more reactive but less selective, leading to excessive side products under coupling conditions. The lack of a methyl group at the 6-position leads to complications in downstream chemistry and sometimes harsh purification requirements.
On the other hand, fluorination at the 3-position (and not elsewhere) guides the electron density in a way that makes nucleophilic aromatic substitution more predictable. This is noticeably different than a ring with no activating methyl or blocking multiple halides at less strategic positions. Outcome consistency and process transparency prove more valuable in ongoing collaborations than the theoretical diversity of structures.
We often help customers differentiate our 2-Bromo-3-Fluoro-6-Picoline from close cousins such as 2-Chloro-3-Fluoro-6-Picoline or the widely used 2-Bromo-6-Methylpyridine. The right match depends on the properties needed downstream. Sometimes it’s a matter of how quickly a substrate reacts under a palladium catalyst, or how well it fits within a particular SAR campaign. Our molecules are not just bottles on a shelf—they are engineered answers to open-ended questions in organic synthesis.
Trust grows over time as buyers see alignment between what we promise and what arrives in the bottle. Manufacturing halogenated pyridines asks for attentiveness from start to finish. It begins with sourcing lots free from trace contamination and extends through controlled reactor conditions, in-line monitoring, and precise timing for intermediate isolation.
Many customers value full traceability more with each passing year—knowing batch records are available for every drum, not just the initial pilot. We put stress on reproducibility beyond just the first release. Process safety, hydrogen bromide containment, and solvent recycling routines determine how steadily and safely the next run matches the last. Analytical chemists on our team keep cross-verifying the NMR and GC-MS fingerprints for each lot, sometimes catching minor variations before a single gram ever leaves our gates.
Scaling from glassware to 500L reactors does not follow a simple proportional relationship. The heat transfer profile, stir rate, and addition order adjust according to the physical properties unique to this product. Our lab’s catalog work is replicated at plant scale only through careful parameter mapping and data collection—molecular consistency across each kilogram produced matters more than the number of kilograms shipped.
What does regulatory compliance mean at the real-world level for this halogenated pyridine? End-users in Europe, the Americas, and Asia look for assurances beyond simple COA review. They ask frank questions about residual solvents, nitrosamine formation risks, and chemical traceability, especially given increased focus on pharmaceutical supply chains. Delivering these answers honestly shapes our reputation more than any flashy marketing claim.
Supply security goes hand-in-hand with this accountability. In recent years, customers face delayed projects from raw material volatility and unplanned supplier shutdowns. By producing 2-Bromo-3-Fluoro-6-Picoline entirely in-house, we avoid dependency on single-source starting materials from distance suppliers. We forecast our input needs seasonally, maintain buffer stocks, and cross-train technicians for every production step. Sharing this approach with partners gives them stability that stretches beyond price negotiations.
Export paperwork has seen a marked increase in scrutiny. Our logistics professionals focus on providing the right shipping certifications needed for your jurisdiction along with appropriate hazard declarations. For dangerous goods, especially those involving halogens, compliance is not an afterthought but baked into our batch release and documentation cycle.
Manufacturing 2-Bromo-3-Fluoro-6-Picoline needs more than recipe execution—it asks for risk minimization at every stage. The hazards of handling brominating agents and fluoride donors require protective measures above routine organic synthesis. We find that investing in air monitoring, contained transfer systems, and individual operator training reduces risks while keeping waste to a minimum.
Waste management calls for a conscious mindset. Rarely does anyone notice the quiet upgrades behind the scenes: parallel distillation, condensation recovery, and closed-loop vent scrubbing. By keeping effluent loads under regulatory thresholds and recycling solvents on-site, we control cost and lessen our environmental footprint. Regular process hazard reviews highlight risks long before an accident or regulatory inspection draws attention.
Over the years, collaboration with customers sparked several process innovations. A research team testing a new coupling strategy needed ultra-low water content; we adjusted our purification steps, introduced in-line drying, and reformulated packaging. For another group fighting column blockage at scale, we altered our filtration and drying stage, balancing cost with end-use risk mitigation.
Feedback loops mean more than word-of-mouth; they build new manufacturing routes. From special requests—like stable isotope labeling or custom impurity thresholds—to practical in-process cleaning advice, these partnerships shape each improvement. Manufacturers learn directly from the hurdles researchers face daily, and in turn, shape products that better fit shifting industry needs.
This active dialogue builds a network of long-term relationships. Price is often a discussion point, but we see quality, responsiveness, and real transparency drive more sustainable wins. Customers who gain time, avoid rework, and shorten development cycles often tie these successes back to chemical intermediates delivered just the way they need.
The journey of 2-Bromo-3-Fluoro-6-Picoline from concept to consistent daily production mirrors the evolution of our industry as a whole. At the outset, a new building block seems promising in abstract terms; over time, what matters most involves the composite of yield, purity, safety, and traceable records. We focus energy and technical development around these priorities—never just on the headline metric of annual volume.
As next-generation pharmaceuticals and advanced crop protectants continue to call for more specific heterocyclic scaffolds, reliable supply of complex intermediates becomes a cornerstone, not a luxury. We confront challenges not just with technical solutions, but by fostering early dialogue, clear communication, and shared learning curves.
For those at the cutting edge of synthesis, 2-Bromo-3-Fluoro-6-Picoline stands out for its uniquely tuned reactivity, reproducible performance, and robust documentation standards. By investing in process integrity, batch consistency, and fully transparent customer support, we aim to keep science moving—one well-made bottle at a time.