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HS Code |
249147 |
| Iupac Name | 3-Bromo-2,6-dimethylpyridine |
| Molecular Formula | C7H8BrN |
| Molecular Weight | 186.05 g/mol |
| Cas Number | 89877-10-3 |
| Appearance | Light yellow to brown liquid |
| Boiling Point | 252-254°C |
| Density | 1.45 g/cm³ |
| Refractive Index | 1.562 |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | Cc1nc(C)ccc1Br |
| Inchi | InChI=1S/C7H8BrN/c1-5-7(2)9-4-3-6(8)10-5/h3-4H,1-2H3 |
| Synonyms | 2,6-Dimethyl-3-bromopyridine |
| Storage Temperature | Store at room temperature |
As an accredited 3-Bromo-2,6-Dimethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of 3-Bromo-2,6-Dimethylpyridine is packaged in an amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 3-Bromo-2,6-Dimethylpyridine is shipped in tightly sealed containers, compliant with local and international chemical transport regulations. It should be handled with care, kept away from heat, sparks, and incompatible substances. Appropriate labeling, documentation, and use of secondary containment ensure safe transit and prevent leaks or accidental exposure during shipping. |
| Storage | 3-Bromo-2,6-dimethylpyridine should be stored in a cool, dry, well-ventilated area, away from sources of heat and ignition. Keep it tightly sealed in a corrosion-resistant container, protected from moisture and incompatible substances such as strong oxidizers. Store away from direct sunlight and handle under a chemical fume hood, following all safety regulations and using appropriate personal protective equipment. |
Applications of 3-Bromo-2,6-Dimethylpyridine in Industrial Manufacturing3-Bromo-2,6-dimethylpyridine serves as a valuable intermediate across several high-precision synthesis sectors. As the original manufacturer, we supply this compound to global leaders in agrochemical, pharmaceutical, and electronics material manufacturing. Below, we detail specific downstream applications based on real-world industrial processing scenarios, compliance expectations, integration stages, and typical end-use products. 1. Agrochemical Active Ingredient SynthesisMajor agrochemical producers utilize this compound as a key halogenated pyridine building block during the synthesis of advanced herbicide and pesticide molecules, where regioselective bromination on the pyridine ring improves biological activity. Production lines incorporate this raw material directly during multi-step active ingredient formation under strict process control for regulatory submission batches. Industry compliance standards
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2. Pharmaceutical Intermediate for API ManufactureMid- and large-scale pharmaceutical manufacturers purchase this compound as a critical intermediate for complex heterocyclic drug molecule synthesis. The material’s specific bromo substitution enables controlled downstream introduction of additional function groups, leading to preparation of selective kinase inhibitors, antivirals, and other patented actives under cGMP regimes. Industry compliance standards
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3. Electronic Materials Precursor (OLED/Display Industry)Electronics and display material manufacturers employ this compound as a building block for constructing advanced nitrogen-containing organic molecules with high purity requirements. Its unique substitution pattern enables synthesis of electron-rich ligands for OLED emitter and host layer materials during fine chemicals manufacturing for display panels and semiconductor devices. Industry compliance standards
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4. Fine Chemical Intermediate for Dye and Pigment ManufactureSpecialty pigment and dye manufacturers rely on this compound as a halogenated pyridine source for producing colorants with improved fastness and unique electronic absorption spectra. The material enters the colorant synthesis chain during formation of N-substituted pyridine chromophores, critical for high-performance textile, plastic, and ink applications. Industry compliance standards
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Producing 3-Bromo-2,6-Dimethylpyridine in our facility has taught us that the value of a fine chemical goes deeper than the label. Through careful process control and continual batch-to-batch tracking, we bring not only a reliable product to market, but also the lessons and improvements gained by years of direct hands-on involvement. We have witnessed shifts in synthesis routes and purification standards over time. Each improvement has come from real-world feedback, transformations in reagent availability, environmental regulations, and performance in the field. This collective knowledge creates a foundation that lets users trust the quality and reproducibility of our pyridine derivatives for demanding applications.
Our 3-Bromo-2,6-Dimethylpyridine carries the chemical formula C7H8BrN and often comes as an off-white crystalline solid. We routinely manufacture multiple kilogram lots under conditions that emphasize purity, homogeneity, and ease of downstream processing. Typical purity by GC exceeds 98% as measured by direct comparison against known standards. Moisture and byproduct levels are controlled through tight process monitoring and, where needed, post-reaction treatments tailored around not just lab validation, but real feedback from formulators and chemists working in challenging synthesis programs.
Many buyers ask about differences between this compound and other substituted pyridines in our catalog. Working side by side with API research groups and fine chemical intermediates developers, we have come to appreciate subtle but crucial distinctions: the bromo group at the 3-position offers a tunable handle for cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Synthetic chemists select our 3-Bromo-2,6-Dimethylpyridine for its unique pattern of substitution. The 2,6-dimethyl arrangement reduces steric hindrance in certain transformations, suppresses unwanted side reactions, and stabilizes intermediates under elevated reaction conditions. Projects in agricultural chemistry, advanced materials, and medicinal research have leveraged this product both in pilot and at production scale.
During scale-up, handling efficiency matters as much as theoretical yield. Consistent melting behavior, low dusting, and predictable solubility in standard solvents allow for greater throughput and less downtime. Over the past decade, process engineers at our facility have swapped stories with users about process bottlenecks and blending issues seen with impure or off-spec lots sourced elsewhere. By investing in dry room protocols, dedicated storage areas, and staged filtration, we have addressed common sources of yield loss and rework. Our goal is never merely to meet a specification on paper, but to ensure that each lot integrates smoothly into multi-step synthetic schemes.
3-Bromo-2,6-Dimethylpyridine serves as an intermediate in a range of chemical industries. Whether as a precursor for more complex pharmaceuticals or as a building block in agrochemical synthesis, users rely on attributes going beyond certificate numbers. For example, the selectivity of the bromo substituent enables clean functionalization under mild conditions in palladium-catalyzed coupling reactions. The dimethyl groups influence electronic properties, affecting both the reactivity of the core ring and the physicochemical profile of finished molecules. Across multiple production campaigns, research partners have reported reduced rates of isomeric side-product formation compared with unsubstituted or singly-substituted analogues.
Medicinal and agricultural researchers have highlighted this compound’s usefulness in generating libraries of N-heterocycle derivatives, especially where solubility and metabolic stability in downstream candidates must be tuned. Several investigational molecules progressing through late-stage development cite our 3-Bromo-2,6-Dimethylpyridine as the critical starting point. The core structure, with its defined substitution, provides a launching pad for introduction of heteroatoms, linking groups, or further halogenation. Routes built on this intermediate frequently reduce the number of protection/deprotection cycles, saving both time and material.
Across the pharmaceutical and specialty chemical space, regulatory documentation, traceability, and impurity profiles carry increasing significance. We recognize this not as a checklist hurdle but as a sign of responsibility in production. Routine analytical data accompanies every shipment. We include not just basic NMR and HPLC, but batch-level impurity mapping, so partners can anticipate and control the propagation of trace components throughout their own sequences. Our years working hands-on with downstream process development teams inform this level of transparency and technical support. No two applications are exactly alike, and we adjust documentation depth according to the phase of a customer’s project—early discovery winners may only want a rapid COA, while filing for regulatory submission demands full analytical packages and historical batch reconciliation.
Fine chemical manufacturing has, over the years, left little room for “good enough.” Our team remembers batches that did not meet expectations—sometimes because of a supplier, sometimes due to weather-induced equipment hiccups, sometimes a raw material grade deviating from spec. Each setback drove us to adjust, to trace root causes, and ultimately to redesign upstream steps or set tighter in-process controls. This everyday problem-solving shapes not only the 3-Bromo-2,6-Dimethylpyridine leaving our plant, but every facet of our model and mind-set. Lessons learned from pilot plant failures as well as breakthroughs get carried forward into each successive production run.
Chemically similar compounds may look like easy substitutes, but reliability depends on understanding the detailed structural impacts. The 3-bromo pattern, combined with methyl groups flanking positions 2 and 6, reduces the probability of unwanted polybromination during subsequent reactions. Synthetic sequences seeking selective ring substitutions often run into issues with broader halogenation profiles in less hindered analogues. The careful choice of this exact substitution pattern provides cleaner separation and easier purification steps downstream.
Compared to simpler bromo-pyridines, the two methyl groups bring more than steric bulk—they alter the basicity of the nitrogen, giving our product a distinctive reactivity profile that is prized in both basic and acid-catalyzed transformation sequences. Experienced chemists seek out such intermediates after running into problems when using cheaper, less well-defined materials, where unpredictable impurity carryover or unanticipated byproduct formation can disrupt process scale-up, mask analytical signals, or degrade end-product stability.
From a process safety and handling perspective, we consider the whole lifecycle, from bulk bagging and drum transfer through to weighing and metering into reactors. We have integrated feedback from plants and glovebox facilities alike. Operators asked for packaging that minimizes static and dust; our team now employs antistatic liners and tamper-evident closures. Maintenance workers suggested improvements to drum labeling for easier scanning and reconciliation at the loading dock; QR-coded tracking replaced paper manifests. These granular adjustments, based on years of lived experience and open channels with our end users, set our 3-Bromo-2,6-Dimethylpyridine apart from generics sourced without manufacturer oversight.
Contemporary expectations for chemical intermediates now mean that documentary controls, audit-readiness, and chain-of-custody verification hold equal weight with core molecular purity. Every batch produced in our plant features full traceability to lot-level inputs. Audit teams have walked our shop floor, sometimes unannounced, to verify not only analytical controls but also internal training records for operators. No two lots of raw bromo source carry exactly the same trace profile—our analytical chemists monitor this and pre-screen in-bound shipments, flagging any deviation rapidly.
We conduct periodic reviews of analytical performance, not just to satisfy internal benchmarks, but to anticipate regulatory shifts and harmonize with ICH guidelines where applicable. Heavy metal traces, residual solvents, and identification of nonintuitive byproducts take precedence. Experienced contract manufacturing and research partners increasingly ask for detailed impurity lists—including those at sub-0.1% thresholds. This not only satisfies documentation requests down the line, but also avoids surprises late in regulatory filings or tech transfer.
We have learned that ongoing conversations with partners, not just at initial order but during tech transfer or troubleshooting, help spot anticipated issues before they reach the point of no return. During more than one process qualification, a user flagged a shift in color or crystallinity. Lab teams responded by adjusting filtration rates and reviewing solvent swap protocols. The sum of these small interventions helps ensure our 3-Bromo-2,6-Dimethylpyridine delivers not only what’s on the data sheet, but consistent experience on the ground.
Our teams feel a sense of responsibility for every kilogram dispatched. Safe handling and stewardship guide our plant operations, starting with controlled ventilation and extending through strict segregations for organohalide waste streams. Equipment operators have received hazard training based not on theory alone, but case studies from our own facility. Past incidents and near-misses have driven equipment tweaks, reel-to-reel transfer redesigns, and the installation of enhanced vapor extraction systems around high-activity pumps.
We minimize our footprint as a principle, not just a requirement. Process water and organic extracts are tested against internal and local discharge standards. Over time, we have replaced older halogenated solvent protocols with more benign substitutes, recycling where purity allows. This attention to process design and environmental monitoring is not just about compliance, but stems from a direct appreciation for the impact our work has on the surrounding community and the downstream industries depending on us. We treat every drum as a long-term relationship—what leaves our dock today establishes credibility for future projects.
Feedback from partners has spurred us to move beyond basic compliance. As new regulations on halogenated intermediates and their manufacturing waste emerge, we keep pace through iterative improvement in our closed-loop systems. Whether it’s reducing brominated waste generation with more precise reactant dosing or installing new in-line sensors to catch process anomalies in real time, the investments pay off in both safety and sustainability. This continuous dialogue between plant floor, lab, and client shapes the present and future for our product and facility alike.
Every batch we ship carries a story—not only of synthesis, but of dialogue with hundreds of chemists, formulators, and project leads around the world. Our support does not end at the loading dock. Customers in pharmaceutical R&D, process development, and pilot plant scale-out have sent requests, samples, and feedback back and forth over the years. Analytical questions, unexpected viscosity changes, or new isolation requests have all led to adjustments in our protocols, documentation, and packaging.
Our line chemists and technical managers routinely provide insight not based on abstract guidelines, but concrete experience. When a partner walked us through a downstream Stille coupling that lagged below target conversion, our chemists suggested solubility tweaks and alternate activation sequences tested first in-house and later at customer sites. A production hiccup in summer humidity spurred a reformulation of our stored product’s secondary containment. Instead of layering on generic advice, our team discusses the “why” and “how” of each fix, grounded in firsthand trial and revision.
A strong technical exchange fosters innovation at both ends of the relationship. Users who received a consistently reliable supply find it easier to push reaction conditions, scale test campaigns, and file robust documentation packages even under pressure. Through years of standing behind every drum and facilitating open, candid troubleshooting, our team has built a reputation as true manufacturing partners. This reputation directly supports regulatory filings, accelerates submission review, and facilitates the scale-up of promising compounds on tight timelines.
The landscape for pyridine intermediates continues to evolve. Demand from pharmaceutical, agricultural, and material science sectors has risen, putting renewed pressure on manufacturing capacity, supply-chain reliability, and innovation in both process and product. Markets face increased scrutiny on impurity profiles, lifecycle analytics, and environmentally sustainable production practices. Our plant has responded by investing in both personnel training and new technology adaptation. This readiness to change stems from lived experience, not a playbook.
We maintain a robust pipeline of process optimization, listening intently to users encountering shifts in their own protocols or needing tailored specifications matching their downstream targets. Our capacity to scale—without compromising batch integrity or traceability—proves its worth as researchers and formulators encounter new challenges in their syntheses. Continuous improvement isn’t a catchy phrase, but a reflection of the accumulated experience within our shop floors and labs, responding quickly, learning from missteps, and carrying those lessons to each new cycle.
As the industry transitions toward greater accountability and transparency, our confidence does not rest on old habits or static procedures. It comes from a culture of hands-on involvement, openness to feedback, and pursuit of betterment seeded throughout our team. Choosing our 3-Bromo-2,6-Dimethylpyridine means working directly with a manufacturer who takes full ownership, from the first raw material drum to the tailored advice after shipping. Every lot encapsulates not just a reaction sequence but a history of partnerships, improvements, and a steadfast commitment to making chemistry work for the people who depend on it most.