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2,6-Dibromopyridin-3-Amine

    • Product Name 2,6-Dibromopyridin-3-Amine
    • Alias 3-Amino-2,6-dibromopyridine
    • Einecs 221-039-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    607791

    Chemicalname 2,6-Dibromopyridin-3-Amine
    Casnumber 5508-30-7
    Molecularformula C5H4Br2N2
    Molecularweight 251.91 g/mol
    Appearance Light yellow to brown solid
    Meltingpoint 109-112°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥ 97%
    Density 2.3 g/cm³ (approximate)
    Smiles C1=C(N=CC(=C1N)Br)Br
    Inchi InChI=1S/C5H4Br2N2/c6-3-1-4(7)9-2-5(3)8/h1-2H,8H2
    Storageconditions Store at room temperature, keep container tightly closed
    Hazardclass Irritant

    As an accredited 2,6-Dibromopyridin-3-Amine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 2,6-Dibromopyridin-3-Amine (5 grams) consists of a sealed amber glass bottle with a clear hazard label.
    Shipping 2,6-Dibromopyridin-3-Amine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transportation complies with chemical safety regulations, typically under UN Class 6.1 (toxic substances), with proper labeling and documentation. Handle with care, ensuring personal protective equipment is worn during handling and storage.
    Storage **2,6-Dibromopyridin-3-Amine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong oxidizing agents. Protect it from direct sunlight and store at room temperature. Ensure proper labeling and prevent access by unauthorized personnel to maintain safety and chemical integrity.
    Application of 2,6-Dibromopyridin-3-Amine

    Applications of 2,6-Dibromopyridin-3-Amine in Industrial Manufacturing

    As an experienced chemical raw material producer, we specialize in supplying high-purity 2,6-Dibromopyridin-3-Amine to organizations driving innovation across specialized downstream sectors. Below we detail precise industrial application scenarios based on actual demand, focusing on technical compliance, integration in formulation, process handling, and the real output products that define each industry segment.

    1. Pharmaceutical Intermediate Manufacturing for Antineoplastic Agents

    Pharmaceutical manufacturers use 2,6-Dibromopyridin-3-Amine as a halogenated aminopyridine intermediate in the synthesis of specific antineoplastic drug candidates. Its unique substitution pattern enables selective construction of heterocyclic rings during API production, particularly in the synthesis of small-molecule kinase inhibitors leveraging pyridine scaffolds. Handling this intermediate demands precise stoichiometric addition, monitored reaction temperatures, and stringent control of residual solvent content, as required under GxP environments.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF Monographs (where applicable)
    • EMA and FDA impurity guidelines
    • ISO 9001:2015 for quality management in pharmaceutical supply

    Typical usage ratio

    • Batch input generally 0.5–1.4 molar equivalents, tailored based on downstream synthetic route and molecular yield targets

    Downstream process integration

    • Added during heterocycle assembly and selective amination/hydrodebromination steps preceding functional API formation

    Final product types

    • Finished oncology APIs for solid oral dosage forms
    • Precursor for pyridinyl-functionalized biologically active pharmaceutical ingredients

    2. Agrochemical Synthesis of Pyridine-Based Crop Protection Agents

    Specialty agrochemical formulators incorporate 2,6-Dibromopyridin-3-Amine primarily in the development of novel pyridine-derived herbicides and fungicides. The dibromo substitution facilitates downstream introduction of various side chains, imparting specific activity profiles while enabling photostability required in field conditions. Material handling takes place in closed-system batch reactors, aligned to regulatory mandates on process traceability and environmental safety.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 on plant protection products
    • OECD guidelines for chemical testing and residue analysis
    • ISO 16140-2:2016 for method validation
    • China GB 4819-2009 for agrochemical raw material purity

    Typical usage ratio

    • Employed at 1–3% by weight in active intermediate synthesis, variation based on targeted product’s substitution pathway

    Downstream process integration

    • Introduced into cyclization reactions and halogen exchange processes during base structure conversion for final active ingredient synthesis

    Final product types

    • Ready-to-use liquid or granular herbicide formulations
    • Active ingredient concentrates for agricultural chemical blends

    3. Dye and Pigment Intermediate for Electron-Donor Modified Dyes

    Dye compound producers utilize 2,6-Dibromopyridin-3-Amine as an intermediate to introduce electron-donating amine groups into complex dyestuff molecules, enhancing photostability and solubility. The dibrominated structure allows for precise Suzuki or Stille coupling in advanced colorant synthesis. Processing involves strictly controlled anhydrous conditions and vacuum management to ensure product consistency, critical for textile and specialty ink applications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for azo dye intermediates
    • OEKO-TEX® Standard 100 for textile dyestuffs
    • ISO 4928:2023 for color fastness testing
    • Local hazardous chemicals control regulations for intermediate storage and transportation

    Typical usage ratio

    • Utilization typically ranges from 2–5% by mass in preparative batch, proportion varies by chromophore complexity and intended color intensity

    Downstream process integration

    • Added during coupling and condensation steps prior to sulfonation or other functionalization according to dye blueprint protocols

    Final product types

    • Synthetic textile dyes with high UV resistance
    • Inkjet printing pigments for specialty packaging

    4. Electronic Materials: Precursor for Organic Semiconductor Synthesis

    Manufacturers in the electronic materials sector specify 2,6-Dibromopyridin-3-Amine for constructing key segments of organic semiconductors, especially in the field of organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). By modifying the amine-pyridine ring system, chemists achieve precise energy level tuning vital to device efficiency and performance. The material must meet ultra-high purity and controlled metal contaminant profiles, necessitating advanced purification post-reactor extraction.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substance restrictions
    • IPC-4101E for base materials qualification
    • IEC 62474 on material declaration for electronics
    • In-house standards for electronic chemical grade purity (typically 99.5%+ GC/HPLC)

    Typical usage ratio

    • Applied at 0.2–0.8 molar equivalents per coupling stage, amount adjusted based on chain architecture and target semiconductor structure

    Downstream process integration

    • Reacted during aryl substitution and ladderization phases that define final layer properties in OLED and OFET device manufacture

    Final product types

    • Thin-film organic semiconductors for display technologies
    • Functionalized precursors for printed electronic circuits

    5. Specialty Chemical Building Block in Advanced Material Research

    Research institutions and specialty chemical producers demand 2,6-Dibromopyridin-3-Amine as a scaffold for structure-activity relationship exploration, enabling late-stage functionalization in advanced material development. The protected amine and reactive dibromo sites contribute to the rapid preparation of molecular libraries for new catalysis or material science applications. Laboratory-scale syntheses require high batch reproducibility and clean spectral verification (NMR, LC-MS).

    Industry compliance standards

    • ISO 17025 for analytical quality control in research use
    • Responsible Care® Program for laboratory chemical stewardship
    • Local university and corporate R&D safety protocols
    • REACH SVHC communication requirements for experimental chemicals

    Typical usage ratio

    • Ratio varies 1:1 to 1:3 with other building blocks, adjusted for target molecular diversity and scale-up feasibility in parallel synthesis

    Downstream process integration

    • Incorporated during iterative cross-coupling, cyclization, or reductive amination for rapid prototyping and library generation

    Final product types

    • Custom intermediate libraries for material science screening
    • Monomers for high-performance polymers and catalysts
    Free Quote

    Competitive 2,6-Dibromopyridin-3-Amine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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    Certification & Compliance
    More Introduction

    Practical Insights from a Chemical Manufacturer: 2,6-Dibromopyridin-3-Amine

    From the Factory Floor: A Closer Look at 2,6-Dibromopyridin-3-Amine

    Every batch we create of 2,6-Dibromopyridin-3-Amine reveals the blend of precision and reliability that matters in chemical production. There’s something satisfying about watching freshly crystallized samples pass the last GC inspection in our lab before packing—knowing the chemicals just met the specs that countless industry chemists rely on every day. The model number for our main grade is simply based on the batch date—for traceability—and that approach keeps us honest about consistency time after time.

    The Role of 2,6-Dibromopyridin-3-Amine in Synthesis

    Across our experience with heterocyclic intermediates, very few building blocks compare to 2,6-Dibromopyridin-3-Amine when it comes to flexibility in pyridine chemistry. Colleagues working in pharmaceuticals and crop protection return to this compound over and over for the same reasons. This molecule offers the two bromine atoms right where cross-coupling chemists want them—at the 2 and 6 positions—while the 3-amino spot lets it click into further reaction scaffolds or protection strategies. You see its relevance most clearly in high-value target syntheses: when someone brings us a difficult custom intermediate, there’s a good chance this amine sits on the retro-synthesis plan somewhere near the top.

    Quality Is Not Just a Number—It’s a Handshake

    It’s easy to list numbers: assay over 98 percent, melting point in the expected range, no sign of halogen exchange byproducts. To those outside the factory, these lines might read like generic lab specs. For us, quality control spells out scrutiny—two pieces of equipment, not one, cross-checking each other: HPLC and GC, always compared to NMR confirmation. Our team learns to recognize faint smells and minor color differences during drying and filtration that can tell more than numbers do. When a chemist calls to ask if this month’s batch will match his reference sample from last winter, we can say, honestly, that our process has stayed the same, and we stand by our crystallization and purification steps. This isn’t just about certificates—it’s about the real-world trust between a manufacturer and a scientist.

    Differences That Matter: Not All Batches Are Created Equal

    There’s a market filled with variations: some cheaper, some a little too damp, others more yellow or inexplicably sticky. We’ve received customer returns from traders whose sources didn’t vacuum dry their material long enough, leading to unpredictable results in Suzuki and Buchwald-Hartwig couplings. Moisture can sabotage palladium-catalyzed reactions; unpredictable residual solvents or starting material traces throw off yields on multi-kilo scales. That’s why our drying events get logged and monitored—every kilogram sealed double-layered under nitrogen, every storage drum desiccated against humidity swings that ruin countless warehouse inventories across the industry.

    Another difference shows up during scale transitions. Labs working from small glassware often don’t notice a trace impurity hiding beneath a certain threshold. Multinational firms scaling up need reproducibility at every step; batch-to-batch variation remains a silent killer of pilot runs and commercial launches. Our focus lands on making each run indistinguishable, so that one kilogram looks like the next whether we’re supplying 500 grams or half a metric ton.

    Specifications That Match Real-World Demands

    What do our customers actually require, not just what looks nice on a paper certificate? In the real world, product that fails a Karl Fischer moisture test above 0.5 percent throws a wrench into sensitive transformations. HPLC purity below 98 percent often means too many unknowns for pharma intermediates. Many of our regulars run tin(II) reduction or palladium couplings; traces of unreacted bromide starting materials spike side-products or gum up catalyst beds. We target each run according to these realities, not just by copy-pasting from previous offerings.

    Inside the Manufacturing Room: Our Perspective on Purity and Process

    The raw materials make or break yield. Bromination steps need careful temperature monitoring, and pressure swings change reaction kinetics. The amination steps rely on slow addition rates to control exotherms. We use only fresh solvents, since recycled lots sometimes drag traces of unrelated halides or tars through the line, leading to downstream contamination that someone has to fix with extra purification—sometimes rendering an entire day’s work wasted. If anything looks off during filtration or crystallization—too much mother liquor, not enough clarity—we go back and tweak parameters, all the way through final drying.

    Product isn’t packed just by numbers: we inspect, weigh, and check for caking or bridging that messes up downstream dosing and handling. There isn’t a shortcut. Our experience shows that every “convenient” time-saver passes a hidden cost along to the next chemist in line.

    Understanding Customer Use: Beyond the Lab Bench

    The main use of 2,6-Dibromopyridin-3-Amine rests in pharmaceutical and agrochemical research as both a connector and hook molecule. Chiral synthesis programs see it flower into new structures. The 2,6-dibromo arrangement means it fits hand-glove into cross-coupling logic, where specific positions unlock selectivity and function. Downstream, it’s transformed into antimalarial, antiviral, or fungicidal agents through exhaustive, sometimes proprietary, steps that our manufacturers rarely get to see.

    Year after year, synthetic groups working in both universities and commercial labs call with questions about optimizing conditions, troubleshooting off-colors, or reducing trace impurities. More than once, we’ve experimented with different crystallization regimes or alternate solvent systems based on direct feedback from a customer: less dust, less static, more handling ease. Our work gets shaped by the hands-on experience we gather and by the people who explain what their own downstream stakes really are.

    Comparing to Other Pyridine Compounds

    You see many pyridine derivatives on the market—monobromo, methylated, or multi-substituted variants. 2,6-Dibromopyridin-3-Amine holds a distinct place because of its symmetry and the electronics of bromine atoms facing across the ring. Alternatives like 2,6-dichloro or 3-bromo analogs often shift reactivity away from what cross-coupling chemists seek. Even minor positional changes, like swapping bromines from the 2,6-positions to the 3,5, throw off downstream functionalization patterns and cut yields. For those working at the limit—where every percent matters—our regulars notice how a different isomer can add a week of work or force a switch in catalyst or process chemistry.

    If someone asks for a comparison, we don’t recite catalog numbers—we provide stories of what failed and what succeeded in real campaigns. One scale-up project in an antiviral intermediate years ago taught us that a similar compound, with a bromine moved just one carbon over, led to a dead-end route under Buchwald-Hartwig conditions. The lesson: don’t just select based on theoretical diagrams. Real material behaves differently, and only experience walking through hundreds of kilo-sized reactions will show you the importance of sticking with the right substitution pattern.

    Adapting to Industry Needs: Listening and Responding

    One lesson learned from years in this business: success comes from staying close to the people using our compounds, not hiding behind paperwork or process diagrams. Over the years, our customers have pointed out recurring problems—such as micro-scale sampling for HPLC interfering with moisture content, or drums exposed to sunlight and experiencing subtle degradation in appearance or solubility. Every warehouse, every transport, every loading dock introduces small story-sized variables that labs rarely think about—unless something goes wrong. We make sure our teams know these pain points and respond with actionable improvements: robust packaging that blocks light and moisture, labeling by both lot and full synthesis history, open access to earlier batch samples for comparison.

    Case-by-case adjustments matter, too. For projects demanding high sensitivity—say, those working with patented catalyst ligands or preparing for regulatory filings—we rerun full impurity profiles or back up samples with second lots. Whenever a synthesis program faces an unexpected bottleneck, the fastest fix often comes from sharing manufacturing logs and historical QC testing with the team, enabling root cause analysis that fits the real chemical context, not just a template answer.

    Process Improvements and Hard Lessons

    We’ve had our share of batches fail to meet internal standards, and those moments teach more than a dozen unbroken successes. The day a filter clogged during a rainy spell, or the power blinked twice mid-distillation, showed us how vulnerable chemical synthesis can be to minute shifts in process variables. Every error costs real money, and every failure pushes us to improve environmental controls, backup systems, and operator training. There’s no short path to competency—just the ongoing practice of tightening procedures, recording what worked and what didn’t, and making sure new staff see where mistakes tend to creep in.

    Improving the nitrogen purge or switching to inerted transfer lines reduced contamination by trace oxygen. Using glass-lined reactors throughout the process reduced unpredictable leaching of dissolved metals, which show up in delicate pharmaceutical applications. These technical tweaks don’t appear in glossy brochures, but our regular users see the difference in downstream assays and regulatory approval rates.

    Our Take on Transparency and Customer Collaboration

    Open communication with chemists downstream stops minor issues from blowing up into production stoppages. We offer direct access to QA and technical staff—not just generic sales lines—so adjustments or clarifications come straight from the people who handled the batch. Sometimes project needs change at the last minute, or a chemist realizes a new impurity must be tracked down ahead of a scale-up milestone. Instead of stonewalling, we publish analytical data, supply samples for further checks, and support customer-driven analysis on their end.

    This approach lets us serve not only R&D and pilot campaigns, but also established manufacturing lines where regulatory agencies demand complete traceability and documentation. Generics manufacturers, for example, need full chain-of-custody for every intermediate in the process. We adapt by strengthening our own documentation—digital logs, batch-by-batch sample retention, and data packages customized to each client’s regulatory and process chemistry needs.

    Moving Toward Fewer Surprises

    Familiarity with the quirks of 2,6-Dibromopyridin-3-Amine saves chemists frustration down the line. There’s an old saying in the plant: “you can’t fix a shortcut with more paperwork.” The smallest unexpected impurity—one that dodged HPLC but revealed itself under GC-MS a week later—can throw production planners off schedule. The more effort we invest in up-front transparency, batch consistency, and attention to customer priorities, the fewer surprises turn up at scale. We commit to revealing the reality, not just what sounds good on a website.

    Bulk Supply and Handling for Real Manufacturing Scenarios

    Many suppliers treat 2,6-Dibromopyridin-3-Amine as a catalog chemical: packed in small glass bottles, sent out by the gram. In our world, real customers order multi-kilo drums, lined and sealed for protection against ambient air and light. We learned early that shipping in inadequately protected tanks causes caking, loss of free-flowing character, and later, headaches for those weighing it out. Every drum gets nitrogen back-filled and vacuum-sealed, without fail. We use UN-rated steel for high-volume shipments, which avoids transit mishaps that have tripped up too many projects running close to deadline.

    Long-term partners sometimes keep stock on consignment; others prefer just-in-time dispatch. We accommodate by adjusting lot sizes and packaging style—easy to say, difficult to do right without compromising integrity. Smaller users receive fresh splits from bulk, documenting full traceability, avoiding cross-contamination risks that plague repackagers.

    What Sets Our 2,6-Dibromopyridin-3-Amine Apart

    Competing products might look similar at first glance: a white to pale yellow crystalline product, seemingly pure, somewhere near specification. Our strength comes not just from the certificate, but from the repeat experience—we are the source, running the same reactor lines, logging every change, knowing which customer expects what minor attribute. We have no resellers in the chain, so inquiries go straight to the people who make and own each batch.

    Our site process produces consistently high purity with minimal residual solvents. The incoming bromine and pyridine derivatives are quality assured onsite, not purchased from a revolving cast of intermediaries. Every parameter, from solvent drying protocols to temperature ramps, reflects years of learning what delivers reliable quality, not just compliance with the base assay.

    Pushing Accident, Impurity, and Supply Risks Down the Line

    Many companies chase the lowest cost, but we’ve seen too much unnecessary pain inflicted by poor quality—projects stalling due to unknown byproducts, catalysis poisoning, or failed registration batches. At the factory, we work to remove these risks. Every day’s work makes the supply line less vulnerable to weather, equipment upsets, or operator error. Our operators see the results first: if they wouldn’t sign off on the batch for their own use, it doesn’t leave the plant.

    Every process tweak to reduce residual dibrominated side-products and limit sodium or potassium salt traces shows up in customer satisfaction. The time saved by avoiding rework, troubleshooting, or revisiting the procurement department outweighs the visible cost of doing the job right the first time.

    Why Consistency Is the True Key

    New users often underestimate how hard it can be to replicate results from lab to factory. Take it from us: Not every 2,6-Dibromopyridin-3-Amine provides the same outcome. Minor unknowns from cheap alternatives might seem trivial—until a pilot plant runs short, or a production run grinds to a halt with obscure analytical blips. Genuine consistency gives chemists freedom to innovate downstream, confident in their materials. That trust comes from our routine—never relaxing standards, never letting complacency slip into the line.

    Continuous Improvement Shapes Every Batch

    We know the pressure on our partners to streamline, minimize supply chain risks, and pass audits for quality. Our own investment in employee training, site upgrades, and process monitoring wouldn’t make sense without that wider context. Every time we finish a successful batch, or find a way to reduce residual solvent below the last record, we hear feedback from senior chemists and managers. These conversations—real and technical, not just sales pitch—guide where we invest in new equipment or rethink an established protocol.

    Every incremental change adds up. Even changes that go unnoticed by newcomers—switching filter media, tweaking drying cycles, rerouting internal movement to avoid cross-contamination—directly improve the product users receive. Repeat business doesn’t come just from a low price, but from the authentic, cumulative record of batches delivered and queries resolved.

    Final Reflections from the Manufacturer’s Desk

    It’s easy to focus on headline metrics: high assay, prompt shipment, regulatory paperwork in order. The real worth—the part that doesn’t show on the spec sheet—comes from every direct conversation, every recovered error, and each time a batch meets or beats the hardest industry scrutiny. When you use 2,6-Dibromopyridin-3-Amine from our line, you’re choosing the dialogue of hundreds of customer calls, years of measured improvements, and the pride of the actual technicians whose hands made it. That’s what makes the difference for scale-ups, patent owners, research labs, and production chemists around the world. We serve as your manufacturing partner, not just a name on a bottle.