Pyridine, 2-bromo-3,5-dichloro-

    • Product Name: Pyridine, 2-bromo-3,5-dichloro-
    • Chemical Name (IUPAC): 2-bromo-3,5-dichloropyridine
    • CAS No.: 182442-73-7
    • Chemical Formula: C5H2BrCl2N
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    664952

    Chemical Name Pyridine, 2-bromo-3,5-dichloro-
    Cas Number 32984-00-6
    Molecular Formula C5H2BrCl2N
    Molecular Weight 242.88
    Appearance Colorless to pale yellow liquid
    Boiling Point 287.5 °C at 760 mmHg (estimated)
    Density 1.78 g/cm3 (estimated)
    Synonyms 2-Bromo-3,5-dichloropyridine
    Smiles C1=C(C(=NC=C1Cl)Br)Cl
    Inchi InChI=1S/C5H2BrCl2N/c6-4-1-3(7)2-5(8)9-4/h1-2H
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Hazard Classification May be harmful if inhaled or swallowed

    As an accredited Pyridine, 2-bromo-3,5-dichloro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 100g amber glass bottle with a secure screw cap, labeled with hazard and handling information.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 12 MT packed in 480 drums, each 25 kg net weight, securely palletized for safe chemical transportation.
    Shipping **Shipping Description:** Pyridine, 2-bromo-3,5-dichloro- should be shipped as a regulated chemical substance, typically under UN 2810 (Toxic Liquid, Organic, N.O.S.). It must be securely packed in chemical-resistant containers, clearly labeled, and accompanied by the appropriate Safety Data Sheet (SDS). Shipping must comply with local, national, and international hazardous materials regulations.
    Storage Store 2-bromo-3,5-dichloropyridine in a cool, dry, and well-ventilated area, tightly sealed in a chemical-resistant container. Keep away from heat, open flames, and direct sunlight. Segregate from incompatible materials such as strong oxidizers, acids, and bases. Ensure proper labeling and access restricted to trained personnel. Follow all local, state, and federal regulations for hazardous chemicals.
    Shelf Life Pyridine, 2-bromo-3,5-dichloro- typically has a shelf life of 2-3 years if stored in a cool, dry place.
    Application of Pyridine, 2-bromo-3,5-dichloro-

    Purity 98%: Pyridine, 2-bromo-3,5-dichloro- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures enhanced reaction yields.

    Melting Point 85°C: Pyridine, 2-bromo-3,5-dichloro- with melting point 85°C is used in custom organic synthesis, where predictable phase behavior facilitates controlled processing.

    Stability Temperature 120°C: Pyridine, 2-bromo-3,5-dichloro- with stability temperature 120°C is used in high-temperature catalytic reactions, where thermal stability maintains structural integrity.

    Molecular Weight 240.34 g/mol: Pyridine, 2-bromo-3,5-dichloro- of molecular weight 240.34 g/mol is used in agrochemical research, where precise molar calculations enable accurate formulation development.

    Particle Size ≤50 µm: Pyridine, 2-bromo-3,5-dichloro- with particle size ≤50 µm is used in lab-scale solid-phase synthesis, where fine particle distribution improves compound dispersion.

    Water Content <0.1%: Pyridine, 2-bromo-3,5-dichloro- with water content <0.1% is used in moisture-sensitive coupling reactions, where low moisture prevents side reactions.

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    Certification & Compliance
    More Introduction

    Pyridine, 2-bromo-3,5-dichloro-: More Than Just a Building Block for Chemical Innovation

    Pyridine, 2-bromo-3,5-dichloro-, also recognized by specialists under chemical abstracts numbers and with distinct identifiers in laboratory catalogues, draws the curiosity of both research and industry circles for good reason. Its particular configuration—a pyridine ring with bromo at the second position and chloros at both the third and fifth—results in unique properties that other derivatives in the pyridine family simply do not offer. Over the years, working in research labs and consulting for fine chemical manufacturers, I have seen this compound’s role evolve beyond a specialty intermediate into an essential part of larger synthesis conversations.

    How Molecular Structure Guides Us Forward

    Behind the scenes, synthetic chemistry depends heavily on being able to nudge a molecule this way or that, opening and closing doors to new compounds. The extra bromo atom at the 2-position on this pyridine ring, in combination with two chloros, creates an opportunity for directed reactivity you just won’t see in basic pyridine, or even in more common mono-halogenated pyridines. These features do more than catch the eye of organic chemists; they influence the pace and predictability of downstream reactions, making a big difference in everything from pharmaceuticals to materials science.

    I’ll give an example: in medicinal chemistry, those halogen atoms can help steer subsequent transformations to install other functional groups selectively. Synthetic pathways become shorter, with cleaner end products and less unwanted side chemistry. Fewer by-products means fewer purification headaches and less waste. Ask anyone who has tried to purify a sticky mess after a poorly directed reaction—this selectivity isn’t just a technical detail, it’s the difference between a scalable process and an expensive dead end.

    Fit for Purpose: Choosing the Right Compound for the Job

    One of the methods that stands out in the lab is Suzuki coupling, and here, the bromo function on 2-bromo-3,5-dichloro-pyridine really shines. The lab techs I’ve worked with prefer bromo over chloro analogues due to easier activation during these cross-coupling reactions. The pathway to introduce more complex aryl or heteroaryl groups becomes both shorter and more reliable than with dichloropyridines or plain 2-chloropyridine. Beyond academic synthesis, contract research organizations and pharmaceutical makers have embraced this compound, precisely because of these technical advantages.

    From my work in process development, I've noticed that these halogenated pyridine derivatives move from milligram scale in research labs to multi-kilo batches in manufacturing surprisingly smoothly. Purity levels—usually specified upwards of 98% by HPLC and NMR—meet most process requirements without reworking. This sort of reliability supports scale-up and regulatory filings. Contrasting it with something like 2,6-dichloropyridine, which might suit agricultural chemistry but stalls in more delicate pharmaceutical contexts, you start appreciating why chemists are so keen to source the right halide patterns.

    Practical Applications in the Real World

    This compound finds its way into a surprising mix of end-products. The chemical structure serves as a stepping stone for agrochemical fungicides, whose patent literature you can read through to see direct applications in keeping crops healthy. More importantly, in pharmaceutical R&D, the ability to fine-tune the aromatic core lends itself to creating pyridine-based scaffolds for enzyme inhibitors and kinase blockers. These are not just theoretical examples; reading peer-reviewed papers and patent filings from the last decade, you encounter this exact structure time and again, marking progress in drug discovery efforts that aim to address cancer, metabolic disease, and neurological disorders.

    The breadth of applications sometimes surprises newcomers. Even electronic materials benefit from such molecules, where fine-tuning halogen substitution can influence crystalline packing and charge mobility in new organic semiconductors. In these fields, a single substitution change on the pyridine ring shifts properties enough to justify a completely new patent. Throughout my time discussing scale-up challenges with chemical engineers, one truth stands out: you can’t invent a better material if you’re missing key starting blocks. That’s why having stable, well-characterized intermediates like 2-bromo-3,5-dichloro-pyridine serves as a quiet backbone to bigger innovations.

    How It Sets Itself Apart from Similar Pyridines

    Talk to a synthetic chemist, and they’ll likely tell you that on paper, any old dichloropyridine could do a similar job—until you get down to actually doing the work. I have seen labs waste months struggling with less reactive chloro analogues, doggedly trying to make a process efficient. In these cases, 2-bromo-3,5-dichloro-pyridine doesn’t just offer a shortcut; it defines the only viable route. The position of the halogens dictates how easily the molecule participates in classic substitution reactions, impacting regioselectivity and yields.

    For instance, in electrophilic substitution, this particular derivative outperforms counterparts like 2,4,6-trichloropyridine, which may not activate as easily for forming more complex rings or attaching large groups. Researchers learned through trial and error that substituting a bromo for a chloro at the 2-position speeds up reactions, making the overall synthesis less harsh on sensitive function groups. This subtle structural decision winds up saving several degrees of reaction temperature and hours off process times, a reality any manufacturing chemist appreciates during scale-up and scale-out studies.

    Handling and Safety: Not to Be Taken Lightly

    Halogenated compounds aren’t a playground for careless operators. From my first days in organic labs, I learned that handling these intermediates, especially when scaling beyond test tube amounts, takes real respect and attention to detail. Safety data for bromo and chloro pyridines typically flags respiratory irritation or the need for solid ventilation and personal protective equipment. Manufacturing plants don’t take shortcuts here—fume hoods, dual sets of gloves, and standard environmental controls exist for a reason. I’ve never seen an experienced operator skip the extra steps, and I wouldn’t trust a vendor or contract plant who did.

    Stability and shelf life are another concern worth mentioning. Once correctly stored—cool, dry, out of direct light—the compound holds up well for months if not years, making it easier on inventory managers. Problems arise only when suppliers cut corners, so sourcing from reputable chemical suppliers, with real batch records and certificates of analysis, protects both the process and the final product’s quality. I’ve seen disastrous delays occur when someone opts for cheaper, poorly documented material, only to fail quality checks further down the line. Chemical traceability and transparency in manufacturing mean these headaches become avoidable, not inevitable, outcomes in serious operations.

    Market Realities and Sourcing Choices

    Today’s global chemical market rewards flexibility and creative sourcing strategies. Given high demand for advanced pyridine derivatives and the occasional supply crunch—especially when upstream building blocks face their own bottlenecks—procurement decisions impact timelines for drug development, agrochemical launches, and even electronics rollouts. Real stories circulate of delays in custom syntheses simply because a halogenated pyridine variant wasn’t available from a reliable source. I’ve been part of meetings where missing a single intermediate postponed launch dates by months. In these moments, having a trusted supplier for 2-bromo-3,5-dichloro-pyridine becomes as critical as having an idea in the first place.

    This era of supply-chain sensitivity pushes organizations to partner only with established vendors who provide transparent logistics and full traceability. I’ve seen companies conduct full supplier audits, not just for quality compliance, but to affirm practices around environment, health, and ethical employment as well. In a world where customers and regulators demand E-E-A-T—experience, expertise, authoritativeness, trustworthiness—chemicals that show up on time, meet purity standards, and are delivered alongside reliable documentation, make all the difference.

    Innovation Through Careful Selection: The Real Value

    Progress in synthetic chemistry relies not just on visionary ideas, but on boring details: shelf-stable compounds, predictable reactivity, and ready compliance with environmental guidelines. 2-bromo-3,5-dichloro-pyridine fits this bill, letting researchers focus on their core projects rather than fighting their feedstock. I’ve worked with teams that nearly doubled their project velocity just by shifting from less reactive analogues to this particular molecule. Productivity gains like that may remain invisible to outsiders, but inside the lab or pilot plant, every chemist recognizes the value of cutting out headaches. The resulting innovation isn’t just about a fancier molecule, but a sharper, more streamlined path from early idea to finished product.

    In my view, the people who weather the storm of commercialization—from patenting all the way through kilo-lab scale—pay close attention to every intermediate in their synthetic routes. They know that changing even one step or one raw material can ripple through a process, changing timelines, costs, and even the regulatory burden. Making informed choices on starting materials can make or break a program’s feasibility. The huge advances in green chemistry and process intensification wouldn’t have happened if practitioners had ignored the way these subtle changes in raw materials open or close doors down the line.

    Room for Improvement—And Where the Industry Should Go Next

    Despite all the practical advantages, halogenated pyridines still pose tough environmental and waste management questions. From the days of my early lab training, the need to capture and properly dispose of halogenated waste was drilled into us. Persistent organic pollutants from improper handling of bromo and chloro compounds have led to stricter controls in both developed and developing nations. Waste minimization strategies—careful solvent choice, recycling of reaction by-products, use of catalytic instead of stoichiometric coupling agents—have made real inroads. But there’s more to do. Biodegradable alternatives aren’t on the horizon for most synthetic intermediates in this class, so pushing for better waste capture and smart process design matters.

    On the regulatory front, I’ve seen more companies push for full safety testing, fate and transport analysis, and life-cycle assessments even for non-drug intermediates. Customers and regulatory agencies alike are wary of any chemical whose fate can’t be traced beyond the doors of the factory or the lab. Public and investor pressure for broader corporate responsibility, including in the realm of specialty chemicals, accelerates the adoption of best practices. Purchasing teams and R&D managers need to work hand in hand—continuously evaluating both the performance of pyridine intermediates like this one and the ethics of their supply chain partners.

    Potential Solutions and the Path Ahead

    Some organizations have responded by closing loops wherever possible. I’ve seen effective programs where halogenated by-products get collected, treated, and even re-purposed or sold, turning a problem into a revenue stream. Innovation in catalytic cycles and continuous flow processing cut down on solvent use and contribute to safer, greener processes. For those investing in technology, automation of analytical monitoring has all but ended “bad batch” surprises, helping both smaller startups and larger contract manufacturers stay competitive and compliant.

    The industry has also begun to share more data and best practices across company borders, recognizing that one plant’s learnings can prevent trouble for many others. I’ve attended conferences where the open discussion of real-world incidents—good and bad—drives collective improvement faster than any regulator’s mandate. New entrants, as well as seasoned chemists, benefit from this expanding culture of transparency, pushing standards in both product consistency and environmental stewardship higher year after year. In practical terms, customers today expect a track record of safe, responsible behavior from their chemical partners. It’s not just the cost or the speed that wins the account, but the entire package of confidence a supplier provides in their process and philosophy.

    Why Choices Matter in the World of Fine Chemicals

    From direct experience, I’ve learned that seemingly small decisions about which intermediate to buy, which vendor to trust, and which process to run can snowball. The people who look beyond price tags to ask “how will this affect my downstream process?” or “will this raise any flags with my QA manager?” are the ones whose projects cross the finish line. For 2-bromo-3,5-dichloro-pyridine, the edge comes down to stability, predictable reactivity, established quality benchmarks, and the track record of both supplier and downstream users. The story of this compound is not just its chemical formula. It's the result of collective, hard-won knowledge from every scale-up, every batch record, and every improvement made along the way.

    As the market continues to shift—with new regulatory changes, environmental pressures, and soaring demand for quality—the foundations of successful innovation stay the same. The right raw materials, sourced from experienced, reputable partners, make every downstream achievement possible. For buyers and users of specialized pyridine derivatives, understanding this reality ensures the decisions made at the start of development pay dividends all the way to the final product.