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5-Bromo-2,4-Dichloropyrimidine

    • Product Name 5-Bromo-2,4-Dichloropyrimidine
    • Alias 5-Bromo-2,4-dichloropyrimidine
    • Einecs 609-720-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    648221

    Product Name 5-Bromo-2,4-Dichloropyrimidine
    Cas Number 19754-28-4
    Molecular Formula C4HBrCl2N2
    Molecular Weight 227.88
    Appearance White to pale yellow crystalline powder
    Melting Point 68-71°C
    Solubility Slightly soluble in water
    Density 2.22 g/cm3
    Purity Typically >98%
    Smiles C1=NC(=NC(=C1Cl)Br)Cl
    Inchi InChI=1S/C4HBrCl2N2/c5-2-1-8-4(7)9-3(2)6
    Storage Conditions Store in a cool, dry, and well-ventilated place

    As an accredited 5-Bromo-2,4-Dichloropyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25-gram 5-Bromo-2,4-Dichloropyrimidine arrives in a sealed amber glass bottle with a tight screw cap and hazard labeling.
    Shipping **5-Bromo-2,4-Dichloropyrimidine** is packed in sealed, chemically-resistant containers and shipped in compliance with international hazardous material regulations. The package includes detailed safety data sheets, proper labeling, and hazard warnings. Transport occurs via certified carriers, ensuring protection from moisture, heat, and physical damage throughout transit to maintain product integrity and safety.
    Storage 5-Bromo-2,4-Dichloropyrimidine 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, away from heat sources and ignition points. Ensure appropriate labeling and restrict access to trained personnel, following all relevant safety and regulatory guidelines.
    Application of 5-Bromo-2,4-Dichloropyrimidine

    Applications of 5-Bromo-2,4-Dichloropyrimidine in Industrial Manufacturing

    As a direct manufacturer of 5-Bromo-2,4-Dichloropyrimidine, we serve high-value chemical synthesis flows in several specialty sectors. Each application described here focuses on genuine, large-volume downstream segments where this intermediate delivers significant structural or process advantages within refined production cycles.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies utilize this pyrimidine derivative as a core building block in the construction of API scaffolds, including various anti-viral, anti-tumor, and anti-inflammatory agents. Its bromine and chlorine substitutions allow selective substitution and coupling reactions, supporting efficient formation of heterocyclic rings critical to finished drug molecules. Our customers employ validated process routes for high-purity transformations, integrating this intermediate at early to mid-stages of API route design for medicinal product pipelines.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for APIs
    • USP, EP, and JP monographs for relevant drug substances
    • US FDA Drug Master File guidelines for registration dossiers
    • EU EudraLex Volume 4, Part II requirements

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target synthesis step, adjusted for route efficiency and byproduct control in API multi-step synthesis

    Downstream process integration

    • Enters as a halogenated core in the pyrimidine ring-building step, participating in Suzuki or Buchwald–Hartwig cross-couplings and nucleophilic substitution steps with amines, alkoxides, or thiols under controlled, anhydrous, and inert conditions

    Final product types

    • Crystalline API intermediates for small-molecule drugs (e.g., kinase inhibitors, HIV treatments)
    • Pharmaceutical final forms including tablets, injectables, and capsules produced from synthesized APIs

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    Leading agrochemical manufacturers integrate this dichloropyrimidine compound as a reactive intermediate for crop protection actives, especially where heterocycle-based scaffolds provide selectivity or resistance management in field applications. The selective halogen profile supports downstream substitution, tailoring functional groups for biological activity, photostability, and soil mobility, without compromising compliance with crop safety legislation.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) pesticide specifications
    • OECD Good Laboratory Practice for agrochemical safety and residue studies
    • REACH chemical registration (EC 1907/2006) for European formulations
    • US EPA inert ingredient assessment for formulation approval

    Typical usage ratio

    • 0.8–1.5 molar equivalents per active ingredient backbone, tailored by downstream chlorination or cross-coupling efficiency

    Downstream process integration

    • Introduced during key heterocycle expansion or substitution reactions in the assembly of pre-herbicidal or pre-fungicidal precursors, often via palladium-catalyzed reactions or direct nucleophilic aromatic substitution steps

    Final product types

    • Technical-grade herbicide and fungicide active ingredients
    • Wettable powders, emulsifiable concentrates, and water-dispersible granules used in formulated crop protection products

    3. Pharmaceutical Intermediate for Antiviral Nucleoside Synthesis

    Nucleoside manufacturers in the global pharmaceutical sector employ this halogenated pyrimidine as an integral intermediate for nucleoside analog development, facilitating high-reactivity pathways for coupling with protected sugars. High specificity in substitution reactions enables synthesis of potent antiviral candidates, including those used in the treatment of hepatitis and other viral infections, where fine control over process impurities is critical.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP, 21 CFR Part 211)
    • ICH Q3A Impurity Guidelines
    • US DMF, EU CEP (Certificate of Suitability) for nucleoside intermediates
    • Ph. Eur. and USP reference standards

    Typical usage ratio

    • 0.6–1.0 molar equivalents relative to sugar coupling agents in nucleoside synthesis; the precise amount depends on the protecting group strategy

    Downstream process integration

    • Utilized in the halogenated nucleobase synthesis stage, reacting directly with protected ribose or deoxyribose units in glycosylation or Mitsunobu-type reactions, followed by deprotection and purification

    Final product types

    • Purified nucleoside intermediates for further conversion into finished antiviral and antineoplastic drugs
    • Bulk APIs containing nucleoside scaffolding for oral and injectable antivirals

    4. Dye and Pigment Intermediate for Electronic Displays

    Specialty dye and pigment companies incorporate this dichlorinated and brominated pyrimidine in multi-step synthesis of advanced chromophores, particularly for organic electronic displays (OLED) and specialized printing inks. The molecule’s precise substitution allows construction of electron-deficient segments that improve charge transport and colorfastness in OLED stacks and inkjet printing substrates.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for restricted substances in electronics
    • EN 71-3:2019 for chemical safety in colorant applications
    • Quality management in ISO 9001-certified pigment manufacturing
    • Registration under TSCA for North American commerce

    Typical usage ratio

    • 0.4–1.0 molar equivalents as a chromophore precursor within dye synthesis, adjusted by final color index and electronic performance targets

    Downstream process integration

    • Reacted at the conjugation and functionalization step of dye or pigment synthesis, where it defines the central segment of extended pi-conjugated systems, followed by palladium-catalyzed couplings and purification

    Final product types

    • OLED dyes and charge transport materials for display production
    • High-stability inks used in inkjet and specialty printing markets

    5. Chemical Intermediate for Advanced Material Coatings

    Producers of high-performance coatings for electronics, aerospace, and specialty polymers employ this compound in the synthesis of cross-linkable intermediates. Its halogenation supports step-growth polymerization and post-functionalization, forming networks with improved barrier properties, flame resistance, and environmental stability, crucial for protective coatings demanding precise structural incorporation without compromise to downstream process control.

    Industry compliance standards

    • ASTM D01 standards for coatings and related materials
    • ISO 14001 for environmental management in production
    • Restriction of Hazardous Substances (RoHS) in manufactured coatings
    • European Chemicals Agency (ECHA) REACH compliance for polymer additives

    Typical usage ratio

    • 0.2–1.0 percent by weight in reactive resin systems or as a prepolymer additive, adjusted according to desired polymer cross-linking density

    Downstream process integration

    • Integrated at the resin blending or copolymerization stage, where it co-reacts with multifunctional monomers to yield high-performance film-forming polymers in batch or continuous reactors

    Final product types

    • Protective coatings for PCBs and electronic modules
    • Barrier films for packaging or insulation in aerospace and electronics
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    Certification & Compliance
    More Introduction

    5-Bromo-2,4-Dichloropyrimidine: Experience from the Manufacturer’s View

    Real-World Insights Behind a Versatile Intermediate

    Within any chemical plant, a handful of raw intermediates end up shaping the successes of crop protection, pharmaceutical, and material science projects. 5-Bromo-2,4-dichloropyrimidine has proven to be that kind of staple over years of actual production. By sharing what goes into consistent, reliable batches, the practical value of this compound becomes clearer, especially for development chemists and scale-up teams searching for dependable building blocks.

    What Makes 5-Bromo-2,4-Dichloropyrimidine Stand Out?

    What gives this molecule relevance in a crowded market? In our reactors, it’s the unique arrangement of two chlorine atoms and one bromine atom on the pyrimidine ring that makes it so appealing. These halogenations open direct access to numerous pathways by facilitating selective cross-couplings or substitutions. Rather than jumping through hoops for odd functional group conversions, researchers pick our product to simplify the journey to more complex heterocyclic targets.

    By focusing production on high assay material and limiting side-reactions, the actual appearance of our intermediate stays consistent—a pale crystalline solid with a benchmark purity often above 99%, checked lot-wise before release. We see that low residual solvent is critical, since certain applications are sensitive to trace impurities. Chasing after that single-digit ppm on related chemicals does mean longer purification times and tighter in-process controls, but it yields a product that receives repeat orders from demanding labs and pilot plants.

    Manufacturing Perspective: Consistency in Every Drum

    Consistency does not just mean matching numbers on a certificate. Coming from real manufacturing, consistency requires a thoughtful response to variable raw material quality, seasonal temperature shifts, and reactor cleanouts that don’t always go as planned. In practice, our operators review not only the halide starting material but water content, which can trigger minor hydrolysis if not held in check. Suppressing these side-reactions leads to brighter, less colored material that passes batch release standards even after months in storage.

    We do not try to push output at the expense of end-use quality. Years ago, trialing a higher-throughput sequence introduced more colored byproducts—some mirrored the target on TLC but trailed off purity standards during actual NMR checks. The feedback from downstream users was instant: reaction yields dropped, and separation steps grew painful. By returning to longer, slightly slower halogenations, clean crystallization, and sharper fraction cuts, we restored both purity and user trust.

    How Our Technical Choices Impact Your Lab or Plant

    Feedback loops with real chemists influence our processes as much as our internal R&D. Clients synthesizing subtle active ingredients want not just halo-pyrimidine content, but freedom from stubborn traces of related halides. For biotechnology screens, trace catalyst residues are a significant concern. Our answer is repeated, validated removal efforts—sometimes with costly scavengers, sometimes through added washings—because even half a percent deviation becomes a major point in final step troubleshooting.

    We also keep a keen eye on particle size and habit. From years of drum handling and transfer experience, we learned that too fine a batch blocks screw feeders, yet oversized crystals introduce long filtration times. We aim for a modest, free-flowing granule. This brings direct impact to batch reactors downstream, where the material can be charged efficiently without caking or loss. For custom orders, we sort particle ranges by sieving, rather than relying solely on crystallization kinetics.

    Where 5-Bromo-2,4-Dichloropyrimidine Really Proves Its Value

    This intermediate underpins a wider web of synthesis work than most outsiders realize. Customers use it as a jumping-off point for arylation, amination, or Suzuki couplings—a favorite in fields ranging from lead compound optimization to scale-up runs for gram-to-kilogram lots. For example, introducing an amino group at C4 selectively becomes straightforward, because the steric and electronic effects of bromo substituent at position 5 and chlorines at positions 2 and 4 are well understood. Researchers achieve these transformations with higher yields and shorter reaction times than they would with other substituted pyrimidines.

    Even in an age of ever-evolving library creation, this classic building block remains useful. It bridges the gap between simple heterocycles and highly decorated, drug-like compounds. This versatility arises directly from its “programmable” substitution pattern—chemists can swap groups with high selectivity and minimal unwanted isomer formation. Unlike more crowded pyrimidine systems, steric hindrance is manageable, with smoother purification steps in downstream reactions.

    Comparing Our Intermediate to the Competition

    Our plant doesn’t just measure success by how many tons exit the dryers. By speaking with both start-ups and established API producers, we’ve seen that other sources often skimp on crucial benchmarks. Slightly elevated levels of 2,4,5-tribromopyrimidine or mixed chlorobromo byproducts sound like minor issues, but they erode the predictability of each run. We invest in full chromatographic profiles and guarantee a single dominant spot by HPLC, not just a passing glance at a melting point or a quick purity estimate by titration.

    Other differences emerge during actual use. Competing grades might carry more trace iron from corroded reactors or glass particles from hasty vacuum transfer. We use inert-lined reactors and disciplined filtration so our shipments stay clear of non-organic detritus. This attentive housekeeping only comes from years of responding to customer complaints and genuinely wanting to reduce troubleshooting calls after delivery. Most traders won’t see the headaches this kind of contamination causes; as a producer, we prioritize it from the ground up.

    Applications Built on Years of Customer Partnership

    We rarely hear the end user talk about wanting “a compound”—they want their process to run right, their research to move forward, and their customers’ projects to meet launch dates. 5-Bromo-2,4-dichloropyrimidine gives formulators a head start in custom herbicides, new kinase inhibitor scaffolds, or as a foundation for fluorescent probes. Synthetic chemists often report successful late-stage functionalizations by incoming nucleophiles, with the bromine offering a clean handle for Pd-catalyzed coupling.

    In our experience supplying both exploratory and commercial-scale batches, effective communication with formulators and process chemists shapes which designs go to market. One research partner needed ruthenium levels below 100 ppb due to regulatory filings—they didn’t get there with off-the-shelf material, but did after our plant adopted a new scavenger protocol. Another project demanded the exclusion of specific solvent residues below 10 ppm—solved at the production level by in-line monitoring. Delivering on these needs cements long-term cooperation and shapes how the product is received industry-wide.

    Sustainability and Regulatory Trends

    Increasing scrutiny over halogenated intermediates has shifted how factories operate. Waste streams, energy footprints, and worker exposure concerns affect even well-established production cycles. For 5-bromo-2,4-dichloropyrimidine, stricter wastewater halide limits required us to overhaul effluent treatment, pushing for two-stage neutralization and closed cooling cycles rather than old once-through water jackets. Real changes come neither cheap nor fast, but these upgrades keep us on speaking terms with inspectors and increasingly with customers’ compliance teams.

    Regulations also reach as far as residual impurities: micron-scale particles, cross-contamination, and trace elements now receive full documentation, impacting both plant life and end-user validation. Our team runs routine cross-checks with reference laboratories, not just internal QC, validating real-world compliance and doubling the trust between us and our customers.

    How End-Users Shape Our Evolution

    Real innovation comes from listening to the actual pain points downstream. A major pharma client switched suppliers until finding our process kept their lines running without frequent shutdowns to clear blockages. For a start-up screening hundreds of analogues, our controlled subsample packaging meant less exposure and fewer lost grams in each transfer.

    More recently, specialty material customers demanded a pre-screening on light stability, since some downstream users noticed sensitivity under UV exposure. We tweaked packaging, tested opaque liners, and introduced fresh desiccant charges in transit—directly improving how the product performed outside our plant. These actions grew from a manufacturer’s direct accountability and open feedback, not a generic response.

    Product Handling: Practical Details Matter

    The entire supply chain benefits from a physical product that stores well, resists clumping, and pours without sticking. Our storerooms favor humidity-controlled environments, and we mapped out the hygroscopic properties over seasons. During rainy spells, sensitivity rises—noticing this, we invested in new barrel liners and expanded our use of molecular sieves.

    Practical handling also applies to scale-up: both chemical engineers and bench chemists value drums that fit into their workflows. We print clear lot numbers, label shelf-life based on rigorous in-house tests, and ship in verified UN-rated packages. Any breach, even microscopic cracks, can cascade into big headaches; we track every return and treat each as a learning opportunity.

    Monitoring and Improving with Every Batch

    We regularly engage in post-mortems after each campaign, not out of formality but to actually reduce error rates and maintain high satisfaction. Unexpected color shifts, slight odor changes, or an outlier in melting range trigger immediate re-tests, since these are often early signs of side reactions not caught by automated data flags.

    We maintain full batch traceability. This counteracts small upstream hiccups that could multiply as re-work or disposal if not flagged early. These steps go beyond what a trading desk considers and reflect a real manufacturer's outlook: the product in the barrel matters as much as the documentation on the label.

    Refining the Product with a Manufacturer’s Discipline

    Speaking from years of batch production and direct customer feedback, most improvements come from lived experience rather than any published method or software implementation. Success depends on recognizing that small adjustments—whether to drying times, purification sequences, or even bag-sealing routines—impact not just the bottom line but how confident a user feels running their own synthesis.

    On occasion, requests for ultra-high purity for regulatory filings or new biological testing spur us to engineer process changes. These can include column upgrades, adjusted crystallization solvents, or even just slower temperature ramps at bottleneck stages. Since such changes take time, clear communication with users helps them anticipate when their new processes will receive precisely updated product lots.

    The Evolving Role of Substituted Pyrimidines

    Few molecules maintain relevance the way substituted pyrimidines have. Demand for their unique properties runs from newly identified protein targets to high-throughput screens for agricultural leads. As new substitution patterns become desirable, most researchers come back to core fragments like 5-bromo-2,4-dichloropyrimidine because of their high selectivity and ease of further elaboration.

    Working directly in production, we see how small molecule optimization teams benefit from a root intermediate that doesn’t introduce added steps or analytical complications. The time savings in method validation—both synthetic and analytical—are real, directly impacting how long it takes for a lab result to move into the hands of a process chemist or formulary designer.

    Continuous Feedback, Continuous Improvement

    As a chemical manufacturer, we learn that sustainable growth and high standards depend on constantly listening, responding, and refining. No two campaigns run identically; raw material sourcing, seasonal energy prices, and new safety protocols keep our playbook flexible. Each client’s challenge—whether a new impurity standard, an unexpected process blockage, or regulatory nuances—pushes us to adapt, troubleshoot, and improve our own understanding of the compound.

    The result is a product that is not static, but evolving—driven by a close partnership with users, attention to compliance and safety, and years of on-the-ground experience working with 5-bromo-2,4-dichloropyrimidine from initial halogenation to drum shipment. Our drive as a manufacturer is not just to sell a compound, but to help others achieve reliable, robust results—one well-made batch at a time.