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2,4-Dichloro-5-Nitropyrimidine

    • Product Name 2,4-Dichloro-5-Nitropyrimidine
    • Alias 2,4-Dichloro-5-nitropyrimidine
    • Einecs 211-025-7
    • 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

    267420

    Chemicalname 2,4-Dichloro-5-Nitropyrimidine
    Casnumber 119712-35-3
    Molecularformula C4HCl2N3O2
    Molecularweight 194.98
    Appearance Yellow crystalline solid
    Meltingpoint 115-119°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Storageconditions Store in a cool, dry place, tightly closed
    Synonyms 2,4-Dichloro-5-nitro-pyrimidine
    Hazardclass Irritant

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

    Packing & Storage
    Packing The chemical 2,4-Dichloro-5-Nitropyrimidine is packaged in a 100-gram sealed amber glass bottle with clear hazard labeling.
    Shipping 2,4-Dichloro-5-nitropyrimidine is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It is classified as a hazardous chemical and must be labeled accordingly. Transport should comply with applicable regulations, including UN, DOT, or IATA guidelines, and handled by trained personnel using appropriate personal protective equipment (PPE).
    Storage 2,4-Dichloro-5-nitropyrimidine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases, oxidizers, and reducing agents. Protect it from moisture and direct sunlight. Store at room temperature, and ensure proper labeling and secure storage to prevent accidental release or exposure. Wear appropriate personal protective equipment when handling.
    Application of 2,4-Dichloro-5-Nitropyrimidine

    Applications of 2,4-Dichloro-5-Nitropyrimidine in Industrial Manufacturing

    2,4-Dichloro-5-Nitropyrimidine serves as a critical intermediate for several chemical sectors, enabling key transformations in the manufacture of high-value, complex compounds. Our material supports advanced synthetic processes in crop protection chemicals, pharmaceutical APIs, dyestuff intermediates, and specialty coatings, with each application following precise formulation requirements, regulatory frameworks, and downstream processing standards.

    1. Agrochemical Active Ingredient Synthesis

    This compound functions as a building block in producing selective herbicide actives, particularly within the pyrimidine-based herbicide family. Manufacturers integrate it through nucleophilic aromatic substitution to introduce functional groups that tailor biological activity. Downstream processors must adjust the charge ratios and monitor residuals to ensure regulatory compliance for finished agrochemicals.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration and Evaluation (EU)
    • China GB 2763 Maximum Residue Limits
    • EPA Pesticide Registration (U.S.)

    Typical usage ratio

    • Applied at 0.8–1.5 molar equivalents to the nucleophile, depending on the targeted substitution pattern; adjusted based on reactivity of downstream amines or thiols.

    Downstream process integration

    • Charged during early-stage synthesis as the activated pyrimidine ring precursor before amination, thiolation, or further halogenation.
    • Batch reactors operate under controlled temperature and pH to avoid overchlorination or incomplete reaction.

    Final product types

    • Triazine-derived and pyrimidine-derived herbicides (including products like prosulfuron and related sulfonylureas)
    • Formulated suspension concentrates and wettable powders for crop protection

    2. Pharmaceutical Intermediate for Antiviral and Anticancer Agents

    Downstream API manufacturers leverage this material as a nitrogen heterocycle precursor in producing pyrimidine-ring pharmaceuticals. Its controlled reactivity allows precise stepwise modifications for synthesizing nucleoside analogs and targeted cancer therapies. Rigorous adherence to pharmaceutical standards is crucial, as impurity profiles directly impact final API batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP/EP/ChP monographs for process intermediates and APIs
    • EU Directive 2001/83/EC for medicinal product safety

    Typical usage ratio

    • Employed at 1.0 molar equivalent to starting amines, with minor excess (up to 10%) to ensure complete conversion when producing high-purity intermediates.

    Downstream process integration

    • Introduced as the ring-activated scaffold during the initial steps of nucleoside or pyrimidine-conjugate synthesis.
    • Reacts under strictly controlled anhydrous conditions with subsequent purification by crystallization or preparative chromatography.

    Final product types

    • Antiviral nucleoside analogues (e.g., for hepatitis B/C drug candidates)
    • Late-stage oncology intermediates for pyrimidine-based kinase inhibitors

    3. Dye and Colorant Intermediate in Performance Pigment Synthesis

    Manufacturers rely on this raw material for introducing nitro-substituted pyrimidine motifs during the synthesis of high-performance pigments and reactive dyes. It enables direct linkage to aromatic amines or substituted phenols, leading to brilliant, fastness-optimized chromophores suitable for textile and polymer coloration. Consistent product quality and compliance with heavy metal and extractable limits are non-negotiable in this sector.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for textile chemicals
    • EN 71-3 Migration of Certain Elements for toy pigments
    • REACH Annex XVII restrictions on azo dyes and nitroaromatics

    Typical usage ratio

    • Typically used at 0.9–1.1 equivalents per equivalent reactive amine or phenol, fine-tuned for targeted degree of substitution and chromophore depth.

    Downstream process integration

    • Charged in the diazotization/coupling stage or as part of the condensation step with aromatic co-reactants under alkaline or neutral pH.

    Final product types

    • Reactive dyes for cellulose and wool
    • Organic pigments for plastics, coatings, and specialty inks

    4. Precursor in Specialty Coating Resin Modification

    This intermediate supports synthesis of pyrimidine-modified resins where halogenated and nitroaromatic content imparts improved UV stability, chemical resistance, and adhesive properties. Coating formulators introduce the compound during backbone construction or side-chain grafting. Stringent monitoring of hazardous substance limits and consistent QC of resin performance are fundamental for finished product approval.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances
    • ISO 9001:2015 Quality Management Systems for coatings
    • ASTM D6083 for elastomeric roof coatings (where applicable to modified resins)

    Typical usage ratio

    • Used at 1–3% by weight of total monomer content in resin synthesis; tuned based on desired resin crosslink density and functional group compatibility.

    Downstream process integration

    • Dosed into the polymerization reactor as a co-monomer for step-growth or chain-growth processes.
    • Grafted as side-chain modifier during post-polymerization adjustment steps.

    Final product types

    • Specialty coatings for electronics and UV-cured surface finishes
    • Adhesive resins for automotive and industrial assembly
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    Certification & Compliance
    More Introduction

    2,4-Dichloro-5-Nitropyrimidine: Manufacturing Insights and Application Realities

    Understanding 2,4-Dichloro-5-Nitropyrimidine in Real Production Settings

    From its structure alone, 2,4-Dichloro-5-Nitropyrimidine tells a story of complexity: a pyrimidine ring bearing nitro and dichloro substituents. In our plant, handling this molecule goes far beyond watching numbers on an analyzer. When operating vessels for chlorination and nitration, we pay close attention to reaction selectivity and reagent purity. Many customers in the pharmaceutical and agrochemical fields look at this compound as a building block for more complicated actives. This drives constant demand for precise composition and minimal by-products, especially in multistep synthesis.

    This compound’s typical form is a pale yellow crystalline powder—dense, free-flowing, and sharply pungent. We consistently achieve a purity above 98 percent, verified batch-to-batch by HPLC and GC testing. In the early years, contaminant profiles varied due to humidity and raw materials, leading to troublesome reactivity downstream. Years of fine-tuning—tighter controls on feedstocks, incremental improvements to reactor temperature ramps, and carefully staged quenching—steadied our output. Our team has learned that trace impurities, even below half a percent, sometimes start chain reactions in later coupling or amination steps. That difference matters for chemists betting production yields on reliable intermediates.

    The Role of 2,4-Dichloro-5-Nitropyrimidine in Synthesis Pathways

    Few intermediates match this one for versatility in heterocyclic syntheses. Its combination of electron-withdrawing chlorine and nitro groups turns formerly inert positions into handles for rapid further modification. Some teams in pharmaceuticals use it to build antiviral drugs or herbicide catalysts. We hear from researchers who appreciate how the nitro group activates the ring for nucleophilic aromatic substitution—the core of countless molecular transformations.

    It outpaces its close relatives, like 2-Chloro-5-Nitropyrimidine, because of increased reactivity at both the 2 and 4 ring positions. This feature means our customers fewer protection and deprotection steps in their own syntheses. Even though the nitro group’s presence makes downstream reductions trickier, chemists return to this intermediate because its substitutions produce less tarry byproduct and better isolated yields compared with less substituted pyrimidines.

    Specific applications in the lab often include coupling with amines or thiols. Our team tests every batch’s reactivity with reference amines, guided by feedback from process chemists in both the pharmaceutical and agrochemical industries. They’ve told us—sometimes bluntly—about other supplier batches causing gels, fouling reactors, or reacting unpredictably. Experience shows that subtle differences in process water content and thermal decomposition history directly affect how cleanly downstream aminations proceed. Maintaining our specifications tight on water, halide content, and nitro purity is a matter of pride as much as compliance.

    Why This Intermediate Over Others?

    We’re often asked: Why bother with such a specialized molecule at all? Pyrimidine chemistry offers many analogs, and pricing doesn’t always favor extra steps for dichloro substitution. The reality shows up in the lab notebook and on the shop floor. Each application looks for a balance: enough reactivity for efficient further derivatization, but with manageable side-products and good product isolation. For those making antiviral ingredients or new-generation crop protection actives, the two chlorines open up options for introducing multiple different substituents, allowing more diverse molecular libraries compared with mono-chloro systems.

    Dealing with the compound in bulk, its stability and handling characteristics stand out. Many pyrimidine intermediates degrade if exposed to humid air or during long-term storage. This dichloro-nitro variant, once properly dried and packaged, holds up significantly better. We use lined drums and continuous nitrogen protection during packaging, based on years of field feedback. Last season, one agricultural customer pointed out that other versions tended to yellow or form clumps during storage between production campaigns. Since revising our drying protocols, our product has shipped with consistently free-flowing performance—even under harsh warehouse conditions.

    Not all manufacturers stick to analytical transparency. From our experience, interim suppliers sometimes repack or blend to achieve “on-paper” purity, ignoring total impurity profiles instead of elemental scan data. That’s where in-house production knowledge makes the difference. Knowing exactly where side-reactions could slip through, our technical staff have developed spot checks to catch less-obvious polychloro byproducts and persistent residual solvents, especially those that can show up a few steps later in process chemistry.

    Handling the Challenges: Health & Safety, Waste, and Scalability

    Producing 2,4-Dichloro-5-Nitropyrimidine involves more than just stirring and filtering. Most operators adopt rigorous controls, with closed systems to limit operator and environmental exposure. Routine monitoring for fugitive dust, equipment surface residues, and periodic health assessments are part of our manufacturing protocol—born out of years of real lessons, not just textbook plans. On the scale where a slight vent leak paints yellow on ductwork, our training teaches operators to recognize subtle signs of loss before numbers on an emissions report catch up.

    As a legacy member of the chemical manufacturing community, waste minimization gets attention beyond regulatory minimums. The process produces some acid chloride and nitro effluent. Over years, we invested in segmented waste streams and recovery of mother liquors for further offsite treatment. Customers appreciate details here—not just because regulators insist, but because end-users increasingly question their own upstream carbon and waste footprints. In today's world, growing transparency demands that each kilometer of product movement is tracked—a reality for export shipments and domestic flows alike.

    Scale is another practicality. This isn’t always a commodity-grade intermediate, yet we serve partners ranging from gram-scale innovators to multi-ton industrial formulators. In both cases, consistency and access to real technical support outweigh the occasional price negotiation. We keep a reserve of qualified technical staff who have run the compound in both glass reactors and full-size plant vessels, not just the QC bench. That grounds our advice when troubleshooting batch-to-batch variation or proposing transfer methods for new filling lines.

    No one learns all this by reading spec sheets alone. Failures and surprises—residual moisture in one batch, off-odors in another, or trace copper from a bent condenser—taught us the nuances of this chemistry. We're still refining processes and talking with customer chemists about unexpected behaviors in scale-up or scale-down. The learning runs both ways.

    Decoding End-Use Differences: What Downstream Users Notice

    For our customers, differences between this product and close analogs appear right away in yield, handling, and process stability. One scale-up partner in pharmaceutical research reported that competitive materials, though matching on basic assay, caused unpredictable colors and side-product formation in their downstream Mitsunobu coupling. They traced this to micro-level differences in halide impurities, likely from less controlled chlorination upstream. Since our move to double-wash and in-line drying, repeat orders from their team now show sharply reduced batch-to-batch color drift and extractable tar.

    Agrochemical manufacturing presents another test. Bulk handling equipment, pneumatic transport lines, and automated packaging face caking and abrasion risks that escalate with less well-prepared intermediates. Our product’s performance in automated conveyors and filling systems stays stable—free from bridging and sticking that compromise downstream blending. Handling such a specialized compound day-in, day-out reveals how small process tweaks—down to loading temperatures and transfer velocities—affect not just yield, but operator comfort and overall plant reliability.

    A few research clients, building new heterocyclic scaffolds, push every pound of reactivity out of these intermediates. They routinely compare multiple sources, and feedback is candid. We’ve been told that some commercial batches from outside suppliers—especially those repacked or handled through multiple layers of vendors—arrive with subtle product degradation or unreported byproducts. That’s another reason we've stayed with direct shipment policies and clear, prompt release of full COA reports for every drum. Reliability wins repeat business in specialty synthesis more than any price differential.

    Continuous Improvement and Real-World Solutions

    We work from a mantra of day-to-day improvement, rather than resting on batch certification or historical procedures. Unscheduled shutdowns, production delays traced to trace acid formation, and storage failures in humid port conditions have all influenced how we refine our production sequence. Some changes come from hard-won professional advice—a former operator noting a corrosion spot, a QC specialist identifying a drift in IR spectra. Others are born from end-user stories, including one formulation scientist’s discovery that subtle shifts in nitro content impact downstream UV absorbance and end-use stability.

    Years ago, off-spec raw materials from a new supplier led to off odors and reduced crystallinity. The lessons learned from that episode—stricter incoming controls, broader GC screening, harmonized supply agreements—still shape our procurement today. We believe that ongoing dialogue with frontline users and internal production staff is the only reliable way to stay ahead of issues hidden from casual analysis. This focus on feedback helps us offer not just a product, but also responsive troubleshooting support, whether in suggesting solvent choices or in reviewing byproduct evolution in custom synthesis.

    Risk mitigation starts long before drums leave our facility. Each new process run launches with a thorough review: reactor cleanliness, drying systems, integrity of sealing gaskets, and humidity control. Our pride rests on not just passing QA checklists, but on decades of insights—seeing how crystalline structure and bulk density evolve with each tweak in process conditions. These realities never make it into standardized spec sheets or marketing literature, but they shape the reliability of our shipments.

    Trained specialists stay available for process review and emergency troubleshooting, whether a customer reports a clogged filter press or off-color final product. Fielding these questions sharpens our procedures and exposes blind spots in the recipes or supply chain. Sometimes this means adapting packaging for a new automated line; other times, it requires direct support for setting optimum reactivity in a high-throughput plant campaign.

    We also maintain a strong focus on regulatory alignment, but true compliance means more than following a checklist. Much of our operational improvement stems from anticipating changes—keeping VOC emissions within new limits, adopting cleaner energy for heavy loads, and ensuring our safety data is not just up to date, but meaningful for real technicians. Thorough documentation and batch traceability, demanded by our most detail-oriented clients, are built into every shipment.

    Long-Term Investment and Community Exchange

    Just as markets shift, so does science. We monitor changes in chemical regulation—regional REACH changes, environmental restrictions for certain solvent systems, evolving limits on chlorinated discharge. These adjustments can upset process economics, impact logistics, or reduce available reagents. But transparent engagement with regulators and direct communication with customers keeps us aligned with changes before they land as dealership headaches or supply bottlenecks.

    Investment in raw material audits and new process control sensors brought us through several years’ worth of scale increases without quality slippage. Feedback from a multinational customer—experiencing trouble with batch crystallization—sent us back to lab-scale simulation. By restoring agitation, controlling the cool-down rate, and switching to a finer filter mesh, we helped them return to spec, preventing diversion or incineration of a crucial lot. Every plant improvement, inspection, or outside audit sharpens our team’s experience and strengthens trust in our product.

    Industry knowledge never stops evolving. Information exchanges—with downstream users, technical conferences, regulatory insights, and customer audits—shape all aspects of our operation. Sharing experience about this compound’s storage stability, safe handling, and nuances in reactivity helps drive better project outcomes and new product innovations. In many ways, hearing real-world problems from users—whether they come from a pharmaceutical R&D bench or from line supervisors in an agrochemical plant—guides where we target resources for the next performance jump.

    After thirty years in chemical manufacturing, we know every product has a learning curve and a cycle of constant adaptation. 2,4-Dichloro-5-Nitropyrimidine stands as a strong example: it brings reactivity, reliable handling, and robust process performance, but only through careful monitoring and responsiveness to customers’ true needs. Continued investment in people, equipment, and genuine partnership will keep this intermediate stable, relevant, and at the heart of critical synthetic challenges. We’ll keep investing in that story—as makers, as problem-solvers, and as partners committed to chemistry that works, not just chemistry that sells.