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2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One

    • Product Name 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One
    • Alias NSC 23180
    • Einecs 682-076-6
    • 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
    VTB
    Specifications

    HS Code

    450950

    Compound Name 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One
    Molecular Formula C12H5Cl3FN2O
    Molecular Weight 335.54 g/mol
    Cas Number Give if known, else unknown
    Appearance Solid (exact color may vary)
    Chemical Class Pyridazine derivative
    Smiles O=C1C(Cl)=C(Cl)N=NC1CC2=C(C=CC=C2Cl)F
    Inchi InChI=1S/C12H5Cl3FN2O/c13-8-2-1-3-9(16)11(8)5-6-10(18)12(14)7(17)4-15-6/h1-4H,5H2
    Synonyms No widely known synonyms

    As an accredited 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with tamper-evident cap, labeled with chemical name, formula, hazard warnings, and manufacturer details.
    Shipping **Shipping Description:** 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One is shipped in tightly sealed containers to prevent moisture and contamination. It is packaged according to chemical safety regulations, typically under cool and dry conditions, with appropriate labeling and hazardous materials documentation for safe domestic and international transport. Handle with care during transit.
    Storage 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3(2H)-one should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Follow all relevant safety regulations and store at controlled room temperature (15–25°C) to ensure chemical stability and prevent degradation.
    Application of 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One

    Applications of 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One in Industrial Manufacturing

    As a direct manufacturer specializing in advanced pyridazine-based intermediates, we supply 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One for multiple specialized downstream segments. Below, we outline its major industrial application areas, specifying regulatory standards, integration practices, and finished products linked to each scenario.

    1. Crop Protection Synthesis: Herbicide Intermediate

    Agrochemical formulators select this compound for direct use in the synthesis of selective herbicide active ingredients targeting broadleaf and grass weed control. Its chemical structure supports efficient coupling in cyclization and halogenation steps, enabling downstream manufacturers to maintain stringent quality and impurity control through all reaction stages as required in registered plant protection products. The intermediate’s high purity profile enables reproducibility in scale-up, helping ensure global market compliance for agro-active compounds.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products Regulation)
    • US EPA 40 CFR Part 180 – Tolerances and Exemptions for Pesticide Chemicals
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 15–30% by molar ratio as a core intermediate in multi-step API synthesis; actual percentage depends on target molecule design and desired yield for active ingredient batch production.

    Downstream process integration

    • Introduced during core ring construction steps or aromatic substitution reactions within herbicide active synthesis chains; feeding occurs prior to final purification and formulation blend steps for technical concentrates.

    Final product types

    • Herbicide technical concentrates
    • Formulated crop protection products (e.g., EC, SC, WG formulations)
    • Pre-mix active ingredient blends
    • Bulk active intermediates for contract manufacturing

    2. Pharmaceutical Intermediate for Anti-Cancer API Synthesis

    Several pharmaceutical manufacturers utilize this dichloropyridazine derivative as a building block for kinase inhibitor drug substances and related antineoplastic API development. Its halogenated scaffold offers synthetic flexibility during Suzuki coupling and amide bond-forming steps. Production relies on full traceability and detailed impurity profiling under ICH and pharmacopoeial guidance. GMP-grade supply is fundamental in regulated drug ingredient manufacturing, ensuring reliability from route scouting through scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP Pharmacopoeias (intermediate grade)
    • EU Guidelines for GMP for Medicinal Products
    • 21 CFR Part 210/211 (US FDA Drug CGMP Regulations)

    Typical usage ratio

    • 5–18% by molar input in stepwise synthesis, precise ratio set by process chemists after route establishment and mass balance validation during process development.

    Downstream process integration

    • Reacted at critical intermediate formation stages—often after core scaffold installation but before derivatization or salt formation in the final drug substance synthesis.

    Final product types

    • Anti-cancer API bulk intermediates
    • Targeted kinase inhibitor drug substances
    • Advanced pharmaceutical intermediates for CDMO supply chains
    • Specialized chemical probes for life sciences research

    3. Fine Chemical Intermediate in Electronic Chemical Manufacturing

    Manufacturers in the electronics supply chain employ this compound as a precursor for specialty fluorinated and chlorinated ligands, used in high-performance electronic material synthesis. It enables reliable introduction of halogenated moieties in semiconductor process chemicals and liquid crystals. Strict analytical monitoring and process management are standard to achieve tight purity levels and minimize trace metal/organic contamination, especially for microelectronic and display segment requirements.

    Industry compliance standards

    • SEMI C3 Standard for Electronic Grade Chemicals
    • IEC 62474 for Material Declaration in Electronics
    • RoHS 3 (EU Directive 2015/863)
    • ISO 14001:2015 Environmental Management

    Typical usage ratio

    • 2–10% by weight in high-purity precursor cocktails for ligand synthesis; levels optimized based on purity and target functionality in final material blend.

    Downstream process integration

    • Added during early-stage nucleophilic substitution and halide exchange reactions for fluorinated aromatic platform constructions; enters streams prior to distillation and purification of final functional molecule.

    Final product types

    • Electronic grade specialty reagents
    • Liquid crystal monomers
    • Photolithography process chemicals
    • Halogenated performance additives for microelectronics production

    4. API Intermediate for Veterinary Pharmaceuticals

    This dichloropyridazine is a valued intermediate in the synthesis of select veterinary drug substances, especially for anti-parasitic and anti-inflammatory APIs. Manufacturers in animal health maintain tight control of residual solvents and heavy metals, in line with VICH and relevant pharmacopoeial monographs. Production uses validated multi-step synthesis routes and batch recordkeeping to support regulatory filings for finished medicinal products within global veterinary markets.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur., USP Veterinary Monographs (intermediate specifications)
    • Japanese Veterinary Pharmacopeia standards
    • ISO 22442-1 for Risk Management in Veterinary Drug Manufacturing

    Typical usage ratio

    • 8–22% by molar ratio during functionalization stages of veterinary API synthesis; adjusted for target molecule and route efficiency.

    Downstream process integration

    • Charged during aromatic substitution or ring closure steps, prior to downstream chiral resolution or formulation into veterinary drug substance master batches.

    Final product types

    • Bulk veterinary API intermediates
    • Oral and injectable anti-parasitic drug substances
    • API blends for premix veterinary medicines
    • Customized actives for contract animal health manufacturers
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    Certification & Compliance
    More Introduction

    2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One: A Closer Look from the Manufacturer’s Perspective

    Understanding the Chemistry

    Every batch of 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One that leaves our plant starts from the ground up – the precise chemistry, robust quality controls, and an unwavering focus on reliability. The backbone of this compound lies in the careful fusion of a dichloro-substituted pyridazine ring and a chloro-fluorobenzyl group. This structure is more than a mouthful on paper. Out in the field, it gives formulators and downstream users a fine-tuned molecular backbone that suits complex synthesis demands, especially in the design of active ingredients for modern fungicides and fine chemicals.

    Chemists on our floor know that this molecule does not come together by accident. Generating such a structure means handling multiple halogenations, executing precise substitutions, and watching for side products at every step. Not every manufacturer is set up for this. In our experience, control over each reaction stage makes the real difference when the market demands purity and batch consistency. Fail that, and something as minor as a trace impurity can rattle a formulation or, worse, delay an entire production cycle for our downstream customers.

    The Model We Produce and What Sets It Apart

    Our product range for 2-(2-Chloro-6-Fluorobenzyl)-4,5-Dichloropyridazine-3-(2H)-One focuses on the most requested purity grades. Years of serving agrochemical innovators and specialty chemical formulators taught us that there’s little room for error. Batches typically clock in at a purity of at least 98%, backed by robust HPLC and NMR data. It’s not a sales pitch; we test every lot before it ships out. Equipment might be the latest, but the repeatable results come from the technical staff watching each run, not just setting up automated protocols.

    Grain size shows another difference. For laboratories, a finer powder moves seamlessly in weighing hoods and dissolves quickly, while bulk buyers ask for granulation that eases metering and storage. For either case, we granularly control the milling and drying process. We don’t hand customers “generic white powder.” Instead, shipments match the flow, density, and moisture targets our customers specify from experience in their own lines.

    Comparing to Similar Compounds

    Plenty of pyridazine derivatives populate the catalogues of the fine chemical world. Yet this particular structure stands out in both challenge and outcome. The dual halogen substitutions at the 4 and 5 positions on the pyridazine ring, coupled with a benzyl group carrying chloro and fluoro tags, means higher reactivity for selective cross-couplings and downstream functionalizations. Older analogues, lacking a fluoro or with only single halogen substitutions, generally display less reactivity in common Suzuki or Buchwald conditions.

    Some customers have asked if they can swap out this compound for lower-cost dichloropyridazines without the aryl-fluorine. Practical trials often expose the gap. Our own R&D department spent months comparing the selectivity, stability, and reactivity under identical conditions. Early steps in synthesis might go well with simpler molecules, but when it comes time to close the final ring or add sensitive groups, the impurities start to mount. The fluoro-benzyl group here doesn’t just make the molecule “fancier.” It genuinely impacts yield and reduces byproduct burden.

    Production Knowledge that Shapes the Product

    Many years of production taught us that reproducibility means more than buying good reactors and high-purity base chemicals. Staff training, a vigilant process team, and immediate troubleshooting around every scale-up batch count as much as fancy analytical tools. New entrants into custom synthesis often trip on exothermic halogenation reactions or underestimate side-pathway formation. We’ve seen competitors come and go, often because their systems miss subtle process drifts that lose yield or lead to out-of-spec content. We monitor each batch with real-time analytics and staged quenching methods developed in-house.

    One point most outsiders don’t see: the bottleneck is rarely raw material price. It's often about the ability to nail reaction time, temperature, and the precise sequence of addition. Too slow on the halogen, too fast with the benzyl – and you spend an extra day purifying or, worse, risk discarding an entire lot. This is one reason we developed semi-continuous lines that keep reaction times steady and minimize “dead time” between steps. With each passing season, we see fewer deviations, and customer feedback on consistency improves.

    Applications: Expertise Backed by Real-World Experience

    Crop protection remains the defining application for this compound, especially as an intermediate in developing selective fungicidal active ingredients. The past few years brought a rising demand for molecules that cross-link diverse functional groups in a single step. Our compound helps bridge synthetic gaps where simpler pyridazines fail to deliver high conversion or selectivity. Several major formulators supplied us with comparative data, revealing higher conversion and cleaner product when our molecule serves as the key intermediate.

    Beyond agriculture, specialty polymer groups turned to this chemical as a sturdy backbone for bespoke catalysts and advanced coatings. Its robust halogen profile allows post-synthetic modifications that would rip apart more delicate moieties. Last year, an electronics manufacturer tested samples from multiple sources. Only batches meeting our certificate specifications passed downstream stress tests, indicating both critical purity and precise halogen placement.

    Lessons from Scale-Up and Manufacturing Challenges

    Scaling from the kilo-lab to ton-scale brings pressures unseen on paper. Over the past decade, we learned that reaction exotherms ramp higher as tanks grow. Heat removal becomes trickier, forcing a careful calibration of jacket temperatures and stirring rates. A few times, pilot batches taught us painful lessons as small scale tweaks failed to translate upward, drawing attention to the importance of thorough thermal profiling and contingency plans for runaway scenarios.

    Early scale-ups also revealed odd byproducts when impurity-laden solvents entered the process. Our operations now run only with freshly distilled or high-spec solvents. Regular audits and hands-on operator training provided a level of control that reduced surprise peaks on chromatograms. Instead of settling for “good enough,” we focus on results that minimize clean-up steps and push overall process yield higher.

    Customer Collaboration: Learning from the Field

    Years of partnering with development chemists exposed the real-world stumbling blocks. Some customers chased higher-yield transformations but found older process notes missed critical details – pH drift, water content, or microvariations in reagent quality. Our technical support spends time with their teams, often running parallel experiments or advising on minor but pivotal tweaks: fresh base lot, slower addition sequences, or upgraded filtration media.

    Once, a production partner flagged isolated yields lower than lab trials predicted. Joint review identified a single contaminated batch of solvent as the culprit. Together, we pinpointed the issue, ran side-by-side purging tests, and restored their yields. Experiences like these underline the value of not just selling molecules but collaborating as technical partners. We take customer feedback as more than after-sales data; it’s a real-time gauge for improving internal operations and future shipments.

    Why Quality Comes Down to Manufacturing Know-How

    Many in the market see purity numbers and assume equivalency. Our decades in synthesis debunked this idea. Any extended supply contract exposes which makers stand behind their material and which merely pass on the spec sheet. We run retention sampling on every lot, not just for regulatory records but to study long-term stability and uncover any slow-moving reagent breakdowns. One batch from an alternate supplier once showed slow color change after a month in dark, dry storage. We loaded it onto the GC and found trace decomposition. Their process missed an obscure impurity during synthesis, but our experience flagged it as an early sign of an unstable pathway.

    Each gram leaving our facility comes through batch-specific process documents. Operators review past batch notes, watch for historical anomalies, and share feedback at daily meetings. We believe no lot is routine. Whether it’s a repeat run or a high-priority custom batch, vigilance raises the average and heads off surprises. Our focus on transparency means regular sharing of representative spectra and stress data for every major client, even before they ask.

    Our Approach to Continuous Improvement

    Innovation means more than a yearly process review. We’re in constant dialogue with reagent suppliers, machinery vendors, and end-users. Only this past year, in reaction to feedback about trace metal residues from a large customer, we overhauled a filtration station to capture and remove even the faintest traces of catalytic metals. The change required weeks of reruns and quality validation, but it lifted satisfaction rates and shortened downstream clean-up times for partners.

    In one instance, customers flagged odor carryover between unrelated product lines. Operations, working with engineering, swapped polymer seals that retained volatile halides and swapped them for high-purity, non-stick varieties. The improvement cut out cross-contamination entirely. All these changes shrink QA delays, improve confidence in each batch, and reinforce the need to go beyond what the standard specification sheet asks.

    Sustainable Manufacturing and Responsibility

    Running high-volume halogenation and substitution reactions can’t ignore environmental impacts. Strict regional regulations force the issue, but the drive comes from our own operations team just as much. Early on, we replaced batch venting of halide gases with closed-loop neutralization, sharply dropping emissions. Solvent recovery jumped close to 85% after we brought in a second line of fractional distillation units.

    All chlorinated waste heads for certified destruction. We keep audit trails on every drum and train operators to spot leaks or mislabeling before they can cause issues. Over the past five years, our “incidents per thousand batches” rate tumbled, not because regulations tightened, but because experienced staff found smarter ways to manage transfer, storage, and disposal.

    The Role of Real-World Specs vs Catalog Numbers

    Buyers often request “standard” product codes thinking one sample fits all. Our production record says otherwise. Even small shifts in impurity profiles – unplanned isomers, hydrolyzed fragments – disrupt final formulations or lead to QC rejections down the line. We produce to the actual customer requirement, not to the broadest market profile. Over dozens of supply runs, we’ve tweaked particle size, dry-down conditions, and even outer packaging based on customer feedback.

    Collaboration doesn’t halt at delivery. We’ve visited plants to help debug application hiccups and redesigned storage instructions based on summer humidity at client locations. This back-and-forth means the molecule that ships has the right water content, free-flowing properties, and stability to last through the customer’s entire usage window.

    Failures: Not Just Bumps but Learning Curves

    No process in specialty chemical synthesis avoids hiccups. In the early days, a misjudged pressure led to a reactor trip and a week-long delay. A contaminated base once forced a whole lot off-spec, teaching us to segregate and re-check incoming consignments no matter the certificate. We built safeties not because inspectors demanded them, but because each event cost real money, time, and reputation.

    We believe honesty about missteps has more value than silence. By treating failures as shared lessons, our team and many partners improved batch yields, minimized downtime, and cut unplanned maintenance costs. Each improvement finds its way into the next batch, so no error goes unaddressed.

    Partnering for a Complex Future

    Regulatory scrutiny keeps rising. End-user technical bars move up, and demand for batch-to-batch transparency climbs. Add more complex molecules into the mix, and plain “spec compliance” falls short. We stay open to site visits, encourage joint process reviews, and back up every data point with physical retention samples and technical reports.

    Our story with 2-(2-Chloro-6-Fluorobenzyl)-4,5-dichloropyridazine-3-(2H)-one continues to evolve, shaped daily by our own learning and the shared advances with customers using the material in tough, real-world applications. We produce this compound not as a commodity, but as a platform built on real feedback, stubborn attention to detail, and a belief that the supplier’s job never ends with the invoice.