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3,6-Dichloropyridazine-4-Carboxylic Acid

    • Product Name 3,6-Dichloropyridazine-4-Carboxylic Acid
    • Alias 3,6-Dichloro-4-pyridazinecarboxylic acid
    • Einecs 616-786-1
    • 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
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    Specifications

    HS Code

    583512

    Chemical Name 3,6-Dichloropyridazine-4-Carboxylic Acid
    Cas Number 356783-16-9
    Molecular Formula C5H2Cl2N2O2
    Molecular Weight 208.99
    Appearance White to off-white solid
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CN=C(C(=N1)Cl)C(=O)OCl
    Iupac Name 3,6-dichloropyridazine-4-carboxylic acid
    Storage Conditions Store at 2-8°C, keep tightly sealed
    Hazard Statements May cause skin and eye irritation
    Synonyms 3,6-Dichloro-4-pyridazinecarboxylic acid

    As an accredited 3,6-Dichloropyridazine-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle labeled "3,6-Dichloropyridazine-4-Carboxylic Acid," sealed with a screw cap and protective parafilm wrap.
    Shipping 3,6-Dichloropyridazine-4-Carboxylic Acid is shipped in tightly sealed containers to prevent moisture exposure and contamination. The package is clearly labeled, handled as a laboratory chemical, and compliant with relevant transport regulations. It is stored at room temperature, away from sunlight and incompatible substances. Shipping may require documentation per local and international guidelines.
    Storage 3,6-Dichloropyridazine-4-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Avoid exposure to moisture and store at room temperature. Ensure proper labelling and follow all recommended safety and handling procedures as outlined in relevant Material Safety Data Sheets (MSDS).
    Application of 3,6-Dichloropyridazine-4-Carboxylic Acid

    Applications of 3,6-Dichloropyridazine-4-Carboxylic Acid in Industrial Manufacturing

    As a primary manufacturer of 3,6-Dichloropyridazine-4-Carboxylic Acid, we supply this compound as a key intermediate to multiple high-value chemical sectors. Its unique structure supports pharmaceutical synthesis, agrochemical manufacturing, specialty pigment production, and advanced material R&D. Below, we present main downstream industrial uses, each with detailed compliance, formulation, process integration, and end product insights.

    1. Pharmaceutical Intermediate for Anti-Viral Drug Synthesis

    Major pharmaceutical enterprises use 3,6-Dichloropyridazine-4-Carboxylic Acid as a core intermediate during multi-step synthesis of nitrogen-containing heterocyclic antiviral agents. The carboxylic acid group enables linkage to amines and alcohols under GMP-compliant conditions. The controlled halogenation pattern supports selectivity in nucleophilic substitution reactions required for active pharmaceutical ingredient (API) development, often under batch or continuous flow regimes.

    Industry compliance standards

    • EU GMP Part II – Basic Requirements for Active Substances Used as Starting Materials
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (for US FDA-regulated manufacturing)
    • Ph. Eur. and USP intermediates guidance (as relevant to specific API dossiers)

    Typical usage ratio

    • 20%–45% molar ratio relative to other major heterocyclic intermediates, depending on substitution pattern required and downstream coupling efficiency; ratio adjusted by process chemists according to route optimization.

    Downstream process integration

    • Enters as a charged solid or solution during Step 3–5 of multistep heterocycle assembly, before final deprotection or salt formation for API finishing steps.

    Final product types

    • Pyridazine-derived antiviral solid oral dosage forms
    • Injectable antiviral APIs for hospital supply
    • Research-only API intermediates for medicinal chemistry programs

    2. Agrochemical Precursor for Selective Herbicide Synthesis

    Agrochemical manufacturers incorporate this chlorinated pyridazine acid as a tailored building block in the synthesis of selective herbicides. The compound’s dichloro substitution enables high selectivity for coupling reactions, pivotal during production of pre-emergent and post-emergent crop protection agents. The product integrates into regulated closed-system synthesis lines, with strict impurity profile controls to meet agricultural use standards.

    Industry compliance standards

    • FAO/WHO Guidelines on Quality Control for Pesticide Ingredients
    • ISO 9001:2015-certified quality management for agrochemical ingredients
    • REACH (EC No 1907/2006) substance registration for EU distribution
    • China GB 2763-2021 MRL compliance for agricultural active ingredients

    Typical usage ratio

    • 14%–32% w/w of active ingredient batch, based on target molecular design of the herbicidal compound and functional group reactivity needed for downstream modifications.

    Downstream process integration

    • Used as a primary starting reagent in Step 1 or 2 of closed-loop, solvent-controlled batch reactors; introduced prior to esterification, alkylation, or cyclization into active herbicide scaffolds.

    Final product types

    • Pyridazine-derived selective post-emergent herbicides
    • Soil-applied pre-emergent weed control actives
    • Herbicide technical concentrates for further downstream formulation

    3. Intermediate for Specialty Pigment and Dye Manufacturing

    In colorant industry operations, chemical processors convert this compound into bespoke pigment intermediates. The highly controlled aromatic substitution pattern supports subsequent diazotization and coupling reactions, yielding chromophoric systems needed for advanced dyes. Producers deploy the material at calibrated addition rates to balance color saturation versus stability, maintaining compliance with end-use safety limits for textile, plastic, and coating applications.

    Industry compliance standards

    • EN 71-3:2021 Safety of Toys—Migration of Certain Elements (for colorants in children’s products)
    • OEKO-TEX® Standard 100 restricted substance list
    • REACH Annex XVII restrictions (colorant-specific)
    • ISO 787 series on pigment testing and evaluation

    Typical usage ratio

    • 5%–18% w/w with other aromatic or azo precursors, proportional to target pigment grade and application—lower end for light-fast textile colorants, higher for plastics or inks requiring enhanced chroma.

    Downstream process integration

    • Initial intermediate for nitrosation or halogen exchange in pigment synthesis lines; loaded before secondary couplings and crystallization to ensure uniform pigment particle formation.

    Final product types

    • Specialty organic pigments for plastics compounding
    • Direct and reactive textile dyes
    • High-performance inks for industrial printing

    4. Precursor for Electronic Materials and Functional Polymer Research

    Advanced materials labs and electronics industry partners utilize this material to engineer pyridazine-linked monomers. Researchers introduce the compound during pilot-scale polymerization of functionalized resins, targeting electronic-grade performance. The raw material supports synthesis of conjugated polymers and specialty resins, focusing on low ionic contamination and high purity prints required for optoelectronic, photovoltaic, or sensor applications.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free base materials used in electronics
    • IPC-4101C for base materials for printed boards (polymer films)
    • ISO 9001:2015 R&D and production traceability
    • RoHS 2 (Directive 2011/65/EU) restrictions regarding hazardous substances

    Typical usage ratio

    • 2%–12% molar basis in resin formulation, depending on desired electronic property tuning and molecular weight specification.

    Downstream process integration

    • Introduced at initial monomer condensation stage or as a side-chain modifier during advanced polymer upscaling; follows stringent solvent and atmosphere controls to maintain molecular integrity.

    Final product types

    • Photopolymer resists for microfabrication
    • Conjugated polymer films for OLED and solar cell layers
    • Sensing membranes for chemical sensor devices
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    Certification & Compliance
    More Introduction

    Introducing 3,6-Dichloropyridazine-4-Carboxylic Acid: Manufacturing Expertise and Practical Insights

    Understanding the Chemistry Behind the Compound

    A lot of lab benches have seen their fair share of 3,6-Dichloropyridazine-4-Carboxylic Acid. As chemical manufacturers, we know this compound inside and out, because we've put in the hours scaling up from five-liter glassware to real plant equipment. The model we typically work with, CAS number 132256-66-7, goes through several quality checkpoints before heading out the door. Each batch is crystalline, with a purity that exceeds 98%. Large-scale synthesis rarely throws surprises any more; our team has honed the process to reproducibility, focusing on minimizing impurities like the mono-chloro and dicarboxylic analogs that crop up in less controlled operations.

    We don’t just push the reaction and hope for the best. Instead, we monitor the blend of reagents — starting with pyridazine intermediates, choosing the right chlorination reagent, and validating the reaction course by HPLC and NMR in every batch. Trace moisture and organic residuals don't stand much chance. Purity matters because small changes can shift reactivity, and when customers use this acid to build agrochemicals or pharmaceuticals, side reactions waste time and money.

    Application Value: Why 3,6-Dichloropyridazine-4-Carboxylic Acid Matters

    Most of the demand for this acid comes from companies developing new herbicide molecules or active pharmaceutical ingredients. The dichloro substitution pattern on the pyridazine ring gives chemists a solid scaffold for downstream modification. We’re seeing research targeting both ring expansions and coupling reactions — either bringing in heterocyclic complexity or tethering other functional groups to craft new bioactive entities.

    Some researchers want its electron-rich nature, letting them steer selectivity in cross-coupling or nucleophilic substitutions. We watch the incoming sample requests from R&D teams who openly share their synthetic challenges with us. It's not just a bench curiosity; it's become an intermediate in several patent-protected syntheses, where both the dichloro positions and the acid present unique handles for medicinal chemistry work. In fact, process chemists optimizing scale-up routes often check in with us about crystallization protocols, solvent compatibility, or suggestions for cost control — another reason why having direct access to the actual producer beats relying on repackaged material with unknown provenance.

    Differences From Other Pyridazine Acids and Competitive Advantages

    Within the pyridazine carboxylic acid family, plenty of variations exist. A single switch in halogen or carboxylic position can make or break the desired downstream transformation. The 3,6-dichloro variant’s reactivity profile outpaces the monochlorinated derivatives, which often display less predictable behavior when exposed to nucleophiles or cross-coupling catalysts. In the process world, inconsistency means risk. That’s why customers keep coming back for this exact specification: it’s reliable, and the yield after reaction workup tends to be higher.

    Some try to substitute generic pyridazine carboxylic acids sourced from brokers who lack direct experience in synthesis. We've seen project managers bring us issues from failed scale-ups where off-spec acids introduce unbreakable side-products or drop catalytic activity to near-zero. After all, these other acids either lack the right placement of electron-withdrawing groups or show unexpected stability under typical coupling conditions, wasting precious development cycles. Our plant operators work closely with QC chemists to keep these issues in check.

    Manufacturing Approach: Keeping Quality and Supply Stable

    Scaling up 3,6-Dichloropyridazine-4-Carboxylic Acid is all about precise temperature control and real-time analytical support. In our experience, small producers taking shortcuts with chlorination quickly run into wall formation, exotherms, or troublesome emulsions that choke off yields. We build robust batch records where each stage—chlorination, purification, acidification, filtration, and drying—receives dedicated monitoring. Manual versus automated feeds sometimes demand compromise, but decades of scale-up work have taught us to spot a runaway reaction before it damages a vessel or upends a production schedule.

    On the practical side, our technicians test each finished lot for not just purity but for solubility in both reaction and recrystallization solvents. If a synthetic route points to DMF, DMSO, or aqueous systems, we run compatibility checks so that downstream users don’t discover headaches when scaling past gram quantities. That’s something traders rarely provide—a firsthand perspective on how this compound behaves after it leaves the drum.

    Ensuring Regulatory Trust and Traceability

    End users in regulated industries deserve full traceability back to raw materials, including solvent and reagent sources. Our in-house documentation tracks each precursor and lot through the synthesis, furnishing full impurity profiles and retention samples matched to each shipment. We stay on top of regional regulations, including RoHS, REACH, and domestic environmental rules. We maintain this diligence because we’ve faced real-world audits ourselves — not just paperwork, but on-site verification. Regulators ask for more than a certificate; they look for clean chain of custody, authenticity, and a credible culture around safety and process control. This transparency lets clients pass their own regulatory reviews more smoothly.

    Sustainable Production and Waste Minimization

    Waste handling in pyridazine chlorination can easily spiral. We’ve invested in optimized distillation, spent acid neutralization, and closed-loop solvent recovery so that most process solvents find new life in future batches. Recovering chlorinating agents is not just a nod to green chemistry but a direct cost control measure. Controlling halogen release into effluent means treating scrubbers as a priority, not an afterthought. By minimizing the number of separate purification steps, we shrink the waste stream and energy demand, which stacks up over hundreds of tons produced per year.

    Skeptical users often ask if this effort makes a real difference. After shifting to more selective reagents and fine-tuning pH adjustments in purification, we cut hydrolysis byproducts by half compared with previous processes. Downstream crystallization produces fewer oily impurities, and the isolated acid has less caking or clumping in storage. These seemingly small changes yield better handling for packagers in hot, humid climates — another lesson we learned via customer feedback and direct returns.

    Storage and Transport: Keeping Material in Top Shape

    One part of our job that often gets overlooked is how the acid behaves in transit and storage. The dichloro-pyridazine structure is stable in sealed containers, but large quantities can absorb ambient air or moisture over long hauls, especially if packaging gets punctured or stacked in containers under unregulated climates. Early on, we saw batches degrade from light exposure or rough handling during international shipping — color changes, varying solubility, weaker downstream reactivity.

    Our packaging team responded by implementing double-layer drum liners and ensuring every unit ships under dry nitrogen. By tracking delivery conditions and shelf-life both at our warehouses and in transit, we earned a reputation for dependable material quality among formulation chemists worldwide. Batches produced during high humidity months get extra moisture analysis and are flagged in our ERP for short-term delivery or local warehousing. The result? Consistently high-performing product, wherever in the world it gets opened.

    Supporting Innovation: Working with R&D and Scale-Up Labs

    We field calls from laboratory heads exploring new transformations—Suzuki couplings, amide bond formation, cyclizations using the dichloro-acid core. In these scenarios, bench scientists rely on reproducible reagents. We've sent technical specialists into customer labs to help troubleshoot crystallization issues or discuss solvent swaps when late-stage development hits a snag. We supply alternate grade lots for non-critical R&D versus GMP-compliant segments, adapting particle size or drying regimens as pilot data emerges.

    Working so closely with innovation teams, we’ve noticed that even small changes in impurity profiles alter the reactivity of catalysts or ligands used in complex transformations. Our chemists routinely collaborate on joint stability studies, both under accelerated temperature and simulated reaction conditions. It’s common to spend weeks developing new isolation protocols for especially sensitive synthetic intermediates. These relationships have helped create entire new workflows not just in fine chemicals, but in crop protection and medical device chemistry.

    Cost Structure and Long-Term Supply Considerations

    Price pressure affects even established products like 3,6-Dichloropyridazine-4-Carboxylic Acid. As a manufacturer, we control overhead by upgrading core processes and eliminating reliance on imported high-cost reagents. In years past, shortages in precursor chemicals forced many suppliers to ration loads, cancel contracts or quietly switch to lower-cost but less effective starting materials, which led to variability batch-to-batch. We learned to buffer our supply inventories, re-certify backup sources quarterly, and set up toll processing contracts for critical steps subject to global market swings.

    Cost control doesn’t only serve us—it steadies the price for long-term customers, especially global formulators locked into multi-year development or manufacture timelines. By keeping capacity flexible and pooling production risk across multiple plants, we’ve avoided sudden supply shocks that might otherwise derail drug rollouts or agrochemical registrations. Large buyers routinely tour our facilities before inking annual supply contracts, and sometimes send technical staff to audit quality or walk the plant floor. The open book approach reassures everybody that what’s ordered matches what's delivered.

    Practical Handling and Safety Tips from the Producer’s Floor

    Day-to-day use of 3,6-Dichloropyridazine-4-Carboxylic Acid is straightforward, but there are lessons learned over years of handling. Fresh batches show a free-flowing crystalline texture, but any sign of caking or discoloration hints at hidden moisture or trace decomposition — we advise against using such material in precision applications. We counsel labs to keep containers tightly sealed, work in fume hoods when sampling, and avoid storing close to base-sensitive compounds that could react with the acid function.

    Our safety officers run annual training for loading and dispensing teams, reducing exposure and maintaining a spotless incident record. Spills get treated promptly with standard neutralization protocols, and all operators have direct lines to plant chemists for technical assistance with out-of-spec products. Field chemists say the same: a manufacturer with firsthand process understanding responds quicker to troubleshooting than any distributor or sales office removed from the reality of large-scale synthesis.

    Learning From Real-World Feedback

    Improving 3,6-Dichloropyridazine-4-Carboxylic Acid doesn’t just happen in isolation. We pay attention to every shipment, every technical query, every complaint or suggestion from formulation chemists and production managers. After all, the lessons that mean the most come from batches that didn’t go exactly as planned — maybe a vial leaked in transit or a new plant engineer flagged a batch for odd odor, triggering an internal check of process tanks that ultimately pointed to a faulty seal under the condenser. These moments drive incremental improvements in both product and service.

    Over the years, users have pushed for more transparency around batch-to-batch variability. We responded by integrating electronic lot tracking, high-resolution impurity mapping, and customer-accessible technical dossiers. Lab specialists can now cross-reference their observations with our archived data and get quick answers about any concern—no lost time, no runaround through sales reps who lack technical grounding.

    Future Directions and Opportunities for End Users

    Customers keep surprising us with new ways to use this acid. Academic groups, contract research organizations, and start-ups testing new crop protection scaffolds see value in both the compound’s reliability and its versatility. Medicinal chemists rely on its dichlorinated skeleton to guide drug candidates through late-stage modification. Our role is to support that process by providing robust, consistent material, along with flexible packaging and documentation support for regulatory filings.

    We keep investing in analytics upgrades, digital manufacturing integration, and sustainability programs for both our staff and our customers. Analytical chemists can now request custom certificate expansions, embedding more performance data and proactive stability tracking.

    Conclusion: Experience from the Manufacturing Line

    Years working hands-on with 3,6-Dichloropyridazine-4-Carboxylic Acid has taught us that direct manufacturing knowledge matters more than any spec sheet or certificate blurb. From sourcing premium raw materials, through validated batch production, to technical and regulatory support, our approach stems from hard-earned process experience and a commitment to continuous improvement. For research groups, industrial scale users, or global formulators, practical details and real-world responsiveness create a dependable supply chain for even subtle reagents like this one.