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6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine

    • Product Name 6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine
    • Alias 6-Chloro-[1,2,4]triazolo[4,3-b]pyridazine
    • Einecs 629-356-9
    • 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

    139194

    Chemical Name 6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine
    Molecular Formula C5H3ClN4
    Molecular Weight 154.56 g/mol
    Cas Number 94204-08-9
    Appearance Off-white to pale yellow solid
    Melting Point 225-230°C
    Solubility Slightly soluble in water; soluble in DMSO and DMF
    Purity Typically >98%
    Smiles Clc1nnc2n1ncc2
    Inchi InChI=1S/C5H3ClN4/c6-3-1-2-9-10-5(8-9)7-4(3)7/h1-2H
    Storage Conditions Store at room temperature, in a dry, well-ventilated place

    As an accredited 6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 10-gram amber glass bottle with a tamper-evident cap, labeled “6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine, 99% purity.”
    Shipping 6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine is shipped in tightly sealed containers, protected from light and moisture. It is typically transported at ambient temperature unless otherwise specified. Proper labeling according to chemical safety regulations is ensured. Handling precautions are followed, and shipping is usually arranged via certified chemical couriers in compliance with international regulations.
    Storage 6-Chloro-[1,2,4]triazolo[4,3-b]pyridazine 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 it from moisture, direct sunlight, and heat sources. Ensure appropriate labelling and secure storage to prevent unauthorized access. Follow all relevant safety protocols and consult the Safety Data Sheet (SDS) for specific guidelines.
    Application of 6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine

    Applications of 6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine in Industrial Manufacturing

    As a direct manufacturer, we supply 6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine to specialized sectors across the chemical and pharmaceutical industries. We focus on stringent quality standards and consistent product specifications, supporting customer requirements for synthesis, formulation, and downstream product consistency. Below we detail key industrial application scenarios with respective compliance, utilization, processing, and end-product information.

    1. Pharmaceutical Active Ingredient Synthesis (API Intermediates)

    Pharmaceutical manufacturers employ this material as a critical building block in the synthesis of advanced intermediates for central nervous system agents and select anti-cancer compounds. Formulation experts appreciate its well-controlled reactivity, which enables targeted derivatization and high-purity intermediate preparation. The compound enters multi-stage synthesis, often following a controlled chlorination or cyclization step. Robust analytical verification accompanies each batch. End users require transparent traceability and alignment to industry quality metrics across the entire supply chain.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <823> and EP monograph readiness for relevant APIs
    • Auditable full batch traceability and regulatory documentation (DMF Type II on request)
    • Registration with applicable national drug master files

    Typical usage ratio

    • 5–20% molar equivalent in target intermediate synthesis (varies per proprietary route)
    • Adjusted to impurity profiling and step yield requirements

    Downstream process integration

    • Stepwise introduction in high-purity synthesis reactors post-esterification or halogenation
    • Stringent solvent and temperature control to limit byproduct formation
    • Applied as a core coupling or condensation reactant

    Final product types

    • Anti-epileptic drug intermediates
    • Triazolopyridazine-based anti-tumor agents
    • CNS modulator raw APIs
    • Custom clinical-stage research compounds

    2. Agrochemical Active Ingredient Manufacturing

    Producers of crop protection solutions rely on this heterocyclic system to build new-generation fungicides, insecticides, and seed treatment actives. Its selective chemical reactivity supports the formation of key action moieties in triazolopyridazine-based agrochemical structures. Industrial reactors must maintain strict reaction conditions, with in-process QC to verify identity and purity, avoiding cross-contaminants that might impact field application. The final ingredients are routinely formulated for efficacy, shelf stability, and environmental safety.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius contamination limits for pesticide synthesis
    • ISO 17025 analytical lab certification for QC
    • REACH Annexes VII–X regulatory framework for raw material registration
    • Local EPA registration requirements for formulated actives

    Typical usage ratio

    • 3–10% w/w in target active ingredient synthesis
    • Adapted by reaction yield, solubility, and degradation analysis

    Downstream process integration

    • Introduced during core ring assembly or late-stage substitution processes
    • Blended under inert atmosphere in dedicated agrochemical reactors
    • Followed by liquid-liquid extraction and crystallization before formulation

    Final product types

    • Seed coating fungicide actives
    • Broad-spectrum triazole insecticides
    • Systemic crop protection agents
    • Stabilized pesticide intermediates for post-formulation packaging

    3. Advanced Materials and Polymer Additives

    Developers of specialty polymers and functional materials utilize this compound as a nucleating agent, crosslinker, or functional group modifier within select engineering plastics and performance coatings. It serves in controlled doping processes that enhance material durability, adherence, or reactivity toward specific substrates such as OLED layers and specialty resins. Process technicians configure thermal and mixing regimes to ensure uniform integration, balancing physical property targets with molecular compatibility.

    Industry compliance standards

    • RoHS Directive for hazardous substance limits in electronics
    • ISO 9001 certified manufacturing or quality management systems
    • REACH-SVHC (Substance of Very High Concern) assessment for polymer additives
    • Customer-mandated physical property validation protocols

    Typical usage ratio

    • 0.1–2% w/w as polymer additive or crosslinker
    • Adjusted by thermal resistance, adhesion and functionalization goals

    Downstream process integration

    • Direct blend into monomer or pre-polymer systems in bulk mixers
    • Pre-dispersion in plasticizer or solvent for high-shear extrusion processes
    • Inline monitored dosing for continuous film or fiber modification

    Final product types

    • OLED component materials
    • High-performance epoxy resins
    • Electrically functionalized polymer coatings
    • Specialty engineering plastics for automotive or electronic applications

    4. Chemical Research and Discovery Synthesis

    Contract research organizations (CROs), university labs, and in-house R&D departments incorporate this heterocycle in early-stage synthesis campaigns targeting new pharmaceuticals, pesticides, and diagnostic probes. Synthetic chemists benefit from reliable physical parameters, batch reproducibility, and comprehensive regulatory documentation. The compound is a favored candidate for library generation or structure-activity relationship (SAR) studies, entering reactions for scaffold diversification and analog creation.

    Industry compliance standards

    • GMP-compliant sample management for compound libraries
    • OECD GLP (Good Laboratory Practice) for regulated discovery work
    • International Air Transport Association (IATA) for chemical shipment
    • Institutional biosafety and chemical hygiene program certification

    Typical usage ratio

    • Varies by protocol: 0.5 mmol–10 mmol per reaction (research scale)
    • Batch size determined by target molecule and SAR throughput

    Downstream process integration

    • Dissolved or suspended in polar aprotic solvents for combinatorial synthesis
    • Used as the scaffold for subsequent halogenation, alkylation, or acylation
    • Introduced in microwave-assisted or batch synthesis under standard laboratory conditions

    Final product types

    • Molecular probe candidates
    • Pharmacologically active analog panels
    • Early discovery pesticide hits
    • Preclinical diagnostic agent precursors
    Free Quote

    Competitive 6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    6-Chloro-[1,2,4]Triazolo[4,3-B]Pyridazine: Reliable Chemistry for R&D and Scale-Up

    Chemical development today leans heavily on structural creativity, ease of scale-up, and process reliability. In our own operations, each compound we scale in-house carries a different history. Among heterocyclic building blocks, 6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine stands out for its stability and flexibility, both in the lab and when moving to larger reactors. Over the years, customer preferences have shifted due to the unique design of this molecule — and we've watched demand rise with new drug discovery routes and advanced material synthesis.

    Understanding Structure: What Makes This Triazolo-Pyridazine Special

    Chemists always keep an eye out for rings that offer performance along with functionalization opportunities. The 6-chloro group locked onto the [1,2,4]triazolo[4,3-b]pyridazine backbone gives synthetic teams predictable reactivity and electronic influence, without bringing instability into the process. For our operations, that single bridging chlorine changes the entire game for downstream chemistry. During method optimization, we find that electrophilic aromatic substitution works as expected but stops short of giving unexpected side products, even at moderate temperatures.

    This foundation broadens the compound’s reach across pharmaceutical, agrochemical, and specialty intermediate fields. Medicinal chemists choose the ring for its rigid scaffold, giving them a well-defined platform for kinase inhibitor development. As a manufacturer, familiar aromatic heterocycles form the backbone of our batch manufacturing — this particular core consistently gives high yields, minimal step loss, and clear isolation procedures.

    Our Model and Specifications: Practical Manufacturing Focus

    Several years back, our process chemists invested long hours in streamlining the synthesis process. We deliver 6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine as a fine, slightly off-white to pale yellow crystalline powder. Packaging is always based on actual project requirements — from pilot studies needing just a few hundred grams, to routine multi-kilogram production batches for clinical development programs. Purity, as determined by HPLC, typically exceeds the usual research threshold, with each lot traceable all the way to raw material batches for regulatory filings.

    Routine analysis keeps us on track. We use NMR, LC-MS, and elemental analysis for full structure confirmation, and we avoid ghost peaks through a multi-solvent wash. Unlike outsourced intermediates, every drum or jar moves directly from our controlled environment — no generic relabeling, no uncertainty about timelines or quality.

    We operate under a philosophy of transparency. The COA reflects reality on the ground; impurity profiles match what we find, not just what a textbook says to expect. In cases where projects need tighter limits, our in-house QMS adapts protocols for extra stringency, without foot-dragging or endless administrative back-and-forth.

    Uses and Applications: Built for the Real World

    Chemists come to us with full pipelines mapped out, looking for versatility and reliable supply. In practice, 6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine forms the cornerstone of SAR (structure-activity relationship) studies. Exploratory teams favor the compound for fast parallel synthesis — chloro substituents make for easy cross-coupling, and the core handles demanding reaction conditions (like Buchwald-Hartwig or Suzuki couplings) without giving up yield or cleanliness.

    Medicinal chemistry groups use this intermediate to slot new substituents on the triazolo side, tuning solubility and bioactivity profiles across several target classes. Its electron-withdrawing chlorine means clean transformations, particularly on the pyridazine, without making purification a nightmare. Real-world feedback from downstream formulators and analytical chemists points time and again to reliable loading on solid-phase supports.

    Pharma process teams, especially those with late-stage projects, have leaned into the scalable simplicity of this scaffold. Several mills and CRO partners use our product after evaluating in-house analogs and find the tighter batch release controls reduce time-to-pilot. We see this molecule move smoothly into agricultural product research and into specialized electronic material streams, where new heterocycles keep popping up in device coatings and resins.

    Advantages Over Other Heterocyclic Building Blocks

    Nothing tells a synthetic chemist more than hands-on experience. Over a decade, we've evaluated hundreds of ring systems. Compared with 3-chloropyridazines, or similar bromo derivatives, the 6-chloro [1,2,4]triazolo[4,3-b]pyridazine preserves labile groups and transitions from small-batch R&D to plant-scale production without extensive reoptimization. Fewer side reactions, like decomposition under heat or hydrolysis, help keep the plant schedule predictable. The single chlorine doesn’t force extra handling steps, so cleaning solvent waste stays manageable — a growing concern for any facility facing stricter environmental audits.

    From our own shop floor, we can attest to the difference between compounds made domestically versus those sourced through third parties. Inconsistent color, trace metallics, or solvent residues often demand costly purification steps if the supply isn’t carefully controlled. Years of direct manufacturing experience mean we can stand behind our batches, ship after ship — from milligrams for boutique firms to the larger quantities that multinational pharma expects.

    On the regulatory front, supplying cGMP lots for advanced pharma APIs starts early with a clean intermediate. Suppliers expect more than a generic import. Our in-house documentation and guaranteed traceability allow easier regulatory approvals down the chain, which reduces friction in dossier submission and client audits. Third-party intermediates that lack this level of documentation and process control often slow down the whole approval process.

    Lessons Learned from the Shop Floor: Consistency Matters

    Every production run teaches something new. Several years ago, an unexpected solvent peak from an outside supplier nearly stopped a late-stage project just hours before the QA release deadline. Fast corrective action from our own staff avoided serious delays — internal batch tracking and rapid-response lot analysis cut the downtime to hours, not days. That event helped cement our focus: no single supplier or outsourced process can match the real-time, in-house oversight of dedicated personnel.

    Process interruptions from unexpected impurity spikes or sudden material backorders threaten tight research timelines. Keeping every batch release under the same roof makes a difference — less finger-pointing, more hands-on responsibility, and immediate problem-solving capability. Importantly, every operator and technician understands the end-use, so every step receives care that offsite, contract suppliers often can’t replicate.

    Supporting Process Chemistry and Development Teams

    Process chemistry has always thrived on close partnerships. Chemists rely not just on chemical purity, but on consistent lot-to-lot performance. We support all customers — whether they’re academic groups chasing SAR hits, formulators preparing scale packs, or pharma teams polishing clinical candidates. No unfamiliar relabeling, no uncertain timelines — direct conversations with our staff drive every custom campaign.

    We receive direct feedback from formulation teams on solubility and filterability. When customers request adjustments in drying time or particle size, we accommodate these needs, not only at R&D scale but also as production scales up. The entire team, from plant manager to QC chemist, stays connected to ongoing projects, sharing best practices and troubleshooting strategies that don’t come from manuals alone.

    Those working in analytical labs appreciate the absence of hard-to-remove residues and contaminants. In practice, this translates to better chromatography baselines, fewer re-measurements, and faster project conclusions. Customers tackling complex reaction systems report higher catalyst turnover numbers and can compare batch outcomes without hidden variables. The research cycle shortens, uncertainty drops, and chemists can act on new data right away.

    Tailored Production and Quality Commitment

    Our customers send challenging questions every day. Some projects need custom kilogram runs; others call for subtle shifts in moisture content, adjusted packaging, or special labeling. We see these as collaborative challenges rather than as complications. Our plant crews retool production parameters actively, working hand-in-hand with process and analytical chemists at every step.

    Maintaining strict humidity and temperature control, employing closed filtration systems, and tracking lot history down to reactor charge and filter aid choice ensures tight product reproducibility. The shift from 50 grams in a pilot synthesis to 25 kilograms for a toxicology lot shouldn’t add headache — seamless communication between production, logistics, and documentation keeps timelines where clients need them.

    Documentation comes built around practical concerns, not just checkboxes for regulatory audits. Clients can request expanded impurity profiling and receive individual chromatograms linking COA data directly to their samples. We offer open access to supporting data for every batch, without the common runaround from faceless distribution centers. It’s an arrangement born from hundreds of real projects and years of direct exposure to the regulatory world.

    Packing, Shipping, and End-User Support

    Real-world shipping logistics rarely give easy days. Depending on the hazard profile and local requirements, shipping partners and modes change. We’ve handled fragile, moisture-sensitive, and cold-chain restricted batches, tracking everything from dispatch to client receipt with complete chain-of-custody transparency. For high-purity lots, we use inert gas blanketing and labor-intensive double-sealed containers to prevent contamination and moisture uptake.

    All packages reflect actual material sensitivity and regulatory framework. Reactive cargo sees extra inert protection. Quantities down to a single gram or up to multi-kilogram lined HDR drums all receive equal care. Standard paperwork looks simple, but attention to transit times, customs prep, and contingency planning for every destination avoids costly border delays. Teams stay reachable, and direct contact lines keep projects moving, even as shipping schedules stretch or customs rules change overnight.

    Technical support never ends with a shipment. Many clients work through scale-up challenges after receipt — questions about solvent compatibility, byproduct formation under different temperature profiles, or cross-reactivity with new catalysts. Hands-on advice comes from years in the plant, not boilerplate call-center scripts. We provide feedback on unusual reactivity, troubleshooting help, and protocol optimization, guiding teams through hurdles from gram-scale through pilot campaigns.

    Looking Ahead: Innovation and Responsiveness in Manufacturing

    Every synthetic facility earns its reputation from building trust project by project. New breakthroughs in electronic materials or pharmaceuticals put pressure on raw material producers to up their game. We routinely upgrade analytical tools, invest in safer reactor hardware, and train teams for new synthesis methods. With 6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine, we've fine-tuned processes based on customer pilot results, feedback from plant trial runs, and in-depth discussions with scale-up chemists.

    End-user expectations keep rising. Transparency in batch data, reliability in shipments, and a genuine willingness to listen outpace legacy, one-size-fits-all models that dominated years ago. We remain focused on rapidly incorporating suggestions from both chemists and operations managers. Whether it’s a tweak in washing cycles, changes in final dryness, or new methods of impurity capture, improvements start from production floor experience and evolve into lasting process upgrades.

    Sustainable Practices in the Real World

    Modern manufacturing cannot ignore environmental responsibility. Our facilities use closed-system vessel transfers, optimize solvent recovery, and actively reduce both energy and water consumption. Switching to more benign cleaning agents and adopting modern filtration helps reduce toxic waste and operator exposure.

    Our 6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine process reflects an ongoing shift to greener chemistry. By lowering process temperatures in key steps and using aqueous-based workups where feasible, we keep production environmentally friendly without giving up on reliability or product quality. Years of practical tweaking and direct observation mean fewer emissions, less hazard, and reduced post-synthesis waste — all while meeting or exceeding end-user expectations.

    Open Channels: Collaboration Over Transactions

    The best projects happen in conversation, not through static forms or endless paperwork rounds. Customers know they can reach our plant operators, QC analysts, or chemists for direct answers, not generic replies. This approach speeds resolution of the inevitable challenges that develop between pilot runs and full-scale production.

    Requests for custom documentation, novel analytical methods, or changes in shipping arrangements come straight to those managing the product daily. Over time, this dialog has taught us how to minimize surprises on all sides. When clients succeed, everyone grows — and every new batch cements the trust built on transparent, honest communication and a willingness to solve — not just supply.

    Conclusion: Manufacturing Beyond the Basics

    Supplying 6-Chloro-[1,2,4]Triazolo[4,3-b]pyridazine means more than shipping out a chemical. It’s about hands-on learning, continuous improvement, and grounded support for every research team relying on our quality and experience. Our track record grows, not by sitting back, but by rolling up sleeves alongside each customer, working through development hurdles and celebrating each milestone reached together.

    What customers receive is more than a bottle of powder — it’s the accumulated know-how, troubleshooting skill, and practical manufacturing expertise of our entire team. Direct engagement, consistent production, and real feedback drive our work, every day, batch after batch.