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5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole

    • Product Name 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole
    • Alias 5-Chloro-6-fluoro-1,2,3-benzothiadiazole
    • Einecs 629-020-2
    • 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

    777126

    Chemical Name 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole
    Molecular Formula C6H2ClFN2S
    Molecular Weight 188.62 g/mol
    Cas Number 84110-29-4
    Appearance White to light yellow solid
    Melting Point 64-68°C
    Solubility Slightly soluble in organic solvents
    Synonyms 5-Chloro-6-fluoro-1,2,3-benzothiadiazole
    Smiles C1=CC2=NSN=C2C(=C1F)Cl
    Inchi InChI=1S/C6H2ClFN2S/c7-4-2-1-3(8)5-6(4)10-11-9-5/h1-2H
    Purity Typically ≥ 98%
    Storage Conditions Store in a cool, dry place, tightly closed
    Hazard Statements May cause skin or eye irritation

    As an accredited 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 100 grams of 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole, sealed in an amber glass bottle with hazard labeling.
    Shipping 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be handled by trained personnel using appropriate protective equipment in accordance with local regulations. Ensure proper labeling and documentation, and transport under ambient temperature, avoiding extremes. Follow all relevant hazardous material shipping guidelines.
    Storage 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Ensure proper labeling and avoid moisture exposure. Handle under inert atmosphere if sensitive to air or moisture, and follow standard laboratory safety procedures during storage and handling.
    Application of 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole

    Applications of 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole in Industrial Manufacturing

    5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole is a key intermediate with niche value in several industrial sectors, particularly where specificity in molecular structure translates directly to functional performance in the final products. As a direct producer with research and pilot scale application data, we outline its principal roles in four validated downstream industries.

    1. Agrochemical Synthesis: Herbicide and Fungicide Active Ingredient

    Large-scale crop protection manufacturers select this thiadiazole derivative when developing modern herbicide and fungicide actives targeting resistant weed and fungal strains. Its electron-donating and withdrawing characteristics enhance binding affinity in new-generation agrochemical APIs. Synthesizers introduce it during API heterocycle formation steps, supporting high selectivity and reactivity. Process chemists can fine-tune structure-activity relationships, using our stringent batch quality controls to ensure minimal variability between campaigns.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • REACH Regulation (EC) No 1907/2006 for use and registration in the EU
    • GLP (Good Laboratory Practice) for safety dossiers
    • National standards: EPA (US) 40 CFR Part 180, ICAMA (China), BPR (EU)

    Typical usage ratio

    • 5–18% by molecular ratio in target heterocycle-forming reactions, depending on target molecule complexity and reactivity balance; chemists may adjust within this band based on downstream substituent requirements.

    Downstream process integration

    • Added during the early-stage coupling and cyclization reactions in API synthesis
    • Reacted with other aromatic or aliphatic building blocks via halogen exchange or nucleophilic substitution
    • Purification and isolation performed after ring closure, prior to formulation

    Final product types

    • Post-patent and novel herbicide actives (e.g., for broadleaf control)
    • Fungicidal actives for cereals, rice, fruits, and vegetables
    • Pre-mixtures and technical concentrates for formulation houses

    2. Pharmaceutical Intermediate: Synthesis of Heterocyclic API Cores

    Several pharmaceutical process developers use 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole as a critical scaffold for introducing regulated heterocyclic moieties into small molecule drug candidates. The dual halogen profile offer unique reactivity for stepwise substitution and further functionalization, important in anti-infective and CNS drug development paths. We support GMP precursor delivery for clinical and commercial projects, facilitating consistent quality lot-to-lot.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, and JP monographs for APIs
    • FDA cGMP regulations under 21 CFR Parts 210/211
    • Chinese Pharmacopoeia compliance for local market access

    Typical usage ratio

    • 3–12 mol% relative to final API core; scale adjusts based on target per-batch yield and downstream derivatization strategy

    Downstream process integration

    • Introduced in the lead scaffold assembly during the initial stage of multi-step synthesis
    • Modified via amination, alkylation, or acylation as required for final API structure
    • QC verified via HPLC/GC before transition to subsequent synthesis step

    Final product types

    • Oral and parenteral small molecule pharmaceuticals with a thiadiazole motif
    • Investigational and commercial drugs for anti-inflammatory and CNS indications
    • Process intermediates for contract manufacturing organizations

    3. Material Science: Advanced Polymer Modifier for Specialty Films

    Manufacturers targeting high-performance polymer composites use this thiadiazole as an electron-withdrawing co-monomer, especially in optical and barrier film technology. Its introduction supports stable charge transfer characteristics and improved chemical resistance, critical in specialty packaging and electronics substrates. Controlled usage during polymerization allows enhanced dielectric or UV-resistance features in end-use films or laminates.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for raw material input
    • RoHS Directive 2011/65/EU for electronic components and barrier films
    • FDA 21 CFR 177.1395 for select food-contact polymeric films (where applicable)
    • ASTM D882 & ASTM D3985 for film mechanical and barrier properties

    Typical usage ratio

    • 0.2–2.5% by weight relative to total monomer blend; adjusted based on required dielectric or barrier enhancement, with higher rates leading to reduced optical clarity but increased performance in critical packaging layers

    Downstream process integration

    • Dispersed in monomer solution or pre-polymer mix prior to in situ polymerization
    • Polymerized by solution or melt process, followed by extrusion or casting into film
    • Quality confirmed by FTIR/NMR analysis of copolymer composition

    Final product types

    • High-barrier packaging films for pharmaceuticals and electronics
    • Flexible printed circuits and dielectric layers
    • Optical and anti-static coatings in specialty substrates

    4. Dye and Pigment Intermediate: Advanced Functional Colorants

    Specialty dye and pigment manufacturers integrate this compound into the synthesis of advanced benzo-thiadiazole-based chromophores, meeting durability and resistance demands in technical textiles and high-performance inks. Its unique halogenation pattern enables precise tuning of absorption spectra and improves resistance to photochemical degradation, allowing for brighter, more persistent coloration in demanding industrial applications.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for textile safety
    • ISO 105 Series for color fastness
    • REACH Regulation (EC) No 1907/2006 Annex XVII for colorant safety
    • EN 71-3 for colorants in toys and children’s articles (where used)

    Typical usage ratio

    • 1–8% by molecular ratio in dye precursor coupling; formulation scientists determine optimal level based on desired hue and fastness performance for the end application

    Downstream process integration

    • Reacted as the core building block in diazotization or electrophilic aromatic substitution during dye synthesis
    • Post-synthesis blending with dispersants or fixatives according to substrate
    • Finished pigment processed by spray drying or granulation for dispersion

    Final product types

    • Technical textile dyes for outdoor gear and industrial fabrics
    • Special-effect printing inks
    • UV-resistant colorants for plastics and polymers
    Free Quote

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    Certification & Compliance
    More Introduction

    5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole: A Manufacturer’s Introduction

    The production of 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole stands on a foundation of real plant work, hands-on chemical handling, and decades of combined experience with heterocyclic compounds. From the start, there’s always a learning curve for each new molecule, but this one has offered up its own lessons. The structure, a fused thiadiazole with chloro and fluoro substituents on the aromatic ring, gives it a distinct profile in synthesis and finished applications.

    Nature of 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole

    Working with this molecule, it quickly becomes clear that structure drives reactivity. The presence of both a chlorine atom and a fluorine atom imparts both electron-withdrawing effects and distinct chemical properties. This doesn’t just matter in chemical theory—it makes a direct impact on how the compound behaves in research and real-world chemistry. We’ve scaled reactions in practice, tested for stability, and learned to control moisture conditions partly because halogenated benzo-thiadiazoles pick up water if quality slips anywhere in storage or transportation.

    Those working the reactor valves get to see up close what counts as a “good batch” and what just qualifies. Maintaining a high level of purity goes beyond just compliance checks—it determines whether the downstream chemistry runs smoothly or hits setbacks. The latest analytical batch at our facility consistently clocks in at above 99% purity by HPLC, with particular attention paid to low levels of residual solvents and chlorinated by-products. Each production run uses validated isolation methods that keep contamination to a minimum.

    Specifications and Handling Practices

    Powdered, light tan or off-white when fully dried and properly stored, the material handles best in a low-humidity environment. Bagging crew members learned early on that sealed double-layer poly bags with secondary fiber drums provide better protection than single-layer sacks, especially in humid environments. Any slip-up leads to clumping, which slows downstream dissolution. For long-term storage, we’ve found that temperature below 25°C prevents surface degradation—a fact our partners in hotter climates appreciate.

    Routine checks in the plant focus on melting point, appearance, and moisture content. By relying on routine Karl Fischer titration, we catch rogue moisture early. This allows customers—especially those downstream in pharmaceutical and agrochemical synthesis—to use the product without running in-process drying steps. That alone simplifies several chemistries by eliminating a common bottleneck.

    Uses Rooted in Real-World Demand

    This intermediate does not find its home on every laboratory bench. Its demand often flows from specialty sectors—mainly agrochemical synthesis, pharmaceutical intermediates, and specific dye work. Our experience shows that the molecule’s halogen pattern offers key advantages in electron-rich environments where further substitution or ring modification is crucial. Process chemists know how a single misplaced impurity can derail plans, so plant operators keep a practical eye on reaction conditions, aiming for the lowest possible impurity profile.

    Pharmaceutical groups have pulled our 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole for use as a building block in heterocyclic frameworks, relying on its reactivity to introduce functionalization at controlled sites. Others in the agrochemical world push for scale, demanding that each drum offers not just the named compound but consistent batch reproducibility. Years in the business have shown that manufacturers who cut corners wind up chasing recurring complaints on batch-to-batch variability. We’ve invested in statistical process control, not just to tick boxes but to answer for our product’s continued role as a trusted input for long synthesis routes.

    How the Compound Compares with Close Relatives

    In the thiadiazole family, many analogues compete for attention. We’ve worked hands-on with 5-chloro variants, 6-fluoro isomers, and benzo-1,2,3-thiadiazoles without both substituents. Experience tells us that the dual halogenation in 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole adjusts the electron density so reactions involving nucleophilic aromatic substitution run smoother under milder conditions compared with single-substituted analogues. Process yields tend to edge higher because both substituents stabilize side reactions.

    The plant runs on this molecule often differ in requirements for waste recovery compared to the simpler benzo-thiadiazole base structure. We find that chlorinated/fluorinated waste demands stricter handling and post-processing treatment. Much of our process development focuses as much on efficient separation and safe waste neutralization as it does on maximizing throughput. Downstream customers get consistent feedback from us when we implement equipment upgrades—simple steps like adding a secondary condenser or replacing transfer hoses with fluoropolymer-lined options have cut batch contamination rates by measurable margins.

    Process Challenges and Progress with Handling

    A decade of plant operations has shown areas where even best-practice workflows still need vigilance. The small molecule size and aromatic nature mean 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole generates dust. Our process engineering team long ago replaced open pouring with closed-system transfers; positive pressure suits became standard when loading reactors. These investments come after first-hand experience with eye and skin irritation reported early in pilot batches.

    Scale-up from pilot plant to tonne-lot production was not seamless. Aggressive process impurities required updated vent scrubbers and secondary containment for batch filtrates. In some cycles, we saw by-product levels spike due to modest swings in temperature control. We’ve solved these issues by running longer, steady-state temperature holds and switching to in-line process analytics for those stages. Every change we make comes from lessons learned, not out of theoretical convenience but from experience gained facing delayed deliveries or costly rework.

    Supporting Consistency through Real QA Efforts

    A chemical like this can only build its reputation if it works every time. Our QA team routinely tracks customer complaints, processing trends, and instrument calibration records. Every time a batch leaves the warehouse, there’s a full trail of certificate analysis and counter-signed release forms—it’s the kind of paperwork that saves arguments later. We’ve worked hard to give customers data that speaks plainly: batch retention samples, long-term stability testing under various storage conditions, and reactivity tests on actual use cases, not just routine lab analysis.

    We have direct relationships with major downstream users who run feedback cycles with us. One pharmaceutical customer flagged an uptick in a trace impurity after a minor process solvent change. Their feedback made us revisit a step, strip out the new solvent, and return to the earlier approach. That working partnership has made the intermediate more robust for a range of the next user’s application routes.

    Safety and Environmental Efforts Born from the Floor

    Manufacturing always comes with risks. We set up routine safety meetings because early days with the compound taught us the consequences of lax material handling. On a late shift many years back, a minor release during filter cake handling made clear the need for full-face shields in unloading as well as loading. We’ve since added real-time air monitoring in the packing rooms, and every new worker learns the specifics of halogen handling as part of their first week.

    Environmentally, the molecule’s halogenated effluents need attention that simpler thiadiazoles do not. We partner with licensed waste processors and carry out in-house neutralization when possible. Over time, we’ve added layered containment to protect groundwater and invested in higher-grade liner materials for effluent channels. No one wants to see a stack of costly compliance paperwork, but proper stewardship comes out of commitment, not convenience. Every update we make, from membrane filtration upgrades to closed-loop water systems, comes from the combined pressure of regulatory standards and company values.

    Continuous Improvement: Evolving with Customer and Regulatory Demands

    Markets shift and so do customer requirements. A decade ago, specs on permissible residual solvents or trace metals in intermediates drew less scrutiny. Today, pharma and agrochemical partners request proof of increasingly strict limits, tracking not just the basics but also “emerging impurity” classes. We’ve adjusted protocols in step with these changes, running additional GC-MS analysis before release and holding inventory on-site until final outside confirmation.

    Plant teams learned to respond to special requests, such as drum labeling by batch or splitting lots for separate analysis. These seem like minor adjustments until a last-minute regulatory review demands separation of consignment lots based on customer application or export destination. By having experienced hands on the floor and a robust digital tracking system, we can meet these demands with less disruption than in the past.

    Turning around unexpected regulatory changes or audit findings used to be a major headache. Now, we’ve dedicated staff whose only job is liaison with QA/QC labs and regulatory affairs, ensuring full traceability from incoming raw material through to delivered product. This level of support doesn’t emerge overnight—it’s born out of years of practical setbacks and close lessons learned from customer and auditor feedback.

    Investing in the Plant and the Team: Long-Term Perspective

    Real improvements to the manufacturing floor don’t only show up in yearly upgrades or in facilities tours. Seeing how equipment choices affect batch quality, training, and uptime is part of daily routines. By switching to newer reactor linings and updating packing conveyor layouts, we eliminated recurring downtime due to abrasive chemical build-up and minimized cross-contamination risk. It took trial and error, not just engineering theory, to get there.

    Worker retention forms a huge part of our consistent quality. People who understand every nuance of a process are less likely to miss possible sources of contamination or irregularities in a batch. There’s strong internal mentoring from senior operators who remember earlier runs with less automation, where all adjustments depended on a steady hand and well-trained eye. These human investments make production of 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole more predictable from run to run.

    How This Compound Stands Out in Everyday Operations

    Having produced related chlorinated and fluorinated heterocyclic intermediates for years, we know where 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole outperforms. The dual halogen pattern offers broader reactivity, especially where downstream steps need specific substitution at defined sites—something not every isomer delivers. In several custom projects, researchers cite the predictable reactivity as reason to stick with our product, even when alternatives seem available.

    From process operators to the QA team, everyone sees the results when a compound performs as expected. Faster reactions, fewer side products, and more robust isolations make for more reliable scheduling and timely deliveries. End users appreciate that steady stream of on-specification material, documented by full trace records and supported by open lines of plant-to-customer technical feedback.

    Meeting Modern Market Expectations

    The push towards more sustainable and responsible chemistry runs deep in the manufacturing world. Energy usage, waste profiles, and raw material sourcing all get regular review. For 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole, process optimization means tighter reaction control, lower solvent requirements, and more efficient batch yields. By capturing and recycling solvents, reusing process water, and investing in energy-saving plant upgrades, we've managed to reduce the resource intensity of every kilogram shipped.

    Customers, especially from regulated markets, bring additional scrutiny. They request background on supply chain stability and ask pointed questions about origin of raw materials, documentation of critical control points, and contingency plans for unexpected outages. That attention to risk, while demanding, makes for a more resilient manufacturing system. We have backup supplier plans, maintain redundant inventories of essentials, and invest in on-site testing capacity to minimize external dependencies and delays.

    Real Feedback, Real Adjustments

    Feedback from partners often shapes ongoing development. One specialty chemicals client reported issues with filtration rate after drum changes introduced different liner materials. Instead of defaulting to standard solutions, our team spent time at the customer’s plant, identifying where packing specifications caused bridging and clumping. Adjusting fill density and switching to an anti-static drum liner not only solved the problem but improved overall handling, reducing dust generation and speeding dissolution in the customer’s process.

    Face-to-face collaboration with other manufacturers, formulators, and research chemists solves more problems than any distant specification sheet. Our technical support staff often fields calls that move beyond what’s listed on a typical COA—ranging from advice on process tweaks to troubleshooting hard-to-isolate side products. This hands-on partnership is what grounds our commitment to quality and ongoing product adaptation.

    Looking Forward: The Continuing Role of 5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole

    Every year, new applications emerge for halogenated thiadiazoles in complex synthesis routes. Facing unpredictable raw material costs, increased regulatory requirements, and shifting customer needs, we keep adapting—experimenting with new reaction media, eyeing continuous production pilots, and improving waste capture and emissions controls. Direct experience, whether through troubleshooting stubborn filtration issues or revising storage protocols, guides these continuous changes.

    As this compound finds new homes in pharmaceutical, agrochemical, and advanced materials sectors, current trends point to more intricate regulatory demands and tougher product specs. We’ve taken those challenges on wholeheartedly, building open lines of communication from plant floor to customer’s bench, and integrating lessons from real setbacks and successes. As suppliers and practitioners, we know that every drum tells a story—of work done right, of problems met honestly, and of a product that keeps earning its way into advanced chemistry.

    Summary

    5-Chloro-6-Fluorobenzo-2,1,3-Thiadiazole stands apart from single-substituted analogues through its dual-halogen versatility and consistent purity, born out of practical, daily plant experience and ongoing engagement with end uses and regulatory shifts. Our plant crews, QA teams, and process engineers push improvements for safety, efficiency, and product performance, drawing lessons from direct feedback and years of hands-on production. All progress made comes not from simple compliance, but from a deep respect for the real-world needs of everyone relying on our chemical in their most critical reactions.