[1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo-

    • Product Name: [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo-
    • Chemical Name (IUPAC): 4,7-dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine
    • CAS No.: 1026781-60-1
    • Chemical Formula: C4Br2N3S
    • Form/Physical State: solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    419137

    Chemical Name [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo-
    Molecular Formula C4Br2N3S
    Molecular Weight 279.94 g/mol
    Cas Number 139094-42-7
    Appearance Pale yellow solid
    Melting Point 174-178 °C
    Purity Typically ≥98%
    Synonyms 4,7-Dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine
    Storage Conditions Store at 2-8 °C in a dry place
    Solubility Soluble in organic solvents like DMSO and DMF
    Inchi InChI=1S/C4Br2N3S/c5-2-1-11-9-4(6)3(2)7-8-11
    Smiles Brc1cn2nsnc2c(Br)n1

    As an accredited [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 5-gram amber glass bottle, sealed with a PTFE-lined cap, and labeled with hazard and identification information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) involves packing [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo- securely in a 20-foot container for safe transport.
    Shipping This chemical, [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo-, is shipped in tightly sealed, chemically resistant containers under ambient temperature conditions. Appropriate hazard labeling and documentation accompany the shipment, complying with relevant local and international transport regulations for potentially hazardous organic compounds. Protective packaging prevents leaks or breakage during transit.
    Storage [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo- should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protect it from light and moisture. Use appropriate chemical-resistant containers, and ensure proper labeling. Handle under a fume hood, using suitable personal protective equipment (PPE) to minimize exposure.
    Shelf Life Shelf life of [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo-: Stable for 2 years if stored dry, cool, and protected from light.
    Application of [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo-

    Purity 98%: [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo- with purity 98% is used in organic semiconductor synthesis, where it enables high charge mobility in electronic devices.

    Melting Point 210°C: [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo- with a melting point of 210°C is used in OLED material manufacturing, where it ensures thermal stability during device fabrication.

    Molecular Weight 276.93 g/mol: [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo- at molecular weight 276.93 g/mol is employed in polymer donor-acceptor systems, where it promotes efficient electron transfer.

    Particle Size <10 μm: [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo- with particle size below 10 μm is used in thin-film processing, where it achieves uniform film morphology.

    Stability Temperature 150°C: [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibroMo- with a stability temperature of 150°C is used in photovoltaic device assembly, where it maintains structural integrity under operational stress.

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    Certification & Compliance
    More Introduction

    [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo-: A Manufacturer’s Perspective

    Understanding the Core: What We Make and Why it Matters

    For years, our team has dedicated itself to producing specialty heterocyclic compounds that drive innovation in research and industry. Among these, [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo- has carved out its own space as a versatile intermediate. As the manufacturer, we interact directly with the chemists and scientists exploring the limits of what this molecule can do, so we’ve gotten to know its strengths, quirks, and wide market applications through daily work at the bench and across the production line.

    What Makes [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo- Stand Out?

    Any new synthetic building block must compete with a crowded field of organic intermediates. In our experience, the dibromo pattern at the 4 and 7 positions on the core heterocycle doesn’t just extend the reactivity window compared to unsubstituted analogs—the carefully controlled bromination gives research chemists more options for targeted functionalization. This makes cross-coupling, such as Suzuki and Stille reactions, much more straightforward, something we’ve seen labs request repeatedly. You simply get more flexibility constructing complex molecular frameworks.

    Not every client is looking for this precise arrangement of halogens, and it isn’t meant for all possible transformations. The core itself, the thiadiazolopyridine skeleton, offers structural rigidity and electronic character that can improve physical properties in downstream materials. In the lab, operators remark on how the dibromo version delivers a consistent hand—no surprise reactivity or polymorph headaches. Technicians in our own quality control labs appreciate how easily they can verify lot purity using straightforward chromatography and NMR techniques, with reliable fingerprint signals. It’s a clean, tractable intermediate, not a fussy or temperamental option.

    Specifications with Practical Implications

    We supply this compound as a crystalline solid, typically ranging from off-white to light tan. Our team tracks every batch through a tight control process. Starting from niche heterocycle synthesis, we use halogenation steps under carefully maintained temperatures. The process yields a product with high purity — consistently verified by NMR, HPLC, and melting point analysis. Why fuss over those details? Labs demand reliable results, batch after batch. Lower-grade intermediates can introduce noise into downstream reactions, affecting yields and reproducibility. Using our product, labs have reported much lower troubleshooting overhead in scale-up or multi-step syntheses.

    Chemists working with this dibromo thiadiazolopyridine often drive subsequent coupling reactions or build it into broader heterocyclic frameworks. Purity matters because residual byproducts or insufficiently substituted precursor can poison palladium catalysts or disrupt selectivity in postfunctionalization. Our staff keeps these downstream issues front of mind, regularly gathering feedback from partners’ experiences.

    Applications In Practice

    What do buyers really do with this molecule? The largest segment comes from advanced materials research. Several clients target organic semiconductors, light-absorbing dyes, and molecular electronics. The unique electronic and steric features of the thiadiazolopyridine scaffold, modulated by twin bromines, encourage charge mobility and tunable optoelectronic behavior in final devices. Polymer chemists often turn to this intermediate when constructing conjugated backbones for new field-effect transistor architectures, solar cell active materials, and high-performance sensors. The dibromo compound stands up well to modifications—aromatic substitution, C–C coupling, or careful nitrogen modification.

    Pharmaceutical discovery groups also draw on this framework occasionally. Project managers in these settings look for unique small-ring compounds that provide bioisosteric alternatives or rigid scaffolds for SAR exploration. The thiadiazolo fragment has proven useful for introducing new hydrogen bonding patterns, and the dibromo substitution expands medicinal chemistry playbooks by allowing late-stage diversification. Over the years, we have supplied this for fragment-based lead finding studies, combinatorial libraries, and even as a tool to introduce site-specific radiolabels for PET imaging probe research.

    Manufacturing Experience: Streamlining Synthesis and Supply

    Working at scale, one notices gaps that rarely appear in the literature. Raw material supply, reaction work-up, and purification bottlenecks—these define whether a batch is successful. We’ve invested substantial capital upgrading our downstream purification systems to deliver high-batch purity and minimize environmental impact. Standard halogenation methods tend to create byproducts, so we developed in-house crystallization protocols that consistently remove colored impurities and residual solvolysis products. Instead of relying on column-heavy purification, we cycle our crude product through staged washes and recrystallizations. This reduces solvent waste and speeds up delivery timelines.

    As the manufacturing workforce involved in each synthesis can tell you, small details like drying conditions, suitable containers, and tight temperature control during bromination affect not just yield but also the stability and processability of the product. Our operators track every lot from kettle to warehouse shelf, with checks at each step: TLC spot analysis, full-spectrum NMR, and regular comparison to reference standards. Any lot falling outside specification is quarantined, retested, or discarded. By handling the entire cycle ourselves, we avoid the cascading issues that often plague resellers, traders, or brokers—such as variable impurity profiles, mixed provenance, or incorrect storage.

    Transport and storage matter too. Many users want the compound shipped in inert conditions or at low moisture content, especially for larger quantities destined for delicate electronic materials. Our logistics crew prepares vac-sealed, foil-lined drums for kilogram shipments, reducing degradation and contamination risk.

    Supporting Innovation Across Sectors

    People developing next-generation photovoltaic materials, OLED emitters, or thin-film transistors come to us looking for more than simple catalog supply. Several university partnerships have relied on our willingness to scale up rapidly for pilot studies. We work closely with technical leads to adjust batch sizes, document control parameters, and even adapt packaging for glovebox transfers when required.

    Innovation doesn’t stop with materials. Life science and diagnostic companies sometimes incorporate the dibromo thiadiazolopyridine into label molecules or screening platforms. The unique reactivity enables integration with peptides, polymers, or small-molecule libraries. Our clients value the rigorous traceability that comes from direct-from-source manufacturing; they know exactly where the material came from, and that allows them to troubleshoot and optimize much faster.

    Researchers exploring catalysis or analytical derivatization also seek out the dibromo compound for its distinctive halide handles. The electron-withdrawing features of the thiadiazole and the placement of the bromines often produce different reactivity profiles compared to plain heteroaromatics, leading to improved yields or expanded substrate compatibility in cross-coupling experiments. By collaborating with us as the originators, clients get early access to new process variations or alternative synthetic routes.

    Comparing With Sibling Molecules

    Some customers ask whether it’s worth buying the dibromo variant over similar compounds—say, the monobromo analog or an unsubstituted thiadiazolopyridine. The answer depends on the synthesis roadmap. Having both 4 and 7 positions brominated lets researchers pursue stepwise or orthogonal chemistry, introducing multiple different substituents or designing molecules for directional assembly. Single bromination limits downstream flexibility. We have seen customers move from an initial program using monobromo starting points to the dibromo form when they needed further customization or modular postfunctionalization.

    From a manufacturing standpoint, producing the dibromo compound requires greater precision and longer reaction times. This drives higher production costs, but it’s balanced by the reduction in synthetic complexity for the end user. Skipping the dibromo intermediate forces chemists to rely on more steps later, often involving cumbersome protection-deprotection strategies or low-yielding, single-substitution reactions. By supplying the dibromo derivative directly, we help streamline our partners' routes, saving them weeks or months in multi-step synthesis efforts.

    Purity and consistency also play a role in the comparison. Analogues with different halogen patterns may show batch variability, especially as side reactions or partial halogenation build up impurities over time. Our production lines are set up to minimize these outcomes, leveraging both in-process analytical feedback and regular process audits.

    Commitment to Quality, Traceability, and Technical Support

    Our company isn’t just a node on a supply chain. We have chemists, engineers, and process analysts maintaining hands-on oversight from first reactant charge to final packaging. Clients frequently remark on the benefits of working with the manufacturer directly. If an issue appears in downstream application—unexpected solubility, reactivity snag, or scale bottleneck—they can talk to scientists who’ve run the same transformations, sometimes hundreds of times. That kind of technical shepherding allows us to recommend simple adjustments in protocol, washing, or solvent composition, all based on real production and R&D lab records.

    We maintain full batch records and can reproduce or scale custom specifications to suit research or pilot scale needs. Whether it’s adapting solvent profiles for more consistent crystallization, adjusting bromination kinetics for improved yield, or providing supporting spectral data for regulatory filings, the team responds quickly and knowledgeably. This hands-on approach, combined with modern process automation, means fewer surprises for downstream projects.

    With research timelines often measured in months rather than years, delays have real-world impact. By controlling raw materials, handling QA in house, and working closely with shipping partners, we provide a responsive supply stream. Researchers move faster, data cycles compress, and commercialization schedules stay intact.

    Challenges in the Broader Market

    Manufacturing heterocyclic, halogenated intermediates introduces more variables than most catalog suppliers admit. Regulatory controls around brominated compounds have tightened, especially in international logistics and waste handling. Our compliance team tracks changing legislation closely, and we’ve responded by retooling waste reclamation routes to minimize environmental risk. Customers sometimes ask about the sustainability of our processes; since we control every step, we can answer confidently about solvent recycling, waste minimization, and responsible handling.

    Supply chain disruptions during the last few years—raw material shortages, freight delays, trade restrictions—spotlighted the risks of depending on fragmented producers or distant brokers. By maintaining in-house inventory and a dedicated technical workforce, we secure supply and shield clients from the risks of missed project deadlines or unexpected price spikes.

    Sometimes, labs run into upscaling snags, often due to subtle differences in crystallinity, particle size, or trace impurity profiles. Because we manage all process parameters, troubleshooting and optimization conversations draw upon both on-the-ground lab insight and years of process data. This reduces time spent fire-fighting and returns focus to development and discovery.

    Improving for Tomorrow’s Needs

    To stay ahead in specialty chemicals, you learn that making one intermediate well opens doors for advances up and down the value chain. We constantly connect with research groups and industrial scale users to anticipate emerging requirements. This feedback loop guides investment in upgraded equipment, smarter automation, and more robust analytical tools.

    Green chemistry matters more today than it did even five years ago. We’ve reworked several parts of our process to lower energy input, cut hazardous solvent usage, and capture evaporative emissions. In some runs, we now employ alternative solvents or greener reagents, nudged along by both partner requirements and our own commitment to sustainability. Our R&D team pilots continuous improvement cycles—tweaking reaction parameters, investigating new purification chemistry, and looking for ways to further minimize waste.

    These changes don’t come at the expense of product reliability. Every process shift comes after weeks or months of validation, side-by-side comparisons, and cross-checks of downstream performance in real customer workflows. The lessons learned from each improvement feed back into training, documentation, and process setup, making the next batch better than the last.

    Final Thoughts from the Manufacturing Floor

    People throughout our organization—from process chemists to packaging staff—take pride in keeping standards high for [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo-. This isn’t simply a commodity or a catalog number; it represents years of refinement, continuous feedback with leading scientists, and a track record of proven utility in advanced research and production. Each batch stands on the accumulated know-how of people who take chemistry and reliability seriously.

    Whether you’re pushing boundaries in electronics, searching for new medicine, or engineering functional polymers, the right building block can save weeks of effort and provide a foundation for success. Backed by process transparency, support from direct manufacturing specialists, and a focus on reliability and sustainability, our [1,2,5]Thiadiazolo[3,4-c]pyridine, 4,7-dibromo- supports your research ambitions at every stage.