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2,4-Dibromothiazole

    • Product Name 2,4-Dibromothiazole
    • Alias 2,4-Dibromo-1,3-thiazole
    • Einecs 221-320-9
    • 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

    526941

    Cas Number 22232-54-8
    Molecular Formula C3HBr2NS
    Molecular Weight 241.92 g/mol
    Iupac Name 2,4-dibromo-1,3-thiazole
    Appearance Solid
    Melting Point 42-44°C
    Boiling Point 210°C (approximate)
    Density 2.37 g/cm³ (estimated)
    Solubility In Water Slightly soluble
    Smiles C1=NC(=CS1Br)Br
    Inchi InChI=1S/C3HBr2NS/c4-1-2-7-3(5)6-1/h2H
    Pubchem Cid 2716130

    As an accredited 2,4-Dibromothiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,4-Dibromothiazole is packaged in a 25-gram amber glass bottle with a secure screw cap and chemical hazard labeling.
    Shipping 2,4-Dibromothiazole is shipped in securely sealed containers to prevent leaks and contamination. It should be packed according to hazardous material regulations, with appropriate labeling and documentation. Store and transport in cool, dry conditions, away from incompatible substances, and handle with care to ensure safety and compliance with all relevant regulations.
    Storage 2,4-Dibromothiazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers. Use in a chemical fume hood to avoid inhalation. Properly label the storage area and container, and follow all relevant safety and regulatory guidelines.
    Application of 2,4-Dibromothiazole

    Applications of 2,4-Dibromothiazole in Industrial Manufacturing

    2,4-Dibromothiazole serves as a key halogenated heterocyclic intermediate in multiple specialized chemical sectors. Our manufacturing clients rely on this compound to drive precision transformations, strict quality control, and reproducibility for advanced processes in crop protection, pharmaceuticals, electronics, and polymer modification. Below we provide an in-depth overview of established downstream applications fully supported by sector standards and best practice integration.

    1. Crop Protection Synthesis: Advanced Herbicide Intermediates

    Leading agrochemical manufacturers utilize this material for building blocks in thiazole-derived herbicides targeting resistant weeds. Its dibromo structure enables highly selective functionalization for next-generation crop protection molecules compliant with international registration requirements. Our customers adjust inputs based on target molecule complexity, allowing for excellent customization at the formulation stage to support unique patent-protected products for regional agriculture markets.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • European Union Regulation (EC) No 1107/2009 for Plant Protection Products
    • US EPA Pesticide Registration Standards
    • OECD Good Laboratory Practice (GLP)

    Typical usage ratio

    • Application input ranges from 0.5–3.0 mol% per synthesis batch; precise charge calculated based on the molecular weight ratio to target active moiety and reaction yield targets.

    Downstream process integration

    • Introduced at the heterocycle construction or halogen-exchange step, often pre-coupling or cyclization, prior to methylation or amination stages in multi-step active ingredient synthesis lines.

    Final product types

    • Systemic and contact herbicide technical concentrates, thiazole-based selective herbicide formulations, pre-emergent weed control actives.

    2. Pharmaceutical API Synthesis: Thiazole-Based Drug Intermediate

    Pharmaceutical manufacturers incorporate this intermediate in the synthesis schemes for targeted anti-infective and anti-inflammatory compounds containing thiazole scaffolds. Our facility supplies material meeting trace impurity thresholds and full documentation to support regulated GMP API production. Process engineers optimize addition rates in response to yield and purity targets for specific drug candidates under clinical pipeline or approved generics with stringent regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia – National Formulary) monographs
    • European Pharmacopoeia (Ph. Eur.) requirements for intermediates
    • US FDA DMF (Drug Master File) referencing

    Typical usage ratio

    • Standard dosing is 1.2–2.0 molar equivalents against the amine or carboxylic functional group targeted for thiazole ring formation. Adjustments reflect process scale-up yields and impurity risk management.

    Downstream process integration

    • Added during the intermediate stage for constructing the bioactive core, typically after initial condensation or amidation, prior to final crystallization and purification of the API.

    Final product types

    • Small-molecule APIs with thiazole or bromothiazole motifs, particularly in anti-infectives, analgesics, and investigational compounds.

    3. Specialty Electronic Materials: OLED and Semiconductor Precursors

    Manufacturers in high-performance electronics rely on dibromothiazole moieties to introduce both electron-withdrawing characters and precise substitution points on functional organic materials. Its dibrominated aromatic core supports cross-coupling (Suzuki, Stille) strategies essential for organic light-emitting diodes and transistor assemblies. We provide electronic-grade batches with QC-driven traceability for integration into substrate or layer-by-layer fabrication in controlled cleanroom environments.

    Industry compliance standards

    • JEITA (Japan Electronics and Information Technology Industries Association) material purity protocols
    • RoHS Directive (EU) 2011/65/EU for hazardous substances
    • IPC-4101 for base materials in electronics
    • ISO 9001:2015 certified electronic materials management

    Typical usage ratio

    • Employed at 0.3–1.5 weight% relative to total monomer weight in sophisticated polymeric or small-molecule device precursors, with loading precisely measured based on desired electronic behavior.

    Downstream process integration

    • Incorporated at the precursor synthesis step for organoboron or organostannane intermediates, immediately before palladium-catalyzed coupling to form extended conjugated systems on an industrial scale.

    Final product types

    • OLED emitter materials, organic thin-film transistors, semiconducting polymer layers for flexible displays and photovoltaic devices.

    4. Modified Engineering Polymers: Specialty Plastics and Copolymer Additives

    Producers of engineering plastics integrate dibromothiazole as a modular building block for introducing flame retardancy and chemical resistance in specialty copolyester and polyamide series. The dibromothiazole unit enhances halogen content at precise locations within the polymer chain, helping converters achieve specific performance classes without using bulk halogen additives. Our supply meets consistency requirements for melt extrusion and continuous polymerization reactors.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics Materials
    • REACH Regulation (EC) No 1907/2006 on chemical safety
    • ISO 1043-4 for polymer composition labeling
    • ASTM D638 for tensile properties of plastics

    Typical usage ratio

    • Integrated at 0.2–1.0 mole% within the comonomer feed for copolymerization, dosage tailored to target oxygen index and mechanical strength.

    Downstream process integration

    • Fed into the initial comonomer or prepolymer stage, enabling in-situ copolymer formation inside continuous stirred-tank reactors or during step-growth batch synthesis.

    Final product types

    • High-temperature resistant copolyesters, flame-retarded polyamide blends, specialty compounded plastic pellets for automotive and electronics applications.
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    Certification & Compliance
    More Introduction

    Introducing 2,4-Dibromothiazole: Experience from Direct Production

    A Direct View from the Manufacturer

    We have been synthesizing 2,4-Dibromothiazole for years, working daily with raw materials and tight process controls. This compound keeps finding its way into new research projects and specialty chemical uses, owing to its structure and functional potential. Having spent so much time in the production halls, we get to witness all its quirks, benefits, and the real-world impact of clean and reliable manufacturing.

    Reliable Quality Starts with Rigorous Sourcing

    Our commitment to quality begins before the first step in synthesis. Brominating reagents and thiazole feedstocks arrive through trusted channels, and inbound quality control never gets compromised. Every batch goes through a battery of purity tests, and if anything falls short of target thresholds, we reject and escalate the incident. These decisions don’t come from an isolated office or marketing material—quality assurance gets woven into the process floor. Inconsistent source materials ripple downstream, compromising both product yield and end-user experience. For 2,4-Dibromothiazole, even slight contamination risks are too great, especially when researchers rely on accuracy at the molecular level.

    Process and Specifications We Stand Behind

    The molecular backbone of 2,4-Dibromothiazole (C3HBr2NS) is simple but stubborn. Achieving high purity depends on precise reaction temperatures and timings, and by monitoring each batch with gas chromatography and NMR, we keep impurities low and traceable. Typical batches reach over 98.5% purity, with tightly-controlled moisture content. The crystalline product gets handled and packaged in climate-stabilized rooms, avoiding both atmospheric moisture and cross-contamination with other aromatic bromides. If you ever need batch data, we log the results and supply them without delay—accuracy and transparency go hand-in-hand.

    The Importance of Consistency in Research and Production

    For chemists and material scientists, batch-to-batch consistency forms the backbone of successful research. One customer uses 2,4-Dibromothiazole for pharmaceutical intermediate synthesis, another develops specialty dyes. Both rely on identical physical properties and reagent content every time. Inconsistent melting points or contamination—the pain points we’ve seen elsewhere—lead to failed reactions or irreproducible results. By sticking to rigorous internal standards and regular equipment calibration, we’ve reduced off-spec variance to a fraction of a percent. Through feedback loops with customers and routine process improvements, we stay alert to even the smallest shifts in chemical profile.

    Why 2,4-Dibromothiazole Matters

    Demand for 2,4-Dibromothiazole isn’t about sheer volume. Demand grows because this compound enables complex syntheses researchers constantly push forward. Being both an electron-rich ring system and a bromo-activated heterocycle, it fits where few other reagents can. In pharmaceutical, dye, and agrochemical development, small molecules with targeted substitutions often outperform larger scaffoldings for selectivity and fine-tuning. 2,4-Dibromothiazole brings two reactive bromines onto a thiazole core. These positions allow for custom transformations—that’s why it sits at the intersection of innovation and necessity.

    Differences from Similar Compounds

    Other brominated thiazoles have their place, but 2,4-Dibromothiazole offers distinct selectivity. Compare it to 2-Bromothiazole or 4-Bromothiazole: monobrominated analogues might seem interchangeable at first, yet practical experience shows the difference. The presence of two bromine atoms (at the 2 and 4 positions) isn’t just academic. It unlocks bifunctional reactivity. Cross-coupling chemistry, for instance, operates more efficiently when two reactive halogens anchor the same aromatic system. Chemists in the field who switch from a mono- to dibrominated thiazole see better yields and cleaner reaction profiles—less side-product, greater selectivity. Lower halogen content often results in extra steps and higher cost downstream.

    On Purity, Stability, and Storage

    Attention to storage details matters with 2,4-Dibromothiazole. Past experience has shown that lapses in moisture control, or even mismatched storage containers, can trigger hydrolytic changes and loss of material. We protect finished lots in amber glass jars or corrosion-resistant polymer drums, depending on order size, and we keep desiccants close at hand. Temperature and humidity both get monitored not just in the warehouse but every point along the packaging line. Some customers store the compound for extended periods. Care at each production step means that if they return to their supply months later, the compound’s physical and chemical properties still show within spec.

    Application Areas: What We See in Practice

    Direct customer feedback shows that 2,4-Dibromothiazole finds use in advanced organic synthesis—think Suzuki and Stille couplings, heterocyclic core modification, and medicinal chemistry scaffold building. One research group turns it into novel thiazole-containing drugs through stepwise arylation. In dye chemistry, it often acts as a key intermediate for colorant molecules with improved lightfastness and chemical stability. Agricultural chemical innovators use it to anchor new pesticide structures. Each application stretches the molecule in a different way, and with the combination of twin bromines and the thiazole ring, our product reliably meets those demands. In formulation or downstream transformation bandwidth, few alternatives keep pace.

    Dependable Supply: Factory Strengths and Learnings

    Chemicals like 2,4-Dibromothiazole don’t come from commodity lines. Handling bromination reactions needs respect—both for safety and for fine control. Early in our scale-up journey, we faced issues balancing throughput with safety systems—chilled systems prevented runaway reactions, but slow line reactivity sometimes introduced unwanted side products. Through refining our temperature control arrays and retrofitting continuous flow reactors, we reduced side-output by almost fifteen percent and improved main product purity. Now, even large-scale orders retain lab-level precision. This direct hands-on knowledge, gained on our shop floor, feeds right back into customer trust and stable long-term supply.

    Why the Right Specifications Make the Difference

    End-users rarely see the raw production site, but our design choices make a clear difference at the bench. Our 2,4-Dibromothiazole appears as an off-white crystalline solid, melting in a tight temperature window. We measure color (almost every day) using calibrated comparator tubes to catch any emerging contaminants. Residual solvent levels are a constant focus—GC traces allow us to tune vacuum drying. These decisions enable researchers to skip pre-purification steps and jump directly into synthesis campaigns. Over time, not needing to troubleshoot batch variance or account for excess impurities provides scientists measurable returns in efficiency and confidence.

    Packaging Direct from the Factory

    We package at the same facility that makes the product. There’s no interim warehouse, no prolonged exposure to atmosphere, and no ambiguous chain of custody. That transparency helps customers track down the source of any problem, if any should occur, and enables us to take accountability and offer support. Wherever our 2,4-Dibromothiazole travels—to university departments or industrial pilot plants—its packaging and labeling conform to the batch data generated right at production. A packaging slip isn’t just administrative; it’s another checkpoint in our work.

    Why Not All 2,4-Dibromothiazole Is Created Equal

    Subtle differences in process show up most sharply after repeated use. We once received a sample from a customer who’d tried a lesser-known supplier only to find their reaction stopped short. Side-by-side, their material and ours looked similar, but GC-MS revealed trace isomer contamination and heavier halogenated byproducts. That story, not so uncommon, led us to double down on in-process control. The extra analytical screening adds upfront cost and time, but it prevents problems for everyone later. Others source 2,4-Dibromothiazole on price alone and risk extra cleanup or failed research.

    Environmental Responsibility in Chemical Manufacturing

    Every step in producing 2,4-Dibromothiazole produces waste streams. Our operations began minimizing bromine content in effluent over a decade ago. Today, we recover and recycle a percentage of spent bromination agent with continuous flow purification systems. Handling hazardous by-products gets the same scrutiny as product control—our discharge water and air emissions stay within ever-tightening legal limits and internal voluntary targets. Chemical synthesis brings unavoidable impact, but every margin we close makes the process safer for both neighboring communities and our own employees.

    Intellectual Property and Technical Support

    We have supported both proprietary and open innovation for clients by tailoring documentation to meet their needs. Sometimes, researchers require detailed process data or spectral interpretation. We keep thorough records and offer our technical team’s insights, from NMR assignments to strategies for post-synthetic modifications. We have watched research teams save months by addressing a subtle impurity or selected a different solvent based on our suggestions. Being present at the actual production line means we know what’s inside each package and can answer practical questions authoritatively.

    Solving Supply Security: Real-World Adjustments

    Chemical supply chains carry risk at every link. Recent global disruptions put strain on upstream feedstock reliability and outbound shipping timelines. To adapt, we expanded our raw material sourcing to include two redundant supplier regions, and we stock critical intermediates in temperature-monitored on-site tanks. These investments shield our clients from delays, which in research can mean missed grant milestones or halted scale-up. We never forward-order from unknown traders—direct vetting of every upstream source gets documented, so traceability stays intact. Our customers value consistency, and we back that up with documented, direct material flow.

    Looking Forward: Broadening Applications and Sustainable Growth

    Every year, new research teams request samples or production runs for unforeseen applications: next-generation polymers, advanced sensors, catalytic systems. The versatility of 2,4-Dibromothiazole continues to invite innovation. As a manufacturer, we see the most creative uses originate from open communication with end users. When a research chemist approaches us about functionalizing another ring, or making a difficult coupling step run more smoothly, those practical conversations drive our iterative process improvements as much as market demand.

    Continuous Improvement: Lessons from the Shop Floor

    No chemical synthesis is ever “done improving.” Every new project reveals small refinements—batch heating curves, solution concentrations, cooling gradients—that ripple through output quality. In our plant, process engineers review daily run logs, flagging even minor anomalies for post-batch evaluation. Internal cross-checks between analytical staff and synthesis teams mean every lot gets real scrutiny. As scale increases, even minor process errors multiply quickly; factory-floor insights stop these problems before they reach the customer. In responding directly to technical issues, our decades of direct experience provide solutions that aren’t available through a simple specification sheet.

    Closing the Loop: Direct Feedback Makes the Difference

    Having a direct connection to 2,4-Dibromothiazole end users shapes the product’s evolution. Chemists want predictability and ease of use. Our team listens when someone uncovers a new use or improvement, and we have acted more than once to alter packaging to better fit a customer’s workflow, or upgrade quality documentation in response to regulatory changes. This isn’t something resellers can match, because we live with the material from molecule to shipment. Our work doesn’t finish at the warehouse loading dock—it follows each order out to the bench, scale-up reactor, or pilot plant.

    Partnering for Progress

    From direct synthesis to bottling, our role centers on dependability—delivering 2,4-Dibromothiazole that matches what your project requires, batch after batch. Every metric we publish stands on direct measurement and hands-on know-how. Not all manufacturers approach it this way, but for us, reputation and trust build over time, on the factory floor as much as in the laboratory.