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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 | 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. |
Applications of 2,4-Dibromothiazole in Industrial Manufacturing2,4-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 IntermediatesLeading 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
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2. Pharmaceutical API Synthesis: Thiazole-Based Drug IntermediatePharmaceutical 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
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3. Specialty Electronic Materials: OLED and Semiconductor PrecursorsManufacturers 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
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4. Modified Engineering Polymers: Specialty Plastics and Copolymer AdditivesProducers 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.