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HS Code |
726990 |
| Productname | 6-Bromo-2-Chlorobenzothiazole |
| Casnumber | 356783-11-2 |
| Molecularformula | C7H3BrClNS |
| Molecularweight | 248.53 g/mol |
| Appearance | Off-white to light yellow solid |
| Solubility | Slightly soluble in organic solvents |
| Purity | Typically ≥98% |
| Storageconditions | Store at room temperature, in a tightly closed container |
| Hazardclass | Irritant |
| Synonyms | 6-Bromo-2-chloro-1,3-benzothiazole |
| Smiles | Clc1nc2ccc(Br)cc2s1 |
| Inchikey | UNWJVOQQNXQXJV-UHFFFAOYSA-N |
As an accredited 6-Bromo-2-Chlorobenzothiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 6-Bromo-2-Chlorobenzothiazole is supplied in a sealed amber glass bottle with a tamper-evident screw cap and label. |
| Shipping | 6-Bromo-2-Chlorobenzothiazole is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. The package is clearly labeled with hazard information and handled according to standard safety protocols for transport of hazardous chemicals. Shipping complies with relevant regulations to ensure safe and secure delivery to the destination. |
| Storage | 6-Bromo-2-Chlorobenzothiazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it away from incompatible substances such as strong oxidizers. Store at room temperature and handle using appropriate personal protective equipment to prevent inhalation, ingestion, or skin contact. Label the container clearly and follow all relevant safety guidelines. |
Applications of 6-Bromo-2-Chlorobenzothiazole in Industrial Manufacturing6-Bromo-2-Chlorobenzothiazole serves as a specialized intermediate in distinct chemical synthesis routes. As a manufacturer, we supply this compound exclusively for established industrial applications in downstream technical sectors that require precise compliance, formulation accuracy, and controlled integration. Each of the applications below details how our customers use this material within well-defined industry boundaries according to practical manufacturing operations. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisThis compound enables the construction of complex benzothiazolyl-based scaffolds during the synthesis of select APIs, where its halogenated core facilitates regioselective substitution in stepwise organic transformations. End users require this intermediate to meet stringent regulatory requirements before proceeding to advanced reaction sequences in the pharmaceutical pipeline. Industry compliance standards
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2. Agrochemical Intermediate for Fungicide ProductionAgricultural formulators utilize this compound as a core building block in the manufacturing of advanced fungicides that require selective synthesis of benzothiazole-based active agents. Its role is essential in the production chains where halogenated heterocycles enhance the biological targeting profile of the final agrochemical product. Industry compliance standards
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3. Dye and Pigment Intermediate for Technical ColorantsProducers of specialty dyes integrate this compound to construct halogen-substituted benzothiazole moieties, imparting resistance to photobleaching and improving chromatic intensity in high-performance technical dyes. Its role lies in the precise sequencing required to achieve tailored molecular properties for demanding industrial coloration processes. Industry compliance standards
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4. Intermediate for Specialty Material Additives in Polymer ModificationManufacturers of polymer additives employ this compound to introduce halogenated thiazole functionalities into advanced stabilizer and flame-retardant additive families, enhancing polymer matrix resistance to degradation or combustion. The downstream pathway leverages the high reactivity of the aromatic system for further derivatization, with attention to compliance in technical-grade plastic processing. Industry compliance standards
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In our experience, few aromatic building blocks support such a broad spectrum of next-stage syntheses as 6-Bromo-2-Chlorobenzothiazole. Our process engineers spend years refining halogenated benzothiazoles, and one thing stands out: every detail—from storage humidity to batch temperature control—impacts not only yield, but downstream applications. With over a decade handling this compound, we have learned that consistency in purity translates to fewer surprises in large-scale pharma and agrochemical R&D labs.
This molecule sees regular demand across custom and standard synthesis applications. Halogenated benzothiazoles never leave much margin for error, but the 6-bromo, 2-chloro combination proves especially sensitive to trace impurities. Our approach, built on repeat reactions and careful solvent management, produces material that analysts regularly verify by HPLC, GC, and NMR. Even tiny differences in the ratio of ortho and para substitutions change how it performs in your lab.
We manufacture 6-Bromo-2-Chlorobenzothiazole under the code BCBT-360, produced in continuous glass-lined reactors. We understand that researchers and process chemists ask much more than “What is the assay?”; they want to rely on material that won’t introduce unneeded variables to their synthesis. By investing in finely tuned separation processes, we regularly reach purity above 98%. When we scale up, we track every new charge for stability and reactivity, since one overlooked step introduces byproducts that can slow a pilot project by weeks.
This lot-to-lot stability means less time spent on troubleshooting chromatography instead of running the actual transformation. Shipping always follows UN transport standards for hazardous organics, but the real headache comes in preventing inadvertent hydrolysis before product reaches our customers’ benches. So each drum and flask receives triple-layer protection before leaving the clean room floor. Our logistics lead won’t sign off on dispatch until moisture content falls below threshold.
A consistent supply of 6-Bromo-2-Chlorobenzothiazole helps research chemists develop innovative pharmaceuticals, crop protection agents, and specialty materials. What makes it so valuable? The unique substitution pattern—especially the ortho-bromo, ortho-chloro configuration on the benzothiazole ring system—gives chemists precise handles to push halogen-exchange, nucleophilic aromatic substitution, or even organometallic coupling. We repeatedly see requests from labs tracing new kinase inhibitors and antifungal scaffolds, or from materials groups building photoactive heterocycles.
Traditional bromo- or chloro-benzothiazoles often lead to side products in certain Buchwald-Hartwig or Suzuki-Miyaura varieties. The dual halogen pattern introduces more selectivity, letting researchers checkpoint each intermediate before converging on the final target. We work with clients who run trial reactions for electron-rich cross-couplings, taking small-scale feedback and translating it to industrial volume synthesis. This dialogue shapes our quality standards—yield and isolation must reflect actual bench outcomes, not just lab data sheets.
As hands-on manufacturers, we have direct comparison data between single-halogenated benzothiazoles and the dual-substituted 6-Bromo-2-Chlorobenzothiazole. Monohalogenated analogues, such as 6-bromobenzothiazole or 2-chlorobenzothiazole, often don’t achieve the same regioselectivity in many cross-coupling or functionalization steps. The extra halogen substitution increases electron-withdrawing character on the heterocycle, and this translates to more controlled activation and reactivity profiles—particularly under microwave or palladium-catalyzed conditions.
In pilot runs, single-halogen intermediates sometimes produce unexpected byproducts during attempted site-selective transformations. Adding the second halogen fine-tunes the molecular electronics—a difference our chemists have seen reflected in higher yields and cleaner conversions, especially for complex-flow processes. In custom synthesis projects, clients have reported easier purification of desired intermediates versus routes that start with solely bromo or chloro analogues. Our technical team routinely consults on route design, advising partners when the extra step of preparing 6-Bromo-2-Chlorobenzothiazole improves process efficiency farther downstream.
Years in the plant have taught us that handling halogenated benzothiazoles can trip up even experienced teams. Laboratory staff see the powder or crystalline solid, but few consider the fines that can escape during uncontrolled transfers. We package each batch under dry, nitrogen-purged conditions. We learned early on that even a few percent moisture content can degrade product quality over days—not months. That lesson came from a customer who flagged crystalline breakdown after extended bench storage. Now every consignment comes with a detailed certificate showing Karl Fischer titration for water content.
Storage guidance comes direct from lab experience. Our technicians always keep the unopened supply below 25°C, and every lot spends minimal time under lights to slow photodecomposition. During scale-up, we demonstrated that typical desiccants fail to control humidity spikes in Asia's rainy season; so we switched to molecular sieves for every shipment exported to tropical climates. Instead of relying on off-the-shelf containers, our packaging team works directly with our suppliers to implement triple-seal liners and custom desiccant packs.
Working with benzothiazole derivatives poses challenges that other aromatic intermediates do not. Achieving high selectivity in halogenation steps takes rigorous control over reaction kinetics and scrupulous batch monitoring. In our plant, the use of halogen carriers and their ratio against the benzothiazole base structure has been tweaked across many campaigns. Overbromination or incomplete chlorination used to sabotage yield until our team shifted to segmented reagent addition, monitored by real-time FTIR and GC-MS sampling.
Waste management deserves as much attention as the reaction itself. Brominated and chlorinated waste streams require neutralization before any further processing; this is managed onsite by our dedicated environmental unit. Local regulators regularly inspect our plant to audit effluent handling. Routine internal training and scheduled environmental audits keep our team aware that putting the product into the market means carrying responsibility for our footprint long after shipping.
Any synthetic chemist running a modified Sandmeyer or electrophilic aromatic substitution knows purity control does not stop at 99%. Even parts-per-million levels of side products can alter catalytic behavior in asymmetric reactions. So every kilogram undergoes a no-shortcuts QC regime, including trace metals analysis—especially for projects in medicinal chemistry, where residual copper or palladium end up flagged during scale-up validation.
Feedback cycles with our clients matter as much as our own plant-based troubleshooting. Research groups often need a quick trial run or custom variant with altered halide ratios. Instead of sticking with fixed process windows, our experienced synthesis team frequently supports early-stage development by adjusting parameters, sometimes as early as kilogram stage. This sort of flexibility keeps our QC chemists directly involved in scale transfer, bridging the gap between bench and bulk.
We’ve also found that certain clients require unique regulatory documentation, especially in the pharmaceutical industry where development timeline can hinge on trace impurity profile. Our regulatory affairs scientists keep detailed records of every batch, supporting compliance documentation with complete traceability of all reagents, suppliers, and waste streams involved in production. This attention to documentation allows customers—especially those pursuing active pharmaceutical ingredient registration—to move forward knowing each intermediate meets project-specific needs.
We have participated in several consortia to share best practices on halogenated aromatic synthesis, learning from international developers about new clean-up protocols and taking part in raw material quality monitoring groups. Each lesson learned—from cleaning glassware following bromo-chloro cycling, to managing continuous supply chain constraints—informs how we design our operations for reliability under tight schedule pressure.
We see how the demand for 6-Bromo-2-Chlorobenzothiazole comes from a wide range of sectors. Industrial applications focus on the need for highly pure intermediates that don’t throw off catalyst performance and reduce product loss. Pharma clients tell us advances rely on benzothiazole fragments that handle further transformation—alkylation, arylation, or nucleophilic attack—without their intermediates accumulating byproducts. Crop science companies rely on the consistency of halogenated building blocks to ensure actives perform under regulated field studies.
Collaboration doesn’t stop after shipping the product. Our team maintains regular dialogue with customer process leads. Sometimes, separating the final product from incompletely halogenated contaminants means revising purification protocols. We test new crystallization solvents and recrystallization conditions based on user feedback. The aim is always to deliver material that lets research programs move faster with fewer unscheduled stops.
Each campaign of 6-Bromo-2-Chlorobenzothiazole begins with verified starting materials, tested for heavy metal content, chiral purity (where applicable), and trace organics. We invest in in-house GC-MS and LC-MS facilities, supporting screening for potential genotoxic impurities. For every batch, full COA and SDS packages accompany shipments, including detailed chromatograms. Our QC team signs off only when all acceptance criteria match specifications confirmed by pilot customers. No shortcuts—if any parameter fails by even half a percent, the system locks the batch and triggers an internal review.
Plant safety shapes every stage. Facility personnel complete annual Hazard and Operability (HAZOP) training. All halogen-handling incidents receive management review and feed into SOP improvements. Employees receive refresher drills on spill control and personal protective equipment use. These procedures come from real-world learning; after a near-miss during batch filtration, our engineering department refitted all pressure filters with redundant seals. By embracing improvement culture, we maintain a reliable, safe supply of this specialized chemical.
Success in specialty chemical manufacturing ties directly to knowing not just how to make a product, but how that product behaves across industries and applications. R&D teams find that dual-halogenated benzothiazoles like 6-Bromo-2-Chlorobenzothiazole support flexibility in designing modular molecules—something less feasible with mono-substituted variants. Production teams value the way high-purity intermediates cut down on reprocessing. Regulatory groups seek suppliers willing to share analytical and validation data for seamless project advancement.
We continue to pay attention to advances in catalysis and reaction engineering, establishing pilot programs for next-generation functional groups and hybrid molecules building on the benzothiazole core. By watching market trends and actively listening to feedback, our manufacturing strategy remains grounded in user experience. It is not enough to deliver just a product; we build technical partnerships aimed at helping our clients push science and innovation. Our confidence in 6-Bromo-2-Chlorobenzothiazole grows—they tell us what works, and we keep improving every stage to make their work smoother, faster, and more predictable.