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HS Code |
704735 |
| Product Name | 5-bromo-6-chloropyridine-3-sulfonyl chloride |
| Cas Number | 141442-53-5 |
| Molecular Formula | C5H2BrClNO2S |
| Molecular Weight | 270.50 g/mol |
| Appearance | white to off-white solid |
| Purity | ≥ 98% |
| Solubility | Slightly soluble in common organic solvents |
| Storage Temperature | 2-8°C |
| Synonyms | 5-Bromo-6-chloropyridine-3-sulfonyl chloride |
| Smiles | C1=C(C(=NC=C1Br)S(=O)(=O)Cl)Cl |
| Inchi | InChI=1S/C5H2BrClNO2S/c6-3-1-4(7)8-2-5(3)12(9,10)11 |
| Hazard Class | Corrosive |
As an accredited 5-bromo-6-chloropyridine-3-sulfonyl chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a red cap, labeled “5-bromo-6-chloropyridine-3-sulfonyl chloride,” stored under nitrogen. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 5-bromo-6-chloropyridine-3-sulfonyl chloride ensures secure packing, moisture protection, and compliance with hazardous materials transport regulations. |
| Shipping | 5-Bromo-6-chloropyridine-3-sulfonyl chloride is shipped in tightly sealed, chemical-resistant containers under dry, cool conditions. It is classified as a hazardous material, requiring proper labeling and documentation. Transport complies with relevant regulations (such as DOT, IATA, or IMDG) to ensure safe handling and prevent moisture or accidental release during transit. |
| Storage | 5-Bromo-6-chloropyridine-3-sulfonyl chloride should be stored in a cool, dry, and well-ventilated area, away from moisture, heat sources, and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and protected from light. Store under an inert atmosphere if possible. Handle with appropriate personal protective equipment due to its reactive and corrosive nature. |
| Shelf Life | 5-bromo-6-chloropyridine-3-sulfonyl chloride is stable for 1–2 years when stored in a cool, dry place under inert atmosphere. |
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Purity 98%: 5-bromo-6-chloropyridine-3-sulfonyl chloride with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side reactions and enhanced yield. Melting point 102°C: 5-bromo-6-chloropyridine-3-sulfonyl chloride with a melting point of 102°C is used in heterocyclic compound manufacturing, where precise thermal properties enable controlled process conditions. Molecular weight 304.54 g/mol: 5-bromo-6-chloropyridine-3-sulfonyl chloride with a molecular weight of 304.54 g/mol is used in academic research, where accurate stoichiometric calculations facilitate reproducible experimental results. Stability temperature up to 45°C: 5-bromo-6-chloropyridine-3-sulfonyl chloride stable up to 45°C is used in agrochemical development, where temperature stability maintains compound integrity during formulation. Particle size <50 microns: 5-bromo-6-chloropyridine-3-sulfonyl chloride with particle size less than 50 microns is used in organic synthesis, where fine particle size allows for improved reactivity and homogeneous mixing. Moisture content ≤0.5%: 5-bromo-6-chloropyridine-3-sulfonyl chloride with moisture content below 0.5% is used in sulfonylation reactions, where low moisture prevents hydrolysis and preserves reagent efficacy. |
Competitive 5-bromo-6-chloropyridine-3-sulfonyl chloride prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch of 5-bromo-6-chloropyridine-3-sulfonyl chloride rolling off the reactor carries the signatures of precision and consistency our team stands for. This molecule stands out as a valuable building block across research, scale-up, and commercial production phases in pharmaceutical and agrochemical applications. Some intermediates stay obscure in labs; this one shows up on the frontlines where selectivity, reactivity, and chemical reliability matter most.
We put a constant focus on purity, typically achieving levels above 98% as determined by HPLC. Our process control team has invested years tuning reaction times, solvent exchange parameters, and handling methods to minimize impurities like sulfonic acid by-products. Moisture control is critical with sulfonyl chlorides, so our packaging line always dries, purges, and seals under nitrogen. We monitor chloro and bromo distribution since halogen scrambling can impact downstream chemistry—each lot comes with a full chromatogram for traceability. Particle size falls within a tight range, avoiding dust issues in handling while keeping flow smooth for automated charge systems. Typical batches show pale yellow to tan crystalline solid, free from caked clumps or foreign matter. Experience shows that users tackling direct sulfonamide coupling or Suzuki-Miyaura cross-coupling want this consistency; it shortens reaction troubleshooting and keeps yields predictable.
In the synthetic world, sulfonyl chlorides offer a marriage of selective reactivity and functional group versatility. 5-bromo-6-chloropyridine-3-sulfonyl chloride, with its bromine and chlorine pattern, unlocks routes into next-generation heterocyclic scaffolds. Medicinal chemists see this as a proven tag for both early-stage activity screens and scale-up stages in active molecules. Sulfonyl chlorides react decisively—no long waiting or complex activation—so lab teams often pick them for time-sensitive projects. Polymer chemists and agrochemical researchers value the stability our material exhibits in storage and transport. This halogenated scaffold makes it a core intermediate for compounds requiring targeted substitution in the 3-position of the pyridine ring, a region notoriously tricky to functionalize.
Not every sulfonyl chloride outperforms in complexity. 5-bromo-6-chloropyridine-3-sulfonyl chloride holds several observed advantages. Its dual halogenation (bromo and chloro) gives a platform for orthogonal functionalization. Standard benzenesulfonyl chloride lacks this versatility in follow-on chemistry; our product opens windows for C–N, C–O, and C–C bond-forming reactions. By choosing this as the core, chemists skip some of the protection/deprotection hurdles and tap into multiple downstream transformations. In trial runs, we’ve observed improved selectivity and lower side-product formation in sulfonamide couplings, due to the electronic effects of the pyridine ring. Unlike unsubstituted analogs or simple mono-halogenated pyridines, the dual halogen handle here helps medicinal chemistry teams rapidly build SAR libraries with differentiated metabolic profiles. Agrochemical teams have noticed the increased weather resistance and bioavailability when their leads use this core versus tolunesulfonyl or phenylsulfonyl counterparts.
Day in and out, our operators emphasize controlled temperature ramps during chlorosulfonation—small deviations bring out color bodies that complicate analytics. Over the years, iterative improvements like slow addition regimes and jacketed reactors have reduced local overheating, which can cause breakdown of the pyridine ring. We staff our line with chemists who understand mechanistic risk, not just equipment operation. They analyze not just the endpoint but the subtle pH changes signaling impending exotherms or impurity formation. Our drying and packaging area handles only fresh product to prevent trace hydrolysis—moisture is a constant risk, and trained hands keep every flange sealed. Logistics learned the hard way that even high-clarity glass can be a weak link, so we only use containers proven to resist sulfonyl chloride attack, lined with inert barriers. Every improvement stems from an on-the-ground incident or persistent observation, not textbook proposals. These practices lead to repeatable product every time, batch after batch.
Sulfonyl chloride chemistry does not forgive shortcuts. Over time we’ve built a safety culture that treats runaway reactions and fuming emissions as ever-present realities. Our maintenance teams verify every scrubber and vent, and we run regular containment drills. Simple steps like double-gloving to prevent skin contact, using extended hoods, and training on instant exposure response keep our numbers strong. Clients benefit too, since a safer, cleaner manufacturing plant leads to lower risk of contamination and more reliable supply. Every outgoing drum travels with transport protocols learned through years of handling these reactive agents.
Most requests for 5-bromo-6-chloropyridine-3-sulfonyl chloride come from researchers pushing new frontiers in medicinal and crop science. In small volumes, it enables rapid parallel synthesis of sulfonamide analogues across hundreds of candidates. Biotech firms regularly scale these leads to pilot batches, and our lot-to-lot reproducibility removes many headaches in crop protection programs where a single failed batch can set a program back weeks. Specialty polymer firms use this intermediate to introduce electron-withdrawing moieties in films and coatings to boost endurance in harsh environments. For methylation and amination reactions needing a sensitive leaving group on a halopyridine, few alternatives offer this balance of reactivity and stability. We see regulatory teams prefer our product since our quality control regime offers full access to batch records, impurity maps, and traceability from raw material to final packout. Partnerships with scale-up chemists have led to modified particle size ranges for pilot plants using charge-by-funnel feeding.
Years ago, we saw bottlenecks for customers scaling from gram-level runs to hundreds of kilos. Voltages, dusting during transfer, and even static buildup created risks that smaller traders and lab suppliers struggled to anticipate. Our process line now accommodates seamless handoff from small-scale synthesis to commercial campaign, with dedicated vessels sized for each stage. Teams carrying projects through each development step find that uniform impurity profiles save time chasing away-of-spec material or performing laborious extra workups. Commercial users gain peace of mind knowing we audit every round of raw material, keep records going back years, and maintain separate lines for halogenated versus non-halogenated streams. Minimal cross-contamination, transparency in documentation, and continuous analyst training have become core parts of our practice, not afterthoughts.
From a synthetic standpoint, the unique halogen arrangement unlocks direct access to wider analog ranges. The electronic push and pull from both bromine and chlorine positions tunes reactivity; this matters when forming new C–N or C–S linkages. Chemists building SAR libraries or filling patent gaps turn to our 5-bromo-6-chloropyridine-3-sulfonyl chloride because it shortens synthetic routes compared to assembling the core through sequential halogenation and sulfonylation. That’s fewer purification steps, less solvent waste, more throughput. The molecule’s polar nature supports solubility in a range of solvents needed for library synthesis, from DMF to CH2Cl2. Teams at new-venture pharma companies have cleared time-to-lead hurdles by jumping straight to scaffold elaboration instead of commissioning custom syntheses for every fragment. The difference is speed, reliability, and access to chemical space unreachable through ordinary sulfonyl chlorides.
We constantly review and refine our synthesis and workup protocols. Not a month passes where a line worker or chemist doesn’t suggest a process tweak—sometimes to save a step, sometimes to tighten a control point, always to serve our partners’ end use. Years back, our lab determined that pushing the post-chlorination drying phase a little longer preserved color and improved downstream crystallization. Even small details like switching filter paper brands, or reconstructing the flow of drum handling, have come from the floor, not management whiteboards. Transparency with clients matters; regular updates and batch histories have become as expected as the product specs. Monitoring global regulatory trends, we’ve shifted supply chains away from high-risk origins for starting materials, and our documentation supports client audits any time, whether they're a Fortune 500 firm or a new university spin-out.
Rare is the plant run that doesn’t throw up surprises. Once, a customer reported slight off-color material even though assays showed purity met spec. The color shift traced back to a change in a minor raw component. Our team collaborated with their chemists, retraced records, and pinpointed the culprit within days. The replacement adjusted not only product appearance, but also improved reaction time for their downstream process. Another example: An international shipment triggered a customs hold because third-party documentation missed a CITES declaration—a paperwork tangle, not a technical fault. Lessons like these get baked into future runs, making operators, shippers, and quality teams sharper each round. Every closed feedback loop builds real-world experience, not just credentialed compliance.
Innovators keep pushing demands higher. Today’s users want purer material, tighter batch consistency, and transparent environmental footprint reporting. Our chemists consult with process users to understand which impurity thresholds matter for bioactivity; after all, not every minor byproduct interferes with function. Environmental compliance drives us to invest in improved waste neutralization for spent chlorosulfonic acid and byproduct halides. Regulators ask for more thorough reporting on site inspections and emission controls; our team builds environmental statements into every material transfer record. Our relationship with environmental managers, waste processors, and clean-up vendors is decades old, giving our clients the confidence that every purchase supports sound stewardship.
Not every issue needs a lab redesign to solve. Sometimes, fixing caking or dust emissions means adjusting indoor humidity or finding stricter maintenance cycles for seals. Introducing barcode tracking for each drum now keeps real-time location records, solving headaches for both trace recall and inventory aging. Training up new staff starts in the lab, where every operator tries pilot scale charge-outs under observation before working live runs. By making near-miss sharing routine, every hand on deck knows they can halt a run the moment odd readings pop up. Real solutions grow from close observation, honest feedback, and staying on the same page as the client’s bench team. Whether a batch needs custom micronization, changed lot sizes for new API projects, or local GMP-grade requirements, our plant relishes the challenge.
Our journey with 5-bromo-6-chloropyridine-3-sulfonyl chloride has always been about more than just meeting specification sheets. Chemists in discovery, scale-up, or commercial production expect reliability, transparency, and shared knowledge from every supplier relationship. For each project, whether it’s a one-off order or a regular supply for blockbuster R&D, we bring the sum of lessons shaped by actual production runs and real-world complications. The unmatched versatility of this molecular scaffold gives clients the confidence to take creative risks in their R&D, knowing product quality isn’t an open question. In every shipment, we send not just a drum or bottle but years of experience finding and refining solutions. That’s how meaningful value builds, from our process floor to your next synthesis.