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HS Code |
332319 |
| Product Name | 3,4-Dibromosulfolane |
| Cas Number | 105097-73-6 |
| Molecular Formula | C4H6Br2O2S |
| Molecular Weight | 277.96 g/mol |
| Appearance | Colorless to yellow liquid |
| Chemical Structure | Sulfolane ring with bromines at positions 3 and 4 |
| Purity | Typically ≥ 95% (may vary by supplier) |
| Smiles | C1C(S(=O)(=O)CC1)(Br)Br |
As an accredited 3,4-Dibromosulfolane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle labeled "3,4-Dibromosulfolane," features hazard warnings, CAS number, and secure red screw cap for safety. |
| Shipping | 3,4-Dibromosulfolane is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified as a hazardous chemical, requiring proper labeling and documentation during transit. Shipping is conducted in compliance with relevant regulations to ensure safe handling and delivery, typically at ambient temperature unless otherwise specified. |
| Storage | **3,4-Dibromosulfolane** should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and appropriately labeled. Store away from incompatible substances such as strong oxidizers and bases. Use proper chemical storage cabinets, and ensure secondary containment to prevent spills or leaks. Handle under inert atmosphere if required. |
Applications of 3,4-Dibromosulfolane in Industrial ManufacturingAs a dedicated manufacturer of 3,4-Dibromosulfolane, we supply this specialized intermediate to a select range of downstream industries that rely on its unique brominated and sulfolane structure. Focusing exclusively on valid market applications, the following scenarios reflect actual commercial demand, detailing compliance frameworks, recommended formulation ratios, operational integration stages, and targeted finished goods derived from this material. 1. Pharmaceutical Intermediate Synthesis for CNS Drug DevelopmentPharmaceutical companies utilize 3,4-Dibromosulfolane in the synthesis of complex heterocyclic intermediates, particularly for central nervous system (CNS) active compounds. Its dual bromine positions enable selective cross-coupling during the late-stage assembly of bioactive scaffolds, fitting strict impurity and regulatory controls required for human therapeutic pipelines. Industry compliance standards
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2. Agrochemical Synthesis for Targeted Fungicide ActivesManufacturers in the crop protection sector incorporate 3,4-Dibromosulfolane as a core intermediate in the synthesis of fungicidal compounds tailored for high-frequency resistance management programs. The dual bromine functionality enhances molecular diversity in generating new sulfolane-based actives for seed treatment and foliar protection chemicals. Industry compliance standards
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3. Electronic Chemical Manufacturing for Photoresist Monomer ProductionAdvanced electronics and semiconductor material makers use 3,4-Dibromosulfolane to synthesize highly purified monomers for photoresist polymers. Its strict chemical traceability and low metal content are essential for sub-micron patterning, where halogen presence enhances the lithographic sensitivity and line edge definition in integrated circuitry fabrication. Industry compliance standards
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4. Specialty Polymer Additive for High-Temperature Performance PlasticsProducers of engineering plastics select 3,4-Dibromosulfolane as a reactive flame-retardant modifier. Its presence in copolymer formulations imparts thermal stability and halogen-mediated char formation during combustion, crucial for aerospace and automotive polymer component performance under demanding thermal loads. Industry compliance standards
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5. Fine Chemicals Sector: Sulfur-Containing Ligand Production for CatalystsChemical manufacturers targeting homogeneous catalysis applications employ 3,4-Dibromosulfolane as a precursor in preparing sulfur- and halogen-functionalized ligands. It provides precise molecular architecture required for transition metal complexation used in next-generation catalytic process design, supporting an expanding portfolio of sustainable, high-activity catalyst platforms. Industry compliance standards
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Over decades of hands-on synthesis and bench experience, our team has seen 3,4-Dibromosulfolane stand out as a robust, versatile intermediate. It always draws interest from chemists who value fine-tuned control over syntheses that hinge on selective bromination. Unlike many brominated compounds, 3,4-Dibromosulfolane carries unique structural characteristics owed to the sulfolane core—something we've grown to appreciate as both a challenge and an advantage in our facility.
This molecule, identified by its two bromine atoms attached to the 3 and 4 positions of the sulfolane ring, doesn’t just mimic the behavior of bulkier, multi-substituted sulfolanes or more common brominated solvents. From our continuous process refinement, we notice that the strong electron-withdrawing nature of the sulfonyl group combined with selective bromination impacts both reactivity and downstream compatibility. 3,4-Dibromosulfolane keeps its integrity in reactions that degrade similar halogenated compounds, a trait our R&D chemists continue to validate in both academic and industrial collaborations.
Extensive feedback from users tells us this sulfolane derivative performs dependably in specialized alkylation, substitution, and cross-coupling chemistries. We work closely with pharmaceutical and agrochemical researchers who require high-purity, low-moisture intermediates for scale-up, and this product consistently meets tight analytical standards. Its particular reactivity profile often enables clean reactions where mono-brominated analogues or non-cyclic brominated compounds show lower selectivity or excessive byproduct formation.
Rather than acting like simple halogen carriers, the two bromine atoms synergize for regioselective transformations, opening routes not readily accessed through traditional sulfolane derivatives. Our lab techs, always attentive to customer trials, observe frequent reports of higher yields and smoother purifications—especially on pilot plant scales—compared to alternatives like 2-bromosulfolane or chlorinated sulfolanes. This means fewer column runs and less time struggling with stubborn residues.
Consistent product quality comes directly from refined synthesis protocols. Over many production campaigns, we focus on limiting side-products through strict temperature and pressure controls. By monitoring batch kinetics (not just at endpoints but also through in-process analytics), we’ve reduced the occurrence of co-brominated or over-brominated impurities. Our in-house team prefers to use freshly distilled starting materials and high-purity bromine sources, based on a long history of improved run-to-run reproducibility.
Each lot ships after GC-MS certification confirms tight cut-off points for purity and target isomer distributions. For end-users worried about trace sulfurous compounds or minor ring-opened contaminants, our process improvements made since 2019 have substantially curbed those risks. This real-world effort resonates most for customers in regulated industries, who cannot accept variation or surprise impurities in kilo-scale syntheses.
From years of plant-floor management, we recognize materials like 3,4-Dibromosulfolane require respect for reactivity and stability. Our formulation team always stores this material under inert atmospheres to avoid moisture-induced decomposition and minimize the risk of slow hydrolysis. In the hands of careful process chemists, the sulfolane core provides a stable platform that doesn’t emit excessive vapors, and the careful packaging preserves the compound’s shelf life well beyond basic industry guidelines.
We share handling insights both in procurement discussions and on the technical support line, since minor lapses in storage conditions at the user’s site still sometimes result in quality claims. Experience tells us that with correct transfer protocols, users avoid sticky byproducts that plague less stable brominated intermediates. Feedback from facilities conducting multi-step syntheses has led to packaging improvements, like double-sealed liners and heavier canisters, which directly reflect common-sense changes adopted to solve real pain points.
In the pharmaceutical sector, we see most requests for this derivative centered on heterocycle construction and selective bromination challenges—especially where avoidance of chlorine or fluorine contamination matters. For crop protection chemistry, scale-up teams repeatedly choose this product for the manufacture of sulfonyl analogues that can’t tolerate more aggressive halogenation conditions. Process engineers report that its solubility profile suits their continuous-flow reactors, an edge over heavier, less polar dibromides.
We’ve worked directly with teams designing routes to sulfones or sulfonamides that benefit from the specific leaving group character of the bromine atoms. Unlike regular dibromides, our compound’s sulfone ring allows for stepwise substitution under basic or transition-metal catalyzed conditions, often displaying less side product formation than linear alternatives or non-brominated sulfolanes. As a manufacturer, these outcomes are especially gratifying, reinforcing our focus on real, laboratory-driven needs rather than theoretical sales promises.
Regular customer questions force us to drill down on why this product outshines close relatives. We’ve compared 3,4-Dibromosulfolane directly with 2,3- or 2,5-dibromo analogues, and each time, physical and reactive behavior diverges sharply. During large-batch synthesis of both, our operators confirm dramatically different viscosity and melting point ranges. In processing, the 3,4-isomer flows better through filtration systems and doesn’t tend to crystallize in transfer lines, which cuts downtime and reduces cleanout costs.
Technical support requests often highlight cases where mono-bromosulfolanes struggled with stability during prolonged high-temperature reactions. Double substitution at 3 and 4 positions offers consistently higher thermal resilience, a feature acknowledged by our customers running high-throughput continuous processing. We routinely hear from analytical chemists that our compound provides sharper NMR, HPLC, and GC signals than those of closely related materials, which supports both QA and regulatory submissions.
As manufacturers, we pay close attention to process safety, material use, and waste minimization. Unlike many halogenated intermediates, our optimized process reduces hazardous waste streams. Real-time process monitoring, cycle efficiency, and close cooperation with local environmental authorities have proven more effective than simply relying on off-the-shelf control technologies. These improvements lower overall production risk and improve our carbon balance, benefits we pass on to customers interested in greener supply chains.
By applying solvent recovery systems and carefully selecting compatible cleaning agents, we can minimize residual bromine and byproducts in our effluent. Our decision to avoid certain antiquated synthesis routes ensures greater safety and compliance from both a worker and environmental health standpoint. These steps stem from the practical difficulties we encountered with less-controlled processes in the past, and the resulting improvement in lot uniformity means less rework and fewer delays for end users.
Our site has faced the same occasional hurdles as any specialty chemical producer: occasional byproduct surges, equipment fouling, and scalability limits. Time after time, systematic troubleshooting—guided by years of collective operator experience—has revealed causes ranging from subtle temperature gradients to overlooked impurities in feedstock. We prefer to solve these issues internally through measured, data-backed adjustments instead of disruptive overhauls.
A notable breakthrough involved the installation of automated in-line purification units, which sharply reduced our historically high caustic waste costs. Team input during batch scale-up led to a redesign of our crystallization train, allowing us to isolate 3,4-Dibromosulfolane with less solvent usage and tighter melting point distribution. Site technicians with decades of hands-on runtime brought forward key ideas during these improvements, showing real value in skilled human oversight.
Given the potential hazards of all brominated compounds, our internal protocols for handling, transfer, and packaging exceed customary industry benchmarks. Training lab staff on spill containment and first-response actions is routine, a practice borne out by early experiences with more hazardous related materials. We also conduct mock drills at our facility for high-volume transfer scenarios, lessons from which prompted enhancements like improved secondary containment and vapor absorption filters.
Documentation always travels with the shipment, but we find that support after delivery remains vital. Customers benefit from direct phone access to our technical staff, who collectively handle dozens of questions about preparation and reaction compatibility every year. Rather than delegating such contacts to generic sales agents, our policy ensures customers reach chemists who understand the compound, its quirks, and how to improve yield or avoid unwanted reactivity.
Market and research trends hint at growing demand for specialty intermediates that enable step-economical synthesis. Projects aimed at building next-generation APIs or specialty polymers seem to seek out molecules like 3,4-Dibromosulfolane for their reactive and selectivity advantages. We watch inquiries from custom manufacturing and contract development firms—who rely on nimble, high-purity supply lines—grow annually. These groups seek to streamline synthetic routes and reduce their inventory exposure to more hazardous reagents.
Product innovation drives us, but customer collaboration shapes our direction most of all. Recent stories from major process chemistry teams focused on minimizing hazardous waste and simplifying purification have guided our R&D priorities. By choosing scalable reaction technologies and piloting improved containment systems, we’re staking out a position where process integrity matches new application areas—without sacrificing safety or product certainty.
Over the years, we’ve resisted the call to license out production or hand off packaging to third-party operators. Our belief: Full accountability for production and QA provides the greatest assurance for everyone downstream. Trading houses and brokers can offer paperwork, but they cannot replicate the persistent technical dialogue and hands-on troubleshooting we deliver. Issues flagged by end-users during scale-ups quickly inform process adjustments—feedback that never reaches us through indirect supply chains.
Only through years at the reactor or distillation unit—tuning cycle efficiency, refining quench timings, or developing specific impurity profiles—do manufacturers earn the trust of demanding process chemists. This material, simple in appearance but complex in behavior, has proven itself repeatedly across reactions that punish generic brominated intermediates. Satisfactory outcomes rely on subtle process details, not marketing gloss or abstract promises.
Our strength lies in tailored process control and the lasting relationships built with chemists who depend on honest problem-solving. We answer questions far beyond those in a catalog: reaction troubleshooting, comparative data, and efficient scaling advice. As chemists ourselves, it matters deeply that our material meets both present and evolving standards for purity and performance. Years of real-world production ensure every lot of 3,4-Dibromosulfolane leaves our plant consistent, reliable, and ready for the advanced chemistry your research or manufacturing work demands.