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Sodium 2-Bromoethanesulfonate

    • Product Name Sodium 2-Bromoethanesulfonate
    • Alias BES
    • Einecs 230-160-4
    • 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
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    Specifications

    HS Code

    383855

    Chemical Name Sodium 2-Bromoethanesulfonate
    Synonyms BES sodium salt
    Cas Number 4721-07-7
    Molecular Formula C2H4BrNaO3S
    Molecular Weight 211.01 g/mol
    Appearance White to off-white solid
    Solubility In Water Freely soluble
    Melting Point Decomposes above 250°C
    Storage Conditions Store at room temperature, keep container tightly closed
    Uses Biochemical research, methanogenesis inhibitor
    Ph Of 1 Percent Solution Approximately 7.0
    Structural Formula BrCH2CH2SO3Na

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

    Packing & Storage
    Packing Sodium 2-Bromoethanesulfonate is packaged in a sealed 100g amber glass bottle with a secure screw cap for moisture protection.
    Shipping Sodium 2-Bromoethanesulfonate should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport in accordance with local, national, and international regulations for hazardous chemicals. Ensure appropriate labeling and documentation, and use secondary containment if necessary to prevent leaks during transit. Avoid exposure to heat and direct sunlight.
    Storage Sodium 2-Bromoethanesulfonate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep it away from moisture and incompatible substances such as strong oxidizing agents. It should be stored at room temperature, protected from light and sources of ignition. Properly label the storage area to prevent accidental exposure or mishandling.
    Application of Sodium 2-Bromoethanesulfonate

    Purity 98%: Sodium 2-Bromoethanesulfonate with a purity of 98% is used in chemical synthesis reactions, where it ensures high reaction yield and product consistency.

    Molecular weight 189.03 g/mol: Sodium 2-Bromoethanesulfonate of molecular weight 189.03 g/mol is used in pharmaceutical research, where accurate dosing and predictable bioactivity are achieved.

    Melting point 285°C: Sodium 2-Bromoethanesulfonate with a melting point of 285°C is used in high-temperature organic transformations, where it provides thermal stability and maintains structural integrity.

    Particle size <50 µm: Sodium 2-Bromoethanesulfonate with particle size less than 50 µm is used in fine chemical formulations, where uniform dispersion and fast dissolution are necessary.

    Stability temperature up to 120°C: Sodium 2-Bromoethanesulfonate stable up to 120°C is used in heat-sensitive manufacturing processes, where it prevents degradation and preserves chemical activity.

    Solubility in water 20 g/L: Sodium 2-Bromoethanesulfonate with water solubility of 20 g/L is used in aqueous-phase bioconjugation, where efficient reactivity and easy handling are important.

    Assay >99% (HPLC): Sodium 2-Bromoethanesulfonate with an assay greater than 99% by HPLC is used in analytical standard preparations, where reliable quantification and traceability are required.

    Low chloride content <0.05%: Sodium 2-Bromoethanesulfonate with low chloride content below 0.05% is used in sensitive catalyst systems, where unwanted side reactions are minimized and product purity is enhanced.

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    Certification & Compliance
    More Introduction

    Sodium 2-Bromoethanesulfonate: A Closer Look at an Indispensable Chemical

    Introduction

    Over the years, researchers and chemists have come to rely on Sodium 2-Bromoethanesulfonate for its unique combination of features and practical value in the laboratory. The compound, sometimes written as BES-Na or sodium bromoethanesulfonate, finds its place among specialty reagents thanks to its distinct reactivity and solubility. If you’ve worked with chemicals that demand stable sulfonate groups in aqueous phase syntheses, you probably already appreciate the difference that Sodium 2-Bromoethanesulfonate can make compared to other bromoalkanes or sulfonate donors.

    Model and Specifications

    In the market, Sodium 2-Bromoethanesulfonate often appears as a white, crystalline powder. With a CAS number of 16273-15-3 and a molecular formula of C2H4BrNaO3S, the material holds a molar mass around 223.01 g/mol. If high purity counts in your process, analytical data typically indicate purity ranges of 98% and above, with trace-level moisture and halide impurities, which goes a long way in sensitive organic transformations. Its melting point, which often sits near 300°C (decomposes), sets it apart in thermal stability from some halide-containing salts. The compound dissolves well in water, so chemists rarely run into solubility headaches during aqueous workups or when prepping standard solutions.

    Key Uses in the Lab and Industry

    Sodium 2-Bromoethanesulfonate draws attention because it acts as a strong alkylating agent—mainly due to the stable bromo group linked to a sulfonate moiety. In many microbiology labs, it’s well-known as a potent methanogenesis inhibitor, where it blocks methane production in microbial cultures. This has been instrumental for research groups studying rumen fermentation or anaerobic digestion, opening up ways to investigate microbial pathways without methane dominating gas profiles. Some environmental scientists credit their breakthroughs in understanding methane cycles to routine applications of this specific compound.

    Outside the study of methane, organic chemists often turn to Sodium 2-Bromoethanesulfonate during nucleophilic substitution (SN2) reactions. Its reactivity ensures that the bromo function reacts swiftly, delivering the ethanesulfonate group to target molecules. Selecting this compound instead of, say, bromoethane or generic sulfonates, often cuts down side reactions. I remember a summer project involving custom sulfonation of heterocycles for pharmaceutical candidates—using Sodium 2-Bromoethanesulfonate, the reactions ran at lower temperatures and consistently gave sharper NMR spectra, compared to earlier runs with alternative alkylating agents.

    Biotechnologists have realized value here, too. During studies on enzyme inhibition, especially those enzymes involved in methyl-coenzyme M reductase pathways in archaea, Sodium 2-Bromoethanesulfonate delivers reliable and reproducible inhibition. Teams in agricultural engineering often deploy this reagent to study and manipulate methanogenic populations, testing feed strategies that limit greenhouse gas emissions from livestock. It has also started to show up in metabolic engineering, where scientists probe alternative biological pathways by disabling methane formation.

    Comparison with Similar Products

    If you are familiar with the family of bromoalkanes and sulfonates, you’ll notice several options on the market. For instance, bromoethane or methyl bromide typically serve as plain alkylating agents, but their reactivity creates safety issues and leaves behind persistent halide residues that complicate downstream processing. Sodium 2-Bromoethanesulfonate, in contrast, brings together a reactive bromo group with a sulfonate that acts more predictably—helpful both in gram-scale research and in larger pilot reactions. Testing a batch of BES-Na next to plain sodium ethanesulfonate rapidly reveals how much more useful the bromo derivative becomes in controlled substitution chemistry because of its dual reactivity and water solubility.

    Another frequent point of comparison comes from methane inhibitors like chlorinated analogs or organic sulfates. BES-Na usually takes precedence due to its specific targeting of methyl-coenzyme M reductase, which preserves other food web functions in microbial communities. Researchers focusing on environmental stewardship appreciate such selectivity. During a recent project aimed at characterizing microbial populations in wetland sediments, switching from generic halogenated inhibitors to Sodium 2-Bromoethanesulfonate improved not only gas reading accuracy but also simplified quantifying non-methanogenic metabolic activity.

    Application Challenges and Solutions

    Sourcing high-quality Sodium 2-Bromoethanesulfonate has stayed consistent as the main challenge. Purity directly affects both reactivity and reproducibility, especially for academic labs with tight funding. Some industry users raised concerns about the stability of long-stored lots, noticing color change or caking over time if storage conditions dipped below manufacturer recommendations. Avoiding humid environments protects product appearance and performance. For those who run long-term experiments or operate bioreactors, regular quality checks help circumvent problems seen with lower-grade alternatives.

    Microbiological users sometimes report incomplete inhibition in highly concentrated cultures. Upping the BES-Na concentration usually restores activity, but at the risk of introducing off-target chemical effects. In graduate research on wastewater digestion, titration experiments helped pin down optimal concentrations where methanogen inhibition hit maximum levels without suppressing acetate or hydrogen production from fermenters. Communication across teams—microbiology, chemistry, and engineering—usually yields better dosing strategies, rather than relying on generic dosing guides.

    Safety, Handling, and Practical Advice

    Anyone handling Sodium 2-Bromoethanesulfonate knows that chemical safety cannot take a backseat. The bromo group offers both desired reactivity and imposes certain handling precautions. Proper gloves, goggles, and fume hood access remain non-negotiable. Based on personal experience, fine dust can cause mild irritation, so working with the material in small increments keeps clean-up manageable. Disposal of unused or spent solutions follows standard halide and sulfonate waste protocols. In systems where trace halides impair sensitive reactions downstream, a good rinse and buffer cycle solve most routine contamination worries.

    Shipping BES-Na presents fewer regulatory headaches than some bromoalkanes, but bulk quantities still draw attention from compliance officers, especially in export scenarios. Teams working with international suppliers should stay current with local regulatory guidelines. Consultation with environmental safety officers streamlines both import and storage procedures for academic institutions and research centers.

    Insights from Routine Lab Use

    A pragmatic approach to Sodium 2-Bromoethanesulfonate always emphasizes attention to detail. The compound’s granularity, for instance, varies by manufacturer. Some lots offer finer crystals, which dissolve more rapidly during solution prep, saving time during scale-up. Laboratories with automated dispensing systems benefit from less dust generation, which keeps bench spaces cleaner. During a run of twenty parallel reactions for alkylation assays, a high-purity, free-flowing BES-Na sample ensured every well reached target concentration, a small but meaningful boost in day-to-day lab work.

    Storage stories float around every research corridor—who hasn’t found a bottle with crystals stuck to the neck from moisture? Investing in tight-sealing containers, periodically dosing with silica gel or other desiccant, and labeling opening dates spare headaches down the line. Some colleagues seal bulk supplies under nitrogen, extending shelf life even further, though most academic labs find a simple screw-cap works if specimens turn over quickly.

    Recent Advances and Evolving Applications

    In the last decade, technological innovations put Sodium 2-Bromoethanesulfonate on the radar of synthetic biologists. Teams engineering microbial consortia for green chemistry applications use BES-Na to regulate methane output in experimental bioreactors. Shortening methane startup also supports trials for alternative energy and synthetic gas production, where rapid shifts in metabolic states prove vital for data gathering. Some groups try to couple BES-Na usage with real-time gas analysis, exporting trace readings directly to cloud databases. This collaborative approach, which merges chemistry and digital monitoring, exemplifies how a familiar reagent adapts alongside scientific advances.

    The push toward sustainable agriculture means researchers revisit tools like Sodium 2-Bromoethanesulfonate to limit farm emissions. Field studies, particularly those involving ruminants, increasingly deploy BES-Na to model different feeding regimes with lower greenhouse gas profiles. Veterinary researchers also examine how BES-Na influences animal gut microbiomes—does temporary inhibition lead to longer-term shifts in microbial balance or does the system recover as soon as the inhibitor phases out? Open questions remain, but the compound continues to inform policy and management decisions as part of broader emissions research.

    Global Availability and Market Trends

    Traditionally, most Sodium 2-Bromoethanesulfonate supply stemmed from a handful of chemical producers, with availability tracking demand from research and specialty chemical sectors. As biotechnological application widens, the compound has become easier to source in smaller and bulk quantities alike. Experienced procurement specialists know that pricing trends fluctuate with raw material costs—mainly bromine derivatives and sulfonate intermediates. Researchers planning long-term studies often benefit from locking in supply contracts with trusted vendors, especially during periods of market volatility.

    Quality standards for BES-Na differ slightly between medical research, basic science, and industrial manufacturers. Some labs require extensive certificates of analysis, including ion chromatography for trace impurity levels, while others focus on broad compliance with analytical-grade benchmarks. Open dialogue between supplier and end-user often reveals subtle differences in lot performance; some manufacturers offer custom purification or sizing, making it easier for specialist needs to be met.

    Environmental Fate and Stewardship

    A focus on environmental impact accompanies almost every stage of chemical use today. BES-Na differs positively from many methylating or alkylating alternatives in that it doesn’t linger or biomagnify in food chains. Its breakdown products rarely accumulate, and laboratory effluent treatments efficiently remove sulfonated compounds without intensive upgrades. During wastewater bioassay work, researchers observed that BES-Na decomposes relatively quickly, a quality that encourages its use where regulatory standards matter.

    Waste minimization, particularly in industrial settings, has shaped how researchers handle BES-Na storage and disposal. Bulk buyers now demand information on downstream treatment and encourage recycling when possible. For small-scale research, sturdy waste-handling practices keep BES-Na out of stormwater and local landfills, and many universities have adopted improved tracking for sulfonate reagents. These practical approaches dovetail with larger efforts in green chemistry, pushing the sector away from persistent, less easily managed alkylating agents.

    Ongoing Research and Future Prospects

    Current research on BES-Na revolves around expanding its use in sustainable energy and environmental biotechnology. Some interdisciplinary teams pursue the compound as a key ingredient in new anaerobic digestion protocols aimed at maximizing hydrogen production while minimizing methane. Advances in microbial genomics, coupled with BES-Na’s selectivity, allow scientists to tease apart the roles of previously uncharacterized species in environmental samples. Early-stage trials suggest BES-Na helps maintain alternative metabolic pathways that hold promise for bio-based plastics and green fuel projects.

    Colleagues in pharmacology experiment with BES-Na-derived intermediates, searching for more robust disease models through selective metabolic inhibition. The fine-tuned suppressive effects of BES-Na, combined with next-generation analytical tools, lend unparalleled clarity to studies on cellular metabolism. Projects like these benefit from the compound’s track record of reliability and reproducibility, laying the groundwork for applications that extend far beyond its original niche.

    Refining Best Practices

    From my experience working on cross-disciplinary research teams, effective usage of Sodium 2-Bromoethanesulfonate boils down to thoughtful calibration and ongoing data review. Laboratories new to the compound sometimes overshoot target concentrations or underestimate solubility limits, leading to rework or inconclusive results. Consulting with colleagues who have run similar experiments proves worthwhile. Outlining clear protocols around storage, solution preparation, and waste disposal minimizes error and streamlines project timelines.

    Workshops or short trainings on specialty reagents, including BES-Na, help younger researchers build practical skills that benefit long-term career growth. Sharing lessons learned—like which local supplier ships the product with minimal clumping or which concentration curve aligns with methanogen suppression in field soils—saves time and money for everyone involved. Sometimes it’s the whispered tip about batch consistency or ease of redissolving granules that tips the balance in favor of BES-Na over older alternatives.

    Conclusion: Why Sodium 2-Bromoethanesulfonate Matters

    Despite its wonky chemical name, Sodium 2-Bromoethanesulfonate earns its keep in the lab through versatility, reliability, and a proven ability to support both routine and experimental science. Whether used in methane blocking in microbiology, targeted alkylation in organic synthesis, or as a regulatory tool in sustainability studies, the compound remains at the intersection of tradition and innovation. Researchers new and seasoned continue to find fresh ways to apply BES-Na’s properties to ever-evolving questions.

    Choosing the right chemical has lasting consequences for research outcomes and laboratory safety. Sodium 2-Bromoethanesulfonate stands out, not just for its unique chemistry, but for how it has helped teams push into new scientific territory. Trends point to ongoing relevance, especially as global attention sharpens around greenhouse gas reduction and the need for sustainable workflows. In places where progress matters most, BES-Na has earned its spot as a staple in the modern scientific toolkit.