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HS Code |
551843 |
| Iupac Name | 2-Bromo-1-[4-(methylsulfonyl)phenyl]ethanone |
| Molecular Formula | C9H9BrO3S |
| Molecular Weight | 277.14 g/mol |
| Cas Number | 862387-80-2 |
| Appearance | White to off-white solid |
| Melting Point | 97-102°C |
| Solubility | Soluble in organic solvents like DMSO, ethanol |
| Smiles | CS(=O)(=O)C1=CC=C(C=C1)C(=O)CBr |
| Inchi | InChI=1S/C9H9BrO3S/c1-14(12,13)9-4-2-8(3-5-9)7(11)6-10/h2-5H,6H2,1H3 |
As an accredited 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25 grams of 2-Bromo-1-[4-(Methylsulfonyl)phenyl]-1-ethanone, labeled with hazard warnings and handling instructions. |
| Shipping | 2-Bromo-1-[4-(Methylsulfonyl)phenyl]-1-ethanone should be shipped in tightly sealed containers, protected from moisture, light, and incompatible substances. Transport must comply with relevant chemical regulations, including labeling as hazardous if applicable. Use secondary containment and appropriate personal protective equipment during handling to prevent exposure or leaks. Store in a cool, dry place during transit. |
| Storage | Store **2-Bromo-1-[4-(Methylsulfonyl)phenyl]-1-ethanone** in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and bases. Ensure proper labeling, and use secondary containment if possible. Handle under an inert atmosphere (e.g., nitrogen or argon) if the compound is air- or moisture-sensitive. |
Applications of 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone in Industrial ManufacturingAs a direct chemical raw material producer, we supply 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone to specialized industrial sectors where its reactivity and functional group specificity offer tangible process benefits. Below we detail target applications where industrial customers have integrated this intermediate, specifying real downstream conformity needs, usage ratios, process entry points, and representative end products manufactured at scale. 1. Pharmaceutical Intermediate SynthesisMajor pharmaceutical manufacturers use 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone as a core intermediate for constructing aryl ketone moieties during the synthesis of various small-molecule therapeutics, especially in the development of kinase inhibitors and certain non-steroidal anti-inflammatory agents. The compound’s bromoacetyl group is introduced at early or mid-stage synthesis routes, allowing for reliable bromine-mediated substitution or coupling under controlled conditions. This drives high-purity yields for regulated downstream APIs within multi-step cGMP production lines. Industry compliance standards
Typical usage ratio
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2. Agrochemical Research & SynthesisLarge agrochemical companies integrate this raw material in the synthesis of advanced herbicidal and fungicidal scaffolds requiring a methylsulfonylphenyl-acetone core. Its chemical structure supports the generation of selective aromatic substitutions vital for intellectual property-protected crop protection substances. As an early-stage intermediate, the compound enables streamlined construction of lead candidates while keeping side reactions minimal, supporting scalable and reproducible process development in pilot and commercial batches. Industry compliance standards
Typical usage ratio
Downstream process integration
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3. Dye and Specialty Pigment IntermediatesChemical manufacturers in the dye and specialty pigment sector rely on this compound as a route to modified phenylacetone derivatives, supporting the development of colorants with enhanced thermal and photostability. The bromo-ketone functionality enables controlled acylation and coupling reactions for synthesizing dyes with high tinctorial strength and solvent resistance, meeting the needs of industrial textile, coating, and plastic coloration processes. Industry compliance standards
Typical usage ratio
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4. Fine Chemicals for Photoinitiator SynthesisManufacturers of photoinitiators for UV-curable resins utilize our material as a key precursor for molecules where aryl ketone substitution patterns are critical to UV absorption profiles. Its integration allows downstream partners to tailor electronic properties and ensure controlled fragmentation rates, permitting the end-use of cured coatings, adhesives, and inks with predictable performance and safety characteristics per industry standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Our experience in organic synthesis tells us that the right building block saves weeks in the lab and adds confidence to scale-up. Over the years, we have optimized the preparation and purification of 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone, making it a go-to intermediate for medicinal chemistry programs and material science research teams. Despite the rise of automated chemistry kits, real-world projects demand custom pathways. This compound has proven itself as a reliable electrophile when standard options like bromoacetophenone or para-substituted acetophenone analogs fall short due to limited reactivity or instability.
2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone draws attention because of its unique combination: the bromo-ketone functionality activates the aromatic ring for further transformations, while the sulfonyl group on the phenyl moiety directs selectivity and influences solubility. This isn’t a theoretical advantage. In actual practice, we’ve watched teams use this molecule to access highly functionalized heterocycles, tap into regioselective alkylation, or introduce diversity in structure-activity relationship (SAR) studies. Unlike unsubstituted bromoacetophenones, the methylsulfonyl para substitution modifies both the electronic profile and handling characteristics, lending greater control to synthetic routes.
We manufacture this compound to a minimum purity of 98%, checked regularly using HPLC and proton NMR—not just by spot-checking a handful of samples, but by consistently tightening our batch protocols. Chemists often request specific crystal forms or particle size cuts, and while solvent compatibility or reactivity remain top priorities, practical matters like bulk handling stability and ease of weighing also affect daily work. In the course of hundreds of batches, we’ve eliminated residual halide contaminants and reduced organic volatile carryover, so teams can focus on their reactions, not on troubleshooting inconsistent material.
Moisture sensitivity often undermines less robust bromo ketones. Our product’s form resists decomposition in ambient conditions long enough for transfer and set-up, but still offers the reactivity needed for smooth downstream transformation. From kilo-scale drums for material science programs to fine-milled prep for medicinal chemistry, we’ve seen partners gain consistent result reproducibility batch after batch, largely because we control every stage—from bromination to post-crystallization handling—on site.
In pharmaceutical projects, this compound has become a strategic choice for constructing diverse libraries. One major reason stems from the ketone acting as a strong electron-withdrawing group, while the bromine provides an excellent leaving group for nucleophilic displacement. Teams leverage this dual functionality to build complex scaffolds. In our own synthesis for custom orders, it has shortened multi-step routes, giving medicinal chemists access to structures that improve lead optimization. Feedback from our industry partners confirms that the sulfonyl handle tolerates a range of conditions that degrade other para-substituted acetophenones.
In agricultural chemistry, 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone offers a stable, high-purity alternative to more hazardous brominated intermediates. Its compatibility across multiple solvent systems—such as DMF, DMSO, and acetonitrile—lets researchers design process-friendly transformations, reducing the bottlenecks caused by solubility problems with other bromo ketones. Commercial clients who run hundreds of reactions each week frequently remark on the cleaner workups and higher isolated yields when using our product compared to others on the market.
Beyond small molecule pharmaceuticals, this compound sees use in advanced material applications. Teams have integrated it in the synthesis of specialty polymers where the methylsulfonyl group imparted desirable dielectric properties and enhanced chemical robustness. Each application places different demands on purity and physical form, so we tune our protocols accordingly. We’ve been called to troubleshoot reactions for university collaborators when off-grade or poorly crystalline lots from other sources led to unmanageable by-products. Our control over every step—bromination, crystallization, drying—has enabled partners to resolve these issues without switching starting materials or redrawing their synthetic plans.
The organic chemicals market has no shortage of bromoacetophenone derivatives, but few match the unique profile of 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone. Simple bromoacetophenones lack the sulfonyl group’s impact on polarity and reaction selectivity. The methylsulfonyl unit, positioned para to the carbonyl group, modulates electron density and shields against unwanted side reactions. We have observed sharper selectivity in cross-coupling and cyclization sequences when chemists pair this electrophile with basic nucleophiles, in contrast to unsubstituted or para-methoxy alternatives that permit side-chain migration or hydrolytic cleavage.
The practical difference also shows up in stability during storage and shipping. Some halogenated acetophenones, especially those with weaker electron-withdrawing substituents, darken or develop off-odors if exposed to light and air. Our formulation, supported by tightly monitored humidity controls, stays clear and free flowing. Customers who have limited cold storage capacity can store this product under ambient warehouse conditions for extended periods, with minimal risk of caking or off-flavor.
Teams running parallel synthesis or developing combinatorial libraries value the reproducibility gained through our supplier-side controls. Rather than accepting lots that vary in crystal habit or purity, we commit to direct process feedback so our customers receive the same reliable intermediate month after month. Differentiation goes beyond purity specs; it’s about making real improvements in day-to-day lab performance. Our team fields technical questions directly—no third-party call desk or scripted responses—so chemists get advice rooted in hands-on production, not generic literature citations.
Any process chemist or R&D group can relate to the frustration of receiving poorly handled or improperly characterized intermediates. We have seen the ripple effect first hand: delays in pilot plant campaigns, cost overruns, analytical headaches. Over time, we built a system that prioritizes traceability and transparency. Each shipment of 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone comes from a dedicated unit that tracks raw material origins, batch-to-batch yields, and final QA results. In many cases, we provide actual analysis reports from the lot being shipped, not generic specs pulled from an archive. Such detail helps our customers plan with confidence, knowing they’ll receive the same high-performance material whether ordering a single bottle for SAR screening or a pallet for production work.
Research projects rarely move in a straight line. Projects hitch, switch direction, or pivot to related compounds based on new data. By offering a flexible ordering system—multiple grades, custom packaging, rush options for urgent deadlines—we’ve allowed customers to match the supply of 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone to the actual flow of their discovery and development efforts. Direct access to our technical team means partners gain advice on specific reaction set-ups, solvent swaps, or alternative protection strategies, all grounded in real-world trial and error, not theoretical best guesses.
Meeting the specific needs of each synthesis often requires small tweaks that only a manufacturer can accommodate. We’ve modified drying cycles in response to customer feedback about static buildup or clumping in automated weighers. We’ve matched particle size specifications to enable finer dosing in parallel reactors. By understanding both the big-picture demands of pharmaceutical development and the fine-grain needs of benchwork, our team avoids the disconnect that sometimes mars relationships with purely distribution-focused suppliers.
Modern chemical manufacturing calls for attention to sustainability and worker safety at every stage. Early routes to bromoaryl ketones relied on hazardous solvents or inefficient workups, putting handlers and the environment at greater risk. Our continuous process improvements substitute greener reagents and recycle process water where feasible. In our plant, waste minimization remains a key metric—not a marketing slogan. Our team has phased out chlorinated solvents for final washes and maintains closed transfers for all halogenated intermediates. With each new product evaluation, we weigh not only cost and reactivity but the impact of impurities and environmental footprint.
For those managing regulatory compliance or concerned with product stewardship, our tightening of residual bromide levels and process by-product tracking supports both in-house QA and downstream audit documentation. We welcome full supply-chain traceability requests from our partners. Our strong record with international material transfer agreements ref lects an ongoing commitment to responsible production. We share best practices across industry groups and welcome direct site visits from technical partners—real access, not just paperwork.
As pharmaceutical, agrochemical, and materials research domains grow more sophisticated, their need for customized building blocks like 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone continues to rise. We stay ahead by integrating technical learning from every successful batch into our next production campaign. Problems flagged during customer use—such as variable crystallinity or low batch yields in downstream coupling—become triggers for manager review and process fine-tuning. Feedback doesn’t rest in a database, it shapes the protocol for the next run.
No standard catalog order matches the demands of innovative research. Some chemists require tighter impurity profiles, others seek alternative forms or custom concentrations in solution for direct dosing. We respond by leveraging our agile plant footprint and experienced synthesis crew. Our decades of accumulated insights guide every specification we set, from choice of purification media to run-times on rotary evaporators.
It’s easy for chemical suppliers to rely on templated product sheets or catalogue entries that mask differences in actual performance. Our approach centers on direct exchange with project teams. Whether it’s troubleshooting a late-stage Suzuki coupling or consulting on stability for shelf-life extension, we engage peers as fellow problem-solvers, not just customers. Many of our collaboration stories began with a phone call about a stalled reaction or an impurity spike uncovered during scale-up, leading to long-term technical partnerships. People in the lab value straight information, not marketing gloss.
We think the role of a true manufacturer goes beyond supplying product. We aim to act as an extension of every research and development program that trusts us with their building block needs. By bringing a long view and persistent curiosity to every project, we help customers keep their attention on innovation—not chasing down raw material issues.
After countless batches, process reviews, and quality audits, the lesson is consistent: excellence in manufacturing is built step by step, from raw material sourcing through to final packing and delivery. 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone reflects this philosophy. Our plant team stands behind each shipment because we have seen first-hand the impact of high-quality raw materials on successful research outcomes and commercial rollout. As the science of synthesis evolves, we keep refining our methods, so that every project gets a stronger head start.
Choosing a partner for your next challenge—whether in pharmaceuticals, materials, or industrial chemistry—should come down to real-world results. With each lot of 2-Bromo-1-[4-(Methylsulfonyl)Phenyl]-1-Ethanone, our commitment is to supply more than just a molecule. We deliver insight, reliability, and a relentless focus on the needs of working chemists. Our doors stay open for technical discussion, feedback, and process improvement, ensuring that the needs of tomorrow’s chemistry are met with today’s practical know-how.