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HS Code |
229454 |
| Chemical Name | 2-(Phenylsulfonyl)acetophenone |
| Cas Number | 16640-52-1 |
| Molecular Formula | C14H12O3S |
| Molecular Weight | 260.31 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 98-101 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | CC(=O)C1=CC=CC=C1S(=O)(=O)C2=CC=CC=C2 |
| Inchi | InChI=1S/C14H12O3S/c15-11(12-7-3-1-4-8-12)18(16,17)14-10-6-5-9-13-14/h1-10H2 |
| Storage Conditions | Store at room temperature, in a tightly closed container |
| Synonyms | 2-(Benzene sulfonyl)acetophenone |
As an accredited 2-(Phenylsulfonyl)Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, labeled "2-(Phenylsulfonyl)Acetophenone, 25g," with hazard pictograms and safety information, sealed with a secure cap. |
| Shipping | 2-(Phenylsulfonyl)acetophenone is shipped in sealed, chemically resistant containers to prevent contamination and moisture ingress. Packaging complies with applicable chemical transport regulations. It is labeled with appropriate hazard information and handled as a non-volatile, stable organic compound. Shipping may require temperature control and documentation per regulatory and safety standards. |
| Storage | 2-(Phenylsulfonyl)acetophenone should be stored in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally in a chemical storage cabinet. Properly label the container and ensure it is kept out of reach of unauthorized personnel and sources of ignition. |
Applications of 2-(Phenylsulfonyl)Acetophenone in Industrial Manufacturing2-(Phenylsulfonyl)Acetophenone supports a range of production scenarios in advanced chemical industries. As a direct manufacturer, we work closely with global partners in specialty intermediates, photoinitiator systems, pharmaceutical research synthesis, and polymer additive formulations. The sections below outline practical implementations and quality assurance considerations for each major downstream sector. 1. Photoinitiator Synthesis for UV-Curable SystemsProducers of UV-curable coatings and inks employ our material as a core intermediate in high-purity photoinitiator compounds, especially where strict light absorption properties and low toxicological impact are required. Chemists integrate it during the synthesis of novel benzoin-type derivatives and related structures for high throughput production lines involving offset inks, overprint varnishes, and 3D printing resins. Strict qualification protocols underpin raw material intake, and customers frequently specify spectral and residue control at each process step. Industry compliance standards
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2. Pharmaceutical Intermediate for Active Ingredient SynthesisMajor pharmaceutical manufacturers utilize 2-(Phenylsulfonyl)Acetophenone as a building block for targeted synthesis of sulfonyl-containing drug molecules, particularly where electron-withdrawing substituents facilitate regioselective ring closures or cross-coupling. It is integrated into stages demanding high isomeric purity, such as synthesis of proprietary anti-infective or anti-inflammatory candidates. Batch documentation aligns with all relevant traceability and impurity profile requirements for pharmaceutical starting materials. Industry compliance standards
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3. Functional Polymer Additive ManufacturingPolymer compounders and masterbatch producers apply this raw material for controlled modification of resin properties, especially when targeting specific UV absorption, mobility, or flavor barrier enhancements. It acts as a modifier in aromatic sulfone polymer blends for technical films, sheets, or molded parts. The compound's purity and consistent molecular weight contribute to predictable downstream compounding, with in-plant specification referencing comprehensive analytical benchmarks. Industry compliance standards
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4. Specialty Agrochemical IntermediateAgrochemical formulators integrate our chemical as a precursor in the synthesis of select arylsulfonyl-based crop protection agents and herbicide candidates. Its consistent sulfonyl activity profile supports development of agrochemicals needing precise selectivity towards weed species or crop-specific benignity. Formulation teams implement in-line analytical confirmation to align with regulatory impurity and residue requirements during multi-stage technical synthesis. Industry compliance standards
Typical usage ratio
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Making specialty organic intermediates goes far beyond filling an order—it requires a sharp eye for raw material sourcing, equipment setup, reaction control, and end-use performance. We have synthesized 2-(Phenylsulfonyl)acetophenone in our facility for years now, backing each batch with hands-on knowledge and critical feedback from customers who put these molecules to work in the real world. This compound holds a unique place among aryl sulfone derivatives, especially in pharmaceutical research and advanced organic synthesis. Its consistent yield and high purity do not happen by chance. Each lot passes scrutiny in our lab, where we rely on modern chromatographic and spectroscopic testing at every critical point. This isn’t just about standards; it’s about knowing what our customers expect after dealing with inconsistent outside suppliers.
Our standard product typically shows a purity over 99% by HPLC, with trace impurities monitored batch by batch. Some rely solely on melting point and TLC; in our experience, these tell only half the story. Full NMR and LC-MS profiling prove the structural integrity and allow for easy batch-to-batch comparison, which many downstream users have come to rely on for reproducible research.
It’s one thing to offer 2-(Phenylsulfonyl)acetophenone on a catalog shelf, another to master its synthesis from raw benzene derivatives and sulfones all the way through to final crystallization. Small variations in temperature, choice of base, or solvent removal technique shift outcomes day to day. Over time, we’ve learned to watch for subtle shifts during the reaction by monitoring color, exotherm profile, and smell—yes, even smell can be a signal when handling certain sulfonyl groups. To cut confusion, our technicians track reaction times and conditions in meticulous logbooks. If a batch doesn’t meet set parameters on GC or NMR, it never ships.
The main process route starts from a Friedel–Crafts acylation, plugging the acyl and sulfonyl groups into the right positions on the aromatic rings under controlled catalysis. Sulfonylation steps must be handled under fume hoods and with real-time monitoring since over-sulfonation leads to tough purification issues downstream. We have dealt with batches from importers in the past where off-odors or colored impurities popped up during reprocessing; those experiences taught us that cutting corners in the early stages shows up later in both yield and downstream reactivity.
2-(Phenylsulfonyl)acetophenone often ends up as a cornerstone in the development of heterocyclic scaffolds, especially in pharmaceutical intermediates. Its methylene group, activated by both electron-withdrawing sulfonyl and carbonyl groups, behaves predictably during enolate formation, an area where unreliable material quality can grind a multi-step synthesis to a halt. Working directly with research chemists, we’ve fielded feedback on solvent compatibility, issues during scale-up, and challenges with byproducts—adjusting our drying and filtration methods as a result.
End-users tell us they value this particular sulfone for its robust performance in C–C bond-forming reactions. For example, the Pd-catalyzed cross-coupling and enolate alkylation go more smoothly with a consistently pure starting material. Several R&D groups use our product for synthesizing biologically active molecules, including new generations of sulfa drugs and specialized ligands for transition metal complexes. Patterns emerge here—solid purity leads to fewer column purifications and higher overall throughput for critical scale-up runs.
Customers buying from a pure manufacturer often remark how they notice real, practical differences compared to offerings from distributors or trading companies. Material from some of those sources comes with extra paperwork but missing analytical transparency. We supply the same comprehensive documentation that our internal QA department uses when validating batches: HPLC traces, NMR spectra, MS data, and impurity profiles. Researchers and process chemists frequently request these before placing new orders.
Every shipment leaves our facility only after repeating QC checks on color, melting point, and residual solvents, not just the listed purity. Oily films or inconsistent crystalline forms signal a process deviation, and our staff knows to halt packing if they pop up. Over the years, batches made under less rigorous processes have returned to us from frustrated customers— often with time-sensitive projects on the line. Those conversations led us to strengthen our final filtration and drying routines to eliminate even trace amounts of moisture and solvents that can affect sensitive downstream applications.
Not every aryl sulfone offers the same synthetic hook as 2-(Phenylsulfonyl)acetophenone. For chemists focused on introducing functional groups onto benzene rings, the dual-activated methylene unit gives a unique set of reactivity patterns compared to generic acetophenones or simple sulfones. The ketone next to the sulfone reinforces acidity, opening the way for strong, clean enolate chemistry under straightforward conditions. Our regular users often comment that alternative phenylsulfonyl derivatives—lacking the specific arrangement of sulfone and carbonyl groups—don’t participate as readily in key transformations, slowing route optimization and prolonging development cycles.
Some resellers mix up isomeric or slightly different sulfonyl-functionalized acetophenones, often after using bulk suppliers who do not clearly separate these close relatives. We consistently separate and reject byproducts or isomers during purification, since even small amounts confuse downstream reaction planning. Analytical clarity here isn’t a marketing buzzword; it’s what enables a reliable synthetic campaign.
Large trading companies sometimes ship off-the-shelf 2-(Phenylsulfonyl)acetophenone with only a cursory set of checks—if that. The manufacturing environment matters. Over the last decade, we have fielded calls from chemists forced to rework syntheses or stop them entirely because trace metal residues, unseen by superficial checks, alter catalytic reactions or polymerization. End-users tend to return to direct manufacturers who monitor every incoming raw material and set aside off-spec solvents before the first charge is added. This approach minimizes trouble blowing back onto the downstream process chemist, especially during fast-paced development sprints where every lost day risks a missed deadline.
Our experience with product recalls shows that well-documented, transparent QC records matter. No researcher wants a month’s work wasted over a contaminant that could have been spotted with proper NMR or HPLC analysis. By keeping technical data on file for every lot and tracking customer complaint patterns, we spot trends early and can tweak synthetic protocols before problems grow larger. These lessons came through hard-won real-world experience, not just glossy quality certificates.
One recurring concern in handling 2-(Phenylsulfonyl)acetophenone, both during production and at the bench, involves stability and storage. The compound retains integrity well under cool, dry conditions. Moisture pick-up or storage at elevated temperature leads to degradation. That sort of feedback pushed us to optimize our packaging over several iterations, testing out different barrier materials and working with end-users in humid regions to monitor stability after long shipments. By auditing not just our own procedures but also following up on how customers handled storage, we learned that a costly compound lost to improper storage is just as bad as an off-spec starting material. At scale, these efficiency losses add up.
Many researchers point out that poor handling or suboptimal shipping can create issues that only become apparent during sophisticated downstream reactions, including sensitive organometallic manipulations or multistep syntheses. This insight pushed us to include desiccants and to adopt more robust sealing protocols, cutting the risk of hydrolysis or byproduct formation over extended storage.
Moving from synthesis on a few grams to tens of kilograms in a plant means grappling with mechanical issues, waste minimization, and worker safety. Anyone can follow a published prep on a small scale and get decent results, but the real work begins scaling up. Reactor fouling, exhaust system challenges, and unanticipated exotherms are daily realities. From our earliest days, plant operators flagged issues with sulfonyl group handling, especially concerning dust and fume management. By working with them side by side, we refined protocols to keep yields dependable and create a safer workspace.
These nitty-gritty details mean a lot to customers whose schedules depend on consistent lead times. Several pharmaceutical partners have shared stories about losing days to batch failures caused by inconsistent sulfone materials from less scrupulous sources. That feedback loop, coupled with our own real-time process monitoring, pushed us to invest in analytical upgrades and fine-tune every process from blending to drying.
On the user side, repeated requests for technical support around solubility profiles and optimal solvent systems told us a one-size-fits-all approach doesn’t cut it. We’ve built a growing library of internal solvent compatibility and reaction condition data, using feedback from groups in medicinal chemistry and process scale-up. By sharing these insights, we have helped users deal with tricky solubilization issues and supported longer, more difficult reaction sequences.
Sticking close to customer needs goes far beyond answering tech support emails. It leads us to uncover recurring bottlenecks, from air-sensitive handling right down to the final product isolation after multi-step transformations. Our in-house team tracks these trends, folding them back into process redesign or packaging tweaks.
We’ve learned through constant iteration that the best fine chemicals only get better with fresh technical input. Accepting criticism from experienced synthetic chemists and plant engineers taught us humility and provides the backbone for ongoing process development. After several years making 2-(Phenylsulfonyl)acetophenone, we still run trials to find ways to streamline steps, cut down solvent waste, and trim costs where possible—without compromising analytical reliability.
Some of the most valuable feedback comes when batches don’t go as planned, either due to a commercial scale-up or because an unusual side reaction popped up in a downstream chemistry application. Rather than hiding these lessons, we record every deviation, review real customer complaints, and publish technical notes to our users explaining how to avoid known issues. Maintaining open lines of communication with medicinal chemists, polymer scientists, and scale-up engineers helps ensure the compound—while robust—isn’t just “technically pure” but really works as intended in challenging new syntheses.
Making 2-(Phenylsulfonyl)acetophenone at industrial scale raises important issues around emissions, waste management, and operator safety. Our factory addresses these concerns not just for regulatory compliance, but because our team’s well-being relies on careful handling and waste minimization. We scrub exhausts, treat effluents with properly sized neutralization systems, and recycle where practical. Waste reduction and solvent recovery form part of our routine cycle—this comes from years of seeing fines or downstream environmental blowback in facilities that neglected these steps.
Enforcing best practices for personal protective equipment, on-site training, and process controls ensures our team keeps exposure below documented thresholds. We continually audit for accidental releases or potential exposure routes, strengthening protocols as needed. This ongoing vigilance has led to a safety record that we believe supports both product quality and the broader community of users and neighbors.
Pharmaceutical partners, university research labs, and specialty material developers frequently share stories about new molecule discoveries and critical process breakthroughs that depended on reliable supplies of 2-(Phenylsulfonyl)acetophenone. Customers pursuing difficult cyclization reactions or planning multi-gram campaigns rely on quick access to consistent lots. On several occasions, our technical team offered input on reaction troubleshooting, enabling smoother scale-ups and improved yields.
In one instance, a medicinal chemist working on sulfa drug analogs required tailored advice on minimizing aldehyde impurities during late-stage functionalization. Our technical staff ran comparative tests, advice that ultimately saved time and resource by adjusting workup routines based on real product performance. This sort of direct back-and-forth rarely happens when working through faceless distributorships lacking hands-on synthesis experience.
Another group, synthesizing ligands for transition metal catalysts, reported that inconsistent isomers from other sources led to unpredictable product reactivity. Our end-to-end process, strict intermediate isolation, and attention to trace isomer separation led to improved overall recovery and fewer wasted runs.
No two chemical manufacturers run identical processes, and those details add up to a product’s real-world performance. We approach every order for 2-(Phenylsulfonyl)acetophenone with an eye toward reproducibility, backed by data and—more importantly—by feedback gained on the ground. Communication with chemists down the line informs next-generation improvements, whether adjusting crystallization solvents or modifying purification steps for swollen downstream specs.
We encourage direct dialogue about the product, including any specific requirements for scale, packaging, or technical data. Over years of experience, this practice has led to meaningful partnerships with customers seeking a reliable, well-characterized intermediate from a source that stands behind every batch shipped.
Direct manufacturing offers more than just a lower price or a shorter supply chain. It means deep familiarity with the underlying chemistry, a commitment to transparency at every step, and respect for both researchers’ time and the safety of everyone involved. Drawing on years of trial, error, and honest dialogue, we continue to supply 2-(Phenylsulfonyl)acetophenone at a standard informed by daily work and enduring customer relationships. Each gram carries the weight of this experience, and we remain committed to supporting our partners in their ongoing research and production campaigns.