|
HS Code |
980322 |
| Iupac Name | 4-{[4-(Prop-2-en-1-yloxy)phenyl]sulfonyl}phenol |
| Molecular Formula | C15H14O4S |
| Molecular Weight | 290.34 g/mol |
| Cas Number | 869869-98-1 |
| Appearance | White to off-white solid |
| Melting Point | 160-162°C |
| Solubility | Soluble in organic solvents such as DMSO and ethanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C in a dry, well-ventilated area |
| Smiles | C=CCOC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(C=C2)O |
| Inchi | InChI=1S/C15H14O4S/c1-2-8-19-13-5-9-15(10-6-13)20(18,21)14-3-7-12(16)11-4-14/h2-7,9-12,16H,1,8H2 |
As an accredited 4-{[4-(Prop-2-En-1-Yloxy)Phenyl]Sulfonyl}Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 g, sealed with tamper-evident cap, labeled with chemical name, hazard pictograms, batch number, and handling instructions. |
| Shipping | The chemical **4-{[4-(Prop-2-en-1-yloxy)phenyl]sulfonyl}phenol** is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with relevant safety guidelines, ensuring stability during transit. The shipment includes proper labeling for hazardous materials, and is handled by trained personnel following chemical transport regulations to ensure safe delivery. |
| Storage | Store **4-{[4-(Prop-2-en-1-yloxy)phenyl]sulfonyl}phenol** in a tightly sealed container, away from moisture and direct sunlight. Keep in a cool, dry, well-ventilated area, separate from incompatible materials such as strong oxidizing agents and bases. Label the container clearly, and handle under a fume hood if possible. Follow all standard laboratory safety procedures during storage and handling. |
Competitive 4-{[4-(Prop-2-En-1-Yloxy)Phenyl]Sulfonyl}Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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For over two decades, our synthesis workshops have focused on making high-grade specialty chemicals for applications where reliability really matters. Among these, 4-{[4-(Prop-2-En-1-Yloxy)Phenyl]Sulfonyl}Phenol has established a reputation, not by hype, but through consistent performance in challenging reaction environments. The product’s unique molecular structure brings a sulfonyl-bridged connection, linking a phenolic segment with a prop-2-en-1-yloxy functional group. This sets it apart from more basic sulfonic acid derivatives and phenolic additives—offering more than just the sum of its parts—it delivers targeted reactivity, cleaner conversion, and, as confirmed in feedback from process chemists, reproducible results in multi-step synthesis work.
Professional users, particularly in the pharmaceutical and fine chemicals sectors, have grown to appreciate specialty intermediates like this one not just for what they are, but for what they help others create downstream. Our current offering reaches chemists seeking a balance between selective reactivity and robust process tolerance. In bench trials and full-scale plant runs, this molecule repeatedly demonstrates resistance to degradation and high-purity retention, reducing concerns about side reactions that can complicate large-scale operations.
In our experience, process optimization is as much about avoiding unnecessary troubleshooting as it is about hitting high theoretical yields. This material streamlines workflows for sulfonylation, cross-coupling, and alkylation steps by producing fewer extraneous byproducts compared to less engineered analogs. Years ago, starting from precursors with a more generic substitution pattern often wasted both time and solvent, especially during iterative purification. Improvements in substitution, specifically the propenyl ether on the phenyl ring and the placement of the phenolic OH, eliminated sources of instability that we observed in our earlier pilot campaigns.
Working at this scale and with this level of fine-tuned reactivity, not even a highly automated plant can sidestep the human imperative: watchfulness at every single unit operation. From initial alkylation through sulfonation and up to the final work-up, the best chemists keep close tabs on purity by direct observation and hands-on analysis—not simply by relying on default settings. Our longstanding control strategy pairs robust reaction monitoring (NMR, HPLC, mass spectrometry) with on-the-fly troubleshooting, because every production batch counts for both research and commercial clients.
For those responsible for sourcing, traceability of starting materials remains a primary concern. From our point of view, tightening up traceability in alkyl-benzenesulfonate manufacture, from reactor charge to finished bagging, has reduced lot-to-lot drift below the threshold many regulatory bodies require. Our technical team has found that improved supplier relationships for our base phenolic feedstocks not only support global compliance but also reduce disruptions caused by upstream quality events—episodes that have, in the past, sent even the best-run plants scrambling for requalification.
The downstream result? Higher yield and lower risk of off-specification material, especially where the risk of over-sulfonation or uncontrolled side-chain cleavage would, with other products, lead to batch rejections or untimely reworks. We control every parameter, from solvents to process temperature to residual catalyst content, to maintain a product profile that users can return to again and again.
The unique connectivity in 4-{[4-(Prop-2-En-1-Yloxy)Phenyl]Sulfonyl}Phenol brings distinct advantages to API intermediate synthesis, performance polymer manufacture, and certain agrochemical projects. Chemists in these fields often talk about headaches caused by reagents that overreact, form sticky emulsions, or load up downstream separations with hard-to-remove tars. By contrast, we find that the electron-withdrawing influence of the sulfonyl group paired with the stabilizing effect of the propenyloxy-phenyl substitution not only supports intended reactions but helps keep unwanted polymerization and resinification out of the picture.
Take, for example, selective sulfonylation—where the wrong substitution leads to overlapping peaks or persistent tailing in chromatographic separations. Our most rigorous in-house runs show that well-prepared material, kept dry and handled carefully, delivers tight melting endpoint ranges and high clarity, speeding up both analytical verification and scale-up. R&D users who've switched from lower-cost generics report cleaner NMR spectra and fewer post-reaction clean-up headaches.
Others in the field have documented improved recovery rates in etherification and carbon-carbon coupling trials, particularly in sodium or potassium carbonate environments that historically eat away at unprotected functionalities. Here, the torsional effects and resonance stabilization found in this compound justify the investment, as yields increase and waste lessens.
From years spent shoulder-to-shoulder with project chemists, the difference between a good sulfonylated phenol and a great one often boils down to how the substitution pattern aligns with intended downstream reactivity. The propenyloxy functional group situated para to the sulfonyl bridge on the phenyl ring can mean a world of difference in certain reaction environments. While some alternatives use simpler alkoxy or just straight-chain alkyl ethers, we’ve measured better processability and shelf-stability when the propenyl group stays intact through a range of moisture and heat exposures.
Anecdotally, one of our partners described a multi-step synthesis where using an older meta-substituted version forced recurrent distillations to remove byproducts. Switching to the para-connected propenyl ether cut waste streams and reduced cycle times, not to mention saving on column solvent orders at plant scale. We often see an advantage when the product’s backbone resists oxidative breakdown—especially relevant for pilot plants operating under tight timelines and modulating conditions.
This molecule’s configuration also means it can withstand basic and mildly acidic conditions that would degrade less robust analogs. Anyone running screening arrays at the microreactor or kilo lab level tends to notice improved conversion predictability and less fouling. That predictability matters whether scaling up for kilograms or running gram-scale library screens.
Through years of hands-on optimization, we refocused process development to give better control over unreacted starting material removal, and tighter specifications for allowable mono- versus di-sulfonylated byproducts. Upgraded purification steps—particularly enhanced phase-separation and automated rotary-vac drying—keep residual solvents well below even the strictest target range our partners demand.
This doesn’t just enhance HPLC purity on paper; it keeps engines running at partner facilities where every deviation or stoppage flows directly into lost opportunity and added cost. By emphasizing training, stepwise documentation, and QC oversight, our facility builds trust batch after batch. Operators know the difference between “on spec” and “done right,” and only batches clearing all checkpoints move forward.
Our customers often need high levels of documentation to satisfy not just internal standards, but also the requirements of international regulatory bodies. Real-world questions about residual metals, trace solvents, and critical impurities get answered in real time, not by form letters or generic certificates. That’s a direct benefit of being both manufacturer and problem-solver: we troubleshoot with the user’s ultimate product in mind, not just the immediate batch.
Many in the industry have settled, over the years, for more traditional monosulfonylates or even bulkier di-functional phenols. But substitutions at ortho or meta positions often compromise reactivity or physical stability. Our experience tells us that moving to p-positioned propenyloxy substitution brings less steric hindrance and better electronic balance. In side-by-side reaction trials, this leads to better selectivity, sharper endpoints, and higher throughput.
Compared to hydroxybenzene sulfonates used in bulk surfactant and colorant industries, this product stands out in terms of chemical specificity. Its enhanced reactivity toward nucleophilic coupling agents opens up possibilities not readily attainable with more basic phenol- or hydroxyl-sulfonate reagents. For organizations focused on synthesizing advanced intermediates, that means less material loss and more certainty in each operation—not to mention simpler post-reaction workup given the absence of gooey oligomers that plague less refined grades.
Even within the specialized context of propenyl ethers, the length and connectivity of the hydrocarbon bridge plays a decisive role. Alternative products where the alkoxy group has longer or branched chains tend to show sluggishness in certain catalytic cycles. Here, the prop-2-en-1-yloxy option offers a sweet spot, ensuring both agility in reactions and resistance to unwanted chain scission.
Trust, in our trade, is built batch by batch and validated every time a customer’s process runs without a hitch. For us, keeping a keen eye on both upstream raw material profiles and subtle downstream usage details drives product development. We routinely manage impurities such as trace alkene or residual chloride well below action limits because small oversights can spiral into major operational headaches.
Raw materials, climate, and transport timelines all pose risks to product consistency. Our in-house approach controls for every variable—selecting only top-grade solvents, controlling reactor pressure ramps, and verifying finished product in duplicate. Packaging lines are set up to minimize moisture ingress and exposure to atmospheric contaminants, real-world measures that make a difference not just in storage, but as soon as the drum reaches a client’s facility for use.
We also realize our clients face mounting expectations for sustainability and responsible sourcing. Whenever possible, we source from renewable phenolic streams and manage energy usage through improved heat integration in plant operations. These aren’t afterthoughts—they directly tie into both product stability and long-haul supply assurance.
Feedback from the field often tells us what the spec sheet cannot: what daily handling, storage, and application of the product looks like across different geographies and climates. Stories from end-users filter back through our team—sometimes highlighting ease of dissolution in tricky formulations or resilience during protracted process holds. We take up these cues for further improvements.
Our QA teams don’t just check boxes—they interrogate every anomaly, trace every deviation, and work closely with our development lab to refine test methods or tweak stabilization protocols as needed. We don’t take shortcuts on batch reviews, and we welcome verification audits from partners, regulatory agencies, and third-party laboratories alike.
The result? A culture of steady improvement, where setbacks become lessons for the next production round, and where successes drive us to even higher expectations. For chemists relying on us for material critical to their pipeline, we commit not just to the letter of quality agreements, but also the spirit of continuous support.
Many technical breakthroughs emerge from settings as varied as single-user R&D labs up to 24/7 fully integrated plants. Our work with 4-{[4-(Prop-2-En-1-Yloxy)Phenyl]Sulfonyl}Phenol has touched every part of this spectrum: catalyzing the launch of new medicinal chemistry programs; underpinning the next generation of functional polymers; supporting green chemistry initiatives that aim to minimize waste. Each client brings their own blend of ambition and caution, and this product has helped drive both productivity gains and cost reductions.
By supporting those scaling new molecules or troubleshooting hard-to-purify intermediates, we enable results—not just reactions. We’ve listened to users describe improved shelf-life for product stock, easier integration into multi-solvent blends, and simplified downstream purifications. Whether gaining regulatory approval for a new product or reducing the cost of established ones, users consistently look for partners who won’t leave them out of the loop during the stakes and stresses of process transfers and changes.
Future technical needs will stretch the capabilities of specialty chemicals and demand more than marginal improvements. We see increased drive for lower residual contaminant levels, higher energy efficiency, and products whose performance doesn’t drop off at higher throughput rates. Continuous upgrades to our plant reduce cycle times and enable finer tolerance in critical reactions. Process modeling and digital verification supplement—even strengthen—the trained judgment of our teams.
No manufacturer succeeds alone. Progress comes from open dialogue with scientists, engineers, and supply chain managers at every point of use. Our doors remain open for technical feedback, collaborative troubleshooting, or tailored solutions with custom run parameters. Supporting innovation and reliability counts for more than hitting monthly targets—it means being part of a global network of makers, problem-solvers, and boundary-pushers.
Ultimately, our reputation grows not from glossy brochures but from sustained results, one campaign at a time. As chemical manufacturing moves into the future, compounds like 4-{[4-(Prop-2-En-1-Yloxy)Phenyl]Sulfonyl}Phenol stand ready to tackle both legacy process challenges and the next wave of scientific advances.