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HS Code |
940958 |
| Productname | Phenylsulfonylacetic Acid Ethyl Ester |
| Casnumber | 17617-57-1 |
| Molecularformula | C10H12O4S |
| Molecularweight | 228.27 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 145-147 °C at 2 mmHg |
| Density | 1.26 g/cm3 |
| Solubility | Soluble in organic solvents |
| Purity | Typically ≥ 98% |
| Smiles | CCOC(=O)CS(=O)2C1=CC=CC=C1 |
| Synonyms | Ethyl phenylsulfonylacetate |
| Refractiveindex | 1.523 (at 20 °C) |
| Storagetemperature | Store at 2-8 °C |
As an accredited Phenylsulfonylacetic Acid Ethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Phenylsulfonylacetic Acid Ethyl Ester is supplied in a 25g amber glass bottle, sealed for protection, with clear labeling. |
| Shipping | Phenylsulfonylacetic Acid Ethyl Ester is shipped in tightly sealed, inert containers under cool, dry conditions. Packages are labeled per regulatory standards, with proper hazard identification. Transportation complies with chemical safety regulations to prevent exposure, contamination, or degradation. Protective packaging ensures stability and integrity throughout transit. Handle with appropriate safety precautions upon arrival. |
| Storage | Phenylsulfonylacetic Acid Ethyl Ester should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. It should be kept in a cool, dry, and well-ventilated area, ideally at room temperature. Protect the compound from direct sunlight and sources of ignition. Follow all relevant safety and storage guidelines for organic chemicals. |
Applications of Phenylsulfonylacetic Acid Ethyl Ester in Industrial ManufacturingPhenylsulfonylacetic Acid Ethyl Ester is a key chemical intermediate with defined roles in specialized sectors of industrial synthesis. Our factory-grade production serves as a direct material for advanced organic and pharmaceutical manufacturing processes where precise formulation and compliance with international standards are required. 1. Pharmaceutical Intermediate SynthesisManufacturers of active pharmaceutical ingredients (APIs) use this ester as a crucial building block in stepwise synthesis of sulfonamide-containing compounds and beta-lactam derivatives for therapeutic applications. Its controlled reactivity supports side-chain modifications and advanced coupling in regulated APIs, which may involve multi-stage reactions and sensitive quality control. Direct input into batch reactors ensures minimized contaminant formation and high yield of desired pharmaceutical precursors. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingProducers of high-performance agrochemicals utilize this ester as a reactive intermediate for constructing herbicide and fungicide molecules with sulfonyl functionalities. It supports precision synthesis for selective crop protection products. Integration enables stepwise modification, allowing downstream formulation of parent actives that require strict impurity profiles and reproducibility. The material drops into closed reactor vessels, with real-time process controls to maintain regulatory specifications and safety. Industry compliance standards
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3. Synthesis of Specialty Organic Electronic MaterialsProducers of advanced electronic chemicals and specialty polymers use this ester as a functional building block for the synthesis of sulfonylated monomers, essential in producing semiconducting and dielectric materials for electronics. The compound enables controlled introduction of sulfonyl groups that modify electronic and thermal properties during monomer design. It enters tightly controlled synthetic steps under anhydrous and oxygen-free conditions, supporting material purity and precise functionality required in thin-film or printed electronics industries. Industry compliance standards
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4. Fine Chemical Synthesis for Dye and Pigment IntermediatesSpecialty dye and pigment manufacturers benefit from the selective reactivity of this ester to introduce sulfonyl-acetate moieties into chromophore frameworks. This functionality increases dye solubility, enhances light fastness, and alters molecular charge for performance textiles and plastics. The ester undergoes substitution and coupling reactions with aromatic amino or hydroxy groups as intermediate steps in high-purity colorant production. Closely controlled thermal and catalytic conditions are essential to maintain color strength and batch reproducibility. Industry compliance standards
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Producing Phenylsulfonylacetic Acid Ethyl Ester starts with a strict approach. We work with carefully sourced raw materials, and the chemistry unfolds in batch reactors built to handle the exacting requirements of aromatic sulfonyl compounds. Over years we have learned that even slight changes in reaction conditions can tip product quality, so our team tracks temperature, pH, and timing to the minute. Our batches run under robust in-process controls, and only clean, perfectly calibrated equipment enters the line.
Each lot of Phenylsulfonylacetic Acid Ethyl Ester (ethyl 2-(phenylsulfonyl)acetate) leaves our floor with an analytical certificate, confirmed by NMR and HPLC. We hold our typical purity to >99% by HPLC, because for downstream users, nothing derails a synthesis run like unexpected byproducts. Moisture and trace acid are both measured and kept below 0.1%. The appearance runs from white to off-white solid, never yellow, which points to trace oxidative degradation. We package directly from bulk to sealed, inert containers that protect from atmospheric moisture, as this ester picks up trace water surprisingly fast.
In organic synthesis, Phenylsulfonylacetic Acid Ethyl Ester offers remarkable control over C–C bond formation. We see our customers using it as a nucleophile for Knoevenagel condensations, Michael additions, and various alkylation protocols. Its combination of sulfonyl activation and the ethyl ester makes it less volatile than methyl analogs but more soluble in common organic solvents. This balance stands out particularly in pilot and scale-up campaigns, where reaction reproducibility takes priority—no stumbling over batch-to-batch variability or sluggish phases.
Bench chemists figure out early on that the ester functionality in this molecule gives them options. They can saponify smoothly to the acid under mild basic conditions, with the phenylsulfonyl group resisting hydrolysis far better than, say, benzoyl-protected acids. This is a trait we confirm by stability testing every year. Shelf-life under proper storage runs past 12 months, avoiding the need to reorder with each synthetic campaign. Our customers who work in pharma intermediates mention how reliable the product proves, even after long storage, avoiding the cloudiness or precipitate growth they sometimes get from cut-rate suppliers.
As manufacturer, we often get drawn into our customers’ process development discussions. Our in-house chemists have fielded questions about substitution with closely related esters, such as methyl or tert-butyl analogs. Besides subtle boiling point and solubility shifts, we know the phenylsulfonylacetic ethyl ester tends to give cleaner reaction profiles with less tendency to transesterify under Lewis acidic or base-promoted conditions. This isn’t a footnote; companies scaling up ADRs or new heterocyclic compounds rely on this property to keep waste counts down.
Some inquiries come from users comparing this ester against unsubstituted ethyl acetic ester or even benzyl protected glycolic esters. We highlight the electron-withdrawing effect of the sulfonyl group, which modifies reactivity compared to more basic esters. For anyone tuning SN2 or enolate chemistry, this shift allows selectivity over competing side reactions and raises the yield ceiling for targeted stepwise syntheses. These are not academic claims; they are borne out in repeated scale-up processes for custom syntheses, from crop protection intermediates to specialty dyes.
We keep detailed process logs in our plant, and transparency with customers is part of our model. Anyone scaling up a transformation knows that trace impurities in esters—especially aromatic-containing esters—can poison Pd and Ni catalysts. We test down to low ppm for possible ring-substituted derivatives, which can otherwise sneak in through secondary side reactions. This often makes the difference in run-to-run selectivity for API or advanced intermediate producers. Our experience points to a need for higher analytical scrutiny in ester manufacture, which we treat as non-negotiable.
We have found, through direct feedback, that customers struggling with stuck reactions or unclear impurity origins often track the issue to raw materials. Phenylsulfonylacetic Acid Ethyl Ester demands a dry, impurity-free process chain, so we built in staged vacuum drying and real-time water analysis at the key points. It is these practical steps, not just analytical claims, that close the gap between theory and what consistently works on the kilo scale.
Some of our repeat customers specialize in building α-sulfonyl carboxylates as starting points for drug candidates. They report that our Phenylsulfonylacetic Acid Ethyl Ester drives downstream yields higher than both methyl and tert-butyl counterparts, especially for multi-step sequences. Due to the sulfonyl group's electron-withdrawing effect, it can stabilize adjacent intermediates, reducing the risk of unexpected decomposition or rearrangement. This helps especially in microwave-assisted runs and batch-to-continuous process transfers.
Users working in fragrance intermediates and agricultural actives use the ester for alkylation protocols, and the clean work-up is a recurring advantage. The ethyl ester’s moderate volatility means less product drag-off during solvent evaporation, keeping recovery rates up and loss factors down. Fragrance producers let us know they are less worried about contamination with trace aromatic aldehydes, due to our closed transfer and packaging system. Again and again, the main point customers stress is consistent input leads to predictable output, and they turn to us because they can trace their problems—or successes—back to the starting materials.
Every production lot is more than a label; it comes with specific numbers, and we never skip a test. Whether it’s IR, NMR, GC, moisture, or melting point, our protocol stacks up experience from previous years and integrates new best practices. We even keep retains from every batch, in case a customer wants to revisit a previous lot’s details. These are not regulatory checkboxes, but habits honed from real-world troubleshooting.
Users in research and scale-up both appreciate direct packaging into HDPE or PTFE units under nitrogen blanket, avoiding unnecessary exposure. Phenylsulfonylacetic Acid Ethyl Ester does not tolerate careless storage; we remind buyers to store in a desiccator or dry room below 25°C. In manufacturing campaigns where one batch can run for weeks, avoiding hydrolysis or color formation is worth the effort. It takes less time and money to prevent a problem than to resolve it mid-run.
The industry leans heavily on experience, and over decades we have matched Phenylsulfonylacetic Acid Ethyl Ester directly against common alternatives. The methyl variant offers higher volatility and easier removal in some reactions, but it often escapes in long-heated runs, leading to lower isolated yields and sometimes introducing a methyl odor to the product. The tert-butyl analog resists acidic conditions, which matters for some syntheses, but its bulkier group slows nucleophilic attack, dragging out reaction times—pinching throughput just when engineers are pushing scale.
In contrast, the ethyl ester strikes a balance: its evaporation rate is moderate so both lab and plant users capture spent solvent easily, and the molecule’s size nestles between speed and stability. Alfa and beta eliminations—problems seen with similar compounds—rarely occur under typical conditions for this product, reducing the risk of downstream polysulfonyl formation or foaming. We built these lessons not from theory but from customer returns and actual troubleshooting alongside chemists, both in-person and over remote support.
Synthetic chemists, especially in medicinal chemistry, count on reliable building blocks. We are often asked if our process enables tracking of origin, batch, and even specific reactor conditions. The reality is, at larger scales, variation sneaks in from solvents and minor thermal swings, so we invest heavily in monitoring and adjust batch protocols to hold tight reproducibility. No customer wants to find a new impurity in an established reaction—changing a single raw material can throw off months of work. User feedback shows that most production upsets stem from unseen shifts in precursor purity, so open lines and rapid response matter to us as much as analytical control.
A lesson we have learned after repeated incidents: a lower-priced ester sourced from an unknown or inconsistent process almost always means more downstream washing, and sometimes, unworkable final product. Our goal is preventing these headaches by staying in the feedback loop. Many formulation facilities, especially in Asia and Europe, note how much time they save by not having to perform additional rework on their incoming esters. This is a cumulative benefit that pays back every single campaign.
As the market evolves, new users bring new questions. We work with both experienced and first-time buyers of Phenylsulfonylacetic Acid Ethyl Ester, and many now require documentation that meets the rising standards for environmental and safety audits. Green chemistry matters, and we invest in scrubber technology and solvent recovery, reducing emissions from our plant. We also support customers with data for process safety—if a user asks for thermal gravimetric analysis, we run it. If there are requests for custom particle size or solvent ratios, we try to adapt within safe and viable production limits.
The push for digitized documentation and supply chain visibility continues to grow. We have moved our tracking systems to electronic batch records; any user who needs certificate reprints or archive information receives it quickly. This isn’t just for accreditation, but to offer the transparency that competitive industries need. As new reaction types develop—continuous flow, photoredox, or new biotransformations—our technical team stays engaged, both as observers and partners.
At the core, making Phenylsulfonylacetic Acid Ethyl Ester comes down to commitment—each batch, customer, and process step matters. We listen to feedback from pharmaceutical, agrochemical, and specialty chemical customers alike, gathering data and experiences to ensure you get a product that does what it says every time. Clean, reproducible, and trusted—this is the foundation that keeps projects on track, from kilo lab to process plant. When you pick a supplier for a critical reagent, the difference between a smooth campaign and an unexpected setback can often be traced back to a maker’s attention and real experience. We stand behind every gram, and we’re ready to help with every run.