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HS Code |
128754 |
| Productname | (Phenylthio)Acetic Acid |
| Casnumber | 2141-17-5 |
| Molecularformula | C8H8O2S |
| Molecularweight | 168.22 |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 52-56°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.27 g/cm³ |
| Smiles | C1=CC=C(C=C1)SCC(=O)O |
| Inchi | InChI=1S/C8H8O2S/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10) |
| Synonyms | 2-(Phenylthio)acetic acid |
| Storagetemperature | Store at room temperature |
As an accredited (Phenylthio)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White polyethylene bottle with screw cap, labeled “(Phenylthio)Acetic Acid, 100g.” Includes hazard symbols, batch number, and storage instructions. |
| Shipping | (Phenylthio)acetic acid is typically shipped in tightly sealed containers, protected from moisture and light, and stored in a cool, well-ventilated area. It is classified as a chemical substance and should be handled in accordance with relevant safety and transportation regulations, including proper labeling and documentation to ensure safe and compliant delivery. |
| Storage | (Phenylthio)acetic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible materials such as strong oxidizers. Protect from direct sunlight and excessive heat. Ensure proper labeling and keep the storage area equipped with appropriate spill containment and safety equipment. Handle using appropriate personal protective equipment. |
Applications of (Phenylthio)Acetic Acid in Industrial ManufacturingAs a specialized manufacturer of (Phenylthio)Acetic Acid, we support multiple industrial segments where this compound serves as a critical intermediate. Our expertise covers strict regulatory standards, technical formulation, process integration, and downstream manufacturing for selected application sectors with established market demand. 1. Pharmaceutical Synthesis of Sulfur-Containing IntermediatesMany pharmaceutical manufacturers incorporate (Phenylthio)Acetic Acid in the multistep synthesis of sulfur-bridged heterocycles and advanced intermediates for APIs, especially within cephalosporin and thiazole derivative series. Direct involvement occurs at the formation of specific thioether linkages, where precision in stoichiometry and purity specifications is essential. Acid chloride activation or coupling agents introduce this material during core structure elaboration, optimizing reactivity while meeting batch-to-batch reproducibility. Finished APIs benefit from traceability and robust quality documentation from origin through validated change control. Industry compliance standards
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2. Agrochemical Intermediate for Thioether Pesticide SynthesisAgricultural chemical producers utilize (Phenylthio)Acetic Acid to manufacture key intermediates for selected herbicides, fungicides, and insecticides with thioether functional groups. The raw material serves as a building block at controlled input ratios during the condensation or cyclization of complex active substances. Factory handling ensures non-contamination, accurate dosing, and compliance with maximum residue level (MRL) expectations in finished crop protection agents. Custom synthesis capabilities allow for scale-up with consistent specification adherence to global agrochemical approval processes. Industry compliance standards
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3. Fine Chemical Synthesis for Specialty Polymer AdditivesChemical manufacturers apply (Phenylthio)Acetic Acid in the production of custom polymer additives and specialty modifiers requiring sulfur-functionalized aromatic groups. This raw material enhances cross-linking, improves anti-oxidative properties, and tunes solubility profiles in engineering plastics and elastomer blends. Factory protocols enforce precise dosing and compatibility studies for each customer’s resin matrix. Sulfur incorporation impacts product reinforcement and weathering characteristics, with all process steps documented for traceability and quality system audit trails. Industry compliance standards
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4. Organic Synthesis of Flavors and Fragrances PrecursorsThe flavor and fragrance industry uses (Phenylthio)Acetic Acid for the synthesis of aroma ingredients embodying sulfur-containing aromatic notes. Producers rely on this material for constructing musky, earthy, or savory profiles through thioalkylation reactions or as a stepping stone to aldehydes, ketones, and alcohols relevant to perfumery and food flavors. Processing lines demand strict compliance with food-grade impurity thresholds and transparent chain of custody covering all input lots processed at our certified facilities. Industry compliance standards
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In our years of producing fine and specialty chemicals, few products draw as much consistent attention as (Phenylthio)Acetic Acid. This compound, recognized by chemists for its specific structure—a phenylthio group attached to an acetic acid moiety—arises within organic synthesis routes that call for both adaptability and reliability. From the production line to the laboratory bench, its presence is not a coincidence but the result of deliberate process engineering and quality-driven decision making.
At our facility, (Phenylthio)Acetic Acid emerges from direct synthesis, guided by secure and finely-tuned reaction conditions. We keep our eyes trained on purity, which forms the backbone of any intermediate used downstream in advanced synthesis. Our standard output consistently exceeds 98.5% assay by HPLC, and over the years we have settled on a crystalline powder with a melting point range of 68–71°C. These numbers did not get selected at random. They grew from hands-on batch monitoring and lessons learned when off-spec lots failed users at the bench.
Moisture is a silent adversary, so we aim for water content well below 0.5% by Karl Fischer titration each time. Unwanted contaminants—phenol, acetic acid, sulfur species—are monitored tightly using both GC and NMR profiles. Each batch tells a story as spectral data build our confidence before a drum leaves the warehouse. Our specification sheets do not hide behind generic claims but deliver on these points, because every technical customer asks for them.
Chemists often question whether one arylthioacetic acid differs from another. In practice, subtle variances in precursor choice and reaction control give rise to big differences at the work-up stage. Phenyl group orientation, side-product management, and sulfur handling demand a steady hand. Over time, the reaction of thiophenol with bromoacetic acid has served us best, affording a cleaner product profile than attempts using lower-cost alternatives. This translates directly into fewer downstream chromatographic purifications for our customers. The bottom line: less time and material wasted, tighter yields, and improved reproducibility.
Consistency is not a slogan but a habit. For every lot, we confirm both the S-configuration and acid function by FTIR and x-ray crystallography spot checks. Our process tuning means end-users do not wrestle with off-color oils or unworkable clumps. Real operators know that a trouble-free intermediate lifts whole projects, not just single reactions.
(Phenylthio)Acetic Acid takes part in a surprising range of transformations. Its thioether linkage introduces both flexibility and selectivity to synthetic campaigns. Medicinal and agricultural researchers frequently use it as a building block for more complex molecules. In our history, gram-scale users in pharmaceutical labs value its performance in nucleophilic substitution and peptide coupling. On a larger scale, some agrochemical manufacturers pursue sulfoxide and sulfone derivatives, drawn by the potent biological profiles those groups often manifest.
We field questions each month from scientists aiming for C–S bond formation. They regularly choose this compound over less accessible arylthio analogues because its structure balances reactivity with manageable safety. Labs see sharp yields in both base- and acid-catalyzed conditions, without degradation typical of some aliphatic thioacids. Our regular clients have shared yields exceeding 90% for specific amide coupling reactions, which only happen when starting material maintains high acid and low impurity levels.
Some users attempt to substitute benzylthioacetic acid or other sulfur-bearing acids. These may seem interchangeable, but results in cyclization or cross-coupling steps show that the electron-donating and steric parameters of the phenyl group adjust the reactivity profile in meaningful ways. As actual producers, we have watched academic groups run comparative studies, and data from our own customer feedback confirm that bringing the phenylthio group to the reaction provides more control and selectivity compared to methyl- or benzylthio analogs.
Manufacturing (Phenylthio)Acetic Acid carries real-world hurdles that shape what end-users receive. The strongest influence over finished product quality is not always the purity of feedstock, but how each process phase gets managed. We have learned not to cut corners with raw material standardization, especially thiophenol. Over the years, running parallel batches with off-brand suppliers routinely led to elevated contamination and greater batch-to-batch fluctuation. Maintenance of reactors and careful pH control extend the lifespan of equipment and ensure uniform batch outcomes.
Another concern arises from shipping and storage. The acid absorbs moisture and tends to agglomerate in damp conditions, which makes even a small slip-up at the packaging stage trouble down the line. We once overestimated the reliability of basic fiber drums, and after a series of sticky, difficult-to-handle returns, switched exclusively to lined drums with tested air-tight liners. Customers noticed quality retained over longer periods; these small process decisions give users real confidence, whether working from small containers or bulk orders.
No matter the season, we never simply “stock and ship.” Each shipment sees a final QC check—moisture, acidity, and color index. Small failings at this point cause major disruptions in research and synthesis downstream. By sticking to routines built over decades in the chemical manufacturing business, the consistency of every bottle genuinely supports progress across projects in research, development, or commercial usage.
In manufacturing, accountability does not end with the door to the plant. Feedback loops with laboratories and industrial partners illuminate areas for process improvement we may overlook from our side. By focusing our investigation and support around real synthesis challenges, we contribute more than just a product—we become participants in each client’s research ambition.
Requests come in for custom particle sizing, or for extra-low-odor lots to meet demands from high-purity application. More rigorous demands, such as combined sulfur speciation alongside high purity, force continual reinvestment in both analytical infrastructure and raw material sourcing. This company-wide dedication shows up directly in the material sent out. New applications in asymmetric transformations and sulfur-based catalysis continue to appear; partnerships between manufacturing and research teams multiply the possibilities.
We face requests for technical guidance on disposal, safety, and green chemistry process alternatives. Rather than rely on generic answers, we leverage our experience handling thousands of kilograms and maintaining SOPs developed in real working plants. Our experts address details that only hands-on production teams notice, such as pressure build-up during bulk acidification or specific hazards in large-scale sulfoxide oxidations, offering recommendations rooted in continuous practice, not just literature.
For any research group or production planner, the right intermediate makes or breaks a process. Alternatives to (Phenylthio)Acetic Acid include simpler thioacetic acids and substituted thioesters. Many seem comparable on paper, but several key observations separate our product in actual use.
First, the phenyl ring provides a stabilizing influence, increasing tolerance to oxidizing conditions. Compared to straight-chain thio acids, the risk of over-oxidation to sulfonic acids or simple degradation is lower. Our team has observed higher shelf-life and less olfactory nuisance—a practical win in many facilities. On the catalytic side, reactions needing sulfur transfer or cross-coupling proceed with less catalyst poisoning compared to cheaper methylthio or benzylthio analogs.
Also, solubility profiles diverge meaningfully. (Phenylthio)Acetic Acid dissolves more freely in standard polar organic solvents, and we have followed solvent selection charts based on years supporting medicinal chemistry teams. Attempts to replace it with p-tolylthio or naphthylthioacetic acids often introduce solubility headaches that require tedious reformulations—a point raised repeatedly among scale-up groups.
One cannot overlook safety, either. Lower molecular weight thioacetic acids produce more volatile sulfur compounds and sharper odors during processing, sometimes violating occupational exposure limits. Long experience allows us to warn clients before they run into trouble on the plant floor. By providing not only the product but insights born from repeated scale handling, we reduce scheduling risks and regulatory headaches for both research and production customers.
Environmental oversight has grown sharper for all sulfur-bearing chemicals. As true producers, we manage real-time effluent treatment and waste minimization in all facilities. Stringent audits invite honest evaluation: we have invested in closed transfer lines and in-line scrubbers that lower fugitive emissions far below regulatory triggers. Real compliance comes from practical engineering rather than theoretical promises.
We receive frequent inquiries about REACH and EPA compliance for (Phenylthio)Acetic Acid. Decades in this sector teach that regulatory compliance cannot be retrofitted. Each process innovation goes through an internal evaluation: every alternate solvent, reactant, or process aid gets checked not only for performance but for downstream waste and recycling. As a result, bulk shipments reach clients with documentation linking each drum back to batch records and analytical runs performed at our own facilities, not paperwork recycled from traders.
Disposal and lifecycle analysis matter in this product line. We help clients develop acid neutralization and sulfur recovery techniques based on setups we have run in our own plants—real solutions, not speculative “best practices.” Each advice stems from our knowing how stubborn sulfur residues can be, how they react in waste streams, and how regulators read manifests for elevated organosulfur content.
As chemical manufacturers, we know progress rarely appears in leaps. Instead, it grows from sustained effort and problem-solving at every step. Our work with (Phenylthio)Acetic Acid continues to evolve. Better catalyst systems, process intensification for greener production, and on-demand blending have all been tested in our pilot units. We document each advance, simplify process controls, and pass on the benefits—material reliability, cost savings, and operational insight—to all downstream users.
Recently, pharmaceutical partners have started exploring enantiopure variants of related thioacetic acids. Drawing on established chiral separation capabilities, we have added these options to our portfolio after first ensuring our output could match quality benchmarks without sacrificing throughput or safety. By resolving real-world problems in catalyst loading, by-product isolation, and odor management, this experience ultimately folds back into our work on the core material.
Collaboration remains a constant. Some of our closest partnerships involve screening new analogues designed to take the best of the phenylthio motif into next-generation medicinal chemistry or materials science. Each project draws on our institutional knowledge—chemical handling, process troubleshooting, purification, and regulatory passage. True manufacturing experience means listening as well as planning, adapting as well as sticking with proven protocols.
For chemists and process engineers alike, material reliability often cuts through technical jargon and product claims. As manufacturers, we see every day how careful process control at the source of supply changes the entire downstream experience. (Phenylthio)Acetic Acid shines not from a single technical specification but from a legacy of hands-on chemistry, investigative spirit, and thoughtful production. Whether enabling a key step in a complex synthesis or supporting production-scale transformations, it deserves attention not simply for what it is, but for what it allows capable teams to achieve.
Each drum, each bottle, each gram carries forward a set of choices—raw material selection, process discipline, environmental stewardship, customer support—baked in over thousands of hours of work. From new drug scaffolds to advanced materials, and from pilot lines to laboratory tests, (Phenylthio)Acetic Acid provides tools to accomplish more, with fewer disruptions and sharper results. That story drives every batch out of our plant and into the hands of chemists who make tomorrow’s progress.