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HS Code |
577725 |
| Productname | (4-Fluorophenylthio)acetic acid |
| Casnumber | 2122-57-4 |
| Molecularformula | C8H7FO2S |
| Molecularweight | 186.21 |
| Appearance | White to off-white solid |
| Meltingpoint | 90-93°C |
| Boilingpoint | 346.7°C at 760 mmHg |
| Solubility | Slightly soluble in water |
| Purity | Typically >98% |
| Storagetemperature | 2-8°C |
| Smiles | FC1=CC=C(C=C1)SCC(=O)O |
| Inchikey | QODOUIMGAYHDLF-UHFFFAOYSA-N |
As an accredited (4-Fluorophenylthio)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of (4-Fluorophenylthio)acetic acid supplied in a clear, sealed glass bottle with a tamper-evident label and hazard markings. |
| Shipping | (4-Fluorophenylthio)acetic acid is typically shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous chemical, following all local, national, and international regulations. The container is clearly labeled and packed with absorbent material, ensuring safe transport and minimizing risk of leaks, spills, or contamination. |
| Storage | (4-Fluorophenylthio)acetic acid should be stored in a tightly sealed container, away from direct sunlight, heat sources, and moisture. Keep it in a cool, dry, well-ventilated area, preferably at room temperature (15–25°C). Ensure it is isolated from incompatible substances such as strong oxidizers and bases. Properly label the container and follow all relevant safety and regulatory guidelines. |
Applications of (4-Fluorophenylthio)Acetic Acid in Industrial Manufacturing(4-Fluorophenylthio)Acetic Acid serves as a critical intermediate for several highly specialized downstream industries. As an established producer of this compound, we supply it for advanced synthesis operations where traceability, regulatory alignment, and precise process parameters are fundamental to ensure efficiency and compliance. Below, we have outlined major application scenarios supported by actual market demand, specifying relevant standards, addition rates, how the material fits into downstream workflows, and the finished products our clients are manufacturing with this raw material. 1. Pharmaceutical Intermediate for Thioether-Containing API SynthesisIn the pharmaceutical sector, (4-Fluorophenylthio)Acetic Acid acts as a building block for several fluorinated and thioether-linked active pharmaceutical ingredients, most notably within the synthesis of central nervous system targeting molecules and certain anti-inflammatory compounds. Production takes place within controlled environments, emphasizing traceable sourcing, solvent management, and GMP batch documentation to support global regulatory submissions. Industry compliance standards
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2. Crop Protection Active Ingredient Synthesis (Herbicides and Fungicides)Agricultural chemical manufacturers use this material as a key intermediate when developing new-generation thioether and fluorinated agrochemical actives. Typical integration occurs during the stepwise assembly of highly substituted aromatic rings, where stringent impurity control and batch traceability underpin compliance for international regulatory submissions. Industry compliance standards
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3. Custom Synthesis for Advanced Polymer AdditivesSpecialty polymer formulators incorporate (4-Fluorophenylthio)Acetic Acid as a functionalizing agent for high-performance engineering plastics, imparting tailored polarity and hydrophobicity. This compound is especially valued in the manufacturing of fluorinated aromatic thioether monomers, which enhance final polymer resistance to thermal degradation and aggressive solvents in automotive, electronics, and aerospace components. Industry compliance standards
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4. Synthesis of Specialty Organic Dyes for Industrial CoatingsDye manufacturers leverage (4-Fluorophenylthio)Acetic Acid in constructing complex aromatic scaffolds used in high-end, weather-resistant coatings. This functional group plays a role in improving dye-substrate affinity, UV stability, and overall fastness. Assurance of raw material traceability and consistent isomeric purity is essential during regulatory review for the automotive and industrial paint sectors. Industry compliance standards
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Over several years of manufacturing specialized aromatic acids, (4-Fluorophenylthio)acetic acid has earned its own place on our production line. The choice to make this compound started with growing demand among researchers and process chemists, who kept looking for robust intermediates in the field of pharmaceutical and agrochemical synthesis. From raw materials to storage, each batch speaks to the discipline behind its precise assembly and consistent delivery.
Our process for (4-Fluorophenylthio)acetic acid follows a route tailored for high-purity yield and batch-to-batch consistency. Structural isomers and analogs have a habit of sneaking into similar reactions, but tight controls and real-time monitoring keep the product on spec. Typical production involves introducing a 4-fluorothiophenol component to an acetic acid backbone under anhydrous conditions, using quality-controlled reagents. Every step allows for real verification—most notably, the final material runs through high-performance liquid chromatography and NMR analysis. Purity generally reaches beyond 98 percent. During packing, careful attention eliminates trace contaminants and preserves the free-flowing crystalline appearance. The experience of multiple campaigns has refined points like solvent removal, crystal washing, and optimal drying, so each container shows the bright white solid our clients expect.
The formula, C8H7FO2S, gives (4-Fluorophenylthio)acetic acid its modest weight and efficient handling profile. Its molecular weight stands at 186.21 g/mol. The dominant feature is the para-fluorine—an atom that can quietly shift the acid’s reactivity and make it more predictable when entering coupling or substitution reactions. Melting point typically ranges from 92°C to 95°C under normal laboratory testing. This property influences storage: keeping the product cool and sealed in moisture-free conditions extends its shelf life and preserves its reactivity. Our customers rely on reproducible physical characteristics for ease of weighing, solution preparation, and downstream formulation. By recognizing trends in how these specifications interact with manufacturing or bench-scale operations, we help minimize wasted steps and material loss.
Chemists will recognize (4-Fluorophenylthio)acetic acid as an intermediate, but over time, its value has shown up in more than narrow specialty work. The most direct use sits in the synthesis of complex building blocks for pharmaceuticals. That subtle fluorine in the para position helps dial in the electronic properties needed for forming carbon-sulfur bonds, especially in aromatic substitution and metal-catalyzed pathways. The extra electron-withdrawing influence modulates both acidity and sulfur nucleophilicity, making the compound a predictable participant in acylation and alkylation procedures.
Large-scale clients in crop protection research point out the acid’s convenience when building new sulfoxides, sulfones, or thioethers. The 4-fluoro handle doesn’t just alter reactivity—it protects the aromatic ring from unwanted side reactions under some oxidizing or reducing conditions. In a handful of custom syntheses, the product has functioned as a stand-in for phenylthioacetic acid, but with tighter control over metabolic or environmental fate. Teams with medicinal research experience have shown greater yield and selectivity when integrating this fluorinated acid, compared to non-fluorinated analogs. Research publications frequently cite its application in new molecule scaffolds for kinase inhibitors, anti-infective agents, or herbicide leads.
The main distinction begins with the para-fluorine atom. On first glance, it sounds like a modest adjustment, but the effects ripple through every aspect of performance. Comparable compounds—like phenylthioacetic acid or variants with ortho/meta fluorination—behave differently under representative conditions. Adding fluorine at the para site subtly increases resistance to acid-base hydrolysis, changes solubility in organic solvents, and in many medicinal chemistry projects, boosts metabolic stability. During one customer’s process review, switching in the 4-fluoro variant reduced side reactions and cleaned up the chromatographic profile of their target intermediate. That kind of feedback highlights the practical payoff of what, structurally, appears a modest change.
In terms of synthetic flexibility, (4-Fluorophenylthio)acetic acid handles well in both nucleophilic and electrophilic transformations. In the hands of skilled process chemists, its characteristics open doors to reactions that might stall or foul using less tailored analogs. Specific projects—like Suzuki coupling or construction of heterocyclic cores—demand high selectivity and reproducibility, and the para-fluoro motif delivers. The acid’s melting point and solid form simplify both manual and automated dosing, something a few bulkier or less stable isomers cannot claim. Whether in parallel synthesis for drug discovery libraries or longer campaign runs, these differences shrink troubleshooting and speed up scale-up phases.
Over numerous batches, the lesson holds: one-off specification is never enough. Manufacturing (4-Fluorophenylthio)acetic acid needs discipline at every stage. The most common challenge during scale-up turns out to be the formation of regioisomeric byproducts, especially if feedstock purity or reaction kinetics drift slightly. Temperature control, nitrogen purging, and solvent quality make or break selectivity. Our team’s experience underlines why analytical checks at mid-points—not just at the end—pay dividends in process reliability. Some newcomers to fine chemical production underestimate how quickly downstream issues accumulate from minor upstream lapses. More than once, tracing a problem in a customer’s lab experiment led back to a trace impurity or mixed melting range in the starting material.
Even experienced hands face the temptation to rush crystallization or reduce drying time, both of which risk leaving latent solvent or mixed-phase material that can alter performance in later steps. By sticking to refined protocols, the line between a reliable compound and an unreliable batch stays clear. This reliability supports partners who need certainty from run to run: weight measurements, solution stability, and reactivity each reflect how tightly production parameters stay within limits. Waste minimization and solvent recycling also depend on these standards, so the discipline applies both for quality and environmental stewardship. Creating habits around monitoring has shown its value when unexpected deviations show up—quick intervention saves whole lots from falling out of spec.
We hear repeatedly from research teams and scale-up engineers about the headaches that come from unreliable supply. Shortages of key intermediates can halt promising projects. In the early days of supplying (4-Fluorophenylthio)acetic acid, bulk customers would flag issues—occasional off-smells, drifting melting points, inconsistent flow. In response, our production team examined each complaint by tracing it directly through the workflow: starting material tests, intermediate QC, packing checks. Often, unexpected issues stemmed from small lapses rather than major failures—slight over-drying, pressure swings during solvent removal, or inconsistencies in filtration media. Over time, tightening these details has cut defects and given end users confidence that their batches translate smoothly from one container to the next.
This responsiveness has shaped both our process and the relationship with professional buyers. Working closely with technical staff—not just procurement channels—makes it easier to spot potential problems early. One direct result has been increased transparency: more detailed batch records, more robust sample retention, and openness when discussing true shelf life or potential off-characteristics. Customer trust builds on experience, and that includes dealing honestly with gray areas: explaining why a rare off-smell might turn up, or why a delivered melting point falls at the lower end of the range. This feedback loop strengthens both the product and the production team, making future manufacturing cycles smoother.
(4-Fluorophenylthio)acetic acid does more than fill a line on a catalog. Its production reflects the collaboration between process know-how and real-world research needs. The journey from first flask to reliable multi-kilogram orders mirrors the shifts in modern organic synthesis, where unique substitutions and targeted modifications create genuine advances. We watch with interest as our product appears in new literature: scientists use it to construct ligands for emerging catalysts, or as a controlled substrate in the design of light-sensitive probes.
Companies developing diagnostic reagents and biotech products remind us that marginal gains in raw material consistency and availability shape their commercial prospects. Their pilot runs need the same reliability as a full-scale launch. Working upstream means we think about risks ahead of time: packaging robust enough for long sea transit, batch labeling that tracks lot histories clear back to first synthesis, document support for regulatory dossiers when requested. The long arc of this support is grounded in viewing each batch as an asset, not just a commodity. Through open channels and practical solutions, problems rarely fester into production or supply bottlenecks.
One repeated point from customer feedback involves handling and solution preparation. The tendency of fine crystalline solids to clump after extended storage has led to small but meaningful process quirks. Adopting upgraded anti-caking liners and revised air-drying cycles improved pourability without additives that could foul sensitive reactions. Regular audits confirm that even with variable ambient humidity, the product remains easy to manage both at the bench and in scale-up scenarios. Training with external partners reinforces safe storage practices and shares best-in-field practice for opening, measuring, and re-sealing bulk containers.
In research settings, clarity on solubility parameters matters. (4-Fluorophenylthio)acetic acid shows reliable solubility in common polar aprotic solvents. Chemists favor this predictability, as it lets them program sequential reactions or automate stages in exploratory synthesis. Fine control over purity and water content means downstream yields are more likely to hit their marks. Carrying out regular stability assays under light, heat, and moisture stress conditions, we update recommendations to reflect real changes in product performance—avoiding overpromises and keeping surprises to a minimum. Spot checks and root cause analysis stay part of the operational toolkit, even after long strings of trouble-free batches. That discipline stands out, especially for clients whose regulatory requirements or traceability needs sit at a higher standard.
Industry always offers alternatives. Direct substitutions for (4-Fluorophenylthio)acetic acid often include non-fluorinated analogs like phenylthioacetic acid or other ring-substituted variants. Yet, these choices rarely match its blend of reactivity, purity, and reproducibility. Detailed comparative tests run at customer sites point to incremental—but meaningful—improvements in yield, stability, and downstream performance. The 4-fluoro effect proves its worth in situations demanding rigorous analytical outcomes, tighter control of metabolism, or higher selectivity. Engineering teams working to reduce side product formation or improve crystallization outcomes appreciate this difference even more during late-stage process development or scale transfer.
For users shifting from non-fluorinated precursors, the transition typically brings a welcome reduction in purification steps. Analytical teams report sharper NMR and LC-MS signals. Downtime drops, and campaign runs move with fewer interruptions. Where substitution does not fit—projects needing other ring electronics or avoiding halogens—we offer honest guidance and technical support for alternatives. It strengthens trust and reduces mismatched expectations, saving everyone time and resources. As the chemical landscape broadens, the core lesson holds: investment in technical clarity and product consistency pays off best when customers shape their synthesis in partnership with the manufacturer.
The field never stands still. Although our current specification and handling regime serves most users well, the push for better green chemistry, reduced waste, and safer transport shapes ongoing improvements. Packaging shifts toward recycle-friendly and lower-impact materials to align with new supply chain standards. We continue to monitor emissions from synthesis—especially solvents and byproducts—looking for economies and new routes that trim environmental load. Piloting microreactor and continuous flow processes for (4-Fluorophenylthio)acetic acid, we watch for efficiencies that will feed back benefits in delivery times, carbon footprint, and cost per kilo.
As synthesis sophistication grows, so does the importance of digitally tracking each lot from start to finish. We back each shipment with digital batch records accessible to audited users, so process engineers and regulatory teams can reference exactly the data points they need. This new transparency supports moves into controlled sectors, such as regulated pharmaceutical development or factory-scale supply for large molecule manufacturing. Detailed COA packages and lifecycle documentation are standard, not add-ons, supporting our customers’ upward drive for quality, transparency, and compliance. Every step in design, production, and delivery leans into demonstrated experience, technical agility, and respect for evolving industry standards.
The role of (4-Fluorophenylthio)acetic acid underscores the evolving demands in discovery science, custom manufacturing, and commercial-scale operations. Years of investment in its reliable, reproducible production pays off for research labs and manufacturing floors alike. Clean process chemistry, transparent communication, and technical flexibility run together through each campaign. Clients expect more than just compound delivery—they expect relational support, strong documentation, and honest guidance when process needs shift. Each improvement in quality or service comes from listening closely to the people using these products at the bench and in the plant. Our commitment stands: shape the chemistry, grow with the science, and build partnerships that last.