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HS Code |
330037 |
| Name | (Ethylthio)acetic acid |
| Cas Number | 3943-89-3 |
| Molecular Formula | C4H8O2S |
| Molecular Weight | 120.17 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 109-110°C (17 mmHg) |
| Melting Point | - |
| Density | 1.12 g/cm³ |
| Solubility | Soluble in water and organic solvents |
| Pka | 3.26 |
| Inchi | InChI=1S/C4H8O2S/c1-2-7-3-4(5)6/h2-3H2,1H3,(H,5,6) |
| Smiles | CCSCC(=O)O |
| Refractive Index | n20/D 1.494 |
| Flash Point | 116°C (closed cup) |
| Odor | Unpleasant, strong |
As an accredited (Ethylthio)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle with secure cap, labeled “(Ethylthio)Acetic Acid, 100g”, hazard symbols, batch number, and handling instructions. |
| Shipping | (Ethylthio)acetic acid must be shipped in tightly sealed, chemically resistant containers. It should be transported in accordance with local and international regulations for hazardous substances. Keep away from incompatible materials, ignition sources, and direct sunlight. Ensure clear labeling and provide a Safety Data Sheet (SDS) during shipping for safe handling and emergency instructions. |
| Storage | (Ethylthio)acetic acid should be stored in a cool, dry, and well-ventilated area. Keep the container tightly closed, away from heat, ignition sources, and incompatible substances such as strong oxidizers. Use corrosion-resistant containers. Label containers clearly and protect them from physical damage. Store away from moisture and direct sunlight. Follow all safety and regulatory guidelines for hazardous chemical storage. |
Applications of (Ethylthio)Acetic Acid in Industrial ManufacturingAs a dedicated manufacturer of (Ethylthio)Acetic Acid, we focus on supporting downstream industries that utilize this specialty intermediate for well-defined technical processes. Our decades of formulation expertise and commitment to direct process integration enable us to supply material that meets stringent requirements in each sector. Below, we outline key real-world industrial application scenarios where (Ethylthio)Acetic Acid delivers value as a raw material in established production streams. 1. Pharmaceutical Intermediate for Thioether-Containing Drug SynthesisMany modern APIs with thioether moieties rely on (Ethylthio)Acetic Acid as a core building block. The compound enters the synthetic sequence at the heterocycle formation or thioalkyl-ethylation step, providing both reactivity and structural control. Production batches demand reproducible quality and compliance, as downstream pharmacopeial analysis scrutinizes both identity and impurity profiles. Manufacturers typically introduce this intermediate under controlled pH and temperature conditions required by multi-step organic synthesis platforms. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisMajor agrochemical producers deploy (Ethylthio)Acetic Acid in the synthesis route for select thioether and thioester-based herbicides and fungicides. Its predictable reactivity and sulfur incorporation make it suited to the multi-step couplings, condensations, or esterifications required for patent-protected crop protection molecules. Precision in input ratio and impurity control is enforced at each stage due to strict national residue regulations on final products. Industry compliance standards
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3. Synthesis of Sulfur-Modified Polymer AdditivesRubber and plastic compounding plants incorporate (Ethylthio)Acetic Acid during the manufacture of sulfur-modified accelerators, antioxidants, and chain transfer agents for elastomers and resins. The ingredient acts as a chain-terminating or flexibility-modifying agent where precise sulfur dosing is required. Typical workflows introduce the material into upstream monomer or pre-polymer blends before finishing or molding stages, ensuring uniform additive distribution and predictable performance in the resultant polymer matrix. Industry compliance standards
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4. Speciality Thioether-Based Corrosion Inhibitors ManufactureProducers of speciality corrosion inhibitors for oilfield, cooling water, and refinery applications require consistent (Ethylthio)Acetic Acid input to synthesize thioether-carboxylate compounds. The acid supplies both the sulfur source and the acetic functional group necessary for targeted metal–surface interactions. Precise metering and reaction control enhance the stability and performance of the downstream inhibitor blends, ensuring adherence to technical standards and environmental discharges. Industry compliance standards
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5. Advanced Organic Synthesis for Laboratory Reagents and Custom ChemicalsSpeciality reagent and custom chemical suppliers source (Ethylthio)Acetic Acid for defined organic transformations, particularly for laboratory-scale syntheses and pilot plant validations where sulfur-alkyl transfer is essential. The compound features in Grignard expansions, nucleophile-initiated substitutions, or as a handle for further derivatization. Quality-sensitive applications scrutinize trace impurities and batch consistency, especially for catalog reagent supply. Industry compliance standards
Typical usage ratio
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As a chemical manufacturer dedicated to synthesis from the molecule up, we’ve watched laboratories and production lines increasingly lean on sulfur-containing building blocks to meet complex synthesis targets. (Ethylthio)Acetic acid has proven itself as a reactive anchor in this space. With our years in the reactors, we’ve seen how the shift toward specialty organosulfur compounds is driven less by catalog wishlists and more by the realities of modern targets. As a manufacturer, the difference lands in every batch, purification, and order shipped: quality isn’t just for the end-user, it starts with us at the ground floor.
At our facility, producing (Ethylthio)acetic acid isn’t about scaling from a dusty protocol. Every lot springs from a line of review, choosing high-purity starting materials—ethanethiol and bromoacetic acid—and driving reactions for full conversion. Through distillation, phase separation, and repeated crystallization, we aim for product that leaves no ambiguity during analytical checks. For many bench chemists and process engineers, this saves hours otherwise lost to unpredictable impurities and batch variation. These steps might look routine, but they lay the groundwork for reproducibility and downstream performance in the hands of a chemist racing against tight deadlines.
Unlike simple analogues, (Ethylthio)acetic acid’s thioether moiety brings a softer nucleophilic pocket to the molecule, differentiating its reactivity profile from mere acetic or mercaptoacetic acid relatives. Chemists looking to introduce ethylthio groups find this acid offers more than a point of attachment—it often enables better solubility in organic media and greater resistance to overoxidation during certain transformations. Compared to raw ethylthiols themselves, the carboxylate functionality tempers volatility and offers a friendlier scent for your team. We know that on the bench, these differences signal less wasted time on side reactions and better downstream yields.
Our batches typically achieve purity above 98%, as confirmed by in-house HPLC and NMR. Melting points cluster reliably within 35-38°C, and we track sulfur and residual solvent content in every lot before release. Our specifications evolve with your process demands. Some users require acetic acid levels below 0.2%, and we have modified recrystallization steps to meet that need without skyrocketing the cost or sacrificing yield. This degree of specificity isn’t just technical fine print—we recognize that when an analytical chemist or synthetic organic group counts on a clean starting point, the consequences ripple through multi-step syntheses, costing weeks if not months if those specs slip.
In over a decade of feedback, we’ve seen requests for (Ethylthio)acetic acid come from diverse corners. Medicinal chemistry teams use it as an intermediate for sulfonamide or thioether linkage development, especially in lead scaffold construction. Agrochemical researchers pursue modified sulfur profiles for pest and weed control agents, counting on stability and fine-tuned reactivity not found with simple thiols. We’ve also watched polymer chemists incorporate (ethylthio) branches to tweak backbone flexibility and UV absorption profiles. Beyond the bench, it serves in pilot plant esterifications, showing good compatibility with both acid chlorides and carbodiimide activation methods.
Many users value the consistent handling properties: compared to volatile alkanethiols, our acid minimizes inhalation risk and forms stable, deliquescent-free salts with most commercial amines. It blends easily with standard organic solvents, enabling one-pot combination with various activating agents, without the thiol oxidation headaches that slow down parallel synthesis or automated library production. These handling improvements are not afterthoughts—they crop up again and again when talking directly with process chemists under GMP conditions. Without the right starting point, the unpredictability multiplies all the way to the end of the run.
Compared with off-the-shelf (ethylthio)acetic acid from non-manufacturing resellers, our material takes a direct route from reactor to drum—each step maintained under our protocols rather than relabeling or blending from disparate sources. We stake our reputation on analytical documentation provided with every delivery: IR, NMR, HPLC, and sulfur analysis. More than one customer has reported chromatographic headaches from non-uniform batches purchased elsewhere, or required reworking after uncharted carbon impurities snowballed in their late-stage reactions. In-house feedback drives us to go beyond technical sheets, fielding calls or emails about your specific routes, troubleshooting why an NMR shift might edge a peak, or helping explore alternate storage solutions to cut moisture uptake.
The advantage of working directly with a synthesis-driven manufacturer manifests in flexibility. Faced with an uptick in requests for deuterium-labeled analogues, we spun up parallel production lines, adapting starting material logistics instead of waiting on long supplier chains. Custom packaging—amber glass or lined drums—met the demands of teams needing multi-kilogram supplies without cross-contamination. Shipping is always coordinated with seasonally appropriate temperature controls because too many years battling heatwaves have taught us not to trust generic carriers with sensitive organosulfur cargo.
Quality in our plant starts with training: our operators and chemists rotate through every phase of synthesis and analytical verification. Each shift logs production data, and deviations prompt immediate review. This isn’t just to satisfy audits—internal yields, sulfur quality, and moisture data feed directly into planning, reducing waste while pushing for cleaner, higher-output runs. We work closely with our analytical development teams, leveraging real-time IR and NMR to spot process drift before it becomes a batch-wide issue.
Repeated scale-up operations have taught us where bottlenecks lurk. Long ago, we encountered issues with ethylthiol purity from regional suppliers, prompting us to insource critical distillations and invest in foulant-resistant glassware. Every modification goes through an impact analysis meeting—often involving both engineering and chemist teams—before reaching the mainline batch sequence. These are not distant supply chain problems but hands-on bottlenecks we clear to give you the reliability you expect when you plan your syntheses months in advance.
Applications for (ethylthio)acetic acid start as simple as thioether alkylations or cross-coupling substrate preparation but rarely remain there. Research users have moved toward direct esterification, benefiting from the acid’s ability to avoid strong odors or polymerization concerns associated with simple thiol routes. Because our batches present defined melting and boiling ranges, users appreciate both the ease of weighing crystalline acid and its predictable response to dissolution or neutralization. No secondary pre-treatments or excessive drying steps slow down workflows, freeing up your lab space for actual chemistry instead of constant batch prepping.
From industrial chemistry contexts, our acid's performance in sulfoxide and sulfone synthesis sets it apart. Close control over sulfur content and silanol byproducts results in streamlined oxidations, allowing teams to push selective functionalization without tripping project timelines. In one long-term project, catalytic teams reported that off-target precipitation—previously blamed on “operator error”—vanished after switching to our higher-purity material. Such case studies come in monthly, reminding us that synthesizing specialty building blocks is more than manufacturing; it’s about how process improvements transfer directly into the resolution of real-world problems.
Demands for green and sustainable reagents continue to shape our manufacturing philosophy. Sulfur-containing components like (ethylthio)acetic acid play vital roles in new, more atom-efficient reactions and renewable matrix development. Our ongoing work explores ways to cut solvent waste and recover side streams for utility reuse, always tracking how tweaks to process parameters affect final customer experience. By focusing on lean process design, we’ve trimmed batch cycle times and reduced excess consumption of throttling agents, passing those cost savings to customers requiring hundreds of kilos for scale-up.
We started re-engineering our synthesis to incorporate biogenic ethylthiols where possible, reducing dependency on traditional hydrocarbon streams. This not only supports ongoing requests from sustainable chemistry teams but strengthens our position against supply volatility. Customers working on bulk agrochemical campaigns or scale-up programs have benefited from early notification of process changes and transparent discussions on risk mitigation. By keeping technical support within our plant, we answer questions on lot consistency or reactivity changes directly, not via a remote chain of customer service scripts.
We built our manufacturing blocks knowing the quirks and hazards of organosulfur compounds. Over the years, we’ve refined containment and transfer methods for hot and cold materials, mitigating release risk through air-locked reactors and multi-stage scrubbers. We enforce not just paper rules but hands-on, daily engagement with safety protocols. Every tanker exit and drum fill is actively supervised and thoroughly logged. Training cycles ensure all onsite staff, new and experienced, understand the irritant profile and handling recommendations of (ethylthio)acetic acid.
We’ve coordinated feedback from transportation partners and end-users to adjust labeling, weight distribution, and loading protocols for safer transfers within the facility and beyond. This doesn’t just satisfy regulatory boxes but addresses the lessons learned from past near-misses and keeps our material flowing to customers on time, minimizing downtime from avoidable hazards. Our monitoring program keeps in close touch with regulatory changes as well, so end users see consistent documentation and labeling during each purchase—making audits smoother for everybody downstream.
Questions often arise about substituting (ethylthio)acetic acid with more common mercaptoacetic or methylthioacetic acids. In our experience, these compounds do not replicate the unique balance of stability and reactivity found in the ethylthio variant. Mercapto group analogues introduce handling difficulties from oxidation and odor, complicating both lab and plant work. Methylthio derivatives offer reduced lipophilicity, sometimes missing the targeted partitioning behavior required in fine chemicals or pharma intermediates. Over a broad range of trials, (ethylthio)acetic acid consistently outperforms others when robust, nucleophilic sulfur atoms are needed for carbon chain elaboration without unwanted cross-linking or byproduct build-up. For those developing new polymers, the ethyl group provides enough bulk to fine-tune material flexibility—something we’ve confirmed with partners prototyping next-generation elastomers.
Our team views product manufacturing not as a static cycle, but as a continuing dialogue—one between those making the chemicals and those applying them amid changing challenges. We see our role as both manufacturer and longtime collaborator, working to supply (ethylthio)acetic acid that advances research and production goals. Regular check-ins with our users drive ongoing improvements: whether it’s a request for higher analytical documentation or specific packaging for large-scale runs, we treat each as a point for direct action. Over years of working directly with teams, we have learned that even small improvements in consistency, documentation, or technical support can mean the difference between a delayed pilot plant run and a product launch.
For us, this approach makes real-world sense. Each year, we audit both the process and the product, incorporating feedback from users ranging from start-up labs to large-scale manufacturers. Adjustments are made immediately—whether to solvent selection, purification, or analytical routine. Staying close to both the chemistry and its end application has helped our plant evolve in tandem with industry shifts. It’s this commitment to continual self-examination and improvement that keeps our batches meeting customer expectations, run after run.
Producing (ethylthio)acetic acid isn’t just about filling an order or achieving a purity threshold. From our perspective at the manufacturing site, the full value comes from understanding how incremental quality improvements surface as real benefits in your work. Each molecule has seen our focus, from drum to bottle, shaped by conversations with those who count on specialty chemical reliability in high-stakes environments. Reliability, hands-on quality control, and deep practical engagement with synthesis needs form the backbone of every shipment we make. Our aim extends beyond specification—delivering (ethylthio)acetic acid as the dependable foundation for the new reactions, products, and discoveries that shape tomorrow’s chemistry.