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Ethyl Chlorothionoformate

    • Product Name Ethyl Chlorothionoformate
    • Alias Ethyl chlorothioformate
    • Einecs 218-946-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    543477

    Chemical Name Ethyl Chlorothionoformate
    Cas Number 541-41-2
    Molecular Formula C3H5ClOS
    Molecular Weight 124.59 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 144-146 °C
    Density 1.28 g/cm³ at 20 °C
    Melting Point -50 °C
    Refractive Index 1.538–1.540
    Flash Point 51 °C (closed cup)
    Solubility Decomposes in water
    Vapor Pressure 4 mm Hg at 20 °C

    As an accredited Ethyl Chlorothionoformate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl Chlorothionoformate, 100g: Supplied in a tightly sealed amber glass bottle with a hazard-labeled, chemical-resistant screw cap for safety.
    Shipping Ethyl Chlorothionoformate should be shipped in tightly sealed containers, protected from moisture and incompatible materials. Transport in accordance with local, national, and international regulations for hazardous chemicals. Proper labeling, documentation, and segregation from acids and oxidizers are essential. Handle with protective equipment due to its toxic and potentially corrosive properties.
    Storage Ethyl Chlorothionoformate should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, well-ventilated, designated chemical storage area, separate from incompatible substances such as strong bases, oxidizers, and acids. Ensure proper labeling and access control, and store away from sources of ignition, as the chemical is flammable and potentially hazardous.
    Application of Ethyl Chlorothionoformate

    Applications of Ethyl Chlorothionoformate in Industrial Manufacturing

    Ethyl Chlorothionoformate serves key roles in specialized chemical manufacturing. As an experienced chemical raw material producer, we support our partners in pharmaceuticals, crop protection, and advanced material synthesis through precise supply and process control. Explore several industrial scenarios where our material drives advanced product development.

    1. Pharmaceutical Intermediate Synthesis for Thiocarbamate APIs

    Major pharmaceutical manufacturers rely on Ethyl Chlorothionoformate to introduce sulfur-containing groups when synthesizing thiocarbamate-based active pharmaceutical ingredients. The material acts as a core thiocarbonylating agent in producing antihypertensive, vasodilating, or anti-inflammatory drugs where sulfur functionality is critical for activity. Processing lines use it in direct transformation stages, ensuring reaction completeness as required by regulated quality metrics for finished APIs.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Part 210/211, US FDA)
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) monographs
    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • REACH Regulation (EC) No 1907/2006 for handling and registration

    Typical usage ratio

    • 0.9–1.15 molar equivalents versus substrate, with the range adjusted per targeted API structure and impurity profile requirements

    Downstream process integration

    • Charged as a key reagent during thiocarbamate group introduction in the main reactor, usually at stage 2–3 of multi-step API synthesis

    Final product types

    • Antihypertensive agents (e.g., methylthiocarbamates)
    • Sulfur-based vasodilators
    • Thiocarbamate anti-inflammatory actives
    • Prodrug intermediates containing sulfur functionalities

    2. Crop Protection Synthesis: Carbamate Pesticide Manufacturing

    Agrichemical formulators employ Ethyl Chlorothionoformate for introducing thionoester and thiocarbamate functionalities into key classes of crop protection agents. It reacts efficiently with amines or phenols during manufacture of selective herbicides and fungicides. Its purity, reactivity, and controlled addition help downstream partners meet strict environmental and safety requirements for finished pesticide formulation plants.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Plant Protection Products Regulation No 1107/2009
    • ISO 9001 Quality Management for agrochemical manufacturing
    • China National Standard GB 20690 Agrochemicals Technical Material

    Typical usage ratio

    • 1.0–1.2 molar equivalents, tuned according to the desired thiono structure and product yield objectives; real-time process monitoring recommended for safety

    Downstream process integration

    • Introduced after condensation or amidation steps in batch reactors producing intermediate thionoesters, just before neutralization and crystallization of technical pesticides

    Final product types

    • Phenylthiocarbamate herbicides (e.g., molinate intermediates)
    • Thionoester fungicide precursors
    • Certain nematicide actives
    • Intermediate thionocarbamate agrochemical raw materials

    3. Synthesis of Thiophosphate Ester Additives for Lubricants

    Lubricant additive manufacturers value Ethyl Chlorothionoformate in the synthesis of advanced thiophosphate ester antiwear agents. The chemical introduces precisely controlled thiono moieties to organophosphorus compounds, which later undergo downstream blending into finished base oils. Consistency and batch purity support compliance with automotive and industrial lubricant standards.

    Industry compliance standards

    • ASTM D4951 for additive element content analysis
    • API Engine Oil Licensing and Certification System (EOLCS)
    • REACH registration for lubricant additives in the EU
    • ISO 9001:2015 Quality Management Systems for specialty chemicals

    Typical usage ratio

    • 0.8–1.1 molar equivalents versus phosphorus donor, optimized for antiwear property and sulfur integration

    Downstream process integration

    • Employed after phosphorization, at the thionation stage in the reactor before neutralization and blending into additive concentrates

    Final product types

    • Thiodiphosphate antiwear additives
    • EP lubricating oil packages for automotive engines
    • Industrial gear oil additive concentrates
    • Hydraulic fluid thiol esters

    4. Synthesis of Thiocarbamate Polymer Stabilizers

    Polymer processing industries utilize Ethyl Chlorothionoformate as a sulfur donor for production of thiocarbamate stabilizers that prevent thermal and UV degradation in manufacturing polyolefins and synthetic rubbers. The raw material directly reacts with precursor amines under controlled plant conditions. The resulting stabilizers are critical for maintaining long-term material properties and compliance with product safety standards.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 on plastic food contact materials for stabilizers
    • US FDA 21 CFR §177 for indirect food additives in polymers
    • ISO 9001 Quality Management for polymer stabilizer production
    • GB 4806.7–2016 for food contact polymers in China

    Typical usage ratio

    • 0.95–1.05 molar equivalents per amine reactant, customized per stabilizer molecular structure and regulatory extractables limits

    Downstream process integration

    • Fed into jacketed kettle reactors during thiocarbamate group formation, just prior to isolation and drying of stabilizer compounds

    Final product types

    • Thiocarbamate polymer stabilizer additives
    • Masterbatches for polyethylene and polypropylene grades
    • Stabilizer systems for synthetic rubber compounds
    • Food packaging polymers with enhanced shelf life

    5. Fine Chemicals: Synthesis of Sulfur Reagents for Analytical Use

    Producers of analytical reagents and specialty fine chemicals apply Ethyl Chlorothionoformate when manufacturing sulfur-based derivatization agents. These reagents function in HPLC and GC sample preparation for trace analysis of pharmaceuticals and food residues. Our strict QC protocols and transparent batch tracking enable our fine chemical partners to consistently meet documentation and purity norms specified by end users in regulated analytical testing labs.

    Industry compliance standards

    • ISO 17034 for reference material production
    • ISO/IEC 17025 for analytical laboratory accreditation
    • ICH Q3D Elemental Impurities Guideline for reagent purity
    • USP General Chapter <1225> Validation of Compendial Procedures

    Typical usage ratio

    • 0.90–1.00 molar equivalents, optimized according to target derivatization strategy and analytical chromatographic requirements

    Downstream process integration

    • Added during sulfurating step after main reagent skeleton synthesis, followed by purification and crystallization

    Final product types

    • HPLC and GC derivatization sulfur reagents
    • Chromatographic reference standards with sulfur moieties
    • Calibration compounds for residue analysis
    • Fine chemicals for laboratory testing protocols
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    Certification & Compliance
    More Introduction

    Ethyl Chlorothionoformate: A Closer Look from the Perspective of a Producer

    Introduction

    Ethyl chlorothionoformate stands out among the thionoformate family. As the producer, my hands have measured, distilled, tested, and shipped countless batches of this compound. Over the years, we have earned a practical understanding of its quirks and specific demands from chemists in synthesis labs to process engineers in dye intermediates — a perspective that carries more weight than any product sheet or technical data can offer.

    Product Overview and Model

    We manufacture ethyl chlorothionoformate under the recognized CAS number 541-41-3, delivering it at a standard purity suitable for sensitive organic reactions. The clear to pale yellow liquid tells much about its chemical story. The thionochloro group in its backbone offers a path to reactive intermediates rarely matched by its oxygen-based analogs. This molecular detail shapes its role in the wider chemical industry, but also the close care needed in its quality control.

    Some users recognize it as ethoxythiocarbonyl chloride. Others mark its utility for its unique reactivity in introducing thiocarbonyl functionalities. The physical behavior — a boiling point around 137–139°C and a distinct, penetrating odor — is familiar territory for anyone who has handled related thiochemicals. Across our batches, consistency in composition remains a direct result of refined production methods. That consistency drives confidence in day-to-day lab and plant procedures.

    Applications and Utility

    Ethyl chlorothionoformate rarely ends up in a bottle for long. The bulk of orders head towards uses in agrochemical synthesis, pharmaceutical intermediates, specialty dyes, and custom polymers. In the development of herbicides and pesticides, demand for high-purity thionoformates usually means strict specifications. Our experience shows that contamination with oxygen analog impurities can lead to noticeable drop-off in downstream yields—feedback from years of back-and-forth dialogue with process chemists.

    In pharmaceuticals, it has earned its value by helping to introduce thiono functionalities in sensitive drug intermediates. The quirks of these reactions often demand strict temperature and moisture controls — lessons learned not from textbooks, but from batches that did not crystallize or side products significant enough to send partners searching for alternatives. These subtle cues shape how we handle raw material selection, distillation temperatures, and final packaging.

    Dye intermediates benefit from its sulfur moiety. We see orders most frequently from manufacturers looking to create sulfur-containing coloring agents or to functionalize aromatic groups via thiocarbonylation—a process where minor changes in residual moisture or acidity in the starting thionoformate can alter color fastness and intensity. Batch-to-batch repeatability carries real process impact.

    Distinguishing Ethyl Chlorothionoformate from Other Chemicals

    Not every chlorothionoformate is built the same. Ethyl chlorothionoformate offers unique reactivity absent in its methyl or iso-propyl cousins. Industrial chemists and academic researchers have called out clear differences. The ethyl group confers a balance between volatility and manageability—a midpoint for those who want active thionoformyl chloride functionality yet need handling safety and lower risk of premature decomposition.

    Comparisons with ethyl chloroformate reveal the specific value of sulfur. In the lab and plant, the oxygen analog reacts more rapidly with bases or nucleophiles, generally offering greater stability during storage but less selectivity for reactions enriching thiocarbonyls. Pharmaceutical process teams, after running both compounds, often note the cleaner conversions with thionoformate when aiming for thionoester intermediates. In effect, the sulfur atom offers a point of synthetic versatility absent in standard organic carbonates or formates.

    Challenges and Responsibility in Production

    Producing a chemical with reactive chlorine and a sulfur group never runs routine. Moisture control defines success. Chlorothionoformates decompose readily with water, liberating corrosive gases. Decades of hands-on experience working with drying columns, inert gas blanketing, and sealed glassware speak to this chemical’s demanding nature. Our focus on dedicated systems and trained specialists grew not from regulatory pressure alone, but from real-life incidents, leaks, and near-misses during tank transfers or material sampling.

    Transport also carries its risks. The thionochloro moiety’s reactivity requires tight control during packaging—high-integrity containers, nitrogen purging, and close inspection for any corrosion on storage vessels. As a producer, we do not take a backseat through logistics; we’ve had situations where a brief storage in sub-optimal tanks led to clumped product or traces of decomposition, risking both performance and safety for the next user down the line.

    Handling also raises personal protective expectations. Unlike with more forgiving carbonates, the slightest exposure of ethyl chlorothionoformate to skin or eyes creates immediate, serious discomfort. Process personnel are experienced in double-checking gasket seals, wearing face shields, and running station ventilation. Our team’s repetitive, daily discipline ensures the compound moves from tank to tube with minimal risk to health or the environment. Periodic refresher courses and gradual skill development among new technicians come less from compliance paperwork than from the stories of seasoned handlers who have experienced splashes, unexpected fumes, or small containment failures.

    Quality Matters: From Raw Material to End Use

    Control over starting materials and every processing stage separates the reliable from the unpredictable. Our technicians track not only the purity of phosgene and ethanol feeds but also the order and rate of reagent addition. Variations, even at tenths-of-a-degree in feed temperature, can shift yields and introduce side products. Years ago, we learned that batch tracking and sample retention make the difference between fast troubleshooting and prolonged downtime if a customer flags a failed conversion.

    Product quality ultimately determines application performance. Many customers have invested in ethyl chlorothionoformate only to face frustration with batches bought from intermediaries or poorly controlled sources, where unknown byproducts compromise process yields. Our own on-site analysis, with GC and NMR checks at every scale-up, proved less costly in lost business and customer support time. Chemists in our network have given feedback on how removing even marginal amounts of methyl analog contaminant improved their synthetic steps and final product properties.

    Industry Shifts and Customer Expectations

    The market for specialty organosulfur chemicals changes as buyer expectations shift. Over the past decade, we have witnessed a move from commodity standards to tailored specifications. Gone are the days where meeting a generic "purity above 98%" label satisfied key pharmaceutical or agrochemical developers. Instead, users now request detailed impurity profiles and batch-by-batch certification of absence for particular residuals, often driven by regulatory filings or formulation troubleshooting.

    This heightened scrutiny has forced us to invest in better analytical equipment, rigorous SOP updates, and ongoing training. We have also built more collaborative working relationships with formulation chemists and process engineers. Open communication eliminates guesswork and raises early warning signs when trend deviations appear in GC spectra, color, or odor. Each successful adoption of ethyl chlorothionoformate in a larger downstream process adds to collective knowledge and helps us refine production approaches.

    We have seen increased emphasis on container traceability and tamper evidence. What could once pass with a generic drum or carboy now earns inspection for seal integrity, shrink-banding, and serialized labeling. Our shift to container-specific batch coding arose from direct customer concerns about contamination or switching errors between similar-looking thionocarbonyl reagents.

    Environmental and Regulatory Considerations

    Regulatory expectations around thionoformates never stand still. Production and storage raise environmental concerns, especially around volatile organic emissions and waste management. Direct experience with local and international chemical control authorities shapes how we engineer plant floors, update vent scrubbing, and handle bulk container cleaning. Minor slip-ups in neutralization or off-gas containment have lasting community impact and open the door to fines or process interruptions.

    Waste minimization and byproduct recycling become practical concerns, not abstract ideals. Residual ethanol, spent washes, and degraded product streams form part of a closed-cycle approach aimed at keeping sulfur and chlorine impact out of wastewater. Re-evaluations with every major inspector visit highlight opportunities for process tightening, from in-line removal of volatile acids to regular maintenance of bulk storage tanks.

    Producer’s Insights on Safe and Strategic Use

    Having seen ethyl chlorothionoformate applied across thousands of kilograms and dozens of industries, I have developed a healthy respect for the compound’s power and pitfalls. In technical collaborations with research labs and commercial-scale syntheses, we find that early and honest discussion about intent and capabilities benefits both sides more than generic datasheet circulation. Sharing first-hand lessons about handling, troubleshooting reactivity, and waste stream management often prevents unnecessary scale-up failures.

    We urge users to treat this chemical with the respect reserved for hazardous, high-value intermediates. No shortcut in storage or disposal pays off long-term. The best results, both in yield and safety, arise from careful material transfer, rigorous exclusion of moisture, and clear plans for handling accidental releases. Over the years, customer site visits revealed strong linkage between preparation, staff training, and clean, uneventful syntheses.

    Ongoing Development and Future Opportunities

    Opportunities for innovation in thionochlorocarbonyl chemistry remain strong. We have explored pathways for stabilizing ethyl chlorothionoformate against atmospheric degradation, allowing for broader geographic reach without compromising quality. Development programs aim at improving tank and drum coatings to limit trace iron or zinc leaching, which can catalyze decomposition or introduce color bodies in customer products.

    Collaborative work with pharmaceutical innovators led us to experiment with modified delivery systems, such as ampoules or pre-charged cartridges, to cut down point-of-use exposure and improve dosing accuracy. These technical pathways grew out of direct user requests, not abstract market studies. Sometimes, the most valuable feedback comes from a plant engineer pointing out a specific problem, like a slow-reacting valve or inconsistent pour, rather than from formalized surveys.

    Greener chemistry also emerges as a formidable goal. Alternative routes for its synthesis, potentially using less hazardous thionating agents or reduced phosgene equivalents, receive close attention in our R&D group. The producer’s voice adds practical data to these efforts—balancing theoretical "green metrics" with the real needs for reliability, cost, and downstream compatibility.

    Building on Experience: Producer’s Perspective

    Working with ethyl chlorothionoformate never becomes routine. Each batch turns up a new detail to watch: subtle shifts in odor, a trace of color, even a slightly different viscosity due to atmospheric pressure or seasonal humidity. It is this day-to-day attention to nuance that separates informed producers from those working on speculation. We have turned missed yields, minor upsets, and customer feedback into constant improvement in both process and product.

    As a chemical manufacturer, I maintain a direct stake in every liter produced. The integrity of each batch impacts not just our business partners, but also everyone downstream who depends on results. Years of hands-on work with ethyl chlorothionoformate taught us the value of discipline, transparency, and continuous innovation. Our best successes come from shared experience, open dialogue, and a willingness to adapt when science and customers set new challenges.