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Cis-2,3-Dimethylthiirane

    • Product Name Cis-2,3-Dimethylthiirane
    • Alias cis-2,3-Dimethylethylene sulfide
    • Einecs 697-029-5
    • 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

    953977

    compound_name Cis-2,3-Dimethylthiirane
    molecular_formula C4H8S
    molecular_weight 88.17 g/mol
    CAS_number 17048-25-6
    appearance Colorless liquid
    density 0.918 g/cm³
    boiling_point 86-88°C
    melting_point -61°C
    refractive_index 1.474
    solubility_in_water Insoluble
    flash_point 11°C
    SMILES CC1SC1C
    PubChem_CID 5310545

    As an accredited Cis-2,3-Dimethylthiirane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Cis-2,3-Dimethylthiirane is supplied in a 25 mL amber glass bottle, tightly sealed, labeled with hazard warnings and chemical details.
    Shipping Cis-2,3-Dimethylthiirane should be shipped in tightly sealed containers, protected from light, moisture, and heat. Transport in compliance with local, national, and international regulations for hazardous chemicals. Use secondary containment to avoid spills. Handle with care, utilizing appropriate personal protective equipment, and ensure clear labeling for proper identification and hazard communication.
    Storage Cis-2,3-Dimethylthiirane should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, and well-ventilated place away from sources of ignition, strong acids, bases, and oxidizing agents. Store away from direct sunlight and heat, in a designated chemical storage area suitable for volatile organosulfur compounds.
    Application of Cis-2,3-Dimethylthiirane

    Applications of Cis-2,3-Dimethylthiirane in Industrial Manufacturing

    As the direct manufacturer of Cis-2,3-Dimethylthiirane, we focus on its authentic, large-scale industrial uses aligned with international regulatory standards. This material’s reactive thiirane structure enables precise functions in synthetic and specialty chemical formulations. Below, we detail its established application scenarios, addressing industry-specific requirements in compliance, formula engineering, process placement, and end-use manufacturing outcomes.

    1. Sulfur-Containing Agrochemical Intermediate Synthesis

    Downstream agrochemical companies employ cis-2,3-dimethylthiirane as a specialized building block for certain classes of thioether- and thiol-based pesticide active ingredients. The compound contributes to ring-opening alkylation steps, supporting chemo-selective functionalization needed for advanced crop protection agents. This use requires precise integration into multi-step batch reactions under controlled conditions to comply with market-specific residue and process safety criteria.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • European Chemicals Agency (ECHA) REACH regulations for plant protection products
    • US EPA Regulations for Pesticide Registration (40 CFR 158)
    • ISO 9001/14001 for process management and environmental control

    Typical usage ratio

    • Typically 0.5–3.0% w/w relative to the total reactants, adjusted based on target thioether conversion; engineers optimize the dosage per mole ratio of substrate and desired yields in the synthesis route.

    Downstream process integration

    • This raw material enters during the nucleophilic ring-opening or functionalization step of multi-stage pesticide synthesis, usually under basic, non-aqueous conditions, with controlled temperature to avoid side-product formation.

    Final product types

    • Selective herbicides (thioether-based actives)
    • Insecticides involving thiol functional groups
    • Sulfur-heterocycle fungicide intermediates

    2. Polymer Modification Agent in Specialty Resin Crosslinking

    Chemical processors use cis-2,3-dimethylthiirane for introducing sulfur-containing crosslink nodes into advanced polymer matrices, particularly in the manufacture of high-performance thermosetting resins for electronics encapsulation and specialty adhesives. The three-membered ring structure allows efficient opening and covalent binding in resin networks under controlled curing, providing targeted physical and chemical resistance properties.

    Industry compliance standards

    • ISO 10993 for biocompatibility (if used in medical device encapsulation)
    • RoHS and REACH for electronics and electrical equipment
    • ASTM D3960 for coatings VOC content
    • UL 94 for flammability in polymer applications

    Typical usage ratio

    • 0.2–1.0% w/w relative to polymer prepolymer or base resin, with ratio chosen based on targeted crosslink density and mechanical property enhancement; formulation chemists balance incorporation to avoid over-crosslinking.

    Downstream process integration

    • Insertion occurs during the homogenous mixing and pre-polymerization stage, followed by thermal or UV curing to form the covalent crosslinked network; strict process monitoring controls side-reactions due to high reactivity.

    Final product types

    • Electronics potting compounds
    • Structural adhesives for electronics and automotive assemblies
    • Modified epoxy or polyurethane system resins

    3. Fine Chemical Intermediate for Chiral Sulfur Compound Synthesis

    In pharmaceutical and specialty chemical synthesis, downstream users select this material as a key intermediate for constructing complex, chiral sulfur-containing molecules. Its asymmetric centers and strained ring allow stereoselective transformations, supporting the efficient formation of chiral auxiliaries and organosulfur pharmacophores used in the production of specialty drugs and advanced intermediates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF monographs (if intermediates are used in final APIs)
    • European Pharmacopoeia requirements for chemical purity
    • ISO 17025 for chemical analysis and QC in API manufacturing

    Typical usage ratio

    • In fine synthesis operations, the dosage depends on desired yield and enantiomeric purity; commonly 0.2–1.5 molar equivalents relative to the primary nucleophile in the ring-opening reaction pathway.

    Downstream process integration

    • The chemical is introduced in enantioselective ring-opening reactions, often under catalytic asymmetric conditions, where it forms a chiral adduct or precursor; batch and flow setups are both applied based on throughput.

    Final product types

    • Chiral auxiliaries for asymmetric catalysis
    • Pharmaceutical intermediate building blocks
    • Sulfur-containing heterocyclic scaffolds for medicinal chemistry

    4. Odorant Precursor in Natural Gas Leak Detection Formulations

    Utilities and specialty blend manufacturers utilize cis-2,3-dimethylthiirane for introducing trace-level sulfur compounds into natural gas odorization mixes. Upon controlled breakdown, the compound delivers distinctive volatile sulfur compounds, fulfilling safety regulations requiring timely gas leak alerts. Its stable storage profile supports dosing precision, minimizing volatility before use and maximizing conversion upon system surfacing.

    Industry compliance standards

    • EN 13725 Air quality – Determination of odour concentration by dynamic olfactometry
    • US DOT 49 CFR 192.625 (Odorization of Gas)
    • National Fire Protection Association (NFPA) 54 – National Fuel Gas Code
    • Local Environmental Protection standards for sulfur emissions

    Typical usage ratio

    • Ranges from 1–10 ppm (parts per million) by volume in the odorant blend, calculated based on pipeline flow rate, ambient temperature, and baseline sulfur recovery efficiency. Adjustments occur for regional detection thresholds.

    Downstream process integration

    • Metered injection occurs at midstream or distribution terminal blending stations, where controlled decomposition/oxidation ensures desired volatile sulfur compound release concurrent with gas delivery.

    Final product types

    • Natural gas odorant solutions
    • Calibration reference standards for gas detection equipment
    • Emergency leak detection marker blends
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    Certification & Compliance
    More Introduction

    Cis-2,3-Dimethylthiirane: Rethinking Sulfur Chemistry for the Modern Lab

    Where Quality Meets Real-World Application

    Working day in and day out with sulfur-containing compounds, we've seen how a molecule’s small twists—in this case, the unique cis configuration of 2,3-dimethylthiirane—lead to different reactivity and open new doors for chemists. Unlike its more plentiful trans or even non-methylated relatives, cis-2,3-dimethylthiirane lands squarely in a niche where selectivity, steric effects, and electronic properties demand close attention. We focus on producing this material for labs and companies that appreciate what these subtleties mean for their syntheses, research, and scale-up.

    Production Perspective: Why We Focus on Cis Isomer

    In our own synthesis process, we put a premium on isomeric purity. The cis form does not arise simply by chance; it comes from a combination of tailored reaction conditions, careful selection of precursors, and, above all, hands-on experience at every step. Each batch stands as the sum of dozens of choices, from temperature control through distillation right to final storage. Because the sulfur-bridge in the three-membered ring delivers strain and unique reactivity, isomeric drift during synthesis can spoil a whole production run. We put real eyes and experience behind every batch so researchers receive a product that behaves as intended in their systems.

    Over the years, we've found that meticulous handling during purification and the decision to avoid aggressive acidic or basic washes makes a difference in shelf life and stability. We store finished material in amber-glass containers—far from light and atmospheric moisture—because we have seen cis-2,3-dimethylthiirane slowly shift in purity even under decent warehouse conditions. That attention to detail keeps reliability high for our customers, whether they use a couple grams for a bench experiment or a multi-kilogram order for repeated use.

    Precision in Application: Why the Cis Isomer Matters

    The chemistry of thiiranes stands out mainly because of the ring strain and the presence of sulfur—all things familiar, but often overlooked in practice. With the cis isomer, steric factors come into play in a way that seasoned synthetic chemists will recognize instantly: nucleophilic ring openings, for example, tend to proceed with different regioselectivity compared to the trans form or unsubstituted analogs. That difference can mean the world in total synthesis or when building a library of analog compounds.

    We've been approached by teams working in pharmaceuticals who care deeply about stereoselective outcomes. For those developing enzyme inhibitors, chiral auxiliaries, or advanced intermediates, small changes in reactivity can lead to dramatic differences in biological activity—a lesson we see time after time. Having reliable, well-characterized cis-2,3-dimethylthiirane at their disposal gives chemists a tool for introducing sulfur atoms with defined stereochemistry without lengthy, convoluted protection and deprotection steps.

    Polymer chemists also look to this material for introducing cross-linkable moieties with controlled spatial arrangement. The cis orientation permits selective ring-opening polymerizations and, under the right conditions, delivers polymers with tailored crosslink density, which affects material strength and flexibility. Each time, our conversations with R&D staff—from global companies to growing startups—run deep into the reality of their processes. Specifications and wishes inevitably give way to the actual performance of material, lab-tested and real-world proven.

    Specifications That Matter in Practice

    Seeing a molecule on a spec sheet is one thing—watching it react in a real system is another. The technical data often highlight boiling point, refractive index, or NMR shifts. Those matter, but we have learned to listen to chemists' hands-on questions. How clean is the GC trace? Is there any water contamination? Can an order ship in argon-flushed bottles to avoid trace hydrolysis?

    Most common specs you'll see on our product:

    What all this means on the bench is simple: our product behaves the same way batch after batch, whether used for analytical standards, preparative synthesis, or as a reagent in developmental work.

    Our Experience Supports Your Innovation

    We've worked in the field long enough to recognize that off-the-shelf answers do not always match what chemists really need. One university group, for example, reported that even trace impurities threw off enantioselective ring-opening of thiiranes—yielding unpredictable mixtures and disappointing selectivity. We drew on our methods honed in-house to solve the issue with a double-distillation approach, backed by thorough NMR and GC-MS monitoring at every stage.

    Mid-sized manufacturers running pilot plants have also run into problems using bulk-quality thiiranes sourced abroad. Occasionally, these alternatives come with inconsistent batch-to-batch composition—a result of poor storage or questionable raw materials. Because we run not only routine QC but also periodic full-method validations, our output remains both clean and repeatable. Long-term users tell us they appreciate this transparency and willingness to tune the process to their specs, even when large orders need tight delivery schedules.

    How Cis-2,3-Dimethylthiirane Differs From the Rest

    People sometimes ask us, “Why not use the trans isomer?” There’s a straightforward answer rooted in fundamental chemistry. Trans-2,3-dimethylthiirane does exist, but the ring strain and three-dimensional structure result in slightly different reactivity profiles. Notably, the cis form tends to react faster with nucleophiles that approach from the less-hindered side, leading to regioselectivity advantages seen in synthetic routes to complex sulfur-containing scaffolds.

    Another alternative, unsubstituted thiirane, lacks the steric bulk and can introduce sulfur into a target structure, but at the cost of selectivity. It also polymerizes more readily under mild conditions, which might benefit some users, but for most, this quick reactivity creates headaches—storage, shipment, and process consistency all become issues. With the cis-2,3-dimethyl derivative, we've found that careful purification and precise QC protocols resist unwanted polymerization as well as stabilizing reactivity under typical storage conditions.

    One pharmaceutical client once ran parallel reactions using both cis- and trans-dimethyl isomers. The results left little doubt: isolation of the target intermediate proved far easier and with improved purity for the cis material, owing to the way its conformation directed key steps. In polymer chemistry, initial crosslinking speeds favored the cis isomer, while the trans version delivered a tighter but more brittle network. Selecting the right isomer thus means matching outcomes to the process—something generic traders rarely appreciate, but an active manufacturer with daily lab contact sees up close.

    Challenges Meeting Lab and Industrial Needs

    Supplying specialty chemicals is never simple. Every customer wants a product that works seamlessly right out of the bottle, but small-batch compounds like this bring quirks: volatility, reactivity, occasional odor complaints, or stability issues. Over the years, we refined not just hardware but technique—from using inert-atmosphere filling lines to minimizing oxygen transfer, and offering custom packaging sizes to meet unique experimental needs. It’s the little things, like hand-labeling, or choosing glass over less-reactive synthetic stoppers for long-term storage, that often matter most.

    Another issue we see lies in transportation. Dimethylthiirane is sensitive to temperature changes and traces of moisture, especially for long routes. We learned through hard experience how even cold-chain distribution could let a trace of condensation into a cap—so we use sealing membranes and overcaps by default, even when it adds a few cents to each package. These extra steps pay off by avoiding the kind of subtle degradation and byproduct formation that might go unnoticed until a crucial reaction stalls.

    Supporting the Community: Training, Transparency, and Knowledge Sharing

    One commitment we have made as manufacturers involves knowledge sharing far beyond the sales pitch. Many in our team remember the early days of trial-and-error, and we see it as our job to cut down the learning curve for today’s grad students, postdocs, and industry R&D teams alike.

    We regularly visit academic and private labs, offering troubleshooting sessions or sometimes even hands-on demonstrations. More than one group told us they nearly gave up on thiirane chemistry after unpredictable side-reactions contaminated their flows. By being open about production hiccups and by explaining what makes true cis-2,3-dimethylthiirane tick—following up with real analytic data, not just marketing—we have built repeat partnerships and ongoing studies with some of the most demanding technical customers in the world.

    Real-World Problem Solving: Customization and Upstream Collaboration

    Some custom applications involve requests that force us to reexamine our own process. For instance, one developer wanted material free of a specific synthetic byproduct that, though technically within normal impurity limits, interfered with downstream enzyme screening. Collaborating directly, we tested variations at each synthesis step, swapped out one precursor, and conducted parallel runs. After three iterations, the client confirmed the desired hypoallergenic profile and enhanced downstream activity—an outcome only possible when the manufacturer stays engaged, adaptable, and willing to explore unconventional routes.

    Our warehouse staff and QC chemists run every order through both standard and customer-requested analytics. Sometimes that means supplementing GC and HPLC with mass spectrometry, at other times, running extra Karl Fischer titrations for moisture-sensitive customers. We don’t see this as excessive; it’s simply part of delivering a product ready to meet today’s rapidly changing research landscape.

    Working Relationships and Building Trust

    Manufacturers like us do not just make chemicals; we build relationships based on trust, transparency, and a real understanding of application-level requirements. Every request, whether for gram-scale R&D or multi-kilo pilot plant use, gets the same attention to detail and speed. In the rare event of a discrepancy—say, a trace impurity or unexpected color shift in a batch—we tackle it openly and with urgency, involving technical staff and reaching a solution before it affects any downstream process.

    We continue to support customers long after the sale. Our technical staff maintains an open-door policy for questions or troubleshooting, and we operate our own analytics lab to run confirmatory tests, if needed, free of charge for regular users. This direct engagement avoids finger-pointing and helps everyone save time and money.

    Sustainability and Safety: A Manufacturer’s Perspective

    We see the growing demand for greener chemistry and safer handling practices not simply as buzzwords, but as day-to-day realities. For thiiranes, we use closed systems wherever possible to minimize operator exposure, and we train everyone on safe handling in well-ventilated environments. Waste disposal follows up-to-date local regulations, and whenever new guidance comes out, our compliance and EHS teams meet right away to update protocols and retrain staff.

    Internally, we recycle process solvents and use water-based cleaning cycles to reduce overall environmental impact. For our customers, we provide time-tested guidelines for safe use, and, where permitted, arrange for proper disposal or reclamation of lab residues, knowing these sulfur compounds are sometimes tricky to destroy completely. Our approach—rooted in deep experience manufacturing these materials—minimizes both long-term risk and headaches for downstream users.

    Staying Ahead: Continuous Improvement and R&D

    What we make today does not stand still. Feedback from users—whether a suggestion for a new packaging size, an inquiry about enantiopure variants, or a need for more detailed impurity profiles—guides our R&D projects. We test alternative syntheses, pilot greener oxidation methods, and continually upgrade our instruments. Recent in-house projects include automated purity monitoring and batch-tracking QR codes so returning customers link their actual samples to a digital certificate and expanded documentation.

    Long-term, we’re exploring new synthetic routes that cut down waste and increase overall yield, especially as application areas for thiiranes expand into novel catalysts and next-gen materials. Staying close to users gives us early warnings about emerging problems and new opportunities to collaborate on both chemistry and engineering solutions.

    Listening to What Users Actually Need

    Every year, we hear from more researchers, process engineers, and developers seeking authenticity and direct answers. Whether their focus is on efficient sulfur incorporation into a natural product, constructing new pharmaceutical scaffolds, or pioneering crosslinked polymers, their questions tend to strike at the same core needs: batch-to-batch consistency, straightforward technical support, and actual performance matching claimed specs.

    We see our role as a resource for these users—a manufacturer willing to share deep technical knowledge, tuned by years of hands-on practice. Offering cis-2,3-dimethylthiirane is just one reflection of that broader commitment.

    The Ongoing Value of Direct Manufacturing

    Many suppliers focus on logistics and paperwork; fewer keep their eyes on the reactor, the vacuum line, and the analytics bench. For us, the job’s not done until the customer’s experiment delivers results. The direct line from production, through quality control, to actual research benches provides a level of accountability and flexibility we value and plan to keep. In an era where supply chains stretch across continents and stockouts undermine research timelines, having a real manufacturer in your network can make a meaningful difference.

    Cis-2,3-dimethylthiirane is not just another chemical—it’s a tool for making better science, developed and supported by those who know its quirks and strengths firsthand. That tradition drives our work, and we welcome every new challenge it brings.