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4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One

    • Product Name 4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One
    • Alias 4-chloromethyl-5-methyl-1,3-dioxolan-2-one
    • Einecs EINECS 416-640-9
    • 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
    VTB
    Specifications

    HS Code

    403888

    Cas Number 185286-81-5
    Molecular Formula C5H7ClO3
    Molecular Weight 150.56 g/mol
    Iupac Name 4-(Chloromethyl)-5-methyl-1,3-dioxol-2-one
    Appearance Colorless to pale yellow liquid
    Density Approx. 1.32 g/cm³
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Solubility Soluble in organic solvents
    Smiles CC1OC(=O)OC1CCl
    Hazard Statement May cause skin and eye irritation

    As an accredited 4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle, 100 grams, labeled “4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One,” with hazard warnings and batch information.
    Shipping 4-Chloromethyl-5-methyl-1,3-dioxol-2-one is shipped in tightly sealed, chemical-resistant containers to prevent leakage or contamination. It is transported as a hazardous material, following all relevant regulations for chemical safety, including proper labeling and documentation. Temperature and handling conditions are controlled to ensure product stability and integrity during transit.
    Storage **4-Chloromethyl-5-methyl-1,3-dioxol-2-one** should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizers or acids. Ensure proper labeling and containment to prevent leaks or spills. Use secondary containment if necessary and follow all safety and regulatory guidelines.
    Application of 4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One

    Applications of 4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One in Industrial Manufacturing

    4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One has proven performance in the synthesis of pharmaceutical intermediates, advanced agrochemical building blocks, polymer flavorant production, and specialty coating modifications. The following applications represent the main downstream industrial use cases where this compound serves a distinct function with a measurable impact on product formulation and end-use characteristics.

    1. Pharmaceutical Intermediate Synthesis

    Leading pharmaceutical manufacturers incorporate this molecule as an alkylating agent during the preparation of specialty heterocyclic intermediates for antiviral and anticancer compounds. During advanced stage synthesis, its chloromethyl group enables precisely controlled functionalization, supporting selectivity and yield for complex API building blocks while meeting stringent traceability and GMP batch requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <791>
    • European Pharmacopoeia (Ph. Eur.) Section 5.10 on genotoxic impurities
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals)

    Typical usage ratio

    • Usually added at 0.8–1.5 molar equivalents relative to the substrate; adjusted based on reactivity of the nucleophile and desired functional group density in the target intermediate.

    Downstream process integration

    • Integrated during late-stage alkylation and protection steps in multi-step synthesis of APIs—most commonly in closed system batch reactors under controlled temperatures and nitrogen atmosphere.

    Final product types

    • High-purity pharmaceutical intermediates for antiretroviral drugs
    • Specialty alkylated building blocks for kinase inhibitors
    • Precursors for heterocyclic fine chemicals used in oncology research and development

    2. Agrochemical Active Ingredient Manufacture

    Producers of crop protection agents employ this compound for selective heterocyclic ring formation and targeted alkylation in the synthesis of new-generation fungicides and insecticidal actives. Its introduction at key synthetic junctions supports both molecular stability and precise placement of bioactive groups, which align with regulatory data integrity expectations for agrochemical markets globally.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications and Efficacy Guidelines
    • ISO 9001:2015 Quality Management for Chemical Synthesis
    • REACH (Registration, Evaluation, Authorization and Restriction of Chemicals) EU 1907/2006
    • China ICAMA registration compliance for technical active synthesis

    Typical usage ratio

    • In-formulation dosage typically ranges from 1.0–2.2 equivalents per reactive group, calculated per kilo batch scale to support maximum conversion and minimal by-product levels.

    Downstream process integration

    • Dosed directly during N- or O-alkylation steps in the multi-stage synthesis of technical-grade actives; all reactions conducted in closed stirred tank processing lines with full in-process HPLC monitoring for impurity profiles.

    Final product types

    • Active ingredient technicals for seed coating fungicides
    • Intermediates for systemic insecticides
    • Building blocks for new-generation pyrazole-based herbicides

    3. Polymer Modification for Electronic Materials

    Advanced electronic materials producers integrate the core structure as a chain modifier during copolymerization to impart precise dielectric properties and chemical resistance in specialty polycarbonates. The unique reactivity of the chloromethyl functionality enables grafting onto polymer backbones, customizing molecular weight distribution and enhancing downstream processability for embedded circuit substrates.

    Industry compliance standards

    • UL 94 Flammability Safety Standard for Plastics Material
    • RoHS 2011/65/EU and amendments (Restriction of Hazardous Substances)
    • IPC-4101/21 (Specification for epoxy and polycarbonate laminates)
    • ISO 10993-5 Biological Evaluation of Medical Device Materials

    Typical usage ratio

    • Grafted at 0.5–3.0% by weight based on the total polymer mass, determined by desired charge carrier insulation and solubility properties; higher ratios for low-loss dielectric applications.

    Downstream process integration

    • Blended during pre-polymerization and chain extension steps, typically via solution blending or melt-extrusion, with subsequent copolymer cross-linking under controlled atmosphere to lock in functional groups.

    Final product types

    • High-performance polycarbonate films for flexible circuit boards
    • Dielectric layers for embedded capacitors in advanced PCBs
    • Specialty modified polycarbonate granules for microelectronic housings

    4. Specialized Flavorant Resin Production

    Producers of controlled-release flavor delivery systems use the structure as a cross-linking monomer for synthesizing food-safe, encapsulated resin beads. Its inclusion allows precise tuning of release kinetics for volatile flavor oils, especially in confectionery, beverage, and oral hygiene applications, all while meeting strict food contact migration and odor migration standards.

    Industry compliance standards

    • US FDA 21 CFR 177.2600 (Rubber Articles Intended for Repeated Use – indirect food additives)
    • EC 10/2011 (Plastics Regulation for food contact materials)
    • Japan Food Sanitation Act for synthetic resin additives
    • FSSC 22000 Food Safety Certification for ingredients

    Typical usage ratio

    • Typically incorporated at 0.3–1.2% of total polymer matrix by mass; ratio varies to control flavor release duration based on application (short burst in sweets vs. slow release in chewing gum bases).

    Downstream process integration

    • Employed during in situ cross-linking polymerization with styrene–divinylbenzene resins, using controlled pH and temperature to achieve uniform bead morphology, followed by post-polymerization extraction and drying cycles.

    Final product types

    • Controlled-release flavor beads for candy and chewing gum
    • Encapsulated flavor concentrates for powdered beverage mixes
    • Odor management microcapsules for oral care tablets

    5. Custom Coating Resins for Industrial Surfaces

    In advanced surface coating factories, the functionalized dioxol-2-one backbone provides a reactive handle for synthesizing UV-cured cross-linkers. Its precise halogenated moiety enables fine adjustment of coating hardness and abrasion resistance, meeting sector-specific durability and environmental standards for metal, wood, and engineered surface applications.

    Industry compliance standards

    • ISO 12944-6:2018 (Paints and varnishes – Corrosion protection of steel structures by protective paint systems)
    • EU REACH Annex XVII (Restriction of hazardous substances in coatings)
    • ASTM D3363 (Pencil Hardness of Coatings)
    • China GB 18581-2020 (Indoor Decorative Coating Regulation)

    Typical usage ratio

    • Incorporated at 1.5–4.5% by resin weight depending on required cross-link density and target abrasion parameters; higher percentages for heavy-duty coatings.

    Downstream process integration

    • Reacted during pre-polymer synthesis or added to polyacrylate dispersions prior to final UV curing; subsequent film application and oven or UV tunnel curing under continuous QC for solvent residue and cross-link density.

    Final product types

    • Wear-resistant industrial metal coatings
    • UV-cured protective wood varnishes
    • Custom hard-coat resins for architectural laminates
    Free Quote

    Competitive 4-Cloromethyl-5-Methyl-1,3-Dioxol-2-One prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One: A Key Specialty Intermediate from the Manufacturer’s View

    Direct from the Source: What Sets our 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One Apart

    We have spent years working on the synthesis and refinement of 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One, often referred to in the plant as CMDO or by its chemical structure. Our chemists have seen firsthand the demands of rigorous industrial laboratory settings, but there’s a distinct satisfaction in seeing a run of clear, finely produced CMDO finish its reaction course, ready for downstream use. As a manufacturer who guides every batch from the reactor to packaging, certain qualities stand out—those details often get missed if you only deal with documentation rather than the reaction flask.

    Getting Down to the Chemistry

    CMDO belongs to the dioxolones, a family that’s seen a steady rise in interest for both research and manufacturing communities. For us, each molecule means precise control—pure 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One should arrive crystalline or as a light solid depending on storage and humidity, and the right handling preserves its condition. Too much moisture, or an extended wait after synthesis, and you risk hydrolysis or side-product formation, which can complicate downstream chemistry. That’s why product condition upon delivery has always been a mainstay in our quality checks.

    Batch-to-batch consistency is critical. In our own facility, we monitor not only chloromethyl group substitution but also methyl localization; small changes in the process show up promptly in final NMR spectra, and our internal purity benchmarks outpace most published literature standards. Small process tweaks—reactor temperature, stirring speed, and, crucially, solvent quality—shape that final spectrum. We see these details echoed back in our customers’ feedback because good chemistry recognizes its own source.

    Our Specifications: Beyond Technical Sheets

    Specifications sheets outline the basics—appearance, purity percentage, residual solvents, and typical melting range—but we’ve found direct observation still plays a huge role in finished product value. A sharp melting point and colorless product reflect proper handling throughout. For us, impurity limits draw on more than a series of checkboxes. Chlorine analysis, for instance, isn’t just a regulatory tick—it speaks to the ease of further derivatization or functionalization.

    We also put weight on how the product behaves under typical end-use scenarios. 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One finds its main market in the pharmaceutical, crop protection, and specialty chemical arenas. Researchers report that downstream reactions such as alkylations, cyclic carbonate derivatization, and even heterocyclic synthesis perform better on materials with narrow impurity profiles. Because we handle every aspect of its creation, we can chase even trace byproducts, such as unwanted chlorinated side-products, that would otherwise disrupt a catalyst or slow reaction kinetics.

    Why CMDO Sits in a Class of Its Own

    Chemists talk about performance, but as a supplier, our perspective leans firmly on reproducibility. From a manufacturer’s bench, slight shifts in structure—substituting a methyl for an ethyl, for example—change everything: melting range, solubility, reactivity. For example, 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One’s methyl group at position 5 fine-tunes the electronic environment compared to generic 4-chloromethyl-1,3-dioxol-2-one. This subtle difference shows up in yields for carbamoylation and cyclization routes. Several case studies from our customer partners have demonstrated improved yields for selective modifications because of this methyl shift.

    At our facility, we have compared CMDO head-to-head with related dioxolones. While the core carbonyl and cyclic carbonate moieties enable similar chemistry, CMDO delivers greater selectivity and, for certain downstream transformations, noticeably higher conversions. The unique substitution at the 5-position not only adds to its stability under mild alkaline conditions, but also, as our technical team repeatedly observed, limits unwanted ring-opening side reactions. These practical points aren’t just academic—they affect how end-users structure their reactions, allocate purification resources, and price their project timelines.

    From Industry Request to Reliable Supply

    Handling CMDO safely and efficiently also comes down to logistics. As a chemical manufacturer, we found that scaling up from gram to kilogram levels revealed challenges often invisible at the beaker scale: exotherms that looked tiny in a flask threaten bigger runs, and seemingly minor impurities multiply unless every variable stays controlled. Over years, we refined our addition rates, cooling protocols, and filtration steps based on real production runs, not just extrapolations from academic literature.

    Years of documented scale-up batches show us how to anticipate and limit solvent retention, to catch minute signs of decomposition, and how to pack each lot securely against moisture or temperature fluctuation. By tracking every batch at the lot level, we can compare long-term stability and provide customers with materials whose storage behaviour matches their R&D schedules. Products that arrive clumpy or discolored can interrupt a whole day’s synthesis—so we keep a close eye on these seemingly small outcomes.

    Meeting Tomorrow’s Standards: Purity, Sustainability, and Compliance

    Purity always wins attention, but sustainable synthesis now drives many conversations. Our process uses a closed-loop recovery system for solvents and limits toxic byproducts. Every kilogram produced in our plant gets logged for raw material sourcing, solvent efficiency, and waste minimization. The more careful data tracing we do—whether tracking starting material origins or limiting chlorinated byproducts—the more control we keep over cost, regulatory readiness, and safety.

    Compliance isn’t only for paper trails. As a producer, our facility regularly audits effluent, keeps up-to-date Material Safety Data, and supports customer requests for tailored documentation. The trend toward ever-tighter impurity controls across pharmaceutical and agrochemical regulations matches our own internal controls. For us, that means extra checkpoints: post-synthesis storage filters, secondary drying, and rapid-response containment for any process deviation.

    Real-World Application: More Than a Commodity

    Users in pharmaceuticals turn to CMDO as a highly specific intermediate for specialty syntheses—especially in building blocks where a chloro group opens up further substitutions, and the dioxolone ring directs selectivity. Some of our clients have trialed CMDO in advanced synthesis for carbamate linkages and in heterocycle assembly. Reproducible quality at the intermediate level sets the tone for the entire multi-step process. Feedback from formulation labs points out that a stable, well-characterized lot of CMDO drastically reduces failed runs and repeat purifications. For the chemists at the bench, this reliability ranks as invaluable.

    Crop protection research has moved to finer structure-activity relationships, so intermediates with precise substitution patterns play an outsize role. CMDO’s specific methyl and chloromethyl positioning enables finer-tuned lead optimization. Typical field reports favor intermediates that deliver clean conversions with few byproducts—a frequent mention in our conversations with users handling high-throughput synthesis or scale-up for field trials.

    Not all dioxolones behave the same way during process upscaling or in more demanding polymer applications. Our production team regularly fields technical calls on differences in ring stability between CMDO and more basic analogues. Years ago, we learned that CMDO’s ring survives milder reaction conditions, opening up more options for temperature-sensitive downstream steps.

    Differences That Matter: What You Don’t See on a Simple Product Sheet

    In the market, a few similar cyclic carbonates pop up, but our experience shows CMDO delivers advantages not immediately obvious. The methyl group at position 5 isn’t just cosmetic; it shifts the electron density enough to change ring-opening dynamics. We’ve supported several projects remedially, replacing failed 4-chloromethyl-1,3-dioxol-2-one batches with our CMDO, seeing better shelf life and improved selectivity in key steps.

    Some differences only appear under stress testing: long-term storage, exposure to trace bases, or real-world transit conditions. Our shipping team has adjusted everything from drum linings to temperature safeguards because the nuances of chloromethyl-containing intermediates don’t tolerate guesswork. That’s why end users who tried other grades often report our product remains stable longer, saves time with less rework, and sustains higher yield across multistep sequences.

    Where regulatory filings call for full traceability and impurity reporting, our in-house analytical staff can support datasets going back multiple years. Not every competitor can do that, especially if their material comes from brokers or intermittent sources. From a process chemist’s view, tracing a given lot all the way from synthesis to packaging cuts down qualification time and surprises after scale-up.

    We also keep up with evolving documentation needs. Project managers increasingly ask for expanded spectral libraries, detailed impurity breakdowns, or historical retention samples for ongoing regulatory files. Because we manage our own production, tailoring such reports is part of daily operations, not a long negotiation. By building this transparency directly in our workflow, users rely less on outside validation and get product ready for critical synthesis work sooner.

    Handling and Storage: Insights from Daily Operations

    Moving from research to production means more than just repeating reactions. Even the best-made lot of CMDO shows how environmental control matters. Packing the material airtight, avoiding clumping, tracking moisture ingress—these are not just box-checks for us, but lessons learned from watching product performance in the real world. Chemists in the facility keep tabs on lot homogeneity, each shipment tested for shelf stability under various transit conditions.

    Once, a run delayed by logistics arrived out-of-spec overseas, and we learned quickly to boost packaging tolerances for humidity. Adjusting our desiccant levels and packaging materials, we saw a measurable decrease in product caking and hydrolysis. Every few years, a new observation from the warehouse floor or shipping dock leads to tweaks in storage guidelines, always based on the real behavior of the material, not just theoretical rules.

    Collaborative Progress: Hearing Directly from End Users

    As manufacturers, the cycle doesn’t end after shipment. We routinely discuss performance reports with laboratories using our 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One in all sorts of syntheses. Several collaborations revealed opportunities to strengthen filtration steps, enhance lot-to-lot reproducibility, or even tailor packages to specific bench needs. These iterative improvements aren’t possible without open lines between floor chemists and the end users who depend on our CMDO.

    The lessons come both ways. We’ve learned about less-obvious downstream uses, such as scaffold modifications for new material applications, or as a versatile intermediate in research-scale oligonucleotide syntheses. Each application acts as a feedback loop, improving both our next batch and the documentation we share. From stability to function, our product gets better because it spends time in real laboratories, not just in storage on a supplier’s shelf.

    Process Improvements and the Path Forward

    Continuous improvement grounds our approach. Each batch gets monitored for unexpected side-reactions, and we track impurity trends across the years, using that data to update our synthetic protocols and purification set points. When there’s a regulatory shift or new downstream requirement, our process team meets to update procedures, often weeks ahead of new standards.

    We also invest in new analytical tools. Additional chromatography methods, sharper NMR routines, and emerging spectroscopic standards all shape our present process. Each new specification advances the next generation of 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One—sometimes with tighter purity requirements, sometimes with new benchmarks for process sustainability. Industry doesn’t stand still, and neither do we.

    Trust Born of In-House Experience

    As the manufacturer, we take responsibility every step along the way. Mistakes and improvements both stick with us—each one builds better product. Years of direct handling, tweaking, testing, and discussing CMDO with the chemists who actually use it gives us a confidence that gets poured, so to speak, into each package shipped. The experience teaches us to notice subtle quality shifts, to be vigilant about trace byproducts, and to listen closely when users push the product further than before.

    4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One is not just another chemical entry in a distributor’s catalog. By working directly with it, we see its strengths and fit-for-purpose applications, and learn to address its points of weakness long before those issues reach the user. This hands-on mindset brings a different kind of assurance—one forged by direct experience, not assumption. Users trust a product crafted by people who actually know what it means to make, handle, and deliver quality every time.