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(R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate

    • Product Name (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate
    • Alias (R)-(-)-TsDMDOM
    • Einecs EINECS 672-947-5
    • 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
    VTB
    Specifications

    HS Code

    727353

    Product Name (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate
    Cas Number 120429-61-6
    Molecular Formula C13H18O5S
    Molecular Weight 286.35
    Physical State Solid
    Appearance White to off-white crystalline powder
    Optical Rotation [α]D20 = -12° (c=1, CHCl3)
    Melting Point 80-84°C
    Purity ≥98%
    Storage Temperature 2-8°C
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Boiling Point Decomposes before boiling
    Smiles CC1(OCC(O1)C)COS(=O)(=O)C2=CC=C(C)C=C2
    Enantiomeric Excess ≥98% ee

    As an accredited (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, sealed with a screw cap, labeled with compound name, hazard symbols, and safety instructions.
    Shipping **Shipping Description:** (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl p-Toluenesulfonate is shipped in tightly sealed containers under cool, dry conditions. The shipment is labeled for chemical use only and complies with regulatory requirements. Avoid exposure to heat, moisture, and incompatible substances. Handle and transport with appropriate protective measures, following all safety guidelines.
    Storage Store (R)-(-)-2,2-Dimethyl-1,3-dioxolan-4-ylmethyl p-toluenesulfonate in a cool, dry, well-ventilated area, tightly sealed in a moisture- and light-resistant container. Keep away from incompatible substances such as strong acids, bases, and oxidizing agents. Avoid heat, ignition sources, and prolonged exposure to air. Use appropriate personal protective equipment when handling. Store according to standard chemical storage regulations.
    Application of (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate

    Applications of (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate in Industrial Manufacturing

    (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate serves as a specialized intermediate across several advanced chemical manufacturing sectors. Its optical purity and reactive functional groups enable scientists and technical managers to meet exacting enantiomeric and purity specifications in process development, API synthesis, and specialty chemical production. The following scenarios reflect established and compliant deployment in downstream industries.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Pharmaceutical producers incorporate this intermediate into stereoselective synthetic routes for active pharmaceutical ingredients where enantiopurity influences drug safety and efficacy. Process chemists employ this compound during the preparation of key API precursors, particularly within routes designed for β-blockers and selective serotonin reuptake inhibitors, leveraging its configurational stability and suitable leaving group for nucleophilic substitution.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP Monographs (when applicable to final molecule)
    • EU EudraLex Volume 4 GMP Parts I & II
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to the nucleophile—adjusted based on batch size, substrate loading, and reactant stoichiometry optimization in scale-up

    Downstream process integration

    • Introduced during the chiral alkylation or ether formation step, following initial protection procedures; used in early- to mid-stage multi-step synthesis of APIs

    Final product types

    • Chiral API cores for cardiovascular medicines
    • Stereodefined pharmaceutical intermediates for CNS agents
    • Protected alcohol derivatives used in advanced clinical molecule synthesis

    2. Fine Chemical Synthesis for Agrochemical R&D

    Research teams in agrochemical companies select this specialty compound to construct stereochemically defined intermediates critical for crop protection actives and pesticide chiral auxiliaries. Its structure facilitates introduction into heterocyclic scaffolds and the creation of advanced building blocks as part of new molecule discovery, supporting SAR studies and pilot batch process modeling.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical R&D and pilot production
    • Regulation (EC) No. 1107/2009 authorizing plant protection products (for actives registration)
    • OECD GLP for agrochemical analytical studies
    • Company-specific analytical test methods (NMR, GC-MS enantiopurity validation)

    Typical usage ratio

    • 1.0 molar ratio to target nucleophile in pilot-scale synthesis; may vary from 0.95–1.1 equivalents depending on route

    Downstream process integration

    • Reacted with nucleophilic synthons following protection stages, usually after initial base-induced functional group manipulations in multistep synthetic schemes

    Final product types

    • Stereochemically defined agrochemical intermediates
    • Prototypes of chiral auxiliary molecules for herbicides and insecticides
    • Test batches of new fungicide actives for greenhouse crop trials

    3. Asymmetric Catalysis Ligand Preparation

    Researchers in homogeneous catalysis leverage this compound when building enantiopure ligand frameworks, especially where rigid protecting groups and steric bulk are beneficial for catalyst performance. Ligand manufacturers use this raw material in the derivatization of alcohol- or amine-based scaffolds, often in the preparation of phosphorus- or oxygen-centered chiral ligands suited for industrial asymmetric hydrogenation and addition reactions.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006 for substance registration
    • ISO 17025 for analytical test methods and product QC
    • CLP Regulation (EC) No. 1272/2008 for hazardous substance classification
    • RoHS compliance where required for export to restricted regions

    Typical usage ratio

    • 0.9–1.05 equivalents in ligand precursor protection; exact dosing based on the functional group availability and designed catalyst framework geometry

    Downstream process integration

    • Utilized in the initial protection of diol or amino alcohol precursors prior to further coupling with metal-coordinating groups, supporting high-purity ligand manufacturing

    Final product types

    • Chiral diphosphine ligands for asymmetric hydrogenation
    • Enantiopure oxazoline or dioxazoline ligands for catalytic enantioselective transformations
    • Bulk ligand supply for pharmaceutical and specialty monomer production

    4. Advanced Monomer Modification for Specialty Polymer Synthesis

    Manufacturers of specialty polymers use this molecule to introduce defined chiral centers and protect challenging alcohol functionalities during synthesis of custom monomers. It aids in the precise assembly of polyesters and polycarbonates with targeted optical activity, supporting the production of engineering resins and biomedical polymers where chirality and chemical resistance are critical.

    Industry compliance standards

    • ISO 9001:2015 for design and production of plastics and polymers
    • FDA 21 CFR 177.1580 (when applicable for polymers contacting food or medical devices)
    • EU Regulation 10/2011 for plastics intended to contact foodstuffs (if downstream use applied)
    • Full supply chain change control documentation as per IATF 16949 for automotive polymers

    Typical usage ratio

    • 1.0 equivalent per target alcohol group in monomer; formulation development may adjust from 0.95 to 1.05 equivalents relevant to batch uniformity and repeatability

    Downstream process integration

    • Added during functional group protection of monomeric diols or triols prior to polymerization, ensuring stereochemical definition and process stability in high-value resin synthesis

    Final product types

    • Chiral polyesters for biomedical diagnostic components
    • Optically active engineering polymers for automotive parts
    • Specialty polymer beads for chromatography
    Free Quote

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    Certification & Compliance
    More Introduction

    (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate: Precision and Reliability from the Manufacturer’s Bench

    The Product We Know from the Ground Up

    Years of navigating the fine details of chiral intermediates and functional reagents have shown how much hinges on consistency and quality. (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-ylmethyl p-toluenesulfonate might look like just another line item to those outside the lab, but as producers, we’re attuned to every shift in its manufacture. We handle not just the chemical synthesis but the spirit of attention—the exact habits, controls, and insight that mean the product shows up each batch the same, batch after batch, vial after vial. Nothing replaces the peace of mind it brings when you know what goes into each step, from raw material sourcing right through to purification and packaging. Clear, repeatable process matters not as a slogan, but as the lived reality for chemists who rely on that next transformation to go exactly as planned.

    What Sets This Reagent Apart in the Laboratory

    Chemo-selectivity lies at the heart of why so many organic chemists turn to this compound. As a manufacturer, we’ve watched projects get derailed by a lack of stereochemical control or the mystery variables introduced by poor or inconsistent sulfonating agents. The (R)-enantiomer of this dioxolane derivative, armed with the p-toluenesulfonate group, steps neatly into asymmetric synthesis and protection-deprotection methodologies. Protecting groups might seem interchangeable on paper, but experienced researchers know the wrong one can lead to byproducts or tedious downstream purification. Here you find high chemical purity, tight optical rotation specifications, clarity on melting points and solubility profiles—details dialed in over years of process refinement so that our customers know exactly what they receive.

    Specifications Matter: How Precision Is Built

    A product like (R)-(-)-2,2-Dimethyl-1,3-dioxolan-4-ylmethyl p-toluenesulfonate is only as good as the evidence that supports each batch’s quality. We focus every step on measurables: percentage enantiomeric excess, absence of key impurities, confirmed spectral data. The product generally presents as a colorless to slightly pale white crystalline solid. Rigorous tracking of residual solvents, thermal stability, and HPLC purity has never been a one-size-fits-all exercise at our site; rather, it means paying attention to how the product will behave—during storage, in transport, and as soon as it enters the synthetic workflow of our client.

    Our in-house team doesn’t just work from literature values; repeated trial, careful process monitoring, and persistent troubleshooting have all refined the optimal route. Often, we engage in dialogue with users to clarify application specifics. Since strict enantiomeric purity can dictate the outcome of a chiral center downstream, customers have come to expect supporting chiral chromatograms and COA transparency. Our analytical team only signs off batches that match industry standards as well as our own higher benchmarks—QA founded on experience, not slogans.

    What the Compound Delivers in Practice

    Protection of diols and alcohols stands as the chief application in many advanced organic syntheses. We see repeated demand from pharmaceutical intermediates, where protecting a sensitive hydroxyl group with a dioxolane ring and carrying it forward through cascades of reactions gives chemists confidence against side reactions. The toluenesulfonate pendant facilitates clean substitution, smooth deprotection, and does so without introducing hard-to-remove byproducts. As manufacturers, we hunt for those details because we want your downstream steps to click into place, not grind to a halt.

    Beyond routine scale protection, this compound steps up as a building block in the hands of peptide scientists, natural products researchers, and medicinal chemists searching for stereochemically pure fragments. Rigorous isolation ensures no risk of the (S)-enantiomer or related undesirables creeping into your transformation, and the ease with which the tosylate can be displaced by nucleophiles gives significant flexibility in route planning. When clients have pushed to scale for pilot or production runs, our technical staff can help inform optimal handling: how best to store, dissolve, or dry down the material to maximize shelf life and reactivity.

    The Value of True, Direct Manufacturing

    There is no substitute for visibility into your own manufacturing process. Our work controlling each facet, from raw material qualification to crystallization solvents, means fewer mysteries and more dependability for chemists. Every kilogram turned out in our plant comes with a story—a team crosschecking glassware, sampling from split batches, pushing for yield and purity simultaneously because we have to live with the outcome. Most frustrations organic chemists encounter can be traced to slippage in the supply chain, where third-party resellers lose track of storage or aliquoting. Direct control means every drum and bottle bears the fingerprints of our own team from start to finish.

    We’ve seen requests for customized specifications driven by unique processes. Some need batch-specific chiral purity, some focus on minimizing certain residual solvents, others look for more water content controls or custom packaging sizes to reduce waste. Our position as a manufacturer lets us react to technical questions and deliver bespoke solutions—or corrections—quickly. It lets us say what we will and will not guarantee, and honor those words with follow-up. A trader or generic label can never match this level of accountability or feedback loop.

    How This Compound Compares to Similar Chemicals

    Within the world of protecting groups and leaving groups, subtle differences bring outsized ripples across complex syntheses. Some customers weigh alternatives such as benzyl or methyl protection, but these options lack the same balance of stability under acid or base and ease of selective removal. Others look at mesylates or other sulfonates for displacement chemistry, yet find the toluenesulfonyl group introduces greater leaving ability and less risk of elimination byproducts.

    Sourcing directly from us, researchers get not just the pure chemical. They also benefit from detailed data: shelf-life stability tracked under real-world lab and warehouse conditions, impurity profiles measured after multiple months, and open lines for discussion about process-specific handling tips. Over years, patterns have emerged—for example, how our product’s melting behavior correlates with ease of dissolution, or the impact of storage humidity on free-flowing powder. Having endured the headaches that subpar batches can cause, we know that predictable performance lets chemists do their real work, not babysit a protection step.

    Key Lessons from the Field: Stories We’ve Seen

    We once worked with a contract pharma lab struggling with byproduct build-up during an alkylation. Closer inspection showed a 3% impurity from a competitive product—trace unreacted acid left over from incomplete neutralization. After switching to our cleaner batch, their byproducts dropped below 0.1%, yield climbed into pilot-production territory, and time spent on column chromatography shrank to a single pass. In another case, a university group used a bulk order over several semesters, reporting the same optical rotation every time. They credited the ability to assign intermediates and run NMRs without fear of racemization. These aren’t just anecdotes—they points to the lived value of getting a compound exactly as specified every time, with no unwanted surprises.

    Such stories reinforce a core lesson: the people using these intermediates do not want to chase uncertainty or repeat a reaction three times just to troubleshoot the basics. The research dollars and work-hours saved by combining sharp analytical controls with internal quality stewardship outweigh all the sales pitches about “premium” or “research grade.” As the source, we stand behind the purity, chirality, and reliability that hundreds of downstream syntheses depend on. This is not simply about transactional supply, but about goods made to be used without worry, with supporting data that matches everyday lab reality.

    Addressing Problems: From Scalability to Handling Challenges

    The jump from gram-scale to multi-kilogram quantities will stress test any supplier. Our investment in equipment designed to handle both small and mid-size orders means fewer bottlenecks. We have seen users run into issues with certain routes—such as incomplete deprotection or low reactivity under mild conditions. In these cases, we work through the underlying chemistry: identifying whether impurities could be acting as inhibitors, considering alternatives in crystallization solvent, or providing advice on the optimal temperature and mixing regime.

    Colleagues globally face similar scale-up problems, and sharing real insight—rather than just referencing a data sheet—brings real results. For example, accidental moisture ingress caused sticking or partial hydrolysis in the past. We improved drum-lining and switched to moisture-barrier bags, published our own water-content data, and coached clients on proper drybox handling where relevant. Concrete fixes arose from understanding not just the product, but the environment in which it would be used. Our lab team stays ready to adapt; raw material purity, storage logistics, and process tweaks are never set-and-forget topics. We treat every batch as a new test of our system.

    Quality Data You Can Trust

    Data transparency underpins our credibility. We stake our reputation on raw analytical numbers: NMR, HPLC purity, chiral GC, LC-MS, melting point, water content, and residual solvent content, every measurement conducted and archived in our own lab. These are not outsourced or purchased from a vendor; they stem from our own instruments, calibrated and cross-validated regularly. Clients often request supporting spectra, past batch records, or documentation of method changes—requests we meet because we know lab managers build their own QA protocols around real data, not assurances. Any question about trace metals or heavy atom analysis draws on years of cumulative in-house experience. Remaining connected and transparent lets us improve batch by batch, root out the tiny corner-cases before they become problems, and sustain trust in every order we ship.

    Why (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate Remains a Go-To

    Organic and medicinal chemists keep returning to this reagent because it simplifies complex protection/deprotection schemes. A good protecting group shields sensitive hydroxyls without complicating later steps. A great protecting group comes off cleanly, with minimal byproducts, under mild conditions, and brings no spectral confusion to final products. This compound walks that line. Routine operations—nucleophilic substitution, alkylation, preparation of stereochemically pure intermediates—see shorter timelines and more robust conversions. In every order, we build in feedback from customers who pushed the limits and reported back, allowing us to bank years of incremental refinements into the current process. These iterative gains matter most for labs who can’t afford failure or downtime.

    Producing (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate in-house gives us a vantage point to spot trends, anticipate needs, and respond when the market shifts. Whether clients prepare APIs, agrochemical leads, or novel small molecules, they count on both immediate performance and ongoing technical dialogue. We recognize the bar keeps rising—regulatory standards, analytical scrutiny, data transparency. Meeting that bar demands process rigor, not just well-written datasheets but deep knowledge built over years in the field, from the people who actually pull the levers and test the output.

    Environmental Considerations and Safety

    Responsibly handling sulfonate esters means understanding potential for environmental impact, operator exposure, and downstream contamination. Our facility integrates closed reactor systems, high-efficiency scrubbers, and specialized waste neutralization for all sulfonate byproducts. Regular audits and internal training ensure every team member, from production chemist to warehouse operator, handles the product safely and knows the proper protocols. By maintaining full oversight, we reduce uncontrolled emissions, avoid cross-contamination, and can guarantee not just the purity of our product, but also our environmental footprint.

    Lab customers often inquire about optimal safety practices, and our technical team stands ready with real-world handling tips—based on what actually works during hundred-kilogram campaigns. This differs from simply passing along off-the-shelf recommendations. Specific details, such as optimal PPE, storage temperature, and spill mitigation tactics, are informed by our day-to-day experiences, not simply generic advice. We recognize responsible stewardship runs in parallel with purity, and both mark the difference between a true manufacturer and a faceless supply chain link.

    Future Directions: Staying Ahead of Need

    The research world rarely stands still. As drug discovery and advanced material science accelerate, we continually monitor for new uses and application notes from global researchers. Sometimes, this means modifying our process in response to a published route that leverages our reagent for an unexpected transformation. It also means working directly with clients to create custom runs with alternate solvents, special packaging, or newly requested analytical data points. The agility and institutional knowledge that comes from handling a single compound over many years puts us in a position to offer not just supply, but true support as synthetic strategies evolve.

    Summing Up: Why Experience in Manufacturing Still Matters

    We’ve built reputation batch by batch, learning where subtle changes in chemistry can make or break a route. Our commitment to (R)-(-)-2,2-Dimethyl-1,3-Dioxolan-4-Ylmethyl P-Toluenesulfonate reflects an old truth: the closer you are to manufacturing, the fewer surprises your customers face. From raw material vetting to analytical validation, to packaging that guards against hydrolytic risk, every detail matters. Labs depend on real, not theoretical, product performance. Our investment, oversight, and technical dialogue means every researcher, from a single-bench operator to a pilot-plant head, finds reliability and precision in each shipment. That is the core value direct manufacturing can deliver, and it shapes every gram we send out into the world.