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(1S)-(+)-(Camphorylsulfonyl)Oxaziridine

    • Product Name (1S)-(+)-(Camphorylsulfonyl)Oxaziridine
    • Alias CSO
    • Einecs 255-841-4
    • 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

    809052

    Name (1S)-(+)-(Camphorylsulfonyl)Oxaziridine
    Cas Number 126029-48-1
    Molecular Formula C10H15NO3S
    Molecular Weight 229.29
    Appearance White to off-white solid
    Melting Point 102-104 °C
    Optical Rotation [α]D20 +77° (c=1, CHCl3)
    Solubility Soluble in common organic solvents like dichloromethane
    Storage Temperature 2-8 °C
    Purity Typically ≥98%
    Smiles CC1(C)C2CC(C1S(=O)(=O)N3COC3)(C2)C
    Inchi InChI=1S/C10H15NO3S/c1-8-5-6(2)10(3,7(8)4-8)15(13,14)11-9-12-11/h6-7H,4-5H2,1-3H3
    Synonyms (1S)-(-)-Camphorsulfonyl Oxaziridine; CSO

    As an accredited (1S)-(+)-(Camphorylsulfonyl)Oxaziridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (1S)-(+)-(Camphorylsulfonyl)Oxaziridine is packaged in a sealed amber glass bottle, containing 5 grams, with hazard labeling.
    Shipping (1S)-(+)-(Camphorylsulfonyl)Oxaziridine is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent moisture or air exposure. The packaging complies with international regulations for hazardous materials, and temperature-control or secondary containment is used if required. Standard shipping includes appropriate labeling and safety documentation to guarantee safe handling and transport.
    Storage (1S)-(+)-(Camphorylsulfonyl)oxaziridine should be stored in a cool, dry, and well-ventilated area away from heat, moisture, and direct sunlight. It must be kept tightly sealed in its original container, protected from air and incompatible substances (like strong acids, bases, and oxidizers). Refrigeration (2–8°C) is recommended to maintain stability and prevent decomposition. Handle under inert atmosphere if possible.
    Application of (1S)-(+)-(Camphorylsulfonyl)Oxaziridine

    Applications of (1S)-(+)-(Camphorylsulfonyl)Oxaziridine in Industrial Manufacturing

    As a global manufacturer of advanced chiral oxidants, we supply (1S)-(+)-(Camphorylsulfonyl)Oxaziridine to leading processors who require reliable enantioselective oxidation for complex molecule production. Below, you will find focused industrial applications where this raw material directly addresses industry needs for asymmetric synthesis, with specific information on compliance, formulation usage, plant integration, and product output, all reflecting our experience supporting downstream scale-up and process transfer.

    1. Asymmetric Synthesis of Pharmaceutical Intermediates

    Pharmaceutical firms routinely implement chiral oxaziridines for enantioselective oxidation in key steps of API intermediate manufacturing, where asymmetric introduction of hydroxyl or amine functionalities is required by patent specifications or process development. Chemists add this reagent typically at the oxidation or amination stage following initial substrate preparation, applying direct monitoring to maximize chiral yield and avoid racemization. Batch and flow systems both benefit from rapid reaction kinetics and ease of removal of byproducts.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • Chinese Pharmacopoeia (ChP) Quality Standards

    Typical usage ratio

    • 0.8–1.2 equivalents per oxidizable site for laboratory and commercial batches; exact stoichiometry adjusted based on conversion kinetics and substrate load, as verified in pilot scale-up trials

    Downstream process integration

    • Added after substrate dissolution in a polar solvent (e.g., dichloromethane, THF, acetonitrile), with precise temperature control (0–25°C); quench and extraction steps follow oxidation to isolate chiral intermediates; in continuous-flow production, dosed via metered pumps aligned with reactant progression in microreactors

    Final product types

    • Chiral β-amino alcohols and β-hydroxy ketones as key intermediates
    • Precursors for antiretroviral and antihypertensive APIs
    • Custom building blocks for CNS-active agents

    2. Enantioselective Production of Agrochemical Building Blocks

    Agrochemical manufacturers apply this chiral oxaziridine during the synthesis of optically pure intermediates, typically in the synthesis of insecticide or herbicide scaffolds where enantiopurity determines field performance and regulatory acceptance. It is employed at the late-stage oxidation of prochiral sulfides or amines, significantly reducing process steps required for active isomer preparation and improving cost efficiency for scale-up under quality management systems.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006
    • US EPA Inert Ingredient Assessment Standards
    • China GB/T 1605-2001 Agrochemical Purity Requirements

    Typical usage ratio

    • 1.05–1.2 equivalents per target functional group; based on substrate size and impurity threshold set by product registration dossiers for global markets

    Downstream process integration

    • Mixed with pre-purified substrate at the last synthetic step pre-crystallization; compliance-mandated in-line HPLC monitoring verifies enantiomeric excess; post-reaction neutralization with standard base or scavenger reagents

    Final product types

    • Chiral sulfoxide and sulfone intermediates for insecticide actives
    • Optically pure amine derivatives for herbicide finalization
    • Pesticidal core agents requiring certificate of analysis (COA) documentation for enantiomeric purity

    3. Fine Chemical Synthesis for Flavors and Fragrance Ingredients

    Major aroma compound producers utilize this oxaziridine for the controlled introduction of chiral oxygen atoms in the creation of naturally labeled flavor or fragrance building blocks, particularly targeting molecules with a stereodefined alcohol or amine functional group. Its selectivity enables cost-effective conversion routes to high value, non-racemic ingredients that meet food and COSMOS fragrance safety standards.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • US FDA 21 CFR §172 (Food Additives Permitted for Direct Addition to Food for Human Consumption)
    • EU Regulation (EC) No 1334/2008 (Flavourings and Certain Food Ingredients)
    • ISO 9235:2013 (Aromatic Natural Raw Materials)

    Typical usage ratio

    • 0.95–1.3 equivalents, with specific dosage verified in pilot batches to maximize selectivity while minimizing unwanted over-oxidation or byproduct formation

    Downstream process integration

    • Usually fed into stirred reactor vessels after initial precursor formation, following pH adjustment; post-reaction, manufacturers perform solvent extraction, filtration, and column purification to isolate target enantiomers; batch QC includes optical rotation and residual reagent check

    Final product types

    • Chiral alcohol flavor ingredients such as (S)-linalool or analogous perfumery bases
    • Fragrance intermediates with defined stereochemistry for luxury fragrance compounds
    • Food-EU-compliant aroma molecules for beverage and confectionery applications

    4. Production of Advanced Material Monomers for Polymer Industry

    Polymer manufacturers focused on functional and specialty polymers rely on this reagent for the asymmetric oxidation of monomer precursors, enabling the synthesis of chiral building blocks that impart unique mechanical or optical properties to end-use resins and advanced functional materials. It enters processes where stereochemistry at a monomer unit is essential for polymer assembly or for achieving target performance attributes in electronics or engineered plastics.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Polymer Production)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH Polymer Registration (Annexes VII–X)
    • UL 94 Flammability Standard for Plastics

    Typical usage ratio

    • 1.0–1.25 equivalents relative to the functional monomer unit; fine-tuned during R&D optimization runs to guarantee chiral integrity at industrial scale

    Downstream process integration

    • Reactive addition at the oxidation or functionalization stage, with online spectroscopic analysis to confirm endpoint; subsequent filtration and stabilization prior to downstream polymerization or polycondensation

    Final product types

    • Chiral monomers for optical active polymers
    • Pre-polymers for specialty plastics in electronics encapsulation
    • High-performance resins for automotive and aerospace components
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    Certification & Compliance
    More Introduction

    (1S)-(+)-(Camphorylsulfonyl)Oxaziridine: Precision in Asymmetric Synthesis from a Manufacturer’s Perspective

    Reliable Performance from a Trusted Factory Floor

    Chemistry is never about shortcuts. Every batch of (1S)-(+)-(Camphorylsulfonyl)Oxaziridine we manufacture reflects years of technical expertise and a workflow that leaves nothing to chance. Through decades of hands-on experience with sensitive, high-value intermediates, we’ve fine-tuned a reliable process for delivering consistent quality with this advanced chiral oxidant. Raw materials are sourced with traceability, handled in stainless systems dedicated to this class of nitrogen heterocycles, and monitored at every step. Our teams know the weight of every deviation—right down to the moisture content and appearance of the final crystalline product.

    Years of production on real industrial scales have shaped our confidence in supplying (1S)-(+)-(Camphorylsulfonyl)Oxaziridine to research labs and kilo-lab campaigns where process controls matter. A minor impurity or a shift in enantiomeric purity has consequences, whether tuning a pharmaceutical candidate’s activity or defining the performance of a specialty material. We understand these stakes from firsthand experience on the production floor. Each package leaving our facility has been checked and rechecked, with analysts who know our customers by name and often adjust QC reporting formats to meet specific downstream needs.

    What Sets This Oxaziridine Apart

    Chiral amine oxidations and enantioselective syntheses depend on reliable reagents, and over the years, many chemists turn to (1S)-(+)-(Camphorylsulfonyl)Oxaziridine as a first-choice asymmetric oxidant. The origins of this molecule in camphor chemistry create a rigid bicyclic backbone and a well-defined chiral environment for transfer reactions. Its utility comes from that unique shape—one proven through published results and hundreds of screening projects over a decade of commercial supply.

    Unlike other oxidants on the shelf, this molecule offers a rare blend of selectivity and manageable reactivity under a broad range of conditions. We’ve worked shoulder-to-shoulder with process chemists scaling up asymmetric amination and epoxidation. Its crystalline stability means a technician can weigh out the product in ordinary laboratory air with minimal loss of activity—even after months in storage. That stability reduces waste and troubleshooting on larger runs, keeping projects efficient and budgets intact. Many competitors chase the same performance with analogues based on simpler peroxides or less-defined chiral auxiliaries, but subtle changes in the sulfonyl group or backbone often reduce selectivity and can introduce challenging byproducts. Our customers regularly return to the authentic camphorylsulfonyl scaffold because it simply works—batch after batch, year after year.

    Consistency Backed by Real-world Testing

    In the competitive space of asymmetric oxidation chemistry, theoretical purity looks good on paper, but real process success comes only with control on a molecular level. We’ve invested in nuclear magnetic resonance (NMR) and chiral high-performance liquid chromatography (HPLC) analysis for in-line checks as well as post-reaction confirmation. Each batch we deliver goes through material validation using actual finished product samples—not just dry certificate reports. Our process teams catch variability quickly. Problems get solved quickly on production day, long before they leave the plant.

    Over the years, customers have shared feedback from their own pilot plant work, noting faster protocol development when working with our material compared to others they tried before. There’s direct evidence in published literature, too: The camphorylsulfonyl oxaziridine scaffold often yields higher stereoselectivity and fewer difficult side reactions than typical cyclic ketone-based alternatives. We’ve continued to refine our manufacturing based on these post-market performance trends, pursuing small but meaningful process tweaks to remove residual byproducts, optimize particle size, and reduce dusting—all based on the input from real-world users, not just lab test results.

    Downstream Impact: More Than Just a Reagent

    For chemists building small molecule drug candidates or complex natural product analogues, every stereocenter matters. (1S)-(+)-(Camphorylsulfonyl)Oxaziridine has shown its value as a reliable asymmetric oxidizing agent—selectively transferring oxygen or a nitrogen atom with tight control and minimal over-oxidation side reactions. In larger batch manufacturing, where consistency over hundreds of kilograms determines project timelines, weak performance or purity drift in a single intermediate creates downstream headaches: wasted materials, off-specification product, delays that cascade through the coordination of synthetic steps. We’ve responded to these realities by assembling dedicated teams for troubleshooting and feedback. Many R&D chemists from our clients have come to appreciate technical exchanges after encountering challenging transformations. Our factory teams develop practical suggestions that account for solvent compatibility, temperature ranges, and even filtration performance after reaction workup.

    We see outcomes not just in final product yields but also in real process uptime—how little time users spend on cleaning up or reworking reactions. This reagent’s crystalline form resists atmospheric oxidation and keeps handling safe and simple, cutting down the risks of undesired decomposition compared to more sensitive or liquid oxidants, a point often raised in process hazard reviews from our user base.

    Experience Drives Our Development

    We haven’t relied on old syntheses. Our original manufacturing process for (1S)-(+)-(Camphorylsulfonyl)Oxaziridine began more than fifteen years ago, but we’ve evolved it to increase efficiency and control at every stage. In the plant, our operators have replaced open glassware with jacketed reactors, installed semi-automated dosing pumps for reagent addition, and improved containment during sulfonyl chloride preparation and work-up stages. These “under the hood” changes reduce variability and improve operator safety. We take pride in our low environmental impact per kilogram of product shipped—reflected in reduced solvent usage and energy input following lean manufacturing audits.

    It’s easy to be content with current procedures, but direct feedback from users keeps us searching for the next improvement. Some years ago, a customer encountered filtration difficulties with a particularly high concentration run; our team proposed a finer cut on particle size distribution, confirmed its stability under thermal stress, and quickly introduced that change into standard production. This isn’t a theoretical story—it’s the day-to-day cycle of process refinement we live and value as a manufacturer.

    Model and Customization—Why Control Matters

    On our line, we target the (1S)-enantiomer exclusively, verified by regular chiral HPLC retention checks. Absolute stereochemistry matters—especially for pharmaceutical end-use and chiral catalyst development. Small molecule chiral purity, as measured by enantiomeric excess, defines downstream biological activity and directly impacts regulatory acceptability for advanced intermediates.

    Customers sometimes ask for tailored batch sizes or custom packaging for moisture and light protection. The need for control over both production and logistics prompted our move to integrated drum filling and sealed single-use packaging options, shielding sensitive materials from atmospheric exposure during transit. On-site storage and timely shipping mean we can deliver within tight lead times, supporting both urgent R&D scouting projects and larger, plan-driven manufacturing campaigns.

    Direct Line to Innovation

    We maintain active collaborations with academic researchers and industrial clients who need variants or specific testing for new application areas. We regularly produce pilot batches for custom derivatives based on changes to the sulfonyl or camphor substituent pattern. Not every modification leads to dramatic improvements, yet these projects give us unmatched insight into what works—both on the bench and in the plant. Real-world testing from our development partners often clarifies which functional group tweaks keep both selectivity and practical yield. This kind of open feedback loop, bridging lab and industry, informs not only our in-house process but also the guidance we give to end-users troubleshooting novel transformations.

    Perceptions of supply reliability—often overlooked by newcomers—carry real consequences. Projects move quickly in pharmaceutical and fine chemicals R&D, but the need for reliable sourcing creates bottlenecks if production schedules or quality shifts. Many of our customers share stories of sudden supply interruptions or lot-to-lot variation with alternative suppliers, and we understand the pressure those setbacks cause when coordinating global research portfolios. As the original manufacturer, we believe clients shouldn’t have to worry about switching between lots, revalidating methods, or dealing with unresponsive third parties. Our direct relationship cuts through the guesswork, providing stable, accountable supply.

    Why (1S)-(+)-(Camphorylsulfonyl)Oxaziridine Stands Out in the Field

    From bench-top exploration to pilot plant runs, we’ve watched trends in chiral reagent technology shift and cycle. Simpler oxaziridines and achiral analogues sometimes find use as stopgap oxidants, but experienced process chemists nearly always return to the camphorylsulfonyl structure when priority shifts to high enantioselectivity and clean product isolation. Comparative screening performed by independent end-users shows that our product, supplied as high-purity crystalline solid, outperforms competitors in conversion rate and stereocontrol. In direct reactions, minor differences in byproduct profile or moisture sensitivity make a major impact on operational simplicity and yield reproducibility.

    We see clear trends—successful projects consistently attribute efficiency gains to the use of the authentic (1S)-(+)-enantiomer, not just in isolated yield, but in reduction of reprocessing and simpler downstream purification. Low solubility in nonpolar and moderate-polarity organic solvents assists in clean workups and easy crystallization, saving labor and materials. We avoid batch-to-batch drift in particle morphology, learning through hard-won experience that even small fluctuations in blend uniformity can complicate everything from dosing to reaction rates.

    Beyond the lab, practical handling matters. Chemists report better ease of manipulation with a well-defined crystalline solid, avoiding sticky residues or oily films that slow down product isolation. Our packing and shipping teams, well versed in the sensitivity of high-value crystalline intermediates, focus on minimizing mechanical abrasion and static buildup, ensuring that product delivered at the point of use matches its state upon leaving our facility.

    Concrete Distinctions: Comparing with Alternative Products

    In the field, we’ve watched users switch from alternative oxidants, including other oxaziridines and peracids, after encountering limits in selectivity or encountering hazardous handling issues. Sulfonyl analogues with less steric bulk or lacking the rigid camphor core often lead to higher byproduct formation and a greater proportion of off-target epoxidation. Handling issues—such as low melting points or hygroscopicity—present further obstacles, especially as scale increases. Liquid or low-melting alternatives also present safety hazards during transportation and bulk storage, a challenge not easily solved at the plant level.

    Our crystal product retains stability over a far broader range of storage conditions than typical peracids or solution-phase oxidants. Over more than a decade, shelf-life studies confirm that properly packaged material holds purity and activity, supporting users in long lead-time projects and allowing deliberate planning for campaigns. Other manufacturers might offer similar molecules, but only deep operational know-how, built through repetition at scale, ensures customers receive reliable, easy-to-use material with each shipment.

    We also provide application support, not as a sales tool, but because chemists in the trenches need nuanced guidance to unlock the best from our materials. Detailed, hands-on support—covering everything from optimizing cooling rates during large-scale runs to guidance on quenching procedures—comes directly from our plant staff and technical managers. This information helps minimize downtime, maximize yields, and keep projects on track, all based on experience no distributor or generic trader can match. Our approach lets users access institutional knowledge built from decades of operations, not just bullet points from an outdated spec sheet.

    Looking Forward: Meeting Tomorrow’s Demands Today

    Innovation in chiral chemistry keeps pushing the boundaries. As drug development projects move deeper into the area of complex natural-product inspired structures or tackle increasingly challenging targets, demand for high-performance, consistent, and safe reagents grows. Our on-the-ground experience tells us that sustainable, transparent supply of (1S)-(+)-(Camphorylsulfonyl)Oxaziridine supports clients seeking to separate themselves from reliance on non-dedicated suppliers or high-variability contract producers.

    Responsive support, continuous process improvement, and a deep technical toolset mean we can offer more than just bulk chemical resupply. When a novel catalyst or a unique method is published, our teams stand ready to test feasibility at production scale, evaluate potential issues, and support custom runs at any stage of development.

    We believe in a future for asymmetric synthesis built on shared knowledge, reliability, and technical competence at every production stage. Our commitment to delivering (1S)-(+)-(Camphorylsulfonyl)Oxaziridine is grounded in years of direct manufacturing experience and close relationships with front-line chemists—ensuring every project, regardless of size or complexity, starts with trusted, consistent materials from source to final product. For teams intent on making every stereocenter count, that difference is not theoretical—it’s a practical reality, made possible by real manufacturers standing behind every shipment.