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(R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone

    • Product Name (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone
    • Einecs 629-463-1
    • 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

    511682

    Chemical Name (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone
    Cas Number 104706-04-3
    Molecular Formula C13H15NO3
    Molecular Weight 233.26
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 126-128°C
    Optical Rotation [α]D20 -52° (c=1, CHCl3)
    Solubility Soluble in chloroform, dichloromethane, and DMF; slightly soluble in water
    Storage Conditions Store at 2-8°C, protect from light
    Iupac Name (R)-3-Propionyl-4-benzyl-1,3-oxazolidin-2-one

    As an accredited (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle with tamper-evident seal, labeled: “(R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone, ≥98% purity.”
    Shipping (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone ships in secure, sealed containers suitable for chemical transport. The package is clearly labeled with hazard and handling information, complying with all applicable regulations. Temperature and environmental controls are maintained as required to ensure product stability during transit, with prompt delivery to maintain compound integrity.
    Storage (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone should be stored in a tightly sealed container, away from moisture and incompatible substances. Keep in a cool, dry, and well-ventilated area, at room temperature or as specified on the product label. Protect from direct sunlight and sources of ignition. Store under inert atmosphere if recommended for enhanced stability.
    Application of (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone

    Applications of (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone in Industrial Manufacturing

    As a dedicated manufacturer, we support a range of specialized manufacturing sectors with stable and high-purity (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone. This chiral building block serves as a critical asymmetric auxiliary in multiple advanced synthesis routes. Below, we provide transparent application data for primary downstream industries, including regulatory context, formulation guidance, integration routes, and finished product classes.

    1. Asymmetric Synthesis of Pharmaceutical Active Ingredients

    Downstream API producers widely use our oxazolidinone derivative as an enantiomerically pure auxiliary for asymmetric synthesis, allowing precise stereoselective acylation, aldol, and alkylation reactions required for manufacturing chiral intermediates in drug APIs. These processes directly impact the enantiopurity and bioactivity of pharmaceutical ingredients, critical for regulatory approval in regulated markets.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • United States Pharmacopeia (USP)
    • European Pharmacopeia (Ph. Eur.)
    • FDA 21 CFR Parts 210/211 for drug substance manufacturing

    Typical usage ratio

    • 5–15% molar equivalent per chiral center in the target molecule; exact quantity is optimized based on desired enantiomeric excess and yield requirements in pilot trials.

    Downstream process integration

    • Introduced at the asymmetric induction or chiral auxiliary stage, followed by condensation, separation of diastereomers, and ultimate auxiliary cleavage to afford pure enantiomer intermediates.

    Final product types

    • Chiral drug intermediates for antibiotics, antivirals, and anticancer therapies
    • Precursor molecules for proprietary API manufacturing in small-molecule pharmaceuticals

    2. Synthesis of Specialty Agrochemical Intermediates

    Agrochemical companies purchasing this chiral auxiliary use it in the synthesis of stereochemically-defined intermediates for selective herbicides and pesticide actives. The role of the oxazolidinone core is critical in achieving high selectivity and reduced off-target effects in the finished agricultural agents, as regulatory agencies increasingly require strict control over isomer ratios to ensure both performance and environmental safety.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Active Ingredients
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH (EC) No 1907/2006 for substance registration
    • ISO 9001:2015 for quality management in chemical synthesis

    Typical usage ratio

    • 3–12% by weight of the chiral auxiliary, depending on the complexity of the target agro-intermediate and crop application spectrum; adjusted per batch based on isomeric purity specifications.

    Downstream process integration

    • Deployed during the key chiral step, such as asymmetric alkylation or acylation, to introduce stereocenters; followed by auxiliary removal via hydrolysis or reduction before final derivatization.

    Final product types

    • Chiral intermediates for sulfonylurea herbicide synthesis
    • Stereospecific building blocks for pyrethroid insecticides

    3. Fine Chemical Custom Synthesis (Toll & CDMO Operations)

    Contract manufacturing organizations and fine chemical processors integrate our material as a key auxiliary in custom synthesis routes for chiral specialty chemicals, where scalable, high-yield enantiocontrol is required over multi-step campaigns. Oxazolidinone auxiliaries help reduce costly chromatographic separations and directly affect the timeline and quality of project deliverables.

    Industry compliance standards

    • Responsible Care® Management System
    • ISO 14001 for Environmental Management
    • Client-specific quality assurance protocols, often aligned to cGMP or ICH Q7 for intermediates
    • Hazardous Substance Process Safety Regulation (where applicable)

    Typical usage ratio

    • 4–10% molar equivalent per target substrate for contract synthesis batches; ratios set via client synthetic route modeling and scaled during process optimization.

    Downstream process integration

    • Charged as a chiral auxiliary in key intermediate steps, monitored by in-process control for auxiliary bonding and removal, with real-time adjustment for scale-up consistency.

    Final product types

    • Chiral specialty chemicals for life science research
    • Intermediate supply for flavor, fragrance, and performance material projects

    4. Manufacturing of Advanced Material Monomers

    Polymer and advanced material innovators employ this oxazolidinone for the synthesis of enantiopure monomers destined for polymers with defined optical activity. These downstream firms require high chiral integrity to support specialty copolymer performance, crucial for applications in medical device coatings and high-precision functional films.

    Industry compliance standards

    • ISO 13485 for materials used in medical devices
    • RoHS Directive 2011/65/EU (for polymer applications in electronics)
    • ASTM D638 and ISO 527 (standard methods for polymer testing)
    • Customer-defined purity and performance specifications for monomers

    Typical usage ratio

    • 1–8% chiral auxiliary relative to the monomer precursor; the proportion determined by desired chirality in the polymer backbone and evaluated through material property testing in QA labs.

    Downstream process integration

    • Applied at the monomer synthesis stage during asymmetric functionalization, followed by cleavage and monomer isolation before polymerization, ensuring chiral information is retained in the final polymer structure.

    Final product types

    • Chiral monomers for high-performance polymers
    • Functional films and medical-grade coatings with enantioselective properties

    5. Research Application in Chiral Catalysis Development

    Chemical research institutions and catalyst technology developers utilize this oxazolidinone variant as a model compound for exploring new asymmetric catalysis protocols. Its performance as a resolving auxiliary supports the screening of new catalytic systems and the development of proprietary chiral ligands, contributing directly to innovation in process chemistry.

    Industry compliance standards

    • Institutional Research Protocols aligned with GLP (Good Laboratory Practice)
    • Internal chemical risk management policies
    • OECD Test Guidelines for chemical research
    • Responsible Care® laboratory safety standards

    Typical usage ratio

    • Generally 2–10% per screening batch; adjusted depending on the type of catalysis being investigated and scale of research trial, with optimization ongoing as new catalyst systems are evaluated.

    Downstream process integration

    • Employed during asymmetric induction experiments, both for auxiliary-based and catalytic transformations, and tracked through analytical methods such as chiral HPLC or NMR for research data integrity.

    Final product types

    • Reference chiral standards for catalysis screening
    • Chiral auxiliaries for the development of new synthetic methodologies in academic and industrial laboratories
    Free Quote

    Competitive (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone: A Reliable Choice for Selective Synthesis

    A Product Born from Precision in Chemical Manufacturing

    Working in chemical production means paying attention to every step. Every process, each purification, the tight control on temperature, and how we handle moisture — all of it shapes what you get in the drum or bottle. Our (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone stands as a prime example of what experience and care bring into your lab, reactor, or pipeline. This chiral auxiliary, commonly recognized for its performance in asymmetric synthesis and fine chemical production, reflects years of steady improvements on the plant floor. Chiral materials face relentless scrutiny, not only for purity but for the actual three-dimensional arrangement of the molecule itself. The wrong isomer, even if present at low levels, throws yield and selectivity off. That is one reason we keep a close eye on the configuration from raw materials through to drying and packing.

    Real Experience Ensures Reliable Specifications

    Anyone who has spent time around an actual oxazolidinone synthesis knows there is little room for unreproducible batches. The properties here matter — not only chiral purity but also trace water, residual solvents, and stability during storage. Routine testing remains one side, but an operator’s judgment tells when to rerun a chromatography column or invest in a longer drying cycle. All our (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone inventory comes from batches checked with polarimetry, NMR, and chiral HPLC. Experience taught us what levels to watch for; it is not just a matter of “meeting the spec”. If a filtration yields a faint color or the crystal habit seems off, we know enough to quarantine the material before it heads to a synthetic step. This vigilance earned trust from customers using the compound in scale-up and pilot runs, where nothing replaces the assurance that batch-to-batch variation stays minimal.

    An Asset Where Asymmetric Synthesis Matters

    There is no secret about why research chemists and pharmaceutical process teams seek out this particular auxiliary. The (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone offers a clear edge for controlling stereochemistry in aldol, Michael, and related enolate-based transformations. The cyclic structure locks conformation. Stereoelectronic effects, honed over decades of Corey’s auxiliary chemistry, let users guide enolizations toward the geometry they require. Our team sees these effects up close. We have worked with early-stage researchers scaling their gram reactions up to the kilogram stage, and heard many stories about the “break point” in a project — sometimes a subtle change in auxiliary source makes all the difference. Not only does the synthetic step run cleaner when the chiral auxiliary remains consistent, but downstream separations benefit from the predictable byproducts.

    Specifications That Reflect Decades in the Lab and Plant

    There is no interest here in hiding behind jargon or paperwork. We run HPLC checks on every lot, and the reasons are simple. Late in a manufacturing campaign, a trace impurity throws off the ratio of products or fouls a Pd-catalyzed step. Experience has taught us that water content, sometimes invisible on a “typical” spec sheet, can heavily influence enolization yields. For this auxiliary, maintaining low water and solvent levels keeps customers productive, especially when reactivity or downstream analyses depend on dry conditions.

    We regularly supply (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone as a solid material for ease of handling, but flexibility allows us to accommodate specific packaging or handling requests — direct from the plant, not via a series of middlemen. Developers appreciate the solid’s stability; moisture and light sensitivity stay manageable with the right container and desiccant. There’s little appetite for compromise if a bottles picks up ambient moisture during transport. Our team knows that pain well: loss of performance, difficulty in weighing, and downstream problems with reactive intermediates.

    Key Differences from Other Chiral Auxiliaries

    Plenty of chiral auxiliaries have crossed our shelves: other oxazolidinone derivatives, pseudoephedrine, camphorsultam variants, and even some custom-synthesized acids. We have run enough head-to-head comparisons to see the differences in purification, ease of recovery, and byproduct cleanup. One clear point stands out — (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone offers strong selectivity for enolate chemistry, typically delivering high diastereoselectivity without the messier work-ups some alternatives require. The scaffold’s rigidity and the electronic influence of the benzyl group make it easier to predict the sense of induction. Chemists focused on pilot and full-scale development care about ease of removal, and our observations confirm that hydrolysis and extraction steps run smoothly in standard process setups.

    From our vantage, alternatives sometimes seem cheaper or easier to source, but the slight savings on the invoice tend to evaporate when extra purification, product loss, or longer cycles erode productivity. Our internal comparison batches, run under matched conditions, consistently generate less auxiliary-derived waste with this product than with several other popular options. Customers who have switched often mention reduced time lost on post-reaction cleanup.

    The Importance of Consistent Quality from Source to Shipment

    Traceability matters. After years spent supporting process chemists and scale-up teams, it has become clear that consistent sourcing saves more than it costs. Our batch logs document every step, from raw material checks to final packing. Customers sometimes request samples from multiple production runs as they develop internal specifications. Our records support these requests with direct batch traceability. There is a world of difference between a drum filled from a single controlled process and a batch pooled from a broker’s dozens of sources.

    Direct collaboration with end users has shaped the way we handle orders. Unexplained color in the product, slight changes in crystal form, or out-of-range rotation values all triggered root-cause investigations in the plant, not just paperwork in an office. These steps prevent repeat issues and build open communication. Over time, we have trimmed unnecessary steps, standardized what works, and responded quickly when things looked off — skills that come only from manufacturing, not trading.

    Supplying for a Spectrum of Uses

    The mainstay applications of (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone center on stereoselective organic synthesis. Researchers building chiral centers in active pharmaceutical ingredients, crop protection agents, or fine chemicals can rely on the material to control molecular shape early in synthesis. We see this in daily orders from small discovery groups up through pre-commercial scale-ups. Some customers focus on classical aldol reactions; others use it for more elaborate cascade transformations. The auxiliary’s compatibility with a variety of Lewis acids and catalytic systems gives process chemists freedom to design around available equipment and solvents.

    Recovery and reuse matter, especially beyond the earliest research stages. Direct feedback from scale-up teams led us to optimize washing and recovery protocols, making sure the auxiliary can be isolated and redeployed with minimal drop in chiral purity — a difference that shows up on both the bottom line and in time saved. Routine supply for these stages often means working with engineering teams to test and refine isolation steps, and we welcome direct plant-to-plant feedback in this area.

    Troubleshooting and Support Grown from Firsthand Manufacturing

    Support for technical troubleshooting takes on real meaning when you have faced process disruptions in your own plant. Challenges with incomplete reactions or nonstandard byproducts sometimes relate as much to the reagent or auxiliary as to the conditions. We draw on our manufacturing logs and real-time monitoring data to help resolve these cases. The right approach may involve extra drying, solvent swaps, or a small tweak to workup that only emerges after repeated cycles. Talking directly with customer chemists — not through intermediaries — often unearths small observations that solve bigger process headaches.

    Supply interruptions, batch recalls, or insurance of regulatory compliance all depend on clarity about sourcing and handling. From the raw benzylamide to the finished oxazolidinone, our documentation remains available for audits or regulatory use. Site visits by customer QA teams have led us to update procedures to reflect customer priorities — from improved secondary containment in storage to batch-specific labeling that makes plant-level tracking easier.

    The Role of (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone in a Changing Chemical Landscape

    With more companies moving toward sustainable practices and tighter process controls, requests for reliable chiral auxiliaries have only increased. Early in our experience, it was enough to achieve target purity and deliver quickly. Now, researchers ask about origin, plant certifications, waste management practices, and tracking of not only the main product but also any byproduct flows. For (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone, our approach includes clear documentation on solvent use, utility consumption, and stewardship of intermediates. It becomes plain that the real cost of specialty chemicals reaches beyond the purchase price, particularly where end-use products face regulatory scrutiny. By embedding these practices early, not in response to market pressures but as part of the plant culture, our whole team keeps up with the evolving expectations of advanced manufacturing.

    We notice trends in requests for smaller or larger packaging sizes, more frequent QA sampling, and even support for alternative paperwork related to green chemistry initiatives. With these have come collaborations aimed at developing closed-loop recovery processes and better return protocols for used packaging, which we believe support not only customers but the safety and integrity of every operator in our supply chain.

    No Substitute for Manufacturer Experience

    It takes more than a spec sheet or a list of regulatory approvals to deliver a product consistently. People in the plant see the differences batch to batch, even in small details: how the crystals filter, what the “feel” of the product reveals about trace solvent, or whether a batch smells faintly of starting material. This kind of vigilance comes only from hands-on work. The collective experience of plant managers, shift operators, and QA staff stands behind every shipment. Comments and concerns from customer chemists don’t end up in a black hole; we work them directly into process adjustments and record-keeping, ensuring the next drum or bottle that leaves our site is better for the dialogue.

    Customers sometimes ask whether there is a cheaper or faster route to similar chiral auxiliaries. From firsthand runs, we know the real savings often come not from the sticker price but from what gets saved in analyst time, failed reactions, or wasted solvent and energy. Our material’s track record reflects how these “hidden costs” drop when quality and consistency stay high. Even projects on tight budgets have recognized that reduced troubleshooting and increased yields rapidly outweigh marginal differences in up-front costs.

    Expertise in Scale Supports Consistency at Lab and Commercial Quantities

    Supplying grams to single researchers and multi-tonne lots for full-scale campaigns means that our processes need to flex without losing quality. Small-scale operations might handle more batch work and respond quickly to special requests, but as volume grows, in-process controls and automation become crucial. Over decades, we have invested in both, knowing that manual checks and operator skill bridge the early pilot work, while controlled plant operations sustain commercial production. Orders for (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone range from research bench through pilot and GMP supply, and our process engineers understand the difference between a ten-gram batch for screening and a multi-kilo campaign for an IND project.

    There are unique demands at each scale. At the research level, splitting lots or providing enhanced batch documentation are common. At pilot and commercial stages, focus shifts to logistics, traceability, and timing — process interruptions cost far more downstream. We plan shipments based on real manufacturing schedules, not distributor lead times. Experience with real-world production schedules means fewer surprises and more honest communication about what’s possible, should an unexpected blip in plant operation occur.

    Building Value Over the Long Term

    We know from long-term partnerships that reliability in specialty chemical supply is about more than today’s batch. It is about supporting new synthetic routes, helping chemists recover and recycle what they can, and staying accountable for every lot shipped. The best way to grow is to develop alongside customers — scaling with them, adapting formulations or specs as they fine-tune their own processes, and being up front about what is and isn’t possible.

    The years have taught us that consistent communication prevents problems that documents alone never reveal. Every batch of (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone sent out reflects not only a protocol followed, but an ongoing critical review from manufacturing and laboratory teams alike. Requests for special testing, alternative containers, or documentation for new regulatory filings are met with the same detailed attention that has defined our approach since our earliest deliveries.

    Supporting Safe, Predictable, and Productive Chemistry

    From the point where raw materials hit receiving to the moment finished product leaves our loading bay, there are many opportunities for errors, inconsistencies, or process improvements. Our team has met project's tight deadlines, last-minute scaling requests, and unusual purity demands head-on, and learned that quick, honest feedback is valued far more than silent compliance to paperwork. Chemists chasing novel transformations, regulatory teams evaluating new impurities, and plant engineers reviewing equipment compatibility all benefit from a direct line to the manufacturer.

    (R)-(-)-4-Benzyl-3-Propionyl-2-Oxazolidinone remains a high-performing tool for enantioselective synthesis — but what makes the difference is not only the molecule’s structure or standard purity claims, but the careful, lived experience behind every step of its production and supply. Our commitment rests on a simple principle: manufacture each lot as if it was going straight back to our own lab. That mind-set keeps us moving forward, one batch, one process improvement, and one satisfied customer at a time.