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(4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone

    • Product Name (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone
    • Alias Evans' chiral auxiliary
    • Einecs 402-320-1
    • 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
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    Specifications

    HS Code

    889674

    Iupac Name (4R,5S)-4-methyl-5-phenyl-1,3-oxazolidin-2-one
    Cas Number 98206-11-0
    Molecular Formula C10H11NO2
    Molecular Weight 177.20
    Appearance White to off-white solid
    Melting Point 118-120°C
    Optical Rotation [α]D20 +45° (c=1, CHCl3)
    Solubility Slightly soluble in water, soluble in organic solvents such as methanol, ethanol, and dichloromethane
    Storage Conditions Store in a cool, dry place in a tightly closed container
    Smiles C[C@H]1COC(=O)N1[C@H]2C=CC=CC2
    Purity Typically ≥98% (may vary by supplier)
    Chirality Chiral, (4R,5S) configuration
    Uses Chiral auxiliary in asymmetric synthesis

    As an accredited (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25-gram amber glass bottle with a tamper-evident seal, labeled clearly with product details and hazards.
    Shipping (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone is shipped in tightly sealed containers to prevent contamination and moisture exposure. Packages are cushioned to minimize physical damage during transit. The chemical is transported with standard labeling and documentation, complying with relevant local and international regulations for handling and storage of laboratory chemicals.
    Storage (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong acids and bases. Protect from moisture and direct sunlight. Store at room temperature (20-25°C). Ensure proper labeling and keep away from sources of ignition. Use appropriate personal protective equipment when handling.
    Application of (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone

    Applications of (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone to critical sectors requiring rigorous process documentation and quality control. Our product supports chiral synthesis throughout regulated chemical and pharmaceutical value chains, meeting process demands for stereochemical control, traceability, and efficiency across demanding industrial operations.

    1. Chiral Auxiliary in Pharmaceutical API Synthesis

    Major API manufacturers rely on this oxazolidinone as a chiral auxiliary for the enantioselective synthesis of β-lactam antibiotics, antidepressants, and other chiral drugs. Production uses its specific configuration to control stereochemistry in asymmetric aldol and acylation reactions, guaranteeing consistent product purity and regulatory compliance during scale-up. Downstream users integrate it into highly scrutinized multistep synthesis routes where batch-level traceability remains essential for submission dossiers and regulatory inspections.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210/211)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) guidelines for chiral purity
    • US FDA Drug Master File (DMF) referencing

    Typical usage ratio

    • 20–35 mol% as chiral auxiliary, depending on target molecule and process yield requirements; exact ratio adjusted according to enantioselectivity targets and downstream reprocessing steps.

    Downstream process integration

    • Chiral auxiliary introduced at early condensation/acylation stage; recovery and recycling performed post-stereoselective step; removed by hydrolysis or reduction before final API isolation.

    Final product types

    • β-lactam antibiotic intermediates
    • Chiral phenylalanine derivatives
    • Enantiomerically pure antidepressant APIs
    • Synthetic amino acid APIs

    2. Fine Chemical Intermediate for Agrochemical Active Ingredient Manufacturing

    Agrochemical producers incorporate this material as a stereochemical control agent during the synthesis of chiral herbicides and fungicides. Its robust configuration controls selectivity in key carbon–carbon bond forming reactions, improving yields of highly regulated active isomers. Processing plants use it to meet regional plant protection product registration requirements during scale-up and repeated campaign manufacturing.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH (Regulation No 1907/2006, ECHA)
    • China ICAMA Pesticide Registration regulation
    • US EPA criteria for pesticide active ingredient registration

    Typical usage ratio

    • 18–28 mol% in asymmetric cyclization or aldol reactions; adjusted per required optical purity and targeted agrochemical active intermediate specifications.

    Downstream process integration

    • Added during chiral step of synthetic route; removed post-isomerization; most agrochemical manufacturing systems recycle the auxiliary to maximize yield and lower waste.

    Final product types

    • Chiral pyrethroid active intermediates
    • Stereospecific fungicide precursors
    • S-phenyl-substituted herbicide actives
    • Intermediates for enantiopure crop protection agents

    3. Synthesis of Specialty Polymer Additives

    Chemical formulators apply this oxazolidinone as a building block in the creation of chiral specialty additives, such as asymmetric stabilizers and optical brighteners, for high-value polymer systems. Its defined stereochemistry enables selective functionalization, ensuring consistent physical and optical properties required for plastics under regulatory monitoring. Final users document material lot and use routes for traceability and validation in food contact and automotive polymer production.

    Industry compliance standards

    • EU No 10/2011: Plastic Materials and Articles intended to come into Contact with Food
    • US FDA 21 CFR 177.1520 for polymer additives
    • ISO 9001:2015 Quality Management Systems for additive manufacturing
    • Automotive Industry Action Group (AIAG) material traceability guidelines

    Typical usage ratio

    • 3–8 wt% incorporated during masterbatch compounding; proportion set per final additive effect and mechanical property tests on base polymer.

    Downstream process integration

    • Feedstock mixed with base monomers pre-polymerization; integrated during melt blending or extrusion; compatibility tests performed to benchmark performance and regulatory limits compliance.

    Final product types

    • Chiral stabilizer concentrates for films
    • Polymer optical brightener additives
    • Plastic masterbatch for automotive interiors
    • Food contact packaging resins

    4. Chiral Ligand Source in Catalytic Fine Chemical Synthesis

    Producers of catalytic ligands and enantioselective process chemicals use this oxazolidinone core for the preparation of chiral ligands employed in asymmetric hydrogenation and organometallic catalysis. It serves as a synthetic platform enabling downstream manufacturers to deliver catalysts that meet demand for high enantiomeric excess in fragrance, electronic chemical, and pharmaceutical intermediate synthesis.

    Industry compliance standards

    • ISO 17025:2017 for analytical competency in chiral purity verification
    • Chemical Facility Anti-Terrorism Standards (CFATS) compliance—US, where applicable
    • REACH Notification (when relevant for export to EEA)
    • Japanese Chemical Substances Control Law (CSCL) notification for organometallic intermediates

    Typical usage ratio

    • 5–15 mol% as chiral precursor or backbone scaffold; fine-tuned to target ligand structure and catalyst activity requirements per end-user process validation.

    Downstream process integration

    • Reacted with metal complexes to build active chiral ligands; downstream coupling or protection-deprotection cycles applied to achieve target catalytic performance and stability.

    Final product types

    • Chiral phosphine oxide ligands
    • Organometallic hydrogenation catalysts
    • Enantioselective catalyst systems for fine chemicals
    • Synthetic intermediates for electronic chemical manufacturing

    5. Building Block for Chiral Aroma Chemicals

    Manufacturers in the aroma and fragrance sector incorporate this compound to construct chiral building blocks for scent molecules requiring strict stereochemical integrity. It enables access to enantiopure intermediates essential for the synthesis of high-end fragrance ingredients, which demand traceable ingredient supply for international consumer product regulations.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association Code of Practice)
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • FDA 21 CFR Part 701 for fragrance ingredients
    • ISO 9001 for ingredient traceability batch records

    Typical usage ratio

    • 5–12 mol% as asymmetric synthesis auxiliary or intermediate; ranges set by desired chiral purity and olfactory profile specifications.

    Downstream process integration

    • Inserted during early-stage fragrance intermediate synthesis; hydrolytically cleaved or modified post-key step before bulk fragrance ingredient assembly.

    Final product types

    • Enantiomerically pure musk aroma intermediates
    • Chiral lactone building blocks
    • High-purity rose oxide derivatives
    • Fragrance signature-ingredient isolates

    6. Research Reagent for Enantioselective Method Development

    Our oxazolidinone supports academic and industrial R&D laboratories developing new enantioselective synthetic methods. Its defined chiral centers provide a test platform for evaluating reaction conditions, reagent reusability, and new catalytic approaches under controlled, reproducible circumstances. Laboratories use our specification-certified batches to support method validation reports, grant submissions, and patent filings.

    Industry compliance standards

    • ISO 17025 for laboratory accreditation
    • GLP compliance for documentation in regulated academic-industrial collaboration
    • Internal SOP documentation for reagent traceability
    • USP Chapter <1058> for analytical equipment qualification

    Typical usage ratio

    • 10–25 mol% in test reactions; determined by scale and analytical detection limits targeting enantiomeric excess profiling.

    Downstream process integration

    • Charged into test flask as chiral source; subjected to novel catalyst screening or reaction development protocols; spent material recorded for full traceability in research notebooks and electronic lab records.

    Final product types

    • Enantioselectively synthesized test compounds
    • Chiral reference standards
    • Patent-protected synthesis intermediates
    • Peer-reviewed research samples
    Free Quote

    Competitive (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone: Practical Takeaways for Lab and Plant

    What Drives Our Commitment to Reliable Chiral Auxiliaries

    Day in and day out, dependable tools keep chemistry moving forward. We have spent years perfecting the reproducibility and scaling of a chemistry that underpins dozens of specialty syntheses: (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone. This compound sits at a crossroads between chiral control and operational reliability. Its popularity has grown with the new wave of enantioselective syntheses, largely because it meets stringent performance standards not only on paper, but batch to batch, at every size.

    Our earliest pilot runs came out of demand from process chemists seeking better control in asymmetric transformations. Then came the boom in demand for cleaner routes to β-lactams and nonracemic amino acid derivatives. Whether you’re researching small-scale library construction or moving toward commercial production, this oxazolidinone adapts to your needs without surprises. We understand that every synthetic step has to justify itself—cost, handling, and reliability matter as much as theoretical yield. We constantly check for byproducts, control trace metal content, and monitor precursor purity—a tedious process, but it pays off in fewer headaches downstream.

    Every Batch Builds on Practical Experience

    Molecular purity means more than ticking a box. During production, our teams track stereochemistry at each checkpoint. By controlling each element—raw materials, reaction conditions, isolation—we minimize risk from rogue diastereomers or shadow impurities. Trace amounts of alternative oxazolidinone configurations can derail enantioselective synthesis. We bear witness to how a few ppm of the wrong stereoisomer can drop the e.e. of your product or increase purification costs. In our facility, real feedback from users shapes our continuous quality adjustments.

    Nobody wants a product that requires endless checking and rechecking just to reach publication quality. Our customers report that our (4R,5S) batch tests are straightforward and repeatable, with NMR and chiral HPLC confirming the purity and e.e. claims. We take that feedback and build it into our process development, closing wasteful loopholes before they impact your timelines or budgets.

    Specifications That Support Real Synthesis Goals

    Every container of (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone leaves our plant with a tight set of specs: stereochemistry confirmed by both polarimetry and HPLC; purity routinely exceeding 99%; residual solvents well below common regulatory thresholds; controlled particle size for reproducible weighing and handling. Over the years, our process engineers have tweaked drying cycles and crystallization rates. The result is a white to off-white crystalline powder with consistent melting behavior and easy transfer in the lab or plant—no sticky residues, no unpredictable lumps.

    Long-term storage sometimes stumps other producers. We screen every lot for suspicion of ring opening, hydrolysis, or oxidative degradation using actual forced aging studies, not just guesswork. Our samples stored for months in lab cabinets or warehouses remain within spec on retest—an essential feature for procurement teams who want to avoid surprise recalls or urgent re-orders.

    Why Our Customers Put Their Trust Here

    We regularly hear that unpredictable sources mean real trouble. Too many batches from "marketplace" vendors arrive with off-spec melting points, marginal e.e., or ambiguous documentation. That’s particularly damaging if you’re optimizing a multi-step synthesis, where a faulty chiral auxiliary throws off product quality at late stages. Synthetic chemists from pharma to materials science rely on us not only for chemical performance, but to save time wasted on troubleshooting supplier inconsistency.

    Everything we know about troubleshooting shows up in our product. Taking granular process notes, listening to customers as they test custom modifications, and keeping close partnerships with research chemists all help us refine each run. Consistency isn’t accidental. We commit to it, batch by batch.

    Applications That Matter

    This oxazolidinone found its niche as a chiral auxiliary in asymmetric alkylations, aldol condensations, and cycloadditions. Whether building blocks for natural product syntheses or platform molecules for agrochemical pipelines, its use cuts down on costly or unreliable chiral separations. We have clients at the bench and process levels who depend on it for everything from exploratory fragment addition to late-stage pharmaceutical intermediates. Its rigid core reliably imparts chirality, while the methyl and phenyl substitutions on the heterocycle fine-tune both reactivity and stereoselectivity.

    In the pharma world, the product’s robustness allows researchers to chase ambitious new routes—protecting against risk at scale-up—and gives production teams breathing space by reducing variability during kilo-scale or even larger runs. At process scale, slight differences in auxiliary quality immediately amplify costs and delays, especially if downstream crystallization or chromatography suffers. Our long-term clients have seen real reductions in rework thanks to predictable performance under a range of solvents and reaction conditions.

    What Sets This Compound Apart

    We worked on substitutions, particle sizes, drying methods, and purification techniques because it’s not enough to mimic other market standards. Compared with both unsubstituted oxazolidinones and racemic offerings, our (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone gives sharper selectivity in common alkylation protocols. The configuration is no accident. Our monitored process delivers the correct pairing of methyl and phenyl groups, turning out auxiliaries that outperform both in reactivity and stability.

    Some labs use racemic or less pure alternatives due to price or local availability. They pay for it in lower stereochemical outcomes, inconsistent NMR patterns, or unexpected byproducts. We see how even top graduate researchers get tripped up sourcing from “all-in-one” suppliers who cut corners on storage and documentation. Process development teams locked into suboptimal auxiliary performance waste time reoptimizing old steps. By contrast, clients running our product rarely revisit their auxiliary step once it’s validated. Their major troubleshooting migrates upstream or downstream, leading to progress, not circular work.

    Supporting Innovation—Not Just Selling a Commodity

    Research teams send us reports of interesting applications every season. Some are classic transformations like Evans aldol reactions yielding key intermediates for statins or glycopeptide antibiotics. Others are in new space—advanced ligands for catalytic enantioselective reactions, or chiral scaffolds for advanced materials. We supply innovators from academia, biotech start-ups, and established fine chemical producers, and we frequently discuss custom modifications, particle forms, or scale needs. Customization fits our strengths—not as an afterthought but as a fundamental design principle from the days we started up.

    Growing collaborations help everyone. A recent custom scale-up improved a customer’s process by allowing lower temperature operation and shorter reaction times. Savings in downstream purification and reduced energy consumption quickly made these improvements essential to their process. For us, feedback loops like this don’t just improve one product. Insights from scale-up, analytical troubleshooting, or logistics adjustments feed back into every lot we produce.

    Facing and Overcoming Challenges in Synthesis

    Knocking out high-quality chiral auxiliaries has its headaches. Raw material fluctuations, periodic shortages of certified precursors, and evolving analytical standards all put pressure on the producer. Years of active troubleshooting—fixing batch color variation, fending off solvated impurities, and managing scale-dependent heat transfer—mean our teams expect, monitor, and fix these issues before they ever impact the customer.

    We run routine reality checks by talking with the people making chemistry happen in the lab, not just managers with spreadsheets. Their input led to adjustable packaging options, detailed batch records, and responsive technical documentation. Our lessons are hard-won: reproducibility isn’t just a number on a certificate, it’s something teams prove daily under real production constraints.

    Operational Experience Touches Each Batch

    We keep all our production steps close to our team, from selection of precursors and solvents to finished product handling. Never outsourcing our core steps means we can quickly respond if a challenge or customer need emerges. Over time, this hands-on approach builds intuition: predicting yield dips from Pacific humidity spikes, knowing which sampling intervals give the best purity picture, or responding to new regulatory details on solvent residue.

    Many of our closest customers value being able to call or meet to discuss process challenges, collaborate on trouble spots, and arrange for rapid sample delivery. That’s only possible through real relationships and a sustainable supply chain. We recognize that every project, whether it’s a milligram for a new methodology or a ton for validated process chemistry, places a unique set of demands on us as both manufacturers and problem solvers.

    The Real Value in Honest Product Support

    Bottles of (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone arrive with ready access to batch documentation, in-depth analytical support, and a point of contact who knows both production and applications. We offer more than numbers on a data sheet; we provide operational history, documented scale-up experience, and application notes that reflect our years supporting synthetic teams.

    On-site pilot runs, shared lessons from failed reactions, and post-delivery troubleshooting create shared understanding. That mutual trust makes it possible to tackle even ambitious new chemistry. Process engineers testing new green chemistry proposals often raise questions about byproduct profile, downstream compatibility, or regeneration. We don’t offer vague assurances—we back up every claim with data, transparency on limitations, and alternatives if needed.

    Where Continuous Improvement Matters

    No production run stands alone. Every batch reflects refinements driven by years of feedback, root-cause analysis, and review of outlier cases. By analyzing both customer feedback and our real-world QC records, we stay ahead of common failure modes. The pain points reported a decade ago—unpredictable melting, variability in enantiomeric excess, solvent residue outside regulatory bounds—now form the backbone of our process controls.

    Current work addresses even finer margins: adjusting shelf life through molecular stability studies, engineering particle size for automated dispensing systems, and squeezing out the last bits of variable yield with newly sourced catalysts. Lessons come not just from technical literature, but by watching how our product works—or stalls—in the hands of practicing chemists. Every misstep becomes a target for process improvement.

    Looking Ahead: Supporting Next-Generation Chemistry

    We’re seeing newcomers push for both more sophisticated chiral chemistry and stricter sustainability targets. Serious synthetic work no longer tolerates “black box” materials. Researchers want proven track records—demonstrated with solid data, not generic claims. Our history manufacturing (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone means we provide a foundation that teams rely on. Through transparent processes, consistent analytics, and responsive technical support, we foster trust in every shipment.

    We know innovation isn’t about rolling out a one-size-fits-all solution. It’s about producing a material that adapts to the next stage—be it process intensification, new asymmetric catalysis, or environmentally friendlier synthetic methods. Our commitment gives researchers and production teams time to focus on their best work: designing the future, not wrestling production glitches or tracing supply chain failures.

    Open Dialogue and Knowledge Sharing—A Different Way Forward

    We look beyond selling or fulfilling contracts. Product support, regular feedback sessions, and hands-on troubleshooting nurture success, both for us and for our customers. We encourage open dialogue, which means not just highlighting strengths but also identifying limitations and paths to improvement. Whether you’re investigating new routes or optimizing legacy processes, the support you receive reflects our long-term, face-to-face experience with real-world needs.

    As demands for more advanced chiral chemistry rise, reliable auxiliary supply proves critical. Our experience manufacturing (4R,5S)-(+)-4-Methyl-5-Phenyl-2-Oxazolidinone gives you a partner rooted in real-world production, ready to face new challenges at the bench or plant with facts, flexibility, and honesty—all backed by evidence built over years in the field.