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HS Code |
850551 |
| Product Name | (S)-4-Benzyl-1,3-Oxazolidine-2-Thione |
| Cas Number | 15171-80-9 |
| Molecular Formula | C10H11NOS |
| Molecular Weight | 193.27 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 77-79°C |
| Optical Activity | Chiral (S-configuration) |
| Solubility | Soluble in organic solvents such as dichloromethane and ethanol |
| Storage Conditions | Store in a cool, dry place; protect from light |
| Density | Approx. 1.2 g/cm³ |
| Purity | Typically ≥98% (commercial) |
As an accredited (S)-4-Benzyl-1,3-Oxazolidine-2-Thione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a screw cap and labeled with (S)-4-Benzyl-1,3-Oxazolidine-2-Thione and hazard information. |
| Shipping | **Shipping Description:** (S)-4-Benzyl-1,3-Oxazolidine-2-Thione is shipped in a sealed, chemical-resistant container to prevent contamination and degradation. It should be protected from moisture and stored at room temperature. Shipments comply with all relevant regulations for chemical transport, ensuring safe and secure delivery for laboratory and research use only. |
| Storage | (S)-4-Benzyl-1,3-Oxazolidine-2-thione should be stored in a tightly sealed container, protected from moisture and light, at a cool, dry place—preferably under inert gas such as nitrogen or argon. Avoid contact with strong oxidizing agents, acids, and bases. Store at room temperature or as specified by the supplier, and ensure proper labeling and chemical segregation according to standard laboratory safety protocols. |
Applications of (S)-4-Benzyl-1,3-Oxazolidine-2-Thione in Industrial Manufacturing(S)-4-Benzyl-1,3-Oxazolidine-2-Thione is a specialty chemical intermediate widely adopted by manufacturers in advanced chemical synthesis pipelines. We leverage our process expertise to deliver high-quality raw material supporting critical downstream production stages. Below we present several focused industrial application scenarios where our product demonstrates technical and compliance-driven value. 1. Chiral Auxiliary in Enantioselective Pharmaceutical SynthesisSpecialty pharmaceutical manufacturers use (S)-4-Benzyl-1,3-Oxazolidine-2-Thione as a chiral auxiliary to introduce stereocontrol in the synthesis of active pharmaceutical ingredients (APIs), particularly in beta-lactam ring construction and asymmetric amination reactions. It is incorporated during key chiral center formation steps, where precise optical purity is essential for API regulatory compliance and therapeutic efficacy. Required specification and handling ensure low impurity profiles in line with industry expectations for regulated pharmaceutical synthesis. Industry compliance standards
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2. Custom Ligand Production for Asymmetric CatalysisFine chemical producers and contract manufacturing organizations utilize this compound as a building block for the synthesis of custom N-heterocyclic ligands applied in metal-catalyzed asymmetric transformations. The introduction of the thione group and rigid chiral scaffold provides high selectivity when integrated into ligand-design workflows, especially for applications needing process reproducibility and batch traceability for regulated catalyst production. Industry compliance standards
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3. Intermediate for Advanced Agrochemical SynthesisAgrochemical manufacturers deploy (S)-4-Benzyl-1,3-Oxazolidine-2-Thione at the intermediate stage for synthesizing enantio-enriched crop protection compounds, especially in the formulation of herbicides and fungicides requiring improved biological selectivity. The material ensures tight control over stereochemical outcomes which directly informs bioactivity and environmental compliance in downstream formulations. Industry compliance standards
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4. Synthesis of Specialty Polymer AdditivesPolymer additive manufacturers employ (S)-4-Benzyl-1,3-Oxazolidine-2-Thione for producing functionalized thione-based polymer modifiers that impart improved stability and controlled crosslinking properties in specialty elastomer and coating systems. Stringent QC and traceability requirements apply at every stage from raw material handling to additive finishing. Industry compliance standards
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Achieving purity and structural reliability in chiral auxiliaries has become one of the more demanding jobs for specialty chemical manufacturers. Through years in the plant and at the benchtop, one material continues to draw repeat attention among chemists driven by selectivity and chiral control: (S)-4-Benzyl-1,3-Oxazolidine-2-Thione. Manufacturers sometimes talk up a molecule without handling it directly. Our perspective runs different—we produce this compound in-house. Persistent effort goes into validating every batch. From the picking of starting materials to the final packaging, we oversee it ourselves.
Chemists exploring asymmetric synthesis constantly ask how to keep optical integrity during transformations. (S)-4-Benzyl-1,3-Oxazolidine-2-Thione solves more than one challenge here. Our teams developed validated, reliable methods to ensure enantiomeric purity and control stereo-outcome—no small feat when you’re dealing with routes where impurities or incorrect enantiomers wreck downstream processes. Synthetic chemists in pharma, specialty chemicals, and research know the headache caused by even low-level racemization. With this compound, the desired (S)-enantiomer dominates, confirmed batch after batch using in-house chiral HPLC and NMR.
With each kilogram and each gram, plenty of analytical data gets logged. There’s nothing speculative about the optical value or elemental analysis; repeat testing tears into every lot to guarantee that stereochemistry stays sharp right through delivery.
Practitioners use (S)-4-Benzyl-1,3-Oxazolidine-2-Thione primarily as a chiral auxiliary, with a big role in enantioselective alkylations and as a precursor in advanced heterocyclic synthesis. Over the years, in-house teams and even a few visiting customers have tested variants, checking reaction yields, byproduct profiles, and ease of workup. From those tests, the feedback was clear: both the benzyl group and the thione moiety are critical for predictable selectivity and functional group tolerance.
There’s an increasing demand from medicinal chemists and flavor and fragrance developers who rely on building blocks both clean and chiral-defined. Rather than running blind with off-the-shelf intermediates, users benefit when structure and enantiomeric purity are not in doubt—every order represents deliverable synthetic value rather than just paperwork and certificates.
Our principal model for this auxiliary centers around a stable, crystalline form with strong batch-to-batch repeatability. We keep moisture and oxygen levels low during both synthesis and storage. That means no unexpected hydrolysis, decomposition, or racemization during shipping or long-term storage.
Our process produces the (S)-enantiomer, not as a generic mix or a racemic conglomeration. For clients needing NMR, MS, or custom chiral purity runs, plant analysts provide the numbers to back up every shipment. Density, melting point, and solubility are available with direct verification—each pulled from measured results, not copied from old papers.
Unlike many chiral auxiliaries that force chemists to compromise between stability and reactivity, this compound tolerates extended storage under standard laboratory conditions and demonstrates robust reactivity in alkylation and functionalization protocols. Customers directly involved in asymmetric synthesis consistently report low side-product formation when using the crystalline material provided straight from our plant.
In the crowded world of chiral auxiliaries and sulfur-containing reagents, both subtle and sweeping differences separate a dependable product from a source of frustration. One frequent competitor: generic oxazolidine-2-thione analogs, often with variability in the alkyl or aryl substitution pattern. Only firsthand manipulation uncovers how the benzyl group’s steric and electronic effects matter. Several tests in our pilot reactors showed that if you swap in another group—say, methyl instead of benzyl—you’ll find not only altered reactivity but significant differences in diastereoselectivity, sometimes even leading to trouble during auxiliary removal.
Additionally, when comparing with racemic or poorly resolved auxiliaries from reseller stock, our house product outperforms in reliability: side reactions from chiral contamination stay well below detectable limits, and the thione unit remains uncompromised even during scale-up. Large-scale users also point out the lack of problematic smell and safety risks that sometimes arise from low-grade thiones. We take extra measures to control for these, both in synthesis and purification.
Competing auxiliaries, especially those with a more flexible substituent or a less stable backbone, occasionally show shelf-life issues or unpredictable solubility in key organic solvents. Ours shows consistent dissolution in common solvents such as DCM, THF, and methanol, making it convenient in multi-step routes. That might seem minor until you’re running parallel reactions and find one batch won’t dissolve or keeps precipitating out—guaranteed to slow down scale-up and optimization.
Manufacturing (S)-4-Benzyl-1,3-Oxazolidine-2-Thione demands close control from step one. We begin with chiral amino alcohols and bench-validated benzyl bromide routes, always under continuous glove-box nitrogen for the sensitive condensation and thione formation steps. Midway, our plant team runs in-process HPLC and tests crude samples with rapid TLC, NMR, and melting point checks. After washing and crystallization—done at controlled, moderate temperature—the result is a resilient crystalline product that holds up to transit, lab handling, and long-term bench storage.
Most clients come with the expectation of kilogram-scale supply, particularly for pilot and scale-up chemistry. We set up production with the flexibility to switch between batch and continuous-flow methods, adjusting to shifting demands from pharmaceutical groups, contract research organizations, and universities. Our direct oversight guarantees both prompt delivery and a short feedback loop—every customer query about solubility, purity, or application reaches the chemist who knows the batch, not a call center clerk reading a script.
We’ve invested in specialized plant infrastructure—think multi-head filtration assemblies for rapid batch swaps and redundant nitrogen lines for extra protection during storage. Any time a client flags an issue, adjustments happen quickly. For example, in the rare event of batch inconsistency, teams review logbooks, test archived samples, and either reprocess material or, in critical settings, rerun the whole batch. The result is ongoing trust: our partners return not because we’re cheapest, but because we deliver on quality and accountability.
Producing high-quality (S)-4-Benzyl-1,3-Oxazolidine-2-Thione goes beyond chasing yields or cut-rate pricing—it’s about delivering a product that’s safe for labs and responsible for our community. Full attention gets paid to containment, emission reduction, and waste treatment. We’ve invested in upgraded scrubber technology and onsite solvent recycling. By cutting down on volatile emissions and maximizing material re-use, both operations inside the plant and partner labs outside see real safety benefits. Some users worry about unpleasant odors or hazardous residues from sulfur-containing materials; our plant’s strict containment and final purification minimize these risks.
We also maintain up-to-date documentation on hazardous labeling, storage requirements, and safe disposal, based on our lived experience in handling and shipping the material. Practicing what we teach, all drivers and handlers receive practical safety training—not just slide decks and sign-offs. Because when your own team risks exposure, there’s incentive to hold standards high and continually improve safety protocols.
Chemists in pharma and advanced materials keep coming back for (S)-4-Benzyl-1,3-Oxazolidine-2-Thione because it helps solve specific selectivity problems other auxiliaries just aggravate. In enantioselective alkylations, its chiral environment and steric shielding grant tight control over the formation of carbon-carbon or carbon-heteroatom bonds. That discipline translates to reduced downstream purification effort, clearer analytical workups, and, most importantly, more consistent production of critical intermediates or end-use materials.
Beyond mainstream enantioselective reactions, research groups have pushed this molecule into new types of cyclizations, radical reactions, and multi-component couplings. Because our product stands up to these demanding tests, labs report fewer headaches—not only in reaction consistency but also during auxiliary removal and recovery steps. We’ve watched as customers tune conditions to maximize yield and then recover and recycle much of the auxiliary for future use. This isn’t just about saving money; it keeps waste streams minimal and lets researchers push for more sustainable, circular chemistry approaches.
Functional group tolerance counts for a lot. Some auxiliaries break down under moderately harsh or oxidizing conditions. Over the years, we’ve proofed our product in protocols involving strong bases, mild oxidants, and even some transition-metal catalysis—little or no degradation or racemization, whether the scale is milligrams or tens of kilos.
Delivering a trustworthy chemical means more than certifying analysis reports—it calls for manufacturer transparency and directly addressing questions from users. We’ve taken feedback from hundreds of distinct syntheses to tweak purification and packaging. Some researchers value screw-cap glass over plastic, some want bulk drums for scale-up. We listen, evaluate, and adapt. If a user spots a problem after delivery—say, particles, clumps, or a color shift—our tech team tracks back every process record and reruns key analyses. This direct, human approach isn’t about ticking compliance boxes. It’s about standing beside every batch and learning from every order.
There’s more to reliable service than shipping on time. We routinely share non-confidential techniques for handling, storage, and even modified protocols that help labs avoid waste or unproductive reaction pathways. Customers appreciate being able to discuss not just theory and data but hands-on troubleshooting, whether they’re in academia or manufacturing themselves. Calls and messages don’t go to a help desk; they land on the desks of our technical team with actual plant experience.
Making (S)-4-Benzyl-1,3-Oxazolidine-2-Thione yourself—rather than buying generic stock—yields insights you can’t find in catalogs. We control variables that often get ignored: reaction time, temperature ramps, and the subtle influence of trace impurities on stability. Our plant teams developed in-process controls so tight that, once a target batch is approved, chemists don’t run into surprises mid-process.
Handling unknowns head-on, we find and fix issues quickly. Raw material supply hiccups are handled with alternate sourcing and continuous quality checks. Nobody gets the luxury of going back to a distributor and blaming upstream suppliers; the onus sits here. This brings a level of accountability that keeps the entire operation honest. We’re proud that our customers return for the technical reliability they’ve experienced firsthand, not simply the lure of a low bid or faster paperwork.
Change in synthetic chemistry doesn’t wait for push-button solutions—users try new methods, shift from small-scale R&D to manufacturing, or jump into green chemistry. We tune our own plant flexibility so partners aren’t limited by supply chain delays or sudden batch-to-batch changes. That includes scheduling around urgent needs, offering technical feedback when someone pushes the chemistry in new directions, and prepping small or custom scales on short notice.
Looking ahead, applications keep evolving. We maintain strong links with both industry consortia and university groups, exchanging insights and finding new synthetic routines. For any chemist trying to maximize synthetic value, reduce cost, or minimize waste, (S)-4-Benzyl-1,3-Oxazolidine-2-Thione stands ready as a tool with proven reactivity, robustness, and ongoing support.
Trust in chemicals grows from two elements: proven quality on the bench, and responsiveness from the people who make them. Our company backs every gram with lived experience—reliable supply, consistent enantiopurity, and hands-on support for challenging synthetic plans. Anyone can print a spec sheet or quote purity figures. We stand ready to discuss, troubleshoot, and update methods based on users’ real-world needs.
The world of chiral synthesis is unforgiving of error, and tolerates little downtime. For teams invested in next-generation pharma, advanced research, or new material synthesis, (S)-4-Benzyl-1,3-Oxazolidine-2-Thione isn’t just a line item. It’s a bridge to more efficient, accurate, and sustainable chemistry, delivered by those committed to not just serving the market—but advancing it.