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HS Code |
590305 |
| Iupac Name | (S)-2-(2-Methoxyphenyl)oxirane |
| Cas Number | 120255-61-8 |
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.18 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 255-257°C |
| Density | 1.13 g/cm3 |
| Optical Rotation | [α]D20 +43° (c=1, CHCl3) |
| Purity | Typically ≥98% |
| Smiles | COc1ccccc1C2OC2 |
| Inchi | InChI=1S/C9H10O2/c1-11-9-5-3-2-4-8(9)7-6-10-7/h2-5,7H,6H2,1H3/t7-/m0/s1 |
| Synonyms | (S)-2-(2-Methoxyphenyl)oxirane, (S)-2-Oxiran-2-ylanisole |
As an accredited (S)-2-Oxiranylanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | (S)-2-Oxiranylanisole, 10g, is supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling. |
| Shipping | **Shipping Description:** (S)-2-Oxiranylanisole is shipped in tightly sealed containers under ambient conditions. The packaging ensures the chemical’s integrity, preventing exposure to moisture and light. Shipment must comply with local and international regulations for safe handling of organic compounds. Appropriate labeling and documentation accompany each shipment to ensure safe and compliant transport. |
| Storage | (S)-2-Oxiranylanisole should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong acids, bases, and oxidizing agents. Refrigeration (2–8°C) is recommended to prevent decomposition. Ensure all storage complies with relevant chemical safety regulations and guidelines. |
Applications of (S)-2-Oxiranylanisole in Industrial ManufacturingAs an established producer of (S)-2-Oxiranylanisole, we supply this chiral epoxide to global manufacturers across high-value sectors. Its precise stereochemistry enables highly specific syntheses and functionalization steps for advanced performance materials and life science applications. Below, we detail core industrial downstream use scenarios, process requirements, integration positionings, and regulatory frameworks verified with major customer projects. 1. Chiral Intermediate for Active Pharmaceutical Ingredient (API) SynthesisThis molecule serves as a key chiral building block in the enantioselective preparation of various pharmaceutical actives, including non-steroidal anti-inflammatory drugs and beta-blockers. Contract manufacturing organizations and originator companies integrate the compound at early or mid-stage synthetic steps to establish required chirality or to facilitate ring-opening with nucleophiles for API core construction. Typical workflows incorporate quality-by-design principles and traceability at every hand-off, integrating our material under validated supply agreements. Industry compliance standards
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2. Advanced Fragrance Ingredient ManufacturingThe compound finds targeted use as a precursor in the synthesis of chiral aroma chemicals, which impart floriental, anisic, or fresh powdery notes to premium perfumery bases. Fine fragrance manufacturers value its chiral purity for producing unique olfactory profiles that are distinguishable from racemic blends. It also enables controlled modifications for functional groups that improve diffusion or tenacity. Integrators prioritize sensory analysis and direct regulatory compliance due to the low inclusion rates required for effect. Industry compliance standards
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3. Chiral Epoxy Resin Modifier for Electronic EncapsulationSelected epoxy resin formulators add the compound as a chiral modulator to enhance cross-link density and thermal performance in specialty electronic encapsulant systems. Its precise epoxide stereochemistry supports improved dielectric properties and customized cure kinetics, especially for microelectronic device protection. The material integrates into proprietary resin blends before hardener dosing, with incoming and outgoing QC for batch-to-batch traceability required by electronics OEMs. Industry compliance standards
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4. Chiral Auxiliary for Agrochemical SynthesisAgrochemical producers exploit the stereoselective features of this compound to introduce specific chirality into active pesticide or herbicide molecules, which can directly influence field performance and environmental dissipation rates. The ingredient is incorporated at chiral introduction steps in multi-stage syntheses, with finished batch monitoring for residual content and optical purity. Regulatory authorities require traceable production records and established conjugation methodologies throughout manufacturing campaigns. Industry compliance standards
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Through years of manufacturing specialty chemicals, (S)-2-Oxiranylanisole has become a staple product thanks to its reliable structure and consistent performance in enantioselective synthesis. Many chemical plants look for reagents with defined stereochemistry when producing high-value pharmaceutical intermediates or calibrating advanced materials, and this compound’s (S)-configuration remains a proven cornerstone in those efforts. In our labs, this enantiomer is produced to minimize racemic impurities and help research teams pursue the selectivity that modern applications demand.
(S)-2-Oxiranylanisole features an epoxide moiety fused directly to an anisole ring, resulting in a chemical with distinct reactivity and dependable stability during both storage and use. In practical terms, this oxirane offers a blend of aromatic reactivity and mild ether character. Chemists seeking chiral building blocks gravitate to (S)-2-Oxiranylanisole because it lets them construct new molecules with predictable stereochemical outcomes. This product regularly anchors the synthesis of active pharmaceutical ingredients, agrochemical candidates, and specialty chemicals requiring strict control over isomeric purity.
Direct from our reactors, every batch of (S)-2-Oxiranylanisole comes from carefully selected raw materials. Over the years, we have optimized our production lines to ensure tight control over stereochemical outcome, not only at the point of chirality induction but all the way through to final purification. In real-world use, chemists often cite contamination by trace enantiomers as a source of excessive downstream purification costs. Through meticulous process design, we have cut those costs for our clients by keeping minor isomer content consistently low. No material leaves our plant without confirmation by chiral HPLC and other robust analytical tools.
Material purity sits at the heart of all we do. After repeated cycles of overhead distillation, low-temperature crystallization, and chromatographic polishing, our outgoing samples deliver both reliability and reproducibility. Facility updates have trimmed solvent consumption and energy draw, but product integrity remains steady, batch after batch. Our experience confirms that keeping close tabs on precursor quality pays off by avoiding surprises during scale-up and reducing waste.
R&D teams turn to (S)-2-Oxiranylanisole when precision matters. Enantiopure epoxides often play a central role in advanced synthetic chemistry, where downstream yields hang on the stereo integrity of core building blocks. In our hands, (S)-2-Oxiranylanisole acts as a selective electrophile, helping users drive reactions with high enantiomeric excess. The slight ring strain in the oxirane supplies enough energy to encourage nucleophilic addition, which is valuable in ring-opening reactions or in forming C—C and C—N bonds under controlled conditions.
Pharma clients frequently discuss how the consistency of our product simplifies both process documentation and regulatory filings. Regulatory professionals appreciate knowing that batch-to-batch variations remain minimal and that QC procedures at the source account for not only chemical content, but also residual solvents and trace metals. Reliable input chemicals directly support robust downstream results: that’s become a recurring trend in client feedback since we brought this product to market.
Reflecting feedback from partners in both industry and academia, we keep specifications practical and in line with actual laboratory needs. All (S)-2-Oxiranylanisole leaving our plant measures at least 99 percent chemical purity, and enantiomeric excess confirms the chiral preference. Since moisture and oxygen sensitivity are moderate, only standard precautions are needed—a simple nitrogen atmosphere during storage is enough for months of stability. It offers a boiling point that suits most pilot-plant distillation set-ups, so solvent removal by rotary evaporation or low-pressure distillation works seamlessly.
Color and odor are not entirely trivial: small changes can often signal degradation or side reactions in storage. We encourage users to monitor for any off-notes, though in our experience, tightly sealed, light-excluded packaging keeps the product lively and colorless. Glass is preferred for small-scale use; for bulk, lined drums have shown no detrimental effect.
Having watched research teams use our product across several continents, the major uptake remains in pharmaceuticals. Medicinal chemists often build chiral amines or β-aryl alcohols by selective opening of the epoxide ring using metal-catalyzed or enzymatic methods. In our own collaborations, one group produced candidate antifungals through direct ring opening with heterocyclic nucleophiles, using our (S)-2-Oxiranylanisole as the starting linchpin. Their overall yield improved not only due to selectivity of the product, but also because batch-to-batch variation dropped sharply after switching to a consistent vendor.
In flavor and fragrance research, the compound delivers a unique intermediate stage in the creation of novel ethers and aromatic alcohols. Newer green chemistry approaches often look for products that tolerate milder reaction conditions, and (S)-2-Oxiranylanisole readily participates in such schemes. The product’s volatility also makes it a manageable player in continuous processes with vapor-phase catalysis.
We have seen the occasional challenge—most commonly, accidental exposure to strong acids or bases can trigger undesired polymerization. Maintaining careful pH control solves this. Temperature excursions are another concern, especially in facilities where control systems see heavy daily use. We stress the importance of continuous monitoring, rather than spot checks, to prevent unpredictable side reactions during large-scale operations.
Not all chiral epoxides deliver the same blend of performance and manageability. Some lack the methylated aromatic structure that makes (S)-2-Oxiranylanisole uniquely versatile. Straightchain or aliphatic chiral epoxides tend to display less aromatic reactivity, while bulkier, more functionalized analogues struggle with solubility in standard solvents. Delicate substrates sometimes need a product like ours, which bridges both aromatic substitution and confident reactivity at the oxirane.
Despite a crowded field of potential chiral starting materials, repeated customer feedback favors (S)-2-Oxiranylanisole because it allows tighter control over downstream regioselectivity and can tolerate mild bases or acids. In head-to-head comparisons, we see chemists choosing our compound over glycidyl ethers, where selectivity or side reactions pose more frequent cleanup hurdles. Compared to symmetrical epoxides, the ortho-methoxy substitution gives reaction designers a new handle for tuning selectivity.
For scale-up, the consistent boiling point and manageable viscosity of our product contrasts with thicker or lower-yielding alternates. From a reactor operator’s standpoint, the ability to track and control color and purity with simple HPLC methods turns everyday maintenance into a streamlined practice. Production facility managers comment that reduced fouling and less residue lead to longer catalyst life and simplified cleaning protocols.
Rising scrutiny around sustainability and raw material traceability has shifted how we source our initial building blocks. Traceability remains a cornerstone in chemical manufacturing. All feedstocks for (S)-2-Oxiranylanisole trace back through verified supply chains with documented origins, typically reflecting responsible practices in aromatics refining. As a direct manufacturer, we understand that shortcutting normal documentation breeds not only compliance risk but also the chance of unpredictable side effects in final product.
We invest in solvent recovery loops, waste minimization tactics, and energy-efficient distillation techniques to reduce the product’s environmental footprint. By collaborating with major partners on green chemistry initiatives, we find ways to drive down hazardous waste without sacrificing throughput. Customers increasingly ask detailed questions about both energy consumption and lifecycle impacts, so transparent reporting has become part of our regular practice.
Future projects seek to close material loops further; one effort involves recovering spent solvents and turning production waste into reusable process inputs. As market needs shift, these investments mean customers won’t face abrupt specification changes. Our commitment to steady, transparent manufacturing standards aims to back every innovation our downstream partners bring to market.
Certainty in chemical purity can’t come just from a product label. In practice, we run GC-MS, NMR, and chiral HPLC analysis for every lot, not just random samples. These checks reveal trends even before a product ever reaches a customer’s shelves. We hold back shipments for review any time outliers appear, regardless of how minor. This may slow down logistics on occasion, but our data shows long-term reliability outpaces short-term gains from aggressive dispatch policies.
Over the years, analytical teams have found the most common off-spec cause comes from subtle increases in byproducts during extended storage. Shifts in container permeability or warehouse climate can unbalance carefully tuned molecular ratios, so detailed records of shipping climate, transit times, and storage environments accompany every consignment. Our technical support stands ready with interpretive guidance in these rare events—something only a direct manufacturer, with deep process insight, can offer in real time.
Our clients provide some of the sharpest eyes for minor deviations in product profile. Directly interacting with process chemists and pilot plant teams uncovers real operational insights. Several improvements to our workflow have come from suggestions made during tech transfer and scale-up support, especially as new regulatory or operational demands enter the field.
Experience shows that user feedback, gathered from both small research labs and large contract manufacturers, brings to light the most actionable insights. For example, a switch from one drum lining material to another only emerged due to spotting trace metal upticks in a handful of client postreaction samples. Taking such reports seriously and converting them into documented process change is built into our continuous improvement philosophy.
No product remains static. The real-world needs of our clients push us to refine protocols, uproot inefficiencies, and share the resulting gains with every new user. Our technical team meets not only compliance checklists but also practical demands from the field: less batch variability, fewer process interruptions, and a clear support path if troubleshooting ever arises.
Industrial chemistry faces ever-tightening rules on both safety and traceability. Our approach balances secure handling, end-to-end documentation, and actionable batch data in an accessible format. Certificates of analysis for (S)-2-Oxiranylanisole address not just physical and chemical parameters but also trace allergen presence, solvent residues, and relevant inorganic ion traces.
Practical compliance means embedding audit-friendly protocols into every stage of production. For years, this mindset has saved our partners days of review time during new supplier QA or regulatory audits. As each new pharmacopoeial standard or updated REACH guideline arrives, our in-house laboratory adapts to make sure every requirement is met ahead of customer requests. When rules change, we update data logs and supply chain documentation in near real-time.
Laboratory syntheses rarely scale without incident. Our technical support team liaises closely with pilot and kilo-lab partners worldwide, offering firsthand insight from our own scaling experience. Variations that seem trivial in hundreds-of-gram batches—such as thermal lag, agitation efficiency, or minor solvent effects—can trigger major downstream problems at tonnage.
We have compiled a database of practical observations based on both in-house experience and external feedback. Many customers report faster time-to-market, owing in part to preemptive troubleshooting tips that avoid common scale-up pitfalls. Some clients leverage this additional support not only during their first trials but also years later as they expand capacity or adapt their own processes. Our willingness to share lessons learned—rather than guard data behind paywalls—has fostered a network of mutual problem solving.
Building and supplying (S)-2-Oxiranylanisole has required ongoing adaptation, not just to market shifts but to the practical challenges faced by real users. Every improvement in product purity, stability, or processing performance reflects dialogue with hands-on chemists and process engineers, not just abstract design goals. Our perspective as a direct manufacturer—staying involved through production, delivery, and customer troubleshooting—drives each new iteration of both product and practice. Each batch shipped stands on years of accumulated technical judgment, tested by daily application across the chemical industry.