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(R)-Styrene Oxide

    • Product Name (R)-Styrene Oxide
    • Alias (R)-Epoxyethlybenzene
    • Einecs 207-433-4
    • 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
    VTB
    Specifications

    HS Code

    968130

    Cas Number 20780-54-5
    Molecular Formula C8H8O
    Molecular Weight 120.15 g/mol
    Iupac Name (R)-2-phenyloxirane
    Appearance Colorless liquid
    Boiling Point 194-195 °C
    Melting Point -60 °C
    Density 1.052 g/cm³ at 25 °C
    Optical Rotation [α]D20 +39° (neat)
    Purity Typically ≥98%
    Solubility Insoluble in water, soluble in ethanol and ether
    Refractive Index n20/D 1.535

    As an accredited (R)-Styrene Oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (R)-Styrene Oxide, 25g, is packaged in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping (R)-Styrene Oxide is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is transported under standard ambient conditions, with clear hazard labeling due to its flammable and irritant properties. Shipping complies with applicable chemical safety regulations, including appropriate documentation and emergency handling instructions.
    Storage (R)-Styrene Oxide should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong acids, bases, and oxidizing agents. Keep the container tightly closed and protected from light. Use a corrosion-resistant container and label it clearly. Store under inert atmosphere, if possible, to prevent unwanted reactions.
    Application of (R)-Styrene Oxide

    Applications of (R)-Styrene Oxide in Industrial Manufacturing

    (R)-Styrene Oxide serves as a valuable chiral intermediate across multiple specialty chemical and pharmaceutical industrial sectors. Our production quality and enantiomeric purity support process-critical demands in each downstream application, from synthetic APIs to advanced material building blocks. The following sections outline verified industrial uses, handling requirements, incorporation ratios, process flows, and resulting end-product types.

    1. Pharmaceutical API Synthesis: Chiral Drug Intermediates

    Manufacturers of active pharmaceutical ingredients rely on this chiral epoxide as a building block for β-blockers, antifungals, and other enantiomerically pure compounds. Our material integrates at the asymmetric synthesis step, offering a controlled stereochemistry source. Downstream couplings or ring-openings require consistent enantiomeric excess and low impurity profiles, as specified by leading pharmacopoeias and regulatory agencies. Customers report lot-to-lot process performance in multi-kilogram batch syntheses for both clinical and commercial production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • USP/NF Monographs for related chiral intermediates
    • 21 CFR Part 210/211 (FDA cGMP for finished pharmaceuticals)
    • EMA Guideline on chiral active substances

    Typical usage ratio

    • 0.85–1.20 molar equivalents per targeted API intermediate
    • Adjusted based on process stoichiometry and desired yield, with excess minimized to reduce purification load

    Downstream process integration

    • Introduced at the enantioselective ring-opening or coupling stage
    • In-line chiral purity testing by HPLC post-addition
    • Followed by downstream functional group transformations
    • Intermediate isolation before final API salt formation or crystallization

    Final product types

    • Metoprolol (β-blocker API)
    • Terconazole (antifungal API intermediate)
    • Enantiopure β-aminoalcohols for CNS drug candidates
    • Custom chiral pharmaceutical building blocks

    2. Agrochemical Actives: Stereoselective Synthesis

    Our (R)-enantiomer enters agrochemical active ingredient synthesis where chirality influences biological activity. Producers select this raw material for construction of pyrethroid insecticides, herbicides, and certain fungicides. In these processes, chemists use asymmetric opening or further functionalization steps to generate crop protection agents with defined stereochemical profiles, critical for regulatory approval and field performance.

    Industry compliance standards

    • ISO 9001:2015 quality management systems
    • FAO/WHO specifications for pesticide actives
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • REACH registration for chemical intermediates

    Typical usage ratio

    • 0.90–1.10 molar equivalents per targeted agrochemical intermediate
    • Ratio adapted to synthesis route and yield optimization per batch

    Downstream process integration

    • Added at chiral ring opening or esterification stages
    • Inline GC/MS confirmation of conversion rates
    • Purification prior to formulation with adjuvants or carriers
    • Pre-final agrochemical formulation blending

    Final product types

    • (R)-Fenpropathrin (pyrethroid insecticide precursor)
    • Chiral herbicide intermediates
    • Fungicidal actives with defined enantiomeric content
    • Chemical standards for residue analysis

    3. Epoxy Resin Modifiers for Fine Polymers

    In the high-performance polymers sector, (R)-Styrene Oxide modifies formulations for specialty epoxy systems. Resin compounders and electronic encapsulation material producers use this chiral epoxide to enhance curing behavior and introduce optical or adhesion properties. The material combines with bisphenol A-based resins under precise ratios and process conditions to control final mechanical and dielectric characteristics in advanced composite applications.

    Industry compliance standards

    • ISO 9001:2015 for quality management in polymer processing
    • RoHS Directive 2011/65/EU for restricted substances
    • UL 94 flammability safety standards (where applicable)
    • Customer-specific resin purity protocols

    Typical usage ratio

    • 2–6 wt% as an epoxy resin modifier
    • Can vary with total epoxy value and targeted performance specifications

    Downstream process integration

    • Blending at prepolymer stage with main resin feedstock
    • Catalyzed ring-opening during resin crosslinking
    • In-situ monitoring for viscosity and exotherm control
    • Post-cure property testing for optical clarity or dielectric breakdown strength

    Final product types

    • Optically clear potting compounds
    • Specialty adhesive films for electronics
    • Structural composite resins for aerospace or automotive
    • Custom dielectric encapsulants

    4. Chiral Fine Chemical Synthesis: Analytical Standards and Reagents

    OEM suppliers and laboratories utilize (R)-Styrene Oxide in standardizing chiral analysis methods and producing certified reference materials. This application requires high enantiomeric excess, full spectral identification, and documented impurity profiles for method validation in regulatory and research environments. Laboratories incorporate the material into custom chemical kits or as controlled reaction precursors for analytical testing.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • ISO 17025 for calibration laboratory accreditation
    • GLP (Good Laboratory Practice) guidelines
    • NIST-traceable analytical certification schemes

    Typical usage ratio

    • 0.1–1.0 wt% when formulating analytical calibration kits
    • Volume precisely adjusted according to test method sensitivity and required quantification limits

    Downstream process integration

    • Directly dispensed into kit reagent vials or HPLC vials
    • Aliquoting and packaging in cleanroom conditions
    • Stability testing for shelf-life documentation
    • Certification alongside co-analytes and internal standards

    Final product types

    • Enantiopure chiral reference standards
    • High-purity analytical reagents
    • Calibration kits for epoxide quantification
    • Chiral chromatography performance benchmarks

    5. Fine Flavors and Fragrance Synthesis: Specialty Aroma Ingredients

    A select number of specialty flavor and fragrance producers utilize the (R)-enantiomer as a precursor for certain aroma compounds modeling styrene oxide’s chiral structure. Chemical synthesis routes incorporate this input at the step generating fragrance alcohols or ethers with specific olfactory notes. Food safety, purity, and batch identity are critical due to direct sensory and regulatory scrutiny, often supported by robust analytical profiling and traceability documentation.

    Industry compliance standards

    • IFRA (International Fragrance Association) codes and purity guidelines
    • FCC (Food Chemicals Codex) flavor ingredient standards
    • ISO 22000 food safety management systems (where food contact is involved)
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients

    Typical usage ratio

    • 0.5–3.0 wt% in fragrance or flavor precursor formulations
    • Proportion optimized for olfactory intensity and downstream synthetic yield

    Downstream process integration

    • Entering the sequence during chiral alcohol or ether synthesis
    • Inline GC-FID monitoring for target molecule appearance
    • Final vacuum distillation and purity assurance post-synthesis
    • Blending with essential oil or alcoholic bases for characterization

    Final product types

    • Chiral aroma compounds (e.g., certain florals, balsamic notes)
    • Flavor bases for confectionery or beverage use
    • Fine perfumery intermediates
    • Traceable food-grade fragrance chemicals
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    Certification & Compliance
    More Introduction

    (R)-Styrene Oxide: Practical Insights from Production and Application

    Introduction to (R)-Styrene Oxide

    At our plant, every batch of (R)-styrene oxide starts with a clear goal: consistent enantiomeric purity and dependable supply for demanding synthesis work. Our experience in stereoselective reactions reveals just how critical the right optical isomer becomes as the building block for pharmaceuticals, agrochemicals, and advanced polymer research. Producers like us see past a catalog number; we pay close attention to real-world effects of impurity profiles, water content, and handling during scale-up. This product doesn’t get made in a vacuum—choices we make during process chemistry shape what customers can achieve at the bench or in the pilot reactor.

    Model and Specifications as a Result of Production Priorities

    We manufacture (R)-styrene oxide with specifications tailored for reliable downstream transformations. Stereochemical integrity stays top-of-mind. Regular batches offer optical purities above 99% ee with GC and chiral HPLC confirmation. Color and clarity matter, especially when the next reaction needs to avoid unknown side products. Our product runs clear and water white, meeting stringent appearance checks from visual assessment to UV-Vis absorbance. We hold moisture below 0.2% w/w, verified by Karl Fischer titration, to minimize problems in epoxide opening steps or Grignard reactions. Many forget the headaches a few tenths of a percent water can create on a pilot line or in an automated reactor—yield drops, longer drying times, and extra troubleshooting. We have learned from each run, knowing that lab-scale specs won’t always survive at hundred-liter volumes unless every variable stays closely watched.

    Manufacturing Approach and Repeatability

    We operate under tight control with validated synthetic routes. Chiral resolution takes center stage, not as a gimmick but as a matter of customer trust—when polymers or APIs require the (R)-enantiomer, even a few percent of (S)-styrene oxide means trouble down the line. Our in-house catalysts and work-up techniques eliminate racemization risk as temperatures scale up or cycle times shift for larger vessels. Every operator knows that a few extra minutes at elevated temperatures influence not just yield, but also optical purity and reaction color. By tracking each production lot, we supply traceable, batch-specific data with every shipment.

    Why (R)-Styrene Oxide Stands Apart

    Customers often ask how our (R)-styrene oxide differs from generic or racemic material found from traders or bulk resellers. The answer sits in the selectivity and documented reproducibility. While some processes tolerate racemic material, most advanced research protocols and chiral synthesis routes require the right isomer every time. We notice the difference in how our product performs under challenging asymmetric catalysis and in-site resolution experiments. Typical batches from commodity sources can display broad optical ranges and uncertain contamination risks—a fact exposed when partners run their own internal controls. Over the years, feedback from process chemists using our lots in API and agrochemical intermediates confirmed that consistent stereospecificity cuts troubleshooting cycles and increases batch yields.

    Applications in Real-world Chemistry

    Our (R)-styrene oxide gets used in diverse research and manufacturing pathways. Most commonly, it serves as a chiral precursor in synthesis of beta-adrenergic agents, select antifungal drugs, and several insecticides. Epoxide ring-opening reactions benefit from high enantiopurity—without it, diastereoselective and regioselective control falters and purification turns into an uphill battle. During polymer development, certain specialty copolymer streams gain improved flexibility or reactivity thanks to the orientation of the (R)-epoxide unit. We learned from a partner working on elastomeric block copolymers that trace racemization led to batch failure at the pilot scale due to unnoticed microstructural defects. In academic research, this molecule helps elucidate reaction mechanisms in asymmetric catalysis and studies of enzyme selectivity. We routinely field technical questions about ring-opening, nucleophilic substitutions, and isomer retention in process development, helping users troubleshoot and plan ahead.

    Practical Manufacturing Challenges and Solutions

    Every synthetic step in our production carries its own risks. Air and moisture management drive daily routines, as styrene oxide can hydrolyze or undergo side-reactions in the presence of trace acids or water. We emphasize sealed systems, rigorous glassware cleaning, and molecular sieves for long-term storage. While these controls seem simple, even a small procedural slip has introduced setbacks in the past—decomposition, yellowing, and inconsistent assay values. To mitigate these risks, we developed internal standards for continuous monitoring and run double checks at each crucial stage, from epoxidation through final distillation. Personnel training cycles include real-world case studies: a single missed vacuum check on the distillation line can set back an entire lot’s schedule or force partial reprocessing.

    Process Improvements Based on Customer Feedback

    End-user feedback drives our improvements. Clients consistently raised purity and reactivity questions that generic vendors often ignore. In one instance, a European customer flagged higher than expected byproduct formation in a key reductive amination due to trace phenylacetaldehyde. We traced the source to an unexpected minor side reaction during pilot-scale oxidation steps. Our technical team re-examined catalyst ratios and oxygenation rates, leading to a process patch that tightened byproduct controls across all future lots. Since then, similar customer observations have further shaped how we conduct quality assurance, from reaction monitoring to post-synthesis workup and packaging.

    The Role of Analytical Techniques in Quality Assurance

    We continually invest in analytical equipment and protocols. Beyond basic GC and HPLC for purity and enantiomer measurement, we rely on NMR, FTIR, and even advanced mass spectrometry to chase after small but significant impurities. Each incoming raw material faces an analytical gauntlet—slight shifts in supplier stocks or storage conditions can influence how the product turns out, sometimes by introducing unexpected trace metals or background oxidation products. Our quality team conducts regular method development reviews, integrating lessons from client and internal applications alike. Only compounds that meet or exceed our reproducibility and selectivity expectations make it out the door to customers relying on batch-to-batch repeatability.

    Shelf Life, Storage, and Shipment Practices

    Maintaining product stability ranks high in our day-to-day operations. (R)-styrene oxide shows a tendency to polymerize or alter color if left exposed to light or air. Every shipment leaves the site in amber glass or coated HDPE containers under nitrogen. Some users overlook the need for careful handling at receipt, so we share detailed storage protocols based on our own long-term stability tests—cool, dry, and oxygen-free environments bring the longest shelf life. After observing a few returns from customers who stored material in open warehouses or near heat sources, we ramped up our technical support and training for safe chemical management. These steps keep projects on track in both major industrial settings and research labs.

    Distinct Features and Differences from Other Epoxide Materials

    Comparing (R)-styrene oxide to related epoxides or the racemic version, we spot several concrete differences that matter in practice. Our enantiopure (R) form delivers predictable reactivity and selectivity in stereospecific transformations, as confirmed in customer pilot runs and our internal scale-up trials. Racemic alternatives lead to double the work during purification and lower process yields for enantioselective syntheses. Industrial projects engaged in chiral pool synthesis report halved downstream reject rates and less troubleshooting with material that matches their intended optical configuration.

    Relative to propylene oxide and other smaller aliphatic epoxides, styrene oxide offers a unique balance of aromatic reactivity and greater handling ease—lower volatility and better stability in most neutral, dry conditions. The aromatic group lets it serve in specialized polymerizations or nucleophilic substitutions where increased reactivity unlocks novel end-products. Our production team keeps records from hundreds of reaction screenings showing where (R)-styrene oxide brings a clear operational advantage. These differences become especially plain during scale-up, where solvent compatibility, product isolation, and waste reduction come under the microscope.

    Supporting Users Facing Application Hurdles

    Our work with users goes far beyond simply shipping material. Customers working on new pharmaceutical actives or bio-catalysis projects often run into snags around solubility, ring-opening rates, or side-product management. We offer detailed application notes drawn from years of process experience—not just generic advice, but problem-specific troubleshooting informed by actual run reports. One example involved a customer’s Grignard addition that produced lower than expected yields, ultimately traced to subtle local heating issues in the reactor and incomplete exclusion of trace water. Drawing from similar events in our own process, we helped model improved addition rates and moisture control, setting the stage for better product consistency. These exchanges help us strengthen both our own production and our customers’ chances of project success.

    Meeting Regulatory and Environmental Expectations

    Chemical manufacturing operates under scrutiny—each molecule, intermediate, and by-product may face local or regional regulatory requirements. Our product records align with both domestic and international expectations for purity and traceability. Strict batch tracking, waste handling, and emission controls limit risk both for us and for our downstream partners. Customers working toward cGMP process compatibility find our documentation and process controls ready for integration into highly-regulated production schemes. Regular audits, internal and external, further encourage a culture of quality and accountability in our ranks.

    Looking Ahead—Evolution in Chiral Epoxide Technology

    The needs for (R)-styrene oxide continue to shift along with advances in pharmaceuticals, agrochemicals, and specialty polymers. New demands around greener synthesis, process intensification, and continuous flow drive us to adapt our scale-up protocols. Our team tracks alternative epoxidation routes, improved chiral catalyst systems, and lower-energy isolation techniques. Several ongoing collaborations with academic and industrial partners aim to enhance yields while cutting down on waste and energy input. We recognize that no product stands still in this landscape—each production batch offers lessons that feed straight into our next improvements, helping secure reliability for customers on tight timescales and stricter regulatory frameworks.

    Conclusion: Why Source from a Direct Manufacturer

    Years of experience show the risks of purchasing critical intermediates like (R)-styrene oxide through third-party channels. Product passing through multiple hands often loses traceability, shifts in purity, or arrives subject to questionable storage. Direct supply from a manufacturer ensures established processes and up-to-date batch data, rapid technical support, and customer-focused improvements. Our investment in production experience, process control, and problem-solving capacity ultimately supports a smoother path from gram-scale concept to commercial rollout. This level of partnership emerges only from direct collaboration—a philosophy that guides our approach to every shipment of (R)-styrene oxide leaving our gates.