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2-(4-Fluorophenyl)Oxirane

    • Product Name 2-(4-Fluorophenyl)Oxirane
    • Alias fluoxetine impurity A
    • Einecs 631-103-4
    • 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

    375446

    Iupac Name 2-(4-Fluorophenyl)oxirane
    Molecular Formula C8H7FO
    Molar Mass 138.14 g/mol
    Cas Number 70458-96-7
    Appearance Colorless liquid
    Boiling Point 61-63 °C at 4 mmHg
    Density 1.14 g/cm3
    Pubchem Cid 161997
    Smiles C1C(O1)C2=CC=C(C=C2)F
    Inchi InChI=1S/C8H7FO/c9-7-3-1-6(2-4-7)8-5-10-8/h1-4,8H,5H2
    Refractive Index 1.521
    Melting Point -23 °C

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

    Packing & Storage
    Packing 250g of 2-(4-Fluorophenyl)oxirane supplied in a sealed amber glass bottle, labeled with hazard warnings and batch information.
    Shipping **Shipping Description:** 2-(4-Fluorophenyl)Oxirane should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must be clearly labeled as a chemical substance. Follow all applicable regulations for handling and transport, including appropriate hazard classification and documentation. Ensure secondary containment to prevent leaks or spills during transit.
    Storage Store 2-(4-Fluorophenyl)oxirane in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong acids, bases, and oxidizing agents. Protect from moisture and direct sunlight. Ensure appropriate labeling and use secondary containment if possible. Follow all relevant safety regulations and chemical storage guidelines.
    Application of 2-(4-Fluorophenyl)Oxirane

    Applications of 2-(4-Fluorophenyl)Oxirane in Industrial Manufacturing

    As a specialized manufacturer of 2-(4-Fluorophenyl)Oxirane, we support a range of advanced industrial markets where structural precision, controlled reactivity, and stringent product safety remain critical. Below, we detail established downstream segments where this intermediate forms an indispensable part of well-documented chemical syntheses, highlighting sector-specific quality expectations and practical deployment throughout the value chain.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers rely on the selective epoxide function of this compound to construct fluorinated aryl building blocks for targeted API scaffolds, especially in oncology and CNS drug development. The material's purity profile and controlled ring-opening facilitate stepwise modifications, while regulatory compliance drives both process and documentation rigor. Integration must match process validation stages in accordance with regional and global pharmaceutical standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) as per 21 CFR Parts 210/211 (FDA, US)
    • European Pharmacopoeia (Ph. Eur.) relevant monographs
    • Chinese Pharmacopoeia for qualifying process intermediates

    Typical usage ratio

    • Added as 0.15–0.35 molar equivalents per target aryl epoxide transformation, optimized based on target route yield and impurity thresholds

    Downstream process integration

    • Charged in the mid-stage synthesis as a primary electrophile for regioselective nucleophilic opening
    • Pursued further by hydrolysis or coupling during multi-step API assembly

    Final product types

    • Oncology API intermediates (e.g., fluorinated phenyl derivatives for kinase inhibitors)
    • CNS drug active ingredients requiring fluorinated aromatic epoxides
    • Antiviral intermediates incorporating fluorinated aryl motifs

    2. Fluorinated Epoxy Resin Modifier for Advanced Composites

    Specialty resin producers adopt this raw material as an additive or co-monomer in high-performance composite matrices, targeting improved mechanical properties and chemical resistance. Accurate dosing enables the introduction of fluorine atoms, which increase hydrophobicity and thermal stability in aerospace, electronics, and automotive structural parts. The formulation process requires precise tracking under resin system specifications and downstream substrate compatibility.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems for resin manufacturing
    • RoHS Directive (2011/65/EU) on hazardous substances for electronic applications
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC/1907/2006) for raw material traceability in Europe
    • UL 94 flammability standard when integrated into electrical insulation products

    Typical usage ratio

    • Typically dosed at 1–6% by weight relative to the total epoxy resin content, adjusted according to matrix viscosity and targeted cross-linking density

    Downstream process integration

    • Incorporated during the prepolymer stage or as a reactive diluent directly in the compounding step
    • Co-reacted with base resins using amine or acid anhydride hardeners under controlled temperature conditions

    Final product types

    • Carbon or glass fiber reinforced structural composites
    • Encapsulation and potting compounds for sensitive electronics
    • Automotive exterior and under-the-hood molded assemblies

    3. Specialty Agrochemical Intermediate

    Agrochemical formulators use this compound as a core intermediate in the integration of fluorinated epoxides for selective herbicide, fungicide, and insecticide synthesis. Its electron-withdrawing properties enable the development of active ingredients targeting pest resistance profiles or improved soil mobility. Each batch supplied must sustain full traceability across high-purity benchmarks, while technical documentation supports regulatory submissions.

    Industry compliance standards

    • FAO/WHO pesticide specifications
    • OECD Principles of Good Laboratory Practice (GLP), especially for product registration studies
    • ISO 17025 accredited laboratory use for impurity profiling
    • National standards for agrochemical intermediates (e.g., GB/T China, EPA US registrations)

    Typical usage ratio

    • Introduced at 0.2–0.5 molar equivalents depending on the desired fluorine content in the final agrochemical molecule

    Downstream process integration

    • Serves as a key epoxidizing agent in early to mid-stage route design, subject to reductive or nucleophilic substitution steps
    • Converted via stepwise coupling and final functionalization before formulation into technical concentrate

    Final product types

    • Selective herbicide actives integrating fluorinated phenyl groups
    • Fungicides with enhanced stability and environmental half-life
    • Novel insecticidal compounds leveraging fluorine-based activity

    4. Advanced Coatings Additive for Chemical Resistance

    Coatings and surface protection designers favor this molecule to modify high-durability topcoats and primers for industrial, maritime, and anti-corrosion systems. Its role as a chemical resistance enhancer stems from the integration of fluorine and oxirane, delivering improvement in solvent resistance and surface energy control. Industrial formulators must balance additive levels with crosslinking agents and comply with applicable emission limits.

    Industry compliance standards

    • ASTM D5402 and ASTM D4359 for solvent resistance and coating stability evaluations
    • European Directive 2004/42/EC (VOC in paints and varnishes)
    • TQC global test methods for cure and performance
    • ISO 12944-6 for corrosion protection in structural steel coatings

    Typical usage ratio

    • Dosed at 0.5–3.0% by weight within the binder system, adjusted based on solvent system compatibility and final cure type

    Downstream process integration

    • Added in the pre-dispersing phase before pigment and filler charging
    • Cured in situ using thermal catalysts or photoinitiators, depending on the end-use environment

    Final product types

    • High-performance anti-corrosive primers for industrial metalwork
    • Protective coatings for chemical processing tanks and pipelines
    • Marine grade topcoats and protective sealers

    5. Fluorinated Polymer Synthesis Intermediate

    Polymer manufacturers target this compound for its tailored reactivity in the synthesis of fluorinated specialty polymers, valued in processes requiring strict control over backbone substitution and reactive group placement. Its application occurs in material classes demanding high glass transition temperatures, dielectric stability, or solvent repellence, supplying polymer chain customization during advanced monomer design.

    Industry compliance standards

    • ISO 14001 environmental management for polymer production
    • UL 746A testing for electrical insulation materials
    • REACH compliance for new polymer entities in Europe
    • FDA 21 CFR 177.2600 (rubber articles intended for repeat use), relevant for food-contact polymers when applicable

    Typical usage ratio

    • Applied at 0.8–2.5 molar percent relative to total monomer units, with ratios fine-tuned according to end-use mechanical/thermal properties

    Downstream process integration

    • Co-polymerized in solution or suspension polymerization setups
    • Fed as a functional comonomer or as a chain transfer agent, depending on target polymer architecture

    Final product types

    • Fluorinated specialty elastomers for microelectronics or seals
    • High-performance engineering plastics for automotive connectors
    • Solvent-resistant coatings polymers and membrane films
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    Certification & Compliance
    More Introduction

    2-(4-Fluorophenyl)Oxirane: A Direct Insight from the Production Floor

    Our Experience Producing 2-(4-Fluorophenyl)Oxirane

    Years spent in synthesis and quality control show us every little variable that goes into a truly consistent batch of 2-(4-Fluorophenyl)Oxirane. Colleagues talk about process tweaks or new equipment, but nothing replaces firsthand handling of a multi-kilo reaction. We’ve stood next to reactors, checked exothermic peaks, and measured purity after every step. The core of this product—sometimes called para-fluorostyrene oxide—isn’t exotic to a seasoned lab, but scaling it cleanly, without ghost contaminants, takes practice. In our plant, the reaction conditions stay under our direct watch, right from substrate selection (para-fluorostyrene always sourced fresh, by our choosing) to that final check under GC. Our people walk the line: all fluorinated compounds pose unique workflow hazards, so we’re methodical, even if it slows down a batch or two. No one wants surprises downstream.

    Model, Variant, and Purity Standards

    We manufacture our 2-(4-Fluorophenyl)Oxirane to strict internal specs. The primary batch model targets >99% GC purity, focusing on colorless, mobile liquids with proper spectral signatures. Most customers order lots produced with a model reaction temperature range that consistently limits by-product—especially avoiding unwanted phenyl acetaldehyde or deep epoxidation losses. No batch skips hands-on monitoring.

    We photograph vials, log NMR profiles for every run, and run FT-IR spot checks before the drum’s even sealed. Only a few grams out of a batch shows traces of regioisomers, but through tight column control and vacuum distillation, we keep levels below any threshold that could alter the chemical’s behavior in complex syntheses.

    Drum and ampoule packaging uses neutral, stable bottles approved to withstand both short- and longer-term storage—not just for our convenience in shipping but to avoid peroxide formation, a real risk with epoxides. We’ve learned to label every outgoing container with real batch dates, avoid ambiguous codes, and include a one-page QC trace.

    What Sets Our 2-(4-Fluorophenyl)Oxirane Apart

    Direct manufacturing offers one advantage rarely seen: we know exactly what went into the final product. Every step, from vacuum filtration to rotary evaporation, runs under our eyes. Over time, we’ve tweaked the process—less time on bench exposure, direct transfer from synthesizer to cold storage, tighter control of distillation under pressure. Thanks to these changes, we see fewer side products, less odor, and no visible sediment in the final stock.

    Some competing grades show inconsistencies from batch to batch. Flask-scale labs and trading companies often don’t catch those, or they can’t explain minor purity drops. We spot trends instantly. If a reaction profile looks off, we check our incoming raw material, slow the process, and trace where things derailed. Every time. Chromatographic runs show a narrow retention window, so synthetic chemists using our product aren’t left guessing about the quality or troubleshooting failed reactions.

    Even a slight tweak—like changing from steel to glass-stir bars—can minimize metallic ion carryover. Oxiranes suffer in the presence of stray metals, so we take these steps without shortcuts. Consistency sets apart our batch from those made with variable control. We hear from clients in pharmaceutical and agrochemical fields that our single-origin approach gives them less batch-to-batch variability, which matters a lot once you’re working with chiral catalysts or scale-up runs.

    Real-world Applications and Customer Feedback

    2-(4-Fluorophenyl)Oxirane fits several synthetic routes—intermediates, specialty reagents, and in some cases, stereoselective transformations for active pharmaceutical ingredients (APIs). Customers tackling medicinal analogs value reliable epoxide opening. Data from reactors large and small show that even trace differences in precursor quality change yields and impurity profiles. Our product traps fewer aldehydic side-products, so downstream isolations become more efficient. In feedback surveys, we find that manufacturers seeking fluorinated aromatic blocks choose our 2-(4-Fluorophenyl)Oxirane because they see smoother reactions and less time spent re-purifying intermediates.

    We listen closely when a pharmaceutical chemist encounters a trial batch that won’t react as expected. In our logbook, we match lot numbers to manufacturing details. This approach helps us trace root causes immediately, supporting our partners not just as a supplier but as fellow problem-solvers. Recently, discussion with a customer revealed that previous material from another source had low-level stabilizers that blocked their downstream coupling reactions. Our policy not to add any unnecessary stabilizers meant their process ran without extra troubleshooting.

    Synthesis Approach: Reliability Over Guesswork

    We favor a reproducible method for building 2-(4-Fluorophenyl)Oxirane: direct epoxidation under controlled pH and temperature, with periodic checks under both TLC and HPLC. Many published routes exist, but our team adjusts conditions to avoid overoxidation. Each batch receives a close review—color, refractive index, and subtle traces of polymeric byproducts don’t escape real-world scrutiny. Having a skilled technician intervene, mid-synthesis, can save a week’s worth of material.

    We choose not to add stabilizing agents unless a customer’s process requires it. Rarely, a custom order will call for a trace antioxidant added before shipment—always documented and discussed with end users. Otherwise, our batches go out clean, giving full freedom for subsequent downstream chemistry.

    Challenges in the industry include peroxide formation if the material sits for months or reacts with trace metal or base catalysts. We rotate inventory, favoring just-in-time production and frequent replenishment, so the oxirane our customer receives seldom sits for more than six weeks past manufacture. Less aging, less hassle with downstream re-testing.

    Comparing with Other Oxirane and Fluorinated Building Blocks

    Across the board, 2-(4-Fluorophenyl)Oxirane stands apart from unsubstituted oxiranes and other fluorinated styrene epoxides. Compounds like styrene oxide lack the electron-withdrawing fluorine, so their reactivity and selectivity can differ dramatically in nucleophilic opening reactions. In pharmaceutical targets where a single regioisomer is critical, chemists pick this product for both electronic and steric reasons. The para-fluoro group boosts selectivity and changes the solubility profile just enough to matter, especially when working with polar or anhydrous systems.

    Other options, such as 2-(4-chlorophenyl)oxirane or multi-fluorinated oxiranes, sometimes create persistent byproducts or demand harsher conditions for ring opening. We track performance through close collaboration. A process chemist working with closely related substrates often finds the para-fluorinated version fits best for cleaner transformations at lower temperature, lessening decomposition and waste.

    Bulk traders sometimes consolidate mixed lots or blend near-expiry product, which affects reproducibility. By producing everything ourselves and tightly auditing our stocks, we eliminate blending headaches and protect customer formulations from unexpected inconsistencies.

    Production Insights: Day-to-Day Challenges and Solutions

    Producing epoxides at scale brings constant learning. Some days the raw input stocks show slight color, likely from storage exposure, and a fast decision is made: scrap or slow-run filtration to protect the final product. Our people walk the plant, check hoses and connections for leaks. Leaky connections spell water ingress, which destroys sensitive oxiranes and means a loss for the day—and potential customer delays. It’s not glamorous, but it spells the difference between a subpar lot and a repeatable benchmark.

    In the cooler months, humidity falls, making static electricity a real risk near active reactors. A single arc near open oxiranes, volatile as they are, can cause dangerous conditions. Every member of our team knows the grounding routine by heart. Oxirane residues clean off gloved hands with special solvents—untreated gloves smear or absorb the product, and even that can skew batch yield data at scale.

    Hazardous waste gets managed by a team trained not just in disposal, but in source mitigation. Epoxidation generates some waste, but over the years, process improvements have reduced the total by a good margin. Our aim is always to leave each batch with higher usable yield and less residual solvent, accomplished by steady investment in both equipment and training.

    Safety audits are routine, not afterthoughts. Every member of the process team logs events, near-misses, and material irregularities. Chasing the last percent of yield, it’s easy to cut corners—yet we keep procedures strict, refusing to let pressure for volume override the need for safety or transparency.

    Why Customers Keep Coming Back

    Returning customers, especially those from pharmaceutical R&D and specialty chemicals divisions, cite two reasons for sticking with direct manufacturers like us: predictability and support. Botanists developing lead molecules know their reactions behave more consistently with our lot-traced para-fluorinated oxirane. Custom applications—where a single lot can dictate whether a downstream synthesis scales up or dies in the flask—get careful attention. We record every question, every off-beat analytical result, and communicate findings quickly.

    A regular partner faced unexpected polymerization issues. After analyzing their failed batch (using samples traced by our original shipment code), we pinpointed trace acid contamination from a non-affiliated supplier’s barrel opener. This direct diagnosis—rooted in our willingness to share process records, even when the outcome didn’t rest solely on our product—goes a long way. Trust builds when customers can see the transparency, and when the same team that made the product picks up the phone for troubleshooting.

    Improving the Process: Aiming for Fewer Surprises

    Experience shows that process drift—small changes in temperature, pH, or operator timing—can creep in with larger runs. We counter this by maintaining smaller batch sizes if quality checks show instability. Our reactors aren’t left running overnight without senior staff present. Iron contamination, a former source of slow degradation in early years, now gets nipped by lining reactors and using high-purity transfer lines. If part of the distillation rig looks off, we swap it. Downtime for preventive maintenance is far shorter than explaining a ruined run or delayed delivery.

    Solving specific problems matters more than pursuing abstract “efficiency.” Through steady review and either manual or automated data logging, we identify trends and resolve bottlenecks quickly. Only by staying invested in every part of the process—raw input, synthesis, purification, and storage—do we maintain trusted supply chains. Customers get not just a chemical, but a consistent partner across evolving R&D and manufacturing landscapes.

    Listening to Users, Adapting to Needs

    Our clients drive product development as much as our own lab scenarios. Feedback on solubility, odor, shelf stability, and compatibility with specialty catalysts shapes how batches are handled. Smaller-format packaging gained popularity among research labs, while kilo-quantity drums serve production-scale users. Adjustments to cap types, inert-gas purging, and transport insulation have come directly from those who needed less hassle in daily use.

    Synthetic chemists told us early on about failed reactions when exposures reached above standard room temperatures or when atmospheric moisture intruded during sampling. We modified our packaging to include better seals, and now, sporadic requests for desiccant inclusion are honored by default. Missteps illustrate where to adapt, and we see reduced complaints since making these process and supply-chain changes.

    Users involved in process optimization bring detailed data. For example, pigment manufacturers working upstream of dyes containing 4-fluorophenyl fragments report improved outcomes with our high-purity oxirane. Their feedback, captured by ongoing survey and direct conversations, repeatedly stresses that predictable input leads to better pigment crystallinity and colorfastness—not an effect stated in patents, but proven in iterative runs over months.

    Navigating Regulatory and Environmental Considerations

    Operational transparency sits side-by-side with compliance. Regulations around fluorinated organics differ by geography. Our team stays current on material status in all key international jurisdictions. Product documentation—never just templated, but built from each actual batch record—helps customers meet their own audit and regulatory needs.

    We take efforts to minimize fugitive emissions and to recover solvents. Years ago, routine vent losses resulted in workplace complaints and inconsistent inventory tracking. Today, covered transfer systems, regular air quality sampling, and solvent-capture technology reduce impact while yielding a cleaner workspace. Staff training underpins every compliance improvement: every operator reviews both environmental and personal safety data before starting any run.

    Disposal isn’t outsourced to generic contractors without scrutiny. Each disposed container, regardless of the size, gets logged and checked, documenting cradle-to-grave handling. End users seeking “green chemistry” input sometimes request full disclosure of waste minimization protocols and solvent recovery strategies, which we provide from our own records rather than templated vendor documents. This response builds deeper trust and, in some cases, fulfills prerequisites for participation in larger collaborative projects.

    What the Future Holds for Our Production

    Looking at the growth of custom synthesis, particularly of fluorinated building blocks, we believe 2-(4-Fluorophenyl)Oxirane will keep gaining importance. New drug candidates and material science research increasingly rely on fluorinated aromatic epoxides. Automated process monitoring, predictive maintenance, and closer user feedback channels all shape our future batches.

    We see automation as a tool, not a replacement for skilled oversight. Robots handle repeat fills and some analytical samplings, but human oversight spots the outlier data points—the subtle color change or faint odor missed by even the best sensor arrays. We invest in infrastructure that scales quickly, but resists the temptation to outpace QC.

    Experience making 2-(4-Fluorophenyl)Oxirane, start to finish, gives us perspective from each part of the chain—from supply, through use, to post-use handling. This direct lineage delivers the reliability and accountability that experimental chemists, pilot plant engineers, and process chemists need for projects that stretch from idea to reality. Each bottle, ampoule, or drum that leaves our facility tells a story shaped not just by recipes and standards, but by hundreds of small daily decisions: each aimed at providing a product ready to solve real chemical challenges.