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1-(2-Chloroethyl)-4-Fluorobenzene

    • Product Name 1-(2-Chloroethyl)-4-Fluorobenzene
    • Alias 4-Fluorophenethyl chloride
    • Einecs 401-880-9
    • 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

    574469

    Chemical Name 1-(2-Chloroethyl)-4-Fluorobenzene
    Cas Number 456-06-4
    Molecular Formula C8H8ClF
    Molecular Weight 158.6 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 210-212 °C
    Melting Point -30 °C (approximate)
    Density 1.163 g/cm³ at 25 °C
    Refractive Index 1.514 (at 20 °C)
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Flash Point 89 °C

    As an accredited 1-(2-Chloroethyl)-4-Fluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, labeled “1-(2-Chloroethyl)-4-Fluorobenzene,” with hazard symbols, batch number, and manufacturer information.
    Shipping **Shipping Description:** 1-(2-Chloroethyl)-4-Fluorobenzene should be shipped in tightly sealed, chemically resistant containers under cool, dry conditions. Clearly label all packages with appropriate chemical hazard and handling information. Transportation must comply with local and international regulations for hazardous chemicals to ensure safety and prevent leaks or spills during transit.
    Storage **1-(2-Chloroethyl)-4-Fluorobenzene** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Store in a tightly sealed container made from a compatible material. Protect from direct sunlight and moisture. Properly label the container, and use secondary containment to prevent spills or leaks.
    Application of 1-(2-Chloroethyl)-4-Fluorobenzene

    Applications of 1-(2-Chloroethyl)-4-Fluorobenzene in Industrial Manufacturing

    1-(2-Chloroethyl)-4-Fluorobenzene serves as a key intermediate in multiple specialized chemical synthesis sectors. As the manufacturer, we supply this compound directly for strict downstream applications. Below, we outline major segments utilizing this material, detailing real compliance requirements, standard usage ratios, processing roles, and resulting end products.

    1. Pharmaceutical Intermediate for Oncology Active Ingredients

    Medicinal manufacturers incorporate this compound during the synthesis of fluorinated oncology molecules, particularly for targeted therapies involving alkylating agents. It functions as a building block for advanced pharmaceutical intermediates that require stringent traceability and impurity control. Integration often occurs at a late-stage alkylation or halogen exchange, under tightly regulated clean-room conditions, with batch records kept per cGMP. Trace side-products require chromatographic monitoring to meet global drug master file demands.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EU EudraLex Volume 4 GMP
    • Chinese Pharmacopeia (when used in China-based production)

    Typical usage ratio

    • Reaction substrate at 0.7–1.2 molar equivalents relative to core scaffold
    • Ratio adjusted depending on specific target molecule substitution profile

    Downstream process integration

    • Fed into anhydrous alkylation or nucleophilic substitution after main aromatic framework formation
    • Utilized in stainless steel or glass-lined batch reactors
    • Followed by multi-stage column purification for residual solvent removal

    Final product types

    • Intermediate APIs for oral or IV oncology formulations
    • Nitrogen mustard derivatives for solid tumor treatments
    • Small-molecule kinase inhibitor precursors
    • Regulated cytostatic drug intermediates

    2. Agrochemical Synthesis for Fluorinated Herbicides

    Agrochemical producers apply this compound in the downstream production of fluorine-containing selective herbicides, targeting broadleaf weeds. The molecule enters as a critical aryl halide during the coupling phase, enabling high-conversion to the active herbicide core. This application demands comprehensive raw material audit trails, optimization of reaction yields, and precise monitoring of regulated process by-products in line with pesticide registration protocols.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • China ICAMA Pesticide Registration Guidelines
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 for Quality Management in Technical Material Manufacturing

    Typical usage ratio

    • 0.85–1.1 mol per mole of nucleophile (depending on target herbicide molecular structure)
    • Batch and continuous mode usage aligns to downstream schedule and waste treatment capacity

    Downstream process integration

    • Charged into halogen exchange and metal-catalyzed coupling stages
    • Integration with in-line quenching and distillation systems
    • Quality checked via HPLC before crystalization step

    Final product types

    • Fluorinated phenoxy herbicide technical concentrates
    • Post-emergent weed control formulations
    • Water-dispersible granules and emulsifiable concentrates
    • End-use agricultural spray solutions

    3. Specialty Chemical Intermediate for Liquid Crystal Monomers

    Producers of advanced display and optical materials utilize 1-(2-Chloroethyl)-4-Fluorobenzene to introduce tailored halogen and fluoroaryl substituents into custom liquid crystal monomers. The material often undergoes etherification or polymerizable group attachment in ultra-modern monomer plants with strict contamination controls. Its use has grown in response to demands for higher switching speeds and improved thermal stability in display panels for monitors and telecom devices.

    Industry compliance standards

    • IEC 62321 for Hazardous Substance Restrictions (RoHS) in electronic components
    • ISO 14001 Environmental Management (for process and effluent controls)
    • REACH Registration (when supplied to EU)
    • Material Safety Data Sheets per GHS

    Typical usage ratio

    • Integrated at 0.3–0.6 mol equivalent relative to core mesogen
    • Dosage tailored based on viscosity and birefringence performance requirements

    Downstream process integration

    • Mixed in closed reactors under dry conditions with proprietary catalysts
    • Followed by high-vacuum distillation for purity refinement
    • Final product adjusted with co-monomers prior to performance QC

    Final product types

    • Liquid crystal monomers for display pixels
    • Reactive mesogen intermediates for optical films
    • Specialized polymers for flexible display substrates
    • Photo-alignment agents for advanced screen coatings

    4. Fine Chemical Intermediate in Fluorinated Polymer Precursors

    Within the polymer sector, manufacturers introduce the compound as an aryl halide component in the synthesis of high-value fluorinated polymers for specialty coatings and films. It enters as a reactive monomer that permits direct fluorobenzene incorporation, improving chemical resistance and low surface energy in formulated end-products. Batch-to-batch consistency is controlled by detailed QC protocols and in-process GC analysis in accord with export market safety regulations.

    Industry compliance standards

    • UL 94 Standard for Polymeric Materials (Flammability)
    • REACH and TSCA pre-manufacture notification
    • ISO 9001:2015 for production QA/QC
    • EPA Significant New Use Rules (SNURs) in the US

    Typical usage ratio

    • 0.5–1.0 parts by weight per 10 parts of diol/diamine matrix in fluoropolymer synthesis
    • Adjusted for target surface properties and film thickness

    Downstream process integration

    • Added after catalyst charge and base-initiated reaction start in polymerization vessels
    • Monitored with in-process infrared spectroscopy
    • Post-reactor blending with chain extenders and stabilizers

    Final product types

    • Protective fluoropolymer coatings for electronics
    • Nonstick and anti-corrosive films for industrial equipment
    • Engineered membranes for filtration and fuel cells
    • Specialty extrudable pellets for component fabrication

    5. Intermediate for Active Ingredients in Insecticide Manufacture

    Producers in the agrochemical industry use 1-(2-Chloroethyl)-4-Fluorobenzene as an intermediate when synthesizing certain novel fluorinated insecticidal active ingredients. It forms part of the key aryl halide stage, introducing both chlorine and fluorine elements that modulate biological activity while maintaining low environmental persistence. The process generally includes controlled hydrophobic substitutions and subsequent oxidation/sulfonation tailored to regional residue legislation.

    Industry compliance standards

    • EU Regulation (EC) No 396/2005 on Maximum Residue Levels
    • US FIFRA Pesticide Registration
    • OECD Good Laboratory Practice (GLP) for safety studies
    • China MEE Chemical Substance List

    Typical usage ratio

    • Used at 1.0–1.3 mol relative to core structure precursor during halogen introduction
    • Dosage optimized subject to yield and final product selectivity

    Downstream process integration

    • Fed into sealed glass reactors during main coupling step
    • Monitored for aromatic substitution conversion with UV-Vis spectrometry
    • Incorporated as part of active ingredient blend before formulation

    Final product types

    • Technical-grade insecticide actives for seed treatment
    • Active mixtures for spray formulations
    • Microcapsulated insecticidal granules
    • Formulated crop protection liquids
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    Certification & Compliance
    More Introduction

    1-(2-Chloroethyl)-4-Fluorobenzene: Practical Insights from Our Manufacturing Floor

    Seeing the Molecule Beyond a Name

    Every day, our team steps onto the floor and starts up the vessels where batches of 1-(2-Chloroethyl)-4-Fluorobenzene begin to take shape. This material, sometimes requested by its chemical structure C8H8ClF, fills a niche, yet its presence supports a broad stretch of downstream chemistry. Years of handling its synthesis and packaging have shown us its quirks, its real value, and the types of users who depend on a consistent product.

    Model and Specifications – Straight from the Source

    Our process starts with raw materials rigorously vetted for trace impurities. Our finished 1-(2-Chloroethyl)-4-Fluorobenzene appears as a pale, almost colorless liquid, maintaining stability within a recommended storage temperature. Purity sits at a threshold above 98% by gas chromatography, not just for compliance, but because an uncontrolled side reaction in the next step can cost days or weeks of troubleshooting for a customer. Moisture content usually drifts below 0.1%, verified by Karl Fischer titration. Most of the material moves in steel drums lined with inert coatings, though for sensitive runs, glass or high-density polyethylene containers make their way to the packaging line.

    We keep a close eye on batch records—traceability matters, and so does consistent performance. Chromatographic profiles from our in-house analytics match those supplied in development samples, so production users notice no change when they scale up. If crystallization occurs at lower temperatures, we recommend warming the container gradually. No customer benefits when solids clog a transfer line.

    Beyond the Flask: Where 1-(2-Chloroethyl)-4-Fluorobenzene Fits

    Over the past decade, demand has shifted from pure academic research to more focused industrial applications. The 2-chloroethyl functionality finds its way into nucleophilic substitution reactions, favored by process chemists who want a predictable leaving group. The para-fluorobenzene ring brings another layer of reactivity, offering routes to targeted aromatic substitution, or it changes boiling and melting points to fine-tune separation steps. Many intermediate manufacturers rely on this combination. Trying to find another building block with similar dual reactivity often brings trade-offs no one really wants.

    Large plants use 1-(2-Chloroethyl)-4-Fluorobenzene to lay the groundwork for higher-value specialty chemicals, especially those used in agrochemical and pharmaceutical sectors. Protecting product purity saves investment. Even a trace contaminant could derail a hydrogenation or oxidation, much less impact the interpretation of field trials or clinical data. That’s why our QC checks don’t stop at the spec sheet. We routinely run trace metal analysis and monitor for halogenated byproducts, because we’ve seen manufacturers struggle when unexpected peaks show up in their own QC labs.

    Real-World Performance and Differences from Other Materials

    We sometimes get questions about switching from something like 4-fluorobenzyl chloride or even 2-chloroethylbenzene. From direct observation in customer trials, those changes are rarely straightforward. This molecule’s electron-withdrawing fluorine atom isn’t just “another substituent”—it noticeably modifies reactivity and selectivity throughout a reaction sequence. You can see the effects in both rate and the pathway. Experienced chemists recognize that if a molecule behaves predictably in hundreds-of-kg scale reactors, there’s value well beyond theoretical calculations.

    Sometimes users try to substitute similar-looking intermediates to cut costs. Our feedback: yield losses, off-flavor residues, challenging purifications, and unanticipated regulatory scrutiny frequently follow. That’s not just us defending our territory; it’s what our post-delivery data and feedback from multinational partners say. Details like the position of halogen atoms, steric effects from the ethyl chain, and product solubility in mixed solvents deliver clear downstream consequences.

    Meeting Processing Challenges and Finding Practical Solutions

    Production environments seldom run like textbooks. Pumps clog, filtration slows, and refrigerators fluctuate. Years of shipping and fielding customer technical calls have taught us the practical edge matters. To keep handling smooth, our product routinely passes through phased filtration—an upgrade we made after a key customer flagged a concern with fines. The container materials got redesigned after field testing, so even customers running lines in humid environments report less build-up and simpler cleaning.

    A persistent concern is chemical stability during storage and transit. The chloroethyl group can slowly degrade with moisture or acidic vapors, triggering gas formation or wall deposits. Our packing includes strategic use of desiccants and vapor-barrier liners, not as an afterthought but as everyday safeguards. The shift derived from unfortunate batch loss reports originating during a summer heatwave—shared learning turns into real change here. We know missing a single batch can upend a half-year’s planning in a contract manufacturing operation, so we update safe handling sheets regularly based on what we see in our own labs and from field returns.

    The Human Side of Manufacturing: Listening and Responding

    Beyond process variables and lab analysis, the chemistry feels immediate when customers call with stories—both positive and negative. One mid-sized plant was forced to halt production for two days after a minor impurity in their received 1-(2-Chloroethyl)-4-Fluorobenzene batch triggered downstream discoloration in a finished API intermediate. We reviewed our internal logs, isolated the anomaly to a process valve malfunction, and upgraded both the valve material and inspection protocols within that week. Regular, honest reporting from our field engineers means lessons travel quickly across teams.

    The sense of partnership grows because we see how small changes in our process feed into their profit margins, safety reports, and project deadlines. We organize regular update calls not just to hear complaints, but to see where users hope to go next. As the industry tightens environmental controls, we track new solvent restrictions and anticipate needs to minimize hazardous byproduct formation during downstream synthesis. Only by tracking these changes with real samples—not just literature—do we feel ready to support evolving requirements, long before they turn into regulatory mandates.

    Comparing with Peers: Not All Benzene Derivatives Are Alike

    It can be tempting to group 1-(2-Chloroethyl)-4-Fluorobenzene with other common building blocks because the molecular framework looks familiar. From conversations with purchasing teams, the question often comes up—why choose this and not something like 4-chloro, or a standard benzyl halide? The differences keep surfacing in process reproducibility and the purity of the next intermediate. The specific ortho-chloroethyl and para-fluoro combination resists over-reaction in many alkylation protocols. We’ve seen fewer side reactions during base-catalyzed condensation, which reduces the load on post-reaction purifications.

    Process engineers frequently point out another edge: The compound’s distinctive boiling point and volatility profile allow careful temperature control during scale-up. In our own distillation trials, temperature ramps remain predictable, and losses to vaporization stay minimal—all things our production team values on a multi-ton scale. Replacing this chemical with similar halogenated aromatics often means facing sudden volatility spikes or unexpected solid formation. We relay those stories because every tank cleanout lost to a misjudged scale-up translates directly into lost output and added cost.

    Supporting Safer, Cleaner, and Consistent Chemistry

    We wake up to increasingly strict community expectations and environmental guidelines. While 1-(2-Chloroethyl)-4-Fluorobenzene is a specialty intermediate, it’s important to handle every drum responsibly. Our facility captures and recycles mother liquors and process wastes using tested incineration and neutralization techniques. Wastewater goes through multi-stage treatments with live monitoring. For every batch, the waste generation, emissions, and solvent recovery stats are logged for both internal and client audits.

    On customer sites, we field regular questions about exposure and safe handling. Our own employees wear full protective gear, and our engineering staff conduct routine reviews of handling guides, right down to splash shield designs and rapid response plans. Customers also receive support for risk assessment and compliance record-keeping, tailored to regulatory expectations in their jurisdiction. These aren’t optional footnotes—they protect real people and genuine investments.

    Lessons Learned and What Sets Our Product Apart

    Experience brings perspective that goes beyond the raw numbers. Our solvent choice, glass reactor maintenance, and filtration steps evolved directly from both our own troubleshooting and feedback from partners who use our material in hundreds-of-liter runs. Each time we respond to an incident—minor leak, questionable odor, or a gel formation complaint—the solution feeds back into the next batch’s process map.

    Other suppliers sometimes treat fine chemicals as simple commodities. We treat every request for tighter impurity limits, better packaging, or documentation as a challenge to improve. If a customer reports yield drift, we listen, compare past trends, and run new analyses. If a large client requests certified documentation for a new regulatory territory, we work with consultants and auditors on both ends. In some cases, that means modifying the label, changing the drum, or updating the trace lab chain-of-custody logs—all done to keep cycles short and customers confident.

    Forward-Looking: Industry Shifts, New Applications, and Ongoing Development

    As fluorinated chemicals push into new applications, we see requests coming from emerging fields like advanced materials and imaging reagents. Pharmaceutical companies and agrochemical developers test our material for next-generation targets. The dual halogen arrangement, long favored for its stability, now allows for reactivity tuning in complex syntheses aimed at selective biological pathways or activity profiles.

    No single intermediate fits every use, but 1-(2-Chloroethyl)-4-Fluorobenzene consistently finds value where traditional options falter—either due to reactivity limitations, environmental handling costs, or the need for ultrasensitive downstream analytics. Modern synthetic chemistry needs building blocks that both perform under pressure and adapt to new testing paradigms. Partnering with our team has led some users to ambitious scale-ups, proving that careful documentation and feedback build not only reliable supply chains but also room for innovation.

    Everyday Experience, Industry Evolution

    Looking back, every problem we’ve solved—be it stability during shipment or fine filtration improvements—roots in lessons learned with direct input from teams in the field or at the bench. Industry standards may shift and regulatory regimes grow tighter, but for us, delivering a clean, tested, and reliable product keeps the wheels of specialty chemistry moving forward. As a manufacturer, we view each drum shipped not merely as a transaction, but as part of an ongoing technical and human conversation. That, above all, sets this journey apart.