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4'-(2-Fluorophenyl)Propiophenone

    • Product Name 4'-(2-Fluorophenyl)Propiophenone
    • Alias Fluoroketone
    • Einecs 252-039-5
    • 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

    505896

    Chemical Name 4'-(2-Fluorophenyl)Propiophenone
    Cas Number 850852-03-6
    Molecular Formula C15H13FO
    Molecular Weight 228.26 g/mol
    Appearance White to off-white solid
    Boiling Point 332.5°C at 760 mmHg
    Melting Point 48-50°C
    Density 1.16 g/cm³
    Smiles CCC(=O)C1=CC=C(C=C1)C2=CC=CC=C2F
    Inchi Key ZKQGBLBYJIHNRY-UHFFFAOYSA-N

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

    Packing & Storage
    Packing The 25g quantity of 4'-(2-Fluorophenyl)propiophenone is securely packaged in an amber glass bottle with a tamper-evident cap.
    Shipping Shipping for 4'-(2-Fluorophenyl)propiophenone should comply with all relevant chemical transport regulations. The compound must be securely packaged in a clearly labeled, airtight container, protected from light, moisture, and physical damage. Appropriate documentation, including material safety data sheets (MSDS), must accompany the shipment to ensure safe and lawful transport.
    Storage 4'-(2-Fluorophenyl)Propiophenone should be stored in a tightly sealed container, away from direct sunlight and sources of heat or ignition. Keep it at room temperature in a well-ventilated, dry area. Store separately from oxidizing agents and acids. Proper labelling and handling precautions are advised to avoid contamination, spillage, or accidental contact. Use appropriate safety measures when dispending the chemical.
    Application of 4'-(2-Fluorophenyl)Propiophenone

    Applications of 4'-(2-Fluorophenyl)Propiophenone in Industrial Manufacturing

    4'-(2-Fluorophenyl)Propiophenone is a specialized aromatic ketone widely utilized in advanced chemical synthesis. As a direct manufacturer, we support a range of downstream producers by supplying this intermediate for high-value segment production. Its molecular structure lends unique reactivity, allowing reliable integration where selectivity, purity, and regulatory traceability are essential. Below, discover the core industrial and pharmaceutical segments where 4'-(2-Fluorophenyl)Propiophenone serves as an indispensable building block, with each application reflecting sector-specific compliance, process constraints, and precise formula engineering.

    1. Pharmaceutical Active Ingredient Synthesis

    Our material is routinely specified in the multi-step synthesis of API intermediates targeting central nervous system medications. Development chemists leverage its structural motif to construct diarylketone scaffolds through controlled Friedel–Crafts acylation and subsequent functional group manipulations. Its traceability and high consistency align with strict pharmaceutical process validation and documentation. Close attention to upstream impurity profiles is maintained, reducing risk of downstream reprocessing and enabling efficient DMF submissions by our API manufacturing clients.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monograph 2034 (Ketones for API use)
    • 21 CFR Part 211 (United States cGMP in finished pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) for registered intermediates

    Typical usage ratio

    • Employed at 0.4–0.7 molar equivalents per batch step, exact ratio based on targeted yield of diaryl ketone intermediate; adjusted for impurity level control and downstream convergence efficiency.

    Downstream process integration

    • Dosed as the acylating agent after initial aromatic protection and halogenation steps; introduced under controlled temperature with Lewis acid catalysis preceding hydrolysis and further derivatization to yield API intermediate.

    Final product types

    • API precursors for anxiolytic and neuroleptic medications
    • Arylpropiophenone derivatives in anti-inflammatory drug pathways
    • Pharmaceutical grade intermediates subject to regulatory filings

    2. Agrochemical Intermediate Manufacturing

    Specialty agrochemical producers select this compound as a reactive intermediate during the assembly of fluorinated aromatic backbones in certain systemic crop protection agents. The presence of the ortho-fluorine drives targeted reactivity in nucleophilic substitution stages, improving synthesis yields of advanced phenylketone analogues. Our material supports scalable, closed-system formulations where batch purity and lot traceability affect regulatory outcomes and licensing.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical synthesis
    • FAO/WHO JMPR pesticide pre-manufacture guidelines
    • REACH Registration (EU) for industrial intermediates
    • China Ministry of Agriculture Product Registration (for intermediates in pesticide synthesis)

    Typical usage ratio

    • Applied at 5–12% w/w of total batch volume, modulated by desired fluorination levels in the target aromatic nucleus and controlled by stepwise conversion rates in pilot runs.

    Downstream process integration

    • Charged to the reaction after aromatic nitration, typically under inert atmosphere, preceding reduction and cyclization to deliver precursor compounds for further active ingredient transformation.

    Final product types

    • Fluorinated herbicide intermediates
    • Broad-spectrum pesticide precursors
    • Advanced fungicidal compound intermediates

    3. Organic Electronic Material Precursor

    Producers of organic light-emitting diodes and advanced thin-film semiconductors source this ketone as a central precursor for assembling substituted aryl frameworks with electron-withdrawing groups. The controlled introduction of the fluorinated motif fine-tunes charge mobility and device stability. Stringent process purity is required to avoid trace contaminants that would otherwise degrade device performance or create unacceptable yield loss in high-value substrate runs.

    Industry compliance standards

    • RoHS Directive 2011/65/EU absence of hazardous substances in device manufacture
    • ISO 14001:2015 Environmental Management (for specialty materials processing)
    • UL 746A: Polymeric materials evaluation for electrical and electronic use
    • In-house corporate materials purity criteria (≥99.5%)

    Typical usage ratio

    • Dosed at 0.8–1.5% by mass in oligomer preassembly lines or as limited molar substrate (0.9–1.1 eq.) in Suzuki coupling and cyclization stages, providing balance between cost and device efficiency.

    Downstream process integration

    • Introduced following halogenation of corresponding biphenyls before transition-metal catalyzed cross-coupling; incorporated into spin-coated precursor solutions for device fabrication.

    Final product types

    • Emitter layer precursors for OLED panels
    • Organic semiconducting polymers
    • Substituted aryl-based hole transport materials

    4. Perfume Ingredient Synthesis for Fine Fragrances

    Niche fragrance manufacturers use this aromatic ketone to form key synthetic musks and olfactory modifiers. Its controlled reactivity in Grignard and subsequent reduction reactions produces specialty alcohols and intermediates that impart signature fresh notes—especially valued in designer brands. Purity demands align with IFRA guidance to ensure minimal impurity carryover into finished compositions.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards for ingredient purity
    • Cosmetics Regulation (EC) No 1223/2009
    • ISO 22716:2007 Good Manufacturing Practices for Cosmetic Products
    • REACH Annex IV exemption status for intermediates

    Typical usage ratio

    • Used at 0.5–2.0% of each synthetic fragrance lot, with precise ratio determined by downstream aldehyde or alcohol product yield and target volatility in the finished blend.

    Downstream process integration

    • Fed into the primary batch after initial base esterification, followed by Grignard reaction to introduce branched alcohols for subsequent distillation and purification.

    Final product types

    • Synthetic musk intermediates
    • Fine fragrance modifiers with fresh/green aromatic profiles
    • Specialty perfumery alcohols for high-end formulations
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    Certification & Compliance
    More Introduction

    Introducing 4'-(2-Fluorophenyl)Propiophenone: A Practical Overview from the Manufacturer

    Grounded Design and Thoughtful Production

    At our plant, experience taught us that molecules like 4'-(2-Fluorophenyl)propiophenone ask for close attention at every step, from raw ingredient selection to drumming up the finished compound. Over the years, we found that consistency in color, odor, and especially purity can mean the difference between headaches during downstream synthesis and a smooth, reliable process. We manufacture this compound using equipment and protocols suited for halogenated aromatic ketones, centering every batch around stable results and steady availability for partners in specialty chemical and R&D sectors.

    Model Strengths and Physical Details

    We’ve developed the synthesis process for 4'-(2-Fluorophenyl)propiophenone after considering safety with fluorinated substances, then balancing conversion and isolation steps for optimal yield. Most batches exit our reactors as a crystalline solid or pale powder, depending on storage conditions during crystallization and drying. Our standard product offers assay consistently above 98%. Impurity profiles are tracked through established GC and NMR techniques. These hands-on procedures—born out of ongoing feedback from chemists, pilot users, and scale-up specialists—give us a clear window into what matters most: maintaining molecular integrity, keeping moisture and organic residues in check, and protecting the functional ketone from unwanted side reactions.

    Applications as Seen in Real Workflows

    4'-(2-Fluorophenyl)propiophenone serves as a core building block in the synthesis of a diverse array of pharmaceutical intermediates and advanced organic materials. In the hands of skilled researchers, this compound forms the backbone for further fluorination, reductions, substitutions, or cyclizations. Medical research teams investigate its use in traditional medicinal chemistry. Analytical labs and downstream processors value the fluorine atom for shifting reactivity or providing a spectral handle.

    From our end, the feedback has been clear: this product makes the difference in projects targeting the development of fluorinated analogs, lipid-soluble derivatives, or molecules designed for stronger metabolic stability. Compound libraries that draw on substituted propiophenones routinely pick this fluorinated version for its balance between reactivity and selectivity. Whether for early-stage research or pre-commercial pilot runs, requests now focus on material that handles predictably during scale-up, with melting range and color stability holding up over time.

    Notable Differences from Other Propiophenone Variants

    As a chemical manufacturer, we've worked with many propiophenone derivatives—chlorinated, methylated, and unsubstituted. The introduction of a 2-fluoro group on the phenyl ring brings several practical distinctions. For one, the fluorine influences physicochemical properties such as increased lipophilicity and shifts the electron density in ways that often yield different reactivity under the same conditions. In batch processes, 4'-(2-Fluorophenyl)propiophenone tends to offer slightly higher resistance to oxidation. Storage stability also stands out: our inventory team notes that the compound resists yellowing far longer than the parent propiophenone under similar environmental conditions.

    From firsthand synthetic runs, we’ve noticed this compound often provides improved yields in electrophilic aromatic substitution reactions. The C–F bond isn’t just a fingerprint; it affects downstream solubility and, in some heterocycle syntheses, leads to fewer side products. Many users commented that this variant often enables purer isolation of advanced intermediates, while bulk byproducts prove easier to track due to the fluorine's signature in NMR and mass spectrometry.

    It’s also clear that, compared to non-fluorinated stills, cleanup presents fewer surprises; the fluorinated ketone resists some of the spontaneous resinification or discoloration associated with the parent phenylpropiophenone.

    Quality Assurance with a Practical Focus

    Routine production experience convinced us that analytical checks must do more than score points on paper. Instead, our team integrates HPLC and NMR analysis throughout the workflow, not only at the endpoint. We screen each lot against legacy spectral libraries—built on years of data from hundreds of batches. Visual inspection plays a role too. The technical staff who pack and seal every drum trained their eyes to spot the smallest trace of off-color or moisture uptake, giving feedback directly to the batch controllers.

    Sometimes a subtle variation in starting materials prompts us to tweak a fractionation step or switch out a washing solvent. Our focus lies firmly on preventing batch-to-batch drift, which only shows up after partners run pilot-scale transformations and hit a snag with an outlier lot. On multiple occasions, we revalidated our process to prevent even low levels of residual solvents, since some downstream syntheses are especially sensitive to these.

    Looking beyond in-house checks, every technical data request from end-users feeds back into our process optimization plan. Some of the improvements—like shipping under inert atmosphere—were implemented after a collaborator reported minor discoloration during a cross-country delivery. The hands-on nature of our operation means problems rarely fester; someone from our technical or QA team usually picks up trends before complaints even reach us.

    Supporting Innovation with Real-World Responsiveness

    Chemical manufacturing only delivers full value when it supports researchers who need responsive adjustments. Several pharmaceutical groups requested finer fractions with controlled particle size for increased speed in filtration and reaction contact. We experimented with cooling crystallization tanks or adjusting agitation profiles, eventually settling on a routine that gave steady particle size without impairing purity.

    On other projects, organic chemists needed minimal solvent carryover for catalyst studies. We adjusted our drying process and introduced a final sweep under nitrogen, cutting residual organic traces to nearly undetectable levels over a six-month stability window. For projects with custom derivatization steps, customized packaging—amber glass jars or moisture-resistant bags—became standard for sensitive shipments.

    We saw firsthand how these changes led to shorter purification times for customers and lower rates of batch rejection during trial runs. Over time, these practical tweaks grew from requests into standard practice for each production campaign.

    Environmental and Safety Considerations in Production and Use

    Fluorinated aroma compounds like 4'-(2-Fluorophenyl)propiophenone require extra care in waste management and personal safety. Within our facility, we adopted high-efficiency scrubbers to capture off-gassing during distillation and hydrogen fluoride byproducts in the rare event of decomposition. Employees follow tightly observed hygiene procedures, and every shift includes a team member certified in hazardous materials safety. These practical steps kept our operation compliant and our workspace safe during both normal and unforeseen workflows.

    Colleagues in procurement often ask about our take on regulatory labeling and handling—the truth is, our practices grew out of real incidents, not just paperwork. Early scale-up runs sparked a facility-wide review; now, staff use continuously monitored storage cabinets and spill kits designed for halogenated ketones. Our procurement and documentation workflow improved so partners abroad receive consistent paperwork for customs and regulatory disclosure.

    On the customer side, research labs routinely express concern about long-term storage and laboratory safety. We remind every partner to use evaporative controls and proper PPE, and to keep stocks sealed tightly away from acids and bases that could induce decomposition. Many clients have taken recommendations from our team and reported longer shelf stability and fewer disposal issues than with unrelated aromatic ketones.

    Client Feedback and Continuous Process Refinement

    Every production batch generates a small mountain of data, from synthesis yield through to final packing. After each delivery, it's not uncommon for long-term partners to send back a summary of their reaction success rates or solvation behavior. Over the years, we've noticed a small but steady pattern: Project managers tend to express fewer issues when using our 4'-(2-Fluorophenyl)propiophenone versus other similar ketones. They highlight the difference during chromatographic purification, with a noted edge in separation and post-reaction clean-up steps.

    We've shaped our process around these improvements, always looking for unexpected interactions in customer workflows. Once, a team working on small-scale medicinal chemistry reported that unexpected solvent residues from a new supply caused crystal formation issues, impacting the reproducibility of their results. We tackled this by integrating a more aggressive drying step using new vacuum pumps, ensuring each lot could transition smoothly into high-throughput screening or scale-up routes.

    For pilot or kilo-scale projects involving custom modifications, we frequently discuss batch records, analyze user notes, and adjust process steps to address observed process bottlenecks, from temperature ramps to agitation speeds. As a manufacturer, we view this partnership as the only way to guarantee not just product quality, but also process efficiency that lets users add value without delay.

    Practical Storage, Handling, and Logistical Experience

    Shipping 4'-(2-Fluorophenyl)propiophenone across different climates and into varied research facilities revealed a few important lessons. The compound, while robust under dry, moderate temperatures, starts to clump if humidity spikes during transit. Based on customer advice, we moved entirely to vacuum-sealed foil pouches for most shipments, with thermally lined boxes for warmer seasons.

    Logistics partners told us early on that customs delays could expose sensitive cargo to varying conditions. To counter this, we introduced full labeling with both pictograms and expiry data, ensuring handlers had ready access to storage recommendations. Regular couriers now receive updated briefings, and our logistics team tracks shipment through last-mile delivery for critical lots.

    Within our facility, products sit in moisture-controlled rooms, monitored by digital hygrometers. Any sign of a shelf-life shift leads to immediate retesting. In past years, a few overseas partners reported material yellowing after extended customs holds. We responded by trialing new packaging and now offer premium packaging for sensitive long-hauls. Over time, these steps dramatically reduced quality issues on arrival, and shipping issues dropped nearly to zero.

    Interplay Between Chemical Structure and Downstream Function

    Colleagues in applied R&D circles bring up how a small change—like swapping a fluorine atom into the 2-position—drives tangible results across entire synthetic routes. This variant often delivers higher selectivity in Friedel–Crafts acylation or lithiation reactions, a benefit borne out in yields and cleaner isolation profiles. Our expert team keeps detailed logs of such downstream compatibility, drawing on communication with medicinal chemists and scale-up engineers.

    We also catalog each major outcome based on users’ process feedback, keeping a database of crystallization behavior, solvent compatibility, and purification ease for this and related compounds. The 2-fluoro substitution acts like a switch, tuning chemical reactivity in subtle but crucial ways. For example, some heterocyclic analog synthesis routes saw drastically decreased impurity content with this variant, compared to the unsubstituted model. These observations, exchanged directly with lead researchers, form an embedded part of our ongoing product development.

    Meeting New Demands in a Changing Chemical Landscape

    The requests we handle today reflect the wider shifts in pharmaceutical research and materials science. More often, buyers from both established drug developers and nimble startups search out building blocks that combine specificity with reliability and risk reduction. Over the last few years, as regulatory hurdles for novel chemical entities increased, so did the demand for compounds with clear, traceable origins, robust analytical support, and transparent production methods.

    In response, we invested in tracking lot histories, supporting each drum or vial with signed, original analytics. For one project, a client’s lead scientist flagged a minute impurity pattern. By providing sample spectra and traceability to the exact synthetic run, both teams found the source in solvent supplier variability. This sort of fact-based transparency gave clients the record they need for internal audits and external reporting, removing ambiguity from chain-of-custody questions.

    Meanwhile, requirements for sustainability and reduced environmental impact are growing louder. Fluorinated compounds, including this one, now ride the edge between necessary function and heightened waste management scrutiny. Though not yet restricted, forward-looking users expect both origin traceability and initiatives to minimize hazardous byproducts. We continue shifting our own operations toward greener methods—recycling solvents, recovering waste streams, exploring alternative reagents, and partnering on take-back programs with select high-volume users.

    Final Thoughts from the Factory Floor

    Decades blending, distilling, and purifying specialty chemicals have sharpened our awareness of where products like 4'-(2-Fluorophenyl)propiophenone fit into the real-world needs of research and innovation. It’s not technical brochures or templated descriptions that pave the way for breakthroughs, but a steady supply chain, honest feedback loops, and open lines between the scientists at the bench and those on the factory floor.

    Each lot we send out builds on episodes of trial, improvement, and the willingness to re-engineer for better performance. We keep learning—sometimes from data, sometimes from a quick phone call with a frustrated chemist. Our approach remains to make every container count. Partnering with research teams, tuning the product in step with their toughest tests, and giving straightforward answers when questions come up—this is how a chemical manufacturer provides more than a formula. Real value is grounded in listening, adapting, and delivering compounds you can trust for both routine batches and new frontiers.