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3-Fluoropropiophenone

    • Product Name 3-Fluoropropiophenone
    • Einecs 238-856-4
    • 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
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    Specifications

    HS Code

    997801

    Chemical Name 3-Fluoropropiophenone
    Cas Number 348-84-5
    Molecular Formula C9H9FO
    Molecular Weight 152.17 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 230-232 °C
    Density 1.12 g/cm3
    Refractive Index 1.521
    Flash Point 97 °C
    Smiles CCC(=O)C1=CC(=CC=C1)F
    Pubchem Cid 152330
    Synonyms m-Fluoropropiophenone

    As an accredited 3-Fluoropropiophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle with a tamper-evident cap, labeled 3-Fluoropropiophenone, includes hazard symbols and product details.
    Shipping 3-Fluoropropiophenone is shipped in tightly sealed containers, protected from moisture and light. It must be handled in compliance with chemical safety regulations and typically transported as a hazardous material. Appropriate labeling and documentation are required to ensure secure and compliant delivery. Storage and shipping conditions should minimize exposure to heat and ignition sources.
    Storage 3-Fluoropropiophenone should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from direct sunlight and moisture. The storage area should be equipped with appropriate spill containment. Keep the substance at room temperature and ensure proper labeling to prevent accidental misuse or exposure.
    Application of 3-Fluoropropiophenone

    Applications of 3-Fluoropropiophenone in Industrial Manufacturing

    As a specialized manufacturer of 3-Fluoropropiophenone, we support multiple segments within the chemical industry where high-purity intermediates are essential for downstream synthesis. Below we detail real-world industrial application scenarios, compliance standards, dosage guidance, integration methods, and examples of final products based on best practices and proven customer usage.

    1. Pharmaceutical Intermediate for Anticonvulsant API Synthesis

    Pharmaceutical companies employ 3-Fluoropropiophenone as a key building block for producing specific anticonvulsant active pharmaceutical ingredients (APIs). This aromatic ketone acts as a starting material in the Friedel–Crafts acylation and subsequent steps for the synthesis of fluorinated diaryl compounds. The process requires careful monitoring of reagent ratios and reaction temperatures to ensure product purity that meets international pharmacopeial standards for APIs. Downstream processors carry out hydrogenation, amination, and cyclization steps, transforming the intermediate into finished APIs which undergo full GMP validation before tableting or capsule filling.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) relevant monographs
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Japan PMDA API import standards

    Typical usage ratio

    • Used at 0.95–1.15 molar equivalents as the limiting reagent; exact ratio modified based on downstream API yield requirements and impurity control determined by in-process QC.

    Downstream process integration

    • Reacted directly in the initial ketone acylation step by batch or flow methods; intermediate isolated, then subjected to sequential hydrogenation and nucleophilic substitution.

    Final product types

    • Pharmaceutical grade anticonvulsant API
    • Bulk intermediate for further modification
    • Finished tablets and capsules (antiseizure medications)

    2. Agrochemical Intermediate for Fungicide Synthesis

    Agrochemical manufacturers integrate 3-Fluoropropiophenone in the production of fluorinated heterocyclic fungicides. It functions as a core intermediate, especially in synthesis routes involving condensation or Grignard coupling to introduce fluorine functionality into the target molecule. Compliance with agrochemical quality controls and active content verification ensures safe downstream processing and regulatory approval for field use. The compound enters pilot and commercial production facilities where batch reactors are optimized for minimal by-products, and downstream solid form conversion yields technical-grade fungicidal actives for end-market formulation.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • China GB 20633 (General Rules for Pesticides Registration)
    • REACH (EC) No 1907/2006 chemical registration for agrochemical precursors
    • ISO 17025 accredited in-house testing for active content

    Typical usage ratio

    • 0.8–1.2 moles per mole of target fungicidal scaffold; ratio adjusted during scale-up to balance cost and stoichiometric conversion. Higher ratios applied for purity assurance in final active content.

    Downstream process integration

    • Fed into closed-system batch reactors for condensation reactions; crude product isolated and recrystallized, followed by integration into granulation or wettable powder lines for formulation.

    Final product types

    • Technical grade fungicide active ingredients
    • Finished crop protection agents (fungicide granules, suspensions, or dispersible powders)

    3. Fine Chemical Synthesis for Aroma Compounds

    Producers of fragrance intermediates employ the fluorinated propiophenone core in synthesis of specialty aromatic chemicals. It serves as a substrate in Friedel–Crafts alkylation or reductive amination patterns, introducing fluorine moieties into high-value aroma molecules used by perfumers. Quality assurance during synthesis relies on adherence to IFRA and IFRA Annex standards for trace impurities and allergen content. Production lines conduct reactive distillation, crystallization, and molecular sieving to obtain high-purity fractions, which are then tailored to perfumery houses for compounding.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Cosmetics Regulation (EC) No 1223/2009 Annex II/III for restricted substances
    • ISO 9235 (Aromatic Natural Raw Materials specifications for the fragrance industry)

    Typical usage ratio

    • 0.9–1.05 molar equivalents in relation to cyclic ketones or aldehydes in route; batches fine-tuned to maintain performance attributes and minimize fluorinated side products in aroma applications.

    Downstream process integration

    • Directly introduced to organic synthesis steps for aromatic ring transformation; extracted or fractionated before compounding and QC testing for sensory profile confirmation.

    Final product types

    • Fluorinated aroma intermediates
    • Complex perfume bases
    • Finished fine fragrances for B2B supply

    4. Specialty Material Monomer for Electronic Grade Polymers

    Manufacturers of specialty polymers utilize 3-Fluoropropiophenone to introduce controlled fluorine atoms into polymer backbones used in advanced electronic and optical applications. The ketone monomer is copolymerized or used in step-growth polymerizations where fluorinated functionalities contribute to enhanced dielectric properties or chemical resistance. Compliance with RoHS and REACH is mandatory, especially for telecom, display, or microelectronic applications. Our customers optimize batch feed ratios to achieve uniform distribution of functional groups, ensuring final polymers meet performance criteria for specialty films or coatings.

    Industry compliance standards

    • RoHS Directive (Restriction of Hazardous Substances) 2011/65/EU
    • REACH Regulation (EC) No 1907/2006 for monomer registration
    • IEC 61249-2-21 (Requirements for base materials for printed boards)

    Typical usage ratio

    • 5–20 mol% when used as a copolymer unit; exact ratio tailored according to electrical/physical properties required by the specialty application.

    Downstream process integration

    • Mixed in pre-polymerization reactors under controlled thermal and inert atmospheres; incorporated as a comonomer or chain end-capper in continuous or batch processes.

    Final product types

    • Electronic grade specialty polymers (e.g., fluorinated polyimides, polyaryl ethers)
    • Flexible printed circuit board substrates
    • Optical films and display coating materials

    5. Laboratory Scale Synthesis for Reference Standards

    Analytical reagent suppliers and pharmaceutical QC laboratories use 3-Fluoropropiophenone as a standard or sample preparation material for analytical validation protocols. Authentic reference standards are essential for LC-MS, GC-MS, and NMR calibration in drug development and forensic toxicology labs. Strict adherence to ISO and GLP ensures traceability from batch synthesis to packaging. Our in-house capabilities guarantee consistent isotopic purity and supply chain provenance, supporting the verification of method performance in regulatory submissions.

    Industry compliance standards

    • ISO 17025 (Testing and calibration laboratory competence)
    • Good Laboratory Practice (OECD GLP) for analytical method validation
    • USP and EP reference standard guidelines

    Typical usage ratio

    • Batches synthesized at 10–100 mg scale per request; concentration for calibration standards between 0.1–10 μg/mL in analytical protocols, determined by detection limits and method sensitivity.

    Downstream process integration

    • Purified and aliquoted into certified safe glassware; delivered to laboratories for QC testing, calibration, or as spiking material in trace analysis.

    Final product types

    • Pharmaceutical and forensic reference standards
    • Analytical calibration solutions for instrument validation
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    Certification & Compliance
    More Introduction

    Understanding and Applying 3-Fluoropropiophenone: Insights from a Chemical Manufacturer

    Introduction to 3-Fluoropropiophenone

    Manufacturing 3-Fluoropropiophenone has brought our technical team countless opportunities to refine processes and listen to the evolving needs of specialty chemical markets. We have a firsthand view of the tight tolerances and process requirements researchers and process engineers face, especially with fluorinated building blocks. The compound, known by the chemical structure C9H9FO, stands out as a versatile intermediate. In the lab, its pale yellow appearance and distinctive aromatic scent signal the start of many specialized syntheses.

    Our batches deliver consistently high purity, with active measures taken at each stage to prevent contamination and unplanned byproduct formation. This product never sees extraneous water or residual acids, and analytical controls confirm it—the attention comes from seeing what even a small impurity can do in a downstream reaction. Having worked through temperature swings, shipping mishaps, and the occasional regulatory update, we have learned that attention to detail in production pays exponential dividends for our downstream partners.

    Technical Qualities and Model Specifications

    We manufacture 3-Fluoropropiophenone using a specifically designed acylation process, tuning both time and temperature to avoid over-fluorination or byproduct formation. Our product is regularly supplied in kilogram to metric ton quantities, meeting minimum GC assay levels of 99%. The boiling range most often falls between 92 and 94°C at 0.6 mmHg, as confirmed by carefully calibrated distillation lines and routine laboratory checks.

    Moisture and acidity count among the major culprits that reduce yields in fluorinated ketone synthesis. In the past decade, improved filtration and inert atmosphere handling have brought down trace water count to less than 0.05%, which many customers require for catalyst-driven conversions or organometallic steps. Color metrics fall within <20 Hazen units, which matter in sectors where even a mild yellow tint implies degradation for their users.

    Not every request is identical—some teams want material in amber glass, others in lined steel drums. We draw from a pool of packaging suited for moisture and air sensitivity: nitrogen-flushed containers, sealed argon atmospheres for bulk, and extra space for expansion if required by shipping. This hands-on knowledge of what material faces outside our plant has changed more than a few decisions about final QA checks and release specifications.

    Applications and Usage in the Field

    Chemical researchers regularly reach out to discuss the place of 3-Fluoropropiophenone in their synthetic roadmaps. Its unique structure integrates a fluorine atom ortho to a phenyl ketone, which opens doors to functional group transformations. Our broad customer base works in pharmaceuticals, crop protection, and advanced material sciences, leveraging the compound’s reactivity in both nucleophilic and electrophilic processes.

    Pharmaceutical development draws especially strong demand. We see repeated requests for 3-Fluoropropiophenone as a core intermediate for synthesizing selective inhibitors, and as a precursor to new classes of CNS-active compounds. Groups working on structure–activity relationships value the position of the fluorine atom: shifting it can have broad impacts on metabolic stability and receptor binding affinity, while preserving the aromatic ring has downstream significance in target-ligand interactions. We’ve watched the late-stage functionalization strategies evolve, and customers confirm the difference in outcome from our consistently pure starting material.

    Agrochemicals also account for a sizable segment of annual orders. Synthetic routes to new fungicidal and herbicidal agents benefit from the fluorine’s subtle electronic effect—conferring resistance to breakdown and altering lipophilicity, which impacts how ingredients move through plant tissue or persist in field conditions. One large collaborator noted that shifting to our 3-Fluoropropiophenone over lower-purity sources improved their downstream yields by nearly 8%, translating to major gains at the pilot scale.

    Several advanced materials labs request this molecule for incorporating fluorinated rings into specialty polymers and copolymers. Research on high-performance coatings and electronics-grade intermediates keeps 3-Fluoropropiophenone in the running as both a reactive site and a property-modifier. Some long-term partners report improved dielectric properties and greater environmental durability in their polymer matrices, giving them a marketing edge in sectors where competition is fierce.

    What Sets 3-Fluoropropiophenone Apart from Similar Chemicals

    Our deep involvement in fluorinated aromatic chemistry has laid bare how subtle some product differences can be—but for the end-user, those differences add up quickly. Comparing 3-Fluoropropiophenone with unsubstituted propiophenone, or even with para-fluoro-substituted analogues, illustrates this well.

    The ortho-fluoro group in 3-Fluoropropiophenone introduces significant electron-withdrawing effects while maintaining reactivity toward conventional carbonyl transformations. Direct substitution on the aromatic ring, and its influence on steric and electronic characteristics, makes certain coupling, reduction, and condensation steps more controlled, with improved selectivity for routes requiring precise regioselectivity. Teams working with palladium-catalyzed cross-coupling have reported fewer unwanted side products and greater yields thanks to these subtle but essential effects.

    Unlike compounds with multiple fluorines, 3-Fluoropropiophenone strikes a unique balance: it offers modified electronic effects without raising volatility or handling hazards to the same degree. At plant scale, this translates into safer working conditions—avoiding the need for ultra-specialized containment or abatement equipment, while still achieving the benefits fluorination can deliver.

    Storage and handling also differ. With some closely related compounds, a shift in the fluoro-substitution pattern changes not just specific reactivity, but also the product’s sensitivity to light, temperature, or oxygen. 3-Fluoropropiophenone tolerates ambient storage better than many competitors. Keeping it in darkness and under nitrogen suffices for most laboratory and production workflows, allowing easier integration into existing process infrastructure. End-users describe less downtime from product failures or instability, which matters when every hour counts in high-throughput labs or pilot facilities.

    In regulatory filings, the documentation trail for single-fluoro substituted ketones is more manageable than for more heavily or differently substituted analogues. Users moving from R&D test tubes to formal IND or product registration appreciate the difference this makes in providing clear safety and environmental impact data. Our quality team regularly works alongside customer regulatory groups, ensuring that data packages addressing purity, residual solvents, and physical properties match what agencies demand.

    Practical Challenges in Supplying and Scaling 3-Fluoropropiophenone

    Chemical manufacturing, especially fluorinated ketone synthesis, rarely goes exactly as planned. We keep the product clean and within spec by controlling everything from raw material sourcing to temperature ramp speed. Fluorination chemistry brings a few unique hurdles—reactivity can spike unexpectedly in the presence of trace acids or water. Careful inspection and pre-treatment of our starting materials became lessons we learned through missed yield targets and the occasional batch rejection. This product’s value really shows during scale-up, where small differences in mixing or heat transfer impact yield and isolation.

    Batch safety takes center stage. Some customers may not realize that direct fluorination of aromatic rings can run away quickly if system heat loss lags. Our team monitors exotherms and adjusts agitation and dosing based on years of data, fine-tuning only possible from standing next to the reactor during each shift. After years on the production line, we respect not just the chemistry, but also the hazards—routine maintenance checks and layered engineering controls protect everyone working with us.

    We also factor in the regulatory and logistical aspects. Global transport of fluorinated ketones means tracking shelf life under different climates and prioritizing robust packaging. Mismanagement leads to product loss or, worse, failed performance at the customer’s plant. For urgent shipments, we keep a reserve inventory validated for rapid release by in-house analytics, which grew out of repeat requests for 48-hour delivery after breakdowns or QC issues at partner factories. Remaining responsive keeps trust high—no matter the industry segment served.

    Customer Support and Collaboration—Direct from the Factory Floor

    Regular dialogue with processors, formulators, and researchers puts us right at the intersection of science and application. Academic labs often have very different needs than a full-scale pharmaceutical synthesis plant. Over the years, we have adapted our offering—sometimes formulating a slightly more dilute solution for ease of use, or supplying test samples for exploratory research. These practices developed from real conversations with end-users who needed quick answers or custom handling to make their processes work.

    Our technical staff does not just process paperwork; they work through analytical questions, synthetic troubleshooting, and future project scoping right alongside customers. One research group fed back detailed kinetics data on fluorinated ketone condensations, identifying how our slightly lower water content boosted their reaction window. Industrial partners, in contrast, focused on drum-to-drum consistency and cycle time reduction, noting shifts in GC retention times as an early warning indicator for batch abnormalities. These real-world touchpoints feed back into our own QC practices.

    For new applications, we frequently collaborate with external chemists to test downstream performance—from novel heterocycle assembly to exploring non-traditional photochemical routes. The insights gained push us to refine area-specific specs, shifting slightly for advanced techniques. This flexible, responsive development approach means less guesswork and more risk reduction across the value chain.

    Environmental and Safety Considerations

    Compliance with local and international standards forms the baseline for our operation—but our tight production controls extend further. We track and minimize waste streams; optimized distillation leads to a drop in overall solvent use and lowers emissions. Internal recycling of wash solvents and periodic reactor clean-out, timed with shipment demands, has almost halved our plant’s total organic discharge over the last five years.

    Worker safety remains a lived reality, not just a set of posters on the wall. Our standard protocols include air and surface monitoring for fluorinated volatiles. Direct engagement with plant operators led to adoption of new filtration masks and emergency response upgrades. Weekly checks keep conditions consistent, and review meetings ensure new regulatory changes do not blindside anyone.

    End-users depend on transparent documentation for downstream approvals or site permitting. Along with basic COAs and MSDS, we offer tailored impurity profiles and batch histories. This resource becomes essential for customers aiming to maintain traceability from raw material input all the way to finished product registry. Regulators, both regional and international, want evidence for both process control and material identity; from our side, investment in timely and accurate record-keeping saves both us and our customers valuable effort during registration or audit phases.

    Continuous Improvement—Learning from Every Batch

    Process improvement in specialty aroma and fluorinated chemicals never truly stops. Gaps—small and large—emerge as project scopes grow and new requirements shift. We identify weaknesses every time a cycle closes, whether that is a feedback call from a customer or a missed efficiency target. For 3-Fluoropropiophenone, the growing demands for lower residual solvents, higher assay, and secure packaging reflect the rapid changes in how and where these molecules get applied.

    Technology upgrades play an essential role. Adding inline spectroscopic monitoring trimmed analysis time during scale-up, and automation in both filling and labeling reduced error rates across all product lines. Industry partners benefit; after a shutdown in mid-winter left one university project without material for an important assay run, we invested in expanded buffer inventory—learning that technical reliability is as valuable as product purity.

    Over the years, customer feedback cycles became a primary driver for reducing order lead times and improving labeling accuracy. Exposure to the challenges and pain points our users face targets our daily improvement meetings. We now build and sustain real-time relationships with our users—using their process flows as a critical reference for how our own steps stack up.

    Looking Forward: Supporting Next-Generation Applications

    Synthetic pathways shift with research progress and regulatory forces. The demand for 3-Fluoropropiophenone now includes not just larger-scale API work, but also new lines of electronic materials and functional monomers. Recent years saw a surge in cross-coupling and photoredox protocols where our ketone plays an enabling role. The shift toward automation and high-throughput experimentation only increases the emphasis on batch-to-batch reproducibility and transparent sourcing.

    Our experience across thousands of shipments and hundreds of project collaborations positions us to anticipate needs and invest where customers will need support next. Unfiltered access to data, honest conversation about production limits, and a relentless focus on continuous improvement form the core of our work.

    With more sectors moving toward sustainability and tight documentation, and as technical documentation and trace impurity concerns take center stage, we build our practices to withstand scrutiny and meet next-generation challenges. The legacy of each batch shipped rests not just on chemical purity, but on the cumulative trust earned from every site visit, technical consultation, and resolved support call.