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2',4'-Difluoropropiophenone

    • Product Name 2',4'-Difluoropropiophenone
    • Alias DFPP
    • Einecs 630-971-0
    • 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

    791188

    Chemical Name 2',4'-Difluoropropiophenone
    Cas Number 350-46-9
    Molecular Formula C9H8F2O
    Molecular Weight 170.16 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 91-93 °C at 16 mmHg
    Density 1.211 g/cm3 at 25 °C
    Refractive Index n20/D 1.494
    Flash Point 113.3 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CCC(=O)C1=CC(=C(C=C1)F)F
    Inchi InChI=1S/C9H8F2O/c1-2-9(12)6-3-4-8(11)7(10)5-6/h3-5H,2H2,1H3

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2',4'-Difluoropropiophenone, sealed with a screw cap, labeled with hazard warnings.
    Shipping 2',4'-Difluoropropiophenone should be shipped in a tightly sealed container, protected from light and moisture. Ensure proper labeling and compliance with local, national, and international transport regulations. Handle as a chemical substance and transport by ground or air according to its hazard class, using appropriate protective packaging to prevent leaks or spills.
    Storage 2',4'-Difluoropropiophenone should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat sources and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and acids. Ensure proper chemical labeling and restrict access to trained personnel. Always follow local regulations and safety guidelines when storing this chemical.
    Application of 2',4'-Difluoropropiophenone

    Applications of 2',4'-Difluoropropiophenone in Industrial Manufacturing

    2',4'-Difluoropropiophenone serves as a critical synthetic intermediate for specialized chemical manufacturing. Its molecular structure supports complex transformations in pharmaceutical, agrochemical, and fine chemical industries. The following industrial application sections reflect real-world downstream sectors where our material integrates into production processes under regulated environments.

    1. Pharmaceutical Intermediate for CNS Active Compounds

    In pharmaceutical manufacturing, 2',4'-Difluoropropiophenone acts as a key building block in the synthesis of central nervous system (CNS) active APIs. Medicinal chemists use it for Friedel–Crafts acylation and reductive amination steps when constructing fluorinated aromatic ketone frameworks. These frameworks form part of the core structure in various CNS candidate molecules researched and produced under controlled conditions for neurological therapies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP)
    • EU GMP Guidelines (EudraLex Volume 4)
    • Chinese Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.6–1.3 molar equivalents; adjusted according to stoichiometry in the API route and byproduct minimization targets

    Downstream process integration

    • Inserted at the initial or secondary synthetic stage as the acylation donor; followed by reductive amination, halogen exchange, or cyclization in multi-step reaction schemes

    Final product types

    • Active pharmaceutical ingredients for antidepressants
    • APIs for anti-epileptic medications
    • Neuroprotective research intermediates
    • Other CNS drug development intermediates

    2. Agrochemical Active Ingredient Precursor

    Crop protection manufacturers utilize this compound for preparing difluorinated analogues of phenylketones, which form the basis of several herbicides and insecticides. Process chemists introduce it in coupling reactions or halogenation steps to yield active ingredients with enhanced metabolic stability and field persistence. The material's purity and controlled isomer distribution support consistent product performance in large-scale field applications.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • ISO 9001:2015 quality management for manufacturing
    • Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA FIFRA registration requirements

    Typical usage ratio

    • 5–12% by weight in active intermediate batch; titration adjusted based on desired substitution and downstream yield calculations

    Downstream process integration

    • Employed post-phenyl acylation as a fluorinated starting block; typically flows into tandem halogenation-oxidation or Suzuki coupling stages for final active molecule formation

    Final product types

    • Herbicide technical concentrate intermediates
    • Insecticide technical grade actives
    • Pre-emergent weed control formulation ingredients
    • Plant protection agent intermediates for proprietary blends

    3. Fine Chemical Synthesis for Specialty Monomers

    In fine chemical production, this difluorinated ketone enables the introduction of unique fluorine-functionalities for downstream monomer and polymer applications. Synthesizers obtain enhanced thermal stability and electronic properties in specialty polymerizable units by deploying this reagent in controlled acylation or fluorination sequences. Automotive, electronics, and high-performance material industries incorporate these monomers for performance coatings and engineered plastics.

    Industry compliance standards

    • REACH registration for chemical substances in the EU
    • ISO 14001:2015 environmental management for chemical sites
    • National Emission Standards for Hazardous Air Pollutants (NESHAP, US EPA)
    • Quality agreement based on customer QC protocol

    Typical usage ratio

    • 0.8–1.6 molar equivalents in acylation reactions; batch-specific based on target monomer chain length and side groups

    Downstream process integration

    • Introduced in the transformation step to create fluorinated aromatic monomer precursors; protocol includes catalytic hydrogenation or base-catalyzed coupling for chain extension

    Final product types

    • Heat-resistant monomers for high-performance polymers
    • Modified resins for powder coatings
    • Specialty materials for electronic encapsulation
    • Surface treatment chemical intermediates

    4. Analytical Reference Standard and Custom Synthesis

    CRO and CDMO laboratories require this molecule as a certified reference standard for method validation and trace impurity detection in regulated synthesis campaigns. Analysts apply it for qualitative and quantitative system suitability checks across pharmaceutical and agrochemical manufacturing chains. Additionally, custom synthesis teams leverage this ketone as a derivatization synthon for isotopically labeled compound preparation used in regulatory studies and bioanalytical research.

    Industry compliance standards

    • ISO/IEC 17025:2017 for laboratory competence
    • GLP (Good Laboratory Practice) for test facility use
    • USP Reference Standard qualification
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 10–200 mg per analytical batch for standard preparation; scale-up to multi-gram levels for custom labeling projects

    Downstream process integration

    • Applied in sample calibration procedures, calibration curve generation, and as a synthetic entry point in custom labeling routes

    Final product types

    • Certified analytical reference standards
    • Isotopically labeled intermediate products
    • Spiking solutions for LC-MS or GC-MS method development
    • Regulatory impurity standards for batch release protocols
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    Certification & Compliance
    More Introduction

    2',4'-Difluoropropiophenone: Practical Insights from the Manufacturer’s Floor

    Chemical Identity, Model, and Technical Specifics

    Manufacturing 2',4'-Difluoropropiophenone starts with choosing quality fluorinated benzene derivatives and applying reliable Friedel-Crafts acylation. Over years of hands-on experience, our production lines have optimized this multi-stage process to deliver strong batch consistency. Each drum—be it 25 or 200 kilograms—offers a material with a firm specification range. In typical batches, the product appears as a clear, colorless to pale yellow liquid, showing a faint aromatic scent that signals proper synthesis. Most analytical labs checking our samples report GC purity in the region of 98.5% or higher, and trace moisture spots under 0.2%, which chemicals in this class often struggle to achieve. The molecular formula C9H8F2O and molecular weight of 170.16 g/mol stay stable as expected from strict process control.

    This ketone, with its propionyl backbone bonded to a difluorinated benzene ring, stands apart from mono-fluorinated or non-fluorinated variants because the two fluorine atoms at ortho and para positions change its reactivity. Those handling analytical characterization will notice the specific NMR and mass spectra that help with clear identification, an advantage in purity assurance versus less distinctly substituted phenones. The liquid state at standard conditions, coupled with a boiling point near 235°C, supports convenient handling, pipetting, and scale-up in plant environments. Viscosity measurements remain steady across working temperatures, so dosing and mixing are predictable even on a large scale.

    Usage and Role in Applied Chemistry

    Within the chemical plant, people ask why we continue producing this compound in volume. Years of feedback from R&D chemists and process engineers show its main value comes from its position as an intermediate in specialty synthesis chains. Most popular use cases originate in the pharmaceutical sector, where the difluoro motif allows medicinal chemists to explore structural analogs of known bioactive compounds. New fluoroaromatics often behave differently in biological systems due to the bond energies and electron distribution brought on by fluorine, so access to this building block opens new directions during lead optimization.

    In custom fine chemical contracts, scale-up technicians look for reaction precursors that behave consistently and deliver high yields during downstream conversions—alkylation, reduction, or halogen exchange. 2',4'-Difluoropropiophenone proves itself here as a straightforward substrate, and production engineers often report that batches allow smooth transformations to more elaborate heterocycles or substituted ketones. This efficiency saves time, lowers waste, and trims process cost. For those concerned about regulatory inspection, our supply lines conform to established QA procedures, and long-time plant staff keep careful batch records, helping with material traceability across multiple years.

    Laboratory teams prefer this compound to less-defined or mixed-fluorinated alternatives. One reason: the consistent electron-withdrawing effect of the two fluorine atoms at the 2 and 4’ positions. This influence on the aromatic ring can stabilize specific intermediates during pharmaceutical synthesis or agrochemical research. It’s not uncommon to see newer research groups switch away from basic phenylpropiophenones to explore the effects of dual fluorination, often discovering improved metabolic stability, greater selectivity in biological testing, or altered physical properties (such as increased lipophilicity or different solubility profiles).

    Quality Will Make or Break Downstream Yields

    From a manufacturing standpoint, 2',4'-Difluoropropiophenone doesn’t tolerate sloppy process conditions. Minor impurities—unreacted starting material, mono-fluorinated isomers, or water—will crash out as losses further down the synthesis line. Over time, our team has tuned every kettle, condenser, and brine wash to avoid contamination. GC analyses help keep the product above competing batches that might cut corners with raw material selection or skip essential purification steps. Years of conversation with customers confirm the difference: tighter starting quality translates into fewer side reactions, cleaner purification of the next intermediate, and stronger confidence during final digests and crystallizations.

    Shipping and storage demand their own discipline. Ketones in this chemical family absorb atmospheric water if left unchecked, so drums arrive with tamper-evident seals and dry nitrogen blankets, a practice we borrowed from pharmaceutical-grade supply. This prevents unnecessary hydrolysis or peroxide formation, both of which have ruined pilot runs in the hands of companies with less attention to shipping detail. Plant managers avoid ruined batches when suppliers match this standard, and our warehouse staff have learned that a simple handheld moisture meter remains a crucial tool before drums leave the loading dock.

    2',4'-Difluoropropiophenone Versus Single Fluorinated and Unsubstituted Analogs

    Many chemists familiar with 2'-fluoropropiophenone or 4'-fluoropropiophenone notice practical tradeoffs moving to the difluorinated version. While all share a similar aromatic core, putting a fluorine at both the ortho and para sites alters the compound’s chemical resistance—a user who has spent long hours at the bench will see fewer unwanted side products in some acid- or base-catalyzed schemes. Yields of downstream fluorinated products often climb by several percentage points compared to single-fluorine analogs; support from our Quality Assurance data confirms this trend, in part due to reduced polychlorinated biphenyl (PCB) formation during ring substitution steps.

    Crystallographers find a slightly tighter lattice structure in intermediate solids, which alters melting points and makes purification by recrystallization more reliable. Physical chemists also note a distinctive change in partition coefficients, so 2',4'-Difluoropropiophenone offers better control for separating products during column chromatography. On the technical side, we hear from formulation chemists attempting scale-up that, with the difluorinated compound, final products show more consistent batch-to-batch analytical signatures, which helps avoid regulatory holdups.

    Unsubstituted propiophenones behave differently under certain synthetic conditions. Without any fluorine, aromatic substitution becomes less selective, and downstream oxidation reactions run hotter, making them trickier to manage in large reactors. Those working in high-throughput pharmaceutical campaigns favor the difluorinated compound for late-stage diversification reactions, where the electron-deficient ring system shapes the product distribution. Our own plant engineers report that, compared to the parent compound, the difluorinated version holds up better under UV irradiation and shows less yellowing during long-term storage.

    Safe and Responsible Handling: Lessons from the Factory

    Over years of routine batch handling, our technical staff have seen firsthand how personal protective equipment and good air management make a difference. The faint aromatic odor can become unpleasant at higher concentrations, making process ventilation and fume hoods standard for transfer and sampling. Although the compound exhibits relatively low acute toxicity, gloves and safety glasses remain must-haves due to the potential for skin and eye irritation.

    Employees report that minor spills clean up easily with standard absorbents, but we always stress the importance of rapid response and thorough disposal. Our hazardous waste streams from clean-up never leave the site untreated, and staff training covers both emergency procedures and environmentally responsible disposal. We notice that business partners with rigorous housekeeping practices see fewer incidents, echoing our own experience that cleanliness prevents both contamination and accidental exposure.

    Production Realities and Market Demand

    Manufacturers like us rarely have the luxury of slowing down, since large-volume users need reliability. Ramping up production to meet growing regional demand means more than adding capacity—it takes rigorous supply chain management, robust incoming material QC, and constant upkeep of reactors and distillation columns. Our facility keeps buffer stock of key precursors, insulating production against supplier hiccups and global logistics slowdowns. Records from the last few years show that this approach shields us from supply shocks that have disrupted more speculative vendors.

    Observing the market, demand for advanced fluorinated intermediates keeps climbing. This trend comes from both branded pharmaceutical projects looking for fresh options in metabolically stable scaffolds, and new entrants in the agrochemicals sector responding to stricter global regulations, which call for lower environmental persistence and improved safety profiles. Over multiple cycles, 2',4'-Difluoropropiophenone fetches steady orders from both market segments, in part due to its unique combination of ease of functionalization and desirable fluorine substitution pattern.

    Competing products hit the market from re-packagers and distributers, yet manufacturers holding control over the process stack consistently outperform. Consistent batch records, non-stop process improvement, and in-house analytical support turn into fewer recalls, better technical support, and faster problem solving. Smaller players sometimes offer discounted material but can’t guarantee the tight product specifications or batch consistency. Decades of accumulated experience warn against price-driven purchasing in this segment, as minor early savings give way to downstream losses, process interruptions, and in some cases, failed regulatory audits.

    Challenges Seen by the Manufacturing Team and Actions for Future Improvement

    Manufacturing any fluorinated aromatic requires specialized infrastructure and strict controls. Hydrofluoric acid management, waste handling, and air emissions monitoring compound the complexity, bumping up both direct operating costs and regulatory obligations. Those new to this field often underestimate the sophistication of the safety precautions and environmental controls—mistakes here can result in both health risks and regulatory penalties.

    Our response: continuous investment. The past few years have seen upgrades to closed-system reactions, more efficient scrubbers for acid-containing exhaust, and process innovations aimed at reducing byproduct formation. Plant operators and lab staff attend routine safety and methods training. Our R&D teams keep tweaking purification steps, squeezing down impurity levels with every year. These actions deliver both cleaner material to clients and improved plant safety.

    On the sustainability front, we pay close attention to waste minimization and resource conservation. Water use audits, solvent recovery, and recycling continue to play an increasing role. Plant engineers report progress in moving toward greener alternatives for auxiliary solvents and have begun studying byproduct valorization options. Larger reactors now recover more heat, translating to both lower energy bills and a smaller carbon footprint. Each of these changes reflects real choices by skilled production teams rather than broad promises from sales departments.

    What End Users Value in Direct-Manufacturer Partnerships

    Direct buyers come to us looking for more than a chemical drum. They seek predictable lead times, accurate paperwork, and timely responses to technical questions. As a direct manufacturer, we can offer real-time process updates, custom batch documentation, and expert advice on storage or transformations. Our technical service staff include veterans from production, R&D, and analytical teams—a far cry from generic call-center responses. This makes a difference for project managers handling GMP synthesis, as they know a live support network stands behind every kilogram delivered.

    Collaborative development projects increasingly account for a share of our schedule. Researchers pushing the boundaries—modifying difluorinated scaffolds, testing new routes—get early access to process data, impurity characterization, and scale-up support, all straight from the source. This direct communication removes many common roadblocks. Over the years, mutual trust forms between the production team and end-users: feedback loops tighten, and both sides adapt faster to changing technical requirements.

    Bulk pharmaceutical users seeking a specific impurity profile or unique isotopic labeling benefit from our willingness to adjust process variables or spearhead one-off campaigns. Academic researchers, meanwhile, value clear technical data and reliable shipping. Requiring all this from a distant distributor usually doesn’t work out, as the voice of the true manufacturer gets lost in layers of reselling. In our experience, the closer the relationship, the faster issues get resolved, and the more rapidly projects move forward.

    Why Real-World Process Experience Matters for 2',4'-Difluoropropiophenone

    A chemical as specific as 2',4'-Difluoropropiophenone carries both potential and pitfalls. Production techniques, analytical skills, and decades of cumulative lessons make the difference between ordinary and great supply. Nuances—from raw material selection to distillation rates, from nitrogen blanketing to shipping container seals—impact not just purity numbers but also the everyday experience of those putting this intermediate into practice.

    Our manufacturing teams know which process steps operate closest to the edge and which offer room for further optimization. They share detailed batch data with QA and regulatory teams, translating operational lessons into batch documentation, impurity profiling, and support for product registrations. Time after time, we see that such direct partnerships offer safer, more predictable project outcomes than less hands-on supply chains. End users in advanced pharmaceutical development and technical research benefit, securing a chemical of uncompromised quality, backed by transparent expertise and long-term investment in safe, reliable, and efficient manufacturing.

    In the world of functionalized aromatics, experience matters. 2',4'-Difluoropropiophenone stands as clear evidence of the difference a knowledgeable manufacturing team delivers over generic intermediates. Day by day, the compound’s value grows—alongside an unwavering commitment to quality, safety, and client-focused support, from synthesis to shipment and ongoing technical partnership.