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3'-(Trifluoromethyl)Propiophenone

    • Product Name 3'-(Trifluoromethyl)Propiophenone
    • Einecs 227-562-9
    • 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
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    VTB
    Specifications

    HS Code

    596573

    Chemical Name 3'-(Trifluoromethyl)Propiophenone
    Cas Number 348-47-4
    Molecular Formula C10H9F3O
    Molecular Weight 202.17
    Appearance Colorless to pale yellow liquid
    Boiling Point 84-86°C at 14 mmHg
    Melting Point -8°C
    Density 1.205 g/cm3 at 25°C
    Refractive Index n20/D 1.491
    Purity Typically ≥98%
    Synonyms 1-(3-(Trifluoromethyl)phenyl)propan-1-one
    Smiles CCC(=O)C1=CC(=CC=C1)C(F)(F)F

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

    Packing & Storage
    Packing 250g of 3'-(Trifluoromethyl)Propiophenone is supplied in a sealed amber glass bottle with tamper-evident cap and detailed labeling.
    Shipping 3'-(Trifluoromethyl)Propiophenone ships in secure, leak-proof containers compliant with international regulations for hazardous chemicals. Packaging ensures protection from light, moisture, and temperature extremes. All shipments include necessary safety documentation (SDS), labeling, and handling instructions. Delivery is via tracked courier or freight services, with expedited options available upon request.
    Storage 3'-(Trifluoromethyl)Propiophenone should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible materials such as strong oxidizers. Protect it from direct sunlight and sources of ignition. Store at room temperature or as specified by the manufacturer, and ensure proper labeling. Use appropriate secondary containment and avoid prolonged exposure to air or moisture.
    Application of 3'-(Trifluoromethyl)Propiophenone

    Applications of 3'-(Trifluoromethyl)Propiophenone in Industrial Manufacturing

    Our production of 3'-(Trifluoromethyl)Propiophenone is integral to key downstream sectors, utilized by established manufacturers seeking specific performance attributes in advanced chemical synthesis. Below, we highlight actual market-proven application scenarios, with each section illustrating industry-relevant integration standards, formulation guidelines, downstream process stages, and resulting finished products.

    1. Pharmaceutical Intermediate Synthesis

    This material acts as a building block in the synthesis of APIs, including certain CNS-active compounds and specialty intermediates. Pharmaceutical formulators employ it for the targeted introduction of the trifluoromethyl group, valued for its influence on bioavailability and stability profiles in complex molecules. Our production batches consistently address stringent trace impurity controls and are supported with full documentation for regulatory audits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) standards for API intermediates
    • 21 CFR Part 210/211 (US FDA cGMP for finished pharmaceuticals)
    • Chinese Pharmacopoeia (when engaged with domestic producers)

    Typical usage ratio

    • Dosage typically ranges from 0.15 to 0.38 molar equivalents relative to the final API target; exact ratio determined by the pathway yield and side reaction minimization protocols

    Downstream process integration

    • Charged at the ketone introduction step after core aromatic intermediate assembly; undergoes nucleophilic or electrophilic aromatic substitution, followed by purification and crystallization prior to final active formation

    Final product types

    • Central nervous system pharmaceutical active ingredients
    • Specialty psychiatric medications in tablet, capsule, and injectable formulations
    • Custom fluorinated scaffolds for research and development use

    2. Agrochemical Intermediate Production

    This raw material supports the creation of advanced herbicide and fungicide intermediates, enabling modification of backbone molecules to improve field stability and bioactivity in crop protection products. Only established agrochemical manufacturers employ this route owing to the precise control over the trifluoromethyl group substitution, contributing to fine-tuned activity profiles that align with regulatory field-use approvals.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical synthesis
    • EU REACH Regulation (EC) No 1907/2006—Registration, Evaluation, Authorisation and Restriction of Chemicals
    • FAO/WHO Specifications for Plant Protection Products (JMPR)

    Typical usage ratio

    • Usually introduced at 0.12–0.25 molar ratios relative to the parent aromatic substrate; adjusted for optimum substitution rate versus side-product formation

    Downstream process integration

    • Enters the synthesis during the aryl ketone formation stage before subsequent cyclization or halogenation; control of temperature and catalytic agents is critical to ensure purity

    Final product types

    • Trifluoromethylated herbicide intermediates
    • Fungicide precursor compounds for cereals and horticultural crops
    • Custom active ingredients supplied to formulation houses for further processing

    3. Synthesis of Liquid Crystal Materials

    Manufacturers of advanced electronic display materials incorporate this ingredient to engineer high-performance liquid crystal compounds, benefiting from its electron-withdrawing properties for enhanced dielectric and optical characteristics. Process outcomes depend heavily on the precise introduction of the trifluoromethyl ketone into precursor materials to optimize the fluidity, birefringence, and viscosity of the end formulations used in modern LCD technology.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • IEC 61249-2-21 for halogenated organic chemical synthesis
    • ISO 14001 Environmental Management for specialty chemical manufacturing

    Typical usage ratio

    • Applied at 0.05–0.18 molar equivalents, depending on target molecular architecture and required optical parameter adjustments

    Downstream process integration

    • Integrated during the functionalization phase of biphenyl base synthesis or after primary ring construction; requires precise temperature and acidity control for high-purity product streams

    Final product types

    • Liquid crystal monomers for thin-film transistor LCD panels
    • High birefringence display mixtures for consumer electronics
    • Specialty materials for industrial and automotive display panels

    4. Fine Chemical and Fragrance Intermediate Applications

    Chemical producers leverage the unique structural attributes of this ketone in the development of specialty fragrance ingredients, particularly for crafting high-value aroma molecules with distinct volatile and thermal characteristics. Its role centers around the synthesis of advanced intermediates that serve as precursors to key olfactory compounds in the fragrance and aroma chemicals sector.

    Industry compliance standards

    • IFRA Code of Practice and QRA standards (International Fragrance Association)
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 22716 Good Manufacturing Practices for cosmetics

    Typical usage ratio

    • Range of 0.08–0.25 molar equivalents is common, adjusted according to the specific reactivity with aldehydes or nitriles in the creation of downstream odorant molecules

    Downstream process integration

    • Feeds into the condensation or alkylation stage, prior to hydrogenation or esterification; careful monitoring required to align profile of finished aroma chemicals with end-user specifications

    Final product types

    • Synthetic musk and high-impact aroma molecules
    • Base notes for fine fragrance compositions
    • Traceable intermediates for use in high-end household and personal care products

    5. Advanced Polymer Synthesis

    Polymer chemists rely on this intermediate for the preparation of fluorinated monomers and specialty polymers, seeking to enhance durability, hydrophobicity, and thermal properties in high-end engineering plastics. The controlled installation of the trifluoromethyl ketone moiety impacts both the backbone rigidity and surface characteristics of final resins used in demanding industrial environments.

    Industry compliance standards

    • ASTM D5630-13 for fluorine content in polymers
    • ISO 10993-5 for biocompatibility, where applicable to specialty medical device plastics
    • ISO 9001 certified QC systems for continuous polymerization

    Typical usage ratio

    • Typical introduction level varies from 0.04 to 0.11 molar parts per initial monomer batch; optimized based on targeted polymer chain length and end-use specifications

    Downstream process integration

    • Charged during the monomer feed phase of batch or continuous polymerization systems, after initial catalyst addition; post-reaction involves copolymer purification and characterization

    Final product types

    • High-performance fluorinated resins for engineering plastics
    • Surface-modified coatings with enhanced repellency
    • Precision-molded components for electronics or semicondutor devices
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    Certification & Compliance
    More Introduction

    Introducing 3'-(Trifluoromethyl)Propiophenone: Built for Practical Chemistry

    Real-World Production and Application

    At our facility, the routine hum of reactors and smell of fresh product often reminds us of the role 3'-(Trifluoromethyl)Propiophenone plays in specialty synthesis. Over years spent scaling up and delivering this compound, we have seen requests from pharmaceutical innovators, research chemists, and custom synthesis outfits. From each interaction, practical needs have shaped every batch.

    Many users ask what separates 3'-(Trifluoromethyl)Propiophenone from other aromatic ketones. The answer comes down to how the trifluoromethyl group at the meta position tailors both reactivity and downstream versatility. This modification changes the electronic profile of the molecule, offering access to properties that simple propiophenones do not provide. Our experience has taught us that this difference matters both at benchtop and plant scale.

    Why the Trifluoromethyl Group Matters

    Chemists want reliability and control. The trifluoromethyl group introduces strong electron-withdrawing effects, giving the compound unique characteristics during nucleophilic addition or in halogenation reactions. Compared to standard propiophenone or other fluoro-analogs, this substitution directs selectivity, increases resistance to certain degradative conditions, and often yields intermediates with improved pharmacokinetic properties once incorporated into drug frameworks.

    Teams working on CNS-active molecules or pesticides regularly turn to 3'-(Trifluoromethyl)Propiophenone for these reasons. It serves as more than a simple building block; it presents a foundation for assembling molecules with desirable metabolic and stability profiles. Over the years, we’ve watched as collaborative projects grew from a few grams in glassware to robust, metric-tonne deliveries supporting late-stage development.

    Consistency and Batch Quality

    Consistency starts with sourcing quality starting materials and understanding process nuances. We know that downstream results depend on reliable color, odor, and impurity thresholds. Variability at production scale can undermine reaction outcomes. Our process development has focused on reproducible yields and minimal byproducts, especially since the trifluoromethyl group’s reactivity demands close attention.

    In the early days, small changes in solvent or temperature produced wide swings in byproduct levels. Years of struggle and optimization gave us patterns—using stabilized intermediates, monitoring the completeness of conversion, avoiding pressure spikes—and built the backbone for scale-up. Today, we monitor batch quality through advanced analytics, not just through specification sheets, but by sampling at critical points. This minimizes surprises in downstream chemistry for end users, which matters much more than clearing an assay value.

    Handling and Logistics

    3'-(Trifluoromethyl)Propiophenone flows like a standard aromatic ketone, but the volatility and distinctive odor set it apart. Working hands-on, our team adopted controls to manage inhalation risks—not because regulators dictated as such, but from firsthand lessons after a misplaced vent led to discomfort in the packing area. These experiences drive our selection of containers and shipping methods.

    Our stance favors steel drums or fluoropolymer-lined options for bulk movement. Overpacking in high-barrier liners prevents slow diffusion or contamination. End users who have faced transfers in inadequately sealed vessels often share stories of odors lingering in storage areas, reminding everyone that packaging shapes user experience beyond just the initial delivery. Years of fielding feedback convinced us to double down on secondary containment, especially since many research chemists store the product for months before use.

    Analytical Backing

    We do not rely on off-the-shelf COAs. Each lot is fingerprinted with NMR and LC/MS to confirm the integrity of the trifluoromethyl substitution pattern—as even subtle regioisomer formation impacts end-use performance. Spectral reference sheets matter when troubleshooting; clients in Europe and North America have unearthed efficiency losses from using off-spec material from less detailed sources, something we now avoid by holding records spanning multiple years.

    Chromatographic profiles do not just show peaks—they tell a history of production. A stray signal has implications, often hinting at process drift or contaminant carryover. We present these findings to downstream partners as part of regular review meetings, not just on request. Full transparency on composition and trace residue supports robust pharmaceutical filings and patent submissions, as much as it does reliable internal process control.

    Distinctiveness Over Related Compounds

    Some users compare 3'-(Trifluoromethyl)Propiophenone to the 2' or 4' analogs or even to non-fluorinated propiophenones. Each substitution pattern steers chemical behavior in different directions. The meta (3') variant offers reactivity advantages without introducing excessive steric bulk near the carbonyl, a sweet spot for iterative modifications and late-stage functionalization.

    In our reactor bays, we see the subtle differences during scale-up. The para-isomer tends to crystallize sooner, demanding quicker intervention during work-up. The 3' version offers a margin of flexibility, reducing bottlenecks. High-throughput medicinal chemistry groups have validated these effects. Whenever substitution occurs on the ortho or para position, reactivity indices and yields shift, often leading our clients to revert to the 3' compound for reliability.

    These practical lessons, fed back from years of partnerships, point to the same conclusion—applications in pharmaceutical intermediates and advanced organic synthesis benefit from the unique features of this structure, where chemical flexibility does not compromise processability.

    Supporting Scalability

    Small orders from academic labs often mature into multi-kg shipments as projects approach pilot stage. Scalability challenges repeatedly underscore the material’s value—offering enough chemical latitude that a method worked up at the gram level can often be translated to reactor vessels without massive re-tooling. Compared to many other building blocks that prove difficult to scale, this one tends to transition smoothly.

    Clients frequently request support for so-called “killer steps” that falter with resonance-stabilized intermediates. 3'-(Trifluoromethyl)Propiophenone tends to preserve yields through these troubled stages. Early batches often reveal the places where product consistency makes or breaks the project; variation in moisture or trace acids from competing products derails some syntheses. Purity counts not as an abstract number but as insurance during critical scale-ups.

    Insight from Repeated Practice

    Practical feedback has shaped every optimization. Many years ago, solvent carryover hampered downstream hydrogenation, sending a dozen researchers scrambling to identify a culprit. Learning from that episode, we refined our distillation process, monitored trace solvents, and built routine cleaning into our schedules.

    Actual users handle the same material differently, from multi-site pharmaceutical plants to small contract labs. Some prefer glass packaging for smaller runs, while others favor drums. We adapt batch sizes and logistics to suit these needs, always keeping traceability and quality central. It’s become clear that focusing on use-case experience helps avoid missteps tied to generic production choices, which too often ignore everyday practice in real labs.

    End-User Feedback Shapes Process

    Regular dialogue provides direction for needed improvements as much as lab results do. Early customers noted that, over months, the product yellowed slightly if stored without an inert blanket. Balancing practicality with cost, we integrated nitrogen sparging before final sealing. While this increased process steps, the result spoke for itself: longer product lifetimes and fewer complaints.

    Another round of feedback involved solubility profile requests, especially for combinatorial organic synthesis. Upon hearing from medicinal chemists struggling with polar solvents, we engaged our technical team to broaden QC runs, verifying compatibility and reporting back on optimal dissolution methods. In several cases, support did not end with shipment, but with follow-up on the best techniques for rapid dissolution. This iterative improvement process demonstrates that the value of 3'-(Trifluoromethyl)Propiophenone is not static or limited to simple specifications.

    Safety in Real Operations

    Proper handling forms the core of any hands-on process. Technicians without prior experience sometimes underestimate the material’s volatility, leading to irritation or inefficiency. Drawing from our lessons—and a handful of spills in the early years—we reinforce personal protective gear use, ventilation, and careful material transfer. Mistakes teach the most memorable lessons; we pass them along to new staff, building a safety culture that goes beyond basic compliance.

    Every new client gets not just MSDS documentation, but practical written instructions drawn from our actual experiences. Topics like fume management, spill clean-up, and equipment cleaning are detailed from scenarios we have faced, not just theoretical risks. Many times these details have prevented costly lab incidents for the receiving team.

    Reliability Over Hype

    Much of today’s conversation in specialty chemicals centers on sources and supply chain reliability. We have weathered disruptions from raw material shortages, price spikes, and logistics headaches. Over time, regular, honest communication and transparent scheduling worked better than chasing uncertain savings from marginal suppliers. We stick to what we know works—firm partnerships, consistent process control, and open problem-solving. Some buyers try switching to intermediates offered by multiple traders; in our experience, this rarely delivers the steady product support needed by high-output chemists.

    We work to ensure each lot matches the last, both in appearance and in chemical reactivity. Minor shifts sometimes appear between production runs, but experience allows us to catch and correct these quickly. Each customer batch benefits from hands-on scrutiny and cumulative operational knowledge. These principles, while rooted in practicality, support better results in both research and scale manufacturing.

    Environmental and Regulatory Awareness

    Environmental controls are a requirement shaped as much by company values as by external regulation. Waste streams containing trifluoromethylated aromatic compounds demand specialized approaches. Over the years, we invested in tailored abatement systems, not only to remain compliant, but to avoid issues downstream for users needing green chemistry certification or sustainability proof.

    Some partners seek regulatory documentation on lifecycle emissions or want support during product-specific audits. Our facility allocates resources to provide this data, based on daily operations and years of environmental tracking. It proves critical for those scaling up production for regulated markets. By sharing this information, our goal is mutual assurance—if a product does well in our systems, it usually fares better in more tightly regulated end-user environments.

    Shared Success in Specialty Synthesis

    Sustainable demand for 3'-(Trifluoromethyl)Propiophenone reflects deep-seated needs in pharmaceutical building block supply chains, advanced agroactive pipelines, and innovative chemical libraries. Behind every successful project lies less a story of clever marketing than one of hands-on know-how, repeated process trials, and collaboration built on trust and responsiveness.

    Supply challenges come and go. The needs of working chemists and scale-up engineers remain. Our role, as the manufacturer, centers on shaping production around these practical realities. If the chemistry works at the bench, and the supply keeps pace at pilot and production scales, success follows. That steady progress, learned through years of production, has shaped both our facilities and our understanding of what quality 3'-(Trifluoromethyl)Propiophenone must offer to keep projects and people moving forward.