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Cyclopropyl 4-Fluorophenyl Ketone

    • Product Name Cyclopropyl 4-Fluorophenyl Ketone
    • Alias 4'-Fluorocyclopropyl Phenyl Ketone
    • Einecs 707-801-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    647811

    Iupac Name 1-(4-fluorophenyl)cyclopropan-1-one
    Molecular Formula C9H7FO
    Molecular Weight 150.15 g/mol
    Cas Number 125126-61-6
    Appearance White to off-white solid
    Melting Point 49-53°C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles O=C1CC1C2=CC=C(C=C2)F
    Inchi InChI=1S/C9H7FO/c10-8-3-1-7(2-4-8)9(11)5-6-9/h1-4H,5-6H2
    Storage Conditions Store in a cool, dry place, protected from light

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

    Packing & Storage
    Packing 100g Cyclopropyl 4-Fluorophenyl Ketone packaged in a sealed, amber glass bottle with tamper-evident cap and detailed hazard labeling.
    Shipping Cyclopropyl 4-Fluorophenyl Ketone is shipped in tightly sealed containers under cool, dry conditions. The packaging ensures protection from light and moisture. Compliant with chemical transport regulations, shipments include proper labeling and documentation. Handling instructions and safety data sheets accompany each order to guarantee safe and secure delivery to the destination.
    Storage Store **Cyclopropyl 4-Fluorophenyl Ketone** in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Ensure proper labeling and secondary containment to prevent leaks or spills. Follow standard chemical storage guidelines and local regulations for handling hazardous materials.
    Application of Cyclopropyl 4-Fluorophenyl Ketone

    Applications of Cyclopropyl 4-Fluorophenyl Ketone in Industrial Manufacturing

    Cyclopropyl 4-Fluorophenyl Ketone serves as a key intermediate in highly specialized downstream sectors. By controlling input specifications and maintaining batch integrity, our manufacturing team ensures stable supply to partners in pharmaceutical APIs, advanced agrochemicals, electronic material syntheses, and specialty polymer additives. Below, we detail practical application routes and end-use formulations for leading industrial tracks, based on verified customer integrations and regulatory frameworks.

    1. Active Pharmaceutical Ingredient (API) Synthesis for CNS Drug Candidates

    Leading pharmaceutical manufacturers incorporate this ketone as a core intermediate during the synthesis of central nervous system (CNS) drug candidates, including anticonvulsants and novel antipsychotics. The manufacturing process utilizes its cyclopropyl moiety for increased metabolic stability, allowing chemists to achieve selective transformation via Friedel–Crafts acylation and nucleophilic addition. Downstream QC teams validate impurity profiles to comply with stringent API release standards prior to tableting or encapsulation.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP <797> Compounding Sterile Preparations
    • European Pharmacopoeia Monographs for CNS APIs
    • FDA 21 CFR Part 210/211

    Typical usage ratio

    • 0.8–1.5 molar equivalents per synthetic cycle, adjusted based on scale-up yields, impurity thresholds, and target batch size

    Downstream process integration

    • Introduced during Step 2/3 of API route following initial ring assembly, enabling direct transformation into substituted amides or secondary alcohols

    Final product types

    • CNS Active Tablets (e.g., antiepileptics)
    • Modified-Release Capsule APIs
    • Clinical-Phase Small Molecule APIs
    • Reference Standards for Regulatory Filing

    2. Building Block in Agrochemical Synthesis (Herbicides & Fungicides)

    Crop protection compound manufacturers utilize this ketone as a precursor to construct newer classes of fluorinated herbicides and fungicides. The structure serves as an electrophilic partner in Suzuki–Miyaura couplings and as a source for bioactive side chains unique to next-generation agrochemicals. Quality control labs closely monitor residual solvent and halide levels per local and international standards.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for Crop Protection Agents
    • EPA 40 CFR Part 180 (US pesticide tolerance)
    • REACH registration (EU)
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 5–20% by weight of total intermediate mass per step, with adjustments based on selectivity and crop-specific toxicity studies

    Downstream process integration

    • Loaded into continuous flow reactors at coupling or condensation stages, directly channeled into compound libraries or technical concentrate blending

    Final product types

    • Granular Systemic Herbicides
    • Fungicidal Emulsifiable Concentrates
    • Pre-mix Adjuvant Formulations
    • Patent-Filed Agrochemical Actives

    3. New Material Precursor in OLED Intermediate Synthesis

    Fabricators in the electronics sector select this chemical for its function as a structural modifier in synthesizing fluorinated intermediates for organic light-emitting diode (OLED) materials. The electron-deficient cyclopropyl ring tailored by this building block imparts increased thermal and oxidative stability to heterocyclic ligands during vapor deposition. Process engineers control the reactivity under nitrogen-purged batch reactors to minimize polymerization risks.

    Industry compliance standards

    • IEC 62321 RoHS Testing for Electronic Materials
    • JEDEC JESD625 for Chemical Contamination Control
    • China RoHS 2 Environmental Protection Management
    • ISO 9001:2015 Quality Management

    Typical usage ratio

    • 2–8% by mass in advanced intermediate synthesis, subject to adjustment based on target photophysical performance and batch quality control

    Downstream process integration

    • Feeds directly into condensation and cyclization stages of OLED emitter production, acting as a chain-terminating or spacing reagent

    Final product types

    • OLED Blue and Green Emitters
    • Electron Transport Layer Materials
    • Small-Molecule Host Compounds for Display Fabrication
    • Photoluminescent Dyes for Flat Panel Displays

    4. Performance-Enhancing Additive in Engineering Plastics

    Producers of high-performance polymers employ this ketone for its capacity to modify mechanical and thermal properties through selective functionalization stages. Integrated into copolymer backbones, the compound confers enhanced impact resistance and chemical robustness—particularly valuable in automotive and aerospace plastics where dimensional stability must meet strict specifications. Strict handling protocols are enforced during pelletization and compounding.

    Industry compliance standards

    • UL 94 Flammability of Plastic Materials
    • ISO 19069-2:2015 Polypropylene Composites
    • ASTM D638 Tensile Properties of Plastics
    • RoHS and REACH Substance Restrictions

    Typical usage ratio

    • 0.5–3.0% by weight in polymer masterbatches, optimized after extrusion trials and end-use simulation tests

    Downstream process integration

    • Introduced during high-shear melt processing or reactive extrusion before molding and post-treatment steps

    Final product types

    • High-Impact Polypropylene Alloys
    • Aerospace-Grade Polyamides
    • Thermally Stable Automotive Housings
    • Custom Polymeric Compounds for Electronics
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    Certification & Compliance
    More Introduction

    Cyclopropyl 4-Fluorophenyl Ketone: What Sets It Apart in Modern Synthesis

    Meeting Real Needs with Practical Chemistry

    In the business of manufacturing specialty chemicals, experience teaches us that real value comes from balancing purity, reliability, and scalable production. Cyclopropyl 4-fluorophenyl ketone, often referenced by its molecular structure, has garnered attention among researchers and process chemists for its role as a versatile building block in pharmaceutical synthesis. Its model stands out due to a unique combination of a cyclopropyl ring attached to a 4-fluorophenyl group, a pairing that presents opportunities for targeted activity or selectivity in compound libraries. We've seen steady demand for this product as more medicinal chemistry teams look for creative scaffolds beyond traditional phenyl or fluorobenzene frameworks.

    This molecule—combining a cyclopropyl unit with a fluorinated aromatic ring—brings a distinct character to reaction planning. Fluorine increases metabolic stability, while the strained ring system can tune a molecule’s interactions in drug targets. In our experience, medicinal chemists appreciate these qualities when constructing new candidates for central nervous system or oncology research. Unlike typical aryl ketones or analogs without fluorination, the 4-fluorophenyl group can profoundly influence a compound’s lipophilicity and electron distribution, often leading to sharper selectivity or improved absorption profiles.

    Production Insights: What We’ve Learned on the Shop Floor

    From the perspective of a manufacturer, achieving consistent quality in cyclopropyl 4-fluorophenyl ketone means more than relying on published literature. Route scouting and reaction optimization often expose subtle differences in raw material quality. We’ve encountered varying behaviors depending on cyclopropanol source, and slight impurities in the starting fluorobenzene can ripple into the end product. The purification steps require keen attention, especially since persistent low-level aromatic byproducts can affect downstream applications. Fully understanding these challenges allows us to refine both the synthesis and isolation, supplying customers with a reliable, high-purity product for research or scale-up.

    Batch reproducibility stands as the mark of a true manufacturer. Traditional routes might use Friedel-Crafts acylation or cross-coupling strategies; we have invested in adapting these methods for environmental safety and operator comfort. Our plant design places a premium on closed-system handling and solvent recovery, because we have learned through audits that protecting worker health and minimizing residual solvents goes hand-in-hand with producing quality material. By managing these factors, we keep waste low and deliver a product that maintains stable physical and analytical characteristics between lots.

    Specifying What Matters: Purity, Residuals, and Handling

    Pharmaceutical and agrochemical companies expect high standards when sourcing intermediates. For cyclopropyl 4-fluorophenyl ketone, users focus not only on assay but also trace residuals such as heavy metals and solvent levels. Our team uses validated HPLC and NMR methods to quantify the main component, and checks for isomer formation, since the cyclopropyl ring can create challenges in synthesis. Bringing this product to over 99% purity for R&D use remains the norm, though some customers ask for even tighter specifications where trace analysis supports late-stage development.

    Solid-state properties—appearance, melting range, and particle size—play a role in customer process choices. Early on, our experience showed large differences in performance between batches produced with different crystallization solvents. After trialing several options, we optimized conditions to ensure consistent free-flowing powder with minimal hygroscopicity. This attention to physical form reduces clumping during shelf life and offers handling advantages in automated dispensing or continuous reactors.

    A point often overlooked by external writers is the product’s behavior under storage. Cyclopropyl 4-fluorophenyl ketone holds up well under controlled temperatures, but we've seen occasional issues in extreme humidity leading to small lumps forming in unsealed packaging. By talking directly with end-users, we tailored our packaging to include robust moisture barriers, which proved to reduce these incidents. Feedback loops between quality assurance and warehouse staff sharpened this approach, underscoring the value of direct manufacturing experience.

    Applications: Insights from Customer Projects

    From years of customer partnerships, we’ve come to understand how cyclopropyl 4-fluorophenyl ketone fits into real projects. Most inquiries come from drug discovery teams, frequently using it as a key fragment in the construction of novel APIs with potential neurological or antiviral activity. Medicinal chemists value the cyclopropyl ring’s role in disrupting metabolic breakdown, extending compound half-life in vivo. The added fluorine at the para position can further direct oxidative metabolism away from vulnerable sites, giving a double advantage not seen in non-fluorinated analogs.

    Some partners investigate its reactivity for the rapid assembly of fused heterocycles or pyrazole derivatives through condensation or cyclization reactions, while others employ late-stage functionalization via selective reduction or halogen exchange. Because the molecule carries both an electrophilic carbonyl and a nucleophilic aromatic ring, formulation teams can test different appendages with predictable site selectivity. These nuances emerge only after extensive benchwork, and we’ve incorporated customer feedback into our technical support documentation to help troubleshoot unexpected side reactions or byproduct formation.

    In agrochemical research, inquiries point to the molecule’s potential as a precursor for fungicides or insecticides where metabolic stability and binding affinity are prized. The combination of three-membered ring strain and aromatic fluorination gives a scaffold not easily achieved by direct fluorobenzene or simple acetophenone variants. We often see innovative catalyst screens or regioselective oxidations attempted by teams aiming to find new structure-activity relationships.

    Why Cyclopropyl and Why the 4-Fluoro Substitution?

    Over time, synthetic chemists have gravitated towards building blocks offering metabolic robustness without sacrificing reactivity. Cyclopropyl groups tend to resist common oxidative or hydrolytic cleavage, compared to unbranched alkyl groups. Adding a fluorine at the para position brings two benefits: increased electron-withdrawing effect and a marked influence on physical properties like solubility and permeability. Both properties help researchers tune their molecules for better biological profiles, such as blood-brain barrier penetration or targeted binding.

    Through collaborative trials with academic and industrial groups, we observed that the 4-fluorophenyl series, when appended with cyclopropyl ketones, often leads to hits in early screening not seen with non-fluorinated or ortho/meta-fluoro substitutions. Specific projects in CNS or antiviral research have shown a measurable uptick in potency or specificity, which tracks well with trends seen in the literature. The distinct combination of reactivity and physiochemical balance makes this product appealing where classic aryl ketones or benzyl derivatives fall short.

    Comparisons to Similar Products

    Traditional phenyl ketones, such as acetophenone or simple cyclopropyl phenyl ketone, lack the enhanced polarity and metabolic tuning that 4-fluorophenyl analogs deliver. We produce a range of aryl ketones in-house; this hands-on perspective sharpens our appreciation for subtle differences in handling and downstream performance. The introduction of fluorine reduces electron density on the aromatic ring, suppressing unwanted side-reactions and creating a more stable core under oxidative conditions common in advanced synthesis.

    Many specialty chemical suppliers list similar molecules with alternative substitution patterns. Our lab trials found that ortho- and meta-fluorinated variants react distinctly during cross-coupling or nucleophilic substitution, often leading to regioisomeric mixtures or lower yields. In contrast, the para-fluorine group found in this product drives uniform transformation, supporting cleaner transformations and simplifying analytical monitoring. The cyclopropyl ring, though strained, offers higher stability in practical workflows than, for example, cyclobutyl or non-cyclic groups, which can break down under processing stress.

    Physical properties set this molecule apart from competitors. Melting point, solubility in organic solvents, and ease of purification all track with our internal benchmarks, providing confidence that material shipped from our line meets target process parameters. Returns and complaints remain negligible due to this tight control, providing assurance to partners running multistep syntheses on tight deadlines.

    Supporting Scale-Up, Green Chemistry, and Safety Improvements

    Drawing from direct feedback, many researchers look for greener options with reduced byproducts and operator risk. Our production method for cyclopropyl 4-fluorophenyl ketone prioritizes solvents with lowered environmental impact, supported by on-site distillation and waste treatment capacities. This investment came after internal hazard reviews identified solvent emissions and acid-catalyzed side reactions as hotspots for improvement.

    Process safety remains central from lot development through full-scale production. Over the years, we’ve modified equipment for enhanced heat exchange and added fail-safe pressure controls after pilot scale runs highlighted thermal runaway risks during cyclopropanation. Repeated safety drills and incident reviews have led us to revise protocols, ensuring that each batch runs smoothly and batch data stays complete. These operational steps improve not only the product’s quality but also the safety data packages required for scale-up or regulatory filings in pharma and agrochemical applications.

    Partner companies send auditors to tour our lines, and this transparency has delivered steady business over the years. By maintaining traceability from raw materials through dispatch, we help downstream clients satisfy their own regulatory needs for supply chain security. Short gaps between production and QA release ensure customers aren’t left waiting when planning their own campaigns.

    Technical Troubleshooting and Continuous Improvement

    Having engineers and chemists under the same roof offers an advantage not always matched by traders or repackers. We’ve learned to listen to real problems arising during mixing, filtration, or storage. More than once, technical support calls have led us to re-examine filtration aids or storage packaging. On one occasion, a client’s unexpected yield drop led our lab team to screen for a residual base in the product, ultimately updating a washing step that resolved the issue.

    Internal communication between production chemists and warehouse teams keeps us nimble. Quarterly reviews of customer feedback—positive and negative—bring improvements throughout the facility. From packing lines through analytical reviews, second-guessing and double checks remain part of our ethos. Practical problems, such as material bridging in drums or stickiness after summer transport, often drive the difference between a reliable supply chain partner and a name on a catalog.

    We host yearly mini-conferences with select R&D clients to share insights. These gatherings invariably highlight small details—a revised drying protocol here, an alternate bottle size there—that sharpen the offering over time. It’s not about hardware or facility size, but the collective willingness to adapt and invest in better performance for those depending on each shipment.

    Looking Forward: Integration with Evolving Research

    Growth in fragment-based and structure-driven drug discovery has sparked interest in tailored building blocks. Cyclopropyl 4-fluorophenyl ketone sits among a class of next-generation fragments that enable faster cycles of synthetic testing with improved biological tractability. By regularly monitoring shifts in patent literature and published screens, we position our supply planning ahead of sudden spikes in demand. This preparation allows research teams to move quickly, knowing their starting materials arrive consistently and match project timelines.

    Collaborations with universities bring fresh approaches to late-stage diversification. We supply research quantities packaged for academic workflows, while also collaborating with industrial scale-up teams designing metric-ton processes. Learning from each sector, we secure feedback about new transformations or safer reagent combinations. It’s a two-way street, benefiting both product evolution and sustainable manufacturing.

    Since regulatory requirements tighten each year, our regulatory group keeps up with changes affecting specialty chemical intermediates. As countries update chemical notification lists or tighten shipping restrictions, we adjust policies and update documentation. Customers appreciate this as it prevents project delays or seizure at customs—a frequent pain point for high-value pharmaceuticals.

    Ethics, Traceability, and Customer Trust

    In the specialty chemical industry, reliability rests on more than current certifications or badges. Trust involves deep inspection—every bottle of cyclopropyl 4-fluorophenyl ketone moving out of the warehouse carries a traceable lot number, with in-house run sheets stored for years. Partners have reached out to verify full supply histories for IND or NDA submissions, and we support those requests promptly, drawing from clear archive protocols.

    We work closely with logistics partners who understand temperature sensitivity and volatile organic compound regulations. Communicating requirements upfront with shipping agents reduces cargo holdups and keeps customer projects running smoothly. For urgent projects, our flexible warehousing allows us to prioritize rush orders, balancing fairness with efficiency.

    Corporate social responsibility has shifted from slogans to actions. Teams engage with communities near manufacturing sites to ensure operations protect shared resources. We have set up roundtables with environmental agencies, responding to local water use concerns and investing in remediation. These investments reduce emissions and support sustained production of specialty intermediates like cyclopropyl 4-fluorophenyl ketone in regions where opportunity and regulation intersect.

    Conclusion: Perspective Born of Experience

    As a manufacturer, we see cyclopropyl 4-fluorophenyl ketone as more than an entry in a catalogue. Its journey—commendable not just for its chemical novelty, but also for the continuous loop of learning and refinement—places it at the forefront of building blocks favored by high-impact research. The smallest details, from crystal habit to packaging tape, matter because somewhere down the line, they shape outcomes for scientists, engineers, and ultimately patients relying on innovative medicines or crop protection agents.

    Each production run brings feedback and improvement. Through close interaction with chemists, technical support, and regulatory groups, the product improves in practical ways. This approach has become second nature, ensuring that cyclopropyl 4-fluorophenyl ketone keeps pace with the rapid evolution of modern science, while earning the trust of the industry’s toughest critics—its end users.