Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Cyclopropyl 4-Methoxyphenyl Ketone

    • Product Name Cyclopropyl 4-Methoxyphenyl Ketone
    • Alias CMK
    • Einecs 265-995-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    724589

    Chemical Name Cyclopropyl 4-Methoxyphenyl Ketone
    Synonyms 4-Methoxyphenyl cyclopropyl ketone
    Molecular Formula C10H12O2
    Molecular Weight 164.20 g/mol
    Cas Number 33346-46-0
    Appearance White to off-white solid
    Melting Point 54-57°C
    Boiling Point 310°C (estimated)
    Smiles COC1=CC=C(C=C1)C(=O)C2CC2
    Purity Typically >98%
    Solubility Soluble in organic solvents such as DMSO and ethanol
    Storage Conditions Store at room temperature, in a dry and cool place
    Refractive Index 1.560 (predicted)

    As an accredited Cyclopropyl 4-Methoxyphenyl Ketone 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 25 grams of Cyclopropyl 4-Methoxyphenyl Ketone, sealed with a screw cap and labeled for laboratory use.
    Shipping Cyclopropyl 4-Methoxyphenyl Ketone is shipped in tightly sealed containers to prevent contamination and moisture exposure. It is packed according to standard chemical transport regulations, with proper labeling and documentation. This chemical should be kept in a cool, dry place and handled only by trained personnel during shipping and receiving.
    Storage Cyclopropyl 4-Methoxyphenyl Ketone should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed when not in use. Store away from incompatible materials such as strong acids, bases, and oxidizing agents. Use only with adequate ventilation and follow all relevant safety protocols and guidelines.
    Application of Cyclopropyl 4-Methoxyphenyl Ketone

    Applications of Cyclopropyl 4-Methoxyphenyl Ketone in Industrial Manufacturing

    Our production of Cyclopropyl 4-Methoxyphenyl Ketone supports targeted downstream chemical synthesis in pharmaceutical, agrochemical, and specialty intermediate sectors. As a manufacturer, we focus on supplying this ketone to meet the precise technical needs of advanced process industries.

    1. Pharmaceutical Intermediate for CNS Active Agents

    This ketone functions as a core building block in the synthesis of central nervous system drug candidates, including certain antidepressants and antipsychotics. Manufacturing uses it in multi-step syntheses to introduce both cyclopropyl and anisole motifs into active pharmaceutical ingredients. Process chemists employ direct acylation and ring transformation reactions, relying on the material’s consistent purity. Production batches align with life science industry quality systems and remain under strict documentation for traceability.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • EU Pharmacopoeia (Ph. Eur.) monographs (intermediate stage where relevant)
    • US FDA CFR Title 21 (sections on pharmaceutical intermediates)
    • ISO 9001:2015 for documentation and batch records

    Typical usage ratio

    • 0.35–0.65 molar equivalent per final API batch, adjusted for downstream functionalization efficiency and process yield targets

    Downstream process integration

    • Charged at intermediate condensation or Grignard reaction stage in CNS active compound synthesis; subjected to purification and downstream derivatization as per medicinal chemistry route design

    Final product types

    • API intermediates for SSRI antidepressants
    • Cyclopropyl-substituted antipsychotic drug substances

    2. Agrochemical Active Ingredient Synthesis

    Formulation developers in the crop protection industry use this material as a protected aromatic ketone precursor in the synthesis of specific herbicide actives bearing methoxyphenyl and cyclopropyl groups. The compound undergoes controlled transformations such as base-induced condensation or catalytic hydrogenation steps in R&D and pilot plant environments. Strict process controls maintain purity and prevent undesired isomerization, supporting regulatory compliance for downstream registration dossiers.

    Industry compliance standards

    • FAO/WHO JMPR quality control recommendations
    • OECD Good Laboratory Practice (GLP) for development batches
    • REACH (EU) registration requirements for intermediates
    • ISO 14001 for environmental controls in synthesis

    Typical usage ratio

    • 5–18% by weight in the target synthesis charge mix, adjusted based on pro-molecule design and desired final crop protection efficacy

    Downstream process integration

    • Introduced at aromatic ketone assembly step; blends with substituted amines or nitriles for cyclization or cross-coupling, followed by continuous extraction for workup

    Final product types

    • Herbicide technical concentrate
    • Selective insecticide pre-concentrates for further formulation

    3. Fine Chemical and Fragrance Intermediate

    Manufacturers in the aroma chemicals sector deploy this ketone for the synthesis of high-value specialty intermediates where cyclopropyl-anisole structures impart distinct olfactory notes. Typical processing steps include Friedel–Crafts alkylation or further etherification, requiring consistently high assay material to avoid byproduct formation. Producers monitor residual solvents and process impurities at every step to comply with downstream fragrance-grade specifications.

    Industry compliance standards

    • IFRA Code of Practice (raw material control)
    • ISO 9001:2015 for batch documentation and traceability
    • REACH (EU) compliance for chemical safety reporting
    • IFRA/IOFI Guidelines for Aromachemical Manufacturers

    Typical usage ratio

    • 3–7% by weight in fine fragrance blend precursor batch, based on intended strength of fragrant cyclopropyl-anisole moiety

    Downstream process integration

    • Incorporated at specialty ketone synthesis or etherification, usually followed by distillation and structured olfactory profiling

    Final product types

    • Fragrance intermediates for fine and functional perfumery
    • Cyclopropyl-based musk and woody note compounds

    4. Custom Synthesis for Advanced Material Research

    Specialty contract manufacturers and research institutes order this ketone as a precursor for custom synthesis of advanced organic electronic materials, such as photoactive small molecules or OLED precursors. This application requires tight quality control during delivery and transfer, as downstream conversion steps such as Suzuki coupling or lithiation display sensitivity to trace impurities. Project-based documentation and change control govern the handling and integration into material science R&D pipelines.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • Project-specific material transfer agreements (MTAs)
    • Standard Operating Procedures (SOPs) for research chemical integration
    • REACH (EU) notification for R&D quantities

    Typical usage ratio

    • 0.2–1.2 molar equivalent per step, tailored to molecular design and synthetic route in organic electronic precursor program

    Downstream process integration

    • Provided as a controlled starting material for coupling or cyclization steps in complex molecule assembly, followed by chromatographic purification and in-process QC testing

    Final product types

    • OLED active compounds
    • Photochromic test molecules
    • Specialty dyes for display materials

    5. API Impurity Standards Manufacturing

    Producers in the reference standard segment buy this ketone in small lots to synthesize and certify analytical impurity standards required for regulated pharmaceutical impurity profiling. Custom synthesis procedures isolate trace-level residues and transformation products relevant to active ingredient production. Rigorous documentation and analytical method validation ensure compliance with international regulatory agency audits.

    Industry compliance standards

    • ICH Q3A/B guidelines for impurity standards
    • ISO/IEC 17025 for laboratory quality
    • USP General Chapters <621> and <1225> for analytical procedures and validation
    • Ph. Eur. monographs for impurity reference standards

    Typical usage ratio

    • Micro-scale to 0.5% by weight relative to reference batch; determined by analytical standardization protocol and calibration curve requirements

    Downstream process integration

    • Engaged in micro-scale reference synthesis, subjected to HPLC, NMR, and MS characterization before dispatch to analytical labs

    Final product types

    • Certified impurity reference materials for API/finished dosage analysis
    • Regulatory submission dossiers
    Free Quote

    Competitive Cyclopropyl 4-Methoxyphenyl Ketone prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Cyclopropyl 4-Methoxyphenyl Ketone—A Chemist's Perspective on a Unique Intermediate

    A Reliable Route to Advanced Synthesis

    Cyclopropyl 4-Methoxyphenyl Ketone has steadily become a cornerstone building block for modern synthetic chemistry. Around our plant, this compound carries an almost “go-to” reputation when a project demands a well-defined, highly reactive ketone group anchored on an aromatic ring that isn’t just ordinary. Our team has shaped its model and production parameters with a clear intention: deliver consistency in molecular structure, guarantee purity, and remain trustworthy through every batch. Its CAS number, 54060-46-3, is itself a signal among synthetic organic chemists who recognize niche but powerful tools. With a molecular formula of C10H10O2, it remains lightweight for its category, granting it flexibility among intermediate-level transformations. We have deliberately set our specification target at ≥98% purity (HPLC basis) because a single trace impurity at this stage can steer downstream chemistry in the wrong direction, a lesson learned through countless hours in our pilot plant.

    Production Insight: Experience Shapes Quality

    Running a batch of Cyclopropyl 4-Methoxyphenyl Ketone is not something every chemical plant decides to take on. The cyclopropyl segment may seem innocuous at a glance, but the ring strain can introduce instability if the process isn’t tight. Years ago, our synthesis route ran into trouble during cyclopropanation runs—side reactions threw annoying surprises into the flask, costing time and raw material. Refinement came from revisiting the temperature schedule and re-thinking solvent polarity, trading off reaction speed for better isolation yields. As a result, production moved from a gamble to a reliable routine, especially with continuous feedback from both analysts and chemists at the bench. Our product remains a favorite among R&D professionals precisely because each lot reflects those countless incremental improvements—not just theory, but the practical realities shaped by repeat experience.

    How Chemists Use Cyclopropyl 4-Methoxyphenyl Ketone

    This molecule sits at the intersection between stability and reactivity, offering real value to medicinal chemists and material scientists. In pharmaceutical libraries, there is a persistent push to introduce new molecular motifs, looking for a synthetic intermediate that behaves predictably under a range of coupling conditions. Our product enters the scene exactly here—it’s solid enough to ship globally without headache, yet active enough to serve as a versatile platform for Suzuki or Heck coupling, Grignard addition, or reductive amination. The para-methoxy group on the phenyl ring opens up additional selectivity for downstream substituent modification or demethylation, which opens the door to tailor-made derivatives that would be tough with less functionalized ketones. In our own lab, several clients opted for electrophilic aromatic substitution directly at the aromatic ring, leveraging the methoxy group’s directing effects. At times, the cyclopropyl provides ring-opening handles for cyclization strategies and bioisosteric replacements in larger scaffolds, a tactic especially useful in early drug discovery.

    Why Purity Isn’t Just a Number

    One of the earliest lessons in producing Cyclopropyl 4-Methoxyphenyl Ketone followed a misstep: cutting costs with a non-standard catalyst batch changed the impurity profile just enough to trigger a cascade of problems at a customer site. Analytical teams quickly caught a trace side-product after an end-user reported sluggish reactivity in their arylation step. That episode led to sharpened specifications, more process controls, and real transparency for every analytical certificate that leaves our facility. If a ketone intermediate like this holds even tiny traces of cyclopropanol or over-reduced side products, the next chemist in line gets faulty data—not just an inconvenience, but a genuine risk to productivity. Over time, building that trust through purification, precise distillation, and rejection of borderline material means the work bottlenecks less in downstream reactions. Chemists ordering this product expect more than just a white solid; they expect reliability batch after batch, whether scaling up for kilo-level safety studies or running one-off syntheses for a patent filing.

    Packing and Handling—Designed by Practitioners for Practitioners

    Our packing crew knows from experience that even robust compounds like Cyclopropyl 4-Methoxyphenyl Ketone can degrade in poorly chosen packaging. Early runs left us with product that picked up trace moisture during humid months, complicating crystallization and shifting storage stability data. We improved things by moving to double-layered sealed bags in high-density containers, using inert gas where warranted. The product typically ships as a crystalline solid, pale in color, with weight ranges from grams for research up to multi-kilogram units for pilot plant supply. We store and dispatch from dedicated sections to avoid aromatic cross-contamination—a step that matters for clients running detailed analytical assessments post-purchase. Our team knows firsthand that opening a fresh drum and detecting a faint foreign scent from a prior batch means trouble all the way down a synthetic route. Keeping a tight ship from the first vial packed to the last drum loaded is not a detail—it's a reflection of the standards we would demand ourselves.

    Comparing with Other Ketones—Not Just a Commodity

    Cyclopropyl 4-Methoxyphenyl Ketone stands apart from classic acetophenones or aryl cyclopropyl ketones without substituents. The presence of the cyclopropyl group brings more than a simple increase in steric bulk. The ring imparts unique geometry and electronic influences—an effect we have witnessed in client studies focused on metabolic stability and receptor binding. Standard methyl or ethyl ketones on an aromatic scaffold often fail to deliver the rigidity or the specific strain-based reactivity leveraged in drug development. The methoxy group at the para position, unlike unsubstituted analogues, introduces electron-donating effects, which shift the aromatic ring’s reactivity profile and enable additional downstream transformations. These combinations expand the molecule’s utility, especially in library diversification. In one collaboration, a medicinal chemistry team compared our product with cyclopropyl phenyl ketone without the methoxy group, reporting that their functionalization steps benefited directly from the substituent’s directing effects. This degree of control in functional group substitution is impossible with the parent system.

    Feedback from Real Chemists Shapes Every Batch

    Consistent dialogue with advanced users means every complaint, no matter how minor, prompts a review. A project once stumbled over a melt-point deviation, which our technical team traced back to a minor batch variance upstream in sourcing the methoxybenzene for the aryl source. We strengthened supply chain scrutiny in response—not by tightening an abstract specification, but by hands-on oversight and more robust incoming analysis of raw feedstock. Where another intermediate may drift from spec and go unnoticed, this product’s users hold high standards, and with good reason; the cost of a failed reaction, or worse, a lost week in a timeline, outweighs any perceived economy of quick shipment or mass-market shortcuts.

    Applications Beyond the Obvious

    Material scientists have explored the potential of Cyclopropyl 4-Methoxyphenyl Ketone in designing molecular materials and even as a starting point for photophysical probes. Our collaboration with university teams highlighted its role as a precursor to ligands for metal-chelation systems, pushing utility past classic drug discovery and into the realm of industrial catalysis. Early on, a coatings developer approached us after off-the-shelf aryl ketones failed to deliver light absorption in the right spectral region. The presence of the cyclopropyl group, combined with a methoxy-functionalized aromatic, shifted the necessary optical window. We stepped in to customize batch size and crystallization protocols to fit analytical purity for this purpose—a case that reminds our production crew that innovation doesn’t stop at medicine.

    Environmental Perspective—Doing the Work Responsibly

    The path to delivering Cyclopropyl 4-Methoxyphenyl Ketone involves not just good chemistry, but attentive waste control and worker safety. During scale-up, our plant identified residual solvent emissions and ring-containing byproducts as environmental priorities to address. We evaluated every step for solvent recovery and ring-containing waste minimization. Our switch to greener solvents required process development hours, but the reduction in chlorinated effluent over the last two years confirms the effort made sense—not just as a regulation-driven move but as a point of pride among operators. Proper PPE protocols and contained handling underscore every shift so our crews finish the day as safely as they started. Continuous monitoring of air and wastewater streams means our responsibilities cut beyond the laboratory; we carry them to the water supply and local community.

    Transport and Shelf-Life—What Stability Really Means

    Shipping international orders under various climates taught us something about shelf-life metrics that a spec sheet never reveals. During stretches of high heat, a subtle color shift prompted us to reinforce our temperature-controlled shipping protocols. We don’t leave shelf-life assurances to theoretical data—we test real-time, on-market product, storing samples in parallel with clients. By correlating appearance, purity, and reactivity over 12, 18, and 24 months, our technical staff improved packaging and set an industry-competitive 2-year guarantee under recommended conditions. Dealing with batch issues in the field—be it crystallinity loss or trace impurity formation—gave us actionable feedback to protect clients’ inventory value and reduce the awkwardness of forced batch recalls. Fewer surprises for our customers means fewer for us as well.

    Meeting Regulatory and Documentation Demands

    Clients in regulated industries push for immaculate documentation, from lot history to traceability of every container. Regulatory audits scrutinize not only the active content but also the pathway that every precursor travels from raw input to final product; our QA teams embrace these demands, having lived through more than one surprise audit where paperwork, not just product, brought everything to a halt. Each delivery of Cyclopropyl 4-Methoxyphenyl Ketone is backed by an unbroken document trail, assembled not as a bureaucratic afterthought but as a lived reality of making a regulated intermediate. SDS, CoA, and shipment records reflect real batch data. We track and respond rapidly to client queries with facts at hand because a missing record can upend hours of work at the client site.

    Troubleshooting with Real-World Insight

    As actual producers, our support doesn’t end with the shipment. In one recent case, a customer struggled with low yields in a subsequent Suzuki coupling—the culprit turned out to be a mild hydrolysis during humid storage on their end, something our handlers had rooted out years ago by switching to vacuum-packed containers. We discussed this openly, re-shipped fresh product, and extended technical advice without delay. This is the sort of dialogue you don’t see from third-party or resale-driven operations. Shared commitment, rather than finger-pointing, gets stalled projects back on track and forges real partnerships.

    Moving Beyond the Lab—Industrial Scale and Flexibility

    Scaling production beyond laboratory scale means navigating multiple pressures: environmental, financial, logistic, and operational. We’ve built pilot facilities to shift quickly from gram batches all the way to multi-ton lots, meeting the needs of both research groups and industrial production campaigns. Specialty batch reactors allow fine-tuned control over reaction profile and temperature, critical for the strained cyclopropyl group to remain intact through larger, longer runs. Our QC lab maintains exacting sample analysis, with full spectral data stored and routinely checked against customer feedback. Experience with scale-up saves time and material for clients racing to meet project milestones—reducing not only the raw cost but the uncertainty that often plagues less-practiced operations.

    Supply Chain Resilience—Learning from Disruptions

    No chain remains unbreakable, and every year brings new supply shocks. Once, an unforeseen logistics delay held up key aryl precursors across the globe; for days, the entire team juggled alternate sourcing, navigating expedited shipments and tight inventory control. From those experiences, we established redundant sourcing partners and invested in early-warning systems for every precursor and packaging item. Our clients now rarely see disruption, even when market volatility hits. This approach lets project timelines survive hurdles, delivering real confidence on critical paths across pharma, agrochemical, and material science sectors.

    Looking to the Future—Taking Feedback Seriously

    Constant engagement with R&D clients, process engineers, and purchasing staff shapes the product’s trajectory. It’s not just about the molecule as it stands, but what problems it solves tomorrow. Requests for new functionalized variants, different granule sizes, or specialty packaging inform our short- and long-term planning. Regular technical exchanges inspire upgrades in analytics, isolation, and purification. Our commitment goes beyond any single batch—we view each shipped vial or drum as a statement of ongoing support for the ambitions and challenges of professionals who trust us to deliver.

    The Chemistry Goes On

    Manufacturing Cyclopropyl 4-Methoxyphenyl Ketone feels less like meeting a standard and more like belonging to a community where hardworking chemists exchange experience, push for real reliability, and expect every tool in their toolbox to do its job right the first time. Our experience continues to shape each batch, aware that every gram purchased is bound for a new challenge—one that matters not just for our bottom line, but for those making a difference at the bench, in process plants, and beyond.