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Cyclopropyl Phenyl Ketone

    • Product Name Cyclopropyl Phenyl Ketone
    • Alias Cyclopropyl benzyl ketone
    • Einecs 209-862-1
    • 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

    784363

    Iupac Name 1-cyclopropyl-2-phenylethan-1-one
    Cas Number 1191-39-1
    Molecular Formula C10H10O
    Molecular Weight 146.19 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 108-110 °C at 15 mmHg
    Density 1.084 g/mL at 25 °C
    Refractive Index 1.545-1.547
    Flash Point 113 °C
    Smiles O=C(C1CC1)C2=CC=CC=C2

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

    Packing & Storage
    Packing Cyclopropyl Phenyl Ketone, 100g, is securely packaged in an amber glass bottle with a tamper-evident cap and safety labeling.
    Shipping Cyclopropyl Phenyl Ketone is shipped in tightly sealed containers, protected against light and moisture, and labeled according to safety and regulatory guidelines. It is transported as a chemical substance, with proper documentation, and handled following standard protocols for flammable solids to prevent exposure, spills, or contamination during transit.
    Storage Cyclopropyl Phenyl Ketone should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Protect it from direct sunlight and moisture. Ensure the storage area is equipped with proper spill containment and that only trained personnel access the chemical.
    Application of Cyclopropyl Phenyl Ketone

    Applications of Cyclopropyl Phenyl Ketone in Industrial Manufacturing

    Cyclopropyl Phenyl Ketone serves as a specialty intermediate in multiple synthesis routes across fine chemical sectors. Its unique cyclopropyl group and aromatic moiety enable chemists to build complex molecular architectures, supporting the manufacture of high-value end products in pharmaceuticals, agrochemicals, and specialty polymers.

    1. Pharmaceutical Active Ingredient Synthesis

    This compound acts as a key building block for the preparation of various central nervous system drug candidates and anti-cancer intermediates. Process chemists use it in controlled Grignard reactions and cross-coupling protocols to form cyclopropyl functional groups in complex APIs. Consistent purity plays a crucial role during multi-step synthesis, particularly where regulatory compliance for trace impurities and solvent residues must be maintained from raw material to final API stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (for intermediates supply to Europe-based drug makers)
    • US FDA 21 CFR Part 211 (if product progresses to drug substance integration)
    • USP/EP/JP general monograph references for raw material control

    Typical usage ratio

    • Batch-level concentration ranges from 5–35% molar, adjusted for target compound scaffold
    • Ratio depends on stoichiometry of Grignard addition, with excess up to 10% for yield optimization in scale-up

    Downstream process integration

    • Introduced at intermediate coupling stage after aromatic halide derivatization
    • Used as the precursor in ring-closing synthesis before chiral resolution or selective reduction steps
    • May require inline purification depending on residue analysis after initial coupling

    Final product types

    • Antipsychotic and antidepressant active pharmaceutical ingredients
    • Kinase inhibitor intermediates for oncology R&D pipelines
    • Novel small-molecule drugs containing cyclopropyl motifs

    2. Agrochemical Intermediate Production

    This intermediate undergoes Friedel–Crafts acylation or cyclopropanation with other agrochemical feedstocks to create unique scaffolds for fungicide and insecticide molecules. Producers in this sector require traceable supply chains and high batch uniformity, ensuring that each lot meets strict detection limit thresholds for by-product content before integration into bulk actives for crop protection.

    Industry compliance standards

    • FAO/WHO guidelines for technical material quality
    • ISO 9001:2015 for raw material traceability in agrochemical synthesis
    • REACH Annex VII-XI (Europe) registration for supply above 1 ton per year
    • China GB2763 for pesticide residue reference if used in domestic formulation plants

    Typical usage ratio

    • Applied in 2–10% weight basis during bulk active synthesis, depending on the cyclopropyl substitution density in the agrochemical molecule
    • Proportion adjusted upwards for target actives requiring multiple cyclopropyl insertions

    Downstream process integration

    • Added directly into chlorination or acylation reaction stages following initial base molecule synthesis
    • May undergo reflux with Lewis acid catalysts to increase reaction throughput
    • Subject to distillation or crystallization for purification ahead of formulation blending

    Final product types

    • Cyclopropyl-containing pyrethroid pesticides
    • Fungicide actives used in cereals and orchard protection
    • Custom insecticides developed for resistance management programs

    3. Specialty Polymer Modifier

    Manufacturers incorporate the ketone as a functional group initiator or crosslinking monomer during the synthesis of advanced performance resins. Its rigid, three-membered ring can enhance heat resistance, impact strength, and low-temperature flexibility in end-use polymer matrices. Regular QC must monitor integration efficiency, as residuals can alter polymerization kinetics or post-cure mechanical properties.

    Industry compliance standards

    • ISO 9001:2015 certified manufacturing process
    • RoHS Directive (2011/65/EU) for electronics and automotive polymers
    • REACH SVHC compliance for downstream European processing
    • ASTM D638 reference for polymer tensile properties

    Typical usage ratio

    • Commonly dosed at 0.2–1.5% by weight in composite resin systems
    • Ratio depends on required crosslink density and final mechanical strength target

    Downstream process integration

    • Incorporated at pre-polymerization stage in batch reactors under inert atmosphere
    • May function as a chain transfer agent or end-group modifier before curing
    • Requires homogenous dispersion to maintain polymer property profile

    Final product types

    • High-performance thermosetting plastics for electronics
    • Impact-resistant automotive interior polymers
    • Heat-stable coatings and adhesives

    4. Fragrance and Flavor Intermediate

    Chemical processors use the compound as an intermediate for building complex aromatic ring systems found in certain bespoke fragrance molecules. Its unique structure enables synthesis routes that access uncommon olfactory notes, applied main in fine fragrance or functional perfume formulations. Given its chemical reactivity, manufacturers must ensure removal of trace residues as per international safety thresholds before downstream blending.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association) for trace and residual screening
    • Food Chemicals Codex (FCC) for flavor intermediate approvals
    • ISO 22716:2007 (Cosmetic GMP) for fragrance blending houses
    • EU Cosmetic Regulation (Regulation (EC) No 1223/2009) for finished blends

    Typical usage ratio

    • Intermediate typically forms 0.5–2.5% of total raw material batch in syntheses
    • Levels adjusted to achieve specific cyclopropyl aromatic notes in base compounds

    Downstream process integration

    • Entered at reaction stage for constructing ring-fused lactones and aromatic ethers
    • Undergoes hydrogenation or selective reduction for odor modulation
    • QC testing for low residuals prior to perfumer’s base blending

    Final product types

    • Fine fragrance intermediates for designer brands
    • Functional scent compounds in personal care and household products
    • Aroma molecule precursors for specialty food flavor houses
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    Competitive Cyclopropyl Phenyl Ketone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Cyclopropyl Phenyl Ketone: Proven Synthesis and Reliable Performance

    Understanding Cyclopropyl Phenyl Ketone from the Factory Floor

    Producing cyclopropyl phenyl ketone feels like working at a crossroads of modern organic chemistry and practical manufacturing. As a factory rooted in specialty ketone production, we have moved beyond the bench-scale textbooks and built methods that keep up with shifting demands in pharmaceutical and fine chemical synthesis. Cyclopropyl phenyl ketone isn’t just another catalog number. Its combination of a cyclopropyl ring fused with a phenyl group through a carbonyl bridge gives it a unique balance of reactivity and stability—an advantage process chemists look for when planning next-generation molecules or scaling up new reactions for industrial purposes.

    Not every ketone brings the same value to the drawing board. Many multi-step synthesis projects stall when intermediates fail to handle a combination of heat, moisture, and repeated purification. Cyclopropyl phenyl ketone provides consistent results because of the strong C–C bonds in its cyclopropyl ring and the familiar behavior of its aryl and carbonyl functionalities. These points come up again and again with our customers, many of whom run continuous stirred-tank reactors over long production runs. They tell us the product keeps impurities low and withstands working conditions better than open-chain analogs or more sensitive cyclic ketones. It’s details like these that truly set it apart in practical chemical process engineering.

    What Cyclopropyl Phenyl Ketone Offers in Synthesis

    One of the chief reasons chemists opt for cyclopropyl phenyl ketone is the reactivity profile needed for efficient C–C bond construction and access to structures rarely available through simpler reagents. In pharmaceutical research, cyclopropyl groups help improve metabolic stability and target selectivity, which is why we see demand rising among both drug discovery teams and scale-up partners. On production lines, consistency matters more than anything; we optimize our purification methods to deliver a clear, colorless liquid that meets purity benchmarks batch after batch. This helps ensure every reaction starts from the same point, making yields and downstream separation more predictable.

    Compared to other cyclic ketones or linear aryl ketones, cyclopropyl phenyl ketone often wins out when toughness is essential. Many open-chain aryl alkyl ketones break down under strong bases or prolonged heating. The three-membered cyclopropyl ring in our product resists ring opening and holds up to a wide assortment of nucleophilic additions, cycloadditions, and Friedel–Crafts acylations. Labs working with diverse reaction types recognize this resilience; it minimizes troubleshooting and supports a wider reaction window during both R&D and commercial production.

    Choosing Reliable Specifications: The Manufacturer’s Perspective

    With years experience producing specialty aromatic ketones, we have seen the difference a few dozen ppm in residual solvent or trace side-products can make in tightly regulated workflows. Drug intermediate supply chains face ever tighter scrutiny, so every step in our manufacturing process includes checks for process-specific byproducts and meticulously tracked solvent residues. In our experience, purity above 98% is the baseline; many projects require higher targets. By controlling columns, solvent switches, and storage conditions in-house, we offer consistency. Strong batch traceability matters both for compliance and for troubleshooting, so every lot comes documented.

    Molecular formula C10H10O gives a clear picture of the product structure, but the feel and smell of the material say much more on the production floor. Cyclopropyl phenyl ketone gives off a faintly sweet, ether-like aroma, which signals quality and low impurity content when handled in well-ventilated process rooms. Our long-standing technicians judge batches both by instrument readout and by these sensory cues—often catching small variations before analytical reporting flags anything. This practical sense is what keeps customer complaints low, and helps us deliver material that integrates smoothly into downstream production.

    End-Uses and Practical Applications

    The specialty market around cyclopropyl phenyl ketone revolves around its role as a building block, especially where the cyclopropyl motif is required. Researchers use it as both a starting material and a structurally interesting substitute for conventional aryl ketones, letting them introduce compact, strained rings into target molecules. This approach is common in agrochemical and pharmaceutical synthesis, where cyclopropyl groups can alter binding dynamics to enzyme targets and slow metabolic degradation. Many of the new-generation kinase inhibitors and enzyme blockers gradually moving through regulatory pipelines today use cyclopropyl cores introduced through intermediates just like this one.

    Other ketones, such as propiophenone or acetophenone, continue to serve as workhorses for many reactions. Still, their open-chain structure misses out on the strain and rigidity the cyclopropyl ring provides. For substitution with highly nucleophilic reagents, cyclopropyl phenyl ketone offers less susceptibility to unwanted side-reactions. Customers often report smoother workup and higher yields, especially in high-throughput array chemistry, where minimizing cleanup streamlines the entire workflow. For chemists scaling up, shaving minutes off each workup and avoiding column fouling can make the difference between a feasible and a dead-end process.

    Process Challenges and Our Solutions

    Large-scale cyclopropylation is not trivial. Many commodity ketones require aggressive reagents or harsh conditions, which can hike up impurity levels or trigger unpleasant side-reactions. Over the years, we’ve experimented with different cyclopropanation routes and optimized our plant to limit chlorinated by-products by using milder cyclopropanation reagents. Advanced distillation and vacuum drying, installed after multiple customer audits, shorten batch turnaround time and drop water content well below 0.5%. These process tweaks come from repeated experience troubleshooting after long night shifts—making corrections not as a result of textbook planning, but real-world pressure from multi-ton campaign failures and in-process stability hiccups.

    Scaling up this intermediate means batch-to-batch reproducibility. In practice, controlling exotherms and ensuring consistent ring closure defines success more than flashy new synthesis pathways. We developed in-house protocols for quenching and filtration that keep colorless product streaming into our bottling line. By keeping the same core team involved from raw material release through to finished product QC, knowledge stays inside the factory, not lost to turnover or outsourcing. This approach cuts back on miscommunications and gives customers a constant, predictable product profile—whether they need a few kilograms or a multi-ton delivery.

    Analytical Backing for Every Shipment

    Instrument data sits at the core of our trust with buyers. Each batch undergoes GC, HPLC, and NMR checks, not just as box ticking, but because we have seen how even minor peaks in chromatograms can derail demanding downstream processes or trigger returns. Our evolved screening protocols weed out not only starting material residues but also breakdown products common to bulk syntheses. On the rare occasion that we identify a drift in the fingerprint, corrections are made in subsequent batches rather than buried under paperwork. Decisive action wins long-term trust and prevents contaminated deliveries sabotaging customer timelines.

    Foreign customers sometimes ask about our testing approach to moisture and trace metal content. Repeated cycles of Karl Fischer titration and ICP-MS screening are standard, based on years supporting pilot plants and GMP campaigns. This level of scrutiny—more than what many generic suppliers offer—grew out of constant feedback from process chemists who noticed how small levels of water or metals affect hydrogenations, Grignard additions, or oxidations. We learned early that it’s better to over-invest in routine controls than face the reputational and financial costs of a botched multi-stage synthesis.

    Comparing with Other Ketone Products: Where Each Belongs

    In a market with an expanding catalog of ketone options, there is no universal winner. Cyclopropyl phenyl ketone offers a tool for introducing defined strain and rigidity into target molecules, giving chemists structural variety and the power to tune physical or biological properties. Where projects need reliable carbonyl chemistry with extra chemical and metabolic resilience, our product stands out. Its cyclopropyl ring stays put under reaction conditions that would cause less robust structures to rearrange or fragment.

    By contrast, acetophenone offers an all-purpose platform for straightforward C–C bond formation or as a solvent, but it lacks the same resistance to nucleophilic attack or enzymatic breakdown. Cyclohexyl phenyl ketone shifts the steric profile but comes with higher molecular weight and somewhat decreased ring strain. Each has a role, but in drug or agrochemical research, cyclopropyl phenyl ketone increasingly anchors routes where a balance of ring tension and aromaticity is prized. Its use continues to rise in molecular libraries, particularly as companies hunt for scaffolds that break from common flat aromatic designs.

    Environmental, Health, and Safety Considerations

    Factory experience has shown that cyclopropyl phenyl ketone handles well under standard laboratory and plant procedures, provided standard PPE and ventilation measures are followed. Over the years, we’ve reviewed incident logs and seldom found issues arising from the bulk material itself. Problems, if they happen, usually link to improper labeling, container choices, or neglecting established storage rules. It pays to remind teams that the product, while manageable, remains flammable and should be protected from both open flames and excessive heat. Our shipping containers reflect these realities, not just regulatory paperwork, with proper closures and secondary containment.

    On the environmental side, local wastewater treatment setups play a role in how safely spent material is handled. Following internal audits, we invested in higher-capacity waste capture and neutralization equipment to better handle cleaning solvent and process rinse-outs. This came not just from compliance pressure but as an investment: preventing environmental releases reassures all parties and keeps our production floor running smoothly.

    Responding to Customer Feedback and Evolution

    Being on the production side keeps us in close touch with how real-world chemists use and adapt the product. Over time, we have adapted packing options from bulk drums to smaller bottles after hearing from academic and start-up customers about material waste and usability. The same logic guides tweaks in delivery schedules and temperature control, especially as shipping lanes shift and timelines tighten. Long-term buyers—many with years of shared history—help drive these changes through regular feedback. Not all suggestions get acted on immediately, but every point gets logged.

    Scale-up processes come with their own lessons. After tackling an unexpected shift in impurity profiles in larger reactors, we integrated on-line monitoring to catch deviations before a batch is finished. Improvements like these mean fewer surprises down the line for users. The difference between a factory that merely makes a chemical and one that stands behind every batch isn’t just QA paperwork; it’s this willingness to pull process learnings back into the day-to-day operation—and to take responsibility for fixing mistakes quickly.

    Stepping into the Future: Opportunities and Shifting Demands

    Industry trends point toward increased adoption of cyclopropyl phenyl ketone and relatives in new chemical space exploration. Companies push for unique building blocks that can’t be easily mimicked by commoditized compounds. As demand shifts, we stay nimble, tweaking inventory to avoid backorders and keeping a pulse on related compounds that might rise in demand. Research into new synthetic methods for adding or modifying the cyclopropyl group keeps expanding. We participate by collaborating with partner labs and piloting safer, greener process upgrades. Learning flows both ways; what others find on the bench helps shape where we push next in manufacturing.

    Finally, the depth of expertise that comes from being the manufacturer—handling production day in and day out—can’t be faked with sales copy or third-party marketing. Our batches track back to every tweak the process team has ever tried, every shipment that came back to be reworked. When we deliver cyclopropyl phenyl ketone, our experience shows up in the consistency of the product, the traceability of its production, and the confidence our customers bring to their next reaction, knowing the intermediate isn’t just another faceless commodity—it’s the result of years of hard-won factory experience.