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4'-Chloro-2-Phenylacetophenone

    • Product Name 4'-Chloro-2-Phenylacetophenone
    • Alias p-Chlorohomoveratryl ketone
    • Einecs 253-037-1
    • 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

    946193

    Chemical Name 4'-Chloro-2-Phenylacetophenone
    Molecular Formula C14H11ClO
    Molecular Weight 230.69 g/mol
    Cas Number 135-19-3
    Appearance White to off-white solid
    Melting Point 97-99°C
    Boiling Point 378.4°C at 760 mmHg
    Purity Typically ≥98%
    Density 1.18 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and ether
    Smiles CC(=O)C1=CC=CC=C1C2=CC=C(C=C2)Cl
    Refractive Index 1.617
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing White, sealed glass bottle containing 25 grams, labeled "4'-Chloro-2-Phenylacetophenone" with CAS number, hazard symbols, and storage instructions.
    Shipping 4'-Chloro-2-Phenylacetophenone is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with chemical safety regulations, ensuring no leaks or contamination. Transport is carried out by certified carriers specializing in hazardous materials, following all relevant local and international regulations for chemical handling and documentation to ensure safe, secure delivery.
    Storage 4'-Chloro-2-Phenylacetophenone should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Avoid contact with strong oxidizing agents. Store at room temperature and label clearly. Ensure proper chemical safety procedures are followed and access is limited to authorized personnel.
    Application of 4'-Chloro-2-Phenylacetophenone

    Applications of 4'-Chloro-2-Phenylacetophenone in Industrial Manufacturing

    As an experienced manufacturer supplying raw chemical materials to global industries, we recognize the critical performance and compliance needs faced by downstream processors. 4'-Chloro-2-Phenylacetophenone functions as a specialty intermediate across advanced chemical synthesis, particularly where high-purity building blocks streamline complex transformation steps. Explore its established industrial roles below.

    1. Pharmaceutical Intermediate for Antipsychotic APIs

    Pharmaceutical manufacturers use 4'-Chloro-2-Phenylacetophenone as a core intermediate in the multi-step synthesis of select antipsychotic active pharmaceutical ingredients (APIs), including compounds such as haloperidol and benperidol. Its chloroacetophenone structure enables regioselective condensation and subsequent functional group transformation, supporting the manufacture of molecules with strict impurity control. Precise molar ratios and documentation of chain of custody are essential for traceability during commercial API production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia / National Formulary) specifications for pharmaceutical starting materials
    • EDQM CEP (European Directorate for the Quality of Medicines, Certificate of Suitability)
    • China Pharmacopoeia for regulated API intermediates (where applicable)

    Typical usage ratio

    • Intermediate conversion: utilized at 1.0–1.2 molar equivalents versus target haloperidol or benperidol yield, with precise adjustment for side reaction minimization.

    Downstream process integration

    • Material introduced at Stage 2–3 in multi-step organic synthesis, commonly after Grignard reaction or Friedel–Crafts acylation and before quaternization or reductive amination.
    • Strict in-process HPLC monitoring for residual starting material and side product control.

    Final product types

    • Haloperidol pharmaceutical API
    • Benperidol pharmaceutical API
    • Related antipsychotic intermediate bulk substances

    2. Agrochemical Intermediate for Selective Herbicides

    Agrochemical formulators choose 4'-Chloro-2-Phenylacetophenone as an intermediate in the synthesis of specific aryl-substituted herbicide actives. Its functionalized aromatic ring supports nucleophilic substitution and further coupling, enabling access to pro-herbicide scaffolds used in crop protection. Process engineers monitor the raw material’s purity and batch traceability throughout scale-up and downstream conversion.

    Industry compliance standards

    • ISO 9001:2015 certified quality management for pesticide intermediates
    • FAO International Code of Conduct on Pesticide Management
    • REACH Regulation (EC 1907/2006) for registration and safe handling
    • OECD Good Laboratory Practice (GLP) for analytical development

    Typical usage ratio

    • Introduced at 0.9–1.3 molar equivalents per downstream coupling partner, dependent on efficiency of condensation and loss during purification.

    Downstream process integration

    • Added during the aromatic acylation or nucleophilic displacement step, prior to saponification or chlorination sequences in herbicide synthesis.

    Final product types

    • Aryloxyacetate herbicide actives
    • Pro-herbicide intermediates
    • Formulated crop protection products after further processing

    3. Specialty Chemical Synthesis for Liquid Crystal Monomers

    Manufacturers in the field of advanced electronics and display technologies utilize 4'-Chloro-2-Phenylacetophenone in the synthesis of key liquid crystal monomer building blocks. The para-chloro functionality provides sites for targeted etherification or amination, generating mesogenic units vital for high-performance display and optical films. The criticality of impurity profile and trace metal content is especially high in this segment.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive) compliance for electronic-grade chemicals
    • IEC 61249-2-21 for halogen-free compositions in electronics
    • Customer-specific in-house QC protocols for liquid crystal purity (residual metals, UV-absorbance, etc.)
    • ISO 9001:2015 process traceability

    Typical usage ratio

    • Reacted at 1.0–1.1 molar equivalents versus downstream nucleophile or amine, excess controlled for complete conversion and minimal byproducts.

    Downstream process integration

    • Introduced during Stage 1–2 of liquid crystal monomer synthesis, before estate formation or Suzuki-type coupling reactions.
    • Batches subjected to fine-filtration and spectral QC prior to polymerization.

    Final product types

    • Liquid crystal monomers
    • Mesogenic oligomers and pre-polymers
    • LC display panels and optical films

    4. Fragrance Intermediates for Fine Chemical Production

    In fragrance and flavor chemistry, 4'-Chloro-2-Phenylacetophenone plays a role as a precursor in constructing aromatic ketone frameworks found in select musky or floral fragrances. The compound’s reactivity supports functionalization via reduction and cyclization, facilitating access to signature aroma molecules. Purity and residual solvent limits remain closely monitored in support of downstream sensory performance and safety.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association) for fragrance raw materials
    • ECHA REACH Substances of Very High Concern (SVHC) review
    • ISO 9001:2015 for flavor and fragrance ingredient production
    • GC/MS analytical validation per customer COA specifications

    Typical usage ratio

    • Used at 0.8–1.2 molar equivalents versus cyclizing agent, flexibly adjusted based on conversion yield and olfactory target purity.

    Downstream process integration

    • Material enters as a functionalized aromatic core in Step 2–3, prior to ring closure or Grignard extension in fragrance molecule synthesis.
    • Inline verification of processed batch for residual halides and organoleptic purity before final blending.

    Final product types

    • Musky aromatic ketones
    • Floral aroma intermediates
    • Complex fragrance bases for fine perfumery
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    Certification & Compliance
    More Introduction

    4'-Chloro-2-Phenylacetophenone: A Manufacturer’s Perspective

    What We Know from Years at the Reactor

    Every product has a story, and each begins far before drums leave the warehouse floor. 4'-Chloro-2-Phenylacetophenone, which you’ll see referenced by its CAS number or as 1-(4-Chlorophenyl)-2-phenyl-ethanone, deserves a thoughtful introduction beyond basic data. Our own journey with this compound stretches across more than a decade, with every batch shaped by daily choices and customer needs. Over time, we’ve seen how subtle differences in incoming raw materials and production decisions can create variations not obvious in a typical data sheet.

    Working with 4'-Chloro-2-Phenylacetophenone: What Sets It Apart

    Chemists often evaluate acetophenones as though they’re interchangeable, but small changes in structure make a big difference. Substituting a chlorine at the 4' (para) position on the phenyl ring isn’t just an academic tweak; it marks a boundary between whole fields of reactivity. In practice, this compound’s chloro group gives it unique polarity, and it behaves slightly differently under reduction, acylation, and cross-coupling conditions. We’ve isolated the product under various routes — Friedel-Crafts acylation, Friedel-Crafts alkylation, and other condensation sequences — and observed that downstream reactions often show a real need for consistent, low-residue material.
    Many customers have specifically reported the improved yields and selectivity observed when working with this variant compared to unchlorinated analogs. In pharmaceutical and agrochemical R&D, that difference is often the only thing standing between a successful campaign and a long reset.

    Manufacturing Details: No Blur or Guesswork

    Raw material origin matters, not just for purity, but for reliability batch after batch. We source critical precursors from long-established partners who operate under strict quality norms. Each synthesis run draws on validated process chemistry developed in-house, with temperature and feeding rates adjusted to control side reactions. The product precipitates as a white crystalline solid, and through years of plant experience, our operators detect shifts in color, particle size, and filterability long before automated instruments chime in. Sometimes the difference between a quick filtration and hours of slow percolation comes down to subtleties in stirring or solvent ratios. We’ve trained the team to spot these nuances, and customers tell us the consistent free-flowing crystals improve their own process operations.

    Quality: More Than a Purity Number

    End users look for quick numbers — GC area percent, HPLC retention times, melting point — but there’s more to quality than hitting a single high mark. Take the trace metal profile: even low ppm levels of iron or copper can interfere with sensitive catalysts, particularly in palladium-catalyzed couplings. For that reason, we test product lots for residual metals every time. Moisture, often neglected, matters just as much. We supply the compound in moisture-barrier packaging, keeping water out of the ketone, since even low levels can cause unexpected coloration or hydrolysis during storage. Numerous customers have reached out after switching from general vendors, specifically mentioning a reduction in colored byproducts in their own multi-step syntheses.

    Why Consistency Drives Innovation Downstream

    Over the years, users have described experiments derailed by tiny process changes — a flask going cloudy too soon, yields dropping unexpectedly, or chromatograms showing mystery peaks. Sometimes a batch of acetophenone from a different plant operates within the stated purity but acts unpredictably, especially in scale-up. Our own plant has worked closely with formulators to understand which characteristics matter most. By tracking not just primary purity but levels of regioisomeric impurities and trace process byproducts, we’ve delivered material that saves our customers hours of troubleshooting. Providing data transparency makes all the difference in rapid route development for new molecules.

    What Industries Use 4'-Chloro-2-Phenylacetophenone?

    We’ve sent drums and sample-sized jars of this compound to clients from North America to Asia, and across a spectrum of applications. Many first encounter it as an intermediate for active pharmaceutical ingredients — especially for molecules that use arylated frameworks where selectivity counts. Research groups also value the compound for structure-activity relationship (SAR) studies, precisely because the chloro group adds both steric and electronic effects. Agricultural chemistry teams use the ketone as a platform for synthesizing advanced herbicidal or fungicidal molecules, often via selective halogenation or cross-coupling. Dye and pigment manufacturers produce vivid, photostable colorants thanks to the high reactivity and purity of our product. We’ve even had materials scientists request the compound for new classes of organic semiconductors, where precise electron-donating properties are essential.

    One thing that unites these industries is the absolute necessity for clean, well-characterized intermediates. Experience tells us that with each new research push, someone tries out an old batch and discovers their yield or selectivity drops. By providing up-to-date COAs (Certificates of Analysis) and batch records, and being upfront about any changes to incoming raw materials, we help labs get results faster and with fewer surprises.

    Handling, Storage, and Real-World Lessons

    Years of storing and moving this product have taught us a lot. 4'-Chloro-2-Phenylacetophenone’s solid form handles smoothly in most standard production environments, but direct exposure to humid air tends to cause slow caking and occasional off-coloration. We pack it under inert atmosphere or use thermal-sealed liners whenever shipping to regions with seasonal humidity fluctuations. These steps, our team discovered, cut down on unnecessary reprocessing at the customer’s facility. Clients sometimes inquire about the impact of packing material — our experience shows that metallic drums without a food-grade liner can cause subtle batch-to-batch disparities. By shipping in high-density polyethylene containers or PE-lined fiber drums, we ensure longer shelf stability and easier re-dispensing.

    On one occasion, a major user shared results from their stability trials after switching to our packaging. Their conclusion: extended shelf life and undiminished purity, even after six months in a non-climate-controlled warehouse. We’ve since adopted this as a standard, and routinely solicit feedback from large and small customers. A small adjustment, like liner thickness or anti-static treatment, has sometimes meant the difference between smooth transfer by automated feeders and hours spent breaking up compacted product.

    Comparisons: How 4'-Chloro-2-Phenylacetophenone Measures Up

    Our plant also produces more common acetophenones and their substituted analogs for a wide swath of industrial buyers. Chemical structure ultimately governs function in the lab as much as in the barrel, and we’ve found the para-chloro group brings distinct advantages that set it apart from unsubstituted acetophenone or ortho/meta-chloro derivatives. This includes a shift in reactivity patterns during Grignard, nucleophilic aromatic substitution, and carbonyl addition reactions. For example, process chemists find our product lets them use milder conditions with better selectivity, cutting down on byproduct formation.

    For downstream users, small differences in purification translate to tangible cost savings. By using our highly controlled batch process, the overhead for subsequent purification, whether by crystallization or chromatography, drops. The position of the chlorine on the aromatic ring affects how the molecule interacts in polar and non-polar systems, as well as compatibility with specific catalysts. Having tested analogs side-by-side, we’ve seen that only the para-chloro version delivers the balance of reactivity and robustness needed for scale-up in multipurpose GMP (Good Manufacturing Practice) plant settings.

    Selectivity isn’t the only asset, though. The crystalline nature of this compound and the narrow melting point window signal a well-defined, low-impurity profile; buyers working in light-sensitive applications or analytical chemistry benefit from the absence of colored and volatile byproducts. Some clients have transitioned entire project series from other acylbenzenes to our offering after observing fewer decomposition events under elevated temperature or prolonged exposure to light.

    Experience with Regulatory and Documentation Challenges

    Navigating evolving compliance frameworks has become a more prominent piece of our daily business. From pre-shipment regulatory reviews to detailed traceability documentation, the landscape changes quickly. We have full batch-level documentation ready for customer audits, including where raw materials originated, operator signatures, and final inspection data. This transparency not only satisfies requirements from pharmaceutical and agrochemical oversight bodies, but also builds trust between our team and clients who rely on our word.

    There have been situations where substituting similar compounds failed due to unnoticed variance in trace contaminants or unreported changes in manufacturing process at other sites. We treat any process change as a consultative issue with end users, giving them a full picture of impact — whether on analytical footprint or on synthetic performance. The feedback loop this creates with our partners in research and industry leads to continuous improvements in both record-keeping and process robustness.

    Customer Support and Troubleshooting

    We run a production site, not just a sales desk. Our technical support is built on direct contact between our process chemists and customers. Requests for milligram-scale samples or analytical details are answered by people who have run the reactors and chromatography columns themselves. We keep communication lines open for troubleshooting and optimization. For example, R&D teams often call about scale-up hazards or complex impurity questions. We document observed issues in both synthesis and storage, so a customer facing an unexpected crystal habit, trace discoloration, or dissolution change gets advice based on thousands of kilograms of real-world production, not just literature or catalog standards.

    Process improvements come from this ongoing feedback. One pharmaceutical developer working with us flagged an unusual recrystallization problem, which we tracked back to slight temperature settings on our end. By coordinating pilot plant runs and open lab time, both sides found a more forgiving process window. This kind of collaboration improves timelines for everyone involved.

    Sustainable Practices and Responsible Sourcing

    Chemicals with halogen atoms, including para-chloro-substituted aromatics, have an environmental legacy that commands respect. Our plant has moved steadily toward reducing effluent volume and switching out hazardous solvents wherever possible. Recycling solvents and reclaiming byproducts, we have cut waste output measurably. These investments come from years of working closely with environmental officers, and from understanding that today’s customer base — especially those supplying regulated global markets — want their suppliers as committed to responsible manufacturing as they are.

    On occasions where certain raw material lots show non-conformance for traceability or sustainability, we’ve halted production, rather than risk product integrity down the line. Repeated in-house training and process audits mean our personnel not only meet external standards but anticipate potential non-compliance before it ever reaches the customer.

    Future Perspectives: Where We’re Headed with 4'-Chloro-2-Phenylacetophenone

    Our lab teams are pursuing continued process improvement, especially with cleaner, more efficient routes. We’ve invested in pilot projects aimed at using greener reagents and reducing batch cycle times. Customers increasingly request documentation that meets tighter regulatory requirements, and we keep our technical files and disclosure records ready. In-house studies continue to compare the properties of new lots with historical data, allowing for ongoing tweak and optimization. The production team regularly reviews feedback from downstream applications, further aligning our offerings with the evolving needs of pharmaceutical, agrochemical, and material science researchers.

    From every drum filled at our site, we know the practical value of 4'-Chloro-2-Phenylacetophenone lies in the details: consistent quality, reliable supply, and responsive technical support. These priorities distinguish our product in a crowded market, enabling customers to work more efficiently, safely, and with less downtime. Direct hands-on experience—combined with proactive information sharing—ultimately secures the trust of those who depend on specialized intermediates for tomorrow’s discoveries.