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4'-Methoxy-2-Phenylacetophenone

    • Product Name 4'-Methoxy-2-Phenylacetophenone
    • Einecs 237-924-0
    • 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

    732803

    Iupac Name 1-(4-methoxyphenyl)-2-phenylethanone
    Molecular Formula C15H14O2
    Molecular Weight 226.27 g/mol
    Cas Number 20548-85-2
    Appearance White to off-white solid
    Melting Point 62-65 °C
    Boiling Point 390.2 °C at 760 mmHg
    Density 1.128 g/cm3
    Solubility In Water Insoluble
    Smiles COC1=CC=C(C=C1)C(=O)CC2=CC=CC=C2

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

    Packing & Storage
    Packing 250g of 4'-Methoxy-2-Phenylacetophenone is packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 4'-Methoxy-2-Phenylacetophenone is shipped in tightly sealed containers, protected from light and moisture. It is packed according to chemical safety regulations, labeled as a laboratory reagent. The package includes a material safety data sheet (MSDS) and is transported via a certified carrier in compliance with local and international regulations for non-hazardous chemicals.
    Storage Store **4'-Methoxy-2-Phenylacetophenone** in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances. Keep it away from strong oxidizing agents and sources of ignition. Store at room temperature and ensure proper labeling. Use personal protective equipment when handling, and follow all relevant safety guidelines.
    Application of 4'-Methoxy-2-Phenylacetophenone

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

    As an established chemical manufacturer, we supply 4'-Methoxy-2-Phenylacetophenone to key sectors where aromatic ketones serve critical synthetic functions. This material offers established reliability for advanced organic synthesis, reflected in its direct uptake by the following downstream industries.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use 4'-Methoxy-2-Phenylacetophenone as a building block in the synthesis of specific active pharmaceutical ingredients, especially for non-steroidal anti-inflammatory drugs (NSAIDs) and certain antihistamines. It acts as a core intermediate where its methoxy-modified aromatic structure facilitates clean substitution during multi-step API development. Production processes frequently operate under stringent GMP conditions to ensure batch-to-batch consistency, with quality documented for every consignment delivered to fine chemical processors.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EU EudraLex Volume 4 (GMP Guidelines)
    • Relevant monographs from the European Pharmacopoeia and US Pharmacopeia for synthesized APIs

    Typical usage ratio

    • In small-molecule API synthesis, used at 0.2–0.7 molar equivalents relative to the final active ingredient; actual charge depends on reaction step yield and required scale

    Downstream process integration

    • Charged during Grignard, Friedel–Crafts acylation, or Suzuki coupling stages
    • Introduced pre-purification, followed by isolation/purification of the intermediate
    • Sequenced for precise stoichiometry control in multi-step reaction cascades

    Final product types

    • NSAID API intermediates (e.g., ketoprofen-type scaffolds)
    • Phenylalkylamine antihistamine intermediates
    • Intermediate compounds for central nervous system (CNS) agents

    2. Scent and Fragrance Intermediates

    Manufacturers of fine fragrances and aroma molecules incorporate 4'-Methoxy-2-Phenylacetophenone in the synthesis of compound esters and aldehydes prized for warm, balsamic notes in high-end perfumes. The material’s aromatic structure provides a scaffold for subsequent functionalization, often via oxidation or reduction reactions, yielding unique fragrance molecules. Operators carry out these transformations within REACH and IFRA frameworks, ensuring all reaction by-products are managed according to industry safety standards.

    Industry compliance standards

    • REACH (EC) No 1907/2006 chemical registration requirements
    • IFRA Code of Practice for fragrance safety
    • Cosmetic Ingredient Review (CIR) Expert Panel guidelines for ingredient safety
    • ISO 9235:2013 (Aromatic raw materials for the fragrance industry)

    Typical usage ratio

    • Acts as a precursor in 1–3% by weight of the target fragrance’s batch mass; the exact ratio depends on target conversion efficiency and desired olfactory profile of the final molecule

    Downstream process integration

    • Introduced at the initial condensation, oxidation, or reduction stage
    • Follows through subsequent esterification or acetylation to develop targeted scent molecules
    • Batch records align with traceability and allergen management systems under IFRA protocols

    Final product types

    • Base aroma chemicals for deodorants and ambient fragrances
    • Intermediates for musk and vanilla notes in fine perfumes
    • Complex esters for personal care product fragrances

    3. Photoinitiator Manufacturing for UV-Curing Systems

    Producers in the coatings, inks, and adhesives sector use 4'-Methoxy-2-Phenylacetophenone as a key intermediate in the synthesis of advanced photoinitiators. Its chromophore enables efficient UV absorption, crucial for formulating photoinitiators designed for rapid polymerization in UV-curable resins. The precise control over bulk material purity and moisture content ensures that the resultant photoinitiators deliver consistent cure rates and film properties, critical for manufacturers offering high-speed printing and specialty coatings.

    Industry compliance standards

    • ISO 9001 (Quality management systems for industrial processes)
    • RoHS compliance for coatings/inks in electronics packaging
    • SGS and TÜV quality audits for specialty photoinitiator manufacturers
    • Food Contact Notification (FCN) requirements for packaging inks (where applicable)

    Typical usage ratio

    • Blended at 2–6% by weight in photoinitiator reaction formulation, adjusted based on optical density and functional group reactivity

    Downstream process integration

    • Charged during the acylation or condensation step in synthesizing benzoin ether or diaryl ketone photoinitiators
    • Processed under argon or nitrogen as required for moisture-sensitive reactions
    • Purified via crystallization before blending into photoinitiator masterbatches

    Final product types

    • UV ink photoinitiators for packaging, labels, and flexible films
    • Photo-reactive coatings for automotive plastics
    • Curing agents in dental composites and 3D printing resins

    4. Fine Chemical Building Block for Agrochemical Synthesis

    Agrochemical producers utilize 4'-Methoxy-2-Phenylacetophenone as a structural intermediate in multi-step syntheses of specific herbicide and fungicide molecules, especially where a substituted acetophenone backbone offers bioactivity or target selectivity. Controlled, high-purity batches are necessary to minimize catalyst poisoning and by-product formation during downstream reactions such as chlorination or alkylation, supporting large-scale field trial batches and eventual registration of new active substances.

    Industry compliance standards

    • FAO/WHO guidelines on specification of pesticide technical material
    • Chinese GB/T chemical quality standards for agricultural inputs
    • OECD Principles of Good Laboratory Practice (GLP) for experimental lots
    • ISO 17025 certification for laboratory testing of new active substances

    Typical usage ratio

    • Incorporated at 0.8–1.2 molar equivalents relative to final active molecules; dosage modulated according to overall process conversion and impurity profiles required by regulatory submission

    Downstream process integration

    • Added during initial ketone introduction in the synthesis of triazole or benzimidazole-based pesticides
    • Utilized as a substrate for selective functionalization in flow or batch reactors
    • Followed by chromatographic purification upstream from final formulation

    Final product types

    • Herbicide technical concentrates (e.g., aryl-ketone-based pre-emergents)
    • Fungicide actives for horticultural use
    • Experimental crop protection molecules for international field testing programs

    5. Intermediate for Specialty Dye Synthesis

    Producers of high-performance organic dyes incorporate 4'-Methoxy-2-Phenylacetophenone as a starting material for synthesizing specific anthraquinone or methoxyaryl dye structures. Its aromatic core enables introduction of extended conjugation during condensation or coupling steps, imparting distinct lightfastness and color strength properties required for technical textile applications and electronic display films. Careful monitoring of residual solvents and color index compliance is essential for these downstream uses.

    Industry compliance standards

    • Oeko-Tex Standard 100 for harmful substances in textiles
    • REACH Annex XVII restrictions for azo dyes and intermediates
    • IEC 62471 for photo-biological safety in electronic display materials
    • GB/T 7573:2009 for color fastness testing of dyed goods

    Typical usage ratio

    • Inserted at 10–20% by weight of dye batch, depending on target shade depth and application substrate; color intensity calibrated by pilot-scale runs

    Downstream process integration

    • Utilized in condensation with anhydrides for anthraquinone dye synthesis
    • Catalytically coupled to diazonium salts for azo dye formation
    • Final purification includes ion-exchange step to control heavy metal content

    Final product types

    • Technical textile dyes (polyester, nylon, and cellulose blends)
    • Display dyes for OLED and LCD backlit screens
    • Specialty printing inks for industrial packaging
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4'-Methoxy-2-Phenylacetophenone from an Experienced Manufacturer's Perspective

    Long Years in Synthesis: What We Have Learned

    A compound like 4'-Methoxy-2-Phenylacetophenone does not arrive by chance. Our team has spent decades fine-tuning its manufacture, understanding how even a slight tweak in temperature or solvent affects purity and reproducibility. This chemical carries the CAS number 5965-83-3, often recognized in fine chemical synthesis circles for its methoxy functional group paired with an acetophenone backbone. Over the years, we have observed market requirements shift towards cleaner reactions and consistency in yields. Specialists working at the bench will find its appearance—white to pale yellow crystalline powder—signals readiness for demanding downstream applications.

    Structure and Features that Matter in Practice

    Not every acetophenone derivative behaves the same. Compared with acetophenone, 4'-Methoxy-2-Phenylacetophenone (sometimes known as 1-(4-Methoxyphenyl)-2-phenylethanone) brings the added electron-donating power of the methoxy group into play, changing both reactivity and solubility. The methoxy group stabilizes intermediates in certain organic syntheses, often allowing for milder conditions and higher selectivity. During scale-up, we have seen that the compound’s melting point stability (typically in the range of 86–88°C) makes it easier to monitor during purification stages, especially in recrystallization processes.

    As seasoned chemists, we take special notice of batch-to-batch consistency. Impurities, no matter how minor, upset reaction schemes in research and bulk production alike. By investing in robust purification columns and high-precision analytical instruments, we hold purity often above 99%. No less important, we observe this compound dissolves smoothly in organic solvents such as ether, dichloromethane, and chloroform, making it compatible with established protocols and minimizing the troubleshooting time in the lab.

    Navigating Applications and Market Demands

    Chemists come to us because their syntheses lean on intermediates that don’t let them down. 4'-Methoxy-2-Phenylacetophenone stands out in the preparation of pharmaceuticals, fragrances, and specialty organic materials. Its reactivity enables carbonyl chemistry, particularly in the formation of complex molecules through Friedel-Crafts acylation or further functional group elaboration.

    Pharmaceutical researchers request this intermediate during synthesis of analgesics, anti-inflammatory drugs, and certain psychoactive agents. Its electronic properties mean they can control subsequent transformations with finer precision. Over time, we also noticed perfumers and fragrance manufacturers drawn to its ability to serve as a core backbone for scent modifiers; the methoxy substitution increases stability and brings hit-after-hit reproducibility even after months in storage.

    Academic clients often comment on cost-to-value balance. Scalability proves essential; graduate students and industrial chemists both require larger quantities that keep physical characteristics identical from pilot runs to larger batches. Because we control the synthesis right from the choice of raw benzene derivatives, unexpected color changes or precipitates are rare during use.

    How Our 4'-Methoxy-2-Phenylacetophenone Differs from the Rest

    Not every producer sticks with the material through every challenge. From raw material selection to final packaging, we have put in the work to ensure each drum, bottle, or vacuum-sealed pouch keeps moisture and contamination at bay. We refuse to accept the trade-off between high purity and good storage stability. Focusing on slow and even cooling during crystallization gives our product a sharp melting profile, which eases downstream solvent stripping and reuse.

    End-users have reported that some suppliers’ batches create problems by introducing color or off-odors in sensitive syntheses. We avoid excess solvent carryover and organic residues. By reviewing infrared spectra and chromatography on every batch, we reduce the risk of process interruptions that can cost researchers precious days or upset manufacture in ton-scale reactors. Customers have told us firsthand that making these steps standard has saved them frustration and helped keep project timelines intact.

    We see differences in handling, too. The compound’s granule size and shape may seem trivial. Through our own trials, we realized agglomeration can clog feeders and disrupt weighing systems. By optimizing the drying and sieving process, our team delivers a free-flowing product that pours and measures with minimal static, keeping workflow smooth.

    Living with the Compound: Practical Perspectives

    Few compounds give such a balance between molecular flexibility and reliable handling. Take storage—while our customers want the convenience of long shelf lives, the least trace of moisture can complicate matters. By double-sealing containers and using desiccants tested for their effectiveness, we ensure the compound remains as described, whether opened right away or set aside for months.

    Handling makes a difference in large production suites. Automated systems draw powder from hoppers or drums, so clogging or bridging wastes operator hours. Our experience flagged that particle fineness impacts not only dissolution in solvents but also pneumatic transfer. By sticking to particle size distribution checks, we make 4'-Methoxy-2-Phenylacetophenone ready for both automated and manual operations, from 500-gram research benchtops up to hundreds of kilos in industrial production.

    Health, Safety, and Environmental Concerns in Real-World Use

    Laboratories and plant environments care about safety and waste management. Over the years, we learned that clear and accurate information on use and disposal protects not just staff but also floors and filtration units. We train our manufacturing team to spot and remove unidentified byproducts and to check that solvent remnants don’t increase exposure or downstream environmental burden. Anhydrous packaging and careful cleaning reduce worker exposure.

    Product stability ties directly to knowledge gained from regular stability studies. By reviewing storage test results routinely, we keep an eye on how the product responds to light, heat, and moisture. This know-how builds confidence for users storing or transporting material across distances or through customs checkpoints. Shipping rules shift often, so our logistics crew keeps up with hazardous material changes and operator feedback to maintain seamless deliveries year-round.

    Supply Chain, Traceability, and Open Communication

    It took years to build reliable supplier networks for our precursors. Each shipment, whether bulk solvents or aromatic building blocks, comes with its own analytical certificate, and we don’t accept shipments until on-site checks pass muster. If any deviation creeps in, we select an alternative batch or supplier—even if it means extra lead time—because end quality relies on foundation stones.

    We know the frustration of interrupted production from late or off-spec shipments. To head off problems, we keep core materials in climate-controlled warehouses and set up buffer stocks based on patterns of previous demand. Our customer support answers directly from the plant floor, not a distant call center; so, problems get resolved straight away. Years of feedback have shaped our standard operating procedures, letting us spot trouble with supply or demand well before it threatens customer deadlines.

    Listening to Chemists and Responding with Real Solutions

    User feedback has shaped the way 4'-Methoxy-2-Phenylacetophenone leaves our plant. Chemists prefer technical details served plain, not buried in jargon. We share NMR, GC-MS, and LC data that matches real samples, not idealized literature values. When research teams need a modification—say, a new solvent residue limit or a shelf-life study for a regulatory filing—we run those tests ourselves, sharing full transparency in the results.

    Recently, customers looked to green chemistry for process improvements. They ask about residual solvents, waste streams, and energy use during production. We addressed this by minimizing chlorinated waste and installing solvent recovery systems. Solvent losses now stay well beneath regional thresholds, and recycle rates climb each quarter. Runoff streams are monitored downstream to prove they meet local discharge rules. This hands-on approach gives confidence not just to auditors but the teams that depend on hassle-free downstream processing.

    Cost, Value, and the Changing Chemical Landscape

    Price competition has changed over the past decade, and our survival has always rested on honest conversations with downstream users. Bulk buyers want reliability, but small labs expect quality at fair cost. We run cost-benefit checks of raw materials each quarter, seeking out efficiencies without shortcuts. Swings in global supply chains trigger contingency protocols, redirecting orders from trouble spots and balancing inventories across regions.

    Smaller customers have their own needs: quick turnaround and no long waits for documentation. Test results go out with every order, and our staff answer technical questions by phone or email. If a shipment doesn’t match expected values, we run extra checks or arrange a replacement promptly. Maintaining that trust means turning away from lowest-cost options whenever reliability gets compromised.

    Our Take on Quality and Continuous Improvement

    We learned long ago not to rest on previously set standards. Each batch gives new insights—sometimes by showing a slightly shifted melting point, sometimes through feedback from a user who noticed an unanticipated effect in their process. Quality isn’t just about certificates and passing tests. It means coming back to the plant floor even after most hands go home, checking that aromas stay clean, and that samples taken from the bottom of a drum match those from the top.

    As regulatory frameworks tighten, product traceability comes under ongoing scrutiny. Records of each step in synthesis, purification, and packaging are now more complete and easier for outside reviewers to audit. If an extra filtration stage can lower trace impurities, or a new mechanical seal can improve container closure, we invest upfront—long before a buyer ever sees a drum or bottle.

    Empowering Research and Innovation

    We know that new discoveries start with solid, predictable inputs. 4'-Methoxy-2-Phenylacetophenone provides a platform for building complexity into high-value end-products. Chemists who need to perform directed ortho metalation, or to couple into biaryl systems, depend on reliable intermediates. Some teams use it for photophysical studies, taking advantage of its optical properties that hint at possible roles in molecular electronics.

    No lab or plant runs on theory alone. We’ve seen process changes demand last-minute scale-ups, sudden switches in supply routes, or rapid reformulations. The compound’s robust characteristics help keep research groups ahead of the curve, no matter how rapid the pivots. We regularly work with teams exploring new coupling methods or looking to lower process mass intensity; our knowledge of the core molecule means those transitions can run smoothly, backed by years gathering data on rate constants, solubility profiles, and compatibility charts.

    Building an Informed Community

    Manufacturing and research thrive when information gets shared freely. Through direct support to university partners, regular roundtable sessions with industry scientists, and training programs for early-career chemists, we work to build a culture where questions about 4'-Methoxy-2-Phenylacetophenone—and related intermediates—get honest answers, not textbook recitations. We invite technical visits, offer plant tours, and bring our process engineers into customer meetings to explain how small changes in synthesis routines can cascade into large savings or smoother workflows.

    In an industry that too often guards its know-how, we see more value in open dialog. We issued technical bulletins discussing practical handling, proper storage, and strategies for contamination mitigation, focusing on the compound’s tendencies as seen directly over years of real-world experience. Even minor tweaks—a humidity-controlled packaging line, a streamlined order form, or rapid analytical turnaround—reflect observation and adaptation to the practical needs voiced by those who count on our chemicals for critical work.

    The Road Ahead and Commitment to Ongoing Excellence

    No single product stands still. Each campaign brings new analytical methods, customer-driven improvements, and changes brought by regulation or supply chains. We approach 4'-Methoxy-2-Phenylacetophenone as a living part of that landscape, shaped as much by lessons learned from partners as by our own accumulated knowledge. By holding ourselves accountable not just to certification agencies but to each buyer, researcher, and operator who uses this compound daily, we strive to deliver a chemical that lives up to its promise and supports a dynamic scientific future.