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4-Chloro-4'-Methoxybutyrophenone

    • Product Name 4-Chloro-4'-Methoxybutyrophenone
    • Einecs 228-492-1
    • 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
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    Specifications

    HS Code

    745904

    Product Name 4-Chloro-4'-Methoxybutyrophenone
    Molecular Formula C11H13ClO2
    Molecular Weight 212.68 g/mol
    Cas Number 2893-03-2
    Appearance White to light yellow crystalline powder
    Purity Typically ≥98%
    Melting Point 57-59°C
    Boiling Point 165-168°C at 3 mmHg
    Solubility Soluble in organic solvents such as ethanol, DMSO, and chloroform
    Density 1.19 g/cm3
    Smiles COC1=CC=C(C=C1)C(=O)CCCCl
    Storage Temperature Store at 2-8°C
    Refractive Index n20/D 1.546

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, with secure screw cap; white label displays chemical name, formula, hazard symbols, and batch number.
    Shipping 4-Chloro-4'-Methoxybutyrophenone is shipped in tightly sealed containers to prevent moisture and contamination. It is transported according to standard chemical safety regulations, usually as a hazardous material. Proper labeling and documentation accompany the shipment, and it is kept away from incompatible substances, with temperature control if required to preserve stability.
    Storage 4-Chloro-4'-Methoxybutyrophenone should be stored in a tightly sealed container, away from direct sunlight and incompatible materials such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a dedicated chemical storage cabinet. Ensure the storage area is clearly labeled and access is restricted to trained personnel to avoid accidental exposure or contamination.
    Application of 4-Chloro-4'-Methoxybutyrophenone

    Applications of 4-Chloro-4'-Methoxybutyrophenone in Industrial Manufacturing

    4-Chloro-4'-Methoxybutyrophenone serves as a specialized intermediate across several segments of the fine chemicals and pharmaceutical manufacturing industry. Its unique reactivity and selectivity allow precise adaptation for the synthesis of downstream products where regulatory demands, process controls, and end-quality are critical. Detailed below are major industrial application scenarios reflecting authentic downstream integration within regulated supply chains.

    1. Pharmaceutical Intermediate for Antipsychotic APIs

    This material is commonly used in the synthesis of certain antipsychotic bulk ingredients, where its functional groups enable key bond formations during the build-out of active pharmaceutical compounds. Adherence to stringent quality systems is mandatory throughout the drug substance manufacturing process. Controlled amounts, determined by the reaction stoichiometry, are introduced during the early or mid-stages of complex multi-step syntheses. Output undergoes rigorous release testing to support end-product registration.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs for API Purity
    • 21 CFR Part 211 cGMP for Finished Pharmaceuticals (FDA)
    • ChP (Chinese Pharmacopoeia) Batch Release Requirements

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents per target API step, adjusted per synthetic pathway and impurity profile targets

    Downstream process integration

    • Introduced post-base framework formation as a key carbonyl donor in API build-up phases
    • Purified via solvent extraction or crystallization immediately after coupling or alkylation reactions

    Final product types

    • Antipsychotic tablets and oral suspensions (finished dosage form)
    • Bulk active pharmaceutical ingredient (API) shipments
    • API intermediates for further modification

    2. Agrochemical Intermediate for Fungicide Synthesis

    Manufacturers utilize this compound to build up selective fungicidal agents, where controlled chlorination and methoxy substitution patterns are crucial for targeting pathogen resistance. Compliance with agrochemical registration guidelines governs raw material characterization, traceability, and documented process routes. The input ratio generally matches the limiting reagent, with downstream yield optimization by analytical monitoring.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines for Constituent Profiling
    • REACH Regulation (EC) No 1907/2006 for intermediate use registration
    • ISO 9001-2015 Quality Management System auditing
    • OECD Good Laboratory Practice for residue trials

    Typical usage ratio

    • 1.0 to 1.1 equivalents per fungicidal core scaffold; reactant balance optimized for downstream purity specification

    Downstream process integration

    • Added during heterocycle ring formation or side-chain functionalization steps in target fungicide synthesis
    • Impurity fingerprinting managed after condensation or substitution phases

    Final product types

    • Packaged fungicide concentrates
    • Technical-grade active substances for formulation
    • Dispersible granules and suspension concentrates

    3. Fine Chemical Intermediate in Photoinitiator Production

    Specialty manufacturers implement this material in the synthesis of photoinitiators for UV-curable resins and inks. Compliance with occupational safety and product performance testing underpins the supply chain, especially where trace residues or by-products are regulated in sensitive applications. Usage ratios depend on the required functionalization grade, with process adjustments to manage reaction kinetics and color stability in the final resin systems.

    Industry compliance standards

    • EN 71-3 Safety of Toys (chemical migration for inks)
    • RoHS Directive 2011/65/EU for electronic and electrical equipment
    • ISO 14001 Environmental Management for specialty chemical processing
    • UL Yellow Card materials certification for cured polymer systems

    Typical usage ratio

    • 5–10% by weight in precursor blends before downstream condensation and purification; adjusted to achieve promoter content control and final absorption peak profile

    Downstream process integration

    • Utilized at the oligo-aromatic coupling stage to introduce structural chromophore elements
    • Followed by controlled hydrogenation and crystallization steps prior to photoinitiator isolation

    Final product types

    • UV-curing photoinitiator powders
    • High-performance UV offset inks
    • Resin additives and curing promoter blends

    4. Synthesis of Specialty Fragrance Intermediates

    The molecule serves as a building block for certain synthetic musk and ether fragrance bases in the flavors and fragrance sector. End-use requires compliance with official fragrance safety standards, controlled by quantitative impurity monitoring and batch record traceability. Input quantities depend on the aroma intensity and compatibility with typical musk architectures, refined by pilot-scale panel screening. Production methods integrate the compound at addition phases to generate functionalized aldehyde or alcohol intermediates, which then undergo downstream distillation and purification.

    Industry compliance standards

    • IFRA Code of Practice for synthetic fragrance manufacture
    • EU Cosmetic Regulation (EC) No 1223/2009 for ingredient purity
    • ISO 22716 Good Manufacturing Practices for cosmetic products (applied to fragrance blending)
    • Food Chemicals Codex if intended for flavor use

    Typical usage ratio

    • 0.5–2% on a mass basis in typical musk or aldehyde intermediate syntheses, customized to final target volatility and organoleptic balance

    Downstream process integration

    • Charged to esterification or alkylation units after initial aromatic ester or ether skeleton assembly
    • Intermediate products undergo fractionated vacuum distillation for odor and purity adjustment

    Final product types

    • Fragrance base oleochemicals
    • Concentrated musk accords for perfumery
    • Synthetic aroma chemicals for compounded flavors

    5. Intermediate for Advanced Polymer Additive Manufacturing

    Manufacturers source this material as a reactant for building tailored polymer additives, especially UV-absorbers and chain stoppers in engineering plastics. Industrial polymers require documented incoming raw material control, validation of absence of hazardous breakdown by-products, and conformity with polyolefin additive safety specifications. Typical addition levels reflect the required chain-termination or absorption properties, adjusted through pilot extrusion line trials. The compound enters either as a separate monomer feed in copolymerization or as a functional group donor during pre-polymer blending. Subsequent modifications adapt the additive profile to specific resin end-use.

    Industry compliance standards

    • GB 9685-2016 (China) – Additive use in food contact plastics
    • FDA 21 CFR 177 (US) – Polymers with additives for indirect food additive approval
    • OEKO-TEX Standard 100 for textile-associated polymers
    • REACH SVHC Risk Assessment (EU) for downstream users

    Typical usage ratio

    • 0.1–1.0% by weight in copolymer or masterbatch formulations, depending on final functional requirement and compatibility assessment

    Downstream process integration

    • Feedstock in the masterbatch compounding line following resin base mixing
    • Functionalized during chain transfer or capping reactions, followed by high-shear dispersion

    Final product types

    • Light-stabilized film and fiber masterbatches
    • UV-protective polyolefin and polyester resins
    • Specialty engineering plastics for automotive and packaging
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    Certification & Compliance
    More Introduction

    4-Chloro-4'-Methoxybutyrophenone: A Manufacturer’s Perspective

    Introducing Our 4-Chloro-4'-Methoxybutyrophenone

    Working on the chemical floor, we have seen firsthand how reliable specialty intermediates keep production on schedule and costs under control. Among all the ketones we manufacture, 4-Chloro-4'-Methoxybutyrophenone stands out. Its unique substitution pattern—having a chlorine atom at the para position and a methoxy group opposite—gives it a distinct profile that has strengthened its reputation in custom synthesis, especially for pharmaceutical and fine chemical clients. Whether our end-user is focused on high-purity research or large-batch commercial output, this compound keeps showing up as a practical solution.

    Model, Specifications, and Production Standards

    Chemists sometimes ask what sets one intermediate apart from another. Experience shows it is not only about the molecular structure, but about how consistently the product performs at scale. Our 4-Chloro-4'-Methoxybutyrophenone is usually supplied as a pale yellow solid, batch-crystallized and filtered right here on the production floor. We achieve a typical purity of 99 percent or higher by gas chromatography, reflecting care taken during distillation, crystallization, and solvent recovery. Trace metals and residual solvents are kept well below recognized thresholds. Moisture gets minimized through vacuum drying, which is part of our post-reaction handling every cycle, so that each drum or kilo pack we ship displays the clarity and integrity expected by research and process chemists in API development or specialty intermediates.

    We have invested years in process optimization—starting with careful raw material sourcing through each individual isolation. When the demand called for kilogram or larger batches, we saw crystal habit begin to matter more. A regular batch quality means faster filtration, fewer headaches with downstream separation, and less rework for our partners. By keeping a routine check on particle size distribution, we avoid fines or agglomerates that can disrupt flow or impact dosing accuracy further down the pipeline.

    Uses in Synthesis and Formulation

    Over the last decade, we have been a go-to supplier for developers creating small molecules, from CNS-active compounds to agrochemical scaffolds. 4-Chloro-4'-Methoxybutyrophenone has turned into an intermediary of choice in building intricate molecules where a balance between electron-donating and electron-withdrawing groups can’t be compromised. Custom and contract research organizations keep returning for this material, especially when downstream products demand careful control of substitution patterns.

    In the lab, this ketone slips smoothly into Friedel-Crafts-type acylations, Grignard reactions, and reductive aminations—not just because of its reactive carbonyl, but due to the para-methoxy group’s ability to drive selectivity in aromatic substitutions. In more routine manufacturing settings, our clients rely on its crisp melting point and manageable solubility for both solid-phase and solution-process chemistries. That kind of versatility rarely comes without a trade-off, but we have not seen major formulation headaches even in applications sensitive to impurities. That is the reward for tight controls, not just on the reaction but across all post-synthesis operations.

    Comparing to Other Phenone Intermediates

    Chemistry does not treat all phenones the same. Over years of feedback, a few distinctions have settled the place of 4-Chloro-4'-Methoxybutyrophenone versus other available options. For example, unchlorinated butyrophenones sometimes invite more side-reactions downstream, especially when subjected to strong nucleophiles. Substituting with a methoxy group or with chlorine alone often leaves out the synergistic benefits seen in certain cross-coupling protocols or halogen-driven activations.

    We routinely benchmark our product against neighboring ketones like 4'-Methoxybutyrophenone and 4-Chlorobutyrophenone. Chemical behavior diverges as soon as one enters catalysis regimes, such as Buchwald-Hartwig aminations or Suzuki couplings. For researchers aiming for highly specialized substitution schemes, our compound’s twin groups open routes where either electron withdrawal or electron donation must be leveraged without extra protection or deprotection steps. That efficiency cuts several days out of syntheses that would otherwise call for more convoluted intermediates or awkward workarounds.

    Process engineers handling pharmaceutical payloads frequently comment on the improved reaction rates for certain arylation chemistries as well as the lower tendency to produce colored byproducts versus monosubstituted analogues. In a facility like ours, walking from raw material intake to finished product, the data lines up: fewer run-time deviations lead to increased output and reduced maintenance. The dual substitution pattern also slows some undesired oxidations, making shelf life less of a concern, even in non-ideal storage.

    Why Quality Means More Than Just Analysis

    As a manufacturer, we cannot ignore the real impact of contamination, inconsistency, or careless packaging. Supply chain volatility and changing global regulations make it even more important that we stay accountable for each batch leaving our plant. That philosophy has shaped our approach to 4-Chloro-4'-Methoxybutyrophenone production. Lot documentation follows every shipment, giving direct traceability from starting materials up through final QA sign-off. Many clients request samples for their in-house methods, and we support this by sending full technical data, not just a generic analysis certificate.

    Our plant managers know that the real price of a “good” intermediate goes beyond figures in a spec sheet. Small problems in purification or particle handling can turn into hours of lost time or even failed campaigns once materials land with our partners. That’s why our process improvement loop always includes feedback from bench chemists, material handlers, and formulation scientists—not just lab analysts. We have learned not to wait for problems to show up downstream, and we regularly review isolation protocols, drying parameters, and storage advisories to minimize those risks.

    Lessons Learned from Decades in Chemical Manufacturing

    Every molecule brought to market teaches its own lessons. Over twenty years, we have witnessed how regulatory expectations tighten and how crucial proper documentation becomes. We saw that without standardized impurity profiles, cross-batch variability creeps up. In one instance, a series of lots with slightly higher residual aromatic content led a customer to request weeks of corrective experiments. Rather than see similar problems repeat, we invested in both new analytical tools and better solvent recovery methods for this and related products.

    We have also adapted as new applications emerge. Ten years ago, requests for 4-Chloro-4'-Methoxybutyrophenone mostly arrived from classic pharmaceutical synthesis labs. Today, inquiries come from advanced material startups, specialty resin producers, and academic teams exploring next-gen drug analogues. Adapting to these new needs has meant pivoting batch sizes, adjusting purification sequences, and sometimes rewriting packing and storage guidelines.

    Safety matters in every part of the process, from handling exothermic reactions during chlorination to filtering and drying solids without introducing static discharge risks. Our operators run routine hazard training and protective system checks. Years of hands-on experience taught us that vigilance—supported by clear standard operating procedures—yields better predictability and safety than any administrative checklist alone.

    Common Technical Hurdles and How We Solve Them

    Scaling up reactive ketones from lab to commercial scale often exposes hurdles that nobody flags in academic papers. For 4-Chloro-4'-Methoxybutyrophenone, solvent choice during crystallization caused the most early headaches. Some solvents encouraged oiling-out or left fine, hard-to-filter particulates. Standardizing on a solvent and control regime took months, but the result was smoother filtration, higher yield, and a more reproducible crystal form.

    Filtration efficiency remains central. Even small changes in crystal size can double filtration time, so we routinely run particle checks and optimize the cooling rate. By sharing detailed batch histories with our end-users, we help them plan for consistent filtration and avoid surprises during formulation. This practical sharing of expertise shortens customer learning curves and supports better outcomes in scale-up labs abroad.

    Another persistent issue is residual solvent management. If drying parameters drift outside best practice, solvent traces linger, sometimes above regulatory cutoff. This slows product release and can present tox or reactivity concerns downstream. Instead of treating this as merely a lab problem, we brought in new vacuum equipment and trained all staff in best practices for loading, tray management, and endpoint testing. Today, our product typically clears even the tightest solvent specs, and customers rarely log deviations.

    Supply, Sustainability, and Meeting Future Needs

    Many ask if chemical manufacturing will keep pace with evolving environmental standards. We took steps toward sustainability before many regulatory deadlines appeared, by recycling solvents on site and minimizing single-use plastics in both lab and production. For 4-Chloro-4'-Methoxybutyrophenone, we have reduced process solvent waste by about 40 percent since launching our latest production line. This came through small changes—reconfigured piping, updated solvent tanks, less water in final washes—each one reducing both cost and environmental burden.

    Wastewater remains a priority. Our team treats every liter before discharge or reuse. Even though chlorinated compounds sometimes demand more vigorous treatment, we have not hesitated to make upgrades where environmental risk appears. We believe that delivering a specialty intermediate does not excuse neglecting water quality or worker safety. We track new global rules and anticipate process changes so clients get uninterrupted supply and regulatory confidence.

    Supporting Product Stewardship and Customer Engagement

    Our approach to selling 4-Chloro-4'-Methoxybutyrophenone goes beyond making a single shipment or providing paperwork. Once a partner designs our material into a new process, we stay connected—troubleshooting batch recovery, swapping best practices in blending, or helping optimize crystallization conditions. Product stewardship means anticipating points where things go off-script and helping avoid or rapidly fix them.

    This direct engagement pays off when process scale-ups run into yield decline or trace impurity spikes. By maintaining tight feedback loops from end-users, we have even refined drying and packing protocols to reduce static generation—a subtle but common cause of yield drop in some large-scale blending lines. We believe shared experience is the most dependable risk control for high-value intermediates—better than any contractual fine print or boilerplate guarantee.

    We train our staff not just to execute routines, but to spot deviations before they become issues. Cross-training is standard in our shop—technicians rotate between reactor setup, quality control, and packaging, so everyone understands how even small oversights can snowball by the time a synthetic sequence wraps up. Our quality leads gather checklists, field direct partner calls, and compile weekly reports. That ongoing loop of insight and action brings value that cannot be matched by only sending spec-compliant drums out the door.

    Continuous Improvement Driven by Real-World Feedback

    Over the years, we have improved both the efficiency and reliability of 4-Chloro-4'-Methoxybutyrophenone production by listening closely to customers across segments—including discovery chemists, process scale-up managers, and quality teams at CDMOs. Supply chain crises, configuration changes, or new analytical requests push our team to update processes, qualify alternate suppliers, or add more in-process checks. This work ultimately defends product reliability in the face of market volatility, regulatory shifts, or new scope from our partners.

    Sharing field failures and recoveries helps set clear expectations and raise standards. Sometimes a customer’s in-line monitoring systems detect color or melting point shifts. Instead of disputing it, we initiate immediate investigation, review our procedures, and, when warranted, initiate rework or recall. In return, we ask our partners to keep open channels, share relevant data, and join process review calls. That’s where trust takes root.

    Conclusion: Delivering Reliability Built on Experience

    Our journey with 4-Chloro-4'-Methoxybutyrophenone has underscored a simple fact: manufacturing specialty intermediates is not about ticking boxes on a technical sheet. It’s about navigating hands-on challenges, maintaining stubborn attention to detail, and acting on feedback from real-world chemists and engineers. Each kilogram shipped carries the trace of our team’s daily discipline, accumulated knowledge, and respect for the practical realities that end-users face from pilot plant to final product.

    As the industries we serve move faster and face higher stakes, upstream diligence makes downstream innovation possible. By refusing shortcuts on quality or environmental compliance, and by cultivating collaboration across departments and with external partners, we have carved out a space as not just a supplier but a true contributor to successful chemical innovation. Our ongoing commitment to customer support, process reliability, and technical agility continues to shape how this product serves its dynamic role in modern synthesis.