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4,4'-Dichlorobutyrophenone

    • Product Name 4,4'-Dichlorobutyrophenone
    • Einecs 214-147-9
    • 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

    810164

    Cas Number 2235-90-7
    Molecular Formula C10H10Cl2O
    Molecular Weight 217.09 g/mol
    Appearance White to light yellow crystalline powder
    Melting Point 56-59 °C
    Density 1.262 g/cm3
    Purity Typically ≥98%
    Solubility In Water Insoluble
    Flash Point 150.6 °C
    Iupac Name 4-(4-chlorophenyl)-4-oxobutanoyl chloride
    Synonyms 4,4'-Dichlorobutyrophenone; 1-(4-Chlorophenyl)-4-chlorobutan-1-one

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

    Packing & Storage
    Packing 250g of 4,4'-Dichlorobutyrophenone is supplied in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4,4'-Dichlorobutyrophenone should be shipped in tightly sealed, chemical-resistant containers, clearly labeled with appropriate hazard warnings. It must be protected from moisture and incompatible substances, and transported according to local, national, and international chemical safety regulations. Use secondary containment and ensure compliance with all relevant shipping guidelines for hazardous chemicals.
    Storage 4,4'-Dichlorobutyrophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizing agents. Protect from direct sunlight and moisture. Clearly label the storage container and keep it in a designated chemical storage cabinet appropriate for hazardous organic compounds.
    Application of 4,4'-Dichlorobutyrophenone

    Applications of 4,4'-Dichlorobutyrophenone in Industrial Manufacturing

    4,4'-Dichlorobutyrophenone serves as a key intermediate in specialty chemical synthesis. Our factory supplies this material directly to major industrial sectors, where it meets rigorous downstream requirements for purity, phase behavior, and consistency. Below we detail specific application routes, processing details, and compliance considerations for active use in real-world manufacturing environments.

    1. Pharmaceutical Synthesis (API Intermediate Production)

    This compound functions as a building block in the creation of several pharmaceutical intermediates, especially for the synthesis of psychoactive agents and analgesics. Chemists integrate the material at the condensation step, ensuring compatibility with sensitive reaction chains. Dedicated GMP production suites handle both input and byproduct management to avoid cross-contamination and preserve traceability across all operations beginning with this input.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP regulations)
    • EU EudraLex Volume 4 GMP (for pharmaceutical production)
    • Relevant monographs in the USP and EP for API intermediates

    Typical usage ratio

    • Implemented at 0.8–1.5 molar equivalents relative to final target structure, adjusted according to desired yield, impurity profile, and downstream route optimization.

    Downstream process integration

    • Added during ketone alkylation or arylation steps prior to ring closure and purification; typically enters after solvent charging but before catalyst introduction.

    Final product types

    • API intermediates for antidepressants
    • Precursors for antipsychotic APIs
    • Key intermediates for local anesthetic agents
    • Specialty starting points for neuroactive compounds

    2. Agrochemical Manufacturing (Herbicide Intermediate)

    The material occupies a tracked step in the formation of several phenoxy and phenyl-based herbicide actives. Process engineers administer it under closed-system reaction conditions, especially where operator exposure or raw material volatility must be managed. It anchors certain condensation cycles central to the manufacturing of highly selective crop protection agents.

    Industry compliance standards

    • ISO 9001:2015 (Process Quality Management for chemical synthesis)
    • REACH registration (for European Union market placement)
    • EPA Pesticide Registration (40 CFR Part 158) for U.S. sales
    • China’s HSE Measures for Agrochemical Production

    Typical usage ratio

    • Normally dosed at 0.5–1.2 parts by weight per part of active ingredient target, modulated based on target molecule substitution pattern and catalyst system.

    Downstream process integration

    • Feeds into the initial aryl ketone synthesis phase; commonly reacted prior to halogen exchange or etherification, sometimes requiring in-line phase separation for impurity control.

    Final product types

    • Phenoxy herbicide actives
    • Selective weed control agents for cereals and rice
    • Cereal crop growth regulators
    • Specialty intermediate bulk agrochemicals for contract manufacturing

    3. Dye and Pigment Intermediate Production

    4,4'-Dichlorobutyrophenone acts as a primary reactant in the synthesis of specialty dyestuffs, especially for thermally stable, halogenated pigment lines. Dye manufacturers incorporate the compound during the arylation or oxidative coupling phase to anchor chromophoric groups efficiently. Strict purity control ensures finished pigment quality essential for long-life commercial inks and plastics coloration.

    Industry compliance standards

    • EN 71-3 (Toy Safety—Migration of Certain Elements) for pigment end uses
    • REACH (Annex XVII—Restriction of certain hazardous substances)
    • ISO 18451 (Pigments and Extenders—Terminology and Classification)
    • GMP for Pigments if used in food contact materials

    Typical usage ratio

    • Employed at 1.0–2.0 equivalents relative to chromophore unit; formulation varies based on intended lightfastness, solvent system, and polymer carrier compatibility.

    Downstream process integration

    • Inputted prior to oxidation; forms the backbone for subsequent halogenation or sulfonation steps, depending on required pigment family.

    Final product types

    • Thermally stable pigment intermediates
    • Specialty dyes for industrial inks
    • Color additives for engineering plastics
    • Pigments for automotive and packaging coatings

    4. Specialty Polymer Modifier Production

    Manufacturers in advanced materials use this compound to tailor-make functionally modified polymers, particularly where halogenated backbones or crosslinked phenyl structures enhance performance. Its integration often follows a batch addition during prepolymer formation, followed by in-situ reaction monitoring to achieve target molecular weights and mechanical properties relevant to customer specifications.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for halogen content limits in polymer additives
    • ISO 9001:2015 (Quality management in polymer manufacturing)
    • UL 94 (Flame retardancy rating for plastic components)
    • FDA 21 CFR (for food contact plastics, specific migration limits)

    Typical usage ratio

    • Ranges from 0.2–3.0 phr (parts per hundred resin) depending on desired functionalization degree, base polymer matrix, and end-use application.

    Downstream process integration

    • Entered at the polymerization stage, prior to chain extension; can be used as a co-monomer or as a chain stopper in thermoset and thermoplastic resin synthesis.

    Final product types

    • Flame-retardant engineering plastics
    • Industrial coatings with enhanced UV resistance
    • High-performance elastomer modifiers
    • Antistatic compounds for electronics enclosures

    5. Fine Chemical Synthesis for Flavors and Fragrances Intermediates

    In the flavors and fragrance sector, this material supports the design of select aromatic intermediates with stable halogenated profiles. Downstream processors use the compound as a controlled input under batch or continuous conditions, with process adjustments for product isolation suited to strict odor and purity thresholds in regulated markets. Manufacturers maintain traceability to fulfill both customer audits and compliance checks.

    Industry compliance standards

    • IFRA Code of Practice for manufacturing aromatic intermediates
    • ISO 9001:2015 (QA systems for flavor and fragrance plants)
    • GMP for food and cosmetic ingredients (where applicable)
    • EU Food Additive Regulation (EC) No 1333/2008—indirect application as intermediate

    Typical usage ratio

    • Added at 0.3–1.0 equivalents to target aromatic core, typically scaled based on downstream aldehyde or ketone reactivity.

    Downstream process integration

    • Feeds into Friedel-Crafts acylation or consecutive oxidation steps; batch purification retains volatile aromatic characteristics.

    Final product types

    • Intermediate aromatic aldehydes for perfumery
    • Flavor precursor molecules for food and beverage applications
    • Cosmetic-grade fragrance intermediates
    • Stable halogenated notes for speciality scent profiles
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    More Introduction

    4,4'-Dichlorobutyrophenone: Practical Insights from Experience

    Introduction to 4,4'-Dichlorobutyrophenone

    In the chemical manufacturing business, reliable specialty products drive real progress for industrial innovation. Among the key intermediates, 4,4'-Dichlorobutyrophenone stands out based on its solid track record in synthesis and its role as a raw material for advanced products, including active pharmaceutical compounds and agrochemical agents. Our experience with its production and application highlights practical points that often get overlooked in standard catalog descriptions but matter every day on the line.

    Model, Purity, and Physical Characteristics

    We produce 4,4'-Dichlorobutyrophenone under tight controls to achieve high consistency in purity and particle size. Its molecular structure—two phenyl rings linked by a four-carbon chain bearing two chlorine atoms and a carbonyl group—brings extra stability and versatile reactivity. The product leaves our facility as a crystalline white solid, checked batch by batch for melting range, color, and trace residuals.

    Our typical grade, with purity levels above 99%, is designed to meet the demands of fine chemical synthesis. Every customer expects results to match paperwork—any deviation in material quality shows up later on through yield losses or unpredictability in downstream reactions. That’s why specification is more than just a number for us. We invest in multiple filtration steps and temperature control throughout both chlorination and condensation to weed out side products such as unreacted starting materials, over-chlorinated fragments, and byproducts from incomplete reactions.

    What Sets 4,4'-Dichlorobutyrophenone Apart?

    The structure of 4,4'-Dichlorobutyrophenone offers two core advantages. The first is its selectivity as an electrophilic agent in carbon-carbon coupling reactions needed to build complex molecular scaffolds. It reacts smoothly in Friedel-Crafts acylations and related steps that can be difficult with simpler or mono-chloro analogs. Users working with 4-chlorobutyrophenone or other lower-chlorinated forms often run into inconsistent yields, unwanted color formation, or the need for excess reagents to force the reaction. With the 4,4'-di-chloro version, those worries get minimized—the extra chlorine atoms lend a balance between reactivity and control during transformation.

    Second, 4,4'-Dichlorobutyrophenone gives an edge in resistance to oxidation and hydrolysis under typical processing conditions. Product losses due to instability represent a real cost to production—shelf life matters as much as purity. In our experience, both warehouse managers and technical staff benefit from the extended storage window and relative inertness during transportation.

    Real-World Application and Feedback

    This compound sees heavy use as a core building block for active pharmaceutical ingredients, herbicides, and selective pesticides. Over the years, both scale-up and pilot batch processes pointed out that 4,4'-Dichlorobutyrophenone handles stepwise synthesis with fewer protection or deprotection steps. That detail saves on time, labor, and the amount of solvents discarded in waste streams. Some of the most productive collaborations with formulation experts evolved after switching from less consistent intermediates—problems with off-odors, yellowing, or batch-to-batch variation in reactivity faded with the shift.

    Feedback from partner manufacturers in Europe and Asia put a spotlight on its role during critical steps such as ring closure, substitution, or chain elongation in complex molecule assembly. Chemists often report improved conversion rates and lesser need for labor-intensive purification. Following upstream with a cleaner intermediate brings down risks in later purification, which matters in a regulated industry where one off-spec shipment can disrupt months of planning.

    Technical Handling and Environmental Notes

    Based on long production runs, we’ve found that certain habits in storing and transferring the compound keep it at peak condition longer. The solid form, stable at room temperature, avoids caking or degradation if kept sealed from atmospheric moisture and strong light. Using high-density, double-bagged containers made a real difference both in packaging longevity and in speeding up material handling during intake at customer plants. We learned a lesson after trialing lesser packaging—the frequency of complaints about lumping or minor contamination dropped once we made the switch.

    Environmental standards for halogenated intermediates continue to rise. 4,4'-Dichlorobutyrophenone falls under scrutiny because of its dual chlorine atoms. We fully treat all waste liquors and byproduct streams to recover or neutralize organochlorine content before discharge, strictly adhering to local and international chemical safety codes. Investment in newer distillation and scrubbing units was not just about compliance—it directly raised process yields and cut down annual chemical losses by several percent. No shortcut replaces cross-system investment and regular audits, which, over many years, taught us the true cost of waste is more than disposal fees—inefficient use of raw materials drains potential from the whole plant.

    Working with the Product in the Lab and at Scale

    On the lab bench, 4,4'-Dichlorobutyrophenone streams as a reliable substrate in multi-step organic synthesis. Its predictable melting point and robust behavior under mild alkali or acidic conditions let chemists control reaction parameters closely. We’ve seen considerable success in scale-up projects where customer specifications demanded tight control of residual solvents and color index—our filtration process and in-line spectroscopic monitoring offered measurable improvements in those metrics.

    For process engineers, handling this compound means less downtime. The consistent crystal morphology helps charge reactors efficiently, avoiding clumping or static build-up, especially during pneumatic or screw-fed transfer. Production lines appreciate reliability—if each batch pours, dissolves, and reacts as expected, there’s less cleanup, less frustration, and fewer process interruptions.

    Where others face repeated start-stop cycles because of fluctuating intermediate quality, steady material flow allows the synthesis train to operate at a predictable pace. Sometimes small details like the right choice in drying or micronization equipment spell the difference between headache and smooth output.

    Comparisons with Other Intermediates

    Experience has shown clear differences between 4,4'-Dichlorobutyrophenone and its close relatives, such as mono-chlorinated butyrophenones or p-chloro analogs. The double substitution on the phenyl rings affects both the ease of reaction and the final purity of products. With single chlorine intermediates, unwanted byproducts can build up especially under variable temperature or extended reaction times, forcing chemists to intervene with extra cleanup steps.

    In multi-step pharmaceutical synthesis, cleaner conversion of 4,4'-Dichlorobutyrophenone in ketone condensation or reduction steps translates into higher final yields and less risk of regulatory rejection due to impurities. Technical operators see the payoff not just in numbers but in day-to-day routine—a more forgiving intermediate keeps campaigns moving, reducing hormone-wrecking surprises during QA and QC.

    For agrochemical formulators, switching from older materials to 4,4'-Dichlorobutyrophenone brought smoother downstream compatibility with solvents, less fouling in reaction vessels, and clearer extraction of targeted active compounds. The time saved on back-end purification added up quickly. Some early skepticism from process veterans faded with repeated positive outcomes in both small-batch and bulk trials.

    Why Consistency Pays Off

    Over decades, it has become clear that consistency always trumps theoretical maximums offered by fancy catalogues. The real rewards show up in reduced error rates, less spoiled inventory, and trust earned from partners repeating year-on-year orders. Our commitment to full lot tracking, in-house testing, and on-record transparency about process changes grew from customer demands, but it pays us back through tighter process control and faster incident resolution when something rare goes off plan.

    There are still plenty of tempting shortcuts in chemical production—lower energy input, older plant hardware, less careful operator training—but these all end up reflected somewhere in material quality and handling ease. Skipping steps with intermediates like 4,4'-Dichlorobutyrophenone guarantees headaches later, whether for us or for the customer downstream.

    Our focus on robust process design—multiple crystallizations, particle conditioning, on-line analytics—came after hard lessons. We poured years into understanding how even small changes to solvent quality or condensation timing ripple through to the final product. Our technical staff routinely reviews run logs and batch data not just for the record, but to isolate common error patterns and correct root causes. We advise customers to treat their own in-house purification and reaction protocols as living processes—constantly subject to refinement, and better tuned with feedback from experience rather than chasing a theoretical ideal.

    Responding to Challenges

    Scaling up production or switching suppliers always brings unpredictable variables. Before a switch, customers often ask us to run pilot-scale samples using their own solvent/reagent combinations. Our lines stay flexible for such trials—we’ve run dozens of these collaborative experiments and routinely share both successes and obstacles. Working side by side with the customer’s technical team during trials often saves weeks of troubleshooting that might arise later.

    Raw material availability, energy price fluctuations, and regulatory shifts remain the largest outside challenges. We address market uncertainty by long-term partnerships with chlorinating agent suppliers, maintaining stockpiles on site, and updating customers on lead times ahead of firm orders. We apply real-time process monitoring to spot early drifts in conversion efficiency, which enables us to minimize the risk of out-of-spec shipments.

    The ground-floor solution to many headaches in specialty chemicals is keeping all parties informed and setting realistic delivery timelines. Overpromising on turnaround or cutoff purity invites problems—delays ripple downstream, and the impact on brand reputation can last far longer than a single contract.

    Future Directions and Continuous Improvement

    Innovation in specialty chemical manufacturing keeps pressure on intermediates producers to improve performance and sustainability. We track emerging routes for making 4,4'-Dichlorobutyrophenone with greener solvents or more selective catalysis. Our R&D group reviews new process literature and benchmarks them via internal pilot runs. Incremental gains—like shaving a few degrees off the required reaction temperature or lowering waste solvent production—may appear small, but in high-volume runs, they spell big gains in resource use and carbon footprint.

    We field regular feedback from pharmaceutical and agrochemical producers pushing for more transparent lifecycle accounting. Clear chain of custody, documented recycling of byproducts, and transparent material sourcing all tie into the future acceptability of all specialty intermediates. Taking these issues seriously has already brought long-term confidence from clients looking to align with sustainable supply guidelines.

    Listening to End-Users: Practical Solutions

    Customers who work with 4,4'-Dichlorobutyrophenone tend to share direct feedback—from blending issues in large glass-lined vessels to isolated color shifts following a new batch. We keep communication lines open for troubleshooting, whether it relates to material compatibility, formulation questions, or longer-term shelf life challenges. A small change in process upstream may only show up as a subtle shift in downstream appearance or performance, but for the right customer, even a minor color tinge or textural difference can spell the need for a workaround. We collect these details, share them back with our process and quality teams, and adjust production logic to lock in best practices.

    Training for both our operations staff and customer QA teams forms another part of our approach. We have seen that hands-on workshops—walking through crystallization, transfer handling, or analytical checks—build user confidence and reduce variability in material use. These face-to-face exchanges help eliminate blame games and turn error incidents into process improvement opportunities rather than disputes.

    Building Better Supply Chains

    Strong supplier-customer relationships keep specialty chemical supply chains resilient. Our team shares regular product bulletins detailing any upcoming process adjustments, raw material shifts, or potential sourcing issues. Monthly quality reports give customers the transparency they need for their own regulatory filings. We keep an open-door policy for on-site audits and sample runs, believing that long-term business always wins from shared learning rather than secrecy.

    The unpredictability of global logistics—border slowdowns, freight disruptions, or force majeure events—pushes us to maintain both buffer stock and alternative transport partners. We partner directly with end-user buyers to agree on contingency plans for urgent deliveries or unexpected spikes in demand. Our own warehouse and distribution planning systems now factor in volatility in both raw material inputs and customer drawdown patterns.

    Summing Up Practical Experience

    After decades of practice, one lesson rings true—chemistry is only as reliable as its building blocks. 4,4'-Dichlorobutyrophenone earns its reputation by delivering both stability and high performance in the hands of capable formulation and synthesis experts. While standard specifications cover the basics, it’s the day-to-day habits—careful analytical checks, transparency about sourcing, and a commitment to regular process improvement—that keep both us and our customers ahead of surprises down the line.

    Where production values consistency, clear communication, and measured investment in process reliability, users of 4,4'-Dichlorobutyrophenone see repeatable success. Those who treat their intermediates as mere commodities often pay the price down the line with lost time, inconsistent output, and avoidable troubleshooting. Our aim remains to keep improving based on both feedback and proven results, carrying the quiet lessons of hundreds of production runs into every new batch and every new customer partnership.