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4-Chlorobutanal Dimethyl Acetal

    • Product Name 4-Chlorobutanal Dimethyl Acetal
    • Alias 1,1-Dimethoxy-4-chlorobutane
    • Einecs 'EINECS 224-365-5'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    920180

    Product Name 4-Chlorobutanal Dimethyl Acetal
    Synonyms 1-Chloro-4,4-dimethoxybutane
    Cas Number 7252-83-7
    Molecular Formula C6H13ClO2
    Molecular Weight 152.62
    Appearance Colorless to pale yellow liquid
    Boiling Point 159-161°C
    Density 1.054 g/cm3
    Refractive Index 1.418-1.420
    Purity Typically ≥ 98%
    Solubility Insoluble in water
    Storage Temperature 2-8°C
    Smiles COC(CCCl)COC
    Inchi InChI=1S/C6H13ClO2/c1-8-6(9-2)4-3-5-7/h6H,3-5H2,1-2H3

    As an accredited 4-Chlorobutanal Dimethyl Acetal 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 mL capacity, tightly sealed with a PTFE-lined cap, labeled with hazard warnings and chemical information.
    Shipping **Shipping Description:** 4-Chlorobutanal Dimethyl Acetal is shipped in tightly sealed, chemical-resistant containers under standard ambient conditions. It is classified as a hazardous material, requiring proper labeling, secure packaging, and adherence to all relevant regulations during transport. Avoid exposure to heat, sparks, or open flames. Handle and store away from incompatible substances.
    Storage 4-Chlorobutanal Dimethyl Acetal should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, sparks, or open flames. Protect from moisture and strong oxidizing agents. Store at room temperature and avoid exposure to light. Ensure appropriate chemical labeling and keep away from incompatible materials to prevent hazardous reactions.
    Application of 4-Chlorobutanal Dimethyl Acetal

    Applications of 4-Chlorobutanal Dimethyl Acetal in Industrial Manufacturing

    4-Chlorobutanal Dimethyl Acetal serves as a specialized intermediate in several complex synthesis routes for fine and performance chemicals. As an original manufacturer, we support established downstream processes in designated sectors requiring precise compliance and predictable reactivity. Industrial users rely on our material for its controlled impurity profile, batch consistency, and documented regulatory conformity throughout consecutive processing stages.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize this intermediate in multi-step syntheses leading toward APIs, especially certain statins and antivirals. Its reactive moiety facilitates heterocycle formation or acts as a masked aldehyde unit under controlled deprotection. The material must meet regulatory guidance on impurity limits and be traceable through all GMP records. Custom usage ratios depend on the targeted molar route and required conversion yields. Downstream processing introduces the intermediate post-activation in a controlled reaction vessel, supporting alkylation or cyclization stages under validated SOPs. Final products include advanced pharmaceutical intermediates and finished APIs with full batch documentation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP)
    • USP and EP impurity thresholds for starting materials
    • EMA Guideline on Starting Materials and Intermediates

    Typical usage ratio

    • 0.85–1.10 equivalents relative to target synthon; precise ratio established per validated route after pilot studies

    Downstream process integration

    • Charged alongside base and solvent after dissolution step; used under inert conditions in closed reactors during stepwise condensation, derivatization, or deprotection

    Final product types

    • Statin pharmaceutical intermediates
    • Antiviral compound precursors
    • Custom API building blocks
    • Regulatory-submitted GMP intermediates

    2. Agrochemical Synthesis

    Agrochemical producers employ this raw material as a key building block in the synthesis of select herbicide and insecticide actives. The acetal's protected form enables safe manipulation during alkylation or halogenation, later unmasking to introduce functional groups crucial for biological activity. Application parameters hinge on the desired crop protection molecule, as stoichiometry and purity directly influence downstream reactivity. Compliance focuses on agrochem-specific guidelines for traceability and allowable impurity profiles, ensuring the final active fits regional regulatory frameworks. The raw material integrates as a staged reactant before or after core scaffold assembly. End products reach the market as high-purity crop protection actives for direct formulation into commercial agrochemical blends.

    Industry compliance standards

    • FAO/WHO Specifications for pesticide active ingredients
    • ISO 9001:2015 for quality management in agrochemical supply
    • REACH (EC No 1907/2006)
    • GLP (Good Laboratory Practice) for registration batches

    Typical usage ratio

    • 1.0–1.3 molar equivalents per target molecule backbone; variable per synthesis step, controlled by titration and analytical QC

    Downstream process integration

    • Added after initial ring formation phase or used for side-chain functionalization; processed under strict batch record and emission control setup

    Final product types

    • Precursor to herbicide actives (e.g., butyric acid derivatives)
    • Intermediates for insecticidal compounds
    • Registered technical-grade crop protection ingredients

    3. Fine Chemical & Flavors Manufacturing

    In the flavor and specialty chemical sector, this material functions as a controlled aldehyde source for synthesizing complex aroma molecules and performance additives. The acetal group allows flavor chemists to manipulate the reactive function under acidic hydrolysis with minimal by-product formation, safeguarding product purity for food additive protocols. End-use ratios depend on target aroma compound yield and downstream blending formulations. Processing typically involves catalytic acid-catalyzed hydrolysis or related transformation under food-grade controls. Resulting fine chemicals serve as finished artificial flavors, olfactory ingredients, or specialty additives subject to international compositional standards.

    Industry compliance standards

    • FCC (Food Chemicals Codex) ingredient standards
    • EU Flavouring Regulation (EC) No 1334/2008
    • IFS Food & BRC Global Standard for flavor ingredients
    • HACCP for critical control in food chain intermediates

    Typical usage ratio

    • 0.5–1.2 equivalents relative to desired aroma target; adjusted for reactivity and downstream purification efficiency

    Downstream process integration

    • Fed into hydrolysis or condensation batch with continuous monitoring; separated by vacuum distillation or chromatographic methods under food-grade protocol

    Final product types

    • Artificial flavoring components
    • Food-grade aldehyde derivatives
    • Fine aroma intermediates for complex fragrance blends

    4. Polymer Additive Synthesis

    Manufacturers of specialty polymers utilize this intermediate to introduce reactive aldehyde functionalities into chain-extender blends or crosslinking agents used in resins and adhesives. Its stable acetal form supports transport and bulk storage, only releasing the active aldehyde during controlled thermal or acidic deprotection in the additive reactor. Dosing ratios respond to molecular weight design and reactivity targets of the finished additive. The intermediate enters the process within closed-system reactors, coordinating with resin feedstock prior to polymerization or as a post-polymerization crosslinker. End products include crosslinking additives for industrial adhesives and tailored resin modifiers enabling advanced performance in end-use applications.

    Industry compliance standards

    • ISO 9001:2015 for polymer additive supply
    • REACH pre-registration and notification for polymer intermediates
    • ASTM D4762 Polymeric Additives Quality Specification
    • OSHA process safety management for polymer operations

    Typical usage ratio

    • 0.2–1.0 wt% of total batch feed in additives formulation; finalized after small-scale performance validation

    Downstream process integration

    • Injected to resin kettle or blending vessel before main polymerization stage, or post-polymerization as reactive blending agent; separated during vacuum stripping if necessary

    Final product types

    • Crosslinking agents for polyurethane and acrylic adhesives
    • Chain extenders for hybrid resins
    • Performance-modifying additives for industrial hot-melt adhesives
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    Certification & Compliance
    More Introduction

    Experience in Supplying 4-Chlorobutanal Dimethyl Acetal - A Manufacturer's Perspective

    Understanding the Backbone of 4-Chlorobutanal Dimethyl Acetal

    Manufacturing 4-Chlorobutanal Dimethyl Acetal, chemical formula C6H13ClO2, brings with it a set of precise challenges, responsibilities, and a satisfaction unique to those who work directly with its synthesis. Unlike traders or intermediaries, we handle the complete chemical lifecycle: from sourcing raw chlorinated butyric acid derivatives, to managing the acetalization process, and finally reaching a product our team can vouch for, batch after batch. Direct manufacturing means that every drum and canister filled has passed through our own distillation lines and hands-on quality checks—not just a paperwork review.

    Why 4-Chlorobutanal Dimethyl Acetal Matters in Industrial Synthesis

    Experience shows that 4-Chlorobutanal Dimethyl Acetal stands out as a key intermediate—not only on paper but in day-to-day plant operations where reliable building blocks drive entire synthetic routes. This acetal’s unique structure, with a four-carbon chain and an acetal functional group capped by a chlorine atom, gives it a versatile reactivity profile. Downstream users count on its stability during storage and handling, yet its ability to unlock butanal and gamma-chlorobutyric acid functionality with mild acidic hydrolysis supports a diverse set of chemistries. Demand comes from the pharmaceutical, agrochemical, and specialized organic manufacturing sectors, all looking for the same thing: reproducibility batch after batch, and a clean, well-documented impurity profile.

    We often receive feedback from formulation chemists highlighting the difference in outcome from acetals produced on larger, uncontrolled lots versus those prepared with attention to distillation cut points and stabilization. Chlorinated intermediates can develop side-products if process conditions drift. Tolerances matter, and downstream synthetic yield magnifies any inconsistencies, with even minor isomer contamination causing headaches in column separations or downstream catalysis. Rework is not just a cost issue—it’s an operational setback.

    Specifications and In-Plant Testing

    Our manufacturing standard for 4-Chlorobutanal Dimethyl Acetal aims for more than just exceeding the baseline 98% purity requested in generic documentation. Each lot receives a full gas chromatography scan, FT-IR tracking for acetal group integrity, and targeted chloride quantification for both free and bound chlorine. Density and refractive index checks round out the testing suite, confirming no unreacted alcohol or aldehyde remains.

    Batch consistency stems from repeatable, closely monitored reaction conditions: we hydrolyze and distill under inert gas to minimize peroxide formation, then cool the recovered product under dry nitrogen to keep oxides at bay. To those outside the plant, these steps rarely show up on the paperwork, but a seasoned production operator knows oxygen exposure can spark slow decomposition or introduce subtle coloring that affects user confidence.

    A keen eye on packaging then plays a role. Tightly closed steel or HDPE drums receive product that’s cooled and stabilized; trace water presence, so often ignored by brokers and CMO’s, sets up the risk of slow hydrolysis during transit. For our direct clients who schedule annual multi-ton block shipments or urgent just-in-time deliveries, shipment quality means trust—the same material in the first kilogram as the last.

    Practical Differences from Similar Acetal Intermediates

    In the world of chloroacetal intermediates, careful choice means everything for process designers. Take 3-chlorobutanal dimethyl acetal as a comparator: its different chlorine placement shifts reactivity, sometimes making it more prone to off-pathway cyclizations or producing regioisomeric impurities that prove tough to separate in pharmaceutical-grade work. We learned early that routine procurement mistakes—selecting 3-chloro instead of 4-chloroacetal—lead to expensive troubleshooting on customer synthesis lines.

    Other acetals, such as butyraldehyde dimethyl acetal, offer a simpler structure but no functionalized handle for further elaboration; without the chloro group, downstream substitution or cyclization reactions require an extra synthetic step. Customers leveraging the 4-chloro variant appreciate an easier nucleophilic substitution route, allowing them not just one pathway, but a toolkit for introducing specialty motifs or side chains.

    We have fine-tuned the removal of trace methyl chloride or formaldehyde, potential byproducts of acetalization, which if left unchecked, can poison catalysts or attack sensitive substrates in later steps. Competitors who overlook these subtle residues risk customer dissatisfaction and technical complaints—topics that inevitably filter back to the manufacturing floor, not the sales office.

    The Role of 4-Chlorobutanal Dimethyl Acetal in End-Use Environments

    The main users of this acetal include medicinal synthesis labs, agrochemical scale-up operators, and fine chemical custom manufacturers. In pharmaceuticals, it frequently anchors the synthesis of beta-lactam intermediates, N-heterocycles, or specialty aldehyde derivatives where selectivity and clean deprotection matter. Feedback from our customers underlines one important reality: unpredictable hydrolysis rates or unidentified secondary peaks in NMR raise flags during new process validation trials. Since regulatory filings depend on impurity profiles and full reproducibility, a consistent reagent supply makes validation smoother.

    Agrochemical producers, focused on active molecule yield for cost control, emphasize a different pain point—material lost to side reactions. Inferior batches accelerate byproduct formation under acidic workup, sapping process efficiency and requiring more absorber capacity or increased washing. For us, it becomes a point of pride when returning users report back on higher molar conversion rates or fewer filtration headaches.

    Long-term users cite the workability of our material during in-plant processing, such as its easy phase separation thanks to a well-maintained water content and a lack of haze. This isn’t just QA jargon: sluggish separation means downtime, and downtime drains project timelines.

    Typical Handling Lessons – Manufacturer’s Advice

    Anyone working with chlorinated acetals soon learns the value of sound storage: cool, dry, and away from acidic vapors. The product’s acetal linkage, robust to mild conditions, breaks down in acidic environments—liberating both formaldehyde and butanal. During a warehouse audit a few years back, a minor drum leak created headaches, and reinforced a zero-tolerance approach to container maintenance and short-term throughput.

    Small-scale customers in research sometimes underestimate the volatility and odor. Spilled droplets on benchtops linger, and the odor draws attention, necessitating strong ventilation even during bench synthesis. In plant settings, we have optimized our loading stations with scrubber units, ensuring that even larger transfer operations match environmental and workplace comfort expectations.

    From a waste stream point of view, spent acetal wash waters require careful neutralization; direct discharge can’t happen without risking halogenated byproducts in effluent. We developed a neutralization sequence involving alkaline hydrolysis followed by activated carbon polish—routine methods that originated in real troubleshooting, not just compliance documentation.

    Realities of Quality Assurance – What Full Traceability Looks Like

    We document each batch from raw materials to final product, using serialized drum tracking and inspection logs. The real benefit of full traceability comes when a question arises years down the line during a regulatory review or a customer’s process change. Rather than scrambling to locate whether a batch originated from recycled solvent lots or had subtle impurity peaks, we can produce documentation detailing every lot ingredient, storage period, and production timestamp.

    When third-party inspectors question our processes, showing a direct fingerprint of every lot and the associated results from IR, GC, and water content gives all parties peace of mind. This reality often gets lost in larger-scale, distributed models where wholesalers lose sight of origins. Customers draw comfort from knowing they can reach out to the plant floor and get direct answers.

    Process Improvements – Balancing Efficiency and Safety

    Manufacturing improvements don’t just drive cost; they help shore up safety and environmental performance. Over several years, we invested in closed-loop reactor systems for our acetalization step, reducing operator exposure and vapor emissions. Filtering through multiple passes with new catalyst scavenging lines cut down trace metal residues in the finished product—a common issue in older processes using high surface area acid catalysts without post-polishing.

    Consistency means verifying not just the main product purity, but residual byproduct profiles. Early troubleshooting found a heat-sensitive epoxide forming under excess acid during distillation; tuning those process parameters improved both final product appearance and downstream reactivity for our clients.

    Solvent recycling became another core team focus, both for environmental compliance and cost recovery. Rather than discharging spent methanol or toluene directly, we pull spent solvent through a multi-stage filtration and redistillation—ensuring no cross-contamination and reducing the risk of chlorinated waste streams.

    Customer Collaboration and Technical Support

    Our value doesn’t stop with drums on the loading dock. Direct manufacturer and end-user relationships foster technical troubleshooting: if a user encounters haze during recrystallization or off-color distillate in process scale-up, we work through the problem together. Questions about storing at sub-zero temperatures, anticipating viscosity changes, or managing accidental hydrolysis reach our technical team, who’ve faced these realities firsthand.

    New formulation trials sometimes reveal the need for further purity or tighter residual solvent specification. Unlike a typical distributor, we can run bench-scale tests, feedback process adjustments, and scale up solutions into the next manufacturing run. A number of industrial partners cite the benefit of rapid response to custom specifications—such as limiting methyl chloride down to low ppm, or broadening drum size offers for their continuous feed systems.

    Our in-house R&D feeds right back to manufacturing planning. Feedback loops with QC teams shorten development cycles and sharpen quality targets. In the past, customer requests for higher purity lots led us to re-examine the entire acetalization route and invest in finer-tuned column packings and analytical standards.

    Looking Ahead – Reliability in a Competitive Market

    The chemical sector shifts rapidly as supply chains realign, bring new specialty applications, and raise environmental expectations. Our ongoing investment in greener processes—a switch to lower-impact catalysts, solvent capture, and minimizing waste—goes hand in hand with a focus on the reproducibility of each batch we send to long-standing and new users. Origin matters; the benefit shows in end-user results. Institutions counting on well-characterized and robust building blocks avoid costly development errors and accelerate their own R&D.

    Every experience making 4-Chlorobutanal Dimethyl Acetal reminds us that robust chemistry and direct engagement with real-world technical requirements remain our best tools for building confidence and partnership. Whether refining reaction parameters, improving logistics for bulk buyers, or troubleshooting at the plant level, the challenges rarely repeat themselves in the same way—and that drives our commitment to both quality and responsive support.

    Conclusion – Trust Earned in Every Batch

    Unlike those who trade on fluctuating prices or distant lab analyses, the manufacturing process for 4-Chlorobutanal Dimethyl Acetal demands an unwavering focus on the details that matter to direct users—batch homogeneity, storage security, and support that goes far beyond the datasheet. The lessons drawn from years handling production, testing, and feedback have forged a commitment to providing a product that helps our partners drive forward their own innovation. That’s the mark of a real manufacturer in specialty chemicals: responsibility from raw materials to delivery, with trust earned one batch at a time.