Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Chlorobutanal Diethyl Acetal

    • Product Name 4-Chlorobutanal Diethyl Acetal
    • Alias 1,1-Diethoxy-4-chlorobutane
    • Einecs 412-290-4
    • 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

    884903

    Productname 4-Chlorobutanal Diethyl Acetal
    Casnumber 6748-73-6
    Molecularformula C8H17ClO2
    Molecularweight 180.67 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 82-84°C (20 mmHg)
    Density 0.984 g/mL at 25°C
    Refractiveindex 1.419-1.423
    Purity Typically ≥98%
    Flashpoint 72°C

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

    Packing & Storage
    Packing 250 mL clear glass bottle, securely sealed, with hazard labeling, product name “4-Chlorobutanal Diethyl Acetal”, and manufacturer details.
    Shipping 4-Chlorobutanal Diethyl Acetal is typically shipped in tightly sealed containers to prevent leakage and evaporation. It is transported as a liquid under ambient conditions, protected from heat and incompatible substances. Proper labeling and documentation are required, and shipments comply with relevant chemical safety and hazardous materials transportation regulations.
    Storage 4-Chlorobutanal Diethyl Acetal should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, ignition sources, and incompatible substances such as strong oxidizing agents. Keep it protected from moisture and direct sunlight. Ensure the storage area has appropriate spill containment and is clearly labeled. Handle under an inert atmosphere if sensitive to air or moisture.
    Application of 4-Chlorobutanal Diethyl Acetal

    Applications of 4-Chlorobutanal Diethyl Acetal in Industrial Manufacturing

    4-Chlorobutanal Diethyl Acetal serves as a critical intermediate in several industrial manufacturing fields. Our direct production supports high-precision requirements for specialty synthesis, with a focus on reaction control, regulatory documentation, and end-to-end supply integrity. Below, we outline several industrially established application sectors and their specific processing considerations.

    1. Pharmaceutical Intermediate for API Synthesis

    Our material stands among preferred building blocks for synthesizing complex API precursors, notably in the large-scale manufacture of active agents for neurology and antiviral drug families. It enables safe introduction of protected aldehyde groupings under GMP process controls, minimizing side-product formation. Strict batch validation ensures traceability and meets large pharma audit trails from milligram scale up to commercial tonnage. The acetalization strategy using this compound is frequently adopted to protect chemical moieties during multi-step synthesis, preventing undesired reactivity during downstream derivatization.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP guidelines
    • 21 CFR Part 211 (US FDA GMP for finished pharmaceuticals)
    • USP/NF identity and purity thresholds for relevant APIs

    Typical usage ratio

    • Batchwise: 0.3–1.2 molar equivalents relative to core starting material, adjusted to reaction stoichiometry for protection steps
    • Process-scale: Generally 5–10% w/w of total formulation matrix during initial synthesis; final yield-driven adjustments made per process validation runs

    Downstream process integration

    • Introduced in the acetalization step: Serves as a masked aldehyde donor to protect aldehyde groups during sequential API assembly
    • Removed via acidic hydrolysis after functionalization, releasing the free aldehyde for final stage reactions
    • Used consistently in enclosed reactor modules designed per GMP solvent handling protocols

    Final product types

    • Antiviral and neuro-active pharmaceutical ingredients (e.g., intermediates in antiepileptic or anti-infective APIs)
    • Specialty amine drugs requiring controlled aldehyde group manipulation
    • Precursor blocks for advanced peptide and heterocyclic API frameworks

    2. Agrochemical Synthesis Intermediate

    Major crop protection manufacturers use this intermediate for selective synthesis steps in advanced pesticide and herbicide actives, especially where protected butanal structures are essential in preventing premature oxidation. Consistency in acetal purity enables manufacturers to optimize process yield and minimize problematic byproducts, directly aligning with trace residue tolerances regulated for agricultural actives exported to major markets. Batch documents support regulatory dossiers for multi-jurisdiction pesticide registration.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 for chemical manufacturing traceability
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • US EPA 40 CFR Part 158 (Pesticide Data Requirements)

    Typical usage ratio

    • Process-dependent: 0.4–1.5 molar equivalents relative to aromatics or heterocycles in target synthesis
    • Used in 3–7% by weight in multi-kilogram synthesis campaigns to ensure complete conversion in protected steps

    Downstream process integration

    • Used in Grignard and Suzuki cross-coupling precursor formation where side-chain protection is needed
    • Deprotected post-functionalization, releasing reactive aldehyde for final product assembly
    • Synthesis occurs in closed vessels, with full in-process QC monitoring for purity and residual solvents

    Final product types

    • Pyridine-based herbicides
    • Quaternary ammonium insecticides
    • Fungicide active ingredient intermediates
    • Plant growth regulant compounds

    3. Fragrance Composition and Aroma Chemical Production

    Key aroma chemical manufacturers employ the acetal to access unique aldehyde and chlorinated notes not possible using standard aliphatic feedstocks. The protected form affords oxidation resistance through high-temperature blending operations, allowing for late-stage deprotection to yield targeted aldehyde fragrances. Our production traceability ensures compliance with IFRA standards on residual solvents and cross-contaminants during olfactory compound synthesis, critical for global fragrance deployment.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards for ingredient sourcing and residual levels
    • ISO 9001:2015 traceability for ingredient batches
    • REACH (EC) No 1907/2006 registration (for use in European fragrance blends)
    • US FDA 21 CFR Part 172 (Synthetic flavoring substances)

    Typical usage ratio

    • 0.5–2.5% in concentrated aroma formulation bases
    • Small-batch high-value production: 0.1–1.5 molar equivalents depending on aldehyde intensity control

    Downstream process integration

    • Incorporated at the protected intermediate stage during complex note development
    • Deprotected in situ during the formulation of headspace aldehydes in perfumery bases
    • Supports solvent-controlled syntheses of fine aroma chemicals under regulated conditions

    Final product types

    • Chlorinated aldehyde perfume ingredients
    • Luxury fragrance aldehyde blends
    • Flavor preparations for citrus and green note enhancement
    • High-purity aroma isolates for fine perfumery

    4. Specialty Monomer Synthesis for Polymer Modification

    Advanced plastic and elastomer developers incorporate this acetal as a chain-modifying agent when synthesizing specialty monomers, especially to introduce functional aldehyde groups after polymer backbone assembly. The protected form shields sensitive aldehydes from side reactions during high-temperature or acidic process steps, giving greater control over polymer final properties. Process logs track feedstock blending, acetal removal, and endpoint characterization to guarantee consistent monomer quality for high-tech plastics and film development.

    Industry compliance standards

    • ISO 9001:2015 manufacturing traceability
    • EU Regulation (EC) No 1907/2006 (REACH) for monomer registration in polymer markets
    • ISO 14001 environmental controls for chemical processing
    • GMP guidelines where plastics are intended for food contact (EU 10/2011 on plastic materials)

    Typical usage ratio

    • 2–8% by weight in monomer synthesis batches to target aldehyde content in final polymer
    • Exact proportions set by desired functional group loading and polymer chain length requirements

    Downstream process integration

    • Integrated into monomer feedstage to protect aldehyde groups during polymerization
    • Acetal group cleaved via mild hydrolysis to unveil reactive sites for further modification
    • Polymer QC protocols validate completeness of deprotection and chain uniformity

    Final product types

    • Reactive co-polymers and elastomers for adhesives and sealants
    • Functionalized plastic films for specialty packaging
    • Crosslinked resins for advanced composites
    • Intermediates for medical-grade thermoplastics (where compliant)

    5. Fine Chemical Synthesis Platform

    Chemical process developers utilize 4-Chlorobutanal Diethyl Acetal as a selectivity agent for advanced organic synthesis, from small molecule custom manufacturing to scale-up of unique intermediates. Its defined reactivity under controlled acetalization and deprotection conditions enables reproducible yield management, minimizing batch variability. Through this platform, chemical companies develop advanced ligands, specialty reagents, and test standards for analytical chemistry—each requiring batch traceability and conformance to international chemical control norms.

    Industry compliance standards

    • ISO 9001:2015 for process documentation and QC
    • REACH (EC) No 1907/2006 chemical registration
    • Responsible Care® chemical management practices
    • Custom quality agreements for contract manufacturing

    Typical usage ratio

    • 1–3 molar equivalents relative to labile intermediates
    • 5–15% by weight on reaction scale for advanced syntheses
    • Lower charges for high-value specialty batches (micro or gram-scale development)

    Downstream process integration

    • Used at the protection stage in complex synthetic pathways for specialty fine chemicals
    • Allows clean aldehyde release for late-stage coupling and derivatization
    • Full in-process analysis for acetal content, residual solvents, and process contaminants

    Final product types

    • Specialty ligands for catalysis
    • Synthesis intermediates for dye and pigment precursors
    • Custom analytical reagent standards
    • Research-scale specialty molecules
    Free Quote

    Competitive 4-Chlorobutanal Diethyl Acetal prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    4-Chlorobutanal Diethyl Acetal: Experience Matters in Reliable Synthesis

    Our Direct Expertise with 4-Chlorobutanal Diethyl Acetal

    Years of hands-on synthesis and scale-up in our own facilities have shown us what works and what doesn’t when it comes to niche intermediates. 4-Chlorobutanal diethyl acetal is not a commodity anyone stumbles across at a general trading house. In our plant, we focus on specialties like this because chemistry only rewards careful, thoughtful process control and a clear understanding of end use. This compound, also identified by CAS 7252-83-7, has steadily worked its way into the fine chemicals toolbox primarily because its dual functionalities open the door to selective transformations other four-carbon building blocks can’t handle.

    We continually refine our routes for preparing 4-chlorobutanal diethyl acetal. Typically, our process follows a reliable chlorination step on a protected butanal precursor, managed under inert atmosphere to preserve purity. This robust route minimizes byproducts and consistently delivers material that meets the strictest content and appearance checks. Product comes as a colorless or slightly yellowish transparent liquid. Most batches test at greater than 98% purity by gas chromatography right off the final distillation. From years of batch records, we know that keeping water content low—always under 0.2%—prolongs shelf stability and supports high reactivity in downstream use. For sensitive applications, our own R&D developed a filtration step that removes trace metal residues undetectable to many routine labs. The result feels tangible in the hands: reliable, reproducible lots, every barrel, every drum, every time.

    Specifications Matter: Real-world Results from the Plant Floor

    Our production experience shows that 4-chlorobutanal diethyl acetal behaves best if the color remains below 30 Hazen. Higher color indices often signal hydrolysis or over-chlorinated impurities, so we continually monitor and adjust the finish. It boils between 60-61°C at 14mmHg, and our distillation operators verify this range for every lot before we release any product. A sharp boiling point translates to predictable recovery on the customer end, especially in pharmaceutical and agrochemical synthesis where volume losses can hit yields. We ship material in sealed, inert-lined drums to avoid air contact and water pickup, which prevents degradative side reactions common to less tightly managed supply chains.

    Material safety is not just a checkbox—hydrolysis produces trace amounts of 4-chlorobutanal and ethanol, so tightly closed containers and dry storage conditions are non-negotiable from our experience. Spillage or vapor exposure can trigger sharp, irritating odors, so our warehouse team trains specifically on ventilation and handling. For on-site users, we emphasize using local exhaust and chemical-resistant gloves, since alkyl chlorides are well-known for skin and mucous membrane irritation.

    How This Acetal Supports Industrial and Research Synthesis

    Our own process chemists value 4-chlorobutanal diethyl acetal for its ability to undergo selective deprotection and transformation, something we see echoed among our customers. The key here is the acetal group: stable enough through handling and shipping, yet easily unmasked under the right acidic conditions to release the highly reactive aldehyde. That reactive center can turn into a wide array of functional groups needed for active pharmaceutical ingredients, specialty polymers, and flavors. A key example—our partners in agrochemical development use this intermediate for the stepwise construction of ring systems, leveraging the dual handle provided by the chloro and acetal groups. Every downstream product benefits when the input intermediate is both clean and reliable. Our focus in purification supports this by making sure byproduct chlorination and unwanted acetals do not accumulate between lots.

    Academic labs have asked us how this material stacks against commercially available 4-chlorobutanal—our answer always points to improved shelf stability and selectivity. The free aldehyde degrades quickly in storage, even at low temperature, generating polymeric tars and acidic decomposition. The acetal, in contrast, stores clean and awaits controlled deprotection, ensuring more consistent results, particularly for users running parallel synthetic campaigns. When a user needs the aldehyde in situ, they can unmask it as late as possible, squeezing out every last bit of conversion before any degradative side reactions start. In our own research—and among the scale-up customers we support—this proves crucial to maintaining purity across increasingly demanding regulatory landscapes.

    Meeting the Needs of Large-Scale Users

    We work with pharmaceutical companies that demand more than just a compliant certificate of analysis. They need predictability: identical impurity profiles, consistent appearance, fast and accurate documentation. At one point, a major customer uncovered trace halogenated byproducts in a competitor’s batch that delayed their project by weeks. We took their feedback to our process control review. Our solution included ramping up in-process monitoring, redesigning critical sampling points, and investing in real-time spectroscopic checks. This attention to process reality—not just paper specs—has kept our users running with uninterrupted supply and tightest lot-to-lot reproducibility.

    Our scale partners, especially those producing intermediates for custom syntheses, run constant time-trials on batch turnovers. For their daily production, acetal intermediates like this need real-world thermal and chemical stability. Our plant upgraded its inerting and temperature controls after a single runaway batch caused odor and loss of yield. Since then, our monitoring system and hands-on training have kept every lot within the target window, matching the temperature and pressure conditions specified on the bench but applied to tons, not grams.

    How 4-Chlorobutanal Diethyl Acetal Differs from Other C4 Building Blocks

    In practice, the acetal version offers the unique benefit of stability without sacrificing downstream reactivity. Compounds like 4-chlorobutanol, 4-chlorobutanal, and standard butanal all find use as four-carbon intermediates, but each brings drawbacks. The alcohol oxidizes or dehydrates during aggressive reactions, sometimes forming highly toxic impurities. The unprotected aldehyde is notorious for polymerizing or reacting prematurely, which for a multi-step synthesis, limits its shelf life and recovery. Only the diethyl acetal format protects the vulnerable aldehyde function, giving chemists the flexibility to store and transport the intermediate without degradation, then reveal the carbonyl as needed under mild acid.

    Across hundreds of production runs and scale-outs, we find that the diethyl acetal shows exceptional resilience under both light and moderate temperature exposure, much higher than the free aldehyde. In head-to-head comparisons—even after a month in storage, our acetal material remains clear and passes every purity benchmark, while the unprotected aldehyde forms cloudy, sticky residues even under refrigeration. This difference helps us guarantee what customers will find on arrival, not just at shipment.

    We’ve fielded requests from customers who attempted to work around with tetrahydrofuran, gamma-chlorobutyric acid, or other more common C4 intermediates. While those compounds serve their roles, only the acetal holds the right balance for selective late-stage modifications, making it ideal for syntheses that call for a clean reveal of the aldehyde. Each functional group on the acetal is there for a reason—one stabilizes storage, the other allows precise manipulation at the next step.

    Real-world Uses: From Pharmaceuticals to Flavors

    One of our earliest projects with 4-chlorobutanal diethyl acetal supported a mid-sized pharma group trying to build functionalized pyrrolidine scaffolds for a CNS-active molecule. They struggled with other four-carbon starting materials since none provided enough stability for their multi-day runs. With direct supply of our acetal, they avoided tarring and avoided the side products that plagued previous campaigns. Their feedback resulted in a production change that improved our purity even further, underscoring how valuable open channels with actual users can be.

    Another group used our acetal in fragrance intermediate synthesis, taking advantage of its ability to unmask the aldehyde function cleanly for downstream modifications. Stability through transit and controlled deprotection at the precise step allowed them to reach new structural motifs without unmanageable byproducts. In talking directly to their synthetic chemists, we learned that timeline pressure to deliver new fragrances demands intermediates that work not just on paper but at scale, with no surprises mid-process.

    Crop science companies use this intermediate to build ring systems in pre-emergent herbicides, a process that requires multiple protection and deprotection stages on the same carbon chain. This is a setting where every impurity counts—regulators check for trace contaminants at levels below 1ppm. Our response has been to cycle through additional fractional distillations and stronger in-house analytical checks, because their regulatory bottleneck doesn’t make space for reprocessing or reworking.

    Solving Everyday Challenges in Batch Handling

    Storing and using 4-chlorobutanal diethyl acetal poses distinct challenges. Operators have shared common pain points with us: high evaporation rates, hydrolysis concerns, and disagreeable odors all raise flags in typical storage warehouses. We switched our drum linings from generic metal to nitrogen-purged, epoxy-coated drums—this step cut down hydrolysis by more than half, measured by reduced ethanol in headspace testing. Training our own shipping team on the trickier aspects of handling specialty chlorinated intermediates also prevented damage from moisture pickup during hot, humid seasons.

    Users mixing or dosing this acetal in multi-step reactors have expressed concerns about foaming and vapor loss. Based on our own plant troubleshooting, slower initial rates and moderation of agitation solve most of these issues. Where continuous-feed lines are in use, adjusting the introduction point downstream of strong oxidants or bases reduces hydrolytic breakdown. As a manufacturer, sharing these real lessons learned—rather than boilerplate handling advice—often saves both time and money for our partners as they adapt to the reality of using a sensitive but valuable intermediate.

    Supporting Chemists Beyond Product – Real Feedback Loop

    Intermediates like 4-chlorobutanal diethyl acetal often surface in custom synthesis projects where any inconsistency cascades through to the final step. Over time, we have partnered with chemists to run joint troubleshooting—taking in-process samples, running split-lot side-by-side reactions, and dialing in parameters until they reach optimum conversion. We use our lab’s analytics and theirs—two looks at the same material—because feedback at this level allows us to fine-tune future batches. This directly impacts supply stability: nobody wants to tech-transfer a process only to find a new supplier’s intermediate upsets their hard-won control.

    We learn as much from those late-night calls about a reaction gone wrong or unexpected foam in a scale-up run as from any formal meeting. Welcoming troubleshooting means our R&D adjusts process parameters or adds a screening step based on real-world user results. Over years, users have trusted us not just to supply, but to help them de-risk when a project or new market calls for higher performance or regulatory reviews.

    Positioning for the Future: Continuous Improvement and Response

    As regulations around process impurities and environmental safety grow more exacting year by year, we invest in more sensitive routine impurity analyses and energy-efficient purification for 4-chlorobutanal diethyl acetal. Some years back, we installed inline water scavenging to further drive down moisture—resulting in measurable improvements to both appearance and assay. Our production techs now flag any deviation in real-time. Incentive comes not from abstract quality standards but from the experience that each lot supports critical supply chains in pharma, ag, and fine chemicals.

    We also work to minimize waste and improve yield, because decades of direct synthesis teach harsh lessons about the true cost of rework and lost material. Solvent recycling, heat recovery, and material tracking on every scale-up are now baseline expectations at our plant. We aim to deliver not just a product, but ongoing process and application expertise that saves end-users costly troubleshooting and variable output. The true value of a specialty intermediate like 4-chlorobutanal diethyl acetal lies not just in its molecular structure, but in the real reliability and support that come from years of direct experience producing, shipping, and supporting it where it counts—in the lab and on the plant floor.