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

2-Bromobenzaldehyde Diethyl Acetal

    • Product Name 2-Bromobenzaldehyde Diethyl Acetal
    • Alias 1-(2-Bromophenyl)-1,1-diethoxyethane
    • Einecs 700-200-8
    • 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

    220776

    Product Name 2-Bromobenzaldehyde Diethyl Acetal
    Cas Number 1564-99-8
    Molecular Formula C11H15BrO2
    Molecular Weight 259.14 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 146-148°C at 13 mmHg
    Density 1.337 g/mL at 25°C
    Purity Typically ≥98%
    Refractive Index n20/D 1.522
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 2-Bromo-1-(diethoxymethyl)benzene
    Smiles CCOC(C1=CC=CC=C1Br)OCC

    As an accredited 2-Bromobenzaldehyde Diethyl Acetal factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2-Bromobenzaldehyde Diethyl Acetal is supplied in a clear, amber glass bottle with a secure screw cap and labeling.
    Shipping 2-Bromobenzaldehyde Diethyl Acetal is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The package is clearly labeled with hazard information and handled according to international transport regulations. Temperature and moisture control may be required, and the substance is shipped by certified carriers specializing in chemical logistics.
    Storage 2-Bromobenzaldehyde Diethyl Acetal should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separate from strong oxidizing agents and acids. Proper labeling and secondary containment are recommended to prevent accidental exposure or spillage. Store at recommended temperatures as indicated on the safety data sheet.
    Application of 2-Bromobenzaldehyde Diethyl Acetal

    Applications of 2-Bromobenzaldehyde Diethyl Acetal in Industrial Manufacturing

    As a direct manufacturer, we supply high-purity 2-Bromobenzaldehyde Diethyl Acetal to key sectors that require this building block for high-value chemical synthesis. Below, we outline specialized application scenarios based on established industrial integration, highlighting compliance, usage control, process steps, and the specific end products achieved.

    1. Pharmaceutical Intermediate Synthesis

    Our material is predominantly used by pharmaceutical producers as a protected formyl source for the construction of complex heterocyclic scaffolds and advanced intermediates. Its stability and controlled deprotection under acidic conditions allow for efficient installation of formyl functionalities in the late-stage drug candidate assembly, minimizing side reactions and loss of yield in high-value APIs such as selective anti-infectives and CNS-active compounds.

    Industry compliance standards

    • Current Good Manufacturing Practice for Active Pharmaceutical Ingredients (ICH Q7)
    • 21 CFR Part 211 (FDA, USA)
    • European Pharmacopoeia (Ph. Eur.) compliance for intermediates
    • China GMP (2010 Revision)

    Typical usage ratio

    • Applied at 0.12–0.35 molar equivalents relative to the core substrate, adjusted based on target molecule complexity and protection step requirements.

    Downstream process integration

    • Dosed during intermediate synthesis via a condensation or protection reaction, followed by controlled hydrolysis to regenerate the aldehyde for subsequent steps.

    Final product types

    • Process intermediates for antiviral agents
    • Precursor stages in antipsychotic drug synthesis
    • Key building blocks for specialty CNS APIs

    2. Agrochemical Raw Material Synthesis

    Producers in the crop protection sector employ our diethyl acetal as a masked benzaldehyde in multi-step synthesis routes for selective herbicides and fungicides. By preventing side reactions at aryl aldehyde positions, manufacturers maintain integrity of halogenated intermediates, allowing controlled introduction of bioactive moieties before final deprotection and formulation of active agrochemicals.

    Industry compliance standards

    • ISO 9001:2015 certified batch production
    • EU Regulation (EC) No 1107/2009 on plant protection product safety
    • EPA Registration (USA) guidelines for technical grade actives

    Typical usage ratio

    • Implemented at 0.10–0.28 molar equivalents, depending on the complexity and sensitivity of downstream halogenation or coupling steps.

    Downstream process integration

    • Introduced at the early stage as a formyl protecting unit, with subsequent hydrolysis after key C–C or C–N couplings are complete, prior to oxidation or formulation steps.

    Final product types

    • Selective pre-emergent herbicide intermediates
    • Fungicidal agent building blocks
    • Technical grade intermediates for active ingredients

    3. OLED and High-Performance Material Synthesis

    Manufacturers serving the organic electronics segment integrate this compound in multi-step synthesis pathways for fine-tuned aryl aldehyde building blocks, which are essential in preparing hole-transport layers and light-emitting compounds for OLED displays. Its acetal group withstands extensive organometallic coupling, ensuring functional group selectivity before controlled acidolysis reveals the reactive functional moiety needed for device performance.

    Industry compliance standards

    • REACH Registration (EC No 1907/2006) for chemical safety
    • ISO 14001 for specialty material production
    • RoHS Directive (2011/65/EU) for electronics

    Typical usage ratio

    • Used at 0.08–0.18 molar equivalents in aryl-based substrate derivatization, altered based on molecular design of the target OLED material.

    Downstream process integration

    • Added during substrate functionalization prior to high-temperature Suzuki or Stille couplings, followed by mild deprotection to reveal the aldehyde for device precursor synthesis.

    Final product types

    • Hole-transport polymers for OLED screens
    • Color-emitting small molecules
    • Functionalized aryl monomers for advanced display components

    4. Fine Fragrance Intermediate Production

    Perfume and aroma chemical manufacturers use this material as a protected precursor for brominated benzaldehyde derivatives, which are subsequently unmasked to provide aldehydic notes vital for luxury fragrance formulations. This approach avoids premature oxidation or undesired polymerization during scale-up, maintaining precise olfactory properties in the final blends.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • ISO 9001:2015 for flavour and fragrance production
    • EU Regulation (EC) No 1223/2009 on cosmetic products

    Typical usage ratio

    • Added at 0.07–0.15 molar equivalents relative to other base aroma reactants, modified according to the intensity and volatility profile required in the end product.

    Downstream process integration

    • Fed into the aroma chemical synthesis stream as a masked functional group, with hydrolysis following etherification or downstream glycosylation, preceding formulation and QC blending.

    Final product types

    • Aldehyde-rich fine fragrance bases
    • Specialty aroma chemicals for perfumers
    • Brominated benzaldehyde analogues for olfactory compounds

    5. Specialty Polymer Initiator Manufacturing

    Chemists in specialty polymer fields incorporate this compound to generate functional initiators for polymerization, specifically where selective introduction of aromatic aldehyde groups is required for grafting or end-capping reactions. Its controlled deprotection under acidic conditions supports batch and continuous processes where functional fidelity and polymer purity are critical for technical applications.

    Industry compliance standards

    • ISO 9001:2015 quality management for speciality chemicals
    • REACH Registration (EC No 1907/2006) for monomers and additives
    • ASTM D6103 for polymer initiator performance

    Typical usage ratio

    • Blended at 0.09–0.20 molar equivalents to tailor initiator charge density, subject to downstream molecular weight and functional group requirements.

    Downstream process integration

    • Activated through acid hydrolysis after initial monomer pre-mixing, enabling the attachment of aldehyde groups as controlled initiation or termination points for the polymer chain.

    Final product types

    • Functionalized polymer initiators for specialty adhesives
    • High-performance end-capped resins
    • Controlled graft copolymers
    Free Quote

    Competitive 2-Bromobenzaldehyde 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

    2-Bromobenzaldehyde Diethyl Acetal: Direct from the Manufacturer’s Line

    Getting Close to the Source

    Walk into any production site handling fine chemicals and you’ll find a story behind every intermediate. Here in the lab, quality doesn’t start on paper—it shows up at the measuring glass, after months or even years refining how to keep a batch pure from start to finish. Working hands-on with 2-Bromobenzaldehyde Diethyl Acetal, known in some circles as a versatile building block for pharmaceuticals and performance materials, we’ve found that the difference always comes down to process control, real chemical insight, and how you treat every variable from raw material choice to the drying process. Only chemical manufacturers who actually run live production know where the bottlenecks sit, and where contaminants try to creep in if you don’t pay attention.

    Our 2-Bromobenzaldehyde Diethyl Acetal, produced within our integrated facility, represents more than just another specialty chemical; it carries the weight of careful method optimization, process monitoring, and a steady focus on actual user needs. Market requests can shift quickly—sometimes demanding small packs for custom syntheses, sometimes expecting scale for larger formulators. Each variant means rethinking parameters like solvent ratios, reaction times, and the point where distillation puts purity ahead of theoretical yield. The material consistently comes in colorless to pale yellow liquid form, easy to judge at a glance and reassuring for anyone familiar with typical acetal characteristics. The specific gravity, boiling point, and GC purity get kept under real scrutiny before ever considering a lot for sale.

    Understanding Its Role in Synthesis

    Most people see 2-Bromobenzaldehyde Diethyl Acetal as just another reagent, but anyone driving an industrial process knows how much trust sits behind the choice to modify a molecule’s backbone. A major fraction of this acetal finds its way into the pharmaceutical field. Developing functionalized benzene rings is always a balance between selectivity and yield. For us, the acetal serves a core purpose: protecting the aldehyde function from side reactions during more complex transformations. That protection, once introduced, gives downstream chemists confidence—no unexpected oxidations or rearrangements muddying up the synthetic plan. It’s one thing to claim high selectivity in theory; it's something else altogether to have customers sending back consistent NMR traces and chromatograms run by their own QA teams.

    People often ask about handling. On our floor, technicians treat every drum with basic respect—ventilation, low moisture exposure, and sealed containers. Spills get neutralized quickly, but with a well-run shop, you can keep loss rates close to zero. Our smaller users, such as R&D-driven pharmaceutical startups, prefer liter-scale packaging that preserves stability over shelf life. At scale, customers request hundreds of kilos for full campaigns, so real traceability and batch records become a big part of the job—a forgotten shipment or mismarked drum causes headaches on both sides.

    Production Realities: Where Quality Emerges

    Making acetal compounds always tests the patience of any chemical engineer. Our batch reactors used for this synthesis operate under strictly controlled conditions because every gram counts, and so does every deviation. You can’t rely just on purchase specifications or COAs—mid-process sampling, routine GC checks, and even manual color observation come into play when downstream applications have no room for guesswork.

    Starting raw materials set the tone, so we only accept supplies that match previous impurity profiles from vendors. Every liter of diethyl acetal comes backed by a record of previous lots; we don’t swap out for convenience since that nearly always shifts yield or color. Bromination conditions in our plant get kept under close lock—excess bromine residues introduce not just regulatory issues, but trace side products that reappear in final NMR spectra. We watch water content in every intermediate step, using both KF titration and visual checks, to ensure stability for extended storage and downstream functional group conversion.

    On the shop floor, a small error like letting the pH drift or running distillation too aggressively can turn a whole day’s output into rework. Process improvements—such as introducing in-line filtration and pressure controls—didn’t just happen from reading standards but came from repeated troubleshooting and actual operator input. Documentation helps, but asking your own team after a run yields real insight on what needs fine tuning.

    Why Not Just Use Benzaldehyde Derivatives Directly?

    Some early-stage chemists or procurement agents wonder why the acetal matters—why not work directly with the 2-bromobenzaldehyde core? Protection, predictability, and cost efficiency drive the choice in practice. Aldehyde groups react easily; they won’t survive exposure to most basic or nucleophilic reagents needed for further modification. The acetal, formed from ethyl groups, shields the site cleanly and can be deprotected under mild acid after all essential transformations finish.

    Compared to straight 2-bromobenzaldehyde, the acetal gives a notably longer shelf life. It avoids the slow air oxidation that turns some aldehydes dark or sticky during storage. The more stable structure plays well not just on paper but in transport and storage—shifting drums between climate zones or across borders raises fewer worries about decomposition. Our experience matching customer returns suggests that handling costs drop by a measurable margin using the acetal intermediate, with less reanalysis and reshipment needed.

    We have compared this diethyl acetal with other acetals, such as dimethyl or dipropyl analogs, and experience shows the ethyl variant strikes the best balance between ease of hydrolysis and resistance to unplanned transacetalization. It’s a subtle edge but deeply appreciated where scale-up comes to the table.

    Purity, Side Products, and Batch Control

    Sitting in production, purity does not simply mean “meets spec”; it reflects everything going on in your reactors, from cooling rates to filtration technique. Each batch of our 2-Bromobenzaldehyde Diethyl Acetal gets checked beyond what standard method cards demand. Aside from confirming GC area purity above 99%, our QC team routinely screens for structural analogs, unreacted starting material, and elemental analysis to catch outliers long before shipment.

    Practically every commercial chemical has its own set of trouble products. For this acetal, common side products include trace brominated impurities or partial hydrolysis fragments, especially if handling or purification gets rushed. We’ve spent years fine-tuning how we dry and wash out these byproducts. Dealing promptly with these issues stops surprises further downstream, saving both users and ourselves from wasted effort.

    We do not simply run samples against a catalog; our lab maintains in-house standards, with reference traces from previous production periods, so inter-lot consistency follows long experience, not just the latest reference. By training all technicians directly on these standards, we keep human error to a minimum.

    Strengths and Real-World Advantages

    Why have customers stayed with our material instead of swapping to alternates? The answer starts with traceability. We track each input, each reactor parameter, and each cleaning step. In the event of a challenge—a question about a peak in an LC-MS run—a single phone call connects direct to the chemist in charge of that actual batch. Fact-based discussions happen daily: the modest upfront attention we give pays off in loyal clients and zero last-minute production stops.

    Some customers have pointed out that our acetal interferes less with downstream coupling reactions than material from other sources, possibly due to trace base content being lower or repeated washing cycles removing unwanted ions. Even small differences, seen only after dozens of transformations on-site, translate to less troubleshooting and revalidation on their end. It’s easy to underestimate how much downstream value comes from a maker’s attention before shipping.

    Every production environment is unique, and a compound like 2-Bromobenzaldehyde Diethyl Acetal acts as a reliable foundation for more complex molecular designs. Whether used in research, process development, or registered active pharmaceutical ingredient pathways, the focus remains on reliability and predictability, not just “meeting spec.”

    Handling, Storage, and Supporting Good Practices

    On our shelves, acetal shipping containers always stay capped tightly. Exposure to air and moisture encourages gradual breakdown—acidic or even just wet conditions can shorten shelf life and, over time, taint the purity of subsequent workups. We advise all partners to follow simple steps: keep drums out of direct sunlight, store at room temperature away from any acids or strong bases, and reseal immediately after sampling.

    To help downstream users, we share detailed insights from our storage and long-haul transport experience: maintain full documentation of every sample, note opening and closing dates, and request fresh lots for critical work when possible. By tracing every shipment, we answer requests on real timelines, not with vague stock answers. This level of detail only comes from repeated direct handling, and it avoids headaches later, especially when audits or regulatory reviews come up.

    We’ve also noticed that with our packaging variants—ranging from glass to HDPE—there is little leaching or reactivity observed, which supports our claim for long shelf life. This reduces operational risk and suits clients operating in tight regulatory or compliance spaces.

    Environmental Realities and Waste Management

    Making and using chemicals responsibly requires more than just ticking checkboxes on an SDS. Throughout production, we’re responsible for every solvent drum that enters, and every drop of waste produced. Our acetal runs involve careful solvent recovery—primarily ethanol and toluene systems—that get distilled and reused. This reduces environmental footprint and impacts not just cost, but actual site sustainability metrics.

    Handling waste from brominated materials gets special attention here. We avoid venting bromine; scrubbers and closed systems keep emissions well below permitted limits. Even wash water receives direct monitoring for total organic bromine, and we document each waste stream from collection to disposal or recycling. Our experience in regulatory inspections proves the point: clean practices and rigid records avoid fines, delays, or shutdowns.

    Where other operators sometimes underestimate the cost of waste treatment when scaling up acetals, we’ve already implemented solvent loops and batch-scale waste minimization. These strategies not only save money but help future-proof downstream processes for customers who value environmental responsibility.

    Feedback Loops and Customer Collaboration

    Everything written above comes from practice, feedback, and years of close work with both small and multinational customers. In direct calls, partners share how the acetal fits (or fails) in their own reactions. When something doesn’t behave as expected, such as a slow hydrolysis or a troublesome byproduct, the best outcome comes from going back to raw data—batch chromatograms, spectral analysis, and open dialogue. For example, we have adjusted dehydration and filtration steps based on recurring comments about one-off cloudiness, finding that a change in filtration pad thickness solved the recurring issue.

    Even after shipping, we keep close tabs on any lot that ends up needing investigation. Traceability means pulling up original records, including intermediate purging logs, instead of offering guesswork. For long-term users, we frequently provide technical bulletins with recommended handling tweaks based on collective user experience—not abstract “best practices,” but actual methods tested across dozens of pharma, agrochemical, and advanced materials labs.

    Customers often note that supplier collaboration rarely goes beyond invoices and COAs, but as a manufacturer we’re able to support even first-time users. We do not shy away from talking real chemistry, from reaction troubleshooting to unusual analytical peaks. This open line wouldn’t exist if we didn’t own the process from end-to-end.

    Comparing with Alternate Protecting Groups and Analogs

    Direct side-by-side evaluation with other protecting group strategies underlines the practical appeal of this diethyl acetal. Compared to methoxy or bulkier acetal variants, users describe our product as easier to deprotect under mild acidic conditions, with fewer byproducts and shorter deprotection times. Many alternative benzaldehyde acetals involve significant downstream tediousness—polymeric tars, strong acid requirements, or mixed byproducts—none of which a scale-up team wants saddled with at the kilogram stage.

    Further, our internal data across hundreds of runs shows that the ethyl acetal form resists transacetalization cross-contamination, especially important for groups working in multi-product facilities. This isn’t something often listed in standard tables; it reflects practical experience handling mixed equipment, shared glassware, or batchwise cleaning. Each structural analog has its use, but our trials reinforce the robustness and predictability in standard workflows seen with the diethyl acetal variant.

    Against non-acetal protected analogs (such as imines or oximes), the difference becomes more distinct. Our users often encounter easier purification routes and more reliable conversions. These small but tangible advantages reduce total project time, lower consumable usage, and simplify analytical verification for registrational filings.

    What Sets Our Product Apart

    Outsiders may not appreciate the subtle differences between similar-looking chemicals on a catalog page, but any producer dealing with repeat customers recognizes persistent patterns. Feedback, real-world troubleshooting, and successful audits shape a reputation—one built less on advertising and more on reproducible outcomes. Our hands-on control over every point in production gives us confidence to stand behind each batch of 2-Bromobenzaldehyde Diethyl Acetal.

    For clients filling high-value vials, running multi-step syntheses, or validating key intermediates for regulatory filings, knowing exactly what goes into each bottle isn’t just comfort—it makes a measurable difference in yield, purity, and process predictability.

    We treat 2-Bromobenzaldehyde Diethyl Acetal as a foundation, not an afterthought. Each order flows from a larger system built on experience and real dialogue, not just commodity movement. The dialogue with customers, the feedback from the production line, and years of direct QC adjustment let us continue offering this material at the highest standard possible.

    Choosing a direct-from-manufacturer chemical means less uncertainty—more feedback, less drift from spec, and greater support for the actual chemistry at hand. For modern, adaptable synthesis workflows—from drug development to complex material manufacturing—the right acetal supporting team makes all the difference.