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2-(2-Chlorobenzyloxy)Benzaldehyde

    • Product Name 2-(2-Chlorobenzyloxy)Benzaldehyde
    • Alias PCBXAL
    • Einecs 422-130-7
    • 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

    224638

    Iupac Name 2-[(2-chlorophenyl)methoxy]benzaldehyde
    Molecular Formula C14H11ClO2
    Molecular Weight 246.69 g/mol
    Cas Number 67913-94-4
    Appearance White to off-white solid
    Melting Point 70-74°C
    Solubility Soluble in organic solvents such as DMSO and ethanol
    Smiles C1=CC=CC=C1COC2=CC=CC=C2C=O
    Inchi InChI=1S/C14H11ClO2/c15-13-7-3-1-6-12(13)10-17-14-8-4-2-5-11(14)9-16/h1-9H,10H2
    Storage Conditions Store in a cool, dry place, away from light
    Purity Typically >98% (as available from suppliers)
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited 2-(2-Chlorobenzyloxy)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package is a sealed amber glass bottle, labeled "2-(2-Chlorobenzyloxy)Benzaldehyde", with hazard symbols and handling instructions.
    Shipping 2-(2-Chlorobenzyloxy)Benzaldehyde is shipped in secure, airtight containers to prevent contamination and moisture exposure. Packages are clearly labeled according to regulatory and hazard requirements. The chemical is transported by certified carriers, adhering to standard safety and environmental guidelines for hazardous materials. Shipping documentation and tracking ensure compliance and safe delivery.
    Storage 2-(2-Chlorobenzyloxy)benzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, open flames, and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Store at room temperature or as specified by the manufacturer. Ensure containers are clearly labeled and kept out of reach of unauthorized personnel.
    Application of 2-(2-Chlorobenzyloxy)Benzaldehyde

    Applications of 2-(2-Chlorobenzyloxy)Benzaldehyde in Industrial Manufacturing

    As a specialized manufacturer of 2-(2-Chlorobenzyloxy)Benzaldehyde, we supply this advanced aromatic building block to downstream sectors that require precise specifications and high standard compliance. Below, we detail the principal industrial routes where our material plays a critical role, with each segment focusing on real, high-value applications, technical processing integration, and regulatory frameworks relevant to our direct B2B partners.

    1. Pharmaceutical Intermediate Synthesis for Antifungal Agents

    Leading pharmaceutical manufacturers incorporate this benzaldehyde derivative as a key aldehyde component when synthesizing azole antifungal drug intermediates. During Medicinal Chemistry R&D and process-scale manufacturing, it reacts at the core step of constructing substituted benzimidazole or triazole scaffolds. The controlled reactivity and halogenated benzylic structure support both yield maximization and impurity profile management in active ingredient pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211, Subpart C—Drugs: Controls of Components
    • European Pharmacopoeia (Ph. Eur.) Monograph 2034—Substances for Pharmaceutical Use
    • Chinese Pharmacopeia General Chapter 0901 for pharmaceutical excipients and intermediates

    Typical usage ratio

    • 0.08 – 0.12 mol per mol of final API target, adjusted based on target molecule conversion rate and scale-up efficiency.

    Downstream process integration

    • Charged during the condensation and cyclization steps following initial solvent charging in stirred reactors, typically after solvent pre-adjustment and prior to catalyst addition. Inline purity checks confirm reaction endpoint before downstream purification.

    Final product types

    • Benzimidazole antifungal intermediates
    • Triazole-based API core structures
    • Crude and purified pharmaceutical intermediates for bulk drug synthesis

    2. Synthesis of Agrochemical Fungicide Intermediates

    Within crop protection sector, formulators use this aromatic aldehyde to introduce targeted functional groups into fungicide lead compounds, especially for the construction of heterocyclic rings in new-generation agricultural fungicides. The chlorinated benzyloxy structure enhances biological activity profiles and improves downstream coupling efficiency, supporting robust process scaling and performance consistency across agrichemical supply chains.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management Systems for Agrochemical Production
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • Chinese National Standards GB 2763—Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.05 – 0.2 mol per mol of active pesticide precursor, determined by final product purity targets and process step selectivity.

    Downstream process integration

    • Dosed into batch reactors during nucleophilic aromatic substitution or acylation stages for the preparation of target fungicide molecules. Excess removal via aqueous work-up controlled by in-line analytical detection.

    Final product types

    • Precursor intermediates for new-generation triazole fungicides
    • Halogenated benzyl ether intermediates used in crop protection formulations
    • Formulated fungicidal finished products for field application

    3. Fragrance and Aroma Chemical Precursor in Fine Chemicals

    Producers of specialty aroma chemicals rely on the controlled oxidation and further derivatization of this benzaldehyde to yield unique aldehydic, floral, or woody notes suitable for luxury perfumery and flavor compounding. Its stability and reactivity as a substituted benzaldehyde ensure batch-to-batch reproducibility required by global fragrance houses and food aroma blenders.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • US FDA 21 CFR 172.515—Flavoring Agents and Related Substances
    • ISO 9235:2013—Aromatic Natural Raw Materials—Vocabulary
    • European Flavour Association (EFFA) Quality & Safety Standards

    Typical usage ratio

    • 0.02 – 0.08 wt% in concentrate blends, adjusted according to sensory intensity and longevity targets of the finished scent profile.

    Downstream process integration

    • Introduced after base note blending during aroma compound formulation, followed by controlled oxidation, acetylation or etherification as required. Final QC includes GC-MS tracing for trace aldehyde management.

    Final product types

    • Specialty aldehyde aroma ingredients
    • Luxury perfume and cologne compositions
    • Flavor and fragrance intermediates for food and beverages

    4. Electronic Chemicals: Photoresist Monomer Synthesis

    High-purity electronics sectors employ this material in the fine synthesis of monomers for photoresist polymers, critical for microelectronic lithography. Its benzaldehyde core enters resin design for UV-sensitive photoresists, delivering highly defined pattern profiles and improved line-edge roughness for semiconductor wafer fabrication at sub-10 nm nodes.

    Industry compliance standards

    • SEMI C57—Specifications for Photoresist Materials
    • ISO 14644—Cleanrooms and associated controlled environments
    • JEITA Guidelines for Electronic Chemicals Purity
    • RoHS Directive (EU) 2011/65/EU if used in semiconductor assemblies

    Typical usage ratio

    • 0.04 – 0.10 mol per mol of final monomer composition, tailored for targeted polymer chain length and ultraviolet absorbance requirements.

    Downstream process integration

    • Introduced during controlled dropwise dosing to anhydrous synthesis environments; post-reaction distillation and filtration ensure sub-ppb contaminant levels. Sequential polymerization follows for precise copolymer assembly.

    Final product types

    • Functional aromatic monomers for photoresist polymers
    • UV-curable resin precursors for semiconductor photolithography
    • High-purity electronic-grade intermediate chemicals
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    Certification & Compliance
    More Introduction

    2-(2-Chlorobenzyloxy)Benzaldehyde: Manufacturing Insights and Practical Uses

    Directly From Our Lines: The Real Deal With 2-(2-Chlorobenzyloxy)Benzaldehyde

    From our production floor, 2-(2-Chlorobenzyloxy)benzaldehyde presents itself as a steady performer for demanding applications in chemical synthesis. This compound, a fine crystalline product with the chemical structure built around a benzaldehyde backbone and a 2-chlorobenzyloxy substitution, stands out in selectivity and versatility during multi-step synthesis. Over years of manufacturing, meticulous attention has gone into optimizing both purity and consistency — batch to batch, kilo to kilo.

    The Backbone of Advanced Synthesis

    Every chemist on site knows that intermediates like 2-(2-chlorobenzyloxy)benzaldehyde often make or break the reliability of downstream products. This isn’t some commodity chemical cranked out to fill warehouse space. Each step, from controlled chlorination to careful purification, is mapped out with downstream users’ feedback in mind. For example, the aldehyde function on the benzene ring gives the intermediate value in constructing more complex frameworks found in pharmaceuticals and advanced materials. The chlorobenzyloxy group, which isn't a random add-on but a precise touch, plays a major part in regioselective reactions; its electronic influence directs synthesis steps that follow. Our senior reactor operators have seen how just a small impurity, unfiltered moisture, or off-base chlorination run can spiral into expensive bottlenecks for clients. That’s why we keep all specs discussed on the production floor rooted in real-life performance, not lab-bench theory.

    Zero-Guesswork Raw Materials and Strict Process Controls

    Not all manufacturers pay equal attention to how their process routes impact the reproducibility of 2-(2-chlorobenzyloxy)benzaldehyde. Over the last decade, we have learned that the quality of raw materials turns up as either reliable yield or stubborn impurities weeks downstream. We source chlorobenzyl alcohol and salicylaldehyde from short-listed suppliers after several years of supplier qualification and on-site audits. After every run, our quality technicians test chromatographic purity and moisture right off the centrifuge, not weeks later in a separate lab. Every shift knows what kind of color, odor, and spectral fingerprint signals a perfect batch. This isn't about passing specs in a file; it's about making sure not a single drum leaves our site unless it stands up to what our clients face under reaction conditions.

    Specifications That Reflect Real Processing Needs

    Our team crossed the bridge from bench-scale to commercial-scale production with an eye on what end-users actually ask for. The finished product typically reaches customers as a white to off-white crystalline solid, often within the melting point range of 94-98°C. A purity spec above 99% (GC) isn't just there for show; it traces back to observing downstream condensation and cross-coupling steps that underperform with lesser grades of material. We manage residual solvents to below 500 ppm and check for chloride content, knowing well these minor details matter most in scaled-up pharma syntheses. Since 2-(2-chlorobenzyloxy)benzaldehyde is sensitive to atmospheric moisture, we pack it under nitrogen in high-barrier bags – the habit taken from months of feedback from chemists who ran reactions only to be tripped up by side-product formation. These aren’t marketing claims; they’re points we verify during every customer audit and several surprise inspections from our own internal compliance team.

    Differences From the Crowd: Comparing With Close Relatives

    In our experience, those new to this building block sometimes confuse it with simpler benzaldehyde derivatives or with 2-chlorobenzyl-protected analogs lacking the specific ether linkage. One frequent competitor, o-chlorobenzaldehyde, appears superficially similar but behaves differently in protecting group strategies, especially where stability against nucleophiles matters. The distinct advantage appears during acid- or base-catalyzed reactions where the benzyloxy linkage insulates the aldehyde moiety better than direct chlorination on ring positions. The subtle electronic properties arising from this arrangement reveal themselves in yields and the cleanliness of product profiles in sophisticated syntheses.

    Comparing it with 4-(2-chlorobenzyloxy)benzaldehyde, our variant shows refined selectivity, especially during the introduction of substitution groups or during oxidative transformations. That means less effort spent on post-reaction cleanups and fewer chromatographic runs needed. For those integrating this compound into multi-stage syntheses, casual swapping between derivatives often leads to unpredictable yields or new byproduct profiles, clogging up both lab-time and solvent waste. We've run side-by-side tests in our plant-scale reactors to see real-world outcomes – and our logs show competitive advantage every time the right assignment of atomic positions matters for catalytic or sequential additions.

    Focus Markets: Pharma, Materials Science, Beyond

    The lion’s share of our output lands with pharmaceutical developers looking for building blocks in small-molecule API synthesis. This isn’t a secret. The technical team regularly fields requests for customization, especially when new regulatory filings require revalidated analytical profiles or demonstration of scalability beyond lab scale. Some specific uses include protection-deprotection sequences and as intermediates in the formation of biaryl or diaryl compounds. Early clients who demanded tight controls on trace impurities have helped us shape every SOP behind our modern lines.

    Material science labs also source this product for work on advanced organic compounds: OLEDs, charge-transport materials, and specialty polymers. In these settings, it’s often trace contaminants that spell disaster; we pack and seal based on lessons learned from a few costly failures in early research consortia. The difference lies in open lines of communication between our process engineers and client teams who aren't shy about sharing unsolved problems with scale-up or batch instability. This direct channel has led to several process adjustments, like looping in double-stage drying and improved in-line filtration, and not just creating specs that look good in a spreadsheet.

    Handling and Practical Processing Tips

    Our manufacturing team has picked up a wealth of practical tips over years handling this product. For instance, it clings to metal in certain conditions, so we recommend PTFE-lined scoops and storage vessels. Our operators monitor the hygroscopic nature on humid days, especially during bagging – this attention avoids caked material or sticky residues. Even after all those years, the best outcomes still start with storing at room temperature in sealed containers, shielded from direct sunlight and kept dry at all times. Heating above 50°C in open vessels leads to degradation, so those running high-temperature reactions do well to add the compound slowly, controlling exotherms and tracking headspace gas composition throughout.

    We don’t keep these tips to ourselves. Many of our repeat clients have grown from relying on datasheets to working directly with our technical team to get the most out of their process chemistry. Adjustments like adding a drying agent to reaction vessels or using anhydrous solvents can make a world of difference scaling from grams to tons. Day-to-day production happens with a feedback loop running from customer complaints straight to shift leaders and back through regular training sessions. We refine not just our compound, but the way our teams and clients use it in diverse settings.

    Why Product Integrity Matters More Than Marketing

    No manufacturer holds out a promise that every batch is flawless – variables still exist, from shifts in atmospheric pressure to subtle changes in solvent lots. Years ago, we pushed past template batch certificates, sitting down with clients to walk through how even examples of so-called “off-spec” material (still passing basic metrics) performed in real synthetic reactions. These partnerships bred improvements like in-process controls for organochlorine residue, feedback-driven shifts in crystallization temperatures, and even a change to higher-grade liners for shipment drums. Money spent on storage upgrades saved countless hours for end users forced to struggle with mysterious side reactions or blocked filters.

    Quality agreements now come after several trial runs where product spends weeks in real-world transit or on-site storage, not just on a QA manager’s desk. What we’ve found is that transparency around methods, testing, and changes to process stir the trust needed to support long-term business instead of single-transaction sales. This is not an attitude born overnight; it roots in thousands of kilograms produced and shipped under meticulous review, every kilogram checked under lights that don’t forgive corner-cutting. Our technical documentation team spends as much time on revision cycles as on the first draft – because the chemistry world keeps evolving, and so does our understanding of best practices.

    Challenges That Demand Attention

    Scaling up this intermediate brings its own set of hurdles. Early on, we noticed emulsion formation during workups, especially when scaling past 500-liter reactors. Aggressive agitation – useful in smaller runs – simply made for tougher separations in a plant setting. By collaborating with production chemists and learning from trial runs, we moved to staged addition of aqueous quench and redesigned our agitators. Yield jumped, and downstream separation headaches dropped to nearly nil. This is the sort of experience that simply doesn’t show up in a generic spec sheet. Anyone working in chemical manufacture understands that the learning never stops and feedback – whether praise or complaints – leads to direct change. We never shy from talking shop about mechanical troubleshooting or chemical quirks with our supply chain partners.

    Transport safety also rose as a real concern, not because the material is classified as particularly hazardous, but more from insight gained through reports of package breaches in high-temperature regions. We overhauled drum insulation and ramped up training for our logistics partners. Every year we pull random samples from storage for re-analysis. The QA team never hesitates to halt a shipment if a test falls outside our self-determined safe range, even if it slows delivery for an impatient customer. Long-term trust simply trumps quick profit.

    Continuous Improvement Backed by Science

    At a manufacturing scale, small changes have large impacts. Data analysis drives our approach; every parameter from raw material traceability to energy input for specific distillations gets logged, tracked, and reviewed. Our process chemists run regular pilot-scale experiments, introducing tweaks that are only approved after clear evidence of benefit. For example, an extractive crystallization step added in 2022, proposed by two of our shift leaders, raised product purity while shaving hours off cycle time. This additive approach keeps us competitive with global suppliers who sometimes cut corners in pursuit of cost savings. Our approach values time, data, and repeated testing over buzzwords or “breakthrough” process claims.

    We stay active in industry circles and regulatory working groups. Not because anyone told us to, but because each group or consortium meeting brings word of new synthetic challenges, regulatory trends, or raw material shifts that genuinely impact our customers’ outcomes. Learning from both victories and mistakes — our own as well as those of our peers — guides every upgrade and SOP revision. This habit of listening more than talking or selling keeps us alert to new pitfalls and new opportunities for improvement.

    Listening to Client Needs: No Half-Measures

    Over years of direct conversations with client chemists, commercial buyers, and R&D leaders, we’ve dropped “one-size-fits-all” language for custom-tailored technical support. Whether assisting with scale-up troubleshooting or guiding the first few kilograms into a new reaction sequence, our technical and production teams stay in close contact, answering real questions, not just reciting documentation. Experience teaches us that a manufacturer marking every phone call with curiosity and honesty wins business for the long haul.

    From our perspective in the plant, each kilo of 2-(2-chlorobenzyloxy)benzaldehyde carries not just a chemical formula, but years’ worth of problem solving and direct lessons learned. Each improvement to our handling, processes, or packaging arises from conversations with source chemists just as much as from regulatory audits or scientific studies. Whether a kilo finds new life in a drug candidate or in a next-generation display material, we feel a responsibility borne from every step of the manufacturing process.

    Looking Ahead: Resilience and Growth Through Real Manufacturing

    Changing market dynamics, new environmental regulations, and supply chain volatility keep the pressure on every manufacturing plant. We stay agile by directly investing in new analytical equipment, workforce education, and cross-training between production and QA teams. Each hire, each new SOP, and each supplier agreement strengthens our ability to offer compounds that meet rising expectations – not just on paper, but in practice.

    This direct approach to manufacturing and customer engagement has shaped all our decisions around 2-(2-chlorobenzyloxy)benzaldehyde. Even as industry shifts, we keep one eye on new synthetic challenges and one on the practical, day-to-day needs of chemists who push the boundaries on discovery and production. In our view, the only way to build and retain trust in chemical manufacturing is to live these lessons every day – inside the plant, in every packed drum, shipped ton, or late-night troubleshooting call. This compound’s performance reflects all those layers of care and know-how, rooted in our ongoing experience and true collaboration with real-world users.