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HS Code |
375101 |
| Productname | 2-Benzyloxy-4,5-Dimethoxybenzaldehyde |
| Casnumber | 74639-74-6 |
| Molecularformula | C16H16O4 |
| Molecularweight | 272.30 |
| Appearance | White to off-white solid |
| Meltingpoint | 89-91°C |
| Solubility | Soluble in organic solvents (e.g., DMSO, chloroform) |
| Purity | Typically ≥98% |
| Smiles | COc1cc(C=O)c(OC)cc1OCc2ccccc2 |
| Inchi | InChI=1S/C16H16O4/c1-18-15-10-12(9-17)16(19-2)11-13(15)20-8-14-6-4-3-5-7-14/h3-7,9-11H,8H2,1-2H3 |
| Storagetemperature | Store at 2-8°C |
As an accredited 2-Benzyloxy-4,5-Dimethoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Benzyloxy-4,5-Dimethoxybenzaldehyde, sealed with a screw cap and labeled with safety information. |
| Shipping | 2-Benzyloxy-4,5-Dimethoxybenzaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. The package complies with relevant chemical transport regulations, clearly labeled with hazard and handling information. Shipping is typically via ground or air, suitable for non-flammable solids, ensuring safe and rapid delivery to the recipient. |
| Storage | 2-Benzyloxy-4,5-Dimethoxybenzaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally in a chemical storage cabinet designated for organic compounds. Avoid exposure to heat and incompatible materials such as strong oxidizing agents. Always label containers clearly and handle with appropriate personal protective equipment. |
Applications of 2-Benzyloxy-4,5-Dimethoxybenzaldehyde in Industrial ManufacturingAs a dedicated manufacturer of 2-Benzyloxy-4,5-dimethoxybenzaldehyde, we have focused our production capabilities and technical expertise on industries that depend on its unique synthetic properties. Our product integrates most prominently in pharmaceutical research, advanced dye synthesis, specialty agrochemical intermediates, and fine fragrance ingredient manufacture. Below, we outline the core application scenarios where manufacturers achieve direct benefits in their downstream operations. 1. Pharmaceutical Intermediate for Antineoplastic Drug SynthesisR&D and production teams in the pharmaceutical sector value this compound as a crucial building block in the synthesis of multiple benzaldehyde-derived small molecules. It is often deployed in medicinal chemistry programs targeting advanced antineoplastic agents, due to its compatibility with protected phenolic groups and reactivity in condensation reactions. Our customers rely on its consistency for heterocyclic assembly and subsequent steps that define final bioactive APIs. Industry compliance standards
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2. Intermediate for Industrial Dye SynthesisDyestuff manufacturers integrate this aldehyde during the synthesis of complex organic dyes requiring methoxy-substituted aromatic frameworks. The benzyloxy and methoxy functionalities enable entry into coupling reactions and subsequent formation of chromophores with excellent color stability and lightfastness—critical for technical, textile, or inkjet dye productions. Industry compliance standards
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3. Building Block for Agrochemical IntermediatesProducers of crop protection active ingredients utilize this benzaldehyde derivative as a precursor in the formation of methoxy-aryl structures found in several modern herbicides and fungicides. The protected phenol group offers synthetic flexibility for downstream coupling, with high-purity batches enabling precise residue control and supporting regulatory submissions in key agricultural markets. Industry compliance standards
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4. Precursor for Specialty Fragrance IngredientsAromachemical manufacturers use this aldehyde as a precursor in the controlled synthesis of perfumery bases and aroma compounds that require precise masking of phenolic odours or fine-tuning of volatility. The protected benzyloxy group and dual methoxy substituents facilitate a select range of transformations yielding high-purity intermediates for fine fragrances, especially for luxury and niche perfumery. Industry compliance standards
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Nothing tells the story of an aromatic intermediate quite like its journey from raw material to a result in the hands of a working chemist. We began scaling up 2-Benzyloxy-4,5-Dimethoxybenzaldehyde (often referred to by its CAS number for clarity in research pipelines) years ago, after constant queries from both life sciences and fine chemical researchers for an aromatic aldehyde with both high purity and robust functional group compatibility. What makes this compound distinctive starts with its very structure: a benzaldehyde core with two methoxy groups in the 4- and 5-positions, plus a benzyloxy substituent on the 2-position. This combination bridges solubility, reactivity, and selectivity in downstream transformations.
Over the past decade, we have watched requests for this compound grow, especially among process chemists aiming at synthesizing complex heterocycles, ligands, or advanced intermediates for pharmaceuticals. By producing this material under our own roof, we keep a sharp eye on every batch—no guesswork and full traceability from starting phenol to packaged aldehyde. Our team understands exactly how slight shifts in reaction temperature or solvent composition during synthesis can affect palladium-catalyzed reactions, or how trace impurities, even at levels below 0.1%, can impact end uses in high-value targets. This experience allows us to guarantee a standard that traders and consolidators cannot, because we drive the manufacturing protocol and can tweak it batch-by-batch for our loyal customers’ evolving needs.
Each lot carries its own unique stamp of analytical data. Typical material comes as a pale solid with a melting point in the expected range for this structure. We confirmed the structure by NMR, and our typical GC-MS chromatograms reveal no extraneous peaks within the limit of detection for our instrumentation. HPLC purity commonly exceeds 99.5%. We do not ship product until it clears our full internal panel, including water content (measured by Karl Fischer, usually below 0.05%), residual solvents, and a panel of UV-Vis and IR checks to prove perfect ring substitution and aldehyde group integrity. This rigorous approach springs from real headaches years ago: a single impure shipment sent a partner’s project back months, because the trace phenol by-product blocked a downstream coupling. That drove us to strengthen our recrystallization regime and install in-line filtration every time.
Particle size sometimes features in our discussions, especially with teams planning solid-phase syntheses or scale-up. Some projects required us to customize granulation, but we discovered that for almost all laboratory and kilo-scale users, a fine crystalline solid with narrow particle size distribution works best for rapid dissolution and predictable reactivity. We package in inert conditions, as aldehydes are notorious for slow oxidation over time in ambient air, especially during long storage. Each shipment receives a tamper-proof seal and comes in chemical-resistant packaging designed after several cycles of customer feedback on product clumping and static attraction.
Similar-looking benzaldehyde derivatives exist, but switching one substituent—even a methoxy for a methyl—produces dramatic shifts in performance. Over the years, synthetic chemists have reached out for the 2-benzyloxy variant specifically because its benzyloxy group protects the adjacent oxygen while remaining removable through gentle hydrogenolysis without impacting the rest of the molecule. Competing molecules, like the 2-methoxy-4,5-dimethoxybenzaldehyde, introduce steric troublers during their transformations. Our customers found that with our product, cross-coupling with heterocycles proceeds with higher yields, and the downstream deprotection runs smoother, requiring milder conditions, saving both time and solvent cost.
Some projects started with the 3,4,5-trimethoxy series, drawn by abundant cheaper sources, but those alternatives supplied no good entry route when benzyloxy deprotection became necessary. Our hands-on feedback shows that this specific arrangement—methoxy, methoxy, benzyloxy—is a sweet spot for balance between solubility in organic reaction media and selectivity toward ortho-directed reactions. We supported a customer through several kilo trials where yield increases by almost 20% compared to earlier, more heavily substituted variants.
Anyone deeply embedded in fine chemicals, custom synthesis, or medicinal chemistry encountered benzaldehyde derivatives at some stage. This compound found its way into advanced intermediates for candidate drugs, specialty dyes, and even chiral catalysis research in top-tier academic settings. Over time, our compound played a role in synthesis projects involving oxidative cyclizations, multi-component assemblies, and as a critical intermediate in natural product analogues. It found value for teams who could not get similar quality or flexibility from a third-party reseller, because we tune our output for their success and applied use.
Our technical support team fields regular feedback from development chemists noting clean NMR after using our batch in their key steps, especially following condensation with nucleophiles or transformations through Wittig routes. Detailed conversations over structure–activity relationships drove us to refine our purification further, tightening every bottleneck in the flow from starting materials to prompt shipment. This approach benefits researchers racing patent clocks: they see fewer false starts, and react at scale with trust in the bridge between design and execution.
Making 2-Benzyloxy-4,5-Dimethoxybenzaldehyde safely and efficiently takes more than following literature descriptions. Early on, we worked through batch-to-batch inconsistency by identifying the biggest culprit: residual moisture picked up during one of the etherification steps. Over dozens of runs, we optimized drying cycles, improved the quality of input benzyloxy reagents, and designed a closed reactor system for the acid-catalyzed steps. We set up routine titanium-based filter checks to eliminate metal ion contamination, as even low parts-per-million iron can catalyze side oxidation, subtly changing the color and slowing downstream reactions.
We avoid cross-contamination by dedicating vessels to aromatic aldehyde synthesis, learned from costly errors trying to multi-task with polyaromatic compounds—trace impurities from earlier campaigns compromise both safety and downstream work. After we implemented full lot tracking and robust electronic batch records, we traced every out-of-spec issue back to a single point, and now run independent checks with each lot, communicating unprompted if anything drops outside our narrow spec window. This habit does more than build trust; it saves both us and our customers wasted time spent debugging unexpected reactivity or contaminant interference.
Our job rarely stops at the packaging line. When a longtime user once experienced unexplained color shifts during aging, our chemists assessed storage, transit, and application conditions together. Tracking back through shipping and lab records, we found direct sunlight during transport was the cause—an often-overlooked factor that degraded product over weeks. We updated our boxes for UV-blocking integrity and worked with the customer on storage protocols, winding up with more stable performance for their transformations.
Years of operational feedback teach more than any process manual. Recently, a customer sent samples of their own synthesized 2-Benzyloxy-4,5-Dimethoxybenzaldehyde that performed poorly; analysis found unusually high water content. Sharing technical know-how, we compared spectra, shared our rigorous Karl Fischer titration process, and helped troubleshoot their in-house setup. This combined effort saw both their process and our understanding deepen, helping us zero in on what matters most—reliably pure product that performs exactly as required, from milligram screening to kilo-scale runs.
Plenty of options exist online for chemical intermediates. Most come filtered through resellers or traders, sometimes repackaged multiple times and handled without context or oversight. Selling what we make, we answer for every atom—customers call and reach chemists who know the process, not a detached call center. Whenever an order fails analytical or application checks, we can dig into exactly when, where, and how it came from the line, and offer replacement or solutions rooted in detailed knowledge of both synthesis and end uses.
Our difference stands in open communication and willingness to re-engineer batches for specialty applications, including heavier lot sizes, tighter impurity controls, and feedback-driven logistics upgrades. Companies developing APIs regularly need regulatory documentation and lot-specific analytics; with manufacturing on-site, we can generate in-depth certificates of analysis showing not only standard purity checks but expanded heavy-metals and trace organic panels as requested. This level of transparency proves essential for moving from lab to pilot plant, and offers the confidence required for buying direct in an ecosystem where shortcutting even a single quality check brings disaster.
Being the producer, we see the direct footprint of every kilogram manufactured, down to the energy used in each distillation column and the recycling loops feeding back any unreacted starting material. Broader global pressures now mean responsible sourcing and waste minimization are not optional—they are baseline. We made major investments in solvent recovery and waste stream management, staying ahead of tightening regulation. During the last five years, we overhauled older processes to reduce both hazardous emissions and overall waste loading, meeting both local and international standards for environmental responsibility.
The chemical industry’s reputation rides on more than compliance; it’s about honest dialogue with users about both product stewardship and exposure risks. A first-time customer once asked for a detailed breakdown on exposure and downstream handling—rather than push a generic data sheet, our safety experts walked through every stage of their likely workflow, flagging points where aldehydes can irritate or where extra PPE means the difference between safe and risky work. Direct manufacturing means we stand behind every package and its safety, not just at receipt, but through the entire journey from synthesis through to waste disposal.
Innovation at the bench drives what we do on the shop floor. Several leading researchers approached us for variants suited to even more selective reactions, or with sterically bulkier protecting groups. Our R&D chemists work hand-in-hand with these teams, adapting our core processes to deliver derivatives on tight timelines, frequently scaling ideas from grams to kilos in less than a quarter. Owning the process lets us respond not only with speed, but with agility, making real-time changes to meet the next-generation synthesis needs.
At every stage, we keep an open line between users and synthesis experts. Process chemists, not call centers, give guidance and receive requests, ensuring product never loses its connection to true end use. By repeating these cycles of improvement, listening, and direct engagement, the result is more than a catalog item—it’s a partnership in advancing research and production alike. When a pharma lab needs rapid scale for pilot synthesis, or an academic group pursues a new reaction pathway, our immediate feedback and technical support lessen downtime and propel science forward, unencumbered by doubt or supply chain fog.
Quality, reliability, and open communication remain the foundation of everything we do with 2-Benzyloxy-4,5-Dimethoxybenzaldehyde. Supplying this compound year after year keeps both us and our customers ahead—through changing regulatory climates, evolving synthesis methods, and every curveball in fine chemical development. Being embedded in every aspect of production lets us respond to market shifts as they happen. The feedback loop from user to factory creates real improvements, whether in technical purity, logistics, packaging, or safety practice.
Our role does not end once product clears the loading dock; it extends through every reaction flask and chromatography column that our aldehyde passes through. Walking alongside customers through each new challenge, we create solutions that work in the real world, batch by batch, kilogram by kilogram, and result by result. That is the real measure of value in manufacturing 2-Benzyloxy-4,5-Dimethoxybenzaldehyde—not only consistent quality, but an ongoing commitment to the needs and realities faced by today’s chemical innovators.