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HS Code |
666749 |
| Iupac Name | 4-[(2,4-dichlorobenzyl)oxy]benzaldehyde |
| Molecular Formula | C14H10Cl2O2 |
| Molecular Weight | 281.14 g/mol |
| Cas Number | 37126-13-3 |
| Appearance | White to off-white solid |
| Melting Point | 109-113°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1)OCC2=C(C=C(C=C2)Cl)Cl)C=O |
| Inchi | InChI=1S/C14H10Cl2O2/c15-12-6-5-11(7-13(12)16)8-18-14-3-1-10(9-17)2-4-14/h1-7,9H,8H2 |
As an accredited 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25 grams of 4-[(2,4-Dichlorobenzyl)oxy]benzaldehyde; sealed, labeled with hazard symbols and product details. |
| Shipping | 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde is shipped in tightly sealed, chemical-resistant containers, clearly labeled with hazard information. The package should be protected from moisture, light, and extreme temperatures. Transport must comply with applicable regulations for hazardous chemicals, ensuring safe handling and storage during transit to prevent leaks or contamination. |
| Storage | Store **4-[(2,4-Dichlorobenzyl)oxy]benzaldehyde** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep it at room temperature and protect from excessive moisture. Ensure proper labeling and store on dedicated shelving to prevent accidental contact or mix-ups with other chemicals. |
Applications of 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde in Industrial Manufacturing4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde is an advanced specialty intermediate widely adopted in targeted high-value synthesis sectors. Below, we detail its industrial applications where the material delivers process-specific benefits and compliance assurance for manufacturers scaling downstream operations. 1. Pharmaceutical Intermediate for Antifungal APIsThis compound functions as a critical intermediate in the multi-step synthesis of certain imidazole- and triazole-structured antifungal active pharmaceutical ingredients. Its specific chemical reactivity supports the introduction of aromatic aldehyde and dichlorobenzyl moieties required for the pharmacophores of proprietary antifungal molecules. Industry compliance standards
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2. Fine Chemical Synthesis for UV-Absorbing AgentsAs a building block in the synthesis of specialized benzaldehyde-derived UV-absorbing agents, this material supports the introduction of dichlorinated aromatic functional groups required in photostable compounds used for industrial and specialty coatings. It enables control of reactivity and compatibility during multi-stage protection and deprotection cycles integral to product recipes. Industry compliance standards
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3. Synthesis of Agrochemical Active IngredientsThe material plays an essential role as a precursor in the tailored synthesis of select fungicide and herbicide actives, where its dichlorinated aromatic structure strengthens bioactivity and supports molecular stability under field exposure. Its reliable batch consistency underpins the scalable synthesis of advanced agrochemical molecules for regulated markets. Industry compliance standards
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4. Functional Dye Intermediate ManufacturingThis benzaldehyde derivative serves as a highly specific functional intermediate in the manufacturing of advanced diarylmethane and triarylmethane dyes. The dichlorobenzyl-oxy segment imparts improved color fastness and enhanced compatibility for electronic display and specialty textile dye formulations, especially where color stability under UV or oxidative environments is critical. Industry compliance standards
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As a producer of specialty intermediates, we often focus our research and daily operations on unique chemical structures that bring clear benefits to formulation scientists and industry partners. 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde stands out as one of these purposeful molecules. Its architecture—a benzaldehyde core connected through an ether bridge to a dichlorinated benzyl group—opens up performance properties you don’t always see in more basic aromatic aldehydes.
In our experience, the presence of the dichloro substitution at the 2 and 4 positions on the benzyl segment imparts distinct physicochemical qualities. It shows greater resistance to oxidative conditions and keeps a reliable melting point over repeated batch production. Chemists notice the subtle differences that these chlorine atoms offer, especially in product stability and overall formulation compatibility.
The journey starts at raw material selection. Controlling isomeric purity is non-negotiable, and our teams have learned not to cut corners. Running this molecule through its paces in acrylic-based coatings, we’ve found that the aldehyde function can participate in targeted reactions, benefiting crosslink density while allowing for phase separation control. Its hydrophobic character, which comes from the dichlorobenzyl group, influences how it disperses and remains stable in water-based suspensions. This pays off in shelf-life and appearance, addressing issues we remember encountering with simple benzaldehyde derivatives in the past.
Customers bring us new ideas, so we’ve seen this molecule show up in more than just coatings. In the synthesis of active pharmaceutical intermediates, the molecule’s unique electronic features mean it behaves predictably during condensation or reduction steps. Protective group chemistry sometimes challenges formulation timeframes, but with current synthetic routes we see this product maintain low variance in impurity profiles. This saves hours of troubleshooting and supports compliance, putting it in another league compared to standard aromatic aldehydes.
We’ve spent years refining our production lines with both small-scale and multi-ton batches. The product commonly appears as an off-white to pale-yellow crystalline solid. We keep minimum purity at 98% as measured by HPLC, with a water content below 0.5%. These are not arbitrary numbers. Early on, we saw how even slight moisture uptake could lead to side reactions during end-use blending, so we reinforced our drying and storage protocols accordingly. Our analytical group runs retention sample checks far past legal requirements, minimizing digressions that can cost time and create waste in downstream processing.
Customers who demand traceability appreciate our consistent spectral fingerprints. UV/VIS, FTIR, and NMR characterization come standard, with each batch retaining a comprehensive profile for at least 5 years. In one instance, a client flagged an unusual odor that traced back not to our batch, but to a contaminated vessel on their production floor—a detail only clarified because of long-term IR recordkeeping on our side.
Handling production ourselves, rather than handing it off to third parties or resellers, gives us direct feedback and control. We know at any hour what’s running through the reactors and what QC is picking up. Adjustment cycles are faster because everyone from R&D to plant maintenance sits down together. A trader or distributor rarely sees what it takes to correct a subtle color drift at the micron scale, but in manufacturing, the reality becomes part of daily decisions.
Chlorination steps require strict safety and environmental vigilance. We use a closed-loop system for handling both reagents and waste streams, informed by years of environmental audits. Effluent is treated in-house. Colleagues in quality management push us to stay ahead of local regulations, and those habits build confidence with customers who ask about supply chain transparency and sustainable practices.
Over decades, the aromatic aldehyde category has become crowded, but few structures offer the unique blend of reactivity and resistance found here. In typical benzaldehyde, oxidizing or reducing conditions can drive unwanted by-products. The dichlorinated benzyl ether connection in our compound steps up stability and shifts electron density throughout the molecule. This has a measurable effect: the rate of aldehyde group side-reactions drops noticeably, particularly when exposed to alkali or in multi-step syntheses under mild heat. At the bench, this translates into fewer surprises for chemists and reduced demands on purification steps.
Some customers have tested direct substitutions in their protocols, swapping out simpler benzaldehydes. They noticed a marked improvement in final yield, due in large part to the reduced volatility and enhanced shelf-life of 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde. In some fine fragrances or flavor intermediates, where trace impurities matter, the cleaner impurity profile has been a recurring advantage.
Our R&D team works with both newcomers and seasoned chemists. In resins, the compound's physical dimensions and polarity reduce compatibility issues across a range of solvents. It keeps particulate size distributions tighter during processes like spray drying or granulation. On one project, a formulation engineer wanted to blend this intermediate with urea-formaldehyde resins for high-performance adhesives. Adjustment of resin ratios yielded a surprising gain in tack time and hot-press stability—improvements directly linked to the molecule’s subtle balance between nucleophilic and electrophilic sites, boosted by the dichloro effect.
Feedback cycles with our customers help identify pain points. For companies trying to extend the life of applied films or coatings, the molecule’s resistance against ambient humidity and UV breakdown shows up as fewer surface defects after accelerated weathering. These experiences repeat across various industries: in pigment dispersions, the product helps prevent precipitation; in biologically active intermediates, its structure reduces unwanted side-reactions, which lowers purification costs and increases throughput.
Chemical safety goes beyond a line on a safety data sheet. Our team recalls early storage tests, where a poorly sealed container led to detectable losses in aldehyde activity. Tight control of temperature and moisture levels became central to preventing hydrolysis or oxidation. Today, all our product leaves the facility in containers internally lined for compatibility, and we recommend consistent cool, dry storage up to two years for best results.
Unloading at customer sites sometimes raises questions about dust caking or container residues. Experience taught us simple switches—using flushable liners and tailored shipping units—prevented technical headaches down the line. Our logistics team checks documentation at every handoff, looking for details that traders often consider outside their scope.
Investing in robust QC labs has changed our business. From benchtop GC-MS units through advanced chromatographic fingerprinting, our facility checks for isomeric identity and potential chlorinated byproducts at every step. In the past, unknown traces in competitor samples led to batch failures on customer lines. Those instances drove our decision to invest in additional quality checkpoints.
By tying analytical output to feedback from our production team, we cut down on recall risk and improve reliability. The process keeps us closely connected not only to our own staff, but also to our end users, who rely on predictable performance in their daily workflows.
It’s all too common in the chemical industry to blame batch variability on upstream supply. Directly controlling both sourcing and final synthesis means problems come straight to us—and get solved within days instead of weeks. In one case, shifting to a higher-purity chlorinating agent eliminated recurring issues with residual odorous compounds that plagued users downstream.
We look for chances to convert minor-process waste into useful by-products, and our plant’s heat-recovery system reflects a move toward smarter, less wasteful manufacturing. Sustainability expectations only get stricter. We have systems in place to track solvent recovery and hazardous emission reductions, reassuring users who document sustainability claims for their customers as well.
In a side-by-side test, downstream partners found that our 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde offered more reliable performance in the synthesis of complex pharmaceuticals and specialty polymers than alternatives sourced from outside manufacturers. A typical benefit stems from lower levels of trace organic residues—each batch showing cleaner chromatograms—driven by meticulous internal controls each step of the way.
By opening our labs to visiting client researchers, we benefit from direct discussion and knowledge sharing. In many cases, customer trials become collaborative projects, with our team offering process tips based on years of reactor troubleshooting and analytical work. Some users in the electronics sector have asked about consistent dielectric properties and surface reactivity; in these settings, the molecule’s dichloro-charged benzyl group offers advantages in chemical stability while bonded to sensitive substrates.
Formulators appreciate access to detailed technical history on every lot delivered. Our documentation covers not only purity but trace residuals down to sub-ppm. The point isn’t to overwhelm, but to back up claims on quality and performance with verifiable data. As regulations shift—especially in health-sensitive uses—this transparency makes the difference for clients whose business relies on documented outcomes.
Managing the complexities of a specialty intermediate like 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde relies on years of hands-on learning. From batch-to-batch scaling, to finding the right conditions for maintaining color and odor stability, our shop-floor teams have identified the recipes and checklists that bring stable, high-quality product every month. This experience translates to fewer headaches for customers who expect reliable supply even during market disruptions.
Equipment maintenance taught us about the importance of minimizing metal contamination in every batch. We upgraded to high-purity liner materials and re-trained operators to recognize the faintest changes in product profile, resulting in the ability to deliver lots with repeatable analytical signatures. Market volatility and supply chain challenges show up regularly. Having the full process under one roof lets us buffer against raw material shortages and address new requests proactively rather than reactively.
Improvement never ends. Our process team attends international conferences and works with academic partners to refine synthetic methods and waste reduction strategies. We’ve incorporated digital monitoring to catch process drifts earlier. This leads to real-world gains for users, including faster order turnaround and fewer concerns over off-spec material.
We’ve learned that detailed, honest dialogue with customers builds long-term trust. If a sample doesn't meet spec—even for reasons outside our control—we communicate quickly and propose corrective actions based on real understanding, not generic apologies.
Through decades of direct manufacturing, our team has seen the business evolve. 4-[(2,4-Dichlorobenzyl)Oxy]Benzaldehyde has played a role in everything from new drug molecules to robust performance coatings. Because we design and operate every step—from synthesis to quality control to delivery—we support product consistency in ways that traders and resellers can’t match.
Direct insight into end-use applications pushes us to anticipate client needs. With every run, we use the latest operational experience to improve outcomes not only for ourselves but for the formulation chemists and process engineers counting on us across industries. In our opinion, the difference isn’t just what the product is, but how it’s made and the experience that stands behind it. This shared learning defines the real value of specialty manufacturing today.