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HS Code |
698933 |
| Iupac Name | 4-[(4-chlorobenzyl)oxy]-3-methoxybenzaldehyde |
| Molecular Formula | C15H13ClO3 |
| Molecular Weight | 276.72 g/mol |
| Appearance | Pale yellow solid |
| Melting Point | 109-111 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents like DMSO, ethanol |
| Cas Number | 287112-65-2 |
| Boiling Point | 419.1 °C at 760 mmHg (estimated) |
| Density | 1.24 g/cm³ (estimated) |
| Smiles | COC1=CC(=C(C=C1)OCC2=CC=C(C=C2)Cl)C=O |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Refractive Index | 1.604 (estimated) |
| Purity | Typically ≥98% (depending on supplier) |
As an accredited 4-[(4-Chlorobenzyl)Oxy]-3-Methoxybenzenecarbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle, securely sealed, labeled with product name, CAS number, and hazard symbols. |
| Shipping | This chemical is shipped in secure, chemical-resistant containers, clearly labeled according to hazardous materials regulations. It is transported in compliance with international guidelines for hazardous substances, with appropriate documentation, ensuring protection from moisture, heat, and direct sunlight during transit. Safety data sheets (SDS) are provided with all shipments. |
| Storage | Store 4-[(4-Chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and incompatible substances such as strong oxidizing agents. Keep the container tightly closed when not in use. Use only with proper ventilation and avoid inhalation, ingestion, or contact with skin and eyes. Store in a chemical safety cabinet if possible. |
Applications of 4-[(4-Chlorobenzyl)Oxy]-3-Methoxybenzenecarbaldehyde in Industrial Manufacturing4-[(4-Chlorobenzyl)Oxy]-3-Methoxybenzenecarbaldehyde is an essential intermediate with targeted applicability in specialty chemical manufacturing. Our facility supplies this material for specific, proven downstream processes where its chemical structure provides value for formulation consistency, product performance, and regulatory compliance. Below, we detail the principal industrial application scenarios for this compound and address the unique processing, quality, and compliance considerations relevant to each sector. 1. Synthesis of Pharmaceutical Building BlocksThis compound serves a critical role as a starting material for advanced pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) used in anti-inflammatory and cardiovascular therapies. Key processing steps require precise control over aldehyde selectivity and aromatic substitution to produce high-purity secondary intermediates that comply with stringent medication safety standards. Industry compliance standards
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2. Fragrance and Aroma Chemicals ProductionThe unique aromatic-ether structure of this material enables its use in the formulation of high-value fragrance bases and aroma compounds for both fine perfumery and functional consumer goods. Its reactivity supports controlled acetalization, allowing manufacturers to build novel aldehyde notes into sophisticated fragrance accords and enhance longevity in end-use products. Industry compliance standards
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3. Agrochemical Intermediate SynthesisThe compound’s chlorinated benzyl moiety and electron-rich aromatic framework support its function in the manufacture of select herbicidal and fungicidal precursors. Agrochemical producers utilize its structural attributes for building bioactive scaffolds that anchor further functionalization steps, ultimately resulting in crop protection molecules with regulated environmental profiles. Industry compliance standards
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4. Specialty Polymer Modifier ManufacturingThis material finds industrial use in the design of performance-modified polymers, imparting controlled polarity and aromaticity to resin matrices. Specialty polymer manufacturers exploit its reactive aldehyde for site-specific attachment, creating chain-terminated or pendant groups within coatings, adhesives, and electrical encapsulation formulations to meet stringent end-use property targets. Industry compliance standards
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As a chemical manufacturer grounded in decades of plant-floor reality and constant feedback from end users, we spend every day refining our understanding of raw materials. 4-[(4-Chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde, a compound with both complexity and utility, emerged from real-world demands characterized by specificity of reactivity, manageable stability, and application requirements traced to pharmaceutical and fine chemical intermediates. Each batch we produce owes its integrity not to automated repetition, but to continuous monitoring, human oversight, and measures that reflect both scientific and operational learning.
Our 4-[(4-chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde appears as an off-white to pale yellow solid, with a molecular formula of C15H13ClO3 and a molecular weight that supports efficient integration into larger molecular architectures. We measure all product lots to confirm melting point within a defined narrow range, maintaining rigorous control over water content, residual solvents, and trace impurities. Consistency from batch to batch is not simply a promise—it is a byproduct of cumulative effort from our in-house analytical and production teams.
Structural features, such as the fused benzyl ether and methoxybenzaldehyde moieties with a para-chlorine atom, allow for specific reactivity that would not be achievable with closely related aldehydes or ethers. Those variations matter; the downstream synthesis steps in client labs often pivot on these differences. Our customers report cleaner coupling reactions and less byproduct formation compared to reactions that rely on less defined or less pure analogues.
Every chemist who enters our workspace brings years of hands-on familiarity with organic synthesis. We know, from monitored trials, that this compound’s reactivity profile can diverge sharply from those of simple benzaldehydes or unsubstituted analogues. This makes direct substitutions risky business; subtle shifts in electronic or steric environment carry outsized impact in scale-up chemistry.
End-users, particularly those in medicinal chemistry, often pursue this compound for its selective role as a key intermediate in synthesizing pharmaceutical candidates and specialty chemicals. Its resonance-stabilized backbone and the electron-withdrawing effect of the chlorine atom often contribute to regioselective reactivity not reproducible with alternative compounds. Attempts to shortcut to other aldehydes or swap the chloro-benzyl ether for less hindered ethers typically show reduced yields and, more importantly, unpredictable side product profiles. Data from direct comparative syntheses highlight lower purification burdens and more straightforward downstream transformations when our 4-[(4-chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde is used over less advanced analogues.
Quality in chemical manufacturing owes more to wisdom gathered through troubleshooting than to adherence to standard operating protocols alone. We recognize that residual solvent levels, water content after crystallization, and trace contaminants like unreacted aldehyde or chlorobenzyl alcohol drive differences at application scale. To prevent downstream operational headaches, we continually refine our work-up and purification cycles. For instance, our improved vacuum drying regimens and solvent washes directly reduce time spent on purification in our customers’ processes.
Years of customer feedback have highlighted avoidable pitfalls in raw material sourcing. Chemists using material sourced from traders or batch aggregators often encounter batch-to-batch volatility—inconsistent purity, fluctuating melting points, haze or off-color appearance, and wide swings in HPLC retention times. Feedback from one pharmaceutical pilot plant revealed that a supplier change led to batch failures traceable directly to invisible contaminants in their intermediate. After switching to our tested production stream, they noted 100 percent pass rates on both analytical and functional benchmarks for over a year of consecutive lots.
Subtle differences define the fate of an entire synthesis route. Our 4-[(4-chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde offers a reliable choice for aromatic substitution and etherification steps, but this reliability is no accident. Within the ether linkage and para-chlorine position lies a balance of stability and reactivity shaped specifically for select synthetic transformations. The methoxy group at the three-position dampens unwanted electrophilic side reactions, while the protected aldehyde function allows for stepwise extension under both basic and acidic conditions, something not matched by less well-defined or more labile aldehydes.
Cost-conscious chemists sometimes try to substitute with generic or less refined analogues—4-chlorobenzaldehyde, or even bulk 4-hydroxybenzaldehyde derivatives. In real-world production, these choices lead to more side-product formation and loss of yield in later reaction stages. More time gets spent troubleshooting, filtering, and trying to salvage intermediate steps. The stability profile and low impurity background in our compound safeguard project timelines and budgets, a fact reported repeatedly by process engineers scaling from gram to multi-kilogram quantities.
Numbers tell a story. Across the last several years, customer audits and internal quality controls have converged around a set of benchmarks. Our material consistently yields a GC purity of 98.5 percent or better, water below 0.2 percent, and minimal detectable levels of related benzyl alcohol and methoxy impurities by HPLC. These numbers were not reached in a vacuum; they stand atop hundreds of process improvement cycles, analytical cross-checks, and collaborative troubleshooting with our partners.
Real chemistry never unfolds in isolation from its supply chain. When our customers describe failed reactions, unexpected byproducts, or inconsistent project outcomes, investigation usually leads back to trace impurities—sometimes below the threshold detectable by routine analysis. We have learned to probe deeper, refining our purification and doing side-by-side reaction trials until benchmarks are truly met. That learning process gives our product real functional value compared to aggregators who blend material from multiple sources, often masking those troublesome variances.
Feedback rhythms from the grassroots of organic synthesis—pilot runs, scale-up trials, lab notebook entries—drive our priorities. Each synthesis project that uses our 4-[(4-chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde feeds a feedback loop: Does the compound perform to expectation? Do side reactions crop up unexpectedly? Have solvent exchange issues affected crystallization, or do isolate yields meet targets?
Through these field reports, we collect actionable data. One pharmaceutical group shared how switching to an alternative supplier delayed project timelines by requiring extra purification at nearly every downstream step, only to discover trace levels of unreacted benzyl chloride contaminant and off-spec melting range. After supply was reestablished with material from our production, those issues disappeared. Such experience builds not just trust, but a process knowledge repository within our team, and it deepens our commitment to both transparency and rigorous internal review.
Real decisions take place at kilo-lab scale, not just in analytical sample vials. Chemists face constraints—equipment, storage, waste, reagent availability. Over the years, we've witnessed pitfalls in storage stability with related benzaldehyde intermediates, particularly those prone to oligomerization or oxidation. This compound, by contrast, shows a favorable shelf-life under routine conditions, retaining its defined melting profile for months, even in uncontrolled environments, such as transport or warehouse storage.
Practical packaging solutions followed from accumulated shipping experience. Standard containers can excess moisture or allow interaction with atmospheric oxygen, neither of which shows up in pure data sheets. Our team trialed multiple closures and liners, selecting those with the lowest moisture migration rates after real-world field tests. These changes resulted in measurably improved product recovery, lower caking, and maintained reactivity profiles on delivery.
Handling practice varies by sector, but our input often involves consultations on safe addition techniques, solvent compatibility, and waste reduction. Feedback helped hone batch production schedules, recommending that users prepare their reaction charge soon after opening to avoid unnecessary exposure and surface area-related decomposition. These details are born from both our experience and collective project data, not hypothetical scenario planning.
We did not set out to simply provide another aromatic aldehyde. Peer comparisons against similar compounds clarify what’s at stake. For instance, manufacturing with 4-hydroxybenzaldehyde derivatives or basic 4-methoxybenzaldehyde often introduces instability under base-catalyzed or strongly acidic conditions. We have tracked syntheses where the difference between success and failure boils down to how the ether linkage mediates both solubility and resistance to unproductive side reactions.
By keeping attention on real-world use and process robustness, we avoid a singular focus on any one property in isolation. Feedback from routine application, such as Suzuki couplings, ether cleavages, or chiral intermediate preparation, demonstrates how slight modifications—an extra methoxy, a para-chlorine, or a different benzyl group—lead to tangible gains or losses in project efficiency. Customers seeking to switch to cheaper or older grade materials often zero in on cost savings, then return to our product after running comparative trials. Purity, though critical, does not substitute for true consistency across process cycles.
We have moved past initial production hurdles and entered a stage of relentless refinement. Every stage, from raw material selection through to packaging, gets shaped by incidents, both positive and negative. A minor oxidation event years ago resulted in an overhaul of our transfer protocols. Occasional off-color crystals prompted an investigation into post-synthesis precipitation solvents, which now undergo annual review. Delays in logistics revealed the value of robust container selection and tracking.
Mixing theory with practice, we recognize that high-purity intermediates serve as linchpins in both pharmaceutical discovery and advanced materials synthesis. Side reactions rob chemists of progress; impurities complicate regulatory submissions and process validation. Our approach to 4-[(4-chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde emphasizes real-world trade-offs: investing upstream to save time and trouble downstream, and refining techniques based on what actually works rather than sticking rigidly to tradition.
Through all these efforts, our product has taken on a life defined by both feedback and adaptation. Distant relational descriptions from third-party spec-sheets rarely measure up to the systems thinking and iterative learning found on a working plant floor. We found that even minor deviations in cleaning protocols could impact LCMS background noise, and we responded by building staff awareness into our ongoing training.
Direct engagement with customers, whether over an R&D bench or via remote troubleshooting, makes up the backbone of our value chain. Our staff’s hands-on interaction with the compound during production—smell, visual cues, solubility checks—helps catch deviations invisible to machine-based QC.
Many users arrive at our doorstep after process failures traceable to uneven quality intermediates or uncertain supply chains. Recurring pain points include unwanted residue after attempted purifications, inconsistent reaction rates, or unpredictable yield reduction. These operational stories shaped our work to strike a balance between high standards and practical deliverables.
Open communication, rooted in a shared language of synthetic chemistry, lets customers relay reaction mishaps or unplanned side reactions. Our production and technical teams dig into both their notebooks and our archives of field feedback, aiming to translate experience into incremental product improvements. Everyone gains: the lab chemist with tighter yields, the process engineer with fewer breakdowns, and regulatory teams who gain confidence through robust reproducibility.
In the rapidly changing landscape of fine chemical manufacturing, adaptation must match technical rigor. Continuous dialogue with end users only grows more important. Rather than chasing the latest marketing trend or technical buzzword, we keep eyes on what matters in on-the-ground chemistry—stability over shipment, predictable reactivity in key transformations, and the ability to support scale-up without unhelpful surprises.
We avoid complacency by anchoring product evolution in process data, field feedback, and targeted laboratory investigation. Each adjustment—finer filtration media, an additional crystallization run, re-tested packaging—arises not from guesswork, but from field-proven need. Finished product that consistently saves chemists from troubleshooting earns loyalty the only way that matters: by freeing projects to move, not clogging workflows with new variables.
The true difference between chemical sources only appears after repeated use under real conditions. Our product stands as a refined, reliable offer because it comes not just from process design, but from lessons gathered batch by batch, challenge by challenge, and success story by success story. Chemistry, as it unfolds in plants, warehouses, and R&D labs, leaves no shortcuts for anyone. Reliable results stem from diligence, learning from setbacks, and constant, informed adaptation.
For us, 4-[(4-chlorobenzyl)oxy]-3-methoxybenzenecarbaldehyde represents not just an entry in a catalog, but a benchmark for how rigorous, iterative, and grounded development keeps the next project moving forward.