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HS Code |
125186 |
| Iupac Name | 4-(3-Methoxyphenyl)benzaldehyde |
| Molecular Formula | C14H12O2 |
| Molar Mass | 212.24 g/mol |
| Cas Number | 51125-36-9 |
| Appearance | White to off-white solid |
| Melting Point | 106-108 °C |
| Solubility In Water | Slightly soluble |
| Functional Groups | Aldehyde, Ether (methoxy), Aromatic rings |
| Smiles | COC1=CC=CC(=C1)C2=CC=C(C=C2)C=O |
| Inchi | InChI=1S/C14H12O2/c1-16-14-6-2-5-13(10-14)12-7-3-11(9-15)4-8-12/h2-10H,1H3 |
As an accredited 4-(3-Methoxyphenyl)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 25 grams of 4-(3-Methoxyphenyl)benzaldehyde, labeled with product and safety information. |
| Shipping | 4-(3-Methoxyphenyl)benzaldehyde is shipped in tightly sealed containers under cool, dry conditions, compliant with standard chemical transportation regulations. Packaging ensures protection from moisture, sunlight, and physical damage. Hazard labeling and documentation accompany the shipment. Handle with care to prevent exposure or leaks during transit. Intended for laboratory and research use only. |
| Storage | 4-(3-Methoxyphenyl)benzaldehyde should be stored in a tightly sealed container, away from light, heat, and moisture. Keep the container in a cool, dry, well-ventilated area, designated for chemicals. Ensure it is separated from oxidizing agents and acids to prevent unwanted reactions. Properly label storage containers and adhere to standard safety guidelines and local chemical storage regulations. |
Applications of 4-(3-Methoxyphenyl)Benzaldehyde in Industrial Manufacturing4-(3-Methoxyphenyl)Benzaldehyde serves as a key intermediate in multiple advanced chemical manufacturing routes. Our facility supplies this compound through validated, high-efficiency processes to support stringent downstream applications. Below, we outline main industrial use-cases with specific compliance, dosing, integration points, and finished goods information relevant for technical decision-makers. 1. Pharmaceutical Intermediate for Antihypertensive Sartan APIsManufacturers of antihypertensive APIs, such as Valsartan and Irbesartan, utilize 4-(3-Methoxyphenyl)Benzaldehyde in the biphenyl synthetic pathway. The compound acts as an essential building block during the condensation and cyclization sequences required for tetrazole ring formation. Dedicated GMP process lines use this intermediate to maintain strict batch reproducibility and meet international API quality benchmarks. All batches undergo full traceability documentation and impurity profiling aligned to current pharmacopoeia standards. Industry compliance standards
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2. Synthesis of High-Performance Liquid Crystal MonomersProducers of advanced liquid crystal display (LCD) materials use this compound as a core aldehyde component for building biphenyl architectures in high-purity liquid crystal monomer synthesis. The unique ring-substituted structure imparts desired optical and phase transition properties. Manufacturing facilities apply advanced purification and multi-step organic conversions to achieve target isomeric ratios and minimize elemental impurities per electronics industry guidelines. Industry compliance standards
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3. Advanced Agrochemical Synthesis – Fungicide IntermediatesAgrochemical formulators incorporate this benzaldehyde as a precursor for producing key active intermediates in the azole and phenyl ether fungicide segments. The methoxy-substituted structure increases process selectivity in Grignard additions and subsequent methoxylation reactions. Manufacturers rely on this intermediate to control final structure-activity relationships in field-ready crop protection chemicals. Industry compliance standards
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4. Scent and Fragrance Aldehyde for Fine ChemicalsFragrance compound blenders use 4-(3-Methoxyphenyl)Benzaldehyde as a specialty ingredient in the synthesis of complex aromatics for high-end consumer fragrances, soaps, and detergents. Its specific aromatic profile enables the development of modern aldehydic notes, supporting product lines that require stable, long-lasting scent. In fully controlled industrial perfumery lines, this ingredient undergoes batch-specific blending and analytical testing for consistency in olfactory and purity profiles. Industry compliance standards
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5. Custom Specialty Polymer Additive ProductionSpecialty chemical producers apply this benzaldehyde derivative to the synthesis of functionalized monomers for niche polymer systems, such as high-performance adhesives, electrically conductive resins, and coated films. The reactive aldehyde group enhances compatibility in free-radical and condensation polymerization processes. Facilities ensure consistency in input material through advanced in-line spectroscopy and batch release according to application-critical polymer property parameters. Industry compliance standards
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Walking through the plant floor, you find a handful of raw materials that truly shape high-value chemistry. 4-(3-Methoxyphenyl)Benzaldehyde stands out. We know it both by molecular structure—C14H12O2—and by the role it plays in fine chemistry. In our operation, we developed process controls to produce it at purity ratings typically above 99%. Most batch yields fall within standard lot tolerances because reactions have been optimized through years of hands-on experience. We engineer our systems to ensure minimal trace metal contamination and tightly track moisture levels, both of which can influence downstream steps in pharmaceuticals, agrochemical intermediates, and specialty polymers.
The backbone of 4-(3-Methoxyphenyl)Benzaldehyde combines a benzaldehyde group with a methoxy-substituted phenyl. This configuration, crafted through controlled oxidation and coupling pathways, gives the molecule versatility. If you compare batches sourced from different manufacturers, even minor differences in purity, residual solvents, and isomeric content end up influencing outcomes for those producing target molecules like active pharmaceutical ingredients or specialty dyestuffs.
Our long-term clients often target synthetic routes where positional selectivity matters. 4-(3-Methoxyphenyl)Benzaldehyde regularly enters into Grignard reactions, Wittig condensations, or aldol additions. In pharmaceutical intermediate labs, chemists count on the clean aromatic profile and stable aldehyde group. With the methoxy moiety at the meta position, steric and electronic effects bring predictable reactivity. That reliability lets downstream processes move without frequent troubleshooting or need for extra purification steps.
In large-scale pharma synthesis, certain building blocks develop reputations for either unpredictable yields or difficult extractions. Through direct plant feedback—often from small pilot runs—we adjusted our synthesis procedure for 4-(3-Methoxyphenyl)Benzaldehyde to limit byproduct formation. We eliminated old distillation techniques with newer, more selective methods, resulting in sharper melting point ranges. Over time, quality managers saw downstream crystallizations become easier to control, with less incidence of colored impurities. Teams developing new dye molecules benefit when aldehyde feeds show consistent color and minimal residual solvents, helping their process chemists avoid time-consuming post-purification.
We assign each production batch a unique internal code, traced from raw material intake to finished product shipment. Typical product appears as an off-white powdery solid, with melting points ranging 82-85°C. Trace analysis for related impurities happens on every lot released for shipment. Consistency here matters—narrow melting range reflects not just good practice but real operational discipline. Some downstream users find even sub-percent variances in melting point affect their own reaction controls. By making such testing routine, we help other chemists rely on uninterrupted flow in their projects.
On the production line, experienced operators stress solvent handling and temperature control. Small variations in reaction exotherms—sometimes missed on paper—affect batch-to-batch uniformity. We learned by running successive kilograms under different agitation rates and heating profiles, which gave us better control over reaction kinetics. These successes stemmed from feedback loops: onsite process chemists track product performance during coupling reactions or reductions, reporting what worked, where blocks happened, or which lots showed best results. Few documents capture these micro-adjustments, yet they make long-term manufacturing reliable.
In chemical manufacturing, process changes ripple throughout the value chain. Some years ago, we faced repeated reports of trace yellowing in benzaldehyde samples, traced back to incomplete scavenging during work-up. Rather than mask the problem, we redesigned the work-up stage—added more selective filtration beds, adjusted pH, and lowered residence time in potentially reactive environments. Once adopted across all reactors, subsequent finished lots showed cleaner appearance measurements, which reduced customer complaints on color-critical applications.
Many buyers, often in pigment synthesis or pharmaceutical R&D, maintain incoming material specs that stretch beyond generic “purity.” They test not just for GC purity but for absence of side-chain isomerization products or unexpected hydrocarbon contaminations. For them, our in-house control over the full synthetic route becomes a mark of trust: they send challenging analytical requests, and we trace down root causes, running side-by-side with their teams. Handling specialty aldehydes, we don’t rely on contract intermediates. This internal control lets us address problems in real time instead of running through bureaucratic bottlenecks or unclear supply chains.
Customers sometimes ask why a compound like 4-(3-Methoxyphenyl)Benzaldehyde falls in price brackets seemingly higher than more basic aromatics. The answer lies in batch controls and facility resources. While we craft hundreds of kilos per month, each lot passes acceptance only after meeting thresholds not everyone enforces. By maintaining small to mid-scale reactors, we keep conditions homogeneous, ensuring consistent heat transfer and stirring. Larger batch sizes often invite uneven temperature profiles, risking hot spots and decomposed product. We stick to what keeps both the plant and customers aligned on quality goals.
Choose a standard chemical supply catalog, and you find technical grade aldehydes made for general industrial use. Yet, most of our-client inquiries chase higher-purity lots, down to parts-per-million for both residual solvents and metal contaminants. For more complex organics synthesis, where each impurity can lead to expensive downstream failures, those last refinements matter. Our plant’s analytical team grew over the years alongside production. Today, each product release comes with a full analytical dossier: GC, HPLC, targeted mass spectrometry, and element-specific ICP analysis. These records take time, but open the doors to sectors like regulatory pharmaceuticals and advanced materials research.
A few years ago, a specialty polymer manufacturer requested a direct comparison with para- or ortho-methoxybenzaldehyde derivatives. Each isomer shifts both the electronic landscape and reactivity, causing varying rates in condensation or addition reactions. We run our own head-to-head syntheses, tracking yields, side reactions, and work-up requirements. The meta-methoxy group in 4-(3-Methoxyphenyl)Benzaldehyde, for instance, balances electronic activation without pushing uncontrolled polymerization or causing faint color bodies. This lets users tune their synthesis parameters—an advantage lost with less tailored benzaldehyde precursors.
Another subtlety: during routine scale up, the meta isomer consistently avoided some of the stubborn resinification or dimer formation often found with alternative substitution patterns. These behaviors matter more than small cost differences; they mean fewer costly reworkings and more predictable purity in the finished products.
Clients increasingly press us about manufacturing sustainability. They ask for information on waste handling, energy consumption, and greener synthesis steps. We take these requests seriously, having converted a portion of our upstream sourcing to include renewable feedstocks. During one such shift, we moved solvent recovery to a closed-loop system and dropped overall VOC emissions by more than half. These investments arise from both regulatory changes and genuine commitment inside our operations team, not just market trends.
We also participate in several collaborative research projects, benchmarking our process streams against industry best practices. Data from these efforts guide real investments—like onsite solvent recycling, energy recovery from exotherms, or transition to lower-impact catalysts. Such real-world implementation only works when engineers, operators, and laboratory chemists have direct say in redesigning process lines. For a relatively niche intermediate, reducing carbon and chemical footprints remains a work in progress, yet tangible reductions now appear year-on-year.
Users in the lab or at pilot scale often face two practical issues: controlling atmospheric exposure during sampling, and solubility for downstream steps. Our team ran storage stability tests in a range of container materials, from standard HDPE to amber-glass and lined steel. Data show the compound holds well under low humidity, sealed conditions, but aldehydes show some natural reactivity to trace oxidants. For formulators, dealing with color drift or precipitation sometimes means redissolving with polar aprotic solvents or adding inert gas blanketing. We provide informal guides built from operator experience—how best to handle short-term storage or avoid cross-contamination, gleaned from running hundreds of lots through actual warehousing and shipping routines.
In our facility, small changes like double-sealing primary containers, using controlled atmosphere rooms, and staging quick transfers between units reduced the frequency of off-color complaints. These low-tech solutions came by listening directly to technical users, not from generic shelf-life tables.
We’ve shipped 4-(3-Methoxyphenyl)Benzaldehyde to dozens of different sectors, but most projects fall into a few categories: pharmaceutical intermediates, advanced pigments, and polymer building blocks. End-users often run exploratory chemistry, modifying this aldehyde into bespoke products. A key expectation—beyond the datasheet properties—is reliability from lot to lot. Organizations running clinical research or scale-up campaigns have no patience for surprises tied to subtle changes in feedstock. For newcomers scaling up for the first time, we offer walkthroughs on adjusting reaction parameters at kilo scale, sharing our own history of both smooth runs and unexpected bottlenecks.
The gap between bench chemistry and full-batch operations always brings hidden risks. Our staff chemists—each with years refining this particular aldehyde—advise both R&D partners and production engineers on how to anticipate subtle shifts in reaction outcomes. Trials run over dozens of scales showed where to expect thermal runaways or secondary colored impurities, which analytical methods flagged these, and how to mitigate them before they become yield-stealing or compliance-blocking.
Such collaborations help both sides: researchers reduce guesswork, while our manufacturing teams find new avenues for incremental improvement. An R&D partner once flagged a trace impurity barely above detection threshold. By cross-referencing archived analytical runs, we reworked part of the isolation step, eliminating a future blockage before it appeared at larger scale. Progress in these projects rarely appears in published literature, but it fundamentally changes both product consistency and end-use confidence.
Markets opening for new medical entities, specialty polymers, or pigments mean regulation grows stricter every year. Our quality and regulatory compliance staff interface with industry groups to understand what documentation end-users expect now and two or three revisions down the line. Each lot of 4-(3-Methoxyphenyl)Benzaldehyde carries traceability down to individual raw material and process step—an approach developed originally for large pharma customers, now adopted everywhere. Our documentation spans the results of process audits, change control logs, and region-specific reporting, drawing from real-world manufacturing data.
We routinely prepare product to comply with audits from European, North American, and Asian regulatory bodies. Such diligence isn’t just about satisfying checklists; it came about as a response to on-site audits, real inspectors, and feedback from users needing paper trails for their own approvals. This practice sets our materials apart from open-market competitors, who sometimes deliver adequate material, but without the robust record-keeping and control frameworks customers here have come to trust.
We see improvement as a cycle, not a box-checking exercise. For 4-(3-Methoxyphenyl)Benzaldehyde, each process update—however small—feeds into production and back out to the users. We keep communication channels open across function lines: R&D chemists, production operators, QA analysts, logistics coordinators. Lessons from challenging batches trigger internal reviews. Operators note unfamiliar thermal profiles, QC flags a drift in GC retention times, or a buyer reports a slight change in solubility profile. Every new data point makes the next lot more secure, creating a culture where updates don’t disrupt, but strengthen, how we define “standard” quality.
Actual manufacturing, distinct from third-party trading or repackaging, brings a unique duty: every production decision shapes both internal safety and external supply reliability. By investing in experience—training, teamwork, shared lessons—we keep our operations nimble enough to evolve as markets and expectations change. While much happens behind closed factory doors, the trace comes out in every batch shipped. We hope this commitment shows, bottle after bottle, project after project.
Chemistry at production scale brings together science and craft. In every lot of 4-(3-Methoxyphenyl)Benzaldehyde, we see the fingerprints of countless incremental improvements suggested by the plant floor, the analytical lab, and conversations with end-users. Every batch is an accumulation of applied knowledge—reflected in its appearance, analytical profile, and behavior in downstream syntheses. Keeping a close hand on the full production lifecycle means we catch problems before they leave our doors, and help our partners reach new confidence in their own finished goods. The pressures of modern regulation, sustainability, and supply assurance are real, but they also drive us toward better practice, better product, and a more direct relationship with the chemists who choose our materials for their most demanding work.