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HS Code |
351978 |
| Cas Number | 37952-52-2 |
| Molecular Formula | C8H7NO4 |
| Molecular Weight | 181.15 |
| Appearance | Yellow solid |
| Melting Point | 110-112°C |
| Purity | Typically >=98% |
| Smiles | COC1=CC(=CC(=C1)[N+](=O)[O-])C=O |
| Solubility | Soluble in organic solvents (e.g., ethanol, DMSO) |
| Iupac Name | 4-methoxy-3-nitrobenzaldehyde |
| Synonyms | p-Methoxy-m-nitrobenzaldehyde |
As an accredited 4-Methoxy-3-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g 4-Methoxy-3-Nitrobenzaldehyde comes in a sealed amber glass bottle with a clear chemical hazard label and details. |
| Shipping | 4-Methoxy-3-Nitrobenzaldehyde is shipped in tightly sealed containers, protected from light, moisture, and physical damage. It must comply with local and international regulations, including appropriate labeling as a hazardous chemical. Shipments typically require documentation for safe handling, and transportation is often via ground or air freight with temperature and safety controls. |
| Storage | 4-Methoxy-3-Nitrobenzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and reducing agents. Protect from direct sunlight and moisture. Ensure appropriate labeling, and keep the storage area equipped with proper spill containment and safety measures. |
Applications of 4-Methoxy-3-Nitrobenzaldehyde in Industrial ManufacturingAs a dedicated manufacturer, we supply 4-Methoxy-3-Nitrobenzaldehyde directly to specialized industries that demand high-purity aromatic aldehydes for precision synthesis. This intermediate directly supports downstream production within the fine chemicals sector, consistently meeting compliance needs in each real-world industry line where it is integrated. Below are focused downstream scenarios reflecting established use cases, with manufacturing practice and application specifics detailed per sector. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers rely on this compound as a building block in advanced heterocyclic and aromatic APIs, especially in the synthesis of cephalosporin side chains and anti-tumor intermediates. Our technical record confirms its integration into multi-stage organic reactions aligned with GMP protocols. Purity and residual solvent content monitored at intake to ensure compliance during the coupling and reductive amination steps. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingAgrochemical producers utilize this aromatic aldehyde to construct specialty nitro-aromatic moieties for herbicide and fungicide active ingredient synthesis. The fine control of substitution patterns supports structure-activity relationship (SAR) studies and commercial actives, fitting the quality management protocols enforced in crop protection chemical plants. Industry compliance standards
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3. Dye and Pigment Intermediate ProductionSpecialty dye and pigment plants adopt this chemical for synthesizing high-fastness azo and anthraquinone dyes in the textile and plastics sectors. The functionalized aromatic ring advances chromophore extension and controls final hue precision. Our material’s narrow impurity profile aligns with stringent controls at pigment synthesis stages. Industry compliance standards
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4. Fine Chemical Synthesis for Analytical StandardsProducers of laboratory reference materials and specialty reagents incorporate this aromatic aldehyde as a foundational intermediate for QC testing compounds, especially where selectivity and purity determine performance in sensitive analytical methods. Reliability in traceability and batch consistency meets advanced laboratory certification controls. Industry compliance standards
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5. Fragrance Intermediate SynthesisWithin the aroma chemical sector, this compound serves as a precursor in specialty aldehyde chain extensions to produce fine fragrance ingredients. Its aromatic structure underpins the production of long-lasting, high-purity fixatives and masked aldehydes required in high-grade perfumery formulations, aligning with IFRA and food contact regulations for downstream integration. Industry compliance standards
Typical usage ratio
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Every batch of 4-Methoxy-3-Nitrobenzaldehyde that carries our label comes out of years of hands-on experience in aromatic intermediates production. This isn’t just about ticking boxes for purity or handing over a certificate of analysis; it’s about knowing why certain specifications matter from the ground up.
We chose a manufacturing route that gives us consistent control over both the ortho- and para-selectivity during the nitration and subsequent oxidation steps. Chemists who handle benzaldehyde derivatives know this isn’t just a theoretical concern — inconsistent regioselectivity ruins yields and introduces byproducts that complicate purification and reaction predictability. Our process minimizes the formation of positional isomers and keeps the content of key impurities well below what influences downstream reactions.
Over the years, we learned that purity isn’t just a talking point: it changes the way the molecule reacts in customer applications. Our standard material comes at a minimum purity of 99% by HPLC, with a moisture content that stays below 0.2%. The color remains clear pale yellow, which reflects the lack of decomposition byproducts like nitrophenols or methoxybenzyl alcohols.
We typically supply this chemical as a free-flowing crystalline solid, which avoids caking and compaction and pours easily. Particulate handling in the warehouse and during reaction quenching stays clean, without the static cling or dusting that cheaper, less controlled products introduce.
This benzaldehyde derivative became a mainstay in our product line because of repeat demand from pharmaceutical R&D groups dealing with active pharmaceutical ingredient (API) synthesis, as well as companies working on functional dyes and advanced materials. The nitro group’s electron-withdrawing effect combines with the methoxy electron-donating ring to create a distinct reactivity profile. This structure directs further functionalization into predictable positions, which cuts down on waste for acylation, alkylation, or cyclization reactions.
For instance, several customers synthesize key imine intermediates starting from our aldehyde, reacting it with amines for downstream applications in both medicinal chemistry and pigment innovation. The controlled reactivity and the absence of interfering byproducts greatly reduce purification headaches.
We’ve also seen strong uptake in laboratories working on solid-phase synthesis, where the performance of the starting material decides the consistency of the solid supports and the outcome of multi-step iterations.
Not all sources of 4-Methoxy-3-Nitrobenzaldehyde end up behaving the same way. We don’t use chloride-catalyzed oxidation, so residual metals do not show up in our product. Some batches from traditional suppliers have trace iron or copper, which can decimate downstream selectivity or introduce color in finished APIs — both costly problems. In our hands, every step, from nitration to crystallization, has been tweaked to minimize hydrolysis, avoid methyl ether cleavage, and stay clear of over-oxidation. We avoid high-temperature distillation steps that break down the aldehyde, so the characteristic sharp aroma and melting point range remain consistent.
We work with both kilo and multi-tonne reactors, making regular process adjustments based on actual feedback from users — not just scaling up from theoretical yields. For some customers, we modified our workup to reduce trace oxidized acids, because they observed subtle effects on subsequent Grignard reactions. These incremental improvements come directly out of listening to chemists using the product in real processes, not just from a standard product sheet.
Other benzaldehyde derivatives can look similar on paper but act very differently in synthesis. Comparing, for instance, 3-methoxy-4-nitrobenzaldehyde or 2-methoxy-5-nitrobenzaldehyde against our 4-Methoxy-3-Nitrobenzaldehyde, you quickly see variation in melting points, reactivity toward nucleophiles, and solubility in common polar solvents.
The para-methoxy group changes both the electron density and the way the nitro group activates the aromatic ring, making this molecule the favored substrate in a range of nucleophilic aromatic substitution (SNAr) reactions and in condensation steps where positional selectivity is critical. The reaction rates can differ noticeably — putting the nitro group at the meta position drops reactivity for these transformations, and switching to the ortho methoxy leads to solubility and stability issues that frustrate isolation yields.
Some users ask if cheaper technical grade alternatives suffice. In our experience, once you move beyond research scale, those grades drag in latent impurities that show up at the pilot- or production-stage as yield loss, color bodies, or even filtration failures. Saving a little up front leads to days’ worth of re-work and additional column chromatography runs, more solvent waste, and costly downtime.
We don’t overlook details that seem small on the spec sheet but show up day-to-day. Our crystalline product comes with consistent bulk density and particle size distribution, so it weighs out and dissolves the same way every time. No gumming up in cold rooms, no fused block at the bottom of the barrel.
We package this product in moisture-resistant, lined fiber drums or HDPE containers, chosen after years of testing to prevent both physical contamination and slow hydrolysis. Our storage advice comes from what actually works: keep containers tightly sealed and away from direct heat to maintain reactivity for long timeframes. We monitor both ambient humidity and temperature in our facilities, so the product lands in your lab in the same condition it left ours.
Beyond just providing a COA, we invest in regular NMR, GC-MS, and LC-MS runs on representative batches. Over the years, this caught the occasional rare impurity that might otherwise make it to a formulation stage. We exchange analytical data with several major research groups, using their synthetic failures as feedback that feeds into our impurity control strategy.
Our technical team has worked with customers to trace problematic transformations down to residual traces of starting anisaldehydes or partial over-oxidation products. We don’t just isolate these cases — we feed them back into our QA/QC routines, adjusting workup and drying protocols in real-time. It’s an investment, but one that pays back in fewer complaints and greater loyalty.
Some customers need the material with ultralow moisture, tight particle specifications, or in specific packaging suited for drum-to-isolator transfers. Our facility runs batch and semi-continuous modes, giving us flexibility to turn around special requests within days, not months. We keep campaign records, so recurring clients see reliable supply with batch-to-batch reproducibility.
Over time, larger buyers came to us after running into persistent issues with variable crystal size and inconsistent melting points from other manufacturers. We upgraded both our crystallization feedstock filtration and solvent recovery so that a 10 kg bag matches last year’s pilot bag — down to the color and free-flowing consistency. This removes any risk of sudden surprises in the middle of a production run.
Safety in production isn’t just about legal compliance — it directly impacts operator morale and workflow. Our protocols rely on practical experience: we stagger nitration feeds and use in situ temperature probes, because runaway exotherm from uncontrolled acid addition not only endangers staff but ruins yield and damages glassware.
We run weekly process hazard analyses and train new technicians live on the shop floor. We use this training not just for formal compliance, but to ensure clean handling without exposure; most staff have at least five years’ experience on our benzaldehyde product lines. Customers get the benefit of this institutional memory, whether with documentation, consultation, or trouble-shooting for unexpected color or odor on arrival.
Even with control, the chemistry behind 4-Methoxy-3-Nitrobenzaldehyde can throw curveballs. We’ve seen crystallization batch failures linked to seasonal humidity spikes and learned to compensate with environmental controls and desiccant-packed packaging. Scale-up always brings surprises — slow oxidation at pilot plant scale brought out new side reactions that never showed up in the lab. We ran rapid-cycle process tweaks, adjusting running solvents, temperature ramps, and stirring profiles to keep the final product in-range every time.
Occasionally, global raw material shortages have forced us to diversify sourcing for starting anisaldehydes. Some batches coming out of spot markets introduced trace contaminants, which led us to invest in more rigorous incoming QC checks and back-integrate several production steps. Now, we test every drum on arrival and have direct insight into the origin and purity profile of each lot.
Shipping presents its own set of obstacles. Our logistics team knows which weeks to avoid for sea freight due to seasonal transit delays, and which packaging options survive cold-chain breakdowns without product degradation. Building direct relationships with carriers cuts down on mishandling and accidental loss; fewer hands between us and the end-user mean fewer chances for contamination.
Many of the process improvements in our 4-Methoxy-3-Nitrobenzaldehyde came directly from customer feedback. Years ago, a medical chemistry lab flagged an unseen impurity peaking on their HPLC — a tiny contaminant that had eluded standard GC screening. Because we could compare batch records, we traced it back to a single upstream solvent change. Adjusting the reagent batch did more than fix the problem; it created a protocol that now keeps this and similar intermediates out of every scale we ship.
We regularly solicit candid reactions from our buyers, not only for troubleshooting but to adapt product handling and delivery schedules. This feedback shapes our training materials, raw material purchasing, and even how we label and pack containers. The net result is a product with fewer surprises — every drum fits seamlessly into the next stage of development.
Our manufacturing team believes in bringing transparency into every batch — not as a buzzword, but because it keeps us sharp and lets our customers benchmark our product against any alternative in the market. We provide full traceability from raw materials to the finished, labeled drum. Lab teams have access to batch-level analytical profiles, atypical impurity disclosures, and direct contact with our process engineers.
Over time, customers stop asking whether our batches will perform: they know from experience that they will. The standard deviations on melting point, purity, and moisture sit where they should — within tight historical ranges. This is a direct result of refusing to lower standards, even when it might have saved us some production time or cost. In our experience, the chemical industry rewards consistency, not shortcuts.
We manufacture 4-Methoxy-3-Nitrobenzaldehyde for every scale: discovery to pilot to full production. Our team’s background covers kilo-lab scaleups, major API rollouts, and plenty of troubleshooting on the fly for unexpected bottlenecks. Over time, our role moved beyond filling orders; we became partners for labs tackling tough synthesis problems. We answer not just to procurement officers, but to the chemists who build products molecule by molecule.
Each change in our process, every quality improvement or handling tweak, reflects this partnership ethos. We learn from every shipment and every complaint to sharpen our process for the next customer, the next batch, and the next challenge. As long as labs keep pushing forward — searching for cleaner reactions, higher yields, and safer products — we’ll keep refining the way 4-Methoxy-3-Nitrobenzaldehyde fits into their toolbox.