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HS Code |
159703 |
| Product Name | 5-(3-Nitrophenyl)-2-Furaldehyde |
| Cas Number | 3696-19-5 |
| Molecular Formula | C11H7NO4 |
| Molecular Weight | 217.18 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 146-148°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
As an accredited 5-(3-Nitrophenyl)-2-Furaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 5-(3-Nitrophenyl)-2-Furaldehyde is securely sealed in an amber glass bottle with a tamper-evident cap and labeled. |
| Shipping | 5-(3-Nitrophenyl)-2-Furaldehyde is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. The chemical is classified as hazardous and packaged according to international safety regulations. Proper labeling ensures safe handling during transport. Delivery is typically via certified carriers specializing in chemicals, with all necessary documentation included. |
| Storage | Store **5-(3-Nitrophenyl)-2-Furaldehyde** in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents or reducing agents. Keep the container tightly closed and clearly labeled. Use appropriate chemical-resistant storage containers. Avoid exposure to moisture and sources of ignition. Ensure access to safety equipment and spill cleanup materials. Store at room temperature unless otherwise specified. |
Applications of 5-(3-Nitrophenyl)-2-Furaldehyde in Industrial Manufacturing5-(3-Nitrophenyl)-2-Furaldehyde is an advanced aromatic aldehyde used in several specialty chemical manufacturing sectors, valued for its unique structural features that enhance selectivity and performance in downstream synthesis. We manufacture this raw material under stringent quality control for direct integration into demanding industrial processes. Below, we present specific application scenarios based on established, verifiable industry use cases, with detailed process and compliance information for each sector. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers incorporate 5-(3-Nitrophenyl)-2-Furaldehyde as a key building block in multi-step synthesis of certain nitrophenyl-furan-based drug candidates and intermediates, facilitating selective condensation and cyclization reactions under controlled process parameters. Advanced reactors enable the compound to serve as a starting aldehyde for constructing heterocyclic pharmacophores, especially in anti-infective and anti-inflammatory drug research pipelines. Industry compliance standards
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2. Agrochemical Active Ingredient DevelopmentCrop protection R&D teams utilize 5-(3-Nitrophenyl)-2-Furaldehyde in synthetic routes for furan-based agrochemicals, especially where electron-withdrawing groups enhance molecular interactions with pest or fungal targets. Integrating this compound into the nitrofuran core design allows development of new modes of action and optimization of formulation compatibility for pilot and scale-up batches. Industry compliance standards
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3. Specialty Dye and Pigment PrecursorsIn specialty dye manufacture, the unique conjugated structure of 5-(3-Nitrophenyl)-2-Furaldehyde provides chromophoric moieties that enable tunable color properties and fastness profiles. Dye and pigment formulators employ the compound in nucleophilic addition and coupling reactions, targeting applications in high-performance textile and industrial coatings where precise absorption properties are required. Industry compliance standards
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4. Electronic Materials: Organic Semiconductor PrecursorsProducers of organic electronic materials exploit the electron-withdrawing nitrophenyl functionality of the compound to modulate molecular orbitals in custom-designed semiconducting oligomers and polymers. Its aldehyde group participates in cross-coupling or polymerization steps essential in forming charge transport layers or emissive blocks for organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). Industry compliance standards
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5. Analytical Reagent FormulationsAnalytical chemistry laboratories and manufacturers of diagnostic kits use 5-(3-Nitrophenyl)-2-Furaldehyde as a derivatization reagent for specific spectrophotometric and chromatographic analyses, where its aldehydic moiety enables sensitive detection or quantification of amines, hydrazines, and related analytes in complex sample matrices. Industry compliance standards
Typical usage ratio
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Working in a factory, you get to see not just raw materials and reactors, but also the daily habits of a molecule—how it crystallizes, how it behaves in storage, and how it responds to scaling. Our team lives with 5-(3-Nitrophenyl)-2-Furaldehyde from batch synthesis to packing. This is not just another furan compound; its nitrophenyl group draws a sharp line between it and relatives like simple furaldehydes. A passing glance at its gold powder may suggest something decorative, but here function and color go hand in hand.
People outside the lab might look at the formula C11H7NO4 and see numbers, but the nitro substituent on the phenyl ring carves out a place for this compound in medicinal research. You get that extra electron-withdrawing force, which, in real chemistry, changes the reactivity entirely. In our reactors, this shift shows up as a steady condensation step and avoids runaway side reactions. Our colleagues working in downstream pharmaceutical synthesis and material science often say they need this “clean break” from less activated furaldehydes, especially for novel heterocyclic intermediates.
Any plant hand knows furan chemistry can be unforgiving. You start with pure starting materials, but the work isn’t done after filtration. At scale, small differences in temperature or agitation show up in the product—crystal color, odour, and even how the powder flows. Our standard batch typically tests above 98% purity by HPLC and NMR checks in. Every piece of equipment, from our glass-lined autoclaves to our moisture meters, gives us feedback. For 5-(3-Nitrophenyl)-2-Furaldehyde, the actual purity matters far more than paperwork suggests. An impurity at the nitro site impacts reactivity during complex stepwise synthesis in agrochemical or drug intermediate work, so we test for specificity.
Customers in the field ask tough questions. Why bother with this compound at all? For some, it’s the way the nitro group opens the door to further functionalization. It attaches metal catalysts differently from an unsubstituted furaldehyde. For others, it’s the material’s stability across temperature shifts. A simple story: a coating company once told us how lesser analogs decomposed too rapidly during their curing process at elevated temperature, with unexpected color bleed. Our 5-(3-Nitrophenyl)-2-Furaldehyde, shipped dry and sealed, kept its properties—even after months in storage. Quality at this level comes from constant feedback between bench-scale work and kilo-scale runs, not theory alone.
Plenty of labs use unsubstituted furfural for polymer applications, but as soon as the chemistry turns complex, the properties of this advanced aldehyde start to show. We see it every day in our customer discussions—peptide builders rely on the electron withdrawal for specific coupling reactions, while dye makers need that precise yellow-straw tone to act as a chromophore precursor. In contrast, standard furaldehydes just don’t activate aromatic substitution with the same precision. Labs pushing for new antibacterial agents have told us straight that alternative starting points either react too sluggishly or introduce unwanted side products. The inclusion of a meta-nitrophenyl moiety in the structure distinguishes it from cousins lacking this group, both in the lab and in the real world.
Our site has handled this compound long enough to advise: the best way to keep 5-(3-Nitrophenyl)-2-Furaldehyde clean is low humidity and avoidance of direct sunlight. It handles short-term room temperatures just fine, but we prefer packing in moisture-resistant liners for anything shipped overseas or warehoused long-term. Not all aldehyde derivatives keep their crisp yellow color—oxidation can darken inferior batches. Early on, we learned that desiccant and barrier packaging don’t just protect reputation; they protect yield for our downstream users.
Some colleagues from outside manufacturing are convinced that a smooth gram-scale synthesis means industrial runs will be just as forgiving. From our experience, that’s not always the case with 5-(3-Nitrophenyl)-2-Furaldehyde. The main oxidation step, for instance, can release more heat in larger vessels, calling for fine-tuned cooling cycles. We’ve modified stirring and solvent selection over time to prevent hot spots that threaten yield or purity. Maintaining color is another tell: a golden yellow powder means our crystallization steps kept the product pure. When color drifts, we investigate—not just by adjusting pH, but by reviewing agitation rates and batch histories.
Compliance shapes every batch. Regulatory agencies don’t compromise on traceability, especially for furan derivatives destined for life science R&D. We thus maintain lot-specific documentation, and audited process logs let users track any shipment back to its reactor date. This is a far cry from trading stock. As manufacturers, our access to historical data—from raw material source to chromatograms—makes risk management possible, especially as downstream applications grow more sophisticated.
Purity targets in our facility come from countless discussions with formulation teams. Some want greater-than-99% readings, arguing their catalysts show more activity with less background. Others use broader specs, comfortable with slightly wider impurity profiles because their application tolerates trace variation. We see the results ourselves: lower impurity batches always mean lower incidence of resin gelling or unexpected emission during scale-up. So we draw a line where performance demands it, not just where the paperwork says to stop. For those who depend on exact melting points or stability across process steps, our QA routines deliver reproducible answers each time.
Sitting across the table from R&D customers reminds any manufacturer how demands change over time. Early adopters were almost always focused on straightforward coupling reactions or testing new N-heterocycles. Genetic researchers have since started probing for new bioactivity profiles, and specialty polymer labs started investigating longer-chain furan derivatives for improved durability. Our process engineers respond by refining filtration and drying steps, and this agility means fewer delays between inquiry and supply—directly from our synthesis line, not through a stack of resellers.
We hear more from customers who report back on actual usage than any sales team ever could. A crop science researcher once pointed out that a batch stored improperly at their site developed clumping and failed to dissolve cleanly. Since then, we’ve improved our consultation, suggesting practical measures for their storage conditions and adapted our packaging for hotter climates. Pharmaceutical partners sometimes come back with results showing subtle differences in NMR based on trace impurities; these reports lead us to enhance purification, reducing not just overall impurity numbers but specifically those that interfere with ring substitutions.
Plenty of distributors offer furaldehydes, but material from non-manufacturing suppliers too often suffers from faded hues, inconsistent melting ranges, or insufficient documentation. Independent labs sending complaint samples confirm what we see in head-to-head analysis: crystal habit, purity, and spectral matching just don’t line up unless you control the process start-to-finish. We offer more than a certificate; we give users direct evidence—matching spectral assays and run histories—because we know these differences matter when chemistry moves from bench to pilot scale.
Running a chemical plant comes with criticism and scrutiny, especially as environmental stakes climb. Our own process engineers look for waste reduction constantly. Nitrophenyl furaldehyde’s synthesis splits fractions of solvent and byproducts—our separation technologies reclaim over 90% of the acetic acid we use, reducing both cost and discharge load. Staff at our site experiment with catalyst recoveries and greener oxidants. These hard-earned adjustments matter not only for compliance but for public trust in specialty chemistry. Years ago, discharge from less efficient workups threatened permit renewals; process improvements kept both permits and downstream partnerships secure.
Recent years taught manufacturers everywhere to prepare for raw material interruptions. Our supply planners favor contracted sources for key starting phenyl compounds, locking in both quality and lead times. Sudden spikes in demand from specialty dye or pharma companies do happen, and in those moments, only direct synthesis capacity protects against shortage. Traceability also comes into play: end users relying on certified chains prefer knowing their 5-(3-Nitrophenyl)-2-Furaldehyde didn’t change hands five times before production. Competitors relying solely on brokers can’t promise the same transparency, and savvy users catch on quickly.
Lab managers and process engineers visiting our site often want to know about day-to-day storage. We recommend using sealed containers with low moisture content—absorbent liners work better than vacuum alone. Opening a container in a humid environment runs the risk of slow hydrolysis, leading to changes that show up in test methods long before a visible change occurs. For frequent access, repackaging in smaller aliquots reduces exposure, protecting not just appearance but performance in downstream chemistry.
High yield means more than simple numbers on a balance sheet. In our reactors, minor deviations in pH, solvent polarity, or heating rates have distinct effects. Factory data collected over time led us to tweak addition rates, sometimes preferring a staged approach over single-pot synthesis. Lowering side product generation not only saves on purification but improves solvent recovery. Our repeat customers see these improvements in lot-to-lot consistency, saving both time and troubleshooting during their process validation steps. We keep detailed logs on every modification, using this data to further dial in the next run.
Scientists exploring new reactions involving heterocyclic aldehydes want certainty with every lot. Many university and industrial partners shared how unpredictable batch quality interrupted their development cycles. By running pilot reactions on every production lot ourselves—testing for side reaction propensity, color stability during heating, and ease of functionalization—we offer more than just reassurance. This practice goes beyond compliance; it protects ongoing research programs from wasted time and cost.
Whether used in small molecule synthesis, custom dye assembly, or advanced materials, the ultimate feedback comes in customer repeat orders. A formulator working in analytical chemistry once commented that our product’s spectral signature stayed constant between supplies, letting them skip time-consuming baseline corrections. These stories reaffirm our belief that factory-controlled synthesis trumps redistribution every time. Ongoing relationships with both local and global partners allow us to continually gather data and tweak process parameters, treating every batch as a fresh opportunity to improve.
Fine chemical production means never making assumptions about how a user’s needs will evolve. Some downstream researchers have begun exploring 5-(3-Nitrophenyl)-2-Furaldehyde for applications outside traditional organic synthesis: developing functionalized coatings, or testing as part of luminescent or conducting polymers. In those fields, purity isn’t just a preference—it determines whether the compound will work at all. We collaborate with advanced users to optimize grade and lot size, ensuring that their cutting-edge work has a stable, predictable foundation.
As a manufacturer, our investment goes beyond the order sheet. We provide long-term batch histories, trace analytics over time, and collaborative development for users requiring adjustments to standard grades. This approach grows trust and technical exchange over quick sales. Working shoulder-to-shoulder with end-users, process chemists, and supply managers has shown us that timely communication and tailored solutions set a real manufacturer apart from trading houses.
Over the years, our focus on 5-(3-Nitrophenyl)-2-Furaldehyde taught us new lessons about what it means to deliver value in the specialty chemicals field. Each step in production, each conversation with an end user, guides our refinements. Technical mastery, regulatory focus, and a hands-on approach to customer feedback shape every batch in a way that only direct manufacturers can provide. We aim to keep building on this foundation, staying responsive to ever-changing demands in science and industry.