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5-(4-Nitrophenyl)-2-Furaldehyde

    • Product Name 5-(4-Nitrophenyl)-2-Furaldehyde
    • Alias 5-(4-Nitrophenyl)-2-furaldehyde
    • Einecs 629-019-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    970256

    Cas Number 656-52-2
    Molecular Formula C11H7NO4
    Molecular Weight 217.18 g/mol
    Iupac Name 5-(4-nitrophenyl)furan-2-carbaldehyde
    Appearance Yellow solid
    Melting Point 185-188°C
    Solubility Slightly soluble in water
    Synonyms 4-Nitrophenylfurfural
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 5-(4-Nitrophenyl)-2-Furaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle labeled "5-(4-Nitrophenyl)-2-Furaldehyde, 25g, For laboratory use only."
    Shipping 5-(4-Nitrophenyl)-2-Furaldehyde is shipped in tightly sealed containers, protected from moisture and light, and clearly labeled as a hazardous chemical. Transport complies with relevant regulations for hazardous substances, typically via ground or air. Safety documentation and material safety data sheets (MSDS) accompany the shipment to ensure safe handling and regulatory compliance.
    Storage 5-(4-Nitrophenyl)-2-Furaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Store at ambient temperature, and ensure proper labeling. Use personal protective equipment when handling and always follow standard laboratory chemical storage guidelines.
    Application of 5-(4-Nitrophenyl)-2-Furaldehyde

    Applications of 5-(4-Nitrophenyl)-2-Furaldehyde in Industrial Manufacturing

    5-(4-Nitrophenyl)-2-Furaldehyde serves as a critical intermediate in sectors such as fine chemical synthesis, specialty pigment production, advanced polymer modification, and pharmaceutical research. As the direct manufacturer, we provide this compound with consistently controlled purity and tightly defined material parameters to meet demanding downstream use scenarios.

    1. Specialty Pigment Precursor for High-Performance Coatings

    Downstream coating manufacturers utilize this material as a starting core for synthesizing chromophore frameworks that impart vibrant yellow to orange hues with lightfastness required for exterior-grade paints and industrial finishes. The compound reacts via electrophilic aromatic substitution and condensation with amine groups to form azomethine pigments, valued for their resistance to UV-induced fading and chemical degradation in architectural and automotive coatings.

    Industry compliance standards

    • REACH Annex XVII (Europe, pigment monomer use in coatings)
    • GHS chemical labeling requirements
    • ISO 787/24 (Pigments and extenders – Evaluation in coatings)
    • ASTM D476 (Standard Classification for Dry Pigmentary Colors Used in Coatings)

    Typical usage ratio

    • 0.5–2.0% by weight of total pigment precursor batch, adjusted based on shade strength and chroma intensity needed in end-use coating

    Downstream process integration

    • Introduced during pigment intermediate condensation and diazotization stage; subsequent coupling with amines forms final pigment which is then milled with resin matrices before letdown

    Final product types

    • Architectural exterior paints
    • Automotive & vehicle OEM finishes
    • Industrial protective coatings
    • High-durability decorative enamels

    2. Intermediate in Synthesis of Targeted Pharmaceutical Building Blocks

    Custom synthesis groups and API manufacturers rely on this aldehyde for constructing heteroaromatic scaffolds, especially in the formation of furan-nitroaniline derivatives for subsequent reduction and cyclization steps. Its high reactivity towards nucleophilic substitution supports the creation of lead compounds in early-phase drug development targeting antimicrobial and antiparasitic agents.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP–NF (United States Pharmacopeia monograph specifications for process impurities)
    • EDQM CEP Guidelines (Residual solvent and impurity controls)
    • ISO 9001 (Quality Management Systems for Manufacturing)

    Typical usage ratio

    • 0.8–2.5 molar equivalent, calculated against partner reagents in the intermediate chemical stage; strictly adjusted based on conversion yields and process mass intensity

    Downstream process integration

    • Added at the initial condensation or ring-closure step for constructing poly-heterocyclic scaffolds; downstream transformation includes nitro group reduction and functional group elaboration in flow or batch reactors

    Final product types

    • Pharmaceutical intermediates for furan-based drug candidates
    • Active ingredient analogues for preclinical research
    • Reference standards for analytical method development
    • API precursors for contract synthesis workflows

    3. Component for Polymeric Material Crosslinkers

    Producers of specialty polymer systems, particularly those developing advanced crosslinked resins for electronics encapsulation and high-performance adhesive tapes, introduce this aldehyde to yield crosslinking agents via aldol condensation and Michael addition routes. Its furaldehyde and aromatic nitro functionalities allow for tailored network density and strong heat and chemical resistance in final thermosetting matrices, supporting the rigorous requirements of high-reliability insulation and bonding materials.

    Industry compliance standards

    • UL 94 (Flammability of Polymer Materials)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • ISO 10993-5 (Cytotoxicity for material biocompatibility, where applicable)
    • IPC-4101 (Specification for Base Materials for Printed Boards)

    Typical usage ratio

    • 0.3–1.2 parts per hundred resin (phr), optimized based on resin backbone reactivity and final glass transition temperature targets

    Downstream process integration

    • Dosed into prepolymer mix during pre-cure blending, followed by thermal or UV-initiated crosslinking; precise ratio adjustment ensures reproducible matrix crosslink density for product performance consistency

    Final product types

    • Epoxy adhesive films for electronics assembly
    • Encapsulation compounds for circuit protection
    • Thermoset laminates for high-frequency PCB substrates
    • Specialty industrial tapes and sealant systems

    4. Precursor for Electrically Conductive Organic Materials

    Advanced materials manufacturers employ this compound in the synthesis of conjugated organic frameworks used in developing conductive oligomers and polymers. Through targeted condensation polymerization with amine and thiol functional co-monomers, the furan-aryl backbone contributes to electronic delocalization and tunable bandgaps suitable for use in flexible organic electronics, light-emitting diodes, and antistatic packaging applications.

    Industry compliance standards

    • IEC 61249-2-21 (Halogen-free electronic materials)
    • ISO 9001 (Quality assurance in specialty material manufacturing)
    • RoHS directive (Electronic component compliance, EU)
    • REACH (Polymers and monomer registration, Europe)

    Typical usage ratio

    • 1.0–3.0% by weight of total monomer charge, tailored to modulate polymer film thickness and resistivity in end-use device assembly

    Downstream process integration

    • Blended with co-monomers during solution or melt-phase polymerization; post-polymerization processing may include solution casting, spin-coating, or extrusion for device fabrication

    Final product types

    • Flexible printed circuit substrates
    • Organic light-emitting diode (OLED) emission or hole transport layers
    • Antistatic coatings for packaging films
    • Low-voltage conductive polymer films

    5. Analytical Reagent for Chromatographic Derivatization

    Specialty laboratory reagent suppliers and analytical labs incorporate this compound in sample preparation protocols as a derivatizing agent for selective detection of amine-containing analytes in high-performance liquid chromatography (HPLC) and gas chromatography (GC) workflows. It facilitates improved detection limits and enhanced method precision for trace-level quantitation of pharmaceuticals, environmental contaminants, and process impurities.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and calibration laboratory accreditation)
    • USP General Chapter <621> (Chromatography system suitability)
    • FDA 21 CFR Part 211 (cGMP for laboratory controls in pharma manufacturing)
    • OECD GLP Principles (Good Laboratory Practice)

    Typical usage ratio

    • 0.02–0.2 mg/mL as derivatization agent, dependent on analyte stoichiometry and instrument sensitivity requirements

    Downstream process integration

    • Added to sample aliquot under controlled pH before chromatographic injection; reacts with analyte under mild heating or mixing, producing UV-visible or electroactive derivatives for quantitation

    Final product types

    • Derivatized analytical standards
    • Validated HPLC and GC method kits
    • Pilot batch QC samples in pharmaceutical manufacturing
    • Analytical reference materials for regulatory submissions
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    Certification & Compliance
    More Introduction

    5-(4-Nitrophenyl)-2-Furaldehyde: A Manufacturer’s Perspective

    Seeing Beyond the Molecule

    Over two decades of chemical production have taught us that sometimes the most valuable compounds aren’t the headline-makers. In our plant, 5-(4-Nitrophenyl)-2-Furaldehyde (sometimes referenced by those in the lab as Model 5NPF-FA) reflects a shift scientists and engineers are driving within specialty synthesis. This molecule owes its value not to broad hype but to focused performance in research, pharmaceuticals, and advanced material testing.

    The Right Balance of Reactivity

    What sets 5-(4-Nitrophenyl)-2-Furaldehyde apart is a careful balance between its nitro-substituted aromatic ring and its reactive aldehyde group. Over our years of scale-up and custom run batches, we found that researchers chasing new intermediates for drug discovery or photoreactive polymers often need a consistently high-purity aldehyde that isn’t disrupted by uncontrolled moisture, oxidizers, or surface-active contaminants. Our skilled team worked out a production route that brings purity to above 98%, maintaining batch-to-batch color and odor profiles within tight boundaries. The furan ring and para-nitro arrangement, as every synthetic chemist learns, opens doors to targeted selectivity. That matters most in labs where one wrong impurity ruins months of synthesis planning.

    From Small-Scale Synthesis to Industrial Lots

    We didn’t land at this product overnight. Originally, the route was tested in beakers with a modest yield, easily degraded by oxygen. Scaling up takes more than theoretical chemistry—it took three years to adapt the protocol, shielding the intermediate in inert atmospheres, managing exothermic steps, and keeping cross-contamination risks near zero. In response to feedback from leading polymer chemistry divisions in Northern Europe, we re-calibrated drying and filtration, shifting from routine rotary evaporation to custom glass lines that kept exposure minimal. This prevents formation of byproducts such as unwanted dinitro compounds, which a GC trace will reveal at even a few hundred parts per million.

    Specifications Shaped by Direct Lab Use

    We work with specifications that matter on the bench. Purity matters—but so do form and consistency. Years ago, complaints arose from a handful of university clients about uneven particle sizes causing heterogeneity in test reactions. Instead of brushing this off, we redesigned crystallization conditions, now offering a fine, near-uniform yellow powder. Each production lot undergoes controlled drying at sub-atmospheric pressure and is vacuum-sealed before shipping to prevent premature aldehyde dehydration.

    Average melting point comes in at between 116-120°C under standard atmospheric pressure. Water content stays under 0.3% by Karl Fischer titration, minimizing hydrolysis. Trace metal profiling by ICP-OES, another process driven by real user concern, now runs on every fifth batch, confirming absence of iron, copper, or zinc at levels relevant to catalyzed reactions. We introduced this after feedback indicated that inconsistent results in photochemical reactions might trace back to metal-catalyzed side steps. This methodical check costs us, but it sustains the trust our buyers put in each delivery.

    Critical Differences: What Sets Real Manufacturing Apart

    Production plants—not brokers—see the reality of contamination control, especially when making a substance like this, which tends to absorb atmospheric moisture or off-gas aldehyde over time. Daily, our operators track mill scale, humidity, and even the shelf-life of storage containers. We take direct responsibility. Labs and industry partners call when a problem arises. Our open-door samples program lets customers review quality long before purchasing; if an impurity or problem emerges, our chemists—not outsourced quality controllers—work directly with clients to troubleshoot.

    The difference shows up in applications. 5-(4-Nitrophenyl)-2-Furaldehyde has been a trusted intermediate for C–C bond formation studies, pro-drug synthesis, and specialty dye production. Most compounds in the same family trade reactivity for stability, or vice versa. We’ve tuned ours to hold up through rigorous conditions encountered in ring-opening reactions and as a core for linking through both heterocyclic and aromatic pathways.

    Real-World Uses: What We’ve Learned from the Field

    Extensive communication with our researchers proves that 5-(4-Nitrophenyl)-2-Furaldehyde functions best as more than a reagent—it’s a building block for innovation. In advanced pharmaceutical synthesis, it serves as a backbone for coupling reactions, especially for those targeting heterocycle-rich libraries. Several biotech partners rely on high-purity lots when screening for anti-inflammatory lead compounds. Low water content helps them avoid hydrolysis-driven breakdown, which saves both time and costly reagents.

    Polymer chemists exploit its dual aromatic–heterocyclic nature. One research group in the energy storage sector, who purchases from us regularly, uses our product to build specialty conjugated polymers designed for flexible electronics. The para-nitro substitution is key, imparting both electron withdrawal and a clear signature for spectroscopic tracking—researchers noted that less pure competitors yield cloudier signal profiles and unpredictable mechanical results.

    Another major area is dye chemistry. The molecule’s conjugated aromatic/nitro/furan backbone has been leveraged in the development of advanced optical brighteners, plus specialty markers for imaging research. In all cases, the ask is the same: reduce extraneous peaks in HPLC/UV spectra and maintain consistent chromophore response. Our hands-on quality systems—daily spot runs, in-process controls—are informed by two decades of batch-to-batch analytical data.

    The Sorts of Challenges We Face—and Face Down

    Not every batch runs perfectly. The organic chemists on our team spend hours hunting down off-odors or coloration shifts that appear in rare runs. Once, a subtle color change tipped us off to a small batch byproduct from a worn reactor seal. By involving both operators and chemists, we pinpointed and replaced the faulty part, wrote new SOPs, and shared our findings across the organization. Mistakes are inevitable in any manufacturing facility, but direct customer reporting and rapid response make the difference—and this is only possible when the manufacturer is hands-on and connected.

    A big challenge unique to aldehydes with nitro groups is stability. Over time, these compounds can self-condense or decompose under poor storage. We run ongoing shelf-life trials under multiple temperature and humidity regimes. Every two months, we open stored drums from previous years and rerun NMR and HPLC profiles to ensure no new contaminants creep in. Based on this data, we finalized an optimal nitrogen blanketing system for storage and shipping, reducing decomposition to levels far below industry-standard benchmarks.

    Why the Model Matters: Application-Centered Advances

    Model 5NPF-FA became our flagship not only due to customer demand but also because we saw repeated hurdles around consistency in the industry. By designing our production around tighter purity control, avoiding batch-to-batch variability, and focusing on research-forward specifications, we help accelerate scientific discovery for our clients.

    Many products sound similar on paper—names and grades get tossed around by distributors chasing volume. Experience shows that only manufacturers who work shoulder-to-shoulder with researchers can adapt properties before and during scale-up, refining solvent removal, neutralizing trace contaminants, and documenting every modification for full transparency.

    After one pharmaceutical pilot project flagged a recurring issue with trace acetone in certain competitive lots, we invested in dedicated solvent handling and extra rinsing of reaction vessels. Cleaner lots soon let a client’s downstream chiral synthesis reaction proceed without byproduct formation, and we made this improvement permanent across future batches.

    Transparency, Traceability, Trust

    Our operations team documents every gram from input to output, retaining reference samples from each production lot for up to five years. Suppliers of starting furan and nitrochlorobenzene must meet our standards for impurity rejection—no batch enters the process without source-based CoAs and in-house verification. This detailed documentation allows us and our customers to investigate any outlier. Some of the world’s largest research organizations and boutique R&D startups have audited our plant based on this open-door approach.

    Supporting compliant institutions also means providing purity certificates, NMR spectra, and HPLC chromatograms direct from our QA team on request. Clients regularly participate in method transfer studies with us: samples shipped under double vacuum, feedback sessions between their analysts and ours, and process improvements that support them in reaching their own regulatory or project milestones.

    What We’ve Learned from Decades of Collaboration

    We don’t pretend to know every application our product might end up in; innovation comes from the ground up. But by keeping lines open—not just sending intermediates into the void—we gain insight into real research bottlenecks. This has led us to push for even greater purity, invest in new detection equipment, and shift our packaging geometry so that even the smallest labs receive manageable, well-sealed sample sizes that don’t degrade on the shelf.

    In many client environments, especially startups and academic labs, budgets are real and margins for error are thin. Losing a drum or even a gram to instability or inconsistency can set back timelines or waste precious funding. Knowing this, our teams make the decision every day to slow down in production when a quality flag arises—even if it means missing an ambitious ship date. Long-term relationships depend on predictable quality, not just on-the-spot pricing or shipment speed.

    Continuous Improvement Grounded in Experience

    Small comments from customers have repeatedly prompted major advances in our process. After one feedback session regarding caking during storage, we adopted anti-static bottling and inert lining. When another client reported volatility on reopening older packages, we switched sealing techniques and now include shelf-life labeling as standard on every container. Investing in these changes proves cost-effective in the long run, both for us and for every scientist relying on high integrity inputs.

    We see manufacturing as much more than a transactional exchange of goods. Every drum, bottle, or ampoule we ship carries the weight of collaborative effort—process innovation, analytical rigor, and open channels for troubleshooting. This approach keeps our team motivated, our partners engaged, and our places as a trusted specialty chemical supplier locked in.

    Looking Forward

    5-(4-Nitrophenyl)-2-Furaldehyde production continues to evolve, driven by emerging needs in advanced R&D. New fields, from precise drug screening to specialty electronics, expand the reach of what this molecule can achieve, and we adapt alongside the researchers. Down the line, as regulatory and environmental pressures rise, our aim remains unchanged—to anticipate hurdles before they disrupt our partners’ work, to root out impurities before they reach the bench, and to take pride in every run, every improvement, and every real-world result.

    Direct feedback for every product cycle has proven invaluable. By staying transparent, prioritizing reproducibility, and connecting quality assurance with daily production realities, we build more than a product—we build trust. Based on our experience, there’s simply no substitute for a real manufacturer’s hands-on, iterative, detail-driven process. True reliability flows not from marketing claims, but from decades of shared success between the plant floor and the researchers driving tomorrow’s breakthroughs.