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5-(2-Nitrophenyl)-2-Furaldehyde

    • Product Name 5-(2-Nitrophenyl)-2-Furaldehyde
    • Alias Nifuraldehyde
    • Einecs 402-170-3
    • 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

    442630

    Chemical Name 5-(2-Nitrophenyl)-2-Furaldehyde
    Molecular Formula C11H7NO4
    Molecular Weight 217.18 g/mol
    Cas Number 10003-61-1
    Appearance Yellow to orange crystalline powder
    Melting Point 123-126 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically >98%
    Synonyms 2-Furfuraldehyde, 5-(2-nitrophenyl)-
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Smiles O=Cc1ccc(Oc2ccccc2[N+](=O)[O-])o1
    Inchi InChI=1S/C11H7NO4/c13-7-9-4-5-16-11(9)8-2-1-3-10(6-8)12(14)15/h1-7H

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams; tightly sealed cap, hazard labels for irritant and oxidizer, chemical name and CAS number displayed.
    Shipping 5-(2-Nitrophenyl)-2-Furaldehyde is shipped in tightly sealed containers to protect from moisture and light. It should be handled with care, avoiding physical damage. The package is clearly labeled with hazard warnings, and transport complies with relevant chemical shipping regulations. Store and ship at ambient temperature unless otherwise specified.
    Storage Store **5-(2-Nitrophenyl)-2-furaldehyde** in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally within a chemical storage cabinet specifically for hazardous organic compounds. Label clearly, follow all local regulations, and avoid sources of ignition, as the compound may be sensitive to heat or spark.
    Application of 5-(2-Nitrophenyl)-2-Furaldehyde

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

    5-(2-Nitrophenyl)-2-furaldehyde serves as a critical specialty intermediate in various industrial manufacturing processes within the agrochemical, pharmaceutical, specialty dye, functional polymer, and advanced material sectors. The integration of this compound directly influences end-product performance, regulatory adherence, and the advancement of targeted synthesis strategies across these downstream industries. Below we outline distinct application scenarios based on real use cases, inclusive of detailed compliance standards, formulation ratios, process positioning, and the resulting product portfolios.

    1. Agrochemical Active Ingredient Synthesis

    Within the crop protection sector, this material acts as a key aldehyde intermediate for synthesizing targeted nitroaromatic pesticides. Its conversion enables selective functional group introduction during the construction of advanced herbicide molecular frameworks. Technical teams rely on its stability and reactivity during multi-step synthesis, especially in processes requiring precise nitration and furanyl segment incorporation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1907/2006 REACH Annex XVII—Pesticide Ingredients
    • United States EPA FIFRA Regulations
    • ISO 9001:2015 Quality Management for Agrochemical Production

    Typical usage ratio

    • 0.8%–3.2% in intermediate step—ratio adjusted based on final molecule complexity and functional group protection demands

    Downstream process integration

    • Charged after the initial nitration and before cyclization or further functionalization; introduced via continuous flow or batch reactors during the heterocyclic backbone formation stage of pesticide synthesis

    Final product types

    • Precursor to selective systemic herbicides (e.g. nitrophenyl-furanyl derivatives)
    • Advanced fungicide candidates under field trials
    • Nitroaromatic insecticidal active substances

    2. Pharmaceutical Intermediate for Heterocyclic Drug Scaffold Construction

    Our material finds dedicated downstream application in the preparation of complex heterocyclic cores during the synthesis of experimental pharmaceutical agents, including antitumor and antimicrobial candidates. Medicinal chemists use its aldehyde and nitroarene moieties for building lead structures, utilizing this compound in convergent routes for enriching target molecule scaffolds with electronic and steric functionalities.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF Monographs (for related impurities and intermediate purity)
    • EDQM Guidance on Intermediates
    • Pharmaceutical Grade Quality Assurance (ISO 15378:2017)

    Typical usage ratio

    • 0.5%–2.5% (w/w in the reaction substrate mix), contingent on scaffold length and molar conversion efficiency of downstream condensation/reduction steps

    Downstream process integration

    • Added post-initial ring formation, following activation of aromatic positions; commonly reacts under controlled conditions with amino components in the key condensation or cyclization reaction vessel

    Final product types

    • Late-stage intermediates for nitrofuran-based antibacterial compounds
    • Synthetic building blocks in research for anti-mycobacterial or antineoplastic agents
    • High-purity reference standards for medicinal chemistry programs

    3. Colorant and Specialty Dye Intermediate

    Manufacturers in the high-performance colorant sector employ this furaldehyde derivative as a core intermediate for synthesizing metal-complex or azo-furan dyes. Its electron-withdrawing nitro group and planar structure support coupling reactions with diazo or keto reagents, enabling advanced dye molecules with high fastness and photostability for applications such as textile and technical fibers.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100 (for dyes on textiles)
    • ZDHC MRSL (Manufacturing Restricted Substances List)
    • REACH Annex XVII & XIV for Dye Chemicals
    • ISO 105-B02 (Color Fastness to Light)

    Typical usage ratio

    • 2.0%–7.0% in dye synthesis reaction mass, tuned by target chromophore strength and overall yield optimization

    Downstream process integration

    • Fed after the diazotization or keto coupling stage; undergoes nucleophilic substitution and subsequent complexation to deepen shade or boost thermal resistance

    Final product types

    • Metal-complex fabric dyes for technical textiles
    • Azo-furan pigments for automotive and industrial coatings
    • Light-stable ink colorants for specialty packaging

    4. Functional Monomer for Advanced Polymer Materials

    In advanced polymer manufacturing, formulators leverage this aldehyde for introducing tailored polarity and aromaticity into specialized polymer chains. It acts as a functional monomer enabling crosslinking and unique thermal properties in niche engineering plastics and high-performance resins, especially where aromaticity and electron density modulate physical or electronic behavior.

    Industry compliance standards

    • ISO 9001:2015 Polymer Manufacturing Quality Management
    • RoHS Directive 2011/65/EU (for electronics-housing polymers)
    • UL 94 (Flame Retardancy Standard)
    • ASTM D638 (Tensile Properties of Plastics)

    Typical usage ratio

    • 0.5%–4.0% (by monomer feed weight), adjusted for balance between rigidity, dielectric, and melt processability requirements

    Downstream process integration

    • Blended with primary monomers during pre-polymerization batching; the compound is covalently bonded during step-growth or chain-growth polymerization using controlled addition protocols ensuring distribution across polymer matrix

    Final product types

    • High-dielectric thermoset resins for electronics
    • Heat-resistant molded engineering plastics
    • Crosslinked fiber-reinforced composite precursors

    5. Photovoltaic Application as Dopant or Modifier

    Researchers in photovoltaic material science have incorporated this compound as a chemical dopant or crosslinking additive for organic photovoltaic layer formulation. Its nitro-furanyl structure can modify surface energy or electron mobility in organic light-absorbing and charge-transport films, offering precise tuning for emerging solar cell materials with novel optoelectronic behaviors.

    Industry compliance standards

    • IEC 61215 (Design Qualification and Type Approval of Solar Modules)
    • RoHS (Restriction of Hazardous Substances for PV Manufacturing)
    • ISO 14001:2015 (Environmental Management for Clean Energy)
    • OEKO-TEX® STeP (Sustainable Textile & Polymer Processing where relevant)

    Typical usage ratio

    • 0.1%–0.8% in the active or dopant layer—calibrated experimentally for device efficiency and long-term photostability targets

    Downstream process integration

    • Added immediately prior to film casting or coating onto substrate; compound interacts molecularly within donor-acceptor polymer blends during solution processing or vacuum deposition

    Final product types

    • Organic photovoltaic absorber layers
    • Hybrid solar cell charge-transport films
    • Experimental flexible solar panel modules
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    Certification & Compliance
    More Introduction

    Introducing 5-(2-Nitrophenyl)-2-Furaldehyde from a Chemist’s Bench

    Real Experience in Synthesis and Application

    Out on the plant floor, surrounded by tanks and fatigue-resistant pumps, I’ve watched the journey of 5-(2-Nitrophenyl)-2-Furaldehyde from raw material order to its final form—deep gold crystals, distinct nitro scent standing out among a cacophony of other chemicals. This isn’t some catalog substance produced anonymously. Each batch passes through our hands, each adjustment in synthesis stemming from years of tinkering and a habit of checking details twice. Anyone stepping into fine chemicals manufacturing quickly learns the real-world difference between bench-scale and production; it’s about process reliability and the consistency of what you deliver.

    Purity Rooted in Real Controls

    We don’t just state purity because certificates demand a number. Monitoring HPLC traces, triple-checking crystallization endpoints, and tweaking column flows always take place with the actual users in mind—the researchers and technicians whose projects ride on the reliability of the input. What sets our 5-(2-Nitrophenyl)-2-Furaldehyde apart lies in this process discipline. On paper, many suppliers claim 98% or 99% purity, but the difference shows when a customer’s reaction mix stalls because of a stubborn byproduct or a contaminant that won’t show on a quick TLC. You see it when new graduate students call up mystified, troubleshooting their first cross-coupling or nucleophilic addition and the only variable turning up is a stray impurity in an acquired bottle. No one wants their project to hiccup over an unreliable building block, especially not after months of grant proposals and late nights.

    During our routine checks, the nitrophenyl group’s susceptibility to reduction, and the aldehyde's tendency toward self-condensation, guide every pH adjustment and choice of solvent. Our team dials in the process so that, batch after batch, users see the same melting point and receive a batch number that matches spectral data from week to week. Someone who has worked up more than a few hundred grams knows subtle yellowing or uneven crystal size signals another hour at the filter—a cost most traders or middlemen never see, but our operators and QC staff do. Those repeated efforts create a product trusted by R&D teams and process chemists who push for reproducibility every day.

    Why Structure Matters in the Workflow

    Chemically, 5-(2-Nitrophenyl)-2-Furaldehyde sits at the intersection of furans and nitroaromatics. The nitro group pulls electron density, shaping reactivity, and the furaldehyde motif gives plenty of synthesis opportunities—a point that’s been explored in numerous heterocycle libraries and combinatorial approaches. For synthetic chemists, these aren’t just structural quirks; they shape yields, selectivity, and compatibility with downstream steps.

    Having worked on method development with hundreds of intermediates, patterns emerge over time. Some aryl aldehydes degrade or react before you want them to. Others lack the batch-to-batch consistency to support scale-up. The 2-nitrophenyl moiety offers both polarity and steric influence, which many appreciate when building more complex scaffolds. In our applications, whether the end users chase pharmaceutical leads, specialty dyes, or new polymer cross-linkers, the base molecule remains steady. That’s the feedback we chase—users who say each bottle works the same as the last. Results like those don’t come from marketing; they come from a discipline ingrained in the manufacturing process, from vessel cleaning down to drying and packaging.

    Comparing Related Intermediates

    Not all aromatic aldehydes behave the same. Try switching from a 2-nitrophenyl to a 4-nitrophenyl, or swapping the furan for a benzene ring, and reactivity profiles change. A 4-nitrophenyl group positions electron-withdrawing effects differently, shifting the nucleophilicity of intermediate products. Furan systems, compared to simple benzenes, introduce more oxygenation and tend to behave less predictably in some condensation reactions. Years at the bench convince anyone that not every synthetic shortcut pays off when scale matters. Clients who’ve swapped similar compounds mid-project often encounter issues ranging from unforeseen byproducts to chromatography headaches.

    In our experience, consistent physical properties anchor process scale-up. Melting point ranges for 5-(2-Nitrophenyl)-2-Furaldehyde tend to stay sharp, meaning fewer surprises when running purification columns or solidification steps after reaction. Wet samples, or compounds absorbing ambient moisture due to improper storage, throw off mass balances and complicate downstream workups. Our real-world controls keep moisture content in check, ensuring every order lands at the dock in optimal condition.

    Applications: What Customers Actually Do

    Over the years, customers have shared dozens of application stories. Pharmaceutical research teams have leveraged the compound in synthesis routes toward anti-inflammatory and antimicrobial agents, utilizing the activated aldehyde function in condensation and cyclization steps. Others tap into the nitro group’s utility in reduction, substitution, or further elaboration—transforming the simple building block into a stepping stone for screening libraries.

    Outside pharma, the compound pops up in materials science functions. Some teams explore its reactivity in developer molecules for advanced photographic applications. Others push boundaries in heterocyclic pigment chemistry, exploiting the furan ring for color fastness improvements and stability tests. In these real-world routes, process reliability becomes mission-critical, because scaling up from milligrams to multi-kilogram orders tests every part of the supply chain. Any issues with batch homogeneity or unexpected impurity drag entire projects off-course, leading not just to delays but also to excess waste and added costs.

    Handling Downstream Challenges

    Few things frustrate end users more than inconsistent physical form. Clumping, inconsistent grain, and static build-up complicate weighing and dosing steps. When pressure builds on a busy lab team, minor annoyances can become workflow bottlenecks. We keep this reality in mind and make judicious use of controlled drying cycles and staged cooling at the tail end of manufacturing. Decades ago, we learned that ignoring these small steps can almost double customer support calls. Customers want ease of transfer—free-flowing powders or predictable crystallites—especially in automated labs or pilot plant settings where manual intervention should be limited.

    Quality Takes Experience, Not Promises

    Many producers claim to offer quality controls, but practical experience shows what actually works. For instance, all suppliers claim to pack under inert gas, but leak checks and double-sealed bags, often overkill in theory, make the biggest difference when a crate sits on a humid loading dock in monsoon season. Our staff has seen truckloads of downgrades avoided this way, chalking up real-world lessons that don’t appear in product datasheets. The same goes for logistics and labeling—what looks like simple documentation evolves into a chain of checks over years of near misses and learning through error.

    Each transfer, each label check, and each recalibrated drying oven play a role in delivering not just a chemical but a guarantee that what’s ordered will perform. For this product, buyers expect sharp melting points, high purity by NMR and HPLC, and stability throughout transit. It’s a trust built up batch after batch, with missed expectations fed back into process improvements, not ignored in the rush to ship out another drum.

    Troubleshooting in Real Labs

    Several times a year, a call or email surfaces describing a stalled route or analytical problem downstream. Sometimes, it’s a question about the impact of trace metal content, other times, unexplained spectral signals. We’ve learned to keep lab notebooks open and answers transparent. Users rely on our willingness to walk back through analytical logs, re-run samples, or even pull retention material for side-by-side testing. Anyone who’s ever had to restart a multi-step synthesis knows the difference it makes when a supplier shows up with real troubleshooting support, not rerouted emails or generic advice.

    Safety From the Ground Up

    Handling nitro compounds comes with clear safety mandates. Both odor and reactivity call for specific ventilation and handling protocols in the production environment. Years of safe manufacturing refine these routines—batch charging order, temperature ramps, and the specific gloves and goggles stocked on the line. When regulatory teams visit for inspections, our records and incident logs speak for themselves. We don’t rely solely on desk audits or promises. Our lines have weathered real incidents, and every procedure update strives to anticipate what can go wrong before it does. End users benefit from this experience, particularly those scaling from milligram trial reactions to pilot or kilogram work. Safety, in this context, isn’t just personal protection but a protocol ensuring both quality and continuity.

    Environmental Responsibility

    Manufacturing aromatic aldehydes and nitro compounds tackles not just technical but environmental concerns. Our team invests heavily in solvent recovery and waste stream controls. Over the past five years, process modifications cut waste water volume by a third for every ton manufactured. That effort keeps operating licenses current and delivers responsible stewardship, but, more importantly, it ducks future disruptions from environmental audits or supply chain interruptions. End users increasingly notice such efforts, not only for compliance but as part of their own sustainability mandates—especially for projects that look ahead to global filings or trademarks.

    Process Adjustments Over the Long Haul

    Every campaign reveals new variables. Solvent sourcing struggles crop up, impacting crystallization on scale. Deep winter chills slow down post-reaction dry downs, meaning yield or drying times fluctuate. Each round offers a learning opportunity; sometimes a tweak in charge rate, sometimes a shift to a different agitation protocol. These adjustments make their way into formalized process instructions, but they grow from on-the-floor learning, not hypothetical modeling. The cumulative effect spills over to the end user—more predictable properties, easier downstream work-up, and fewer unpleasant surprises in both analytical and preparative settings.

    Real Value in Reliability

    In the specialty chemical world, value rarely comes from grand claims. It takes on-the-ground discipline—batch logbooks, standard operating procedures honed through trial and error, and a staff incentivized to take pride in each drum released. Many customers return for this reason alone. They’ve seen projects pushed off-schedule due to unreliable intermediates. Those who rely on our 5-(2-Nitrophenyl)-2-Furaldehyde count on being able to replicate results, send regulatory registrations overseas, or line up new multi-step syntheses without hiccups related to the starting material.

    When we’re asked what differentiates our product from those offered by bulk suppliers or traders, we talk about response time, willingness to review production notes, and transparency in every spec. Anyone relying on this compound appreciates clear answers to impurity questions and readiness for peer-level technical discussions. We’ve supplied researchers from lab-bench gram scales through metric ton pilots, and in each phase, feedback loops drive further improvement.

    Building on Customer Feedback

    Continuous improvement isn’t just a slogan hung on a factory wall. Every end-user report—whether complaint or praise—feeds straight into worksite meetings and process updates. Maybe a recent order arrived with crystals too fine for the end user’s semi-automated equipment. That event triggers quick dialogue across production, quality, and dispatch, prompting adjustments in final sieving or packaging protocols next round. This dynamic feedback strengthens the downstream workflow, saving cumulative time and cost for both sides.

    Sometimes, customer suggestions spark broader innovation. Over the past decade, new applications in photoresist chemistry came directly from a partner’s willingness to share their own challenges and goals. Our technical team responded with recommendations for intermediate purification, resulting in co-published application notes and, eventually, broader utility for other customers in electronics intermediates. This spirit of collaboration and transparency creates better products, makes jobs easier, and cements longstanding partnerships.

    What Lab Teams Need From Suppliers

    In real lab environments, staff care about more than a spec sheet. They need to know what’s in the bottle, what’s possible in a rush order, and that the manufacturer stands behind every lot shipped out. Our technical support reflects this reality: experienced chemists and analysts answer calls and emails directly. Requests to cross-check spectral forms, provide historic batch details, or send application-specific recommendations receive earnest attention, as we recognize every research timeline runs on tight deadlines.

    Where suppliers fall short on technical dialogue, researchers chase answers in the dark, wasting effort and grinding through repetitive troubleshooting. Our process, developed over years, allows teams to plan syntheses around predictable results and a known supply chain—critical on projects where IP and regulatory filings come next. Customer priorities have informed everything from how we validate our analytical suite to the incremental environmental upgrades we’ve built into the site.

    Closing: Why Experience Makes a Difference

    Working down in the factory, where real material gets made and shipped, teaches the importance of every seemingly minor detail—double-walled drums, redundant analytical checks, responsive logistics. No amount of promotional language compares to the trust that comes from delivering reliable intermediates project after project. Our focus on 5-(2-Nitrophenyl)-2-Furaldehyde comes back to this ethos: hands-on oversight, open channels for honest feedback, and respect for the chemists and engineers who rely on unambiguous, performance-backed building blocks. Every kilogram reflects years of accumulated experience, safety discipline, and lessons hard-learned on plant floors and in laboratories around the world.