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3-Nitrodibenzofuran

    • Product Name 3-Nitrodibenzofuran
    • Alias 3-Nitro-dibenzofuran
    • Einecs 217-611-0
    • 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

    700406

    Iupac Name 3-nitrodibenzofuran
    Cas Number 1011-94-1
    Molecular Formula C12H7NO3
    Molecular Weight 213.19 g/mol
    Appearance Yellow solid
    Melting Point 136-138°C
    Solubility In Water Insoluble
    Pubchem Cid 79727
    Smiles c1ccc2c(c1)oc3ccccc3c2[N+](=O)[O-]
    Inchi InChI=1S/C12H7NO3/c14-13(15)9-6-7-3-1-2-4-8(7)12-11(9)5-10(12)16-12/h1-6H

    As an accredited 3-Nitrodibenzofuran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A sturdy amber glass bottle containing 25 grams of 3-Nitrodibenzofuran, tightly sealed with safety cap, labeled with hazard warnings.
    Shipping 3-Nitrodibenzofuran should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must comply with regulations for hazardous chemicals, typically under UN numbers relevant to organic compounds. Handle with appropriate labeling and documentation, and ship via certified carriers specializing in chemical transport to ensure safety and regulatory compliance.
    Storage 3-Nitrodibenzofuran 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 it from light and moisture. Properly label the storage container, and keep it away from heat or direct sunlight to avoid decomposition. Store according to local chemical safety regulations.
    Application of 3-Nitrodibenzofuran

    Applications of 3-Nitrodibenzofuran in Industrial Manufacturing

    As an established manufacturer of 3-Nitrodibenzofuran, we deliver advanced-grade material for high-precision industrial segments. This application section details the real-world utilization of 3-Nitrodibenzofuran across several demanding value chains, focusing on compliant formulation, integration in industrial processes, and specification-driven end products.

    1. Electronic Material Intermediates for High-purity OLED Emissive Layers

    Specialty electronics manufacturers use 3-Nitrodibenzofuran as an intermediate for developing organic emissive molecules in the fabrication of OLED display and lighting panels. In this context, the compound provides critical aromatic ring stability and electron-withdrawing properties that influence blue-emitting layer performance. Typically, R&D and production labs incorporate it during the synthesis of host and dopant molecules for high-brightness, longer-lifetime OLED devices, with precise process control to meet exacting display OEM requirements.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive, EU)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU)
    • IEC 61249-2-21: Halogen-Free Substance Limitation for Substrates
    • ISO 9001-certified integrated management systems

    Typical usage ratio

    • 0.5–2 mol% as an upstream intermediate in host compound synthesis; the exact amount depends on the targeted photophysical properties and final compound purity needs.

    Downstream process integration

    • Incorporated at the monomer synthesis stage for OLED material development—specifically, used in the preparation of dibenzofuran-based small molecules via nitration/derivatization reactions prior to purification and vacuum deposition.

    Final product types

    • OLED display panels (TV, mobile, automotive clusters)
    • OLED lighting sheets
    • Emission layer organic precursors

    2. Pharmaceutical Intermediate for Heterocyclic Drug Synthesis

    Active pharmaceutical ingredient (API) manufacturers employ 3-Nitrodibenzofuran as a tightly specified intermediate during multi-step heterocyclic drug molecule synthesis, especially in the preparation of benzofuran or related cores for central nervous system therapeutics and oncology candidates. Demand for this compound centers on its consistent purity, trace impurity control, and reactivity under nucleophilic substitution or reduction steps, directly impacting final API quality attributes validated in GMP facilities.

    Industry compliance standards

    • ICH Q7 (EU/US GMP for Active Pharmaceutical Ingredients)
    • Ph. Eur. and USP monographs (for final APIs, where applicable)
    • 21 CFR Part 211 (Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; US FDA)
    • Traceability under ISO 13485 for medical usage pathways

    Typical usage ratio

    • Varies by synthesis scheme; 0.2–5 mol equivalent, based on target molecular scaffold and scale-up parameters during intermediate coupling, reduction, or core-building stages.

    Downstream process integration

    • Introduced during early- to mid-stage multi-step synthesis, commonly reduced or further functionalized before API intermediate assembly and purification through crystallization or column chromatography.

    Final product types

    • CNS active pharmaceutical ingredients (benzofuran- or related-based)
    • Research-stage oncology drug candidates
    • Reference standards for medicinal chemistry labs

    3. Functional Dye and Pigment Building Block for Technical Applications

    Advanced dye and pigment manufacturers integrate 3-Nitrodibenzofuran as a key aromatic nitro compound in the backbone development of high-performance colorants, particularly in constructing stable, functionalized dye molecules for industrial textile finishes, polymer coloration, and UV-resistant technical inks. The electron-withdrawing nitro group allows subsequent amination or coupling reactions, consistently supporting batch-to-batch pigment reproducibility and long-term performance.

    Industry compliance standards

    • EN 71-3 (Migration of Certain Elements, for textiles and toys; EU)
    • OEKO-TEX Standard 100 (Textile Ecology Labelling, restricted substance list)
    • ASTM D4300-03 (Standard Test Methods for Lightfastness of Colorants)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List, textile sector)

    Typical usage ratio

    • Adjusted in the range of 1–15 weight% per batch, depending on required shade depth, solubility, and fastness properties of the target dye or pigment system.

    Downstream process integration

    • Employed during the initial diazotization and coupling stages to generate nitro- or amino-functionalized aromatic dye intermediates ahead of downstream solubilization, salt formation, and micronization steps for the finished colorant.

    Final product types

    • High-stability disperse dyes for polyester fiber coloration
    • Technical-grade printing inks
    • UV-stable polymer pigment masterbatches

    4. Specialty Polymer Synthesis for Advanced Material Composites

    Producers of advanced specialty polymers incorporate 3-Nitrodibenzofuran for introducing rigid aromatic segments and nitro functionalities during the polycondensation or copolymerization of high-performance engineering plastics. Its use modulates backbone polarity and thermal stability, which can be tuned for end-use demands in sectors such as microelectronics encapsulation, high-strength coatings, or fiber-reinforced composites approved for critical infrastructure.

    Industry compliance standards

    • ISO 9001 and ISO 14001 (Quality and Environmental Management for Polymer Manufacturing)
    • UL 94 (Standard for Safety of Flammability of Plastic Materials for Parts in Devices and Appliances, US)
    • EN ISO 11357 (Thermal analysis of polymers by DSC)
    • RoHS and REACH compliance for final composite materials

    Typical usage ratio

    • Set at 0.5–10 weight% in prepolymer resin blends; dosage refined in R&D and pilot lines to balance glass transition temperature, dielectric constant, and end-use processing requirements.

    Downstream process integration

    • Added in initial feed or co-polymerization reactors when preparing engineered resin base, followed by post-polymerization blending, granulation, and extrusion tailored to application performance specs.

    Final product types

    • High-temperature encapsulation resins for microelectronics
    • Polymer matrix composites in aerospace and automotive parts
    • High-gloss functional coatings with tailored dielectric/thermal profiles
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    Certification & Compliance
    More Introduction

    Introducing 3-Nitrodibenzofuran: Chemical Character and Application Insights

    What Sets 3-Nitrodibenzofuran Apart in Precision Synthesis

    As a manufacturer deeply involved in preparing high-purity aromatics, we have learned that certain molecules turn out to be quietly essential despite their lack of headline fame. 3-Nitrodibenzofuran carries that modest importance. As a derivative of dibenzofuran, this compound introduces nitro functionality into the fused ring system. Its structure—dibenzofuran substituted at the third position with a nitro group—offers a matching blend of stability and reactivity, attracting specialized research and advanced synthesis labs.

    On our shop floors and inside the pilot bays, we listen to customers describe what conventional dibenzofuran can’t do. Many standard-grade aromatics can’t take part in selective downstream reactions. They lack sufficient activation points or leave too much noise in analysis because their impurity profiles travel stubbornly through the production pipeline. 3-Nitrodibenzofuran steps up with its rich electron-withdrawing nitro group, delivering a compound capable of forming a range of new bonds, especially where electrophilic or nucleophilic aromatic substitution gets tricky otherwise.

    Manufacturing Process: A Matter of Control and Confidence

    We take our responsibility for quality seriously. Our process starts from carefully qualified precursors, often monitored from the day they arrive. Each stage, from initial nitration to workup, requires diligent temperature and pH control. Yield drifts threaten to pull unwanted byproducts into the finished batch, so we build checkpoints into our sequence. The fate of side products—often chlorinated or multiply nitrated cousins—dictates careful fractionation and purification. This hands-on vigilance pays off downstream. Researchers and formulators who depend on us know how irritating a stubborn impurity becomes when a reaction fails or when one signal refuses to disappear from spectroscopy.

    Given a sample of our typical run, 3-Nitrodibenzofuran appears as a faintly yellow crystalline powder, melting above 140°C. We routinely target purities greater than 98.0% as confirmed by GC-MS and NMR. Handling properties—administrated flowability and minimal static adherence—reflect our continual process refinement. After years running batches of this and similar heterocyclic nitroaromatics, our team recognizes the details that matter: limiting peroxide buildup, controlling VOCs, and capping residual acids. Over time, we have reduced solvent consumption and waste by optimizing not only the main reaction but also its workup, which customers seldom see but benefit from through traceability and batch consistency.

    Working with 3-Nitrodibenzofuran: Bench Experience and Scale-Up Factors

    Academic teams, contract labs, and intermediate producers come to us with operational questions. In the field, chemists and engineers seek reliability and practical feedback—not just paperwork specs. We have seen 3-Nitrodibenzofuran become crucial in the creation of specialty dyes and advanced electronic materials. Its reactivity at the 3-nitro position allows regioselective reductions, leading to amino-derivatives, or it serves as a core for additional substitutions and cross-coupling experiments. In pharmaceutical research, its unique backbone can introduce non-trivial electronic interactions—helpful for structure-activity investigations where unsubstituted dibenzofurans fall short.

    Careful users note that while 3-Nitrodibenzofuran works efficiently in certain reactions, it resists over-activation and rarely undergoes uncontrolled decomposition under well-chosen process conditions. We advise colleagues in the field about solvent choices, typical temperatures, and common pitfalls in scaling up from grams in the lab to multi-kilo runs. Using hydrogenation methods, for instance, selectivity favors the 3-nitro group without disturbing the fused core, provided pressure and catalyst type are chosen wisely. Small errors in the atmosphere or agitation can mean unwanted side products, which our experience helps preempt.

    Experience also teaches us not to underestimate cleaning issues. Even trace residues pose risks in high-sensitivity instruments. Our solutions involve not only conventional wash solvents but also dedicated vessel finishes and process cycles. This investment may not show on the invoice, but our regular customers see it in the consistency they receive across batches and the rare necessity for rework.

    Comparable Compounds and Why Customers Choose This Route

    Some customers wonder whether to choose 3-nitrodibenzofuran, with its number 3-position functionalization, over similar products in our aromatic nitro series. For instance, 2- or 4-nitro analogs shift the reactivity map. Small as that structural variation may seem, it shapes the molecule's influence in downstream chemistry. The difference matters in everything from ligand coordination to the directionality of further functionalizations.

    From a manufacturing viewpoint, we find that the 3-nitro substitution brings advantages in reproducibility and shelf stability compared to positions more prone to delocalization effects. Colleagues assessing whether to adopt an ortho- or para- functionalized dibenzofuran often run comparative tests in parallel. With our batches, select analyses reveal the relative purity and ease of isolation between these analogs. In 3-nitro, those seeking to preserve the aromatic core and direct new substitutions efficiently get best results.

    Applications for 3-nitrodibenzofuran diverge sharply from those suited to unsubstituted compounds or chlorinated relatives. In dye synthesis, the nitro group enables color tuning through electron distribution, unavailable in simple dibenzofurans. For materials developing high-performance organic semiconductors, the presence in the molecule opens up new pathways for charge transfer or molecular stacking, as confirmed by our partners using final blends for device fabrication.

    Handling and hazard profiles differ as well. We have refined our preparative controls to minimize dusting and to reduce the residual volatility of the final product, lowering risk during drum loading and transfer. Feedback from customers running analytical validations shows that our tighter particle size distribution and lower impurity levels specifically in the 3-nitro compound rack up fewer instrument maintenance issues, keeping long-term R&D on schedule.

    Market Trends: Sourcing, Demand, and Prioritizing Quality

    The demand for 3-nitrodibenzofuran remains steady among those whose syntheses depend on unique aromatic building blocks. Unlike commodity chemicals, the end-users in this segment prioritize traceability and batch-level certification. We see customers in both established academic consortia and agile start-up labs moving to purchase by multi-kilo lots, especially for advanced material pursuits. They want supplier relationships that can guarantee stable supply over long timelines, not just a single transaction.

    Our manufacturing cycles have adapted to this need for consistency. Larger batches retain the same quality benchmarks as small R&D samples. We validate each lot prior to shipping, providing not just purity confirmation but a breakdown of trace byproducts and a documented processing trail. This commitment allows our downstream users to meet their own quality assurance requirements—often under regulatory oversight or for demanding patent disclosures.

    Those who have been in the business long enough recall times when certain nitroaromatics drifted in quality and supply, afterthoughts of crowded supplier lists. Today, we actively work with partners to forecast orders in line with real-world project pacing. Where possible, we offer flexible production slots and ramp up for temporary surges without compromising established standards.

    Environmental Standards, Safety, and the Value of Specialized Know-How

    Producing nitroaromatic compounds in bulk is not without its challenges, especially as regulatory expectations shift. Years of experience have made us alert to the hazards posed by nitro group-containing substances—from their thermal stability windows to their persistent nature in the environment. We invest in capture and treatment steps for process water and waste vapors. Modern nitration steps, when managed by practiced hands, keep releases low and secondary pollution minimal.

    By directly operating our own facilities, we avoid the delays and complications that sometimes turn up with traders or outsourcing. If a customer raises concerns about trace solvents or regulatory compliance on trace byproducts, we can implement feedback on-site, adapting purification or controls and documenting the improvements. Emerging disposal norms or substance registration rules do not catch us off guard. These continuous efforts secure us a place among preferred manufacturers for users surveying the market not only for price but for responsible stewardship.

    Safety remains a practical reality, not theory. We maintain team training with real incident reviews, and our plant-level incident rate falls below industry averages for nitroaromatic production. Not every customer sees the fire suppression systems or the real-time air monitoring stations, but those precautions underpin the trust they place in each drum and package.

    With years spent troubleshooting filtration or monitoring heat-up curves for nitroaromatic chemistry, we believe know-how makes a measurable difference. This expertise benefits not only custom projects but also everyday production. We build routines that preserve both the chemical’s integrity and the safety of our teams—tightening cleanout, inspecting protective layers on vessels, and ensuring routine maintenance never slips by undetected.

    Supporting Advanced R&D with Reliable Supply

    Researchers and material developers depend on more than just a bottle or bag of chemical. They need the documented assurance that each batch is what it claims, every time. Our in-house analytics run far beyond minimum standards. We archive chromatograms, NMR spectra, and impurity fingerprints for traceability. When a customer reaches out about a spectral anomaly or an unexpected result, we provide actual batch data, not just a generic certificate. This reduces downtime and restores confidence.

    In recent projects, we have watched 3-nitrodibenzofuran become a linchpin for the synthesis of new chiral ligands and specialty intermediates. Its role as a building block for OLED precursor molecules has grown—driven by the appetite for next-generation displays. In these emerging areas, raw material purity is everything. Even a small contaminant propagates through purification columns, threatens device stability, or results in regulatory holdbacks. Knowing this, manufacturers like us deliver more than a transaction. We stake our name and reputation on each kilogram delivered.

    Our relationship with the communities of scientists, engineers, and formulation chemists using 3-nitrodibenzofuran is grounded in open feedback and solution-oriented support. We don’t just ship, we listen. Sometimes customers expose a recurring challenge—a side reaction, a tough isolation, or an incompatibility with an existing step. We use this dialogue to review our own process, sometimes tuning the synthetic route or altering a drying protocol. This partnership approach isn’t always visible in the product write-up, but it matters for successful long-term collaborations.

    Process Improvements: Meeting High-Grade Expectations and Reducing Footprint

    With pressure mounting in the chemical sector to prove both performance and responsibility, we continue investing in process improvement. Upgraded reactors with better agitation and controlled addition keep yields consistent and minimize batch-to-batch variability. Inline analysis, including automated gas analysis and liquid chromatography, stops batch problems before they scale up.

    Solvent recovery loops and energy-efficient distillation save on input costs and lower our environmental load. For compounds like 3-nitrodibenzofuran, the manufacturing window is tight. Hydrolysis or reduction can degrade product before final isolation. Our team has refined not only core synthesis but also the post-reaction handling to capture target product at its best.

    By pursuing continuous feedback loops—both from instrumentation and real-world customer responses—we’ve rooted out inefficiencies from filter media selection to vacuum pump calibration. Reducing chemical handling risk starts on the shop floor and tracks all the way to storage and shipment.

    Process safety is a topic we address every shift, not just at audit times. Residual static, charging speeds during drum packing, and cross-contamination risks—these operational realities respond not to policy but to awareness cultivated by years of direct production.

    Understanding Supply Chain and Batch Logistics for R&D and Production

    As more users demand transparency up and down the chain, we document sources, pre-shipment tests, and transport conditions. By controlling our own logistics, we prevent last-minute delays or exposure to temperature swings. Nitrofuran derivatives travel best with moisture barriers and careful stacking; we routinely inspect all outbound shipments for compliance with current DG regulations.

    Bulk and sample orders both receive the same scrutiny, with cross-referencing against customer-specific standards, if available. As a result, those ordering for critical path projects — such as in advanced polymer synthesis or chiral auxiliary research — receive not only the product but also peace of mind about reproducibility and safety.

    Documented chain-of-custody and electronic batch records maintain traceability from raw feedstock to customer shelf. This level of attention makes the difference between speculation about quality and real-world assurance when customers set out to validate new routes or scale up to pilot.

    Final Thoughts on the Role of 3-Nitrodibenzofuran in Modern Chemistry

    From the vantage point of an engaged manufacturer, we recognize that chemicals such as 3-nitrodibenzofuran support new technologies, facilitate discoveries, and form the quiet backbone of niche industries. The blend of selectivity, reliability, and hands-on process knowledge shapes its adoption by serious research and commercial teams alike. By committing to best-in-class practices, responsive support, and continuous improvement, we do right by those advancing science at the edge of what’s possible.

    People choosing our product do so because they want more than a substance—they value the certainty built into every gram shipped. In this sector, trust is made not by grand claims but by consistent, proven results batch after batch.