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5-Fluoro-2-Iodonitrobenzene

    • Product Name 5-Fluoro-2-Iodonitrobenzene
    • Alias 5-Fluoro-2-nitroiodobenzene
    • Einecs 840-055-5
    • 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

    951381

    Product Name 5-Fluoro-2-Iodonitrobenzene
    Cas Number 321-29-1
    Molecular Formula C6H3FINO2
    Molecular Weight 265.99
    Appearance Light yellow to beige solid
    Melting Point 61-64 °C
    Density 2.14 g/cm³ (estimated)
    Purity Typically >97%
    Solubility Slightly soluble in organic solvents; insoluble in water
    Smiles c1cc([N+](=O)[O-])cc(F)c1I
    Inchi InChI=1S/C6H3FINO2/c7-4-1-2-5(9(11)12)3-6(4)8/h1-3H
    Storage Conditions Store at 2-8°C, protect from light
    Hazard Statements May cause irritation; handle with care

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 5-Fluoro-2-Iodonitrobenzene, sealed with PTFE cap, labeled with hazard and product information.
    Shipping 5-Fluoro-2-Iodonitrobenzene is shipped in tightly sealed, chemical-resistant containers, clearly labeled according to regulatory requirements. The packaging safeguards against moisture and physical damage. It is transported as a hazardous material, ensuring compliance with international shipping regulations, including documentation and safety data sheets, to guarantee safe handling, transit, and delivery.
    Storage 5-Fluoro-2-iodonitrobenzene should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. The storage area should be free from incompatible substances, such as strong bases or reducing agents. Properly label the container, and access should be limited to trained personnel using appropriate personal protective equipment.
    Application of 5-Fluoro-2-Iodonitrobenzene

    Applications of 5-Fluoro-2-Iodonitrobenzene in Industrial Manufacturing

    5-Fluoro-2-Iodonitrobenzene serves as a critical intermediate in specialized chemical synthesis, supporting downstream manufacturing for pharmaceuticals, agrochemicals, advanced materials, and electronics. As a direct producer, we supply high-purity batches designed for stringent industrial requirements and global standard compliance in each application area.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use 5-Fluoro-2-Iodonitrobenzene primarily within the synthesis of selective kinase inhibitors, antiviral agents, and cardiovascular drugs. It enters the process as a halogenated nitrobenzene intermediate during multi-step organic synthesis, often for constructing fluorinated aromatic scaffolds via palladium-catalyzed cross-coupling or nucleophilic aromatic substitution. Downstream users integrate this building block to achieve specific molecular frameworks, ensuring traceability and batch consistency to meet regulatory review. Typical formulations require controlled stoichiometry to minimize byproduct contamination and maximize batch yields, guided by active ingredient synthesis routes.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapter <85> Bacterial Endotoxins Test
    • European Pharmacopoeia monographs section 2.2.46 (Chromatographic separation techniques)
    • FDA 21 CFR Part 211 cGMP for finished pharmaceuticals

    Typical usage ratio

    • 0.5–2.0 molar equivalents per batch, adjusted based on target molecular scaffold
    • Controlled addition (dropwise or staged) to minimize side products

    Downstream process integration

    • Introduced at the early synthetic route as a core halogenated aromatic unit
    • Reaction step: Suzuki, Buchwald–Hartwig, or Ullmann-type coupling
    • Followed by hydrogenation or reduction and deprotection where required
    • Integrated into automated or continuous API synthesis systems

    Final product types

    • Kinase inhibitor drug compounds
    • Pyridine-based cardiovascular agents
    • Amino-fluorobenzene core antivirals
    • Clinical trial API batches (phase I-III)

    2. Agrochemical Intermediate Synthesis

    Producers in the agrochemical sector employ our material as a specialized intermediate when synthesizing pre-emergent herbicides and novel fungicidal active components. The nitrofluorinated aromatic ring offers improved selectivity and resistance profiles in target compounds. The integration occurs within closed, monitored reactors under controlled temperature and pressure, supporting scalability for both pilot and commercial production runs. Quality assurance confirms residual solvent and halide content align with agrochemical residue regulations.

    Industry compliance standards

    • OECD Guideline 107: Partition Coefficient (n-octanol/water)
    • FAO/WHO Codex Alimentarius pesticide residue definitions
    • ISO 9001:2015 Quality Management Systems for process validation
    • European Union Regulation (EC) No 1107/2009 for plant protection product approval

    Typical usage ratio

    • 0.4–1.2 equivalents relative to main nucleophile in synthesis
    • Adjusted per specific crop protection molecule and regulatory-driven impurity limits

    Downstream process integration

    • Primary aromatic ring source early in active ingredient (AI) synthesis
    • Employed during nitro reduction, halide substitution, or coupling with heterocyclic amines
    • Batch monitoring with in-process HPLC purity analysis
    • Residue removal and isolation steps before AI formulation

    Final product types

    • Pre-emergent herbicides (e.g., fluorinated benzamide derivatives)
    • Triazole-based fungicides
    • Sulfonylurea herbicidal precursors
    • Registered active ingredients for agrochemical product lines

    3. OLED and Liquid Crystal Material Precursors

    The electronics manufacturing sector utilizes 5-Fluoro-2-Iodonitrobenzene as a core precursor in some OLED emitter synthesis pathways and advanced liquid crystal materials for display applications. The material contributes to construction of highly conjugated molecular segments with defined fluorine functionality, directly influencing electron transport and emission properties. Precision control of the incorporation step is critical for achieving batch-to-batch uniformity of the resulting optoelectronic properties. Manufacturers validate these batches for trace metal and residual solvent content to comply with electronics-grade material standards.

    Industry compliance standards

    • IEC 61249-2-21 for halogen content measurement
    • JEITA ED-7307 Environmental Standards for Electronics
    • RoHS (Restriction of Hazardous Substances) Directive 2011/65/EU
    • TUV SUD QM system certification for display materials

    Typical usage ratio

    • 0.8–1.3 molar equivalents in conjugated segment synthesis
    • Often limited by batch scale and desired emission spectrum tuning

    Downstream process integration

    • Input for Buchwald–Hartwig amination to generate OLED emitter building blocks
    • Reactive halogen source in Stille or Suzuki coupling to build π-conjugated backbones
    • Liquid crystal host or dopant synthesis under rigorously dry, inert conditions
    • Purification and polymorph selectivity tuning before panel assembly

    Final product types

    • Blue/green OLED emitter molecules
    • Index-matching liquid crystal materials
    • Transistor-grade organic semiconductors
    • Specialty display active layers

    4. Organic Synthesis for Dye and Pigment Manufacturing

    Dye and specialty pigment producers value this compound as a key raw material in the synthesis of high-performance, halogenated azo and anthraquinone dyes. The nitro and iodine functionalities enable effective regioselective substitution, supporting the introduction of electron-donating or -withdrawing groups around the aromatic ring. Process chemists apply calibrated reaction profiles to ensure color consistency, light fastness, and thermal stability in the final product. Manufacturing lines operate under environmental permits that control emissions from halogenated intermediates.

    Industry compliance standards

    • REACH Annex XVII restrictions for hazardous aromatic amines
    • Oeko-Tex Standard 100 regarding use of halogenated intermediates
    • ISO 9001 process and traceability documentation
    • ZDHC (Zero Discharge of Hazardous Chemicals) Manufacturing Restricted Substances List

    Typical usage ratio

    • 0.3–1.0 equivalents per pigment or dye molecule synthesized
    • Varies with chromophore structure and color target (range: 5–15% input relative to total batch)

    Downstream process integration

    • Introduced during diazotization or coupling step with aromatic amines
    • Enables coupling with functionalized amino or hydroxy derivatives
    • Monitored by TLC/HPLC to track complete reaction and minimize residual halide
    • Employed in specialized lines for deep-color, synthetic pigment production

    Final product types

    • Halogenated azo dyes for textile applications
    • Anthraquinone-based pigments for plastics and coatings
    • Specialty ink colorants
    • Technical grade dye intermediates for export
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 5-Fluoro-2-Iodonitrobenzene: A Manufacturer’s Perspective

    What Sets 5-Fluoro-2-Iodonitrobenzene Apart

    Working directly with the synthesis of 5-Fluoro-2-Iodonitrobenzene, we see its value both in the laboratory and for its downstream applications. The chemical structure—made up of a fluorine atom, an iodine atom, and a nitro group attached to a benzene ring—gives this molecule a niche that is hard to fill with substitutes. Chemists looking to build more complex molecules out of robust aromatic intermediates have singled out this compound for its reactivity and unique properties. We prioritize its purity and consistency batch after batch, because even minor changes can affect research output and manufacturing results.

    Core Identity and Model Information

    We classify this material as 5-Fluoro-2-Iodonitrobenzene, with the molecular formula C6H3FINO2 and the CAS registry number where available. Our focus has always been on producing greater than 98% pure product, but we monitor other quality parameters during every lot’s creation—such as moisture content, melting range, and solvent residues. Not all providers approach compliance with the same discipline. From decades of handling hazardous aromatic compounds, we've learned the importance of monitoring every input, reaction time, and purification step. This approach brings confidence to customers who need reliable performance. For packaging, we select materials that minimize degradation without introducing leachables. Tightly closed amber glass bottles, lined with PTFE gaskets, make sense for this solid.

    Where It Finds Its Use

    Much of 5-Fluoro-2-Iodonitrobenzene serves the pharmaceutical industry, particularly in drug discovery and development programs seeking fluorinated building blocks. Medicinal chemists favor this compound in creating lead molecules and optimized drug candidates. The fluorine atom can influence metabolic stability in potential medicines, while the nitro and iodine functions open up diverse reaction routes—Suzuki-Miyaura couplings, nucleophilic aromatic substitutions, and other methodologies are well-supported here. Our customers, mainly in Asia, Europe, and North America, share case studies showing that the aromatic iodo functionality reacts with palladium catalysts under relatively mild conditions, which often eases scale-up. These details trickle back to us from process engineers, who routinely ask for 5, 25, and 100 kg lots, not just gram quantities for research.

    Comparisons to Other Nitrobenzenes and Halogenated Benzenes

    5-Fluoro-2-Iodonitrobenzene often gets compared to easier-to-source compounds, such as 2-iodonitrobenzene or 4-fluoro-2-nitroaniline. The fluoro-iodo substitution pattern offers nuances that neither a mono-halogenated nor a pure nitroaromatic can replicate. In some reactions, the combination of fluorine and iodine provides a switchable reactivity. For nucleophilic substitution, the fluorine can serve as either a leaving group or as a steric and electronic modulator, guiding where transformation takes place. Conversely, the iodo group remains a favorite for those looking to transition towards further C–C coupling chemistry—which isn’t something 2-nitroaniline can deliver. For researchers, seeing how subtle changes like the addition of a fluorine atom affects downstream yields or toxicity makes the difference between a successful patent or another failed trial. Our technical support staff have helped bench scientists tailor purification strategies that account for trace impurities, which can behave very differently depending on which halogen dominates the ring.

    Sourcing and Manufacturing Considerations

    Producing 5-Fluoro-2-Iodonitrobenzene gives us a window into the limits and opportunities in aromatic halogen chemistry. Starting from fluorinated toluenes and careful introduction of the nitro group, our production line runs small test batches before committing to full-scale drums. Each lot brings its own surprises—variable yields, the occasional byproduct, and safety risks linked with exothermic reactions. Our reactor operators carefully monitor temperatures, addition rates, and pressures to minimize runaway reactions, drawing on a culture of safety that would be hard to match at smaller or less disciplined plants. We’ve invested in gas scrubbing and wastewater treatment tailored to the odds and ends produced during mixing and purification, which in our experience, has smoothed our regulatory audits and made our site easier to insure.

    On the analytical side, differential scanning calorimetry and various chromatographic methods keep us abreast of minor process shifts. What customers rarely see are the incremental adjustments demanded by every year’s change in raw material supplier or tweaks in regional regulatory thresholds. We often hear from our partners who tried material sourced from brokers or lesser-known traders—when a product with similar naming but inferior quality ends up causing costly batch failures or low yields. That kind of disappointment pushes users toward direct engagement with those of us who actually run the reactors and do the real troubleshooting.

    Consistency, Research, and Scalability

    Controlling crystalline form, particle size, and trace contaminant levels defines what separates a research-grade supplier from a true manufacturing partner. Our experience hits home during discussions about scale-up—the step between bench and pilot plant, or between pilot and full production. Inconsistent batches can halt an entire drug screening program or trigger regulatory questions. We don’t just meet an arbitrary specification but work with clients to tune every parameter that matters for downstream processing: solubility in reactors, reactivity in flow chemistry, and even image analysis for powder flow. These points become particularly relevant when life sciences clients submit documentation to regulatory agencies. Our stability studies and retained samples smooth that process, and we react promptly if clients detect any issue that could reflect back on our raw material.

    There’s a temptation, especially for some chemical users, to chase lower quoted prices. When those same customers compare our detailed batch traceability, retention of analytical samples for years, and willingness to troubleshoot technical problems, they routinely come back to long-term supply agreements. That loyalty hasn’t grown overnight—it’s something that developed because we’ve solved problems in real-world environments. Once, a customer’s HPLC method picked up a low-level impurity—similar to 4-fluoro-2-iodonitrobenzene, detected only after a particularly sensitive downstream reaction. We collaborated by sending additional analytical data and adjusting purification parameters to suppress this byproduct in future lots. In these moments, the direct experience of a manufacturer pays dividends, both for us and for our partners.

    Transport and Storage Challenges

    Not all chemical intermediates travel well. 5-Fluoro-2-Iodonitrobenzene, while stable under ambient conditions, does have risks associated with improper storage. We keep our temperatures under 25°C and guard against moisture, since traces of water speed up hydrolysis in certain halogenated aromatics. Our logistics team has learned to pre-cool storage areas in tropical zones and to stagger deliveries around the wet season when humidity spikes. With global customers, we follow region-specific rules—in Europe, single-use packaging may be mandatory, while American clients sometimes require tamper-evident seals. By keeping all loads tightly crated and tracking humidity indicators, we prevent clumping and oxidation. Warehouses often ask about shelf-life. We pulled samples held for over 24 months and observed no significant hydrolysis or color darkening—validating the care taken in our handling, but also a testament to the stability of the product when protected from the elements.

    Sustainability and Responsible Manufacturing

    As manufacturing standards evolve, chlorinated solvents and hazardous waste from nitrobenzene chemistry have moved under stricter regulatory scrutiny. We responded early by switching to solvents with easier end-of-life treatment, and by capturing halogenated emissions for safe disposal. Our process engineers designed a closed-system protocol for addition and transfer, which almost halved yearly solvent consumption. The leadership team committed to upgrading our incineration and distillation facilities, not under external pressure, but because we saw leaking value in wasted reagents and residual mother liquors.

    Some years back, a client in Scandinavia required documentation showing every input’s country of origin and a complete hazardous waste manifest. We invested in digital tracking systems tied to lot numbers—from raw fluorinated material supply through to finished, packaged product. This transparency cut down on compliance headaches and reassured partners who face rising environmental, social, and corporate governance demands. Corporate clients increasingly ask whether our batch processes are “green,” and while the chemistry of halogenated aromatics isn’t going fully bio-based tomorrow, the steps to minimize environmental impact are ongoing.

    Worker Safety and Process Reliability

    After handling thousands of kilos each year, our lab and plant staff have a clear sense that aromatic iodides and nitrobenzenes need strict handling protocols. Airborne dust suppression, continuous monitoring, and personal protective equipment define daily routines. In our main plant, safety interlocks monitor glove box pressure and emergency shutoffs surround the nitration units. Staff training covers chemical hygiene, spills, and first response. One missed day of safety protocol can cost more than any single shipment of product. We’ve learned to invest more in staff retention and safety culture than in automation alone, because most incidents in similar factories happen when training lapses or fatigue sets in. Our attention to workplace health supports overall consistency and product quality, confirming again that reliable chemistry emerges only from reliable teams.

    Changing Markets and Research Needs

    Drug screening programs continue to demand more complex and functionalized aromatic intermediates. We keep a close eye on patent trends and technical journals to update our synthesis and purification strategies. In the early 2010s, biopharma customers raised their demands for higher assay, lower halogen contamination, and tighter particle size ranges. Instead of treating these requests as add-ons, we integrated feedback directly into our production processes, leading to improved batch reproducibility. Our technical team is available to assist with custom transformations involving 5-Fluoro-2-Iodonitrobenzene, and we keep detailed reaction notes on hand when designing protocols for new coupling reactions or downstream derivatization. Rather than work from a standard recipe, we listen and adjust, providing more utility for advanced research.

    Market Trends and Quality Assurance

    Most researchers come to us when their internal teams reach a bottleneck on scalability or synthesis control. Quality assurance underpins every step, right down to the logs we keep for solvent lot number, reactor pressure curves, and yield histories. There’s a direct link between plant conditions and end product performance. A spike in downtime or an out-of-spec raw material batch ripples through to every customer, so our maintenance schedules are set up to prevent, not react. We maintain retain samples and offer partners access to our archived analytical data, so they’re never in the dark about what went into the intermediates entering their processes.

    Demand for halogenated nitrobenzenes sees periodic surges, often following a round of new patent filings or research breakthroughs. Research consortia and contract development organizations frequently request technical documentation beyond safety data sheets—spectral data, impurity profiles, and advice on downstream compatibility. Our R&D group responds to questions about cross-coupling yields, handling protocols, and residue removal, and we share insights based on our batch records rather than generic literature data.

    Opportunities for Improvement and Collaboration

    As chemistry scales to new frontiers—continuous flow reactors, in situ monitoring, and greener synthesis—our team remains deeply involved in both pilot and industrial production. Our close relationships with catalyst vendors and process technology partners help us suggest improvements that pay off in yield, waste reduction, and compliance. We see opportunities to swap out legacy reagents for less hazardous substitutes and to reinvent how nitroaromatic intermediates are produced at scale. Every improvement in upstream raw materials or synthesis conditions has ripple effects, from worker safety to customer satisfaction and downstream innovation.

    Direct communication between manufacturer and end user has proven to be the most reliable path to long-term improvement. We take every technical feedback loop seriously—from minor color shifts, through solubility testing, to concerns about residual solvents—and turn these observations into process upgrades. Our best collaborative successes came from customers willing to share raw data or provide early warning on issues, so we could fine-tune production before the problem became costly. This relationship-centered approach stands apart from what traders or brokers can offer, since only direct handling of the chemistry provides such deep expertise.

    Working With Us: Closing Thoughts on Making the Right Choice

    Selecting a source for 5-Fluoro-2-Iodonitrobenzene means more than comparing purity numbers or batch sizes. We have learned—sometimes the hard way—that the true value lies in the consistency of communication, the willingness to share technical knowledge, and the investment in long-term quality. Our roots as an actual manufacturer, not merely a distributor, underline every shipment and every answer we offer to partner questions. 5-Fluoro-2-Iodonitrobenzene may look like one compound among many to the uninitiated, but it brings subtle properties that set it apart from the crowd—and only real manufacturing experience uncovers those secrets. By maintaining deep integrity in our processes, a responsive approach to customer needs, and an unwavering focus on safe, sustainable, high-quality manufacturing, we support a broad spectrum of research, development, and industrial goals.