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2,6-Diiodo-4-Nitroaniline

    • Product Name 2,6-Diiodo-4-Nitroaniline
    • Alias 2,6-Diiodo-4-nitrobenzenamine
    • Einecs 221-879-1
    • 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
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    Specifications

    HS Code

    732233

    Iupac Name 2,6-diiodo-4-nitroaniline
    Molecular Formula C6H4I2N2O2
    Molar Mass 421.92 g/mol
    Cas Number 698-96-6
    Appearance Yellow crystalline solid
    Melting Point 232-235°C
    Boiling Point Decomposes before boiling
    Density 2.64 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically > 95%
    Smiles Nc1c(I)cc([N+](=O)[O-])cc1I

    As an accredited 2,6-Diiodo-4-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, sealed with a screw cap, labeled "2,6-Diiodo-4-Nitroaniline," with hazard and handling information displayed.
    Shipping 2,6-Diiodo-4-Nitroaniline should be shipped in tightly sealed containers, protected from light, heat, and moisture. Ensure compliance with all local, national, and international regulations. Label as a hazardous chemical and include necessary documentation, such as Safety Data Sheet (SDS). Transport with appropriate hazard labeling and proper cushioning to prevent physical damage.
    Storage 2,6-Diiodo-4-Nitroaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and direct sunlight. Keep separate from incompatible substances such as strong oxidizers and reducing agents. Protect from physical damage and moisture. Ensure containers are clearly labeled and kept in a designated chemical storage area.
    Application of 2,6-Diiodo-4-Nitroaniline

    Applications of 2,6-Diiodo-4-Nitroaniline in Industrial Manufacturing

    2,6-Diiodo-4-nitroaniline serves as a specialty intermediate in industrial fine chemical synthesis, contributing to targeted downstream formulations in pharmaceuticals, agrochemicals, photographic materials, and specialty pigments. As a direct manufacturer, we control the quality and purity crucial for sensitive applications, ensuring compatibility with precise production environments and formulation protocols.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical companies utilize this compound as an iodo-substituted aniline intermediate for synthesizing various active pharmaceutical ingredients (APIs), especially where halogenation enhances molecular specificity and biological activity. The compound participates primarily in multi-step organic syntheses for targeted iodinated drug substances where nitroaniline derivatives are needed during the construction of aromatic systems with precise electronic and steric requirements. Every batch undergoes strict analytical validation to meet regulatory standards for impurity levels and residual solvents at each integration stage.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <1086> for Impurities in Drug Substances
    • EU EMA Guideline on the Chemistry of Active Substances
    • Current Good Manufacturing Practice (cGMP), US FDA 21 CFR Part 210/211

    Typical usage ratio

    • 0.8%–2.5% molar ratio in reaction mixture, adjusted based on desired degree of iodination and downstream functional group transformations.

    Downstream process integration

    • Charged during early-stage condensation or amidation when forming aromatic API scaffolds
    • Acts as a halogen source and aniline donor in the main synthetic step
    • Typically used under strictly anhydrous, controlled temperature conditions in glass-lined reactors
    • Product isolation employs solvent extraction and crystallization before further derivatization

    Final product types

    • Radiopaque contrast agents
    • Thyroid disorder pharmaceuticals (iodine-based APIs)
    • Iodinated antimicrobial agents
    • Iodinated oncology candidates for targeted therapies

    2. Crop Protection Synthesis (Agrochemicals)

    Specialty agrochemical producers use this material to synthesize advanced nitroaniline herbicides and fungicides where diiodo substitution confers selectivity and soil persistence. The nitro function supports downstream reductions to amines while maintaining electron-withdrawing character for specific heterocyclic couplings. Formulation teams monitor material integration at the intermediate stage to ensure accurate impurity profiles and consistent crop safety margins for regulatory approval.

    Industry compliance standards

    • FAO/WHO JMPR Pesticide Specifications and Quality Control Standards
    • ISO 1750: Pesticides and other agrochemicals – Common names
    • EU Regulation (EC) No 1107/2009 concerning plant protection products
    • REACH Registration compliance for intermediate handling

    Typical usage ratio

    • 1.5%–4% by mass in the primary reaction step, varying with target herbicide structure, soil bioavailability, and subsequent derivatization losses.

    Downstream process integration

    • Introduced during nucleophilic aromatic substitution for building the core nitroaniline structure
    • Post-reaction purification utilizes column chromatography to optimize final active substance purity
    • Amine reduction steps employ stringent pH control and metal catalyst safety protocols
    • Staging integrates trace element monitoring and solvent removal prior to downstream blending

    Final product types

    • Nitroaniline-based selective herbicides
    • Diiodinated fungicides
    • Seed treatment formulations
    • Crop-specific pre-emergent weed control agents

    3. Photographic Chemical Formulation

    In photographic film and imaging material production, 2,6-diiodo-4-nitroaniline functions as a precise color coupler intermediate, where the iodinated aniline unit provides radiant sensitivity and controlled reactivity for dye formation under light exposure. This chemical is introduced into multilayer film manufacturing to generate image-forming dyes with tailored absorption spectra and photostability essential for high-fidelity imaging. Quality assurance teams emphasize trace contaminant screening and color stability assessments at each batch scale-up.

    Industry compliance standards

    • ISO 18902: Imaging materials – Processed films – Physical property standards
    • ANSI/NAPM IT9.1: Photographic image stability guidelines
    • REACH Annex IX: Polymer and colorant use and restrictions
    • Japan Industrial Standards (JIS K7139) for colorant safety in sensitive media

    Typical usage ratio

    • 0.2%–1.0% by weight of color coupler premix, proportion based on final dye absorbance and required color intensity during emulsion coating.

    Downstream process integration

    • Added to gelatin or polymer binder premix for silver halide emulsion blending
    • Compound undergoes controlled in-situ reduction as a precursor to photoactive dye molecules
    • Emulsion coating utilizes precision dosing valves and temperature-controlled mixers
    • QC employs spectrophotometric validation and accelerated aging tests for each production run

    Final product types

    • Professional silver halide photographic films
    • Color photographic papers
    • Specialty imaging plates for X-ray and scientific use
    • Archival photographic display materials

    4. High-Performance Pigment Intermediates

    In the pigment and specialty dye industry, formulators use this diiodo-nitroaniline as an advanced intermediate for synthesizing complex organic pigments where halogenation improves weather fastness and enhances chroma in demanding environments. The molecule enters proprietary multi-step synthesis pathways for azo, azo-metal, and quinacridone pigment structures, contributing to tuned absorption and reflection profiles required by OEM coatings and plastics. In-process checks focus on controlling substitution patterns to ensure consistent pigment performance in the final matrix.

    Industry compliance standards

    • EN 71-3: Migration of certain elements in pigments for toys and childcare items
    • ASTM D476: Standard Classification for Dry Pigmentary TiO2 Products
    • ISO 9001:2015 Quality Management for pigment manufacturing
    • REACH Annex XVII: Limitation of hazardous substances in colorants

    Typical usage ratio

    • 0.5%–1.7% by weight in pigment precursor batch, tailored according to target halogen density and matrix compatibility.

    Downstream process integration

    • Participates in the diazotization coupling step to form stable aromatic amine dyes
    • Integrated before final pigment metallization or oxidation processes
    • Intermediate purification achieved via continuous solvent extraction and pH-controlled precipitation
    • Batches monitored for iodine retention during heat and light fastness testing

    Final product types

    • Automotive and industrial coatings pigments
    • High-durability plastic colorants
    • Printing inks requiring superior light resistance
    • Special effect pigments for security and anti-counterfeiting applications
    Free Quote

    Competitive 2,6-Diiodo-4-Nitroaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,6-Diiodo-4-Nitroaniline: A Closer Look from the Chemical Manufacturer's Bench

    Understanding the New Breed of Specialty Intermediates

    In the chemical manufacturing world, not every intermediate holds the same value for those of us who have our hands on the glass and steel. Here on our plant floors, 2,6-Diiodo-4-Nitroaniline (CAS 6635-24-5) stands apart from the standard range of aniline derivatives because we see its depth of character before it even leaves the drying oven. The dense orange-yellow crystalline powder serves as a reliable backbone in synthetic routes where fine iodine manipulation is called for. As manufacturers, we track purity and manage batch consistency with real focus, since even minor process shifts echo downstream with intermediates this specialized.

    The Workings Behind the Product

    Every batch of 2,6-Diiodo-4-Nitroaniline we produce takes shape through stringent control of temperature, pH, and precursor sourcing. The process calls for pinpoint handling of halogenation—each molecule gets its two iodine atoms at the 2 and 6 positions on the aniline ring, with a nitro group carefully placed in position four. The choice of methods, whether starting from the plain aniline base or shifting from another halogenated aromatic, affects everything from yield to residual solvent content. Our teams favor routes that offer stability and minimize byproducts, since the downstream steps for our customers can be sensitive to trace contamination or color bodies.

    Key Specifications We Rely On

    As manufacturers, we always measure purity with HPLC and confirm structure and substitution patterns through NMR and mass spectrometry. Our experience shows that correct melting point—usually in the 242–245°C range—signals a clean product. Off-melting batches almost always suggest a hitch either in crystallization or washing, and we act fast to correct it. Handling moisture content and insolubles proves critical; if the powder carries too much water or is slow to dissolve in polar organics, problems surface during customer synthesis. We've found that certain producers cut steps, leading to yellow-brown hues or residual starting material— shortcuts that always catch up with you in later stages.

    Comparing 2,6-Diiodo-4-Nitroaniline with Other Nitroanilines

    A lot of chemists ask us about differences between our product and simpler nitroaniline derivatives, like p-nitroaniline or its mono-iodo cousins. The addition of the extra iodine brings new reactivity and a heavier molecular weight—important factors in high-precision pharmaceutical, agricultural, and academic research. The electron-rich nature of the aromatic ring, balanced by two heavy iodo substituents and a strong nitro group, creates reactivity that mono-iodinated compounds just can’t match. The large iodine atoms influence crystal packing and solubility, which allows for different selectivity in downstream synthesis. Chemists often pursue this compound because it helps introduce complex iodinated scaffolds that simple nitroanilines can’t provide.

    Why Accurate Sourcing Matters

    We see a difference between materials made with methodical, on-site batch production and those sourced through loosely controlled outsourcing. We get purchase requests from buyers who had issues with inconsistent product from brokers: discoloration, unexpected side products, and batches that behave differently from kilo to kilo. As producers, we keep technical records for every step, running parameter histories and impurity profiles, knowing that any deviation shapes user success miles away. Even a fraction of unreacted aniline or unremoved solvent lingers through synthesis routes; we’ve heard from clients that a single untested lot can throw an entire process validation back to square one.

    Applications and End Uses

    Much of the 2,6-Diiodo-4-Nitroaniline we manufacture finds its way into early-phase pharmaceutical research, where it acts as a key intermediate in iodine-based diagnostics or radiolabeling agents. It comes up in medicinal chemistry projects—those chasing selective kinase inhibition or antibody conjugation. Others use the compound in organic pigments or as a building block for specialty dyes that need robust lightfastness and unique electron density arrangements. From the manufacturers’ side, we interact most with technical officers who need traceable, high-integrity material when their internal teams ramp batches or investigate new nitroaniline derivatizations.

    Academic users often probe these molecules for new reactivity modes—C–I bonds bring site-selective modifications through palladium-catalyzed couplings or sonogashira reactions. Our feedback loops with these researchers grant us early warning of process challenges that can pop up as new catalysis protocols get adopted. With each run, we feed those insights back into cleaning protocols, crystallizations, and even packaging methods.

    Handling, Storage, and Plant Safety: A Manufacturer’s Perspective

    We work directly with the compound’s chemical quirks every day. Through hard lessons, we know that even dry-room storage and special packing don’t always stop a sensitive nitroaniline from picking up ambient humidity. Packing is designed for both accident mitigation and convenience—double-layer, static-resistant liners block light and air. We test batch stability under real-world conditions, since our customers need shelf life measured in months, not just weeks. Warehouse staff keep substances separated from oxidizers or bases and avoid stacking heavy drums. It’s details like full ventilation and daily equipment checks that help keep both product and people safe—a point only long-term operators learn from handling volatile nitro compounds repeatedly.

    The Impact of Manufacturing Scale

    Scaling up from a beaker to a multi-kilo reactor introduces challenges that trade-focused companies seldom appreciate. We fine-tune agitation speeds so solids don’t clump; we stage additions of reagent to dodge runaway reactions and control exotherms that risk shifting selectivity. Real operators tackle filtration rates and dryer loads, not to mention preemptive maintenance so contamination doesn’t backtrack into prized reactors. It sometimes feels like running a small city—with every parameter, from water quality to ambient humidity, feeding into the next outcome. We see a marked improvement in downstream customer results once we iron out these wrinkles, reinforcing the importance of in-house scale-up before any promises reach the marketplace.

    Reliability Over Marketing Hype

    We value transparency and real test data more than fancy sales descriptions. Buyers frequently approach us with bad memories of inconsistency from rebagged, resold lots. Instead, we run extra quality tests and chase every outlier sample back to its production log. Repeat business grows from this habit. Laboratory and procurement teams often tell us that consistent analytical results and full traceability matter far more than hyperbolic claims. We encourage technical discussions with professional chemists, rather than sales talk, to ensure the fit for any given synthetic job.

    Market Trends and Shifts in Demand

    During the last few years, broader demand for halogenated intermediates shifted as radio-pharma and specialty pigment sectors pushed for tighter controls and better documentation. As research in targeted cancer therapies and advanced imaging grows, specifiers have demanded traceability to every drum. A decade ago, many viewed 2,6-Diiodo-4-Nitroaniline as a niche offering—now, reliable sources get pre-orders six months in advance. We plot production schedules around seasonal trends and carry excess raw materials to manage the swings linked to academic and industrial grant cycles. Shoring up supply chains for precursors like iodine and nitro aromatics can take weeks—or even months—so manufacturer agility makes a big difference during rapid surges in demand.

    Differences That Come from Production Approach

    Manufacturer methods shape downstream success far beyond what catalog specs convey. Our quality team looks at every aspect: precursor traceability, process water pH checks, and even the cleaning records for glass reactors. Many products from trading houses or third-tier sources cut these corners, leaving customers exposed to fluctuating reactivity or assay drift between batches. In direct feedback loops, we discovered some buyers came to us after trashing entire campaigns over off-specification product, often because a subtle process change in a foreign facility went undisclosed. As manufacturers, we own both process risks and successes, and we communicate changes months in advance to partners who rely on consistent supply for validated processes.

    Ease of Integration in Research and Production

    We routinely talk with chemists in pharma, dye, and materials labs who ask about filtration, solubility, or color stability in their intended applications. Some want to know about downstream compatibility with boronic acids or other functional groups for advanced coupling reactions. Our answer draws from our hands-on experience: each production batch has a slightly unique physical ‘feel’, but with advanced purification and careful crystallization, we hit the targets our long-time clients expect. Filtration times and re-dissolution rates are not abstract—they matter to the people standing at the bench just as much as to procurement officers crunching numbers.

    Some new users want flexible packaging, while established pharma buyers stick to traditional drums with multi-layer liners. We weigh these requests against our knowledge of the compound’s true shelf-life, hygroscopicity, and how long it’ll hold up through variable shipping routes. What gets written in a lab notebook rarely mirrors what happens in a real factory or during a cross-ocean transit. As a team, we call on both lab and plant veterans to vet every change before implementation.

    Issues Facing the Industry: What to Watch Out For

    Lately, raw material supply sees regular shocks—shifting export regulations, weather-driven route closures, and swings in precursor pricing. As direct manufacturers, we navigate this by holding back-up supplier agreements and maintaining protocol flexibility. Standard risk planning looks good on paper, but it doesn’t substitute for decades of supplier trust and quick technical troubleshooting of batches affected by minor contaminant upticks. Each new synthetic method developed in academic circles gets stress-tested in our pilot lines before adoption for production scale, reducing unforeseen stoppages for our customers.

    Environmental controls also play a rising part. With two iodine atoms per molecule, waste management for spent process streams can't get shortchanged. We’ve invested in updated filtration and recovery lines, diverting side streams into reprocessing rather than simple neutralization. This makes a difference on both regulatory standing and operating cost—a front rarely seen by those outside the operator’s role.

    New Developments and Pursuit of Higher Standards

    Industry demands greater analytical documentation with every new contract. We’ve moved from simple assay certificates to full trace impurity profiling, including microanalysis and environmental residue tracking to align with new pharmacopoeial standards. Clients in medical research bring questions about every last known impurity, driving us to invest in more sophisticated chromatography and validated test methods. Being the direct manufacturer puts us in the position to adapt quickly; we design new protocols in-house and validate them before wider rollout.

    For specialty pigment or electronics applications, end users want confirmation of physical attributes—particle size, flow properties, and even static charge sensitivity—since their handling needs differ from bulk chemical users. We adjusted our milling and packaging practice over time based on these conversations, keeping product fresh and avoiding caking during months-long shipping periods.

    Building Knowledge Across the Supply Chain

    Producers live with every detail of a compound’s story, from raw material intake to the shipping dock. Our teams often visit partner facilities, running joint trials to see firsthand how each batch performs outside our own QA lab. Direct cooperation offers a feedback loop that trading agencies cannot duplicate. Problems with off-odor, slow dissolution, or color shifts feedback to us instantly, giving us space to fix next runs before larger issues mount. Shoring up process transparency and sharing results empowers partners beyond what specification sheets alone can achieve.

    On the training front, we focus on planting institutional memory across shifts. Every worker, from incoming chemists to logistics planners, learns to spot the hidden cues of process drift early. Batches that show fraction-of-a-percent yield loss prompt meetings to check upstream activities—raw material quality, refrigeration settings, even utility outages. This internal vigilance makes the difference in providing a product that actually performs in the hands of those who need it.

    What the Future Holds for 2,6-Diiodo-4-Nitroaniline

    We see no sign of market interest waning; more sectors value highly specialized aniline derivatives each quarter. Whether as research intermediates, building blocks for diagnostics, or feedstocks for advanced materials, the need for stable, predictable quality persists. As a manufacturer, nothing brings more satisfaction than hearing that a client’s downstream campaign moved forward without a hitch—especially knowing all the discipline and detail that precede that outcome.

    Long experience teaches that success in supplying these specialty compounds comes from patient attention to detail, robust plant protocols, and a willingness to adapt to what real users need, not what the market press releases claim. In a world where synthetic targets grow tougher and regulatory requirements tighten, we’ll keep shaping our practices to make sure every run of 2,6-Diiodo-4-Nitroaniline consistently meets the needs—and ambitions—of those who trust us with their projects.