|
HS Code |
932873 |
| Chemical Name | 2-Iodophenyl Isocyanate |
| Cas Number | 16470-58-7 |
| Molecular Formula | C7H4INO |
| Molecular Weight | 245.02 g/mol |
| Appearance | Yellow to brown liquid |
| Boiling Point | 120-124 °C at 15 mmHg |
| Density | 1.76 g/cm³ |
| Purity | Typically ≥98% |
| Refractive Index | 1.657 |
| Smiles | C1=CC=C(C(=C1)N=C=O)I |
| Synonyms | 2-Iodo-1-isocyanatobenzene |
| Solubility | Reacts with water, soluble in organic solvents |
| Storage Conditions | Store under inert gas, cool and dry place |
| Hazard Statements | Irritant, harmful if inhaled |
As an accredited 2-Iodophenyl Isocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Iodophenyl Isocyanate, tightly sealed with a tamper-evident cap and hazard labeling. |
| Shipping | 2-Iodophenyl isocyanate should be shipped in tightly sealed containers under cool, dry conditions. It must be packaged according to hazardous material regulations, labeled appropriately, and protected from moisture and incompatible substances. Avoid exposure to heat and direct sunlight. Shipment typically requires ground transportation with all relevant safety and hazard documentation included. |
| Storage | 2-Iodophenyl Isocyanate should be stored in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible substances such as strong acids, bases, and oxidizing agents. Keep the container tightly closed and protected from light. Store under inert gas (e.g., nitrogen) if possible to prevent decomposition. Properly label storage areas and handle using suitable personal protective equipment. |
Applications of 2-Iodophenyl Isocyanate in Industrial ManufacturingAs a direct manufacturer of 2-Iodophenyl Isocyanate, we supply this specialty chemical intermediate for downstream synthesis in advanced materials, pharmaceuticals, and organic electronics. To support customer process design and regulatory needs, we outline below the end-use segments where this molecule serves critical roles based on actual industry practice. 1. Pharmaceutical API Intermediate SynthesisIn the pharmaceutical sector, 2-Iodophenyl Isocyanate acts as a reactive building block during multi-step synthesis of targeted small molecule drug candidates. It facilitates selective urea, amide, and heterocycle formation, with iodinated aromatic ring structures required in numerous kinase inhibitors and CNS-active drug API scaffolds. Its purity and trace metal controls directly affect API yield and downstream impurity profiling, demanding conformance to stringent regulatory expectations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)Crop science manufacturers rely on 2-Iodophenyl Isocyanate as a selective reagent for synthesizing complex aromatic ureas and carbamates found in systemic herbicide and fungicide actives. The chemical’s reactivity offers structural advantages in the introduction of iodine-substituted benzene rings, which are critical for selectivity and persistence in modern agrochemical formulations, and must align with environmental residue controls and stewardship regulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Organic Electronic Materials (OLED and Semiconductor Precursors)Makers of organic light-emitting diodes and advanced functional materials incorporate 2-Iodophenyl Isocyanate into cross-coupling chemistry to generate electron-transporting and emissive frameworks containing phenyl-urea linkages. The isocyanate group enables site-specific extension of rigid-rod molecular structures, while iodine functionality supports subsequent palladium-catalyzed C–C and C–N bond formation. Device reliability and batch reproducibility depend on material input traceability and consistent reactivity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymer Synthesis (High-Performance Polymers)Producers of specialty and high-performance polymers add 2-Iodophenyl Isocyanate during the polymerization of aryl-urea and polyamide chains when advanced thermal or flame retardancy and controlled halogen content is required. The compound’s dual reactivity allows for well-defined chain incorporation, enabling tailored property profiles in demanding coatings, aerospace composites, and advanced wire insulation. Each batch’s halogen analysis and reactive group content must comply with downstream converter specifications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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In the daily grind of chemical manufacturing, subtle shifts in molecular structure create all the difference between a specialty intermediate and a batch that stalls a synthesis pathway. 2-Iodophenyl isocyanate stands out as a clear example of molecular design paired with a focused purpose. It comes as a pale to off-white solid, already giving hints of its careful preparation. Laboratories, research plants, and commercial syntheses all crave reliability and purity; over the years, we've watched customers and partners lean on 2-iodophenyl isocyanate because it consistently opens doors to new compounds that other isocyanates just can’t unlock.
What really separates 2-iodophenyl isocyanate from a crowd of similar compounds isn’t just its reactivity—though the phenyl isocyanate backbone supports that claim—but its selectivity in organic synthesis. The iodinated position on the aromatic ring offers more than just a heavier atom or a quirky substitution; it provides a versatile site for further modification. In cross-coupling reactions, particularly the palladium-catalyzed variants, 2-iodophenyl isocyanate becomes more than a building block. It acts as a true gateway, opening access to libraries of functionalized aromatic ureas and carbamates, or helping researchers gently navigate the tricky waters of pharmaceutical intermediate synthesis without heavy side-product burdens.
As manufacturers, we recognize that subtle impurities or residual moisture can distort a batch outcome—not only at research scales, but even more so in industrial syntheses. That means our direct control over the crystallization and purification process for 2-iodophenyl isocyanate isn’t just a procedural checkbox. It becomes a daily act. We've learned to maintain batch reproducibility by rigorously drying raw materials, maintaining sealed, moisture-inert packaging, and testing each lot to ensure iodine content, isocyanate purity, and absence of phenolic or urea byproducts. Without this consistency, downstream chemistries start to falter, reaction times lengthen, and researchers lose valuable time.
The typical chemist looking for a reliable isocyanate tracks down purity first. For this compound, 98% minimum purity is a must—an expectation we meet and surpass with properly handled storage and verified HPLC retention times. Handling precautions gain attention, too: packs arrive cold and sealed to fend off hydrolysis, avoiding the slow creep of impurities that alter NCO content.
There’s always that worry with specialized aryl isocyanates about hidden pitfalls. They strike as powerfully nucleophilic, but degrade if left open to air or water. Removing traces of moisture before use goes from advice to necessity. As makers, we’ve adopted sealed ampoule packaging for those who need every last trace of integrity. We field regular calls about order sizes: “Can you ship in 1-gram vials?”, “Will a 250-gram drum stay stable for three months?” Our experience tells us clear packaging, prompt delivery, and routine in-house batch retesting head off nearly all user challenges.
Compared to common aryl isocyanates—look at phenyl isocyanate or even 4-methylphenyl isocyanate—the iodine-substituted variant unlocks new synthetic possibilities. Cross-coupling activity springs to life with the addition of the heavy halogen. In Suzuki, Sonogashira, and Buchwald-Hartwig couplings, the iodo group activates the ring for better conversion rates. Chemists aiming for functionalized aromatic intermediates keep coming back for this trait, and we’ve watched more patents cite its use as an electrophilic partner, especially where scarcities of other haloarene isocyanates limit development or cost control.
We have supplied to academic labs investigating kinase inhibitors, and to custom synthesis groups pushing the edge on heterocycle derivatization. The stories coming back are surprisingly consistent: phenyl isocyanate can form carbamates, but 2-iodophenyl isocyanate lets them tack on another aryl, alkyne, or amine with much less side scrambling. Results turn up clearer, impurity profiles slim down, and purification challenges drop.
As for safety, compared to isocyanates like methyl isocyanate or even isophorone diisocyanate, the aromatic backbone and large substituent on 2-iodophenyl isocyanate bring a much lower volatility profile. That gives users a margin to work in fume hoods without instant evaporation or tricky airborne hazards. Even so, we always stress full PPE, careful weighing, and dedicated glassware rinses—just as we do on our own plant floors.
Modern synthetic chemistry keeps upping its requirements for traceability and batch documentation. Our own customers—from pilot plants in Europe to pharmaceutical groups in Asia—trace every molecule’s journey. While years ago a simple batch sheet satisfied most requests, we now ship our 2-iodophenyl isocyanate with complete certificates of analysis: NMR, IR, GC-MS where needed, and recent HPLC curves showing peak purity. Customers digging into reaction reproducibility in CRO settings have shown us how even tiny drifts in residual water or halide content throw off their entire analytical cycles. Our solution is straightforward: continuous in-process checks during manufacture, and final post-purification submissions for every major shipment.
Long-term stability in storage marks another sharp difference between 2-iodophenyl isocyanate and lower-grade aromatic isocyanates found elsewhere. Our consistent cold-chain logistics and moisture-barrier packaging stretch shelf life and reduce worries over decomposition, which is an advantage especially for those aiming to scale up from grams to tens of kilograms. Bulk warehouses never look kind on hygroscopic solids; getting dry, sealed stock in at the start pays dividends over the whole supply chain. Reports from our partners—CMOs and advanced research units alike—underline that batches held under argon retain purity over a year or more, while typical competitors’ “standard” stocks can degrade in a matter of weeks.
Listening to chemists using 2-iodophenyl isocyanate at scale has changed the way we produce and package. One of the bigger challenges used to be static charging of the fluffy solid and clumping outside gloveboxes. We addressed this by moving to wider-mouthed, static-dispersing PTFE bottles and minimizing unnecessary headspace. Each feedback cycle drilled home the importance of product flow and ease of weighing. Customers handling hundreds of grams at a time noticed immediate improvements, and we implemented these changes as a result of their frank assessments, not just our own lab trials.
There’s also been plenty of conversation around matching the packing density and flake size for automated weighing devices. Some large pharma companies prefer slit septum bottles for direct robotic resampling. Others want broad, flat vials for manual crystal scraping. We tune batch crystallization to produce slightly larger crystal sizes for easier handling—acknowledging that the odd dusting during transfer doesn’t go unnoticed. Years of experience making, packaging, and moving batches taught us these details can save untold hours in the lab and keep a project on schedule.
Explaining to a new chemist why 2-iodophenyl isocyanate should get the call over plain phenyl isocyanate, or why it fits better than triflate analogs, really comes down to the chemistry. The ortho-iodo group opens extra cross-coupling doors, particularly for complex biaryl or heterocyclic structures. In many advanced syntheses, researchers turn to this compound where direct functionalization is key—contracting time, raising yields, and delivering cleaner profiles than tri-halogenated or meta-substituted isocyanates.
As a manufacturer, we’ve seen that, while phenyl isocyanate might seem interchangeable at first glance, the purity and targeted reactivity of 2-iodophenyl isocyanate sharply reduce the time and cost invested in downstream purification. New users have commented on consistent melting point and spectral profiles after months in storage—one of those small advantages that compounds into noticeable savings and smoother project workflows.
Transporting isocyanates always draws a tighter circle of scrutiny. Over the years, we’ve built a direct-to-lab, license-compliant supply chain, making sure each shipment meets applicable international transit and customs requirements. Users in regions with still tightening chemical controls—think California’s Prop 65, EU REACH—have asked for stripped-down documentation, including detailed impurity panels and handling certifications. Our facility holds active registrations where required; these records, coupled with direct manufacturer access, streamline audit requests and reduce procurement delays.
This hands-on experience shapes how we approach regulatory change or new demands. We have adjusted our SDS sheets to address not just workplace safety, but the nuances of academic versus commercial use. Our logistics team, tuned in to the peculiarities of customs for hazardous materials, pre-warns about any seasonal backlogs on high-value routes, helping labs avoid costly interruptions. That direct connection reduces third-party mishandling and maintains our reputation with customs and science managers alike.
Drawing on our years supplying this compound, we see clear strategies making the difference in overall efficiency. Those working at the benchtop invest in argon- or nitrogen-swept vials, scooping and weighing quickly to reduce exposure. For batch syntheses above 10 grams, dissolving the solid into dry solvents and immediately using reduces hydrolysis. Several customers standardize with THF or acetonitrile, since these solvents both dissolve the isocyanate rapidly and hold it inert long enough for downstream addition.
Waste handling comes up frequently, especially for clients tightening compliance with newer environmental controls. We offer guidance based on our own experiences running full-cycle disposal: neutralizing excess solid under mild acid scavengers, filtering off spent iodine, and tracking disposal paperwork. That open communication about residue minimization or recovery—rather than sidestepping the issue—helps everyone, from the single-user lab to the multi-tonne processor.
The world of chemical synthesis shifts quickly. By remaining grounded in our experience, adjusting production, and responding to real-world lab feedback, we continue improving the handling and reliability of 2-iodophenyl isocyanate. New combinatorial methods, controlled-release pharmaceuticals, or emerging material sciences can all demand slightly different purity profiles or packing protocols. Each request rolls back into product development: adapting synthetic routes, accelerating purification cycles, or testing alternative packaging for long-distance cold transit.
Over the last two decades, our plant teams and technical advisors have seen the practical realities behind isocyanate manufacturing and delivery—from rush jobs during grant deadlines to bulk inventories requiring stable, year-long storage. The emphasis always settles on trust: labs depend on the consistent performance of their building blocks, and as manufacturers, we hold ourselves to that standard every batch.
At the core, chemists need confidence—confidence that each bottle or drum of 2-iodophenyl isocyanate lines up to specification, offers real-time stability, and supports their innovation. Years in the manufacturing trenches taught us that shortcuts never pay, especially with nuanced intermediates like this one. Every lot that leaves our facility reflects countless refinements, stressing down-to-earth reliability over flash or empty claims.
Whether you’re pioneering a new molecular scaffold, investigating unexplored reaction terrain, or just trying to keep a synthetic run on time, 2-iodophenyl isocyanate stands ready. Through direct experience and an open dialog with those in the field, we keep this compound not just available, but purpose-fit for the ever-changing pulse of real-world synthetic chemistry.