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2-Fluoro-6-Iodobenzonitrile

    • Product Name 2-Fluoro-6-Iodobenzonitrile
    • Alias 2-Fluoro-6-cyanoiodobenzene
    • Einecs 841-957-8
    • 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

    106318

    Productname 2-Fluoro-6-Iodobenzonitrile
    Casnumber 57381-52-9
    Molecularformula C7H3FIN
    Molecularweight 263.01 g/mol
    Appearance White to off-white solid
    Meltingpoint 54-58°C
    Density 1.97 g/cm³ (estimated)
    Purity Typically >98%
    Smiles C1=CC(=C(C(=C1)F)I)C#N
    Inchi InChI=1S/C7H3FIN/c8-6-3-1-2-5(9)7(6)4-10/h1-3H
    Solubility Slightly soluble in organic solvents (e.g., DMSO, DMF)
    Storage Store at 2-8°C, keep container tightly closed
    Synonyms 2-Fluoro-6-iodobenzene-1-carbonitrile

    As an accredited 2-Fluoro-6-Iodobenzonitrile 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 5 grams of 2-Fluoro-6-Iodobenzonitrile, tightly sealed with a screw cap, labeled with hazard symbols.
    Shipping 2-Fluoro-6-iodobenzonitrile is shipped in tightly sealed containers to prevent moisture and light exposure. It is handled as a hazardous material, following all relevant regulations for transport. Labeling includes hazard identification, and shipping documentation accompanies the package. Appropriate protective packaging ensures safety during transit to prevent leaks or spills.
    Storage 2-Fluoro-6-Iodobenzonitrile should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated chemical storage area, separate from incompatible substances such as strong oxidizers. Ensure proper labeling and restrict access to trained personnel. Follow all relevant safety guidelines and local regulations for hazardous chemicals.
    Application of 2-Fluoro-6-Iodobenzonitrile

    Applications of 2-Fluoro-6-Iodobenzonitrile in Industrial Manufacturing

    As a direct factory producer, we supply 2-Fluoro-6-Iodobenzonitrile to industrial customers involved in advanced molecule construction, where its fluoro and iodo groups offer strategic utility in regulated, application-specific synthesis. We focus on the downstream sectors where this intermediate is established in controlled processes. The following sections detail its integration across pharmaceutical intermediates, agrochemical actives, electronic chemicals, and specialty dye synthesis, addressing operational compliance, technical ratios, workflow position, and end product outcomes in each case.

    1. Pharmaceutical Intermediate Synthesis

    Major research-driven and generics manufacturers use this compound to build fluorinated and iodinated scaffolds for active pharmaceutical ingredient (API) development and late-stage intermediate transformations, following strict ICH Q7 and cGMP principles. In API route design, chemists take advantage of site-selective functionalization enabled by both fluoro and iodo moieties, typically during Suzuki-Miyaura or Buchwald-Hartwig cross-coupling steps. Our product enters in validated stages, contributing to the success of molecules targeting CNS, antineoplastic, or anti-infective indications.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA CFR Title 21 Parts 210/211 (for medicinal end use in USA)
    • EU GMP Part II (for EU markets)
    • NMPA (China): Measures for Administration of Drug Manufacturing

    Typical usage ratio

    • 0.8–1.2 molar equivalents in coupling or cyclization reactions, adjusted according to yield optimization and side reaction profiles

    Downstream process integration

    • Charged at mid-stage or late-stage transformation step, following halogen-metal exchange or direct C–C/C–N coupling setup, followed by purification to API or advanced intermediate

    Final product types

    • CNS drug intermediates (e.g., for fluorinated benzene building blocks)
    • Oncology small molecule intermediates with direct aromatic substitutions
    • Anti-viral or anti-infective advanced intermediates

    2. Agrochemical Active Ingredient Synthesis

    Manufacturers of crop protection agents integrate this raw material in the synthesis of selective herbicide and insecticide candidates, facilitated by its ease of further halogen exchange or metal-catalyzed coupling. Regulatory systems, such as FAO/WHO guidelines, define purity and synthetic controls for actives registration. Target structures often undergo late-stage introduction of the aromatic nitrile with dual halogen functionality to yield distinctive bioactivity profiles.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 concerning plant protection product approval
    • China GB/T 1600-2001 for pesticide intermediates

    Typical usage ratio

    • 1.0 equivalent in final step halogen exchange or 0.5–1.5 equivalents in tandem cyclization–coupling processes; batch size and downstream sensitivity influence loading

    Downstream process integration

    • Introduced in the penultimate or final functionalization stages before formulation and crystallization of the active, after pre-activation by transition metal catalysis or by nucleophilic aromatic substitution

    Final product types

    • Select broadleaf weed control herbicide intermediates
    • Pyridine-based insecticide actives with fluorinated aryl motifs
    • Fungicidal agents with iodoaromatic structures

    3. Electronic Chemicals & OLED Intermediate Production

    Electronic chemicals manufacturers use this compound for introducing specialty aryl systems in the construction of light-emitting or charge-transport segments in OLED and advanced display materials. The unique pattern of substitution supports precise tuning for physical and photonic properties needed in next-generation displays. Stringent cleanroom and purity standards govern its use, especially when final products must meet RoHS and REACH requirements for electronics.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • REACH Regulation (EC) No 1907/2006
    • SEMATECH Chemical Management Guidelines

    Typical usage ratio

    • 0.2–0.8 equivalents in functionalization or cross-coupling, often as a limiting reagent for maximizing electronic performance and minimizing byproduct formation

    Downstream process integration

    • Used as a precursor in aryl extension and cross-coupling sequence to form the core structures for emissive or charge-transfer moieties, prior to device material purification and thin-film deposition

    Final product types

    • OLED emitter layer intermediates
    • Photonic modulator pre-polymers
    • Small-molecule semiconductors incorporating halogenated arenes

    4. Specialty Dyes and Fluorescent Marker Synthesis

    Producers of specialty dyes and molecular markers rely on this material to introduce both fluorinated and iodinated aromatic rings for precise wavelength adjustment and enhanced photostability, notably for biochemical detection or high-performance inks. The sector demands full traceability and compliance with chemical registration, particularly for applications in laboratory diagnostics or industrial quality control reagents.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals and Traceability
    • GHS (Globally Harmonized System for Classification and Labelling)
    • EU REACH for chemical substances used in dyes and colorants

    Typical usage ratio

    • Stoichiometric use (1.0 equivalent) in directed aromatic substitution or ring-building; sometimes higher loading applied when targeting complex multi-ring products

    Downstream process integration

    • Added in the scaffold construction or chromophore modification phases, prior to salt formation, solvent exchange and colorant stabilization steps

    Final product types

    • Specialized fluorescent tags for bioimaging
    • Security inks with halogenated dye components
    • Industrial markers and tracers requiring robust aromatic stability
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    Certification & Compliance
    More Introduction

    2-Fluoro-6-Iodobenzonitrile: Experience from the Manufacturing Floor

    Understanding the Core: What Makes 2-Fluoro-6-Iodobenzonitrile Stand Out

    In the world of industrial chemistry, specialty halogenated benzonitriles serve as versatile building blocks for a range of high-value applications, especially pharmaceuticals and advanced agrochemicals. As manufacturers who have worked firsthand with aryl halides and nitriles for decades, we know what it takes to produce a compound like 2-Fluoro-6-Iodobenzonitrile that meets both strict industry expectations and practical challenges that come up in the real world. Whether chemists are pursuing synthesis routes with specific reactivity or regulatory scrutiny, this particular benzene derivative often finds itself opening critical doors that other intermediates keep closed.

    2-Fluoro-6-Iodobenzonitrile offers a unique combination of electronic and structural features. The molecular formula, C7H3FIN, may look simple on paper, but the way fluorine and iodine atoms interact with the nitrile group on the benzene ring creates a distinct reactivity profile. The ortho relationship between the nitrile function and those two halogen substituents directly shapes how the molecule reacts during subsequent synthetic steps. The precision required in its creation means we invest in high-purity precursors, precise control over reaction temperature, and careful handling of sensitive reagents. Our experience has shown that minor shifts in reaction conditions can mean the difference between a pure lot and an expensive batch loss.

    Unlike its close relatives—6-fluorobenzonitrile, 2-iodobenzonitrile, or similar di-halogenated benzonitriles—this compound's two-point substitution pattern gives chemists access to a toolbox that meets modern medicinal chemistry needs. Often, research and process chemists point out that the flexibility in further functionalization allows for custom-tailored small molecules with better performance in bioactivity screens, which helps shorten the development time for advanced candidates. In our facilities, we adapted our purification steps to keep trace metals and organic byproducts well below industry limits, supporting downstream synthesis that calls for high reactivity and narrow side product profiles.

    Our Manufacturing Perspective: Quality, Safety, and Consistency

    Years of direct manufacturing have taught us that the road to a successful batch begins before the first reagent ever meets the reactor. The decision to source raw iodine from well-audited mines, to invest in advanced containment systems for fluorinated intermediates, and to validate every step in the process doesn’t just help us meet regulatory standards. It keeps our operators safe, protects our local community, and means the end-user gets a reproducible product every time. Not all facilities can claim such a track record. Reliable access to critical intermediates can make or break entire research projects in the pharmaceuticals and fine chemicals sector, so we treat every consignment of 2-Fluoro-6-Iodobenzonitrile as if it was destined for a clinical supply chain—because sometimes it is.

    We continuously track the target specs that truly matter: moisture below 0.2%, heavy metals under globally recognized thresholds, and chromatographic purity that consistently reads above 99%. It’s not uncommon for customers to circle back and ask if we can adjust certain impurity levels to fit a patented route or to line up with supply chain shifts. Our technical team sits directly with production engineers; we adapt production in-house, not through wordy emails or distant contract partners. This integration makes it possible to respect sensitive intellectual property boundaries and optimize lots according to the needs of specific medicinal chemistry campaigns or regulatory filings.

    Handling and transporting halogenated benzonitriles is not without risk. Our staff trains exhaustively on both process containment and environmental controls. You won't find generic packaging here—every container and bulk drum is designed with actual on-site storage feedback, chemical compatibility reports, and ongoing customer experiences. We see the value in learning from incidents, both our own and those reported across the wider chemical manufacturing community. These lessons get incorporated into everything from our waste scrubbing units to our documentation practices.

    The Value for Chemical Synthesis and Beyond

    Most of the 2-Fluoro-6-Iodobenzonitrile we deliver goes into the hands of process chemists looking to build sophisticated new scaffolds. The dual halogen substituents greatly expand the palette for cross-coupling chemistry—Suzuki, Sonogashira, and Buchwald–Hartwig protocols are just some of the methods made possible by having both fluorine and iodine at exactly the right positions. The electronic differences between the two substituents mean chemists can fine-tune the coupling sequence, select which halogen is displaced first, and reduce side reactions caused by over-reactivity or ring activation. Those who have run scale-ups or kilo-lab campaigns for pharmaceutical actives know how one impure intermediate or inconsistent batch can sink a project timeline. By holding tight tolerances, we give teams one less variable to troubleshoot.

    R&D groups, especially those developing kinase inhibitors or other small-molecule drug candidates, come back to these halogenated intermediates over and over. The ability to introduce or modify aryl halide patterns precisely is not just about diversity—it frequently translates to improved metabolic stability, enhanced potency, or even patentability. On the agrochemical side, the stability offered by the nitrile and the reactivity of the iodo and fluoro positions open up new opportunities for crop protection products, especially those aimed at emergent pest resistance or improved environmental profiles.

    Our involvement in their workflows often extends to method development. We’ve cooperated directly with client scientists to simplify workups, implement solvent swaps, and design steps that minimize generation of hazardous waste. It’s easy to underestimate the time and savings that come from starting with a properly purified intermediate—costly rework, repeated column chromatography, and wasted man-hours can all be traced back to the initial building block. We prefer to solve these upstream, so that the focus can stay on core innovation. After shipping tons of this compound year after year, each batch makes its mark in research papers, patents, and regulatory submissions worldwide. Our process improvements often come back to us indirectly, reported as smooth reactions and fewer purification headaches down the line.

    How 2-Fluoro-6-Iodobenzonitrile Compares to Its Peers

    Those who have worked with other halogenated benzonitriles know that subtle differences add up. Pure 2-iodobenzonitrile delivers good reactivity for many Pd-catalyzed couplings, but lacks the electronic modulation of the ortho-fluorine needed for certain downstream chemistry. The presence of fluorine not only shifts the electron density around the ring but changes the solubility, stability, and even the handling experience on the plant floor. In demanding syntheses, the lower activation required to displace the iodo group—thanks to the adjacent fluoro group—lets researchers run reactions under milder conditions, which means fewer side products and more sensitive functionality tolerated. Similarly, the nitrile offers a robust handle for further derivatization, and its position matters for both physical properties and chemical selectivity.

    Working with 2,6-dihalogenated benzonitriles that lack a nitrile at the ortho position, or that substitute other halogens, doesn’t produce the same scope or yield when carrying forward to more complex final compounds. We’ve run these head-to-head in our own kilo labs; 2-Fluoro-6-Iodobenzonitrile stands out for offering predictable, robust behavior under a range of cross-coupling protocols and less troublesome byproduct generation. Beyond routine project work, this also means easier troubleshooting when schedules tighten and development windows close in.

    Global Trends and Market Realities

    Shifts in pharmaceutical innovation and supply chain strategy have altered how specialty intermediates are valued and sourced. Our customers ask not only for consistent product and analytical support, but also for proof of ethical sourcing, safe production, and robust supply contingency. In recent years, increased regulatory pressure around per- and polyfluoroalkyl substances (PFAS) and iodo-containing intermediates forced us to reevaluate effluent handling, trace impurity monitoring, and cross-facility communication on incident reporting.

    We track regulatory changes on two continents, often before they become industry norms. This means each outgoing drum carries the right paperwork, test results, and traceability, avoiding upstream headaches for our partners facing tighter inspections. Open dialogue with environmental authorities, coupled with infrastructure investment, keeps our emissions and residual iodine losses within permissible bounds. For the longest time, industry development overlooked non-product value—worker safety, sustainable raw material management, and transparent record-keeping. Now, our experience matches our product’s technical value, because authorities and customers demand both.

    In times of raw material crunches, it’s not unusual for buyers to turn to online markets and global traders, chasing lower prices. Based on years of handling the unique hazards of fluorinated and iodo-intermediates, we’ve seen the consequences: degraded purity, undisclosed byproducts, mislabeled containers, and much higher waste streams in downstream processing. Our decision to manufacture 2-Fluoro-6-Iodobenzonitrile under strict on-site controls, with real batch release oversight, has protected many chemical projects from failure at the start line. Repeat business and word-of-mouth recommendations don’t stem from sales pitches—they are built on reliability proven out by ship-to-ship, year after year.

    Meeting Custom Needs without Compromise

    A one-size-fits-all approach never lasts in specialty chemicals. Each researcher or formulator brings unique requirements to the table. Some demand solvent systems free from chlorinated residues, a lesson we learned after a costly shipping mishap erased weeks of R&D work for a pharmaceutical client. Others want to explore alternative salt forms for improved solubility or packaging compatible with automated dosing rigs. These aren’t burdens—they’re opportunities for us to draw on deep in-house experiences, built up across decades. Our technical teams receive requests to create tailored lots with modified particle sizes or to strip out hard-to-remove organic side products developed during prolonged or non-standard storage. We don’t outsource the problem or shy from small-lot custom runs; we solve them directly, sharing knowledge and approaches along the way.

    Often, downstream users want insights into actual production lot data—residual solvents, acidity profiles, or trends noticed over successive batches. We respond with full transparency and recorded data, not just aggregated statistics. It’s common to set up direct communication between our production chemists and customer technical leads, ensuring that no request or concern gets lost in transmission. By working together, projects avoid costly do-overs and each iteration moves a little closer to a streamlined, reproducible outcome. Whether shipping 500 grams in glass bottles or bulk containers tipping past a hundred kilograms, these details add up to one smooth, reliable delivery each time.

    Continuous Improvement Based on Field Experience

    Gaps between R&D claims and plant-floor realities emerge quickly when global weather disrupts raw material supply, or when a long-term customer suddenly needs an emergency lot moved across borders. The lessons we draw come as much from failures as from successes—unexpected hot spots in reactors, variations in feeds, or new impurity peaks discovered in quality review. We built our process for 2-Fluoro-6-Iodobenzonitrile through painstaking trial and error, using real batch histories to revise procedures and train staff on error prevention. That commitment to improvement, right down to our labeling standards and waste tracking, sets us apart.

    We regularly solicit feedback, both solicited and unsolicited, from those who use our chemicals in their labs or factories. It’s natural for complaints or questions to arise about solubility, dosing, or reaction compatibility under unusual circumstances. Rather than deflect, our teams see these queries as data points, helping us adapt or refine how we crystallize, filter, or dry the product at scale. Sometimes, small adjustments to our agitation or loading protocol cut hours off a batch cycle, letting us deliver on short lead times without quality sacrifice. By treating each new challenge as a puzzle worth solving, we keep 2-Fluoro-6-Iodobenzonitrile aligned not only with technical spec sheets but also with practical, lived experience in the field.

    Looking to the Future

    As the boundaries of chemical manufacturing shift and new synthetic needs emerge, the demand for robust, well-characterized intermediates like 2-Fluoro-6-Iodobenzonitrile keeps growing. With continued advances in green chemistry, regulatory frameworks, and global logistics, we see an ongoing need to adapt practices and equipment to anticipate not just what’s needed today but also tomorrow’s challenges. Over the years, collaborations with academic groups and feedback from global R&D leaders have sharpened our focus. Safety, quality, and supply reliability remain nonnegotiable.

    Every kilogram that leaves our site is the result of careful planning, systematic checking, and a shared respect for the hands and minds that will put it to use. Our commitment means offering genuine partnership, not just another stop in the supply chain. The market will always demand innovation, efficiency, and accountability. We choose to deliver all three, with every lot of 2-Fluoro-6-Iodobenzonitrile. Proven by results, improved by feedback, trusted by those who put their names on the line in research, manufacturing, and beyond.