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4-Fluoro-2-Iodobenzoic Acid

    • Product Name 4-Fluoro-2-Iodobenzoic Acid
    • Alias 4-Fluoro-2-Iodobenzoic acid
    • Einecs 607-166-5
    • 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
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    Specifications

    HS Code

    531860

    Product Name 4-Fluoro-2-Iodobenzoic Acid
    Cas Number 57381-52-9
    Molecular Formula C7H4FIO2
    Molecular Weight 266.01 g/mol
    Appearance White to off-white powder
    Melting Point 178-182°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC(=C(C=C1F)I)C(=O)O
    Inchi InChI=1S/C7H4FIO2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,(H,10,11)
    Storage Temperature Store at 2-8°C
    Synonyms 2-Iodo-4-fluorobenzoic acid

    As an accredited 4-Fluoro-2-Iodobenzoic Acid 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 with a secure screw cap, labeled "4-Fluoro-2-Iodobenzoic Acid, ≥99% purity, CAS: 403-39-0."
    Shipping 4-Fluoro-2-Iodobenzoic Acid is shipped in secure, tightly sealed containers to prevent contamination and moisture exposure. Packaging complies with relevant chemical and hazardous material regulations. Containers are clearly labeled with hazard information, and shipping is conducted via certified carriers specializing in chemical transport, ensuring safety and regulatory compliance throughout transit.
    Storage 4-Fluoro-2-Iodobenzoic Acid should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature or as specified by the manufacturer. Properly label the container, and ensure it is handled only by trained personnel using appropriate personal protective equipment.
    Application of 4-Fluoro-2-Iodobenzoic Acid

    Applications of 4-Fluoro-2-Iodobenzoic Acid in Industrial Manufacturing

    As a specialized manufacturer of 4-Fluoro-2-Iodobenzoic Acid, we supply this advanced halogenated benzoic acid derivative to precision-driven sectors. Our product supports demanding synthesis processes across selected downstream markets where tightly regulated inputs and controlled conversions are critical to end use. Below, we detail verified industrial application scenarios, each with full compliance, process, and product integration information.

    1. Pharmaceutical Intermediates for Fluorinated Drug Synthesis

    4-Fluoro-2-Iodobenzoic Acid enters pharmaceutical manufacturing as a building block for active pharmaceutical ingredient (API) intermediates, especially for fluorinated drug candidates such as anti-inflammatory and oncological therapeutics. The compound's functional groups enable palladium-catalyzed carbon-heteroatom coupling and Suzuki-Miyaura cross-coupling. Synthesizers integrate it into multi-step organic syntheses targeting key benzene derivatives required by clinical-stage and commercial pharmaceutical companies. Strict change control, in-process QC, and material traceability apply from goods-in through active batch records.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF and European Pharmacopoeia (for final API intermediates)
    • 21 CFR Part 211 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs
    • REACH Regulation (EC) No 1907/2006 (Substance registration and communication downstream)

    Typical usage ratio

    • 0.5–2.5 molar equivalents as a coupling precursor within multi-step batch synthesis, adjusted by substrate molarity and stoichiometric design

    Downstream process integration

    • Material charged at controlled temperature into reaction vessels for direct coupling, amidation, or acylation steps in intermediate synthesis

    Final product types

    • Fluorinated molecular API intermediates (e.g., for kinase inhibitors, anti-inflammatory APIs)
    • Biosimilar pharmaceutical intermediate compounds
    • Research reference compounds for clinical studies

    2. Agrochemical Intermediate Synthesis

    This compound is widely adopted by agrochemical manufacturers for producing halogenated benzene intermediates needed in advanced crop protection agents, such as herbicides and fungicides. The dual halogen functionality enables selective aromatic substitutions and ring transformations to yield agrochemical actives with enhanced stability or targeted biological activity. Agrochemical QC systems require raw material identification, batch-to-batch consistency, and non-GMO verification through analytical testing before use in scale-up and formulation.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Production Facilities
    • Regulation (EC) No 1107/2009 concerning Plant Protection Products (EU)
    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • Mandatory Certificate of Analysis with impurity profiling per customer request

    Typical usage ratio

    • 1–10 wt% relative to combined aromatic precursors; tuned to process conversion efficiency and scale

    Downstream process integration

    • Charged at the first or second synthetic step in multi-stage active ingredient synthesis; applied in selective coupling or halogen exchange reactions under controlled conditions

    Final product types

    • Halogenated benzene intermediates for triazole fungicides
    • Selective herbicidal actives targeting broadleaf weeds
    • Pyridine-based insect control agents

    3. Advanced Materials: OLED and Liquid Crystal Monomers

    Key electronics and optoelectronics material developers use this raw material to produce highly functionalized aromatic monomers applied in organic light-emitting diode (OLED) devices and liquid crystal displays. The fluorine group provides electron-withdrawing capability, while the iodine position allows custom cross-coupling, resulting in monomers with tunable electrical and optical properties. Strict EHS and purity requirements demand GMP-like documentation, real-time analytics, and full supplier disclosure.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 Environment Management Standards
    • Restriction of Hazardous Substances Directive (RoHS) for electronics manufacturing
    • Japan Industrial Standards (JIS) For Electronics Substrates

    Typical usage ratio

    • 5–20 mol% in monomer feed for polymer synthesis; ratio set according to desired device performance and emission wavelength tuning

    Downstream process integration

    • Dosed into catalytic cross-coupling reactors for oligomer chain building or monomer functionalization; followed by solvent removal and monomer isolation

    Final product types

    • OLED emitting layer materials
    • Liquid crystal alignment agents
    • High-performance organic semiconductors

    4. Specialty Chemical Manufacturing: Dye and Pigment Precursors

    The fine chemicals sector employs 4-Fluoro-2-Iodobenzoic Acid for the synthesis of specialty dyes and pigments, especially as a precursor for introducing fluorine into aromatic colorant frameworks. Material purity, particle sizing, and absence of residual halides are critical QC checkpoints. Experienced dye manufacturers design reaction schemes where the compound functions as an electrophilic aromatic substitution substrate or participates in nucleophilic displacement to yield high-intensity dyes with enhanced weather resistance.

    Industry compliance standards

    • ISO 9001:2015 for Quality Control in Colorant Production
    • EN 71-3 Safety of Toys — Migration of certain elements (for pigments in toys and plastics)
    • REACH Annex XVII for dye precursor chemicals

    Typical usage ratio

    • 2–5 molar equivalents in batch dye synthesis; adjusted for molecular conversion and waste minimization

    Downstream process integration

    • Transferred to closed reactors for stepwise build-up of colorant cores, often under nitrogen atmosphere

    Final product types

    • Fluorinated azo and anthraquinone dyes for polyester fibers
    • High-durability pigments for engineering plastics
    • Industrial inkjet colorant dispersions

    5. Research Chemicals for Custom Synthesis

    Contract research organizations (CROs), reference standard labs, and advanced materials R&D facilities routinely order this compound for targeted aromatic halogenation studies or as a substrate in combinatorial chemistry. These users demand reproducible physical characteristics, documented impurity profiles, and full traceability. Material often undergoes custom purification before incorporation into short-run synthetic projects and complex scaffold building.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for research-grade production and handling
    • Material transfer according to institutional chemical hygiene plans
    • Documentation in line with ISO/IEC 17025 for reference standards

    Typical usage ratio

    • 0.1–2.0 mmol scale in automated or manual synthesis modules, batch size set by target compound requirements

    Downstream process integration

    • Dispensed by precision delivery for route scouting, pathway validation, and generation of compound libraries for screening

    Final product types

    • Specialty halogenated scaffolds for medicinal chemistry
    • Research screening compounds (lead identification or SAR studies)
    • Custom calibration and analytical reference materials

    6. Fluorinated Monomer Production for Polymer Additives

    4-Fluoro-2-Iodobenzoic Acid supports polymer manufacturers in synthesizing fluorinated monomers that serve as controlled additives or co-monomers for engineering plastics. This application leverages both fluorination for chemical stability and the ortho-iodo function’s reactivity in installing complex pendant groups. Plant SOPs specify multi-stage distillation and in-line analysis to ensure suitable reactivity and downstream integration in high-molecular-weight polymerization.

    Industry compliance standards

    • ISO 9001:2015 for process and material consistency
    • ASTM D2567 for Additive Manufacturing Compounds
    • Restriction of Hazardous Substances (RoHS) for end-use in consumer plastics

    Typical usage ratio

    • 1–15 mol% as co-monomer starter, regulated by polymer property targets and catalyst activity

    Downstream process integration

    • Continuous feed into bulk monomer reactors, followed by staged purification and additive blending before extrusion or pelletizing

    Final product types

    • Fluorinated engineering polymers for automotive and electronics
    • Weather-resistant coatings and specialty films
    • Functionalized plastic modifiers for high-value industrial parts
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4-Fluoro-2-Iodobenzoic Acid: Real-World Insights from Manufacturing

    Crafting 4-Fluoro-2-Iodobenzoic Acid: A Look Inside Our Process

    Manufacturing fine organofluorine compounds takes years of expertise, and this holds true with 4-Fluoro-2-Iodobenzoic Acid. This specialty chemical, with the CAS number 403-39-6, brings together a unique pairing of fluorine and iodine on a benzoic acid backbone. We follow strict handling and purification parameters through every batch—thinking back over dozens of campaigns, this approach helps maintain excellent purity and meet what chemists demand for advanced synthesis. It’s not a general-purpose chemical; the design of this molecule opens up selectivity in coupling, cross-coupling, and other functional-group transformations.

    Material Specifications and Batch Consistency

    Our 4-Fluoro-2-Iodobenzoic Acid appears as an off-white to light tan crystalline powder. We see most batches exceed 98% HPLC purity, with lot-to-lot consistency monitored through NMR, IR, and HRMS. Water content stays tightly controlled by Karl Fischer titration—typically below 0.5%. This isn’t just to satisfy a certificate; even small changes in trace moisture leave ripples through downstream reactions. Chemists on the bench have mentioned how our tighter moisture and impurity standards reduce background signals during sensitive metal-catalyzed processes.

    Particle sizing has an impact, especially for companies that feed this acid through automated solid-dosing equipment. We keep a close eye on milling, since oversized pieces slow down dissolution rates, while fine dust makes for messy handling. Through hundreds of kilograms of processing, we have honed in on particle ranges that suit automated equipment but also allow for manual weighing when needed.

    Where This Compound Delivers Value

    Beyond lab-scale curiosity, 4-Fluoro-2-Iodobenzoic Acid drives real-world value in pharmaceutical intermediate production and research. Medicinal chemists favor its dual halogen handles, allowing site-selective Suzuki, Sonogashira, and other coupling reactions. Across projects developing kinase inhibitors or agrochemicals, our partners point out that having a reliable iodine leaving group alongside a non-reactive fluorine offers strategic freedom for late-stage diversification. This isn’t something achieved with plain fluoro or iodo benzoic acids, as the precise substitution pattern influences reactivity and regioselectivity.

    From a formulation perspective, the acid moiety supports effective salt formation and offers good compatibility with both polar and non-polar solvents. Researchers working on small molecule scaffolds have described how the compound dissolves easily in DMF and DMSO, but also suspends without clumping in ether or hexane. This fluid solubility profile gives process chemists direct control of concentration and crystallization parameters, helping to minimize waste and maximize yield, even under scale-up pressures.

    Challenges in Manufacturing: Why It Matters

    Producing 4-Fluoro-2-Iodobenzoic Acid isn’t just about combining reagents. Source materials for fluoro- and iodo-aromatics come with their own supply chain quirks, as volatility in iodine pricing or purity swings can upend planning. Over the years, we have built direct relationships with upstream suppliers of high-purity fluorobenzene derivatives and maintain buffer inventory for critical iodination agents. This forward planning isn't always visible to customers, but it keeps supplies flowing during periods of raw material shortages or market disruption.

    Safety and environmental stewardship mean everything with organohalides. Our waste streams, especially from iodination steps, require careful neutralization and trace monitoring before discharge. In our plant, every batch run includes pre-dump testing for residual halogens and organics, because water board compliance hangs in the balance. Auditors from large drug companies sometimes visit to inspect these systems; their feedback helps us refine emissions control, which upstream manufacturers can overlook.

    Real-World Experience with Application Demands

    Most requests for this compound come from R&D labs scaling up toward pilot batches. Our regular customers work at the discovery end of new active pharmaceutical ingredients, as well as at contract development firms running kilogram-scale preclinical campaigns. The technical teams behind these projects often share feedback. For example, inconsistent GC or LC residual solvent profiles in starting materials make havoc in crystallization and filtration steps. That’s why solvent selection—both for reaction and final isolation—can’t be an afterthought. We invest time in purge studies, replicating customer protocol conditions, to help narrow down any risk of cross-contamination or recalcitrant by-products.

    Downtime in kilo labs hurts timelines and budgets. We field routine questions about powder flow, off-gassing, and shelf stability. With long-term storage, the acid moiety may absorb atmospheric moisture, so we recommend (and ourselves use) double-bagged, nitrogen-flushed packaging for shipments over 500g. For multi-month storage, our own trials in controlled humidity chambers reveal little degradation, provided containers remain sealed below 25°C.

    Differences from Other Halogenated Benzoic Acids

    True benefit comes by comparing 4-Fluoro-2-Iodobenzoic Acid against its close cousins. 2-Iodobenzoic acid serves well in standard cross-couplings, but lacks the electron-withdrawing balance needed for advanced medicinal chemistry. A pure fluorobenzoic acid resists activation, making functionalization tricky past early steps. This compound, with its para-fluoro and ortho-iodo pairing, creates both electronic and positional leverage: the fluorine reduces susceptibility to unwanted side-reactions, while the iodine acts as a dependable reactive handle for bond formation. This has shown enhanced selectivity during regioisomer preparation, something customers in process chemistry cite in technical debriefings.

    Commercial offerings of this compound, especially from resellers, sometimes show variable batch purity or less than optimal particle sizing. As a direct manufacturer, our team holds the levers for reaction time, quench technique, and purification cycles. This direct control means lower risk of off-spec batches or untrackable impurity profiles. We’ve seen researchers run into trouble with repurified materials sourced from brokers, finding trace halide contaminants that introduce color or reactivity issues. By owning the production—from raw material intake up through final packaging—we build in full traceability.

    Continuous Improvement and Responsiveness

    Through feedback loops with customers, we adapt specifications and process controls as applications evolve. Specific projects in crop science and specialty polymers, for instance, have required custom grading or tighter trace metals limits. Our R&D team stays in close communication with technical liaisons on the customer side so that modifications don’t introduce unpredictable performance on the bench. Those relationships, often built over years of back-and-forth on dozens of projects, give us a clear sense of where others may fall short.

    A few years back, several partners in Europe highlighted instability issues when storing open packs of halogenated benzoic acids over humid summers. The solution came from refining both gasket sealing and adding extra desiccant charges. The result proved more dependable shelf life, giving formulators flexibility even when projects pause or samples sit for months before full use.

    Technical Support Born from Daily Plant Operation

    Real technical support means seeing the process as a partner, not just sending a spec sheet. Our plant’s operators and QC chemists tackle troubleshooting for each order—whether it’s scaling a standard 250g pack up to a 20kg drum or dialing in the purity grade for a new application. Customers developing complex heterocycles from our acid often call seeking insight on side-product suppression or residue-free washing protocols. We draw on cumulative process logs, archived NMRs, and real-world run data to offer specifics, not generic answers. This approach helps speed up customer development and slashes trial-and-error waste at the bench.

    On-site, we focus on stacked quality control points, not just final product checks. Intermediate samples go for interim HPLC, LC-MS, and titration. This records a chain of custody across each lot, invaluable for tracing any anomalies if they pop up later. For contract scale-up work, these internal archives let us quickly address questions about minute batch differences and adjust future runs based on customer input rather than just compliance pressure.

    Transport, Documentation, and Global Context

    Shipping 4-Fluoro-2-Iodobenzoic Acid across borders means navigating evolving regulations on dual-use chemicals and halogenated aromatics. Some destinations require detailed impurity profiles and transport certificates tied directly to production records. To comply, we generate certificates of analysis referencing exact lot data, not recycled templates. Labelling and document archiving connect to our ERP system, ensuring every shipment ties back to an auditable batch record. Audits over the past five years by pharmaceutical and academic partners have helped identify gaps in documentation, which our technical team integrates into updated protocols.

    Customs seizures and inspection delays occasionally occur, especially in countries tightening scrutiny on halogenated building blocks. By staying in active dialogue with regulatory agencies and third-party validators, we minimize the chance of products languishing at port or being flagged for untracked compliance claims. Customers often comment on this attention to detail after experiencing shipment hang-ups with less regulated channels.

    Where We Learn—and Where the Market Evolves

    No process stays stagnant. As medicinal chemistry, process chemistry, and material science fields advance, so do their demands for starting materials. The shift toward greener chemistry stretches how halogenated intermediates get produced and disposed of. We invest in route development aimed at reducing harsh reagents and minimizing halogen waste. Solvent recovery, spent acid neutralization, and halide reclamation have all become routine parts of our process review cycle, not just afterthoughts tacked onto compliance paperwork.

    Some of the most useful product improvements come straight from bench chemists. For instance, one pharma customer’s pilot group flagged batch color variations that hinted at minor side-product carryover. Shared NMRs and IR traces from our lab and theirs gave the clues we needed to add an extra short-path distillation at the pre-crystallization stage, which cut out the subtle impurities. These kinds of incremental fixes add up over years and hundreds of batches, building reliability that far exceeds what anonymous resellers provide.

    Supporting Innovation through Reliable Chemistry

    Whether used in early discovery or as a late-stage intermediate, 4-Fluoro-2-Iodobenzoic Acid plays a unique role in shaping new molecules with therapeutic or material utility. Demand continues to rise for more precision in starting material quality. Standard analytical panels—HPLC, NMR, GC—only tell part of the story. True consistency and problem-free scale-up come from years of tuning, plant-level control, and firsthand knowledge of chemical behavior every step of the way.

    Having sat across from chemists frustrated by slow dissolving solids, or struggled with out-of-spec shipments that derailed a critical synthesis, we keep our focus on the details. Every kilogram produced, every protocol refined, and every technical bullet point included on the report reflects years of cumulative effort and collaboration.

    Commitment on the Factory Floor

    Behind every pack of 4-Fluoro-2-Iodobenzoic Acid stands not just a manufacturing workflow, but a team dedicated to constant improvement. We balance complex supply economics, global regulatory shifts, and hands-on problem solving. The future of this specialty acid, and of aromatic halogen chemistry more broadly, will rely on integrating feedback and embracing smarter, cleaner, more adaptable processes.

    With a footprint covering both small, custom-lot R&D scale and full-scale commercial output, every batch of our acid carries the touchpoints of years of direct plant and lab experience. It’s this blend of responsiveness, transparency, and technical know-how that shapes what makes our 4-Fluoro-2-Iodobenzoic Acid a dependable foundation for scientific and industrial progress.