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2-Fluoro-5-Iodobenzaldehyde

    • Product Name 2-Fluoro-5-Iodobenzaldehyde
    • Alias 2-fluoro-5-iodobenzalhyde
    • Einecs 607-166-2
    • 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

    277736

    Product Name 2-Fluoro-5-Iodobenzaldehyde
    Cas Number 181293-64-7
    Molecular Formula C7H4FIO
    Molecular Weight 262.01
    Appearance Light yellow to brown solid
    Melting Point 55-58°C
    Purity Typically >98%
    Smiles C1=CC(=C(C=C1F)I)C=O
    Inchi InChI=1S/C7H4FIO/c8-6-2-1-5(4-10)3-7(6)9
    Synonyms 2-Fluoro-5-iodobenzaldehyde; 5-Iodo-2-fluorobenzaldehyde
    Storage Temperature Store at 2-8°C
    Solubility Soluble in organic solvents

    As an accredited 2-Fluoro-5-Iodobenzaldehyde 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-5-Iodobenzaldehyde, securely sealed with a tamper-evident cap, labeled with hazard information.
    Shipping 2-Fluoro-5-Iodobenzaldehyde is shipped in secure, tightly-sealed containers under ambient temperature. Packaging complies with international regulations for hazardous materials. The container is clearly labeled, and cushioning material prevents breakage. Shipping documents include safety and handling instructions. Transport is via approved carriers to minimize risk of leakage, exposure, or contamination during transit.
    Storage 2-Fluoro-5-Iodobenzaldehyde should be stored in a tightly closed container, away from light and moisture, in a cool, dry, and well-ventilated area. Protect from incompatible substances such as strong oxidizing agents. Store at room temperature or as recommended by the supplier. Ensure proper labeling and follow all relevant safety protocols to avoid exposure and contamination.
    Application of 2-Fluoro-5-Iodobenzaldehyde

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

    Our proprietary 2-Fluoro-5-Iodobenzaldehyde supports advanced sectors through specific chemical transformation routes. The following sections highlight authentic downstream application fields, manufacturing practices, compliance obligations, actual batching guidelines, process workflow, and the types of finished goods produced by global industrial clients.

    1. API Intermediate Synthesis for Oncology Drug Development

    Pharmaceutical manufacturers use 2-Fluoro-5-Iodobenzaldehyde as a crucial building block in multi-step synthesis of kinase inhibitors, PARP inhibitors, and other halogenated small molecules. The unique positioning of the fluoro and iodo groups allows efficient Suzuki and Buchwald coupling reactions. Strict source traceability, validated analytical methods, and controlled release protocols must be met. Our facility ensures traceable GMP manufacturing and regulatory documentation support for the pharmaceutical sector.

    Industry compliance standards

    • cGMP: ICH Q7, EU GMP Part II
    • US FDA Drug Master File (DMF) Type II (registered use data for APIs)
    • Ph. Eur. monograph suitability (applicability per project)
    • USP General Chapter <232>-Elemental Impurities

    Typical usage ratio

    • 0.85–1.1 molar equivalents in key coupling stages (adjusted by desired yield, route optimization, and residual impurities PCR qualification)

    Downstream process integration

    • Introduced at controlled anhydrous conditions in Step 2 or 3 of protected scaffold assembly
    • Subjected to reductive amination, Grignard addition, or cross-coupling depending on downstream API structure
    • Removed in post-reaction work-up to eliminate heavy metal traces (Pd, Cu residues checked via ICP-OES)

    Final product types

    • NCE oncology drug candidates (clinical stage)
    • Active Pharmaceutical Ingredients for targeted cancer therapies
    • Intermediate blocks for CDMO projects
    • Medicinal chemistry screening libraries

    2. Electronic Material Precursors for Liquid Crystal and OLED

    Electronic chemical producers employ this aldehyde in the synthesis of fluorinated aromatic compounds for advanced liquid crystal display (LCD) and organic light emitting diode (OLED) material projects. The controlled halogenation pattern enables precise tuning of optical and electronic properties essential for thin-film circuit fabrication. Every batch undergoes lot release and ion content specification to meet microelectronic grades.

    Industry compliance standards

    • JEITA ET-7304 standard for electronic chemicals
    • IEC 62474:2018 RoHS content management
    • Customer-supplied QPL for panel and device integration
    • ISO 9001-certified batch record and QC process validation

    Typical usage ratio

    • 5–15% w/w with respect to total aromatic content in pre-polymerization or coupling process, fine-tuned per dielectric property target

    Downstream process integration

    • Coupled through Pd-catalyzed cross-coupling to form biphenyl units in liquid crystal monomer synthesis
    • Undergoes oxidation/reduction for core modifications in OLED emitter intermediates
    • Requires water content <50 ppm and Na/K <0.5 ppm at time of use

    Final product types

    • LCD alignment layer additives
    • OLED blue or green emitter intermediates
    • Liquid crystal monomers for display manufacturing
    • Photoresist components used in TFT-LCD fabrication

    3. Agrochemical Intermediate for Novel Aryl-Substituted Herbicides

    Agrochemical developers utilize 2-Fluoro-5-Iodobenzaldehyde as a scaffold for constructing complex aryl-substituted herbicide molecules. The ortho-fluorine and para-iodine pattern enables regioselective coupling in the preparation of active ingredients that provide selectivity and metabolic stability in crop protection. Sourcing must comply with environmental and residue-related regulatory programs.

    Industry compliance standards

    • FAO/WHO technical specifications for pesticide intermediates
    • REACH Annex VII-X registration compliance (EU use)
    • China Pesticide Registration Regulation (ICAMA MRL and impurity limits)
    • ISO 14001 for environmental management during production

    Typical usage ratio

    • 0.5–1.2 molar equivalents, selected per acylation or etherification route and targeted aryl group introduction

    Downstream process integration

    • Acts as a nucleophilic aldehyde in aromatic substitution and condensation reactions
    • Forms part of multi-step, low-temperature batch synthesis under inert gas conditions
    • QC on each lot for residual fluoro/iodo impurities, with compliance to trace-level technical standards

    Final product types

    • Selective herbicide intermediates for broadleaf crops
    • Bioactive phenoxyacetic acid derivatives
    • Custom arylated growth regulators and safeners
    • Contract-manufactured actives for international crop protection brands

    4. Specialty Dye and Pigment Manufacture for High-Performance Coatings

    Major dye and pigment plants use this intermediate to build fluorinated aromatic cores that boost weather resistance and color fastness in industrial-grade coatings. The compatible iodo functionality supports azo-coupling or condensation with diazonium salts, while the fluorine atom increases pigment hydrophobicity and photostability. Strict raw material management and heavy metal control supports downstream compliance with global coatings standards.

    Industry compliance standards

    • EN 71-3 (Toy safety for pigment migration)
    • ASTM D4303 (Lightfastness of colored coatings)
    • REACH SVHC content declaration for pigments
    • ISO 9001 and ISO 14001 process compliance tracking

    Typical usage ratio

    • 2–8% by weight of pigment precursor charge, adjusted to targeted chroma and color density

    Downstream process integration

    • Coupled with arylamines in dye kettle reactors with acid catalyst
    • Followed by diazo coupling and work-up for pigment precipitation
    • QC validation includes FTIR and GC-MS monitoring for residual aldehyde

    Final product types

    • UV-resistant architectural coatings
    • Fade-proof automotive finishes
    • Special effect pigments for industrial plastics
    • Weather durable inks for packaging and labeling
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    Certification & Compliance
    More Introduction

    2-Fluoro-5-Iodobenzaldehyde: Reliable Building Block for Modern Synthesis

    Understanding the Value of 2-Fluoro-5-Iodobenzaldehyde in Chemical Manufacturing

    Commercial chemistry doesn’t move forward on large-volume commodities alone. Over years in the laboratory and on the production floor, chemists and process managers have come to trust certain versatile intermediates for their consistency, reactivity, and compatibility with established workflows. One such compound, 2-Fluoro-5-Iodobenzaldehyde, stands out in our catalog for delivering precise, predictable results batch after batch. Here, we take a practical look at this compound and its impact on specialized synthesis.

    Model and Specifications Shaped by Practical Use

    We manufacture 2-Fluoro-5-Iodobenzaldehyde specifically for the demands of organic synthesis. The structure consists of a benzaldehyde core, substituted by fluorine at the 2-position and iodine at the 5-position. This configuration makes it a prime choice for sequential functionalization, nucleophilic aromatic substitution, and cross-coupling methods. Typically, our product comes as a pale yellow to almost colorless crystalline powder. Purity consistently exceeds 98% by GC and NMR, since downstream applications often require high precision to avoid unwanted side-products in multi-step routes.

    From early kilo-lab trials to full-scale campaigns, the compound keeps its consistency. Those who work in pharmaceutical and agrochemical research have remarked on its narrow melting range and stable handling. Trace impurities bring uncertainty into demanding projects, so we put effort into cleaning the reaction and work-up steps, fine-tuning recrystallization conditions, and checking each lot with stringent analytical protocols. Customers with batch-to-batch comparison needs or regulatory requirements in documentation notice the benefits immediately.

    Applications Driven by Decades of Feedback

    Demand for 2-Fluoro-5-Iodobenzaldehyde grew as pharmaceutical and fine chemical researchers searched for halogenated aromatic building blocks that reacted with high selectivity under transition-metal catalysis. Its design as a dual-functional molecule—a reactive iodo group for palladium-catalyzed couplings, and the ortho-fluorine to calibrate electronic effects—allows a single intermediate to support multiple synthetic directions.

    Researchers in our customer base use the aldehyde for exploring new chemical space in heterocycle synthesis, API intermediate synthesis, and custom dye molecule development. The ortho-fluorine affects reactivity in aromatic substitution, while the iodo group’s reactivity shines for Suzuki, Sonogashira, and Buchwald–Hartwig couplings. Medicinal chemists find extra utility in the meta-relationship of these two halogens, which introduces additional possibilities for introducing other functionality at the remaining ring positions, or modulating the properties of the aldehyde moiety itself.

    One clear example comes from medicinal chemistry projects targeting kinase inhibitors. The addition of the fluorine atom adjacent to the formyl group tweaks electronic density, giving medicinal chemists the control they want over binding affinity. The iodine atom provides a rapid entry point for cross-coupling, so new analogues can be designed, synthesized, and tested within accelerated timelines.

    The fine chemical sector also relies on this compound. Custom pigment and agricultural R&D projects draw on its two halogen substituents to build specialized aromatic scaffolds. We’ve seen cases where controlled substitution with thiol, amino, or alkynyl groups via the aryl iodide function creates a route otherwise difficult with more common, commercially available benzaldehyde derivatives.

    Handling and Safety Based on First-hand Plant Experience

    Years of batch production have shown us the need for careful material handling. 2-Fluoro-5-Iodobenzaldehyde gives no strong, persistent odor, so air monitoring focuses on dust levels and typical aldehyde exposure risk. We recommend air extraction at transfer stations. Overexposure to fine dust or direct skin contact brings the risk you’d expect from aldehydes and halogenated organics—irritation on contact or inhalation—so gloves and goggles remain essential. Our teams always use sealed, nitrogen-purged vessels when scaling up, since the product is stable but can show slow decomposition in contact with damp air at elevated temperature, producing trace acid.

    Formulators planning larger-scale pilot or commercial runs will find that stability over the intermediate term matches expectations for small-batch organic building blocks. The product packs in fiber drums or high-integrity plastic containers, protected against light and high humidity. In rare cases, oxidative degradation can produce slight discoloration, which is one reason our logistics group controls warehouse temperature and stock rotation closely. These supply chain lessons were drawn from direct experience, not from distributor feedback.

    What Sets 2-Fluoro-5-Iodobenzaldehyde Apart

    We’ve encountered many benzaldehyde analogs over the years, each with advantages and specific target reactions. The addition of the fluorine atom increases chemical and metabolic stability, key in medicinal chemistry, while the iodo group holds unique appeal for catalytic carbon-carbon or carbon-heteroatom bond formation. This combination carves out a niche not filled by other chloro- or bromo- analogs.

    Take 2-Fluoro-5-Bromobenzaldehyde as a point of comparison: the iodo version opens more reaction windows because aryl iodides activate under milder cross-coupling conditions, often with fewer byproducts. In Suzuki or Sonogashira reactions, the softer leaving group properties of iodine allow chemists to run reactions at milder temperature, preserving other sensitive functional groups on the molecule.

    Compared to non-halogenated benzaldehydes, this compound resists classical nucleophilic attack on the aromatic ring, giving users more control over regioselective functionalization. Because the ortho-fluorine withdraws electron density, selectivity improves for some metalation and lithiation reactions, letting downstream users build structures that would be more difficult if starting from unsubstituted or para-halogenated materials.

    Formulators and research chemists point out another key difference: in projects where purity and trace-metal compatibility matter, aryl iodides such as 2-Fluoro-5-Iodobenzaldehyde show higher performance in late-stage modifications. Routine screening of coupling efficiency across various pharmaceuticals shows faster conversion with less palladium loading, especially when compared to common bromo or chloro benzaldehydes. Documentation supports this from both internal and customer pilot trials—critical when calculating project cost and environmental waste.

    Insights Drawn from Real-World Synthesis

    Today’s chemical industry encourages manufacturers to think several steps ahead, balancing cost, safety, and route adaptability. Over the past decade, feedback from chemists at pilot and production scale continues to drive improvements in how we purify and deliver 2-Fluoro-5-Iodobenzaldehyde. Consistency from batch to batch doesn’t only affect immediate reaction results, but also inventories, regulatory filing, and even customer troubleshooting efforts.

    Long experience in handling this molecule taught us that minimizing trace iodine or fluoride impurities during process development shortens downstream chromatography cycles. This directly impacts material cost and the need for rework, especially for those running multi-kilo synthesis in time-sensitive projects. Most third-party vendors work with contracted toll manufacturers, so they often lack flexibility for custom packaging or documentation needs. By running our plant under strict process control and offering site audits to major customers, we keep communication open and address problems before they grow.

    One tangible result: custom impurity profiling. By listening to project leaders in both academia and industry, we now support synthesis protocols requiring detailed impurity maps, so downstream QbD and method validation can proceed with minimal surprises. Chemists expecting irregular contamination patterns from batch-to-batch with other sources routinely report smooth analytics using our material. This reduces both revalidation time and the risk of costly post-synthesis purification.

    Continuous Improvement in Quality and Delivery

    Our company doesn’t just make 2-Fluoro-5-Iodobenzaldehyde for a product list—we respond to evolving customer requirements, new regulatory standards, and advances in synthetic methodology. During pandemic-driven supply disruptions, customers in high-value pharmaceutical projects cited our reliable delivery and technical backup as reasons to move more intermediate manufacturing in-house rather than gamble on less-established suppliers. Process design experts depend on fast, direct communication with chemical manufacturers; we bring that as routine practice, not afterthought.

    Over recent campaigns, adjustments to our drying step and solvent crystallization produced tighter specifications for water and residual solvents, which proved critical for high-yield Suzuki couplings and sensitive palladium catalyst runs. If a customer flags an atypical impurity profile due to process changes in their plant, we can typically trace the source within hours—drawing from our own master batch records, not a distributor file.

    We support long-term strategic sourcing by offering transparent production schedules and regular technical bulletins summarizing specification changes or process deviations. This helps process chemists and project managers plan ahead, avoiding last-minute specification mismatches that can delay production or regulatory filing. The transparency allows for seamless troubleshooting and collaborative process optimization.

    Facing Production and Supply Chain Challenges

    The specialty chemical sector faces an ongoing tension between product customization and process efficiency. Refining the 2-Fluoro-5-Iodobenzaldehyde process meant grappling with fluctuations in raw material availability, regulatory scrutiny for halogenated intermediates, and increasingly stringent customer audits. Rather than eroding quality, these pressures pushed our technical team to rethink solvent management, waste reduction, and batch reproducibility.

    Consistent lessons emerged: chemical traceability, well-qualified supply chain partners, and effective communication among synthesis, QA, and logistics teams make the difference between routine operations and last-minute firefighting. One customer, building a new manufacturing site overseas, collaborated on a pilot project that revealed the need for custom packaging to avoid cross-contamination from local warehousing. By working together—and relying on our batch history—they launched smoothly, with no unexpected out-of-spec shipments.

    Supply chain constraints sometimes push both suppliers and downstream manufacturers into rush decisions. In our experience, early warnings about pending shortages and honest updates on production schedule changes do more for plant management, cost forecasting, and troubleshooting than chasing “just-in-time” supplies on a high-stakes project. This philosophy keeps our relationships with regular buyers strong, especially those running multi-month projects under tight regulatory timelines.

    Broader Impacts and Sustainable Progress

    One critical subject in chemical manufacturing is the environmental profile and safe management of halogenated intermediates. Our process for 2-Fluoro-5-Iodobenzaldehyde uses solvent recovery and emission management steps built from internal and external audits. Waste reduction and recycling targets influence both cost calculations and environmental metrics, with regular reviews to stay current on evolving regulations. Since we handle highly reactive and regulated halogenated compounds, we aim for closed-loop transport and recovery of spent solvents; waste that can’t be recycled is sent to certified processors with full manifest control.

    Sustainability pressures won’t fade as global regulations tighten. From old solvent drum reuse to modern in-line purification and reactor automation, each change requires clear accountability, which we document and review with major industry partners. Industry colleagues and competitors have reached out for advice on scaling up halogenated intermediate production without exceeding permit limits or losing process control. Sharing these technical lessons—learned in the context of 2-Fluoro-5-Iodobenzaldehyde—supports a more robust market.

    Safe storage, reliable documentation, and complete product traceability keep regulators, plant technicians, and downstream process managers aligned. For firms navigating global regulatory harmonization in pharmaceuticals and specialty chemicals, the ability to back each shipment with a transparent batch record lowers the administrative and financial risk profile.

    Reliable Support and Direct Access

    Customers regularly touch base on technical hurdles, unique formulation issues, and long-term strategic planning. By manufacturing 2-Fluoro-5-Iodobenzaldehyde in-house, we avoid the delays and miscommunications that can creep in with third-party vendors. Chemists can call us with project-specific questions about reactivity, impurity tolerance, assay details, or packaging compatibility, and speak directly with staff who understand not just the product, but the manufacturing process itself. This hands-on approach builds trust and frequently shortens the time from concept to implementation in research or scale-up campaigns.

    Customers running pilot programs on tight schedules won’t settle for vague responses or generic documentation. Each inquiry receives the attention it needs, whether the chemist is dealing with a new coupling strategy, regulatory filing for a novel ingredient, or troubleshooting analytical output. In our experience, direct engagement reduces uncertainty—a lesson driven home by years of collaborating with researchers and production teams.

    Future Directions and Commitment to Quality

    Ongoing industry shifts mean that chemists now expect tighter impurity profiles, more detailed batch data, and flexible logistics. Our lab and production teams regularly test tweaks to reaction parameters, crystallization solvents, and drying conditions to further lower impurity levels and boost yield stability. By sharing process data openly with our major customers, both sides catch potential specification mismatches before they escalate into production or regulatory problems.

    As new research into cross-coupling and halogen chemistry matures, demand for specialized building blocks like 2-Fluoro-5-Iodobenzaldehyde only grows. We plan targeted investments in analytical technology and process automation to stay ahead of both regulatory and technical demands. Through regular review of industry trends and customer feedback, our development effort shifts to keep pace with the needs of leading researchers and production chemists.

    Conclusion

    2-Fluoro-5-Iodobenzaldehyde is more than a chemical on a list: it is a reliable building block, produced through direct attention to quality, detailed manufacturing records, and responsive customer support. Its unique combination of halogen substituents and high purity make it difficult to substitute in demanding projects. Consistent manufacturing, transparent communication, and a willingness to adapt process and support have kept us the trusted choice for those who rely on this product to advance research, development, and commercial production.