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3-Fluoro-5-Iodoaniline

    • Product Name 3-Fluoro-5-Iodoaniline
    • Alias 3-Fluoro-5-iodobenzenamine
    • Einecs 841-232-3
    • 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

    538616

    Product Name 3-Fluoro-5-Iodoaniline
    Cas Number 187024-65-1
    Molecular Formula C6H5FIN
    Molecular Weight 237.02 g/mol
    Appearance Light brown to beige solid
    Melting Point 70-74°C
    Density 2.06 g/cm³
    Purity Typically ≥97%
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Smiles Nc1cc(F)cc(I)c1
    Inchi InChI=1S/C6H5FIN/c7-4-1-5(8)3-6(9)2-4/h1-3H,9H2
    Synonyms 3-Fluoro-5-iodobenzenamine

    As an accredited 3-Fluoro-5-Iodoaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "3-Fluoro-5-Iodoaniline, 25g, CAS 399-52-0." Features hazard symbols and safety information.
    Shipping 3-Fluoro-5-Iodoaniline is shipped in tightly sealed, chemically resistant containers to prevent contamination and exposure. The package is labeled with appropriate hazard warnings and handled according to relevant regulations for hazardous chemicals, typically under controlled temperature and away from incompatible substances. Shipping complies with international and domestic transport safety guidelines.
    Storage 3-Fluoro-5-iodoaniline should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as oxidizing agents. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical-resistant containers, and store at room temperature unless otherwise specified. Ensure the storage area is clearly labeled and access is restricted to authorized personnel.
    Application of 3-Fluoro-5-Iodoaniline

    Applications of 3-Fluoro-5-Iodoaniline in Industrial Manufacturing

    As a direct manufacturer of 3-Fluoro-5-Iodoaniline, we supply high-purity material for specialized downstream sectors where precision and consistency are critical. Below are key application areas where this intermediate supports advanced production, adhering to current industry protocols and process expectations.

    1. Pharmaceutical Intermediate for Advanced API Synthesis

    3-Fluoro-5-Iodoaniline serves as an essential building block in the synthesis of next-generation active pharmaceutical ingredients, especially for targeted therapies and oncology compounds. Process R&D teams integrate this aniline derivative to introduce fluoro-iodo motifs, enabling specific molecular modifications that influence potency and selectivity in drug candidates for both small-molecule and heterocyclic API development pipelines. Production relies on stringently controlled steps, from N-arylation to Suzuki-Miyaura cross-coupling reactions, to ensure compliance with regulatory authorities and reliable scalability from pilot to commercial batches.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP for Intermediates & APIs
    • US FDA 21 CFR Part 211
    • Chinese Pharmacopoeia 2025 (API intermediate chapters)

    Typical usage ratio

    • 0.8–2.5 molar equivalents per target API batch, adjusted by stoichiometric demands for the specific synthetic pathway

    Downstream process integration

    • Introduced after initial core ring assembly; used in amination, halogen exchange, or biaryl coupling stages; incorporated via closed-system reactors with in-process purity checks

    Final product types

    • Small-molecule APIs for oncology
    • Kinase inhibitor intermediates
    • Fluorinated heterocyclic scaffolds
    • Custom-developed bioactive molecules

    2. Agrochemical Synthesis: Herbicide and Fungicide Intermediates

    3-Fluoro-5-Iodoaniline actively supports the agrochemicals sector as an intermediate in the multi-step synthesis of selective herbicides and fungicides. Its dual halogen substitution pattern enables further downstream substitution, acylation, and N-functionalization, tailoring active molecules for mode-of-action studies by crop science formulators. Industrial-scale integration occurs in continuous-flow and batch reactors with robust environmental management and full traceability from raw material receipt to finished agrochemical intermediates.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems (agrochemical sector clause adaptations)
    • REACH Regulation (EC) No 1907/2006 for chemical intermediates
    • OECD Good Laboratory Practice (GLP) Guidelines (for active substance synthesis)

    Typical usage ratio

    • 1.2–3.0 molar equivalents per active intermediate batch, fine-tuned for structure–activity project requirements and impurity threshold targets

    Downstream process integration

    • Charged into the N-substitution or coupling step following aromatic halogenation; processed under inert-gas blanketing with automated metering to maintain selectivity and minimize by-product formation

    Final product types

    • Novel triazole or triazine herbicide intermediates
    • Fungicidal amine derivatives
    • Pyridine-based agrochemical actives
    • Seed treatment pre-formulations

    3. Specialty Dye and Pigment Manufacture

    3-Fluoro-5-Iodoaniline plays a targeted role in the synthesis of fluorinated azo dyes and specialty pigments, enhancing color fastness and resistance profiles for high-end technical and textile applications. Dyestuff producers incorporate this raw material in diazotization and coupling reactions, yielding colorants with stable C–F and C–I bonds. Strict control of impurity profiles and shade consistency is maintained through in-line monitoring and batch-specific analytical release testing, ensuring compliance with international textile chemicals standards.

    Industry compliance standards

    • ZDHC Manufacturing Restricted Substances List (MRSL) v3.0
    • OEKO-TEX® STANDARD 100 Compliance (Class I and II textiles)
    • REACH Annex XVII (Azo colorant restrictions)
    • ISO 105-C06:2010 (Textiles — Tests for colour fastness)

    Typical usage ratio

    • 0.5–1.1 molar equivalents per pigment or dye molecule, optimized for target chroma and lightfastness parameters

    Downstream process integration

    • Engaged at the diazonium salt preparation or coupling agent stage; handled in jacketed glass-lined vessels to optimize yield and color homogeneity; process monitored by UV-Vis and HPLC techniques

    Final product types

    • High-stability textile dyes
    • Technical-grade marker pigments
    • Industrial colorants for plastics and films
    • Specialty inkjet dyes

    4. Electronic Chemical Synthesis for High-Performance Materials

    Chosen by advanced electronics and materials manufacturers, 3-Fluoro-5-Iodoaniline delivers precise halogen incorporation in the synthesis of organic semiconductors and photonic polymers. Downstream producers value its structural contribution when fabricating insulating layers, hole-transport materials, and specialized photoresist systems, where molecular design affects charge mobility and thermal resistance. Rigorous supply chain documentation and lot-release analytical data support integration into validated electronics workflows.

    Industry compliance standards

    • IEC 61249-2-21:2017 (Halogenated materials content for PCBs)
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances in electronics)
    • ISO 9001:2015 (Process control for functional materials synthesis)
    • SEMI C94-0217 (Semiconductor Material Standards)

    Typical usage ratio

    • 0.6–1.6 molar equivalents per custom monomer or oligomer batch, adjusted depending on engineering specification for dielectric constant or optical performance

    Downstream process integration

    • Charged at the monomer functionalization or halogen exchange stage; handled in controlled-atmosphere synthesis modules; product fraction validated using GC-MS and NMR prior to use in formulation

    Final product types

    • Organic electronic semiconductors
    • Photoresist monomers for lithography
    • High-dielectric polymer blends
    • Electronic-grade performance films
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    Certification & Compliance
    More Introduction

    3-Fluoro-5-Iodoaniline: Practical Experience, Real-World Benefits

    Production Insights and Purity Standards

    3-Fluoro-5-Iodoaniline, known in our workshop as Model 3F5IA, represents a specific building block that turns up in a variety of fine chemical syntheses. Our team has developed this product using a carefully controlled batch process. The raw materials, starting with fluorinated nitrobenzene intermediates and high-purity iodinating agents, pass through sequential reductions and halogenations—steps where crystal form, moisture control, and even reaction vessel cleanliness steer the outcome. Our technicians continually monitor color, particle size, and impurity profile at each stage with both TLC and GC-MS checks. With this chemical, purity affects not just outcome, but the safety and yield in people’s downstream work.

    We see orders mostly for 3-Fluoro-5-Iodoaniline at greater than 98% HPLC or GC area purity, with water content held below 0.5%. The fine, off-white to very pale pink powder flows easily, avoiding bridging or clumping during handling. We don’t use pressing or granulation, as these steps could stress—or degrade—the iodo group. Tackling contamination is part of daily workflow, and even small levels of isomeric impurities can throw off selectivity in planned coupling reactions. Our daily reality involves checking that residual solvents like DMF or acetonitrile land well beneath the 500 ppm mark by the final dry-down.

    Key Uses From Real Customer Projects

    Over the past five years, pharmaceutical labs have become our primary partners for this product. 3-Fluoro-5-Iodoaniline enables formation of C-N and C-C bonds, through Suzuki, Buchwald-Hartwig, or Ullmann couplings. What sets it apart isn’t just the combined electron effects of the fluorine and iodine—it’s their specific arrangement. The fluorine adds metabolic stability and modulates aromatic electron density, which helps medicinal chemists fine-tune both reactivity and biological profile. People rely on the iodo moiety primarily because of its lability under palladium catalysis, making this product a go-to intermediate for late-stage functionalization.

    We’ve supplied this chemical for everything from oncology R&D to specialty pigment projects. On the pharma side, lead optimization teams draw on our batches to access novel kinase inhibitors and CNS-active scaffolds. Researchers report that the selectivity in halide coupling helps minimize competing side products and shortens post-reaction purifications. In pigment synthesis, 3-Fluoro-5-Iodoaniline brings about colorants with particular lightfastness and tinctorial strength. Its presence in dendrimer and photoresist projects stems from a reactivity window not found in the more common bromo or chloro analogs.

    Comparison to Other Halogenated Anilines

    Within our facility, we’ve run kilo-scale lots of halogen-aniline derivatives ranging from 2-fluoro-4-iodoaniline to 4-chloro-3-fluoroaniline. The 3-fluoro-5-iodo isomer consistently delivers a higher selectivity during cross-coupling in aromatic substitution, especially where steric bulk upsets reactivity. For scale-up, this isomer’s difference shows not just in bench chemistry, but in kilos flowing through a fixed-geometry reactor. Colleagues tell us they see consistently higher yields compared to 3-bromo-5-fluoroaniline, reducing the carryover of unreacted starting material in column separations.

    We’ve noted that iodo compounds like ours bring added sensitivity to oxidants and sometimes cost more per mole due to the price of elemental iodine and the time-consuming purification. Balancing that extra cost against improved reactivity has been a frequent point of discussion when customers run process economics for pilot-scale manufacturing. For those who worked mainly with bromo or chloro derivatives, initial skepticism over iodine’s reactivity dissipated once reactions consistently delivered the targeted diaryl amines or biaryl motifs faster, and with less catalyst weight.

    Practical Handling and Storage

    From a manufacturer’s perspective, storage concerns focus on stable packaging and periodic retesting. 3-Fluoro-5-Iodoaniline needs protection from heat and humidity, so we supply it in foil-lined drums, with purged nitrogen atmospheres to slow any decomposition. Over a couple of years, we’ve seen that moisture ingress leads to color changes and minor degradation, which is rare but real—so we encourage our partners to store at or below ambient temperature and seal containers well after each use.

    Technicians appreciate the dry powder's tendency to resist static and its manageable dust levels, so direct weighing on scales doesn’t introduce measurable loss. Where people run into trouble is grinding or compounding with bases—strong bases prompt deamination or halide displacement, underlining that 3-Fluoro-5-Iodoaniline finds its proper home under controlled, mostly neutral-to-mildly acidic reactors. Shipping to North America and Europe hasn’t produced any customs issues due to regulatory compliance, but we maintain that certifications match each region’s chemical control requirements.

    Creating Value Through Consistency

    Developing this intermediate wasn’t just about bench chemistry. From the earliest gram-scale trials, we realized that controlling halogenation at both the 3 and 5 positions on aniline demands strict feedstock quality. Our staff now pre-screens every incoming lot for heavy metals and trace organic byproducts, since these trace elements in raw nitrobenzenes or amines can spoil batch outcomes. As a result, our product shows minimal lot-to-lot variability; HPLC and NMR batch records back up this claim.

    Medicinal chemistry projects move quickly, with design-make-test cycles often running monthly. A single batch delay because of intermediate variability risks not just lost time, but wasted screening resources. We keep this in mind, and for years have aligned our QC not just with pharmacopeia recommendations, but with actual blinded submissions to several multinational pharma labs—they assay our lots alongside their reference standards, and we take corrective steps whenever an outlier appears, even if well under commercial rejection thresholds.

    Industry Demand and Feedback

    The main demand drivers stem from drug discovery and materials science. Oncology research has zeroed in on aryl amines with fluorine and iodine for enhanced interaction with protein pockets and tailored pharmacokinetics. Over a dozen feedback surveys from CROs highlight that our 3-Fluoro-5-Iodoaniline offers reliable coupling, owing to its reproducible melting point (typically in the 60–65°C range) and squared-away crystalline form. Several process chemists commented that our lots land them within 1-2% of projected yields batch after batch.

    Over the years, a small set of new customers arrived after trying cheaper alternatives from traders who sourced via secondary markets. The reported headache was inconsistent color, a lingering "chlorine smell," or solubility issues—all traced to partial halogen exchange and improper purification. Many of these custom syntheses got back on track after switching to pure, manufacturer-quality material. This kind of practical, hands-on feedback shapes every run we make today.

    Environmental and Safety Considerations

    Working with halogenated aromatic amines calls for attention to both process safety and environmental stewardship. Within production, exhaust air scrubbing and solvent recovery have become core routines. Our local treatment systems remove not just organic residues, but also control iodine and fluoride release. Waste streams move into specialized treatment—no simple incineration or landfill. Technicians in the plant wear Class A PPE, and we keep records of potential skin or respiratory irritations even though such incidents remain rare.

    On the shipping end, clear labeling and documented MSDS reviews keep logistics predictable. Partners in pharma and materials science have come back for pointers on safe handling, and we don't shy away from sharing plant-level tips—avoiding strong oxidizers, controlling for static, and immediate spill sweep-up fall into well-worn routines.

    Scaling Up: Challenges and Solutions

    Bringing 3-Fluoro-5-Iodoaniline from pilot lab to ton-scale demanded more than just larger reactors. Our technical staff wrestled with batch exotherms, as halogen exchange releases significant heat, and jacketed vessels with rapid quench lines now steady those surges. One early setback came from underestimating iodine volatilization; some product drifts off into the vent stream during final icing. We tweaked conditions by lowering quench temperature and recondensing vent gases, boosting overall yield by more than eight percent.

    Another challenge lay in mother liquor recyclability. Whether to capture partially halogenated byproducts or strip solvents for reuse, our facilities installed single-column distillation units. This lowered both costs and chemical waste. These details matter because pharmaceutical firms want confirmation that, beyond price, a supplier invests in cleaner, more reproducible chemistry.

    Pathways for Process Improvement

    Continuous improvement forms the backbone of sustainable operation, and in 2022, we launched a lean-driven review focused on reducing process solvent use by 20%. Initial efforts centered on stepwise or one-pot condensation, minimizing wash cycles, and optimizing the solvent-to-feed ratio. After recalibrating filter beds and switching to less water-intensive crystallization solvents, we reduced production waste by approximately fifteen percent over the year.

    Learning from feedback, we also evolved our drying stage—our earlier tray ovens sometimes failed to reach the sub-ppm moisture readings that pharma requires. Now, forced-circulation vacuum dryers paired with online moisture analyzers have become our norm. Batch records reflect real-world values, and customers routinely report better behavior in reactions that require anhydrous starting material—especially in metal-catalyzed couplings or oxidative steps.

    Collaborating With Scientists and Buyers

    Frequent calls come from new users seeking advice on integrating 3-Fluoro-5-Iodoaniline into multi-step syntheses. We believe open dialogue gives buyers more than a digital catalog—actual experience from plant and lab helps demystify which solvent combinations or catalyst choices best suit our material. In some cases, customers rerun small-scale pilots or tweak their analytical protocols to align with our suggested parameters—like precise heating rates, alternative palladium sources, or the use of mild reducing agents during scale-up.

    What’s become clear over the years: broad product selection means little without technical support. Our team stays available for troubleshooting—by sharing batch history, impurity fingerprints, or drying times, we help users navigate the grey zones between academic literature and large-scale reactors. We view success not just as on-time shipments, but as seeing our partners report improved yield, purer endpoints, and fewer “unknowns” in their final spectra.

    Quality Control Beyond Compliance

    Industry expectations keep rising; batch uniformity counts, yet so does transparency. We routinely review analytical data beyond COA minimums: UV-Vis, IR, and elemental analysis supplement routine HPLC and NMR, as even trace polyhalogenated contaminants can affect downstream reactivity. As regulatory agencies in Europe and the US raise scrutiny over both residual solvents and trace metals, we future-proof production by investing in better detection and reporting protocols.

    We’ve also built in periodic spot-checking, where third-party labs corroborate in-house QC reports. Several candid conversations with long-term partners led to additional client-requested stability trials—suitable both for regulatory filings and for peace of mind in temperature-stressed territories.

    Trends and Outlook

    The shifting landscape of drug discovery and performance materials keeps demand high for specific halogenated anilines. Researchers continue exploring new coupling partners, green chemistry substitutes, and late-stage functionalization. As manufacturing scales up to meet these trends, access to pure and consistent 3-Fluoro-5-Iodoaniline becomes central to project success, whether in gram-scale medicinal chemistry or multi-ton pigment lines.

    Drawing from production floor and lab communications, the difference boils down to trust: customers have a right to full transparency, on-site support, and iterative improvements. By focusing on batch quality, responsible manufacturing, and sharing practical know-how, our approach puts each order of 3-Fluoro-5-Iodoaniline in the hands of scientists with the confidence to create their next breakthrough—without the setbacks that come from inconsistent supply or vague technical answers.