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3-Fluoro-4-Iodotoluene

    • Product Name 3-Fluoro-4-Iodotoluene
    • Alias 3-Fluoro-4-Iodotoluene
    • Einecs 841-639-1
    • 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

    651680

    Cas Number 57311-88-7
    Molecular Formula C7H6FI
    Molecular Weight 252.03 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Melting Point -5°C
    Boiling Point 226-228°C
    Density 1.800 g/mL at 25°C
    Refractive Index 1.585 (20°C)
    Flash Point 90°C
    Smiles CC1=CC(=C(C=C1)F)I
    Inchi InChI=1S/C7H6FI/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 3-Fluoro-4-iodotoluene; 1-Iodo-2-fluoro-4-methylbenzene
    Storage Temperature Store at 2-8°C

    As an accredited 3-Fluoro-4-Iodotoluene 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 10 grams of 3-Fluoro-4-Iodotoluene, sealed, with hazard labeling and detailed product information on the label.
    Shipping **Shipping Description:** 3-Fluoro-4-Iodotoluene should be shipped in accordance with relevant chemical regulations. It must be packed in tightly sealed, inert containers, protected from light and moisture. Proper labeling and documentation are required. During transport, keep away from incompatible substances and handle as a hazardous material according to local and international guidelines.
    Storage 3-Fluoro-4-Iodotoluene should be stored in a tightly sealed container, away from direct sunlight, sources of ignition, and incompatible materials such as strong oxidizers. Store it in a cool, dry, and well-ventilated area designated for hazardous chemicals. Ensure the storage area has appropriate spill containment and clearly labeled containers to prevent accidental misuse or exposure.
    Application of 3-Fluoro-4-Iodotoluene

    Applications of 3-Fluoro-4-Iodotoluene in Industrial Manufacturing

    3-Fluoro-4-Iodotoluene serves as a highly specialized intermediate that supports advanced synthetic needs in fine chemical manufacturing. Our material, produced under tightly controlled quality systems, enables precision in pharmaceutical, crop protection, and specialty materials workflows. Below we present its key downstream industrial applications, detailing compliance requirements, practical formulations, processing integration points, and the exact types of finished goods delivered by our global manufacturing clients.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Major pharmaceutical companies employ this raw material as a halogenated building block for targeted synthesis of complex API molecules, especially in oncology and antiviral candidates that demand precise substitution patterns on aromatic rings. The aromatic iodine and fluorine atoms provide unique reactivity for subsequent cross-coupling, often supporting the construction of highly regulated, patent-protected molecular fragments. Quality assurance aligns with current GMP and strictly controls residual process impurities to meet ICH Q11 guidance during final API production.

    Industry compliance standards

    • ICH Q7/Q11 Good Manufacturing Practices for APIs
    • 21 CFR Part 211 - Current Good Manufacturing Practices in Pharmaceutical Manufacturing
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) monographs for process chemicals
    • REACH/TSCA registration for pharmaceutical use chemicals

    Typical usage ratio

    • 0.3–1.5 equivalents relative to the target aryl substrate in coupling reactions; exact stoichiometry based on target structure and process yield requirements

    Downstream process integration

    • Enters at the initial or mid-stage Suzuki-Miyaura, Buchwald–Hartwig, or Sonogashira coupling steps, providing the halogen-activated ring for further elaboration; after coupling, the protected intermediate advances to late-stage API assembly and crystallization

    Final product types

    • Small-molecule APIs for oncology, CNS therapeutics, and antivirals
    • Proprietary pharmaceutical intermediates in custom synthesis programs
    • High-value registered pharmaceutical substances for clinical development

    2. Agrochemical Synthesis: Herbicide and Insecticide Intermediates

    Leading agricultural chemical companies select this raw material for synthesizing fluorinated aryl building blocks included in next-generation herbicide and insecticide active compounds. The chemical structure enhances persistence and selectivity, meeting industry demands for environmental safety and efficacy of crop protection products. Batch records and analytical testing support compliance with hazardous substance and residue control directives critical to the agrochemical sector.

    Industry compliance standards

    • FAO/WHO Guidelines on Good Manufacturing Practices (GMP) for Pesticide Production
    • ISO 9001:2015 Quality Management System for chemical process control
    • REACH (EC 1907/2006) registration for plant protection product intermediates
    • US EPA Pesticide Registration and evaluation protocols (40 CFR Parts 150–189)

    Typical usage ratio

    • 0.2–1.2 molar equivalents as a coupling partner in the synthesis of specific herbicide scaffolds; loading level adjusted by desired substitution pattern and process conversion rate

    Downstream process integration

    • Dosed as the halogenated aromatic precursor during Pd-catalyzed coupling or Grignard functionalization; processed intermediates undergo further esterification or amidation to become final active ingredients

    Final product types

    • Triazole herbicides and insecticides with selective action on cereal or cotton crops
    • Novel fluorinated aryl-based crop protection agents specified for resistant weed management
    • Registered technical grade agrochemical actives for formulation into commercial end-use products

    3. Advanced Liquid Crystal Material Synthesis for Display Technology

    Producers of specialty liquid crystal materials incorporate this compound to construct high-purity aromatic intermediates offering unique dielectric and refractive index properties, essential for manufacturing advanced TFT-LCD and OLED panel components. The presence of both fluorine and iodine enables precise tuning of molecular geometry and ensures compatibility with stringent electronics industry requirements for purity and trace metal content.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) on hazardous substance control in electronic components
    • IEC 62474 material declaration for display electronics
    • JIS/JQA (Japanese Standards) for liquid crystal quality and purity in electronic applications
    • ISO 9001:2015 Quality Management for functional material production

    Typical usage ratio

    • 0.05–0.5 molar equivalents to the target aryl substrate, optimized per structural design of the display material; higher ratios apply for high-fluorine content formulations

    Downstream process integration

    • Introduced during the sequential aromatic substitution stage of liquid crystal monomer synthesis; coupled intermediates advance to hydrogenation and final purification ahead of panel material compounding

    Final product types

    • Custom-designed liquid crystal mixtures for LCD and OLED displays
    • High-performance panel films for consumer electronics screens
    • Specialty functional materials for precision optical devices

    4. Custom Fine Chemical Synthesis for Performance Polymers

    Manufacturers engaged in the development of high-performance specialty polymers utilize this aromatic building block to introduce halogenated substituents at targeted ring positions within polymer backbones. Its reactivity allows for the creation of advanced engineered plastics with customized mechanical and thermal properties. Strict raw material traceability and in-process QC ensure polymer batches meet critical application demands in aerospace and electronics industries.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for specialty polymer manufacturing
    • UL 94 flammability standards for plastics in electrical and electronic devices
    • REACH substance management for monomer feedstocks
    • RoHS compliance for polymers used in tech hardware assemblies

    Typical usage ratio

    • 0.1–0.8% by weight of total monomer feed; dosage tuned for intended halogen content and end-use property specification in the polymer matrix

    Downstream process integration

    • Integrated at the monomer synthesis or pre-polymer functionalization stage, undergoing coupling or direct polymerization to embed halogenated motifs within the polymer chain; followed by extrusion or molding of finished material

    Final product types

    • Fluorinated engineering plastics for aviation or microelectronics assemblies
    • Custom halogenated copolymers for high-durability industrial components
    • Polymer-based films and sheets with enhanced chemical resistance and fire retardancy

    5. Synthesis of Specialty Dyes and Pigments for Electronic and Industrial Applications

    Leading dye and pigment manufacturers employ this building block for the synthesis of electronically active diazo and azo compounds, especially those requiring specific halogen positions for controlling colorfastness, solubility, and conductivity. This approach supports the growing demand for high-purity pigments in OLED, printer ink, and specialty marking technologies, all of which require rigorous control of trace halogen compounds and heavy metals.

    Industry compliance standards

    • EN 71-3 Safety standards for colorants in electronics and industrial applications
    • ISO 1248 Pigments—Specifications and test methods
    • RoHS Directive (2011/65/EU) for pigments used in electronics
    • REACH SVHC assessment for colorant chemicals

    Typical usage ratio

    • 0.1–1.0 molar equivalents in diazotization or azo coupling reactions; ratio adjusted for intensity, hue, and solubility performance in the formulated dye

    Downstream process integration

    • Used during the early diazotization and coupling stages, where the fluoroiodotoluene acts as a halogen donor to the pigment backbone; after synthesis and purification, the pigments undergo formulation and dispersion based on application

    Final product types

    • Electroactive pigments for OLED and display coatings
    • Precision dyes for industrial inkjet and toner
    • Functional colorants for high-specification marking systems
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    Certification & Compliance
    More Introduction

    3-Fluoro-4-Iodotoluene: Practical Experience from the Manufacturer’s Floor

    Real-World Chemistry, Not Theoretical Talk

    In daily operations at our plant, we see countless aromatic compounds come down the line. Over years of running glassware and steel, some intermediates prove themselves in unique ways. 3-Fluoro-4-Iodotoluene stands out for both its reactivity and its practical role in pharmaceutical and agrochemical synthesis. Out here, we don’t judge a product by spec sheets alone. We see how it behaves in reactors, what yields it supports, how it handles scale-up, and how downstream partners trust its consistency.

    Every batch of 3-Fluoro-4-Iodotoluene we make traces back to our experience managing multi-step halogenations reliably. Many in the market focus on classic bromo or chloro toluene derivatives, both for cost and familiarity. Yet, introduction of a fluorine at the meta position changes both the electron density on the ring and the stability of downstream intermediates. These differences aren’t just academic. In day-to-day batch processing, fluorinated aryl iodides offer clear benefits that become more obvious as processes stretch from gram lab work to multi-ton campaigns.

    Consistent Quality From Raw Material In

    Our typical synthesis relies on toluene as a starting material, and we source fluorinating agents with strict impurity controls. Skipping steps or relaxing controls at just one stage can hit the final purity hard, and purification here is no joke — even trace isomers or residual oxidants push a project off track. Our team has learned the hard way that each wash, extraction, and distillation matters. Consistent appearance, melting point, and GC-HPLC profile don’t come free. They come from years at the bench and constant feedback from clients scaling up in tight regulatory windows.

    For analytical enthusiasts out there, 3-Fluoro-4-Iodotoluene usually hits a purity above 98%, measured by both GC and NMR. Over time, we have clocked how small differences show up in different assays: a minor byproduct that looks harmless in initial screens may create headaches during Suzuki coupling or lithiation further down the process. We solve these challenges by keeping raw materials clean and fine-tuning our distillation steps. We spend real time, not just because specs demand it, but because one misstep means a week lost on a reactor — and no chemist has patience for that.

    Distinctive Properties in the Toolbox

    On the bench, 3-Fluoro-4-Iodotoluene manifests as a pale yellow liquid, much more manageable than some sticky aromatic halides. The melting and boiling point ranges, and its neat handling, make it simpler during transfers and purges. You won’t find it fuming or decomposing under ordinary storage, which our warehouse crew appreciates. But the real kicker lies in that functional group arrangement.

    The meta-fluorine shifts the electron density, so electrophilic aromatic substitution on this scaffold responds differently compared to unsubstituted or di-halogen toluenes. With the para-iodine, our product supports efficient metal-catalyzed couplings. You get both the reactivity of aryl iodides—renowned for their strong leaving group character—and the unique electronic tweak from the fluorine. This shows up in the selectivity of many catalyzed cross-coupling reactions, where yields climb and side products drop, especially as you scale up to kilo lots. We’ve seen firsthand how partners working on kinase inhibitors or other fluorinated heterocycle projects lean hard on this combination.

    The Difference From Other Toluene Derivatives

    Plenty of chemists start with plain 4-iodotoluene or the 3-fluoro variant, but once you see how tough some cross-coupling steps become, the value of having both halogens in place grows obvious. We have tracked performance data across multiple reaction series: with just the iodine, certain Sonogashira reactions limp along or fail to reach completion with finicky aryl alkynes; with just the fluorine, plenty of modern steps become difficult to control.

    The true edge appears when both are present. The ortho/para directivity from the methyl and halogen pairing also supports downstream diversification, something not readily matched by lower-cost alternatives. Synthetic biologists and medicinal chemists want options: being able to tweak, substitute, or functionalize at other positions without losing the utility of their handle at carbon four. Our product proves its mettle in these flexible design needs, supporting both high throughput discovery and manufacturing scale-up.

    Compared to monohalogenated toluenes, dihalogen analogs bring complexity. Storage, compatibility with base-sensitive intermediates, and solubility take center stage. Our process addresses these by dialling in small tweaks—solvent choices, drying procedures, and tank material selection—so partner organizations don’t have to. By the time shipments leave our facility, their quality and shelf-stability has been validated, not guessed.

    Applications and Real-World Impact

    In the pharmaceutical world, 3-Fluoro-4-Iodotoluene often sounds niche, but time proves otherwise. Fluorinated molecules have dominated new drug applications for their role in modulating potency, metabolic stability, and receptor selectivity. Many kinase inhibitor scaffolds feature related motifs, and medicinal chemists working on next-generation oncology drugs ask for this precise compound to speed their SAR (structure-activity relationship) cycles. Some agrochemical partners consume even more. Crop protection chemicals push innovation year-round, with ever-changing regulatory and environmental requirements. Including electron-withdrawing groups at strategic points delivers improved persistence and reduced toxicity in target organisms – the meta-fluorine arrangement fits snug into such strategies.

    The beauty of this molecule isn’t just on paper. We work hands-on with teams optimizing C–N, C–C, and C–O couplings. Late-stage functionalizations, such as Suzuki-Miyaura or Buchwald–Hartwig reactions, need reliable inputs. A single inconsistent raw material can derail a sequence, setting a team back days. With our product, users find smooth solubility profiles in DMF, DMSO, and even less polar solvents thanks to that subtle fluorine tweak. The molecule holds up under a range of temperature and catalyst conditions, avoiding the surprises—precipitation, decomposition, or stubborn residues—that plague poorly controlled alternatives.

    Manufacturing Hurdles and Why They Matter

    Small differences in process chemistry make a big impact on final performance. Every plant operator knows fluorination and iodination don’t always play nicely in the same pot. Too much water or trace metal contamination can lower yields and introduce tough impurities—some nearly impossible to wash out. As a manufacturer, we battle these gremlins in real time, not sitting back waiting for QC results from someone else’s plant. Each stage, whether chlorination, fluorination, or substitution, receives direct oversight. If a batch veers from plan, our operators catch it during heat-up or transfer, and adjustments come fast.

    Not every facility cares to run small lots with high-cost reagents, especially when a client demands tonnage with month-to-month consistency. We make these investments at our site: upgraded containment, air handling, and distillation units sized to preserve purity and avoid cross-contamination. The smell of chemical processes, the warmth of a running column, the never-ending clamp-tightening—these create a setting where batch-to-batch quality stops being a boardroom talking point and becomes second nature.

    Safety and Handling from Our Perspective

    Talking safety, years spent moving halogenated aromatics have taught us the importance of both containment and employee protection. 3-Fluoro-4-Iodotoluene gives fewer headaches than some of its cousins. Its relatively manageable vapor pressure and thermal stability let us focus on the essentials: clean transfer lines, filtered ventilation, and frequent operator training. We’ve designed storage and transport protocols by looking not just at the regulations but at how drums and containers behave across winter and summer cycles. Over time, small tweaks in gasket materials or temperature thresholds have kept both product and team safe during transit. Customers often overlook the real-world effects of small formulation differences; we see them every shipping cycle.

    Collaboration and Feedback Loops

    Many of the world’s most discussed drugs or protecting agents never get off the ground without consistent, high-purity intermediates. 3-Fluoro-4-Iodotoluene rarely claims headlines, yet it stands behind major product launches and patent filings. Collaborating with both established pharmaceutical giants and fresh research labs, we gather feedback at every handoff. When a customer flags a new downstream incompatibility or requests a shift in bulk handling, we listen, adjust, and document outcomes. This attitude—learned over years of honest mistakes and small victories—keeps our product ahead while retaining costs and timelines partners appreciate.

    Knowing how a compound performs in real reactors, with challenging impurities and under tough timelines, grounds every improvement. Scale brings fresh problems: heat transfer, crystallization, or solvent recovery. We have modified protocols based on repeat feedback. Sometimes this means spending weeks reworking distillation columns or tweaking filtration methodologies, all aiming for more reliable product in more demanding chemistries.

    Looking Forward: Supporting Innovative Chemistry

    We pay close attention to the evolving needs of those developing next-generation molecules, whether in drug discovery, crop protection, or advanced material science. Fluorinated aromatic iodides form building blocks for new chemical libraries—a surge of activity follows every innovation in coupling catalysts or reaction platforms. Getting ahead here means not just chasing new products, but locking in the details: process safety, analytical consistency, and practical handling.

    In the R&D pipeline, some partners stay laser-focused on current method optimization, seeking higher yields or milder reaction conditions. Others push boundaries, looking for compatible solvents, lower catalyst loads, or alternative activation strategies. Groups using photoredox, nickel catalysis, or even enzymatic halogenation have provided feedback that shapes our SOPs. We believe real progress emerges from these two-way dialogues, not top-down dictates or distant procurement cycles.

    Supporting Compliance and Environmental Responsibility

    Maintaining environmental stewardship means high capture rates for volatile organics and serious investment in emissions abatement. With every batch of 3-Fluoro-4-Iodotoluene, our waste streams get careful monitoring: scrubbers, carbon beds, and solvent recyclers capture halogenated emissions and cut down offsite disposal. Improved process mapping, informed by frontline experience, reduces the chance of offscale chemistry. We avoid corner-cutting on safety data, not just to tick boxes but because anyone working with halogenated aromatics knows surprises hurt both bottom line and workforce morale. Our crew, trained and equipped, has seen the differences this makes over long shifts and annual audits.

    Inspection bodies and third-party auditors see our work up close. Instead of merely showing paperwork, we invite them onto the plant floor: real exposure, running samples, verifying containment and documentation, and confirming waste treatment. Such openness turns audit day from stressful to ordinary, allowing us to respond fast to regulatory shifts and maintain customer trust month over month.

    Lessons Learned on the Manufacturing Floor

    Chemistry at scale, especially when new, never looks exactly like the plan. Equipment fouling, unexpected pressure spikes, or slight color drift tell stories not covered in textbooks. Over the years, even minor operator insight—tweaks in heat ramp rates, patience during vacuum applications—can make or break batch outcomes. Our team swaps stories during shift changeovers, cataloguing odd smells, viscosities, or unexpected reflux characteristics. Each is logged and, over time, brings stepped improvements in both product and plant safety.

    Data gathered from thousands of kilos across different reactor trains creates feedback we feed forward, shaping how production unfolds. By sharing both wins and stumbles, the plant floor team builds a resilient process. They know the stakes: for chemists pushing the boundaries of medicinal or agricultural innovation, raw material failure wrecks timelines, strains budgets, and erodes trust in ways that take years to fix.

    Why 3-Fluoro-4-Iodotoluene Keeps Its Value

    Plenty of alternatives want a slice of the market. Monohalogenated toluenes sometimes fill the gap at lower upfront cost, while certain trifluorotoluene products tempt those in early-stage screening. What we see, batch by batch, is the persistence and selectivity edge the 3-Fluoro-4-Iodotoluene variant provides. Time saved on purification, boosts in final product yield, and fewer cycles back to the drawing board — these benefits add up tangibly, not just in R&D, but in the hard numbers after multi-ton deliveries.

    Over time, we have fielded calls and emails from process leads who tried to cut costs or cycle times with off-spec or alternative materials. Occasionally, one shortcut works until a new impurity pops up or a yield drops unexpectedly. We take these lessons seriously, feeding them back into our own reviews and lab meetings. Sometimes the market rewards cheapness; but for repeated campaigns, or any regulated chemistry, reliability always wins out.

    Direct Connection to the Science, Not Just the Market

    Too often, intermediates like 3-Fluoro-4-Iodotoluene look anonymous in shipping manifests or corporate procurement runs. For those of us making it, each batch reflects dozens of choices, refinements, and hard-won lessons. We stay closely tuned to what the molecule does both upstream and down — spending extra on clean reagents, dialing in glassware and reactors, even modifying site infrastructure to boost throughput or handle new synthesis routes. This isn’t theoretical or arms-length production; it’s daily work, mixing persistent curiosity with real technical standards.

    In the future, as new catalysts and reaction schemes continue to expand the chemistry possible with fluorinated aromatic iodides, we expect the demand and usage scope of this molecule will only grow. Every new drug pipeline, every regulatory shift in agrochemical approvals, brings a new set of standards for consistency, documentation, and sustainable practice. We plan to keep matching our own process improvements to these needs, just as we have for the past decade.

    Building On Experience, Delivering Real Value

    For us, making 3-Fluoro-4-Iodotoluene isn’t about hitting a quota or meeting the minimum standard. It’s about working with chemists across the world, sharing insight on process and scale, and delivering a molecule that does its part in challenging projects. Our pride isn’t in the gloss of a data sheet, but in knowing the next advance in medicine or materials might just rest on a barrel of product from our plant — consistent, known, and ready for the real challenges of modern chemistry.