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HS Code |
334837 |
| Product Name | 1-Iodo-4,4,4-Trifluorobutane |
| Cas Number | 429-65-2 |
| Molecular Formula | C4H6F3I |
| Molecular Weight | 239.99 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 121-123 °C |
| Density | 1.81 g/cm³ at 25 °C |
| Refractive Index | 1.410-1.415 |
| Purity | Typically ≥ 97% |
| Smiles | C(CCI)CC(F)(F)F |
As an accredited 1-Iodo-4,4,4-Trifluorobutane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 1-Iodo-4,4,4-Trifluorobutane; tightly sealed cap with hazard labeling and product details. |
| Shipping | **Shipping Description:** 1-Iodo-4,4,4-Trifluorobutane is shipped in tightly sealed, chemical-resistant containers, protected from heat, moisture, and direct sunlight. Transport complies with relevant hazardous material regulations (such as DOT or IATA). Proper labeling and documentation are required, and handling by trained personnel using suitable personal protective equipment is mandatory to ensure safety. |
| Storage | **1-Iodo-4,4,4-Trifluorobutane** should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Store in a cool, dry, and well-ventilated area away from sources of ignition, heat, strong acids, or bases. Keep away from incompatible materials and handle using appropriate personal protective equipment to ensure safety. |
Applications of 1-Iodo-4,4,4-Trifluorobutane in Industrial Manufacturing1-Iodo-4,4,4-Trifluorobutane is a highly specialized intermediate, primarily recognized for its selective reactivity in the synthesis of advanced chemical compounds. We support customers in several defined sectors where this material is fundamental for the development of specialty products that require strict process control, regulatory compliance, and precise formulation parameters. 1. Active Pharmaceutical Ingredient (API) Intermediate for Fluorinated DrugsPharmaceutical manufacturers use 1-Iodo-4,4,4-Trifluorobutane as a building block for synthesizing fluorinated side chains in next-generation pharmaceuticals. The material participates in carbon-iodine substitution reactions during the active ingredient synthesis, contributing to the drug’s metabolic stability and bioavailability. This step typically occurs after core scaffold assembly and undergoes stringent process validation to meet regulatory requirements for traceability and impurity control. Industry compliance standards
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2. Agrochemical Synthesis for Herbicide and Fungicide FormulationsAgrochemical formulators utilize this material to create active ingredients that require terminal trifluorinated groups for enhanced environmental stability and regulated degradation rates. It enters the chlorination or coupling reaction stages for the manufacture of target molecules designed for crop protection, imparting improved field persistence and desired toxicological profiles. Industry compliance standards
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3. Specialty Monomer and Polymer Modification in Performance Material ManufacturingPerformance polymer manufacturers integrate 1-Iodo-4,4,4-Trifluorobutane into polymer backbones to introduce fluorinated side chains that provide enhanced chemical resistance, hydrophobicity, and dielectric stability. The material’s iodo functionality enables precise grafting through controlled radical polymerization or substitution reactions during polymer modification processes in advanced material facilities. Industry compliance standards
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4. Synthesis of Fluorous Phase Transfer Catalysts and Extraction MediaProducers of fluorous media employ this compound as an alkylating agent to introduce trifluorobutyl chains into phase transfer catalyst structures, enhancing their fluorophilicity and separability. The material typically reacts with polyether or quaternary ammonium scaffolds, resulting in catalysts and extraction agents used in industrial-scale multiphase synthesis and purification processes. Industry compliance standards
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On our shop floor, we see demand shift every year—still, few products stand out for their repeat requests from R&D, scale-up groups, and process managers, quite like 1-Iodo-4,4,4-Trifluorobutane. As the manufacturer, we have watched customers chase reliability in halogenated intermediates, only to land on this compound when precision and reactivity matter. Our expertise starts at the reactors, where every batch tells you something about chemical behavior and operator finesse, and the science behind this compound keeps us pushing for tighter specs and cleaner end product.
The essential feature here is the compound’s structure: C4H6F3I, a straight-chain butane with three fluorines on terminal carbon and one iodine on the other end. We produce this product at consistently high purity—most recent analyses show GC area normalizations consistently above 98.5%. Chemists value that figure, but what’s more relevant for us is how the material looks and pours. Our operators watch color and odor for deviations, analyzing trace impurities that common distillation processes let slip through elsewhere. Our QA team remains on top of every step, pulling samples through the day—to guarantee no batch will let you down on selectivity.
From a handling perspective, the product arrives as a colorless to pale liquid, density heavier than water at about 1.8 g/mL, and a boiling point just over 130°C at normal pressure. Stability under inert gas lets chemists hold inventory on shelf for weeks, which sets it apart from less stable iodoalkanes that break down on exposure. Every drum we ship receives a final round of NMR scrutiny for chain-length identity and a halide test to check for side reactions that sneak in if temperature or mixing falters.
1-Iodo-4,4,4-Trifluorobutane earns its keep in the lab by working as a highly selective alkylating agent and as a versatile handle for introducing trifluorobutyl groups or iodine into new structures. We field requests from agrochemical manufacturers, pharmaceutical discovery teams, and fluoropolymer innovators. Most care about how quickly and cleanly the reagent couples, especially in metal-catalyzed cross-couplings or nucleophilic substitutions.
Traditional halobutanes and trifluoromethylated compounds can stall out in reactions, giving you mixtures that complicate scale-up. By contrast, 1-Iodo-4,4,4-Trifluorobutane shows brisk reactivity—iodine provides an excellent leaving group, while the trifluoromethyl terminus shields reactions from overactivity and narrows product ranges. In Suzuki or Ullmann-type couplings, for example, yields stay high and byproduct generation remains low, especially under mild base or copper assistance. It never fails to surprise new users how controlled the reactivity is compared to other iodoalkanes, where beta-elimination and impurities are more frequent.
Not all iodoalkanes deliver on this promise. Length tweaks or chlorine substitutions can yield off-target reactions or degrade product performance, particularly during pharmaceutical API synthesis. Chemists report tighter batch-to-batch reproducibility and easier purification—chains with extra methylene or without fluorines have less selectivity, while the full trifluorobutyl substitution manages steric and electronic pressures exactly as needed.
We build safety and consistency into shipping and storage protocols. Bottles and drums leave our site nitrogen-blanketed to lock out oxidation, and every label specifies date of filling so you know its history. In customer plants, anhydrous handling gives chemists flexibility to try new ligands or catalysts without fouling the reaction or introducing hydroiodic acid. Waste management tends to be more straightforward as well, since the compound generates less halogenated byproduct and separates easily during workup. Routine GLC and halide screening by our lab catches any drift in composition from run to run, which means customers spot fewer surprises at the end.
Production does not come easy. Operators must control heating ramps, maintain reactor cleanliness, and track iodine equivalents precisely. Early on, we struggled with trace iodide and low-level olefinic byproducts—over time, switching glassware, updating purification steps, and refining NMR targets has brought us closer to theoretical purity every season. Our technical team fields questions about process tweaks and troubleshooting, especially from scale-up clients or pilot plants who notice even tiny shifts in reactivity or product quality from other suppliers.
As a manufacturer, we directly witness how small changes in input quality ripple through supply chains. Pharmaceutical projects have told us how superior quality 1-Iodo-4,4,4-Trifluorobutane unlocks cleaner C–C bond formations in their active intermediates, supporting green chemistry goals and reducing clean-up steps. In agrochemical routes, selectivity of this molecule prevents fingerprints of unknowns in finished products, where regulatory limits bite hard on impurity levels.
Engineers in the electronics sector pick this material for dielectric modification and as a precursor in custom fluoropolymers. Modest volumes can yield big shifts in final component reliability—especially once you pass pilot scaling. Experience tells us that other halobutanes or brominated analogs simply do not match the reactivity profile, often at the cost of fouled catalysts or incomplete conversions.
Our own process improvement stories stem from practical realities. Early client feedback flagged odor complaints, so we invested in vent recovery and sealed sampling. Another time, a rare shipment broke emulsion stability during distillation—now we triple-check surfactant contamination before filling. Each correction finds its way into our SOPs. Over the years, as the product earned its role in specialized syntheses, we have heard from customers reporting double-digit time savings just from the improved reactivity and work-up times this compound offers over lesser alternatives.
We make several halogenated butanes and their fluorinated counterparts, but few have the balanced utility of 1-Iodo-4,4,4-Trifluorobutane. The C4 carbon chain sits at a sweet spot between excessive volatility and unmanageable viscosity. Add three fluorines, and you secure metabolic stability and chemical inertness at the terminus, which improves translation from laboratory to industrial process.
Chlorinated or brominated versions are available, but reaction rates slow and yields can struggle with side reactions—something few chemists have patience for when deadlines loom. Longer chain analogs can show solubility or volatility issues, while shorter chains falter in compatibility with complex molecules. The iodine atom here does more than allow coupling—it sets up efficient transformations, cleans up byproducts, and supports one-pot procedures.
Our bench teams see the learning curve in new customers who switch from similar-looking halides or from shotgun approaches with cheaper substitutes. Once they feel the improvement in ease and control, they stop looking elsewhere. For experienced synthetic chemists, small gains in yield or simpler separation steps mean fewer headaches and better economics over dozens of batches each year.
On the sustainability front, embracing 1-Iodo-4,4,4-Trifluorobutane creates less downstream waste than standard chloro- or bromo-alkanes. The product’s high conversion rates and selectivity reduce halogenated waste, making end-of-pipe management more efficient. Less energy is burned on purification, and operators minimize solvent washes—good outcomes for plants prioritizing green chemistry or ISO certifications.
Quality control does not just mean a hard number—we maintain traceability from batch start to drum fill, so customers have confidence in both performance and compliance. Detailed COAs follow the material, reflecting investments in analytical infrastructure—GC-FID, NMR, and halide titration all come into play. No drum leaves our site without sign-off from technical management, who understand that a misstep in raw material means a product recall or failed pilot run months later.
Like most fluorinated iodoalkanes, the price of raw materials—iodine and fluorinated building blocks—has spiked with global supply disruptions. Years back, we locked in multiple vetted sources for iodine and put aside tonnage when possible. Customers benefit when we can deliver to schedule even under market shocks; our history gives us leverage smaller operators or late-stage traders simply do not have.
Operationally, large-scale production means careful waste trapping and vent management. A few years ago, vented iodine threatened a local nuisance, leading us to boost recovery systems and retrain staff for leak checks. These process upgrades protect worker health and push our compliance metrics higher. As a manufacturer, regulatory demands around halogenated compounds only tighten; staying ahead with responsible batching, containment, and employee training reduces risk and keeps approval pathways open.
Shipping across climate zones poses storage challenges—some analogs degrade or darken, especially on long journeys. We now use inerted, UV-protective drums for international orders, verified by photos and logged with RFID tracking. On arrival, most drums retain specification without remediation; deviations trigger a replacement plan without haggling. Consistent communication with customers—not automated emails, but real operator phone calls—helps us spot trouble areas and tweak logistics.
Chemists who rely on our 1-Iodo-4,4,4-Trifluorobutane have not all faced the same synthesis or regulatory pressure. Some optimize for reactor throughput, others chase down ppm-level residue specs, and a few design one-off transformations for patent races. Our staff understand how process questions differ: one group may need scale-up documents, another looks for unique work-up suggestions or blending clarity. Our technical team has handled dozens of troubleshooting requests—NMR signal ambiguities, coupling side-reactions, or advice on complementary base systems.
By cultivating open feedback—visits to customer pilot suites, joint RCA reports following rare quality deviations, and consistent tech notes shared online—we continue to improve our process and drive the science in productive directions. We treat these relationships as extensions of our R&D, and have pointed two clients to alternate coupling agents that streamline their process, cutting both cycle time and halide stress.
Having worked through cycles of scarcity, price volatility, and tightening regulatory standards, our team has learned that close attention to quality, supply chain, and customer partnership will define the next generation of specialty alkylating agents. 1-Iodo-4,4,4-Trifluorobutane wins loyalty from experienced chemists and engineers, not because it is the cheapest option, but because its predictability, purity, and supply assurance keep projects moving and innovation on track.
We continue to upgrade our plant safety, automate more analytics, and layer in new operator training for emerging synthesis demands. Future plans include on-site custom synthesis support, a client-sourced innovations log, and more real-time inventory tracking for urgent requests. Each of these investments comes from hands-on lessons in handling, shipper compliance, and technical problem solving—not from trade fair marketing or spreadsheet algorithms.
To our team, producing 1-Iodo-4,4,4-Trifluorobutane is not a theoretical exercise. It is chemistry done under pressure, for people who understand what a superb intermediate can do on the plant floor or in a discovery suite. Our experience flows through every drum that leaves the site—each batch carrying lessons from the last and building consistency that customers depend on. By standing behind every container, working closely with users, and never losing sight of process reliability, we see this product anchoring more breakthrough syntheses and supporting the future of fluorinated chemistry for years to come.