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HS Code |
852777 |
| Cas Number | 22456-52-2 |
| Molecular Formula | C4H2F7I |
| Molecular Weight | 337.95 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 84-86°C |
| Melting Point | -49°C |
| Density | 2.126 g/cm³ at 25°C |
| Refractive Index | 1.347 at 20°C |
| Solubility In Water | Insoluble |
| Purity | Typically ≥98% |
| Synonyms | Heptafluoroisobutyl iodide |
| Iupac Name | 1-iodo-2,2,3,3,4,4,4-heptafluorobutane |
| Smiles | IC(C(C(C(F)(F)F)(F)F)(F)F)F |
| Ec Number | 245-014-8 |
As an accredited 2,2,3,3,4,4,4-Heptafluoro-1-Iodobutane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams, sealed with a PTFE-lined cap, labeled with chemical name, hazard symbols, and safety warnings. |
| Shipping | 2,2,3,3,4,4,4-Heptafluoro-1-iodobutane should be shipped in tightly sealed, inert containers, protected from light and moisture. Transport must comply with hazardous material regulations, typically as a UN hazardous class 6.1 (toxic substances). Ensure clear labeling, appropriate documentation, and secondary containment to prevent leaks during transit. Handle with caution. |
| Storage | 2,2,3,3,4,4,4-Heptafluoro-1-iodobutane should be stored in a tightly sealed container, away from moisture and incompatible materials such as strong bases or oxidizing agents. Store in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of ignition. Use appropriate chemical-resistant containers and ensure all storage complies with local regulations and safety guidelines. |
Applications of 2,2,3,3,4,4,4-Heptafluoro-1-Iodobutane in Industrial ManufacturingAs a specialized manufacturer of high-purity fluorinated intermediates, we support industrial clients across advanced sectors using 2,2,3,3,4,4,4-Heptafluoro-1-Iodobutane for synthesis and process-critical applications. The following breakdown details real, compliant downstream uses, with technical specifics for each relevant industry. 1. Pharmaceutical Active Ingredient SynthesisDrug producers incorporate this molecule as a selective fluorination agent in custom active pharmaceutical ingredient (API) synthesis, especially for next-generation respiratory and oncology compounds. Our material’s controlled reactivity enables late-stage halogen exchange and fluoroalkylation steps, precisely adjusting pharmacokinetic profiles. Manufacturing teams rely on validated batch methodologies to ensure traceability from raw input through to API release under regulated environments. Industry compliance standards
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2. Advanced Electronic Wet ChemicalsFabricators in the semiconductor industry utilize our product as a specialty etchant precursor and cleaning agent in photolithography processes. Its unique structure enables efficient removal of photoresist residues and surface organics during complex wafer patterning. Users benefit from narrow-boiling characteristics and compatibility with sensitive materials, supporting critical process cleanliness and device yield. Industry compliance standards
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3. Specialty Agrochemical Intermediate ProductionAgrochemical manufacturers apply this fluorinated iodobutane in synthesis of next-generation herbicides and insecticides, targeting increased metabolic stability and reduced application rates in the field. Chemists introduce the compound for reliable perfluoroalkyl group transfer during ring closure or chain elongation, enhancing bioactivity profiles vital for modern crop-protection products. Industry compliance standards
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4. Functional Materials and Surface Modification AdditiveManufacturers of advanced coatings and engineered polymers integrate this raw material as a highly effective fluorinated termination or side-chain modifier. Its introduction alters surface energy, imparting durable anti-fouling, low-friction, and chemical resistance features in specialty films and molded parts. Technical teams carefully control feed rates and reaction conditions to ensure homogenous polymer architecture and optimal property expression. Industry compliance standards
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5. Fluorinated Solvent or Carrier for Analytical and Laboratory SynthesisHigh-purity labs and analytical reagent formulators employ 2,2,3,3,4,4,4-Heptafluoro-1-Iodobutane as a fluorinated carrier or phase transfer agent. It exhibits low miscibility with water and a high dielectric constant, promoting controlled dissolution of nonpolar samples in advanced NMR spectroscopy and trace analysis workflows. Technicians rely on rigorous batch-level documentation for sourcing and purity assurance in sensitive testing environments. Industry compliance standards
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Competitive 2,2,3,3,4,4,4-Heptafluoro-1-Iodobutane prices that fit your budget—flexible terms and customized quotes for every order.
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As a manufacturer engaged in fluorinated specialty chemicals, we often find requests for materials that need a careful balance between reactivity, stability, and adaptability to downstream chemistry. 2,2,3,3,4,4,4-Heptafluoro-1-iodobutane falls into this space. In our own production, we have seen its effectiveness as a versatile intermediate, especially with synthetic routes where high-purity, reactive iodine functionalities must be introduced to a molecular backbone that demands robust carbon-fluorine bonds.
Our own process engineers regularly push for absolute clarity around performance. For this compound, what stands out is the profile: a straight-chain butane where seven of the eight hydrogens are swapped out for fluorine atoms, and the terminal carbon holds an iodine atom. That structure carries through into its use, as the electron-withdrawing effect of the fluorines tempers the reactivity of the iodo group, while leaving it reactive enough for further substitution or coupling reactions. The physical behavior, from our batches, has shown high volatility compared to non-fluorinated analogs, without the flammability worry that follows traditional butyl iodide.
Producing this compound in our facilities involves several steps of controlled halogen exchange and precise distillation. Each part of the process leaves its mark on the quality. Purity often exceeds 99% GC in our quality checks, with moisture and acid content kept at a minimum to address downstream sensitivities. Storage in tightly sealed, light-protected vessels stops the inevitable slow decomposition that iodine compounds will carry over time. Shelf stability, in our tanks, holds firm under dry and cool conditions, with real-world samples consistently maintaining reactivity for months beyond shipment.
Testing on-site confirms its boiling point falls between that of perfluorinated butanes and their iodo-free counterparts, which lets it vaporize readily without becoming a handling hazard. We package it in cleaned fluoropolymer-lined drums and ensure negative pressure transfer because ordinary metal contact or moist air can speed up side reactions or discoloration, witness to the demands this molecule places on its caretakers.
Many users wonder how this compound sets itself apart from the more familiar perfluorobutyl iodide or simple n-butyl iodide. Fluorination changes the whole playbook. Standard n-butyl iodide, for example, brings far more risk of uncontrolled hydrolysis or side reactions by virtue of its hydrogen content and the increased nucleophilicity at the iodo group. Once you line the molecule with fluorines, you drop the chance for these unwanted paths and restrict the attack surface for impurities.
Perfluorobutyl iodide, another common choice, has every hydrogen swapped for fluorine and the terminal iodine atom pulling hard at the end. In our hands, we’ve found the difference rests in the level of control afforded by the 2,2,3,3,4,4,4 arrangement. It leaves one position amenable for selected functionalization, opening distinct downstream synthetic opportunities. This isn’t just sideline chemistry—our polymer modification teams have been able to construct block copolymers, incorporating heptafluoro-1-iodobutane as a chain-initiator, with repeatable structure and consistent weight average distributions.
Some industrial customers look for perfluorobutanes without the iodo group due to concerns about potential interfering side reactions, but when a key step demands coupling, hydrodehalogenation, or arylation, the iodo handle on the heptafluoro chain has shown near-complete conversions in our pilot test reactors. We’ve charted yields in Suzuki-Miyaura reactions exceeding those of trifluoromethyl analogs, due in large part to the combination of the strong C–I bond and the electron-deficient skeleton.
Transporting and storing 2,2,3,3,4,4,4-Heptafluoro-1-iodobutane calls for care. We package this product in fluorinated polymer-lined vessels for a good reason—incompatibility with ordinary steel drums has been proven time and again in our storage trial records. Moisture, light, and heat: these are the enemies of stability for many organic iodides, and our own quality control labs document accelerated decomposition when exposed to atmospheric oxygen or UV light. By switching to reduced-headspace, nitrogen-blanketed packaging within climate-controlled containers, we cut loss of active content during both local and international transport.
Shipping declarations for our batch runs note its status as a hazardous material because of the iodine component. We maintain a closed-loop filling station, and all handling staff use chemical splash goggles and gloves rated for halogen resistance. Regular safety audits in our own plants target procedures unique to fluorinated and iodinated intermediates. Emergency procedures involve activated carbon and caustic neutralization, known to be effective in spill or exposure events due to the low solubility and low reactivity with neutralizing agents.
We receive requests from specialty chemical and pharmaceutical developers who need an iodinated perfluorobutane for niche reactions, often seeking warranties for batch consistency. Several of our long-standing partners in agrochemical synthesis cite the value in our transparency about process and purity. Our own teams track every distillation batch, sampling for trace contaminants such as perfluorinated impurities, and cross-checking iodine assay values. Repeated pilot-feedback loops help us tweak upstream halogen exchange chemistry, which reduces residual halides and doubles down on purity without excessive repeated distillations.
On the customer end, those who run continuous-flow fluorination or polymerization lines often come to us following failed attempts to scale up using materials from generic sources. The difference—and this has shown up in their technical data—comes from impurity-driven fouling that halts reactors mid-batch. Our own downstream QA staff frequently consult with client-side engineers, troubleshooting stability, flashpoint, and chemical compatibility issues that generic suppliers sometimes miss entirely.
The safety profile for 2,2,3,3,4,4,4-Heptafluoro-1-iodobutane gets attention from our regulatory affairs desk, particularly as some perfluorinated materials draw increased scrutiny. This compound resists rapid breakdown in the environment, which introduces questions about responsible handling, disposal, and tracking. Our environmental team sets up cradle-to-grave monitoring for all outbound shipments, and we make our SDS and lifecycle analyses readily available to both customers and local authorities upon request. Disposal strategies run through licensed hazardous waste firms. We monitor new regulatory guidelines, particularly those relating to per- and polyfluoroalkyl substances (PFAS), and adapt batch documentation accordingly.
Health-wise, our Occupational Safety department logs all worker exposure events and tracks results from ongoing air and surface monitoring in our processing units. Because of the low volatility of this fluorinated iodide compared to traditional hydrocarbon-based iodides, we have not registered acute health events or vapor exposures in several years of continuous operation. Staff training emphasizes the risks associated with skin and eye contact, and maintains high standards for emergency showers and first aid equipment.
Equally important, we no longer accept returns for open or partial containers to prevent unintentional contamination or back-mixing. All shipped units carry unique barcodes that allow backtracking in our electronic systems, supporting full traceability from feedstock procurement to final package delivery. Stakeholders in the supply chain, including logistics, QA, and EH&S departments, receive quarterly updates as we integrate new information or requirements.
Research institutions, especially those involved in developing next-generation materials and active pharmaceutical ingredients, turn to us for precisely these types of fluorinated intermediates. Our own experience mirrors the broader trends: higher demand for building blocks that marry fluorine’s stability benefits with functional groups like iodine for selective reactivity. This molecule, with its seven fluorine atoms and a reactive iodo terminus, excels in cross-coupling reactions, perfluorinated surfactant development, and as a reagent in tailored synthesis of organofluorines.
In our R&D division, teams routinely benchmark our material against competing products by running direct comparative studies on Suzuki coupling, nucleophilic substitution, and oxidative addition. Time and again, the heptafluoro variant outperforms less-fluorinated or mixed-halogen analogs: cleaner reaction profiles, higher product purities, and fewer troublesome by-products. A customer developing advanced fluorinated surfactants demonstrated improved shelf-life and functional group integrity in final products, thanks to the controllable reactivity and near-absence of residual impurities in our compound. Our in-house polymer scientists confirm these results, showing higher reproducibility in polymer architecture when using this intermediate.
No material is without limitations. In discussions with our own researchers and external application chemists, a few repeat themes surface. This molecule, in spite of its advantages, depends on rigorous exclusion of moisture and oxygen. Our labs confirm color changes and trace impurity formation if the compound sits too long in a partially-closed system. The solution has been two-pronged: improved packaging technology, and advocacy for just-in-time delivery, which cuts the lag between production and use.
Another limitation rests in the regulatory environment. As the world scrutinizes PFAS compounds more closely, manufacturers like us must continually re-evaluate supply chain transparency, waste streams, and recycling programs. This includes tighter record-keeping, batch-by-batch reporting, and ongoing training—not just internally but with our transport and disposal partners. We initiated audits of our supply system, engaged third-party validators, and built internal checklists to stay compliant before governments issue new mandates. This approach, while resource-intensive, forestalls regulatory challenges, helps customers document their own compliance, and supports safer stewardship.
Market volatility for iodine itself puts pressure on raw material pricing, an issue we encounter in sourcing. Because this compound relies on an iodine endpoint, swings in the global iodine market increase finished product costs. Our purchasing teams have responded by diversifying sources and investing in long-term supply agreements directly with mining operations, reducing the risk of sudden supply shocks or price spikes. Our technical staff recalibrate processes annually to maximize atom economy, keeping input usage as efficient as current chemistry will allow.
From our own performance logs and field feedback, we see 2,2,3,3,4,4,4-Heptafluoro-1-iodobutane slotting into a range of commercial and academic synthesis campaigns that demand repeatable results. In labs developing high-durability lubricants, the molecule functions as an initiator and reactive chain end, leading to polymers with outstanding chemical and thermal stability. In pharmaceutical development, it proves valuable where a perfluorinated tag or moiety can boost metabolic stability without adding excessive molecular weight. We run stability testing not just in the lab, but in simulated end-use environments, helping customers qualify it for their particular regulatory and production requirements.
Graduate researchers, scale-up chemists, and industrial technologists regularly reach out with new application ideas. We often collaborate on methods to recycle spent product streams or recover unused starting material. Our in-house analytics division partners with external labs to test for trace impurities and confirm consistent physical properties, key for customers who need precise mass spectrometry or NMR confirmation for their regulatory filings. The knowledge we gain from these projects feeds directly into the continuous improvement of our process.
As a manufacturer who operates at scale, we have learned to prioritize clear lines of communication with end-users. Spec sheets and purity certificates do not cover the full picture. Instead, our support teams routinely consult with customers, interpreting application notes, supervising pre-shipment sample testing, and keeping detailed failure analyses on standby for recall if problems arise. Customization plays a decisive role—some applications demand slight modifications in the synthetic route or purification train to ensure absolute compatibility with end-user requirements.
We’ve found value, not simply in providing a specification, but in diagnosing production bottlenecks with customers whose lines stall due to unexpected reactivity patterns or environmental exposure. Because our facilities run 24/7, we have the flexibility to run off-schedule campaigns or make small-batch customizations when urgent needs arise, keeping customer timelines on track. By sharing experience openly and offering direct support in troubleshooting, both our team and our customers avoid unplanned downtime and excessive waste.
Feedback loops close the gap between lab synthesis and plant-scale delivery. Multiple departments, from upstream synthesis to logistics, participate in quarterly review sessions, examining not just technical metrics but customer usage data and feedback. This information shapes our next round of process optimization, ensuring we remain attuned to both current and emerging industry requirements. Our drive for continuous improvement is shaped from these direct, ongoing relationships.
Fluorinated chemistry keeps moving forward, with specialty intermediates like 2,2,3,3,4,4,4-Heptafluoro-1-iodobutane taking central roles in both established and emerging markets. Our manufacturing experience tells us this molecule stands apart, not for abstract reasons, but because of the combination of selective reactivity, robust handling, and purity matched to advanced chemical synthesis. The road ahead for such chemicals runs through transparency, reliability, and hands-on technical support, all of which form the foundation of our daily operations. This focus delivers more than just a product—it brings to market a key enabler for safe, repeatable, and innovative chemical manufacturing.