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HS Code |
231469 |
| Chemical Name | 1-Chloro-6-Iodohexane |
| Molecular Formula | C6H12ClI |
| Molar Mass | 246.52 g/mol |
| Cas Number | 207048-22-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 269-271 °C (estimated) |
| Density | 1.72 g/cm³ (at 20°C, estimated) |
| Refractive Index | 1.525 (estimated) |
| Solubility In Water | Insoluble |
| Smiles | ClCCCCCI |
As an accredited 1-Chloro-6-Iodohexane 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-Chloro-6-Iodohexane, sealed with a screw cap and labeled with hazard information. |
| Shipping | **Shipping Description for 1-Chloro-6-Iodohexane:** Shipped in sealed, chemical-resistant containers to prevent leaks and contamination. Store and transport away from heat and incompatible materials. Complies with relevant hazardous material regulations (UN/NA, DOT/IATA). Proper labeling and documentation required. Use only with trained personnel and appropriate protective equipment to ensure safe handling. |
| Storage | 1-Chloro-6-iodohexane should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it separate from incompatible substances like strong bases and oxidizers. Store under inert atmosphere if possible to prevent decomposition. Properly label the container and ensure easy access to safety equipment in the storage area. |
Applications of 1-Chloro-6-Iodohexane in Industrial ManufacturingAs a direct manufacturer, we supply 1-Chloro-6-Iodohexane to multiple established industries where its unique halogen functionalities enable targeted synthetic transformations. We work closely with formulation and process engineers to ensure integration into complex downstream processes, supporting reliable scale-up and compliance with sector-specific standards. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers employ 1-Chloro-6-Iodohexane for stepwise regioselective alkylation, especially in the construction of specialty heterocyclic building blocks and as a linker in active pharmaceutical ingredient (API) development. Controlled reaction parameters maximize selectivity at both halogen positions, supporting custom route design in new molecule synthesis. Industry compliance standards
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2. Agrochemical Fine SynthesisProducers in crop protection exploit the reactivity of 1-Chloro-6-Iodohexane as a key alkylating agent for introducing mono- or bifunctional side chains into herbicide and fungicide molecules. Its defined chain length and controlled halogen content aid structure–activity optimization campaigns required by modern regulatory dossiers. Industry compliance standards
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3. Advanced Material Science: Polymer ModificationSpecialty polymer developers use 1-Chloro-6-Iodohexane to functionalize polymer backbones or introduce specific terminal halogen moieties during copolymerization. The dual-halogen structure enables grafting and subsequent click chemistry steps, ensuring fine-tuning of physicochemical performance in engineered materials for transport and electronics. Industry compliance standards
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4. Organic Electronics SynthesisProducers of organic semiconductors incorporate 1-Chloro-6-Iodohexane to introduce halogenated alkyl chains onto aromatic cores, improving electron transport and film-forming characteristics in device-grade molecular materials. The material’s dual reactivity enables downstream Suzuki or Stille coupling for tuning charge mobility profiles. Industry compliance standards
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5. Custom Surfactant and Specialty Chemical SynthesisManufacturers of custom surfactants utilize 1-Chloro-6-Iodohexane for precision halogen insertion, designing specialty surfactant molecules required for challenging emulsification environments, such as pharmaceutical microemulsions or advanced oil recovery. The primary halide reactivity enables sequential conversion to sulfonates or quaternary ammonium derivatives. Industry compliance standards
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Since we first put 1-Chloro-6-Iodohexane into active production lines, it has stood out as a go-to intermediate for alkyl halide chemistry. With our experience in halogenated hexanes, we recognize that 1-Chloro-6-Iodohexane fills a crucial spot: a six-carbon chain capped at each end with different halogens—chlorine and iodine. This unique setup shapes how the molecule interacts within both organic synthesis and scale-up manufacturing routines.
Producing 1-Chloro-6-Iodohexane calls for close attention to purity levels, isomer content, and, above all, control of by-products through both optimization and real-world troubleshooting. Labs and workshops using this material count on it to be free of extraneous halides or chain-shortened side products, and every batch tells its own story about consistency and improvement.
We manufacture 1-Chloro-6-Iodohexane with a targeted purity above 98%, as this threshold means fewer headaches when scaling-up or working downstream. The model we follow relies on long-chain electrophilic substitution, performed under precise process control. Each molecule needs to possess an intact six-carbon backbone, without branching that could create off-specification reactivity.
Careful analysis of each lot involves gas chromatography and NMR methods. High-purity 1-Chloro-6-Iodohexane offers double benefits: the iodo terminus reacts efficiently in classic alkylation, while the chloro group resists side reactions that could otherwise compromise more sensitive functional groups. Moisture control and inert packaging come as standard, reflecting repeated experience in the sometimes-fickle storage behavior of this sort of alkyl halide.
Over years of customer feedback and project partnerships, we’ve seen 1-Chloro-6-Iodohexane move beyond papers and catalogs into practical synthesis. Chemists on university benches reach for it to build larger, more complex molecules efficiently. Its iodo group delivers high reactivity in nucleophilic substitutions, so coupling reactions proceed quickly without high temperatures. The chloro end waits patiently for later steps, opening the door to orthogonal strategies where sequence matters.
In custom synthesis, our partners find its selective reactivity reduces waste and simplifies their purification work. Halide metathesis, Grignard preparations, and carbon chain elongation all benefit from the difference in reactivity between the two halogen atoms. Our quality means that reactions run cleanly—fewer by-products show up on the chromatograms, and users spend less time troubleshooting.
Some may look at 1-Chloro-6-Iodohexane and expect it to follow the rules for other six-carbon alkyl halides, like 1-Chlorohexane or 1-Iodohexane. Our direct manufacturing experience points to important differences—chief among them, its bifunctional nature. The combination of iodo and chloro ends yields properties and reaction profiles distinct from mono-halogenated chains.
Compared to 1-Chlorohexane, which offers only moderate leaving group ability, adding an iodine atom at the sixth carbon supercharges the molecule’s ability to participate in cross-coupling. Return to traditional hexane, and the linking options drop off; the dual-halide molecule offers access to both early and late-stage functionalization, not to mention extra value as a building block for asymmetric and orthogonal synthetic schemes.
The closest alternative, 1-Iodohexane, doesn’t allow the same staged approach—the presence of only iodine makes it highly reactive, but it limits the selectivity and control that dual-halide molecules provide. We’ve witnessed research groups save time and resources by using 1-Chloro-6-Iodohexane, especially where a one-pot reaction isn’t realistic.
We view sourcing and quality management as ongoing priorities, not one-time actions. Commercial reliability, shelf stability, and performance in sensitive transformations can’t be left to chance. This means feedback from hundreds of distributors, direct users, and research partners, all aimed at continuous refinement—from procurement of base hexanol, to in-line monitoring during halogenation, and full traceability through batch records.
Delays in raw material supply have taught us to look for multiple sources for starting materials. Keeping control at each stage prevents interruptions during halogen exchange and minimizes risk of contamination that smaller labs or trading companies sometimes overlook. This approach isn’t about cutting corners for margin—it’s about understanding what our end users face when a faulty batch sets back a complex synthesis campaign.
A fair share of real-world stories shape our approach to production. Academic groups often report that the purity, halide ratio, and packaging condition each influence their reaction outcomes. If water or light exposure degrade the iodo group, reaction yields can drop significantly. Using the right container and shipping protocol reduces this risk, and it’s built into our logistics—no matter whether the order goes across town or overseas.
Our analytical chemists pay close attention to the formation of minor by-products, especially those from over-iodination or incomplete substitution. Years of iterative process improvement, based on batch outcomes and user reports, help us hold the line on specifications. We have watched downstream results improve as we dialed in conditions to minimize these so-called invisible impurities.
Large-scale users, from CROs to small pharmaceutical units, judge us less by price and more by batch-to-batch consistency. When you scale up to 10 liters or 100 liters, minor lapses in purity can translate into hours or days of lost effort. One of the hard lessons we learned from early scale-up runs: even trace amounts of isomeric by-products or unreacted hexanol skew the efficiency of catalytic stages, which trickles down into lost yield and analytical headaches.
Our investment in robust instrumentation and experienced technical staff responds directly to those needs. Blending hands-on practical knowledge with process monitoring, not just quality management checklists, keeps users coming back. Troubleshooting often involves a direct line back to our bench scientists, who know how the product behaves in coupling, substitution, and even in less-common applications like radiolabeling building blocks.
Year after year, the same issues circle back in the conversations we have with new customers: safe handling, avoidance of darkening or decomposition, and how small factors influence storage and shelf life. Our technical team has learned that 1-Chloro-6-Iodohexane responds well to cool, dry storage, with opaque containers that limit light exposure. We push for speedy transit and emphasize clear labeling not for bureaucratic reasons but for real chemical stability.
Some early-career chemists want to reduce solvent volumes or handle the compound in open air to save time. Past reports—sometimes with failed batches—demonstrate that this isn’t the right corner to cut. Controlled conditions and working setups, outlined in pre-shipment instructions, actually protect downstream results and safety in the lab.
For over a decade, environmental responsibility has become more than just a box on compliance forms. Our production lines incorporate solvent recovery, reduced-waste synthesis routes, and continuous monitoring. Halogenated waste streams don’t get a free pass—each lot is tracked through waste management processes in line with local and international requirements.
We also support customers targeting green chemistry goals. Those working toward biomass-based transformations or energy-efficient syntheses know that a reliable intermediate can spare both resources and time. Through direct dialogue with R&D partners, we continue to look for routes that generate less halogen residual and selectivity for the desired halogen exchange, based on both experience and new technical possibilities.
Each season brings a new influx of questions, troubleshooting reports, and real results from across the globe. This feedback loop drives our methods as much as any technical reference. End users want quick, honest answers when things don’t go as planned. Issues with minor color changes or slightly shifted NMR peaks get treated as actionable events—our process engineers adjust, communicate back, and keep solutions front and center.
Long-term collaborations shape ongoing investment. When a leading synthetic group switched to our product during an especially demanding coupling campaign, both sides saw the value in real-world communication. We refined purification steps to minimize trace contaminants that, though invisible in initial tests, influenced downstream yields after months in storage.
Mastering a specialty chemical often seems like a technical problem, but after years of making and delivering 1-Chloro-6-Iodohexane, it’s more of a people problem: listening, learning, and adapting. From the operators who monitor reaction temperatures, to the PhDs who interpret the NMR data, our team learns from every step. Our finished product isn’t just a bottle of clear liquid—it’s the sum of lab scale-up trials, missed yields, improvements in handling, and honest conversations with users who want something better next quarter.
New applications regularly emerge. A few seasons ago, a development team highlighted the utility of 1-Chloro-6-Iodohexane as a radiolabel precursor, leveraging its dual halide reactivity to streamline isotope incorporation. This wasn’t a published method but an innovation driven by the needs of a small group looking for both reactivity and control in their radiolabeling work. Experience tells us to listen and respond, even when a new feature or property isn’t part of a standard specification.
Chemistry doesn’t stand still. Demand for 1-Chloro-6-Iodohexane continues to shift as new coupling technologies, automated syntheses, and regulatory requirements evolve. By aligning production closely with feedback and open dialogue, we’ve helped users transition smoothly, even as methodologies in the literature move forward.
Researchers developing new heterocyclic drugs or probing post-synthetic modification find ways to use the dual-reactivity of this compound for challenges that classic mono-halide hexanes simply can’t tackle. Our continuing investment in process stability and analytical depth responds directly to real-world use—not just formal standards or catalog descriptions.
Producing 1-Chloro-6-Iodohexane calls for more than technical skill. It comes down to care—double-checking each batch, tweaking processes for a cleaner end result, and taking responsibility for what reaches your bench or reactor. Each order reflects years of lab work, production tweaks, analytical runs, and above all, conversations with the people who depend on this chemical as a foundation for bigger ambitions.
As manufacturers, our incentive isn’t just to ship another drum; it’s to keep earning the trust of chemists, engineers, and entrepreneurs who anchor their own projects on the reliable performance of our product. Every lot comes with that commitment built in.