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1-Chloro-5-Iodopentane

    • Product Name 1-Chloro-5-Iodopentane
    • Alias 5-Chloro-1-iodopentane
    • Einecs 211-952-8
    • 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

    195667

    Chemical Name 1-Chloro-5-Iodopentane
    Molecular Formula C5H10ClI
    Molecular Weight 232.49 g/mol
    Cas Number 20748-57-8
    Appearance Colorless to pale yellow liquid
    Boiling Point 246-248 °C
    Density 1.68 g/mL at 25 °C
    Refractive Index 1.537
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents

    As an accredited 1-Chloro-5-Iodopentane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25-gram amber glass bottle, tightly sealed, labeled "1-Chloro-5-Iodopentane," with hazard symbols and handling instructions.
    Shipping **Shipping Information for 1-Chloro-5-Iodopentane:** 1-Chloro-5-Iodopentane should be shipped in tightly sealed containers under cool, dry conditions, away from sources of ignition. It is classified as a hazardous material, requiring appropriate labeling and packaging per international regulations. Ground or air shipment must comply with DOT, IATA, and IMDG guidelines for dangerous goods.
    Storage 1-Chloro-5-iodopentane should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizing agents. Store away from moisture to prevent degradation. Proper chemical labeling and secondary containment are recommended to prevent spills and exposure. Use appropriate personal protective equipment when handling.
    Application of 1-Chloro-5-Iodopentane

    Applications of 1-Chloro-5-Iodopentane in Industrial Manufacturing

    As a specialized manufacturer, we supply 1-Chloro-5-Iodopentane to downstream enterprises utilizing its unique halogen-substituted alkane structure for high-value synthesis steps. Verified industrial consumption occurs in pharmaceutical intermediates, agrochemical intermediates, specialty polymer additives, and advanced material research. The following outlines industrial application scenarios with detailed integration data based on real-world commercial practice.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    Process chemists in pharmaceutical plants rely on this compound as a targeted alkylating agent or functional group precursor during multi-step manufacturing of central nervous system and antiviral active pharmaceutical ingredients. Its reactivity, arising from dual halogen substitution, supports selective nucleophilic substitution steps under inert conditions, enabling the construction of carbon chains or heterocycle attachments within the synthetic route.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • Applicable regional pharmacopoeias (USP, Ph. Eur., JP)
    • FDA DMF and CEP documentation as per product destination
    • REACH registration (for EU supply chain)

    Typical usage ratio

    • 0.02–0.15 molar equivalents per step in multi-stage routes; stoichiometry adjusted by desired alkylation level and process yield optimization

    Downstream process integration

    • Introduced during the early to late-stage intermediate coupling, directly reacting with nucleophilic substrates under monitored temperature control and in dry polar aprotic solvents

    Final product types

    • API intermediates such as alkylated amines and ethers
    • Chiral building blocks incorporated into psychiatric and antiviral pharmaceuticals
    • Protected alcohol/amine derivatives for GMP route scale-ups

    2. Agrochemical Intermediate Manufacturing (Herbicides and Fungicides)

    Crop protection formulators use this halogenated pentyl derivative as a precision intermediate for the stepwise assembly of selective herbicide and fungicide molecules. It offers chain extension capabilities and halogen exchange flexibility, enabling synthesis of active molecules that require exact spatial arrangement of substituents for field performance.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems for agrochemical ingredients
    • OECD Good Laboratory Practice (GLP) for intermediate stage validation
    • FAO/WHO specifications for formulation constituents

    Typical usage ratio

    • 3–8% by weight of reaction mixture in coupling and halogen exchange steps, optimized by desired intermediate concentration and downstream conversion efficiency

    Downstream process integration

    • Participates in nucleophilic substitution or elimination reactions with aromatic or heterocyclic cores under controlled base-mediated or phase-transfer catalytic conditions

    Final product types

    • Hexyl-substituted triazoles
    • Alkylpyridine herbicide bases
    • Key intermediates for triazinone fungicides

    3. Specialty Polymer Modifier Introduction

    Polymer formulators require halogenated alkanes such as 1-Chloro-5-Iodopentane for introducing precisely placed functional handles along polymer backbones, impacting final resin properties like surface energy, chemical resistance, and adhesion. This molecule acts as a co-monomer, especially in custom synthesis of block copolymers, under free-radical or anionic polymerization regimes, and as a chain stopper or crosslinking site pre-cursor.

    Industry compliance standards

    • ISO 9001:2015 (polymer production)
    • RoHS and REACH compliance for downstream plastics
    • ASTM D256, D638 for plastic mechanical property validation

    Typical usage ratio

    • 0.5–2% by weight of total monomer feed; ratio determined by targeted modification density, desired final molecular weight, and processing compatibility

    Downstream process integration

    • Direct addition to monomer mix before initiation phase, or post-polymerization grafting within solvent or melt-phase systems at precisely regulated temperatures

    Final product types

    • Halogen-functionalized block copolymers
    • Specialty adhesives with enhanced substrate bonding
    • Antistatic or hydrophobic films and coatings

    4. Advanced Material and Structural Modification in Organic Electronic Component Fabrication

    Research-driven fabricators incorporate this halogenated pentane as a precursor for the late-stage introduction of iodo or chloro side chains in organic semiconductors and photoactive materials. The compound’s halide functional groups enable further cross-coupling or substitution enabling tunable bandgap and improved charge carrier mobility in thin-film electronics or OLED segments.

    Industry compliance standards

    • ISO 14644 (cleanroom processing)
    • IEC 60068-2 for material and device reliability testing
    • REACH Annex XVII for hazardous substance control

    Typical usage ratio

    • 0.01–0.10 molar ratio to core organic substrate, dosage optimized for intended electronic/optical property shift and scalability

    Downstream process integration

    • Appended during final synthesis step for material functionalization through palladium-catalyzed coupling or direct substitution chemistry prior to device patterning and deposition

    Final product types

    • High-mobility organic semiconductors for thin-film transistors
    • OLED active layer molecules with engineered side chains
    • Photoresponsive polymers for solar energy research
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    Certification & Compliance
    More Introduction

    1-Chloro-5-Iodopentane: Directly from the Manufacturing Floor

    Working with 1-Chloro-5-Iodopentane in Modern Chemistry

    A lot of people ask what it’s like producing 1-Chloro-5-Iodopentane on the manufacturing floor, and why chemists keep coming back for this compound. We don’t just batch it for the sake of filling an order; the workers here see how often this alkyl halide sits at the crossroads of chemical innovation, particularly where selectivity and reactivity really matter. Every step we take on the line–from handling raw iodine to bottling the finished product–reflects a commitment to giving research and industry a building block that consistently performs where others don’t quite deliver.

    What Sets Our Synthesis Apart

    For us, production isn’t a process of just following a recipe. Each batch of 1-Chloro-5-Iodopentane, known by its CAS number 207317-81-3, means double-checking purity and monitoring for byproducts. We’ve seen over and over that even trace amounts of dihalopentane isomers or unreacted starting material can trip up downstream reactions. So we invest time and labor at the purification stage, not just for regulatory compliance, but because customers report cleaner conversions and higher yields in their work.

    Having the right specification matters more than many buyers realize. Iodinated chloropentanes show a range of volatilities and reactivity, and our regular feedback from returning customers always focuses on repeatability. For instance, when we talk to pharmaceutical teams, their process chemists expect a compound with minimal impurity drift between shipments; that consistency gives them confidence whether they’re scaling pilot runs or tweaking ligand syntheses.

    Understanding Physical and Chemical Merit

    Out of all the halopentane derivatives we’ve made in this plant, 1-Chloro-5-Iodopentane stands out because its chlorine and iodine functional groups sit at opposite ends of the pentyl chain. This structural uniqueness opens up options for selective substitution in multi-step syntheses. Iodine’s lability lets it participate in cross-coupling or metalation, while that chlorine atom can often hold its position for several steps, surviving until later functionalization.

    You can’t always count on that kind of controlled dual reactivity in similar molecules. We’ve tried altering positions–iodo or chloro in the middle of the chain, or swapping the halogens. Most of the time, people come back with solubility headaches, or find that their NMR spectra fill up with undesirable side products. The 1,5-derivative keeps showing us the sweet spot for chain length and halogen spacing in practical work.

    Applications Shaped by Real-World Demands

    We see our product head all over the globe. Each market values something a bit different. Pharmaceutical chemists often rely on 1-Chloro-5-Iodopentane to introduce functionalized side chains into small molecules, especially where stepwise deprotection, substitution, or cyclization calls for differentiation between reactive groups. Agrochemical clients tend to focus on its stability until a final transformation step, where forming a new carbon-nitrogen or carbon-sulfur bond makes the molecule’s activity pop.

    From our end, there’s a certain satisfaction in hearing about new heterocycle syntheses or advanced intermediates that start with our product as a cornerstone. We get lab reports and field data back from collaborators that reference lower contamination, higher selectivity, and faster work-ups compared to similar chain halides purchased from resellers or low-grade sources. The downstream value multiplies if you take extra time at the source–a lesson every operator on our line learns from day one.

    Differences Compared to Other Halogenated Pentanes

    Handling enough of these halopentanes side by side in production, we see differences not just in the paperwork, but in day-to-day operations and end performance. 1-Chloro-5-Iodopentane behaves differently under sunlight than straight diiodopentanes or dichloropentanes. We store ours under nitrogen to reduce risk of oxidation or radical formation, and find that batches kept strict to protocol rarely degrade or discolor–a telltale sign colleagues at other sites complain about with lower-spec material.

    In synthesis, iodine’s larger atomic radius and higher leaving group ability makes the 5-iodo group predictably reactive, while the chloro group on the terminal carbon holds steady through more reaction conditions. Colleagues tell us this dual handle gives them more control for designing semi-rigid ligands, attaching labels, or building up ring structures where substitution pattern matters. Compare this to, say, 1,5-dichloropentane, which brings two less reactive leaving groups to the table and often pushes process chemists to harsher reaction conditions or longer run times. And for 1,5-diiodopentane, you end up fighting issues with volatility, expense, and premature elimination.

    Quality Management Based on Lessons Learned

    Even the most established process can run into hiccups. We saw during an equipment upgrade that micro-dosing of water in the final reaction wasn’t drying out as completely as before, nudging up our acid content and threatening shelf-life stability. Walking the plant, pulling every valve and filter apart, checking each drum and sample, we isolated the culprit and dialed the system back to our usual sub-200 ppm water spec. Chemists who have been burned by wet, colored halopentanes know how finicky they can be with aluminum and iron traces from cheap glassware or unlined reactors. We learned early this can tank an entire synthetic route if ignored.

    Documentation goes beyond formal checklists for us. Line managers here have a standing rule–every operator has to sign off on visual clarity, no exceptions. That means no cloudiness, suspended solids, or brown tints. We train every new hire on how to spot the faintest sulfurous fog or unusual glints, since those markers signal something’s gone off, and those mistakes end up compounding for whoever’s next in the synthetic pipeline.

    Usage Patterns Across the Chemical Sector

    If you survey the literature, 1-Chloro-5-Iodopentane is more than a specialty product. It appears in transition-metal catalysis, nucleophilic substitution, and polymer precursor work. From our personal logs, research groups often call back reporting better coupling efficiency compared to analogues where the chain length is shorter or halogens are both on the same end. In the flavor and fragrance industry, those rare cases where a halogenated intermediate is required, the product’s relative stability and straightforward purification encourage new test projects.

    Over the past decade, interest in radioiodination has seen a surge, and labs now ship requests for this compound as a precursor because the terminal iodine can be exchanged for isotopic I-125 or I-131. We get walked through new techniques directly from R&D teams using imaging workflows, and our plant keeps pace in order to support repeatable, safe outcomes for their whole radio-labeling timelines. It’s not just about shipping a commodity; the compound’s use in PET tracer synthesis and advanced molecular imaging puts a high premium on true batch traceability, which we document all the way down to raw iodine sourcing and chronologically logged spectral data.

    Practical Handling Insights From Production Experience

    A specialty halide like this never feels routine on the floor. Straight out of synthesis, the crude product picks up the smell of hot halogen and hydrocarbons. Careful distillation strips away most of the extraneous notes, and takes the product toward a colorless or pale-straw liquid if done correctly. Every batch needs a calibrated detector for halide purity, especially since customer groups vary–a gram-scale research order has different baseline needs than a drum shipped to a contract manufacturer ramping up a new process.

    We handle every lot with attention to air exclusion and headspace minimization. Years of accidental contamination from air, trace ammonia, or light exposure can teach a harsh lesson. There’s still a hands-on element: operators manually check the tightness of drum seals, and a separate team logs weights and headspaces twice at dispatch. This old-school attention to detail pays back by keeping NMR purity readings high and minimizing the need for post-delivery clarification calls.

    Supporting Sustainability and Supply Chain Security

    The chemistry world has shifted its focus toward sustainability and reliable supply. We’ve felt the squeeze on iodine markets during geopolitical events, just like most manufacturers. We source as directly as we can, staying close to known-and-trusted mining sites and refining partners. A few years back, a spike in demand for medical imaging molecules led dozens of labs to scramble for alkyl iodides, and price hikes forced some to turn to cheaper mixed-halide blends that gave inconsistent results. We keep our procurement team tuned in to upcoming trends, and avoid speculative inventory so labs can plan projects without sudden price jumps or uncertain quality.

    We take solvent and energy recycling to heart, routinely reprocessing waste during the workup and distillation phases. Not just for compliance or cost savings, but because small changes on the floor–better filtration, improved caustic washing, tighter vacuum seals–add up in the operation over time. The result is a smaller solvent footprint per kilogram shipped, along with a process that produces less off-gas and waste halogenated streams. New synthetic technologies using milder bases or phase-transfer catalysis further support green chemistry commitments in the industry.

    Anticipating New Applications and Future Challenges

    There’s no sign yet that demand will slow. With the continual expansion of combinatorial libraries and the push for more innovative drug scaffolds, chemists are always clamoring for unique, versatile building blocks with selective functional handles. We field phone calls and emails asking about longer and shorter chain variants, enantiomeric enrichment, and customized purity levels. Sometimes this means tuning our process for trace metal control, other times we rework purification for stricter halogen ratios.

    Our group tackles each new request as an opportunity to build trust. Over time, our QA logs and side-by-side spectroscopic comparisons have guided new clients through problematic syntheses they couldn’t finish with off-the-shelf suppliers. It’s rewarding to see pilot projects using our 1-Chloro-5-Iodopentane template evolve into full-scale active ingredient manufacturing. We keep up with academic collaborations, pilot plant tests, and continuous flow methods, since new process technology often reshapes what’s demanded at the kilogram scale.

    Comparing User Experiences: What Real Feedback Shows

    Clients rarely mince words. On one occasion, a regular customer switching from another supplier called to report that their previous batches dissolved sluggishly in acetonitrile, introducing foaming at the extraction step. After trialing our product, they cited a complete change in consistency: clean phase separation, no sticking residue, and a quick reaction start. We hear about other cases where polymer chemists avoid high-iodine analogues because of off-gassing during curing, but do well with our spec, which shows lower loss at elevated temperatures.

    Sometimes, the biggest advantage comes from the little things. Shipments sealed against moisture, detailed GC and NMR paperwork, on-call support from an actual chemist–these factors save hours and dollars compared to the frustration of repeated troubleshooting. We’ve heard about abandoned trials using off-spec material sourced from indeterminate lots, leading to waste and project delays. By being upfront about specifications and achievable purities, we help customers avoid headaches before a single milliliter gets delivered.

    Summary of the Value Manufacturing Adds

    At its best, our work is about more than volume or throughput. It’s about showing that careful attention during every run leads to a product that gives researchers a clear edge. Whether it’s the strategic functional group spacing, the chain length, or the minimization of impurities and batch variability, 1-Chloro-5-Iodopentane provides a robust answer to tough synthetic problems. Having stood over the reaction vessel, checking TLC plates and smelling the change in fractions as a column runs, we’ve internalized what matters for customers who put our work to the test in the lab.

    Each bottle or drum that leaves our doors stands as an invitation: bring your toughest synthetic problems, and you’ll find support forged from years of practical experience, not just theory. We look forward to seeing what our partners will build next from this versatile intermediate, ready for the next challenge, whatever direction today’s chemistry takes.