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1-Iodohexane

    • Product Name 1-Iodohexane
    • Alias 1-iodohexane
    • Einecs 211-105-1
    • 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

    403032

    Cas Number 628-17-1
    Molecular Formula C6H13I
    Molar Mass 212.07 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 187 °C
    Melting Point -54 °C
    Density 1.455 g/cm³
    Refractive Index 1.486
    Flash Point 63 °C
    Solubility In Water Insoluble
    Purity Typically ≥ 98%
    Vapor Pressure 0.3 mmHg (25 °C)

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

    Packing & Storage
    Packing 1-Iodohexane is supplied in a 100 mL amber glass bottle with a secure, airtight cap and a safety warning label.
    Shipping 1-Iodohexane is classified as a hazardous chemical for transport. It is shipped in tightly sealed containers, protected from light and moisture, and packaged according to regulations for flammable liquids and toxic substances. Proper labeling and documentation are required, and it should be handled by trained personnel using appropriate safety measures.
    Storage 1-Iodohexane should be stored in a tightly closed, clearly labeled container, away from sunlight, moisture, and incompatible substances such as strong oxidizers and bases. Store it in a cool, dry, and well-ventilated area designated for hazardous chemicals. Ensure that appropriate spill containment is available, and that access is limited to trained personnel using suitable personal protective equipment.
    Application of 1-Iodohexane

    Applications of 1-Iodohexane in Industrial Manufacturing

    1-Iodohexane plays a crucial role as an alkylating intermediate across multiple chemical production sectors. Our in-house manufacturing processes ensure controlled iodine incorporation and strict batch consistency, supporting demanding downstream requirements. Below are specific industrial applications and technical integration details from actual client industries.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical producers rely on 1-iodohexane in the preparation of cationic surfactants, local anesthetics, and building blocks for API side chains. Reacting it with nucleophilic agents enables the formation of alkylated derivatives during multi-step synthesis. Our product supports both small- and large-scale cGMP production lines where high-purity alkyl iodides ensure process reliability. QC is tailored for minimal halogen impurities to meet kinase inhibitor and central nervous system drug precursor synthesis needs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • 21 CFR Part 211 United States cGMP
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • USP <795> and <797> for compounding and process cleanliness

    Typical usage ratio

    • 0.9–1.1 molar equivalents per reaction step, adjusted for purity and batch size
    • Stoichiometry varies by target side chain length and nucleophile excess

    Downstream process integration

    • Fed into alkylation reactors after base deprotonation steps
    • Used during SN2 displacement reactions in multi-step API synthesis
    • Post-reaction QC monitoring for residual iodide content and byproducts
    • Purification via vacuum distillation or recrystallization before downstream coupling

    Final product types

    • Cationic surfactant intermediates
    • Pharmaceutical active compound side chains
    • Local anesthetic building blocks (e.g., hexyl derivatives)
    • Antibacterial quaternary ammonium compound intermediates

    2. Agrochemical Active Ingredient Preparation

    Leading crop protection manufacturers employ 1-iodohexane to synthesize specific herbicide and insecticide precursors. The straight-chain C6-iodide group allows controlled alkylation when forming imidazole, triazole, and carbamate molecules. Consistent reactivity and assay levels prevent unwanted side products in scale-up, enhancing isolation yields and downstream formulation reliability. This intermediate remains critical for alkyl imidazole and heterocyclic pesticide synthesis plants.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • REACH Registration for Environmental Safety
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 4–12% w/w in active ingredient precursor batches
    • Adjustment depends on alkylation step yield and reactant excess margin

    Downstream process integration

    • Dosed as an alkylating agent in heterocycle ring closure reactors
    • Fed into jacketed vessels for exothermic displacement reactions
    • Inline analytical monitoring for residual unreacted iodide
    • Isolated with base hydrolysis or extraction for formulation plants

    Final product types

    • Imidazole-based fungicide intermediates
    • Triazole herbicide alkylating agents
    • Carbamate pesticide precursors
    • Hexyl-substituted crop protection actives

    3. Specialty Surfactant Manufacturing

    Our direct industrial customers utilize 1-iodohexane in synthesizing custom surfactants for EOR (Enhanced Oil Recovery), textile processing, and personal care additives. It delivers a tailored hexyl chain via alkylation, increasing hydrophobicity and tuning emulsion stability. Integration into amine, phosphine, or ether group reactions occurs under precisely controlled batch titration, providing reactors with rapid and selective C6 group attachment. Every lot is checked for halide residue and side-chain uniformity, supporting rigorous QA for advanced surfactant applications.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in chemical production
    • OECD Guideline 301B for biodegradability of surfactants
    • REACH (EC No 1907/2006) registration for environmental safety
    • U.S. EPA 40 CFR 721 Subpart E — Significant New Use Rules for surfactants

    Typical usage ratio

    • 5–15 mole% based on total amine or alcohol feedstock
    • Ratio set according to hydrophobic-lipophilic balance (HLB) targets

    Downstream process integration

    • Added during primary alkylation phases under nitrogen atmosphere
    • Combined with base and alcohols in stepwise temperature ramping
    • Excess iodide neutralized prior to final surfactant cleanup
    • QC on cloud point and foaming properties following chain introduction

    Final product types

    • Hexyl-substituted ammonium surfactants
    • Nonionic surfactants for textile scouring
    • Alkyl ether sulfates for personal care blends
    • Cationic surfactants for EOR foam stability

    4. Organic Electronic Material Fabrication

    Producers of conductive polymers and advanced electronic coatings adopt 1-iodohexane in the functionalization of thiophene, benzene, and pyrrole monomers. Its straight-chain C6 tail modifies solubility and electronic properties, improving film uniformity and device performance. Reactors employ controlled stoichiometry to achieve desired side-chain grafting, targeting precise film flexibility and conductivity in OLEDs or flexible display applications. Our supply ensures high-purity and trace-halide analysis, meeting custom monomer specifications for electronics-grade synthesis.

    Industry compliance standards

    • IEC 62321-7-2:2017 (IEC RoHS halogen testing for electronics)
    • ISO 14644-1 Cleanroom Standards (for coatings and device assembly)
    • REACH Annex XVII compliance for restricted substances
    • IPC-4101 for base material quality in electronics laminates

    Typical usage ratio

    • 0.8–1.2 equivalents per functional group on the target monomer
    • Fine-tuned to maintain electronic behavior and process compatibility

    Downstream process integration

    • Dosed in monomer alkylation with metal-catalyzed coupling
    • Employed at low temperature to limit side reactions and oligomerization
    • Post-reaction removal of iodide ions via vacuum stripping
    • Integrated with in-line FTIR and GPC analysis for polymer chain verification

    Final product types

    • Hexyl-functionalized polythiophenes
    • Flexible electrode coatings for OLED displays
    • Organic photovoltaics with tailored solubility profiles
    • Conductive polymer blends for printed electronics

    5. Flavors and Fragrances Synthesis

    Within specialty fragrance and food ingredient sectors, manufacturers introduce 1-iodohexane as an intermediate in synthesizing musky and green hexyl aroma compounds. The C6 iodide structure provides a reactive site for esterification and etherification, enhancing olfactory notes in high-purity flavor/fragrance molecules. Process engineers optimize dosing at tightly controlled temperatures to prevent off-odors or color issues during final distillation, and all lots adhere to flavor house trace-iodine specifications for supplier acceptance.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • ISO 9235:2013 (Essential oils definition, production, labeling for natural aroma ingredients)
    • US FDA 21 CFR 172.515 (Flavoring substances permitted for direct addition to food)
    • EU Regulation (EC) No 1334/2008 on flavorings and food ingredients

    Typical usage ratio

    • 1–5% molar input relative to aldehyde or alcohol substrate
    • Varies according to batch scale and final aroma intensity adjustment

    Downstream process integration

    • Fed during targeted hexylation reactions in closed reactors with condensation control
    • Integrated pre-esterification or etherification for aroma tailoring
    • Refined post-reaction by column chromatography to limit residual iodide traces
    • Analytical testing for purity, unsaturation, and flavor house standards

    Final product types

    • Hexyl esters in luxury fine fragrances
    • Green floral ether derivatives for personal care scents
    • Musky hexyl alcohols for food flavoring blends
    • Naturally-derived aroma chemicals for beverage bases
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    Competitive 1-Iodohexane prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-Iodohexane – Practical Insights From The Manufacturer

    An Introduction Built on Daily Practice

    In our line of work, 1-iodohexane stands out as a valued compound for several clear reasons. Over the years, teams in our synthesis halls have handled plenty of halogenated organics, but 1-iodohexane, also called hexyl iodide, has a real knack for simplifying reaction pathways. Its straightforward structure—a six-carbon alkyl chain with an iodine atom at the terminal carbon—gives it the versatility researchers chase in organic transformations. Each batch that comes out of our reactors traces its lineage back through carefully monitored steps: controlled iodination, tight purification, and unbroken cold chain logistics. These things mean our product isn’t just a reagent on a shelf; it’s a tool people reach for when reliability matters.

    Specifications: From Raw Materials to Finished Product

    Consistent performance starts with quality inputs. Our 1-iodohexane, with the standard molecular formula C6H13I and molecular weight of 212.08 g/mol, is produced using pharmaceutical-grade n-hexanol or n-hexyl bromide. The colorless to pale yellow liquid we package always shows iodine as the sole halogen, confirmed by direct analytical tests. In our facility, routine gas chromatography checks monitor purity, regularly confirming it at or above 98.5%. Water content runs low—Moisture doesn’t play well with alkyl iodides, so Karl Fischer method checks always happen before packaging.

    We keep user safety squarely in view. Engineers run weekly checks for peroxide formation, given the sensitivity of alkyl iodides to light and oxygen. All storage containers are made of high density polyethylene or borosilicate glass and clear labeling boasts hazard and purity details in plain print. We produce 1-iodohexane at research and pilot scale, tailoring batch sizes to suit academic users and specialty manufacturers. Before leaving our facility, each drum or bottle gets a Certificate of Analysis, matched batch number on every label, and a secure tamper-evident seal. There’s never any compromise on those basics.

    Field Applications: It’s Not Just a Lab Reagent

    People often think of 1-iodohexane as just a staple for basic research, but its reach stretches further. Chemical synthesis routes benefit most. This alkyl iodide often appears in nucleophilic substitution and metal-catalyzed coupling reactions. Those in pharmaceutical labs know the speed and clean yields possible when using iodine as a leaving group. Compared with the bromides and chlorides, 1-iodohexane brings a lower activation energy, letting reactions run milder and cleaner—which matters for sensitive building blocks and precious intermediates.

    We see requests for specialties like labeled compounds for radiochemistry. Our process engineers accommodate custom isotopic specification, always with direct collaboration between us and users to match radio-purity levels and regulatory needs. At larger scales, our industrial customers value hexyl iodide in surfactant precursor synthesis and as a core raw material for specialty lubricants. Specific crop-protection agents, fragrance chain-building, and specialty polymer fields all make use of this alkyl iodide’s clean reaction record. There’s a practical angle to every batch we ship.

    Standing Apart From Other Alkyl Halides

    Our customers sometimes question the point of choosing 1-iodohexane over easier-to-find hexyl bromide or hexyl chloride. What changes in their chemistry with just a halogen swap? Direct experience in scale-up synthesis shows the clear edge. Iodine carries a larger atomic radius and forms weaker carbon-halogen bonds, making the molecule far more reactive—even at room temperature. Researchers switching from bromide to iodide tell us about shorter reaction times, fewer side products, and much cleaner separations.

    In the world of organic synthesis, 1-iodohexane shines in scenarios where steric bulk, lower reactivity, or problematic elimination reactions from bromides or chlorides stall progress. We’ve heard from teams working on combinatorial libraries and difficult Suzuki couplings, who chose our iodide to break through bottlenecks. It isn’t just a matter of cost or availability; it’s a calculated choice when time, precision, and higher yields matter.

    Production Knowledge: What Sets a Manufacturer Apart

    Turning out high-purity 1-iodohexane is rarely a fully automated process, no matter how efficient the plant. From raw feedstock selection to by-product removal, there’s hands-on oversight at every junction. Our plant managers tweak reaction temperatures and monitor iodine source purity—iodine quality swings influence side reactions and degrade final quality fast. By years of calibrating reaction kinetics, our engineers cut down iodine overuse and minimize the formation of undesired secondary iodinated products.

    Typical synthesis uses n-hexanol or n-hexyl bromide, hit with a controlled dose of iodinating agent, in closed reactors swept with inert gas. Any trace oxygen or moisture inside spells headaches: side reactions, colored by-products, and polymerized residues. After the reaction, fractional vacuum distillation polishes off the last impurities. Our chemists monitor each run with periodic GC, and by the time 1-iodohexane hits the fill lines, it’s been checked for both organic by-products and residual elemental iodine. Only hands-on checks guarantee batches keep their light color and shelf stability.

    Stability and Handling – Practical Lessons Learned

    Field experience goes a long way in handling alkyl iodides. Even at the highest purities, 1-iodohexane can pick up color over time without cold, dark storage. Customers often ask about color shifts—slight yellowing indicates light exposure or trace peroxides, not always a sign of lowered performance, but always a trigger to test before running scale-up. We share handling advice up front: store tightly capped, keep dry, and refrigerate if possible. Exposure to air, light, and high temperature shortens shelf life and can drive unwanted side chemistry. In our plant, bottles move from fill lines to storage in insulated bins, with batch samples retested periodically.

    Bulk users sometimes request anti-oxidant stabilizers or special packaging formats. We accommodate vacuum-sealed ampoules, nitrogen flushing, and smaller bottles for sensitive work. Transport remains cold chain, and our logistics teams track every batch from dispatch to receipt, including temperature loggers when autumn turns warm or spring hits early. Through these steps, we make sure product reliability doesn’t depend on luck.

    Beyond the Reaction Flask: Value for Chemists and Industry

    Academic and industrial research groups return to 1-iodohexane for a reason. It unlocks transformations that stall with other halides. In our own in-house testing, we compare reaction yields using hexyl iodide, bromide, and chloride under identical conditions. The iodide consistently produces fewer side products in SN2 reactions, and runs cleaner in Grignard formations. For those using it to introduce six-carbon chains onto nucleophiles, the switch from bromide or chloride saves time on purification and lowers the need for repeated chromatographic cleanup.

    At larger scales, cost always comes up. Iodides, including 1-iodohexane, cost more to produce and handle, but process developers see long-term gains in yield and reliability. Teams working in fine chemicals and advanced materials often share feedback on consistency across lots. We make a habit of collecting this data—reaction reproducibility matters. Each time we tighten in-process controls, lower batch-to-batch variance, or cut trace contaminants, research partners gain more predictable outcomes.

    Supporting Responsible Chemistry

    Responsible manufacturing shapes every stage we operate. Halogenated organic synthesis generates waste streams, so our environmental teams run effluent monitoring around the clock. We recover and recycle process iodine and solvents wherever practical—cutting both costs and the total load on our waste streams. Our health and safety teams train every operator, from vessel loading through material transfer, because exposure to volatiles or iodine fumes spells risk for people and product alike. Even quality control focuses on more than analytical numbers; the physical fitness of each container gets checked routinely.

    Customers turning to us often need help scaling up or meeting regulatory compliance. We work side by side to document traceability, support hazard assessment, and prepare clean shipping documentation. International shipments follow the most stringent control schedules. Border crossings for controlled precursors never slow up our regular customers, because each batch ships with a document trail tying raw materials to certificates and analytical results.

    Crafting Solutions: Meeting the Challenges

    We don’t just ship standard bottles. The most productive projects start with a technical call—from custom volume requests to analytical tweaks, because not all synthetic routes tolerate the slightest impurity or variation. Our chemists collaborate directly with researchers, verifying that our process parameters line up with their reactivity windows. This hands-on problem solving keeps projects on track, especially for time-sensitive runs or those at risk for trace-by-product formation.

    Sustainability plays into our plans for every new order. Our plant invests in recovery columns, off-gas scrubbing, and single-use plastic reduction. Not just slogans; these are the lessons that matter to those who count on long-term supply relationships. On the shipping side, temperature loggers and sealed containers reduce spoilage. Every time a customer flags an issue, our teams trace it back, analyze the batch and process, and adjust protocols as needed—not just for the complaint at hand, but for all subsequent runs.

    Case Experiences: Listening to the End Users

    Feedback loops fuel our best improvements. In one case, a pharmaceutical lab reported subtle yellowing on two out of ten 500-ml bottles, despite tight controls. Investigation tracked a minor heat spike during loading—our process engineers fine-tuned coolant system setpoints. Afterward, outage rates dropped, batches stayed colorless for twice as long in storage, and returns became rare.

    Another user, running high-throughput SN2 alkylations, pushed us to supply multiple lots with sub-10 ppm water content. We revamped our vacuum drying step, invested in batch-specific Karl Fischer titration before shipment, and saw the switch ease customer workflow—no more pre-use drying or failed first runs. Over time these direct improvements sharpen not just our product, but the reliability of the finished goods built on it.

    Regulatory and Safety Focus

    Chemical handling runs safest with no secrets. We maintain MSDS and technical support ready for quick response. All material arrives with hazard labeling as required by international shipping codes and aligns with the latest requirements under GHS and related frameworks. Production staff at our plant work through annual safety refreshers, including lessons learned from real-world incidents. This investment safeguards people, product, facility, and end user alike.

    Shipments directly trace from incoming raw iodine to outgoing final product through barcoded batch records. Process deviations, even minor, trigger internal review. This constant self-audit process lets us spot patterns—like small losses of yield, trace water incursions, or seasonal shifts in color stability—before customers ever experience a supply blip.

    Innovation and Future Outlook

    Markets evolve, and so does our work on 1-iodohexane. Customers push the boundaries with radio-labeling, new surfactant chemistries, or trace impurity reductions for next-generation electronics. Every year, our R&D group tests improvements in reactor throughput, solvent recovery, and crystal filtration. We partner with users around the world to tune process scale, batch size, and quality metrics. By lining up internal projects with customer needs, we not only deliver batches that perform, but tougher documentation packages that help new product applications launch on schedule.

    We also track and invest in greener alternatives for solvents, process energy, and waste. New packing formats reduce per-bottle waste. Continuous process tweaks drop the environmental impact—and we welcome those conversations from users, since their inputs direct our improvement cycles.

    Why Direct Manufacturer Collaboration Matters

    Working straight with us cuts the fog surround of origin and handling details. Our customers know what to expect: each drum, bottle, or ampoule links directly to a production batch and a real process record. For those looking to trial a new reaction, scale up, or run regulatory submissions, that confidence carries through. If issues arise—be they physical, analytical, or regulatory—our technical and customer service teams pick up the phone, log the challenge, and track it through resolution. This partnership model stands apart from a pass-through distributor relationship, since we own and continuously improve every step, from raw material to finished good.

    Choosing 1-iodohexane straight from a maker means tighter purity, real accountability, and shared purpose in the success of projects. As chemistry grows ever more demanding, those points turn from luxuries to necessities.