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2-Octyl Iodide

    • Product Name 2-Octyl Iodide
    • Alias 1-Iodooctane
    • Einecs 242-893-6
    • 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
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    Specifications

    HS Code

    210484

    chemical_name 2-Octyl Iodide
    molecular_formula C8H17I
    molar_mass 240.13 g/mol
    cas_number 1520-67-6
    appearance Colorless to pale yellow liquid
    boiling_point 207-209 °C
    density 1.384 g/mL at 25°C
    refractive_index 1.5130-1.5170
    purity Typically ≥98%
    flash_point 85 °C (closed cup)
    smiles CCCCCC(C)CI
    storage_temperature Store at 2-8°C
    synonyms 1-Iodo-2-octane

    As an accredited 2-Octyl Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Octyl Iodide is supplied in a 25g amber glass bottle with a secure screw cap, labeled with product details and hazard warnings.
    Shipping 2-Octyl Iodide must be shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous material, following all relevant regulations for flammable and potentially harmful organic chemicals. Use appropriate labels and documentation. Transport under temperature-controlled conditions if recommended by the supplier or SDS.
    Storage 2-Octyl Iodide should be stored in a cool, dry, well-ventilated area away from sources of heat, ignition, and direct sunlight. Keep the container tightly closed and protect it from moisture. Store separately from oxidizing agents and strong bases. Use chemical-resistant containers and clearly label them. Ensure secondary containment to prevent leaks or spills and follow local regulations for storage of hazardous chemicals.
    Application of 2-Octyl Iodide

    Applications of 2-Octyl Iodide in Industrial Manufacturing

    2-Octyl Iodide serves as a specialized intermediate and reactant in several high-value industrial segments. Its performance, reactivity, and selectivity support advanced synthesis and process optimization along regulated downstream sectors. Below we outline real-world application fields, practical compliance, industrial dosing, processing points, and final manufactured outcomes.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    API manufacturers select 2-Octyl Iodide as an alkylating agent for introducing octyl chains into complex molecules under tightly controlled synthesis steps. The material enables site-specific halogenation and side-chain extension, particularly within custom antiviral and anti-inflammatory drug precursor routes. Integration occurs in small-molecule synthesis lines, where trace-level impurities and by-product formation face strict oversight. The compound’s reliability in batch and continuous flow pharma facilities supports consistent lot release and regulatory submissions.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) guidelines for API production (ICH Q7, EU GMP Part II)
    • United States Pharmacopeia (USP General Chapters <823>, <1058>)
    • European Pharmacopeia monographs for intermediates
    • FDA 21 CFR Part 211: finished pharmaceuticals CGMP

    Typical usage ratio

    • Reaction charge: 5–15 mol% relative to the intended active core, adjusted for chain incorporation efficiency and process yield targets

    Downstream process integration

    • Added during late-stage intermediate transformation or halogen exchange steps within the multi-step synthetic sequence
    • Maintains color and impurity profile control via in situ monitoring

    Final product types

    • Active ingredients for antivirals
    • Non-steroidal anti-inflammatory APIs with extended side chains
    • Precursor blocks for next-generation oncology agents

    2. Agrochemical Intermediate Manufacturing

    The agrochemical sector demands targeted iodinated intermediates for the synthesis of specific herbicides and fungicides. 2-Octyl Iodide provides a reactive octyl group source for constructing ether and ester functionalities via nucleophilic substitution pathways. Formulators rely on the material’s high purity and batch consistency to meet stringent agrochemical registration and toxicological scrutiny, ensuring regulatory acceptance and downstream reproducibility.

    Industry compliance standards

    • FAO/WHO specification for pesticide technical materials
    • OECD Good Laboratory Practice (GLP) for intermediate testing
    • EU REACH Annex VII–IX for intermediate substances
    • ISO 9001:2015 for quality management in fine chemicals

    Typical usage ratio

    • Intermediate synthesis: 10–25 mol% depending on the target molecule and scale-up process design, often tuned via pre-reaction titration assays

    Downstream process integration

    • Feeds charge tanks in batch reactors for substitution or cross-coupling
    • Critical control in quaternization and alkylation phases for final active construct

    Final product types

    • Alkyl ether fungicide scaffolds
    • Iodoalkane-modified herbicides
    • Precursor molecules for seed coating agents

    3. Specialty Material Synthesis (Liquid Crystals and Advanced Polymers)

    Makers of specialty polymers and liquid crystal display (LCD) components utilize 2-Octyl Iodide for introducing long, branched alkyl chains via controlled substitution. The material’s reactivity profile facilitates the synthesis of cleared nematic and smectic phases in display monomers, as well as impact modification in advanced polymer backbones. Practitioners maintain tight batch acceptance and MSDS compliance, reflecting the advanced electronic and display sector’s performance and safety demands.

    Industry compliance standards

    • IEC 62474: Material declaration for electronics manufacturing
    • RoHS 2 (EU Directive 2011/65/EU) for material restriction
    • ISO 14001 for environmental management during specialty polymer synthesis
    • REACH substance registration requirements (EC 1907/2006)

    Typical usage ratio

    • Polymer feedstock: 2–7 wt% by mass in monomer charge, ratio adjusted based on chain length influence and device specification

    Downstream process integration

    • Dosed into monomer polymerization kettles during chain initiation or halogen exchange steps
    • Process monitored by inline spectrometric hydrodynamic analysis

    Final product types

    • Nematic and smectic phase liquid crystal monomers for LCDs
    • Alkyl-modified rigid or flexible specialty polymers
    • Advanced dielectric films for electronics

    4. Fine Chemical and Fragrance Intermediate Synthesis

    Manufacturers serving fine chemical and specialty fragrance sectors employ this raw material for introducing bulky octyl side chains via halide displacement reactions. The compound enables pronounced alteration of volatility, partition, and olfactory structure in designer molecules. Manufacturing lines ensure traceability, in-process QC, and maintain IFRA safety standards, given the low-impurity expectation for downstream blending into consumer compositions.

    Industry compliance standards

    • IFRA Code of Practice for safe fragrance compound production
    • ISO 22716 for cosmetic GMP in associated supply chains
    • EU Cosmetics Regulation (EC) No 1223/2009 for ingredient sourcing
    • Purity control under IFRA and RIFM analytical guidelines

    Typical usage ratio

    • Fine chemical synthesis: typically 1–8 mol% of total reactant pool, set based on volatility targets and fragrance profile development tests

    Downstream process integration

    • Introduced during Grignard or nucleophilic substitution steps in small-batch reactors
    • Monitored by GC-MS to ensure aromatic and alkyl content control

    Final product types

    • Bulky ether and ester fragrance intermediates
    • Synthetic musk and woody odorant compounds
    • Flavor precursor molecules for regulated blends
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    Certification & Compliance
    More Introduction

    2-Octyl Iodide: Building Better Organic Synthesis Through Practical Chemistry

    Introduction to Our Direct Approach

    Being in the thick of chemical manufacturing has meant a daily conversation with both the product and the problems chemists face in the lab and on the floor. Among our workhorse alkyl halides, 2-Octyl Iodide stands out by its consistency and the reliability it brings to synthesis. This particular iodide, backed by technical grade preparation, features in projects across pharmaceutical research, agricultural intermediates, and advanced surface coatings. We focus on producing this compound at the right concentration and purity, supporting those who work in real labs with hands-on formulation and analytical experience.

    Spotlighting Its Role in Synthesis

    Few reagents fill their niche as cleanly as 2-Octyl Iodide. We see it in Grignard reactions, as its iodo group gives it a strong leaving ability compared with similar chlorides or bromides. It pushes the coupling reactions forward with less byproduct and shows particularly high conversion rates. Chemists working with 2-Octyl Iodide can count on it when designing carbon frameworks or preparing sidechains for specialty molecules. The longer alkyl chain compared with butyl or hexyl iodides allows for a balance between steric bulk and reactivity, with an eye toward both selectivity and ease of purification. In our production, we monitor not just for the main product but for trace impurities—so the user isn’t caught off guard by residual iodine or lower chain analogs.

    Differences Compared to Other Alkyl Iodides and Halides

    Those driving large batch syntheses know the headache that comes from using lower homologues. For example, methyl or ethyl iodides can bring excessive volatility and present inhalation risks during handling. Heavier homologues like dodecyl iodide tend to have limited solubility and can complicate workup. 2-Octyl Iodide sits in the pocket: liquid at room temperature, easily manipulated, and less prone to gassing off or sticking around in the waste stream. Our teams have run side-by-side trials, and the performance gap widens when you move from bench scale to plant scale—losses to evaporation, clean-up time, and downstream purity all see clear improvements.

    Product Quality Backed by Experience

    Having operated our own reactors for years, we count on reproducible methods. Our 2-Octyl Iodide consistently tests at or above typical purity benchmarks for organic synthesis. During workup, we target minimizes residual moisture and keep halide content tightly within specification. When customers have reported unusual chromatographic profiles, we’ve traced it directly to trace halogen content or unexpected oxidation products in competitor samples. Our process avoids over-iodination and leverages fractional distillation under controlled atmospheres. No matter the size of your batch, you see that attention in NMR and GC analyses, not just a spec sheet.

    Real-World Use Cases in Laboratories and Production Lines

    Organic chemists appreciate how 2-Octyl Iodide helps shape novel molecules. In our collaborations, we’ve observed how it serves as an effective alkylating agent in constructing carbon skeletons, particularly in synthesizing pharmaceutical precursors and specialty monomers. On occasion, process engineers have shared feedback about scale-up challenges with lower-alkyl iodides, noting that the 2-octyl variant offers fewer losses during transfer and reacts efficiently under standard lab conditions. From gram to kilogram quantities, users find they waste less time fighting volatilization or byproduct formation.

    In agricultural R&D, researchers use 2-Octyl Iodide as a stepping stone toward specific crop protection agents. Its longer chain confers increased hydrophobicity, important in fine-tuning the delivery and environmental persistence of actives. Suppliers to the electronics sector have shared success stories where they’ve incorporated this reagent in specialty coatings, taking advantage of its unique balance between chain length and halide reactivity.

    Safe Handling and Environmental Controls

    Years of shipping, storing, and splitting up alkyl iodides have taught us a few hard lessons. 2-Octyl Iodide brings less volatility into the warehouse; experienced handlers quickly notice the difference as soon as they crack open a drum. Less vapor means fewer fugitive emissions and a steadier work environment. Spills and clean-up are less challenging than with more volatile analogues. Our facility stays meticulous about waste collection and air scrubbing, both to comply and because our own staff work at the loading dock and production line. Users down the chain benefit from a product less likely to flash off or react with open air.

    For teams working in confined spaces or at scale, this difference has practical impact. Lower rates of occupational exposure mean fewer headaches and safer routine operations. In our experience, neither gloves nor fume hoods alone offer enough certainty with methyl or ethyl iodide; 2-Octyl Iodide’s heavier nature allows for safer handling routines. We’ve altered our own internal procedures based on lessons learned—what worked on the bench doesn’t always cut it in a staging area with forklifts moving thousands of liters. We give honest feedback to customers about both the chemistry and the day-to-day realities of using and storing this reagent.

    Product Consistency and Delivery

    The repeatability of a chemical batch becomes more than a footnote to those who’ve been burned by out-of-spec barrels mid-campaign. With 2-Octyl Iodide, we source raw octanol chain precursors in bulk and follow an in-house halogenation protocol. Our teams standardize for reaction conditions, atmosphere, and purification, keeping moisture and oxidants away. Multiple in-line checks spot color, density and halide content before shipping. Customers often take samples for their own analytics, and we encourage this scrutiny. Feedback returns to our lab staff, not just management, so minor departures from ideal never become routine slip-ups.

    From time to time, logistical bottlenecks have threatened to slow deliveries. We have learned to keep buffer stocks of finished and pre-purified intermediates, so orders stay on track through supply hiccups. Instead of chasing a short-term sale, we focus on steady output and treating repeat customers less like numbers and more like partners. Clear communication about product lead times, purity, and if necessary, real-world handling tips, sets up better outcomes for everyone involved.

    Industry Trends: Regulatory Landscape and Future Demand

    The regulatory climate around organoiodide manufacturing continues shifting. We see this up close, not as a rumor mill but as new registration requirements and purification documentation. Some regions push for tighter limits on residual iodine, while others measure batch traceability all the way back to source alcohols. Having invested in in-house analytics, we can actually meet audits and spot checks without scrambling. This also avoids putting our customers at risk of compliance violations or recalls.

    Market demand for 2-Octyl Iodide connects tightly to expanding needs in pharmaceutical and materials chemistry. Drug developers want longer sidechains for improved pharmacokinetics, and advanced polymer designers aim to customize new backbone structures. Nearly every inquiry asks for assurance that the supplied product can be tracked and traced; working with shorter supply chains, we are able to answer directly. Experience tells us that transparent sourcing and detailed production records matter more than just quoting specs off a sheet.

    Meeting Innovation with Practical Processes

    As chemistry innovation speeds up, the smallest details in a synthesis route mean the difference between a scalable process and a costly dead-end. Many academic and industrial labs ask for bulk samples or custom purities. We adjust our end product to their method, not just “sell what we make.” Recently, a polymer manufacturer needed low-moisture, high-purity 2-Octyl Iodide for living radical polymerization. They provided explicit NMR and IR signatures to hit. Our technical crew dialed back moisture using repeat distillation and nitrogen blanketing, delivering a batch that slotted straight into their workflow. Neither the customer nor our production line had to accept compromise.

    We invest in feedback and collaborative troubleshooting, not just as an add-on, but because every tweak—whether in reaction temperature or isolation technique—matters down the supply chain. Researchers don’t have time or budgets for off-spec reagents. They rely on a supplier who knows their needs and can dig into failures, not just dodge the issue.

    Supporting Custom Synthesis and Scale-Up R&D

    Custom synthesis groups need the flexibility to request volumes or tweaking of impurity profiles. Our experience with 2-Octyl Iodide makes it clear where trade-offs land. Shorter-chained iodides often bring more volatility and require extra distillation. Our product, with its medium-length chain, simplifies logistics and reduces evaporative losses. Teams implementing continuous flow reactions often lean into this balance—one client reported halving their need for in-line scrubbers by switching over. Batch record transparency and supporting documentation make audits and research reviews much less painful for them.

    For startup biotechs, rapid iteration with reliable intermediates often decides the pace of development. We’ve participated in project launches where the timeline from PO to first gram must be counted in days, not weeks. Carrying inventory of 2-Octyl Iodide, especially in custom packaging or slight grade adjustments, comes from real relationships—not just inventory control.

    Environmental Responsibility and Resource Management

    Modern manufacturing isn’t all about output. Environmental scrutiny increases each year. We apply real waste management practices from our own experiences handling alkyl iodides. Every kilogram of 2-Octyl Iodide that leaves our facility passes through closed-loop solvent recovery and halide-neutralizing reactors. This eliminates persistent organic residue and returns solvents to the loop, lowering both disposal costs and environmental risk.

    Incidents in the sector, such as legacy spills or failing air controls, remind us that best practices aren’t optional. We keep environmental responsibility embedded in every step—not as a marketing afterthought but from basic operational necessity. Compliance isn’t just satisfying auditors; it protects our team and our customers from liabilities down the line. If a new regulation or ecological necessity calls for process adjustment, our development chemists update protocols and audit new approaches before they affect external supply.

    Troubleshooting Real-World Synthesis Hurdles

    Customers hit snags from time to time—incomplete conversion, side-reactions, or product instability. In these moments, direct conversation with a manufacturer makes all the difference. Having faced similar challenges ourselves, we walk through reaction conditions and suggest tweaks. A pharma team struggling with yield drop in carbon coupling once supplied us their exact protocol. Reviewing their solvent ratios and order of addition, we suggested adjusting both to minimize side iodination. Direct feedback shaved days off their optimization and saved thousands in starting material costs.

    These exchanges build trust across projects and seasons. We engage, not from theory, but as operators who face the same equipment, impurities, and downtime. When a customer can call someone who’s run the reaction and managed the byproducts, they skip past generic advice.

    2-Octyl Iodide in Process Optimization

    No process remains static in chemical manufacturing. On the ground, shifting production scales, new reactor configurations, or tweaks in downstream purification call for revisiting the properties of every intermediate. With 2-Octyl Iodide, process engineers report increased reliability during phase separations and extractions. Its reduced volatility contributes to fewer headaches tracking mass balances. In multi-step syntheses, selectivity rises—there’s less unreacted halide left to drag down product quality. We build in extra analytics at key points to document each batch, which matters when investigations or audits look back at the record. This diligence sets apart batches that merely “pass” from those that avoid future troubleshooting headaches.

    Long-Term Relationships Drive Quality

    Over years, we’ve noticed retention relies less on flashy claims and more on keeping promises about repeat delivery and quality. Word spreads among professional chemists about the reliability and practical benefits of one source over another. Consistent batches, honest answers, and a readiness to go beyond the spec sheet win more trust than temporary discounts.

    Final Thoughts: Chemistry Grounded in Everyday Reality

    A manufacturer’s view of 2-Octyl Iodide matches neither the abstract catalog description nor a mere sales pitch. Chemists on our own shop floor see the impact of process choices—for reaction scale-up, for daily operations, and for the safety and health of both users and the surrounding community. We recognize the difference between a product made to pass QC and one that enables confident progress down the next synthetic pathway. Our team stands behind each drum and flask, focused on the next advancement, responding with both experience and care.