2-Iodobutane

    • Product Name: 2-Iodobutane
    • Alias: sec-Butyl iodide
    • Einecs: 208-912-9
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    791282

    Chemical Name 2-Iodobutane
    Molecular Formula C4H9I
    Molar Mass 184.02 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.66 g/cm3
    Boiling Point 110-112 °C
    Melting Point -110 °C
    Refractive Index 1.495
    Cas Number 513-48-4
    Flash Point 18 °C
    Solubility In Water Insoluble
    Pubchem Cid 10451

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

    Packing & Storage
    Packing Amber glass bottle with a secure cap, labeled "2-Iodobutane, 100 mL," featuring hazard symbols and handling instructions.
    Shipping 2-Iodobutane is shipped in tightly sealed containers, typically amber glass bottles or specialized drums, to prevent light and moisture exposure. It must be labeled as a hazardous material, handled with appropriate safety precautions, and transported according to local and international regulations for flammable and toxic chemicals. Store in a cool, well-ventilated area.
    Storage 2-Iodobutane should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances, such as strong oxidizers. Keep the container tightly closed and clearly labeled. Store away from direct sunlight and moisture, and avoid prolonged exposure to air to prevent decomposition. Appropriate safety precautions and storage protocols should be followed as per regulatory guidelines.
    Application of 2-Iodobutane

    Purity 99%: 2-Iodobutane with purity 99% is used in organic synthesis laboratories, where it enables high-yield alkylation reactions.

    Reagent Grade: 2-Iodobutane of reagent grade is used in pharmaceutical intermediate production, where it ensures consistent product quality and reliability.

    Boiling Point 91°C: 2-Iodobutane with a boiling point of 91°C is used in halogen exchange reactions, where it offers efficient vapor-phase processing.

    CAS Number 513-48-4: 2-Iodobutane identified by CAS Number 513-48-4 is used in analytical chemistry standards, where it supports precise compound identification.

    Density 1.616 g/cm³: 2-Iodobutane with density 1.616 g/cm³ is used in separation processes, where it provides predictable phase behavior for solvent extraction.

    Light Sensitivity: 2-Iodobutane sensitive to light is used in controlled environment reactions, where it minimizes degradation and maximizes storage stability.

    Molecular Weight 184.0 g/mol: 2-Iodobutane with molecular weight 184.0 g/mol is used in NMR spectroscopy studies, where it delivers accurate spectral interpretation.

    Stability Temperature Below 25°C: 2-Iodobutane stable below 25°C is used in long-term reagent storage, where it guarantees preserved reactivity over time.

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    Certification & Compliance
    More Introduction

    2-Iodobutane: Practical Insights from a Chemical Manufacturer’s Perspective

    Introduction to 2-Iodobutane

    At our manufacturing facility, 2-iodobutane doesn’t just occupy a place on the product lineup—this alkyl halide serves as a cornerstone for various synthesis pathways and creative chemical work in both research and industrial settings. As a company involved in the actual production process, not simply moving goods between hands or relying on packaged claims, we see 2-iodobutane day in and day out, tested by the real needs of labs and factories. Our experience spans decades, growing with the rhythm of market demand and scientific necessity.

    2-Iodobutane, also known as sec-butyl iodide or 1-iodo-2-butane, carries the CAS number 513-48-4 and a molecular formula of C4H9I. The molecule features a four-carbon butane backbone, with the iodine atom attached to the second carbon. This unique arrangement shapes both the reactivity and the usability of the compound. In physical form, pure 2-iodobutane presents as a colorless to faintly yellow liquid under ambient conditions. During large-scale batches at our site, the product is produced and handled under strict environmental and occupational safety standards, with trace moisture, acid, and impurity levels monitored continuously to ensure reliable product performance.

    The Manufacturing Approach

    We synthesize 2-iodobutane in-house using well-controlled halogenation methods. Most often, this hinges on the reaction of 2-butanol with hydroiodic acid under optimized temperatures, enabling direct substitution on the desired carbon center. Every batch runs through exhaustive washing, drying, and distillation to strip away side-products and any unreacted starting material. Our process parameters have evolved under years of hands-on refinement.

    Personnel with a background in organic chemistry and plant operations handle the actual conversion steps, ensure batch consistency, and apply statistical process control to keep impurity profiles to a minimum. We utilize automated chromatographic techniques for batch certification, giving chemical buyers a consistent Iodine content often exceeding 99%. In practice, this translates to fewer headaches for downstream chemists, whether they're running gram-scale synthesis or feeding reactors on a much larger scale.

    Applications Shaped by Real-World Chemistry

    2-Iodobutane plays a key role in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its strength lies in the strength of the carbon-iodine bond, which breaks apart more readily than those in chlorinated or brominated butanes. This high reactivity means the compound excels in nucleophilic substitution and elimination reactions—a point that experienced chemists exploit for efficient carbon-carbon or carbon-heteroatom bond formation.

    We ship this product to facilities focusing on drug discovery, where substitution reactions unlock molecular diversity for library screening. Others use 2-iodobutane to introduce butyl functional groups into complex molecules, or as an alkylating agent to build up carbon chains and append pendant groups to aromatic rings. For those involved in the creation of chiral compounds, the secondary structure lends itself well to stereochemical modifications, meaning downstream intermediates can carry over the configuration, a crucial feature in medicinal chemistry.

    Research institutions rely on our 2-iodobutane for teaching, practical lab demonstrations, and method evaluation. Each time, feedback loops from hands-on users drive process adjustments and technical support. When a batch hits a particular purity snag, we investigate the origin firsthand and modify either raw material sourcing or purification runs. Our investment in robust analytics means even small changes in impurity profile are caught early, reducing risk for process hiccups during scale-up or application development.

    2-Iodobutane vs. Other Alkyl Iodides

    Many in our industry ask how 2-iodobutane compares to related alkyl iodides, such as 1-iodobutane or tert-butyl iodide. From our manufacturing vantage point, the differences run deeper than simple naming. The position of the iodine atom completely changes the chemistry. In 1-iodobutane, the iodine sits on a primary carbon. This means the molecule undergoes substitutions with different rates and often yields different products under otherwise identical conditions. Tert-butyl iodide, featuring a tertiary carbon center, can react so rapidly in some cases that handling stability drops, and storage requirements ramp up. That brings extra safety measures and cost.

    2-Iodobutane offers a middle ground. As a secondary alkyl iodide, it combines strong reactivity with more predictable handling. In our facility, we store and ship it under inert gas to reduce oxidation and elimination risks. Compared to alkyl bromides and chlorides, the iodide variant works at milder temperatures and often needs less catalyst loading. Customers chasing higher efficiency in nucleophilic substitution processes usually gravitate to the iodide derivative for that reason.

    Another point stems from stereochemistry. The secondary center in 2-iodobutane supports both retention and inversion reactions, depending on conditions. With a good chiral resolving agent, skilled chemists can build up enantioenriched intermediates. This gives 2-iodobutane advantages in asymmetric synthesis not as readily available from most primary or tertiary analogs, where the reaction scope tends to narrow.

    Specifications That Matter in Practice

    Laboratory and production teams consistently flag certain properties of 2-iodobutane for attention. Purity, color, and odor point to the most direct signals of a successful batch. Our technical data centers on GC area percentage for major and minor components. Customers running HPLC or NMR on supplied samples often echo our own findings, bringing mutual trust in the integrity of transfer and final use.

    Water content draws another focus, as residual moisture can promote hydrolysis or unwanted by-products during heating. Our drying regimens employ molecular sieves and vacuum stripping after distillation, consistently pulling water content under 150 ppm when measured by Karl Fischer titration. Storage bottles come sealed with PTFE and topped under argon before packaging leaves the floor. That small procedural difference often separates genuine manufacturers from third-party suppliers, whose transfer protocols and container quality may not always match the compound’s sensitivity.

    Each batch produces a practical refractive index, boiling point, and specific gravity that tie closely to product quality. High iodine content can accelerate darkening if not stabilized, especially during storage in humid or sunlit conditions. We circulate supplies in amber-glass bottles and recommend quick transfer into smaller, air-free vials for multi-user environments. Customers running sensitive pharmaceutical or electronic applications may request extra documentation, such as trace metal analysis or volatiles screening. As a chemical manufacturer with internal analytics, we answer those needs directly rather than passing requests down a chain.

    Hands-On Handling and Safety Remarks

    Direct handling of 2-iodobutane calls for both basic chemical know-how and respect for its unique hazard profile. Our plant operators receive annual safety training, centered on practical scenarios involving exposure, containment, and spill control. The chemical’s vapors possess a distinct sharp odor, associated with halogenated hydrocarbons, and rapid inhalation or skin contact can cause irritation. Eyes bear the greatest risk from splashes.

    Our on-site storage areas feature explosion-proof ventilation, leak detectors, and segregated containers. Even small leaks prompt immediate containment and cleanup because of the volatility and the potential for slow decomposition. Emergency protocols don’t come from checklists alone; they grow from real situations—occasional pressure buildup, unplanned spills, or drum integrity checks. Technicians in our facility keep a steady supply of spill absorbents, neutralizers, and personal protective equipment graded specifically for halogenated hydrocarbon exposure. We never treat these as ‘optional extras’—the right gear sets the foundation for increased operational confidence and lower incident rates.

    Shipping preparation involves inert gas purging and double-sealed containers. We coordinate with certified couriers experienced in dangerous goods logistics, and our shipping documents include up-to-date hazard classification as per current regulatory standards. Though standard in our facility, these extra measures help repeat customers feel secure that product quality and safety don’t end at the shipping dock.

    Challenges in Manufacturing and Distribution

    Producing 2-iodobutane at scale is rarely free from obstacles. The iodine feedstock market suffers from price swings, prompted by global supply shortages, regulatory hiccups, or industrial accidents at primary iodine sources. We mitigate this through long-term relationships with miners and refining partners, locking in secondary supply lines against disruptions. Nevertheless, cost pressures remain real, and they filter through into final customer pricing.

    Contaminant control ranks high among operational headaches. Even minor trace levels of byproduct iodides or sulfate ions can provoke batch rejections, especially for high-value applications where customers demand low single-digit ppm levels for anything except the target product. We constantly invest in more selective filtration and distillation equipment, expanding our analytic instrumentation as needs evolve. Our team actively tracks feedback from users implementing 2-iodobutane in new synthetic routes. If a performance problem or incompatibility surfaces, we collaborate to adjust purification or recommend storage tweaks.

    Transportation carries its own risks. Regulatory changes covering halogenated organics can disrupt routes overnight. Weather events, customs scrutiny, and geopolitical tensions have all brought delays in recent memory. Our distribution network remains nimble by design, with multiple forwarders authorized for expedited processing and contingency plans in case borders close or specific trade lanes seize up. Longstanding supply contracts for critical pharmaceuticals or agricultural intermediates always receive uninterrupted priority.

    Supporting Sustainable Chemical Production

    The chemical industry faces mounting pressure to minimize environmental impact, driver of both regulatory change and internal operational improvement. In 2-iodobutane manufacturing, the energy input for distillation and the environmental load from spent reaction media stand as significant contributors. We strategize reductions through solvent recovery, in-house recycling of unreacted iodine compounds, and shift scheduling to reduce energy spikes.

    Waste solvent and aqueous streams from our halogenation processes undergo multi-stage treatment, neutralization, and—in regulated jurisdictions—off-site incineration or stabilization. Even the chosen drum liners, seals, and boxes follow environmental documentation, keeping cradle-to-grave tracing active through each shipment lot and drum. Our R&D wing experiments with greener synthetic routes, such as catalytic iodination using less corrosive agents or minimization of waste streams through process intensification. Some routes struggle with technical feasibility at commercial scale; incremental improvement, though, remains a continuous goal.

    On packaging, we emphasize recyclable or returnable glassware wherever customer operations permit. For critical use-cases demanding single-use packing—such as trace impurity analysis or contamination-sensitive pharmaceutical projects—we specify clear waste-reduction guidelines, enabling customer sites to process empty containers through compliant recycling or return programs.

    Quality Assurance and Traceability

    Customers increasingly expect not just a chemical, but the story and traceability behind it. Our quality assurance runs deeper than a batch certificate. Full lot-level traceability connects raw material lot, production log, analysis result, and customer feedback together. Any concern raised downstream—whether about color drift, odor abnormality, or reactivity loss—triggers not just internal investigations, but also collaborative troubleshooting with our client’s technical teams. Over years, this approach has built mutual trust and repeat orders.

    Routine audits and process reviews keep our operations consistent with best practices. External certification bodies confirm chemical identity, manage audit trails, and provide transparent reporting available to our strategic partners. All process changes receive backward compatibility checks—the team re-tests historical batches and synthetic intermediates so process improvements don’t introduce new risk into old applications.

    Customers benefit from this system through greater confidence in reproducibility. Researchers scaling from the gram bench to industrial plant floors find that our material grades behave as expected, reducing process optimization time. If critical deviations appear, be they supply chain disruptions or specification shifts, rapid real-time updates go straight to affected users. Accountability functions as both a risk management and a reliability tool in a global chemical market facing ever higher expectations.

    Research and Collaborative Development

    We maintain close relationships with universities, startups, and R&D divisions exploring innovative chemistry involving 2-iodobutane. Our technical support team doesn’t just answer inquiries; they collaborate on unusual applications, sometimes creating custom batches with defined impurity profiles or specific isotopic labels. These partnerships often begin with mutual curiosity—could a new catalytic route reduce off-gassing, or might a subtle shift in storage practice extend shelf stability for high-volume users?

    Open dialogue with scientists in the trenches enables us to optimize not only the quality of output, but the suitability for emerging techniques. With advances in cross-coupling chemistry and the demand for cleaner C–C and C–N bond formation, 2-iodobutane’s unique balance of reactivity and stability draws increased interest. Training and shared pilot studies often reveal process details that lab manuals alone don’t capture, giving applied chemists stronger results at scale.

    Feedback from R&D users directly influences ongoing product development. New synthetic demands—such as the need for ultra-low trace metals, or persistent solvent residue concerns—inspire iterative retooling in analysis and purification. By closing the loop between manufacturer and end-user, we help create materials that enable new science, delivered at commercial scale and speed.

    Conclusion

    Our direct experience with 2-iodobutane, forged through daily production, customer service, and technical troubleshooting, grants us a practical outlook that shapes every bottle shipped from our facility. This secondary alkyl iodide serves the creative, analytical, and industrial needs of chemists across the world, offering an optimal mix of reactivity, selectivity, and safe handling—qualities forged not by marketing but by lived expertise.

    Sourcing quality 2-iodobutane involves more than pointing to purity numbers or certification marks. It means working with a manufacturer who knows the pathways, recognizes the hazards and opportunities, and builds chemistry on a foundation of trust and transparency. That approach, rooted in days and years spent on the production floor and in the lab, guides our ongoing commitment to both scientific advancement and responsible chemical stewardship.

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