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(S)-(+)-1-Iodo-2-Methylbutane

    • Product Name (S)-(+)-1-Iodo-2-Methylbutane
    • Alias (S)-(+)-1-Iodo-2-methylbutane
    • Einecs 609-255-2
    • 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

    557037

    Chemical Name (S)-(+)-1-Iodo-2-Methylbutane
    Molecular Formula C5H11I
    Molecular Weight 198.05 g/mol
    Cas Number 22434-44-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 130-132 °C (at 760 mmHg)
    Density 1.594 g/mL at 25°C
    Optical Rotation [α]D20 +18° (neat)
    Refractive Index n20/D 1.507
    Storage Conditions Store at room temperature, in a tightly closed container, protected from light
    Purity Typically ≥98%
    Solubility Insoluble in water, soluble in organic solvents

    As an accredited (S)-(+)-1-Iodo-2-Methylbutane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Clear glass bottle with a yellow and black hazard label, tightly sealed, containing 25 mL of (S)-(+)-1-Iodo-2-Methylbutane.
    Shipping (S)-(+)-1-Iodo-2-Methylbutane is shipped in tightly sealed containers, protected from light and moisture. It is transported according to ADR, IATA, and IMDG regulations as a hazardous material. Ensure secure packaging to prevent leaks or breakage, and label with appropriate hazard symbols. Store and ship at room temperature, away from incompatible substances.
    Storage (S)-(+)-1-Iodo-2-Methylbutane should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from light and moisture. Proper chemical labeling is essential. Store under inert atmosphere (such as nitrogen) if recommended by the manufacturer. Use appropriate secondary containment to prevent accidental release.
    Application of (S)-(+)-1-Iodo-2-Methylbutane

    Applications of (S)-(+)-1-Iodo-2-Methylbutane in Industrial Manufacturing

    Our facility produces (S)-(+)-1-Iodo-2-Methylbutane at scale, maintaining strict process and quality controls for a range of industrial sectors. Below are the key application pathways recognized by downstream technical manufacturers and formulation specialists globally.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Process manufacturers in the pharmaceutical industry rely on this raw material as a privileged chiral alkylating agent for constructing complex stereocenters in active pharmaceutical ingredient (API) intermediates. It is widely integrated in multi-step syntheses such as asymmetric alkylation, employing enantiomeric purity to guarantee the required molecular configuration in advanced intermediates for chiral beta-blockers, antiviral compounds, and central nervous system agents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and EP monograph requirements for related chiral intermediates
    • EMA and FDA guidelines on residual solvents and enantiomeric purity
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.8–1.2 molar equivalents, adjusted by route optimization studies and target molecule configuration

    Downstream process integration

    • Charged in early to mid-stage synthesis after base-catalyzed deprotonation; reacts under controlled temperature in anhydrous conditions

    Final product types

    • Chiral intermediate esters
    • Enantiomerically pure amines
    • Pharmaceutical API precursors for beta-adrenergic antagonists
    • Stereodefined heterocycles for CNS therapeutics

    2. Agrochemical Active Ingredient Preparation

    Prime agrochemical companies use this compound for the targeted alkylation of nitrogen and sulfur heterocycles during crop protection agent synthesis. Its stereospecific structure is vital in producing selective and residue-compliant herbicides and insecticides. It often participates in late-stage functional group introduction, directly influencing the biological activity and regulatory acceptance of the end product.

    Industry compliance standards

    • FAO/WHO Maximum Residue Limit guidelines
    • EPA 40 CFR Part 180 for pesticide chemical residues
    • ISO 14001 Environmental Management Systems
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals

    Typical usage ratio

    • 1.0–1.3 molar equivalents, tailored based on the functionalization step and active moiety

    Downstream process integration

    • Introduced post-core ring assembly via nucleophilic substitution, under inert atmosphere for minimum by-product formation

    Final product types

    • Chiral aniline herbicides
    • Selective chiral insecticidal amides
    • Registered pesticide actives requiring enantiomeric purity certification
    • Chiral fungicide intermediates

    3. Flavor and Fragrance Chiral Building Block

    Specialty chemical formulators incorporate this material as a stereocontrolled alkylating agent in the production of aroma chemicals and essence building blocks. It provides synthesis routes for chiral branched alcohols and lactones used in high-value flavors and fine fragrances, where sensory activity is closely tied to optical purity and regulatory conformity.

    Industry compliance standards

    • IFRA Code of Practice
    • US FDA 21 CFR 172.515 (Flavoring Substances)
    • EU Regulation (EC) No 1334/2008 (Flavourings and Certain Food Ingredients)
    • ISO 22000 Food Safety Management Systems

    Typical usage ratio

    • 0.7–1.0 molar equivalents, dependent on downstream alkylation requirements and structure–activity relationship protocols

    Downstream process integration

    • Deployed in the enantioselective alkylation of aldehydes or ketones to yield chiral precursors, followed by reduction or cyclization steps

    Final product types

    • Chiral branched alcohol flavors
    • Stereospecific lactone fragrance molecules
    • High-purity aroma chemical intermediates
    • Food-grade flavor enhancers with defined enantiomeric distribution

    4. Fine Chemical Research & Custom Synthesis

    Synthetic chemistry contract labs and R&D centers obtain this substance to develop new ligand systems, catalysts, and reference standards. The defined S-configuration enables the study of stereoselective transformations and the exploration of new reaction methodologies in academic and pilot-industrial settings. It frequently serves in the alkylation of model substrates to develop process-optimized, scalable synthetic routes.

    Industry compliance standards

    • GLP (Good Laboratory Practice) OECD Principles
    • ISO 17025 Accreditation for Testing and Calibration Laboratories
    • Institutional Review Board guidelines for non-clinical research materials
    • REACH Annex XVII Restricted Substances Protocols

    Typical usage ratio

    • 0.5–1.5 molar equivalents, depending on reaction model, scale, and optimization trials

    Downstream process integration

    • Applied in the initial substrate alkylation during research chemical development, often under inert gas and customized reagents

    Final product types

    • Reference chiral catalysts
    • Screening compounds for new chemical entities
    • Certified research standards for method validation
    • Custom intermediates for small-scale pilot production
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    Certification & Compliance
    More Introduction

    (S)-(+)-1-Iodo-2-Methylbutane: A Perspective from the Manufacturer

    Building Reliability in Chiral Alkyl Halide Production

    At the heart of our daily work in chemical manufacturing, we see the impact of each batch, each choice of reagent, and every small improvement on the industries and research institutions we support. Our (S)-(+)-1-Iodo-2-Methylbutane is not just a product moving off the shelves—it stands for decades of process refinement, investment in high-purity precursors, and an ongoing dialogue with chemists across pharmaceuticals, agrochemicals, and advanced materials.

    Understanding (S)-(+)-1-Iodo-2-Methylbutane from the Factory Floor

    Years ago, chiral alkyl iodides like this compound were hard to obtain in enantiomerically pure forms. Today, our team routinely prepares this molecule using modern asymmetric methods. From selecting raw materials free from racemization-prone impurities, to optimizing PTC (phase transfer catalysis) step conditions, attention to detail guides every phase.

    Our production model for (S)-(+)-1-Iodo-2-Methylbutane centers on batch processing in glass-lined reactors with precision temperature control. Final enantiopurity assessment uses chiral HPLC, backed by continuous calibration. We have learned, often through costly trial and error, that cutting corners at any stage—iodination, separation, or purification—means headaches for downstream users. Whether a pharmaceutical developer needs a starting material for chiral amine synthesis or an academic needs it for method benchmarking, consistency in optical purity and trace impurity profile are make-or-break features.

    Specifications: What Matters Most to Those Who Use It

    Chemicals like (S)-(+)-1-Iodo-2-Methylbutane are only as valuable as their predictability batch-to-batch. From our own QC records and feedback from customers, we keep optical rotation above 98% ee for all commercial lots. Water content gets tested using Karl Fischer titration, and we ensure iodine-related byproducts never cross set limits, using both GC and ICP-MS. In our experience, the most frustrating delays for a bench chemist come not from major impurities, but from those under 0.2% that sneak through less careful processes. We commit to tracking even low-level halide residues and handling each complaint as a signal to tighten controls.

    Using (S)-(+)-1-Iodo-2-Methylbutane: Insights from Synthesis Work

    Our customers employ this molecule mostly as a key intermediate or chiral alkylating agent. Over the years, we have traced its adoption in several asymmetric synthesis routes: preparations of chiral amines, accesses to alpha-branched carboxylic acids, and formation of enantiomerically pure building blocks for active pharmaceutical ingredients. In some large-scale pharmaceutical pilot projects, the marginal difference between 99% ee and 97% ee fed into downstream cost and regulatory hurdles—highlighting just how tight specs must stay.

    We know chemists expect reliable reactivity from this iodide, given the lability of the iodide leaving group. For enantioselective alkylation reactions, less steric hindrance—paired with an electron-rich backbone—lets this compound improve yields and facilitate mild reaction temperatures, which are critical in scale-up. We see particularly strong demand from teams developing beta-blocker intermediates and certain steroid analogues.

    Comparative Experience with Other Alkyl Halides

    Hand-on production experience has taught us much about the nuances between (S)-(+)-1-Iodo-2-Methylbutane and its analogues. Handling its brominated cousins, we notice lower reactivity in typical SN2 displacements, sometimes leading to sluggish conversion and increased byproduct formation. Chlorinated counterparts are even less reactive and often push chemists to harsher conditions, risking racemization. The iodo variant consistently delivers cleaner conversions under milder conditions, especially in cases needing copper or palladium catalysis.

    Compared to the racemic mixture, which often finds limited application in non-chiral settings, the optically active variant enables highly selective synthesis. In high-stakes pharmaceutical settings, regulatory filings call for proof not just of yield, but of enantiopurity and minimized side product burden. For one customer scaling up a CNS-active intermediate, our chiral iodide allowed a one-pot transformation, reducing solvent use and waste—practical gains that only a truly reliable supply can support.

    Modern Manufacturing: From Raw Material to Rigorous Testing

    Continuous improvement sits at the core of our value as a manufacturer. Tracking sources of our starting alkyl alcohol, keeping analytical logs up to date, and revalidating reactor cleanliness after every batch—all these habits were honed through years of troubleshooting. To make (S)-(+)-1-Iodo-2-Methylbutane, we invest in pre-validated supply routes, with contracts requiring full traceability and chain-of-custody documentation. All iodine comes from sustainable suppliers, and we screen lots for trace metals at intake, not just at final release.

    Our QA procedures include double-checking each step’s output, not simply inspecting final product. Taking lessons from production setbacks, we maintain cross-functional teams that respond rapidly to any deviation. Factors like humidity, cross-contamination, and subtle batch-to-batch pressure differences have all left their mark on our SOPs—pushing us to continually train our operators and invest in facility upgrades.

    Handling and Delivering Quality

    Users in research or GMP settings face enough uncertainty from reaction optimization and regulatory questions; the raw material should not introduce extra risk. We employ glass ampoules or UN-certified containers as needed for shipping, minimizing light and air exposure that could foster degradation or unwanted hydrolysis. Storage at 2-8°C preserves integrity, based on stability testing over years of shipment monitoring.

    Handling an organoiodine like (S)-(+)-1-Iodo-2-Methylbutane, we advise against relying on old stock, as even sealed material can slowly change in storage, affecting the reactivity profile. For large-scale users, we adjust packaging and logistics to align with specific inventory turnover rates and validated shelf-life studies. Decades of customer engagement inform every tweak; our logistics never simply mirror those of “major” sources, but rather reflect the real flow of research demand.

    Supporting Consistent Application Across Industries

    We see some trends in the way this chiral iodide gets used. In pharmaceutical labs, it usually reaches the bench as a connecting point for synthesizing biologically active molecules—often as a reactant for transition-metal catalyzed couplings or as a chiral alkylating agent in amine formation. In agrochemical development, it supports crop protection agent synthesis—routes that require the same level of traceability and purity. Advanced materials teams ask about broader impurity profiles, worried about dopant interference and polymer consistency.

    Each sector wants something slightly different from the material: speed, cost-savings, or regulatory documentation. As actual producers, we stay flexible in our approach but do not compromise on consistency; our history with major pharmaceutical approvals has shown how one bad batch can undermine a program’s prospects, forcing us to hold ourselves to the highest standards even when shortcuts seem tempting.

    Addressing Challenges Unique to Large-Scale Chiral Alkyl Iodide Manufacture

    Iodinated chemicals come with handling and safety implications, as well as pricing risks that many on the outside might not fully appreciate. Volatility in iodine markets, regulatory developments in hazardous goods transit, and periodic supply chain logjams each leave an imprint on every ton we produce. We work directly with global partners to buffer stocks and diversify suppliers, keeping disruptions away from customers’ doors.

    In our own history, cleaning up side-products—such as traces of diiodide or minor over-iodinated byproducts—demanded investment in additional chromatographic and recrystallization capacity. Unlike less “active” halide reagents, small impurities in chiral iodides often escape typical QC traps. We maintain a program of staff upskilling and frequent technology upgrades, as our users rely on knowing exactly what they are adding to pivotal reactions.

    Perspective on Sustainability and Regulatory Expectations

    Modern chemical manufacturing does not stop at purity or yield. Our process development team keeps green chemistry principles in focus: reduction in hazardous byproducts, optimized solvent management, and waste capture. For (S)-(+)-1-Iodo-2-Methylbutane, upgrades in our halogenating steps over the past decade have cut waste volume and improved downstream resin recovery. Customers pushing for REACH or other regulatory filings want more than COAs—they ask for lifecycle analyses and carbon footprint statements.

    Meeting these expectations, we partner closely with regulatory consultants and maintain clear records for audits. Feedback from enterprise clients in API development guided recent investments in digital tracking of batch histories and raw material provenance. Regulatory questions, once rare in this product category, now shape how we design every production run.

    Differences That Matter: From Our Bench to Yours

    The market for alkyl iodides remains crowded, with many sources offering seemingly “the same” product. Our product stands apart because of how deeply we engage with every customer’s application, learning from granular feedback and never treating batches like undifferentiated commodities. People from scale-up chemists at midsize pharma to graduate students at teaching universities have sent feedback on solubility, impurity spectra, and even just the convenience of our packaging.

    Observed firsthand, the optical purity of (S)-(+)-1-Iodo-2-Methylbutane has knock-on effects down stream, impacting not just isolated yield but the waste burden and even operator safety. A less pure batch, even by a couple of percentage points of enantiomeric excess, can throw off reaction selectivity and require double runs or purification steps downstream. We learned through field complaints decades ago that investing early in a tighter optical rotation range prevented endless “troubleshooting” after-the-fact at the customer site.

    Continuous Learning: Listening to the End Users

    Our perspective as manufacturers is shaped most by the stories coming back to us—batches that helped a new drug candidate progress into late-stage trials, or conversely, delays that traced back to contaminants we had thought irrelevant. We encourage feedback and invest in both analytical upgrades and process tweaks when new problems arise. Sourcing iodine from auditable mines, choosing greener solvents, and streamlining packaging have each stemmed from direct end-user engagement.

    Unlike trading firms that simply broker lots, our in-house knowhow lets us respond dynamically. A query about solubility in a new reaction system led us to tweak drying parameters for several lots. A report of batch-to-batch variation led to a rigorous root cause analysis, sparking a change in filtration process and a reduction in the number of steps between iodination and final packaging.

    Looking Ahead: Reliable Supply in a Changing Industry

    Operating as the producer of (S)-(+)-1-Iodo-2-Methylbutane carries a certain responsibility. We stay vigilant about changes in regulatory frameworks, market expectations, and technology. Our commitment means tracking analytical advances—such as NMR spectroscopy for detailed impurity mapping and portable IR probes for in-line monitoring. Digitalization of manufacturing and supply chain records gives our customers the transparency they increasingly demand.

    Supply chain shocks are no longer rare. We build resilience through cross-training staff, staging raw material buffers, and partnering with shipping firms experienced in hazardous material transit. Our close ties with clients—pharmaceutical firms, specialty chemical houses, and academic teams—adjust our own priorities, keeping our focus on what matters most: clean, consistent, and reliable chiral building blocks delivered on time.

    Summary of What Sets Our (S)-(+)-1-Iodo-2-Methylbutane Apart

    In our daily practice, purity and performance go hand in hand. Our team’s experience shows that paying attention to every phase—raw material sourcing, process optimization, individualized packaging, and rigorous QC—builds lasting trust. The subtle ways impurities and enantiomeric composition shape the outcome of major syntheses cannot be understated; our track record in supporting critical missions, whether drug development or advanced materials discovery, hinges on never getting complacent.

    Real-world manufacturing is challenging, with markets, regulations, and technologies all in motion. Relying on feedback not just from our own teams but from users worldwide, we sharpen both production and service, knowing that the quality of (S)-(+)-1-Iodo-2-Methylbutane makes a meaningful difference in hundreds of labs and factories each year. We remain committed to bringing safer, purer, and more predictable chemistry—one batch at a time.