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Allyltributyltin

    • Product Name Allyltributyltin
    • Alias Tributylallylstannane
    • Einecs 219-371-7
    • 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

    691703

    Cas Number 533-68-6
    Molecular Formula C12H28Sn
    Molecular Weight 291.07 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.13 g/mL at 25°C
    Boiling Point 123-126°C at 8 mmHg
    Melting Point -28°C
    Refractive Index 1.489-1.492 at 20°C
    Solubility Insoluble in water; soluble in organic solvents
    Flash Point 107°C (closed cup)
    Purity Typically ≥97%
    Storage Temperature Store at 2-8°C

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

    Packing & Storage
    Packing Allyltributyltin is packaged in a 100 mL amber glass bottle with a secure screw cap, labeled with safety and chemical information.
    Shipping Allyltributyltin should be shipped in tightly sealed containers, protected from light and moisture, and clearly labeled as a hazardous material. It must be transported according to relevant international and local regulations for toxic and environmentally hazardous substances, typically under UN number 2788. Proper personal protective equipment (PPE) is required during handling.
    Storage Allyltributyltin 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 and acids. Protect from light and moisture. Store under nitrogen or inert atmosphere if possible, and keep away from direct sunlight and heat. Use appropriate chemical storage cabinets for organometallic compounds.
    Application of Allyltributyltin

    Applications of Allyltributyltin in Industrial Manufacturing

    Allyltributyltin is an organotin compound used primarily in the synthesis of specialty polymers and organometallic intermediates. As a direct manufacturer, we support a range of established industrial application areas where this raw material delivers specific functional advantages, with clearly defined usage and compliance practices tailored to each sector.

    1. Specialty Silicone Rubber Additive Production

    In the silicone rubber manufacturing sector, allyltributyltin serves as an efficient crosslinking agent for vinyl-functional polysiloxanes. Manufacturers use this material to enable controlled curing of liquid silicone rubbers (LSR) and high-consistency rubbers (HCR), particularly when producing heat-resistant or flexible rubber components. Its performance enables precise modification of viscoelastic properties, targeting applications where conventional crosslinkers cannot deliver the needed combination of thermal stability and mechanical flexibility.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • IEC 60811 and ISO 37 (Rubber and Elastomer Physical Testing)
    • REACH Annex XVII (Organotin Compound Use Restrictions)
    • GB/T 531.1-2008 (China Rubber Testing Standards)

    Typical usage ratio

    • 0.1–1.0 phr (parts per hundred rubber), with adjustments based on desired crosslink density and final product hardness

    Downstream process integration

    • Chemists incorporate allyltributyltin during the initial rubber compound mixing, prior to addition of catalyst. The material remains active through the kneading and pre-curing stages, impacting network formation during final heat curing in compression or injection molds.

    Final product types

    • Heat-resistant silicone gaskets
    • Flexible membranes for medical and automotive assemblies
    • High-performance insulating sleeves
    • Surgical and laboratory silicone tubing

    2. Advanced Polymer Synthesis—Organotin Intermediates

    Chemical manufacturers utilize allyltributyltin as a building block for synthesizing organotin-based intermediates required in preparing high-value specialty polymers, such as tin-containing polyethers and polyesters. Its unique reactivity enables the introduction of tin moieties to the polymer backbone, essential for applications requiring precise electronic properties or catalytic activity in materials science research and advanced manufacturing.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management Systems for chemical synthesis)
    • OECD Guidelines for Testing of Chemicals
    • REACH Regulation (EC) No. 1907/2006
    • APIC GMP Guide (for polymer intermediates in regulated sectors)

    Typical usage ratio

    • Varies from 0.05 to 0.5 molar equivalent per monomer functional group, depending on the target polymer structure and catalyst system

    Downstream process integration

    • Engineers add allyltributyltin during the monomer or prepolymer stage, typically under inert atmosphere. The reaction pathway involves hydrometallation or radical addition, forming organotin-functional repeating units as the polymer backbone develops.

    Final product types

    • Organotin-functional polyethers for antistatic layers
    • Conductive thin-film materials
    • Precursor resins for microelectronic encapsulation
    • Specialty polyesters for research and custom formulations

    3. Organic Synthesis—Stille Cross-Coupling Reactions

    Allyltributyltin is recognized in the fine chemical industry as a key reagent for Stille cross-coupling, used extensively for synthesizing complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its allyl group enables selective transfer to organic halides under palladium catalysis, providing synthetic chemists with valuable access to extended carbon skeletons and functionalized products without unwanted side reactions common with similar tin reagents.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (US FDA cGMP regulations for pharmaceuticals)
    • REACH Registration and Safety Data Sheet compliance
    • EU EMA guidelines for genotoxic impurities monitoring

    Typical usage ratio

    • Molar equivalents typically range 1.05–1.2 (stoichiometric excess), adjusted based on substrate reactivity and yield optimization

    Downstream process integration

    • Process chemists charge allyltributyltin to the reaction vessel together with the halide substrate and palladium catalyst. This step is performed after preliminary protection or activation of reactive groups, and is usually followed by aqueous workup and purification fractions to recover the desired coupled product.

    Final product types

    • Pharmaceutical intermediates and active ingredients
    • Bioactive agrochemical chains
    • Liquid crystal precursors
    • Complex fragrances and specialty organics

    4. Synthesis of Tin-based Catalysts for Polyurethane Manufacture

    Industrial polyurethane manufacturers use allyltributyltin as a raw material for creating custom tin-organic catalysts applied in the production of specialized foams and elastomers. The compound provides a controlled source of allyl and tin atoms, critical for preparing catalysts with specific activity profiles, pot life parameters, and resistance to hydrolysis in formulated systems where traditional stannous octoate or dibutyltin dilaurate show limitations due to regulatory or technical issues.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for Polyurethane Production)
    • GHS/CLP (Safety and handling of organotin compounds)
    • Chinese GB/T 2567-2008 (Polyurethane Specification)
    • REACH authorization for intermediates

    Typical usage ratio

    • Used as precursor at 0.05–0.25 wt% of total polyurethane batch, with loading tailored to targeted catalyst performance in flexible vs. rigid foam and elastomeric systems

    Downstream process integration

    • Chemists synthesize the tin catalyst from allyltributyltin via ligand exchange or modification steps; production teams introduce the finished catalyst into polyol and isocyanate blending tanks before foam or elastomer forming operations commence

    Final product types

    • Flexible slabstock polyurethane foam for automotive seating
    • Integral skin foams for dashboards
    • High-durability elastomer rollers
    • Specialty sealants and adhesives with low-leaching catalyst residues

    5. Low-Temperature Curing Agents for Epoxy Systems

    In advanced coatings and composite manufacturing, allyltributyltin is employed as a niche curing accelerator in epoxy resin systems requiring fast, low-temperature set and controlled exotherm during thermoset processing. Its action enables formulators to achieve thorough curing at sub-ambient or moderate conditions, targeting electronics encapsulants or specialty adhesives where heat-sensitive inclusions are present or fast cycle times are essential for productivity.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastics Components)
    • ISO 9001:2015 (Procurement and QC in Electronics Manufacturing)
    • IEC 61249 (Epoxy laminate material standards)
    • REACH registration as substance for industrial use

    Typical usage ratio

    • 0.02–0.08 wt% relative to total resin mass, adjusted according to required gel time and filler content in the final formula

    Downstream process integration

    • Production staff meter the compound into pre-mixed epoxy systems, following dispersion of core fill materials but before catalyst and accelerator addition; this sequence ensures consistent reactivity and final mechanical stability

    Final product types

    • Electronics potting compounds
    • Low-temperature curing adhesives
    • Fiber-reinforced epoxy laminates for circuit boards
    • Thermal management encapsulants for automotive electronics
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    Certification & Compliance
    More Introduction

    Allyltributyltin: Unlocking Versatility in Organic Synthesis

    Insight from the Workshop: Beyond Standard Chemicals

    Down on the factory floor, the day starts with a whiff of alkene and the steady hum of glass reactors. Over the years, the practical challenges―not just the paperwork and formulas, but the day-to-day, hands-on problem solving―shape how chemists approach every batch. No one here reaches for Allyltributyltin out of habit or to fill a shelf; each time, it fills a real need in the flow of synthetic organic chemistry. If you look for a reagent able to deliver allyl groups cleanly and predictably, the name comes up often.

    We produce Allyltributyltin because the demands for quality and reliability in functional group transfer are as high as they come. This organotin compound, known in the lab as tributyallyl stannane, serves as more than just a niche reagent. Its model, defined by the simple formula C15H32Sn, stands out both for its efficacy in allylation reactions and for its manageable reactivity profile.

    On the Line: Purity and Consistency Matter in Every Flask

    No two reactions behave exactly the same. Even the smallest inconsistency in a chemical like Allyltributyltin can derail optimization and scale-up. That is why we scrutinize each batch for both physical appearance and spectroscopic fingerprints. The colorless to pale-yellow liquid isn’t just a sign of quality; it tells you the sample hasn’t degraded or picked up impurities from joint grease or careless exposure to air.

    With a molecular weight of 347.12 g/mol and a density close to 1.1 g/cm³ at room temperature, its handling characteristics differ noticeably from lighter, more volatile organometallic reagents. In our experience, these physical traits give it an edge in operational safety and reproducibility on a practical scale. Over the years, raw data from countless runs backs up this choice—it does not seem easily influenced by minor changes in the workup or storage environment, so long as one respects its susceptibility to decomposition by strong acids or oxidizing agents.

    Real-World Use: Trusted by Experienced Synthetic Chemists

    Allyltributyltin remains a preferred partner for introducing an allyl group into a molecule without the violent unpredictability that comes with highly reactive Grignards or the air-sensitive fussiness of lithium reagents. This reliability grows most apparent in selective carbon–carbon bond formations, such as the Stille coupling and related cross-coupling methodologies. Here, the reagent rarely loses its nerve in the face of halides, esters, or electron-rich partners. Efficient transfer of the allyl group—without significant isomerization or unwanted side reactions—means higher yields and reduced by-products for downstream purification.

    When experimenting with or upscaling allylation protocols, an organotin allyl compound allows chemists to proceed under neutral or mildly basic conditions. If a substrate carries sensitive functional groups, this flexibility spells less chance of collateral damage. These reactions tolerate water and atmospheric oxygen to some extent, unlike many transition-metal catalyzed processes, broadening the window for robust routine operation.

    Crafting Every Drop for Industry Demands

    From the control room to the end of the bottling line, years of observation highlight how consistency makes or breaks a synthetic campaign. Batches of Allyltributyltin see use both in small pharma labs pushing out milligrams and major manufacturers aiming for multi-step, kilogram-scale synthesis. Repeat customers share similar reports: reaction reproducibility ties directly to reliable input materials. Uniform allyl transfer translates to time saved in troubleshooting, less waste, and more predictable cost-of-goods calculations downstream.

    Unlike off-the-shelf traders or resellers, our position as an actual manufacturer brings with it direct feedback from those with real process skin in the game, not just catalog numbers. Product runs respond to detailed input from bench chemists, not just technical specs written by committee. If a batch shipped out with even minor deviation in impurity profile, it would come right back as real-world process inefficiency or, worse, a failed lot.

    The Practical Value: Comparing Alternatives with Real Experience

    Plenty of reagents promise similar functionality in literature or patent searches: Grignard reagents, allyl halides, allylboronates, and more. Still, as anyone who’s tried each in a tightly scheduled production knows, the devil lies in the details. Take allylmagnesium chloride, for instance. It tends to overreact, can destroy sensitive esters, and doesn’t play well with moisture. Allylboron compounds, while more benign, sometimes lack the versatility needed for specific cross-coupling protocols or require stricter anhydrous technique, which raises operational costs.

    Allyltributyltin distinguishes itself with a measured, moderate reactivity and compatibility across a broader scope of catalysis. For most of the palladium-catalyzed Stille-type couplings and certain additions to carbonyl compounds, it enables fine-tuning of selectivity and conversion rates through conditions that remain accessible on a factory floor or university bench. A lot of laboratories settle on this compound after painful experience with alternatives that initially look good on paper but don’t hold up across repeated scaleups or shifting substrate demands.

    Safety Is Part of the Story

    Running a chemical manufacturing facility teaches the value of safety through real events, not just training brochures. Tributyltin compounds require respect and protective measures—the same goes for Allyltributyltin. The stannane backbone and three butyl arms mean personnel stay protected behind their gloves and goggles, with good ventilation across the board. Proper storage—cool, away from direct sunlight, and tightly sealed—keeps quality up and personnel safe. With no unnecessary risks tolerated, the practical know-how that trickles down from years of production becomes part of every bottle we fill.

    Regulatory, Environmental, and Disposal Considerations

    Tin compounds face closer attention worldwide due to their environmental persistence and potential toxicity. Our operation designs each lot with these regulatory realities in mind, using purification and waste management protocols that stand up to audit and environmental health concerns. Disposal isn’t an afterthought, but an integral part of operations—scripts learned through years of working with organotin waste are baked into plant procedures. Working with onsite specialists and external partners, our focus includes both environmental responsibility and maintaining regulatory compliance across domestic and international markets.

    Direct Dialogue with Chemists: Meeting Unique Needs

    Over time, customer stories shape our understanding of what works and what falls short. Some reach out with questions on fine-tuning catalyst ratios. Others bring up specific substrates that resist coupling except with a certain grade or age of Allyltributyltin. By maintaining a process that listens before acting, our facility stays nimble—able to tweak distillation parameters, adjust bottling logistics, or refine quality assurance to address bottleneck issues.

    This continuous feedback loop, running from kilo-lab to plant-scale synthesis and back, forms a competitive edge that purely trading operations rarely manage. Each process improvement or adjustment grows out of direct exchanges—not just anonymous feedback forms, but real troubleshooting with real consequences for timelines and budgets.

    The Competitive Edge in Larger-Scale Synthesis

    Much of the world’s pharmaceutical and specialty chemical production depends on reagents that work as hard on the reactor as they do in the literature. Scaling from gram to kilogram amplifies every flaw or hidden impurity. Over the years, we have seen that Allyltributyltin stands up to these tests by offering straightforward handling and consistently clean workups. Its moderate boiling point makes for smoother removal post-reaction, and its reactivity keeps downstream use of transition metal residues at manageable concentrations.

    Unlike exotic or privatized molecules that carry short-term supply risk and high prices, Allyltributyltin offers proven, long-history performance. Supply chains favor core reagents with broad regulatory approval, well-developed production protocols, and decades of accumulated safety and storage data behind them.

    Future Development: Responding to Changing Industry Demands

    The chemistry industry evolves fast, with new synthetic routes and greener processes always on the near horizon. Our plant’s experience builds not only in quantity, but in the real pursuit of safer, more sustainable alternatives. Demand rises each year for less hazardous options and more environmentally friendly production methods. We invest in advanced distillation techniques and green-chemistry-inspired purification to reduce the need for halogenated solvents during product isolation. Close ties to academia and industrial research partners make early adoption of innovations possible, as long as they serve the needs for scalability and reliability.

    Even as newer, less toxic organometallic reagents come under development, Allyltributyltin remains a linchpin in the current state of practical synthesis. Most alternative reagents do not yet deliver the same balance of selectivity, robustness, and predictability at the manufacturing scale. Our R&D team tracks every relevant publication and regulatory announcement worldwide, optimizing both product and process to head off foreseeable supply or compliance issues.

    Practical Advice for Handling and Use

    Just as important as what goes in is how you manage what comes out. Residual stannanes after a reaction call for careful removal and waste treatment. We encourage users to consult internal safety data, not just rely on past procedures, so the environmental footprint per batch remains low. Years in production have shown that careful phase separation, followed by activated carbon and careful distillation steps, can reclaim substantial value from spent process streams, keeping both waste and cost in check.

    In the search for optimal reaction conditions, not all glassware or instruments treat Allyltributyltin equally. Side-arm flasks and well-greased joints minimize sample loss and air ingress—details learned the hard way through sporadic product degradation under less-than-airtight setups. Standard Schlenk techniques give the best results for stoichiometric transfer, especially in research and custom synthesis, where endpoint precision makes or breaks a project.

    Building Trust, One Batch at a Time

    Every liter shipped is the result of months of feedback, process improvement, and iteration. Engineering teams study product stability not as a textbook problem, but as a real-world challenge directly tied to cost, safety, and customer success. This forward-thinking approach, rooted in hard-won experience with Allyltributyltin and similar reagents, shapes the next innovation while safeguarding daily operations.

    With a knowledge base built on years of hands-on manufacturing, and a listening post embedded at every level—floor, lab, management—our Allyltributyltin leaves the line ready for use in processes ranging from new route development to GMP synthesis. Its place is secure not due to marketing alone, but because it earns trust batch by batch, synthesis by synthesis.