Products

Tributyltin Hydride

    • Product Name: Tributyltin Hydride
    • Alias: TBTH
    • Einecs: 245-727-4
    • 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

    225838

    Chemicalname Tributyltin Hydride
    Chemicalformula C12H28Sn
    Molarmass 291.06 g/mol
    Casnumber 688-73-3
    Appearance Colorless to pale yellow liquid
    Boilingpoint 78-80°C at 0.3 mmHg
    Density 1.17 g/cm³ at 25°C
    Meltingpoint -60°C
    Solubilityinwater Insoluble
    Flashpoint 55°C (closed cup)
    Odor Mild, unpleasant odor
    Refractiveindex 1.491

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

    Packing & Storage
    Packing Tributyltin Hydride, 100g, supplied in an amber glass bottle with a tight-seal cap, labeled with hazard and safety information.
    Shipping Tributyltin hydride is shipped as a hazardous material. It must be packed in tightly sealed containers, protected from light and moisture, and transported under inert gas. Proper hazard labels—including flammable liquid and toxic—are required. Shipment must comply with regulations for toxic and environmentally hazardous substances (UN number: 2929).
    Storage Tributyltin hydride should be stored in a tightly closed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, well-ventilated area, away from heat, light, and sources of ignition. Store separately from oxidizing agents, acids, and strong bases. Glass containers with PTFE-lined caps are recommended for safe storage.
    Application of Tributyltin Hydride

    Applications of Tributyltin Hydride in Industrial Manufacturing

    Tributyltin hydride serves key roles in specialized chemical synthesis across a range of industrial sectors. Our production supports high-purity demands and regulatory traceability, supplying critical material for targeted downstream applications. The following sections detail principal segments, based on actual usage in manufacturing processes.

    1. Pharmaceutical Intermediate Synthesis

    Tributyltin hydride acts as a selective reducing agent in the synthesis of complex pharmaceutical intermediates. Manufacturers employ it for radical dehalogenation, reduction of functional groups, and specific coupling reactions where conventional hydride donors fail to provide adequate selectivity or yield. Its application is closely regulated due to potential toxicological impact, demanding controlled reaction environments and waste management. Process engineers integrate tributyltin hydride to streamline synthetic paths for APIs such as alkaloids, nucleoside analogs, and custom drug scaffolds requiring precise dehalogenation, minimizing by-product formation and improving downstream purification.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • EU REACH Regulation (EC) No 1907/2006
    • US EPA TSCA guidelines for organotin compounds
    • Pharmacopoeia monograph conformity for related process impurities

    Typical usage ratio

    • Used at 1-2 molar equivalents relative to substrate halide mass
    • Optimized ratio based on substrate reactivity and required selectivity
    • Pilot and production scaling adjusts dosage per batch size and residual content testing
    • Residual tin regulated below 1 ppm in final API following purification

    Downstream process integration

    • Added during mid-stage synthetic transformation after substrate introduction
    • Reaction performed under inert gas, typically at 25-40°C
    • Post-reaction, phase separation removes tin-containing by-products before final isolation
    • Waste streams directed to organotin treatment plants for compliant disposal

    Final product types

    • Antiviral and anticancer drug intermediates
    • Steroid derivatives with defined dehalogenated positions
    • Custom chiral building blocks
    • Nucleoside and nucleotide analogs

    2. Agrochemical Active Ingredient Production

    In agrochemical manufacturing, tributyltin hydride functions as a dehalogenation and reduction agent in the preparation of certain protected intermediates for herbicides and fungicide actives. Its use enables the production of specialty molecules where classic hydrogenation results in over-reduction or loss of product integrity. Downstream operators incorporate tributyltin hydride in tightly controlled, closed-loop batches, meeting strict regulatory oversight due to potential environmental persistence of organotin residues.

    Industry compliance standards

    • OECD Test Guideline 508 for organotin residues
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • China’s GB 2763 Maximum Residue Limits
    • Product-specific stewardship programs requiring documented destruction of residues

    Typical usage ratio

    • Applied at 0.5–1.5 equivalents relative to active precursor
    • Adjusted downward if field residue levels challenge compliance
    • Excess reagent removed via liquid–liquid extraction prior to downstream conversion
    • Final formulation ensures non-detectable tin residue in technical concentrate

    Downstream process integration

    • Dosed into glass-lined batch reactors equipped with internal temperature control
    • Reaction endpoint monitored by GC or HPLC with on-line tin analysis
    • Spent catalyst and residuals moved to specialized hazardous waste streams
    • Material balance tracked for environmental and operator safety audits

    Final product types

    • S-triazine herbicide intermediates
    • Substituted pyridine-based actives
    • Specialty antifungal agents
    • Protected aromatic compounds for post-processing

    3. Specialty Polymer and Material Modification

    Within advanced materials manufacturing, tributyltin hydride acts as a chain-transfer agent and functional group modifier during polymer synthesis. Its high selectivity for radical-mediated reactions allows introduction or removal of halogen groups for tailored molecular weight and end-group functionality. Material scientists utilize it in laboratory and pilot environments for engineered silicones, polysilanes, and specialty resins where end-group specification or thermal stability improvements are essential.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management in chemical manufacturing)
    • US EPA SARA Title III for toxic chemical release inventory
    • WEEE/RoHS (2011/65/EU) limiting organotin compounds in electronics-related resins
    • Customer-specific restricted substance lists for automotive and semiconductor sectors

    Typical usage ratio

    • Typically 0.1–1 mole% relative to total monomer mass
    • Adjusted to target degree of polymerization or specific functionalization needs
    • Minimized to achieve regulatory thresholds for organotin content in end-use
    • Scaling from R&D to production validates carry-over and decomposition profiles

    Downstream process integration

    • Blended in during initial monomer charge or introduced by continuous dosing
    • Careful temperature ramping prevents loss of activity and unwanted side reactions
    • Residues removed by high-vacuum stripping or Soxhlet extraction
    • Polymer QC includes organotin residue quantification and spectroscopic verification

    Final product types

    • Functionalized specialty silicones
    • End-capped electronic resins for conformal coating
    • Molecularly tailored polysilane wires
    • Heat-resistant engineered plastics

    4. Organic Laboratory Synthesis and Research Applications

    Tributyltin hydride sees widespread use in chemical research and pilot-scale process development, especially within academic, contract research, and advanced materials R&D labs. Its utility in chemoselective radical reactions, such as stannane-mediated cyclizations, deprotection steps, and skeletal modifications, supports the exploration of new synthetic strategies and structure-activity relationships. Researchers adhere to rigorous handling and decontamination routines to ensure laboratory safety and research reproducibility.

    Industry compliance standards

    • Good Laboratory Practice (GLP, OECD Principles)
    • Local environmental health and safety (EHS) protocols for organotin management
    • Institutional hazardous material waste tracking and documentation
    • Annual certification under Responsible Care® or local equivalents

    Typical usage ratio

    • Commonly used at 1–3 equivalents in exploratory synthesis
    • Dose determined by substrate reactivity and desired conversion
    • Small-scale quench step at reaction endpoint neutralizes unreacted reagent
    • Residue monitored by ICP-MS or AAS before disposal or scaling

    Downstream process integration

    • Charged directly into small-volume flasks under argon/nitrogen
    • Employed in stepwise addition for multi-step synthetic sequences
    • Post-reaction extraction ensures removal of tin from organic layer
    • Laboratory-scale distillation or chromatographic separation for intermediate purification

    Final product types

    • Experimental small-molecule libraries
    • Custom deprotected scaffolds for SAR studies
    • Complex natural product analogs
    • Patentable intermediates for pharmaceutical and materials research

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    Certification & Compliance
    More Introduction

    Tributyltin Hydride: Insights and Experience from a Chemical Producer

    Understanding Our Production: A Look at Tributyltin Hydride

    Producing tributyltin hydride is as much about consistency as it is about quality, especially for chemists who hunt for reliability batch after batch. Our team spends countless hours refining each stage—right from the butylation reactions to the careful distillation processes—because even minor shifts in procedure shape the final outcome. The model we produce is known for its fine handling in bench-scale and scale-up synthesis, where high-purity organotin reagents aren’t replaced easily. Tributyltin hydride in its purest form appears as a water-white, faintly viscous liquid, typically handled in glass or lined steel to avoid surface reaction during storage and transfer.

    Our specifications target a purity of 97% or greater. Gas chromatographic purity checks aren’t there for show—they’re a front-line check on unexpected byproducts. Within every run, our operators keep one eye on yields and the other on contaminants like tributyltin oxide, which can creep in at the wrong temperature or with incomplete exclusion of air and water. The smallest impurity can affect sensitive reductions in pharmaceutical or polymer chemistry. Sometimes, another batch needs rerunning rather than risk a shipment that doesn’t meet a chromatogram’s tightest peaks.

    Pushing Boundaries With Organotin Chemistry

    Tributyltin hydride plays a central role in radical chemistry for both academia and industry. We’ve had direct conversations with research groups who trust it for dehalogenations, single-electron transfer reactions, and selective reductions. Its radical generation pathway is robust, giving synthetic chemists a reliable tool for cleaving carbon-halogen bonds where milder or less selective reagents fall flat. This puts tributyltin hydride at the center of medicinal chemistry and materials science labs where time and patience are thin resources.

    We manufacture this organotin in volumes suited for both pilot and full-scale applications, tapping into scale-up experience that bridges a few dozen grams for catalog work to drums shipped for continuous process operations. What this means at our plant is a focus on temperature stability, airtight systems, and quality checks that anticipate field questions chemists ask: How stable is your product in transit? Does it contain corrosive tin halides or traces of water? Will it catalyze side reactions that kill yields downstream?

    Distinguishing Tributyltin Hydride From Other Reagents

    Tributyltin hydride stands apart from classic hydrogen donors and other organotin compounds like tributyltin chloride or trimethyltin hydride. We have frequent discussions with buyers keen on understanding these differences, because the wrong choice can derail an entire research campaign or industrial batch. Where tributyltin chloride serves as a precursor for biocides or antifouling paints, hydride finds a niche in high-precision organic synthesis, avoiding the strong acid or electrophilic properties that complicate workups or equipment cleaning.

    One distinctive example from recent work came from a customer in contract research needing large-scale dehalogenations for an advanced pharmaceutical building block. They weighed alternatives such as silanes and sodium borohydride, but those yielded persistent byproducts—often requiring intensive purification that added weeks to timelines. Our product delivered a cleaner reduction profile. It produced none of the off-smells or heavy oils that sometimes appear with less controlled hydride grades or outdated production routes. Such results don’t come from luck, but from skilled operators who know every quirk of our reactors and those of upstream monomer producers.

    Everyday Manufacturing Challenges—And Solutions Drawn From Experience

    Making tributyltin hydride daily is about managing risk and optimizing flow as much as about chemistry itself. Our operators have backgrounds in both organic synthesis and process control, letting us spot trouble signs early. Air-sensitive processes demand constant vigilance. Even a pinhole in a transfer line, or humidity creeping into a tank, risks oxidation that saps potency and leaves persistent tin(IV) byproducts. Such incidents taught us the value of double-sealing systems, dry nitrogen sweeps, and inline water-scrubbing.

    Shipping policies stem from hard-won lessons about how tributyltin hydride behaves in different climates and transit times. Bottles never sail loosely in containers—they ride in shatterproof, sealed packaging, with desiccant packets and shock-absorbing cradles. There are no shortcuts with an organometallic compound that can react unpredictably outside tightly controlled conditions. These protocols originated after a long-ago shipment arrived with yellowing and minor decomposition thanks to vibration and heat. Since then, quality never ends at the factory gate; any returned or delayed goods prompt a root-cause analysis and a plant-wide review—no matter how small the incident.

    Applications and Feedback from Industry

    Medicine, crop protection, and materials development keep tributyltin hydride in steady demand, yet every industry calls for unique handling and documentation. Our product’s greatest value emerges in roles such as tin hydride-mediated radical cyclization. Peptide synthesis customers favor its selectivity and ability to perform in solvents ranging from toluene to THF with minimal tin contamination of final products. Industrial scale users press us for detailed MSDS and shipping certifications, reflecting regulatory oversight of organotin compounds.

    A decade’s worth of collaboration has taught us where our product outpeforms others. In fine chemical manufacturing, any edge in selectivity reduces both waste and troubleshooting. Several agrochemical manufacturers have shared reports—overcoming incomplete reactions or side-product formation with tributyltin hydride instead of older, less consistent hydride sources. This feedback loop returns directly into how we refine and scale up: downstream user data translates into adjusted batch sizes, filtration protocols, and equipment retrofits.

    Handling, Storage, and Worker Safety: Practice Over Policy

    Focusing on safety shapes our workflow as much as regulatory compliance. Operators on our lines wear full organic vapor cartridges, puncture-resistant gloves, and eye shields because experience shows how splattered droplets or leaks can evolve into mishaps. Tributyltin hydride’s reactivity mandates that any handling—sampling, transfer, or blending—runs under strictly anhydrous, inert conditions. Laboratory and filling area design favors negative-pressure hoods and quick-access decontamination points, not just for compliance but because one forgotten step means lost product or, worse, sending a colleague to the health center.

    Every shift ends with a cross-check: instrument calibration, batch verification, and visual inspection of transfer lines. A clean workspace cuts both contamination and the likelihood of cross-product mistakes. Storing tributyltin hydride in amber glass-lined drums reduces light-driven degradation, and each drum rests away from oxidizing agents. Shipping teams get real-time feedback from our internal audits, closing the loop with manufacturing to keep standards measurable and transparent.

    Regulations and Accountability: More Than Paperwork

    Organotin chemistry often finds itself under the microscope of local, federal, and international authorities. As a manufacturer, we don’t treat these standards as box-ticking exercises; they map to practical daily realities. Waste streams get segregated at the source, and off-gas is treated with wet scrubbers tuned for tin compounds. Documentation travels with every shipment—full certificates of analysis, results from each relevant toxicity panel, and transport manifests for safety inspections and border checking.

    Auditors from health, environment, and transport agencies have visited our site enough times that our team welcomes them as an extension of the industry. That constant interaction means our environmental releases, air monitoring and onsite spill management remain at the forefront of guidelines and, where possible, even ahead of new rulemaking. From labeling to disposal, regulations do shape our workflow, but the drive for transparency and sustainability is about reputation and trust as much as meeting basic legal thresholds.

    Research, Collaboration, and Continuous Improvement

    A steady partnership with academia and end-users pushes us to evolve tributyltin hydride production. Research teams send us feedback not just on the chemical’s effectiveness, but on how packaging, documentation, or even MSDS clarity impacted their projects. Process chemists who scale discoveries from gram to kilogram quantities demand robust supply and consistency, something that only a well-tuned plant and open dialogue can deliver. Every few years, we review upstream supply chain practices, partner with raw material producers for tighter specs, and bring in new analytical tools to catch the faintest impurity or process drift.

    Tributyltin hydride’s standing in radical reactions—everything from tin hydride reductions in new agrochemicals to chiral auxiliary removal in advanced organics—keeps us vigilant. Feedback from successful pilot runs and the occasional failed project alike builds a living playbook. One recent shift change led to a full reevaluation of filtration and packaging procedures after a filtration column fouled with unexpected tin residues. Instead of chalking it up to operator error, we modified tank cleaning schedules for the entire plant.

    Comparisons: Tributyltin Hydride Versus Other Organotins

    While there are many tin compounds available, tributyltin hydride remains in a unique class due to its radical-based reduction capabilities. Tributyltin chloride and tributyltin oxide excel elsewhere—disinfection and antifouling—but lack the selectivity and gentle hydrogen atom transfer that the hydride delivers. For organic chemists, this means cleaner products, fewer downstream treatments, and improved yields. Trimethyltin and triphenyltin derivatives also exist, but our teams have seen the stronger toxicity and less stability complicate handling, shipping, and waste disposal.

    Chemists we serve regularly point out that “generic” hydride products or “tin reagents” supplied by traders or importers often lag in shelf life and purity. We hear stories about failed polymerizations or sensitive dehalogenations, typically traced to sub-optimal hydride lots or unclear storage histories. Our commitment as a direct producer is straightforward: nothing ships that hasn’t been through valid, reproducible analysis, because a failed organostannane reaction wastes time and trust across the board. Other hydrogen donors show up in the literature, but their selectivity and lower toxicity don’t bridge the same performance gap, especially for sensitive crop protection and medicine intermediates.

    Responsible Manufacturing: Sustainability in Organotin Production

    Sustainability is more than a marketing banner in our facility. Over the years, we reduced the use of chlorinated solvents and redirected heat from exothermic reactions into steam recovery and plant heating. Waste tin is collected, processed, and sold as a byproduct, closing a loop that keeps hazardous disposal safely managed and allows downstream applications to benefit. We frequently analyze wastewater for trace tin, adjusting treatment protocols based on live monitoring data pulled from the discharge lines. These adjustments aren’t just “green compliance”—they save energy costs, boost plant morale, and reduce risk of regulatory fines or pressuring from local authorities.

    For us, responsible manufacturing feeds directly into worker retention and market reputation. Many operators stay on for decades because they see tangible progress: fewer health incidents, lower exposure scores, and positive reviews from inspectors. As a team, we review new organic additives and stabilizers suggested by academic partners, evaluating both their impact on product consistency and their downstream fate in environment and human health. If a process or formulation fails to match these goals, it’s dropped—no matter the short-term cost or disruption.

    Looking to the Future: Adapting to Market and Science Changes

    The landscape for tributyltin hydride never stands still. Regulations cycle, green chemistry advances, and end-user demand fluctuates with trends in pharmaceuticals, agriculture, and advanced materials. Our plant evolves in stride, taking on new distillation technologies, advanced filtration, and more rigorous process audits. Future-proofing organotin supply means working upstream with raw materials and downstream with disposal partners—as shortages or regulatory shifts can ripple quickly through the sector.

    Rather than chasing short-term gains, investments stay rooted in building redundancy, operator expertise, and transparency. Bulk users can trace the batch history, operator chain, and analytic profile for every drum that ships. Yearly upgrades, like real-time process analytics and batch tracking software, come from the shared view that mistakes—either from contamination, handling missteps, or supply misalignment—cost more in lost trust than in upfront spend. Every year, new chemistries and reduced-toxicity alternatives surface, but our clients count on careful transition planning, head-to-head performance testing, and open communication about what these changes mean for production schedules or synthetic outcomes.

    Trust Built on Day-In, Day-Out Chemistry

    The discipline of making tributyltin hydride is grounded in the realities of organometallic chemistry—easy to mishandle, fussy about air and moisture, and less forgiving than bulk commodity reagents. We have learned to adapt, innovate, and support the scientists and manufacturers who trust every drum and bottle we deliver. This job requires long hours, sharp attention, and respect for both the product and the people who use it. Feedback, even the toughest, leads us into better practice and deeper understanding. Through this approach, tributyltin hydride shifts from a specialty reagent to a foundation for progress—in the hands of those who demand results without compromise.

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