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(4-Bromophenoxy)Trimethylsilane

    • Product Name (4-Bromophenoxy)Trimethylsilane
    • Alias (4-Bromophenoxy)trimethylsilane
    • Einecs 'EINECS 627-178-8'
    • 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

    390605

    Chemical Name (4-Bromophenoxy)trimethylsilane
    Molecular Formula C9H13BrOSi
    Molecular Weight 245.19 g/mol
    Cas Number 72634-71-6
    Appearance Colorless to pale yellow liquid
    Boiling Point 109-111°C at 13 mmHg
    Density 1.25 g/mL at 25°C
    Refractive Index 1.543-1.545
    Purity Typically >97%
    Solubility Insoluble in water; soluble in organic solvents
    Storage Temperature Store at 2-8°C
    Smiles C[Si](C)(C)Oc1ccc(Br)cc1
    Inchi InChI=1S/C9H13BrOSi/c1-12(2,3)11-9-6-4-8(10)5-7-9/h4-7H,1-3H3

    As an accredited (4-Bromophenoxy)Trimethylsilane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of (4-Bromophenoxy)trimethylsilane, tightly sealed with a tamper-evident cap and hazard labeling.
    Shipping (4-Bromophenoxy)trimethylsilane is shipped in tightly sealed, inert containers to prevent moisture and air exposure. The package is labeled in accordance with chemical safety regulations and transported as a non-hazardous material, away from strong oxidizers and incompatible substances, with protections to prevent breakage, leaks, and environmental contamination during transit.
    Storage (4-Bromophenoxy)trimethylsilane should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, sources of ignition, and incompatible substances such as strong oxidizers and acids. It should be kept under inert atmosphere (nitrogen or argon) if possible, and protected from moisture to prevent hydrolysis. Use appropriate chemical-resistant containers.
    Application of (4-Bromophenoxy)Trimethylsilane

    Applications of (4-Bromophenoxy)Trimethylsilane in Industrial Manufacturing

    As the original manufacturer, we supply (4-Bromophenoxy)Trimethylsilane to specialized chemical producers worldwide. This compound enables precision transformations in advanced sectors, supporting strict quality requirements in pharmaceuticals, agrochemicals, advanced electronics, and specialty polymer manufacturing.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies use this material to introduce bromophenoxy groups during the synthesis of complex drug intermediates, such as ether-linked heterocycles and arylsilane-functional moieties. It is primarily applied in batch reactions for the coupling or protection of phenolic hydroxyls under Schlenk or glovebox conditions. The product's purity complies with multi-stage GMP synthesis, minimizing metal and moisture content to prevent process contamination. Typical applications include anti-cancer agent scaffolds, CNS-active intermediates, and aryl silane building blocks for targeted synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP General Chapter <941>
    • EMA Guideline on the Chemistry of Active Substances
    • FDA 21 CFR Part 210/211 (pharma process controls)

    Typical usage ratio

    • 0.8–1.3 molar equivalents, typically adjusted based on targeted coupling efficiency and yield; exact amounts depend on substrate reactivity.

    Downstream process integration

    • Charged into reaction vessels during coupling, etherification, or silylation steps. Reaction performed under inert nitrogen protection, monitored for endpoint via HPLC, and followed by standard isolation and purification workups.

    Final product types

    • Pharmaceutical intermediates (e.g., aryl ether drug scaffolds)
    • API building blocks
    • Biosynthetic enzyme reaction substrates
    • Custom research molecules for clinical pipelines

    2. Agrochemical Active Ingredient Synthesis

    In agrochemical sector, R&D pipelines rely on this compound for the development of brominated silane-modified phenoxy structures, which are core components in the synthesis of pre- and post-emergence herbicides as well as certain insecticidal molecules. The material often acts as an intermediate in catalyst-mediated coupling reactions, followed by transformations such as hydrolysis or further functionalization. Production plants follow specific residue and impurity profiles suited for crop protection actives.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO PPP)
    • ISO 9001:2015 (chemical production management)
    • REACH Regulation (EC) No 1907/2006 registration (EU agrochemical import)
    • EPA 40 CFR Part 169 (U.S. pesticide records)

    Typical usage ratio

    • 1.0–1.5 mol equivalents relative to phenolic substrate, adjusted for conversion or residual bromide specification in the synthesis batch.

    Downstream process integration

    • Introduced in early-phase synthesis, often in palladium- or copper-catalyzed arylation or ether formation. Post-reaction mixture processed through neutralization, phase separation, and further hydrolytic cleavage if required.

    Final product types

    • Herbicide active compounds (e.g., aryl ether triazines)
    • Insecticidal intermediates (e.g., bromophenoxy pyrethroids)
    • Bioactive silane precursors
    • Fine chemical intermediates for seed treatment

    3. Organic Electronic Material Synthesis

    Advanced material firms use this chemical as a mono-functional silanizing agent to create customized arylsilane derivatives for organic light-emitting diode (OLED) and organic photovoltaic (OPV) applications. It participates in Grignard-type and transition metal-catalyzed routes to modify surface binding and charge transport properties of photoactive polymers or small-molecule semiconductors. Stringent protocols ensure electronic-grade purity and minimal ionic contamination.

    Industry compliance standards

    • JEITA EM-3601 (Japanese Electronic Industry Standards for organic materials)
    • ISO 9001:2015 Quality Management Systems
    • RoHS Directive 2011/65/EU (for electronic components)
    • IEC 62474 (Material declaration for electrical/electronic products)

    Typical usage ratio

    • 0.2–1.0 mol fraction, determined by molecular weight distribution targets and performance in optical/electrical testing; usage tailored for each product’s formulation.

    Downstream process integration

    • Reacted during precursor stage synthesis of arylsilane-incorporating monomers. Often followed by purification (chromatography or distillation) prior to blending into polymerization or thin-film deposition lines.

    Final product types

    • OLED emitter materials
    • Charge transport layer additives
    • Aryl silane monomers for OPVs
    • Specialty light guide films

    4. Specialty Polymer Modification

    Producers in the high-performance materials sector apply (4-Bromophenoxy)Trimethylsilane for end-group modification or as a crosslinking agent in polysiloxane, polyimide, and epoxy polymer matrices. It introduces functionality to improve hydrophobicity, adhesion, or chemical durability of molded and extruded components. Applications require strict control of residual bromine and siloxane profile for consistent performance.

    Industry compliance standards

    • ASTM D6287 (Silane-treated silica in polymer applications)
    • ISO 14001:2015 (environmental management)
    • UL 94 (plastic flammability safety)
    • REACH Annex XVII (chemical restrictions for consumer goods)

    Typical usage ratio

    • 0.5–5.0% by weight of polymer feedstock, customized according to required modification level and downstream mechanical strength standards.

    Downstream process integration

    • Added during extrusion or melt blending for modification or grafting reactions; sometimes incorporated during solvent casting, followed by cure or crosslinking under controlled temperature/humidity conditions.

    Final product types

    • Electronics encapsulation resins
    • High-durability silicones
    • Polymer-based barrier films
    • Custom-engineered composite parts
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    Certification & Compliance
    More Introduction

    (4-Bromophenoxy)Trimethylsilane: Advancing Synthesis with Reliable Performance

    The Role of (4-Bromophenoxy)Trimethylsilane in Innovation

    As chemists who spend their days in the heart of production, we see firsthand the significance of each choice in building blocks for synthesis. (4-Bromophenoxy)Trimethylsilane, with the model designation BPTS, has earned a place in our lineup through actual need rather than marketing. Chemists in research and pilot scale processes often challenge us to deliver molecules that push boundaries. BPTS stands out for its function in selective silylation, aiding in protecting groups during multi-step synthesis and in facilitating transformations involving organosilicon intermediates.

    We produce BPTS with a consistent purity over 98 percent. This matters during reactions requiring clear selectivity and reproducibility. Any impurity in the starting material can introduce unpredictable side reactions. Our own teams run weekly analyses on batch samples to ensure actual delivered quality matches stated specifications. Over the years, process feedback has honed how we manage moisture and temperature during packing—a critical factor since this compound absorbs moisture and loses reactivity if handled carelessly.

    Comparative Properties and Practical Impact

    In the field of aryl silyl ethers, (4-Bromophenoxy)Trimethylsilane brings together two features: a trimethylsilyl group bonded to oxygen, and a bromine positioned para to the ether. The silyl ether linkage offers a temporarily masked phenol, while the bromine opens possibilities for further cross-coupling, such as Suzuki or Buchwald–Hartwig reactions. Customers running fragment-based drug discovery have relied on this unique arrangement to allow for stepwise diversification, rather than committing to irreversible steps up front.

    The so-called simple silyl ethers—like trimethylsilyl phenyl ether—may suffice for some protection or masking protocols. Yet, these lack the reactive handle that BPTS provides. By integrating the bromine function, the door opens to palladium-catalyzed cross-coupling, a mainstay in complex molecule assembly. In pharmaceutical labs where every step brings the cost and time pressures of discovery into sharp relief, these added layers of reactivity can mean one less purification or a reduced need for expensive reagents downstream. We have grown BPTS in our own development campaigns for custom intermediates, often using the bromine to introduce new aromatic fragments, saving entire rounds of protection and deprotection.

    Materials Handling: Lessons from Scaling Up

    Through years of upscaling, the challenges in manufacturing BPTS differ notably from less functionalized silanes. Small differences in moisture content of silane and phenol feedstock cause pronounced hydrolysis, impacting yield and even shipping stability. Standard phenoxytrimethylsilane, for example, lets the process run at higher throughput; with BPTS, our reactor operators exercise close control when introducing the bromo group to prevent the unnecessary formation of side products. Every batch receives finite attention at the hydrolysis mitigation stage, and any product showing signs of off-color or viscosity change gets diverted out of saleable stock. Chemical manufacturing for research and process intermediates calls for reliability—buyers expect the compound’s reactivity, not surprises, to drive their discoveries forward.

    Some customers compare BPTS with other aryl bromides or silylated materials. The classic bromoanisole, while widely used, lacks a masked phenolic site, and can produce more by-products during coupling. Silyl ethers without a halogen, though good in multi-step syntheses, require additional manipulations before cross-coupling or introduction of other fragments. This has practical implications—for any chemist optimizing a synthetic route, every removed deprotection or extra activation helps accelerate projects. Producers like us cannot just offer a molecule; we must make sure its properties translate to reliable outcomes in the customer’s hands.

    Piloting Applications and Real-world Outcomes

    Our own experience with BPTS has grown out of requests from both academic collaborations and specialty pharma clients. Many sought a versatile intermediate for preparing diversified biaryls or functionalized phenols. The silyl group holds up well under basic and moderately acidic conditions, and can be cleaved under milder conditions than the more stubborn tert-butyldimethylsilyl analogs. In one recent pilot, university researchers used BPTS to prepare novel ligands by cleaving the silyl ether post-coupling. They commented on the lower occurrence of protodesilylation, which otherwise plagued parallel reactions with less stable silyl ethers.

    We have heard from process chemists who switched from bromo derivatives without silyl masking, reporting cleaner isolation of product and less workup time after aqueous extractions. The trimethylsilyl group’s susceptibility to fluoride or strong acid cleavage allowed for gentle removal, protecting even sensitive functional groups elsewhere in the molecule. In contrast, classical person-hour draining protocols such as hydrogenolysis or harsh acidolysis cost more in solvent, time, and often led to compromised yields. In our own scale-up practice, we have seen these advantages multiply, making a difference during time-sensitive pilot campaigns for new APIs or high-value building blocks.

    Stability, Storage, and Direct Experience

    Proper storage cannot be overlooked. BPTS calls for strictly anhydrous conditions, preferably under nitrogen or argon. In our warehouse, handlers use septum-capped glass bottles with desiccant packs, and the logistics team tracks every consignment for cold-chain documentation during summer shipments. Neglecting such practices saw batches aged during transit, with hydrolysis visible by the time they reached customers in more humid climates. Over the past two years, we have implemented silica gel monitoring during storage and advise partners not to break original seals unless ready for immediate use. Once, a research group ran a control sample showing product drift when stored open at room humidity—this reinforced why process feedback cycles matter at the production level.

    We regularly review analytical methods for monitoring BPTS during long-term storage, checking not just by NMR for purity, but by residual water and halide content. Physical properties—such as color and refractive index—serve as practical first checks. Once, a minor impurity in a fresh feedstock batch led to a persistent discoloration; closing in on its source required us to upgrade a distillation stage rather than simply tweaking the specification. While large ingredient distributors sometimes accept minor off-color material for aromatic chemicals, we treat color shifts as a process problem, opting for root-cause review over expediency.

    Feedback and Continuous Improvement

    We solicit frank feedback from both regular and one-time users. Complaints typically revolve around variability in silyl cleavage rates and humidity sensitivity during handling in glove boxes. Several academic teams told us about inconsistent cleavage yields when working with fluoride reagents from different suppliers. The lesson—control upstream factors in both production and lab use—became clear after joint troubleshooting sessions, where impurities traced to shipping led us to introduce in-line sample points just before the packing step. As a chemical manufacturer, we stay directly engaged with forensic support rather than relying only on after-sales technical service. Commitment to continuous improvement shapes how we approach every batch, rooted in both factory learning and user experience.

    Our scale-up specialists keep open notebooks on process trends. Non-routine production runs trigger group reviews, especially when solving material compatibility issues in equipment exposed to silyl ethers and brominated aromatics. Deposits inside glass-lined reactors required a change in cleaning protocols—a practical outcome of experiencing new reactivity profiles from BPTS compared to classic phenolic ethers. We believe such stories around technical lessons and fixes have value, shining a light on the realities of growing specialty chemical products beyond mere catalog status.

    Strategies for Reducing Bottlenecks and Maximizing Utility

    To ensure every researcher or manufacturer using BPTS gets predictable results, we apply clear, simple packaging standards. No open bulk containers leave the site—sealed glass vessels with vapor-proof caps address the real risks from environmental water. Our internal logistics fill orders only after confirming storage requirements with new customers, saving both sides headaches from accidental spoilage. Laboratories that invested in dry-use hoods reported fewer failures, and collaborations with integrated supply chain partners enabled shipment with calibrated desiccant packs on demand.

    We share best practices with clients during technical exchanges. Small changes, such as storing BPTS in secondary sealed bags or using inert transfer lines, often shave hours off project timelines by minimizing rework. In a recent custom run for a biotech startup, close consultation during the method transfer stage trimmed an entire week from their synthetic route. These process improvements are shared internally and documented for future batches, reflecting how direct manufacturing experience feeds back into better customer outcomes and smarter product evolution.

    Working with (4-Bromophenoxy)Trimethylsilane: Considerations and Opportunities

    Down in the plant, the familiarity with its nuances has translated into smoother runs and fewer surprises. We encourage clients to review their reaction protocols in light of our latest batch data. Inputs such as solvent grade, base, and atmosphere control bear directly on yields. Unlike off-the-shelf phenolic silyl ethers, the bromo functionality here interacts with metal catalysts as cross-coupling scale increases, so minor operational details—such as efficient stirring or strict control of catalyst loading—pay dividends in both output and product integrity.

    One pharmaceutical partner found that integrating BPTS enabled a more streamlined convergent synthesis, producing novel drug candidates two steps sooner than their older protocol. These real-world impacts underscore the competitive advantages that come from using thoughtfully designed building blocks. We see similar stories repeated in specialty materials: clients working on electronic dyes or polymerizable aromatics use BPTS’s silyl ether to mask and then reveal hydroxyl functions with only minimal handling, sidestepping common degradation challenges.

    Addressing potential bottlenecks before they arise is key. Scale-up campaigns involving (4-Bromophenoxy)Trimethylsilane progress faster when the manufacturing side maintains transparent communication with research teams about any new impurity profile or batch-specific attribute. If a customer plans to vary coupling partners or modify cleavage approaches, we recommend advance discussions to align on analytical methods. Our technical team maintains up-to-date information from each production round, supporting custom batch requirements as projects evolve from bench to pilot scale.

    Product Differentiation: More Than Just a Catalog Entry

    We have met requests for detailed batch histories more than once, usually because a subtle difference arising during synthesis caused a downstream effect in client workflows. Unlike generic suppliers, we maintain a record of each batch’s journey, using that data to adjust process conditions and, if needed, reproduce optimal lots. This level of traceability reflects years of learning through direct handling—something only direct producers with a plant floor presence can provide. Unique properties like dual reactivity, stability under defined conditions, and reliable masking power set BPTS apart from over-simplified silyl ethers or general aryl bromides crowding the market.

    Changes in downstream regulations—such as REACH or local environmental rules—prompt us to review not just compliance, but also process safety and sustainability. Drumming up safety improvements, we periodically invest in waste stream mitigation to reduce halogenated by-products. Such investments arise from both regulatory realities and the desire to keep production robust in a changing regulatory landscape.

    Looking Ahead: Continuous Adaptation

    As demand for high-purity reactive intermediates like (4-Bromophenoxy)Trimethylsilane grows, we expect more applications to arise from outside the classic fine chemical and pharma base. Early-stage material science teams have begun to tap compounds like this for new generations of organic electronics and specialty coatings. We stand ready to adjust production methods and scale, with planning cycles built on honest reporting of process limits and opportunities.

    Success in supplying specialty compounds requires more than filling a drum or flask. It means building actual technical relationships, sharing timely observations from factory processes, and investing in real-time analytical control. Clients rely on not just the purity or the stated specifications, but also on the practical reliability and honest guidance that comes from teams with hands-on exposure to each step, every day. For us, every kilogram represents a collaborative point in a much larger journey—linking raw material handlers, plant operators, QC chemists, and the research minds pushing every field forward.

    In summary, (4-Bromophenoxy)Trimethylsilane’s value arises from both chemical design and manufacturing know-how. Its specific features—trimethylsilyl masking, para-bromo reactivity, sensitivity to handling—translate into measured advantages in real-world synthesis. Our focus remains on providing not just a specialty reagent, but an integrated experience—one grounded in field-tested procedures, transparent feedback loops, and long-term partnerships across the research and manufacturing landscape. We continually adapt, learn, and improve, knowing that every batch shipped must meet both present and evolving needs of those driving discovery and innovation.