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HS Code |
478171 |
| Cas Number | 33981-73-4 |
| Molecular Formula | C10H14O2Si |
| Molecular Weight | 194.31 |
| Iupac Name | 2-[(Trimethylsilyl)oxy]benzaldehyde |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 86-88°C at 0.1 mmHg |
| Density | 1.02 g/mL at 25°C |
| Refractive Index | 1.514-1.520 |
| Smiles | C[Si](C)(C)OC1=CC=CC=C1C=O |
| Melting Point | -26°C |
As an accredited 2-(Trimethylsiloxy)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g bottle of 2-(Trimethylsiloxy)benzaldehyde is securely sealed in an amber glass container with a tamper-evident cap. |
| Shipping | 2-(Trimethylsiloxy)Benzaldehyde is shipped in tightly sealed, inert containers to prevent moisture and air exposure. It should be packaged in accordance with relevant chemical safety regulations, using appropriate cushioning and secondary containment. The shipment must be clearly labeled as a chemical substance and handled by authorized personnel only. |
| Storage | 2-(Trimethylsiloxy)benzaldehyde should be stored in a tightly sealed container, under an inert atmosphere (such as nitrogen or argon), and kept in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Store away from oxidizing agents and acids to prevent decomposition or unwanted reactions. Handle using appropriate personal protective equipment. |
Applications of 2-(Trimethylsiloxy)Benzaldehyde in Industrial Manufacturing2-(Trimethylsiloxy)Benzaldehyde serves as a key intermediate for multiple advanced industrial sectors, supporting both high-performance chemical synthesis and the development of downstream specialty materials. As an original manufacturer, we supply this compound for use in stringent, regulated systems, ensuring controlled incorporation in processes that demand consistency, traceability, and compliance. 1. Pharmaceutical Intermediate SynthesisThis compound finds targeted application as a protected aromatic aldehyde within the pharmaceutical industry, enabling the stepwise construction of aromatic heterocycles and complex molecular scaffolds. Researchers and production chemists incorporate this reagent during multi-stage synthetic pathways where the trimethylsiloxy group provides steric protection, enhancing selectivity in Grignard additions and other nucleophilic substitutions. Our industrial partners in active pharmaceutical ingredient (API) manufacturing utilize this material during regulated synthesis campaigns to support the creation of antihypertensive agents, anti-inflammatory drugs, and other regulated molecules. The process requires consistent GMP-grade raw materials to meet both internal quality metrics and external regulatory audit expectations. Industry compliance standards
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2. Electronic Chemicals for Display Materials2-(Trimethylsiloxy)Benzaldehyde is employed in upstream synthesis of organic light-emitting diode (OLED) emitters and charge-transport materials for high-definition flat panel displays. Display material manufacturers utilize this compound during palladium-catalyzed cross-coupling reactions or controlled lithiation, where the siloxy-protected benzaldehyde enables precise placement and uniformity of electron-accepting groups. The resulting intermediates possess enhanced processability and reduced risk of side reactions, contributing to yield improvement and purity control in electronic material production lines. Industry compliance standards
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3. Agrochemical Synthesis for Selective HerbicidesThis compound serves as a synthetic building block in the preparation of key intermediates for modern selective herbicides. Major agrochemical formulators leverage its protected form to introduce functional groups without unwanted side reactions, especially when working with multi-functional aromatic rings in crop protection active ingredients. Integration occurs during the manufacture of pyridine- or benzamide-based actives, where precise selectivity and protection against oxidation or uncontrolled condensation is essential for consistent biological performance. Our supply chain supports traceability and batch consistency for seasonal production schedules tied to global agricultural demand. Industry compliance standards
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4. Advanced Fragrance Ingredient DevelopmentOur material is utilized by fragrance compounders and specialty chemical houses for the stepwise creation of rare, high-value aromatic aldehyde derivatives. The siloxy-protection feature allows for controlled functionalization and customization of the benzaldehyde structure, enhancing stability during multi-step synthesis. Fine fragrance and aroma manufacturers often deploy this compound for synthesizing unique musk and floral aldehydes where regulatory traceability, identity, and purity is critical for high-end consumer applications, including IFRA-compliant fragrances for luxury personal care formulations. Industry compliance standards
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In the field of organic synthesis, every step along a synthetic route leaves its mark on the final results. One compound I’ve seen researchers come back to time after time is 2-(Trimethylsiloxy)Benzaldehyde. We’ve spent years perfecting its production, making sure every batch delivers tight specifications on purity and consistent reactivity. Customers who regularly work with aldehyde building blocks notice the influence even slight trace impurities can have on their yields, so we don’t cut corners here. Our experience making specialty siloxybenzaldehydes for pharmaceutical and agrochemical labs has taught us how minor process tweaks can change the handling and outcome at scales both large and small.
The chemical, also known as o-(Trimethylsiloxy)benzaldehyde or 2-(TMSO)benzaldehyde, features an aldehyde function ortho to a trimethylsiloxy group on the benzene ring. This structure brings a unique balance of reactivity and stability. We’re often asked to explain why customers might choose this compound over a plain benzaldehyde or silyl-protected analogs with bulkier substituents. Experience shows that our product’s mild protecting group offers a smart balance: it shields the adjacent phenolic oxygen just enough to survive moderate reaction conditions, yet deprotects with mild acid or fluoride ion sources, avoiding harsh post-synthetic steps.
Over several years manufacturing this aldehyde, we’ve found researchers in both discovery and scale-up appreciate this precise tuning. The ortho arrangement lets chemists steer selectivity in cyclization or substitution reactions. Labs working with multi-step syntheses for active pharmaceutical ingredients (APIs) often need robust intermediates that won’t introduce extra noise in downstream characterization. By producing material at scales from gram bags to full drum orders, we see up close how important clean, reliable building blocks are for hitting demanding project timelines.
Heavy experience in organosilicon chemistry has taught us to watch out for common pitfalls. Trimethylsilyl groups can be sensitive; introducing them to a benzaldehyde backbone means controlling moisture at every step. We maintain tightly controlled environments: air-free techniques and careful purification routines. With each batch, we run thorough NMR, GC, and LC analyses against our own years of accumulated benchmarks. Even subtle color shifts or unexpected minor peaks tell us to dig deeper—many of our partners rely on these insights to trace issues back to their sources.
While cheaper commodity grades exist, we focus on high-purity 2-(Trimethylsiloxy)benzaldehyde for synthetic applications that can’t tolerate unknowns. This commitment comes from years of fielding customer support calls, walking through analytical oddities, and working with partners to pinpoint and solve stubborn downstream issues. We supply detailed certificates of analysis and, where needed, direct conversations with our technical team—something few suppliers offer, but which our customers have come to depend on.
We see this compound used most often in complex aromatic substitutions, modified Friedel-Crafts acylations, and specialized protecting group strategies in both academic and industrial R&D. The ortho-trimethylsiloxy arrangement isn’t just decorative; it helps guide reactivity and offers a handle for further functionalization. Researchers synthesizing biphenyl ligands, heterocyclic frameworks, or intermediates for specialty dyes often share how switching to our form of this benzaldehyde simplifies purification and improves overall process yields.
Even with the best reagents, we know bottlenecks can sneak in when scale changes from milligrams to multi-kilogram. Over years working directly with process engineers, we’ve optimized bulk crystallization, solvent exchanges, and packaging options so our customers get the same material behavior across scales. We always encourage those ramping up to discuss feedback: insight from a kilo run has helped us tweak everything from drying times to the way we seal drum liners.
In academic circles, this compound enters as a building block for natural product mimicry or as a precursor in the construction of tailored polyaromatic compounds. Postdoctoral scientists have reviewed our lots benchside and provided direct input, especially on how minor byproducts influence isolation steps—a level of technical communication that’s only possible when the manufacturer and end-user speak the same language.
Synthesizing substituted benzaldehydes is straightforward on paper, but real-world scale brings out subtle challenges. Some impurities, such as siloxane oligomers or partially hydrolyzed forms, slip through basic TLC or visual tests. Over years refining our techniques, we’ve learned that maintaining tight pH control, gentle handling, and careful monitoring at every stage pays off. Quality starts with the raw silanizing agents—but it’s vigilance, honed over hundreds of batches, that supports the downstream chemist.
A lot can happen through transit and storage. The trimethylsiloxy group resists hydrolysis, but not indefinitely, especially in poorly sealed containers. For that reason, we developed packaging designed for both bench access and long-term inventory management. Some of our clients have built sophisticated stockrooms for quick retrieval; others store months’ worth in bulk. Listening to their stories has led us to rethink how we label, box, and even offer technical tips for opening drums without moisture infiltration.
Making tailored building blocks requires attention to every point along the production and delivery chain. A single failed batch on the end-user’s bench can set entire projects back weeks or months. From our perspective, the real proof of value is repeat business and open technical conversations. We try to be proactive, asking for feedback on chromatographic performance or solubility during method development, not just when issues arise.
Direct comparisons to parent benzaldehyde or less-substituted analogs illustrate both the strengths and the trade-offs. Standard benzaldehyde stays highly reactive, but uncontrolled side reactions often plague multi-step syntheses where selective functionalization is required. Adding the ortho-trimethylsiloxy group restricts side reactions at the phenolic position and introduces a silyl group easily removed when no longer needed. This subtle protection—neither as robust as a tert-butyldimethylsilyl nor as labile as a free phenol—enables synthetic chemists to chart new pathways, achieving regioselectivity or chemoselectivity otherwise unattainable.
Other silyl-protected benzaldehydes, such as those using bulkier or less common silylation agents, create their own problems. The trimethylsilyl group offers the lowest steric hindrance while maintaining solid resistance against many reaction conditions. Labs tired of wrestling with deprotection steps or of finding oddball byproducts in their NMR spectra often switch to our material after seeing stronger batch uniformity and easier downstream handling.
Another aspect our customers appreciate concerns handling and volatility. The compound’s relatively low boiling point and moderate volatility demand careful packaging to prevent sublimation and loss. Having walked through many storage rooms and seen firsthand the challenges with evaporation losses, we invest in airtight seals and, for larger orders, vacuum transfer protocols to ensure every gram reaches its destination intact. We don’t leave these decisions to chance: whether the order is for several grams or dozens of kilos, we match container size and closure design to project-specific demands.
Sustainability in chemical production doesn’t always attract attention, especially with specialty intermediates. Yet in recent years, environmental impact has become central to our planning. By sourcing silanizing agents from audited suppliers and continuously investing in solvent recovery, we reduce waste and minimize volatile organic compound emissions. We track solvent use with dedicated meters in all production lines and pass along our findings to customers, some of whom need this data for their internal environmental audits.
Minimizing energy use during silylation and refinement steps forms a big part of our daily operations. We plan batch sizes to optimize reactor loading, keeping energy per kilo produced as low as possible. Points that seem minor—like reusing packaging drums or sending scrap containers for closed-loop recycling—accumulate over time. Working directly with customers planning DOE (Design of Experiments) or large-scale optimization, we share both challenges and solutions openly because mutual learning leads to less waste on both sides of the supply chain.
No two production runs are truly identical. Temperature fluctuations, seasonal humidity, and even minor changes in upstream reagents introduce complexity. We rely on a steady flow of feedback from downstream users—sometimes through formal channels, sometimes via quick phone calls with trusted partners—to refine our processes. Regular participation in external proficiency testing and annual reviews of test methods help us compare our product’s performance with both in-house and industry standards. We see this as an opportunity, not a burden. Mistakes in our facility can become lessons that improve our approach, not just for this compound but for every related line.
Each year, we designate time for reviewing synthetic routes. We’ve tinkered with catalysts, adjusted quenching steps, and retrained staff based on the latest customer input and published literature. Technical training doesn’t just stop at the chemist’s bench. Our logistic supervisors learn the importance of timely, temperature-controlled shipments, and our warehouse team knows exactly how to spot moisture ingress in outgoing shipments. All of this comes from a simple reality: at the manufacturing scale, every link in the chain matters.
We make it a habit to regularly visit partner labs and attend technical meetings where feedback flows straight from bench chemists. Customers using 2-(Trimethylsiloxy)Benzaldehyde in exploratory medicinal chemistry can share subtleties from their latest structure-activity relationship studies. Raw feedback—on solubility changes under stress, or how a particular impurity played havoc with a screen—gets communicated back to our own development team. Sometimes, improvements are straightforward, such as rebalancing solvent composition in purification. Other times, novel use cases drive us to prototype entirely new process tweaks.
On the industry side, teams scaling up for regulatory filings value predictability in their raw material. They don’t just need documentation; they want a real connection with the maker when scale-up blips or compliance issues occur. We never look at these connections as an obligation; our own learning deepens when we hear directly from those pushing the frontiers of synthesis.
International shipment brings its own learning curve. Variations in transit conditions—temperature swings, customs hold times—shape both packaging design and our advice for post-delivery storage. Over time, we’ve updated our shipment logistics to offer tracking detailed enough that customers seldom see unexpected delays or storage mishaps.
Demand for complex aromatics rises with the evolution of advanced materials and pharmaceutical R&D. Even small tweaks in functional group arrangement, as seen with 2-(Trimethylsiloxy)Benzaldehyde, unlock new strategies in synthesis and discovery. Our ongoing challenge is to refine production—not just for volume or price, but to ensure that every batch helps researchers take bold steps forward, rather than chasing down unknown variables.
Product improvement, from our perspective, never sits still. Each year we invest in more sensitive instrumentation for purity checks, and revisit our training programs to bring the latest field knowledge in-house. Technical exchanges with academic and industry partners have sharpened our ability to spot and resolve root causes before they hit customer pipelines.
The feedback loop built through our close contact with end-users runs both ways. We’re not just making a reagent; we’re building a foundation that helps chemists translate ideas into discoveries, reliably and safely, year after year. 2-(Trimethylsiloxy)Benzaldehyde, perfected by the experience and learning within our team and among our partners, demonstrates how deep expertise and continuous refinement make the difference for innovators everywhere.