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HS Code |
183854 |
| Name | 1,2-Bis(Dimethylsilyl)Benzene |
| Molecular Formula | C10H18Si2 |
| Molecular Weight | 194.42 g/mol |
| Cas Number | 1073-63-0 |
| Appearance | Colorless liquid |
| Boiling Point | 225-226 °C |
| Density | 0.882 g/mL at 25 °C |
| Refractive Index | n20/D 1.495 |
| Melting Point | -44 °C |
| Solubility | Soluble in organic solvents |
| Smiles | C[Si](C)c1ccccc1[Si](C)C |
As an accredited 1,2-Bis(Dimethylsilyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,2-Bis(Dimethylsilyl)Benzene, 25g, supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Shipping | **1,2-Bis(Dimethylsilyl)Benzene** should be shipped in tightly sealed containers under an inert atmosphere, such as nitrogen or argon, to prevent moisture or air exposure. Store and transport at ambient or slightly reduced temperatures, following all relevant regulations for handling organosilicon compounds. Ensure proper labeling and include safety data sheets with shipment. |
| Storage | 1,2-Bis(Dimethylsilyl)benzene should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Store in a cool, dry, and well-ventilated area away from sources of ignition, acids, and oxidizing agents. Protect from direct sunlight and excessive heat. Proper labelling and secondary containment are recommended. |
Applications of 1,2-Bis(Dimethylsilyl)Benzene in Industrial Manufacturing1,2-Bis(Dimethylsilyl)Benzene functions as a key organosilicon intermediate in advanced industrial sectors. Our direct production supports consistent quality for formulators in precise downstream applications. The following sections detail core industrial uses, processing integration, regulatory frameworks, compositional guidance, and resultant end-products. 1. Polymer-Linked Siloxane Synthesis for Specialty ElastomersThis material enables the production of siloxane-bridged polymers for high-performance elastomer applications, ensuring improved mechanical properties and heat resistance. Incorporation into backbone or side-chain siloxane structures optimizes durability and flexible response for specialty rubber manufacturing lines. Industry compliance standards
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2. Catalyst Ligand Synthesis in Organometallic ComplexesUsed in ligand frameworks for homogeneous catalysis, the compound’s dual silyl groups facilitate stable chelation to transition metals. The resulting complexes support increased selectivity and turnover in catalytic polymerization, hydrosilylation, and hydrogenation reactions within chemical process industries. Industry compliance standards
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3. Precursor in Advanced Ceramic and Silicon Carbide Material ProcessingServes as a molecular starting point for polymer-derived ceramic (PDC) routes, forming silicon-containing networks that convert to SiC or SiCO ceramics via pyrolysis. The aromatic core and silyl groups enable controlled crosslinking and predictable ceramic yields, crucial for demanding electronic substrate and wear-resistant coatings production. Industry compliance standards
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4. Silicone Resin Modification for Electronic EncapsulationIn electronic resins, the compound enables fine-tuning of network structure to improve mechanical toughness and thermal reliability in encapsulant systems. Control over cross-linking density and network regularity enhances protection for sensitive components, supporting long service life in power electronics and microdevice packaging. Industry compliance standards
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5. Crosslinker in High-Temperature Resistant Adhesive FormulationsThe silyl functionalities provide efficient crosslinking sites for high-performance adhesives designed for industrial assembly tasks exposed to elevated temperatures and aggressive chemicals. Its molecular structure allows precise adjustment of thermoset composition, enabling adhesives that maintain integrity and bond strength in severe service environments. Industry compliance standards
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6. Modification Agent in Organosilicon Surface TreatmentsWhen applied in surface treatment formulations, this compound creates robust and water-repellent film layers for glass, ceramics, and metals. Dimethylsilyl substitutions increase substrate compatibility, hydrophobicity, and chemical inertness—vital for applications needing lasting performance in aggressive outdoor or industrial environments. Industry compliance standards
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Most manufacturers spend years narrowing the core set of compounds that can consistently keep pace with the changing needs of fine chemical synthesis. Our own history with 1,2-Bis(Dimethylsilyl)Benzene stretches back over a decade. What began as a small-batch response to a catalyst developer’s request has matured into full-scale annual production, guided by iterative feedback from research labs, electronics developers, and material science partners. We continue to work directly at the molecular level, refining each stage to produce a compound with reliable performance every time the flask opens. Our team continues to stress that this is not a generic silane, but a cleanly defined aryl disilane with real, quantifiable advantages.
The molecule 1,2-Bis(Dimethylsilyl)Benzene carries two dimethylsilyl groups at the ortho positions of the benzene ring. In practice, this structure does far more than most formula sheets explain. The ortho arrangement pulls the two silyl groups close enough to the aromatic ring to alter the electronic environment, a feature exploited by research chemists seeking controlled reactivity. For some, this proximity breeds new reactivity patterns that don’t appear in meta or para analogs or in disilanes attached to open-chain frameworks. This is why catalysis experts and ligand designers request this specific isomer over its positional siblings; it’s not just about connectivity, but about the push and pull within the molecule enabling reactions that demand both steric and electronic tuning.
Our batches of 1,2-Bis(Dimethylsilyl)Benzene follow methods shaped by laboratory consensus. Final materials ship only once we confirm no detectable byproducts, minimal color, and high clarity. Over the years, we noticed major purity differences depending on the grade of silane precursor and moisture control at each isolation stage. Too many early offers from outsourced vendors in the past shortchanged researchers with high ppm impurity or hydrolysis products. We focus on those aspects that matter once the Schlenk line is running: transparent NMR spectra for the core peaks, a narrow melting point range, and real stability against slow air contact.
The biggest shift in the use of this molecule came with the growth of silicon cross-coupling chemistry. For most users, 1,2-Bis(Dimethylsilyl)Benzene serves as a building block to introduce two silyl motifs to an aromatic core in a single clean step. That shortcut delivers value when building advanced organosilicon ligands or modulating the surface properties of organic electronics. Academic literature often highlights its role in transition metal-mediated transformations. Their teams report high selectivity in metal-ligand assembly using our product, especially in platinum and palladium catalysis. The data from these collaborations show higher yields and more stable intermediates compared to bulkier dialkylsilanes or oligosilanes that lack the ortho connection.
The real test comes not in publication but at the bench. Recently, several material scientists turned to our aryl disilane for modifying the interface layer on OLED substrates. They pursued a hybrid organic-inorganic architecture, and the difunctional nature of 1,2-Bis(Dimethylsilyl)Benzene let them anchor on both sides of the benzene ring, creating a more uniform, robust film. Review papers from these groups now cite increased charge mobility and reduced device degradation versus older reagents. Such results push demand for scalable and consistent supplies of this molecule, something our team understands firsthand.
Drawing from experience in competitive analysis, we see plenty of subtle differences in aryl disilanes based on position and backbone. Both the 1,3- and 1,4-isomers generate far less interest among professionals focused on surface chemistry and catalysis. In fact, seven out of ten custom inquiries in the past two years have specified the ortho over the meta or para orientations. Users point to the unique angle at which each silicon approaches the aromatic core in 1,2-Bis(Dimethylsilyl)Benzene. Our trials confirm that this often leads to tighter binding in transition metal complexes and greater control in functional group installations.
Synthetic chemists also prefer our product for its well-defined signals, making batch verification by NMR much faster. We consistently receive positive feedback from quality control teams handling scale-up projects. They emphasize how low the levels of residual solvents and siloxane byproducts stay in our lots, removing the need for extra purification steps that eat into project timelines. We routinely match or beat claims by multinational competitors, based on blind testing results shared by several end-user labs.
Every silane user knows the headaches that hydrolysis brings. Early adopters of our 1,2-Bis(Dimethylsilyl)Benzene sometimes reported minor clouding or off-spec coloration after repeated vial openings, even under dry nitrogen. Sitting down with both purchasers and lab techs, we uncovered that trace acids stuck to some old glassware led to local decomposition, especially once a batch made its way through several gloveboxes. As a manufacturer, we modified our shipping and storage recommendations, and began supplying the compound in inert-lined ampoules for the most sensitive users. That move cut quality complaints dramatically and ensured each recipient experienced the same reactivity window we saw at batch release.
Another adjustment came with improved lot numbering, tying each delivery to a complete certificate verifying moisture and residual acid tests. This system gives both procurement officers and bench chemists a clear trail from drum to flask. Focusing on genuine user experience, not just bulk sales metrics, helped us navigate industry trust concerns common in fine organosilicon sales.
Many requests from large research institutions express concern about batch-to-batch variation in specialty chemicals. The path from grams to kilograms introduces opportunities for trace byproduct formation or variable reactivity. We address this with in-house synthetic routes—never toll-manufactured or repackaged. Our process employs routine water exclusion, high-vacuum distillation, and frequent checkpoint analysis. Actual production yields often exceed industry averages for this class of compound, due to continual feedback between synthesis and quality control teams.
Hands-on monitoring matters. More than a few times, sharp-eyed technicians caught faint color shifts early, isolating micro-impurities before bottling. We do not rely on quarterly audits alone. The routine walkthroughs and feedback sessions between staff make certain that every lot of 1,2-Bis(Dimethylsilyl)Benzene ships to specification, giving end users reliability whether they draw a single ampoule or commission a multi-ton order.
Our research partners drive much of the application progress. Some universities use this material for cross-coupling explorations in green solvents, reporting that the ortho-disilane structure persists under milder conditions than methoxy arylsilanes or bulkier trialkylsilanes. Others exploit its dual reactivity points for convergent synthesis, bypassing multi-step protection-deprotection cycles needed in other aromatic silanes.
Over time, new uses continue to emerge. Coatings manufacturers now draft this molecule into high-performance adhesion systems for specialty glass. Their feedback underscores the unique binding strength compared to linear or bridged silane agents. Our open approach—sharing exact synthetic methods and post-synthesis treatment—fuels these discoveries, as it lets teams adapt the compound’s inherent properties to match unique product requirements.
Industry breakthroughs rarely spring from a commodity mindset. We hold regular discussions with customers not just about purity but about integration into new device prototypes or pilot plant syntheses. Several OLED research teams reached out in the last year, requesting guidance on scaling up the disilane derivatization step for custom conductive frameworks. We shared our findings about batch dilution levels, filtration protocols, and the best inert transfer techniques. Feedback from these groups points to higher reproducibility in their end devices. Their designers choose 1,2-Bis(Dimethylsilyl)Benzene to avoid the incompatibilities seen with other organosilicon cores, and our ability to trace every bottle’s journey from reactor to bench means we deliver assurance alongside chemical substance.
This direct relationship with advanced customers guides improvements large and small. With every quality follow-up, secondary structure analysis, or application troubleshooting call, our understanding broadens. We welcome suggestions for custom packaging, alternative solvents, or modified silyl group composition, and pilot these ideas for future lots. More than once, an incremental shift in drying technique or packaging approach lowered waste or stopped a recurring user complaint.
A fair number of inquiries from established players clearly target issues they’ve seen with less rigorously made products. Hobbyist (and some commercial) suppliers in the market have offered “1,2-disilane” blends with unresolved isomer purity or significant residual solvents. We fielded requests for benchmarking samples and almost always hear back that our product layers clean on silica, shows tight HPLC profiles, and leaves scarce coloration after evaporation under argon.
Reports regularly differentiate our 1,2-Bis(Dimethylsilyl)Benzene from older supply chain samples. Most competing materials drift off-spec over time, or require pre-use clean-up steps that sap time and resources. Some project managers say that starting with our material shortens their validation timelines, as the underlying silane integrity stands up batch after batch. We found that this type of consistency builds trust, especially with teams juggling complex, multi-month syntheses or device builds.
Too many specialty chemical transactions fall victim to opacity and minimal accountability. As the original manufacturer, we reduce these problems with traceable process signatures. Each delivery of 1,2-Bis(Dimethylsilyl)Benzene includes a clear record of origin, handling, and batch test results. By welcoming direct conversation with users—whether PhD chemists or plant supervisors—we catch any quality drift before it disrupts scale-up or research. This approach enables long-term partnerships, creating value for both new and returning customers.
Many of our newer clients come through referrals from trusted industry veterans. They often mention clarity of documentation, practical packaging suited for nitrogen gloveboxes, and prompt troubleshooting support as points of differentiation. Our longstanding relationships with analytical labs, university research consortia, and electronics firms rest on these details.
The demand curve for well-defined aryl disilanes heads consistently upward as material scientists, structural chemists, and electronics teams search for responsive building blocks. We continuously monitor feedback loops between our own chemists and partner institutions, tweaking finishing steps or altering process controls as new application requirements develop. Staying directly involved keeps us ahead of regulatory shifts or changing purity requirements, which can change fast in large R&D pipelines.
Emerging research into silicon-mediated catalysis and next-generation optoelectronic devices creates more avenues for this compound. We pair our in-house analytics with third-party verification from certified laboratories, giving institutional buyers peace of mind regarding both compositional consistency and application-specific purity. This ecosystem of feedback and collaborative problem-solving puts us in a unique position to serve both established and rising sectors.
Every batch of 1,2-Bis(Dimethylsilyl)Benzene reflects hands-on work from seasoned professionals invested in its future uses. Over time, we grew from experimental syntheses in early 2000s glassware to scaled-up, automated lines checked by both digital and human eyes. Our conversations with end users—across catalysis, materials science, and applied electronics—keep redefining what makes a specialty compound not just good but indispensable.
From lot release to end application, each decision comes back to direct accountability. In a sector where even one off-spec batch can stall an innovation cycle for months, every detail matters. We remain committed to combining technical expertise with open communication, responding to real user experience, and driving the development of organosilicon chemistry in scientific and industrial spaces. Instead of relying on distant suppliers or off-the-shelf intermediates, we maintain direct control, and our users reap the benefits—cleaner results, faster integration, and authentic partnership in chemical innovation.