|
HS Code |
854858 |
| Name | Diphenylmercury |
| Chemical Formula | C12H10Hg |
| Molecular Weight | 354.80 g/mol |
| Appearance | White crystalline solid |
| Melting Point | 121-124 °C |
| Solubility In Water | Insoluble |
| Density | 3.249 g/cm³ |
| Cas Number | 587-85-9 |
| Pubchem Cid | 13266 |
| Toxicity | Highly toxic |
| Odor | Odorless |
| Storage Conditions | Store in a cool, dry, well-ventilated area away from incompatible substances |
As an accredited Diphenylmercury factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Diphenylmercury, 25 grams, is supplied in a tightly sealed amber glass bottle with hazard labels, inside a protective secondary container. |
| Shipping | Diphenylmercury should be shipped as a hazardous material in accordance with international regulations. It must be packed in tightly sealed glass containers, cushioned within a sturdy, leak-proof outer packaging. Shipping labels indicating toxic and environmental hazards are required. Use air-tight, moisture-resistant packaging, and avoid exposure to heat, shock, and direct sunlight. |
| Storage | Diphenylmercury should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong acids, bases, and oxidizing agents. Keep it in a cool, dry, and well-ventilated area, preferably in a designated poison or toxic chemical cabinet. Clearly label the container and restrict access to trained personnel only, using secondary containment if possible. |
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Purity 98%: Diphenylmercury with purity 98% is used in organic synthesis reactions, where high-purity reagents ensure minimal side reactions and increased yield. Melting Point 121°C: Diphenylmercury with a melting point of 121°C is used in thermal analysis calibration, where precise phase transition temperatures enhance experimental accuracy. Molecular Weight 401.8 g/mol: Diphenylmercury of molecular weight 401.8 g/mol is used in organomercury compound preparation, where consistent molar ratios facilitate reproducibility. Stability Temperature 150°C: Diphenylmercury stable up to 150°C is used in high-temperature catalyst studies, where thermal stability allows extended reaction times. Particle Size < 5 µm: Diphenylmercury with particle size less than 5 µm is used in dispersion tests, where fine particles promote uniform distribution in solvents. Solubility in Benzene 5 g/L: Diphenylmercury with solubility in benzene at 5 g/L is used in preparative chromatography, where efficient dissolution improves separation performance. Moisture Content < 0.1%: Diphenylmercury with moisture content below 0.1% is used in sensitive metal-organic syntheses, where low moisture prevents hydrolysis and degradation. Analytical Grade: Diphenylmercury of analytical grade is used in trace mercury analysis protocols, where reagent purity reduces background signal and interference. |
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Diphenylmercury stands out as a unique organomercury compound, shaped by decades of experience manufacturing specialty chemicals for demanding applications. In our own production environment, chemists encounter Diphenylmercury most often as a precise, specialty reagent that serves roles few alternatives can fill. Over the years, this product has been part of several breakthroughs, particularly where chemoselectivity and controlled reactivity set strict parameters that more conventional organometallics cannot match.
We produce Diphenylmercury to high standards required by research and industrial settings. The product’s model depends mainly on purity and particulate profile, as specified by each project. Typical batches reach purity above 99%, always confirmed by multiple analytical methods. Physical form often takes shape as white to light-yellow crystalline solids, with stability that comes from careful exclusion of moisture and air during production. Melting point, solubility range, and moisture content are not left to assumption; these parameters receive consistent testing and continuous improvement based on direct feedback from chemists pushing the limits of their synthesis routes.
Chemical manufacturers know no universal substitute exists for organomercurials in many reactions. Diphenylmercury demonstrates an extraordinary ability to transfer phenyl groups to a range of substrates, with reactivity surpassing that of inorganic mercury salts. Where other reagents may form intractable side products, or fail due to uncontrolled reaction rates, Diphenylmercury typically brings tight, predictable yields. This property makes it favored in the synthesis of specialized phenylated compounds, including those for pharmaceutical research, material science prototypes, and the development of certain ligands and catalysts. Researchers in our own labs report that the product allows fine-tuned control over stoichiometry and can offer more selectivity than related diarylmercury compounds, such as Dimesitylmercury, which they find more challenging to handle and less predictable in many common organic substrates.
Years of experience navigating regulatory landscapes have shaped our approach to Diphenylmercury. This compound’s mercury content brings responsibility. We invest in dedicated containment, redundant quality control, and continuous staff training to protect workers, the environment, and downstream users. Strict compliance with international protocols directs both manufacturing and shipping. Close collaboration with customers helps ensure safe end-use, particularly for clients developing new synthetic methods. Our teams proactively consult with regulatory authorities and regularly update safety practices to keep up with global policy shifts driven by concerns over mercury exposure.
The specialty organomercury market has never been static. As new synthetic challenges emerge, chemists working with us often describe gaps left by more common reagents. For example, in specific aryl-aryl coupling reactions, palladium or copper catalysts draw out undesirable side-products, and even Grignard reagents may offer only trace yields. Diphenylmercury’s single-step utilization in homolytic substitution often forms the cleanest path to novel targets. Recent collaborative projects have involved custom-tailoring the physical form of Diphenylmercury, such as adjusting crystal size for batch reactor compatibility or refining solubility parameters for solution-phase synthesis. These optimizations integrate direct user feedback, instead of relying on theoretical assumptions or literature precedent alone. Over time, this has let us adapt the product’s specification envelope in tune with actual laboratory practice.
Among organomercury products, there are critical performance and handling differences. Monophenylmercury chloride often serves as a more accessible precursor in simple alkylation or acylation steps, but for researchers prioritizing highly specific phenylation, it frequently comes up short—yielding lower selectivity or creating persistent environmental residues. By contrast, Dimesitylmercury, sometimes chosen for extreme air or moisture stability, imposes handling risks that many labs cannot justify and rarely matches our product’s reliability in most common synthetic contexts.
We have found that Diphenylmercury’s phenyl transfer efficiency consistently exceeds that of alternative mercury-based reagents, especially under milder reaction conditions. This is why the compound often holds a niche place in advanced synthetic chemistry, while the market for more “mainstream” aryl transfer agents stays broader but less adaptable. Our technical teams routinely analyze comparative performance data from multiple collaborations, leveraging those findings to guide future improvements. The result: customers experience more predictable troubleshooting and faster time-to-result during method development.
Scaling Diphenylmercury from bench to kilogram quantities demands close process control. Continuous purification steps, in-line monitoring, and precision dosing prevent contamination, which in turn safeguards reproducibility—a top concern for research and pilot-scale clients. Manual and automated systems both contribute to the reliability of each batch. This dual approach traces back to lessons learned handling other air- and moisture-sensitive reagents, where even a momentary lapse in inert atmosphere integrity can undermine an entire production run.
New manufacturing runs often start with customer consultation. Laboratories specifying unique purity, particle size, or packaging draw on our team’s practical experience. For certain customers, bulk quantities require not just technical support but also logistics adapted to heightened environmental and safety restrictions. These ongoing relationships build mutual confidence and support efficient troubleshooting.
Manufacturing Diphenylmercury brings practical insight into the importance of safety culture. Our operators and chemists share seasoned perspectives with customers facing similar risks. Mercury compounds demand protocols exceeding general chemical best practice. For Diphenylmercury, double containment, minimal exposure windows, and rigorous air monitoring are standard, along with full personal protective equipment specific to mercury organics. We invest in continual retraining and prompt incident reporting. This focus stems not from regulation alone but from real-world incidents early in our manufacturing history, which shaped our zero-tolerance approach to risk.
Disposal and spill response plans draw on lessons from past incidents and ongoing simulation drills. Our site maintains redundant mercury vapor monitoring, and we collaborate with emergency teams to review procedures after any near-miss or abnormal reading. This practical foundation informs the documentation and training shared with our clients, many of whom have successfully applied customized recommendations to improve their own lab safety records.
Our goal for Diphenylmercury production does not end at satisfying immediate research needs. Mercury stewardship shapes every step, from raw material sourcing to finished product shipment and downstream waste tracking. Facing mounting global pressure to restrict mercury, we focus on minimizing emissions, using closed-loop systems for mercury recovery, and planning for chemical reclamation. Regulatory pressure is not just an obligation; it drives ongoing innovation in both process and waste minimization, ensuring that our customers access only what they truly require and receive up-to-date guidance on best disposal or recovery options.
Several clients partner with us on environmentally conscious project planning, using joint data to anticipate not only possible compliance challenges but also community impact and long-term liability. More than one major research initiative has succeeded because upstream and downstream users worked together to keep mercury within closed-yield circuits, sharing both safety improvements and cost savings.
Product development using Diphenylmercury often sits at the frontier of applied synthetic chemistry. Pharmaceutical firms, university laboratories, and specialty materials developers rely on us not just for supply chain dependability but as a flexible partner in method troubleshooting. Past participation in high-performance material syntheses, such as ligand frameworks or exotic dye intermediates, has reinforced the value of precise, repeatable Diphenylmercury performance.
Our technical support includes more than traditional specification sheets. Application support covers process adaptation, literature consultation, and access to experience-based troubleshooting. Many clients access our bench-scale findings to validate or refine their own experimental design, particularly when shifting from model reactions to pilot-scale runs. This feedback loop not only aids innovation but also builds resilience into research programs otherwise hampered by unreliable or inconsistent reagent supplies.
Diphenylmercury’s status as a specialty reagent means supply chain resilience matters. Over the past decade, global disruptions in mercury mining and transportation have periodically affected availability and cost. Our response has focused on deep vertical integration—sourcing raw mercury under strict compliance, investing in buffer stocks, and maintaining a transparent, predictably timed order fulfillment process. Documentation flows with every shipment and includes substance origin and chain-of-custody verification designed to meet both research quality and legal compliance.
We have also built supply relationships that help customers weather abrupt market shifts. In cases where regional regulation or logistics cause delays, alternative fulfillment paths activate, minimizing lab downtime. Ongoing dialogue with all stakeholders helps to anticipate coming policy changes, and to adapt both inventory and documentation pipelines well ahead of new market standards. Large-volume customers benefit from individualized stock tracking and projected delivery schedules, while smaller research groups gain assurance that critical batch orders will not be bumped for major contracts.
Feedback never stops shaping our approach to manufacturing Diphenylmercury. Each research collaboration, pilot-scale trial, or field report brings opportunities to reduce impurities, optimize handling, or suggest refinements to our customer training. Sometimes, innovation comes directly from a client’s experimental setback—a batch with unexpected byproducts leads to co-designing new purification protocols or post-synthesis work-up instructions that become part of our knowledge pool.
Periodic process audits mine our own operational data for repeat sources of exposure risk, long-term stability issues, or minor deviations from specification. We invest savings from reduced waste or improved reliability right back into process innovation. This cycle ensures our Diphenylmercury matches current research goals, adapts to emergent synthetic needs, and supports users aiming for new frontiers in chemistry.
As global chemistry continues shifting toward more sustainable and high-precision synthesis, compounds like Diphenylmercury maintain their relevance in highly specialized segments. Market trends forecast a gradual reduction in broad use of mercury reagents, but high-value, low-volume applications—such as the selective arylation of challenging substrates or the development of next-generation ligands—keep demand steady for the right product, the right purity, and the right handling support.
Continued dialogue between manufacturers, regulating bodies, and researchers ensures careful balancing of innovation and responsibility. Our own efforts focus on strengthening this network, always seeking new ways to provide not just chemicals but knowledge, safety, and problem-solving capacity.
Diphenylmercury is more than just a name on a product list for our manufacturing team. It represents years of technical experience, regulatory diligence, and direct collaboration with world-class chemists advancing the limits of synthesis. Each batch reflects not only exacting in-process standards but also a shared ethic of risk reduction and knowledge transfer. As manufacturers with a chemical background, we know few reagents test process discipline and technical versatility quite like Diphenylmercury—and few offer quite the same breakthrough potential at the synthesis bench. Our door remains open to practitioners seeking real-world chemical partners who understand both the product and its broader impacts.