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HS Code |
966297 |
| Chemical Name | 2-Chloromercuriphenol |
| Molecular Formula | C6H5ClHgO |
| Molar Mass | 345.16 g/mol |
| Appearance | White to yellowish powder |
| Melting Point | 160-165°C |
| Solubility In Water | Slightly soluble |
| Cas Number | 593-89-5 |
| Density | 3.49 g/cm3 |
| Pubchem Cid | 10813 |
| Synonyms | o-Chloromercuriphenol |
As an accredited 2-Chloromercuriphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Chloromercuriphenol, 25g, packaged in a sealed amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 2-Chloromercuriphenol must be shipped as a hazardous material, following regulations for toxic and environmentally hazardous substances. It should be packaged in airtight, corrosion-resistant containers with appropriate labeling. Transport must comply with international and local hazardous chemical transport rules, ensuring protection against leaks, spills, and exposure during handling and transit. |
| Storage | 2-Chloromercuriphenol should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong acids, bases, and oxidizing agents. Store in a cool, dry, well-ventilated area, designated for toxic and mercury-containing chemicals. Proper labeling and secondary containment are recommended to prevent spills. Handle and store using appropriate personal protective equipment due to its toxicity and environmental hazards. |
Applications of 2-Chloromercuriphenol in Industrial Manufacturing2-Chloromercuriphenol is a specialized industrial reagent with established roles in pharmaceutical synthesis, enzyme inhibition applications, diagnostic reagent production, and as a process additive for polymer chemistry. The downstream usage scenarios outlined below reflect the current landscape of commercial practices, quality requirements, and regulatory frameworks observed by our direct manufacturing partners. 1. Pharmaceutical Intermediate for Enzyme Inhibitor SynthesisOur clients in pharmaceutical manufacturing implement 2-chloromercuriphenol as a key reagent during the synthesis of enzyme inhibitors, especially those targeting thiol-containing proteins. The compound participates as an alkylating agent in the functionalization of molecular scaffolds, consistently forming part of advanced stage process routes for regulated API production. Its high reactivity toward sulfhydryl groups makes it especially valued in the stepwise assembly of molecules designed to modulate enzymatic activity, where batch traceability and reproducible purity are mandatory. Industry compliance standards
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2. Analytical Reagent for Laboratory DiagnosticsChemical diagnostics manufacturers utilize 2-chloromercuriphenol in gram-to-kilogram scale as a selectivity agent in the preparation of protein or enzyme detection kits. Its function relies on specific binding to sulfhydryl moieties, serving as a foundational component in test strip and microplate reagent formulations for both spectrophotometric and chromatographic analyses. End-use laboratories require traceability records, demonstrated low-level impurity, and verification of batch-specific performance against validated calibration standards. Industry compliance standards
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3. Polymer Processing Additive for Specialty Resin ManufacturingProducers of specialty polymers, particularly those manufacturing engineered resins for electronics or sensor components, use 2-chloromercuriphenol in the role of a chain transfer agent or crosslinking facilitator. The compound modifies polymer architecture by interacting with thiol-functionalized monomers, directly influencing structural characteristics necessary for tailored conductivity, chemical resistance, or mechanical flexibility. Each batch undergoes rigorous specification testing to ensure it meets the desired polymer matrix performance metrics required by component OEMs. Industry compliance standards
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4. Biochemical Research and Enzyme Studying ReagentBiotechnology and academic laboratories incorporate 2-chloromercuriphenol as a biochemical tool for investigating the roles of cysteine residues in protein structure/function and enzyme catalysis. Researchers leverage its site-specific inhibition properties to dissect protein reactivity in complex mixtures, frequently under stringent quality and documentation requirements. Supply batches must accompany certificates of analysis with trace impurity mapping, given the sensitivity of analytical protocols in proteomics and structural biology research. Industry compliance standards
Typical usage ratio
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Over decades working with organomercury chemistry, we have shaped the practical standards for 2-Chloromercuriphenol production. We follow strict process control, batch consistency, and in-house analytical testing to meet real-world application needs. We listen to researchers and formulating chemists—learning from their toughest project challenges and adapting our specifications to meet not only purity benchmarks but also real usability in the field.
At the core of our 2-Chloromercuriphenol line sits a synthesis developed after years of lab observation and equipment design. We never take shortcuts with raw materials; phenol sources undergo double distillation for clarity and trace contaminants never get past ICP spectrometry. Chloromercuration, as a reaction, depends on careful temperature staging and steady-state mixing, because incomplete reaction creates side products that show up days later on customers’ thin layer chromatography.
Once the organomercury bond forms, we guide the product through staged crystallization in glass-lined reactors, avoiding batch-to-batch contamination and circumventing unwanted polymer residues. Granulation and filtration happen under constant nitrogen, not to show off but to protect reactivity and avoid oxygen-based breakdowns. Only then do our staff draw samples for in-house purity checks and water content analysis.
2-Chloromercuriphenol, an organomercury compound, has found value as an analytical reagent, in organic synthesis, and as a biochemical research tool. Each lot releases with GC-MS trace impurity profiles, confirming identity and spotlighting even faint aromatic or inorganic contaminants. A standard batch exhibits a white to faintly yellow crystalline powder, melting in the 140–145°C range.
Moisture content is held below 0.1%, because hydrolysis risks both yields and shelf stability for demanding users. Mercury content is verified by cold vapor atomic absorption, so both major and minor component levels are always traceable to NIST standards. Packing occurs in PTFE-lined, amber glass, making sure no light or plasticizer contact alters chemical performance. Our team stores and ships all lots under controlled temperature to defend against slow decomposition—a real-world detail that shows up in customer feedback, not just on paper.
Through long partnerships with organic chemists, we have learned the major headaches and occasional frustrations in sourcing research-grade organomercurials. Trace sodium, copper, or chlorine impurities can alter key steps in the synthetic sequence—sometimes masking mechanisms or causing false positives. Chemists trust our batches for their regularity, avoiding day-to-day guessing and replicating results across months or even years. Our technical support is handled by the same team who make and test the product, delivering advice grounded in lab experience and not generic scripts.
Our ongoing batch log records symptom-level feedback from users working on peptide mapping, safeguarding peptide ends, or introducing labeled markers for protein analysis. This feedback shapes how we set batch purity, moisture levels, and even packaging types. Researchers have shared with us how slight purity drops can cause downstream NMR baseline shifts or unexpected side bands on the LC-MS—reality in the field, not theory.
In analytical chemistry, 2-Chloromercuriphenol serves as more than a building block—it’s often a selective precipitating agent for identifying sulfhydryl compounds, crucial in proteomics and environmental analysis. Any unwanted halide ion leftover from synthesis can give false positives in spectroscopic assays. Our customers rely on us for batches where halide byproducts sit below the standard detection threshold. In our own research division, we see how a minute level of alkali contamination can overturn the selectivity benchmark for thiol detection, requiring us to refine our purification steps long before the market asks for it.
For organic synthesis, the role of 2-Chloromercuriphenol ranges from aryl transfer reactions to peptide chain protection, where both nucleophilic substitution rates and end-point yields rely on high chemical fidelity. Through hands-on synthon applications and iterative pilot runs, we have tuned our product’s free phenol content since even slight over-methylation or hydrolysis residues will cripple synthetic plans. These lessons have come not from abstract guidelines but from real-time monitoring and fixing the very same issues ourselves.
In biochemical and pharmaceutical projects, where trace metal control can spell the difference between signal and noise, we realized simple filtration did not cut it. By using multi-stage recrystallization and high-purity solvent systems, we reach a product profile designed for protein binding studies, enzymatic labeling, and downstream conjugates that require sensitivity—ensuring open reporting of trace elements in every batch certificate.
Some users ask about differences between 2-Chloromercuriphenol and traditional aryl mercury compounds like p-hydroxymercuribenzoate or 4(Chloromercuri)phenol sodium salt. As the group manufacturing both, we see distinct response profiles in application. 2-Chloromercuriphenol offers a more predictable solubility in organic and mixed aqueous-organic systems, which matters when researchers tackle multi-phase extractions. Its melting range and solid phase stability exceed what you see with non-chlorinated organomercurials—an advantage for both storage and formulation.
Compared with para-substituted analogs, meta and ortho substitution in 2-Chloromercuriphenol promotes a sharper reactivity with protein thiols and polynucleotides, due to the specific electronic environment around the mercurial and hydroxyl group. Synthetic routines benefit from these features when selectivity, and not just reactivity, matters—like in selective inhibition or site-specific labeling. Fellow chemists have credited the sharp endpoint clarity and ease of product separation, which speeds up complex synthetic routes.
We avoid marketing hype and stick with lived experience: many clients have switched from sodium or potassium salt forms to neutral 2-Chloromercuriphenol, targeting applications that cannot tolerate excess ionic strength or where sodium ions cause analytical interference. Our product’s neutral behavior in a range of buffered or organic matrices means less troubleshooting and more consistency in demanding assays.
Chemists with any organomercury experience respect the compound’s toxicity and handle the material with maximum diligence. Our factories maintain negative-pressure isolation, automated powder handling, and on-site mercury spill protocols. Training and regular reviews ensure every technician knows the procedures for small-scale formulation and spill response. We do not treat handling procedures as paperwork—we base them on years of hands-on industrial hygiene and real workplace experience.
Our team regularly audits handling and production waste protocols and has implemented mercury recovery using in-house designed chelation systems. We don’t release any product that could potentially add unnecessary mercury load to the customer lab or the environment. Packing and batch shipping meet all current hazard transport requirements, and we consult with supply chain partners to ensure all documentation reflects up-to-date regulatory compliance.
External factors have shaped how we produce, store, and ship organomercury chemicals. The best example is raw material volatility: upswings in ultra-pure phenol or chloride reagents can force production rescheduling, but our standing supplier contracts smooth out price swings for end-users. We keep a rolling stock in fixed conditions, so order lead times stay short, regardless of market blips—something distributors usually struggle with.
Years of direct dialogue with pilot plant chemists taught us the critical need to avoid intermediate storage delays or shipping breaks, since even brief exposure to ambient conditions can shift product color, purity, or reactivity. We maintain our own climate-controlled transport, avoiding third-party mishandling and giving direct tracking information for each outgoing batch.
Some users ask about cost parity with alternative markers or reagents. Direct synthesis from the raw feedstock eliminates reprocessing steps and let us keep tight rein on operational costs; we pass these efficiencies to customers rather than using them as margin boosters. Even when dealing with tough regulatory hurdles or temporary import/export restrictions, our in-house compliance team keeps product lines moving and customers informed.
New demands face organomercury research: lower detection limits for analytical labs, higher purity for pharmaceutical trials, and environmentally friendly waste streams. Our continuous improvement process draws from customer feedback, field reports, and third-party audits. We adapt our process—not just in response to requests, but from real failures and troubleshooting moments in the field. Every minor process adjustment is tested in parallel with current stock, ensuring no surprises for long-time clients.
Recently, we have launched trials of recycled packaging systems for hazardous compounds, reducing the environmental footprint of glass and polymer waste. With improved recovery and recycling at both production and client sites, the carbon and mercury footprints shrink without shifting safety burdens. Our technical staff continue to monitor the effects of residual impurities on high-sensitivity applications, partnering with academic researchers on test runs and refining analytical protocols where necessary.
We know regulation will only grow stricter. We welcome audits and are transparent with inspectors, anticipating new control requirements and developing trace documentation systems with verifiable chain of custody. These steps keep us—and our customers—ahead of growing compliance expectations, protecting the integrity of research and public safety.
Beyond the product, what truly sets our 2-Chloromercuriphenol apart is manufacturer-led support. Chemists and technical staff, who have worked through the same synthesis and application hurdles, offer guidance based on actual production experience. We pursue honest feedback, respond quickly to corrections, and recognize the value of two-way communication with our customers.
We help clients evaluate application suitability, troubleshoot process questions, and even assist with regulatory documentation for shipping or disposal. Whether supporting high-volume production labs or academic research groups, our focus rests on practical, direct solutions. This approach keeps projects moving, deadlines met, and research published faster.
We value safety as a constant, not a checkbox. We update users on new hazard data, application notes from the field, and practical tips for safe handling and disposal. Adherence to evolving regulatory standards comes from a belief in continuous learning—not just compliance for its own sake. Customers trust our openness, and this trust guides ongoing collaboration for both new and established users.
Each lot of 2-Chloromercuriphenol is linked back to detailed batch records, raw material sources, and analytical profiles. We share data proactively, knowing that transparency builds confidence. We do not use generic labels—product details are traceable to specific production lines, with all data certified by our internal QA lab. Regular reviews with technical and safety experts guide our continuous development, allowing us to anticipate rather than react to user needs.
Feedback from partners using our compound for proteomic mapping, polymer modification, or biochemical signal probes forms a critical input in our improvement process. Listening to customers and acting on what we hear lets us spot minor impurities, streamline handling, and even rethink how we approach bulk and specialized applications. This partnership builds more than sales; it builds new research directions.
Through years of direct manufacturing, batch releases, and regular conversation with research teams, our approach to 2-Chloromercuriphenol reflects experience, care, and chemical expertise. We know that the little details—crystal size, batch homogeneity, real purity checks—matter as much as the headline figures. Our staff learns from setbacks, supports others with honest data, and keeps looking for ways to do better.
By putting technical skill and real communication ahead of salesmanship, we’ve earned trust throughout the chemical, pharmaceutical, and research communities. With every lot released, shipped, and supported, we remain committed to quality, transparency, and continuous improvement—not as buzzwords, but as daily practices shaped by real manufacturing and user collaboration.