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4-Chloromercuribenzoic Acid

    • Product Name 4-Chloromercuribenzoic Acid
    • Alias p-Chloromercuribenzoic acid
    • Einecs 204-881-7
    • 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

    784349

    Name 4-Chloromercuribenzoic acid
    Synonyms p-Chloromercuribenzoic acid, p-CMB
    Chemical Formula C7H5ClHgO2
    Molecular Weight 355.16 g/mol
    Cas Number 1070-89-9
    Appearance White to off-white powder
    Melting Point 229-232 °C (decomposes)
    Solubility Slightly soluble in water
    Storage Temperature 2-8°C
    Purity Typically ≥98%

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

    Packing & Storage
    Packing The 25g bottle of 4-Chloromercuribenzoic Acid comes in a tightly sealed amber glass container with a hazard-labeled screw cap.
    Shipping 4-Chloromercuribenzoic Acid is shipped in tightly sealed containers, compliant with hazardous materials regulations, due to its toxic and environmentally hazardous properties. Packaging ensures protection from moisture, damage, and mercury contamination risk. Shipment includes appropriate hazard labels, documentation, and adheres to local, national, and international transport regulations—including DOT, IATA, and IMDG guidelines.
    Storage 4-Chloromercuribenzoic acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong acids or bases. Keep it in a cool, dry, well-ventilated area, preferably in a dedicated poisons or toxic chemicals cabinet. Proper labeling is essential, and it should be protected from light and sources of ignition. Handle using appropriate personal protective equipment.
    Application of 4-Chloromercuribenzoic Acid

    Applications of 4-Chloromercuribenzoic Acid in Industrial Manufacturing

    As a specialized manufacturer, we supply 4-Chloromercuribenzoic Acid to downstream sectors where its unique reactivity, specificity, and inhibition properties have reliable, well-documented technical value in complex process environments. Below, we outline the primary industrial fields utilizing this compound, with clear detail on regulatory requirements, operational formulation, downstream integration, and the major classes of end-use products.

    1. Enzyme Activity Assays in Biotech Quality Control

    4-Chloromercuribenzoic Acid serves a critical assay function in biopharmaceutical and biochemical manufacturing by acting as a selective inhibitor of sulfhydryl group-containing enzymes, enabling precise characterization and in-process control of enzyme preparations. Regulatory environments in these sectors mandate specification of reagents to avoid cross-contamination and ensure validated analytical protocols across batch release and process development.

    Industry compliance standards

    • USP General Chapter Enzyme Activity Assays
    • 21 CFR Part 211 – Good Manufacturing Practice for Finished Pharmaceuticals
    • EU GMP Annex 13 – Manufacture of Investigational Medicinal Products
    • ISO 17025 – General Requirements for the Competence of Testing Laboratories

    Typical usage ratio

    • Final reaction concentrations between 0.1 mM and 5 mM, precisely optimized against enzyme unit activity, substrate concentration, and detection method; adjusted specifically per protein target and assay format

    Downstream process integration

    • Added as a test reagent during QC analysis phases for activity quantification and stability studies of enzyme batches, post-fermentation and prior to formulation fill–finish

    Final product types

    • Biological reference standards, certified enzyme lots, and validated clinical assay kits

    2. Protein Structural Modification in Laboratory Reagent Production

    This compound acts as a targeted thiol modifier during analytical-grade reagent and protein sample preparation. It enables selective modification of free cysteine groups in polypeptides to facilitate detailed protein structure–function analysis, mapping disulfide linkages, and preparing derivatized proteins for downstream biophysical and immunoassay use. QC teams rely on strictly documented workflow integration and process residue controls for compliance.

    Industry compliance standards

    • ICH Q6B – Specifications: Test Procedures and Acceptance Criteria for Biotechnological/Biological Products
    • REACH Regulation (EC) No 1907/2006 for laboratory chemicals
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • Commonly applied at 0.5–10 molar equivalents relative to accessible cysteine residues; concentration tailored to protein size, degree of modification required, and solvent system

    Downstream process integration

    • Introduced in solution after buffer exchange, and prior to protein labeling, crystallization, or conjugation workflows in reagent-grade protein production

    Final product types

    • Derivatized protein reagents, cysteine-mapped peptides, and analytical protein standards

    3. Inhibitor Component in Diagnostic Kit Formulation

    Within the diagnostics industry, 4-Chloromercuribenzoic Acid serves as a selective reagent in kit systems requiring the suppression of undesired enzyme or protease activity, which could otherwise produce false readings or degrade biosensor elements. Diagnostic kit manufacturers must declare reagent identity and concentration for each kit batch, in compliance with regulated device documentation and safety stewardship requirements.

    Industry compliance standards

    • IVDR (EU 2017/746) – In Vitro Diagnostic Medical Devices Regulation
    • ISO 13485 – Quality Management Systems for Medical Devices
    • FDA 21 CFR 820 – Quality System Regulation

    Typical usage ratio

    • Integrated at final concentrations between 0.05–1 mM, based on target analyte, sample matrix, and specific kit architecture; adjusted according to batch verification results

    Downstream process integration

    • Added to stabilizing buffer solutions post-bulk reagent blending but prior to aliquoting and kit assembly under cleanroom conditions

    Final product types

    • Enzyme-linked immunosorbent assay (ELISA) kits, protease-inhibited nucleic acid detection kits, and biosensor-based clinical diagnostics

    4. Analytical Reference Material Preparation for Instrument Calibration

    Reference material producers integrate 4-Chloromercuribenzoic Acid as a calibrant or reaction marker in standards designed for spectrophotometric, chromatographic, or enzyme kinetic instrumentation. Its highly documented, quantifiable thiol reactivity ensures traceability and reproducibility needed for accredited laboratory calibration programs. Downstream users require clear demonstration of identity, purity, and batch reproducibility for compliance with international analytical standards.

    Industry compliance standards

    • ISO Guide 34 – General Requirements for the Competence of Reference Material Producers
    • ISO/IEC 17025 laboratory accreditation guidelines
    • USP General Chapter <11> – Reference Standards

    Typical usage ratio

    • Stock standards comprised of 1–100 μg/mL in specified solvent; end-user dilution determined by target calibration range and instrument specification

    Downstream process integration

    • Employed during reference material blend preparation, either as a primary quantitation analyte or a spike-in control for instrument calibration routines

    Final product types

    • Chemical reference material sets, instrument calibration solutions, and certified analytical standards for assay system validation
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    Certification & Compliance
    More Introduction

    4-Chloromercuribenzoic Acid: Direct from the Manufacturer

    Introduction to 4-Chloromercuribenzoic Acid

    For years, our daily work has revolved around developing and refining key organomercury compounds, and 4-chloromercuribenzoic acid holds a special place in our product line. Chemists who require sensitive, targeted reagents for biochemical and analytical applications often turn to this powerhouse. Its chemical profile (model: C7H4ClHgO2, CAS: 133-57-1) remains distinctive, with a unique combination of aromatic and mercurial functionality. This molecule consistently delivers high reactivity where selective binding to sulfhydryl groups matters most. Whether in protein modification, enzyme mechanism studies, or analytical detection, its ability to form strong covalent bonds sets it apart from generic benzoic acid derivatives.

    What Makes this Compound Stand Out

    From our vantage point at the reactor and the bench, the most striking feature of 4-chloromercuribenzoic acid lies in its performance reliability and targeting. Unlike standard benzoic acids or other halogenated aromatics, the addition of a tightly bound mercury atom opens the door to highly selective chemical reactions. In protein chemistry, this reagent offers a robust, predictable means of inhibiting thiol-containing enzymes. Researchers in our own pilot laboratories often comment that it gives a reproducible, rapid response not seen with other compounds that lack this mercurial functionality.

    Handling a compound like this requires a respect founded on both experience and science. As a direct manufacturer, we have long-established control over quality and purity, reaching a minimum of 98% as consistently confirmed by both titrimetric and chromatographic methods. Our facility staff knows from daily batches that classic issues like trace impurity, solvent residue, or batch variability simply don’t show up in our finished material. We do this with our own process, with all steps—from synthesis, washing, and drying to final vialing—contained inside a single production block. We do not outsource, and we track the entire process, batch by batch. This guarantees traceability and repeatability for chemists who need results, not surprises.

    Real-World Examples: Our Compound in Use

    In practical reality, 4-chloromercuribenzoic acid enjoys continued demand among researchers studying enzyme catalysis and protein-ligand interactions. It has become a classic tool for probing cysteine residues within complex proteins. For instance, in mitochondrial enzyme studies, the compound easily forms stable mercaptide bonds with active site cysteines, revealing detailed function with less ambiguity. Several clients in pharmaceuticals use our acid to determine the presence and accessibility of sulfhydryl groups. The sharp color change seen during reaction—a visual confirmation of the compound’s power—has made troubleshooting much more manageable.

    A further example can be found in membrane biochemistry. 4-chloromercuribenzoic acid has proven invaluable for characterizing membrane protein topology, especially in separating cytosolic from membrane-facing thiols. Our in-house technical team has supported countless projects that rely on this reagent for pinpoint selectivity in the modification of proteins under mild, aqueous conditions. Such selectivity cannot be achieved with more common, broader-acting reagents like iodoacetamide or N-ethylmaleimide; the specificity stems directly from the mercurial moiety.

    Product Handling and Storage Based on Firsthand Knowledge

    Over time, we have learned the nuances of safe, effective handling of this material. Users benefit from our insights as primary producers. The solid appears as a white to off-white powder, very slightly hygroscopic. This is not a compound for just any lab shelf: secure storage in tightly sealed containers, out of direct sunlight, and away from strong acids or bases keeps it at top quality for months. We recommend glass for long-term storage—plastic containers can leach or shed trace contaminants that no researcher wants added to a sensitive reaction. Cold rooms or dry cabinets extend shelf life, but repeated freeze-thaw cycles are unnecessary. These facts come not from safety data sheets alone, but our direct audits and batch monitoring in production and downstream applications.

    We don't simply sell a chemical—we provide clear, informed recommendations based on decades of daily handling. Because 4-chloromercuribenzoic acid presents moderate toxicity due to its mercury content, direct contact with skin or inhalation of dust is something to truly avoid. This seems like common sense to a trained chemist, but we often get questions about best work practices. From our experience, routine glove and laboratory coat use is non-negotiable. Effective ventilation and the use of a fume hood become standard procedure both in synthesis and analytical work-up. We strive to eliminate known hazards at the manufacturing stage, but safe lab technique never loses its value.

    Differences from Related Compounds

    Much of the confusion in the market comes from misidentification—traders and resellers sometimes offer benzoic acid compounds or even unrelated mercurials where genuine 4-chloromercuribenzoic acid is requested. As direct manufacturers and users, we have learned to spot true distinctions immediately. Standard mercury benzoates, for instance, lack the electron-withdrawing chloride substituent seen in the 4- position, which gives our product a distinct spectral signature and a sharper, more reliable binding profile in biological assays.

    Iodo- and nitro-substituted benzoic acids sometimes compete for attention in literature reports, but in practice, their reactivity toward protein thiols lacks the tuning provided by the chloride-mercury combination. Our product's strong preference for cysteine over other amino acid residues gives scientists confidence to interpret their results without second-guessing the integrity of their modifications. This specificity minimizes side reactions which might obscure experimental outcomes—a concern echoed repeatedly by our clientele and our own laboratory chemists.

    Some laboratories inexperienced with organomercurials try broad application of more aggressive agents like mercuric chloride. From our observations, these reagents fail to discriminate between subtle structural differences in proteins or small molecule targets. 4-chloromercuribenzoic acid delivers a measured potency—enough to fully engage with reactive thiols yet gentle enough to avoid complete protein denaturation in most settings.

    Where a project demands reversibility, our compound operates under clear protocols that allow downstream de-mercuration, preserving protein activity for further analysis. We always advise on the latest literature-supported protocols in our technical documents, but real-world troubleshooting remains our specialty. Researchers value our transparency and the guarantee that what arrives in their laboratory is precisely what is specified, without “substitution” or “analogue” confusion.

    Our Experience with Synthesis and Manufacturing Quality

    Decades inside our own plant bring a perspective you won’t hear at a trade desk or sales booth. The synthesis of 4-chloromercuribenzoic acid poses unique challenges; improper reaction control can drive up unwanted side-products, like diphenylmercury or mercury oxides, which degrade both activity and lab safety. Through multi-stage reaction monitoring and end-point analytical testing, we keep each crystal batch within strict specification. Every barrel, every jar comes with our documented record of analytical verification going back to source materials.

    We have learned that even the minute presence of water or peroxide by-products can disrupt the performance of the compound in downstream enzyme assays. Recrystallization, slow-cooling, and vacuum drying protocols—all handled in-house—assure a consistent material. Repeated feedback from academic and pharmaceutical laboratories confirms their satisfaction. Unlike generalized approaches, we only use high-purity precursors with certificates tracked by batch number in our digital system.

    These practical standards create trust, not simply a checklist or formula. We do not cut corners, blend with cheaper analogues, or substitute raw materials. By retaining full control over every step, we guarantee both product identity and robust supply continuity, even as global logistics fluctuate. Colleagues in quality control and technical service know the faces and records behind each outgoing shipment, not just a bar code or product code.

    Application Insights from Customer Feedback

    Working close with academic consortia and biotech firms, we receive regular reports on project successes and challenges. Many teams share their concern over batch consistency, especially given the delicate kinetics involved in protein modification. Our chemists have collaborated to optimize not only the synthesis, but also detailed application notes that clarify molar ratios, optimal solvents (typically aqueous buffer at pH 6–7.5), and compatible co-reagents. This knowledge goes well beyond any printed specification sheet—it's built on repeated, hands-on project troubleshooting.

    We have watched researchers frustrate themselves with less-pure or poorly stored reagent from non-manufacturer sources. The outcomes can range from spurious assay inhibition to complete enzyme inactivation. Reliable inhibition or labeling, with full reversibility and minimal background reactivity, requires genuine compound and careful handling.

    Our own in-house investigations validated performance with a wide range of protein targets, under both denaturing and native conditions. We routinely test every production batch using model enzymes like papain or alcohol dehydrogenase to verify reaction speed and endpoint color change. Collaborative work with leading biochemists has shaped the training we provide; we've established protocols for both standard and advanced labeling, always with the intention of taking unnecessary mystery out of the process.

    Environmental and Regulatory Perspective

    As organomercury compounds rightfully draw close attention for environmental safety, we recognize the responsibility borne by a direct producer. Over the years, regulatory standards concerning mercury handling and waste management have become much stricter. Unlike brokers or resellers, we design all process streams to capture, recycle, and safely neutralize merited waste. We run closed-cycle production, preventing condensation or aerosol escapes at every stage.

    Waste disposal partners undergo rigorous review and materials tracking to meet evolving local and global requirements. Every kilogram shipped is accounted for with precise documentation. These oversight systems started long before recent regulatory changes, building on decades of responsible production. Our experience proves that compliance and high quality do not conflict—if anything, our customers’ trust only grows when they know their supplier invests in zero-discharge process technology.

    On the customer side, we offer detailed disposal advice and ready access to material safety expertise drawn from our own plant protocols. We never treat this as an afterthought, and we keep channels open for ongoing support. An informed user makes for a safer laboratory, and the commitment extends from our plant gate all the way to the researcher’s bench.

    Challenges and Ongoing Solutions

    No chemical manufacturer can ignore the challenges that come with organomercury compounds. Supply chain fluctuations, evolving transport regulations, and the growing need for transparency all shape our ongoing improvements. As global carriers revisit their allowable lists for hazardous products, we continually adapt our packaging to meet strict international shipping codes. Each drum and ampoule includes tamper-proof seals, serialized tracking, and robust shock-proof housing to prevent in-transit degradation.

    From a user’s perspective, some laboratories face difficulty disposing of expired chemical stock due to regional regulations. Our team is on call to advise on compliant disposal pathways, including consolidation and certified neutralization. We know from our own experience that early planning for end-of-life management reduces both environmental impact and administrative headaches.

    Supply continuity remains at the heart of production planning. Our site invests in buffer stock and raw material sourcing from dual suppliers in different geographic zones. We found years ago that this strategy prevents interruption, even during market volatility or transport restrictions. By making sure our production line never stops, our partnerships with universities and industry stay reliable and productive.

    Looking Forward: Sustainable Manufacturing and Advanced Research

    We never rest on tradition alone. Ongoing investment in process automation, in-line sensors, and real-time analytics has deepened our insights into every step of production and purification. These advances help to catch issues before they manifest downstream, allowing us to assure each client that the material they order today matches what they received a year—or even a decade—before.

    Our technical staff regularly engage with the research community to evaluate emerging needs. As new biochemistry techniques develop, we participate in roundtable discussions and collaborative research aimed at optimizing the design, handling, and disposal of organomercurials. Our input draws directly from real manufacturing challenges, not hypothetical scenarios, providing practical guidance for greener chemistry and enhanced safety measures.

    Development projects are ongoing in trace-impurity testing, finding new ways to minimize background noise in advanced proteomics workflows. Work on solvent-free production routes, alongside closed-cycle mercury recovery, reflects both environmental awareness and production efficiency. Direct manufacturer experience steps up here: We can test, pilot, and implement changes much faster than third-party marketers or contract manufacturers, rolling out innovations in quality and sustainability at scale.

    Conclusion: Why Experience Matters in Choosing 4-Chloromercuribenzoic Acid

    4-chloromercuribenzoic acid stands as more than a catalog number or a name on a label. Our years of direct experience have given us a nuanced understanding of what matters in production, quality control, and end-user application. Customers who choose our compound know that they gain more than a bottle of reagent—they receive a commitment to consistent performance, real safety, and practical advice. Our continuous hands-on involvement, unwavering attention to purity, and active engagement with both technical standards and environmental best practices set us apart in a crowded and often confusing global market. With every batch, we build not only on past successes but on a living, working partnership between our plant and the world’s scientific community.