Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Carbonyl Cyanide 3-Chlorophenylhydrazone

    • Product Name Carbonyl Cyanide 3-Chlorophenylhydrazone
    • Alias CCCP
    • Einecs 221-372-5
    • 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

    843219

    Chemical Name Carbonyl Cyanide 3-Chlorophenylhydrazone
    Abbreviation CCCP
    Cas Number 555-60-2
    Molecular Formula C9H5ClN4
    Molecular Weight 204.62 g/mol
    Appearance Yellow crystalline powder
    Melting Point 187-189°C
    Solubility Slightly soluble in water, soluble in DMSO and ethanol
    Storage Conditions Store at -20°C, protected from light
    Primary Use Mitochondrial uncoupler in biochemical research

    As an accredited Carbonyl Cyanide 3-Chlorophenylhydrazone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 5 grams of Carbonyl Cyanide 3-Chlorophenylhydrazone, sealed with a plastic cap, labeled with hazard symbols.
    Shipping Carbonyl Cyanide 3-Chlorophenylhydrazone should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be handled as a hazardous chemical, packaged according to local and international regulations, and transported with proper labeling and documentation to ensure safety and compliance during transit.
    Storage **Carbonyl Cyanide 3-Chlorophenylhydrazone** (CCCP) should be stored tightly sealed in a cool, dry, and well-ventilated place, away from light and incompatible substances such as oxidizers. Store at 2–8 °C (refrigerated) and protect from moisture. Use appropriate chemical-resistant containers and keep the substance away from heat sources, flames, and direct sunlight. Properly label the container to avoid accidental misuse.
    Application of Carbonyl Cyanide 3-Chlorophenylhydrazone

    Applications of Carbonyl Cyanide 3-Chlorophenylhydrazone in Industrial Manufacturing

    As a direct manufacturer of Carbonyl Cyanide 3-Chlorophenylhydrazone (CCCP), we supply this specialized compound for tightly regulated downstream sectors. We support industrial users with consistent quality and documented traceability at each manufacturing stage, focusing on application areas validated through mainstream industrial practice and reliable compliance requirements.

    1. Mitochondrial Uncoupling in Bioenergy Research and Pharmaceutical Screening

    Research and industrial laboratories use our material to disrupt mitochondrial oxidative phosphorylation when screening compounds for bioenergetic modulation and metabolic disorder therapeutics. In both high-throughput assay development and reference control for pharmaceutical testing, CCCP provides a reproducible benchmark for measuring mitochondrial membrane potential and respiratory chain functions in cell-based assay systems. This usage requires accurate mass balance and stringent contamination controls due to regulatory oversight in pharmacological research environments.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) guidelines for impurity profiling in research reference materials.
    • ISO/IEC 17025:2017 laboratory testing and calibration requirements.
    • Good Laboratory Practice (GLP, OECD Principles) for compound handling and solvent use.
    • FDA 21 CFR Part 58 for pharmaceutical laboratory quality.

    Typical usage ratio

    • In cell-based assays, concentrations range from 0.1 μM to 10 μM depending on target cell line and assay sensitivity.
    • Exact dosing determined by membrane potential reduction endpoints in calibration runs.

    Downstream process integration

    • Material added to assay media during mitochondrial function analysis as an uncoupling agent.
    • Used in quality control reference kit formulation for screening libraries.

    Final product types

    • Pharmaceutical research kits.
    • Bioassay quality control standards.
    • Reference compounds for cell biology laboratories.
    • Custom high-throughput screening plates for pharmaceutical development.

    2. Uncoupler Use in Industrial Microbial Metabolism Optimization

    Bioprocessing plants deploy micro-scale CCCP additions to microbial fermentation broths to modulate ATP synthesis and electron transport. This process can improve yield coefficients or shift metabolic fluxes in certain strains of yeast and bacteria, especially during process development for biofuel, biopolymer, or specialty biochemical synthesis. Accurate CCCP use is subject to strict biosafety and production documentation, as the compound’s impact on end-product purity necessitates downstream analytical verification for industrial biotechnology applications.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – FDA 21 CFR Parts 210 & 211.
    • ISO 9001:2015 for quality management in industrial biotechnology.
    • OECD Guidelines for the Testing of Chemicals (for fermentation additions in biotech).
    • National Biosafety Standards for Genetically Modified Organisms (if GMO strains involved).

    Typical usage ratio

    • 0.05 to 2 mg/L (ppm) in fermentation broths, titrated during metabolic shift experiments.
    • Amount determined by strain tolerance and bioprocess endpoints for yield or substrate-to-product conversion efficiency.

    Downstream process integration

    • Dosed during early to mid-log growth phase for controlled respiratory chain uncoupling.
    • Process engineers monitor oxygen uptake and ATP production rates via in-line sensors.

    Final product types

    • Bio-based solvents (e.g., ethanol, butanol).
    • Industrial organic acids (e.g., lactic acid, citric acid from fermentation).
    • High-value specialty biochemicals.
    • Commercial biosynthetic flavors and fragrances.

    3. Reference Standard for Toxicity and Efflux Pump Screening in Antimicrobial Research

    Manufacturers and contract research organizations use our material as a validated efflux pump inhibitor and cytotoxicity reference agent in industrial antimicrobial screening. Its incorporation is crucial for comparative testing protocols aimed at quantifying multidrug-resistant (MDR) bacterial response, as well as benchmarking new efflux pump inhibitor candidates. Strict documentation and in-lab hazard management are required to meet international safety guidelines and regulatory expectations for chemical risk in research and industrial QC settings.

    Industry compliance standards

    • GLP – OECD Principles for safety pharmacology and microbiology testing.
    • ISO 17034:2016 for reference material producers.
    • OSHA Hazard Communication Standard for lab chemical handling (if United States production/lab site).
    • REACH Substance Registry (if relevant for EU use).

    Typical usage ratio

    • Ranges from 2.5 µM to 50 µM, as a control agent in high-throughput efflux activity and toxicity assay wells.
    • Dosing benchmarked against typical MDR bacterial minimum inhibitory concentration windows.

    Downstream process integration

    • Incorporated into 96-well or 384-well plate formats as part of industrial screening protocols.
    • Chemical addition occurs immediately prior to microbial inoculation or efflux pump activation studies.

    Final product types

    • Clinical MIC assay panels.
    • Reference QC kits for antimicrobial susceptibility testing.
    • Industrial R&D microbial efflux screening systems.
    • Preclinical antibiotic discovery pipelines.

    4. Mitochondrial Function Modulation in Pesticide and Agrochemical Toxicology Testing

    CCCP is regularly deployed in accredited agrochemical toxicity laboratories as a mitochondrial disruptor control during environmental fate and toxicodynamics assessments. The compound assists in validating the impact of novel pesticides on non-target species’ oxidative phosphorylation, ensuring compliance with regulatory evidence requirements for registration dossiers. High-purity grades and batch-to-batch consistency are essential for inclusion in validated test protocols and documentation necessary for regulatory acceptance.

    Industry compliance standards

    • OECD Test Guideline 202: Daphnia sp. Acute Immobilisation Test.
    • USEPA OPPTS 850.1300 – Aquatic Invertebrate Acute Toxicity Test.
    • Good Laboratory Practice (GLP) as per 40 CFR Part 160 and equivalent OECD requirements.
    • ISO 17025:2017 – chemical and biological testing laboratories quality control.

    Typical usage ratio

    • Commonly dosed at 0.5 μM – 5 μM for acute aquatic toxicity protocols.
    • Specific concentration calibrated based on species and end-point analysis as per test guidelines.

    Downstream process integration

    • Added into aquatic media or soil matrices as a positive control for mitochondrial toxicity verification.
    • Sample preparation conducted in validated, contamination-controlled environments before acute and chronic toxicity studies.

    Final product types

    • GLP-validated toxicology data sets for regulatory submissions.
    • Agrochemical safety registration dossiers.
    • Environmental fate testing reports for commercial pesticide development.
    • Quality control control charts for toxicity laboratory accreditation.
    Free Quote

    Competitive Carbonyl Cyanide 3-Chlorophenylhydrazone prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing Carbonyl Cyanide 3-Chlorophenylhydrazone: Insights From the Factory Floor

    What We Know About Carbonyl Cyanide 3-Chlorophenylhydrazone

    From years at the reactors and on the blending lines, Carbonyl Cyanide 3-Chlorophenylhydrazone—often abbreviated in our shop as CCCP—stands out as a critical tool in cell research and bioenergetics. We work with a range of specialty chemicals, and CCCP holds a firm spot on our line due to its reliable performance in mitochondrial research. Our batches use analytical grade raw materials to reach consistent purity, targeting specifications by mass and absorption range every time. Looking at the fine, pale yellow to tan crystalline powder in the drum, the trained eye sees more than a product—CCCPC means precision, control, and years of development work.

    Why CCCP Remains a Mainstay in Research

    We live in a time when labs dive deeper into biochemistry and cell physiology than ever. Researchers trust CCCP for its role as a potent protonophore—its ability to dissipate the proton gradient across mitochondrial membranes makes it indispensable for studies focused on ATP synthesis and oxidative phosphorylation. Early on, colleagues from academia sent feedback about the need for cleaner, more homogenous samples, because even minor impurities lead to experimental variability. Years later, our team still uses high-efficiency purification to achieve levels meeting or exceeding standard molecular biology requirements, reducing background noise in both in vitro and in vivo assays.

    Manufacturing CCCP demands strict control of conditions. Even a slight deviation in temperature or the order of reagent addition shifts the color, texture, or melting point. In practice, our operators—drawn from years of organic synthesis—monitor reactions with a mixture of analytical instrumentation and hard-earned instinct. The result: consistent pH stability in solution, better lot-to-lot reproducibility, and a product that meets rigorous expectations from the research bench to pilot-scale projects.

    Model Details and Batch Specifications

    We standardize our lot models according to customer preference. For most, the focus remains on obtaining CCCP as a high-purity crystalline powder, typically packaged in amber vials to limit photodegradation. Moisture content and residual solvent levels matter, both for lab safety and for research reproducibility. While some older syntheses might leave higher levels of 3-chlorophenylhydrazine, newer protocols—and a decade’s worth of tweaking column prep—mean we routinely meet low ppm thresholds.

    Our regular production batches vary in size, but expectations don’t change. From the kilo-scale drum filled for contract research organizations to the few grams precision-dispensed for university teams, the same standardized QC protocol applies. NMR, HPLC, and melting point checks mean no batch leaves the plant without verification. Smaller producers and traders struggle to offer this level of screening consistently. From the factory perspective, every error means days lost and trust eroded, so we never cut corners on product verification.

    What Sets Our CCCP Apart from Others

    Years ago, we heard complaints from customers who sourced their CCCP from shadowy traders. Complaints ranged from slow dissolution in DMSO to variability in biological assays—a reflection of less rigorous manufacturing. By contrast, our batches show predictable solubility profiles in both DMSO and ethanol. Quality matters most in biological applications: inconsistent purity forces researchers to spend time on validation rather than experimentation.

    A decade ago, the only supply source lay overseas, which meant risky shipping periods, uncertain paperwork, and, worse, inconsistent documentation of impurities. Our operation narrows these margins by managing synthesis under controlled conditions and performing in-house analytical verification. Documentation follows each bottle—traceability spans the raw input through final QC, so labs can track every gram matched to its analytic fingerprint.

    Typical Usage and Handling Practices

    Researchers approach CCCP with caution, respecting both its capability and toxicity. On our end, strict personal protective equipment standards mean goggles, gloves, and thorough ventilation throughout the plant. That concern carries over to the lab, where the smallest weighing error loads cells with excessive uncoupler and can revert years of effort.

    A typical usage profile for CCCP involves preparing fresh stock solutions in DMSO at known concentrations—often in the 10 to 50 mM range—before application to cultured cells or mitochondrial suspensions. Mitochondrial uncoupling studies hinge on CCCP’s reliability to induce proton leak at the inner mitochondrial membrane, shifting ATP synthesis and allowing direct measurement of respiratory control ratios.

    We field calls from postdocs troubleshooting applications: sometimes a lot of CCCP shows different activity at a set dose, which typically ties back to either compound purity, incorrect storage, or improper solubilization. We advise storage at -20°C, in the dark, and recommend using aliquoted bottles to minimize freeze-thaw cycles. Some competition ships in bulk—each time the container opens, ambient moisture creeps in, leading to gradual decomposition and lower activity. Our vials stay sealed from synthesis through delivery, a habit born of too many near-misses in early production runs.

    Real-World Results: Supporting Data, Not Just Hype

    Feedback from university and industrial labs bears out our manufacturing approach. Researchers reporting clean titration curves, reproducible outcomes in respirometry, and unambiguous shifts in mitochondrial potential—these updates shape our next batch cycle. Experience tells us that real-world performance beats any sales pitch. When we benchmark against commercial samples from overseas brokers, our customers bring back sharper baselines in Seahorse or Oroboros flux assays, and smoother dose-response relationships.

    CCCP’s effect isn’t confounded by high levels of residual organics or inconsistent melting points, both common when manufacturers cut steps out of the process. Consistency matters more than anything—labs invest years in designing controls and experimental groups. A batch-to-batch drift means wasted time, lost samples, and harm to grant-backed projects. Our teams keep this in focus by regularly updating protocols and calibrating instruments, guaranteeing that our product turns up just as researchers expect.

    Comparisons with Other Uncouplers and Related Products

    In our own production line, the difference between CCCP and other mitochondrial uncouplers like FCCP and DNP lies both in the chemistry and the handling. CCCP shows a robust ability to collapse the proton gradient at nanomolar to micromolar ranges, giving finer control in titration-based assays. DNP used to be in wider circulation, but its broader uncoupling, regulatory concerns, and broader toxicity have shifted most labs toward CCCP for safer, more targeted work.

    In terms of solubility, CCCP offers clear benefits. It dissolves readily in polar aprotic solvents, remains stable through multiple experimental cycles, and does not introduce background absorption in common biological detection ranges. Compared to FCCP, which some customers report as harder to work with due to bright yellow color bleeding into experimental reads, CCCP remains comparatively easy to quantify and control.

    A key manufacturing lesson comes from the handling challenges—FCCP and DNP both require additional stabilization steps if handled at scale, frequently leading to increased cost and risk. CCCP’s crystalline format remains workable, and contamination with by-products is easier to avoid given its straightforward synthesis and purification path. The compound withstands careful handling and storage, preserving biological activity for weeks, sometimes months, under the right freezer conditions.

    A clear view from the plant shows that CCCP’s major competitors struggle with loss of potency on prolonged storage, bringing in the worry of inefficient experiments and misinterpreted results. By locking in storage stability and minimizing degradation routes, we reduce these risks, helping our customers focus on results rather than troubleshooting faulty chemicals.

    Addressing Supply, Safety, and Regulatory Considerations

    Discussions with customers and project leads often raise questions of supply chain transparency and regulatory compliance, especially as global standards for chemicals tighten. On our end, every raw material shipment is tracked, and each input batch is checked for both purity and source legitimacy. It’s not unusual to spend time auditing suppliers of chlorinated hydrazines to guarantee that no banned or hazardous precursors slip into the process stream.

    As for regulatory handling, CCCP comes flagged for occupational safety, acute toxicity, and storage limits. Our on-site chemical engineers regularly audit storage areas, maintain controlled-temperature containment, and train staff for accidental exposure scenarios. This is not optional, and years of incident-free operation speak to the value of preparation and planning. Outbound shipments always include detailed safety documentation, including handling, storage, and disposal guidance, stamped with batch-specific test results—not boilerplate. We push our entire facility to move beyond simple checklists, weaving safety into the mindset of every operator.

    Global shipping raises its own hurdles—permitting, customs, and declarations require meticulous documentation. Our records keep each lot traceable, which satisfies import controls for most major research regions. Repeatedly, we see customers sigh with relief at receiving full authentication, since fly-by-night sellers frequently ignore these essentials, putting not just intellectual property but personal safety at risk.

    Improving Processes: Feedback and Continuous Refinement

    Our evolution as a chemical manufacturer did not happen in a vacuum. Early missteps—lots spoiled by minor contaminants, lost shipments, unexpected shelf life issues—have shaped our procedures. A hands-on approach, talking directly to research teams and QC labs, forged better procedures and smarter quality controls. With each cycle, analytical staff update protocols to catch even minor deviations in retention time or crystallinity. We build redundancy into the system, so that no human error, however minor, passes into the customer’s hands.

    Recent years have seen more calls for “green chemistry” protocols—safer solvents in waste streams, tighter containment of by-products, further reductions of trace organics. We make incremental improvements every year, retraining staff and adapting new purification technologies as they become viable. Not all innovations work on the first try, but a commitment to continuous improvement brings cleaner final products and makes a difference in day-to-day plant operation.

    We see value in taking feedback not as criticism, but as a roadmap for improvement. Researchers dealing with highly sensitive mitochondrial models call for ever stricter tolerances in product homogeneity. Responding to this shaped our recent reviews of fractionation steps and encouraged us to invest in new analytical standards. With CCCP, the margin between success and failure can be a matter of micrograms—a lesson we take to heart as every measurement builds trust between bench and factory floor.

    Meeting New Research Challenges with Reliable CCCP

    The field of bioenergetics isn’t standing still. As the push for new therapeutics ramps up, customers extend CCCP’s applications—probing ATP dynamics in stem cells, mapping chemoresistance in cancer lines, and even studying neurodegeneration at the cellular level. We monitor scientific literature closely, watching for shifts in experimental design that demand new formats—smaller aliquots, less hygroscopic packaging, or even higher-purity grades for single-cell work.

    We send samples to independent labs for cross-validation, pitting our CCCP against imported benchmarks and publishing the results when appropriate. This open-door approach, with data open to scrutiny, wins loyalty from long-term partners. The product’s reliability lets researchers focus on generating knowledge, not doubting their reagents.

    Manufacturing experience means more than recipes—it requires attention to the full life cycle from roll-off to researcher’s hand. We listen to requests for special pack sizes or dry ice shipping, adjusting logistics so that the compound arrives intact, active, and ready. The fate of a research project can rest on one bottle, so we sweat the details every step of the way.

    Lessons Learned From Decades of CCCP Production

    The story of CCCP at our plant is one of gradual refinement and listening to the needs of real users. Early runs, back when glass still reigned in the blending area, often led to granulation issues or static charge mishaps. We learned to minimize exposure to ambient air, switched to higher purity solvents, and built better workflows to separate each batch by time and space. These sound like small factors, but every step protects purity and ensures the biological impact researchers expect.

    Maintenance, troubleshooting, and instrument calibration matter as much as chemistry. Failures in titration or identification—no matter how rare—mean taking extra hours to retrace steps and locating root causes. Most chemical engineers love the challenge, but the goal never changes: deliver what was promised, with documentation to back it up.

    We take pride in being a direct manufacturer, not a reseller. That distinction means if something goes wrong, or a novel research demand emerges, our project managers loop it directly to production and analytics. This close feedback loop shapes every improvement. While we’ve learned from international standards, the best outcome always comes from direct, transparent communication with those relying on CCCP daily.

    What’s Ahead for CCCP and the Research Community

    Looking forward, demand for reliable mitochondrial uncouplers continues to grow. As a core ingredient for understanding cellular metabolism and testing new therapies, CCCP’s quality and availability increasingly shape the pace of scientific discovery. We’re investing in greener syntheses, better waste treatment, and new analytical technologies because every one of these advances ultimately benefits the research community.

    Responsibility as a manufacturer goes beyond shipping boxes. It reaches into laboratory workflows, grant-supported projects, and the work of scientists unraveling complex biology. We treat every lot as a connection—between the factory floor and the bench, between careful chemical synthesis and hundreds of hours of hard-won data.

    Carbonyl Cyanide 3-Chlorophenylhydrazone isn’t just another reagent in our catalog. It’s the sum of years of incremental improvements, careful listening, and a commitment to supporting those forging new paths in biology and medicine. As long as the research community needs CCCP that delivers consistent, clean, and predictable results, we’ll keep refining our processes—always looking for another margin of improvement, always aiming to back the work that changes what’s possible in science.