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Dithizone

    • Product Name Dithizone
    • Alias Diphenylthiocarbazone
    • Einecs 202-065-7
    • 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
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    Specifications

    HS Code

    623747

    Chemical Name Dithizone
    Synonyms Diphenylthiocarbazone
    Cas Number 60-10-6
    Molecular Formula C13H12N4S
    Molecular Weight 256.33 g/mol
    Appearance Dark green powder
    Melting Point 168-170°C
    Solubility Slightly soluble in water, soluble in organic solvents such as chloroform and carbon tetrachloride
    Color Change Forms colored complexes (typically green to red) with certain metal ions
    Usage Used as an analytical reagent for detection of heavy metals
    Storage Conditions Store in a cool, dry place, protected from light

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

    Packing & Storage
    Packing Dithizone is packaged in a 25g amber glass bottle with a tightly sealed cap, labeled with hazard warnings and product details.
    Shipping Dithizone should be shipped in tightly sealed containers, protected from light and moisture. It must be kept cool, dry, and away from incompatible materials such as strong oxidizers. During transit, proper labeling and documentation are required due to its hazardous nature. Handle according to relevant chemical safety and transportation regulations.
    Storage Dithizone should be stored in a tightly sealed container, protected from light, moisture, and air to prevent degradation. Keep it in a cool, dry place, ideally in a desiccator or a refrigerator (2–8°C). Ensure storage is separate from incompatible substances such as strong oxidizing agents and acids. Always follow safety guidelines and local regulations for chemical storage.
    Application of Dithizone

    Purity 99%: Dithizone with 99% purity is used in heavy metal ion detection assays, where it enables high-sensitivity quantification of trace metals.

    Melting Point 130°C: Dithizone with a melting point of 130°C is used in solvent extraction processes, where it ensures thermal stability during metal separation.

    Particle Size <10 μm: Dithizone with particle size below 10 μm is used in thin-layer chromatography, where it provides enhanced resolution for metal chelate separation.

    Stability Temperature up to 80°C: Dithizone stable up to 80°C is used in automated spectrophotometric analyzers, where it maintains consistent complexation for reliable analytical results.

    Molecular Weight 256.33 g/mol: Dithizone with molecular weight of 256.33 g/mol is used in quantitative titration procedures, where it allows precise stoichiometric reaction with metal ions.

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    Certification & Compliance
    More Introduction

    Dithizone: A Closer Look at a Time-Tested Reagent

    In laboratories across the globe, researchers seek tools that deliver reliability, clarity, and results they can trust. Dithizone, known chemically as diphenylthiocarbazone, has built a quiet legacy among classic analytical reagents. Its story begins early in the twentieth century, when a handful of chemists discovered its uncanny knack for binding heavy metals with a distinct, colorful touch. Unlike many technical chemicals that fade into obscurity as new compounds arrive, Dithizone keeps drawing interest, especially from those who value a method that works as hard as they do. Turning to this reagent for qualitative and quantitative heavy metal analysis reflects both science’s stubbornness and its appreciation for elegant solutions. The latest model, appearing as either a green crystalline powder or solution, shows respect for its roots while meeting today’s lab requirements.

    Every researcher I’ve met who works with trace metal analysis tells stories about their “Aha!” moment with Dithizone. Its sharp green hue in the bottle piques curiosity, but its real allure shows up in action: It changes colors when it interacts with metals like lead, zinc, mercury, or cadmium, acting as a sort of chemical litmus test. In my graduate days, I watched an old-school chemist swirl a solution of lead and Dithizone under dim florescent lights. The mix turned crimson, a visual cue so vivid it left no room for doubt. Nature rarely delivers such generous signals, which explains why scientists and technicians, confronted with complex samples in water, soil, or food, return to Dithizone time and again. There are more advanced instruments now, boasting detection at terrifyingly low parts per trillion, but the straightforward color reaction Dithizone gives remains tough to beat for directness.

    How Dithizone Stands Out in Practical Terms

    There’s no shortage of reagents on lab shelves, yet few operate like Dithizone. Many modern detection kits come hermetically sealed, paired with a step-by-step Android app that guides users through every motion. That slick efficiency certainly matters, but these aren’t always the answer when you need to go off the grid, analyze a remote river, or teach students the basics of inorganic chemistry. Dithizone asks for patience and care. It dissolves best in carbon tetrachloride or chloroform, and from there it meets samples through liquid-liquid extraction, a process that might seem quaint by today’s standards but proves remarkably effective. It’s in those moments, pipette in hand, that the hands-on nature of classical chemistry comes alive.

    For those used to complex calibration curves on a multimillion-dollar atomic absorption spectrometer, Dithizone’s colorimetric response feels like a return to a physical language anyone can sense. Pink from lead, orange from zinc, blue with cobalt. You don’t need a technical manual to guess what’s in your beaker; your eyes do the work. In my own teaching experience, students always reacted with amazement, realizing that the transition from invisible ions to visible color bridges the gap between the microscopic and the everyday.

    Some will argue that more sophisticated digital systems measure metals with greater precision, even down to single molecules. That’s true. Yet with Dithizone, you get speed, and you get an honesty about the presence–or absence–of contaminants that no machine noise or arcane computer calibration can obscure. The kit can be carried in a pocket, no batteries needed, and delivers results without specialized training. In field work, this matters more than pixel-perfect precision.

    Core Model and Specifications: What You’ll Find in the Bottle

    Every bottle labeled Dithizone contains diphenylthiocarbazone as its active component. Most suppliers offer it at 98% or greater purity, ensuring that reactions in the test tube reflect the real presence of target metals in a sample, not background impurities. Chemists typically find it as a green to dark-green crystalline powder, though some prefer it in pre-diluted solution for ease of use. The compound boasts a melting point around 150°C, far above room temperature, adding to shelf stability. Light and air can degrade it, so old hands know to keep bottles tightly sealed and away from sunlight. Experience has taught me how a little neglect on the shelf can dim Dithizone’s potency, so attention to storage keeps analyses sharp.

    Typically, Dithizone reacts with cationic metals in mildly acidic conditions. Its real strength lies not just in the beauty of the colors, but the specificity: its strong binding affinity for divalent and higher cations means it gives clearer results for lead, zinc, and mercury than organic analogs. The molecular system forms colored chelates–complexes any undergraduate organic chemistry student would recognize in a heartbeat–whose distinct shades tell you exactly what you’re looking at. That speed and selectivity set it apart from simpler indicators, which blur distinctions or give muted hints rather than direct answers.

    No one would call Dithizone foolproof; false positives creep in if samples contain interfering ions, especially copper or other transition metals. Over the years, tricks of the trade have emerged: masking solutions, pre-treatment of samples, the use of buffer solutions to hold pH steady during extraction. These refinements owe much to patient practitioners who experimented within the confines of cramped, underfunded labs and whose marginal notes in textbooks still guide best practice today.

    Beyond the Bench: Dithizone’s Place in Environmental and Food Testing

    With growing alarm over heavy metal pollution in water, soil, and even staple foods, robust screening takes on extra importance. Dithizone slips easily into this role, supplying quick visual clues about contamination. During a summer internship with an environmental lab, I watched field scientists patrol rivers downstream from mining sites, Dithizone kits in hand. Without the luxury of laboratory conditions, they added a few drops to river samples and looked for the telltale hues. Within minutes, they could flag problem areas and decide where to send more detailed samples. Not every locality can fund continuous monitoring with advanced spectrometers, but Dithizone opens the door to watchdog efforts anywhere vigilance matters.

    This accessibility is not lost on food safety experts. A colleague in agricultural science described using Dithizone to test fresh produce for lead and cadmium contamination, a widespread worry where irrigation water is not strictly controlled. While official confirmation still follows with standardized laboratory methods, a Dithizone screening gives farm inspectors and exporters enough information to block unsafe shipments early in the chain. For communities at risk of tainted food passing undetected, that rapid check becomes a lifeline.

    What Makes Dithizone Different from the Rest

    Looking at the broader landscape, Dithizone belongs to a category of reagents called organic ligands–compounds that pair with target ions to signal their presence through changes you can see. Rivals include diethyldithiocarbamate, Eriochrome Black T, and 8-hydroxyquinoline, all with merits based on the element tested and the environment involved.

    Most alternatives lean harder on solubility in water, whereas Dithizone demands separation from aqueous solutions into organic solvents. This quirk draws complaints from environmentalists worried about chlorinated solvents. Some organizations have moved toward greener alternatives, yet for the tough calls–especially at low concentrations or in complex matrices–Dithizone’s selectivity and clear color formation keep it relevant. It also stands out in situations where sample volumes run low or conditions are unpredictable. As anyone who’s worked with complicated wastewater, industrial streams, or contaminated soils knows, simple, rugged techniques still deliver real value.

    Digital test kits and expensive atomic spectroscopic analyzers talk a good game. They promise trace detection and printouts with seven decimal places. But these methods depend on calibration standards, a steady power supply, and sophisticated troubleshooting skills. Dithizone, by contrast, lets field operators, students, and seasoned analysts work on a shoestring–with instant feedback that doesn’t disappear when the lights go out or the WiFi cuts off.

    Over the years, Dithizone has kept one foot in both worlds: practical enough for everyday use, respected enough to make appearances in regulatory and quality-control protocols. A regulatory manager once told me their team still trains new inspectors on the Dithizone test, even as their main protocol specifies spectrometric confirmation. “You’d be amazed,” he said, “at the things we catch before a sample even gets near a machine.”

    Learning Curve and Safe Use

    No one should handle Dithizone without a basic understanding of laboratory hygiene. Its solvents carry hazards, and careless handling invites contamination or misleading results. My own early missteps taught fast lessons: gloves protect skin, and fume hoods protect lungs. Proper disposal remains a top concern among today’s environmentally conscious labs, and moving toward greener solvent systems has made progress, though never quite matching Dithizone’s performance in all scenarios.

    In training sessions, I’ve emphasized to students and new technicians that the magic of this chemistry depends as much on sharp technique as on the properties of the powder. Careful pipetting, patient mixing, and awareness of cross-contamination set apart reliable results from guesswork. Even on days when automated detectors churn through hundreds of samples, the personal act of running a Dithizone test draws laboratory science back to a human scale.

    Challenges and Solutions in Today’s Analytical Environment

    Despite its strong points, Dithizone faces criticism. Some users point to the toxicity of the solvents it favors. Regulatory agencies watch with growing scrutiny, urging labs to cut back on chlorinated and aromatic organics. In response, research teams are experimenting with new modes of delivery–microencapsulation, alternative carriers, or even biodegradable solvent systems. These approaches have made some headway, but they don’t always deliver Dithizone’s distinct sensitivity and instant visual readout.

    Another concern centers on technique. Unlike plug-and-play test kits, Dithizone works best with careful attention to pH, solvent ratios, and the order of mixing. The learning curve can discourage less-experienced users. More experienced personnel suggest pairing newcomers with veteran mentors during the first few attempts and building troubleshooting flowcharts that target the most common pitfalls–over-extraction, emulsification, or interference from unexpected ions. Investing in practical training helps new analysts gain confidence, and labs committed to intergenerational knowledge-sharing keep this classic method alive.

    Cost pressures always influence technology choices, especially in resource-constrained settings. Dithizone’s advantage comes from a low per-sample expense and equipment-free operation. For many schools, NGOs, and small inspection labs, this matters far more than the slickest spectrometer or cloud-linked reporting app could ever match. It democratizes chemical analysis, letting even the most remote or modestly funded teams spot-check for hazardous metals before they become headlines.

    Personal Experience: Lessons from Field and Lab

    My relationship with Dithizone spans years in university teaching labs, consulting work in industrial quality control, and unplanned adventures in environmental monitoring. Each context threw up different challenges–unlabeled tap water in a crowded city, ambiguous wastewater samples from a textile factory, or questions raised by residents about possible lead in their backyard soil. While complicated, automated systems later confirmed results, the initial answers so often came from a dropper, a bottle of Dithizone solution, and the unmistakable shift from green to red or orange in a glass tube.

    One story comes to mind from a small farming community near an old mining district. Residents, worried about their drinking water, pooled funds for a round of tests. A small portable kit, Dithizone at its heart, let us screen dozens of wells in a single weekend. Spots with hints of pink drew extra attention, and subsequent confirmation by government labs proved the early warning had been justified. No one forgot the lesson that power, in science, doesn’t just come from high-end technology. Sometimes, an affordable, portable chemical kit brings answers and reassurance much faster–and with more impact on the ground.

    There are still sharp debates within analytical circles over how often to use Dithizone–whether it’s best reserved for training and rapid screening or deserves more prominent status in regulatory frameworks. The world will doubtless keep marching toward more automation, smaller and smarter devices, and ever-lower detection limits. Yet the future for classical reagents like Dithizone isn’t fading so fast. Its clear signal, rugged handling, and proven track record keep it in play, especially where budgets are limited or decisions can’t wait for the lab report to come back.

    Potential Solutions and Future Directions

    To extend Dithizone’s value into the next generation of chemical testing, teams are rolling out a mix of improvements and workarounds. In some regions, labs have adopted single-use Dithizone test strips, which use stabilized formulations and greener solvents to minimize hazards while preserving sensitivity. This streamlines handling, reduces exposure, and delivers more reliable results when used under field conditions.

    There’s growing interest in coupling classic reagents like Dithizone with digital readers. Smartphone-based color analysis apps help reduce human error when distinguishing between subtle shades, while QR-coded reporting brings field results straight into centralized tracking systems. Combining these advances with the time-tested chemistry underlying Dithizone promises a best-of-both-worlds approach. Younger analysts–raised on digital technology but appreciative of chemistry’s intuitive beauty–can blend these tools to reach broader audiences and quicker action on emerging threats.

    Teacher training programs can use Dithizone as a gateway into hands-on, inquiry-based science learning, where outcomes are visible and skills are transferrable. For the many countries ramping up efforts to screen water and food sources for heavy metals, this approach can multiply the impact of limited resources.

    On the environmental side, research ongoing in alternative, less toxic extraction solvents points to a future where Dithizone’s sensitivity is matched with reduced ecological impact. Collaboration between reagent makers, analytical chemists, and environmental protection agencies remains key. Sharing field-based data, refining protocols in light of local realities, and keeping honest records of shortcomings will all help push Dithizone’s role ahead.

    Conclusion: Dithizone’s Lasting Significance

    Working in science rarely turns up single answers for complex questions. Dithizone’s continued use demonstrates how a classic method, grounded in sharp chemistry and wide experience, can anchor practice in both old-school and cutting-edge labs. Where speed counts, budgets strain, or simple answers hold urgent importance, this humble reagent delivers. Its limitations demand honest attention and practical solutions, but throwing out Dithizone for shinier options would overlook what fieldwork, hands-on education, and grassroots public health demand: tools that work, tell the truth, and bring knowledge directly to where it matters most.