|
HS Code |
184175 |
| Chemical Name | 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone |
| Molecular Formula | C10H10N2O4S |
| Molar Mass | 254.26 g/mol |
| Appearance | Yellow to orange powder |
| Solubility In Water | Soluble |
| Cas Number | 89-36-1 |
| Melting Point | >300°C (decomposes) |
| Synonyms | Metolazone, Chromotropic Acid A |
| Pubchem Cid | 68548 |
| Inchi Key | BZMZMTZIMHHIPC-UHFFFAOYSA-N |
As an accredited 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a sealed, amber glass bottle containing 100 grams, clearly labeled with hazard warnings and product details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 10 MT palletized; securely packed in 25 kg fiber drums with inner PE bags, suited for chemical transport. |
| Shipping | 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Packaging complies with relevant regulations for chemical transport. It is shipped at ambient temperature and clearly labeled for laboratory use only. Safety data and handling instructions accompany each shipment for secure and compliant delivery. |
| Storage | Store **3-Methyl-1-(4-sulfophenyl)-5-pyrazolone** in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, and well-ventilated area, away from strong oxidizers and acids. Ensure storage temperature is controlled, ideally at room temperature (15–25°C). Practice proper chemical hygiene and clearly label the storage area and container for safety. |
| Shelf Life | 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone is stable under recommended storage conditions; shelf life is typically two to three years. |
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3-Methyl-1-(4-sulfophenyl)-5-pyrazolone stands as a curious compound, popping up in places you might not expect unless your job involves deep dives into analytical chemistry, clinical testing, or colorimetric assays. I’ve spent enough time in research labs and volunteer clinics to spot its name on reagent labels for specific diagnostic kits, especially where precise color changes hold the answer to some important health questions. It carries more weight than a simple additive; it’s a part of the larger story of measurement and diagnostics in chemical and biological sciences.
Each chemical has its quirks and special talents, and 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone brings both to the table. The molecular structure—C10H9N2O4S—tells only half the story. The part that matters is the ability to interact with specific metal ions and generate measurable shifts in color. In the lab, this isn't just a visual trick; these changes can be tracked at precise wavelengths, enabling accurate concentration measurements. I recall during my time in clinical diagnostics, our team relied on this compound for assays that demanded consistent and repeatable reactions without interference from solvents or common ions.
Where other similar compounds might lose grip in the presence of sulfate or chloride ions, this one holds steady. Researchers and industry specialists with experience in biochemical analysis appreciate this kind of reliability, particularly when you’re pushing for reproducibility and trust in your daily results. At the bench, you notice the difference between compounds that work every time and those that force you to rerun a test or question a data point.
This pyrazolone derivative doesn’t just fade into the background of chemical stores. Its signature use shows up in the field of diagnostic reagents, especially where colorimetric measurement matters. Medical laboratories harness it in the detection of phenols, aldehydes, and a range of cations. It also stakes a claim in water analysis, particularly for iron detection. When we were working on public water safety projects, our spectrophotometry tests often included this compound because of its consistent sensitivity and the absence of false positives in tough sample matrices.
An added layer comes from its easy solubility in water, enhanced by the sulfo group. Laboratories appreciate this characteristic since it removes the fuss of dissolving the reagent or ending up with cloudy solutions that tank test accuracy. Years ago, we tested alternate reagents; some fought dissolution, wasting time and precious sample. Teams that want their workflow streamlined tend to stick with the compounds that give them clean solubility up front.
I’ve always believed purity matters as much as the method. If you’ve ever scoped the signal-posted differences between reagent and technical grade choices, you know what a small impurity can do to a result. In 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone, that purity is used for benchmark assays such as the measurement of serum iron via the ferrozine method. You don’t want a shadowy baseline or drifting calibration curve. The difference between an accurate result and a puzzle of unexplained numbers often comes back to starting material integrity.
Some people might not think about the glassware or the quality behind each bottle on the shelf, but any seasoned chemist or lab tech will share stories of a botched experiment due to a subpar batch. For regulatory compliance, the most trusted models keep strict tolerances for contaminant levels and moisture, two factors with outsized influence on outcomes. Big diagnostic kit manufacturers invest in traceable lots and standardize around suppliers with proven records—no one wants variability when patients are waiting for answers.
A close look at the molecule explains its power. Its aromatic ring works in balance with the sulfonic acid group, delivering acidity and water compatibility. The five-member pyrazolone ring anchors the electronic behavior, creating a foundation for chelation. In practice, this means effective coordination with iron and copper, among other metals.
This coordination explains why it finds its main home in iron tests. The stability constants achieved with certain metal ions allow for sensitive detection at low concentrations, with color hues that distinguish between positive and negative results—even with aged reagents. During my own stints teaching undergraduate chemistry, I’d see students light up when complex formation turned a faint solution into a visible signal; the molecule does not shy from showing its work.
Labs often debate between 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone and alternatives like 1-phenyl-2-pyrazolin-5-one, ferrozine, or bipyridine. Each compound offers a unique flavor in both sensitivity and selectivity. My experience with ferrozine—a classic choice for iron determination—taught me about specificity at the cost of cross-reactivity in mixed samples. This methyl-pyrazolone, on the other hand, draws clearer lines in colored or contaminated matrices, making it a better choice for certain clinical chemistry panels and water monitoring.
Cost factors also come into play. Pricing at the reagent grade may look higher for this compound compared to older pyrazolone-based dyes, but returns in reliability and technical support keep budgets on track. Purchasing managers with tight margins sometimes flirt with lesser-known generics, yet most quality control officers gravitate back to the consistent performer after a few failed runs or unexplained blanks.
Performance across temperature swings makes another point of difference. This compound retains measurement properties in room temperature labs or on ice, which isn’t true for all competitors. During a drought monitoring project during an unseasonably hot summer, our crew found less degradation and less need to adjust calibration curves compared to similar dyes. Less drama, less downtime.
A good chemical tool opens up accurate science, but it also supports the larger goals of public safety and patient care. Labs using 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone aren’t just counting ions; they’re answering regulatory demands for clean water, untangling medical puzzles for clinicians, or setting baselines in environmental monitoring. It can be easy to take such reliability for granted, but people working close to those processes know how rare it is.
Hands-on professionals, from chemists in water utilities to clinical technologists, rely on the results these reactions produce. I’ve heard stories from municipal monitoring staff using this compound for trace iron, often sharing the same message: if the test runs right the first time, it saves more than money—it builds community trust. In clinical settings, a rapid and unwavering red-purple shift in a test determines if a patient needs urgent follow-up. This is not academic; real lives run through these analytical pipelines.
No chemical is perfect. Manufacturing quality, batch-to-batch consistency, and the need for safe handling all present hurdles in daily use. Supply chain interruptions sometimes throw off testing protocols, forcing substitutions that erode hard-won accuracy. Laboratories hungry for improvement request suppliers to up their game in terms of transparency and traceability, seeking documented reviews and batch analytics along with each delivery.
In the bigger picture, I’ve seen more conversation around the environmental impact of chemical reagents. Disposal protocols and efforts to lower residuals matter a great deal, especially in large-volume water testing facilities. Some new research efforts are even looking at greener analogs or at recycling methods after primary use. Still, these changes move slowly while legacy tests rely on compounds like this pyrazolone to keep the old protocols alive and relevant.
Training is another overlooked angle. I once trained a team of new interns on basic colorimetric iron determination and realized some had never handled sulfonated compounds. Workshops devoted a surprising amount of time to handling and disposal, ensuring up-to-date practices for both safety and compliance. This level of care breeds confidence, leading to better science and fewer mistakes.
Regulatory agencies continue to tighten standards for laboratory reagents, especially in diagnostic and environmental chemistry. This means traceability and clear documentation sit at the center of every reliable product supply. 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone comes with an expectation: every bottle must trace back to a lot, with independently verified assay values and impurity profiles. As occupational standards evolve, labs show increasing preference for products from sources that publish transparent manufacturing methods and comply with major international guidelines.
End users—myself included, in hospital and academic labs—have come to expect these layers of trust. Product recalls and audit trails keep the pressure on for tight oversight. Experienced technicians often drive purchasing decisions in small facilities, opting for products with thorough published safety data and reliable lot history. This trend helps create a safer work environment and a more predictable workflow, where sudden surprises are the exception rather than the rule.
Availability is a pressing concern for stakeholders in both developed and resource-limited settings. I’ve heard from overseas colleagues who struggle to keep enough supply during peak field seasons, with delays threatening to break continuity in public water projects and community health campaigns. At the same time, demand has climbed in emerging economies, turning formerly niche compounds into staples of routine diagnostics.
Established suppliers now work to build regional partnerships and support faster response times. Online ordering, real-time inventory visibility, and local distribution hubs form an increasingly important part of the supply equation. Seasoned lab managers value the ability to predict delivery, monitor shelf-life, and access technical service without waiting on overseas responses.
New developments in colorimetric analysis and automated chemistry systems continue to shape the destiny of compounds like 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone. Automation has shifted the workload from manual to semi-automated and fully digital spectrophotometry, ratcheting up demand for even higher batch-to-batch consistency and a tighter focus on trace impurities. My time working with automation in university research units taught me that small manufacturing differences can balloon into system errors when magnified by thousands of tests per day.
One promising direction lies in integrating this compound into microfluidic devices and point-of-care diagnostics. Researchers explore kit formats that blend stability and ease of use, packaging precise reagent doses ready for deployment in rural or emergency settings. This opens paths for expanded monitoring efforts without needing high-maintenance laboratory facilities.
Every chemical product carries risks and requires respectful handling. Experienced chemists and environmental health officers keep close watch on protocols for safeguarding both staff and the environment. Current best practices involve specialized training and clear labeling, not only to comply with regulations but to foster a culture of trust within the lab setting. Suppliers familiar with these realities now offer robust safety documentation and updated recommendations for handling, storage, and disposal.
People on the ground need practical guides, not just technical sheets. I remember sending out adapted protocols for on-site personnel who couldn’t access the latest journals, adjusting disposal methods for local regulations. With the shift toward sustainable chemistry, more organizations balance traditional use with new waste reduction strategies and recycling initiatives, keeping stewardship at the front of their operational plans.
The story of 3-Methyl-1-(4-sulfophenyl)-5-pyrazolone shows how chemical tools power practical solutions for science and society. Its unique combination of purity, solubility, and clear reaction endpoints make it a valuable asset in sectors where trust and reproducibility form the backbone of progress—this value grows as labs push for more accurate, efficient, and responsible practices.
Experience on the ground, from teaching chemistry to managing testing protocols in the field, highlights how this compound has carved out a role through honest performance and steady innovation. The future holds new demands for transparency, safety, and environmental stewardship. The professionals and organizations willing to face these challenges will shape the next chapter for chemical reagents and the roles they fill in safeguarding health, water, and the quality of scientific discovery.