|
HS Code |
296992 |
| Iupac Name | 1-(2,4,6-dichlorophenyl)-3-(2-chloro-5-nitrophenylamino)-1H-pyrazol-5(4H)-one |
| Molecular Formula | C15H8Cl3N5O3 |
| Molar Mass | 413.62 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | Approx. 265-270°C |
| Solubility | Slightly soluble in water |
| Cas Number | 16867-43-5 |
| Density | 1.64 g/cm3 (approximate) |
| Chemical Class | Pyrazolone derivative |
| Application | Analytical reagent and dye intermediate |
| Boiling Point | Decomposes before boiling |
| Structure Type | Monocyclic pyrazolone core with aromatic substitutions |
As an accredited 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone, with tamper-evident screw cap and hazard labels. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packs 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone in drums or bags, maximizing space and safety. |
| Shipping | The chemical **1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone** should be shipped in tightly sealed containers, clearly labeled, and protected from light and moisture. It must comply with all relevant regulations for hazardous materials, including use of suitable cushioning and secondary containment to prevent leaks or contamination during transit. |
| Storage | Store **1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone** in a tightly sealed container, away from direct sunlight, heat, moisture, and incompatible substances such as strong oxidizers. Keep in a cool, dry, well-ventilated area designated for chemical storage. Clearly label the container and restrict storage access to trained personnel. Always follow institutional and safety guidelines for handling hazardous chemicals. |
| Shelf Life | Shelf life: Stable for at least 2 years when stored in a tightly sealed container, protected from light, heat, and moisture. |
Competitive 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone prices that fit your budget—flexible terms and customized quotes for every order.
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Every day in our lab, practical decisions drive the direction of what we produce. We look for technical relevance, performance benchmarks, and steady demand before we scale up any specialty chemical. 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone came about through a combination of practical observation and requests from formulators searching for reliable dye intermediates and analytical reagents. This compound offers a structure designed for reactivity and color development that stands out against other similar molecules.
We recognize the history of pyrazolone chemistry and its importance in both color formation and pharmaceutical design. In this case, inserting three chlorine atoms on the phenyl ring and positioning a nitro group on the aniline moiety shifts its reactivity and stability profile in a way that most substitutions just can’t match. The dual presence of electron-withdrawing groups has a pronounced effect on the electron density, influencing how the molecule interacts with substrates in dyeing processes, complexometric chemistry, or analytical coloration. Over the years on our line, we have noticed this compound shows greater resistance to thermal degradation and a consistent shade formation when compared to simpler pyrazolones or anilino derivatives lacking these multiple halogen substitutions.
There are always practical issues with specialty chemicals: solubility, stability, compatibility with solvents, shelf life, and ease of formulation into industrial processes. Over repeated production runs, we have watched this compound retain its integrity under typical processing environments. At ambient temperatures, it holds a crystalline form that does not attract excessive moisture nor degrade under indoor lighting, which simplifies storage requirements. During our quality inspections, we rely on HPLC and NMR data to confirm structure and purity, but our most important feedback comes from process technicians who handle it daily. They confirm that the fine, consistent particle size flows well in feeder systems, and it integrates into typical organic solvent systems without forming clumps or leaving undissolved residues.
Chemists rely on this pyrazolone for several reasons grounded in practical outcomes. Historically, the backbone of the molecule forms stable complexes with transition metals, which matters for colorimetric analysis and industrial dyeing baths. In controlled trials, we have seen it produce sharper and deeper shades than less substituted analogues. Analytical laboratories appreciate its use in color development, especially where precision matters in detecting trace metals. Our clients in pigment and dye manufacture highlight its tinctorial strength and shade consistency batch after batch, which translates to reduced waste and lowered reprocessing costs. We have supplied kilo lots for direct use in colorant formulations where other molecules require surface treatments or additional stabilizers just to remain viable.
There is more to specialty chemical manufacturing than simply specifying assay, loss on drying, and melting point. Sure, every batch meets our internal specifications, but ongoing feedback from users often drives minor process tweaks. Some customers require free-flowing powder for direct feed into reactors; others need exceptional clarity in organic solutions. When we receive consistent reports that our material integrates smoothly with minimal residue, resulting in almost zero filter load during dye synthesis, we know the process is working. Our experience suggests that small improvements to particle morphology can make a surprising difference for those downstream. With 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone, years of feedback have allowed us to offer an optimized form that behaves reliably both as a powder and in mixture.
Over decades, our technical staff has trialed every closely related molecule that has appeared in the literature. It is easy for outside observers to overlook the functional differences, but hands-on users notice quickly. For example, standard 3-anilino-5-pyrazolones usually lack thermal stability and have lower affinity for metal complexation, limiting their consistency in spectral analysis or pigment dispersion. Those with only a single halogen substituent do not offer the same tuneable color depth or wash fastness in textile dyeing processes. The triple-chloro pattern on the phenyl ring and the nitro group both push the limits of electron-withdrawing power, allowing for more defined color boundaries between finished dyes. Manufacturers worried about oxidative decomposition or irregular crystal habit find this compound resolves most of those long-standing technical headaches.
We rarely see repeat orders unless a product brings something unique to the table. This pyrazolone presents strong selling points in stability, purity, and measurable performance within formulated products. Textile dye houses find the color fastness and sharpness of shade particularly valuable, especially when working under industrial-scale equipment conditions that can turn any small impurity into a large lot failure. In analytical chemistry, sensitivity and selectivity take the front seat. Purity must reach the parts-per-million level, or false signals and poor repeatability creep into results. We have invested in refining upstream purification steps to keep residual organics, halides, and water contents below the thresholds demanded by these highly regulated sectors. The result is a product that does not interfere with detection systems nor introduce uncertainty in quality control labs.
Modern manufacturing runs on more than just process yield or product properties. Compliance with environmental controls, safety practices, and waste handling shape how we run our facility. With 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone, in-plant handling protocols cover both worker exposure and reagent compatibility. Chlorinated intermediates and nitro compounds demand strict attention to waste stream control. We have installed vapor capture and solvent recovery units for every step using volatile chlorinated components. All water-based effluent enters our central treatment plant, where we destroy any residual organics before release. Our safety training programs walk new operators through material handling and emergency procedures, not just to comply with regulators, but to safeguard every employee’s health. Our incident record shows that with systematic attention and robust technical know-how, these high-value intermediates can be handled and produced safely in a modern installation.
Nothing in our chemical line remains static. Demand for high-performing coloring agents and analytical reagents drives our R&D to push beyond yesterday’s limits. Close ties with end-users across dye, pigment, and analytical sectors help us anticipate what characteristics really matter. Customers helped us fine-tune particle size, flow, and solubility. For many, batch reproducibility remains the top concern. We keep pilot batches regularly in production, testing various process tweaks to see if we can shave minutes off a reaction or lower trace impurities without sacrificing yield.
Once, during a scale-up, a client in the dye industry mentioned issues with agglomeration. Our technical team adjusted solvent polarity and spray-drying profiles, resulting in a finished product that flowed better through their automated feeders. That feedback loop from hands-on partners is what lets us keep ahead of the curve, offering a tailored product that meets real-world processing needs rather than just theoretical targets.
Producing 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone for international markets comes with both opportunity and responsibility. Global textile and pigment markets count on strict documentation and batch tracking. Every drum carries a unique lot number, backed by analytical reports produced in-house. Transparency in material source and traceability offers peace of mind from our gate all the way to the customer’s production line.
Local downstream processing partners often visit our plant to review production or run co-validation on final samples. These open-door sessions reveal where our work succeeds and where it can improve. We learn the expectations and constraints of downstream processors, and they see first-hand how we interpret their feedback into concrete process decisions. We make our documentation clear and accessible, laying out the full test history for review. One recurring theme from partners runs through every conversation: consistency beats innovation if you cannot do both. Through layered quality control, we manage to deliver both custom modifications and unwavering compliance with all major certification requirements.
Batch synthesis of this compound begins with carefully controlled chlorination steps, monitored for both selectivity and completeness. Reactor operators keep reaction temperature and reagent feed tightly in balance. Over-chlorination creates difficult-to-purify by-products, so extra attention in these early stages lays the groundwork for later purity.
Once the dichlorophenyl fragment is prepared, our team completes the anilino-nitro substitution, blending these moieties within a fixed stoichiometric window. Process chemists track endpoint conversions through both spot TLC and more precise LC-MS assays. A final crystallization sequence ensures that even at scale, the product falls out of solution in the desired habit and particle size, avoiding sticky by-products or fine powders that cause dusting hazards.
Every major synthesis run ends with a combination of filtration, drying in vacuum ovens, and staged sieving, so each kilo of material shows the same handling characteristics in both pilot and commercial loads. The extra work pays off for both us and our customers, who report fewer clogged lines and less downtime.
People who work with dyes and colorimetric reagents notice the difference that extra halogenation and strategic nitration make. You see cleaner colors, stronger shelf stability, and simplified downstream processing. The analytical sector values high batch reproducibility and clean background spectra. Over years of repeat production and post-shipment testing, 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone keeps a strong position due to proven technical value backed by consistent user experience. We rely on real feedback, constant testing, and incremental improvement – all driven by what industrial and analytical chemists expect from a specialist manufacturer.
Future developments always focus on better safety, tighter process controls, and ongoing environmental improvements. User-driven adjustments in physical form, impurity profile, or supply chain tracking do not happen overnight but grow from each season’s practical lessons and sector-specific demands. We remain committed to working in step with industry partners to optimize every detail of 1-(2',4',6'-Dichlorophenyl)-3-(2'-chloro-5-nitroanilino)-5-pyrazolone, supporting progress across color science, analytical chemistry, and precision manufacturing.