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HS Code |
804545 |
| Chemicalname | 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One |
| Molecularformula | C10H10N2O |
| Molecularweight | 174.20 g/mol |
| Casnumber | 5461-28-1 |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | approximately 158-162°C |
| Solubility | Slightly soluble in water, soluble in ethanol and DMSO |
| Purity | Typically ≥98% (may vary by supplier) |
As an accredited 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One is supplied in a 25-gram amber glass bottle with a secure screw cap. |
| Shipping | Shipping for **5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One** should comply with all relevant chemical transport regulations. The compound must be packed in tightly sealed, labeled containers, protected from moisture and light. Transport requires appropriate documentation, and carriers should handle it as a laboratory chemical, ensuring safety protocols to prevent leakage or accidental exposure. |
| Storage | Store **5-Methyl-2-Phenyl-1,2-dihydropyrazol-3-one** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Keep container tightly closed when not in use. Follow standard laboratory safety protocols and use appropriate personal protective equipment when handling. |
Applications of 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One in Industrial ManufacturingAs a direct manufacturer of 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One, we supply this specialty pyrazolone derivative to established industries requiring high purity intermediates for synthesis. The compound exhibits reliable performance as a building block for advanced organic processes across pharmaceuticals, agrochemicals, pigments, and specialty chemical domains. Downstream partners rely on our consistent quality for integration into regulated product pipelines. 1. Active Pharmaceutical Ingredient (API) Intermediate for Analgesic DrugsPharmaceutical formulation teams use 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One as a core intermediate in non-opioid analgesic drug synthesis, focused on pyrazolone-based structures. Production lines leverage its high chemical purity to ensure controlled molecular modification steps, supporting the creation of finished APIs that meet international regulatory protocols. Batch control and traceability during each synthetic step are integral due to strict compliance requirements. Industry compliance standards
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2. Colorant Intermediate for High-Fastness Organic PigmentsColor chemical producers integrate 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One in pigment synthesis for automotive coatings, plastics coloration, and printing inks. The molecule's defined substitution pattern delivers key chromophore formation, increasing light and weather resistance of the pigment. Our product’s batch-to-batch reproducibility enables reliable performance in large-scale blending and dispersing applications. Industry compliance standards
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3. Agrochemical Synthesis Component for Selective HerbicidesAgrochemical formulators select this pyrazolone derivative for crafting selective herbicides targeting broadleaf weeds. Its defined reactivity and substitution pattern enable synthesis of active compounds demonstrating high crop safety profiles. Documented traceability within our supply chain facilitates downstream audits, while our technical support assists with process adjustments during scale-up and registration phases. Industry compliance standards
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4. Fine Chemicals Intermediate for Custom Synthesis Service ProvidersChemical contract manufacturers deploy our material as a reliable intermediate within custom synthesis workflows for academic, biotech, and life science clients. Its defined aromatic and pyrazolone functionality supports a wide range of downstream derivatizations, including metal complexation and ligand preparation. Regulatory documentation and consistent analytical data support seamless integration into validated contract manufacturing agreements. Industry compliance standards
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At our facility, we have developed a strong reputation for building reliable, high-quality intermediates. Among these, 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One stands out. We have put years into refining the synthesis path and purification process for this compound, which often goes by its synonym, 5MPDP. Not every manufacturer approaches this molecule with the same attention to detail; scale and care influence both the end product’s performance and its impact on downstream processes.
This particular compound features a pyrazolone core with a methyl group at position five and a phenyl ring at position two. The structure originates from a series of reactions involving substituted hydrazines and β-ketoesters. On production lines, we pay special attention to reagent quality and reaction monitoring, since even minor impurities can complicate work in pharmaceutical, agrochemical, or dye chemistry labs.
Our standard specification model produces 5MPDP in a fine crystalline powder. Throughout each batch, we target a minimum purity of 99%. That value comes from direct HPLC tracking (using our standard in-house test methods), not from rounding up or relying on external third-party certifications. We’ve learned that keeping actual user needs in focus leads to better, more consistent output. Pure powder translates into dependable results for those working on synthesis or formulation further down the road.
5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One has earned trust as an effective building block. From first-hand experience, customers turn to this product when they need a foundation for anti-inflammatory, analgesic, or antipyretic agents. Some key nonsteroidal anti-inflammatory drugs draw on the pyrazolone framework, and derivative chemistries often rely on the methyl group for providing selectivity or regulatory recognition. Our chemical engineers recognize that seemingly subtle choices at the molecular design stage directly impact solubility, binding behavior, and final product safety.
Beyond pharmaceuticals, our partners in pigment and dye sectors value 5MPDP for different reasons. Its chemical backbone helps build vivid color-fast pigments with good heat and light stability. Having a consistent, untainted raw material shapes both usability in manufacturing and shelf life in end products. We work closely with these industries to guarantee our synthesis keeps up with shifting needs—whether technical (as certain dye formulations evolve) or regulatory (with standards tightening).
Plenty of manufacturers claim to offer “high-quality” 5MPDP. Over the years, we have seen varied experiences with reagents, solvent quality, and equipment cleaning routines. We carry out full traceability for each batch, from the raw material acquisition right up to shipment. Our team monitors the reaction course, using small-scale piloting before every scale-up. Small decisions—such as temperature ramp rates or agitation speed—lead to big gains in finished product clarity, filtration ease, and even the final color of the dry solid.
During filtration and drying, attention to time, airflow, and solvent removal directly influences not just the look and odor, but how the compound behaves down the line. Moisture or solvent left over can wreck an analyst’s chromatography, or worse, interfere during downstream syntheses. Over the years, our chemists have dealt with every manner of “invisible” impurity—unexpected side products that didn’t show up in basic analysis, but later complicated scale-up for customers. We use this experience to inform our own production checks, and we continuously update protocols to reflect sensitivity to seemingly minor factors.
Many offerings in the marketplace look similar on paper, but hands-on work tells another story. We stick to a consistently single-crystal morphology. This provides repeatable performance—for researchers, it ensures easier weighing, dissolution, and precise aliquoting. Compound morphology makes a real-world difference during downstream processing or when scaling protocols from bench to pilot plant.
We also avoid certain auxiliary agents and stabilizers during purification. Instead, our solution focuses on slow recrystallization and gentle solvent removal. This dramatically reduces residues, making our batches more suitable for sensitive organic transformations and for use in regulated settings.
The difference shows up during QC checks: our GC-MS and TLC assays routinely exhibit minimal background, so our partners rarely encounter ghost peaks or unexplained interferences.
Our team has tested various container materials and storage conditions over years of shipments. We found that high-barrier, sealed poly bottles work best. Glass occasionally leads to microcontamination from surface etching or atmospheric water ingress. Plastic liners, combined with a low-humidity storage room, keep our 5MPDP dry and fresh. These details rarely get captured in standard product sheets, but they reduce hassle for both our packers and the laboratory staff at the receiving end.
Most users buy 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One in kilogram-scale lots. Scale-up projects especially highlight the difference between batches produced in-house and grams sourced from research catalogs. Some clients focus on solid-phase synthesis; others dissolve our product for solution-based coupling reactions. Reproducibility comes from reliable solubility and minimal variability in crystal form.
One of the subtle challenges our customers face: even slight batch-to-batch differences may disrupt reproducibility of pharmacological or dye-formation tests. Over our years in chemical manufacturing, we’ve sought direct feedback and consistently incorporate it to improve yield and appearance. Clients told us outright that filtration speed, dust formation, and even static cling can affect their workflow. Tweaking drying profiles and antistatic procedures has helped, as has reviewing packaging for dust minimization.
In the pharmaceutical field, some processes hinge on predictable reactivity, especially for introducing the methyl group or carrying out selective oxidations. Our high-purity version improves consistency in both laboratory-scale and process-scale experiments. We encourage customer visits and technical discussions at our site, emphasizing transparency about production specifics that influence reactivity or byproduct formation.
Chemicals with the pyrazolone core structure have drawn increased attention from health and environmental agencies. The methyl and phenyl substituents change the toxicological and environmental profile, but oversight remains tight. Our compliance group keeps up with shifting guidelines worldwide—specifically focusing on restrictions regarding downstream metabolites, permitted uses, and labeling requirements.
Documenting every step lets us deliver trustworthy batch histories to those who need them for regulatory filings or audits. By keeping impurities under tight control, our team helps everyone downstream to build convincing safety and environmental assessment packages using robust data, not guesswork.
No manufacturing process stands still. In our experience, regular feedback has driven meaningful improvements over the years. A decade ago, most process tweaks aimed to increase yield or reduce waste for in-house reasons. As customer labs grew more sophisticated, feedback centered on batch homogeneity, precise trace impurity levels, and improved lot-to-lot color stability. We take this input to heart. For example, early batches sometimes showed faint yellow tint due to minor side product uptake; fine-tuning filtration has since eliminated this.
We’ve seen research teams run into clogging of reaction vessels due to micro-particles; switching grind and drying routines provided cleaner product that handles smoothly even at the kilo scale. This direct dialogue with customers—in person, at conferences, or over detailed project calls—has made our offering more robust for today’s demanding applications.
Compared with generic or multi-vendor 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One sources, our product draws strength from thoughtful process control and user-first packaging. Most competitors focus solely on purity, and some underplay packaging, crystal form, or trace impurity profiles. Our focus on single-morphology crystals, moisture control, and solvent-free drying pays off where it matters—at the laboratory bench or in production reactors.
For projects where speed matters, our experience streamlines scale-up and supports fast, reliable analytical transfer. Programs running in regulated manufacturing environments need full documentary support; we keep backup samples for each shipment, adding a further layer of quality assurance few can match.
5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One continues to enable advances in both small-molecule drugs and specialty pigment manufacturing. Our research and process engineering teams are steadily developing extended grades for emerging fields, including new API development and organic electronics. Work continues on even higher purity lots, color-improved versions, and easier-to-handle granulated forms.
New research points to potential applications in advanced diagnostics and targeted therapy vehicles, where the interplay between the methyl and phenyl groups becomes even more critical. We partner with select customers to support research protocols, ensuring that feedback loops back to our development arm. Reduced environmental footprint, waste minimization, and circular chemistry approaches also shape our ongoing process reviews.
Over years of hands-on experience, our team learned how minor details make a large impact for chemists, process engineers, and quality specialists using 5MPDP. Single-sourcing from a trusted manufacturer has become a common request from our partners, as this minimizes confusion and lets their staff focus on science, not troubleshooting.
For those who need critical reagent supply, batch descriptions describing only “white solid, 98% purity” do not cut it. We offer full transparency, open communication about the production process, and encourage technical dialogue at every step. It’s a demanding market, shaped by advances in science and by tightening regulatory pressure. Our approach puts the user—chemist, engineer, analyst—at the forefront, with every decision about raw material control, process safety, and innovation traced back to the real needs of those who rely on our product.
By bringing together skilled people, modern analytics, and old-fashioned dedication to continuous improvement, we continue to deliver 5-Methyl-2-Phenyl-1,2-Dihydropyrazol-3-One for the next generation of science and industry. For those seeking reliable, transparent supply and a partner willing to share knowledge and improvement, our door remains open.