|
HS Code |
457200 |
| Chemical Name | 1-Phenyl-5-pyrazolone-3-carboxylic acid ethyl ester |
| Molecular Formula | C12H12N2O3 |
| Molecular Weight | 232.24 g/mol |
| Cas Number | 3464-70-8 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 135-138 °C |
| Solubility | Soluble in organic solvents such as ethanol and acetone |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place; keep tightly closed |
| Synonyms | Ethyl 1-phenyl-5-pyrazolone-3-carboxylate |
As an accredited 1-PHENYL-5-PYRAZOLONE-3-CARBOXYLIC ACID ETHYL ESTER factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams; labeled with chemical name, formula, hazard pictograms, batch number, and storage instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 8,000 kg packed in 160 fiber drums (50 kg each), securely loaded for safe sea transport. |
| Shipping | This chemical, 1-Phenyl-5-pyrazolone-3-carboxylic acid ethyl ester, is shipped in tightly sealed containers, protected from moisture, light, and heat. Standard shipping is via ground or air, following all local and international chemical safety regulations. Ensure proper labeling and handling, using compatible packaging materials to prevent leaks or contamination during transit. |
| Storage | Store **1-Phenyl-5-pyrazolone-3-carboxylic acid ethyl ester** in a tightly sealed container in a cool, dry, and well-ventilated area. Protect from heat, moisture, and direct sunlight. Keep away from incompatible substances such as strong oxidizing agents. Ensure appropriate labeling and restrict access to authorized personnel. Use appropriate personal protective equipment when handling the chemical. |
| Shelf Life | Shelf life: Store 1-Phenyl-5-pyrazolone-3-carboxylic acid ethyl ester in a cool, dry place; stable for 2 years. |
Competitive 1-PHENYL-5-PYRAZOLONE-3-CARBOXYLIC ACID ETHYL ESTER prices that fit your budget—flexible terms and customized quotes for every order.
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Working hands-on with 1-Phenyl-5-Pyrazolone-3-Carboxylic Acid Ethyl Ester for many years, I’ve gained a clear sense of its practical value and influence across chemical manufacturing. Experience on the production floor shapes every batch we prepare; observing its reactivity, purity, and performance in labs and industry gives us a direct perspective you can count on.
Our core product steps off the line under the model PPEE-303. This designation reflects an optimized synthesis protocol, refined after many cycles of production feedback from research partners and bulk-processing clients. Even slight adjustments at the synthesis stage reflect in the structural clarity and reaction reliability, and we have always prioritized that stability. Our batches maintain strict control over the substitution at the phenyl and pyrazolone positions, giving consistent molecule-to-molecule interaction with intended reactants.
Standard batches come with a purity level kept above 99% by HPLC, a color consistently between off-white and pale yellow depending on trace hydrate levels, and bulk densities favoring flow during handling. We use validated ethanol intermediates in esterification to avoid side-chain residues that trouble certain downstream products. Granulometry lies in a range preferred by formulators integrating the ester in hydrophilic suspensions.
Here’s where being the manufacturer matters. Not all pyrazolone derivatives behave the same in real-world syntheses — and this ester’s profile stands apart from other variants in common circulation. Plenty of alternate carboxylic acid esters of 1-phenyl-5-pyrazolone have made their rounds, but subtle substitutions and synthesis routes change thermal stability and reactivity. We nail down the batch consistency by tracking not just the main structure but also the trace side-products common with incomplete esterification.
For example, our ethyl ester shows markedly better compatibility with alkaline media than methyl esters, reducing unwanted byproducts in dye intermediates and active pharmaceutical ingredient (API) routes. You’ll notice this as a drop in process impurities during scale-up. Compared to free acid forms, which require neutralization and can lead to salt formation in unwanted steps, the esterified product maintains better solubility and smoother protection/deprotection transitions in multi-step synthetic routes. Chemists working on large-scale reactions give consistent feedback that they see fewer side reactions and easier workups.
Years ago, we worked with a midsize API developer seeking to synthesize pyrazolone-based compounds while avoiding the recurring chromatographic purification bottleneck seen with the raw acid. By shifting them to our ethyl ester, they shortened purification times and yielded a cleaner product stream — the slight price difference more than justified by time and material savings.
In dye synthesis, particularly with azo derivatives, our PPEE-303 feeds reliably into coupling reactions. Competing products often left residual phenylhydrazine or incomplete esters, leading to color inconsistencies and batch rejections. Our process, fine-tuned over successive annual production reviews, gives customers direct assurance of batch-to-batch reliability. Not all producers will spend weeks investigating where a byproduct comes from, but direct dialogue with end-users led us to tweak our condensation catalyst choice years ago. Since then, our product gained a reputation in textile intermediates thanks to lower background absorption in cyan and orange dye ranges.
Lab scientists have told us outright that handling is easier compared to the analogous methyl and propyl esters. With ours, you’ll see even flow and rapid dissolution in common polar solvents. Some customers prefer the traditional acid form for short-run, high-purity needs, but once you scale up, the handling improvements and lower toxicity component — thanks to ethyl over methyl substitution — matter much more in terms of operator exposure and downstream treatment costs.
One lesson we reinforce in our plant is that quality shows up not just in purity numbers but in how cleanly a product integrates into the next stage of a process. Chemical manufacturers with their own reactors recognize the difference between a “specification” and real-world performance. Cutting down on micelle formation, dust, and low-mass impurities makes all the difference at production scale, especially when filtration and recovery enter play. In direct feedback calls and occasional in-person audits, veteran chemists highlight our low levels of residual starting material and low-odor profile — making it easier for colleagues handling batches in enclosed spaces.
As manufacturers, we look beyond a Certificate of Analysis. Batch logs record trend data for key process parameters, giving us a real sense of where unwanted variability might creep in. Over the years, this attention has paid off: for each parameter, from color index to water content, we’ve shaved off variation with each process cycle. This builds trust for customers scaling technical syntheses who might not see issues until after expensive downstream steps.
At our site, operator safety means more than compliance checklists. The slightly higher boiling point and lower vapor pressure of the ethyl ester help minimize fugitive emissions, leading to better air quality and smoother handling compared to lighter alkyl esters of the same core molecule. Waste stream audits show consistently lower levels of unreacted precursor, stemming from the reaction path tuned for high conversion.
Post-use, the compound’s biodegradation pathways run cleaner — not every synthetic route can claim that. Disposal teams and process managers appreciate reduced air and water emissions, an outcome born from real dialogue between our production staff and our wastewater treatment team. For plants operating on increasingly strict local regulations, this translates to real long-term cost savings and a lighter compliance load.
Over the years, direct user feedback shaped our PPEE-303. Several clients, scaling up from pilot to commercial production, reported thermal stability as a make-or-break issue for certain batch reactors. By fine-tuning the crystallization and drying stages, we target a product with minimal transition range — you get a uniform melting profile and smoother flow without unexpected agglomeration.
Another practical insight: blends with polar aprotic solvents show excellent dissolution rates, with rapid mixing observed across both lab- and plant-scale glass lines. This trait, not widely publicized by resellers, gives our users greater latitude in feedstock preparation and time management. Unexpected delays and batch loss often boil down to incompatibility and slow or incomplete dissolution; hearing direct comparisons with competitive products, we always ask where process pain points lie and look for tweaks to minimize batch failures.
One of our longtime clients in central Europe noticed that reduced trace hydrazine impurity mattered more in summer operations — improved shelf life and fewer odors during high-heat transport kept materials managers satisfied, cutting down complaints and returns that plagued earlier seasonal shipments.
Experience tells us that no two pyrazolone esters behave the same way outside tightly controlled bench experiments. Our ethyl ester presents a blend of reactivity, storage stability, and user-friendliness that we rarely see in methyl, propyl, or free acid forms. Storage for over six months in standard drum packaging shows minimal mass loss or discoloration, a real advantage over free acid analogues, which often clump or degrade.
Process chemists working with methyl esters sometimes report faster reaction rates but increased volatility and more evaporation loss during large-scale handling; propyl esters, on the other hand, run into solubility challenges. Over decades, we’ve refined our process toward ethyl esters because customer experience tells us the trade-offs work better for most industrial schemes. Time and again, users report fewer headaches with filtration and waste handling, two areas where the free acid variant drags efficiency down.
Choosing suitable packaging and logistics means understanding how the product behaves from our tank to your reactor. Our clients don’t want sticky, compacted powders or drums caked with byproduct resin. Packaging lines incorporate nitrogen-blanketed drums and lined bags, heading off oxidative changes during storage. Shipping teams keep real-time logs on temperature and humidity during transport, so we can anticipate and prevent issues on arrival. Less time is lost reopening containers or dealing with returns, and materials managers see lower loss rates outside controlled storage.
Feedback from sites in more humid or warm climates led to tweaks in our final drying protocol — product arrives in better condition and stores longer even without climate-controlled warehousing. Season after season, this means you can run predictable operations and plan for your next campaign without surprise adjustments.
The pyrazolone family continues to draw attention in both pharmaceutical and specialty chemical research. We get advance notice of evolving applications — sometimes from clients trialing new synthetic routes, other times from internal R&D pushing for higher reaction yield or greener process chemistry. Insights from our production floor often inspire tweaks: we may test different starting phenylhydrazine sources to reduce rare trace contaminants or alter our esterification catalyst to optimize conversion.
We keep channels open with our partners. Direct production and process feedback often triggers small but critical changes. Our quality team meets every week to review trial runs, spot new trends, and tackle unusual analytical results from client labs. This close relationship means we don’t just stick with a batch process because it works; we adapt and improve, recognizing that the end use may drive shifts in preferred specifications.
Being the manufacturer gives our team unique insight. Distributors may talk about theoretical specs, but nothing replaces seeing the reaction in person or listening to the production team troubleshooting a mixing issue on a hot summer morning. The details of crystallinity, trace contaminants, dusting, and handling quirks show up in day-to-day plant work, not just in sales brochures.
Through years of shipping material globally, from Asia to the Americas, we gained understanding of logistics, seasonal changes, and different customer preferences. Manufacturers can act on these lessons in a way trading houses can’t match. In visits to customer plants, we watch for bottlenecks — material sticking in hoppers, unexpected residual from cleaning, handling concerns from operators — and bring those lessons back to our own process team. Adjustments made based on these practical experiences keep our materials preferred by those who have to make processes run smoothly from start to finish.
Every batch we make starts and ends with real-world constraints. Pyrazolone esters, including this product, carry their own quirks — some customers encounter slow dissolution in strongly nonpolar solvents, or occasional sensitivity to dust and static during packaging in drier climates. Our staff routinely refines sieving and drying methods to aim for a balance between free-flowing product and minimizing fine particulate carryover into downstream processes.
Though we invest heavily in product stability, long-term storage in non-ideal conditions — like exposure to direct sunlight or repeated temperature swings — can still cause discoloration or minor degradation, especially after many months. We track customer feedback and work with sites to dial in warehouse protocols where needed, providing storage advice informed by direct batch performance rather than theory.
Every drum of 1-Phenyl-5-Pyrazolone-3-Carboxylic Acid Ethyl Ester we ship reflects a line of decisions shaped by chemistry, feedback, and practical handling experience. We see how process chemists, materials managers, and operators interact with the product. Morning QA meetings review outlier batch samples, while late-night process reviews pore over chromatograms and customer notes. Out of this cycle grows a product line that meets shifting industry needs, not just on paper but in the actual flows of everyday chemical production.
Bringing true manufacturer insight to the table lets us focus on solving real-world challenges — reducing impurities that didn’t show up in old QC routines, improving handling across seasons and climate zones, listening to actual process concerns, and building relationships where feedback transforms into action. With each improvement, we see a compound that not only meets technical benchmarks but keeps evolving as the industries we serve change and expand.