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HS Code |
403348 |
| Chemical Name | 1-Phenylmethyl-5-Phenyl-Barbituric Acid |
| Molecular Formula | C17H14N2O3 |
| Molecular Weight | 294.31 g/mol |
| Appearance | White to off-white solid |
| Melting Point | Approximately 210-215°C |
| Solubility In Water | Slightly soluble |
| Smiles | O=C1NC(=O)NC(=O)C1Cc2ccccc2c3ccccc3 |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store in a cool, dry place |
| Purity | Typically >98% |
| Synonyms | Benzylphenylbarbituric acid |
| Application | Intermediate for pharmaceutical synthesis |
As an accredited 1-Phenylmethyl-5-Phenyl-Barbituric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque plastic bottle labeled "1-Phenylmethyl-5-Phenyl-Barbituric Acid, 25g"; includes hazard warnings, batch number, and manufacturer details. |
| Shipping | Shipping for **1-Phenylmethyl-5-Phenyl-Barbituric Acid** must comply with all applicable chemical safety regulations. The substance should be securely packaged in sealed containers, clearly labeled, and cushioned to prevent breakage. Include relevant Safety Data Sheets (SDS), and ship via authorized carriers, ensuring proper documentation and temperature control if required. |
| Storage | 1-Phenylmethyl-5-Phenyl-Barbituric Acid should be stored 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 moisture and direct sunlight. Clearly label the container and avoid dust formation. Store according to relevant chemical safety regulations and handle with appropriate personal protective equipment. |
Applications of 1-Phenylmethyl-5-Phenyl-Barbituric Acid in Industrial ManufacturingAs a direct manufacturer of 1-Phenylmethyl-5-Phenyl-Barbituric Acid, we supply this specialty chemical exclusively to downstream sectors where its chemical profile and reaction kinetics meet precise industrial formulation, quality, and regulatory standards. The following sections detail its primary, proven application arenas, along with key compliance metrics, practical usage proportions, integration into production processes, and reference end-use products developed by downstream partners. 1. Pharmaceutical Intermediate Synthesis for Barbiturate DerivativesThis compound serves as a core intermediate in producing certain barbiturate-structured pharmaceuticals, where its specific substitution pattern contributes to the synthesis of anticonvulsant or sedative-hypnotic active ingredients. Pharmaceutical manufacturers utilize it to introduce phenylmethyl and phenyl functionalities at key scaffold positions during multi-step API synthesis processes, where the chemical’s purity and controlled reactivity are essential for yield and final product quality. Industry compliance standards
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2. Chemical Reference Standards ProductionProducers of analytical chemistry tools and quality standards source this compound for use as a certified reference material, where its stable structure and distinct chromatographic properties make it valuable for system suitability testing, calibration, and impurity profiling in regulated drug laboratories. Industry compliance standards
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3. Specialty Agrochemical R&D IntermediatesAdvanced agrochemical developers incorporate this barbituric acid derivative during targeted synthesis of novel crop protection agents, where the unique aromatic substitution pattern is used to investigate lead compounds with improved pest-selectivity or environmental stability in early-stage screening programs. Industry compliance standards
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4. Photographic Chemical Formulation IntermediatesIn high-end photographic and imaging chemical manufacturing, the compound’s structure is valuable in synthesizing customized stabilizer or sensitizer molecules, contributing to emulsion durability, image density, and controlled grain size in specialty film and x-ray plate production processes where batch-to-batch consistency is tightly controlled. Industry compliance standards
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Every day in our chemical plant, stainless steel vessels hum and jacketed reactors keep precise temperatures. For over two decades, we have specialized in manufacturing barbituric acid derivatives, and among these, 1-Phenylmethyl-5-Phenyl-Barbituric Acid holds a unique place in both our production line and our sense of pride. With a chemical structure that features both a phenylmethyl and a phenyl group, this compound offers unique properties that set it apart in both laboratory research and specialized pharmaceutical synthesis.
Many clients ask what difference a single substitution or molecular tweak makes in practice. Years back, we took on the challenge of synthesizing this molecule at scale, moving beyond small-batch experimentation. The handling, reaction kinetics, and purification processes differ enough from standard barbituric acid derivatives that experience built over many years really matters, especially when it comes to producing consistent, high-purity batches.
Within our own facility, we offer 1-Phenylmethyl-5-Phenyl-Barbituric Acid under a specific model that reflects our proprietary purification standard. Over time, we streamlined our crystallization and filtration steps, targeting an assay purity consistently above 99%. We discovered that batch consistency does not simply depend on raw material quality, but also reactor type, mixing rates, and solvent choice. Many manufacturers overlook these details— we see the results in final product samples that don’t perform as expected during downstream reactions.
We offer a white to off-white crystalline powder, free from residual solvents and below-threshold levels of heavy metals and related impurities. Analytical methods, including HPLC and NMR, support both our internal quality checks and the exacting requirements our customers present. Developing our in-house standard operating procedures, we worked alongside rigorous chemists who understand not just barbituric acid chemistry in theory, but routinely confront the practical issues that arise in every run – yield plateaus, impurity profiles, and filtration behavior.
The journey of 1-Phenylmethyl-5-Phenyl-Barbituric Acid does not end in our warehouse. It moves through hands of pharmaceutical innovators, academic researchers, and experts in specialty organic synthesis. Our compound typically serves as an intermediate, forming part of larger, more complex structures for pharmacological studies. Its unique substituent pattern introduces both steric and electronic effects, influencing reactivity and the properties of targeted molecules.
In our discussions with research clients, we have seen how subtle changes in a barbituric scaffold unlock differences in downstream biological activity. Sometimes, clients ask about using close alternatives, such as 5,5-diphenyl barbituric acid or simple phenyl barbituric acids. Over the years we observed that substituting a benzyl group at the N1 position both changes solubility and shifts the melting point, compared to straight diphenyl substitutions. Synthesis downstream often requires this precise motif, and our clients return for our product when reactions with commercial alternatives repeatedly underperform or cause side-product headaches.
Synthesizing any barbituric acid derivative at scale brings lessons. Recirculating chilled reactors in the right sequence optimizes yield yet misses some issues that only show up batch after batch. Over the years, we have fine-tuned reaction temperatures and solvent volumes to improve consistency.
What separates us from traders or middlemen is not salesmanship, but production experience. For example, we learned that slight fluctuations in the cooling rate favor needle crystallization over plate-like forms; this matters during filtration and drying. Residual mother liquors that hold even a small percentage of impurity need further washing cycles, which we designed into our custom washing protocols. We track each batch from raw to finished product through careful record-keeping, enabling traceability right down to the reactor operator who ran the synthesis.
On the open market, countless resellers offer this and similar barbituric acid products. Few have production insight into what causes sample color shifts, why the odor sometimes changes with off-spec batches, or how to quickly adjust processing when reaction kinetics change across seasons.
We do not source from third parties, so clients are assured their product comes from a controlled, single-production source. Our quality record draws from hundreds of production campaigns. Whenever we evaluate incoming raw materials, we do more than peak at certificates of analysis. Our team runs validation syntheses to confirm the impact on downstream reactions. Years ago, changing a solvent supplier without these steps led to a batch that underperformed during Fischer esterification – a costly lesson that shaped our current quality regime.
In research or process development, even a slight deviation in input quality can sideline weeks of work. Customers come back to us not because of bullet-pointed specifications, but because they have run our material through their own critical steps and see a drop in by-products or a higher isolated yield. We are often asked to advise on solvent compatibilities and reactivity sequences, not because we publish technical whitepapers, but because our chemists spent years producing this compound in the field, not just behind a bench.
Our staff knows that a barbituric acid derivative’s true value emerges during practical use. Whether it’s being built into large heterocyclic rings or coupling with other aromatic cores, customers constantly report fewer issues with our batches slotting into their processes. Many mention greater batch-to-batch consistency compared to off-the-shelf alternatives. We encourage ongoing dialogue— our technical team answers questions directly, suggesting adjustments if small differences in particle size distribution influence slurry handling or charging in process vessels.
Sustainable chemistry is not an abstract goal— it shapes day-to-day production choices. We monitor our emissions and effluent profiles using both in-house testing and external audits. Achieving a consistent product with minimal waste has always driven improvement in our process. Handling barbituric acid derivatives safely means investing in adequate ventilation, solvent recovery, and safe employee practices. Our facility adheres strictly to safety protocols, using sealed systems and appropriate PPE for every batch.
We limit exposure to hazardous solvents by investigating alternative reaction pathways and by capturing and treating emissions on-site. After several process optimization cycles, we achieved a 15% reduction in overall solvent usage over three years, cutting costs while lightening our environmental footprint— something that matters when regulatory landscapes keep tightening.
Many clients ask about alternatives. We have manufactured a full spectrum of barbituric acid derivatives, from 5,5-diphenyl to 5,5-dialkyl or diallyl systems. What often tips the balance are not values in a technical data sheet, but real-world behaviors— loss on drying, dusting tendencies, downstream reactivity, and practical purity. Several research teams have told us that even though the cost appears slightly higher for our fine chemical over a generic source, their real savings come from lower rates of side reactions and fewer purification steps downstream.
For those considering different barbituric scaffolds, we highlight the chemical consequences. Adding a benzyl moiety to the nitrogen shifts both reactivity and solubility compared to relying only on 5,5-disubstitution. When testing alternatives in multi-step sequences, research reports sometimes attribute drops in overall yield to "input variability." Through repeat campaigns and routine feedback from academic labs, we see how input precision simplifies entire research projects, letting teams focus on discovery over troubleshooting.
A barbituric acid derivative is only as valuable as the consistency and safety of the process behind it. Each scale-limited run gives way to pilot scale, then full production scale— and this is where manufacturer knowledge sets real boundaries. Process safety teams validate each reaction step, recalibrate process control sensors, and routinely monitor key exotherms or pH swings during addition steps.
We know well that deviations in raw material quality cause cascading failures only hours or days after a batch is started. For this reason, every lot undergoes full-spectrum QC— not just for purity, but also for off-odors, moisture content, and crystal form. Only repeated experience highlights where to focus— for instance, a certain methyl substitution pattern may need more rigorous drying to avoid caking during packing, whereas another form shifts under standard desiccation.
We have built relationships with scientists who return to us with good, candid feedback. Some find that, for their bioactive molecule development, swapping in a more generic barbituric acid variant causes product losses or complexification during synthesis. Others, working in medicinal chemistry, choose our 1-Phenylmethyl-5-Phenyl-Barbituric Acid for its unique compatibility with their reaction partners.
Genuine manufacturing expertise helps here. We track not just current demand, but listen for the next advances in chemical synthesis. Where possible, we tweak physical properties— adjusting drying conditions, particle size, or storage methods to better suit a customer’s synthesis route. Because we stand behind our manufacturing, clients gain both a product and a technical resource— guiding troubleshooting and scaling up new reactions.
Our facility never stands still. Each analytic breakthrough or idea from our chemists leads to small changes— more sensitive impurity detection, improved crystallization control, greater solvent recovery. As pharmaceutical and fine chemical applications evolve, so does our process. Audits and certifications keep us sharp, while client-driven projects bring new learning opportunities. This commitment to betterment means our batches only get better, year after year.
Tradition matters as much as innovation. We keep detailed logs on all past batches, learning from both trouble-free campaigns and those that taught us about sticking points. Our production staff direct their expertise into daily routines, not just overseeing process steps but noticing small things—a honeyed odor, an unusual pressure spike, or a subtle change in filtration. Each lesson gets folded back into standard operating procedures, meaning that clients benefit from decades of collective knowledge in every shipment.
Nothing replaces first-hand knowledge when producing a complex organic intermediate. We see the difference every day, whether responding to technical questions, supporting a synthesis team wrestling with an impurity, or making urgent adjustments to plant schedules to meet a project deadline.
In a world where chemical sourcing can often mean trading emails with unknown contacts, our partners value both our transparency and our willingness to invite them into our production environment— virtually or in-person. Many of our clients have visited our facility, observed a run from beginning to end, and learned why details such as the stirrer speed or cooling rate alter final product characteristics.
Rare molecules like this one owe their value to practical, real-world manufacturing. Academic and pharmaceutical teams continue to probe the boundaries of barbituric acid chemistry, with our material playing a supporting role in new compounds and ideas.
We watch emerging research into new pharmacophores, structure-activity relationships, and synthetic routes, and we stand ready to adapt our process, measurement techniques, or offerings as needed. Our commitment remains the same: keep quality at the core, support innovation, and blend tradition and progress. Every shipment tells the story of years of work, mindful process control, and a stubborn belief in doing things the right way, batch after batch.