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HS Code |
347077 |
| Chemical Name | 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid |
| Molecular Formula | C12H11NO3 |
| Molecular Weight | 217.23 g/mol |
| Cas Number | 136458-98-7 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=NC(=C(O1)CC(=O)O)C2=CC=CC=C2 |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g quantity of 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid, sealed in an amber glass bottle with safety labeling. |
| Shipping | This chemical is shipped in a sealed, chemically-resistant container, cushioned and clearly labeled according to all relevant regulations. Temperature control and protection from light/moisture are maintained during transit. Proper documentation and hazard information accompany the package to ensure safe and compliant delivery in accordance with local and international shipping guidelines. |
| Storage | 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)acetic acid should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizing agents. Recommended storage temperature is typically 2-8°C (refrigerator), unless otherwise specified by the manufacturer. Label containers clearly and handle with appropriate personal protective equipment. |
Applications of 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid in Industrial ManufacturingAs a chemical raw material manufacturer, we supply 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid directly to industrial users across multiple specialized sectors. Below, you will find the principal downstream application segments with detailed, scenario-specific insights reflecting real commercial use cases, technical formulations, and regulatory requirements. 1. Pharmaceutical Intermediate for Heterocyclic Drug SynthesisPharmaceutical companies utilize this oxazole derivative as an advanced building block in the synthesis of heterocyclic compounds. It plays a pivotal role in constructing molecular frameworks for small-molecule APIs, particularly targeting anti-inflammatory and central nervous system segments. Our customers require consistently high purity for tight process control in multistep synthesis, with batch traceability per cGMP. The material typically enters at the stage of intermediate acylation when establishing the oxazole core within the full API route. Formulators optimize feed ratios based on downstream coupling partner reactivity and the required impurity profile. Final target molecules mainly include patent-protected agents and generic API bulk. Industry compliance standards
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2. Agrochemical R&D for Heterocyclic Herbicide DevelopmentAgrochemical research organizations incorporate this compound as a reagent in the synthesis of novel herbicidal candidates based on oxazole and acetic acid scaffolds. At the lab and pilot scale, formulation chemists select this material for its ability to introduce rigidity and electronic properties favorable for target-site inhibition. The typical workflow involves SM coupling or side-chain derivatization, where this acid component is a limiting or excess reagent depending on desired selectivity. Strict documentation aligns with global agrochemical certification demands, including stewardship over process by-products and solvent residues. Industry compliance standards
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3. Fine Chemical Intermediate for Specialty Dye SynthesisSpecialty dye manufacturers rely on this oxazolyl-acetic acid to construct chromophore backbones used in premium textile and technical applications. The compound offers a pathway for N-acylation or as a coupling component in the creation of highly conjugated molecules, particularly for fluorescent and pH-responsive dyes. It enters batch reactors at the color precursor stage, with critical monitoring for unreacted acid and color purity via UV/Vis analysis. Users tailor the charge relative to dye base to modulate hue and lightfastness properties in the finished batch. Industry compliance standards
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4. Organic Electronics: Advanced Material for OLED Emitter SynthesisManufacturers in the organic electronics sector leverage this oxazole derivative during the synthesis of OLED emitter molecules. Research and commercial development teams utilize it to introduce specific electronic and steric attributes within emitter precursors, improving charge mobility and spectral properties. The acid is generally introduced during the intermediate condensation phase, with precise stoichiometry aligned to molecular design and desired quantum yield. Final purification requires stringent control over metal residues and optical defect level before integration into emitter system scale-up. Industry compliance standards
Typical usage ratio
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Among the growing families of oxazole derivatives, 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid stands out due to its unique structure and functional potential. Within our production area, the air regularly takes on the faint notes of aromatic heterocycles—an unmistakable fingerprint—and this compound is one of those complex molecules that demands both precision and experience at every step.
The process often starts far from the plant site, traced to raw material selection: prosaic phenylacetic acids, methylations, careful protection, subtle ring closures on the oxazole core. Every gram that leaves our reactors carries evidence of real-world variables: batch temperature swings in summer, humidity in the process air, and the constant push to eliminate trace byproducts that can compromise downstream reactions. Our operators know that this sort of acetic acid derivative doesn’t forgive poor attention. That’s the difference between textbook chemistry and the real thing on the shop floor.
On the analytical side, characterizing 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid requires more than just hitting purity thresholds—a typical batch moves through an HPLC and NMR workflow, not because someone in an office asks for it, but because unknown signals and trace peaks hurt more than they help. These checks protect every partner down the line. No distributor enjoys an unplanned purification. No research chemist expects side-products lurking in their syntheses. We don’t either.
Ordering a kilogram or several metric tons looks easy on paper, but specifications change based on end-use. The most experienced customers—those at pharmaceutical labs or custom synthesis outfits—demand clear profiles. We ship material at ≥98% purity (as dictated by HPLC), and scale that spec all the way up to pilot tons. Melt point, color, and particle size—every batch comes with a real COA, signed by a chemist who’s invested more than a formality.
Some groups request tailored lots calibrated to finer specifications. Process parameters—water content by Karl Fischer, residual solvents quantified by GC-MS, optical purity—matter for downstream catalysts or API intermediates. Years ago, a medicinal chemistry group flagged inconsistent melting points unrelated to bulk phase. We re-examined our filtration and drying stages to make the batch reproducible and to remove minor hydrate forms. Factory knowledge, not procurement, fixed the issue. These are not points you’ll find in glossy brochures, but they keep long-term relationships alive.
The 5-methyl and 2-phenyl groups on the oxazole ring change more than just the molecule’s mass. Take similar acetic acid derivatives—for instance, compounds without a methyl at the 5-position, or a simple alkyl in place of the phenyl—the electronic environment shifts, altering both reactivity and stability under a range of conditions. In a production run, these differences show up as more (or less) ease in crystallization, tendency to absorb moisture, even the smell upon isolation. Years of running batches back to back with close analogs taught us that not all oxazole acetic acids behave the same across the same work-up procedure.
During formulation or coupling in pharmaceutical R&D, the difference often surfaces in solubility. Our 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid dissolves differently in mixed organic-aqueous systems. The substituted ring system increases compatibility with DMSO and lowers volatility, which can influence both reaction kinetics and analytical recovery. That change—subtracting guesswork from a potentially fragile project—gives our clients more certainty. Some customers ran side-by-side trials and reported back: this variant provided yields more consistently, especially when using solid-liquid phase transfer catalysis.
What doesn’t show up on a simplified spec sheet is the operator know-how. Acetic acids with bulkier oxazole moieties tend to cake or clump more easily, which can obstruct both scaling up and downstream processing. We learned to anticipate these minor but real handling differences, tuning crystallization rates and adjusting drying protocols. If you’re moving from a less-substituted analog to this molecule, something as simple as flow rates or blending regimes needs adjustment. We have seen lab-to-plant discrepancies resolved by walking through a production area, not in an R&D presentation.
The main users for this compound are research centers focusing on pharmaceuticals, fine chemicals, and advanced materials. Some projects target peptidomimetics, others build small-molecule scaffolds for patentable drugs. A few explore agricultural chemistry. Each application runs on tight deadlines and often even tighter budgets.
No matter the scale, performance means something different to every chemist. Some value sharp melting points as a target for formulation or chromatography development. They care about stability after several weeks at room temperature. Others want consistent reactivity for scale-up—a batch that works on gram and kilogram levels with equivalent conversion rates.
Process development teams focus less on the name and more on how the compound flows in their systems. Sticky lots can block pneumatic transfer. Hygroscopic grades draw moisture and upset balance in stoichiometry-sensitive couplings. Over the years, feedback loops between our QA unit and plant floor have led to very real changes—extra sieving steps, improved packaging, or revision in the compaction procedure, all based on direct reports from the end-user.
Sometimes the best insight doesn’t show up until after a shipment lands several thousand kilometers from where it left our site. One firm focused on selective, high-yield amidation turned up a side impurity only after scaling tenfold. Quick phone calls at odd hours, batches reanalyzed in real-time, and a new batch dispatched—this kind of support isn’t a commodity. That’s been part of how our team has built the right trust, even with new chemical entities that push the envelope.
Most of what makes this material valuable isn’t visible in the number string or molecular drawing. It appears in the methodologies—old and new—that we refine with every campaign. The classic batch mode for oxazole formation still covers most runs, but semi-continuous setups have started to gain favor for trickier lots. Scratching at a stuck filtration late on a Saturday might never make a case study, but it becomes part of how the next campaign succeeds.
Through the years, seasonal shifts show their own hand. Winters pull more moisture from the air, favoring certain crystal morphologies, while warmer months extend drying times and encourage side-formation. Tracking this, the team keeps process logs tracing each shift, learning what small changes anchor consistent outcomes. We have moved more than one process step off-line, just to keep a batch from stalling at the wrong time.
Supply assurance means staying ahead of interrupted raw material trains and regulatory interruptions. Lead times, once measured in weeks, can now pivot fast. We stock and buffer enough key intermediates for oxazoles, knowing that shortages or shipping delays elsewhere in the world ripple straight down to the end-user. After a regional solvent restriction a year back, most distributors scrambled. We didn’t miss a delivery—the stockpiles held up, and our customers rarely saw the drama.
From a sustainability standpoint, careful solvent recovery matters as much as an extra percentage point in yield. While regulatory targets tighten year upon year, the on-ground focus always circles back to minimizing exposure, recycling streams where practical, and documenting every chemical use as local and international bodies demand. No operator wants to work in a space clouded by poor ventilation or behind on best practices—our protocols stay reviewed and upgraded, responding to real feedback from auditors and, more importantly, from the plant floor.
Certain solvents used in the oxazole process carry stricter danger labels every year. Shifting to greener alternatives never feels painless at first—compatibility requires new pilot trials, more analytical development, sometimes entire control system updates. Still, the payoff comes in easier compliance and, often, improved product properties. The production chain often grows more robust as a result, less prone to sudden disruptions from supply chain or policy shocks.
Over several years of manufacturing, the finished product brings back quality inspections from independent labs, not just internal controls. Twice, quality assurance teams flagged small changes in the chemical shift values in the NMR, leading us to run extra impurity profiling. In both cases, early intervention stopped minor problems from ballooning.
In performance testing, batches consistently met or exceeded minimum established standards. A sequence of recent customer-supplied surveys matched our internal QA trends, with on-spec delivery rates surpassing 99%. Product returns due to spec variance sit below 0.5% annually, and nearly every issue that arose came down to logistics, not core process flaws. In competitive benchmarks, the oxazole-acetic acid backbone gives certain routes—especially peptide-like assemblies and polar aromatic drugs—an edge that continues to draw repeat orders.
Handling moisture sensitivity crops up as a perennial problem, especially in containerized transit to more humid climates. Rather than leave the issue with the customer, our packaging technicians have converted all bulk lots to include both sealed liners and desiccant pouches. Monthly review cycles track stability out to six months, quantifying weight change and impurity drift during storage. For buyers working in climates with more than 70% RH, tailored instructions and best-practice videos supplement the physical product, all lessons compiled from years of customer interaction and, sometimes, troubleshooting in a hurry.
Shipping and customs clearances create further bottlenecks, especially for flagged precursors. The regulatory team walks through MSDS paperwork and pre-clears lot documentation so the material moves without customs hold-ups. Early communication takes much of the stress out of handling advanced intermediates—more than once, we’ve seen fast-tracked material miss a critical deadline due to a translation slip or missing page. By staying directly involved until the cargo clears, we keep these headaches from multiplying.
Some buyers express concern with patent infringement or research blockades around advanced oxazole scaffolds. Our legal and technical division continuously reviews published literature and local filings to ensure both our team and customers work within a safe, compliant environment. Occasionally, regulatory ambiguities require us to seek external counsel, pass on process updates, and collaborate on non-infringement certifications. No manufacturer wants to operate with a short-sighted view—by collaborating with industry consortia, we improve transparency and protect both our interests and those of our partners.
Running a full-scale plant for 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid is about more than checking boxes. Every tank charge, every filtration, and every packing step ties together years of experience with each new customer project. The team learns from each campaign—the failures as much as the smooth runs. Our goal is to move beyond raw molecule production to become a reliable partner: one that spots trouble before it lands, adapts to changing specifications, and remains accessible for real-time support.
Consistency, at its core, grows from strict process control and transparent feedback between production and application. A new project never comes down to just a quoted purity or a price per kilo. Instead, the client’s timeline, handling needs, and downstream application influence every thin-layer chromatography spot, every color check, every tweak to packing. Those hour-by-hour changes rarely appear in summary reports but drive success in the field.
The chemical industry is always changing, never satisfied with yesterday’s protocols or expectations. New guidelines, evolving markets, raw material bottlenecks—each one pushes us to innovate while maintaining the high standards long-term partners count on. That process never stops. By growing institutional memory and engaging with everyone from the factory floor operator to the customer’s most junior research scientist, we ensure the product—2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetic Acid—remains both predictable and robust in the face of challenge.
Trust only comes from doing the hard work, batch after batch, and learning at every stage. That reality—the unpredictable, rough-edged demands of scale chemistry—drives our commitment to honest production, clear communication, and ongoing improvement, for this product and every molecule that follows.