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HS Code |
430453 |
| Chemical Name | 5-Phenylisoxazole-3-carboxylic acid |
| Molecular Formula | C10H7NO3 |
| Molecular Weight | 189.17 g/mol |
| Cas Number | 59258-56-5 |
| Appearance | White to off-white solid |
| Melting Point | 170-174°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
| Smiles | C1=CC=C(C=C1)C2=CC(=NO2)C(=O)O |
| Inchi | InChI=1S/C10H7NO3/c12-10(13)8-6-11-14-9(8)7-4-2-1-3-5-7/h1-6H,(H,12,13) |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Pka | Approximately 3.7 |
As an accredited 5-Phenylisoxazole-3-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 25 grams of 5-Phenylisoxazole-3-Carboxylic Acid, labeled with safety and chemical details. |
| Shipping | 5-Phenylisoxazole-3-Carboxylic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is typically packed according to chemical safety regulations, with clear labeling and documentation. The package is handled with care and shipped via certified carriers to ensure compliance with relevant hazardous materials transportation guidelines. |
| Storage | 5-Phenylisoxazole-3-Carboxylic Acid should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect from light and excessive heat. Label the container clearly, and keep it out of reach of unauthorized personnel. Follow all relevant safety and regulatory guidelines for storage. |
Applications of 5-Phenylisoxazole-3-Carboxylic Acid in Industrial Manufacturing5-Phenylisoxazole-3-Carboxylic Acid serves as a critical intermediate in several specialized manufacturing sectors. Its unique isoxazole structure enables selective functionalization and active group modification, supporting high-value products in regulated industries. Below are key downstream application scenarios with detailed technical requirements. 1. Pharmaceutical Intermediates for Anticonvulsant APIsPharmaceutical manufacturers rely on this compound as a critical building block during the synthesis of novel isoxazole-based anticonvulsant active pharmaceutical ingredients. The carboxylic acid group allows formation of amide or ester derivatives which function as key moieties in API molecules. Compliant conversion and impurity control remain essential throughout process scale-up. Pharmaceutical producers strictly manage input concentration and byproduct removal to fulfill drug master file (DMF) submissions and commercial supply agreements. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisAgrochemical producers incorporate this raw material during synthesis of herbicide and fungicide actives within the isoxazole chemical class. The phenylated carboxylic acid enables modification of biological activity via selective substitution and salt formation. Integration into the process flow requires attention to residual solvent control and isomer ratios per agricultural chemical regulations. Industry compliance standards
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3. Advanced Organic Electronic MaterialsSpecialty chemical manufacturers working with organic semiconductors utilize 5-Phenylisoxazole-3-Carboxylic Acid in the fabrication of functional organic building blocks for OLED and OFET devices. Its electron-rich structure supports formation of π-conjugated frameworks, enabling high mobility pathways in thin-film applications. Material purity and residual metal content receive strict oversight to meet device yield targets. Industry compliance standards
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4. Analytical Standards and Research ReagentsProducers of analytical testing kits and certified reference materials employ this carboxylic acid as a standard for HPLC, GC-MS, and NMR-based quantification in pharmaceutical research and environmental monitoring. High-purity batches undergo rigorous final QC to ensure lot-to-lot consistency as required for certified reference materials (CRMs). Batch traceability and impurity profiling are maintained through validated analytical protocols. Industry compliance standards
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5. Heterocyclic Ligand Synthesis for CatalysisManufacturers producing specialty catalysts and organometallic complexes for fine chemical or pharmaceutical synthesis integrate this acid in constructing N,O-donor ligands. Its rigid backbone and aromatic substituent facilitate metal coordination and catalytic activity, especially in C–N bond formation reactions. Control of chelation pathway and ligand purity remains essential for catalytic performance and selectivity. Industry compliance standards
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Working with 5-Phenylisoxazole-3-Carboxylic Acid daily means seeing its strengths up close and putting those qualities to the test through each synthesis batch. We have spent years refining its production, correcting the error margins, improving yield, and consistently delivering a product that chemists can rely on. This approach gives insight not only into the molecule’s structure but also into the real-world challenges researchers and manufacturers face in the lab and on the factory floor.
We produce 5-Phenylisoxazole-3-Carboxylic Acid in our dedicated plant. Its structural backbone—an isoxazole ring with a phenyl at position 5 and a carboxyl group at position 3—reflects a well-designed scaffold for applications in organic synthesis. Someone with hands-on experience quickly identifies the slightly off-white to pale tan crystalline powder that results from our proprietary processes.
Routine purity records using HPLC and NMR show our product usually exceeds 98.0% purity, and benchmarking tests line up closely batch after batch. Tight melting range, typically between 170–175°C, confirms consistency in the manufacturing process. We monitor moisture content and residue on ignition, targeting values well below thresholds that would interfere with downstream chemistry. Every lot undergoes the same comprehensive battery of in-process controls, and our lab team routinely runs further identity confirmations by mass spec and IR.
High purity and low contaminant profiles arise not just from careful solvent choices and filtration, but from daily practice of watching reactions and learning to spot the telltale signs of byproduct formation. Some things only years of handling the material teach you: the subtle shifts in color, the way filters slow when impurity load increases, the ease with which the material stirs or cakes at certain points in the drying line. These are signals automation can't catch alone, and they feed back into process corrections for the next batch.
Our customers—pharmaceutical labs, agrochemical developers, and advanced material researchers—depend on 5-Phenylisoxazole-3-Carboxylic Acid for more than academic interest. We talk regularly with formulation chemists who appreciate how the carboxylic acid group enables versatile downstream manipulation: amidation, esterification, or salt formation. Others use it as a core fragment for heterocyclic building, finding the phenylisoxazole moiety valuable for its fit in kinase inhibitor frameworks and other bioactive scaffolds.
Having exported material to dozens of countries, we see the difference that reliable supply brings. A missed shipment or an out-of-spec batch holds up more than just a bench experiment; it can delay clinical studies or disrupt process scaleups costing thousands in labor and wasted time. On-site, we recognize how important lot-to-lot reproducibility is for those running sensitive reactions, so we blend and mill the powder to maintain a controlled particle size distribution and flowability for easy handling.
We keep samples from every batch long-term and perform retrospective analyses as process upgrades come online. This habit reflects not just regulatory compliance, but a broader commitment to the labs and teams who rely on our product holding true to its certificate of analysis long after delivery.
There’s a world of difference between material made in-house and that acquired from anonymous supply chains. Direct manufacturing means full control over source reagents, synthesis route, and final product handling—critical when the product enters advanced screening or pilot production for pharmaceuticals. We’ve designed our process to minimize batch-to-batch drift in both impurity fingerprint and color profile. That helps medicinal chemists avoid re-validation headaches caused by mysterious variances in starting materials that can crop up in lots from traders or resellers.
Experience with alternate suppliers, especially for a ring system as particular as isoxazole, teaches you caution. Over the years, we’ve run parallel checks comparing our acid’s reactivity profile with samples sourced elsewhere. We noticed that impurities in some outside lots slowed amide coupling steps or triggered side reactions in heterocycle formation, leading to lower yields or the need for extensive purification. Our own product, freshly manufactured and monitored in-house, demonstrates smoother conversion and cleaner crude products at workup, helping customers save time during scale-up.
The tactile properties matter, too. Our material typically presents as a uniformly milled, free-flowing crystalline powder that pours and weighs out with ease. It stays stable in long-term storage under recommended conditions, with minimal degradation or color changes even after months at ambient temperature due to well-established drying techniques and solid packaging. We have received unsolicited feedback from researchers noting the predictable behavior in solvent, the clean melting, and the absence of any off-odors or visible impurities.
Chemical manufacturing is more than drawing up a protocol and letting it run. Factory workers, shift managers, and process chemists gain an instinct for the pulse of the plant. Our production lines have been retooled over time in response to real-world demands: scaling up to metric ton production, adapting environmental controls for weather swings, and streamlining transfer systems for safer material handling. Minimized dust generation and proper fume handling are lessons learned through both trial and regulatory scrutiny.
We take maintenance of each reactor, hydrogenator, and dryer seriously. Quality comes from equipment that runs reliably and stays clean. Team members regularly run small-scale test syntheses using factory-floor product pulled at random to spot-check for possible cross-reactivity or contamination. The feedback loop between the QA lab and the production floor ensures no bottleneck gets ignored.
Safety and traceability are baked into every manufacturing run. All solvents and reagents receive strict inspection before reaching the reactors. Final product release is contingent on documented test results—nothing ships out without meeting specification, as we recognize the risk downstream users face if a substandard lot enters a regulated environment.
Customers gain from knowing that every drum and kilo stems from a process under the manufacturer’s direct supervision, not just sourced from an unknown origin and relabeled. We believe transparency in process and documentation forms the backbone of supplier trust. Raw data, retention samples, and process records remain available for inspection or audit as needed, providing peace of mind to those building high-value projects on our materials.
Decades in active production reveal the pressure points where the right chemical makes or breaks a research project. In the medicinal chemistry field, the ability to quickly order multiple kilograms of 5-Phenylisoxazole-3-Carboxylic Acid at research- or GMP-grade purity opens doors to structure-activity relationship studies, library synthesis, and lead optimization runs without schedule creep. The speed and reliability of getting fresh lots matters more than abstract statements about supply capability.
We have worked alongside clients developing new synthetic routes and shared direct feedback on reactivity, solubility, and compatibility with other synthetic intermediates. Such support goes beyond supplying a product—it means comparing analytical data, discussing observed side product formation, and suggesting minor tweaks based on experience with reaction conditions and workups. If a project hits an unforeseen impurity problem, our access to archived analytical runs allows us to quickly pinpoint batch history and resolve discrepancies.
For solid formulations and pilot-scale work, consistent powder characteristics lower the risk of unwanted surprises during blending, compaction, or processing. Our experience in controlling drying cycles, milling settings, and storage conditions shapes product that remains stable under typical warehouse conditions, minimizing losses to degradation or chalking.
We recognize that streamlined documentation, robust test protocols, and openness to technical review help our customers clear their own regulatory and internal review hurdles more efficiently. Being a manufacturer means we can back up every shipped lot with full traceability and technical context.
In an era of supply chain disruptions and rapid market shifts, direct manufacturing offers meaningful advantages. We predict demand swings and plan raw material procurement months in advance, keeping enough buffer stock to bridge gaps in international supply. The flexibility to adjust batch sizes or switch between research and industrial specification reduces lead times and means we can support urgent programs when timelines grow tight.
The ability to flex production capacity comes from in-house process mastery, optimized work schedules, and longstanding relationships with trusted suppliers. We work from a foundation of full process knowledge—from reaction conditions to final QA—rather than depending on vague promises from distant intermediaries.
Transport and packaging standards reflect feedback from years listening to laboratory and production line users. We select packaging materials for sturdiness and inertness, confirming with accelerated aging tests that the product arrives in the same condition it left our dock. Each label carries comprehensive batch information, allowing for seamless traceability and integration into both research inventories and regulated manufacturing records.
By refining shipping documentation, optimizing customs routines, and keeping communication lines open, we minimize the type of hiccups that slow international deliveries. For urgent deliveries, we maintain a flexible logistics network, adjusting between sea, air, and bonded warehouse options based on client needs and border requirements.
Ongoing experience shows that sustainability and compliance must move hand-in-hand with production improvements. Our clean-up systems and emissions controls have evolved alongside our best practices for solvent recycling and waste minimization. Every process change is evaluated not just for estimated environmental impact, but for long-term ability to remain ahead of new regulatory expectations.
In manufacturing 5-Phenylisoxazole-3-Carboxylic Acid, waste stream reduction and closed-system handling help limit both environmental footprint and operator exposure. We transparently document recycling efficiency and have worked to phase out less environmentally friendly reagents in favor of safer alternatives, aligning process chemistry with global best practices.
Certification and regular third-party audits keep our facility up to standard on environmental, safety, and quality management systems. Customers ask more pointed questions about supply chain transparency and sustainability than ever before, and as a manufacturer, we share our progress, roadmap, and any challenges encountered in routine communications—not through impersonal annual reports, but in direct discussion with those relying on our supply.
As manufacturers of 5-Phenylisoxazole-3-Carboxylic Acid, our knowledge comes from both the plant floor and daily interactions with researchers, purchasing managers, and process engineers. We respond directly to urgent technical questions, troubleshoot reactivity problems when they appear, and hold follow-up calls to resolve unexpected application issues. This level of technical partnership grows only from years of face-to-face feedback, honest error reporting, and shared commitment to problem-solving.
Regular feedback from long-term partners underscores the value of consistently high quality. We document even minor process adjustments and share them proactively with key customers, supporting uninterrupted project flows. For new applications—whether in drug discovery, high-end polymers, or specialty agrochemicals—we ensure open channels for request and adjustment, recognizing that novel projects often mean unique demands on materials, sensitivity, or documentation.
We do not stop improving after shipment. Post-shipment support, prompt replacement in rare cases of transit loss or damage, and clear accountability all underline how much we value direct relationships over volume-based supply deals. Repeat business comes from steady performance over many years, not from short-term pricing wins.
Producing 5-Phenylisoxazole-3-Carboxylic Acid is more than a technical exercise or transactional business. Our plant teams, QA chemists, and client service managers see every shipment as a chance to affirm trust in manufacturing know-how and the value that comes with direct, traceable supply. Every improvement, safeguard, and technical support policy links back to first-hand experience and the daily reality of building both product and relationship for the next project that depends on our compound.