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Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate

    • Product Name Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate
    • Alias methyl 2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)acetate
    • Einecs EINECS 695-714-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    220994

    Chemical Name Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate
    Molecular Formula C13H13NO3
    Molecular Weight 231.25 g/mol
    Cas Number 1073355-93-7
    Appearance Off-white to pale yellow solid
    Purity Typically ≥98%
    Boiling Point No data available
    Melting Point No data available
    Solubility Soluble in DMSO, methanol
    Storage Temperature Store at 2-8°C
    Smiles CC1=C(N=C(O1)C2=CC=CC=C2)CC(=O)OC
    Inchi InChI=1S/C13H13NO3/c1-9-12(8-13(15)17-2)16-11(14-9)10-6-4-3-5-7-10/h3-7H,8H2,1-2H3
    Refractive Index No data available

    As an accredited Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with tamper-evident cap, labeled with chemical name, hazard information, and batch details, 25 grams net content.
    Shipping Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate is shipped in tightly sealed containers, protected from moisture and light. It is transported in accordance with chemical safety regulations, using appropriate hazard labeling. During transit, it is kept at controlled room temperature and handled by trained personnel to ensure safety and maintain compound integrity.
    Storage Store **Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-yl)acetate** in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, well-ventilated area away from sources of heat or ignition and incompatible substances such as strong oxidizers. Properly label the container and ensure access is restricted to authorized personnel. Follow all safety protocols and local regulations for chemical storage.
    Application of Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate

    Applications of Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate in Industrial Manufacturing

    As an original manufacturer, we supply Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate to industrial partners with proven utility in specialty chemical syntheses, pharmaceutical development, fine agrochemical intermediates, and advanced coatings production. Our downstream clients utilize this compound for targeted transformations driven by high-value end-product requirements and regulated industry frameworks.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers integrate this oxazoline ester as a key intermediate in multi-step syntheses, especially for active pharmaceutical ingredient (API) building blocks involving heterocyclic frameworks. Its functional groups are well-suited for selective transformations, including alkylation and amidation, forming the core structures of advanced CNS, anti-infective, and oncology molecules. Process chemists use this material at controlled stages to meet strict residue and purity limits following current Good Manufacturing Practices (cGMP).

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF monographs for relevant APIs
    • European Pharmacopoeia 11.0–Active Substances
    • FDA 21 CFR Part 211: Finished Pharmaceuticals

    Typical usage ratio

    • 0.5–2.5 molar equivalents per API synthesis step, adjusted per route complexity and final impurity targets

    Downstream process integration

    • Introduced after core scaffold formation at pre-final intermediate stage
    • Undergoes ring-opening, nucleophilic substitution, or amidation under controlled temperature with validated work-up protocols
    • Residual solvent and by-product removal via phase separation and crystallization

    Final product types

    • Active pharmaceutical ingredients (APIs) for CNS therapeutics
    • Oncology drug candidate intermediates
    • Multi-ring heterocyclic reference standards
    • Contract-manufactured small molecule intermediates

    2. Fine Agrochemical Intermediate Production

    Agrochemical companies adopt this molecule as an intermediate for designing selective fungicide and herbicide actives. The oxazoline core participates in downstream acylation or thiolation, yielding unique molecular scaffolds optimized for plant protection. Formulators control impurity profiles by including this material at stages that ensure environmental and toxicological compliance in resulting crop-protection agents.

    Industry compliance standards

    • FAO/WHO–International Code of Conduct on Pesticide Management
    • ISO 9001:2015 Quality Management in Agrochemical Manufacturing
    • OECD Guidelines for the Testing of Chemicals
    • REACH (EC No 1907/2006) registration for agro-intermediates

    Typical usage ratio

    • 0.9–1.8 molar equivalents depending on the desired conversion yield and downstream pesticide structure

    Downstream process integration

    • Charged in batch or semi-continuous synthesis reactors post-coupling phase
    • Oxazoline ring modification or substitution reactions performed at 60–110°C with defined stoichiometry
    • Purification follows to remove residual intermediates influencing environmental safety

    Final product types

    • Precursor compounds for commercial herbicides
    • Key molecules in fungicide active ingredient synthesis
    • Intermediate blends for branded crop-protection formulations
    • Reference compounds for agrochemical R&D validation

    3. Electronic Chemicals and Photoresist Additives

    Leading electronic material producers use this compound as a specialty intermediate for photoresist enhancement and semiconductor process chemicals. Its compact oxazoline ring and aromatic substituents support novel resin backbones and light-sensitive agents for lithographic patterning. Strict control over trace metals and organic residues is mandatory for use in electronic-grade formulations.

    Industry compliance standards

    • SEMI C1–Specification for Electronic Grade Chemicals
    • IEC 62474: Materials declaration for electrical and electronic products
    • RoHS Directive 2011/65/EU (lead, cadmium, mercury content limits)
    • Company-specific low-purity contaminants thresholds

    Typical usage ratio

    • 0.2–1.0% weight fraction for resin modification in positive or negative photoresist formulas

    Downstream process integration

    • Blended during pre-polymer synthesis in solvent-controlled reactors
    • Initiates esterification or etherification to improve adhesion and imaging contrast
    • Excess is removed after polymerization via vacuum distillation or solvent extraction

    Final product types

    • Photoresist base polymers for PCB manufacturing
    • Resin additives for high-resolution lithography
    • Dielectric layer materials for integrated circuits
    • Packaged electronic-grade mother liquors

    4. Specialty Coating and Reactive Resin Formulation

    In advanced coatings manufacturing, formulators use this compound as a reactive building block to engineer bespoke functionalities into high-performance paints, varnishes, and sealants. The ester and heterocycle moieties support covalent cross-linking and improved hardness. Specifications for VOC content, residual monomers, and cross-link density drive process controls from raw feedstock onward.

    Industry compliance standards

    • ASTM D5402–Solvent Content in Coatings
    • ISO 16000-9:2016–VOC Regulations
    • EN 71-3: Safety of Toys (Migration of certain elements for consumer coatings)
    • REACH Annex XVII (restrictions on hazardous substances)

    Typical usage ratio

    • 1.0–7.5% weight fraction, modulated per film thickness and target cross-link density

    Downstream process integration

    • Added as a primary or secondary cross-linker in blending tanks prior to final stirring
    • Engages in free-radical or step-growth polymerizations under controlled temperature profiles
    • Unreacted material quantified post-cure as part of batch release

    Final product types

    • Hard-wearing industrial coatings for metal or plastics
    • Specialty urethane or epoxy resin systems
    • Protective sealants with enhanced chemical resistance
    • Performance varnishes with tailored gloss
    Free Quote

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    Certification & Compliance
    More Introduction

    Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate: Meeting the Demands of Fine Chemical Synthesis

    From Our Manufacturing Floor: Quality and Consistency at The Core

    Working up close with Methyl 2-(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)Acetate gives our team insight into how fine details impact chemical processes and, by extension, the final products that reach the market. Our product—commonly abbreviated as MPOA—serves not just as an intermediate but often as a linchpin in specialized pharmaceutical and agrochemical syntheses. Week in, week out, batches leave our reactors with the sort of purity and lot-to-lot consistency that serious manufacturers rely on for reproducible results. This doesn’t happen by accident; it comes through dialing in every stage, from raw material checks through to solvent selection, purification, and packaging.

    Understanding MPOA: Chemical Background and Analytical Focus

    In our experience, the structure of MPOA—with its oxazole ring fused to both methyl and phenyl substituents—offers unique electronic and steric properties. The ester group at the end of the molecule has proven its worth as a strategic handle for chemists. Our chemists pay attention to every minor variable, because these can decide whether a downstream reaction succeeds or ends up an expensive mess. Analytical protocols here walk a tight line between thoroughness and efficiency: titration for endpoint confirmation, chromatography for trace impurity removal, and spectrometric checks to ensure every lot reflects the expected signature. Our team rarely encounters the kind of deviation that sends you scrambling for answers; it’s not a luxury, it’s the foundation of trust between maker and client.

    What Sets Our MPOA Apart: Decisions from Decades of Practice

    One thing we often discuss in production meetings is that MPOA is a product where over-simplification causes headaches on the customer side. Two containers labeled with the same name can behave quite differently in a real-world lab, especially if crystallinity, residual solvents, or trace metals are off. From day one, our focus turned to achieving a product that's not just high in purity content, but free from troublesome isomers or by-products that slow reaction steps or confound subsequent purification. You can tell a batch that came off old equipment and wasn’t properly dried—like clarity in glassware, little things reveal who actually knows their craft.

    Any seasoned chemist will tell you that in heterocyclic intermediates, a little moisture, a touch of catalyst carryover, or bulk-phase impurities from solvents open the door to inconsistency. For this ester, our vacuum drying parameters make the difference between a pale, free-flowing solid and a sticky, marginally impure material that gums up process yields downstream. We ship out only material that meets our own established benchmarks—benchmarks shaped by the hard lessons picked up working not just in the lab but alongside customers retooling their syntheses in response to regulatory or market shifts.

    Real-World Usage: Downstream Chemistry Demands Real Reliability

    MPOA’s main demand grows from its ability to slot into a range of functionalizations and coupling reactions. For certain pharmaceutical targets, we’ve seen our material serve as the crucial carbon backbone in early-stage synthesis of novel pyridines, oxazoles, and benzoxazoles. Some of our longtime clients use MPOA for transitioning into phthalimide derivatives, taking advantage of its methyl and phenyl substitutions for selectivity in alkylation or cross-coupling steps. Researchers who build out new scaffolds for agrochemistry tap into the unique reactivity brought by the oxazole core, and the nearby ester group lends itself for subsequent hydrolysis or transesterification without excessive side reactions.

    While many ester intermediates line up to compete in this segment, MPOA’s definitive edge comes from its electronic profile. As operators in the plant, we observe that selective substitution on the oxazole ring dramatically shifts its behavior, whether in a classical nucleophilic substitution or in a metal-catalyzed C-H activation. That nuance puts our version of MPOA in a place where our hands-on approach helps chemists get their job done—whether they're in a global pharmaceutical pipeline or at a fast-moving CRO churning out dozens of analogs at bench scale.

    MPOA As Used by Chemists—A Direct Line from Reactor to Lab Bench

    Our feedback channels stay active for a reason. Not every synthetic step lands as expected—even with textbook intermediates. Over the years, we've fielded requests for custom bulk quantities, high-purity fractions, and specific particle sizes. Each request has sharpened our understanding of what chemists juggle in their day-to-day. Fine-milled MPOA helps labs achieve complete dissolution in low-boiling solvents where clumps create frustrating filtration issues. Our larger granule formulation caters to continuous flow systems, where rapid, even metering controls make all the difference in automation.

    Where we see chemists run into speed bumps is often in solvent handling and work-up. Some vendors release material barely dried and packed in gas-barrier but moisture-permeable bags, betting that most users will accommodate. We took a different path after seeing actual accounts of failed crystallizations, poor reproducibility, or inexplicable color in finished APIs traced right back to poorly controlled raw materials.

    Practical Differences: MPOA Versus Other Ester Intermediates

    We’ve handled requests for both methyl and ethyl esters of related oxazole compounds and tested several alternatives head-to-head in pilot-scale trials. Most of our industrial customers learn quickly that methyl esters like MPOA offer easier hydrolysis kinetics under basic or acidic conditions, allowing cleaner product profiles. Ethyl and bulkier esters often stick around unreacted, demanding longer reaction times or harsher work-ups. The positioning of the methyl and phenyl groups in this molecule further tune its reactivity—yielding intermediates that perform predictably in cyclization or Suzuki coupling steps, unlike some less sterically-defined alternatives.

    Subtle differences in substituent placement can matter. We’ve seen some cases where switching to an isomer with the methyl on a different position throws off the desired regioselectivity, pushing yields off target and muddying up chromatograms. Across dozens of production campaigns, using consistent substitution patterns paid off in higher, more reproducible yields for key client targets and a dramatic reduction in post-reaction remediation.

    The Human Element: Operators Matter as Much as Labs

    No formulation, no degree of automation replaces an operator whose eye catches subtle changes in batch texture or crumping, the hint of off-odor, or unexpected color development in a final lot. We keep experienced hands on our reactors because every synthesis has a way of surprising even seasoned chemists if you let complacency set in. Some vendors cut corners by shipping untested product and relying only on COAs for the paper trail. In our shop, we run confirmatory physical checks—sampling not just at the final drying but after packaging, looking for shifts in melting point, consistency, or solubility that might tip us off to hidden process drift.

    Practical chemistry still demands attention to those lived details. For MPOA, this means packaging that stands up to storage—even in less-than-ideal warehouse conditions—because lost material or degraded purity ripples downstream into compounded cost and delays. Each month, we review feedback and iterate on both synthesis and logistics to match the changing demands from clients, especially those grappling with regulatory or market-driven shifts.

    Beyond the Catalog: Customization and Scale-Up Learnings

    We’ve spent years evolving how we tailor MPOA productions, starting from 100-gram bench runs right up to 100-kilo bulk orders. Each scale brings its own headaches. Bench scale makes it easy to manage solvent removal, but as you move to plant scale, heat transfer, mixing, and gas evolution need constant checking. It’s easy to miss a batch’s endpoint, leading to over-alkylation or truncated yields. Running numerous campaigns gave our team the practical experience to tighten tolerances, anticipate exotherms, and maintain purity as batches go up in volume. We don’t advertise “off-the-shelf” because users don’t operate in one-size-fits-all conditions. Where a client requests a different particle size or a tighter-by weight purity window, we draw on this practical project trail to deliver what works in the field.

    Applications in Advanced Synthesis: MPOA At Work

    We see MPOA used downstream for several classes of pharmaceuticals and advanced agrochemicals—moving from pilot studies through to scaled lots. Chemists leverage the product’s electron-rich oxazole ring as a reliable platform for cross-coupling, creating complex molecular architectures necessary for new-generation therapeutics. Some reactions favor the stability of the phenyl-substituted oxazole core, where others utilize the acetate ester group for controlled modification or extension. MPOA’s balance between stability and reactivity keeps it relevant not just in straightforward coupling but also multi-step synthetic campaigns aiming at high-value targets.

    The journey from raw materials through to MPOA involves dozens of subtle choices. We’ve learned which solvents produce the cleanest crystallizations and how slow-controlled cooling secures ideal particle distributions. Each adjustment on our manufacturing line echoes in downstream campaigns, affecting everything from yields to ambient shelf life. Research clients return for MPOA supply because having foundational intermediates produced in exacting conditions moves their projects forward, relieves reproducibility headaches, and avoids surprises in scale-up or formulation.

    Assuring Purity and Processability: Beyond Standard COA Results

    Lab reports never tell the full story. Purity by HPLC is only part of the equation—solubility, hygroscopicity, thermal stability, and ease of filtration take equal priority for chemists using the product in synthesis. While working through process improvements, we’ve had to balance aggressive drying with the risk of caking or particle fusion, which creates downstream solubility headaches. Our final protocol uses gradient-vacuum drying and staged cooling, which secures a fine powder or free-flowing granule, depending on client need.

    Solvent residues often trip up new suppliers; even minor amounts of chlorinated solvents can poison palladium-catalyzed reactions or confound API impurity profiles. We keep a strict in-house ban on halogenated solvent use on the MPOA line, and any campaign that previously used these agents undergoes a complete line clean-down. Clients mention their relief in avoiding last-minute process redevelopment due to hidden contaminants linked back to earlier-stage intermediates.

    Meeting the Needs of Regulated Markets: Documentation and Transparency

    Clients in regulated markets—active pharma, regulated crop protection, and specialty chemical sectors—rely on thorough batch records and traceable documentation. Early on, we tuned our quality management workflow so every lot of MPOA comes with batch-level traceability, covering all raw materials, batch logs, and analytical verifications. This foundation helps project teams avoid compliance scrambles should regulators come knocking. Over the years, our records have supplied reference data for dozens of successful regulatory filings, and that feedback loop has only strengthened our quality-by-design approach. We won’t call it “value-added”—it’s just the way real manufacturers keep trust and repeat business alive.

    Dialogue With Chemists: Where Feedback Drives Change

    If there’s one thing we stand by, it’s that open dialogue reveals quality gaps sooner than any solitary analyst ever can. Rapid feedback from a client trying to scale a Suzuki coupling, or struggling with a tricky recrystallization, has pointed us toward meaningful process tweaks. Some of our most impactful improvements—like the shift to custom-milled particle sizing, or the upgrade to triple-layered barrier drums for export—came from users reporting on-site headaches, not from glossy marketing research. Manufacturing isn’t a one-way street; practical guidance from experienced chemists helped move us from simple supply to actual solution finding.

    That persistent two-way channel encourages a culture of improvement. Some requests go beyond straightforward changes—clients have invited us into process audits or collaborative development projects aimed at tightening every link in the chain from raw material to finished compound. Supporting innovation on the synthesis front requires a willingness to admit when your process falls short and a flexibility to adapt quickly, not just quote another standard line item.

    Environmental Considerations and Waste Reduction

    The chemical industry faces growing pressure to curb waste and trim the environmental drag that can arise with complex synthetic intermediates. Our work with MPOA hasn't been immune to this trend. Review after review, we’ve focused on cutting solvent use, recycling mother liquors, and optimizing reaction conditions to lower energy use. It's not just that this supports sustainability; by cutting input costs and waste disposal fees, we strengthen our business and safeguard our role in the wider chemical ecosystem.

    Improvements aren’t just headlines—they’re the product of seeing reaction waste, distillation cuts, and batch rework stack up, then going back to the lab bench to re-optimize. Our approach minimizes mother liquor volume, reclaims solvents for internal re-use, and shifts reagents toward options that won’t create persistent byproducts. These steps not only lower the environmental footprint but contribute to cleaner, more cost-effective output for every customer up the line.

    Shipping and Storage: From Batchroom Door to End User

    Many issues traced to raw material supply end up linked to poor handling between the production floor and the end user. Improper storage can turn pristine MPOA into a compromised material after weeks en route or in a humid warehouse. We pack finished lots in moisture-resistant drums, always with labeled secondary containment, and have revised our logistics strategy to avoid prolonged exposure that’s all too common shipping through multiple climate zones. It took feedback and real incident experience to create rules for how long material sits before shipment or what triggers a re-test before release; we wouldn’t risk a customer’s project on a shortcut here.

    Our philosophy of continuous improvement means lessons from each campaign or shipping challenge get incorporated across the board. New user requests get the same scrutiny, and we maintain a rapid reporting system for any in-transit or storage issues. That way, we maintain confidence from our customers that each new lot will arrive ready to use for whatever specification their synthesis demands.

    Challenges and Solutions: Staying Ahead in a Volatile Market

    No manufacturer can sidestep the reality of supply volatility, whether in upstream reagent availability or shifting downstream demand. Inflationary trends, new regulations, and sudden demand spikes have all tested our ability to keep MPOA flowing without letting quality slip or costs spiral. At times, we tap an expanded supplier network or pull from safety stock to buffer customers against delayed shipments. We’ve found direct relationships—meeting refineries, vetting secondary precursor lines—cut through risk better than any third-hand distributor ever could. Sustaining supply in turbulent markets requires forthrightness when changes occur and swift, transparent communication if timelines shift.

    Across our portfolio, solutions come from persistent investment in backward integration, on-site testing, and a management culture that anticipates market or regulatory headwinds rather than waiting for a crisis to hit. We’ve never believed in papering over cracks with heavy language—just steady, incremental fixes and hands-on experience. The result: a predictable partner for emerging industries and established players alike, one batch of MPOA at a time, meeting the everyday challenges of laboratory and commercial synthesis environments head-on.