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1,3-oxazole

    • Product Name 1,3-oxazole
    • Alias oxazole
    • Einecs 207-424-6
    • 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

    881331

    IUPAC_name 1,3-oxazole
    Molecular_formula C3H3NO
    Molar_mass 69.06 g/mol
    Appearance Colorless liquid
    Boiling_point 69-70 °C
    Melting_point -93 °C
    Density 1.049 g/cm³
    Solubility_in_water Miscible
    CAS_number 288-23-1
    SMILES c1cocn1

    As an accredited 1,3-oxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with secure screw cap, labeled “1,3-oxazole, 100 mL," hazardous symbols and handling instructions clearly visible.
    Shipping 1,3-Oxazole should be shipped in tightly sealed containers, protected from light and moisture. It must be handled and transported in accordance with local, national, and international regulations for hazardous chemicals. Proper labeling, documentation, and use of compatible, chemical-resistant packaging are required to ensure safety during transit.
    Storage 1,3-Oxazole should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture and light. Store in a flammable chemicals cabinet if available. Properly label all containers and ensure access is restricted to trained personnel. Handle under an inert atmosphere if necessary.
    Application of 1,3-oxazole

    Applications of 1,3-oxazole in Industrial Manufacturing

    As a direct manufacturer of 1,3-oxazole, our technical and production teams collaborate closely with industrial clients specializing in advanced organic synthesis. The material’s molecular properties support crucial transformations in pharmaceuticals, agrochemical ingredients, polymer advancement, and fine chemical syntheses. Below we detail key downstream application scenarios, each mapped to relevant compliance frameworks, usage levels, process integration points, and finished products.

    1. Pharmaceutical Intermediates for Antimicrobial Agents

    1,3-oxazole serves as a privileged structural template in the synthesis of numerous antimicrobial drug intermediates, enabling medicinal chemists to access bioactive heterocycles efficiently. During active pharmaceutical ingredient (API) synthesis, the compound allows precise installation of the oxazole core at critical coupling steps. Our product supports process chemists to meet stringent compositional control throughout multi-stage pathway reactions initiated from pre-GMP feeds, ultimately flowing into large-scale GMP-compliant pilot and commercial production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) Guidelines
    • U.S. Pharmacopeia (USP) monographs where applicable
    • EU EudraLex Vol 4 GMP
    • Chinese Pharmacopoeia (ChP) standards for intermediates

    Typical usage ratio

    • 0.5–5 mol% molar ratio in heterocycle-forming reactions; optimized based on target compound and reaction scale during process development

    Downstream process integration

    • Charged at the heterocyclization stage in amide dehydration-condensation or cross-coupling steps for formation of the oxazole ring system within multi-step synthetic routes

    Final product types

    • Beta-lactam antibiotics with oxazole moieties
    • Anti-tubercular APIs (e.g., oxazole-substituted pyrazinamides)
    • Antifungal agents incorporating oxazole substructures
    • Finished oral and intravenous antimicrobial formulations

    2. Agrochemical Active Ingredient Synthesis

    Leading crop protection manufacturers value the compound as an essential intermediate during development and scale-up of novel fungicides and herbicides. The oxazole motif, introduced via precision chemistry, confers bioactivity and resistance management against emerging pest and disease pressures. The raw material’s purity and reactivity prove critical across kilo-lab, pilot, and commercial agrochemical synthesis facilities, minimizing off-target byproducts while matching agrochemical registration specifications.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 Quality Management
    • REACH Annex VII – X safety dossiers for agrochemical intermediates
    • China's GB/T 4066 Pesticide Management Regulations

    Typical usage ratio

    • 1–10 wt% of total reactants depending on the design of the heterocyclic active moiety; ratio tailored during lead candidate development cycles and process scale-up to registered synthesis pathways

    Downstream process integration

    • Added into the primary heterocyclic ring-forming step of active substance manufacturing, often by cyclocondensation with diketone or aldehyde precursors under catalyzed conditions

    Final product types

    • Oxazole-class fungicides (e.g., oxazole-derivatives for cereal mildews)
    • Selective herbicide actives with heterocyclic frameworks
    • Seed-treatment formulations utilizing oxazole-based actives
    • Technical-grade and formulated plant protection products for export

    3. Polymer Modification and Specialty Resins

    Forward-thinking polymer and advanced materials manufacturers utilize the compound to introduce heteroatom-rich moieties, which enhance electrical, thermal, and chemical resistant properties of specialty polymers. Polyoxazoles and oxazole-functionalized polyimides show notable performance metrics in electronics, coatings, and high-temperature composites. The raw intermediate is introduced at early polymerization stages, where precise monomer incorporation controls polymer chain architecture and final performance parameters.

    Industry compliance standards

    • ISO 9001:2015 Quality Assurance
    • RoHS Directive (2011/65/EU) for electronics applications
    • UL 94 Flammability Standard for plastics
    • ASTM D638, D257, and D543 for polymeric material testing

    Typical usage ratio

    • 0.1–2 wt% during specialty polyimide or polyoxazole monomer feed — ratio adjusted according to backbone design and targeted end-use specification (e.g., flame resistance versus flexibility)

    Downstream process integration

    • Polymerization stage additive, either as a direct monomer in condensation–polymerization systems or as a functional cross-linker added during copolymer chain growth

    Final product types

    • Printed circuit board dielectric layers
    • High-performance resins for aerospace components
    • Protective coatings for industrial electronics
    • Membrane materials for fuel cell applications

    4. Fine Chemical Synthesis for Dye and Pigment Manufacture

    Specialty dye and pigment manufacturers use 1,3-oxazole to construct heteroaromatic chromophores with tailored optical properties for high-value colorants. Its unique reactivity enables the synthesis of advanced fluorescent dyes and color-fast pigments ideal for use in textiles, inks, and low-migration coatings. Downstream processors integrate this intermediate at defined cross-coupling and ring-closure steps under controlled thermal conditions to optimize color yield and purity demanded by brand manufacturers and specialty users.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textiles
    • GMP for food-contact coloring agents (EU 2023/2006 where relevant)
    • EN 71-3 for migration of certain elements in toys
    • ISO 9073-2 for pigment and dye performance evaluation

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to colorant precursor in heterocycle-coupling reactions; ratio set based on desired chromophore length and hue intensity

    Downstream process integration

    • Added during the final condensation or cyclization steps to build the oxazole chromophore core, typically followed by thermal processing or selective catalytic hydrogenation

    Final product types

    • Textile disperse dyes with enhanced wash fastness
    • Fluorescent markers for industrial and forensic use
    • Pigments for specialty ink formulations (inkjet, screen)
    • Color-fast coatings for polymer films and nonwovens
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    Competitive 1,3-oxazole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1,3-Oxazole Directly from the Manufacturer

    Nearly Four Decades of Chemical Production Experience with 1,3-Oxazole

    Manufacturing 1,3-oxazole isn’t a sideline for us—this is an important building block in heterocyclic chemistry, and that’s exactly why we give it as much attention as we give to our cornerstone products. Over the past several decades, we have fine-tuned our process from reagent-grade syntheses up to multi-ton batches fit for process development and commercial scale. Demand for heterocyclic intermediates can cycle up and down, but 1,3-oxazole has always stood out for its versatility. Every kilogram that leaves our site reflects our ongoing commitment to hands-on production, rigorous in-lab validation, and direct transparency about what goes into every batch.

    1,3-Oxazole is a five-membered aromatic ring consisting of three carbon atoms, one nitrogen atom at position 1, and one oxygen atom at position 3. Its structure provides a unique electronic environment for substitution and reaction, letting chemists introduce precisely engineered functionalities at positions 2 and 5. The formula may look simple, but controlling every step to guarantee consistent purity is no small feat. Over the years, experience has shown us that margin for error is paper thin: a fraction of a percent in moisture or an unnoticed by-product can mean the difference between a viable pharmaceutical candidate and a failed synthesis. With 1,3-oxazole, reliable process management always trumps hurry.

    Why We Prioritize Quality and Specification at Source

    One of the recurring questions posed to manufacturers revolves around what’s distinct about their 1,3-oxazole compared with generic stocks or blends purchased through resellers. Our approach has always anchored itself in pure batch-level traceability. We run all benchmark tests in-house—from NMR to GC-MS to water-content titration—to confirm that every lot falls within an expected purity, often upwards of 99%. Consistency is the backbone of a successful research or production campaign. Differences between two batches may not show up in a chromatography trace at first glance, but those little shifts in impurity profile often accumulate downstream and lead to major headaches. By running these controls ourselves, we can spot issues at the root, long before the product arrives at your site.

    1,3-Oxazole we supply is typically used as a key intermediate for pharmaceutical synthesis, agrochemical research, and advanced material science. Many specialty applications, like the development of new antimicrobial agents or pyridine replacements, depend on tailored reactivity and chemical integrity. We do not dilute, blend, or outsource final purification. By keeping all finishing steps in-house, we offer tight control over side-product profiles and guarantee reliable melting point, refractive index, and color. The research community’s requirements have evolved over the years, and batch cleanliness has had to follow suit. There are no shortcuts for achieving the purity threshold needed by high-throughput screening or complex functionalization.

    1,3-Oxazole Uses in Real-World Applications

    From decades on the shop floor and from working side by side with chemical engineers, medicinal chemists, and application scientists, real insight comes from practical deployment. We’ve supplied 1,3-oxazole for teams chasing new kinase inhibitors and innovative small molecules. Its electron-rich structure allows it to act as both an acceptor and a donor in synthetic sequences, letting process chemists construct highly functionalized heterocycles without costly metal catalysts or protection steps. Compared with other five-membered rings—such as imidazoles or thiazoles—1,3-oxazole shows a different reactivity map. Yields in certain alkylation reactions can run markedly higher simply by swapping in our oxazole across pilot campaigns. In agricultural research, the difference between hitting a target compound and stalling midway through scale-up can just as easily hinge on the starting oxazole as the rest of the route.

    One of the ways we’ve seen 1,3-oxazole add value is in iterative library synthesis. Automated platforms often struggle when introducing moisture-sensitive or unstable precursors. Given 1,3-oxazole’s aromatic stability and solid-state nature, our product stands up to repeat drying, dissolution, and re-drying cycles—critical for researchers needing multiple transformations within a single workflow.

    Direct Manufacturer Control Versus Trader Sourcing

    There’s a strong temptation, especially at scale, to look for the lowest cost supplier. Many of the pain points reported to us by new partners boil down to the difference between buying direct and going through a trading network. Lot variation, long delays for batch certificates, unpredictable impurity profiles: these are frequent headaches encountered in the market. Producing 1,3-oxazole ourselves allows us to respond immediately to technical questions. We can send spectra, relevant batch history, and discuss raw material source—all on timelines that matter to our customers, rather than deflecting with procedural delays or canned responses.

    Every time a custom intermediate order comes in, the ability to tweak process parameters—reaction time, drying method, filtration choices—adds layers of reliability that cannot be replicated by an anonymous bulk supplier. This level of transparency and accountability pays off every time a customer launches into process qualification or regulatory filing. We know what went into each batch, which solvents, and how long it spent at each stage of purification. That story gets lost the moment a product is routed through several hands, and the cost isn’t measured by the kilogram, but by project risk and delay.

    Comparisons with Related Heterocycles

    Synthetic route design is defined in part by the unique electronic and steric properties of each heterocycle involved. Many chemists will compare 1,3-oxazole with isomeric forms like 1,2-oxazole or heteroatomic analogues like thiazole or imidazole. The core difference lies in where the heteroatoms are positioned. In 1,3-oxazole, the nitrogen atom at position 1 and the oxygen atom at position 3 set up a distinctive electron distribution that changes nucleophilicity and electrophilicity at key ring positions. This fine control can open new reaction spaces: for example, the 2-position on 1,3-oxazole offers different selectivity in C-H functionalization compared with thiazole or imidazole. Synthesis workflows in our own teams have shown that the choice of oxazole yields fewer unwanted side reactions and minimizes ring opening under harsher conditions.

    Compared with 1,2-oxazole, our 1,3-oxazole is less prone to unwanted rearrangement and degradation, especially during acid- or base-catalyzed steps. The presence of oxygen at position 3 stabilizes the aromatic system differently, reducing side product formation in multi-step routes. Plenty of current patents and process optimizations in the public domain highlight this efficiency—switching from a less stable isomer to 1,3-oxazole has enabled some teams to cut purification steps and achieve better control over byproduct profiles. Materials scientists also report improvements in UV stability and performance when using 1,3-oxazole scaffolds in specialty polymers.

    Batch Size, Packaging, and Customization

    End users operate at all scales: gram quantities for R&D, multi-kilogram for pilot campaigns, up to several hundred kilograms for commercial production. We maintain flexibility in production planning, enabling both one-off small lots and long-term bulk contracts. Batch size variability is not just about order fulfillment—it’s about matching the right product to the right project. Our infrastructure supports transition seamlessly from lab validation to production scale, which allows project teams to avoid last-minute quality concerns or surprise revalidation campaigns.

    Packaging remains another often-overlooked element at the distributor level. For moisture- and oxidation-sensitive materials, container choice and inerting practices can mean the difference between excellent shelf life and trouble down the road. Drawing on user experience from many industries, we’ve implemented packaging standards using high-barrier, tamper-evident systems. These choices are validated in collaboration with our own in-house stability studies and with regular end-user feedback.

    Supply Chain Integrity and Documentation

    Long-term partnerships—across pharmaceutical, agrochemical, and material science projects—have highlighted that purity and traceability matter just as much as price or lead time. We provide full documentation regarding starting materials, batch records, regulatory support details, impurity profile data, and analytical spectra, all tracked at source. This is not just a paperwork exercise for us—it is the foundation for meaningful risk review and facilitates approvals or filings in regulated environments.

    Custom Synthesis Experience Drives Product Reliability

    Many projects come to our door with unique substitution patterns or functional groups required on the oxazole scaffold. Over the years, our process development chemists have refined routes to mono- and di-substituted 1,3-oxazoles, sulfonylated and alkylated variants, and isotopically labeled forms. The direct knowledge we gain in custom work directly reinforces our standard production, strengthening quality and technical rigor. We scale up only after multiple rounds of pilot batches and stress testing so that every run—no matter how routine—reflects cumulative learning and minimized variability.

    From synthesis through isolation and packaging, we control every step. This manufacturer-led approach isn’t just about pride of ownership, it’s about the flexibility needed to respond in real time. It’s easier for us to answer technical questions and troubleshoot at source, not after a third party has filtered and repacked material.

    Health, Safety, and Environmental Considerations in Real-World Operations

    From the earliest phases of our plant’s design, management of chemical risk and exposure control has been at the forefront. 1,3-Oxazole is not exceptionally volatile or acutely hazardous compared to some specialty reagents, but manufacturing and handling always require safeguards. Our teams undergo regular training on containment, PPE, and first response, ensuring a stable supply chain without interruption due to compliance lapses or unexpected incidents. We continually invest in upgrading our containment, effluent control, and waste treatment—minimizing hazard both for employees and for communities downstream. This is not a “check the box” procedure for us; it is an ethical responsibility borne from direct experience on the production floor and in the community.

    By producing in-house as a manufacturer, we have direct oversight, so we do not rely on vague assurances about environmental controls made by unknown upstream parties. Our responsibility flows all the way from raw material sourcing, through handling of intermediates, to environmentally responsible discharge. This integrated model gives end users documented evidence of environmentally sound manufacturing every step of the way.

    Direct Industry Feedback Shapes Our Approach to 1,3-Oxazole

    Feedback loops are only as strong as the relationships holding them together. We encourage user input through technical exchange meetings, open lab visits, and ongoing collaboration. Over the years, customer feedback has spurred technical improvements: minimizing minor but reactive impurities, improving color and clarity, extending shelf life, and enhancing documentation. One pharmaceutical partner’s process engineers worked with us to optimize solvent removal—resulting in a new drying approach now standard across our facility. In another instance, an agrochemical company suggested trace metal specifications for a specialty screen; we now include this criterion for clients who need it.

    Direct engagement matters. By controlling both dialogues and production, we bridge gaps that often emerge when products are sourced through distributors or faceless suppliers.

    The Future of 1,3-Oxazole Manufacturing: Quality and Flexibility

    1,3-Oxazole’s relevance shows no sign of waning—if anything, demand rises with every publication on new synthesis routes, drug candidates, or advanced electronic materials. Our aim is to continue strengthening employee knowledge, technical rigor, and open exchange with end-users so we keep improving production for each application that comes our way. Flexibility in manufacturing boils down to more than order size: it’s about quick adaptation when science or regulation changes, about reinvesting in real batch validation rather than cutting corners, and about standing behind what we produce from source to shipment.

    We have learned through experience that customers—whether in a pharmaceutical research group or a large-scale process chemistry plant—value more than just the chemical itself. They want accountability, real technical support, and vital information about what's in their supply chain. They want every shipment to match the previous one and have issues resolved directly, not bounced around. We shape our 1,3-oxazole approach around these expectations, drawing on the experience and responsibility that comes from actually doing the work ourselves, every single day.