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HS Code |
533349 |
| name | 3-Oxetanone |
| CAS_number | 6704-31-0 |
| molecular_formula | C3H4O2 |
| molar_mass | 72.06 g/mol |
| appearance | Colorless liquid |
| boiling_point | 63-65 °C |
| melting_point | -47 °C |
| density | 1.162 g/cm3 |
| refractive_index | 1.426 |
| flash_point | 8 °C |
| SMILES | C1COC1=O |
| PubChem_CID | 11533 |
As an accredited 3-Oxetanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Oxetanone is supplied in a 25g amber glass bottle with a secure screw cap, featuring hazard labels and product identification. |
| Shipping | 3-Oxetanone is shipped in tightly sealed containers, protected from light and moisture, under cool and dry conditions. It is classified as a hazardous material, so transportation follows relevant safety regulations, including proper labeling and documentation. Packaging ensures containment to prevent leaks and exposure during transit for both air and ground shipping. |
| Storage | 3-Oxetanone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and sources of ignition. It must be kept separate from incompatible substances such as strong acids, bases, and oxidizers. Store under inert atmosphere, such as nitrogen, if recommended. Always follow safety guidelines and use appropriate personal protective equipment. |
Applications of 3-Oxetanone in Industrial Manufacturing3-Oxetanone is a high-value cyclic ketone widely recognized for its role in precision organic synthesis and advanced polymer engineering. Our manufacturing expertise delivers 3-Oxetanone in consistent quality, supporting downstream customers in the specialty chemicals, pharmaceutical intermediates, and advanced materials sectors. The following application scenarios outline critical downstream uses based on real-world industrial practice, describing direct integration in key sectors. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisIn pharmaceutical manufacturing, 3-Oxetanone acts as a core intermediate for heterocyclic ring construction in beta-lactam and small-molecule scaffolds. Customers employ it in multistep synthesis flows, essential for producing active moieties present in novel anti-infective and CNS therapeutic APIs. Manufacturers incorporate 3-Oxetanone into protected ring-opening reactions, followed by installation of specific side chains for target molecule assembly. Tight control of input purity and reaction profiles directly impacts the pharmacological profile and regulatory acceptability of the resulting API batch. Industry compliance standards
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2. UV-Curable Oligomer and Monomer ModifierProducers of specialty UV-cured coatings, adhesives, and inks utilize 3-Oxetanone as a reactive diluent and ring-opening comonomer to enhance crosslink density and modify cure kinetics. In oligomer synthesis, formulators introduce the oxetane group to increase reactivity toward acrylate or maleimide systems, driving improvements in scratch resistance, gloss, and thermal stability of UV-cured films. The precise input level depends on the desired polymer matrix rigidity and final performance specifications demanded by electronics or automotive sector clients. Industry compliance standards
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3. Advanced Polyether and Polyester Polyol SynthesisSome downstream polyurethane and flexible foam specialists use 3-Oxetanone in controlled ring-opening polymerization to generate structurally defined polyether or polyester diols. The oxetane ring serves as a source of unique backbone regularity, imparting improved mechanical strength, specific modulus, and reduced creep to specialty elastomers and high-performance sponges. Leading applications demand tight process controls to manage molecular weight distribution with downstream partners customizing copolymer ratios to meet application-specific modulus and rebound criteria. Industry compliance standards
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4. Chiral Building Block in Agrochemical Intermediate ProductionSynthetic agrochemical manufacturers use 3-Oxetanone in the preparation of high-value chiral intermediates integrated into modern crop protection ingredients, such as advanced herbicide and insecticide scaffolds. The unique ring structure facilitates enantioselective synthesis routes, enabling control over stereochemistry critical for biological activity and environmental break-down rates. Chemical engineers strictly modulate reaction parameters and integration points to achieve regulatory-compliant impurity profiles and throughput efficiency in large-batch production. Industry compliance standards
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5. Fine Chemicals Synthesis for Fragrance IntermediatesIn the fine fragrance and specialty chemical sector, processors employ 3-Oxetanone for constructing oxygen-rich bicyclic structures used as key intermediates in synthetic musk, lactone, and macrocyclic odorant compounds. The reactivity profile supports precise insertion into multi-step synthetic sequences, essential for controlling volatility and olfactory profile in final blends. Stringent batch traceability and contaminant control are crucial, with compounding ratios tailored based on the sensory target and downstream distillation yields. Industry compliance standards
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Every shift in the chemical plant teaches hard lessons, none more so than working with specialty intermediates like 3-Oxetanone. Our team has handled this compound from raw precursor right to the packaged product. This molecule grabs attention in the lab for its strained four-membered ring—reactive enough to make synthesis interesting, but sturdy enough to ship and store without a parade of safety warnings. The molecular formula, C3H4O2, makes it a small molecule but one with outsized impact in both research and process chemistry.
The real value of 3-Oxetanone turns up in its unwillingness to behave like other cyclic ketones or lactones. Researchers want it for its unique reactivity in ring-expansion and ring-opening work, often where larger and more sluggish rings won’t do the job cleanly. In practice, we’ve seen teams use it to build complex scaffolds, as an acylating reagent, or as a starting material for modified carbocycles and heterocycles. The strain in the ring boosts its energy, which means it participates in transformations that are slow or impossible with five- or six-membered relatives.
Our facility produces 3-Oxetanone under tightly monitored batch conditions—not just as a bulk commodity, but in grades tailored to synthesis, from technical grade up to 99% purity. The compound appears as a clear, colorless liquid at room temperature and carries a boiling point around 108°C. Handling demands care, especially since the material’s volatility means storage containers need vapor controls. We monitor every drum and bottle for moisture and acidity before shipping, since small defects cause big downstream headaches.
Some cyclic ketones drift toward polymerization if storage conditions slip. Our 3-Oxetanone stays reliably monomeric under nitrogen and in cool, dry conditions. Regularly, we test retention times and spectrum—infrared, NMR, and GC-MS—against certified reference standards. Analytical chemists trust these numbers for troubleshooting reactions. If the ring opens prematurely, the batch demands scrapping, so stability isn’t an abstract target; it is a real demand from both the synthetic chemists inside our labs and the formulators relying on our consistency.
Medicinal chemists claim much of the yearly output. They leverage 3-Oxetanone as a core scaffold in small molecule design. Consider the kind of SAR (structure-activity relationship) campaigns where minute changes in backbone flexibility shift binding affinities dramatically; 3-Oxetanone’s three-carbon ring enables just that sort of fine tuning. Polymer chemists also draw from our stocks, introducing oxetane motifs into chain polymers or block-copolymers, resulting in tailor-made materials for electronics or advanced coatings.
Colleagues with deep experience in asymmetric catalysis enjoy the possibilities for conversion. The compound offers points of attachment that let ligands or auxiliaries orient themselves for facial selectivity, producing chiral building blocks where no clear alternative exists. In bioconjugation, the functionality of 3-Oxetanone produces robust links between peptides or proteins and small labels without the instability seen with some rival reagents. In each of these roles, the real feedback has come from process tweaks and customer feedback that reach us directly, unfiltered by intermediaries.
In our time producing 3-Oxetanone, we’ve fielded countless questions about differences between this and similar cyclic lactones or ketones such as γ-Butyrolactone or β-Propiolactone. Each compound fills its own space. γ-Butyrolactone offers less ring strain and stands up as a common solvent where reactivity should stay low. β-Propiolactone, on the other hand, brings up worker safety considerations due to its carcinogenicity; 3-Oxetanone remains a safer, more manageable option for many users. What sets 3-Oxetanone apart isn’t just the chemistry but the feedback from researchers: they achieve cleaner ring expansions, more selective acylation, and fewer side-products.
Every batch presents the same puzzle—repeatability and safety. Small changes in precursor purity translate to headaches during purification and packaging. We’ve streamlined our drying and filtration process to keep water well below 500 ppm, since hydrolysis damages both shelf life and reactivity. A small team oversees each run, using inline sensors and regular spot sampling to confirm consistency. In years of practice, quick intervention proves crucial; if the color or smell drifts, production pauses and technical staff dig in, rather than pushing possible off-spec product to market.
Users in the field want confidence they haven’t wasted a week’s work due to hidden impurities. Every feedback call we receive means another chance to tweak process conditions or improve our document trail. This back-and-forth, often frustrating in the moment, leads us to refine reactor controls and to tighten our filling procedures, especially when packaging smaller lots for research use.
3-Oxetanone avoids the most hazardous reputation of certain cyclic carbonyls, though it carries enough reactivity to demand respect. Proper PPE, good ventilation, and vapor containment stay non-negotiable for our operators handling drums and bottles. Our experience matches with literature: the material can irritate skin and lungs at vapor concentrations found in poorly ventilated storerooms or during spills. Regular refresher training ensures everyone from the cleaning staff to the process chemists understands the risks and immediate steps if something goes wrong.
We see new regulations on the horizon every year, with evolving expectations for waste handling, allowable workplace concentrations, and international shipment. Engineers and compliance staff update our facility’s safety logic accordingly. As international demand grows, we maintain close dialogue with customs authorities and shipping partners to avoid mislabeling or unnecessary delays at borders.
In the early days, turnaround times for custom 3-Oxetanone grades stretched longer than anyone liked. After hearing from researchers frustrated with extended lead times and batch variety, we reorganized supply chains and expanded storage capacity. This lets us fill small, high-purity research orders quickly, while meeting bulk requests for industry partners on their own timetables. In direct conversations with bench chemists, requests often boil down to, “reproducibility over everything else.” We view our role not just as a producer, but as a close partner for labs pushing synthetic boundaries, from academic groups to industrial R&D centers.
Several customers shared case studies where an unexpected impurity crashed novel syntheses. Each time, we conducted trace impurity analysis alongside them, and in some cases adjusted upstream processing or bulk purification to eliminate halides, peroxides, or solvent residues. These cases demand hours of cross-testing and data sharing—without walls between their labs and our QC team, the answers come sooner.
Early batches of 3-Oxetanone came from flask-scale synthesis, in runs no larger than a few hundred grams. Today, our continuous reactors turn out multi-kilogram lots while preserving the same analytical specs that defined our early reputation. Behind every reactor are operators who understand the quirks of volatile, strained-ring chemistry. Hot spots in the reactor laminate can introduce by-products, so we track jacket temperatures at multiple points, not just at the wall.
We adapted continuous-flow processing for critical steps, improving both throughput and process control. This shift paid dividends in purity—fewer thermal decomposition products and an easier separation job for the distillation team. For contract customers, we can adjust the end-point to deliver blends free from specific solvents or tailored for downstream reactions without extra purification steps.
Low-cost producers occasionally promise cut-rate 3-Oxetanone, but users soon report variable reactivity, mystery peaks in the analytical data, or unexpected shelf-life issues. Our pricing structure reflects the backbone of regular QA, robust documentation, and batch-traceable lot numbers. It’s not marketing spin—dozens of synthetic campaigns have ground to a halt due to penny-wise, pound-foolish sourcing. We work to prevent these scenarios by deploying third-party assays for select lots, having learned the hard way that trust built over years vanishes with a single contaminated drum.
Waste reduction strategies keep costs viable. By reclaiming off-spec material in select reprocessing lines, we cut losses and prevent avoidable disposal. Operators get bonuses for suggestions that improve yield or reduce variance, turning every member of production into both worker and watchdog. These systems let us keep supply consistent, even as global conditions create wild swings in precursor cost or transportation.
In open communication with partners, troubleshooting never stays inside one organization. A research group alerted us to minor glyoxal contamination that only emerged during scale-up. Their insight led our QC team to amplify a specific checkpoint in our analytic flow—a fix that held benefits for every downstream batch since. These corrective actions seldom come from theory alone. They rely on day-in, day-out observation, room for honest critique, and a willingness from both sides to see error reporting as pathway, not a blame game.
Our commitment to feedback means maintaining permanent records of all deviation events, along with root-cause documentation shared with impacted clients. Over the years, this practice fostered improvements in both product quality and speed of delivery, earning us long-term loyalty from labs who rely on 3-Oxetanone’s consistency for grant-funded programs or pilot-scale synthesis.
In recent years, as the pharmaceutical sector targets molecules with higher functional complexity, 3-Oxetanone finds new life in rapidly diversifying synthetic pathways. Internal efforts have aimed at developing new derivatives—such as halogenated or alkyl-substituted oxetanones—in response to requests from contract research and manufacturing organizations. Most feedback notes the benefit of having both the parent structure and functionalized analogues available from a single, dedicated supplier.
All innovation occurs in the context of end-user dialogue. Before launching a process change or new product variant, test lots move directly to trusted research partners for evaluation. Back-and-forth during pilot runs reveals surprises that theoretical models cannot capture. In several cases, slightly modified distillation protocols or targeted phase-separation steps made the difference between bench-scale interest and large-scale adoption.
We stay alert to market signals about raw material sourcing, particularly as customers shift toward green chemistry goals. Our team reviews options for bio-based acetates and low-impact oxidants in precursor synthesis each year. Even if these steps introduce incremental cost, reducing the environmental load matters both to us and to downstream users who face tighter ESG disclosures and regulatory audits.
On the plant side, closed-loop solvent recovery and water minimization feature in each production cycle. Waste generated by 3-Oxetanone production falls carefully within land disposal and incineration limits, and we publish these numbers for review by auditors. The short supply chain allows us to commit to batch traceability back to raw material origins, which appeals to buyers facing both public and investor scrutiny.
As new fields touch advanced materials, demand for reliable, high-purity cyclic ketones like 3-Oxetanone will only grow. Startups and established firms in drug discovery, agrochemical synthesis, and specialty polymers look to us for assurance that sourcing won’t interrupt research or production. From our vantage point inside the manufacturer’s walls, success looks like uninterrupted feedback, relentless process control, and transparent dialogue with every user.
The story of 3-Oxetanone continues to shift as industry demands and regulations evolve. Choice in grade, consistent logistics, and technical guidance will matter even more. We dedicate ourselves to improving these touchpoints, mindful that the compound’s promise in the laboratory only translates to real-world results with responsive, experienced support from the manufacturer at every turn.