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HS Code |
257174 |
| Chemicalname | 3-Acetyl-2-Benzoxazolinone |
| Casnumber | 85-25-8 |
| Molecularformula | C9H7NO3 |
| Molecularweight | 177.16 |
| Appearance | Off-white to pale yellow powder |
| Meltingpoint | 170-174°C |
| Solubility | Slightly soluble in water, soluble in ethanol and acetone |
| Purity | Typically ≥98% |
| Smiles | CC(=O)N1C2=CC=CC=C2OC1=O |
| Synonyms | 3-Acetylbenzoxazolin-2-one; 2-Benzoxazolinone, 3-acetyl- |
| Storagetemperature | Room temperature, tightly sealed |
| Hscode | 29349990 |
As an accredited 3-Acetyl-2-Benzoxazolinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-Acetyl-2-Benzoxazolinone is packaged in a 25g amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | 3-Acetyl-2-Benzoxazolinone is shipped in secure, sealed containers to prevent contamination and moisture exposure. Standard packaging includes amber glass bottles or high-density polyethylene containers. The product is transported under ambient conditions with appropriate labeling, and adherence to all relevant safety regulations for its handling and storage during transit is ensured. |
| Storage | 3-Acetyl-2-Benzoxazolinone should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances, such as strong oxidizing agents. Ensure the storage area is equipped for chemical safety, avoid extreme temperatures, and label the container clearly. Follow standard laboratory practices for safe chemical storage. |
Applications of 3-Acetyl-2-Benzoxazolinone in Industrial ManufacturingAs a direct manufacturer and bulk supplier, we supply 3-Acetyl-2-Benzoxazolinone for specialized downstream industries where its structure and chemical properties serve precise technical roles. Each of the following segments highlights a major end-use application, with detailed insights into compliance, process integration, formulation parameters, and the specific types of finished products produced by our customers. 1. Plant Growth Regulator Synthesis for Paddy Crop ProtectionLeading agrochemical formulators utilize 3-Acetyl-2-Benzoxazolinone as a key intermediate in the synthesis of benzoxazinoid-based plant growth regulators, especially those targeting pest and fungal resistance in rice cultivation. This compound enters critical coupling and cyclization steps, where its purity directly impacts yield consistency and downstream quality requirements for agricultural active ingredients. Industry compliance standards
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2. Specialty Chemical Intermediate for Optical Brightener ManufacturingProducers of advanced optical brighteners select 3-Acetyl-2-Benzoxazolinone for constructing heterocyclic frameworks that enhance the fluorescence properties in detergent and paper application segments. Downstream synthesis leverages this molecule in multi-step reactions including aminolysis and etherification, where accurate feedstock control is vital to achieve brightness uniformity and batch reproducibility in the end products. Industry compliance standards
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3. Photostabilizer Intermediate for Polymeric MaterialsOur material functions as a precursor chemical for the manufacture of UV-absorbing photostabilizers integrated into plastics, coatings, and films. Formulation chemists value tight molecular weight and residue specifications that enable precise tuning of photo-protective agent structures, serving sectors where long-term color retention and surface durability are fundamental performance benchmarks. Industry compliance standards
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4. Fine Chemical Intermediate in Pharmaceutical Synthesis (Research & Development Only)Pharmaceutical R&D institutes and pilot-scale manufacturers incorporate 3-Acetyl-2-Benzoxazolinone in the preparation of specific benzoxazinone scaffolds, which can serve as protected core units or reference structures during lead compound development. These applications demand traceable supply documentation and batch-level analytical support to comply with strict research-grade standards. Industry compliance standards
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Working with 3-Acetyl-2-Benzoxazolinone isn’t just a matter of putting out another aromatic heterocycle. From years on the production floor and in the lab, the differences this compound brings are clear. Offering CAS number 85-09-6 and a tightly monitored melting range, each batch comes through the final checks after thorough crystallization and careful removal of by-products. Some plants cut corners to push out intermediates quickly, but that leads to yellow tints, heavier impurity loads, and unpredictable reactivity. Our team sees these mistakes all too often in third-party samples that reach customer labs. We take a hands-on approach, and that commitment runs through every kilogram.
Similar benoxazolinone analogues crowd the chemical listings, but 3-Acetyl-2-Benzoxazolinone stands out due to its unique reactivity, its use in specialty agrochemicals, and as a scaffold in pharmaceuticals research. The acetyl group at position 3 significantly affects how the benzoxazolinone core interacts with electrophiles and nucleophiles. This subtle difference changes downstream possibilities—a point some overlook when they compare it to parent benzoxazolinone or 2-mercaptobenzoxazoles. Years of analytical records and customer feedback confirm: downstream yield, reproducibility, and solubility track closely to starting purity and crystal habit.
Sourcing reliable 3-Acetyl-2-Benzoxazolinone can challenge even established labs. Shelf-life expectations in our industry do not just mean quoting a best-before date. After production, we store material under inert gas, in brown glass, avoiding unnecessary milling that would increase surface area and pick up atmospheric moisture or CO2. Several European clients over the past decade found out the hard way that improper packaging—thin bags, translucent bottles—leads to product downgrade. The hydrolysis profile of 3-Acetyl-2-Benzoxazolinone differs from less substituted benzoxazolinones, thanks in part to the electron-withdrawing nature of the acetyl group. As a manufacturer, we track these environmental risks batch by batch, not just by catalog number.
Spec sheets often list assay and melting point, but practical quality assurance takes more: chromatography for trace by-products, routine particle size checks (avoiding lumps that signal hydrolysis or condensation), even FTIR baselines to catch subtle differences between plant runs. We have routinely sent half a ton of material through additional purification if an uptick in a single NMR peak suggests instability. Sometimes traders won’t catch these changes, but in a synthetic pathway, they matter.
The largest draw for 3-Acetyl-2-Benzoxazolinone runs through two pipelines: agricultural protection products and advanced intermediates for small molecule synthesis. Formulators in the crop sector care deeply about stability and dispersibility, especially when using this compound as a precursor to herbicidal or antifungal actives. Only a few sites can keep both purity and moisture low enough for routine success in scale-up. Years ago, we worked closely with an agrochemical client who needed reproducible dissolution kinetics; only after extensive drying, custom packaging, and adjusted cryomilling did the final formulation meet their spray uniformity targets.
Pharmaceutical projects take another angle: reliable structure for scaffold modification. Medicinal chemists often step from 3-Acetyl-2-Benzoxazolinone into specific heterocycle libraries (oxazoles, quinolones, even indole derivatives). In these applications, the difference between visible contamination and clean, solid-state material yields measurable project outcomes. We learned not to underestimate the ripple effect from a few percent more crystal hydrate or a handful of colored fines. Even newer uses like photoinitiators and specialty pigments have appeared on our production schedule—a sign of continual evolution in this core chemistry.
We once fielded feedback on a failed synthesis from a European customer. Chromatograms showed scattered low-level impurities that could have passed most spec sheets. After working with their technical team, we tuned our purification process, swapped glassware for borosilicate in distillation, and lengthened the dry-room cycle. Their process performance shot up and turnover times shortened. Bringing those learnings back to the factory, we changed more than batch records; our team meetings now dig into downstream fields, and we routinely check with long-term users before tweaking anything.
Clients pushing the scale from gram samples to multi-kilogram production highlight another hard-earned truth: pilot lots might look identical by classic tests, but operational quirks—filterability, dusting, slight caking after weeks in storage—show up on larger scales. More than once, we had to retool our dryers or extend sieve cycles to get the consistency bulk customers demand. Unchecked moisture can create subtle issues that only surface when setting up a downstream condensation. Only by tracking yield cycles in customer pilot plants and running mock-ups here in our own blending rooms do we keep pace with modern process expectations.
In decades of synthetic chemistry, nuances between analogues do not always leap off a catalog page. We hear clients often mention benzoxazolinone interchangeably with 3-Acetyl-2-Benzoxazolinone, yet the chemical’s moderate polarity, higher melting, and steric shielding translate to real advantages in selectivity and yield. Some analogues degrade too easily or give off odors in finished products. Our batch records show 3-Acetyl’s color and odor stability outperform simpler variants, especially in storage and during extraction. Once, a coatings manufacturer tried substituting in a cheaper benzoxazolinone variant—spend on reformulation and waste disposal far outweighed any initial savings. Meticulous consistency at the raw stage wards off these downstream headaches.
We don’t just follow textbook methods. Every year, we run a round of stability tests in simulated end-use conditions (freeze-thaw, high-humidity, even forced UV). Our notes show that 3-Acetyl-2-Benzoxazolinone stands up better in long-term storage and handling stress. Clients in high-throughput research call out the manageable dust, the lack of caking, and the clean melting profile that makes their work repeatable. Even small details matter: particle size affects automated dispensing; trace acetic acid can tip off downstream couplings or ring closures.
The choice of starting materials sets the stage for everything downstream. We prefer sourcing the highest-purity, traceable anilines and acetic anhydride for our key steps. Lower grades of starting material introduce more trouble later—off-odors, stubborn side-reactions, and batch variability. In our experience, changing a solvent or reactor vessel changes impurity profiles, and only by locking down these details have we earned long-term contracts with research and manufacturing clients. Auditors that walk our plant see labeled drums, clear line diagrams, and operators trained to notice subtle shifts before they become costly problems.
Process safety can't be an afterthought. The intermediates before final cyclization show a stubborn tendency to react with trace iron or even silicone. We coordinate with our vessel supplier to inspect linings yearly, and we designed jacketed reactors specifically to hold tight temperature windows. More than once, shifting air humidity pushed us to recalibrate our dehumidifiers, ensuring the end product survives long warehouse stays overseas. We engage with quality specialists, not just for compliance, but to spot blind spots we might overlook—knowledge we have built batch after batch, year after year.
Sustainability discussions go beyond marketing. Minimizing organic solvents saves money, reduces corrosion in the plant infrastructure, and cuts hazardous waste. We have spent years swapping out certain chlorinated solvents for high-boiling, recyclable options—up front, this increased costs, but over time, efficiency and safety gains made it worthwhile. We reclaim and purify solvent streams, pushing waste close to the minimum practical level. The heat exchangers on our cyclization section now feed process water heating further down the factory line. Plant audits with major clients always ask about these steps, as do local regulators.
The supply chain for high-purity benzoxazolinone intermediates can swing on global events. Fluctuating prices for key feedstocks, shipping disruptions, and evolving import controls in destination countries all filter down to our production plans. We hedge risk by multi-sourcing at least three grades of every critical input—not always easy, but necessary for reliability. In the past few years, this policy saved weeks of downtime and allowed us to fill rush orders even when upstream logistics slowed to a crawl. Only consistent, on-time delivery builds the trust that brings back repeat business from process development and manufacturing clients.
Our best process improvements have grown out of close client collaboration. Some product developers come to us looking for a tweak: tighter particle specs, custom packaging, or a dedicated impurity profile. Over the years, we have added specialty sieving, extra in-process analytics, and even small-scale crystallization trials—all tailored to specific partners who shared data and real-world observations. In one case, a customer needed sterility for a downstream pharmaceutical step. We built a dedicated, filtered crystallization vessel to guarantee a pyrogen-free intermediate. That project taught us as much about our own process as it did about lab spec requirements.
Direct engagement with technical users means ongoing learning. Our in-house chemists regularly run application tests: solubility in a matrix of solvents, compatibility with resin binders, dissolution curves for new product forms. These tests not only verify our own quality, but also often uncover issues early—batch-to-batch drift, rare contaminant spikes, or packaging weaknesses that only emerge after shipping overseas. This feedback feed directly into our next production cycles, adjusting protocols and documentation. We see technical support as crucial, not just an after-sales obligation.
Chemistry progresses fast. Reactivity trends shift, and new derivatives often appear on patent filings within months. Our R&D team has explored alternative acetylation strategies, tried green catalysis routes using reusable organometallics, and tested solvent-free syntheses. These investments go beyond creating a better brochure—they solve real headaches for scale-up teams by trimming steps, cutting hazardous handling, and enabling lighter environmental footprints. Few outside the plant see the number of hours spent tweaking water content, selecting decolorants, or screening for slow-forming polymorphs—all of which influence the viability of 3-Acetyl-2-Benzoxazolinone as a robust building block.
We keep close contact with research clients using our material in early-stage studies on biological activity—antibacterial screens, crop protection mechanism work, and material science. Requests for ever-tighter impurity limits and documentation now outnumber questions about price. Only steady upgrades to our analytical and production equipment allow this progress.
Behind every batch lies real expertise, not just a procedure file. Staff turnover threatens consistency, so our approach leans on continuous training, peer mentorship, and clear performance feedback. Old-timers who remember the plant layout from two decades ago share insights with our newest hires. After a tricky scale-up, we get all hands together, review errors, and update protocols for the next run. It’s not always glamorous work, but that commitment turns out the color-stable, high-purity compound our partners depend on.
Industry standards evolve, and so must our in-house practices. Certification audits, customer visits, and supply chain reviews constantly put our systems to the test. We found the best preparation comes from simulated drill runs—walking our team through what-ifs, from power loss to raw material delays. Just-in-time learning, applied in dozens of small plant improvements, gets our products out the door with the right balance of safety, quality, and speed.
End-use markets keep changing, and adaptations in manufacturing follow close behind. Shifts in agroscience may put 3-Acetyl-2-Benzoxazolinone into biocompatible formulations or slow-release carriers; pharmaceutical interest might drive demand for ultra-high-purity, multi-step intermediates, or enable functionalization routes new to the literature. Each new inquiry, each audit, and each pilot request brings another opportunity to improve long-standing processes. Our investment goes not only into steel and reactors but into relationships, skills, and technical learning that turn raw materials into reliable tools for the innovators who buy our products.
3-Acetyl-2-Benzoxazolinone does not just fill a product number on our books—it reflects a history of lessons learned, processes honed, and partnerships forged at the intersection of chemistry and manufacturing discipline. Every day, our team brings that experience to bear, building confidence for customers who need assurance that their critical intermediate will perform—consistently, safely, and reliably—no matter how the industry or market shifts next.