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6-Chloro-1,3-Benzoxazol-2(3H)-One

    • Product Name 6-Chloro-1,3-Benzoxazol-2(3H)-One
    • Alias 6-Chloro-2(3H)-benzoxazolone
    • Einecs 265-934-0
    • 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

    512665

    Chemical Name 6-Chloro-1,3-Benzoxazol-2(3H)-One
    Cas Number 25861-28-1
    Molecular Formula C7H4ClNO2
    Molecular Weight 169.57
    Appearance White to light beige solid
    Melting Point 148-151°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Structure Benzoxazole ring with a chlorine atom at position 6 and a ketone at position 2

    As an accredited 6-Chloro-1,3-Benzoxazol-2(3H)-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 6-Chloro-1,3-Benzoxazol-2(3H)-One, sealed with a tamper-evident screw cap.
    Shipping **Shipping Description:** 6-Chloro-1,3-Benzoxazol-2(3H)-One is shipped in tightly sealed, labeled containers, protected from moisture and light. Standard chemical transport regulations apply. Handle with care to avoid spills or exposure. Suitable for land, air, or sea shipping, depending on destination and compliance with local, national, and international hazardous materials guidelines.
    Storage 6-Chloro-1,3-Benzoxazol-2(3H)-One should be stored in a cool, dry, well-ventilated area, away from heat sources and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong acids and bases. Use appropriate chemical-resistant containers to prevent contamination or degradation of the compound. Follow all relevant safety and storage regulations.
    Application of 6-Chloro-1,3-Benzoxazol-2(3H)-One

    Applications of 6-Chloro-1,3-Benzoxazol-2(3H)-One in Industrial Manufacturing

    6-Chloro-1,3-Benzoxazol-2(3H)-One is a crucial chemical intermediate serving specialized roles in the synthesis of advanced materials and compounds. Our clients incorporate this molecule in tightly regulated sectors demanding high chemical purity, documented traceability, and repeatable integration into established process routes. Below, we detail the core industrial applications with scenario-specific regulatory, formulation, process, and product insights reflecting real-world manufacturing practice.

    1. Synthesis of Pharmaceutical Intermediates for Antibacterial APIs

    This material acts as a protected core structure in several synthetic routes for modern heterocyclic antibacterial pharmaceuticals, often utilized downstream to introduce chloro or benzoxazole moieties into advanced intermediates. Sourcing from an audited manufacturer ensures batch traceability and validated impurity control, critical in regulated active molecule production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US cGMP for finished pharmaceuticals)
    • Ph.Eur. 5.10 for control of impurities in APIs
    • ISO 9001:2015 Quality Management Systems (for supply chain documentation)

    Typical usage ratio

    • 0.1–0.4 molar equivalents per stage, depending on the protection requirements and active ingredient yield targets in multi-step syntheses

    Downstream process integration

    • Charged during acylation or cyclization steps, following initial condensation; often deprotected or further functionalized in subsequent coupling reactions under strict temperature and pH monitoring

    Final product types

    • Benzoxazole-based antibacterial intermediates
    • Finished antibacterial APIs (e.g., related to quinolone or benzoxazole classes)
    • Active intermediates for antimicrobial research libraries

    2. Optical Brightener Precursor in Synthetic Fibers

    Downstream manufacturers introduce this compound in the synthesis of specialized benzoxazole-derived optical brightening agents for polyester, polyamide, and polyacrylonitrile fiber applications. Its halogenated structure provides enhanced stability under high-temperature melt-spinning and withstands repeated laundering cycles in the final textile products.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for restricted substances in textiles)
    • REACH Regulation (EC) No. 1907/2006 (EU chemical safety requirements)
    • ISO 14001 Environmental Management Systems (textile supply chain)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)

    Typical usage ratio

    • 0.05–0.12% w/w in prepolymer batch, adjusted according to targeted whiteness index and fiber matrix compatibility; higher ratios may reduce fiber tensile strength or alter dye uptake

    Downstream process integration

    • Reacted with condensation agents during the preparation of optical brightener masterbatches; integrated in melt compounding prior to spinning continuous filaments

    Final product types

    • Brightener masterbatches for PET and PA6/PA66 fibers
    • Whitened apparel textiles
    • High-brightness industrial filaments (conveyor, webbing)

    3. Intermediate for Agrochemical Synthesis (Herbicide Actives)

    Chemical producers synthesize halo-benzoxazole frameworks as key intermediates for several classes of selective herbicides. The precise introduction of a chloro substituent at the benzoxazole ring impacts both the biological target specificity and the downstream regulatory dossier for environmental compatibility.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (TC/TK)
    • US EPA 40 CFR Part 158 (pesticide registration data requirements)
    • ISO 9001:2015 (process and batch consistency)
    • European Directive 2019/782/EU for limits on pesticide by-products

    Typical usage ratio

    • 0.3–0.6 molar equivalents per coupling reaction, modified by desired active moiety and target final herbicide molecular weight

    Downstream process integration

    • Charged as a nucleophilic substrate during heterocycle elaboration in bulk herbicide synthesis, typically immediately prior to halogen-exchange or sulfonation steps

    Final product types

    • Formulated herbicide actives with selective crop protection modes
    • Precursor concentrate granules for direct farm supply blending

    4. Monomer Building Block in Polybenzoxazole (PBO) High-Performance Fiber Production

    PBO fiber manufacturers employ halo-benzoxazole derivatives at controlled feed ratios during monomer preparation, which directly affects polymer chain uniformity and final tensile properties of the spun fiber. Precise control of halogenation degree and precursor purity is essential for flame-resistant and ultra-high strength applications in aerospace and protective wear industries.

    Industry compliance standards

    • ASTM D7017 (Standard Specification for High-Performance PBO Fibers)
    • EN 1149 (protective clothing, electrostatic properties)
    • ISO 9001 and ISO 14001 (for fiber production and environmental compliance)
    • NIOSH 42 CFR Part 84 (for protective apparel certification)

    Typical usage ratio

    • 0.15–0.3 molar equivalents during co-monomer synthesis; slight feed adjustments based on target intrinsic viscosity and spinning process parameters

    Downstream process integration

    • Reacted during the polymerization of the PBO backbone; introduced as a halogenated monomer to the condensation reactor under nitrogen and high-pressure conditions before fiber spinning

    Final product types

    • PBO staple fibers
    • High-strength continuous yarns
    • Fire-resistant textiles for industrial, aerospace, and military use

    5. Active Moiety in Specialty Pigments for Coatings and Inks

    Pigment manufacturers utilize this compound's benzoxazole core to synthesize high-chroma, solvent-resistant specialty colorants aimed at industrial coatings and inkjet formulations. Its introduction modulates color fastness and improves suspension stability in advanced printing and automotive finishing products.

    Industry compliance standards

    • ISO 2846-1 (graphic technology—ink color measurement)
    • EN 71-3 (safety requirements for toy coatings)
    • REACH Regulation (EC) No. 1907/2006 (substance registration and use)
    • ASTM D4302 (Standard Specification for Artists’ Oil, Resin-Oil, and Alkyd Paints)

    Typical usage ratio

    • 0.02–0.08% by pigment batch mass for specialty pigment syntheses, tailored for shade intensity and solution stability

    Downstream process integration

    • Reacted with diazonium or azo agents during pigment molecule assembly; introduced prior to neutralization and precipitation in pigment milling stages for consistent particle size

    Final product types

    • High-performance pigments for automotive basecoats
    • Solvent-based and aqueous industrial inks
    • Decorative architectural coatings
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    Certification & Compliance
    More Introduction

    6-Chloro-1,3-Benzoxazol-2(3H)-One: A Closer Look from the Manufacturing Floor

    Understanding Our Product and Its Role

    In production environments where precision synthesis determines the quality of downstream goods, 6-Chloro-1,3-benzoxazol-2(3H)-one finds real value. We handle it at scale every month in our own plant, watching it go from basic raw materials to the clean, crystalline powder that moves into active pharmaceutical ingredients, dyes, and performance additives. Chemists in our plant know this compound mainly by its CAS number, 2387-41-5, and by the way each batch crystallizes when processed correctly. As a direct manufacturer, we have seen this intermediate unlock steps in pharmaceutical research that nothing else quite manages, thanks to a structure combining stability and reactive points in the same molecule.

    Unlike more general-purpose chlorinated benzo-heterocycles, the 6-chloro substitution on the benzoxazol-2-one core delivers a balance of activity our downstream clients often ask for. Over years of feedback from R&D partners, it’s become clear this substituent pattern supports selective reactivity — particularly useful in the design of new drugs that require both aromatic nitrogen and oxygen atoms, with the halogen in a controlled site. We have seen its applications expand as medicinal research hunts new scaffolds for treatments in oncology and anti-infective candidates.

    Manufacturing Experience and Quality Commitment

    Every kilo starts as a precise batch in our reactors. We do not permit deviations from the process developed through experience on this floor. Sourcing only high-purity starting chlorinated anilines and making sure solvents and reagents always meet our internal thresholds keeps the impurities down. Factory staff monitor reaction pH, agitation rates, and cooling curves. Any off-colour or off-odour material gets flagged before drying. Each batch, before we pack and seal the final material, must pass analysis using both HPLC and NMR, not just minimum HPLC area percent.

    Product consistency matters, especially where our customers run multi-step syntheses without space for batch-to-batch variation. Inconsistent feedstock leads to extra purification or failed transformations. Our technical team routinely works with our partners to analyze the side products from their transformations, tracing them back to tiny changes in our process. This closed feedback loop has shaped our protocols, making our 6-Chloro-1,3-benzoxazol-2(3H)-one stand out for tight bulk purity, low residual solvents, and robust phase transition points. The powder flows comfortably, homogenizes easily, and dissolves without haze in most organic solvents our clients report.

    Specification and Batch Control — Beyond the Numbers

    A big part of why this compound remains in demand comes from our attention to reproducibility. Typical product specs on our floor show purity above 99% by HPLC, moisture content below 0.5%, and a well-defined single melting point in the range expected for this scaffold. We run lots between 1kg and multi-ton, never shifting equipment between lots to maintain integrity. Technicians manage every batch by scrutinizing yields and impurity profiles, then adjusting the next run as needed based on analytic data. Rather than simply chasing a product specification, our routine is woven into the rhythm of continuous verification.

    Where 6-Chloro-1,3-Benzoxazol-2(3H)-One Stands Out Among Benzoxazolones

    Some clients ask how it stacks up to unsubstituted benzoxazol-2-one or sibling molecules like 5-chloro variants. Over time, we have tracked requests from drug discovery teams, dye developers, and agrochemical innovators for the 6-chloro version because its electron distribution drives higher selectivity in key reactions. Placement of the chlorine at the 6-position influences downstream amination and condensation reactions, anchoring it as a better intermediate for routes leading to some proprietary drugs. Its reactivity profile—differentiated from analogs by the halogen’s effect on electron density—has made it a more flexible choice for library synthesis compared to simpler benzoxazolones.

    Within our facility, its manufacturing pathway involves specific conditions not needed for the base molecule. We learned, after early runs several years back, that the 6-position substitution changes crystallization dynamics, so the drying and particle sizing steps require extra vigilance. The end result is a powder with improved shelf stability and lower tendency to pick up solvent residues compared to some other isomers.

    The Real-World Usage: Factories, Research Labs, and Production Lines

    Pharmaceutical research labs rely on our compound as a building block—either as a masked functionality or scaffolding for new drug candidates. Its dual heteroatom core offers ways to create either nucleophilic or electrophilic centers depending on the downstream process. Technical teams tell us that using our crystalline powder speeds up purification and waste reduction in later steps. More than one major project has credited their successful route optimization to the reproducibility of our material, allowing them to move from small bench synthesis to kilo campaigns without having to reformulate purification procedures.

    More than just a pharmaceutical intermediate, our batches end up in pigment labs too. 6-chloro-1,3-benzoxazol-2-one allows vibrant and durable color profiles in advanced dyes. The chlorine atom, by altering the core’s electronic properties, brings improved lightfastness to certain dye formulations, something our customers in textiles and polymers point out repeatedly. Working with pigment specialists, we have optimized batch drying and micronization for pigment use, enabling efficient blending without caking or agglomeration.

    Agrochemistry customers incorporate this intermediate for high-selectivity protective agents and specialty formulations. Lower impurity profiles mean cleaner transformations when they build target fungicides or growth regulators. Market trends in sustainable agriculture have pushed us to adapt our process to reduce waste and avoid heavy-metal contaminants, a demand we hear directly from production managers at major agricultural chemistry makers.

    Differences that Shape Each Batch

    Experience shows that subtle differences in how a compound is synthesized and purified translate directly to processability downstream. By trial and error, we discovered that temperature control during ring closure defines the starting point for optimal crystallization. Running over-temperature or pushing reaction times too far introduces unwanted side products. Our QA team measures and scraps any lot with off-spec color, haze, or melting point. These insights are not theoretical—they’ve been refined with every campaign, informing our parameters for agitation, solvent load, and filtration.

    Our technical team meets quarterly with select clients to review how our batches performed in their manufacturing runs. Pattern recognition in these meetings has shaped our continuous improvement. A pigment manufacturer once flagged flow issues in their extruder traced back to excessive fines in our lot; now, we control sieve cut-off more tightly. Academics using our product for cross-coupling reactions contributed notes on how our material’s purity influenced their isolation yields, feeding directly into our revised analytic regime.

    Supporting Evidence from Our Shop Floor

    Every year, our plant goes through third-party audits, including those for cGMP compliance and more basic ISO checks, depending on our end-markets. Rather than treating certification as a rubber-stamp, we compare internal metrics to industry best practices. For our 6-chloro-1,3-benzoxazol-2-one, this includes analyzing impurity profiles with state-of-the-art chromatography and confirming structure using not just single-point IR but full-spectrum NMR. These tests run on every lot as a matter of course, not exception. Bulk chemical stocks get full reanalysis every quarter, even before customer feedback, so age or warehouse conditions don’t shift material behavior.

    New employees learn directly from senior operators about edge-cases in production—how to identify subtle viscosity shifts during ring closure, or what to look for when drying the powder to ensure no residual moisture remains. Each operator logs their batch data into a closed system accessible to technical management. Any deviation brings an immediate corrective action request, often leading to process updates shared throughout the team. This workplace culture means each shipment of 6-chloro-1,3-benzoxazol-2-one draws on real-world insight, not just protocol.

    Environmental and Regulatory Responsibilities

    Modern chemical manufacturing cannot ignore the environmental footprint left by the process. Handling chlorinated intermediates, we take waste minimization and emission controls as core responsibilities. Solvent recovery sits at over 85%, with recovered streams going back into secondary reactions or, where purity allows, back into the main production route. Chlorine waste streams and off-gas scrubbers follow agreed protocols, documented for our environmental audit records. Our manufacturing site complies with current safety legislation and tracks any update in requirements on a rolling basis.

    We also keep a line open with transport partners to ensure packaged drums meet current regulatory demands and client-specific transit needs. Each drum or bag runs through barcoded checks, ensuring traceability. Within customer projects, the ability to trace every lot back to raw material certificate, production timing, and QC sample means any inquiry receives answers without delay or guesswork.

    Feedback from the Field

    Pharmaceutical partners who scale up their synthetic projects have commented on both the cleanliness of our intermediate and the minimal batch-to-batch variation, allowing seamless integration into their established synthesis routes. Dye manufacturers mention the brightness and edge-definition our product provides, and their lack of need to add stabilizers during processing. Reports from agriculture R&D teams show confidence in the reliability of results when using our intermediate as precursor, especially where regulatory filings require exact repeatability and transparency.

    Over the years, close customer partnerships shaped the process by which we isolate, dry, and package 6-chloro-1,3-benzoxazol-2-one. This isn’t the result of one-off requests; it’s an ongoing cycle of feedback, testing, and adjustment. In technical calls, we share not just standard certificates of analysis but, when necessary, advanced spectral data, and we archive powder morphology to support reproducibility claims.

    Industry Trends and the Role of Direct Manufacturing Expertise

    Direct manufacturing expertise proves itself as regulations on material traceability tighten. End users increasingly want to know exactly how source intermediates are made, not just their numeric specifications. By keeping all synthesis and purification in-house, we provide more than just an anonymous bulk chemical. Our team’s knowledge—drawn from hands-on practice, not paperwork—translates into a material that integrates smoothly with modern R&D needs and next-generation performance targets. As global standards evolve and new forms of chemical scrutiny emerge, our flexible, feedback-driven process ensures our batches stay in tune with what customers need.

    Requests keep growing from small-molecule pharmaceuticals demanding tighter traceability, and material science groups are calling for purer, more consistent intermediates. These trends play to our strengths. Our philosophy does not chase lowest cost per ton at the expense of batch control or reliability. Instead, we focus on outcomes in the lab, in the manufacturing plant, and in real-world product deployment.

    Improvement and Collaboration—Looking Ahead

    Manufacturing 6-chloro-1,3-benzoxazol-2(3H)-one is more than a recipe; it’s an evolving practice shaped by chemistry and collaboration. Ongoing improvement depends on keeping process details open between our stages and the client side. Regular technical exchange—whether in routine quarterly calls or in troubleshooting investigations—keeps our procedures tightly linked to how the world’s best labs use our reagents.

    We believe this compound’s future lies not just with our current partners in pharmaceuticals, pigments, and agrochemistry. Its unique combination of stability, reactivity, and purity supports emerging uses in new materials research, analytical standards, and green chemistry efforts. Direct dialogue with innovators in these spaces will continue to refine both our process and the product purification regimen.

    Conclusion: The Manufacturer’s Perspective on Lasting Value

    Years spent manufacturing 6-chloro-1,3-benzoxazol-2(3H)-one have made one fact clear—it is results on the bench and the plant floor that define value. Downstream teams work more efficiently when intermediates arrive on spec, free from headache-inducing variation. Subtle differences in synthetic route, particle treatment, and packaging control build trust batch after batch. This trust drives repeat business, supports product registrations, and gives research teams confidence to push the boundaries of discovery. As manufacturing partners, we bring hard-won technical knowledge, real operational discipline, and a commitment to continued improvement—characteristics shaped not by marketing claims, but by the hands-on realities of daily production.