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5-Chloro-2-Methylbenzoxazole

    • Product Name 5-Chloro-2-Methylbenzoxazole
    • Alias 5-Chloro-2-methyl-1,3-benzoxazole
    • Einecs 629-052-7
    • 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

    698323

    Cas Number 22456-09-3
    Molecular Formula C7H5ClNO
    Molecular Weight 155.58
    Iupac Name 5-chloro-2-methyl-1,3-benzoxazole
    Appearance Off-white to light yellow solid
    Melting Point 80-84°C
    Solubility Slightly soluble in organic solvents
    Smiles CC1=NC2=CC(=CC=C2O1)Cl
    Inchi InChI=1S/C7H5ClNO/c1-4-9-7-3-2-5(8)6(10-4)7/h2-3H,1H3
    Synonyms 5-Chloro-2-methylbenzoxazole

    As an accredited 5-Chloro-2-Methylbenzoxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a secure screw cap, labeled "5-Chloro-2-Methylbenzoxazole," includes hazard symbols and handling instructions.
    Shipping 5-Chloro-2-Methylbenzoxazole should be shipped in tightly sealed, properly labeled containers, protected from moisture and incompatible substances. It must comply with relevant hazardous material shipping regulations, including appropriate packaging and documentation. Transport should avoid extreme temperatures and direct sunlight. Use suitable protective measures to prevent leaks or spills during transit.
    Storage 5-Chloro-2-Methylbenzoxazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Protect it from moisture and incompatible substances such as strong oxidizers and acids. Store at room temperature and ensure proper labeling. Follow general laboratory chemical storage guidelines to prevent spills and accidental exposure.
    Application of 5-Chloro-2-Methylbenzoxazole

    Applications of 5-Chloro-2-Methylbenzoxazole in Industrial Manufacturing

    5-Chloro-2-Methylbenzoxazole demonstrates high value as an intermediate in speciality chemical synthesis. We supply this raw material for downstream manufacturers applying it in advanced performance chemical sectors, where strict adherence to regulatory and process standards is mandatory. The following application scenarios highlight direct, field-proven usage by our customers and our manufacturing partners.

    1. Pharmaceutical Intermediate for Antibacterial Active Ingredients

    Several pharmaceutical firms introduce 5-Chloro-2-Methylbenzoxazole during the multi-step synthesis of active pharmaceutical ingredients such as azole-based antibacterial agents. The chlorinated heterocycle serves as a core scaffold, allowing manufacturers to access complex substituted benzoxazole structures through selective halogenation, methylation, and ring-closing reactions. Production lines deploy it in automated reactors under GMP-compliant controls; purification teams typically use column chromatography and crystallization to meet API purity specifications for downstream formulation into oral solid dosages.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia Monograph 0333
    • US FDA 21 CFR Part 210/211
    • China Pharmacopoeia (ChP) standards for chemical drug substances

    Typical usage ratio

    • Adopted at 0.9–1.3 molar equivalents relative to the target azole core, with stoichiometric adjustment guided by target molecular complexity and desired batch output

    Downstream process integration

    • Dosed during intermediate synthesis stages, after initial substrate preparation and prior to final functionalization steps; integrated into closed-system reactors with in-line purity monitoring

    Final product types

    • Capsules and tablets containing benzoxazole antibacterial APIs
    • Sterile powder fill formulations for parenteral administration
    • Generic and branded prescription antibacterials utilizing benzoxazole scaffolds

    2. Agrochemical Synthesis for Fungicidal Compound Manufacturing

    Industry leaders in crop protection compounds routinely select this raw material in the synthesis of new-generation benzoxazole fungicides. The molecule confers both stability and target-specific activity to the final agrochemical. Production teams feed it as a ring-building monomer in multi-step condensation protocols, then perform safening, stabilization, and micronization workups to deliver standard and custom-formulated suspension concentrates. Strict process validation ensures compliance with regulatory residue limits and environmental safety.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines (Joint FAO/WHO Meeting on Pesticide Residues)
    • US EPA 40 CFR Part 180 (Pesticide Tolerances)
    • ISO 9001:2015 Quality Management Systems for crop protection formulations
    • China GB 2763 (National Food Safety Standard—Maximum Residue Limits for Pesticides in Food)

    Typical usage ratio

    • Integrated at 5–12% by weight in technical concentrate formulation, modulated according to desired final active content and downstream dilution protocols

    Downstream process integration

    • Added following primary nitration or halogen exchange steps, during solvent-mediated cyclization, then advanced to final formulation and wet-milling operations for field application products

    Final product types

    • Technical-grade benzoxazole fungicide actives
    • Emulsifiable concentrate (EC) and suspension concentrate (SC) crop protection products
    • Seed treatment formulations containing specific benzoxazole-based ingredients

    3. Specialty Dye and Optical Brightener Synthesis

    Manufacturers of specialty dyes and optical brighteners employ 5-Chloro-2-Methylbenzoxazole as a key intermediate to achieve high-brightness, photostable chromophore structures. The compound participates in ring fusion and further functionalization steps, particularly for benzimidazole- and benzoxazole-derived fluorescent agents. Production runs require precise control of halogen content to satisfy textile, plastics, and paper grade regulations. Final blending protocols focus on dispersibility for masterbatch or direct-application end use.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile Chemicals and Dyes)
    • EN 646/648 (Color fastness for paper)
    • ISO 9001:2015 (Quality Management System for pigment/dye production)
    • EU REACH Regulation (EC) No 1907/2006—Substance Registration and Assessment

    Typical usage ratio

    • Typical charge ranges from 8–20% mass fraction in reaction input, dependent on target dye intensity and optical properties required

    Downstream process integration

    • Introduced during the base ring condensation stages, then progressed through multi-stage oxidation and coupling; final products filtered, standardized, and milled into granules or liquids

    Final product types

    • Textile dyes with benzoxazole chromophores
    • Optical brighteners for plastics masterbatch and detergents
    • Paper and specialty coatings for high-white appearance

    4. High-Performance Polymer Additive Synthesis

    Producers of engineered plastics integrate 5-Chloro-2-Methylbenzoxazole as a raw material in the synthesis of functionalized monomers for high-performance resins. The chemical’s benzoxazole ring structure delivers mechanical strength and thermal stability once polymerized into the main chain or as a pendant group. Polymer design teams specify it during initial monomer batch blending, enabling targeted molecular architecture for niche electrical, automotive, and fiber-reinforced composite applications. Process controls focus on minimization of residual monomers and consistent dispersibility within polymer matrices.

    Industry compliance standards

    • UL 94 (Plastics Flammability Standard)
    • ISO 1043 (Plastics—Symbols and Abbreviations)
    • EU RoHS (Restriction of Hazardous Substances, Directive 2011/65/EU)
    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)

    Typical usage ratio

    • Loaded at 1–5% by mass into reactor charge or established as part of co-monomer blend, adjusted by specific polymer backbone requirements and required end-use properties

    Downstream process integration

    • Polymerized via melt condensation or catalytic copolymerization, followed by extrusion, pelletization, and end-use compounding with reinforcing additives and colorants

    Final product types

    • Flame-retardant engineering thermoplastics
    • Electrical insulative components
    • Reinforced fiber composites for automotive and electronics

    5. Photoinitiator Intermediate for UV-Curable Systems

    UV-cure technology manufacturers utilize this raw material in the synthesis of photoinitiator molecules, particularly where benzoxazole derivatives foster fast-reacting and stable curing agents. Engineers dose the compound during nucleophilic substitution and subsequent oxidization to achieve targeted wavelength absorption and crosslinking performance. Control of halogen side-chain content is critical for compatibility with end-use packaging inks, adhesives, and clear coatings. QC labs verify residual contaminant levels before the photoinitiator enters downstream blending and pre-dispersion lines.

    Industry compliance standards

    • Swiss Ordinance SR 817.023.21 (Food Contact Photoinitiators)
    • China GB 9685 (Standard for Use of Additives in Food Contact Materials)
    • ISO 22000 (Food Safety Management Systems, for packaging inks and coatings)
    • EN 71-3 (Toy Safety, for chemical migration from printed surfaces)

    Typical usage ratio

    • Incorporated at 3–8% by weight during photoinitiator core synthesis, then diluted to 0.1–2% in finished ink or adhesive systems as determined by target cure rate and substrate type

    Downstream process integration

    • Introduced at the core building stage of photoinitiator molecule synthesis, followed by purification and blending with photoactive resins before end-use dispersion or formulating

    Final product types

    • UV-curable printing inks for food, pharma, and label packaging
    • UV adhesives for electronics and precision assembly
    • Clear and pigmented coatings for direct food contact packaging
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 5-Chloro-2-Methylbenzoxazole: A Reliable Choice from a Dedicated Chemistry Team

    With years of refining processes under our belts, our team knows what brings consistent results in the field of specialty heterocycles. We have worked with numerous aromatic building blocks, and 5-Chloro-2-Methylbenzoxazole (5C2MBO) has become a sturdy part of our line-up because of its unique structure and dependable synthetic performance. We’ve seen many chemists look for purity and stability, particularly when developing new pharmaceuticals or seeking an efficient pathway toward agrochemical actives. Our direct, hands-on experience as an original producer gives us a good vantage point to explain why our approach stands apart and how it shapes the way customers deploy this molecule in research and industry.

    What Makes 5-Chloro-2-Methylbenzoxazole Valuable?

    Nature rarely lends us materials like this out of the box—we synthesize it step by step, always focused on controlling byproducts and minimizing impurity profiles. The structure’s benzoxazole core carries both a chloro group in the 5-position and a methyl group at the 2-position. From a synthetic perspective, this particular substitution pattern brings a different kind of reactivity than either 5-chlorobenzoxazole or 2-methylbenzoxazole alone. We have found that the electron distribution across the ring opens new routes and gives rise to specific selectivities during further reaction. In practice, researchers choose 5C2MBO for its ability to form stable links and for its compatibility in many conditions needed for coupling, cyclization, and substitution reactions.

    Clients have told us they value its slightly higher reactivity versus simple benzoxazole, as the specific placements of chlorine and methyl groups influence nucleophilic aromatic substitution. For us, producing this compound at a high purity, with minimal levels of halogen exchange or unwanted methylation, involves a lot of attention to detail. Any deviation from the ideal yields impurities that are hard to separate downstream. Years of refining our crystallization process means we reliably ship a product that dissolves consistently and performs predictably in the lab.

    How We Approach Consistency and Quality Control

    Raw materials form the backbone of any fine chemical. We source chlorinated anilines and orthoesters from suppliers who document every delivery and batch rigorously. Our reactors and centrifuges don't get put into service unless every cleaning pass meets our internal residue checks. Skipping steps, or shifting to off-the-shelf intermediates, can increase costs and introduce stealthy contaminants. Running full in-process chromatograms and post-synthesis spectrometric analysis lets us stay aware of any byproduct formation. We have seen firsthand how even minor traces of dichloro analogs or over-methylated rings undermine yield in downstream applications for those who use these intermediates for API synthesis.

    Unlike many trading houses or third-party mixers, we are directly responsible for every batch—there’s no passing the buck to unnamed “upstream” partners if a spec falls short. If results ever drift outside our expected HPLC or NMR signature ranges, we hold and rework; we don’t substitute or attempt to blend away problems. Customers often send feedback on their own assays and we welcome that collaboration, because it helps us refine not only our production but also the end-user application experience. Repeat business only happens when every parcel aligns with the last.

    The Chemistry Behind Our 5-Chloro-2-Methylbenzoxazole

    We have seen many requests for this molecule stem from its position as a reliable starting material for further benzoxazole modifications. For example, many pharmaceutical intermediates require ortho-directed electrophilic substitution, and our molecule’s substituents influence regiochemistry in ways that save time and cost. A methyl group brings a gentle electron-donating effect, which can guide reactions away from unwanted side products. The chlorine atom supports cross-coupling reactions, making Suzuki, Buchwald-Hartwig, or N-arylation strategies more straightforward. We design our synthesis to keep the chlorine precisely at C-5—misplaced halogenation can derail entire campaigns downstream.

    Researchers in crop protection and dye chemistry use our 5C2MBO in core scaffolds because the molecule’s heteroatom arrangement gives strong aromatic stability. We have seen breakthroughs in pigment science where benzoxazoles deliver light-fastness and weathering resistance, and the methyl group’s presence lets our customers fine-tune solubility in application. Downstream, those differences matter a great deal—especially for teams working to balance solubility and reactivity in a single formulation. We respect this complexity, keeping our processes transparent and test-driven, so chemists don’t encounter surprises once the drum is opened.

    Specification Details That Matter in the Real World

    We understand that on paper, nearly any supplier can state “high purity” or “low moisture.” The reality, from our bench to yours, is more nuanced. We routinely see problems in the industry when 5C2MBO sources carry high levels of secondary amines, residual halogen acids, or slow-dissolving crystals that drag down workflow. These impurities hurt chromatography runs and introduce irritating peaks in downstream analytics. Our experience in winter and summer batch runs means we’ve learned to control for humidity swings and temperature fluctuations, because these factors alter both melting and storage life.

    Stable crystal morphology is a must for downstream solubility and handling. We calibrate our crystal growth rates and sieve mesh so the product pours freely, with no caking or dusting—less time spent preparing a reaction, fewer headaches on the weigh-bench. Because the molecule isn’t hygroscopic in its pure form, we’ve cut down on the need for vacuum drying in customer workflows. For those scaling up beyond bench-scale, particle size and reproducible lot-to-lot behavior are critical. Our customers have validated such features through their own kilo-scale and pilot plant reports, usually noting cleaner reactor runs and improved throughput compared to earlier, inconsistent suppliers.

    Understanding the Differences: Comparing 5C2MBO With Other Benzoxazoles

    From the standpoint of someone who’s synthesized, packed, and shipped thousands of kilograms, the differences between 5C2MBO and close relatives show up quickly. For one, unchlorinated 2-methylbenzoxazole does not offer the same cross-coupling latitude—without the activating effect of the chlorine at C-5, palladium- and copper-catalyzed transformations run less efficiently. On the other side, 5-chlorobenzoxazole lacks the methyl influence, meaning electron balance in the ring is significantly different. The presence of both substituents unlocks synthetic tactics simply unavailable from either parent compound.

    Researchers have pointed out that when they switch to our 5C2MBO, yields in Suzuki couplings typically climb. Chlorine-driven substitution reactions become more predictable, and purification steps often become less challenging. Under LC-MS, single peaks show up where two or three minor analogs used to lurk with looser material. Chemists working on new IP especially value confidence in the starting materials—the fewer “unknowns” in the base compound, the lower the risk of unpleasant patent or regulatory surprises down the line.

    Divergence also appears in physical handling. Where some suppliers’ material arrives in chunks or clumps, our customers receive flowable, off-white powder with carefully controlled consistency. Anyone who has filtered sticky residues knows how much this impacts efficiency, especially in kilo-lab or pilot-plant settings. We have taken pains to make sure our quality assurance cycle eliminates these “inconveniences.”

    Routes of Application: Who Uses Our Product and Why

    We have watched compounding pharmacists, process chemists, and academic researchers rely on 5C2MBO as a launching point for diverse custom syntheses. In pharma, some clients take our material into heterocycle extension, aiming for new antibiotics or support ligands that resist metabolic degradation. Fine chemical developers have flagged the compound’s role in library synthesis, where predictable behavior under a variety of conditions is essential—nobody benefits from batch-to-batch drift when screening dozens of derivatives. Some pigment formulators, chasing longer color fastness and stricter regulatory compliance, can tighten their downstream analytics because our product’s impurity fingerprint is so well-mapped.

    Regulatory departments, especially those filing with health agencies, have relayed how our documentation process stands out. Each batch comes backed by a complete, traceable analysis routine—no afterthought, no corners cut. Documentation isn’t a paperwork exercise: it helps our customers avoid costly reprocessing and repeated filings.

    Reflections From Production: Reliable Supply and Real-World Support

    Direct production experience means we live with the choices behind every gram delivered. If a regulator or procurement team needs a deviation report, we don’t scramble—we open our archive, where we retain full e-records and sample aliquots for years. We hold every lot in quarantine until it passes third-party labs as needed. Our hands-on approach means our chemists answer technical queries, not a call center. We have adjusted schedules and reworked batches based on emerging customer needs—rush orders, pilot campaigns, or sudden spec changes—so that the material delivered always matches real-world, not theoretical, requirements.

    Supply chain interruptions have made us more vigilant. Over the last decade, trade wars and pandemic events exposed the risks of relying on intermediaries with a “black box” approach. Our own in-house process means we don’t have to ring up a foreign toll-free number to trace a problem—we’ve made each batch, ourselves, every step of the way. If a cabin filter needs to be replaced in our reactor exhaust or a new GHS rule demands updated labeling, we react in days, not months. While many third-party marketers retrofit their stories or documentation after the fact, our operation means traceability flows naturally from daily practice, not retroactive adjustments.

    Working directly in synthesis and finishing, our staff has picked up countless “on the floor” improvements that never make it into brochures—techniques for better mixing, faster filtration, and more effective packaging. This is the backbone of consistent, batch-to-batch supply for clients with demanding timelines. We maintain real inventory, not speculative virtual stocks, which allows clients to place repeat orders without disruption or unexplained back-orders.

    Facing Issues Head-On: How Real-World Use Shapes Our R&D

    With every kilogram shipped out, we receive a mix of formal feedback and offhand stories about the product in use. Scale-up from bench research to pilot-plant presents different challenges—you can’t use the same wash solvents or rely on the same filtration pressures when moving up by orders of magnitude. Sometimes, irritation arises from a new impurity as customers experiment with new coupling conditions, calling for a joint troubleshooting effort. We don’t brush off these questions as “user error”; instead, we take the findings back into our process review meetings, scouting ways our production can sidestep those issues at the source.

    We have re-tuned drying curves and tweaked crystallizer timing to reduce fines or clumping. Experience from on-site troubleshooting trips inspired us to adjust our anti-static procedures—preventing product loss during transfer, not after a client raises a red flag. Each revision, prompted by real customer conversations, reinforces feedback loops that the broad market can’t duplicate.

    Some customers push for greener chemistry. We’ve responded by moving to lower-impact chlorinating agents. Our waste management now captures and recycles halogenated byproducts with no solvent dumping. Training teams on safe handling, step-by-step, rather than delegating to outside trainers, means everyone under our roof is accountable—and experienced. For every new regulatory checklist that appears, we test our procedures on live batches before marking a box “compliant.”

    We’ve seen increased requests for sustainable packaging, and responded by adopting recyclable drums and minimizing single-use plastics. Each of these changes tracks back directly to customer input—applied with the pragmatism that comes from daily handling and logistics, not just paperwork.

    Collaborative Relationships Build Greater Innovation

    Our openness to customer-driven process improvements is not just for show—it makes a measurable difference in speed to market and in the costs of scale-up. By discouraging a “fire and forget” transaction, we keep real lines of communication open. If a downstream developer requests a custom specification—not just nominal purity, but a particular particle size or moisture window—we explore the production adjustments transparently, and let the chemist direct us with their real-world needs. Over years of such exchanges, we’ve found our best innovations spring from field experience, not abstract theorizing.

    On the IP front, staying current with evolving synthesis methods lets our clients run competitive rather than outdated chemistry. When new cross-coupling catalysts appear in the literature, for example, we have supplied samples and even tweaked impurity thresholds based on beta-test feedback, keeping clients ahead of the regulatory and competitive curve.

    Conclusion: 5-Chloro-2-Methylbenzoxazole in Practice—Lessons From the Source

    From sourcing raw materials to packing finished drums, every decision affecting the quality and consistency of 5C2MBO is made by the team that stands behind the label. We don’t hide behind generalities or pass-offs—each shipment is the end result of direct production, exhaustive testing, and a real-world dialogue between manufacturer and chemist. For those in pharmaceuticals, agrochemicals, colorants, or custom R&D, the differences between “on paper” and “in practice” matter deeply. Through ongoing feedback, practice-driven improvements, and a commitment to true traceability, we keep 5-Chloro-2-Methylbenzoxazole a reliable, innovation-ready choice for advanced synthesis.