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HS Code |
449186 |
| Chemical Name | 6-Nitro Benzoxazolinone |
| Cas Number | 700-41-0 |
| Molecular Formula | C7H4N2O4 |
| Molecular Weight | 180.12 g/mol |
| Appearance | Yellow solid |
| Melting Point | 199-202 °C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, dry and ventilated place |
| Synonyms | 6-Nitro-2-benzoxazolinone |
As an accredited 6-Nitro Benzoxazolinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, 25g label. Marked "6-Nitro Benzoxazolinone," CAS number, purity, hazard warnings, supplier details. |
| Shipping | 6-Nitro Benzoxazolinone should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must comply with relevant chemical transport regulations, including appropriate labeling and documentation. Handle with care, using protective equipment, and avoid shipping with strong oxidizing or reducing agents to ensure safety during transit. |
| Storage | 6-Nitro Benzoxazolinone should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong acids and bases. Protect it from light, moisture, and sources of ignition. Proper labeling and handling precautions are essential to prevent accidental exposure or degradation of the chemical. Store according to local regulations and safety guidelines. |
Applications of 6-Nitro Benzoxazolinone in Industrial ManufacturingAs a direct manufacturer specialized in the synthesis and supply of 6-Nitro Benzoxazolinone, we support global partners in sectors where its unique properties provide functional value in established commercial downstream applications. Below we present verified industrial usage scenarios, with precise integration details for formulation, regulatory compliance, process position, and anticipated product outcomes. 1. UV Stabilizers for Plastics and Polymer Additives6-Nitro Benzoxazolinone is widely introduced into resin compounding for engineering plastics where it acts as a photostabilizer to enhance the UV resistance of finished components. Its specific aromatic structure contributes to absorbing UV radiation and minimizing physical degradation, highly valued in outdoor and technical polymer applications such as automotive or electrical housing. Manufacturers rely on this additive to extend lifespan and prevent yellowing of exposed polymers while maintaining compliance in safety-critical environments. Industry compliance standards
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2. Agricultural Pre-Emergent Herbicide IntermediatesIn agrochemical downstream plants, 6-Nitro Benzoxazolinone serves as a key heterocyclic intermediate for the synthesis of pre-emergent herbicides targeting broadleaf weeds and grass control in major field crops. Its molecular scaffold incorporates highly specific nitro substitution patterns required for efficient bioactivity, with downstream partners typically employing it during final-stage coupling or as a precursor to active ingredient production through reduction and cyclization steps. This integration guarantees selective weed management while meeting regulatory purity and residue expectations. Industry compliance standards
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3. Chemical Probe Synthesis for Plant Physiology ResearchResearch and development facilities in plant sciences adopt 6-Nitro Benzoxazolinone as a building block to develop specialized probes for studying allelopathic compounds and plant defense mechanisms. Its role as a reference standard or probe agent assists in quantifying and tracking specific biochemical pathways in laboratory assays and field studies, enabling precise elucidation of metabolic activity involving benzoxazolinone derivatives. The supplied product must meet strict analytical criteria for reproducibility and contaminant control. Industry compliance standards
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4. Dye Intermediate for Specialty Textile ColorantsSpecialty dye manufacturers incorporate 6-Nitro Benzoxazolinone as a functional group source in the synthesis of high-performance disperse dyes for polyester and polyamide textiles. Its electron-rich nitro group modifies chromophore properties, achieving target hues and fastness profiles not easily accessible through traditional intermediates. Integration into the diazotization or coupling step ensures secure attachment of the nitro-benzoxazole moiety to the aromatic dye system, ultimately supporting colorfast synthetic fibers for technical or fashion-oriented textiles. Industry compliance standards
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