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6-Nitro Benzoxazolinone

    • Product Name 6-Nitro Benzoxazolinone
    • Alias 6-Nitro-2(3H)-benzoxazolone
    • Einecs 249-445-7
    • 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

    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 & Storage
    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.
    Application of 6-Nitro Benzoxazolinone

    Applications of 6-Nitro Benzoxazolinone in Industrial Manufacturing

    As 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 Additives

    6-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

    • REACH (EC 1907/2006) registration for chemicals in EU polymer processing
    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU) for electrical and electronic applications
    • UL 746C for polymeric materials exposed to outdoor environments
    • ISO 4892 for plastic weathering and light exposure requirements

    Typical usage ratio

    • 0.05%–0.25% w/w in masterbatch formulations or direct compounding, adjusted per light stabilization needs and polymer type

    Downstream process integration

    • Dispersed during extrusion or injection molding pre-mixing, often as part of a concentrated additive blend incorporated before pelletizing or at the compounding stage; can be also added during solvent-based coatings for flexible films

    Final product types

    • Automotive exterior trim parts and dashboards
    • Outdoor wiring and cable insulation sheaths
    • Solar light housing polymers
    • Weatherable plastic films and sheets for signage

    2. Agricultural Pre-Emergent Herbicide Intermediates

    In 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

    • FAO/WHO Specifications for Plant Protection Products
    • EPA 40 CFR Part 180: Tolerances and Exemptions for Pesticide Chemical Residues in US
    • EU Regulation No 1107/2009 for placing plant protection products on the market
    • ISO 9001:2015 for agrochemical formulation and batch traceability

    Typical usage ratio

    • 10%–25% as precursor input on a molar basis during final-stage active ingredient synthesis; actual mass share varies based on synthetic pathway

    Downstream process integration

    • Charged into the reaction vessel after initial alkylation steps, serving as a skeleton structure for constructing the active moiety of various benzoxazolinone-derived herbicides; post-reaction purification precedes blending into formulation dispersions

    Final product types

    • Granular and liquid herbicide formulations for broadacre crop protection
    • Selective non-crop herbicide products
    • Pre-treated crop seeds with controlled-release herbicidal coating

    3. Chemical Probe Synthesis for Plant Physiology Research

    Research 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

    • ISO/IEC 17025: Laboratory Testing and Calibration
    • GLP (Good Laboratory Practice) as required by OECD guidelines
    • Standard Methods for the Examination of Water and Wastewater (where plant research involves hydroponic assays)
    • Applicable university and research institute procurement guidelines

    Typical usage ratio

    • Generally 20–50 μM in hydroponic plant medium or as 0.1–2.5 mg per assay batch, adjusted based on targeted detection limits and experimental design

    Downstream process integration

    • Dissolved in aqueous or buffer solutions, utilized as a spike or control reagent in metabolic tracking, biosensor calibration, or mass-spec reference calibration during physiological or environmental impact assessments

    Final product types

    • Reference standards for HPLC or GC-MS plant metabolite analysis
    • Chemical assay kits for allelopathic compound quantification
    • Functionalized chemical probes for academic research supply

    4. Dye Intermediate for Specialty Textile Colorants

    Specialty 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

    • OEKO-TEX® Standard 100 for restricted substances in textile dyes
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • REACH Annex XVII compliance for dyes used in the EU
    • ISO 105 series for textile color fastness testing

    Typical usage ratio

    • 0.5%–2.0% in the total batch of dye intermediates, depending on desired chromophore strength and brightness; precisely titrated during synthetic processing

    Downstream process integration

    • Introduced post-nitration, participating in the build-up of azo- or anthraquinone-based dye molecules during coupling reactions, followed by purification and granulation for end-use dyeing preparation

    Final product types

    • Disperse dyes for polyester yarns and fabrics
    • Modified colorant solutions for high-intensity inkjet textile printing
    • Pigment precursor blends for technical textile coatings
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