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2-Nitrophenyl Isocyanate

    • Product Name 2-Nitrophenyl Isocyanate
    • Alias o-Nitrophenyl isocyanate
    • Einecs 247-757-1
    • 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

    834304

    Cas Number 2929-40-6
    Molecular Formula C7H4N2O3
    Molecular Weight 164.12 g/mol
    Appearance Yellow to brown crystalline solid
    Melting Point 45-47°C
    Boiling Point 150°C at 13 mmHg
    Density 1.39 g/cm³
    Solubility In Water Reacts with water
    Purity Typically ≥98%
    Refractive Index 1.615
    Flash Point 129°C
    Smiles O=C=Nc1ccccc1[N+](=O)[O-]

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, with secure screw cap; labeled with chemical name, hazard warnings, and handling instructions for laboratory use.
    Shipping 2-Nitrophenyl Isocyanate should be shipped in tightly sealed containers, away from moisture and incompatible substances. It must be labeled as a hazardous material, handled according to UN 2206 regulations, and transported under controlled temperatures. Adequate protective packaging is essential to prevent leaks, with documentation included for emergency and safety compliance.
    Storage 2-Nitrophenyl Isocyanate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible substances such as acids, bases, and strong oxidizers. Protect from direct sunlight and ignition sources. Use chemical-resistant containers, clearly labeled, and keep it under an inert atmosphere if possible to prevent hydrolysis and degradation.
    Application of 2-Nitrophenyl Isocyanate

    Applications of 2-Nitrophenyl Isocyanate in Industrial Manufacturing

    2-Nitrophenyl Isocyanate is an essential intermediate applied across specialized industrial sectors for its reactivity and selectivity in targeted synthesis. As a manufacturer with direct integration into diverse chemical production chains, we ensure precise quality control and documentation for all downstream uses. The following industry applications showcase concrete implementation scenarios reflecting real-world usage and compliance expectations.

    1. Pharmaceutical Intermediate Synthesis (API Precursors)

    In pharmaceutical manufacturing, companies use 2-nitrophenyl isocyanate as a building block for synthesizing substituted urea and carbamate groups within complex API structures, including anti-inflammatory and anti-tumor agents. Its reactivity towards nucleophiles enables controlled modification of core intermediates under monitored reaction environments. Downstream integrations require tight impurity control, batch traceability, and compliance with global pharmacopoeial guidelines at each step, from coupling to purification.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP; ICH Q7)
    • USP, EP, JP monographs for related APIs
    • FDA 21 CFR Part 210/211 requirements
    • REACH Annex XVII restrictions

    Typical usage ratio

    • 0.8-1.2 molar equivalents relative to nucleophile substrate; ratio adjusted based on specific API precursor loading and target yield optimization

    Downstream process integration

    • Charged in alkylation or acylation stage of intermediate synthesis
    • Reacted in temperature-controlled, moisture-free environment using inert carrier solvents (e.g., acetonitrile, NMP)
    • Followed by product isolation through sequential quench, aqueous workup, and purification by column chromatography or crystallization

    Final product types

    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Pyrimidine-based antitumor agent building blocks
    • Benzothiazole and quinoline advanced intermediates
    • Custom fine chemicals for specialty pharma pipelines

    2. Agrochemical Synthesis (Herbicide and Fungicide Actives)

    Major crop protection manufacturers apply 2-nitrophenyl isocyanate to introduce nitroaryl and urea functionalities within selective herbicide and fungicide actives. Its high selectivity for amine group coupling enables precise formation of biologically active structures. Batch consistency and trace impurity management are crucial for downstream environmental approvals and compliance with pesticide registration frameworks.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • European Regulation (EC) No 1107/2009 on Plant Protection
    • ISO 16140 for QC and impurity analysis
    • GLP-compliant production documentation

    Typical usage ratio

    • 5–12% by weight in core synthetic step, optimized against active molecule conversion and impurity formation

    Downstream process integration

    • Coupling step with primary aryl amines or anilines in polar aprotic solvents
    • Sequence typically follows diazotization or nitro-group reduction in multi-step actives assembly
    • Subsequent hydrolysis, extraction, and formulation into wettable powders or emulsifiable concentrates

    Final product types

    • Urea-based pre-emergence herbicides
    • Selective rice field herbicide actives
    • Triazole fungicide intermediates
    • Custom pesticide analogues for resistance management

    3. Polymer Modifier for Specialty Polyurethanes

    Manufacturers in the specialty polymer sector deploy this compound as a chain extender or end-capper in the formulation of aromatic polyurethanes where unique molecular architectures are needed for advanced coatings, adhesives, or elastomers. Its application supports tailored hardness, flexibility, and chemical resistance, while formulation engineering must monitor unreacted isocyanate content for workplace safety and end-use compliance.

    Industry compliance standards

    • ISO 9001:2015 for quality management systems
    • EN 71-3 on migration of certain elements (when used in consumer products)
    • REACH Regulation (EC) No 1907/2006 for registration and safety data
    • OSHA PEL and ACGIH TLV guidelines for isocyanate handling

    Typical usage ratio

    • 0.5–3.0% by weight as a chain modifier in prepolymer formulations; usage determined by target functional group balance (NCO:OH ratio) and desired polymer end-use

    Downstream process integration

    • Dosed during polyaddition step after prepolymerization of polyol and diisocyanate cores
    • Blended at controlled temperatures under anhydrous conditions with continuous NCO titration
    • Residue minimized by subsequent curing, with isocyanate termination monitored by FTIR

    Final product types

    • High-performance industrial coatings
    • Elastomeric gaskets and technical parts
    • Advanced adhesive systems for electronics
    • Custom polyurethane dispersions for textile lamination

    4. Analytical Reagents for Chromatography and Derivatization

    Analytical laboratories employ 2-nitrophenyl isocyanate as a precolumn derivatization agent for amino acid and peptide analysis by HPLC and LC-MS. Its capacity to form stable urea derivatives with primary and secondary amines increases detection sensitivity and selectivity in both pharmaceutical and food testing workflows. The reagent must meet high purity and trace impurity requirements to prevent analytical background interference.

    Industry compliance standards

    • ISO/IEC 17025:2017 for laboratory competence
    • FDA Guidance for Analytical Procedures and Methods Validation
    • Pharmacopoeial protocols for amino acid content (USP, EP, JP)
    • AOAC Official Methods for food testing

    Typical usage ratio

    • 10–20 molar equivalents relative to the amino compound under study; adjusted based on substrate abundance and target derivatization efficiency

    Downstream process integration

    • Prepared as a stock solution in acetonitrile or DMF under anhydrous conditions
    • Added directly to reaction vials with sample matrix and buffer at room temperature, with incubation and direct injection into HPLC
    • Post-derivatization samples quenched prior to chromatographic separation

    Final product types

    • Analytical-grade derivatized amino acid standards
    • Quantitative peptide mapping reagents
    • HPLC/LC-MS calibration solutions
    • Reference kits for laboratory proficiency testing

    5. Dye Intermediate Manufacturing (Specialty Azodye Precursors)

    Specialty dye producers incorporate this compound for the synthesis of nitrophenyl-urea intermediates, which are further transformed into chromophoric structures required in fiber-reactive and acid dye manufacturing. Tight control of batch coloration, by-product profile, and heavy metal content is essential as products enter downstream coloring or textile finishing processes. Each process stage is subject to textile chemical approval lists and export regulatory requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)
    • REACH SVHC screening
    • ISO 14001 for environmental management (where relevant)

    Typical usage ratio

    • 3–7% by weight of total amine reactant, adjusted for target shade intensity and chromophore structure

    Downstream process integration

    • Introduced post-reduction of nitro-anilines, reacting with amino sulfonic acid derivatives
    • Coupling reactions held under controlled temperature and pH to maximize yield and purity
    • After isolation, intermediates proceed to diazotization and azo-coupling to generate final dyes

    Final product types

    • Reactive dyes for cotton and cellulosic fibers
    • Acid dyes for wool and polyamide textiles
    • Custom dye intermediates for specialty printing inks
    • High-purity intermediates for research and development use
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