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3-Nitrobenzhydrazide

    • Product Name 3-Nitrobenzhydrazide
    • Alias m-Nitrobenzhydrazide
    • Einecs 221-838-9
    • 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

    643038

    Compound Name 3-Nitrobenzhydrazide
    Cas Number 619-96-9
    Molecular Formula C7H7N3O3
    Molecular Weight 181.15
    Appearance Yellow crystalline powder
    Melting Point 198-201°C
    Solubility Slightly soluble in water, soluble in ethanol
    Boiling Point Decomposes
    Density 1.49 g/cm3
    Storage Conditions Store in a cool, dry place, tightly closed
    Purity Typically ≥98%
    Synonyms m-Nitrobenzhydrazide
    Smiles C1=CC(=CC(=C1C(=O)NN)[N+](=O)[O-])

    As an accredited 3-Nitrobenzhydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Nitrobenzhydrazide, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and detailed hazard labeling.
    Shipping 3-Nitrobenzhydrazide is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging meets regulatory standards for hazardous chemicals. Shipping is via ground or air, adhering to applicable safety and labeling regulations. Appropriate documentation and safety data sheets (SDS) are included to comply with international and local transport guidelines.
    Storage 3-Nitrobenzhydrazide should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers or acids. Keep it in a cool, dry, well-ventilated area, preferably in a chemical storage cabinet. Label containers clearly, and handle with appropriate personal protective equipment to prevent exposure. Store at ambient temperature, and avoid heat or ignition sources.
    Application of 3-Nitrobenzhydrazide

    Applications of 3-Nitrobenzhydrazide in Industrial Manufacturing

    3-Nitrobenzhydrazide has critical roles as an organic synthesis intermediate across pharmaceuticals, agrochemicals, pigment manufacturing, and polymer modification. Our direct production processes ensure consistent quality for demanding downstream uses. Below we detail core application pathways and practical considerations for industrial users.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers routinely employ 3-nitrobenzhydrazide as a key intermediate in the construction of complex pharmacophores, particularly for anti-tuberculosis and anti-inflammatory agents. The material participates in targeted hydrazinolysis and cyclization steps during the multi-stage synthesis of pyrazole, triazole, and related heterocyclic scaffolds. Close attention to impurity control and process validation is required at scale-up stages, as the hydrazide group’s reactivity can introduce critical pathway-specific byproducts. Our supply supports continuous production needs with documented batch-to-batch uniformity to fit GMP manufacturing and regulatory submission batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) Chapter <795> and <1225> for chemical intermediates
    • European Pharmacopoeia 11.0 for API synthesis controls
    • FDA cGMP (21 CFR Part 211) as applicable to API manufacturing

    Typical usage ratio

    • 0.90 to 1.15 mol per mol of target API intermediate, tuned to yield and purity needs per process route
    • Excess factor adjusted based on downstream conversion efficiency and impurity filtering strategy

    Downstream process integration

    • Added at step two or three during formation of N-heterocycles after precursor activation
    • Hydrazinolysis conducted in sealed vessels at controlled temperature with automated pH monitoring
    • Integration with continuous purification protocols to meet residual solvent and trace metal specifications

    Final product types

    • Pyrazole-based anti-tubercular agents
    • Triazole and tetrazole derivatives for research and API development
    • Off-patent anti-inflammatory product intermediates
    • Precursor building blocks for generic and custom APIs

    2. Agricultural Chemical Synthesis

    Leading crop science companies utilize 3-nitrobenzhydrazide as a key intermediate in the synthesis of select herbicides, fungicides, and insecticide actives. The material’s nitro and hydrazide functionalities enable versatile condensation reactions, supporting the construction of hydrazone and semicarbazide derivatives found in modern agrochemical active ingredients. Production lines demand high stability, reproducibility, and proper waste stream management when employing this hydrazide to ensure regulatory compliance and consistent field efficacy in the final agrochemical formulation.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for technical and formulated crop protection products
    • EPA 40 CFR Part 158—Data Requirements for Registration (USA)
    • China GB/T 1603-2007 Technical Specification for Raw Pesticides
    • OECD Guideline Series for Testing of Chemicals—degradability and residue analyses

    Typical usage ratio

    • Utilized at 0.70 to 1.10 equivalents per principal intermediate depending on the condensation route selected
    • Adjustment based on formation yield and downstream biological performance of formulated pesticide

    Downstream process integration

    • Charged during preformulation or reactive synthesis of the hydrazone bridge in the technical active material
    • Process conducted in semi-batch reactors with in-process HPLC verification for endpoint confirmation
    • Subsequent integration into formulation plants for dispersible granule or EC concentrate products

    Final product types

    • Hydrazone-based selective herbicide technicals
    • Fungicide actives with improved environmental stability
    • Novel insecticide intermediates under pilot-scale evaluation
    • Precursors for new-generation combination agrochemicals

    3. Organic Pigment Manufacturing

    3-Nitrobenzhydrazide finds established use in azo pigment manufacturing, where it functions as a key coupling component during the synthesis of yellow and orange pigments for plastics, coatings, and specialty inks. The hydrazide enables precise diazotization-coupling reactions to generate high tint-strength pigments with controlled particle morphology. Fine-tuning process parameters ensures high purity and reproducible batch color shade, in accordance with application-driven color fastness and dispersibility criteria.

    Industry compliance standards

    • EN 71-3 Safety of Toys—Migration of Certain Elements (pigments for children’s products)
    • ISO 9001:2015 certified colorant manufacturing quality management
    • RoHS Directive (2011/65/EU) for electronic and electrical equipment
    • REACH (EC 1907/2006) requirements for industrial pigment use

    Typical usage ratio

    • 30–60% by weight in coupling component stream, adjusted to target specific chromophore loads for C.I. Pigment Yellow or Orange series
    • Optimized for end-use substrate compatibility and dispersibility properties

    Downstream process integration

    • Introduced during initial diazotization coupling stage under controlled pH and low temperature
    • Integrated with in-line filtration and washing steps to remove trace nitro compounds
    • Subsequent micronization and surface treatment to meet end-use standards

    Final product types

    • Organic pigment concentrates for plastics and fibers
    • Water-based and solvent-based pigment dispersions
    • High-performance printing inks for industrial applications
    • Coloring agents in automotive and architectural coatings

    4. Functional Polymer Modification

    Specialty polymer producers utilize 3-nitrobenzhydrazide for introducing nitroaromatic and hydrazide functional groups into high-performance resins, films, and fibers. The compound participates in post-polymerization modifications or as a reactive end-capper to improve chemical resistance and adhesive properties. Strict moisture control and continuous monitoring of reaction endpoints allow for uniform functionalization, important for applications with demanding stability and durability requirements in coatings and engineered materials sectors.

    Industry compliance standards

    • ASTM D1974 for film and resin additive quality control
    • ISO 7822 Polymer Additives—Test Methods for Chemical Analysis
    • REACH SVHC (Substances of Very High Concern) reporting for downstream users
    • UL 94 for flammability of plastic materials in end-use products

    Typical usage ratio

    • Added at 0.3–1.0% by weight of base polymer batch for targeted functional group incorporation
    • Ratio determined by end-use durability, polarity, and thermal property requirements

    Downstream process integration

    • Charged post-polymerization or during melt blending in compounding extruders
    • Chemically bonded via radical or nucleophilic substitution under monitored thermal conditions
    • Final film or fiber processed via solvent casting or extrusion and subjected to QC assays for residual monomer

    Final product types

    • Chemically resistant engineering films
    • Adhesion-promoting polymer additives
    • Modified polyamide and polyester fibers
    • Advanced polymer blends in high-wear industrial applications
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