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2-Nitrobenzhydrazide

    • Product Name 2-Nitrobenzhydrazide
    • Alias 2-Nitrobenzhydrazide
    • Einecs 219-259-6
    • 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

    488294

    Iupac Name 2-nitrobenzohydrazide
    Molecular Formula C7H7N3O3
    Molar Mass 181.15 g/mol
    Cas Number 610-94-6
    Appearance Yellow crystalline powder
    Melting Point 185-188 °C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes before boiling
    Purity Typically ≥98%
    Synonyms o-Nitrobenzohydrazide, 2-nitrobenzoic acid hydrazide
    Smiles C1=CC=C(C(=C1)C(=O)NN)[N+](=O)[O-]
    Inchi InChI=1S/C7H7N3O3/c8-9-7(11)5-3-1-2-4-6(5)10(12)13/h1-4H,8H2,(H,9,11)
    Storage Conditions Store at 2-8 °C, protected from light

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

    Packing & Storage
    Packing The 25g package of 2-Nitrobenzhydrazide comes in a tightly sealed amber glass bottle with a hazard label and product details.
    Shipping **Shipping Description for 2-Nitrobenzhydrazide:** 2-Nitrobenzhydrazide should be shipped in tightly sealed containers, protected from light, heat, and moisture. Label according to hazardous materials regulations, as it may be harmful if inhaled or ingested. Ensure compliance with local and international transport guidelines, and include proper documentation for chemical safety and emergency response.
    Storage 2-Nitrobenzhydrazide should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong acids, bases, or oxidizers. Store it away from direct sunlight and moisture. Appropriate chemical safety labeling is essential, and access should be restricted to trained personnel.
    Application of 2-Nitrobenzhydrazide

    Applications of 2-Nitrobenzhydrazide in Industrial Manufacturing

    2-Nitrobenzhydrazide serves as a critical intermediate across niche segments of industrial manufacturing, enabling precise chemical transformations in fine chemicals synthesis, active pharmaceutical ingredient (API) development, agrochemical production, electronic materials, and advanced dye manufacturing. Our direct manufacturing experience ensures tight control over purity, trace metals, and batch consistency to support stringent customer requirements across diverse downstream processes.

    1. Pharmaceutical Intermediate Synthesis

    2-Nitrobenzhydrazide functions as a key building block in the multi-step synthesis of certain APIs, such as antimicrobials and anti-tuberculosis agents. Manufacturers use this hydrazide to introduce nitro and hydrazide functionalities into complex molecules during intermediate stages, with focus on reaction specificity, impurity control, and adherence to stringent quality standards. It is incorporated at condensation, cyclization, and derivatization steps of custom drug molecule production, driven by validated process routes and full traceability throughout the batch record system.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. monographs for relevant intermediates
    • FDA 21 CFR Part 211 regulations on drug substance manufacturing
    • ISO 9001:2015 Quality Management for chemical processes

    Typical usage ratio

    • 5–20% molar equivalent versus the target intermediate, fine-tuned per medicinal chemist specification and material balance for multi-kilogram campaigns

    Downstream process integration

    • Added during initial bench-scale synthesis for route scouting
    • Transferred to kilo labs and pilot plants for scaling up—inline HPLC analytics for conversion tracking
    • Deployed in condensation, hydrazinolysis, or cyclization steps—critical in the transformation of aromatic nitro precursors
    • Sampling connected to in-process QC for nitrosamine and residual solvent analysis

    Final product types

    • API intermediates for anti-infective drugs
    • Building blocks for anti-tuberculosis therapeutics
    • Heterocyclic scaffolds for new chemical entities
    • Pilot-to-commercial scale custom molecules for CDMOs

    2. Agrochemical Active Ingredient Precursor

    This compound plays a focused role as a synthetic intermediate in the preparation of select herbicidal and fungicidal actives containing substituted benzene and hydrazide moieties. Agrochemical producers incorporate it during the construction of complex aromatic backbones and subsequent functionalization steps, where reproducibility and absence of chlorinated by-products directly affect registration dossiers and field performance. Material compatibility with formulation lines and solvent systems is essential, with provisions for traceability and full safety documentation for field deployment.

    Industry compliance standards

    • ISO 9001:2015 Quality Assurance for agrochemical intermediates
    • FAO/WHO specification directives for active ingredients
    • REACH (EC 1907/2006) registration for precursor supply
    • China ICAMA regulations for pesticide production

    Typical usage ratio

    • 3–10% w/w in synthesis steps, adjusted according to yield optimization and specificity of end product profile during route development and hazardous reaction scale-up

    Downstream process integration

    • Introduced in early aromatic nitration and hydrazide derivatization stages
    • Processed via solvent extraction, crystallization, and distillation to control side reactions
    • Monitored for residual hydrazine content before transition to active ingredient formulation
    • Integration points mapped in site HAZOP studies and scale validation

    Final product types

    • Selective herbicide intermediates
    • Fungicidal scaffold compounds
    • Precursor materials for process-patented pesticide molecules
    • Custom contract synthesis intermediates for agrochemical innovators

    3. Specialty Dye and Pigment Synthesis

    2-Nitrobenzhydrazide is utilized in advanced dye manufacturing lines for the synthesis of specialty azo dyes and pigment precursors, where controlled introduction of nitro and hydrazide functional groups provides enhanced fastness, light stability, and distinct colorimetric properties. Its performance in selective coupling and diazotization reactions enables the production of fine dyes for premium textile, leather, and ink applications. Manufacturers demand transparency in supply chain and robust documentation to meet global compliance for textile chemical safety and environmental regulations.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile chemical inputs
    • REACH Annex XVII restrictions on azo dyes
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 14001 for environmental management in dye operations

    Typical usage ratio

    • 2–7% mass percent relative to the total reaction charge, fine-tuned by desired color strength, shade uniformity, and coupling efficiency

    Downstream process integration

    • Added during key diazotization or azo coupling reactions
    • Integrated in multi-step pigment syntheses involving hydrazide derivatization
    • Subject to high-performance liquid chromatography (HPLC) checks on batch dye purity
    • Washed and filtered for removal of non-reacted intermediates prior to downstream blending

    Final product types

    • High-purity azo dyes for textiles
    • Custom pigment intermediates
    • Special effect dyes for inks and coatings
    • Performance pigments for plastics coloration

    4. Advanced Electronic Material Manufacturing

    This hydrazide acts as a niche precursor in electronic materials manufacture where it helps form nitrogen-rich heterocycles and aromatic intermediates required for specialty photoresist chemicals, OLED emitters, and semiconductor surface modifiers. Producers rely on consistent batch quality and trace contaminant control to achieve demanding purity thresholds essential for high-performance device fabrication. Integration occurs at pre-polymerization or molecular functionalization steps under tightly controlled cleanroom environments, with continuous quality assurance through analytical and physical property testing.

    Industry compliance standards

    • SEMI S2 standards for semiconductor materials safety
    • IEC 62474 reporting requirements for declarable substances
    • ISO 14644 Cleanroom Standards for electronic materials production
    • REACH SVHC conformity for supply into electronics manufacturing

    Typical usage ratio

    • 0.5–2% molar proportion relative to the monomer or matrix, accurately determined by device performance targets and layer thickness control

    Downstream process integration

    • Direct charge-in to molecular design labs for functionalization reactions
    • Blended into pre-polymer resins for high-precision photoresist fabrication
    • Feeding into surface activation treatments and doping processes for semiconductor wafers
    • Accompanied by FTIR, NMR, and particle size analysis for in-process quality and contamination monitoring

    Final product types

    • Photoresist precursor materials
    • OLED small molecule intermediates
    • Semiconductor device surface modifiers
    • Functionalized high-purity chemicals for printed electronics
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