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3,5-Dinitrobenzamide

    • Product Name 3,5-Dinitrobenzamide
    • Alias m-Nitrobenzamide
    • Einecs 208-535-4
    • 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

    356922

    Cas Number 4132-60-3
    Molecular Formula C7H5N3O5
    Molecular Weight 211.13 g/mol
    Appearance Yellow crystalline powder
    Melting Point 193-196°C
    Solubility In Water Slightly soluble
    Density 1.65 g/cm³ (approximate)
    Purity Typically ≥98%
    Synonyms 3,5-Dinitrobenzamide, m,dinitrobenzamide

    As an accredited 3,5-Dinitrobenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3,5-Dinitrobenzamide is packaged in a 100g amber glass bottle with a white screw cap, labeled with hazard warnings.
    Shipping 3,5-Dinitrobenzamide is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Packaging complies with relevant safety and regulatory guidelines for hazardous substances. It is labeled with appropriate hazard warnings and transported via certified carriers specializing in chemical shipments, ensuring safe and secure delivery according to UN and DOT regulations.
    Storage 3,5-Dinitrobenzamide should be stored in a tightly sealed container, protected from light, moisture, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong reducing agents and bases. Ensure appropriate labeling and access only to trained personnel, following all relevant safety and regulatory guidelines for hazardous materials.
    Application of 3,5-Dinitrobenzamide

    Applications of 3,5-Dinitrobenzamide in Industrial Manufacturing

    As the direct producer of 3,5-dinitrobenzamide, we supply this compound to specialized sectors where its high purity and precise chemical profile enable critical transformations. The following real-world application pathways reflect established uses in advanced organic synthesis, including pharmaceutical intermediates, agrochemical actives, pigment manufacturing, and polymer modification. Each scenario details sector-specific compliance, recommended formulation ratios, integration steps in downstream workflow, and the range of end products from our global industrial partners.

    1. Pharmaceutical Intermediate Synthesis

    3,5-Dinitrobenzamide acts as a crucial building block in the synthesis of active pharmaceutical ingredients, particularly for drugs that require a nitroaromatic backbone. Medicinal chemists use it in multi-step synthesis routes, where controlled reduction and subsequent functionalization lead to targeted APIs. Precision in purity and trace element control is essential for downstream conversion, ensuring batch consistency from early pilot scale to commercial process validation. Our production maintains batch-to-batch reproducibility, minimizing risk in regulated pharmaceutical workflows.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. monograph guidance for related substances (where applicable in custom synthetics)
    • 21 CFR Part 211 US cGMP regulations for pharmaceuticals
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 5-25% of total intermediate mass in targeted coupling, acylation, or reduction steps, adjusted according to molecular pathway and stoichiometry
    • Precise excess for high-yield conversions, verified by HPLC and NMR in every batch

    Downstream process integration

    • Integrated at the initial aromatic nitration or amidation stage
    • Subjected to selective reduction, acylation, or further derivatization in pharma synthesis lines
    • QC checked on incoming lots for trace metal, residual solvents, and heavy nitro impurities

    Final product types

    • Nitroaromatic API intermediates
    • Antimicrobial and anti-inflammatory agent precursors
    • Specialty medicinal compound scaffolds for oncology and CNS agents
    • Clinical-stage custom organic molecules

    2. Agrochemical Active Ingredient Manufacturing

    Formulators in agrochemical manufacturing utilize 3,5-dinitrobenzamide for constructing key structural motifs in herbicide and fungicide actives. By participating in core condensation and substitution reactions, the compound supports creation of highly selective actives that meet regulatory profiles for environmental persistence and target specificity. Rigorous impurity profiling and dust management are maintained during ingredient handling to reduce occupational and environmental exposure, and all production follows sector-specific stewardship guidelines.

    Industry compliance standards

    • FAO/WHO Manual on the Development and Use of FAO and WHO Specifications for Chemical Pesticides
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH registration–hazard assessment and toxicological evaluation (EC/1907/2006)
    • China GB2763 Pesticide Residue Standards for agro-related processing

    Typical usage ratio

    • 10-22% of precursor blend, depending on crop-selectivity requirements
    • Adjusted for reaction pathway to balance cost, yield, and conversion efficacy

    Downstream process integration

    • Introduced at the stage of key active synthesis—especially for nitrobenzamide-derived triazole or amide herbicides
    • Direct use in cyclization or as amine donor in N-substituted nitroaniline downstream derivatives
    • Rigorous residue monitoring in final crop protection formulations

    Final product types

    • Selective herbicidal actives (e.g., amide-based inhibitors)
    • Fungicidal ingredient scaffolds
    • Pesticide intermediates with controlled degradability
    • Custom crop protection blends for specific geographies

    3. Organic Pigment and Dye Intermediate

    Producers of high-performance pigments and specialty dyes incorporate 3,5-dinitrobenzamide for introducing nitro groups critical to chromophore development and lightfastness. Manufacturers in this segment carry out reduction or coupling transformations, forming stable azo or anthraquinone derivatives with tuned spectral properties. Process engineers maintain strict environmental and occupational safety controls, consistent with advanced pigment production for coatings, plastics, and textile applications where color fastness and chemical stability are mandatory.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys – migration of certain elements (for pigments in consumer-facing products)
    • Restriction of Hazardous Substances (RoHS) Directive 2011/65/EU for electronic coatings
    • ISO 9001 Certified pigment production facilities
    • Zero Discharge of Hazardous Chemicals (ZDHC) standards for the textile supply chain

    Typical usage ratio

    • 8-15% by weight of colorant precursor formulation
    • Varies by desired hue intensity, lightfastness, and substrate compatibility

    Downstream process integration

    • Initial coupling or diazotization step to introduce chromogenic groups
    • Subsequent integration in pigment milling and finishing for dispersion in binders
    • On-line coloristic and particle-size QC to meet tight batch standards

    Final product types

    • Azo and anthraquinone dyes for textile and fiber applications
    • Organic pigments for paints, printing inks, and plastics
    • Colored masterbatches for polymer compounding
    • High-stability dispersions for specialty coatings

    4. Monomer and Polymer Modification Agent

    Engineers in advanced polymer R&D and compounding employ 3,5-dinitrobenzamide to introduce aromatic nitro groups that impart thermal resistance, flame retardance, and modified dielectric properties to specialty resins. This raw material fits directly into the polymer chain via co-monomer feeding or acts as a tailored functionalizing agent for surface modification. Production follows strict polymer quality and safety systems, ensuring compliance for applications in electronics, aerospace, and specialty coating sectors. Operations maintain closed-system feeding and automated release control for safety assurance at industrial scale.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical production
    • UL 94 Flammability standards for polymers
    • EN 45545-2:2020 Fire protection for railway vehicle components
    • RoHS and REACH substance control for end-use compliance in electronics and transport

    Typical usage ratio

    • 0.5-3% w/w as co-monomer or chain modifier, optimized for required property enhancement
    • Higher ratios possible for specialty high-performance blends subject to rheological review

    Downstream process integration

    • Direct feeding to bulk or solution polymerization reactors
    • Reactive extrusion for functionalized compounding
    • Post-polymerization surface grafting for advanced engineered plastics

    Final product types

    • Flame-retardant polyester or polyamide resins
    • High-temperature stable engineering plastics
    • Specialty insulation and encapsulation compounds for electronics
    • Functional surface modified composites
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    Competitive 3,5-Dinitrobenzamide prices that fit your budget—flexible terms and customized quotes for every order.

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