Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3,3'-Dinitrobenzophenone

    • Product Name 3,3'-Dinitrobenzophenone
    • Alias m-(Dinitrophenyl)phenyl ketone
    • Einecs 213-708-7
    • 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

    654825

    Cas Number 573-97-5
    Iupac Name 3,3'-Dinitrobenzophenone
    Molecular Formula C13H8N2O5
    Molecular Weight 272.21 g/mol
    Appearance Yellow crystalline solid
    Melting Point 184-186°C
    Density 1.43 g/cm³ (approximate)
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in organic solvents such as ethanol, acetone, and chloroform
    Chemical Structure O2N-C6H4-CO-C6H4-NO2 (3,3'-substitution on benzophenone core)
    Pubchem Cid 108633
    Synonyms m,m'-Dinitrobenzophenone

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a tightly sealed cap, clear hazard labeling, and chemical identification: 3,3'-Dinitrobenzophenone.
    Shipping 3,3'-Dinitrobenzophenone is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Packaging complies with regulations for hazardous chemicals. It is classified as a potentially harmful substance and is transported under controlled conditions with appropriate labeling, documentation, and handling precautions to ensure safety during transit and delivery.
    Storage 3,3'-Dinitrobenzophenone should be stored in a cool, dry, well-ventilated area, away from sources of heat, sparks, and open flame. Keep the container tightly closed and protected from physical damage and moisture. Store separately from incompatible substances such as strong acids, bases, and reducing agents. Use appropriate chemical-resistant containers and ensure labeling for safety and identification.
    Application of 3,3'-Dinitrobenzophenone

    Applications of 3,3'-Dinitrobenzophenone in Industrial Manufacturing

    As a direct manufacturer, we supply 3,3'-Dinitrobenzophenone for well-established downstream industries focused on advanced material synthesis and specialty chemistry. The following sections highlight major application scenarios validated by industrial practice and regulated by targeted standards, each with a dedicated breakdown of compliance requirements, typical dosage, integration points in downstream workflows, and resulting end products.

    1. Intermediate for High-Performance Pigment Synthesis

    Our material finds prevalent use in the specialty pigment industry, primarily as a key intermediate for synthesizing benzophenone-derived pigments intended for automotive, plastic, and coating applications. Manufacturers select this compound for its reliable nitro substitution pattern, contributing to chromophore development and color fastness in final dispersions. Integrators adjust the dosage according to required color properties and substrate compatibility, often tuning the process to ensure compliance with end-use safety and stability standards. The intermediate typically enters the process at the coupling or cyclization stage, facilitating the introduction of key functional groups that elevate pigment stability and brilliance.

    Industry compliance standards

    • ISO 787 General Methods of Test for Pigments and Extenders
    • ASTM D476 Standard Classification for Dry Pigmentary Titanium Dioxide Products
    • EN 71-3:2021 Safety of Toys – Migration of Certain Elements (relevant for finished goods used in toys and consumer products)
    • REACH Regulation (EC) No 1907/2006 – Registration for Chemicals Used in Pigments

    Typical usage ratio

    • 5–18% of the intermediate feedstock mass; ratio adjusted based on targeted shade, desired lightfastness, and intermediary conversion efficiency

    Downstream process integration

    • Introduced during nitro-coupling or condensation reaction stage prior to chromophore ring closure, supporting the formation of modern organic pigment structures with high weather resistance

    Final product types

    • Automotive and industrial coatings pigments
    • High-stability plastics colorants
    • Printing ink pigments
    • Masterbatch color concentrates

    2. Building Block for Pharmaceutical Intermediate Synthesis

    This compound acts as a controlled intermediate in the multi-step manufacture of certain benzophenone-based pharmaceutical active ingredients, where nitro-aromatic substitution is foundational for bioactive scaffold assembly. Leading API firms use it during early synthesis where precise nitro-positional isomerism is essential for biological targeting. The addition ratio depends on the scale, batch yield optimization, and downstream protection-deprotection steps. Regulatory adherence, especially to ICH guidelines and local GMP requirements, governs every stage, including in-process residue monitoring and fate-tracing in final APIs.

    Industry compliance standards

    • ICH Q7 “Good Manufacturing Practice for Active Pharmaceutical Ingredients”
    • USP General Chapter <1072> “Disinfectants and Antiseptics” (for residue controls)
    • 21 CFR 210/211 (FDA cGMP for finished pharmaceuticals)
    • European Pharmacopoeia, Monograph 01/2023:2000

    Typical usage ratio

    • 0.7–3.5 molar equivalents per batch, adjusted for desired conversion yield and to minimize downstream purification burdens

    Downstream process integration

    • Fed into controlled alkylation or reduction stages, which introduce the necessary nitro-reduction or cross-coupling with amines prior to core functionalization of the API’s chemical structure

    Final product types

    • Benzophenone-derived pharmaceutical intermediates
    • Targeted anti-inflammatory or analgesic APIs
    • Precursors for antihistamine API synthesis
    • Active antimicrobial compounds

    3. Precursor for High-Temperature Polymer Additive Manufacturing

    In specialty polymer industries, formulators apply this compound as a precursor in synthesizing thermally stable diaryl ketone additives used for engineering plastics and high-temperature elastomer systems. Its introduction allows precise modification of backbone rigidity and thermal breakdown resistance for downstream users involved in aerospace, electronics, or performance textile segments. The material typically enters at the pre-polymerization functionalization stage, enabling enhanced matrix integration. Compliance primarily targets RoHS and process-fluency documented under ISO standards for plastics additive evaluation.

    Industry compliance standards

    • ISO 11357 “Plastics — Differential Scanning Calorimetry (DSC) Method”
    • IEC 62321 Determination of Certain Substances in Electrotechnical Products (RoHS category)
    • UL-94 Flammability Standard (for resulting compounds in electrical appliance plastics)
    • REACH Regulation (Annex XVII, regarding restricted substances in polymers)

    Typical usage ratio

    • 2–8% by total monomer feed mass; range selected to balance crosslink density and thermal decomposition onset temperatures

    Downstream process integration

    • Blended in during functional monomer synthesis, usually via Friedel–Crafts acylation or nucleophilic substitution, before chain extension and final polymerization

    Final product types

    • PBT and PET high-performance flame retardant plastics
    • Thermoplastic composite parts for automotive and electrical housings
    • Aerospace-grade insulation layers
    • High-resilience textile fibers

    4. Controlled Agent in Explosives and Propellant Intermediate Manufacturing

    Downstream energetic materials producers utilize this compound as a controlled precursor in the synthesis of advanced nitroaromatic intermediates for select explosives and rocket propellant formulations. Its use focuses on sites where precise nitro placement is critical for tailored decomposition rates and energy yield. Handling, storage, and usage strictly follow government and military regulatory protocols, with batch-level documentation for each production cycle, especially during the formation of multifunctional energetic molecules.

    Industry compliance standards

    • UN Recommendations on the Transport of Dangerous Goods – Model Regulations
    • Federal Register 27 CFR Part 555 (US Bureau of Alcohol, Tobacco, Firearms and Explosives Regulations)
    • International Ammunition Technical Guidelines (IATG series)
    • Responsible Care Security Code for chemical handling

    Typical usage ratio

    • 0.5–2.2% by energetic compound mass; exact percentage varies according to performance profile and sensitivity limits

    Downstream process integration

    • Incorporated at the condensation or nitration phase, serving as a substrate for further functional group additions or controlled reduction to activate molecular energy storage capacity before propellant blending

    Final product types

    • Nitroaromatic-based explosive intermediates
    • Rocket propellant formulation precursors
    • Detonator charge component bases
    • Military-grade booster substances
    Free Quote

    Competitive 3,3'-Dinitrobenzophenone prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance