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2-Amino-2',5'-Dichlorobenzophenone

    • Product Name 2-Amino-2',5'-Dichlorobenzophenone
    • Alias ADB-D
    • Einecs 249-468-3
    • 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

    213453

    Iupac Name 2-amino-2',5'-dichlorobenzophenone
    Molecular Formula C13H9Cl2NO
    Molecular Weight 266.12
    Cas Number 40836-74-8
    Appearance Light yellow to beige solid
    Melting Point 122-124°C
    Solubility Slightly soluble in organic solvents
    Purity Typically >98%
    Smiles C1=CC(=C(C=C1Cl)Cl)C(=O)C2=CC=CC=C2N
    Inchi InChI=1S/C13H9Cl2NO/c14-9-6-7-11(13(16)8-9)12-4-2-1-3-10(12)15/h1-8H,16H2

    As an accredited 2-Amino-2',5'-Dichlorobenzophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 2-Amino-2',5'-Dichlorobenzophenone is supplied in a sealed, amber glass bottle with a tamper-evident cap.
    Shipping 2-Amino-2',5'-Dichlorobenzophenone is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material; proper labeling and documentation are required. Transport follows applicable regulations, ensuring safe handling and storage to prevent spills, degradation, or exposure during transit. Personal protective equipment is recommended when handling.
    Storage Store 2-Amino-2',5'-Dichlorobenzophenone in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. Keep container tightly closed in a chemical-resistant, clearly labeled container. Avoid moisture and prevent physical damage. Ensure access to appropriate spill containment and personal protective equipment, and follow all relevant safety and regulatory guidelines.
    Application of 2-Amino-2',5'-Dichlorobenzophenone

    Applications of 2-Amino-2',5'-Dichlorobenzophenone in Industrial Manufacturing

    2-Amino-2',5'-Dichlorobenzophenone functions as a specialized intermediate in multiple chemical manufacturing sectors. We supply this raw material with consistent batch quality, facilitating precise integration into defined industrial processes downstream. Below, we detail real-world application scenarios, each with compliance, ratio, process, and final product insights derived from active manufacturer use cases.

    1. Pharmaceutical Intermediates for API Synthesis

    Major pharmaceutical companies utilize this material as a key building block in the synthesis of specific active pharmaceutical ingredients, especially for anti-inflammatory and analgesic drug classes. Production requires adherence to strict regulatory controls, as the intermediate enters the reaction stage prior to final molecular assembly. Quality traceability and purity at this step directly impact main stage yield and impurity profile, critically influencing both cost and regulatory acceptance of the end API.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <922> “Pharmaceutical Ingredients”
    • European Pharmacopoeia (Ph. Eur.) for intermediates, applicable to API registration
    • China Drug Master File (DMF) electronic audit traceability

    Typical usage ratio

    • Dosage generally 0.94–1.05 molar equivalents within stepwise syntheses
    • Adjustment according to impurity profile or downstream stoichiometry requirements
    • Excess feed (up to 10%) utilized for reactions with yield-limiting transformation steps

    Downstream process integration

    • Introduced at intermediate condensation or acylation stages
    • Purified and isolated before API final coupling steps
    • Undergoes quality control release before batch transfer to finishing reactors

    Final product types

    • Non-steroidal anti-inflammatory drugs (NSAIDs) APIs
    • Specific analgesic pharmaceutical ingredients
    • Anti-allergic and antihistamine drug actives

    2. Agrochemical Synthesis: Selective Herbicide Precursors

    Agrochemical manufacturers employ this intermediate when producing classes of selective herbicides used in cereal and broadleaf crop protection. The aromatic backbone enables tailored substitutions in the lead molecule, directly affecting mode of action and environmental breakdown rate. Precision in ratio and contaminant control safeguards downstream product safety and regulatory acceptance, especially in markets with residue monitoring.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 for chemical raw material production and custom synthesis
    • REACH Regulation (EC) No 1907/2006 for agricultural chemicals in the EU
    • China National Standards for Pesticide Intermediates (GB/T 20695-2006)

    Typical usage ratio

    • 1.0–1.2 molar equivalent in primary active pesticide synthesis step
    • Decrease possible if using process intensification or alternative solvent routes
    • Batch-specific ratio based on impurity monitoring and desired herbicide isomer

    Downstream process integration

    • Dosed prior to cyclization or aromatic ring-modification stages
    • Purity checked before conversion to final herbicidal acid or salt form
    • Byproducts isolated and recycled depending on plant setup

    Final product types

    • Benzophenone-based selective herbicides
    • Pre-emergent weed control formulations
    • Post-emergence grass and broadleaf weed control agents

    3. Specialty Dye and Pigment Intermediates

    Manufacturers active in the high-performance coloration sector use 2-Amino-2',5'-Dichlorobenzophenone as a key intermediate to produce specialized disperse and solvent dyes. Modifying the aromatic amine structure at this juncture controls the resulting dye’s shade, solubility, and fastness properties, essential for demanding textile and industrial coatings applications. QC sampling and in-process adjustment prevent unwanted dye byproducts and enable precise batch-to-batch reproducibility.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 4 for textile dye intermediates
    • ISO 9001:2015 and ISO 14001:2015 (environmental impact)
    • ZDHC MRSL (Manufacturing Restricted Substances List) for textile auxiliaries
    • EU REACH Annex XVII for restricted aromatic amines in finished dyes

    Typical usage ratio

    • 0.9–1.1 molar equivalents per dye molecule backbone synthesis
    • Adjustments up to 15% if deeper chromophore integration required
    • Dose refined via pilot trials for target hue and stability

    Downstream process integration

    • Charged into aromatic amination or coupling stage of dye synthesis
    • Monitored for reactivity and shade development at interim QC points
    • Waste minimization strategies applied at byproduct separation step

    Final product types

    • High dispersion textile dyes
    • Solvent-based pigments for plastics and coatings
    • Specialty colorants for industrial and automotive sectors

    4. Advanced Polymer Additive Synthesis (UV Stabilizers)

    Chemical processors incorporate this intermediate in the synthesis of advanced UV absorber and stabilizer additives, which protect polymers and coatings from photo-degradation. Selection and process adaptation depend on targeted polymer systems—such as polyurethanes or polyesters—impacting both longevity and regulatory clearance. Material traceability is vital to confirm long-term stability and compliance with safety limits for additives used in goods with direct human contact or outdoor exposure.

    Industry compliance standards

    • US FDA 21 CFR 178.2010 for indirect food contact additives (polymer stabilizers)
    • EU Regulation (EC) No 10/2011 on materials and articles intended to come into contact with food (as applicable to polymer additives)
    • EN 71-3:2019 for additives in toys (migration of certain elements)
    • ISO 4892-2:2013 for plastics—exposure to laboratory light sources

    Typical usage ratio

    • Used at 0.8–1.3 molar equivalents per stabilizer batch formulation
    • Adjusted relative to UV absorption performance requirements by resin type
    • Lab/pilot-use range refined before commercial plant-scale deployment

    Downstream process integration

    • Charged into stabilizer precursor synthesis reactors
    • Purity controlled before blending with final masterbatch formulations
    • Integrated in extrusion or compounding step for finished plastics

    Final product types

    • UV stabilizer masterbatches for plastic films
    • Weathering-resistant polymer additives for outdoor applications
    • Processing aids for paints and industrial coatings
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